Cited by 97Soil Carbon and Nitrogen DynamicsMycorrhizal Fungi and Plant InteractionsMicrobial Community Ecology and Physiology

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Microbial crop residue decomposition dynamics in organic and conventionally managed soils

Abstract

Agricultural practices can influence soil microbial communities, which are the primary regulators of soil carbon and nutrient cycling processes. Differences in microbial community composition have the potential to affect the fate of carbon and nutrients during decomposition and may therefore influence the retention of C and provisioning of crop nutrients in agroecosystems. Long term management-induced shifts in microbial communities and resource availability may interact to affect the microbial utilization of fresh inputs of crop residues in the short term, with lasting impacts on soil C accrual and fertility. The objective of this study was to investigate whether long-term organic and conventional management resulted in differences in microbial residue decomposition. Soils under conventional and organic management planted with annual crops or with a mix of annual crops and three years of perennial alfalfa were collected from a long-term (19 y) field study in Saskatchewan, Canada and were incubated in the laboratory with and without 13C-labelled barley residues for 98d. We measured extracellular enzyme activities (EEAs) and the incorporation of crop residue-derived C within major microbial groups (fungi, actinobacteria, and Gram positive and negative bacteria) during decomposition. Total PLFA biomass and EEAs were highest in soils from the conventional-annual system, similar between the conventional and organic perennial systems, and similar or lowest in the organic-annual system. Crop residue additions alleviated these differences; that is, in residue-amended soils total PLFA biomass, EEAs, and the abundance of the fungal biomarker increased in the organic systems compared to the unamended soils to become similar to the conventional systems. In contrast, residue additions induced small or no changes in biomass and EEAs in the conventional-annual soils. Using 13C-PLFA-SIP we showed that the general pattern of microbial succession during decomposition was similar among soils, but that fungi and especially actinobacteria were relatively more dominant in organic compared to conventionally managed soils during early and later stages of decomposition, respectively. Thus, shifts in the decomposer community composition were greater in soils originating from organic management, possibly as a result of larger changes in resource availability during the incubation that advanced the rate of microbial succession. This may reinforce long term differences in SOC quality and nutrient availability between management regimes. Organically-managed cropping systems are particularly reliant on biological cycling of organic nutrients to support crop growth. This work reinforces the importance of adequate crop residue returns for maintaining soil function, particularly where external organic amendments are not applied to balance nutrients exported as crop products.

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Research works printed but not linked: 72

  1. Allison, 2005, Cheaters, diffusion and nutrients constrain decomposition by microbial enzymes in spatially structured environments, Ecol. Lett., 8, 626, 10.1111/j.1461-0248.2005.00756.x · DOI
  2. Allison, 2005, Responses of extracellular enzymes to simple and complex nutrient inputs, Soil Biol. Biochem., 37, 937, 10.1016/j.soilbio.2004.09.014 · DOI
  3. Allison, 2013, Microbial abundance and composition influence litter decomposition response to environmental change, Ecology, 94, 714, 10.1890/12-1243.1 · DOI
