Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out?
Open accessAbstract
Soil organic carbon (SOC) changes associated with land conversion to energy crops are central to the debate on bioenergy and their potential carbon neutrality. Here, the experimental evidence on SOC under perennial energy crops (PECs) is synthesised to parameterise a whole systems model and to identify uncertainties and knowledge gaps determining PECs being a sink or source of greenhouse gas (GHG). For Miscanthus and willow ( Salix spp.) and their analogues (switchgrass, poplar), we examine carbon (C) allocation to above- and belowground residue inputs, turnover rates and retention in the soil. A meta-analysis showed that studies on dry matter partitioning and C inputs to soils are plentiful, whilst data on turnover are rare and rely on few isotopic C tracer studies. Comprehensive studies on SOC dynamics and GHG emissions under PECs are limited and subsoil processes and C losses through leaching remain unknown. Data showed dynamic changes of gross C inputs and SOC stocks depending on stand age. C inputs and turnover can now be specifically parameterised in whole PEC system models, whilst dependencies on soil texture, moisture and temperature remain empirical. In conclusion, the annual net SOC storage change exceeds the minimum mitigation requirement (0.25 Mg C ha −1 year −1 ) under herbaceous and woody perennials by far (1.14 to 1.88 and 0.63 to 0.72 Mg C ha −1 year −1 , respectively). However, long-term time series of field data are needed to verify sustainable SOC enrichment, as the physical and chemical stabilities of SOC pools remain uncertain, although they are essential in defining the sustainability of C sequestration (half-life >25 years).
AI snapshot
Written from the paper’s full text.
TL;DR
This review synthesises experimental evidence on soil organic carbon (SOC) under perennial energy crops (PECs) and parameterises a whole-systems model to assess whether PECs are a carbon sink or source. It concludes that annual net SOC storage exceeds the minimum mitigation requirement, but long-term SOC stability and key turnover, subsoil and leaching processes remain uncertain.
Key findings
- Annual net SOC storage change exceeds the minimum mitigation requirement of 0.25 Mg C ha−1 year−1 under herbaceous and woody perennials by far: 1.14–1.88 and 0.63–0.72 Mg C ha−1 year−1, respectively.
- Both herbaceous crops/grasses and short-rotation woody crops can deliver up to 40–50 % of captured C to soil as litter and belowground biomass, varying from <1 to >4 Mg C ha−1 year−1.
- Switchgrass showed an overall 25 % higher average stock change than Miscanthus (1.59 vs. 1.21 Mg C ha−1 year−1), likely due to lower root inputs from Miscanthus; willow and poplar averaged 0.56 and 0.63 Mg C ha−1 year−1, respectively.
- C retention was higher in herbaceous systems (30–55 %) than in woody systems (19–33 %), but data on turnover are rare and rely on few isotopic C tracer studies, while subsoil processes and C losses through leaching remain unknown.
Methods
- Literature search used ISI Web of Knowledge and Google Scholar for 1994–2014, refined by key genera; papers were grouped into global inventory/GIS/LCA, process-based modelling, and experimental evidence. Experimental evidence was reported in 85 papers, including 44 specific field trials and 57 studies with data useful for parameterising C sequestration; 25 modelling papers from 2000–2013 used RothC, CENTURY/DayCENT, or both.
- Data were extracted from tables and figures and scaled to Mg C ha−1 year−1; C inputs were measured directly or estimated from dry biomass assuming 45 % C unless stated otherwise. Mean residence time was calculated from mass loss assuming zero-order kinetics, with first-order laboratory rates scaled for temperature using a Q10 of 2.
- RothC was expanded to accept disaggregated C inputs (litter, rhizomes, roots, root exudates) and calibrated using a 14-year-old Miscanthus experiment at Rothamsted, UK, followed by sensitivity analysis of SOC response to input and turnover rates.
Limitations
- The paper states that long-term time series of field data are needed to verify sustainable SOC enrichment, as the physical and chemical stabilities of SOC pools remain uncertain; a half-life >25 years is considered essential for sustainable C sequestration.
- The paper states that severe restrictions apply to the validity of current in situ residue turnover rates due to technical limitations (litter bags) and steady-state assumptions, and that alternative methods described dynamics in young plantations that may not be extrapolated to mature stands.
- The paper states that environmental, fertility and management effects (e.g. harvest intensity) are not covered in dose–response experiments, and evidence for target ecosystems such as marginal land is underrepresented; the text also notes that the synthesis did not account for differences in temperature or other experimental variables.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 469 cited sources checked · 0 supported · 0 flagged
- Findingown data
The annual net soil organic carbon storage change under woody perennials exceeds the minimum mitigation requirement of 0.25 Mg C ha−1 year−1 by far, ranging from 0.63 to 0.72 Mg C ha−1 year−1.
“the annual net SOC storage change exceeds the minimum mitigation requirement (0.25 Mg C ha−1 year−1) under herbaceous and woody perennials by far (1.14 to 1.88 and 0.63 to 0.72 Mg C ha−1 year−1, respectively)”
Quote in the paperSubstantial claim - Findingreasoning
Comprehensive studies on soil organic carbon dynamics and greenhouse gas emissions under perennial energy crops are limited.
“Comprehensive studies on SOC dynamics and GHG emissions under PECs are limited”
Quote in the paperSubstantial claim - Findingnone given
Dependencies of carbon inputs and turnover on soil texture, moisture and temperature remain empirical.
“whilst dependencies on soil texture, moisture and temperature remain empirical”
Quote in the paperSubstantial claim - Findingown data
Gross carbon inputs and soil organic carbon stocks change dynamically depending on stand age.
“Data showed dynamic changes of gross C inputs and SOC stocks depending on stand age.”
Quote in the paperNot a substantial claim - Findingnone given
Little experimental evidence is available to describe carbon sequestration after land use change to perennial energy crops, including where in the soil and when soil organic carbon will reach equilibrium and how long it will last if perennial energy crops are replaced by other crops.
“little experimental evidence is available to describe C sequestration after land use change (LUC) to PECs, where in the soil and when SOC will reach its equilibrium and how long it will last if PECs are replaced by other crops.”
Quote in the paperNot a substantial claim- Rests on an assumption: Data from switchgrass and poplar are appropriate proxies for Miscanthus and willow.
- Findingown data
The annual net soil organic carbon storage change under herbaceous perennials exceeds the minimum mitigation requirement of 0.25 Mg C ha−1 year−1 by far, ranging from 1.14 to 1.88 Mg C ha−1 year−1.
“the annual net SOC storage change exceeds the minimum mitigation requirement (0.25 Mg C ha−1 year−1) under herbaceous and woody perennials by far (1.14 to 1.88 and 0.63 to 0.72 Mg C ha−1 year−1, respectively)”
Quote in the paperSubstantial claim - Findingnone given
Data on carbon inputs and turnover rates are very limited in perennial energy crop systems.
“The critical components that affect C sequestration rate are inputs and turnover rates, but data on these are very limited in PEC systems.”
Quote in the paperSubstantial claim- Rests on an assumption: Inputs and turnover rates are the critical components affecting carbon sequestration rate.
- Findingcitation
Little information was available on parameters affecting soil organic carbon accumulation in slowly decomposable or recalcitrant forms.
“Although some papers recorded specific fractions of SOC [11, 45, 46], little information was available on parameters affecting SOC accumulation in slowly decomposable or ‘recalcitrant’ forms [25, 35, 47].”
Quote in the paperNot a substantial claim0 of 6 sources checked- cites [11] Poeplau C, Don A (2014) Soil carbon changes under Miscanthus driven by C4 accumulation and C3 decomposition—toward a default sequestration function. GCB Bioenergy 6(4):327–338. doi: 10.1111/gcbb.12043 source
Not checked in the free run.
- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [46] Zimmermann J, Styles D, Hastings A, Dauber J, Jones MB (2014) Assessing the impact of within crop heterogeneity (‘patchiness’) in young Miscanthus × giganteus fields on economic feasibility and soil carbon sequestration. GCB Bioenergy 6(5):566–576. doi: 10.1111/gcbb.12084 source
Not checked in the free run.
- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- cites [47] Collins HP, Smith JL, Fransen S, Alva AK, Kruger CE, Granatstein DM (2010) Carbon sequestration under irrigated switchgrass (Panicum virgatum L.) production. Soil Sci Soc Am J 74(6):2049–2058. doi: 10.2136/sssaj2010.0020 source
Not checked in the free run.
- Findingnone given
On average, the carbon input to soil from herbaceous crop litter ranges from less than 1 to 3 Mg C ha−1 year−1.
“On average, the C input to soil from HCG litter ranges from <1 to 3 Mg C ha−1 year−1.”
Quote in the paperNot a substantial claim - Findingown data
Fine roots contribute less than 25% of the apparent annual belowground biomass input under Miscanthus.
“The latter contributes less than 25 % of the apparent annual BGB input under Miscanthus (Table 1 and Fig. 4).”
Quote in the paperNot a substantial claim - Findingcitation
Carbon inputs from Miscanthus rhizomes (1.01 to 2.66 Mg C ha−1 year−1) were generally greater than those from roots (0.19-0.86 Mg C ha−1 year−1).
“The C inputs from Miscanthus rhizomes (1.01 to 2.66 Mg C ha−1 year−1) were generally greater [57, 61, 66, 80, 85] than those from roots (0.19–0.86 Mg C ha−1 year−1, Table 1).”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- cites [61] Monti A, Zatta A (2009) Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy. Agric Ecosyst Environ 132(3–4):252–259. doi: 10.1016/j.agee.2009.04.007 source
Not checked in the free run.
- cites [66] Dohleman FG, Heaton EA, Arundale RA, Long SP (2012) Seasonal dynamics of above- and below-ground biomass and nitrogen partitioning in Miscanthus x giganteus and Panicum virgatum across three growing seasons. Glob Chang Biol Bionergy 4(5):534–544 source
Not checked in the free run.
- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
- cites [85] Himken M, Lammel J, Neukirchen D, Czypionka-Krause U, Olfs H-W (1997) Cultivation of Miscanthus under West European conditions: seasonal. Plant and Soil 189 (117–126) source
Not checked in the free run.
- Findingcitation
For switchgrass, more carbon was allocated to the roots than to the rhizomes.
“For switchgrass, more C was allocated to the roots than to the rhizomes [25, 66, 71].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [66] Dohleman FG, Heaton EA, Arundale RA, Long SP (2012) Seasonal dynamics of above- and below-ground biomass and nitrogen partitioning in Miscanthus x giganteus and Panicum virgatum across three growing seasons. Glob Chang Biol Bionergy 4(5):534–544 source
Not checked in the free run.
- cites [71] Garten CT Jr, Smith JL, Tyler DD, Amonette JE, Bailey VL, Brice DJ, Castro HF, Graham RL, Gunderson CA, Izaurralde RC, Jardine PM, Jastrow JD, Kerley MK, Matamala R, Mayes MA, Metting FB, Miller RM, Moran KK, Post WM III, Sands RD, Schadt CW, Phillips JR, Thomson AM, Vugteveen T, West TO, Wullschleger SD (2010) Intra-annual changes in biomass, carbon, and nitrogen dynamics at 4-year old switchgrass field trials in west Tennessee, USA. Agric Ecosyst Environ 136(1/2):177–184. doi: 10.1016/j.agee.2009.12.019 source
Not checked in the free run.
- Findingcitation
There is some indication that belowground biomass inputs increase over time.
“There is some indication that inputs increase over time [60].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- Findingcitation
Due to differences in stand age, depth and sampling frequency, belowground biomass inputs appear very variable.
“Due to differences in stand age, depth and sampling frequency inputs appear very variable [65, 66, 84].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [65] Christian DG, Poulton PR, Riche AB, Yates NE, Todd AD (2006) The recovery over several seasons of N-15-labelled fertilizer applied to Miscanthus x giganteus ranging from 1 to 3 years old. Biomass Bioenergy 30(2):125–133 source
Not checked in the free run.
- cites [66] Dohleman FG, Heaton EA, Arundale RA, Long SP (2012) Seasonal dynamics of above- and below-ground biomass and nitrogen partitioning in Miscanthus x giganteus and Panicum virgatum across three growing seasons. Glob Chang Biol Bionergy 4(5):534–544 source
Not checked in the free run.
- cites [84] Neukirchen D, Himken M, Lammel J, Czypionka-Krause U, Olfs H-W (1999) Spatial and temporal distribution of the root system and root nutrient content of an established Miscanthus crop. Eur J Agron 11:301–309 source
Not checked in the free run.
- Findingcitation
Values for fine roots from willow and poplar grown as short-rotation forestry are lower than for short-rotation coppice.
“Several authors investigated fine roots from willow and poplar grown as SRC [5, 30, 81, 82, 88, 89] and SRF [72, 90–93], values for the latter being lower (Table 1).”
Quote in the paperNot a substantial claim0 of 10 sources checked- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- cites [88] Rytter R, Hansson A (1996) Seasonal amount, growth and depth distribution of fine roots in an irrigated and fertilized Salix viminalis L. plantation. Biomass Bioenergy 11:129–137 source
Not checked in the free run.
- cites [89] Zhang J, Shangguan T, Meng Z (2011) Changes in soil carbon flux and carbon stock over a rotation of poplar plantations in northwest China. Ecol Res 26(1):153–161. doi: 10.1007/s11284-010-0772-5 source
Not checked in the free run.
- cites [72] Tufekcioglu A, Raich JW, Isenhart TM, Schultz RC (2003) Biomass, carbon and nitrogen dynamics of multi-species riparian buffers within an agricultural watershed in Iowa, USA. Agrofor Syst 57(3):187–198. doi: 10.1023/a:1024898615284 source
Not checked in the free run.
- cites [90] Calfapietra C, Gielen B, Galema ANJ, Lukac M, De Angelis P, Moscatelli MC, Ceulemans R, Scarascia-Mugnozza G (2003) Free-air CO2 enrichment (FACE) enhances biomass production in a short-rotation poplar plantation. Tree Physiol 23(12):805–814 source
Not checked in the free run.
- cites [91] Tufekcioglu A, Raich JW, Isenhart TM, Schultz RC (1998) Fine root dynamics, coarse root biomass, root distribution, and soil respiration in a multispecies riparian buffer in Central Iowa, USA. Agrofor Syst 44(2–3):163–174. doi: 10.1023/a:1006221921806 source
Not checked in the free run.
- cites [92] Upson MA, Burgess PJ (2013) Soil organic carbon and root distribution in a temperate arable agroforestry system. Plant Soil 373(1–2):43–58. doi: 10.1007/s11104-013-1733-x source
Not checked in the free run.
- Findingnone given
The range of carbon inputs from litter in short-rotation woody crops (0.63 to 4.68 Mg C ha−1 year−1) is only slightly larger than those from herbaceous crops.
“The range of C inputs from litter in SRWC (0.63 to 4.68 Mg C ha−1 year−1) is only slightly larger than those from HCG.”
Quote in the paperNot a substantial claim - Findingreasoning
Based on root biomass data, carbon exudates and 2-year mean residence time, and assuming a 210-day season with an average 12-h day length, roots could contribute between 0.4 and 1.7 Mg C ha−1 year−1 to the carbon balance.
“Based on root biomass data (Table 1), C exudates and 2-year MRT (Table 2) and assuming 210-day season with an average 12-h day length roots could contribute between 0.4 and 1.7 Mg C ha−1 year−1 to the C balance.”
Quote in the paperNot a substantial claim - Findingcitation
Based on hourly flux measurements, carbon exudate inputs from Miscanthus could be up to 0.5 g g−1 living root produced annually.
“Based on their hourly flux measurements, C exudate inputs from Miscanthus could be up to 0.5 g g−1 living root produced annually.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [97] Kaňova H, Carre J, Vranova V, Rejšek K (2010) Organic compounds in root exudates of Miscanthus × giganteus Greef Et Deu and limitation of microorganisms in its rhizosphere by nutrients. Acta Univ Agric Et Silviculturae Mendelianae Brunensis LVIII 5:203–210 source
Not checked in the free run.
- Findingcitation
Carbon measured in the rhizosphere of 2-year-old willows pointed to high rhizodeposition of carbon in older plants which was not proportional to root production.
“C measured in the rhizosphere of 2-year-old willows, grown in the glasshouse using stable isotopes (14C) pointed to high rhizodeposition of C in older plants which was not proportional to the root production [98].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [98] De Neergaard A, Porter JR, Gorissen A (2002) Distribution of assimilated carbon in plants and rhizosphere soil of basket willow (Salix viminalis L.). Plant Soil 245(2):307–314 source
Not checked in the free run.
- Findingnone given
Only two papers have been published with root exudate data from Miscanthus.
“Only two papers have been published with root exudate data from Miscanthus [96, 97].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [96] Hromadko L, Vranova V, Techer D, Laval-Gilly P (2010) Composition of root exudates of Miscanthus × giganteus Greef Et Deu. Acta Universitatis Agriculturae Et Silviculturae Mendelianae Brunensis LVIII 1:71–76 source
Not checked in the free run.
- cites [97] Kaňova H, Carre J, Vranova V, Rejšek K (2010) Organic compounds in root exudates of Miscanthus × giganteus Greef Et Deu and limitation of microorganisms in its rhizosphere by nutrients. Acta Univ Agric Et Silviculturae Mendelianae Brunensis LVIII 5:203–210 source
Not checked in the free run.
- Findingnone given
Average fine root inputs are higher under willow than poplar.
“Average fine root inputs are higher under willow than poplar (Fig. 3b).”
Quote in the paperNot a substantial claim - Findingcitation
The C/N ratio of Miscanthus litter increases from 28 to 34 in leaves at the end of season to 43-52 or even more than 100 in mature litter.
“The C/N ratio of Miscanthus litter increases from 28 to 34 in leaves at the end of season to 43–52 [65] or even >100 [110] in mature litter.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [65] Christian DG, Poulton PR, Riche AB, Yates NE, Todd AD (2006) The recovery over several seasons of N-15-labelled fertilizer applied to Miscanthus x giganteus ranging from 1 to 3 years old. Biomass Bioenergy 30(2):125–133 source
Not checked in the free run.
- cites [110] Ernst G, Henseler I, Felten D, Emmerling C (2009) Decomposition and mineralization of energy crop residues governed by earthworms. Soil Biol Biochem 41(7):1548–1554. doi: 10.1016/j.soilbio.2009.04.015 source
Not checked in the free run.
- Findingcitation
11% of rhizodeposits were retained in the soil organic matter.
“However, 11 % of rhizodeposits were retained in the soil organic matter.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [98] De Neergaard A, Porter JR, Gorissen A (2002) Distribution of assimilated carbon in plants and rhizosphere soil of basket willow (Salix viminalis L.). Plant Soil 245(2):307–314 source
Not checked in the free run.
- Findingcitation
From the composition of belowground biomass under a 15-year-old Miscanthus crop, a relative annual death rate of rhizome can be approximated as 3%.
“From the composition of BGB under a 15-year-old Miscanthus crop (19 % dead rhizome, 66 % live rhizome and 15 % live root [19], one could approximate a relative annual death rate of 3 %.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- Findingcitation
Coarse and dense roots of old undisturbed grassland turn over much more slowly (0.92-1.32 years) than fresh inputs.
“Coarse and dense roots of old undisturbed grassland turn over much more slowly (0.92–1.32 years) than fresh inputs [125].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [125] Klumpp K, Soussana JF, Falcimagne R (2007) Long-term steady state C-13 labelling to investigate soil carbon turnover in grasslands. Biogeosciences 4(3):385–394 source
Not checked in the free run.
- Findingcitation
In vitro decomposition of Miscanthus litter was affected by nitrogen added as pig slurry rather than nitrogen added as fertiliser.
“In vitro decomposition of Miscanthus litter was affected by N added as pig slurry [115] rather than N added as fertiliser [116].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [115] Eiland F, Klamer M, Lind AM, Leth M, Baath E (2001) Influence of initial C/N ratio on chemical and microbial composition during long term composting of straw. Microb Ecol 41(3):272–280 source
Not checked in the free run.
- cites [116] Foereid B, de Neergaard A, Høgh-Jensen H (2004) Turnover of organic matter in a Miscanthus field: effect of time in Miscanthus cultivation and inorganic nitrogen supply. Soil Biol Biochem 36(7):1075–1085. doi: 10.1016/j.soilbio.2004.03.002 source
Not checked in the free run.
- Findingcitation
A microcosm experiment showed that free access by soil fauna increased litter turnover by an order of magnitude compared to litter bags.
“A microcosm experiment showed that free access by soil fauna increased litter turnover by an order of magnitude [110] compared to those observed in litter bags [64, 123].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [110] Ernst G, Henseler I, Felten D, Emmerling C (2009) Decomposition and mineralization of energy crop residues governed by earthworms. Soil Biol Biochem 41(7):1548–1554. doi: 10.1016/j.soilbio.2009.04.015 source
Not checked in the free run.
- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [123] Yamane I (1974) Decomposition of litter of Miscanthus sinesins during five years under semi-natural conditions. Rep Inst Agr Res 25:25–30
Not checked in the free run.
- Findingcitation
The most obvious factor is the effect of temperature on the mean residence time of leaf Miscanthus litter derived in litter bags and laboratory incubations.
“Most obvious is the effect of temperature on the MRT of leaf Miscanthus litter derived in litter bags and laboratory incubations [62, 64, 69, 108, 122].”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [69] Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus × giganteus leaf senescence, decomposition and C and N inputs to soil. Glob Chang Biol Bionergy 4(6):698–707. doi: 10.1111/j.1757-1707.2012.01192.x source
Not checked in the free run.
- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
- cites [122] Kim S, Kim JG (2009) Humulus japonicus accelerates the decomposition of Miscanthus sacchariflorus and Phragmites australis in a floodplain. J Plant Biol 52(5):466–474. doi: 10.1007/s12374-009-9060-8 source
Not checked in the free run.
- Findingcitation
Similar longevity values were found for fine poplar roots.
“Similar values were found for fine poplar roots [30].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- Findingcitation
The longevity of fine willow roots can range between 55 and 350 days.
“The longevity of fine willow roots can range between 55 and 350 days [32, 58, 83].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- cites [58] Rytter RM (2001) Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows. For Ecol Manag 140:177–192 source
Not checked in the free run.
- cites [83] Rytter RM, Rytter L (1998) Growth, decay, and turnover rates of fine roots of basket willows. Can J For Res-Revue Can De Rech Forestiere 28(6):893–902 source
Not checked in the free run.
- Findingcitation
Turnover times for willow roots determined from a mass loss (15-25%) in litter bags were much longer than those determined using other methods.
“Turnover times for willow roots [127] determined from a mass loss (15–25 %) in litter bags were much longer than those determined using other methods (Table 2).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [127] Püttsepp Ü, Lõhmus K, Koppel A (2007) Decomposition of fine roots and α-cellulose in a short rotation willow (Salix spp.) plantation on abandoned agricultural land. Silva Fennica 41(2):247–258 source
Not checked in the free run.
- Findingcitation
Within the short-rotation coppice data, there is more quantitative evidence from poplar than for willow.
“Within the SRC data, there is more quantitative evidence from poplar [60, 72, 78, 79, 99, 109] than for willow [58, 111, 131].”
Quote in the paperNot a substantial claim0 of 9 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [72] Tufekcioglu A, Raich JW, Isenhart TM, Schultz RC (2003) Biomass, carbon and nitrogen dynamics of multi-species riparian buffers within an agricultural watershed in Iowa, USA. Agrofor Syst 57(3):187–198. doi: 10.1023/a:1024898615284 source
Not checked in the free run.
- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [79] Fang S, Xue J, Tang L (2007) Biomass production and carbon sequestration potential in poplar plantations with different management patterns. J Environ Manag 85(3):672–679. doi: 10.1016/j.jenvman.2006.09.014 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- cites [58] Rytter RM (2001) Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows. For Ecol Manag 140:177–192 source
Not checked in the free run.
- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
- cites [131] Pacaldo RS, Volk TA, Briggs RD (2013) Greenhouse gas potentials of shrub willow biomass crops based on below- and aboveground biomass inventory along a 19-year chronosequence. Bioenergy Res 6(1):252–262. doi: 10.1007/s12155-012-9250-y source
Not checked in the free run.
- Findingcitation
Integrated studies on carbon enrichment such as POPFACE have shown that increased atmospheric CO2 can induce a decrease of soil organic carbon attributed to a priming effect.
“Integrated studies on C enrichment, e.g. POPFACE, have shown that increased atmospheric CO2 can induce a decrease of SOC [78] attributed to a priming effect [99, 102, 129, 130].”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
- cites [102] Kuzyakov Y (2002) Review: factors affecting rhizosphere priming effects. J Plant Nutr Soil Sci 165:382–396 source
Not checked in the free run.
- cites [129] Niklaus PA, Falloon P (2006) Estimating soil carbon sequestration under elevated CO2 by combining carbon isotope labelling with soil carbon cycle modelling. Glob Chang Biol 12(10):1909–1921. doi: 10.1111/j.1365-2486.2006.01215.x source
Not checked in the free run.
- cites [130] Hoosbeek MR, Vos JM, Meinders MBJ, Velthorst EJ, Scarascia-Mugnozza GE (2007) Free atmospheric CO2 enrichment (FACE) increased respiration and humification in the mineral soil of a poplar plantation. Geoderma 138(3–4):204–212. doi: 10.1016/j.geoderma.2006.11.008 source
Not checked in the free run.
- Findingcitation
Fine willow and poplar roots were characterised by a high turnover rate.
“However, fine willow [58] and poplar roots [81] were characterised by a high turnover rate (Table 2).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [58] Rytter RM (2001) Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows. For Ecol Manag 140:177–192 source
Not checked in the free run.
- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- Findingcitation
In situ decay rates of leaves were much higher when using large instead of small mesh litter bags.
“In situ decay rates of leaves were much higher when using large instead of small mesh litter bags [111].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
- Findingown data
The average production of fine roots under poplar was smaller compared to willow (0.56 vs. 0.99 Mg C ha−1 year−1).
“However, the average production of fine roots under poplar was smaller compared to willow (Fig. 3b; 0.56 vs. 0.99 Mg C ha−1 year−1).”
Quote in the paperNot a substantial claim - Findingcitation
High rates of soil organic carbon were sequestered in a soil very low in carbon compared to those established on grassland sites.
“High rates of SOC were sequestered in a soil very low in C [135] compared to those established on grassland sites (e.g. [19, 86].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- Findingcitation
With increasing age of 9- to 16-year-old Miscanthus stands, the amount of annual soil organic carbon increment rises by more than 40%.
“However, a comparison across similar environments indicates that with increasing age (9- to 16-year-old Miscanthus stands), the amount of annual SOC increment rises by more than 40 % [106].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
- Findingnone given
Annual carbon inputs from Miscanthus roots are about half that of switchgrass with similar turnover time.
“Annual C inputs from Miscanthus roots are about half that of switchgrass with similar turnover time.”
Quote in the paperSubstantial claim - Findingcitation
The carbon effectively sequestered under Miscanthus (percentage retention) ranges between 21% and about 70% of the gross carbon inputs.
“The C effectively sequestered under Miscanthus (% retention) ranges between 21 % [19] and ∼70 % [57] of the gross C inputs.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- Findingown data
Based on long-term field trials for short-rotation woody crops and accounting for all residues, overall lower carbon sequestration rates were calculated for willow and poplar (average 0.56 and 0.63 Mg C ha−1 year−1, respectively) than for herbaceous crop systems.
“Based on long-term field trials for SRWC and accounting for all residues, overall lower C sequestration rates were calculated for willow and poplar (Table 3; average 0.56 and 0.63 Mg C ha−1 year−1, respectively) than for HCG systems.”
Quote in the paperSubstantial claim - Findingown data
In spite of methodological uncertainty regarding turnover of fine roots, the mean residence time of herbaceous crops was about four to five times longer than that of short-rotation woody crops.
“In spite of methodological uncertainty regarding turnover of fine roots, the MRT of HCG was about four to five times longer than that of SRWC (Fig. 3b).”
Quote in the paperNot a substantial claim - Findingown data
The net soil organic carbon storage change under perennial energy crops observed in most recent studies exceeds the default sequestration rates for arable crops, grassland and forests.
“The net SOC storage change under PECs observed in most recent studies exceeds these values (Table 3).”
Quote in the paperSubstantial claim - Findingcitation
Across different environments and time periods, quite similar net storage changes could be found over 3 to 15 years.
“Across different environments and time periods, quite similar net storage changes could be found (3 to 15 years) [19, 134].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [134] Zimmermann J, Dauber J, Jones MB (2012) Soil carbon sequestration during the establishment phase of Miscanthus × giganteus: a regional-scale study on commercial farms using 13C natural abundance. GCB Bioenergy 4(4):453–461. doi: 10.1111/j.1757-1707.2011.01117.x source
Not checked in the free run.
- Findingcitation
ΔSOC under short-rotation forestry/coppice changed within 11 years from an initial loss of 0.74 during the first 2 years to an increase of 5.82 Mg ha−1 year−1 during the last 2 years.
“However, ∆SOC under SRF/SRC changed within 11 years from an initial loss of 0.74 during the first 2 years to an increase of 5.82 Mg ha−1 year−1, during the last 2 years [60].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- Findingcitation
These numbers are similar to the average gains reported for short-rotation coppice poplar earlier (1.63 to 2.43 Mg C ha−1 year−1).
“These numbers are similar to the average gains reported for SRC poplar earlier (1.63 [68] to 2.43 C Mg ha−1 year−1 [10]).”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [68] Hansen EM (1993) Soil carbon sequestration beneath hybrid poplar plantations in the North Central United States. Biomass Bioenergy 5(6):431–436 source
Not checked in the free run.
- cites [10] Garten CT, Wullschleger SD, Classen AT (2011) Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar. Biomass Bioenergy 35(1):214–226. doi: 10.1016/j.biombioe.2010.08.013 source
Not checked in the free run.
- Findingcitation
Hansen found 65% of Miscanthus-derived carbon stabilised in particulate organic matter.
“Hansen [106] found 65 % of Miscanthus-derived C stabilised in POM.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
- Findingcitation
An increased annual soil organic carbon storage change was observed in response to fertilisation, particularly in poplar stands.
“An increased annual SOC storage change was observed in response to fertilisation, particularly in poplar stands [54].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [54] Hellebrand HJ, Straehle M, Scholz V, Kern J (2010) Soil carbon, soil nitrate, and soil emissions of nitrous oxide during cultivation of energy crops. Nutr Cycl Agroecosyst 87(2):175–186. doi: 10.1007/s10705-009-9326-z source
Not checked in the free run.
