Carbon input belowground is the major C flux contributing to leaf litter mass loss: Evidences from a 13C labelled-leaf litter experiment
Abstract
Partitioning of the quantities of C lost by leaf litter through decomposition into (i) CO2 efflux to the atmosphere and (ii) C input to soil organic matter (SOM) is essential in order to develop a deeper understanding of the litter-soil biogeochemical continuum. However, this is a challenging task due to the occurrence of many different processes contributing to litter biomass loss. With the aim of quantifying different fluxes of C lost by leaf litter decomposition, a field experiment was performed at a short rotation coppice poplar plantation in central Italy. Populus nigra leaf litter, enriched in 13C (δ13C approximately +160 per thousand) was placed within collars to decompose in direct contact with the soil (δ13C approximately −26 per thousand) for 11 months. CO2 efflux from within the collars and its isotopic composition were determined at monthly intervals. After 11 months, remaining litter and soil profiles (0–20 cm) were sampled and analysed for their total C and 13C content. Gas chromatography (GC), GC–mass spectrometry (MS) and GC-combustion-isotope ratio (GC/C/IRMS) were used to analyse phospholipid fatty acids (PLFA) extracted from soil samples to identify the groups of soil micro-organisms that had incorporated litter-derived C and to determine the quantity of C incorporated by the soil microbial biomass (SMB). By the end of the experiment, the litter had lost about 80% of its original weight. The fraction of litter C lost as an input into the soil (67 ± 12% of the total C loss) was found to be twice as much as the fraction released as CO2 to the atmosphere (30 ± 3%), thus demonstrating the importance of quantifying litter-derived C input to soils, in litter decomposition studies. The mean δ13C values of PLFAs in soil (δ13C = −12.5 per thousand) showed sustained incorporation of litter-derived C after one year (7.8 ± 1.6% of total PLFA-C). Thus, through the application of stable 13C isotope analyses, we have quantified two major C fluxes contributing to litter decomposition, at macroscopic and microscopic levels.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
Carbon 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.”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
In 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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
These 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.”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
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.”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
Decomposition 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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
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].”
From Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out? (2015) · cites this paper as [109]
Cites
Review of mechanisms and quantification of priming effects
Kuzyakov, Y., Friedel, J. K., & Stahr, K. (2000) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00084-5 · Cited by 3,040 · see citing works
Zelles, L. (1999) · Biology and Fertility of Soils · doi:10.1007/s003740050533 · Cited by 2,040 · see citing works
Frostegård, Å., Tunlid, A., & Bååth, E. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.11.3605-3617.1993 · Cited by 1,360 · see citing works
Harris, D., Horwath, W., & van Kessel, C. (2001) · Soil Science Society of America Journal · doi:10.2136/sssaj2001.1853 · Cited by 1,283 · see citing works
Gholz, H. L., Wedin, D. A., Smitherman, S. M., Harmon, M. E., & Parton, W. J. (2000) · Global Change Biology · doi:10.1046/j.1365-2486.2000.00349.x · Cited by 950 · see citing works
Olsson, P. A. (1999) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.1999.tb00621.x · Cited by 826 · see citing works
Phospholipid fatty acid profiles in selected members of soil microbial communities
Zelles, L. (1997) · Chemosphere · doi:10.1016/s0045-6535(97)00155-0 · Cited by 781 · see citing works
Natural 13C abundance as a tracer for studies of soil organic matter dynamics
Balesdent, J., Mariotti, A. A., & Guillet, B. (1987) · Soil Biology and Biochemistry · doi:10.1016/0038-0717(87)90120-9 · Cited by 720 · see citing works
Adair, E. C., Parton, W. J., GROSSO, S. J. D., Silver, W. L., Harmon, M. E., Hall, S. A., Burke, I. C., & Hart, S. C. (2008) · Global Change Biology · doi:10.1111/j.1365-2486.2008.01674.x · Cited by 530 · see citing works