  4. Awada, 2015, The benefits and costs of zero tillage RD&E on the canadian prairies, Can. J. Agric. Econ., 00, 1
  5. Bai, 2016, Phospholipid 13C stable isotopic probing during decomposition of wheat residues, Appl. Soil Ecol., 98, 65, 10.1016/j.apsoil.2015.09.009 · DOI
  6. Bastian, 2009, Impact of wheat straw decomposition on successional patterns of soil microbial community structure, Soil Biol. Biochem., 41, 262, 10.1016/j.soilbio.2008.10.024 · DOI · Paper page
  7. Bell, 2012, Soil profile carbon and nutrient stocks under long-term conventional and organic crop and alfalfa-crop rotations and re-established grassland, Agric. Ecosyst. Environ., 158, 156, 10.1016/j.agee.2012.06.006 · DOI
  8. Bernard, 2007, Dynamics and identification of soil microbial populations actively assimilating carbon from 13C-labelled wheat residue as estimated by DNA- and RNA-SIP techniques, Environ. Microbiol., 9, 752, 10.1111/j.1462-2920.2006.01197.x · DOI
  9. Brandt, 2010, Design, rationale and methodological considerations for a long term alternative cropping experiment in the Canadian plain region, Eur. J. Agron., 32, 73, 10.1016/j.eja.2009.07.006 · DOI
  10. Dai, 2014, Negative and positive contributions of arbuscular mycorrhizal fungal taxa to wheat production and nutrient uptake efficiency in organic and conventional systems in the Canadian prairie, Soil Biol. Biochem., 74, 156, 10.1016/j.soilbio.2014.03.016 · DOI
  11. de Boer, 2005, Living in a fungal world: impact of fungi on soil bacterial niche development, FEMS Microbiol. Rev., 29, 795, 10.1016/j.femsre.2004.11.005 · DOI
  12. Dungait, 2013, The variable response of soil microorganisms to trace concentrations of low molecular weight organic substrates of increasing complexity, Soil Biol. Biochem., 64, 57, 10.1016/j.soilbio.2013.03.036 · DOI
  13. Eivazi, 1977, Phosphatases in soils, Soil Biol. Biochem., 9, 167, 10.1016/0038-0717(77)90070-0 · DOI
  14. Eivazi, 1988, Glucosidases and galactosidases in soils, Soil Biol. Biochem., 20, 601, 10.1016/0038-0717(88)90141-1 · DOI
  15. Fierer, 2007, Toward an ecological classification of soil bacteria, Ecology, 88, 1354, 10.1890/05-1839 · DOI
  16. Fierer, 2012, Comparative metagenomic, phylogenetic and physiological analyses of soil microbial communities across nitrogen gradients, ISME J., 6, 1007, 10.1038/ismej.2011.159 · DOI
  17. Fließbach, 2007, Soil organic matter and biological soil quality indicators after 21 years of organic and conventional farming, Agric. Ecosyst. Environ., 118, 273, 10.1016/j.agee.2006.05.022 · DOI
  18. Fraser, 2015, Linking alkaline phosphatase activity with bacterial phoD gene abundance in soil from a long-term management trial, Geoderma, 257-258, 115, 10.1016/j.geoderma.2014.10.016 · DOI
  19. García-Ruiz, 2008, Suitability of enzyme activities for the monitoring of soil quality improvement in organic agricultural systems, Soil Biol. Biochem., 40, 2137, 10.1016/j.soilbio.2008.03.023 · DOI
  20. Gattinger, 2012, Enhanced top soil carbon stocks under organic farming, Proc. Natl. Acad. Sci., 109, 18226, 10.1073/pnas.1209429109 · DOI
  21. Grogan, 1997, Cyclopropane ring formation in membrane lipids of bacteria, Microbiol. Mol. Biol. Rev., 61, 429
  22. Hartmann, 2014, Distinct soil microbial diversity under long-term organic and conventional farming, ISME J., 9, 1177, 10.1038/ismej.2014.210 · DOI · Paper page
  23. Helfrich, 2015, The role of soil fungi and bacteria in plant litter decomposition and macroaggregate formation determined using phospholipid fatty acids, Appl. Soil Ecol., 96, 261, 10.1016/j.apsoil.2015.08.023 · DOI
  24. Helgason, 2009, Fungal and bacterial abundance in long-term no-till and intensive-till soils of the Northern Great Plains, Soil Sci. Soc. Am. J., 73, 120, 10.2136/sssaj2007.0392 · DOI