- Findingown data
For a 1 % change of respective residue MRT, simulated SOC changed by 0.02, 0.01 and 0.05 % for root, litter and rhizome, respectively.
“For a 1 % change of respective residue MRT, the simulated SOC changed by 0.02, 0.01 and 0.05 % for root, litter and rhizome, respectively (Fig. 5b).”
Quote in the paperNot a substantial claim - Findingown data
Using reviewed parameters for residue deposition and decomposition under SRC willow, simulated ∆SOC was very similar to that under Miscanthus.
“Using reviewed parameters for residue deposition and decomposition under SRC willow (Tables 1 and 2), we simulated a very similar ∆SOC as under Miscanthus.”
Quote in the paperNot a substantial claim - Findingcitation
There are very few data for Miscanthus, switchgrass, willow or poplar available.
“There are very few data for Miscanthus [62, 65, 150], switchgrass [178, 179], willow [143, 180] or poplar [22] available.”
Quote in the paperSubstantial claim0 of 7 sources checked- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- cites [65] Christian DG, Poulton PR, Riche AB, Yates NE, Todd AD (2006) The recovery over several seasons of N-15-labelled fertilizer applied to Miscanthus x giganteus ranging from 1 to 3 years old. Biomass Bioenergy 30(2):125–133 source
Not checked in the free run.
- cites [150] Kahle P, Beuch S, Boelcke B, Leinweber P, Schulten HR (2001) Cropping of Miscanthus in Central Europe: biomass production and influence on nutrients and soil organic matter. Eur J Agron 15(3):171–184 source
Not checked in the free run.
- cites [178] Anderson-Teixeira KJ, Davis SC, Masters MD, Delucia EH (2009) Changes in soil organic carbon under biofuel crops. GCB Bioenergy 1(1):75–96. doi: 10.1111/j.1757-1707.2008.01001.x source
Not checked in the free run.
- cites [179] Varvel GE, Vogel KP, Mitchell RB, Follett RF, Kimble JM (2008) Comparison of corn and switchgrass on marginal soils for bioenergy. Biomass Bioenergy 32(1):18–21. doi: 10.1016/j.biombioe.2007.07.003 source
Not checked in the free run.
- cites [143] Pacaldo RS, Volk TA, Briggs RD (2013) No significant differences in soil organic carbon contents along a chronosequence of shrub willow biomass crop fields. Biomass Bioenergy 58:136–142. doi: 10.1016/j.biombioe.2013.10.018 source
Not checked in the free run.
- cites [180] Pacaldo RS, Volk TA, Briggs RD (2014) Carbon sequestration in fine roots and foliage biomass offsets soil CO2 effluxes along a 19-year chronosequence of shrub willow (Salix x dasyclados) biomass crops. Bioenergy Res 7(3):769–776. doi: 10.1007/s12155-014-9416-x source
Not checked in the free run.
- Findingown data
Our scenario analysis of a compartmentalised residue input and turnover model shows that differentiation in turnover rates can impact on the dynamics.
“Our scenario analysis of a compartmentalised residue input and turnover model shows that differentiation in turnover rates can impact on the dynamics.”
Quote in the paperNot a substantial claim - Findingown data
For each 1 % change of gross residue C input, simulated SOC changed by 0.13, 0.11 and 0.1 % for root, litter and rhizome, respectively.
“The sensitivity analysis showed that for each 1 % change of gross residue C input, the simulated SOC changed by 0.13, 0.11 and 0.1 % for root, litter and rhizome, respectively (Fig. 5a).”
Quote in the paperNot a substantial claim - Findingown data
Based on C inputs retained, one can distinguish retentive HCG (30-55 %) from transformative SRWC (19-33 %) systems.
“Based on the C inputs retained, ∆SOC (Fig. 4), one can distinguish retentive HCG (30–55 %) from transformative SRWC (19–33 %) systems.”
Quote in the paperSubstantial claim - Findingown data
Our review shows annual ∆SOC of HCG and SRWC exceeding the minimum sequestration rate.
“First, our review shows annual ∆SOC of HCG and SRWC exceeding the minimum sequestration rate, and more certainty applies to C4-HCG than C3-SRWC due to isotope (13C) use.”
Quote in the paperSubstantial claim - Premisecitation
Management of perennial systems greatly affects residue inputs because harvest practices vary the amount of aboveground biomass removed depending on harvest date and harvest method.
“The management of such systems greatly affects residue inputs as harvest practices vary the amount of aboveground biomass (AGB) removed depending on harvest date [19, 20] and harvest method [21, 22].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [20] Larsen SU, Jorgensen U, Kjeldsen JB, Laerke PE (2014) Long-term Miscanthus yields influenced by location, genotype, row distance, fertilization and harvest season. Bioenergy Res 7(2):620–635. doi: 10.1007/s12155-013-9389-1 source
Not checked in the free run.
- cites [21] Meehan PG, McDonnell KP, Finnan JM (2013) An assessment of the effect of harvest time and harvest method on biomass loss for Miscanthus × giganteus. Glob Chang Biol Bioenergy 5(4):400–407. doi: 10.1111/j.1757-1707.2012.01205.x source
Not checked in the free run.
- cites [22] Berhongaray G, El Kasmioui O, Ceulemans R (2013) Comparative analysis of harvesting machines on an operational high-density short rotation woody crop (SRWC) culture: one-process versus two-process harvest operation. Biomass Bioenergy 58:333–342. doi: 10.1016/j.biombioe.2013.07.003 source
Not checked in the free run.
- Premisecitation
Estimates of carbon sequestered under perennial energy crops range between 0.6 and 3.0 Mg C ha−1 year−1.
“To date, estimates of C sequestered under PECs range between 0.6 and 3.0 Mg C ha−1 year−1 [1, 5].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] Lemus R, Lal R (2005) Bioenergy crops and carbon sequestration. Crit Rev Plant Sci 24(1):1–21. doi: 10.1080/07352680590910393 source
Not checked in the free run.
- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
- Premisecitation
The main input of carbon from switchgrass to soil organic carbon comes from its dense root system in the top 30 cm.
“The main input of C from switchgrass to SOC comes from its dense root system in the top 30 cm [24]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [24] Zan CS, Fyles JW, Girouard P, Samson RA (2001) Carbon sequestration in perennial bioenergy, annual corn and uncultivated systems in southern Quebec. Agric Ecosyst Environ 86(2):135–144 source
Not checked in the free run.
- Premisecitation
Switchgrass residues have a fast carbon turnover.
“although its residues have a fast C turnover [25]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- Premisecitation
Miscanthus, switchgrass, willow and poplar may increase long-term soil organic carbon pools due to their extensive root systems.
“Miscanthus, switchgrass, willow and poplar may increase long-term SOC pools due to their extensive root systems [1].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [1] Lemus R, Lal R (2005) Bioenergy crops and carbon sequestration. Crit Rev Plant Sci 24(1):1–21. doi: 10.1080/07352680590910393 source
Not checked in the free run.
- Interpretationreasoning
Carbon inputs and turnover can now be specifically parameterised in whole perennial energy crop system models.
“C inputs and turnover can now be specifically parameterised in whole PEC system models”
Quote in the paperSubstantial claim- The authors state this as an assumption: The carbon cycle of perennial energy crops can be divided into qualitatively different inputs from aboveground biomass and belowground biomass.
- Premisecitation
On average, for each 0.6 kg of fossil fuel carbon used in cultivation, 1 kg of carbon is produced as biomass.
“on average, for each 0.6 kg of fossil fuel C used in cultivation, 1 kg of C is produced as biomass [5]”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
- Premisecitation
Switchgrass could be a better choice for dry areas and relatively poor soil quality.
“If Miscanthus is the best option for temperate Europe, switchgrass could be a better choice for dry areas and relatively poor soil quality [2].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [2] Lewandowski I, Scurlock JMO, Lindvall E, Christou M (2003) The development and current status of perennial rhizomatous grasses as energy crops in the US and Europe. Biomass Bioenergy 25(4):335–361 source
Not checked in the free run.
- Premisecitation
The amount of litter deposition is likely influenced by yield potential.
“It is likely that the amount of litter deposition is influenced by yield potential [8, 10, 29].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
- cites [10] Garten CT, Wullschleger SD, Classen AT (2011) Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar. Biomass Bioenergy 35(1):214–226. doi: 10.1016/j.biombioe.2010.08.013 source
Not checked in the free run.
- cites [29] Kollas CP, Lasch JR, Suckow F (2009) Bioenergy potential in Germany—assessing spatial patterns of biomass production. Int Agrophysics 23:343–352
Not checked in the free run.
- Premisecitation
Belowground biomass components enter soil organic carbon pools dependent on their mortality and longevity.
“BGB components will enter the SOC pools dependent on their mortality/longevity [30–32].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- cites [31] Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159(2):241–251. doi: 10.1023/A:1015529507670 source
Not checked in the free run.
- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- Premisecitation
Fresh and easily decomposable matter such as fine roots and leaves has a slightly smaller biomass carbon fraction (43%) than woody material (46%).
“In general, fresh and easily decomposable matter, like fine roots and leaves, have a slightly smaller biomass C fraction (43 %) than woody material (46 %) [60, 62].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- Premisecitation
The amount of carbon transferred to soil is a function of litter and harvest residues and their decomposition rates, belowground biomass longevity, composition and decomposition rates, and depth and distribution of the root system.
“The amount of C transferred to soil is a function of several system components [10] such as (i) litter and harvest residues and their decomposition rates; (ii) BGB, its longevity, composition and decomposition rates; and (iii) depth and distribution of the root system.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [10] Garten CT, Wullschleger SD, Classen AT (2011) Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar. Biomass Bioenergy 35(1):214–226. doi: 10.1016/j.biombioe.2010.08.013 source
Not checked in the free run.
- Premisecitation
Residue quantity, quality, decomposition rates and soil organic carbon dynamics differ between herbaceous crop/grass and short-rotation woody crop systems.
“Residue quantity, quality, decomposition rates and, hence, SOC dynamics differ between HCG and SRWC systems [33]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [33] Lettens S, Muys B, Ceulemans R, Moons E, Garcia J, Coppin P (2003) Energy budget and greenhouse gas balance evaluation of sustainable coppice systems for electricity production. Biomass and Bioenergy 24 (3):179–197. doi:Pii S0961-9534(02)00104-6 source
Not checked in the free run.
- Premisecitation
Each perennial energy crop system affects soil organic carbon directly through the composition and mass of plant residues and indirectly through its impact on the soil environment.
“Therefore, each PEC system will affect SOC both directly through the composition and mass of plant residues and indirectly through its impact on the soil environment [36, 37].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [36] Lal R (2003) Offsetting global CO2 emissions by restoration of degraded soils and intensification of world agriculture and forestry. Land Degrad Dev 14(3):309–322 source
Not checked in the free run.
- cites [37] Lal R (2008) Carbon sequestration. Philos Trans R Soc Lond Ser B Biol Sci 363(1492):815–830. doi: 10.1098/rstb.2007.2185 source
Not checked in the free run.
- Premisecitation
Environmental variables such as soil water dynamics, temperature, litter incorporation, dissolved organic carbon transport and nitrogen affect carbon cycling under perennial vegetation.
“Environmental variables, such as soil water dynamics [40], temperature [38, 41], litter incorporation and dissolved organic C (DOC) transport [42] and nitrogen [14, 43], affect C cycling under perennial vegetation.”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [40] Jenkinson DS, Coleman K (2008) The turnover of organic carbon in subsoils. Part 2. Modelling carbon turnover. Eur J Soil Sci 59(2):400–413. doi: 10.1111/j.1365-2389.2008.01026.x source
Not checked in the free run.
- cites [38] Bauer J, Kirschbaum MUF, Weihermuller L, Huisman JA, Herbst M, Vereecken H (2008) Temperature response of wheat decomposition is more complex than the common approaches of most multi-pool models. Soil Biol Biochem 40(11):2780–2786. doi: 10.1016/j.soilbio.2008.07.024 source
Not checked in the free run.
- cites [41] Bauer J, Herbst M, Huisman JA, Weihermuller L, Vereecken H (2008) Sensitivity of simulated soil heterotrophic respiration to temperature and moisture reduction functions. Geoderma 145(1–2):17–27. doi: 10.1016/j.geoderma.2008.01.026 source
Not checked in the free run.
- cites [42] Braakhekke MC, Christian Beer M, Hoosbeek MR, Reichstein M, Kruijt B, Schrumpf M, Kabat P (2011) SOMPROF: a vertically explicit soil organic matter model. Ecol Model 222:1712–1730 source
Not checked in the free run.
- Premisecitation
Short-rotation woody crop perennial energy crop systems can increase the carbon stored belowground for a relatively long time, with contributions from dead wood.
“SRWC PEC systems can increase the C stored belowground for a relatively long time, with contributions from dead wood [16].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [16] Sartori F, Lal R, Ebinger MH, Parrish DJ (2006) Potential soil carbon sequestration and CO2 offset by dedicated energy crops in the USA. Crit Rev Plant Sci 25(25):441–472 source
Not checked in the free run.
- Premisecitation
Residues decompose according to a decay rate k dependent on composition, soil protective characteristics, microbial biomass and environmental conditions, which determine the system- and compound-specific mean residence time.
“Residues decompose according to a decay rate (k), dependent on composition, soil protective characteristics, microbial biomass and environmental conditions (temperature, precipitation, soil texture and water availability), which determine the system and compound specific mean residence time (MRT) [34, 35].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [34] Dungait J, Hopkins D, Gregory A, Whitmore A (2012) Soil organic matter turnover is governed by accessibility not recalcitrance. Glob Chang Biol 18:1781–1796 source
Not checked in the free run.
- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- Interpretationcitation
The reliability of some carbon input data is reduced when inputs are approximated from biomass yield and an average carbon content of residues.
“The reliability of some data is reduced when C inputs are approximated from biomass yield and an average C content of the residues [30, 62].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- Interpretationreasoning
Fewer data were available for short-rotation woody crop systems due to the practical difficulties of excavating and studying tree roots.
“Fewer data were available for SRWC systems due to the practical difficulties of excavating and studying tree roots.”
Quote in the paperNot a substantial claim - Premisecitation
There is dieback of smaller stems especially during the first year, which can be a few percent of the biomass.
“There is also dieback of smaller stems especially during the first year [79] which can be a few percent of the biomass.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [79] Fang S, Xue J, Tang L (2007) Biomass production and carbon sequestration potential in poplar plantations with different management patterns. J Environ Manag 85(3):672–679. doi: 10.1016/j.jenvman.2006.09.014 source
Not checked in the free run.
- Interpretationcitation
Data for carbon inputs from belowground biomass are difficult to interpret, especially for roots, because they are based on many single observations rather than time series.
“Data for C inputs from BGB are difficult to interpret, especially for roots because they are based on many single observations [45, 61, 62, 64, 80] rather than time series [26, 32, 81–83].”
Quote in the paperNot a substantial claim0 of 10 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [61] Monti A, Zatta A (2009) Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy. Agric Ecosyst Environ 132(3–4):252–259. doi: 10.1016/j.agee.2009.04.007 source
Not checked in the free run.
- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
- cites [26] Rytter RM (2012) The potential of willow and poplar plantations as carbon sinks in Sweden. Biomass Bioenergy 36:86–95 source
Not checked in the free run.
- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- cites [83] Rytter RM, Rytter L (1998) Growth, decay, and turnover rates of fine roots of basket willows. Can J For Res-Revue Can De Rech Forestiere 28(6):893–902 source
Not checked in the free run.
- Premisecitation
Longevity of roots and their turnover depends on root diameter.
“however, longevity of roots and their turnover depends on root diameter [30, 31].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- cites [31] Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159(2):241–251. doi: 10.1023/A:1015529507670 source
Not checked in the free run.
- Premisecitation
Lignin physically controls decomposition of litter by reducing the surface available for enzymatic attack.
“Lignin, however, seems to physically control decomposition of the litter by reducing the surface available for enzymatic attack [4].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [4] Johnson JMF, Barbour NW, Weyers SL (2007) Chemical composition of crop biomass impacts its decomposition. Soil Sci Soc Am J 71(1):155–162 source
Not checked in the free run.
- Interpretationreasoning
The assessment of decomposition rates of belowground biomass of herbaceous and woody species presents a conceptual problem.
“The assessment of decomposition rates of BGB of herbaceous and woody species presents a conceptual problem.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Gross inputs from leaf and stem litter and harvest residues are more tangible than from belowground biomass.
“In summary, gross inputs from leaf and stem litter and harvest residues are more tangible than from BGB.”
Quote in the paperNot a substantial claim - Premisecitation
Belowground biomass can die and start to decompose at different ages with different decay rates dependent on size and environmental conditions.
“BGB can die and start to decompose at different ages with different decay rates dependent on size and environmental conditions [31, 104].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [31] Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159(2):241–251. doi: 10.1023/A:1015529507670 source
Not checked in the free run.
- cites [104] Gill RA, Jackson RB (2000) Global patterns of root turnover for terrestrial ecosystems. New Phytol 147:13–31 source
Not checked in the free run.
- Interpretationnone given
There is little quantitative knowledge about the site-specific interaction between the size of residue inputs and soil organic carbon and how they are affected by management.
“There is little quantitative knowledge about the site-specific interaction between the size of the residue inputs and SOC and how they were affected by management (e.g. fertiliser, soil fertility, harvest).”
Quote in the paperNot a substantial claim - Interpretationreasoning
The impact of carbon inputs from perennial energy crop systems on soil organic carbon cannot be assessed without quantification of the longevity or mortality before turnover of each component.
“The impact of C inputs from PEC systems on SOC cannot be assessed without quantification of the longevity or mortality before turnover of each component (leaves, shoots, rhizome, stool and coarse and fine roots).”
Quote in the paperNot a substantial claim - Interpretationcitation
Decomposition rates established by using litter bags underestimate the flux of carbon from residues to soil pools, as shown for Miscanthus and poplar.
“The decomposition rates established by using litter bags will underestimate the flux of C from the residues to the soil pools, as shown for Miscanthus [108] and poplar [78, 109].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- Interpretationreasoning
The increased C/N ratio is likely to reduce turnover rates of mature Miscanthus litter.
“This is likely to reduce turnover rates of mature Miscanthus litter [108, 114].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
- cites [114] Luxhoi J, Magid J, Tscherko D, Kandeler E (2002) Dynamics of invertase, xylanase and coupled quality indices of decomposing green and brown plant residues. Soil Biol Biochem 34(4):501–508 source
Not checked in the free run.
- Interpretationreasoning
This suggested the importance of microbial biomass colonising litter.
“This suggested the importance of microbial biomass colonising litter [117, 118].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [117] Frey SD, Six J, Elliott ET (2003) Reciprocal transfer of carbon and nitrogen by decomposer fungi at the soil litter interface. Soil Biol Biochem 35(1001):1004
Not checked in the free run.
- cites [118] Rovira P, Vallejo VR (2007) Labile, recalcitrant, and inert organic matter in Mediterranean forest soils. Soil Biol Biochem 39(1):202–215 source
Not checked in the free run.
- Interpretationcitation
The use of isotopic methods gives a much better account for the in situ complexity of soil systems.
“The use of isotopic methods gives a much better account for the in situ complexity of soil systems [109].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- Premisecitation
Litter rich in lignin and poor in nitrogen is more sensitive to temperature changes than protein-rich litter, as shown for Miscanthus residues.
“Litter rich in lignin and poor in N was more sensitive to temperature changes than protein-rich litter [38] as shown for Miscanthus residues [108, 114].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [38] Bauer J, Kirschbaum MUF, Weihermuller L, Huisman JA, Herbst M, Vereecken H (2008) Temperature response of wheat decomposition is more complex than the common approaches of most multi-pool models. Soil Biol Biochem 40(11):2780–2786. doi: 10.1016/j.soilbio.2008.07.024 source
Not checked in the free run.
- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
- cites [114] Luxhoi J, Magid J, Tscherko D, Kandeler E (2002) Dynamics of invertase, xylanase and coupled quality indices of decomposing green and brown plant residues. Soil Biol Biochem 34(4):501–508 source
Not checked in the free run.
- Interpretationcitation
It is difficult to estimate in situ litter decomposition in both short-rotation woody crops and herbaceous crops.
“It is difficult to estimate in situ litter decomposition, both in SRWC [78, 109] and in HCG [108].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
- Interpretationreasoning
Discrepancies regarding the experimental evidence for the same residue type were found due to the methods used and the experimental setup.
“Discrepancies regarding the experimental evidence for the same residue type were found due to the methods used and the experimental setup.”
Quote in the paperSubstantial claim - Interpretationcitation
In situ decomposition rates of roots could be low as both switchgrass and Miscanthus roots penetrate into deeper, cooler and less aerated soil layers.
“In situ decomposition rates of roots could be low as both switchgrass [70] and Miscanthus [61] roots penetrate into deeper, cooler and less aerated soil layers.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [70] Liebig MA, Johnson HA, Hanson JD, Frank AB (2005) Soil carbon under switchgrass stands and cultivated cropland. Biomass Bioenergy 28:347–354 source
Not checked in the free run.
- cites [61] Monti A, Zatta A (2009) Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy. Agric Ecosyst Environ 132(3–4):252–259. doi: 10.1016/j.agee.2009.04.007 source
Not checked in the free run.
- Interpretationcitation
Inputs were often based on snapshots, while detailed time series were the exception, especially with regard to root production and turnover.
“It is important to realise that inputs were often based on snapshots, whilst detailed time series were the exception, especially with regard to root production and turnover [32, 81, 82].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- Interpretationreasoning
A good number of contrasting results regarding residue turnover was compiled from the literature, enabling initial parameterisation of plant-soil interaction and carbon flux models.
“In summary, a good number of contrasting results regarding residue turnover was compiled from the literature, which enables initial parameterisation of plant–soil interaction and C flux models (see below).”
Quote in the paperSubstantial claim - Interpretationcitation
For belowground biomass, inputs from herbaceous crop roots and rhizomes needed to be separated, which was not always done.
“For the BGB, inputs from HCG roots and rhizomes needed to be separated, which was not always done [45, 57, 86, 106].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
- Interpretationcitation
A small number of studies using isotopes, model systems and field sampling allow scaling of mean residence times to in situ rates.
“However, a small number of studies using isotopes [109], model systems [110, 111] and field sampling [32, 81, 82] allow their scaling to in situ rates.”
Quote in the paperNot a substantial claim0 of 6 sources checked- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- cites [110] Ernst G, Henseler I, Felten D, Emmerling C (2009) Decomposition and mineralization of energy crop residues governed by earthworms. Soil Biol Biochem 41(7):1548–1554. doi: 10.1016/j.soilbio.2009.04.015 source
Not checked in the free run.
- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- Premisecitation
The factors affecting the soil carbon balance are numerous and vary depending on climate, soil conditions and crop management, such as harvest date and residue removal.
“The factors affecting the soil C balance are numerous and vary depending on climate, soil conditions and crop management, e.g. harvest date and residue removal [62, 128].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- cites [128] Saffih-Hdadi K, Mary B (2008) Modeling consequences of straw residues export on soil organic carbon. Soil Biol Biochem 40(3):594–607. doi: 10.1016/j.soilbio.2007.08.022 source
Not checked in the free run.
- Interpretationreasoning
There is relatively little known about the in situ turnover of live rhizomes and coarse roots as longevity becomes an additional level of complexity.
“However, there is relatively little known about the in situ turnover of live rhizomes and coarse roots as longevity becomes an additional level of complexity.”
Quote in the paperNot a substantial claim - Interpretationcitation
Assuming steady-state carbon inputs could lead to an underestimation of mean residence time.
“Assuming steady-state C inputs [135] could lead to an underestimation of MRT [136].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
- cites [136] Derrien D, Amelung W (2011) Computing the mean residence time of soil carbon fractions using stable isotopes: impacts of the model framework. Eur J Soil Sci 62(2):237–252. doi: 10.1111/j.1365-2389.2010.01333.x source
Not checked in the free run.
- Interpretationreasoning
What really makes the difference between herbaceous and short-rotation woody crop systems, in addition to the difference of short-rotation coppice fine roots turnover, is the dynamic of the rhizome.
“However, what really makes the difference between the two systems in addition to the difference of SRC fine roots turnover is the dynamic of the rhizome.”
Quote in the paperSubstantial claim - Interpretationcitation
Especially when planted into grassland soils, the initial residue input and turnover rates from perennial energy crops are too low to compensate for the loss.
“Especially when planted into grassland soils [86, 139], the initial residue input and turnover rates from PEC are too low to compensate for the loss.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- Interpretationreasoning
In-depth analysis supports the concept of an initial resilience phase of soil organic carbon after land-use change to perennial energy crops in which Miscanthus-derived soil organic carbon did not fully replace the continuing turnover of resident carbon during early establishment.
“In-depth analysis supports the concept of an initial resilience phase of SOC after LUC to PEC in which Miscanthus-derived SOC did not fully replace the continuing turnover of resident C during early establishment.”
Quote in the paperSubstantial claim - Interpretationcitation
This could explain the lack of real enrichment of recalcitrant or mineral-associated soil organic carbon during the first 4 or even 6 years under Miscanthus, especially when planted into former grassland.
“This could explain the lack of real enrichment of recalcitrant or mineral-associated SOC during the first 4 or even 6 years under Miscanthus, especially when planted into former grassland [86].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- Premisecitation
Very little CO2 is emitted from Miscanthus stands of different ages.
“typically very little CO2 is emitted from Miscanthus stands of different ages [59].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [59] Davis SC, Parton WJ, Dohleman FG, Smith CM, Grosso SD, Kent AD, DeLucia EH (2009) Comparative biogeochemical cycles of bioenergy crops reveal nitrogen-fixation and low greenhouse gas emissions in a Miscanthus × giganteus agro-ecosystem. Ecosystems 13(1):144–156. doi: 10.1007/s10021-009-9306-9 source
Not checked in the free run.
- Premisecitation
For forest systems, new carbon inputs from plant residues can enter relatively fast decomposable soil organic carbon pools, particularly if the soil had a low clay content.
“For forest systems [142], it has been shown that new C inputs from plant residues can enter relatively fast decomposable SOC pools, particularly if the soil had a low clay content [148].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [142] Lichter J, Barron SH, Bevacqua CE, Finzi AC, Irving KE, Stemmler EA, Schlesinger WH (2005) Soil carbon sequestration and turnover in a pine forest. Ecology 86 (7):1835–1847. doi: 10.1890/04-1205 source
Not checked in the free run.
- cites [148] Mueller L, Carsten W, Koegel-Knabner I (2008) Soil organic carbon stocks, distribution, and composition affected by historic land use changes on adjacent sites. Biol Fertil Soils 45(4):347–359. doi: 10.1007/s00374-008-0336-9 source
Not checked in the free run.
- Premisecitation
Root respiration increases in SRWC systems under enhanced atmospheric CO2 concentrations.
“Root respiration has also been found to increase in SRWC systems under enhanced atmospheric CO2 concentrations [130], which seems to be generally valid for FACE experiments under older (12–16 %) and recently established (22–46 %) systems [153].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [130] Hoosbeek MR, Vos JM, Meinders MBJ, Velthorst EJ, Scarascia-Mugnozza GE (2007) Free atmospheric CO2 enrichment (FACE) increased respiration and humification in the mineral soil of a poplar plantation. Geoderma 138(3–4):204–212. doi: 10.1016/j.geoderma.2006.11.008 source
Not checked in the free run.
- Premisecitation
The increase in root respiration under enhanced CO2 is generally valid for FACE experiments under older (12-16 %) and recently established (22-46 %) systems.
“Root respiration has also been found to increase in SRWC systems under enhanced atmospheric CO2 concentrations [130], which seems to be generally valid for FACE experiments under older (12–16 %) and recently established (22–46 %) systems [153].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [153] Lukac M, Lagomarsino A, Moscatelli MC, De Angelis P, Cotrufo MF, Godbold DL (2009) Forest soil carbon cycle under elevated CO2—a case of increased throughput? Forestry 82(1):75–86. doi: 10.1093/forestry/cpn041 source
Not checked in the free run.
- Premisecitation
Lignin as a biomass component together with polyphenols reduces decomposition rates.
“Lignin as a biomass component together with polyphenols reduces decomposition rates [149].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [149] Thevenot M, Dignac MF, Rumpel C (2010) Fate of lignins in soils: a review. Soil Biol Biochem 42(8):1200–1211. doi: 10.1016/j.soilbio.2010.03.017 source
Not checked in the free run.
- Premisecitation
Under SRWC systems, coppicing can result in a 50 % increase in CO2 emission, mainly due to live root respiration.
“Under SRWC systems, coppicing itself can result in a 50 % increase in CO2 emission, mainly due to live root respiration [152].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [152] Abou Jaoude R, Lagomarsino A, De Angelis P (2011) Impacts of nitrogen fertilisation and coppicing on total and heterotrophic soil CO2 efflux in a short rotation poplar plantation. Plant Soil 339(1–2):219–230. doi: 10.1007/s11104-010-0570-4 source
Not checked in the free run.
- Premisecitation
The least decomposable residues seem to be the most sensitive to temperature.
“The least decomposable residues seem to be the most sensitive to temperature [120].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [120] Felten D, Emmerling C (2011) Effects of bioenergy crop cultivation on earthworm communities—a comparative study of perennial (Miscanthus) and annual crops with consideration of graded land-use intensity. Appl Soil Ecol 49:167–177. doi: 10.1016/j.apsoil.2011.06.001 source
Not checked in the free run.
- Premisecitation
Recalcitrant soil organic carbon components like lignin increase with depth and clay content due to chemical binding.
“Recalcitrant SOC components, like lignin, increase with depth and clay content due to chemical binding [35, 149].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- cites [149] Thevenot M, Dignac MF, Rumpel C (2010) Fate of lignins in soils: a review. Soil Biol Biochem 42(8):1200–1211. doi: 10.1016/j.soilbio.2010.03.017 source
Not checked in the free run.
- Premisecitation
N2O emission was 4 to 6 Mg CO2-equivalent higher after grassland conversion to willow and poplar.
“N2O emission was 4 to 6 Mg CO2-equivalent higher after grassland conversion to willow and poplar, but CO2 fluxes were 30 to 40 % less than on the grass reference [55].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [55] Nikiema P, Rothstein DE, Miller RO (2012) Initial greenhouse gas emissions and nitrogen leaching losses associated with converting pastureland to short-rotation woody bioenergy crops in northern Michigan, USA. Biomass Bioenergy 39:413–426. doi: 10.1016/j.biombioe.2012.01.037 source
Not checked in the free run.
- Premisecitation
N fertilisation in switchgrass reduced the GHG emission per unit harvested biomass.