Accounting for variability in soil microbial communities of temperate upland grassland ecosystems
Grayston, S. J., Griffith, G. S., Mawdsley, J. L., et al. (2001) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00194-2 · Cited by 492 · see citing works
Global Biogeochemical Cycles in the Climate System
(2001) · Elsevier eBooks · doi:10.1016/b978-0-12-631260-7.x5000-6 · Cited by 458 · see citing works
Microbiota, fauna, and mesh size interactions in litter decomposition
Bradford, M. A., Tordoff, G. M., Eggers, T., Jones, T. H., & Newington, J. E. (2002) · Oikos · doi:10.1034/j.1600-0706.2002.990212.x · Cited by 433 · see citing works
The disappearance of leaf litter under different woodland conditions
Bocock, K. L., & GILBERT, O. (1957) · Plant and Soil · doi:10.1007/bf01398924 · Cited by 385 · see citing works
Galdo, I. D., Six, J., Peressotti, A., & Cotrufo, M. F. (2003) · Global Change Biology · doi:10.1046/j.1365-2486.2003.00657.x · Cited by 374 · see citing works
Increasing carbon stocks in the forest soils of western Europe
Liski, J., Perruchoud, D., & Karjalainen, T. (2002) · Forest Ecology and Management · doi:10.1016/s0378-1127(02)00306-7 · Cited by 323 · 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
Ecosystem properties and microbial community changes in primary succession on a glacier forefront
Ohtonen, R., Fritze, H., Pennanen, T., et al. (1999) · Oecologia · doi:10.1007/s004420050782 · Cited by 282 · see citing works
Free‐air CO2 enrichment (FACE) of a poplar plantation: the POPFACE fumigation system
Miglietta, F., Peressotti, A., Vaccari, F. P., Zaldei, A., Angelis, P. D., & Mugnozza, G. S. (2001) · New Phytologist · doi:10.1046/j.1469-8137.2001.00115.x · Cited by 266 · see citing works
Soil Microbial Communities Beneath Populus Grandidentata Grown Under Elevated Atmospheric CO2
Zak, D. R., Ringelberg, D. B., Pregitzer, K. S., et al. (1996) · Ecological Applications · doi:10.2307/2269568 · Cited by 232 · see citing works
Carbon isotopic fractionation during decomposition of plant materials of different quality
Fernández, I., Mahieu, N., & Cadisch, G. (2003) · Global Biogeochemical Cycles · doi:10.1029/2001gb001834 · Cited by 229 · see citing works
Feedback interactions between needle litter decomposition and rhizosphere activity
Subke, J., Hahn, V., Battipaglia, G., Linder, S., Buchmann, N., & Cotrufo, M. F. (2004) · Oecologia · doi:10.1007/s00442-004-1540-4 · Cited by 229 · see citing works
Dignac, M., Bahri, H., Rumpel, C., Rasse, D. P., Bardoux, G., Balesdent, J., Girardin, C., Chenu, C., & Mariotti, A. A. (2005) · Geoderma · doi:10.1016/j.geoderma.2004.12.022 · Cited by 224 · see citing works
Bacterial Diversity in Agricultural Soils during Litter Decomposition
Dilly, O. M., Bloem, J., Vos, A., & Munch, J. C. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.1.468-474.2004 · Cited by 205 · see citing works
Phillips, R., Zak, D. R., Holmes, W. E., & White, D. C. (2002) · Oecologia · doi:10.1007/s00442-002-0868-x · Cited by 184 · see citing works
Sundh, I., Nilsson, M., & Borgå, P. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.4.1476-1482.1997 · Cited by 174 · see citing works
Bird, J. A., Kleber, M., & Torn, M. S. (2008) · Organic Geochemistry · doi:10.1016/j.orggeochem.2007.12.003 · Cited by 169 · see citing works
Turnover of carbon through the microbial biomass in soils with different texture
Gregorich, E. G., Voroney, R. P., & Kachanoski, R. G. (1991) · Soil Biology and Biochemistry · doi:10.1016/0038-0717(91)90152-a · Cited by 167 · see citing works
Hoosbeek, M. R., Lukáč, M., Dam, D. V., Godbold, D. L., Velthorst, E. J., Biondi, F., Peressotti, A., Cotrufo, M. F., Angelis, P. D., & Mugnozza, G. S. (2004) · Global Biogeochemical Cycles · doi:10.1029/2003gb002127 · Cited by 166 · see citing works
Plant Compounds and Their Turnover and Stabilization as Soil Organic Matter
Gleixner, G., CZIMCZIK, C. I., Kramer, C., Lühker, B., & Schmidt, M. W. I. (2001) · Elsevier eBooks · doi:10.1016/b978-012631260-7/50017-0 · Cited by 165 · see citing works
Smith, V. C., & Bradford, M. A. (2003) · Applied Soil Ecology · doi:10.1016/s0929-1393(03)00094-5 · Cited by 144 · see citing works
Frostegård, Å., Petersen, S. O., Bååth, E., & Nielsen, T. H. (1997) · Applied and Environmental Microbiology · doi:10.1128/aem.63.6.2224-2231.1997 · Cited by 125 · see citing works
Cortez, J. (1998) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(97)00163-6 · Cited by 121 · see citing works
Do invertebrate decomposers affect the disappearance rate of litter mixtures?