  25. Helgason, 2010, No-till soil management increases microbial biomass and alters community profiles in soil aggregates, Appl. Soil Ecol., 46, 390, 10.1016/j.apsoil.2010.10.002 · DOI
  26. Helgason, 2014, Long-term microbial retention of residue C is site-specific and depends on residue placement, Soil Biol. Biochem., 68, 231, 10.1016/j.soilbio.2013.10.002 · DOI
  27. Herman, 2012, Interactions between an arbuscular mycorrhizal fungus and a soil microbial community mediating litter decomposition, FEMS Microbiol. Ecol., 80, 236, 10.1111/j.1574-6941.2011.01292.x · DOI
  28. Janzen, 1992, Light-fraction organic matter in soils from long-term crop rotations, Soil Sci. Soc. Am. J., 56, 1799, 10.2136/sssaj1992.03615995005600060025x · DOI
  29. Knight, 2010, Classification and fertility status of organically managed fields across Saskatchewan, Canada, Can. J. Soil Sci., 90, 667, 10.4141/cjss09082 · DOI
  30. Kong, 2010, Tracing root vs. residue carbon into soils from conventional and alternative cropping systems, Soil Sci. Soc. Am. J., 74, 1201, 10.2136/sssaj2009.0346 · DOI
  31. Kong, 2012, Microbial community assimilation of cover crop rhizodeposition within soil microenvironments in alternative and conventional cropping systems, Plant Soil, 356, 315, 10.1007/s11104-011-1120-4 · DOI
  32. Kong, 2011, Microbial community composition and carbon cycling within soil microenvironments of conventional, low-input, and organic cropping systems, Soil Biol. Biochem., 43, 20, 10.1016/j.soilbio.2010.09.005 · DOI
  33. Koranda, 2014, Fungal and bacterial utilization of organic substrates depends on substrate complexity and N availability, FEMS Microbiol. Ecol., 87, 142, 10.1111/1574-6941.12214 · DOI
  34. Lagomarsino, 2009, Soil biochemical indicators as a tool to assess the short-term impact of agricultural management on changes in organic C in a Mediterranean environment, Ecol. Indic., 9, 518, 10.1016/j.ecolind.2008.07.003 · DOI
  35. Leifeld, 2013, Organic farming gives no climate change benefit through soil carbon sequestration, Proc. Natl. Acad. Sci., 110, E984, 10.1073/pnas.1220724110 · DOI
  36. Leithold, 2015, Organic matter returns to soils must be higher under organic compared to conventional farming, J. Plant Nutrit. Soil Sci., 178, 4, 10.1002/jpln.201400133 · DOI
  37. Li, 2012, Pyrosequencing reveals the influence of organic and conventional farming systems on bacterial communities, PLoS One, 7, e51897, 10.1371/journal.pone.0051897 · DOI
  38. Linn, 1984, Aerobic and anaerobic microbial populations in no-till and plowed soils 1, Soil Sci. Soc. Am. J., 48, 794, 10.2136/sssaj1984.03615995004800040019x · DOI
  39. Mäder, 2002, Soil fertility and biodiversity in organic farming, Science, 296, 1694, 10.1126/science.1071148 · DOI
  40. Malhi, 2009, Effects of input level and crop diversity on soil nitrate-N, extractable P, aggregation, organic C and N, and nutrient balance in the Canadian Prairie, Nutr. Cycl. Agroecosyst., 84, 1, 10.1007/s10705-008-9220-0 · DOI
  41. Marschner, 2011, The microbial community composition changes rapidly in the early stages of decomposition of wheat residue, Soil Biol. Biochem., 43, 445, 10.1016/j.soilbio.2010.11.015 · DOI
  42. McDaniel, 2014, Crop rotation complexity regulates the decomposition of high and low quality residues, Soil Biol. Biochem., 78, 243, 10.1016/j.soilbio.2014.07.027 · DOI
  43. McGuire, 2010, Microbial communities and their relevance for ecosystem models: decomposition as a case study, Soil Biol. Biochem., 42, 529, 10.1016/j.soilbio.2009.11.016 · DOI
  44. McMahon, 2005, Dynamics of microbial communities during decomposition of carbon-13 labeled ryegrass fractions in soil, Soil Sci. Soc. Am. J., 69, 1238, 10.2136/sssaj2004.0289 · DOI
  45. Moore-Kucera, 2008, Application of 13C-labeled litter and root materials for in situ decomposition studies using phospholipid fatty acids, Soil Biol. Biochem., 40, 2485, 10.1016/j.soilbio.2008.06.002 · DOI