“N fertilisation in switchgrass actually reduced the GHG emission per unit harvested biomass [53].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [53] Schmer MR, Liebig MA, Hendrickson JR, Tanaka DL, Phillips RL (2012) Growing season greenhouse gas flux from switchgrass in the northern Great Plains. Biomass Bioenergy 45:315–319. doi: 10.1016/j.biombioe.2012.05.026 source
Not checked in the free run.
- Premisecitation
Conversion from arable to Miscanthus or switchgrass confirms higher CO2 emissions under grassland such as prairie.
“Conversion from arable to Miscanthus or switchgrass confirms higher CO2 emissions under grassland (e.g. prairie) [57] reflecting its higher biological activity which eventually increased SOC stocks.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- Premisecitation
The stabilisation of soil organic carbon pools depends essentially on the relation between soil temperature, chemical composition and physical protection.
“The stabilisation of SOC pools depends essentially on the relation between soil temperature [41], chemical composition [144] and physical protection.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [41] Bauer J, Herbst M, Huisman JA, Weihermuller L, Vereecken H (2008) Sensitivity of simulated soil heterotrophic respiration to temperature and moisture reduction functions. Geoderma 145(1–2):17–27. doi: 10.1016/j.geoderma.2008.01.026 source
Not checked in the free run.
- cites [144] Conant RT, Ryan MG, Ran IG, Gren A, Birge HE, Davidson EA, Eliasson PE (2011) Temperature and soil organic matter decomposition rates—synthesis of current knowledge and a way forward. Glob Chang Biol 17:3392–3404 source
Not checked in the free run.
- Premisecitation
CO2 fluxes were 30 to 40 % less after grassland conversion to willow and poplar than on the grass reference.
“N2O emission was 4 to 6 Mg CO2-equivalent higher after grassland conversion to willow and poplar, but CO2 fluxes were 30 to 40 % less than on the grass reference [55].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [55] Nikiema P, Rothstein DE, Miller RO (2012) Initial greenhouse gas emissions and nitrogen leaching losses associated with converting pastureland to short-rotation woody bioenergy crops in northern Michigan, USA. Biomass Bioenergy 39:413–426. doi: 10.1016/j.biombioe.2012.01.037 source
Not checked in the free run.
- Interpretationreasoning
The variability of ΔSOC under perennial energy crops reflects uncertainty due to limited periods of measurements, simplifying assumptions such as linearity and steady state, and environmental variability.
“In conclusion, the variability of ∆SOC under PECs reflects the uncertainty due to the limited periods of measurements, a series of simplifying assumptions (linearity, steady state) and environmental variability (see above).”
Quote in the paperSubstantial claim - Interpretationown data
Discrimination between inputs from above- and belowground residues suggests input- and plant-specific carbon retention factors.
“Discrimination between inputs from above- and belowground residues (Tables 1 and 2) suggests input- and plant-specific C retention factors (Fig. 3).”
Quote in the paperNot a substantial claim - Premisecitation
Physical protection defines the kinetic properties and temperature sensitivity of soil organic carbon pools.
“The latter defines their kinetic properties and temperature sensitivity [145, 146].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [145] Aber J, Melillo J, Mcclaugher C (1990) Predicting long-term patterns of mass loss, nitrogen dynamics, and soil organic matter. Can J Bot 68:2201–2208 source
Not checked in the free run.
- cites [146] Davidson EA, Janssens IA (2006) Temperature sensitivity of soil carbon decomposition and feedbacks to climate change. Nature 440(7081):165–173. doi: 10.1038/nature04514 source
Not checked in the free run.
- Interpretationcitation
For PEC systems, the evidence base is too sparse to model process dynamics or predict a state of equilibrium.
“For PEC systems, the evidence base is still emerging and is too sparse to model the process dynamics, let alone to predict a state of equilibrium [8].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
- Premisecitation
The principles of C fluxes under land use change from arable to grassland and forestry systems apply to the transition to PEC.
“The principles of C fluxes under land use change from arable to grassland and forestry systems certainly apply to the transition to PEC as shown recently using a hybrid C and N model including routines of CENTURY [162].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [162] Shibu ME, Matthews RB, Bakam I, Moffat AJ, Baggaley NJ (2012) Estimating greenhouse gas abatement potential of biomass crops in Scotland under various management options. Biomass Bioenergy 47:211–227. doi: 10.1016/j.biombioe.2012.09.039 source
Not checked in the free run.
- Premisecitation
RothC has been coupled with specific crop growth and litter degradation models to simulate SOC dynamics under Miscanthus, willow and poplar SRC.
“RothC has been coupled with specific crop growth and litter degradation models to simulate SOC dynamics under Miscanthus, willow and poplar SRC [166].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [166] Paul KI, Polglase PJ (2004) Prediction of decomposition of litter under eucalypts and pines using the FullCAM model. For Ecol Manag 191(1–3):73–92. doi: 10.1016/j.foreco.2003.11.007 source
Not checked in the free run.
- Premisecitation
C turnover derived from laboratory incubation of soil and residues overestimates those in undisturbed, natural systems.
“Further, C turnover derived from laboratory incubation of soil and residues overestimate those in undisturbed, natural systems [168, 171, 172]).”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [168] Paul KI, Polglase PJ, Richards GP (2003) Predicted change in soil carbon following afforestation or reforestation, and analysis of controlling factors by linking a C accounting model (CAMFor) to models of forest growth (3PG), litter decomposition (GENDEC) and soil C turnover (RothC). For Ecol Manag 177(1–3):485–501 source
Not checked in the free run.
- cites [171] Hashimoto S, Wattenbach M, Smith P (2011) Litter carbon inputs to the mineral soil of Japanese Brown forest soils: comparing estimates from the RothC model with estimates from MODIS. J For Res 16(1):16–25. doi: 10.1007/s10310-010-0209-6 source
Not checked in the free run.
- cites [172] Paul KI, Polglase PJ, Richards GP (2003) Sensitivity analysis of predicted change in soil carbon following afforestation. Ecol Model 164(2–3):137–152. doi: 10.1016/s0304-3800(03)00027-9 source
Not checked in the free run.
- Interpretationcitation
The stability of SOC pools defines the sustainability of soil C sequestration and eventually the effective C neutrality of the system.
“It is the stability of these pools which defines the sustainability of soil C sequestration and eventually the effective C neutrality of the system [125, 142].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [125] Klumpp K, Soussana JF, Falcimagne R (2007) Long-term steady state C-13 labelling to investigate soil carbon turnover in grasslands. Biogeosciences 4(3):385–394 source
Not checked in the free run.
- cites [142] Lichter J, Barron SH, Bevacqua CE, Finzi AC, Irving KE, Stemmler EA, Schlesinger WH (2005) Soil carbon sequestration and turnover in a pine forest. Ecology 86 (7):1835–1847. doi: 10.1890/04-1205 source
Not checked in the free run.
- Premisecitation
Willows allocate between 1 and 10 % of plant C to root turnover and exudation.
“De Neergaard et al. [98] found that willows allocate between 1 and 10 % of plant C to root turnover and exudation, similar to those found for other plants [154].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [98] De Neergaard A, Porter JR, Gorissen A (2002) Distribution of assimilated carbon in plants and rhizosphere soil of basket willow (Salix viminalis L.). Plant Soil 245(2):307–314 source
Not checked in the free run.
- Premisecitation
Surface litter in a SRWC system managed as SRC seems to be incorporated within a season despite its chemical composition.
“as surface litter in spite of its chemical composition seems to be incorporated within a season [111].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
- Premisecitation
For large-scale applications, process-based models were simplified based on assumptions such as steady state and controlled by empirical inputs such as yield maps.
“For large-scale applications, process-based models were simplified, based on a series of assumptions (e.g. steady state) and controlled by empirical inputs (e.g. yield maps [63]).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Hillier J, Dailey G, Aylott M, Whittaker C, Richter G, Riche A, Murphy R, Taylor G, Smith P (2009) Greenhouse gas emissions from four bioenergy crops in England and Wales: integrating spatial estimates of yield and soil carbon balance in life cycle analyses. Glob Chang Biol Bioenergy 1(4):267–281. doi: 10.1111/j.1757-1707.2009.01021.x source
Not checked in the free run.
- Interpretationreasoning
Under PECs, the main difficulty in assessing C turnover and retention is uncertainty regarding the physical and chemical stability of SOC pools.
“In summary, under PECs, the main difficulty in assessing C turnover and retention is the uncertainty regarding the physical and chemical stability of SOC pools.”
Quote in the paperSubstantial claim - Premisecitation
Soil water dynamics are considered a key parameter in all SOC models applied to PECs.
“Soil water dynamics are considered a key parameter in all SOC models applied to PECs [14, 15].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [14] Battle-Aguilar J, Brovelli A, Porporato A, Barry DA (2010) Modelling soil carbon and nitrogen cycles during land use change. A review. Agron Sustain Dev 31(2):251–274. doi: 10.1051/agro/2010007 source
Not checked in the free run.
- cites [15] Thomas ARC, Bond AJ, Hiscock KM (2013) A multi-criteria based review of models that predict environmental impacts of land use-change for perennial energy crops on water, carbon and nitrogen cycling. GCB Bioenergy 5(3):227–242. doi: 10.1111/j.1757-1707.2012.01198.x source
Not checked in the free run.
- Interpretationreasoning
The use of more pools increases the uncertainty of the model.
“The use of more pools implies more calibrating parameters which improve long-term prediction [8] but increase the uncertainty of the model.”
Quote in the paperNot a substantial claim - Premisecitation
Most process-based SOC models assume that degradation of residues from biomass can be represented by a continuum or two or more pools of plant or soil OM of similar chemical composition and degradability.
“Most process-based SOC models assume that degradation of residues from biomass can be represented by a continuum or two or more pools of plant or soil OM of similar chemical composition and degradability [161].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [161] Manzoni S, Porporato A (2009) Soil carbon and nitrogen mineralization: theory and models across scales. Soil Biol Biochem 41:1355–1379 source
Not checked in the free run.
- Premisecitation
Chemical or physical identification of specific pools with defined decomposition rates is very difficult.
“First, chemical or physical identification of specific pools with defined decomposition rates is very difficult [141, 163].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [141] Zimmermann M, Leifeld J, Schmidt MWI, Smith P, Fuhrer J (2007) Measured soil organic matter fractions can be related to pools in the RothC model. Eur J Soil Sci 58(3):658–667. doi: 10.1111/j.1365-2389.2006.00855.x source
Not checked in the free run.
- cites [163] Xianli X, Liu W, Kiely G (2011) Modeling the change in soil organic carbon of grassland in response to climate change: effects of measured versus modelled carbon pools for initializing the Rothamsted Carbon model. Agric Ecosyst Environ 140(3–4):372–381. doi: 10.1016/j.agee.2010.12.018
Not checked in the free run.
- Premisecitation
Within FullCAM, RothC was used in woodland systems by applying debris partitioning and decomposition rates measured in agricultural soils.
“Within FullCAM [166, 167], RothC was used in woodland systems by applying debris partitioning and decomposition rates measured in agricultural soils.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [166] Paul KI, Polglase PJ (2004) Prediction of decomposition of litter under eucalypts and pines using the FullCAM model. For Ecol Manag 191(1–3):73–92. doi: 10.1016/j.foreco.2003.11.007 source
Not checked in the free run.
- cites [167] Paul KI, Polglase PJ (2004) Calibration of the RothC model to turnover of soil carbon under eucalypts and pines. Aust J Soil Res 42(8):883–895. doi: 10.1071/sr04025 source
Not checked in the free run.
- Premisereasoning
The release of C from litter decomposition is mainly controlled by its incorporation into the soil and by soil depth, which induces temperature and soil moisture gradients.
“The release of C from litter decomposition is a function of different factors, mainly controlled by its incorporation into the soil and by soil depth, which induces temperature and soil moisture gradients.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Multi-pool or compartment models present challenges when applied to ligno-cellulosic plants.
“Multi-pool or compartment models present challenges when applied to ligno-cellulosic (LC) plants.”
Quote in the paperNot a substantial claim - Premisecitation
Much longer times are assumed for the inert and stabilised humus fractions in SOC turnover models.
“They are in contrast to much longer times assumed for the ‘inert’ and stabilised humus fractions in SOC turnover models [159, 160].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [159] Coleman K, Jenkinson DS, Crocker GJ, Grace PR, Klir J, Korschens M, Poulton PR, Richter DD (1997) Simulating trends in soil organic carbon in long-term experiments using RothC-26.3. Geoderma 81(1–2):29–44 source
Not checked in the free run.
- cites [160] Parton WJ, Hartman M, Ojima D, Schimel D (1998) DAYCENT and its land surface submodel: description and testing. Glob Planet Chang 19(1–4):35–48. doi: 10.1016/S0921-8181(98)00040-X source
Not checked in the free run.
- Premisecitation
It has never been proven experimentally that a multi-pool chain model can represent the decreasing decomposition of residues due to chemical and physical protection.
“Second, it has never been proven experimentally that a multi-pool chain model can represent the decreasing decomposition of residues due to chemical and physical protection [118, 148, 170].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [118] Rovira P, Vallejo VR (2007) Labile, recalcitrant, and inert organic matter in Mediterranean forest soils. Soil Biol Biochem 39(1):202–215 source
Not checked in the free run.
- cites [148] Mueller L, Carsten W, Koegel-Knabner I (2008) Soil organic carbon stocks, distribution, and composition affected by historic land use changes on adjacent sites. Biol Fertil Soils 45(4):347–359. doi: 10.1007/s00374-008-0336-9 source
Not checked in the free run.
- cites [170] Rethemeyer J, Grootes PM, Brodowski S, Ludwig B (2007) Evaluation of soil C-14 data for estimating inert organic matter in the RothC model. Radiocarbon 49(2):1079–1091 source
Not checked in the free run.
- Premisecitation
Root dry matter in the surface horizon is an order of magnitude larger than in the subsoil.
“Root dry matter in the surface horizon is an order of magnitude larger than in the subsoil [31, 32, 80, 84].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [31] Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159(2):241–251. doi: 10.1023/A:1015529507670 source
Not checked in the free run.
- cites [32] Rytter RM (1999) Fine-root production and turnover in a willow plantation estimated by different calculation methods. Scand J For Res 14(6):526–537 source
Not checked in the free run.
- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
- cites [84] Neukirchen D, Himken M, Lammel J, Czypionka-Krause U, Olfs H-W (1999) Spatial and temporal distribution of the root system and root nutrient content of an established Miscanthus crop. Eur J Agron 11:301–309 source
Not checked in the free run.
- Interpretationreasoning
None of these data would allow deriving a dose-response function.
“None of these would allow deriving a dose–response function.”
Quote in the paperSubstantial claim - Interpretationcitation
The modelling of SOC fractionation seems essential for the persistence and sustainability of C sequestration.
“The modelling of SOC fractionation seems essential for the persistence and sustainability of C sequestration, showing that initially new SOC is part of easily decomposable POM [139] and later part of the inter-aggregate fraction [25, 45].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- Premisecitation
Simulations were greatly improved when decomposition rates were calibrated using labelled C measurements and applied to experimental evidence for poplar litter.
“Simulations were greatly improved when decomposition rates were calibrated using labelled C measurements [173–175] and applied to the experimental evidence presented for poplar litter [78, 109].”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [173] Leifeld J (2008) Biased C-14-derived organic carbon turnover estimates following black carbon input to soil: an exploration with RothC. Biogeochemistry 88(3):205–211. doi: 10.1007/s10533-008-9209-4 source
Not checked in the free run.
- cites [174] Leifeld J, Zimmermann M, Fuhrer J (2008) Simulating decomposition of labile soil organic carbon: effects of pH. Soil Biol Biochem 40(12):2948–2951. doi: 10.1016/j.soilbio.2008.08.019 source
Not checked in the free run.
- cites [175] Leifeld J, Zimmermann M, Fuhrer J, Conen F (2009) Storage and turnover of carbon in grassland soils along an elevation gradient in the Swiss Alps. Glob Chang Biol 15(3):668–679. doi: 10.1111/j.1365-2486.2008.01782.x source
Not checked in the free run.
- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- Premisecitation
No change of SOC was measured under 19-year-old willow SRC.
“A long resilience phase for SOC was seen under Miscanthus established on former grassland [86], and no change of SOC was measured under 19-year-old willow SRC [143].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [143] Pacaldo RS, Volk TA, Briggs RD (2013) No significant differences in soil organic carbon contents along a chronosequence of shrub willow biomass crop fields. Biomass Bioenergy 58:136–142. doi: 10.1016/j.biombioe.2013.10.018 source
Not checked in the free run.
- Premisecitation
So far, modelling SOC under biofuel crops has mainly relied on C inputs approximated from crop yields.
“So far, modelling SOC under biofuel crops has mainly relied on C inputs approximated from crop yields [19, 45, 86, 139].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- Interpretationown data
The assumption of a single input source of residues may not be adequate to describe C turnover and retention in the PEC soil system.
“It is clear from the experimental evidence synthesised above (Tables 1 and 3 and Fig. 4) that the assumption of a single input source of residues may not be adequate to describe the C turnover and retention in the PEC soil system.”
Quote in the paperSubstantial claim - Interpretationcitation
Initial sequestration rates are low due to small inputs during the establishing phase.
“The opposite is evident: initial sequestration rates are low due to small inputs during the establishing phase [25, 43, 46, 60, 86, 106, 134], which could depend on the productivity and fertility of the soil, its former land use and planting material/success.”
Quote in the paperSubstantial claim0 of 7 sources checked- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [43] Ma Z, Wood CW, Bransby DI (2000) Carbon dynamics subsequent to establishment of switchgrass. Biomass Bioenergy 18(2):93–104 source
Not checked in the free run.
- cites [46] Zimmermann J, Styles D, Hastings A, Dauber J, Jones MB (2014) Assessing the impact of within crop heterogeneity (‘patchiness’) in young Miscanthus × giganteus fields on economic feasibility and soil carbon sequestration. GCB Bioenergy 6(5):566–576. doi: 10.1111/gcbb.12084 source
Not checked in the free run.
- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
- cites [134] Zimmermann J, Dauber J, Jones MB (2012) Soil carbon sequestration during the establishment phase of Miscanthus × giganteus: a regional-scale study on commercial farms using 13C natural abundance. GCB Bioenergy 4(4):453–461. doi: 10.1111/j.1757-1707.2011.01117.x source
Not checked in the free run.
- Interpretationreasoning
There is no justification for the assumption of a steady-state sequestration rate.
“The evidence presented above clearly shows that there is no justification for the assumption of a steady-state sequestration rate as stated by others [8, 136].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
- cites [136] Derrien D, Amelung W (2011) Computing the mean residence time of soil carbon fractions using stable isotopes: impacts of the model framework. Eur J Soil Sci 62(2):237–252. doi: 10.1111/j.1365-2389.2010.01333.x source
Not checked in the free run.
- Interpretationreasoning
Considering a single input source does not account for surface accumulation of litter and longevity of BGB.
“Considering a single input source does not account for the surface accumulation of the litter and the longevity of the BGB.”
Quote in the paperSubstantial claim - Interpretationnone given
The assumption of another 10 % of roots to be accounted for as residue input is not supported by any evidence.
“However, the assumption of another 10 % of roots to be accounted for as residue input [135] is not supported by any evidence.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
- Interpretationown data
Not only yield but harvest management, such as removal of residues in Miscanthus, would affect SOC through the input rate of surface litter.
“Figure 5a clearly implies that not only yield but harvest management (e.g. removal of residues in Miscanthus) would affect SOC through the input rate of surface litter which is an important input of ecosystem models [151, 168] and LCA for energy crops [177].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [151] Smith PL, Kutsch G, Werner L et al (2010) Measurements necessary for assessing the net ecosystem carbon budget of croplands. Agric Ecosyst Environ 139(3):302–315. doi: 10.1016/j.agee.2010.04.004 source
Not checked in the free run.
- cites [168] Paul KI, Polglase PJ, Richards GP (2003) Predicted change in soil carbon following afforestation or reforestation, and analysis of controlling factors by linking a C accounting model (CAMFor) to models of forest growth (3PG), litter decomposition (GENDEC) and soil C turnover (RothC). For Ecol Manag 177(1–3):485–501 source
Not checked in the free run.
- cites [177] Hamelin L, Jorgensen U, Petersen BM, Olesen JE, Wenzel H (2012) Modelling the carbon and nitrogen balances of direct land use changes from energy crops in Denmark: a consequential life cycle inventory. Glob Chang Biol Bioenergy 4(6):889–907. doi: 10.1111/j.1757-1707.2012.01174.x source
Not checked in the free run.
- Premisecitation
A long resilience phase for SOC was seen under Miscanthus established on former grassland.
“A long resilience phase for SOC was seen under Miscanthus established on former grassland [86], and no change of SOC was measured under 19-year-old willow SRC [143].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- Premisecitation
A generalised link between yields and residues is plausible.
“A generalised link between yields and residues is plausible [63].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Hillier J, Dailey G, Aylott M, Whittaker C, Richter G, Riche A, Murphy R, Taylor G, Smith P (2009) Greenhouse gas emissions from four bioenergy crops in England and Wales: integrating spatial estimates of yield and soil carbon balance in life cycle analyses. Glob Chang Biol Bioenergy 1(4):267–281. doi: 10.1111/j.1757-1707.2009.01021.x source
Not checked in the free run.
- Interpretationreasoning
Severe restrictions apply to the validity of current in situ residue turnover rates due to technical limitations (litter bags) and steady-state assumptions.
“Third, severe restrictions apply to the validity of current in situ residue turnover rates due to technical limitations (litter bags) and steady-state assumptions.”
Quote in the paperSubstantial claim - Premisecitation
Uncertainty of soil moisture derived from pedotransfer functions can affect C flux simulations.
“The uncertainty of soil moisture derived from pedotransfer functions can affect C flux simulations [183].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [183] Guber AK, Pachepsky YA, van Genuchten MT, Rawls WJ, Simunek J, Jacques D, Nicholson TJ, Cady RE (2006) Field-scale water flow simulations using ensembles of pedotransfer functions for soil water retention. Vadose Zone J 5(1):234–247 source
Not checked in the free run.
- Premisenone given
Litter fall and harvest residues are more easily measured than roots and rhizomes/stool.
“Second, underpinning evidence for the C balance components is more certain for AGB than BGB inputs: (a) litter fall and harvest residues are more easily measured than roots and rhizomes/stool and (b) gross inputs of BGB components profoundly depend on their MRT.”
Quote in the paperSubstantial claim - Interpretationcitation
Currently, experimental evidence for the effect of soil texture and baseline SOC on sequestration potential is so small that a general relationship for spatial extrapolation is not credible.
“Currently, the experimental evidence for the effect of soil texture and baseline SOC on sequestration potential [63] is so small that a general relationship for its spatial extrapolation is not credible.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [63] Hillier J, Dailey G, Aylott M, Whittaker C, Richter G, Riche A, Murphy R, Taylor G, Smith P (2009) Greenhouse gas emissions from four bioenergy crops in England and Wales: integrating spatial estimates of yield and soil carbon balance in life cycle analyses. Glob Chang Biol Bioenergy 1(4):267–281. doi: 10.1111/j.1757-1707.2009.01021.x source
Not checked in the free run.
- Interpretationreasoning
More certainty applies to C4-HCG than C3-SRWC due to isotope (13C) use.
“First, our review shows annual ∆SOC of HCG and SRWC exceeding the minimum sequestration rate, and more certainty applies to C4-HCG than C3-SRWC due to isotope (13C) use.”
Quote in the paperSubstantial claim - Interpretationcitation
Limitations of process-based models become more apparent at larger scales regarding soil depth, temporal resolution, and surface litter decomposition.
“However, the limitations of process-based models become more apparent when simulating at larger scales with regard to their limits to consider the effect of soil depth [168], adequate temporal resolution [171] and surface litter decomposition [173, 174].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [168] Paul KI, Polglase PJ, Richards GP (2003) Predicted change in soil carbon following afforestation or reforestation, and analysis of controlling factors by linking a C accounting model (CAMFor) to models of forest growth (3PG), litter decomposition (GENDEC) and soil C turnover (RothC). For Ecol Manag 177(1–3):485–501 source
Not checked in the free run.
- cites [171] Hashimoto S, Wattenbach M, Smith P (2011) Litter carbon inputs to the mineral soil of Japanese Brown forest soils: comparing estimates from the RothC model with estimates from MODIS. J For Res 16(1):16–25. doi: 10.1007/s10310-010-0209-6 source
Not checked in the free run.
- cites [173] Leifeld J (2008) Biased C-14-derived organic carbon turnover estimates following black carbon input to soil: an exploration with RothC. Biogeochemistry 88(3):205–211. doi: 10.1007/s10533-008-9209-4 source
Not checked in the free run.
- cites [174] Leifeld J, Zimmermann M, Fuhrer J (2008) Simulating decomposition of labile soil organic carbon: effects of pH. Soil Biol Biochem 40(12):2948–2951. doi: 10.1016/j.soilbio.2008.08.019 source
Not checked in the free run.
- Premisecitation
Spatial variation accounted for by GIS-based simulation provides yield-dependent potential C inputs and sequestration in soils.
“Spatial variation accounted for by GIS-based simulation provides yield-dependent potential C inputs and sequestration in soils [63].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [63] Hillier J, Dailey G, Aylott M, Whittaker C, Richter G, Riche A, Murphy R, Taylor G, Smith P (2009) Greenhouse gas emissions from four bioenergy crops in England and Wales: integrating spatial estimates of yield and soil carbon balance in life cycle analyses. Glob Chang Biol Bioenergy 1(4):267–281. doi: 10.1111/j.1757-1707.2009.01021.x source
Not checked in the free run.
- Interpretationcitation
Technically, various plant ecosystems and a SOC decomposition model of desired complexity can be integrated with some empirical method for assessing site/soil-specific SOC stock changes.
“There is no doubt that, technically, various plant ecosystems and a SOC decomposition model of desired complexity can be integrated with some empirical method for assessing site/soil-specific SOC stock changes, as shown for the GEFSOC system [39].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [39] Easter M, Paustian K, Killian K, Williams S, Feng T, Al-Adamat R, Batjes NH, Bernoux M, Bhattacharyya T, Cerri CC, Cerri CEP, Coleman K, Falloon P, Feller C, Gicheru P, Kamoni P, Milne E, Pal DK, Powlson DS, Rawajfih Z, Sessay M, Wokabi S (2007) The GEFSOC soil carbon modelling system: a tool for conducting regional-scale soil carbon inventories and assessing the impacts of land use change on soil carbon. Agric Ecosyst Environ 122(1):13–25. doi: 10.1016/j.agee.2007.01.004 source
Not checked in the free run.
- Interpretationreasoning
Underpinning evidence for C balance components is more certain for AGB than BGB inputs.
“Second, underpinning evidence for the C balance components is more certain for AGB than BGB inputs: (a) litter fall and harvest residues are more easily measured than roots and rhizomes/stool and (b) gross inputs of BGB components profoundly depend on their MRT.”
Quote in the paperSubstantial claim - Premisenone given
Gross inputs of BGB components profoundly depend on their MRT.
“Second, underpinning evidence for the C balance components is more certain for AGB than BGB inputs: (a) litter fall and harvest residues are more easily measured than roots and rhizomes/stool and (b) gross inputs of BGB components profoundly depend on their MRT.”
Quote in the paperNot a substantial claim - Interpretationcitation
Empirical coefficients such as those used in the IPCC Tier 1 method are insufficient to account for SOC sequestration under PECs.
“Empirical coefficients, such as those used in the IPCC Tier 1 method [39], are insufficient to account for SOC sequestration under PECs.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [39] Easter M, Paustian K, Killian K, Williams S, Feng T, Al-Adamat R, Batjes NH, Bernoux M, Bhattacharyya T, Cerri CC, Cerri CEP, Coleman K, Falloon P, Feller C, Gicheru P, Kamoni P, Milne E, Pal DK, Powlson DS, Rawajfih Z, Sessay M, Wokabi S (2007) The GEFSOC soil carbon modelling system: a tool for conducting regional-scale soil carbon inventories and assessing the impacts of land use change on soil carbon. Agric Ecosyst Environ 122(1):13–25. doi: 10.1016/j.agee.2007.01.004 source
Not checked in the free run.
- Premisecitation
Bulk density is a dynamic property when changing from arable to perennial agricultural systems.
“Bulk density in particular is a dynamic property when changing from arable to perennial agricultural systems [24], and its variation increases the uncertainty of stock changes [80, 164, 184] and needs to be accounted for to capture the effect of spatial heterogeneity on SOC dynamics and sequestration.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [24] Zan CS, Fyles JW, Girouard P, Samson RA (2001) Carbon sequestration in perennial bioenergy, annual corn and uncultivated systems in southern Quebec. Agric Ecosyst Environ 86(2):135–144 source
Not checked in the free run.
- May combine two claims. 103
- Classified as probably not a substantial claim. 50
May combine two claims.
Findingown dataA meta-analysis showed that studies on dry matter partitioning and carbon inputs to soils are plentiful, while data on turnover are rare and rely on few isotopic carbon tracer studies.
“A meta-analysis showed that studies on dry matter partitioning and C inputs to soils are plentiful, whilst data on turnover are rare and rely on few isotopic C tracer studies.”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationPrevious reviews on carbon sequestration under perennial energy crops include some unrelated to soil organic carbon, some without experimental evidence, and some focused on specific geographical regions.
“Although there have been previous reviews on C sequestration under PECs [8–11], some of these were either unrelated to SOC [12, 13], or did not report any experimental evidence [1, 14, 15], or focused on specific geographical regions [16].”
Quote in the paperSubstantial claim0 of 9 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
- cites [9] Bransby DI, McLaughlin SB, Parrish DJ (1998) A review of carbon and nitrogen balances in switchgrass grown for energy. Biomass Bioenergy 14(4):379–384 source
Not checked in the free run.
- cites [10] Garten CT, Wullschleger SD, Classen AT (2011) Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar. Biomass Bioenergy 35(1):214–226. doi: 10.1016/j.biombioe.2010.08.013 source
Not checked in the free run.
- cites [11] Poeplau C, Don A (2014) Soil carbon changes under Miscanthus driven by C4 accumulation and C3 decomposition—toward a default sequestration function. GCB Bioenergy 6(4):327–338. doi: 10.1111/gcbb.12043 source
Not checked in the free run.
- cites [12] Don A, Osborne B, Hastings A (2011) Land-use change to bioenergy production in Europe: implications for the greenhouse gas balance and soil carbon. Glob Chang Biol Bionergy 4:372–391 source
Not checked in the free run.