Schädler, M., & Brandl, R. (2004) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2004.07.042 · Cited by 119 · see citing works
13C-Labelling of lipids to investigate microbial communities in the environment
Evershed, R. P., Crossman, Z., Bull, I. D., Mottram, H. R., Dungait, J. A. J., Maxfield, P. J., & Brennand, E. L. (2006) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2006.01.003 · Cited by 119 · see citing works
Self-citationCotrufo, 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
Self-citationIsotopic discrimination during long-term decomposition in an arid land ecosystem
Connin, S., Feng, X.-H., & Virginia, R. (2001) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00113-9 · Cited by 92 · see citing works
Stabilization of 13 C‐Carbon and Immobilization of 15 N‐Nitrogen from Rice Straw in Humic Fractions
Bird, J. A., van Kessel, C., & Horwáth, W. R. (2003) · Soil Science Society of America Journal · doi:10.2136/sssaj2003.8060 · Cited by 83 · see citing works
Crossman, Z., Abraham, F., & Evershed, R. P. (2004) · Environmental Science & Technology · doi:10.1021/es034619n · Cited by 74 · see citing works
Self-citationDecomposition of Pinus sylvestris litter in litter bags: Influence of underlying native litter layer
Chadwick, D. R., Ineson, P., Woods, C., & Piearce, T. G. (1998) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(97)00090-4 · Cited by 69 · see citing works
Soil microbial activity and biomass in the primary succession of a dry heath forest
Aikio, S., Väre, H., & Strömmer, R. (2000) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(00)00019-5 · Cited by 67 · see citing works
Litter type and soil minerals control temperate forest soil carbon response to climate change
Rasmussen, C., Southard, R. J., & Horwath, W. (2008) · Global Change Biology · doi:10.1111/j.1365-2486.2008.01639.x · Cited by 62 · see citing works
Calfapietra, C., Angelis, P. D., Gielen, B., et al. (2007) · Tree Physiology · doi:10.1093/treephys/27.8.1153 · Cited by 55 · see citing works
Ross, D. J., TATE, K. R., Newton, P. C. D., et al. (2002) · Plant and Soil · doi:10.1023/a:1015779431271 · Cited by 53 · see citing works
Mixed litter decomposition in a managed Missouri Ozark forest ecosystem
Li, Q., Moorhead, D., DeForest, J., Henderson, R., Chen, J.-Q., & Jensen, R. G. (2009) · Forest Ecology and Management · doi:10.1016/j.foreco.2008.09.043 · Cited by 52 · see citing works
Litter decomposition, ectomycorrhizal roots and the ‘Gadgil’ effect
Bending, G. D. (2003) · New Phytologist · doi:10.1046/j.1469-8137.2003.00752.x · Cited by 51 · see citing works
Field decomposition of leaf litters: earthworm–microorganism interactions —the ploughing-in effect
Cortez, J., & Bouché, M. B. (1998) · Soil Biology and Biochemistry · doi:10.1016/s0038-0717(97)00164-8 · Cited by 47 · see citing works
Influence of litterbags on growth of fungal vegetative structures
John, T. V. S. (1980) · Oecologia · doi:10.1007/bf00346977 · Cited by 47 · see citing works
Dungait, J. A. J., Bol, R. A., & Evershed, R. P. (2005) · Isotopes in Environmental and Health Studies · doi:10.1080/10256010500053516 · Cited by 43 · see citing works
Self-citationYamashita, T., & Takeda, H. (1998) · Pedobiologia · doi:10.1016/s0031-4056(24)00386-x · Cited by 39 · see citing works
Derrien, D., Balesdent, J., Marol, C., et al. (2003) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.1269 · Cited by 37 · see citing works