- cites [13] Heaton E, Dohleman FG, Miguez AF (2010) Miscanthus: a promising biomass crop. Adv Bot Res 56:75–137 source
Not checked in the free run.
- cites [1] Lemus R, Lal R (2005) Bioenergy crops and carbon sequestration. Crit Rev Plant Sci 24(1):1–21. doi: 10.1080/07352680590910393 source
Not checked in the free run.
- cites [14] Battle-Aguilar J, Brovelli A, Porporato A, Barry DA (2010) Modelling soil carbon and nitrogen cycles during land use change. A review. Agron Sustain Dev 31(2):251–274. doi: 10.1051/agro/2010007 source
Not checked in the free run.
- cites [15] Thomas ARC, Bond AJ, Hiscock KM (2013) A multi-criteria based review of models that predict environmental impacts of land use-change for perennial energy crops on water, carbon and nitrogen cycling. GCB Bioenergy 5(3):227–242. doi: 10.1111/j.1757-1707.2012.01198.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S4 (based).
Findingnone givenThe physical and chemical stabilities of soil organic carbon pools remain uncertain.
“the physical and chemical stabilities of SOC pools remain uncertain”
Quote in the paperNot a substantial claim- Rests on an assumption: The physical and chemical stabilities of soil organic carbon pools are essential in defining the sustainability of carbon sequestration, with a half-life greater than 25 years.
May combine two claims.
Findingnone givenSubsoil processes and carbon losses through leaching under perennial energy crops remain unknown.
“subsoil processes and C losses through leaching remain unknown”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationExperimental evidence for directly measured greenhouse gas emissions was found in 12 papers from eight different experiments, mainly on nitrous oxide from Miscanthus, switchgrass, short-rotation coppice willow and/or short-rotation coppice poplar, mainly following arable but some also after grassland.
“Experimental evidence for directly measured GHG emissions was found in 12 papers from eight different experiments, mainly on nitrous oxide (N2O) from Miscanthus [48–51], switchgrass [52, 53], SRC willow and/or SRC poplar, mainly following arable [48, 49, 54] but some also after grassland [55, 56].”
Quote in the paperNot a substantial claim0 of 7 sources checked- cites [48] Drewer J, Finch J, Lloyd R, Baggs E, Skiba U (2011) How do soil emission of N20, CH4 and CO2 from perennial bioenergy crops differ from arable annual crops? GCB Bioenergy. doi: 10.1111/j.1757-1707.2011.01136
Not checked in the free run.
- cites [49] Gauder M, Butterbach-Bahl K, Graeff-Hoenninger S, Claupein W, Wiegel R (2012) Soil-derived trace gas fluxes from different energy crops-results from a field experiment in Southwest Germany. Glob Chang Biol Bioenergy 4(3):289–301. doi: 10.1111/j.1757-1707.2011.01135.x source
Not checked in the free run.
- cites [50] Jorgensen RN, Jorgensen BJ, Nielsen NE, Maag M, Lind AM (1997) N2O emission from energy crop fields of Miscanthus “Giganteus” and winter rye. Atmos Environ 31(18):2899–2904 source
Not checked in the free run.
- cites [51] Toma Y, Fernandez FG, Sato S, Izumi M, Hatano R, Yamada T, Nishiwaki A, Bollero G, Stewart JR (2011) Carbon budget and methane and nitrous oxide emissions over the growing season in a Miscanthus sinensis grassland in Tomakomai, Hokkaido, Japan. Glob Chang Biol Bioenergy 3(2):116–134. doi: 10.1111/j.1757-1707.2010.01070.x source
Not checked in the free run.
- cites [52] Nikiema P, Rothstein DE, Min D-H, Kapp CJ (2011) Nitrogen fertilization of switchgrass increases biomass yield and improves net greenhouse gas balance in northern Michigan, USA. Biomass Bioenergy 35(10):4356–4367. doi: 10.1016/j.biombioe.2011.08.006 source
Not checked in the free run.
- cites [53] Schmer MR, Liebig MA, Hendrickson JR, Tanaka DL, Phillips RL (2012) Growing season greenhouse gas flux from switchgrass in the northern Great Plains. Biomass Bioenergy 45:315–319. doi: 10.1016/j.biombioe.2012.05.026 source
Not checked in the free run.
- cites [54] Hellebrand HJ, Straehle M, Scholz V, Kern J (2010) Soil carbon, soil nitrate, and soil emissions of nitrous oxide during cultivation of energy crops. Nutr Cycl Agroecosyst 87(2):175–186. doi: 10.1007/s10705-009-9326-z source
Not checked in the free run.
May combine two claims.
Findingown dataA considerable number of papers using process models were published (47), but few studies modelled carbon specifically under Miscanthus (nine) and willow (six).
“A considerable number of papers using process models were published (47), but few studies modelled C specifically under Miscanthus (nine) and willow (six).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationLitter inputs from leaves under switchgrass vary greatly due to management, being highest in riparian buffer strips and lowest under subsoil amelioration, and are affected by land quality or water.
“Litter inputs from leaves vary greatly under switchgrass due to management; they were highest in riparian buffer strips [72] and lowest under subsoil amelioration [73] and were affected by land quality [74–76] or water [47].”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [72] Tufekcioglu A, Raich JW, Isenhart TM, Schultz RC (2003) Biomass, carbon and nitrogen dynamics of multi-species riparian buffers within an agricultural watershed in Iowa, USA. Agrofor Syst 57(3):187–198. doi: 10.1023/a:1024898615284 source
Not checked in the free run.
- cites [73] Al-Kaisi MM, Grote JB (2007) Cropping systems effects on improving soil carbon stocks of exposed subsoil. Soil Sci Soc Am J 71(4):1381–1388. doi: 10.2136/sssaj2006.0200 source
Not checked in the free run.
- cites [74] Hartman JC, Nippert JB, Orozco RA, Springer CJ (2011) Potential ecological impacts of switchgrass (Panicum virgatum L.) biofuel cultivation in the Central Great Plains, USA. Biomass Bioenergy 35(8):3415–3421. doi: 10.1016/j.biombioe.2011.04.055 source
Not checked in the free run.
- cites [75] Lee DK, Owens VN, Doolittle JJ (2007) Switchgrass and soil carbon sequestration response to ammonium nitrate, manure, and harvest frequency on conservation reserve program land. Agron J 99(2):462–468. doi: 10.2134/agronj2006.0152 source
Not checked in the free run.
- cites [76] Zenone T, Gelfand I, Chen J, Hamilton SK, Robertson GP (2013) From set-aside grassland to annual and perennial cellulosic biofuel crops: effects of land use change on carbon balance. Agric For Meteorol 182:1–12. doi: 10.1016/j.agrformet.2013.07.015 source
Not checked in the free run.
May combine two claims.
FindingreasoningCarbon inputs from perennial energy crops differ considerably in the literature even for the same kind of residue, mainly due to environment but also due to differences in sampling and analytical methods.
“Such inputs differ considerably in the literature (Table 1), even for the same kind of residue, mainly due to environment but also due to differences in sampling and analytical methods.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
FindingcitationSome papers cover other greenhouse gases, such as carbon dioxide and/or methane.
“Some papers cover other GHGs, like CO2 and/or methane [48, 49, 53–55, 57].”
Quote in the paperNot a substantial claim0 of 6 sources checked- cites [48] Drewer J, Finch J, Lloyd R, Baggs E, Skiba U (2011) How do soil emission of N20, CH4 and CO2 from perennial bioenergy crops differ from arable annual crops? GCB Bioenergy. doi: 10.1111/j.1757-1707.2011.01136
Not checked in the free run.
- cites [49] Gauder M, Butterbach-Bahl K, Graeff-Hoenninger S, Claupein W, Wiegel R (2012) Soil-derived trace gas fluxes from different energy crops-results from a field experiment in Southwest Germany. Glob Chang Biol Bioenergy 4(3):289–301. doi: 10.1111/j.1757-1707.2011.01135.x source
Not checked in the free run.
- cites [53] Schmer MR, Liebig MA, Hendrickson JR, Tanaka DL, Phillips RL (2012) Growing season greenhouse gas flux from switchgrass in the northern Great Plains. Biomass Bioenergy 45:315–319. doi: 10.1016/j.biombioe.2012.05.026 source
Not checked in the free run.
- cites [54] Hellebrand HJ, Straehle M, Scholz V, Kern J (2010) Soil carbon, soil nitrate, and soil emissions of nitrous oxide during cultivation of energy crops. Nutr Cycl Agroecosyst 87(2):175–186. doi: 10.1007/s10705-009-9326-z source
Not checked in the free run.
- cites [55] Nikiema P, Rothstein DE, Miller RO (2012) Initial greenhouse gas emissions and nitrogen leaching losses associated with converting pastureland to short-rotation woody bioenergy crops in northern Michigan, USA. Biomass Bioenergy 39:413–426. doi: 10.1016/j.biombioe.2012.01.037 source
Not checked in the free run.
- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
May combine two claims.
FindingcitationThe largest number of papers dealt with assessing greenhouse gas emissions or offsets based on life cycle assessment or GIS modelling, which carry the main uncertainty that underlying carbon sequestration models were not specifically calibrated for perennial energy crops.
“Initially, the largest number of papers dealt with assessing GHG emissions or offsets based on LCA or GIS modelling, which carry the main uncertainty that underlying C sequestration models were not specifically calibrated for PECs [44].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [44] Andrén O, Kätterer T (2001) Basic principles for soil carbon sequestration and calculating dynamic country-level balances including future scenarios. Assessment methods for soil carbon. Edited by R. Lal, J.M. Kimble, R.F. Follett, and B. A. Stewart, Lewis Publishers:495–511
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenAnother large subset of papers took a global perspective extrapolating field trials using models assuming a generalised management.
“Another large subset of papers took a global perspective extrapolating field trials using models assuming a generalised management.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataExperimental evidence was reported in 85 papers, of which 44 were specific field trials for the perennial energy crops under consideration and 57 studies had data useful for parameterising carbon sequestration.
“Experimental evidence was reported in 85 papers, of which 44 were specific field trials for the PECs under consideration and a total of 57 studies had data useful for parameterising C sequestration (Tables 1, 2 and 3).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationBelowground biomass is concentrated in the upper part of the profile; despite large amounts of roots under M. giganteus observed down to 1 to 1.8 m, more than 50% were in the top 30 cm.
“BGB is concentrated in the upper part of the profile [61]; in spite of large amounts of roots under M. giganteus observed down to 1 to 1.8 m [57, 61, 66, 80, 84], more than 50 % were in the top 30 cm.”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [61] Monti A, Zatta A (2009) Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy. Agric Ecosyst Environ 132(3–4):252–259. doi: 10.1016/j.agee.2009.04.007 source
Not checked in the free run.
- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- cites [66] Dohleman FG, Heaton EA, Arundale RA, Long SP (2012) Seasonal dynamics of above- and below-ground biomass and nitrogen partitioning in Miscanthus x giganteus and Panicum virgatum across three growing seasons. Glob Chang Biol Bionergy 4(5):534–544 source
Not checked in the free run.
- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
- cites [84] Neukirchen D, Himken M, Lammel J, Czypionka-Krause U, Olfs H-W (1999) Spatial and temporal distribution of the root system and root nutrient content of an established Miscanthus crop. Eur J Agron 11:301–309 source
Not checked in the free run.
May combine two claims.
Findingnone givenOn average, belowground biomass inputs appear similar to litter under Miscanthus, switchgrass and willow but much smaller under poplar.
“On average, BGB inputs appear similar to that from litter under Miscanthus, switchgrass and willow but much smaller under poplar.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationVariable fractions of willow biomass can be found belowground dependent on stand age and soil texture; 48-58% of total biomass was allocated in the first year and 40% in succeeding years.
“Variable fractions of willow biomass can be found belowground dependent on stand age and soil texture [58]; 48–58 % of total biomass was allocated in the first year and 40 % allocated in succeeding years [26].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [58] Rytter RM (2001) Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows. For Ecol Manag 140:177–192 source
Not checked in the free run.
- cites [26] Rytter RM (2012) The potential of willow and poplar plantations as carbon sinks in Sweden. Biomass Bioenergy 36:86–95 source
Not checked in the free run.
May combine two claims.
FindingcitationObserved litter inputs in short-rotation woody crops increase with stand age, which is not reflected in long-term extrapolations.
“Consistent across species and different locations, observed inputs seem to increase with stand age [60, 78], which is not reflected in long-term extrapolations [26].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [26] Rytter RM (2012) The potential of willow and poplar plantations as carbon sinks in Sweden. Biomass Bioenergy 36:86–95 source
Not checked in the free run.
May combine two claims.
FindingcitationObserved carbon input from fine roots of short-rotation coppice poplar ranges between 0.46 and 1.28 Mg C ha−1 year−1, and between 0.16 and 1.45 Mg C ha−1 year−1 can be found in coarse roots.
“Observed values of C input from fine roots of SRWC poplar range between 0.46 and 1.28 Mg C ha−1 year−1, and between 0.16 and 1.45 Mg C ha−1 year−1 can be found in coarse roots (Table 1).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationFor different species in short-rotation woody crop systems, 25-35% of total tree biomass was found in the roots, with 10% specified as fine roots, confirmed for a 10-year-old poplar plantation.
“For different species in SRWC systems, 25–35 % of total tree biomass was found in the roots [87], with 10 % specified as fine roots, confirmed for a 10-year-old poplar plantation [5].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [87] Whittaker RH, Marks PL (1975) Methods of assessing terrestrial productivity. In: Primary productivity of the biosphere, ed H Lieth and R Whittaker:55–118 source
Not checked in the free run.
- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
May combine two claims.
FindingcitationThis carbon turned over very fast and only 2% was found in the soil microbial biomass.
“This C turned over very fast and only 2 % was found in the soil microbial biomass.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [98] De Neergaard A, Porter JR, Gorissen A (2002) Distribution of assimilated carbon in plants and rhizosphere soil of basket willow (Salix viminalis L.). Plant Soil 245(2):307–314 source
Not checked in the free run.
May combine two claims.
FindingcitationLiving roots can decrease (50%) or increase (380%) soil organic carbon mineralisation rates, causing losses equivalent to the root carbon input to soil, with the range depending on plant species and age.
“However, living roots can decrease (50 %) or increase (380 %) SOC mineralisation rates causing losses equivalent to the root C input to soil, the range depending on plant species and age [103].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [103] Cheng W (2009) Rhizosphere priming effect: its functional relationships with microbial turnover, evapotranspiration, and C-N budgets. Soil Biol Biochem 41:1795–1801 source
Not checked in the free run.
May combine two claims.
FindingcitationThe loss of existing soil organic carbon increased with root biomass in a poplar plantation subjected to free air carbon enrichment but did not appear to impair soil organic carbon increase.
“The loss of existing SOC increased with root biomass in a poplar plantation subjected to free air C enrichment (FACE) [99] but did not appear to impair SOC increase.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
May combine two claims.
FindingcitationIn short-rotation woody crop systems, only 15-18% of original mass was lost from litter bags over 8 months, while a loss of 80% of the same litter was estimated during an 11-month period using 13C-labelled material.
“In SRWC systems, similar discrepancies due to experimental procedures occur: Only 15–18 % of the original mass was lost from litter bags over 8 months [78], whilst a loss of 80 % of the same litter was estimated during an 11-month period using 13C-labelled material [109].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
May combine two claims.
Findingnone givenAvailable literature on decomposition rates for perennial energy crops was patchy, and usable data were limited to 15 experimental papers.
“Available literature on decomposition rates for PECs was patchy, and usable data were limited to 15 experimental papers (Table 2).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationMean residence time for leaves, alone or combined with other aboveground residues, ranged between 0.9 and 3.19 years and was longer under drier and colder conditions.
“MRT for leaves, alone or combined with other aboveground residues, ranged between 0.9 and 3.19 years and were longer under drier [62] and colder conditions [108].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
May combine two claims.
FindingcitationAbout 35% of leaf carbon was stabilised as recalcitrant plant debris or as microbial biomass, but the amount of carbon stabilised in humus remains unknown.
“About 35 % of leaf C was stabilised as recalcitrant plant debris or as microbial biomass [64], but the amount of C stabilised in humus remains unknown.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
May combine two claims.
FindingcitationPotential decomposition rates of Miscanthus residues decreased in order from young rhizome to litter and roots, with mean residence time ranging from 1.2 to 2.4 years.
“Potential decomposition rates of Miscanthus residues, both in situ (litter bags) and by laboratory incubation, decreased in order from young rhizome to litter and roots, with MRT ranging from 1.2 to 2.4 years [64, 69], similar to other results [62].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [69] Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus × giganteus leaf senescence, decomposition and C and N inputs to soil. Glob Chang Biol Bionergy 4(6):698–707. doi: 10.1111/j.1757-1707.2012.01192.x source
Not checked in the free run.
- cites [62] Beuch S, Boelcke B, Belau L (2000) Effect of the organic residues of Miscanthus x giganteus on the soil organic matter level of arable soils. J Agron Crop Sci-Z-Acker Pflanzenbau 184(2):111–119 source
Not checked in the free run.
May combine two claims.
FindingreasoningThese losses translated into mean residence times about four times longer (4.3-5.3 years) than those determined from isotope ratios (1.15 years) and about twice those calculated when accounting for the 10°C difference in incubation temperatures.
“These losses translated into MRTs about four times longer (4.3–5.3 years) than those determined from isotope ratios (1.15 years) and about twice those calculated when accounting for the 10 °C difference in incubation temperatures.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
May combine two claims.
FindingcitationLeaf material accessible to earthworms almost completely disappeared from large mesh litter bags within 1 year (95%; MRT about 1 year), while material accessible only to fungal decomposition lost between 40 and 80% (MRT 2.5 to 1.25 years).
“Leaf material accessible to earthworms almost completely disappeared from the large mesh litter bags within 1 year (95 %; MRT ∼1 year), whilst material accessible only to fungal decomposition only lost between 40 and 80 % (MRT 2.5 to 1.25 years).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
May combine two claims.
Findingown dataGrasses and poplar have similar carbon inputs from aboveground litter, larger than willow short-rotation coppice (about 2 vs. 1 Mg C ha−1 year−1), with a wide range of mean residence time (less than 1 to more than 4 years), some of which may be overestimated.
“Grasses and poplar have similar C inputs from AGB litter, larger than willow SRC (∼2 vs. 1 Mg C ha−1 year−1) with a wide range of MRT (<1 to >4 years), some of which may be overestimated.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationCoarse roots represent a variable fraction of the root biomass (10 and 40%), but much smaller values emerged recently.
“Coarse roots (CR) represent a variable fraction of the root biomass (10 and 40 %; [58, 99]), but much smaller values emerged recently [82].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [58] Rytter RM (2001) Biomass production and allocation, including fine-root turnover, and annual N uptake in lysimeter-grown basket willows. For Ecol Manag 140:177–192 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
May combine two claims.
FindingreasoningFor switchgrass, similar average inputs appear to cause an overall 25% higher average stock change than Miscanthus (1.59 vs. 1.21 Mg C ha−1 year−1), likely due to the lower root inputs from Miscanthus.
“For switchgrass, similar average inputs appear to cause an overall 25 % higher average stock change (∆SOC, Fig. 4) than Miscanthus (1.59 vs 1.21 Mg C ha−1 year−1), likely due to the lower root inputs from Miscanthus (Fig. 3b).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationThe annual average carbon input to the soil as fine root under short-rotation woody crops is between 0.4 and 1 Mg C ha−1 year−1, but their fast turnover diminishes the contribution to soil organic carbon storage and retention to about 10%.
“The annual average C input to the soil as fine root under SRWC is between 0.4 and 1 Mg C ha−1 year−1, but their fast turnover is diminishing the contribution to SOC storage and retention to about 10 % [82].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
May combine two claims.
FindingcitationUnder switchgrass, a large number of studies showed sequestration rates that were similar but higher on average.
“Under switchgrass, a large number of studies [8, 9, 47, 57, 75, 77, 137, 138] showed sequestration rates, which were similar (Table 3) but higher on average (Fig. 4).”
Quote in the paperNot a substantial claim0 of 8 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
- cites [9] Bransby DI, McLaughlin SB, Parrish DJ (1998) A review of carbon and nitrogen balances in switchgrass grown for energy. Biomass Bioenergy 14(4):379–384 source
Not checked in the free run.
- cites [47] Collins HP, Smith JL, Fransen S, Alva AK, Kruger CE, Granatstein DM (2010) Carbon sequestration under irrigated switchgrass (Panicum virgatum L.) production. Soil Sci Soc Am J 74(6):2049–2058. doi: 10.2136/sssaj2010.0020 source
Not checked in the free run.
- cites [57] Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems 16(3):508–520. doi: 10.1007/s10021-012-9628-x source
Not checked in the free run.
- cites [75] Lee DK, Owens VN, Doolittle JJ (2007) Switchgrass and soil carbon sequestration response to ammonium nitrate, manure, and harvest frequency on conservation reserve program land. Agron J 99(2):462–468. doi: 10.2134/agronj2006.0152 source
Not checked in the free run.
- cites [77] Wienhold BJ, Varvel GE, Johnson JMF, Wilhelm WW (2013) Carbon source quality and placement effects on soil organic carbon status. Bioenergy Res 6(2):786–796. doi: 10.1007/s12155-013-9301-z source
Not checked in the free run.
- cites [137] Bonin CL, Lal R (2014) Aboveground productivity and soil carbon storage of biofuel crops in Ohio. Glob Chang Biol Bioenergy 6(1):67–75. doi: 10.1111/gcbb.12041 source
Not checked in the free run.
- cites [138] Follett RF, Vogel KP, Varvel GE, Mitchell RB, Kimble J (2012) Soil carbon sequestration by switchgrass and no-till maize grown for bioenergy. Bioenergy Res 5(4):866–875. doi: 10.1007/s12155-012-9198-y source
Not checked in the free run.
May combine two claims.
FindingcitationLow-storage changes for short-rotation woody crops were supported by findings for short-rotation forestry using labelled carbon, which also showed that new carbon accumulated in soil organic carbon pools was characterised by high turnover rates.
“These low-storage changes were supported by findings for SRF using labelled C [142], which also showed that new C accumulated in SOC pools was characterised by high turnover rates.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [142] Lichter J, Barron SH, Bevacqua CE, Finzi AC, Irving KE, Stemmler EA, Schlesinger WH (2005) Soil carbon sequestration and turnover in a pine forest. Ecology 86 (7):1835–1847. doi: 10.1890/04-1205 source
Not checked in the free run.
May combine two claims.
Findingown dataBased on Table 3, carbon retention is higher in herbaceous (Miscanthus) than woody perennial energy crop systems (21-72% vs. 12-23% retained of original input), confirmed by comparing independent averages.
“Based on Table 3, the C retention is higher in herbaceous (Miscanthus) than woody PEC systems (21–72 vs. 12–23 % retained of original input), which is confirmed by comparing independent averages (Fig. 4).”
Quote in the paperSubstantial claimMay combine two claims.
FindingcitationA priming effect was suggested for Miscanthus root exudates, and a two- to fourfold increase in the mineralisation rate was reported after establishment of switchgrass.
“On the other hand, a priming effect was suggested for Miscanthus root exudates [86], and a two- to fourfold increase in the mineralisation rate was reported after establishment of switchgrass [43].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [43] Ma Z, Wood CW, Bransby DI (2000) Carbon dynamics subsequent to establishment of switchgrass. Biomass Bioenergy 18(2):93–104 source
Not checked in the free run.
May combine two claims.
FindingcitationNew data show high sequestration rates for switchgrass on arable soils but no long-term change for short-rotation coppice willow on former grassland soils.
“New data show high sequestration rates for switchgrass on arable soils [137] but no long-term change for SRC-willow on former grassland soils [143].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [137] Bonin CL, Lal R (2014) Aboveground productivity and soil carbon storage of biofuel crops in Ohio. Glob Chang Biol Bioenergy 6(1):67–75. doi: 10.1111/gcbb.12041 source
Not checked in the free run.
- cites [143] Pacaldo RS, Volk TA, Briggs RD (2013) No significant differences in soil organic carbon contents along a chronosequence of shrub willow biomass crop fields. Biomass Bioenergy 58:136–142. doi: 10.1016/j.biombioe.2013.10.018 source
Not checked in the free run.
May combine two claims.
FindingreasoningFor Table 3, after the initial loss an average annual soil organic carbon gain of 2.29 Mg ha−1 year−1 was interpolated between years 4 and 11, which over the whole period would have been an increase of only 1.87 Mg ha−1 year−1.
“For Table 3, we interpolated after the initial loss an average annual SOC gain of 2.29 Mg ha−1 year−1 between years 4 and 11, which over the whole period would have been an increase of only 1.87 Mg ha−1 year−1.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingnone givenTwo papers dealt with a generic description of the C balance under poplar and switchgrass.
“Two papers dealt with a generic description of the C balance under poplar [10] and switchgrass [8].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [10] Garten CT, Wullschleger SD, Classen AT (2011) Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar. Biomass Bioenergy 35(1):214–226. doi: 10.1016/j.biombioe.2010.08.013 source
Not checked in the free run.
- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
May combine two claims.
Findingown dataA total of 25 papers modelling C in PEC systems were published between 2000 and 2013; 16 used RothC and derived models, five used CENTURY or DayCENT, and two used both models.
“A total of 25 papers modelling C in PECs systems were published between 2000 and 2013: 16 used RothC and derived models, five used CENTURY or DayCENT and two used both models (Table 4).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingreasoningThe simulated cumulative CO2 emission under SRC willow was 20 % higher than under Miscanthus because the turnover of fine willow roots is 17 times faster than Miscanthus roots.
“However, the simulated cumulative CO2 emission was 20 % higher than under Miscanthus, because the turnover of fine willow roots is 17 times faster than Miscanthus roots.”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationInitial SOC gains are greater on former arable than on former grassland when planted with Miscanthus, although not significant.
“Although not significant, initial SOC gains are greater on former arable than on former grassland when planted with Miscanthus in spite of greater—probably yield-dependent—sequestration rates on grassland [134].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [134] Zimmermann J, Dauber J, Jones MB (2012) Soil carbon sequestration during the establishment phase of Miscanthus × giganteus: a regional-scale study on commercial farms using 13C natural abundance. GCB Bioenergy 4(4):453–461. doi: 10.1111/j.1757-1707.2011.01117.x source
Not checked in the free run.
Classified as probably not a substantial claim.
PremisecitationPerennial energy crops are considered to be a nearly carbon-neutral source of energy.
“PECs are considered to be a nearly C-neutral source of energy [4]”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [4] Johnson JMF, Barbour NW, Weyers SL (2007) Chemical composition of crop biomass impacts its decomposition. Soil Sci Soc Am J 71(1):155–162 source
Not checked in the free run.
May combine two claims.
Interpretationnone givenReversion of perennials to arable will destroy belowground biomass in the plough layer, which could be removed or retained, decomposed and humified to become part of soil organic carbon.
“Eventually, the reversion of the perennials to arable will destroy the BGB in the plough layer, which could be removed or retained, decomposed and humified to become part of SOC (Fig. 1).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S1 (asserted), S3 (load-bearing).
PremisecitationCarbon sequestration under perennial energy crops should be at least 0.25 Mg C ha−1 year−1 to make the crop carbon-neutral when converted to biofuel.
“It has been proposed that C sequestration under PECs should be at least 0.25 Mg C ha−1 year−1 in order to make the crop C-neutral when converted to biofuel [7].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [7] Volk TA, Verwijst T, Tharakan PJ, Abrahamson LP, White EH (2004) Growing fuel a sustainability assessment of willow biomass crops. Front Ecol Environ 2(8):411–418 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationPerennial energy crops are fast-growing perennial species that can be grown on marginal soils with low inputs to generate energy either by direct combustion or via conversion to liquid fuels.
“PECs are fast-growing (perennial) species that can be grown on marginal soils with low inputs [1, 2] to generate energy either from direct combustion or via conversion to liquid fuels.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] Lemus R, Lal R (2005) Bioenergy crops and carbon sequestration. Crit Rev Plant Sci 24(1):1–21. doi: 10.1080/07352680590910393 source
Not checked in the free run.
- cites [2] Lewandowski I, Scurlock JMO, Lindvall E, Christou M (2003) The development and current status of perennial rhizomatous grasses as energy crops in the US and Europe. Biomass Bioenergy 25(4):335–361 source
Not checked in the free run.
- Rests on an assumption: The area of land devoted to perennial energy crops is likely to increase.
May combine two claims.
PremisecitationLife cycle assessment on data from the USA found poplar and switchgrass provided the largest overall greenhouse gas sinks, with poplar superior because in grass systems nearly all aboveground biomass is removed.
“LCA on data from the USA found poplar and switchgrass provided the largest overall GHG sinks [18], with poplar superior due to the fact that in grass systems, nearly all AGB is removed.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [18] Adler PR, Del Grosso SJ, Parton WJ (2007) Life-cycle assessment of net greenhouse-gas flux for bioenergy cropping systems. Ecol Appl 17(3):675–691 source
Not checked in the free run.
May combine two claims.
PremisecitationMiscanthus seems to be the best choice in terms of carbon sequestration and input efficiency due to its slow decay of residues and high belowground biomass.
“Miscanthus seems to be the best choice in terms of C sequestration and input efficiency [23] due to its slow decay of residues and high BGB [13].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [23] Lewandowski I, Schmidt U (2006) Nitrogen, energy and land use efficiencies of Miscanthus, reed canary grass and triticale as determined by the boundary line approach. Agric Ecosyst Environ 112(4):335–346 source
Not checked in the free run.
- cites [13] Heaton E, Dohleman FG, Miguez AF (2010) Miscanthus: a promising biomass crop. Adv Bot Res 56:75–137 source
Not checked in the free run.
May combine two claims.
PremisecitationBoth herbaceous crops/grasses and short-rotation woody crops can potentially deliver up to 40-50% of the carbon they capture from the atmosphere to the soil as litter and belowground biomass, with inputs varying from less than 1 to more than 4 Mg C ha−1 year−1.
“Both HCG and SRWC can potentially deliver up to 40–50 % of the C they capture from the atmosphere to the soil as litter and BGB, which can vary from <1 to >4 Mg C ha−1 year−1 [59–61].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [59] Davis SC, Parton WJ, Dohleman FG, Smith CM, Grosso SD, Kent AD, DeLucia EH (2009) Comparative biogeochemical cycles of bioenergy crops reveal nitrogen-fixation and low greenhouse gas emissions in a Miscanthus × giganteus agro-ecosystem. Ecosystems 13(1):144–156. doi: 10.1007/s10021-009-9306-9 source
Not checked in the free run.
- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [61] Monti A, Zatta A (2009) Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy. Agric Ecosyst Environ 132(3–4):252–259. doi: 10.1016/j.agee.2009.04.007 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Premisenone givenHarvested aboveground biomass is converted to atmospheric carbon dioxide by combustion, while litter and harvest residues undergo a phase of surface decomposition and incorporation.
“Whilst harvested AGB will be converted to atmospheric CO2 by combustion, litter and harvest residues undergo a phase of surface decomposition and incorporation.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationWillow and poplar are favoured for short-rotation coppice due to their high growth rates and broad genetic variability, which allows adaptation to different soil and climate conditions.
“Willow and poplar are favoured for SRC due to their high growth rates and broad genetic variability, which allows adaptation to different soil and climate conditions [27, 28].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [27] Kuzovkina YA, Volk TA (2009) The characterization of willow (Salix L.) varieties for use in ecological engineering applications: co-ordination of structure, function and autecology. Ecol Eng 35(8):1178–1189. doi: 10.1016/j.ecoleng.2009.03.010 source
Not checked in the free run.
- cites [28] Lasch P, Kollas C, Rock J, Suckow F (2009) Potentials and impacts of short-rotation coppice plantation with aspen in Eastern Germany under conditions of climate change. Reg Environ Chang 10(2):83–94. doi: 10.1007/s10113-009-0095-7 source
Not checked in the free run.
May combine two claims.
InterpretationreasoningSome parameter gaps could be filled using data in papers on switchgrass and poplar, but it is questionable whether parameters from other woody systems were appropriate for this purpose.
“Some parameter gaps could be filled using data in papers on switchgrass (four) and poplar (four), but it is questionable whether parameters from other woody systems (e.g. evergreen forest) were appropriate for this purpose.”
Quote in the paperNot a substantial claim- Rests on an assumption: Data from switchgrass and poplar are appropriate proxies for Miscanthus and willow.
May combine two claims.
PremisecitationUnder short-rotation woody crops, litter production varies across species and genotypes, is proportional to leaf area index, and generally accumulates at the end of the season before being progressively incorporated into the top 10 to 15 cm of soil.
“Under SRWC, litter production varies across species and genotypes, as leaf litter is proportional to LAI, and generally accumulates at the end of the season in a layer on the soil surface before being progressively incorporated into the top 10 to 15 cm of soil [78].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
May combine two claims.
PremisecitationHarvest method can have a profound impact on losses, but woody harvest residues below 5% seem achievable.
“Harvest method can have a profound impact on losses, but woody harvest residues <5 % seem achievable [22].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [22] Berhongaray G, El Kasmioui O, Ceulemans R (2013) Comparative analysis of harvesting machines on an operational high-density short rotation woody crop (SRWC) culture: one-process versus two-process harvest operation. Biomass Bioenergy 58:333–342. doi: 10.1016/j.biombioe.2013.07.003 source
Not checked in the free run.
May combine two claims.
PremisecitationAbout 20% of short-rotation coppice poplar biomass was allocated to structural roots, which may contribute significantly to biomass carbon, while fine roots contribute to soil organic carbon due to faster turnover.
“It was suggested that about 20 % of SRC poplar biomass was allocated to structural roots [95] which may contribute significantly to biomass C, whilst fine roots contribute to SOC due to their faster turnover compared to structural components [26, 82].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [95] Grigal DF, Berguson WE (1998) Soil carbon changes associated with short-rotation systems. Biomass Bioenergy 14(4):371–377 source
Not checked in the free run.
- cites [26] Rytter RM (2012) The potential of willow and poplar plantations as carbon sinks in Sweden. Biomass Bioenergy 36:86–95 source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationQuantification of fine roots is challenging, and roots concentrate in the upper 5-10 cm of soil.
“Quantification of fine roots is challenging, and indirect methods were proposed although roots concentrate in the upper 5–10 cm of soil [94].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [94] Al Afas N, Marron N, Zavalloni C, Ceulemans R (2008) Growth and production of a short-rotation coppice culture of poplar-IV: fine root characteristics of five poplar clones. Biomass Bioenergy 32(6):494–502. doi: 10.1016/j.biombioe.2007.11.007 source
Not checked in the free run.
May combine two claims.
InterpretationreasoningInputs from roots may depend on soil texture and other environmental factors, but the dataset is too small to derive a rule.
“Inputs from roots may depend on soil texture and other environmental factors, but the dataset is too small to derive a rule; however, longevity of roots and their turnover depends on root diameter [30, 31].”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationThe longevity of aboveground plant parts is defined by abscission, but the decay of aboveground litter depends on its incorporation into the soil and accessibility.
“The longevity of aboveground plant parts is clearly defined by their abscission, but the decay of aboveground litter depends on its incorporation into the soil [107] and accessibility [34].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [107] Moorhead DL, Currie WS, Rastetter BW, Parton J, Harmon ME (1999) Climate and litter quality controls on decomposition: an analysis of modeling approaches. Glob Biogechemical Cycles 13(2):575–589 source
Not checked in the free run.
- cites [34] Dungait J, Hopkins D, Gregory A, Whitmore A (2012) Soil organic matter turnover is governed by accessibility not recalcitrance. Glob Chang Biol 18:1781–1796 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationFor a 3-year-old poplar stand, carbon from fine roots including exudates could stimulate the microbial biomass and induce turnover of already stored soil organic carbon.
“For a 3-year-old poplar stand, it was suggested that C from fine roots (including exudates) could stimulate the microbial biomass and induce turnover of already stored SOC [99].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
May combine two claims.
Interpretationnone givenHromadko's data were an order of magnitude larger than those presented by Kaňova and seem unrealistically large.
“Hromadko’s data [96] were an order of magnitude larger than those presented by Kaňova [97] which seems unrealistically large.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [96] Hromadko L, Vranova V, Techer D, Laval-Gilly P (2010) Composition of root exudates of Miscanthus × giganteus Greef Et Deu. Acta Universitatis Agriculturae Et Silviculturae Mendelianae Brunensis LVIII 1:71–76 source
Not checked in the free run.
- cites [97] Kaňova H, Carre J, Vranova V, Rejšek K (2010) Organic compounds in root exudates of Miscanthus × giganteus Greef Et Deu and limitation of microorganisms in its rhizosphere by nutrients. Acta Univ Agric Et Silviculturae Mendelianae Brunensis LVIII 5:203–210 source
Not checked in the free run.
May combine two claims.
PremisecitationEarthworms enhance the incorporation of residues into the soil and accelerate their decay.
“Earthworms clearly enhance the incorporation of residues into the soil and accelerate their decay [110, 111].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [110] Ernst G, Henseler I, Felten D, Emmerling C (2009) Decomposition and mineralization of energy crop residues governed by earthworms. Soil Biol Biochem 41(7):1548–1554. doi: 10.1016/j.soilbio.2009.04.015 source
Not checked in the free run.
- cites [111] Slapokas T, Granhall U (1991) Decomposition of willow-leaf litter in a short-rotation forest in relation to fungal colonization and palatability for earthworms. Biol Fertil Soils 10:241–248 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Interpretationnone givenLittle is known about the effect of root exudates on soil organic carbon.
“Little is known about the effect of root exudates on SOC.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationRhizodeposition and root exudates can cause a priming effect on the turnover of stored soil carbon, which could increase soil carbon emission and lower the sequestration rate.
“Rhizodeposition and root exudates can cause a priming effect on the turnover of C stored in the soil [100], which could increase soil C emission [101, 102] and lower the sequestration rate.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [100] Rasse DP, Rumpel C, Digna MF (2005) Is soil carbon mostly root carbon? Mechanisms for a specific stabilisation. Plant Soil 269:341–356 source
Not checked in the free run.
- cites [101] Kell DB (2011) Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration. Ann Bot 108:407–418 source
Not checked in the free run.
- cites [102] Kuzyakov Y (2002) Review: factors affecting rhizosphere priming effects. J Plant Nutr Soil Sci 165:382–396 source
Not checked in the free run.
May combine two claims.
PremisecitationLitter decay is proportional to its nutrient content and inversely proportional to lignin content, and is also controlled by nutrient availability, particularly nitrogen, in the soil.
“In general terms, litter decay is proportional to its nutrient content and inversely proportional to lignin content [64]; it is also controlled by nutrient availability (particularly N) in the soil [112, 113].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [112] Oren R, Ellsworth DS, Johnsen KH (2001) Soil fertility limits carbon sequestration by forest ecosystems in a CO2-enriched atmosphere. Nature 411:469–471 source
Not checked in the free run.
- cites [113] Hoffmann B, Muller T, Joergensen RG (2010) Carbon dioxide production and oxygen consumption during the early decomposition of different litter types over a range of temperatures in soil-inoculated quartz sand. J Plant Nutr Soil Sci 173(2):217–223. doi: 10.1002/jpln.200800187 source
Not checked in the free run.
May combine two claims.
Premisenone givenWith age and distance to the growing edge, old parts of the rhizome lose vitality, become inert and start decomposing while younger parts remain alive and store carbon for a long time before it becomes available to soil.
“With age and distance to the ‘growing edge’, old parts of the rhizome lose their vitality, become inert and start decomposing whilst the younger parts remain alive and store C for quite a long time before this can be available to soil.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationMiscanthus rhizomes and roots are potentially the most easily decomposable parts, but the rhizome's carbohydrate and crude protein content changes seasonally to support spring regrowth.
“Miscanthus rhizomes and roots are potentially the most easily decomposable parts [64], but in its [19] function as a storage organ, the carbohydrate and crude protein content of the rhizome changes seasonally to support regrowth of the plants in spring [105].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [105] Masuzawa T, Hogetsu K (1977) Seasonal changes in amount of carbohydrate and crude protein in rhizome of Miscanthus sacchariflorus. Bot Mag-Tokyo 90(1019):181–191 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Interpretationnone givenRoot exudates contributed to soil respiration and may affect soil organic carbon pools in multiple ways.
“Further investigations showed that these root exudates contributed to soil respiration and may affect SOC pools in multiple ways.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationLongevity of roots varies greatly and is likely controlled by diameter.
“Longevity of roots was found to vary greatly [30], likely to be controlled by diameter [31].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [30] Block RMA, Rees KCJ, Knight JD (2006) A review of fine root dynamics in Populus plantations. Agrofor Syst 67(1):73–84. doi: 10.1007/s10457-005-2002-7 source
Not checked in the free run.
- cites [31] Gill RA, Burke IC, Lauenroth WK, Milchunas DG (2002) Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth. Plant Ecol 159(2):241–251. doi: 10.1023/A:1015529507670 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenThe production of fine roots and root exudates could vary greatly between species, genotypes, management and age of the perennial and is tedious to assess.
“The production of fine roots and root exudates could vary greatly between species, genotypes, management and the age of the perennial and is tedious to assess.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing), S4 (based). May combine two claims.
Interpretationnone givenInputs from perennials are continuous, vary over their lifetime, and their variable size and composition are likely to affect their decomposition.
“Inputs from perennials are continuous, vary over their life time and their variable size and composition are likely to affect their decomposition.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationLitter mineralisation depends also on soil fauna, which may vary according to location.
“Litter mineralisation depends also on the soil fauna [119, 120], which may vary according to location [113].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [119] Falloon P, Smith P, Szabo J, Pasztor L (2002) Comparison of approaches for estimating carbon sequestration at the regional scale. Soil Use Manag 18(3):164–174. doi: 10.1079/sum2002118 source
Not checked in the free run.
- cites [120] Felten D, Emmerling C (2011) Effects of bioenergy crop cultivation on earthworm communities—a comparative study of perennial (Miscanthus) and annual crops with consideration of graded land-use intensity. Appl Soil Ecol 49:167–177. doi: 10.1016/j.apsoil.2011.06.001 source
Not checked in the free run.
- cites [113] Hoffmann B, Muller T, Joergensen RG (2010) Carbon dioxide production and oxygen consumption during the early decomposition of different litter types over a range of temperatures in soil-inoculated quartz sand. J Plant Nutr Soil Sci 173(2):217–223. doi: 10.1002/jpln.200800187 source
Not checked in the free run.
May combine two claims.
PremisecitationThe commonly used litter bag method prevents physical incorporation of debris into the soil and does not allow access of larger biota such as earthworms.
“The commonly used litter bag method [64, 69, 78] prevents physical incorporation of the debris into the soil and does not allow access of larger biota (e.g. earthworms).”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [64] Amougou N, Bertrand I, Machet JM, Recous S (2011) Quality and decomposition in soil of rhizome, root and senescent leaf from Miscanthus x giganteus, as affected by harvest date and N fertilization. Plant Soil 338(1–2):83–97. doi: 10.1007/s11104-010-0443-x source
Not checked in the free run.
- cites [69] Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus × giganteus leaf senescence, decomposition and C and N inputs to soil. Glob Chang Biol Bionergy 4(6):698–707. doi: 10.1111/j.1757-1707.2012.01192.x source
Not checked in the free run.
- cites [78] Cotrufo MF, De Angelis P, Polle A (2005) Leaf litter production and decomposition in a poplar short-rotation coppice exposed to free air CO2 enrichment (POPFACE). Glob Chang Biol 11:971–982 source
Not checked in the free run.
May combine two claims.
InterpretationcitationCarbon losses in litter bags may be solely a function of microbial respiration, and other fundamental soil processes affecting turnover such as adsorption to clay and occlusion within the soil matrix were not accounted for.
“C losses may be solely a function of microbial respiration within the litter bag [109], and other fundamental soil processes affecting turnover, such as adsorption to clay and occlusion within the soil matrix [35, 121], were not accounted for.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- cites [121] von Lützow M, Kögel-Knabner I, Ekschmitt K, Flessa H, Guggenberger G, Matzner E, Marschner B (2007) SOM fractionation methods: relevance to functional pools and to stabilization mechanisms. Soil Biol Biochem 39(9):2183–2207. doi: 10.1016/j.soilbio.2007.03.007 source
Not checked in the free run.
May combine two claims.
PremisecitationPhysical protection and chemical adsorption, both controlled by soil texture such as clay content and cation exchange capacity, may play an important role for long-term carbon retention.
“However, physical protection and chemical adsorption, both controlled by soil texture (e.g. clay content and cation exchange capacity), may play an important role for long-term C retention [4, 34, 35, 101].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [4] Johnson JMF, Barbour NW, Weyers SL (2007) Chemical composition of crop biomass impacts its decomposition. Soil Sci Soc Am J 71(1):155–162 source
Not checked in the free run.
- cites [34] Dungait J, Hopkins D, Gregory A, Whitmore A (2012) Soil organic matter turnover is governed by accessibility not recalcitrance. Glob Chang Biol 18:1781–1796 source
Not checked in the free run.
- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- cites [101] Kell DB (2011) Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration. Ann Bot 108:407–418 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenCarbon retention is the net result of annual gross inputs/production, mortality and turnover of the components.
“C retention is the net result of annual gross inputs/production, mortality and turnover of the components.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationVery coarse anchoring roots are likely to have a long mean residence time, such as the lifetime of the stand, but there are no reports on decomposition of those.
“Very coarse, anchoring roots are likely to have a long MRT (e.g. lifetime of the stand), but there are no reports on decomposition of those [81, 82, 99].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [81] Berhongaray G, Janssens IA, King JS, Ceulemans R (2013) Fine root biomass and turnover of two fast-growing poplar genotypes in a short-rotation coppice culture. Plant Soil 373(1–2):269–283. doi: 10.1007/s11104-013-1778-x source
Not checked in the free run.
- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
May combine two claims.
Interpretationnone givenThe large range of mean residence time reflects the experimental conditions, with long mean residence time being an artefact of litter bag usage.
“The large range of MRT reflects the experimental conditions, long MRT being an artefact of litter bag usage.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationIt is disputed whether fine roots contribute most to soil organic carbon in woody systems due to their relatively rapid decomposition.
“It is disputed whether fine roots contribute most to SOC in woody systems due to their relatively rapid decomposition [5, 99, 126].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
- cites [126] Nadelhoffeer KJ, Aber JD, Melillo JM (1985) Fine roots, net primary production, and soil nitrogen availability: a new hypothesis. Ecology 66:1377–1390. doi: 10.2307/1939190 source
Not checked in the free run.
May combine two claims.
InterpretationreasoningRhizome inputs from switchgrass were much smaller than from Miscanthus, which explains the evidence that switchgrass sequestered twice the amount of soil organic carbon.
“Rhizome inputs from switchgrass were much smaller than from Miscanthus which explains the evidence that switchgrass sequestered twice the amount of SOC (Fig. 4).”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationPotential default carbon sequestration rates for arable crops, grassland and forests have been estimated to be 0.3, 0.5-0.7 and 0.1-0.2 Mg C ha−1 year−1, respectively; others found 0.33 Mg C ha−1 year−1 for both grassland and forest systems.
“Potential, default C sequestration rates for arable crops, grassland and forests have been estimated to be 0.3, 0.5–0.7 and 0.1–0.2 Mg C ha−1 year−1, respectively [132]; others found 0.33 Mg C ha−1 year−1 for both grassland and forest systems [133].”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [132] Soussana JF, Loiseau P, Vuichard N, Ceschia E, Balesdent J, Chevallier T, Arrouays D (2004) Carbon cycling and sequestration opportunities in temperate grasslands. Soil Use Manag 20:219–230 source
Not checked in the free run.
- cites [133] Post WM, Kwon KC (2000) Soil carbon sequestration and land-use change: processes and potential. Glob Chang Biol 6:317–328 source
Not checked in the free run.
May combine two claims.
InterpretationcitationSequestration rates are not predictive when based on single early or late observations, average carbon inputs and turnover rates.
“Sequestration rates are not predictive when based on single early or late observations [19, 135, 140], average C inputs and turnover rates.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
- cites [140] Cattaneo F, Barbanti L, Gioacchini P, Ciavatta C, Marzadori C (2014) C-13 abundance shows effective soil carbon sequestration in Miscanthus and giant reed compared to arable crops under Mediterranean climate. Biol Fertil Soils 50(7):1121–1128. doi: 10.1007/s00374-014-0931-x source
Not checked in the free run.
May combine two claims.
InterpretationcitationYields and litter inputs increased during the establishment phase and the postulated delay for rhizome decomposition contradict steady-state assumptions.
“Yields and litter inputs increased during the establishment phase [65] and the postulated delay for rhizome decomposition [106] contradict such assumptions.”
Quote in the paperSubstantial claim0 of 2 sources checked- cites [65] Christian DG, Poulton PR, Riche AB, Yates NE, Todd AD (2006) The recovery over several seasons of N-15-labelled fertilizer applied to Miscanthus x giganteus ranging from 1 to 3 years old. Biomass Bioenergy 30(2):125–133 source
Not checked in the free run.
- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
May combine two claims.
InterpretationcitationThe analogue in short-rotation woody crop systems is coarse roots (1-2 mm) with longer mean residence time or woody roots, the stump or stool, for which no evidence of turnover and retention exists.
“The analogue in the SRWC system is to be found in the coarse roots (1–2 mm) with longer MRT [82] or woody roots, the stump or stool [4] for which no evidence of turnover and retention exists.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [82] Rytter RM (2013) The effect of limited availability of N or water on C allocation to fine roots and annual fine root turnover in Alnus incana and Salix viminalis. Tree Physiol 33(9):924–939. doi: 10.1093/treephys/tpt060 source
Not checked in the free run.
- cites [4] Johnson JMF, Barbour NW, Weyers SL (2007) Chemical composition of crop biomass impacts its decomposition. Soil Sci Soc Am J 71(1):155–162 source
Not checked in the free run.
May combine two claims.
InterpretationcitationBelowground biomass has a greater effect on soil organic carbon than litter inputs, possibly due to delayed incorporation of litter.
“Zimmermann et al. [141] also showed that BGB has a greater effect on SOC than litter inputs, possibly due to delayed incorporation of the latter.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [141] Zimmermann M, Leifeld J, Schmidt MWI, Smith P, Fuhrer J (2007) Measured soil organic matter fractions can be related to pools in the RothC model. Eur J Soil Sci 58(3):658–667. doi: 10.1111/j.1365-2389.2006.00855.x source
Not checked in the free run.
May combine two claims.
InterpretationreasoningRetention rates under switchgrass were higher on average (50%), probably due to a large fraction of root inputs.
“Retention rates were also higher on average (50 %), probably due to large fraction of root inputs.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
InterpretationcitationConsidering the enrichment in the labile fraction, it was suggested that at least 20 years was needed to evaluate the impact of Miscanthus in terms of sustainable soil organic carbon enrichment, which contradicted earlier estimates.
“Considering the enrichment in the labile fraction [86, 135, 139], it was suggested that at least 20 years was needed to evaluate the impact of Miscanthus in terms of sustainable SOC enrichment, which contradicted earlier estimates [19, 45, 106, 135].”
Quote in the paperSubstantial claim0 of 6 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- cites [19] Clifton-Brown JC, Breuer J, Jones MB (2007) Carbon mitigation by the energy crop, Miscanthus. Glob Chang Biol 13(11):2296–2307 source
Not checked in the free run.
- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [106] Hansen EM, Christensen BT, Jensen LS, Kristensen K (2004) Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by 13C abundance. Biomass Bioenergy 26(2):97–105. doi: 10.1016/s0961-9534(03)00102-8 source
Not checked in the free run.
May combine two claims.
PremisecitationCarbon inputs originate from and feed into pools of different stability, and initially carbon is stored as particulate organic matter, which is a relatively slow soil organic carbon pool under switchgrass.
“C inputs originate from and feed into pools of different stability [45, 141], and initially, C is stored as particulate organic matter (POM) [139], which is a relatively slow SOC pool under switchgrass [25, 47].”
Quote in the paperSubstantial claim0 of 5 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [141] Zimmermann M, Leifeld J, Schmidt MWI, Smith P, Fuhrer J (2007) Measured soil organic matter fractions can be related to pools in the RothC model. Eur J Soil Sci 58(3):658–667. doi: 10.1111/j.1365-2389.2006.00855.x source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [47] Collins HP, Smith JL, Fransen S, Alva AK, Kruger CE, Granatstein DM (2010) Carbon sequestration under irrigated switchgrass (Panicum virgatum L.) production. Soil Sci Soc Am J 74(6):2049–2058. doi: 10.2136/sssaj2010.0020 source
Not checked in the free run.
May combine two claims.
InterpretationcitationAlthough annual rhizome inputs are similar to those from litter, its mean residence time is large due to its longevity, which delays decomposition and incorporation into soil organic carbon.
“Although annual rhizome inputs are similar to those from litter, its MRT is large due to its longevity [1, 68] which delays their decomposition and incorporation into SOC.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [1] Lemus R, Lal R (2005) Bioenergy crops and carbon sequestration. Crit Rev Plant Sci 24(1):1–21. doi: 10.1080/07352680590910393 source
Not checked in the free run.
- cites [68] Hansen EM (1993) Soil carbon sequestration beneath hybrid poplar plantations in the North Central United States. Biomass Bioenergy 5(6):431–436 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationLosses of soil organic carbon under Miscanthus genotypes with higher belowground biomass were suggested to indicate higher soil respiration rate and carbon turnover induced by root exudates, causing a priming effect.
“Losses of SOC under Miscanthus genotypes with higher BGB were suggested to indicate higher soil respiration rate and C turnover induced by root exudates, causing a priming effect [86].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
May combine two claims.
PremisecitationLignin decomposition rates are highly variable depending on soils and land use and are not necessarily linked to the stability of the derived soil carbon pool.
“However, lignin decomposition rates are highly variable depending on soils and land use and are not necessarily linked to the stability of the derived soil C pool [146, 149].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [146] Davidson EA, Janssens IA (2006) Temperature sensitivity of soil carbon decomposition and feedbacks to climate change. Nature 440(7081):165–173. doi: 10.1038/nature04514 source
Not checked in the free run.
- cites [149] Thevenot M, Dignac MF, Rumpel C (2010) Fate of lignins in soils: a review. Soil Biol Biochem 42(8):1200–1211. doi: 10.1016/j.soilbio.2010.03.017 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationcitationThe amount of carbon occluded, considered a main index of long-term sequestered carbon in soils under forest and under Miscanthus, remains to be quantified.
“The amount of C occluded, which is considered as a main index of long-term sequestered C in soils under forest [148] as well under Miscanthus [11], remains to be quantified.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [148] Mueller L, Carsten W, Koegel-Knabner I (2008) Soil organic carbon stocks, distribution, and composition affected by historic land use changes on adjacent sites. Biol Fertil Soils 45(4):347–359. doi: 10.1007/s00374-008-0336-9 source
Not checked in the free run.
- cites [11] Poeplau C, Don A (2014) Soil carbon changes under Miscanthus driven by C4 accumulation and C3 decomposition—toward a default sequestration function. GCB Bioenergy 6(4):327–338. doi: 10.1111/gcbb.12043 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationreasoningThe average sequestration rates are largely based on all residues and require further analysis in terms of component-specific contributions.
“The average sequestration rates (Fig. 4) are largely based on all residues and require further analysis in terms of component-specific contributions.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationMiscanthus litter is higher in lignin than other grasses and seems to reduce the turnover rate of existing soil organic carbon by increasing the insoluble carbon fraction resistant to microbial attack.
“Miscanthus, whose litter is higher in lignin than other grasses [69], seems to reduce the turnover rate of existing SOC by increasing the insoluble C fraction resistant to microbial attack [116, 150].”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [69] Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus × giganteus leaf senescence, decomposition and C and N inputs to soil. Glob Chang Biol Bionergy 4(6):698–707. doi: 10.1111/j.1757-1707.2012.01192.x source
Not checked in the free run.
- cites [116] Foereid B, de Neergaard A, Høgh-Jensen H (2004) Turnover of organic matter in a Miscanthus field: effect of time in Miscanthus cultivation and inorganic nitrogen supply. Soil Biol Biochem 36(7):1075–1085. doi: 10.1016/j.soilbio.2004.03.002 source
Not checked in the free run.
- cites [150] Kahle P, Beuch S, Boelcke B, Leinweber P, Schulten HR (2001) Cropping of Miscanthus in Central Europe: biomass production and influence on nutrients and soil organic matter. Eur J Agron 15(3):171–184 source
Not checked in the free run.
May combine two claims.
InterpretationcitationUnder short-rotation woody crop systems, the predominance of decomposable fine roots could explain the initial loss of soil organic carbon and higher losses under free air carbon enrichment.
“Under SRWC systems, the predominance of decomposable fine roots could explain the initial loss of SOC [60] and higher losses under FACE [99].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [60] Arevalo CBM, Bhatti JS, Chang SX, Sidders D (2011) Land use change effects on ecosystem carbon balance: from agricultural to hybrid poplar plantation. Agric Ecosyst Environ 141(3–4):342–349. doi: 10.1016/j.agee.2011.03.013 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationThe intra-aggregate fraction of particulate organic matter is small but could be a close approximation.
“The intra-aggregate fraction of POM [45, 139] is small but could be a close approximation.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
May combine two claims.
InterpretationcitationThe view that roots contribute more to soil organic carbon than aboveground sources seems reflected in the figures, and recent data showed a tight relationship between root and Miscanthus-derived soil organic carbon.
“The view that roots contribute more to SOC than aboveground sources [100] seems to be reflected in Figs. 3b and 4, and recent data showed a tight relationship between root and Miscanthus-derived SOC [80].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [100] Rasse DP, Rumpel C, Digna MF (2005) Is soil carbon mostly root carbon? Mechanisms for a specific stabilisation. Plant Soil 269:341–356 source
Not checked in the free run.
- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
May combine two claims.
PremisecitationOccluded particulate organic matter is particularly stable, and root carbon has been found to accumulate in this pool even under arable crops.
“Occluded POM is particularly stable, and root C has been found to accumulate in this pool even under arable crops [147].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [147] Wander M, Xueming Y (2000) Influence of tillage on the dynamics of loose- and occluded-particulate and humified organic matter fractions. Soil Biol Biochem 32:1151–1160 source
Not checked in the free run.
May combine two claims.
PremisecitationC losses from soil come from root respiration, microbial respiration, and leaching of dissolved organic carbon.
“In general terms, C losses from soil come from root respiration (ca. 20–40 % of plant-fixed C; [151]), microbial respiration (40 % of SOC in decomposable pools [151]) and leaching of DOC.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [151] Smith PL, Kutsch G, Werner L et al (2010) Measurements necessary for assessing the net ecosystem carbon budget of croplands. Agric Ecosyst Environ 139(3):302–315. doi: 10.1016/j.agee.2010.04.004 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThe synthesis did not account for differences in temperature or other experimental variables.
“We did not account for differences in temperature or other experimental variables.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningThe bio-physicochemical complexity of soil organic carbon could explain its turnover variability under perennial energy crops.
“The bio-physicochemical complexity of SOC could explain its turnover variability under PECs.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationParticulate and mineral-associated organic matter are formed in the soil and stabilise soil organic carbon by limiting the access of soil microbes.
“Particulate (POM) and mineral-associated organic matter (MOM) are formed in the soil, which stabilise SOC, e.g. limiting the access of soil microbes [25].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationcitationThe popularity of RothC may lie in its minimal data requirement, adaptability, and easier calibration of residue pools compared to CENTURY.
“The popularity of RothC may lie in the minimal data requirement, its adaptability, which allows its integration, and the easier calibration of residue pools compared to CENTURY [163].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [163] Xianli X, Liu W, Kiely G (2011) Modeling the change in soil organic carbon of grassland in response to climate change: effects of measured versus modelled carbon pools for initializing the Rothamsted Carbon model. Agric Ecosyst Environ 140(3–4):372–381. doi: 10.1016/j.agee.2010.12.018
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationCENTURY and RothC were identified as especially important models for PEC systems.
“CENTURY [160] and RothC [159] were identified as especially important.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [160] Parton WJ, Hartman M, Ojima D, Schimel D (1998) DAYCENT and its land surface submodel: description and testing. Glob Planet Chang 19(1–4):35–48. doi: 10.1016/S0921-8181(98)00040-X source
Not checked in the free run.
- cites [159] Coleman K, Jenkinson DS, Crocker GJ, Grace PR, Klir J, Korschens M, Poulton PR, Richter DD (1997) Simulating trends in soil organic carbon in long-term experiments using RothC-26.3. Geoderma 81(1–2):29–44 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationDondini et al. applied a soil fractionation technique to improve calibration of SOC pools and account for the recalcitrant nature of plant residues.