Standardization for oxygen isotope ratio measurement - still an unsolved problem
Kornexl, B. E., Werner, R. A., & Gehre, M. (1999) · Rapid Communications in Mass Spectrometry · doi:10.1002/(sici)1097-0231(19990715)13:13 · Cited by 35 · see citing works
Kheirallah, A. M. (1990) · Biology and Fertility of Soils · doi:10.1007/bf00336137 · Cited by 30 · see citing works
Mugnozza, G. S., Angelis, P. D., Sabatti, M., Calfapietra, C., Ceulemans, R., Peressotti, A., & Miglietta, F. (2000) · Cited by 29 · see citing works
Rubino, M., Lubritto, C., D’Onofrio, A., Terrasi, F., Gleixner, G., & Cotrufo, M. F. (2007) · Oecologia · doi:10.1007/s00442-007-0815-y · Cited by 26 · see citing works
Self-citationBertolini, T., Rubino, M., Lubritto, C., et al. (2005) · Journal of Mass Spectrometry · doi:10.1002/jms.888 · Cited by 17 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Cotrufo, M. F., Wallenstein, M. D., Boot, C. M., Denef, K., & Paul, E. (2013) · Global Change Biology · doi:10.1111/gcb.12113 · Cited by 3,552 · see citing works
Formation of soil organic matter via biochemical and physical pathways of litter mass loss
Cotrufo, M. F., Soong, J. L., Horton, A. J., Campbell, E. E., Haddix, M. L., Wall, D. H., & Parton, W. J. (2015) · Nature Geoscience · doi:10.1038/ngeo2520 · Cited by 1,874 · see citing works
Kell, D. B. (2011) · Annals of Botany · doi:10.1093/aob/mcr175 · Cited by 439 · see citing works
Carbon Sequestration by Perennial Energy Crops: Is the Jury Still Out?
Agostini, F., Gregory, A. S., & Richter, G. M. (2015) · BioEnergy Research · doi:10.1007/s12155-014-9571-0 · Cited by 155 · see citing works
Yang, X., Szlavecz, K., Pitz, S. L., Langley, J. A., & Chang, C.-H. (2020) · Biogeochemistry · doi:10.1007/s10533-020-00651-0 · Cited by 26 · see citing works
- Authors
- 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.
- Affiliations
- University of Campania "Luigi Vanvitelli" (IT)
- University of Bristol (GB)
- Università degli Studi della Tuscia (IT)
- ORCID
- Venue
- Soil Biology and Biochemistry
- Publisher
- Elsevier BV
- Published
- 2010-07
- Volume
- 42
- Issue
- 7
- Pages
- 1009-1016
- ISSN
- 0038-0717 (ISSN-L)
- OpenAlex
- W2072159772
- Cited by
- 166
- References
- 55
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 11 · 2023: 9 · 2022: 13 · 2021: 10 · 2020: 15 · 2019: 5 · 2018: 14 · 2017: 5 · 2016: 15 · 2015: 7 · 2014: 16 · 2013: 10 · 2012: 6
- FWCI
- 15.88
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Soil Biology and Biochemistry (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (publishedVersion)
- Rothamsted Repository (Rothamsted Repository) (submittedVersion)
- UnitusOpen (Tuscia University) (submittedVersion)
- Archivio Istituzionale della Ricerca - Università degli Studi della Campania "Luigi Vanvitelli" (submittedVersion)
- Funders
- Natural Environment Research Council (lsmsf010001)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Soil Science › Soil Carbon and Nitrogen Dynamics
- Physical Sciences › Environmental Science › Ecology › Environmental and biological studies
- Life Sciences › Agricultural and Biological Sciences › Soil Science › Soil erosion and sediment transport
- Keywords
- leaf litter decomposition, carbon flux, soil organic matter, CO2 efflux, 13C labeling, phospholipid fatty acids, soil microbial biomass, soil microbes, poplar plantations, Populus nigra, short rotation coppice
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.
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