“Dondini et al. [45] applied a soil fractionation technique [141] to improve the calibration of SOC pools and to account for the recalcitrant nature of plant residues.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
- cites [141] Zimmermann M, Leifeld J, Schmidt MWI, Smith P, Fuhrer J (2007) Measured soil organic matter fractions can be related to pools in the RothC model. Eur J Soil Sci 58(3):658–667. doi: 10.1111/j.1365-2389.2006.00855.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenThe models APSIM, CENTURY and STICS include a component for litter decomposition using a rate-modifying function for soil depth, accounting for changes of temperature and moisture along the soil profile.
“The models APSIM, CENTURY and STICS include a component for litter decomposition using a rate-modifying function for soil depth, which account for changes of temperature and moisture along the soil profile.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationLocally calibrated decomposition rates are suggested to account for soil temperature and water content gradients.
“They also suggested locally calibrated decomposition rates to account for soil temperature and water content gradients [166].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [166] Paul KI, Polglase PJ (2004) Prediction of decomposition of litter under eucalypts and pines using the FullCAM model. For Ecol Manag 191(1–3):73–92. doi: 10.1016/j.foreco.2003.11.007 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationThe use of more pools implies more calibrating parameters which improve long-term prediction.
“The use of more pools implies more calibrating parameters which improve long-term prediction [8] but increase the uncertainty of the model.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [8] Garten CT (2012) Review and model-based analysis of factors influencing soil carbon sequestration beneath switchgrass (Panicum virgatum). Bioenergy Res 5(1):124–138. doi: 10.1007/s12155-011-9154-2 source
Not checked in the free run.
May combine two claims.
PremisecitationDecomposition of old SOM can be affected by root priming, which varies with root density along the soil profile and crop C balance.
“In addition, decomposition of old SOM can be affected by root priming [103], which varies with root density along the soil profile and crop C balance [99].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [103] Cheng W (2009) Rhizosphere priming effect: its functional relationships with microbial turnover, evapotranspiration, and C-N budgets. Soil Biol Biochem 41:1795–1801 source
Not checked in the free run.
- cites [99] Gielen B, Calfapietra C, Lukac M, Wittig VE, De Angelis P, Janssens IA, Moscatelli MC, Grego S, Cotrufo MF, Godbold DL, Hoosbeek MR, Long SP, Miglietta F, Polle A, Bernacchi CJ, Davey PA, Ceulemans R, Scarascia-Mugnozza GE (2005) Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment. Tree Physiol 25(11):1399–1408 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationIn forest soils, the soil microbial biomass assimilated 70 % of the DOC and respired the remaining 30 %.
“Similar conclusions were reached for DOC in forest soils [157], where the soil microbial biomass assimilated 70 % of the DOC and respired the remaining 30 %.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [157] van Hees PAW, Jones DL, Finlay R, Godbold DL, Lundström US (2005) The carbon we do not see—the impact of low molecular weight compounds on carbon dynamics and respiration in forest soils: a review. Soil Biol Biochem 37(1):1–13. doi: 10.1016/j.soilbio.2004.06.010 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationNon-linear interactions between decomposition rate and temperature can exist for different pools, with the effect greatest at lower temperatures and for slowly decomposable compounds but least for old SOC.
“Finally, non-linear interactions between decomposition rate and temperature can exist for different pools, with the effect being greatest at lower temperatures and for ‘slowly decomposable’ compounds but least for ‘old’ SOC [14].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [14] Battle-Aguilar J, Brovelli A, Porporato A, Barry DA (2010) Modelling soil carbon and nitrogen cycles during land use change. A review. Agron Sustain Dev 31(2):251–274. doi: 10.1051/agro/2010007 source
Not checked in the free run.
May combine two claims.
PremisecitationUnder grassland, 20-30 % of DOC was rapidly decomposed by microbial respiration, <5 % was retained in the soil, and the rest was assimilated by the soil microbial biomass.
“However, under grassland, 20–30 % of DOC was rapidly decomposed by microbial respiration, <5 % was retained in the soil, whilst the rest was assimilated by the soil microbial biomass [156].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [156] Boddy E, Hill PW, Farrar J, Jones DL (2007) Fast turnover of low molecular weight components of the dissolved organic carbon pool of temperate grassland field soils. Soil Biol Biochem 39(4):827–835 source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningThe half-life of >25 years considered for a C pool to be inert, and similar times as a criterion for SOC sequestration, seems rather short.
“The half-life of >25 years considered for a C pool to be ‘inert’ [121], and similar times as a criterion for SOC sequestration [5, 35, 151, 158] seems rather short.”
Quote in the paperNot a substantial claim0 of 5 sources checked- cites [121] von Lützow M, Kögel-Knabner I, Ekschmitt K, Flessa H, Guggenberger G, Matzner E, Marschner B (2007) SOM fractionation methods: relevance to functional pools and to stabilization mechanisms. Soil Biol Biochem 39(9):2183–2207. doi: 10.1016/j.soilbio.2007.03.007 source
Not checked in the free run.
- cites [5] Sartori F, Lal R, Ebinger MH, Eaton JA (2007) Changes in soil carbon and nutrient pools along a chronosequence of poplar plantations in the Columbia Plateau, Oregon, USA. Agric Ecosyst Environ 122(3):325–339. doi: 10.1016/j.agee.2007.01.026 source
Not checked in the free run.
- cites [35] Marschner B, Brodowski S, Dreves A, Gleixner G, Gude A, Grootes P (2008) How relevant is recalcitrance for the stabilization of organic matter in soils? J Plant Nutr Soil Sci 171:91–110 source
Not checked in the free run.
- cites [151] Smith PL, Kutsch G, Werner L et al (2010) Measurements necessary for assessing the net ecosystem carbon budget of croplands. Agric Ecosyst Environ 139(3):302–315. doi: 10.1016/j.agee.2010.04.004 source
Not checked in the free run.
- cites [158] McLaughlin SB, Kszos LA (2005) Development of switchgrass (Panicum virgatum) as a bioenergy feedstock in the United States. Biomass Bioenergy 28(6):515–535 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationJenkinson and Coleman introduced an empirical coefficient to reduce SOM decomposition in the subsoil.
“Jenkinson and Coleman [40] introduced a similar empirical coefficient to reduce SOM decomposition in the subsoil.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [40] Jenkinson DS, Coleman K (2008) The turnover of organic carbon in subsoils. Part 2. Modelling carbon turnover. Eur J Soil Sci 59(2):400–413. doi: 10.1111/j.1365-2389.2008.01026.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Premisenone givenCENTURY and APSIM decrease the decomposition rate of litter accumulating on the soil surface.
“CENTURY and APSIM decrease the decomposition rate of litter accumulating on the soil surface.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAuthors have modified and coupled RothC by adding and calibrating new specific soil and residue C pools, accounting for tree and crop residues.
“Authors have modified and coupled RothC by adding and calibrating new specific soil and residue C pools, accounting for tree [164] and crop [165] residues.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [164] Nieto OM, Castro J, Fernandez E, Smith P (2010) Simulation of soil organic carbon stocks in a Mediterranean olive grove under different soil-management systems using the RothC model. Soil Use Manag 26(2):118–125. doi: 10.1111/j.1475-2743.2010.00265.x source
Not checked in the free run.
- cites [165] Powlson DS, Glendining MJ, Coleman K, Whitmore AP (2011) Implications for soil properties of removing cereal straw: results from long-term studies. Agron J 103(1):279–287. doi: 10.2134/agronj2010.0146s source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationPrevious work showed that the C cycle in forest systems needed a chemical model for litter decomposition to integrate RothC with plant residues.
“However, previous work [168] showed that the C cycle in forest systems needed a chemical model for litter decomposition to integrate RothC with plant residues.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [168] Paul KI, Polglase PJ, Richards GP (2003) Predicted change in soil carbon following afforestation or reforestation, and analysis of controlling factors by linking a C accounting model (CAMFor) to models of forest growth (3PG), litter decomposition (GENDEC) and soil C turnover (RothC). For Ecol Manag 177(1–3):485–501 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisenone givenEach pool decomposes following first-order kinetics integrated with temperature and moisture functions.
“Each pool decomposes following first-order kinetics integrated with temperature and moisture functions.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationDepth-dependent decomposition has been implemented by water and heat flux models, empirical coefficients, or including C transport such as diffusion and adsorption of DOC.
“In summary, depth-dependent decomposition has been implemented by introducing (i) water and heat flux models [14, 169] or (ii) empirical coefficients [40] or (iii) including C transport, i.e. diffusion and adsorption of DOC [42].”
Quote in the paperNot a substantial claim0 of 4 sources checked- cites [14] Battle-Aguilar J, Brovelli A, Porporato A, Barry DA (2010) Modelling soil carbon and nitrogen cycles during land use change. A review. Agron Sustain Dev 31(2):251–274. doi: 10.1051/agro/2010007 source
Not checked in the free run.
- cites [169] Herbst M, Hellebrand HJ, Bauer J, Huisman JA, Simunek J, Weihermuller L, Graf A, Vanderborght J, Vereecken H (2008) Multiyear heterotrophic soil respiration: evaluation of a coupled CO2 transport and carbon turnover model. Ecol Model 214(2–4):271–283. doi: 10.1016/j.ecolmodel.2008.02.007 source
Not checked in the free run.
- cites [40] Jenkinson DS, Coleman K (2008) The turnover of organic carbon in subsoils. Part 2. Modelling carbon turnover. Eur J Soil Sci 59(2):400–413. doi: 10.1111/j.1365-2389.2008.01026.x source
Not checked in the free run.
- cites [42] Braakhekke MC, Christian Beer M, Hoosbeek MR, Reichstein M, Kruijt B, Schrumpf M, Kabat P (2011) SOMPROF: a vertically explicit soil organic matter model. Ecol Model 222:1712–1730 source
Not checked in the free run.
May combine two claims.
PremisecitationInitially new SOC is part of easily decomposable POM and later part of the inter-aggregate fraction.
“The modelling of SOC fractionation seems essential for the persistence and sustainability of C sequestration, showing that initially new SOC is part of easily decomposable POM [139] and later part of the inter-aggregate fraction [25, 45].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- cites [25] Garten CT, Wullschleger SD (2000) Soil carbon dynamics beneath switchgrass as indicated by stable isotope analysis. J Environ Qual 29(2):645–653. doi: 10.2134/jeq2000.00472425002900020036x source
Not checked in the free run.
- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationOther research differentiated inter- and intra-aggregate and particulate OM to derive pools fitting different model concepts.
“Other research differentiated inter- and intra-aggregate and particulate OM to derive pools fitting the different model concepts [45].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [45] Dondini M, Van Groenigen KJ, Del Galdo I, Jones MB (2009) Carbon sequestration under Miscanthus: a study of 13C distribution in soil aggregates. Glob Chang Biol Bioenergy 1(5):321–330. doi: 10.1111/j.1757-1707.2009.01025.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationDecomposition rates of LC residues can vary with temperature, or through interaction between temperature and recalcitrance, which could depend on their chemical composition.
“Decomposition rates of LC residues can vary with temperature, or through interaction between temperature and ‘recalcitrance’, which could depend on their chemical composition [4, 109].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [4] Johnson JMF, Barbour NW, Weyers SL (2007) Chemical composition of crop biomass impacts its decomposition. Soil Sci Soc Am J 71(1):155–162 source
Not checked in the free run.
- cites [109] Rubino M, Dungait JAJ, Evershed RP, Bertolini T, De Angelis P, D’Onofrio A, Lagomarsino A, Lubritto C, Merola A, Terrasi F (2010) Carbon input belowground is the major C flux contributing to leaf litter mass loss: evidences from a 13C labelled-leaf litter experiment. Soil Biol Biochem 42(7):1009–1016. doi: 10.1016/j.soilbio.2010.02.018 source
Not checked in the free run.
May combine two claims.
PremisecitationThe effect of soil moisture on SOC decomposition is complex and non-linear; a single moisture threshold for decreased microbial activity and soil respiration does not exist.
“The effect of soil moisture is complex and non-linear; a single moisture threshold for decreased microbial activity and soil respiration does not exist [14].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [14] Battle-Aguilar J, Brovelli A, Porporato A, Barry DA (2010) Modelling soil carbon and nitrogen cycles during land use change. A review. Agron Sustain Dev 31(2):251–274. doi: 10.1051/agro/2010007 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationRecalcitrance can be modelled using a delay time of decomposition depending on accessible soil pore space, simulating physical protection from microbial activity.
“Recalcitrance can also be modelled using a delay time of decomposition in dependence of accessible soil pore space, which simulate the physical protective effect of soil from microbial activity [176].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [176] Ludwig B, Kuka K, Franko U, von Luetzow M (2008) Comparison of two quantitative soil organic carbon models with a conceptual model using data from an agricultural long-term experiment. J Plant Nutr Soil Sci 171(1):83–90. doi: 10.1002/jpln.200700053 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing), S4 (based).
Interpretationnone givenIn perennials, biological protection (longevity) of coarse roots, stool and rhizomes is a major conceptual challenge that has not been met.
“In perennials, however, biological protection (longevity) of coarse roots, stool and rhizomes (see above) is a major conceptual challenge that has not been met.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenEffects from the environment, fertility and management, such as harvest intensity, are not covered in dose-response experiments, and evidence for target ecosystems like marginal land is underrepresented.
“Fourth, effects from the environment, fertility and management, e.g. harvest intensity of the systems, are not covered in dose–response experiments, and evidence for target ecosystems, like marginal land, is underrepresented.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationData for ∆SOC from marginal soils with low baseline SOC are target areas but are not available to validate a generalised model.
“Data for ∆SOC from marginal soils with a low baseline SOC, such as the site in Ireland [135], are target areas but are not available to validate a generalised model.”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [135] Dondini M, Hastings A, Saiz G, Jones MB, Smith P (2009) The potential of Miscanthus to sequester carbon in soils: comparing field measurements in Carlow, Ireland to model predictions. Glob Chang Biol Bioenergy 1(6):413–425. doi: 10.1111/j.1757-1707.2010.01033.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based).
InterpretationreasoningExperimental evidence for SOC dynamics, size and persistence of SOC pools prior to establishment, during the lifetime and after termination of PECs must underpin modelling.
“Experimental evidence for the SOC dynamics, size and persistence of the SOC pools prior to establishment, during the lifetime and after termination of the PECs must underpin modelling.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationVariation in bulk density increases uncertainty of stock changes and needs to be accounted for to capture spatial heterogeneity effects on SOC dynamics and sequestration.
“Bulk density in particular is a dynamic property when changing from arable to perennial agricultural systems [24], and its variation increases the uncertainty of stock changes [80, 164, 184] and needs to be accounted for to capture the effect of spatial heterogeneity on SOC dynamics and sequestration.”
Quote in the paperNot a substantial claim0 of 3 sources checked- cites [80] Richter GM, Agostini F, Redmile-Gordon M, White R, Goulding KWT (2015) Sequestration of C in soils under Miscanthus can be marginal and is affected by genotype-specific root distribution. Agric Ecosyst Environ 200(1):169–177. doi: 10.1016/j.agee.2014.11.011 source
Not checked in the free run.
- cites [164] Nieto OM, Castro J, Fernandez E, Smith P (2010) Simulation of soil organic carbon stocks in a Mediterranean olive grove under different soil-management systems using the RothC model. Soil Use Manag 26(2):118–125. doi: 10.1111/j.1475-2743.2010.00265.x source
Not checked in the free run.
- cites [184] Schmer MR, Liebig MA, Vogel KP, Mitchell RB (2011) Field-scale soil property changes under switchgrass managed for bioenergy. Glob Chang Biol Bioenergy 3(6):439–448. doi: 10.1111/j.1757-1707.2011.01099.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S2 (checkable), S4 (based).
Interpretationnone givenC sequestration implies a long-term view and analysis on SOC fractions that represent a turnover time in excess of 25 to 50 years.
“C sequestration implies a long-term view and analysis on SOC fractions that represent a turnover time in excess of 25 to 50 years.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationProcess-based SOC models usually have decomposition reduction functions based on soil moisture, derived from soil water potential or soil water content.
“Usually, process-based SOC models [41, 182] have decomposition reduction functions based on soil moisture, derived from the soil water potential or soil water content.”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [41] Bauer J, Herbst M, Huisman JA, Weihermuller L, Vereecken H (2008) Sensitivity of simulated soil heterotrophic respiration to temperature and moisture reduction functions. Geoderma 145(1–2):17–27. doi: 10.1016/j.geoderma.2008.01.026 source
Not checked in the free run.
- cites [182] Findeling A, Garnier P, Coppens F, Lafolie F, Recous S (2007) Modelling water, carbon and nitrogen dynamics in soil covered with decomposing mulch. Eur J Soil Sci 58:196–206 source
Not checked in the free run.
May combine two claims.
InterpretationreasoningLaborious alternative methods have filled knowledge gaps but described dynamics in young plantations, which may not be extrapolated to mature stands.
“Laborious alternative methods have filled knowledge gaps but described dynamics in young plantations, which may not be extrapolated to mature stands.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationAn alternative up-scaling technique is to run C process models at small scales to initialise larger spatial regression models.
“An alternative up-scaling technique is to run C process models (i.e. RothC) at small scales to initialise larger spatial regression models [185].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [185] Guo L, Falloon P, Coleman K, Zhou B, Li Y, Lin E, Zhang F (2007) Application of the RothC model to the results of long-term experiments on typical upland soils in northern China. Soil Use Manag 23(1):63–70. doi: 10.1111/j.1475-2743.2006.00056.x source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationBauer et al. compared decomposition routines in a modified RothC and showed 2 % sensitivity of CO2 emissions due to soil moisture variation.
“Bauer et al. [41] compared various decomposition routines in a unique modified version of RothC and showed 2 % sensitivity of CO2 emissions due to soil moisture variation.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [41] Bauer J, Herbst M, Huisman JA, Weihermuller L, Vereecken H (2008) Sensitivity of simulated soil heterotrophic respiration to temperature and moisture reduction functions. Geoderma 145(1–2):17–27. doi: 10.1016/j.geoderma.2008.01.026 source
Not checked in the free run.
May combine two claims.
InterpretationcitationAssumptions that the soil-crop system was at potential productivity and equilibrium could be wrong where net SOC formation is delayed, cover is patchy, or residues vary in decomposability.
“Their assumptions that the soil-crop system was at potential productivity, and equilibrium could be wrong where net SOC formation is delayed [86], cover is patchy [46, 139] or residues vary in their decomposability [108].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [86] Zatta A, Clifton-Brown J, Robson P, Hastings A, Monti A (2014) Land use change from C3 grassland to C4 Miscanthus: effects on soil carbon content and estimated mitigation benefit after six years. GCB Bioenergy 6(4):360–370. doi: 10.1111/gcbb.12054 source
Not checked in the free run.
- cites [46] Zimmermann J, Styles D, Hastings A, Dauber J, Jones MB (2014) Assessing the impact of within crop heterogeneity (‘patchiness’) in young Miscanthus × giganteus fields on economic feasibility and soil carbon sequestration. GCB Bioenergy 6(5):566–576. doi: 10.1111/gcbb.12084 source
Not checked in the free run.
- cites [139] Zimmermann J, Dondini M, Jones MB (2013) Assessing the impacts of the establishment of Miscanthus on soil organic carbon on two contrasting land-use types in Ireland. Eur J Soil Sci 64(6):747–756. doi: 10.1111/ejss.12087 source
Not checked in the free run.
- cites [108] Magid J, Luxhoi J, Lyshede OB (2004) Decomposition of plant residues at low temperatures separates turnover of nitrogen and energy rich tissue components in time. Plant Soil 258(1):351–365 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
InterpretationreasoningTopography and soil distribution maps can be included as inputs to process-based models to simulate impacts on growth and SOC for PECs.
“Indeed, topography and soil distribution maps can be included as inputs to process-based models to simulate the impacts on growth and SOC for PECs.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
Interpretationnone givenIt is difficult to obtain sufficiently detailed and widespread data to generalise and verify a generic process description.
“It is difficult to obtain sufficiently detailed and widespread data to generalise and verify a generic process description.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S4 (based).
Interpretationnone givenReliable projections can only be achieved if simulations capture short- and long-term dynamics, synthesising data from chrono-sequences, disaggregating inputs and understanding C fluxes within SOC fractions.
“In terms of modelling, reliable projections can only be achieved if simulations capture short- and long-term dynamics, synthesising data from chrono-sequences, disaggregating inputs and understanding C fluxes within SOC fractions.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationnone givenTurnover is derived from time series estimating productivity/mortality over standing biomass, but time series are the exception over single snapshot observations.
“Turnover is derived from time series estimating productivity/mortality over standing biomass, but time series are the exception over single ‘snapshot’ observations.”
Quote in the paperNot a substantial claim
The authors state this as an assumption.
The carbon cycle of perennial energy crops can be divided into qualitatively different inputs from aboveground biomass and belowground biomass.
“The C cycle of PECs is assumed to be divided into qualitatively different inputs from AGB and BGB (Fig. 1).”
The paper relies on this without support.
Data from switchgrass and poplar are appropriate proxies for Miscanthus and willow.
“due to the scarcity of some direct experimental evidence in these crops, data from two proxy crops, switchgrass and poplar, have also been used.”
The paper relies on this without support.
Inputs and turnover rates are the critical components affecting carbon sequestration rate.
“The critical components that affect C sequestration rate are inputs and turnover rates”
The paper relies on this without support.
The area of land devoted to perennial energy crops is likely to increase.
“The area of land devoted to PECs is likely to increase as countries seek to reduce their dependence on fossil fuels and greenhouse gas (GHG) emissions for climate change mitigation.”
The paper relies on this without support.
The physical and chemical stabilities of soil organic carbon pools are essential in defining the sustainability of carbon sequestration, with a half-life greater than 25 years.
“although they are essential in defining the sustainability of C sequestration (half-life >25 years).”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Soil organic carbon increase by switchgrass ranges from -0.6 to 4.3 Mg C ha−1 year−1, depending on climate, soil properties, land use history and so on.
“Soil organic carbon increase by switchgrass ranges from -0.6 to 4.3 Mg C ha -1 year -1 , depending on climate, soil properties, land use history and so on (Agostini et al., 2015; Dheri et al., 2022; Follett et al., 2012; Jin et al., 2019; Lee et al., 2007; Lemus & Lal, 2005; Liebig et al., 2008; Slessarev et al., 2020; Valdez et al., 2017).”
From Global warming intensity of biofuel derived from switchgrass grown on marginal land in Michigan (2023) · cites this paper as Agostini et al., 2015
Table 3 (Review Method: Meta-Analysis and Data Synthesis; page unavailable) reports switchgrass soil-carbon changes across differing soils and environmental conditions, supporting the general point that rates vary. It does not report the claimed −0.6 to 4.3 Mg C ha−1 year−1 range: its listed switchgrass values are positive and reach 3.71 at most. (LLM, conf=0.88)
Experimental — accuracy not yet measuredAs a result of high C input to the soil, PECs have shown high soil C sequestration rates.
“As a result of this high C input to the soil (Agostini et al., 2015; Klimešová & Martínková, 2018), PECs have shown high soil C sequestration rates (Chimento et al., 2016; Lemus & Lal, 2005; Sartori et al., 2006).”
From Belowground biomass C outweighs soil organic C of perennial energy crops: Insights from a long‐term multispecies trial (2021) · cites this paper as Agostini et al., 2015
These values are well above the proposed sequestration requirement of 0.25 tC/ha/year to make the crop carbon neutral once converted to biofuels.
“It is reported that these values are well above the proposed sequestration requirement (0.25 tCha -1 year -1 ) to make the crop carbon neutral once converted to biofuels (Agostini et al. 2015).”
From Strategies for mitigation of climate change: a review (2020) · cites this paper as Agostini et al. 2015
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Stated poplar fine-root input range omits lower tabulated values
MinorThe stated lower bound is 0.46 Mg C ha−1 year−1, but Table 1 lists a poplar fine-root input of 0.17 in the same units.
“Observed values of C input from fine roots of SRWC poplar range between 0.46 and 1.28 Mg C ha−1 year−1”
“| SRWC | P | Fine root | 2 | 0–15 cm | Sandy | 9.5 °C; 726 mm | Soil coring | 0.17 | Berhongaray [81] | |”
Switchgrass is not shown to sequester twice as much SOC
MinorThe paper says switchgrass sequestered twice as much SOC as Miscanthus, but its stated averages are 1.59 and 1.21, a ratio of about 1.31.
“Rhizome inputs from switchgrass were much smaller than from Miscanthus which explains the evidence that switchgrass sequestered twice the amount of SOC (Fig. 4).”
“For switchgrass, similar average inputs appear to cause an overall 25 % higher average stock change (∆SOC, Fig. 4) than Miscanthus (1.59 vs 1.21 Mg C ha−1 year−1)”
Cites
Temperature sensitivity of soil carbon decomposition and feedbacks to climate change
Davidson, E. A., & Janssens, I. A. (2006) · Nature · doi:10.1038/nature04514 · Cited by 6,919 · see citing works
Soil carbon sequestration and land‐use change: processes and potential
Post, W. M., & Kwon, K. C. (2000) · Global Change Biology · doi:10.1046/j.1365-2486.2000.00308.x · Cited by 2,602 · see citing works
Is soil carbon mostly root carbon? Mechanisms for a specific stabilisation
Rasse, D. P., Rumpel, C., & Dignac, M.-F. (2005) · Plant and Soil · doi:10.1007/s11104-004-0907-y · Cited by 1,861 · see citing works
Conant, R. T., Ryan, M. G., Ågren, G. I., Birge, H. E., Davidson, E. A., Eliasson, P. E., Evans, S. E., Frey, S. D., Giardina, C. P., Hopkins, F. M., et al. (2011) · Global Change Biology · doi:10.1111/j.1365-2486.2011.02496.x · Cited by 1,635 · see citing works
Soil organic matter turnover is governed by accessibility not recalcitrance
Dungait, J. A. J., Hopkins, D. W., Gregory, A. S., & Whitmore, A. P. (2012) · Global Change Biology · doi:10.1111/j.1365-2486.2012.02665.x · Cited by 1,616 · see citing works
Self-citationSOM fractionation methods: Relevance to functional pools and to stabilization mechanisms
von Lützow, M., Kögel-Knabner, I., Ekschmitt, K., Flessa, H., Guggenberger, G., Matzner, E., & Marschner, B. (2007) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2007.03.007 · Cited by 1,590 · see citing works
Lal, R. (2008) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2185 · Cited by 1,413 · see citing works
Lewandowski, I., Scurlock, J. M. O., Lindvall, E., & Christou, M. (2003) · Biomass and Bioenergy · doi:10.1016/s0961-9534(03)00030-8 · Cited by 1,360 · see citing works
Global patterns of root turnover for terrestrial ecosystems
GILL, R. A., & JACKSON, R. B. (2000) · New Phytologist · doi:10.1046/j.1469-8137.2000.00681.x · Cited by 1,300 · see citing works
Assessment Methods for Soil Carbon
Kimble, J. M., Follett, R. F., & Stewart, B. A. (2000) · CRC Press eBooks · doi:10.1201/9781482278644 · Cited by 1,095 · see citing works
Development of switchgrass (Panicum virgatum) as a bioenergy feedstock in the United States
McLaughlin, S. B., & Adams Kszos, L. (2005) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2004.05.006 · Cited by 1,091 · see citing works
Soil fertility limits carbon sequestration by forest ecosystems in a CO2-enriched atmosphere
Oren, R., Ellsworth, D. S., Johnsen, K. H., Phillips, N., Ewers, B. E., Maier, C., Schäfer, K. V. R., McCarthy, H., Hendrey, G., McNulty, S. G., et al. (2001) · Nature · doi:10.1038/35078064 · Cited by 1,084 · see citing works
DAYCENT and its land surface submodel: description and testing
Parton, W. J., Hartman, M., Ojima, D., & Schimel, D. (1998) · Global and Planetary Change · doi:10.1016/s0921-8181(98)00040-x · Cited by 865 · see citing works
Fate of lignins in soils: A review
Thevenot, M., Dignac, M.-F., & Rumpel, C. (2010) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2010.03.017 · Cited by 796 · see citing works
Soil carbon and nitrogen mineralization: Theory and models across scales
Manzoni, S., & Porporato, A. (2009) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2009.02.031 · Cited by 788 · see citing works
How relevant is recalcitrance for the stabilization of organic matter in soils?
Marschner, B., Brodowski, S., Dreves, A., Gleixner, G., Gude, A., Grootes, P. M., Hamer, U., Heim, A., Jandl, G., Ji, R., et al. (2008) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.200700049 · Cited by 743 · see citing works
van Hees, P. A. W., Jones, D. L., Finlay, R., Godbold, D. L., & Lundström, U. S. (2005) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2004.06.010 · Cited by 653 · see citing works
LIFE-CYCLE ASSESSMENT OF NET GREENHOUSE-GAS FLUX FOR BIOENERGY CROPPING SYSTEMS
Adler, P. R., Grosso, S. J. D., & Parton, W. J. (2007) · Ecological Applications · doi:10.1890/05-2018 · Cited by 652 · see citing works
Carbon cycling and sequestration opportunities in temperate grasslands
Soussana, J.-F., Soussana, J.-F., Loiseau, P., Vuichard, N., Ceschia, E., Balesdent, J., Chevallier, T., & Arrouays, D. (2004) · Soil Use and Management · doi:10.1079/sum2003234 · Cited by 563 · see citing works
Fine Roots, Net Primary Production, and Soil Nitrogen Availability: A New Hypothesis
Nadelhoffer, K. J., Aber, J. D., & Melillo, J. M. (1985) · Ecology · doi:10.2307/1939190 · Cited by 546 · see citing works
Aber, J. D., Melillo, J. M., & McClaugherty, C. A. (1990) · Canadian Journal of Botany · doi:10.1139/b90-287 · Cited by 529 · see citing works
Measured soil organic matter fractions can be related to pools in the RothC model
Zimmermann, M., Leifeld, J., Schmidt, M. W. I., Smith, P., & Fuhrer, J. (2007) · European Journal of Soil Science · doi:10.1111/j.1365-2389.2006.00855.x · Cited by 469 · see citing works
Bioenergy crops and carbon sequestration
Lemus, R., & Lal, R. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680590910393 · Cited by 455 · see citing works
Kell, D. B. (2011) · Annals of Botany · doi:10.1093/aob/mcr175 · Cited by 439 · see citing works
Simulating trends in soil organic carbon in long-term experiments using RothC-26.3
Coleman, K., Jenkinson, D. S., Crocker, G. J., Grace, P. R., Klír, J., Körschens, M., Poulton, P. R., & Richter, D. D. (1997) · Geoderma · doi:10.1016/s0016-7061(97)00079-7 · Cited by 420 · see citing works
Carbon mitigation by the energy crop, <i>Miscanthus</i>
CLIFTON‐BROWN, J. C., BREUER, J., & JONES, M. B. (2007) · Global Change Biology · doi:10.1111/j.1365-2486.2007.01438.x · Cited by 393 · see citing works
Changes in soil organic carbon under biofuel crops
ANDERSON‐TEIXEIRA, K. J., DAVIS, S. C., MASTERS, M. D., & DELUCIA, E. H. (2009) · GCB Bioenergy · doi:10.1111/j.1757-1707.2008.01001.x · Cited by 391 · see citing works
Don, A., Osborne, B., Hastings, A., Skiba, U., Carter, M. S., Drewer, J., Flessa, H., Freibauer, A., Hyvönen, N., Jones, M. B., et al. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01116.x · Cited by 363 · see citing works
Chemical Composition of Crop Biomass Impacts Its Decomposition
Johnson, J. M.-F., Barbour, N. W., & Weyers, S. L. (2007) · Soil Science Society of America Journal · doi:10.2136/sssaj2005.0419 · Cited by 336 · see citing works
Cheng, W. (2009) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2008.04.018 · Cited by 323 · see citing works
Lewandowski, I., & Schmidt, U. (2006) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2005.08.003 · Cited by 310 · see citing works
Measurements necessary for assessing the net ecosystem carbon budget of croplands
Smith, P., Lanigan, G., Kutsch, W. L., Buchmann, N., Eugster, W., Aubinet, M., Ceschia, E., Béziat, P., Yeluripati, J. B., Osborne, B., et al. (2010) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2010.04.004 · Cited by 308 · see citing works
Eiland, F., Klamer, M., Lind, A.-M., Leth, M., & Bååth, E. (2001) · Microbial Ecology · doi:10.1007/s002480000071 · Cited by 302 · see citing works
Reciprocal transfer of carbon and nitrogen by decomposer fungi at the soil–litter interface
Frey, S. D., Six, J., & Elliott, E. T. (2003) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(03)00155-x · Cited by 291 · see citing works
Lewandowski, I., & Heinz, A. (2003) · European Journal of Agronomy · doi:10.1016/s1161-0301(02)00018-7 · Cited by 280 · see citing works
Heaton, E. A., Dohleman, F. G., Miguez, A. F., Juvik, J. A., Lozovaya, V., Widholm, J., Zabotina, O. A., McIsaac, G. F., David, M. B., Voigt, T. B., et al. (2010) · Advances in Botanical Research · doi:10.1016/b978-0-12-381518-7.00003-0 · Cited by 258 · see citing works
BODDY, E., HILL, P., FARRAR, J., & JONES, D. (2007) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2006.09.030 · Cited by 251 · see citing works
Biomass and Carbon Partitioning in Switchgrass
Frank, A. B., Berdahl, J. D., Hanson, J. D., Liebig, M. A., & Johnson, H. A. (2004) · Crop Science · doi:10.2135/cropsci2004.1391 · Cited by 243 · see citing works
Kuzovkina, Y. A., & Volk, T. A. (2009) · Ecological Engineering · doi:10.1016/j.ecoleng.2009.03.010 · Cited by 242 · see citing works
The turnover of organic carbon in subsoils. Part 2. Modelling carbon turnover
Jenkinson, D. S., & Coleman, K. (2008) · European Journal of Soil Science · doi:10.1111/j.1365-2389.2008.01026.x · Cited by 241 · see citing works
Labile, recalcitrant, and inert organic matter in Mediterranean forest soils
Rovira, P., & Ramón Vallejo, V. (2007) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2006.07.021 · Cited by 235 · see citing works
Growing fuel: a sustainability assessment of willow biomass crops
Volk, T. A., Verwijst, T., Tharakan, P. J., Abrahamson, L. P., & White, E. H. (2004) · Frontiers in Ecology and the Environment · doi:10.1890/1540-9295(2004)002[0411:gfasao]2.0.co;2 · Cited by 232 · see citing works
Davis, S. C., Parton, W. J., Dohleman, F. G., Smith, C. M., Grosso, S. D., Kent, A. D., & DeLucia, E. H. (2010) · Ecosystems · doi:10.1007/s10021-009-9306-9 · Cited by 232 · see citing works
Soil carbon under switchgrass stands and cultivated cropland
Liebig, M. A., Johnson, H. A., Hanson, J. D., & Frank, A. B. (2005) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2004.11.004 · Cited by 225 · see citing works
Himken, M., Lammel, J., Neukirchen, D., Czypionka-Krause, U., & Olfs, H.-W. (1997) · Plant and Soil · doi:10.1023/a:1004244614537 · Cited by 218 · see citing works
Carbon sequestration in perennial bioenergy, annual corn and uncultivated systems in southern Quebec
Zan, C. S., Fyles, J. W., Girouard, P., & Samson, R. A. (2001) · Agriculture, Ecosystems & Environment · doi:10.1016/s0167-8809(00)00273-5 · Cited by 218 · see citing works
Root distribution and soil moisture retrieval in perennial and annual energy crops in Northern Italy
Monti, A., & Zatta, A. (2009) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2009.04.007 · Cited by 213 · see citing works
Kahle, P., Beuch, S., Boelcke, B., Leinweber, P., & Schulten, H.-R. (2001) · European Journal of Agronomy · doi:10.1016/s1161-0301(01)00102-2 · Cited by 208 · see citing works
Tufekcioglu, A., Raich, J. W., Isenhart, T. M., & Schultz, R. C. (1998) · Agroforestry Systems · doi:10.1023/a:1006221921806 · Cited by 207 · see citing works
Powlson, D. S., Glendining, M. J., Coleman, K., & Whitmore, A. P. (2011) · Agronomy Journal · doi:10.2134/agronj2010.0146s · Cited by 206 · see citing works
Soil Carbon Storage by Switchgrass Grown for Bioenergy
Liebig, M. A., Schmer, M. R., Vogel, K. P., & Mitchell, R. B. (2008) · BioEnergy Research · doi:10.1007/s12155-008-9019-5 · Cited by 203 · see citing works
Carbon sequestration in soil beneath long-term Miscanthus plantations as determined by abundance
Hansen, E. M., Christensen, B. T., Jensen, L. S., & Kristensen, K. (2004) · Biomass and Bioenergy · doi:10.1016/s0961-9534(03)00102-8 · Cited by 197 · see citing works
Comparison of corn and switchgrass on marginal soils for bioenergy
Varvel, G. E., Vogel, K. P., Mitchell, R. B., Follett, R. F., & Kimble, J. M. (2008) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2007.07.003 · Cited by 197 · see citing works
Sartori, F., Lal, R., Ebinger, M. H., & Eaton, J. A. (2007) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2007.01.026 · Cited by 190 · see citing works
Lee, D. K., Owens, V. N., & Doolittle, J. J. (2007) · Agronomy Journal · doi:10.2134/agronj2006.0152 · Cited by 181 · see citing works
Modeling consequences of straw residues export on soil organic carbon
Saffih-Hdadi, K., & Mary, B. (2008) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2007.08.022 · Cited by 179 · see citing works
Fang, S., Xue, J., & Tang, L. (2007) · Journal of Environmental Management · doi:10.1016/j.jenvman.2006.09.014 · Cited by 179 · see citing works
Soil carbon changes associated with short-rotation systems
Grigal, D. F., & Berguson, W. E. (1998) · Biomass and Bioenergy · doi:10.1016/s0961-9534(97)10073-3 · Cited by 176 · see citing works
Altered Belowground Carbon Cycling Following Land-Use Change to Perennial Bioenergy Crops
Anderson-Teixeira, K. J., Masters, M. D., Black, C. K., Zeri, M., Hussain, M. Z., Bernacchi, C. J., & DeLucia, E. H. (2013) · Ecosystems · doi:10.1007/s10021-012-9628-x · Cited by 175 · see citing works
Dohleman, F. G., Heaton, E. A., Arundale, R. A., & Long, S. P. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01153.x · Cited by 175 · see citing works
HILLIER, J., WHITTAKER, C., DAILEY, G., AYLOTT, M., CASELLA, E., RICHTER, G. M., RICHE, A., MURPHY, R., TAYLOR, G., & SMITH, P. (2009) · GCB Bioenergy · doi:10.1111/j.1757-1707.2009.01021.x · Cited by 169 · see citing works
Self-citationTufekcioglu, A., Raich, J. W., Isenhart, T. M., & Schultz, R. C. (2003) · Agroforestry Systems · doi:10.1023/a:1024898615284 · Cited by 168 · see citing works
Soil carbon sequestration beneath hybrid poplar plantations in the north central United States
Hansen, E. A. (1993) · Biomass and Bioenergy · doi:10.1016/0961-9534(93)90038-6 · Cited by 167 · see citing works
Rubino, M., Dungait, J. A. J., Evershed, R. P., Bertolini, T., De Angelis, P., D’Onofrio, A., Lagomarsino, A., Lubritto, C., Merola, A., & Terrasi, F. (2010) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2010.02.018 · Cited by 166 · see citing works
Neukirchen, D., Himken, M., Lammel, J., Czypionka-Krause, U., & Olfs, H.-W. (1999) · European Journal of Agronomy · doi:10.1016/s1161-0301(99)00031-3 · Cited by 159 · see citing works
Paul, K. I., Polglase, P. J., & Richards, G. P. (2003) · Forest Ecology and Management · doi:10.1016/s0378-1127(02)00454-1 · Cited by 158 · see citing works
Soil Carbon Dynamics beneath Switchgrass as Indicated by Stable Isotope Analysis
Garten, C. T., & Wullschleger, S. D. (2000) · Journal of Environmental Quality · doi:10.2134/jeq2000.00472425002900020036x · Cited by 154 · see citing works
Methods of Assessing Terrestrial Productivty
Whittaker, R. H., & Marks, P. L. (1975) · Ecological Studies · doi:10.1007/978-3-642-80913-2_4 · Cited by 153 · see citing works
Lovett, A. A., Sünnenberg, G., Richter, G. M., Dailey, A. G., Riche, A. B., & Karp, A. (2009) · BioEnergy Research · doi:10.1007/s12155-008-9030-x · Cited by 151 · see citing works
Self-citationStorage and turnover of carbon in grassland soils along an elevation gradient in the Swiss Alps
LEIFELD, J., ZIMMERMANN, M., FUHRER, J., & CONEN, F. (2009) · Global Change Biology · doi:10.1111/j.1365-2486.2008.01782.x · Cited by 148 · see citing works
Soil carbon sequestration by switchgrass and no-till maize grown for bioenergy
Follett, R. F., Vogel, K. P., Varvel, G. E., Mitchell, R. B., & Kimble, J. (2012) · BioEnergy Research · doi:10.1007/s12155-012-9198-y · Cited by 146 · see citing works
Land use change effects on ecosystem carbon balance: From agricultural to hybrid poplar plantation
Arevalo, C. B. M., Bhatti, J. S., Chang, S. X., & Sidders, D. (2011) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2011.03.013 · Cited by 140 · see citing works
A review of carbon and nitrogen balances in switchgrass grown for energy
Bransby, D. I., McLaughlin, S. B., & Parrish, D. J. (1998) · Biomass and Bioenergy · doi:10.1016/s0961-9534(97)10074-5 · Cited by 136 · see citing works
Lichter, J., Barron, S. H., Bevacqua, C. E., Finzi, A. C., Irving, K. F., Stemmler, E. A., & Schlesinger, W. H. (2005) · Ecology · doi:10.1890/04-1205 · Cited by 134 · see citing works
Drewer, J., Finch, J. W., Lloyd, C. R., Baggs, E. M., & Skiba, U. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01136.x · Cited by 133 · see citing works
Potential Soil Carbon Sequestration and CO <sub>2</sub> Offset by Dedicated Energy Crops in the USA
Sartori, F., Lal, R., Ebinger, M. H., & Parrish, D. J. (2006) · Critical Reviews in Plant Sciences · doi:10.1080/07352680600961021 · Cited by 131 · see citing works
Bauer, J., Herbst, M., Huisman, J. A., Weihermüller, L., & Vereecken, H. (2008) · Geoderma · doi:10.1016/j.geoderma.2008.01.026 · Cited by 131 · see citing works
DONDINI, M., HASTINGS, A., SAIZ, G., JONES, M. B., & SMITH, P. (2009) · GCB Bioenergy · doi:10.1111/j.1757-1707.2010.01033.x · Cited by 131 · see citing works
Nieto, O. M., Castro, J., Fernández, E., & Smith, P. (2010) · Soil Use and Management · doi:10.1111/j.1475-2743.2010.00265.x · Cited by 130 · see citing works
A Review of Fine Root Dynamics in Populus Plantations
Block, R. M. A., Van Rees, K. C. J., & Knight, J. D. (2006) · Agroforestry Systems · doi:10.1007/s10457-005-2002-7 · Cited by 129 · see citing works
Mueller, C. W., & Koegel-Knabner, I. (2009) · Biology and Fertility of Soils · doi:10.1007/s00374-008-0336-9 · Cited by 127 · see citing works
Lal, R. (2003) · Land Degradation & Development · doi:10.1002/ldr.562 · Cited by 127 · see citing works
Climate and litter quality controls on decomposition: An analysis of modeling approaches
Moorhead, D. L., Currie, W. S., Rastetter, E. B., Parton, W. J., & Harmon, M. E. (1999) · Global Biogeochemical Cycles · doi:10.1029/1998gb900014 · Cited by 123 · see citing works
Differences in rhizosphere carbon-partitioning among plant species of different families
Warembourg, F. R., Roumet, C., & Lafont, F. (2003) · Plant and Soil · doi:10.1023/a:1026147622800 · Cited by 117 · see citing works
Derrien, D., & Amelung, W. (2011) · European Journal of Soil Science · doi:10.1111/j.1365-2389.2010.01333.x · Cited by 114 · see citing works
Hartman, J. C., Nippert, J. B., Orozco, R. A., & Springer, C. J. (2011) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2011.04.055 · Cited by 112 · see citing works
Amougou, N., Bertrand, I., Machet, J.-M., & Recous, S. (2011) · Plant and Soil · doi:10.1007/s11104-010-0443-x · Cited by 111 · see citing works
Longevity and turnover of roots in the shortgrass steppe: influence of diameter and depth
Gill, R. A., Burke, I. C., Lauenroth, W. K., & Milchunas, D. G. (2002) · Plant Ecology · doi:10.1023/a:1015529507670 · Cited by 110 · see citing works
Soil organic carbon and root distribution in a temperate arable agroforestry system
Upson, M. A., & Burgess, P. J. (2013) · Plant and Soil · doi:10.1007/s11104-013-1733-x · Cited by 109 · see citing works
Wander, M. M., & Yang, X. (2000) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00031-6 · Cited by 106 · see citing works
The potential of willow and poplar plantations as carbon sinks in Sweden
Rytter, R.-M. (2012) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2011.10.012 · Cited by 105 · see citing works
Free-air CO2 enrichment (FACE) enhances biomass production in a short-rotation poplar plantation
Calfapietra, C., Gielen, B., Galema, A. N. J., Lukac, M., De Angelis, P., Moscatelli, M. C., Ceulemans, R., & Scarascia-Mugnozza, G. (2003) · Tree Physiology · doi:10.1093/treephys/23.12.805 · Cited by 105 · see citing works
Zatta, A., Clifton‐Brown, J., Robson, P., Hastings, A., & Monti, A. (2014) · GCB Bioenergy · doi:10.1111/gcbb.12054 · Cited by 104 · see citing works
Modelling soil carbon and nitrogen cycles during land use change. A review
Batlle-Aguilar, J., Brovelli, A., Porporato, A., & Barry, D. A. (2011) · Agronomy for Sustainable Development · doi:10.1051/agro/2010007 · Cited by 101 · see citing works
Variation in root architecture among switchgrass cultivars impacts root decomposition rates
de Graaff, M., Six, J., JASTROW, J. D., Schadt, C. W., & Wullschleger, S. D. (2012) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2012.11.015 · Cited by 100 · see citing works
Cotrufo, M. F., De Angelis, P., & Polle, A. (2005) · Global Change Biology · doi:10.1111/j.1365-2486.2005.00958.x · Cited by 100 · see citing works
SOMPROF: A vertically explicit soil organic matter model
Braakhekke, M. C., Beer, C., Hoosbeek, M. R., Reichstein, M., Kruijt, B., Schrumpf, M., & Kabat, P. (2011) · Ecological Modelling · doi:10.1016/j.ecolmodel.2011.02.015 · Cited by 98 · see citing works
Xu, X., Liu, W., & Kiely, G. (2011) · Agriculture Ecosystems & Environment · doi:10.1016/j.agee.2010.12.018 · Cited by 97 · see citing works
Romanyà, J., Cortina, J., Falloon, P., Coleman, K., & Smith, P. (2000) · European Journal of Soil Science · doi:10.1111/j.1365-2389.2000.00343.x · Cited by 96 · see citing works
Rytter, R.-M. (2001) · Forest Ecology and Management · doi:10.1016/s0378-1127(00)00319-4 · Cited by 94 · see citing works
Guber, A. K., Pachepsky, Y. A., van Genuchten, M. T., Rawls, W. J., Simunek, J., Jacques, D., Nicholson, T. J., & Cady, R. E. (2006) · Vadose Zone Journal · doi:10.2136/vzj2005.0111 · Cited by 91 · see citing works
Poeplau, C., & Don, A. (2014) · GCB Bioenergy · doi:10.1111/gcbb.12043 · Cited by 89 · see citing works
Rytter, R.-M., & Hansson, A.-C. (1996) · Biomass and Bioenergy · doi:10.1016/0961-9534(96)00023-2 · Cited by 86 · see citing works
Felten, D., & Emmerling, C. (2011) · Applied Soil Ecology · doi:10.1016/j.apsoil.2011.06.001 · Cited by 83 · see citing works
Field-scale soil property changes under switchgrass managed for bioenergy
SCHMER, M. R., LIEBIG, M. A., VOGEL, K. P., & MITCHELL, R. B. (2011) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01099.x · Cited by 82 · see citing works
Zimmermann, J., Dauber, J., & Jones, M. B. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01117.x · Cited by 80 · see citing works
Grogan, P., & Matthews, R. (2002) · Soil Use and Management · doi:10.1111/j.1475-2743.2002.tb00237.x · Cited by 80 · see citing works
Guo, L., Falloon, P., Coleman, K., Zhou, B., Li, Y., Lin, E., & Zhang, F. (2007) · Soil Use and Management · doi:10.1111/j.1475-2743.2006.00056.x · Cited by 80 · see citing works
Foereid, B., de Neergaard, A., & Høgh-Jensen, H. (2004) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2004.03.002 · Cited by 80 · see citing works
Herbst, M., Hellebrand, H. J., Bauer, J., Huisman, J. A., Šimůnek, J., Weihermüller, L., Graf, A., Vanderborght, J., & Vereecken, H. (2008) · Ecological Modelling · doi:10.1016/j.ecolmodel.2008.02.007 · Cited by 80 · see citing works
Simulating decomposition of labile soil organic carbon: Effects of pH
LEIFELD, J., ZIMMERMANN, M., & FUHRER, J. (2008) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2008.08.019 · Cited by 79 · see citing works
Garten, C. T., Smith, J. L., Tyler, D. D., Amonette, J. E., Bailey, V. L., Brice, D. J., Castro, H. F., Graham, R. L., Gunderson, C. A., Izaurralde, R. C., et al. (2010) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2009.12.019 · Cited by 79 · see citing works
Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment
Gielen, B., Calfapietra, C., Lukac, M., Wittig, V. E., De Angelis, P., Janssens, I. A., Moscatelli, M. C., Grego, S., Cotrufo, M. F., Godbold, D. L., et al. (2005) · Tree Physiology · doi:10.1093/treephys/25.11.1399 · Cited by 78 · see citing works
Sensitivity analysis of predicted change in soil carbon following afforestation
Paul, K. I., Polglase, P. J., & Richards, G. P. (2003) · Ecological Modelling · doi:10.1016/s0304-3800(03)00027-9 · Cited by 77 · see citing works
Al Afas, N., Marron, N., Zavalloni, C., & Ceulemans, R. (2008) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2007.11.007 · Cited by 77 · see citing works
Hamelin, L., Jørgensen, U., Petersen, B. M., Olesen, J. E., & Wenzel, H. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2012.01174.x · Cited by 77 · see citing works
Easter, M., Paustian, K., Killian, K., Williams, S., Feng, T., Al-Adamat, R., Batjes, N. H., Bernoux, M., Bhattacharyya, T., Cerri, C. C., et al. (2007) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2007.01.004 · Cited by 76 · see citing works
Beuch, S., Boelcke, B., & Belau, L. (2000) · Journal of Agronomy and Crop Science · doi:10.1046/j.1439-037x.2000.00367.x · Cited by 76 · see citing works
Pacaldo, R. S., Volk, T. A., & Briggs, R. D. (2013) · BioEnergy Research · doi:10.1007/s12155-012-9250-y · Cited by 75 · see citing works
Carbon dynamics subsequent to establishment of switchgrass
Ma, Z., Wood, C. W., & Bransby, D. I. (2000) · Biomass and Bioenergy · doi:10.1016/s0961-9534(99)00077-x · Cited by 75 · see citing works
Decomposition and mineralization of energy crop residues governed by earthworms
Ernst, G., Henseler, I., Felten, D., & Emmerling, C. (2009) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2009.04.015 · Cited by 74 · see citing works
Larsen, S. U., Jørgensen, U., Kjeldsen, J. B., & Lærke, P. E. (2014) · BioEnergy Research · doi:10.1007/s12155-013-9389-1 · Cited by 73 · see citing works
Comparison of approaches for estimating carbon sequestration at the regional scale
Falloon, P., Smith, P., Szabó, J., & Pásztor, L. (2002) · Soil Use and Management · doi:10.1111/j.1475-2743.2002.tb00236.x · Cited by 71 · see citing works
Cropping systems effects on improving soil carbon stocks of exposed subsoil
Al-Kaisi, M. M., & Grote, J. B. (2007) · Soil Science Society of America Journal · doi:10.2136/sssaj2006.0200 · Cited by 71 · see citing works
DONDINI, M., VAN GROENIGEN, K., DEL GALDO, I., & JONES, M. B. (2009) · GCB Bioenergy · doi:10.1111/j.1757-1707.2009.01025.x · Cited by 70 · see citing works
Nikièma, P., Rothstein, D. E., Min, D.-H., & Kapp, C. J. (2011) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2011.08.006 · Cited by 70 · see citing works
Christian, D. G., Poulton, P. R., Riche, A. B., Yates, N. E., & Todd, A. D. (2006) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2005.11.002 · Cited by 69 · see citing works
Magid, J., Luxhøi, J., & Lyshede, O. B. (2004) · Plant and Soil · doi:10.1023/b:plso.0000016565.14718.4b · Cited by 69 · see citing works
Lettens, S. (2003) · Biomass and Bioenergy · doi:10.1016/s0961-9534(02)00104-6 · Cited by 67 · see citing works
Gauder, M., Butterbach‐Bahl, K., Graeff‐Hönninger, S., Claupein, W., & Wiegel, R. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2011.01135.x · Cited by 64 · see citing works
<i>Miscanthus × giganteus</i> leaf senescence, decomposition and C and N inputs to soil
Amougou, N., Bertrand, I., Cadoux, S., & Recous, S. (2012) · GCB Bioenergy · doi:10.1111/j.1757-1707.2012.01192.x · Cited by 64 · see citing works
Berhongaray, G., El Kasmioui, O., & Ceulemans, R. (2013) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2013.07.003 · Cited by 61 · see citing works
Review and model-based analysis of factors influencing soil carbon sequestration under hybrid poplar
Garten, C. T., Wullschleger, S. D., & Classen, A. T. (2011) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2010.08.013 · Cited by 58 · see citing works
Richter, G. M., Agostini, F., Redmile-Gordon, M., White, R., & Goulding, K. W. T. (2015) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2014.11.011 · Cited by 57 · see citing works
Self-citationCarbon Sequestration under Irrigated Switchgrass ( <i>Panicum virgatum</i> L.) Production
Collins, H. P., Smith, J. L., Fransen, S., Alva, A. K., Kruger, C. E., & Granatstein, D. M. (2010) · Soil Science Society of America Journal · doi:10.2136/sssaj2010.0020 · Cited by 56 · see citing works
N2O emission from energy crop fields of Miscanthus “Giganteus” and winter rye
Jørgensen, R. N., Jørgensen, B. J., Nielsen, N. E., Maag, M., & Lind, A.-M. (1997) · Atmospheric Environment · doi:10.1016/s1352-2310(97)00128-3 · Cited by 55 · see citing works
Berhongaray, G., Janssens, I. A., King, J. S., & Ceulemans, R. (2013) · Plant and Soil · doi:10.1007/s11104-013-1778-x · Cited by 54 · see citing works
Modelling water, carbon and nitrogen dynamics in soil covered with decomposing mulch
Findeling, A., Garnier, P., Coppens, F., Lafolie, F., & Recous, S. (2007) · European Journal of Soil Science · doi:10.1111/j.1365-2389.2006.00826.x · Cited by 53 · see citing works
Lasch, P., Kollas, C., Rock, J., & Suckow, F. (2010) · Regional Environmental Change · doi:10.1007/s10113-009-0095-7 · Cited by 51 · see citing works
Fine-root Production and Turnover in a Willow Plantation Estimated by Different Calculation Methods
Rytter, R.-M. (1999) · Scandinavian Journal of Forest Research · doi:10.1080/02827589908540817 · Cited by 50 · see citing works
Evaluation of carbon sequestration in energetic crops (Miscanthus and coppice willow)
Borzęcka, M., Faber, A., & Borek, R. (2008) · International Agrophysics · Cited by 49 · see citing works
Prediction of decomposition of litter under eucalypts and pines using the FullCAM model
Paul, K. I., & Polglase, P. J. (2004) · Forest Ecology and Management · doi:10.1016/j.foreco.2003.11.007 · Cited by 48 · see citing works
Nikièma, P., Rothstein, D. E., & Miller, R. O. (2012) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2012.01.037 · Cited by 47 · see citing works
Šlapokas, T., & Granhall, U. (1991) · Biology and Fertility of Soils · doi:10.1007/bf00337374 · Cited by 45 · see citing works
NIKLAUS, P. A., & FALLOON, P. (2006) · Global Change Biology · doi:10.1111/j.1365-2486.2006.01215.x · Cited by 44 · see citing works
Growth, decay, and turnover rates of fine roots of basket willows
Rytter, R.-M., & Rytter, L. (1998) · Canadian Journal of Forest Research · doi:10.1139/x98-063 · Cited by 44 · see citing works
Luxhøi, J., Magid, J., Tscherko, D., & Kandeler, E. (2002) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(01)00208-5 · Cited by 44 · see citing works
Zenone, T., Gelfand, I., Chen, J., Hamilton, S. K., & Robertson, G. P. (2013) · Agricultural and Forest Meteorology · doi:10.1016/j.agrformet.2013.07.015 · Cited by 44 · see citing works
Rytter, R.-M. (2013) · Tree Physiology · doi:10.1093/treephys/tpt060 · Cited by 43 · see citing works
Soil carbon, soil nitrate, and soil emissions of nitrous oxide during cultivation of energy crops
Hellebrand, H. J., Strähle, M., Scholz, V., & Kern, J. (2010) · Nutrient Cycling in Agroecosystems · doi:10.1007/s10705-009-9326-z · Cited by 42 · see citing works
Aboveground productivity and soil carbon storage of biofuel crops in<scp>O</scp>hio
Bonin, C. L., & Lal, R. (2014) · GCB Bioenergy · doi:10.1111/gcbb.12041 · Cited by 41 · see citing works
Calibration of the RothC model to turnover of soil carbon under eucalypts and pines
Paul, K. I., & Polglase, P. J. (2004) · Soil Research · doi:10.1071/sr04025 · Cited by 41 · see citing works
Cattaneo, F., Barbanti, L., Gioacchini, P., Ciavatta, C., & Marzadori, C. (2014) · Biology and Fertility of Soils · doi:10.1007/s00374-014-0931-x · Cited by 40 · see citing works
TOMA, Y., FERNÁNDEZ, F. G., SATO, S., IZUMI, M., HATANO, R., YAMADA, T., NISHIWAKI, A., BOLLERO, G., & STEWART, J. R. (2011) · GCB Bioenergy · doi:10.1111/j.1757-1707.2010.01070.x · Cited by 40 · see citing works
Modelling Soil Carbon and Nitrogen Cycles During Land Use Change
Batlle‐Aguilar, J., Brovelli, A., Porporato, A. M., & Barry, D. A. (2011) · Springer eBooks · doi:10.1007/978-94-007-0394-0_23 · Cited by 39 · see citing works
Growing season greenhouse gas flux from switchgrass in the northern great plains
Schmer, M. R., Liebig, M. A., Hendrickson, J. R., Tanaka, D. L., & Phillips, R. L. (2012) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2012.05.026 · Cited by 38 · see citing works
Pacaldo, R. S., Volk, T. A., & Briggs, R. D. (2013) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2013.10.018 · Cited by 38 · see citing works
Forest soil carbon cycle under elevated CO2 - a case of increased throughput?
Lukac, M., Lagomarsino, A., Moscatelli, M. C., De Angelis, P., Cotrufo, M. F., & Godbold, D. L. (2009) · Forestry · doi:10.1093/forestry/cpn041 · Cited by 38 · see citing works
Kimble, J. M., Follett, R. F., & Stewart, B. A. (2000) · CRC Press eBooks · doi:10.1201/9781482278644-46 · Cited by 37 · see citing works
de Neergaard, A., Porter, J. R., & Gorissen, A. (2002) · Plant and Soil · doi:10.1023/a:1020414819264 · Cited by 33 · see citing works
Hoosbeek, M. R., Vos, J. M., Meinders, M. B. J., Velthorst, E. J., & Scarascia-Mugnozza, G. E. (2007) · Geoderma · doi:10.1016/j.geoderma.2006.11.008 · Cited by 32 · see citing works
Zimmermann, J., Styles, D., Hastings, A., Dauber, J., & Jones, M. B. (2014) · GCB Bioenergy · doi:10.1111/gcbb.12084 · Cited by 32 · see citing works
Thomas, A. R. C., Bond, A. J., & Hiscock, K. M. (2013) · GCB Bioenergy · doi:10.1111/j.1757-1707.2012.01198.x · Cited by 31 · see citing works
Pacaldo, R. S., Volk, T. A., & Briggs, R. D. (2014) · BioEnergy Research · doi:10.1007/s12155-014-9416-x · Cited by 30 · see citing works
Bauer, J., Kirschbaum, M. U. F., Weihermüller, L., Huisman, J. A., Herbst, M., & Vereecken, H. (2008) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2008.07.024 · Cited by 29 · see citing works
Yan, M., Zhang, X., Zhou, G., Gong, J., & You, X. (2010) · Journal of Arid Environments · doi:10.1016/j.jaridenv.2010.09.005 · Cited by 29 · see citing works
Long-term steady state <sup>13</sup> C labelling to investigate soil carbon turnover in grasslands
Klumpp, K., Soussana, J. F., & Falcimagne, R. (2007) · Biogeosciences · doi:10.5194/bg-4-385-2007 · Cited by 27 · see citing works
Carbon Source Quality and Placement Effects on Soil Organic Carbon Status
Wienhold, B. J., Varvel, G. E., Johnson, J. M. F., & Wilhelm, W. W. (2013) · BioEnergy Research · doi:10.1007/s12155-013-9301-z · Cited by 24 · see citing works
Zimmermann, J., Dondini, M., & Jones, M. B. (2013) · European Journal of Soil Science · doi:10.1111/ejss.12087 · Cited by 23 · see citing works
Masuzawa, T., & Hogetsu, K. (1977) · The Botanical Magazine Tokyo · doi:10.1007/bf02488356 · Cited by 23 · see citing works
Zhang, J., Shangguan, T., & Meng, Z. (2011) · Ecological Research · doi:10.1007/s11284-010-0772-5 · Cited by 23 · see citing works
Effects of elevated CO2 on below-ground processes in temperate marsh microcosms
Kim, S.-Y., & Kang, H. (2008) · Hydrobiologia · doi:10.1007/s10750-008-9325-0 · Cited by 23 · see citing works
Composition of root exudates of Miscanthus × Giganteus Greef et Deu
Hromádko, L., Vranová, V., Techer, D., Laval-Gilly, P., Rejšek, K., Formánek, P., & Falla, J. (2014) · Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis · doi:10.11118/actaun201058010071 · Cited by 21 · see citing works
Püttsepp, Ü., Lõhmus, K., & Koppel, A. (2007) · Silva Fennica · doi:10.14214/sf.294 · Cited by 16 · see citing works
Hashimoto, S., Wattenbach, M., & Smith, P. (2011) · Journal of Forest Research · doi:10.1007/s10310-010-0209-6 · Cited by 16 · see citing works
Kaňová, H., Carre, J., Vranová, V., Rejšek, K., & Formánek, P. (2014) · Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis · doi:10.11118/actaun201058050203 · Cited by 16 · see citing works
Abou Jaoudé, R., Lagomarsino, A., & De Angelis, P. (2011) · Plant and Soil · doi:10.1007/s11104-010-0570-4 · Cited by 16 · see citing works
Garten, C. T. (2012) · BioEnergy Research · doi:10.1007/s12155-011-9154-2 · Cited by 16 · see citing works
Leifeld, J. (2008) · Biogeochemistry · doi:10.1007/s10533-008-9209-4 · Cited by 16 · see citing works
Palmer, M. M., Forrester, J. A., Rothstein, D. E., & Mladenoff, D. J. (2014) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2014.01.021 · Cited by 16 · see citing works
Ludwig, B., Kuka, K., Franko, U., & von Lützow, M. (2008) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.200700053 · Cited by 15 · see citing works
Hoffmann, B., Müller, T., & Joergensen, R. G. (2010) · Journal of Plant Nutrition and Soil Science · doi:10.1002/jpln.200800187 · Cited by 15 · see citing works
Meehan, P. G., McDonnell, K. P., & Finnan, J. M. (2013) · GCB Bioenergy · doi:10.1111/j.1757-1707.2012.01205.x · Cited by 14 · see citing works
Kim, S., & Kim, J. G. (2009) · Journal of Plant Biology · doi:10.1007/s12374-009-9060-8 · Cited by 14 · see citing works
Kollas, C., Lasch‐Born, P., Rock, J., & Suckow, F. (2009) · Publication Database PIK (Potsdam Institute for Climate Impact Research (PIK)) · Cited by 13 · see citing works
Evaluation of Soil<sup>14</sup>C Data for Estimating Inert Organic Matter in the Rothc Model
Rethemeyer, J., Grootes, P. M., Brodowski, S., & Ludwig, B. (2007) · Radiocarbon · doi:10.1017/s0033822200042934 · Cited by 11 · see citing works
Yan, M., Zhang, X., Jiang, Y., & Zhou, G. (2011) · Soil Science & Plant Nutrition · doi:10.1080/00380768.2011.590943 · Cited by 8 · see citing works
Grogan, P., & Matthews, R. (2002) · Soil Use and Management · doi:10.1079/sum2002119 · Cited by 6 · see citing works
Shibu, M. E., Matthews, R. B., Bakam, I., Moffat, A. J., & Baggaley, N. J. (2012) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2012.09.039 · Cited by 5 · see citing works
Decomposition of Litter of Miscanthus sinensis during Five Years under Semi-natural Conditions
Yamane, I. (1974) · Institutional Repositories DataBase (IRDB) · Cited by 2 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- Kollas CP, Lasch JR, Suckow F (2009) Bioenergy potential in Germany—assessing spatial patterns of biomass production. Int Agrophysics 23:343–352
- Drewer J, Finch J, Lloyd R, Baggs E, Skiba U (2011) How do soil emission of N20, CH4 and CO2 from perennial bioenergy crops differ from arable annual crops? GCB Bioenergy. doi: 10.1111/j.1757-1707.2011.01136 · DOI
Cited by
Sorted by citations
Strategies for mitigation of climate change: a review
Fawzy, S., Osman, A. I., Doran, J., & Rooney, D. W. (2020) · Environmental Chemistry Letters · doi:10.1007/s10311-020-01059-w · Cited by 1,522 · see citing works
Environmental costs and benefits of growing<i>Miscanthus</i>for bioenergy in the<scp>UK</scp>
McCalmont, J. P., Hastings, A., McNamara, N. P., Richter, G. M., Robson, P., Donnison, I. S., & Clifton‐Brown, J. (2017) · GCB Bioenergy · doi:10.1111/gcbb.12294 · Cited by 244 · see citing works
Self-citationMicrobial competition for nitrogen and carbon is as intense in the subsoil as in the topsoil
Jones, D. L., Magthab, E. A., Gleeson, D. B., Hill, P. W., Sánchez‐Rodríguez, A. R., Roberts, P., Ge, T., & Murphy, D. V. (2017) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2017.10.024 · Cited by 193 · see citing works
Beneficial management of biomass combustion ashes
Zhai, J., Burke, I. T., & Stewart, D. I. (2021) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2021.111555 · Cited by 158 · see citing works
What Agriculture Can Learn from Native Ecosystems in Building Soil Organic Matter: A Review
Crews, T. E., & Rumsey, B. (2017) · Sustainability · doi:10.3390/su9040578 · Cited by 157 · see citing works
Mosier, S. L., Córdova, S. C., & Robertson, G. P. (2021) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2021.706142 · Cited by 144 · see citing works
Pulighe, G., Bonati, G., Colangeli, M., Morese, M. M., Traverso, L., Lupia, F., Khawaja, C., Janssen, R., & Fava, F. (2019) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2018.12.043 · Cited by 101 · see citing works
Amaducci, S., Facciotto, G., Bergante, S., Perego, A., Serra, P., Ferrarini, A., & Chimento, C. (2016) · GCB Bioenergy · doi:10.1111/gcbb.12341 · Cited by 98 · see citing works
Kluts, I. N., Wicke, B., Leemans, R., & Faaij, A. P. C. (2016) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2016.11.036 · Cited by 92 · see citing works
Ferrarini, A., Serra, P., Almagro, M., Trevisan, M., & Amaducci, S. (2017) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2017.01.052 · Cited by 89 · see citing works
Cunniff, J., Purdy, S., Barraclough, T. J. P., Castle, M., Maddison, A. L., Jones, L. E., Shield, I. F., Gregory, A. S., & Karp, A. (2015) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2015.04.020 · Cited by 88 · see citing works
Self-citationFuture landscapes: opportunities and challenges
Stanturf, J. A. (2015) · New Forests · doi:10.1007/s11056-015-9500-x · Cited by 78 · see citing works
Cost-optimal pathways towards net-zero chemicals and plastics based on a circular carbon economy
Zibunas, C., Meys, R., Kätelhön, A., & Bardow, A. (2022) · Computers & Chemical Engineering · doi:10.1016/j.compchemeng.2022.107798 · Cited by 72 · see citing works
Ferrarini, A., Fornasier, F., Serra, P., Ferrari, F., Trevisan, M., & Amaducci, S. (2017) · GCB Bioenergy · doi:10.1111/gcbb.12340 · Cited by 60 · see citing works
Kane, J. L., Schartiger, R. G., Daniels, N. K., Freedman, Z. B., McDonald, L. M., Skousen, J. G., & Morrissey, E. M. (2023) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2023.109178 · Cited by 59 · see citing works
Soil Erosion Mitigation by Perennial Species Under Mediterranean Environment
Cosentino, S. L., Copani, V., Scalici, G., Scordia, D., & Testa, G. (2015) · BioEnergy Research · doi:10.1007/s12155-015-9690-2 · Cited by 56 · see citing works
Berhongaray, G., Verlinden, M. S., Broeckx, L. S., Janssens, I. A., & Ceulemans, R. (2016) · GCB Bioenergy · doi:10.1111/gcbb.12369 · Cited by 54 · see citing works
A <i>Miscanthus</i> plantation can be carbon neutral without increasing soil carbon stocks
Robertson, A. D., Whitaker, J., Morrison, R., Davies, C. A., Smith, P., & McNamara, N. P. (2017) · GCB Bioenergy · doi:10.1111/gcbb.12397 · Cited by 52 · see citing works
Accumulation of soil organic carbon after cropland conversion to short‐rotation willow and poplar
Georgiadis, P., Vesterdal, L., Stupak, I., & Raulund‐Rasmussen, K. (2017) · GCB Bioenergy · doi:10.1111/gcbb.12416 · Cited by 52 · see citing works
Oliveira, N., Rodríguez‐Soalleiro, R., Pérez‐Cruzado, C., Cañellas, I., Sixto, H., & Ceulemans, R. (2018) · Forest Ecology and Management · doi:10.1016/j.foreco.2018.06.031 · Cited by 48 · see citing works
The role of temperate agroforestry in mitigating climate change: A review
Dmuchowski, W., Baczewska-Dąbrowska, A. H., & Gworek, B. (2023) · Forest Policy and Economics · doi:10.1016/j.forpol.2023.103136 · Cited by 46 · see citing works
Martani, E., Ferrarini, A., Serra, P., Pilla, M., Marcone, A., & Amaducci, S. (2021) · GCB Bioenergy · doi:10.1111/gcbb.12785 · Cited by 43 · see citing works
Giant reed for selenium phytoremediation under changing climate
El-Ramady, H. R., Abdalla, N. A., Alshaal, T., El-Henawy, A. S., Shams, M. S., Faizy, S. E.-D. A., Belal, E. B., Shehata, S. A., Ragab, M. I., Amer, M. M., et al. (2015) · Environmental Chemistry Letters · doi:10.1007/s10311-015-0523-5 · Cited by 43 · see citing works
Danelli, T., Sepulcri, A., Masetti, G., Colombo, F., Sangiorgio, S., Cassani, E., Anelli, S., Adani, F., & Pilu, R. (2021) · Applied Sciences · doi:10.3390/app11031147 · Cited by 42 · see citing works
Bosco, S., Nasso, N. N. O. D., Roncucci, N., Mazzoncini, M., & Bonari, E. (2016) · European Journal of Agronomy · doi:10.1016/j.eja.2016.04.006 · Cited by 40 · see citing works
Environmental assessment of the Ecuadorian cocoa value chain with statistics-based LCA
Avadí, Á. (2023) · The International Journal of Life Cycle Assessment · doi:10.1007/s11367-023-02142-4 · Cited by 39 · see citing works
Ruf, T., Makselon, J., Udelhoven, T., & Emmerling, C. (2018) · GCB Bioenergy · doi:10.1111/gcbb.12513 · Cited by 38 · see citing works
Martinez‐Feria, R., & Basso, B. (2020) · GCB Bioenergy · doi:10.1111/gcbb.12726 · Cited by 38 · see citing works
Carbon farming practices for European cropland: A review on the effect on soil organic carbon
Petersson, T., Antoniella, G., Perugini, L., Chiriacò, M. V., & Chiti, T. (2024) · Soil and Tillage Research · doi:10.1016/j.still.2024.106353 · Cited by 37 · see citing works
Rytter, R.-M. (2015) · Forest Ecology and Management · doi:10.1016/j.foreco.2015.12.026 · Cited by 37 · see citing works
Rytter, R.-M., Rytter, L., & Högbom, L. (2015) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2015.10.009 · Cited by 36 · see citing works
Climate impact and energy efficiency of woody bioenergy systems from a landscape perspective
Hammar, T., Stendahl, J., Sundberg, C., Holmström, H., & Hansson, P. (2018) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2018.11.026 · Cited by 36 · see citing works
Fortier, J., Truax, B., Gagnon, D., & Lambert, F. (2016) · Forests · doi:10.3390/f7020037 · Cited by 33 · see citing works
Plastic Allometry in Coarse Root Biomass of Mature Hybrid Poplar Plantations
Fortier, J., Truax, B., Gagnon, D., & Lambert, F. (2015) · BioEnergy Research · doi:10.1007/s12155-015-9621-2 · Cited by 32 · see citing works
Das, N., Maheshwari, D. K., & Pandey, P. (2024) · Progress in Energy and Combustion Science · doi:10.1016/j.pecs.2024.101161 · Cited by 31 · see citing works
Albers, A., Avadí, Á., Benoist, A., Collet, P., & Hélias, A. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.135278 · Cited by 31 · see citing works
Bazrgar, A. B., Ng, A., Coleman, B., Ashiq, M. W., Gordon, A. D., & Thevathasan, N. V. (2020) · Sustainability · doi:10.3390/su12093901 · Cited by 31 · see citing works
Gregory, A. S., Dungait, J. A. J., Shield, I. F., Macalpine, W. J., Cunniff, J., Durenkamp, M., White, R. P., Joynes, A., & Richter, G. M. (2018) · BioEnergy Research · doi:10.1007/s12155-018-9903-6 · Cited by 31 · see citing works
Self-citationIncreasing Dairy Sustainability with Integrated Crop–Livestock Farming
Wiesner, S., Duff, A. J., Desai, A. R., & Panke-Buisse, K. (2020) · Sustainability · doi:10.3390/su12030765 · Cited by 30 · see citing works
McCalmont, J. P., McNamara, N. P., Donnison, I. S., Farrar, K., & Brown, J. C. (2015) · GCB Bioenergy · doi:10.1111/gcbb.12323 · Cited by 29 · see citing works
Storage of <i>Miscanthus</i> -derived carbon in rhizomes, roots, and soil
Christensen, B. T., Lærke, P. E., Jørgensen, U., Kandel, T. P., & Thomsen, I. K. (2016) · Canadian Journal of Soil Science · doi:10.1139/cjss-2015-0135 · Cited by 29 · see citing works
Ventura, M., Panzacchi, P., Muzzi, E., Magnani, F., & Tonon, G. (2019) · New Forests · doi:10.1007/s11056-019-09709-w · Cited by 29 · see citing works
Bioenergy carbon emissions footprint considering the biogenic carbon and secondary effects
Fan, Y. V., Klemeš, J. J., & Ko, C. (2020) · International Journal of Energy Research · doi:10.1002/er.5409 · Cited by 29 · see citing works
Zahorec, A., Reid, M. L., Tiemann, L. K., & Landis, D. A. (2021) · GCB Bioenergy · doi:10.1111/gcbb.12903 · Cited by 29 · see citing works
Sumiyoshi, Y., Crow, S. E., Litton, C. M., Deenik, J. L., Taylor, A. D., Turano, B., & Ogoshi, R. M. (2016) · GCB Bioenergy · doi:10.1111/gcbb.12379 · Cited by 30 · see citing works
Wiesner, S., Desai, A. R., Duff, A. J., Metzger, S., & Stoy, P. C. (2022) · Journal of Geophysical Research Biogeosciences · doi:10.1029/2022jg006895 · Cited by 28 · see citing works
Black, C. K., Masters, M. D., LeBauer, D. S., Anderson‐Teixeira, K. J., & DeLucia, E. H. (2017) · Plant and Soil · doi:10.1007/s11104-017-3333-7 · Cited by 27 · see citing works
Boros-Lajszner, E., Wyszkowska, J., Borowik, A., & Kucharski, J. (2021) · Energies · doi:10.3390/en14164903 · Cited by 27 · see citing works
Biomass Yield of 37 Different SRC Poplar Varieties Grown on a Typical Site in North Eastern Germany
Landgraf, D., Carl, C., & Neupert, M. (2020) · Forests · doi:10.3390/f11101048 · Cited by 26 · see citing works
Rytter, R.-M., & Rytter, L. (2020) · Forest Ecology and Management · doi:10.1016/j.foreco.2020.118129 · Cited by 25 · see citing works
Ferrarini, A., Martani, E., Fornasier, F., & Amaducci, S. (2021) · Agriculture, Ecosystems & Environment · doi:10.1016/j.agee.2020.107247 · Cited by 25 · see citing works
Maddhesiya, P. K., Singh, K., & Singh, R. P. (2020) · Land Degradation and Development · doi:10.1002/ldr.3742 · Cited by 24 · see citing works
Manouchehrinejad, M., Sahoo, K., Kaliyan, N., Singh, H., & Mani, S. (2019) · The International Journal of Life Cycle Assessment · doi:10.1007/s11367-019-01667-x · Cited by 24 · see citing works
Global warming intensity of biofuel derived from switchgrass grown on marginal land in Michigan
Kim, S., Dale, B. E., Martinez‐Feria, R., Basso, B., Thelen, K., Maravelias, C. T., Landis, D., Lark, T. J., & Robertson, G. P. (2023) · GCB Bioenergy · doi:10.1111/gcbb.13024 · Cited by 21 · see citing works
Panoutsou, C., von Cossel, M., Ciria, P., Ciria, C. S., Baraniecki, P., Monti, A., Zanetti, F., & Dubois, J. (2022) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.2376 · Cited by 21 · see citing works
Martani, E., Ferrarini, A., Hastings, A., & Amaducci, S. (2023) · Agronomy · doi:10.3390/agronomy13020447 · Cited by 21 · see citing works
DeBruyn, J. M., Bevard, D. A., Essington, M. E., McKnight, J. Y., Schaeffer, S. M., Baxter, H. L., Mazarei, M., Mann, D. G. J., Dixon, R. A., Chen, F., et al. (2016) · GCB Bioenergy · doi:10.1111/gcbb.12407 · Cited by 21 · see citing works
Dynamic, Intermediate Soil Carbon Pools May Drive Future Responsiveness to Environmental Change
Crow, S. E., & Sierra, C. A. (2018) · Journal of Environmental Quality · doi:10.2134/jeq2017.07.0280 · Cited by 21 · see citing works
Grace, O. M., Lovett, J. C., Gore, C. J. N., Moat, J. F., Ondo, I., Pironon, S., Langat, M. K., Pérez-Escobar, O. A., Ross, A. B., Abbo, M. S., et al. (2020) · Plants People Planet · doi:10.1002/ppp3.10147 · Cited by 20 · see citing works
Biotechnology towards energy crops
Dida, G. (2024) · CABI Agriculture and Bioscience · doi:10.1186/s43170-024-00245-y · Cited by 19 · see citing works
Impact of agroforestry ecosystem on carbon sequestration potential and climate change
Patel, R., Patel, B., Jaison, M., Dash, B., & Mukherjee, S. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95911-7.00002-5 · Cited by 18 · see citing works
Nocentini, A., Field, J., Monti, A., & Paustian, K. H. (2017) · Food and Energy Security · doi:10.1002/fes3.125 · Cited by 18 · see citing works
Reversion of Perennial Biomass Crops to Conserve C and N: A Meta-Analysis
Martani, E., Ferrarini, A., & Amaducci, S. (2022) · Agronomy · doi:10.3390/agronomy12020232 · Cited by 18 · see citing works
Economic comparative advantage of willow biomass in the Northeast USA
Langholtz, M., Eaton, L., Davis, M., Shedden, M., Brandt, C., Volk, T., & Richard, T. (2019) · Biofuels, Bioproducts and Biorefining · doi:10.1002/bbb.1939 · Cited by 17 · see citing works
Zumkeller, M., Yu, R., Torres, N., Marigliano, L. E., Zaccaria, D., & Kurtural, S. K. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.1024606 · Cited by 17 · see citing works
Jarecki, M. K., Kariyapperuma, K. A., Deen, B., Graham, J., Bazrgar, A. B., Vijayakumar, S., Thimmanagari, M., Gordon, A., Voroney, P. R., & Thevathasan, N. V. (2020) · Land · doi:10.3390/land9120509 · Cited by 17 · see citing works
Cerasuolo, M., Richter, G. M., Richard, B., Cunniff, J., Girbau, S., Shield, I. F., Purdy, S., & Karp, A. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv507 · Cited by 17 · see citing works
Self-citationUpscaling miscanthus production in the United Kingdom : The benefits, challenges, and trade‐offs
Hodgson, E., McCalmont, J. P., Rowe, R. L., Whitaker, J., Holder, A. J., Brown, J. C., Thornton, J., Hastings, A., Robson, P. R. H., Webster, R., et al. (2024) · GCB Bioenergy · doi:10.1111/gcbb.13177 · Cited by 16 · see citing works
Ishimoto, Y., Yabuta, S., Kgokong, S., Motsepe, M., Tominaga, J., Teramoto, S., Konaka, T., Mmopelwa, G., Kawamitsu, Y., Akashi, K., et al. (2018) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2017.12.026 · Cited by 16 · see citing works
Luo, Y., Zhao, X., Li, Y., Liu, X., Wang, L., Wang, X., & Du, Z. (2021) · Ecological Engineering · doi:10.1016/j.ecoleng.2021.106373 · Cited by 16 · see citing works
Land-use change from poplar to switchgrass and giant reed increases soil organic carbon
Nocentini, A., & Monti, A. (2017) · Agronomy for Sustainable Development · doi:10.1007/s13593-017-0435-9 · Cited by 16 · see citing works
Quantifying soil organic carbon stocks in herbaceous biomass crops grown in Ontario, Canada
Graham, J., Voroney, P. R., Coleman, B., Deen, B., Gordon, A. D., Thimmanagari, M., & Thevathasan, N. V. (2018) · Agroforestry Systems · doi:10.1007/s10457-018-0272-0 · Cited by 16 · see citing works
Plant roots and GHG mitigation in native perennial bioenergy cropping systems
Jungers, J. M., Eckberg, J. O., Betts, K. J., Mangan, M. E., Wyse, D. L., & Sheaffer, C. C. (2015) · GCB Bioenergy · doi:10.1111/gcbb.12321 · Cited by 16 · see citing works
Rössert, S., Gosling, E., Gandorfer, M., & Knoke, T. (2022) · Agricultural Systems · doi:10.1016/j.agsy.2022.103372 · Cited by 15 · see citing works
Ciria, C. S., Barro, R., Gallego, M. S., & Ciria, P. (2020) · Agronomy · doi:10.3390/agronomy10071051 · Cited by 15 · see citing works
Kalita, S., Karlsson, H., Weih, M., Baum, C., Nordberg, Å., & Hansson, P. (2021) · Forests · doi:10.3390/f12111529 · Cited by 14 · see citing works
Namoi, N., Jang, C., Behnke, G. D., Lee, J. W., Yang, W., & Lee, D. (2024) · GCB Bioenergy · doi:10.1111/gcbb.13139 · Cited by 13 · see citing works
Zucaro, A., Forte, A., Faugno, S., Impagliazzo, A., & Fierro, A. (2016) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2016.12.017 · Cited by 13 · see citing works
Is switchgrass good for carbon savings? Long‐term results in marginal land
Zegada‐Lizarazu, W., Zanetti, F., Virgilio, N. D., & Monti, A. (2022) · GCB Bioenergy · doi:10.1111/gcbb.12944 · Cited by 13 · see citing works
Wästljung, A.-C. R., Dufour, L., Gao, J., Hansson, P., Herrmann, A. M., Jebrane, M., Johansson, A., Kalita, S., Molinder, R., Nordh, N., et al. (2022) · GCB Bioenergy · doi:10.1111/gcbb.12991 · Cited by 12 · see citing works
Biofuel consumption and global climate change: Solutions and challenges
Usmani, R. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-91159-7.00019-9 · Cited by 12 · see citing works
Life-Cycle Assessment of Agricultural Feedstock for Biorefineries
Dufossé, K., Aoun, W. B., & Gabrielle, B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-444-63585-3.00003-6 · Cited by 12 · see citing works
Multidimensional Aspects of Sustainable Biofuel Feedstock Production
Raschke, A., Hernandez‐Suarez, J. S., Nejadhashemi, A. P., & Deb, K. (2021) · Sustainability · doi:10.3390/su13031424 · Cited by 12 · see citing works
Menefee, D. S., Collins, H. P., Smith, D. R., Haney, R. L., Fay, P. A., & Polley, W. (2021) · Journal of Environmental Quality · doi:10.1002/jeq2.20315 · Cited by 12 · see citing works
Hassall, K. L., Coleman, K., Dixit, P. N., Granger, S. J., Zhang, Y., Sharp, R. T., Wu, L., Whitmore, A. P., Richter, G. M., Collins, A. L., et al. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.153824 · Cited by 12 · see citing works
Self-citationLife cycle inventory of Miscanthus production on a commercial farm in the US
Adler, P. R. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1029141 · Cited by 11 · see citing works
Ruf, T., & Emmerling, C. (2021) · GCB Bioenergy · doi:10.1111/gcbb.12830 · Cited by 11 · see citing works
Global land-use and sustainability implications of enhanced bioenergy import of China
Wu, Y., Депперманн, А., Havlík, P., Frank, S., Ren, M., Zhao, H., Ma, L., Fang, C., Chen, Q., & Dai, H. (2023) · Applied Energy · doi:10.1016/j.apenergy.2023.120769 · Cited by 11 · see citing works
Multi‐year carbon budget of a mature commercial short rotation coppice willow plantation
Morrison, R., Rowe, R. L., Cooper, H. K., & McNamara, N. P. (2019) · GCB Bioenergy · doi:10.1111/gcbb.12608 · Cited by 11 · see citing works
Wilts, H. D. M., Burton, D. L., Farooque, A. A., Schroeder, W. R., Murray, B. J., Murphy, E. K., & Ramsay, M. (2024) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2024.107118 · Cited by 10 · see citing works
Hou, W., Xu, Y., Xue, S., Li, J., Yang, Y., Yi, Z., & Fu, T. (2022) · GCB Bioenergy · doi:10.1111/gcbb.13019 · Cited by 10 · see citing works
Advancing the SWAT model to simulate perennial bioenergy crops: A case study on switchgrass growth
Dangol, S., Zhang, X., Liang, X., & Blanc‐Betes, E. (2023) · Environmental Modelling & Software · doi:10.1016/j.envsoft.2023.105834 · Cited by 11 · see citing works
Chen, H., Dong, X. Y., Lei, J., Zhang, N., Wang, Q., Shi, Z., & Yang, J. (2024) · Sustainability · doi:10.3390/su16020697 · Cited by 10 · see citing works
Martinez‐Feria, R. A., Basso, B., & Kim, S. (2022) · Environmental Research Letters · doi:10.1088/1748-9326/ac541b · Cited by 10 · see citing works
Di Virgilio, N., Facini, O., Nocentini, A., Nardino, M., Rossi, F., & Monti, A. (2019) · GCB Bioenergy · doi:10.1111/gcbb.12523 · Cited by 9 · see citing works
Bertola, M., Magenau, E., Martani, E., Kontek, M., Ashman, C., Jurišić, V., Lamy, I., Kam, J., Fornasier, F., McCalmont, J. P., et al. (2024) · GCB Bioenergy · doi:10.1111/gcbb.13145 · Cited by 9 · see citing works
Dixit, P. N., Richter, G. M., Coleman, K., & Collins, A. L. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.166390 · Cited by 9 · see citing works
Self-citationMafa‐Attoye, T., Thevathasan, N. V., & Dunfield, K. E. (2019) · Agroforestry Systems · doi:10.1007/s10457-019-00445-w · Cited by 9 · see citing works
Zhou, W., Qian, M., Wang, S., Li, S., & Cao, Y. (2022) · Forests · doi:10.3390/f13020345 · Cited by 9 · see citing works
Wöhl, L., Ruf, T., Emmerling, C., Thiele, J., & Schrader, S. (2023) · Agriculture · doi:10.3390/agriculture13020494 · Cited by 8 · see citing works
- Authors
- Agostini, F., Gregory, A. S., & Richter, G. M.
- Affiliations
- Rothamsted Research (GB)
- Corresponding author
- Richter, Goetz M.
- Venue
- BioEnergy Research
- Published
- 2015-01-15
- Volume
- 8
- Issue
- 3
- Pages
- 1057-1080
- ISSN
- 1939-1234 (ISSN-L)
- 1939-1242
- PMC
- PMC4732603
- OpenAlex
- W2026172647
- Cited by
- 155
- References
- 191
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 17 · 2023: 19 · 2022: 18 · 2021: 15 · 2020: 15 · 2019: 7 · 2018: 14 · 2017: 12 · 2016: 13 · 2015: 11
- FWCI
- 2.89
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- BioEnergy Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Rothamsted Repository (Rothamsted Repository) (submittedVersion)
- Funders
- Directorate for Biological Sciences
- Engineering and Physical Sciences Research Council (EP/K036734/1)
- Biotechnology and Biological Sciences Research Council (BBS/E/C/00005214, BBS/E/C/00005201)
- Natural Environment Research Council (NE/H010718/1, NE/H010742/1)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Agronomy and Crop Science › Bioenergy crop production and management
- Life Sciences › Agricultural and Biological Sciences › Soil Science › Soil Carbon and Nitrogen Dynamics
- Life Sciences › Agricultural and Biological Sciences › Soil Science › Soil erosion and sediment transport
- Keywords
- carbon sequestration, perennial energy crops, soil organic carbon, bioenergy, Miscanthus, willow, switchgrass, poplar, carbon allocation, carbon turnover, greenhouse gas emissions, land conversion, carbon leaching, stand age, carbon neutrality
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review