  46. Moorhead, 2013, Dynamic relationships between microbial biomass, respiration, inorganic nutrients and enzyme activities: informing enzyme-based decomposition models, Front. Microbiol., 4, 1, 10.3389/fmicb.2013.00223 · DOI
  47. Ng, 2014, Does the chemical nature of soil carbon drive the structure and functioning of soil microbial communities?, Soil Biol. Biochem., 70, 54, 10.1016/j.soilbio.2013.12.004 · DOI
  48. Parham, 2000, Detection, quantification and characterization of β-glucosaminidase activity in soil, Soil Biol. Biochem., 32, 1183, 10.1016/S0038-0717(00)00034-1 · DOI
  49. Pascault, 2010, In situ dynamics of microbial communities during decomposition of wheat, rape, and alfalfa residues, Microb. Ecol., 60, 816, 10.1007/s00248-010-9705-7 · DOI
  50. Paterson, 2007, Rhizodeposition shapes rhizosphere microbial community structure in organic soil, New Phytol., 173, 600, 10.1111/j.1469-8137.2006.01931.x · DOI
  51. Poll, 2008, Dynamics of litter carbon turnover and microbial abundance in a rye detritusphere, Soil Biol. Biochem., 40, 1306, 10.1016/j.soilbio.2007.04.002 · DOI
  52. Purahong, 2014, Uncoupling of microbial community structure and function in decomposing litter across beech forest ecosystems in Central Europe, Sci. Rep., 4, 1, 10.1038/srep07014 · DOI
  53. Reeve, 2010, Effects of soil type and farm management on soil ecological functional genes and microbial activities, ISME J., 4, 1099, 10.1038/ismej.2010.42 · DOI
  54. Rinkes, 2013, Interactions between leaf litter quality, particle size, and microbial community during the earliest stage of decay, Biogeochemistry, 1
  55. Rubino, 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, 1009, 10.1016/j.soilbio.2010.02.018 · DOI · Paper page
  56. Schimel, 2012, Microbial control over carbon cycling in soil, Front. Microbiol., 3, 348, 10.3389/fmicb.2012.00348 · DOI
  57. Schneider, 2012, Who is who in litter decomposition? Metaproteomics reveals major microbial players and their biogeochemical functions, ISME J., 6, 1749, 10.1038/ismej.2012.11 · DOI
  58. Spohn, 2013, Phosphorus mineralization can be driven by microbial need for carbon, Soil Biol. Biochem., 61, 69, 10.1016/j.soilbio.2013.02.013 · DOI
  59. Strickland, 2009, Testing the functional significance of microbial community composition, Ecology, 90, 441, 10.1890/08-0296.1 · DOI
  60. Tabatabai, 1969, Use of p-nitrophenyl phosphate for assay of soil phosphatase activity, Soil Biol. Biochem., 1, 301, 10.1016/0038-0717(69)90012-1 · DOI
  61. Tiemann, 2015, Crop rotational diversity enhances belowground communities and functions in an agroecosystem, Ecol. Lett., 18, 761, 10.1111/ele.12453 · DOI
  62. VandenBygaart, 2003, Influence of agricultural management on soil organic carbon: a compendium and assessment of Canadian studies, Can. J. Soil Sci., 83, 363, 10.4141/S03-009 · DOI
  63. Veres, 2015, Soil extracellular enzyme activities are sensitive indicators of detrital inputs and carbon availability, Appl. Soil Ecol., 92, 18, 10.1016/j.apsoil.2015.03.006 · DOI
  64. Wardle, 1999, Response of soil microbial biomass dynamics, activity and plant litter decomposition to agricultural intensification over a seven-year period, Soil Biol. Biochem., 31, 1707, 10.1016/S0038-0717(99)00090-5 · DOI
  65. Waring, 2013, Differences in fungal and bacterial physiology alter soil carbon and nitrogen cycling: insights from meta-analysis and theoretical models, Ecol. Lett., 16, 887, 10.1111/ele.12125 · DOI
  66. Watzinger, 2015, Microbial phospholipid biomarkers and stable isotope methods help reveal soil functions, Soil Biol. Biochem., 86, 98, 10.1016/j.soilbio.2015.03.019 · DOI
  67. Wickings, 2010, Management intensity alters decomposition via biological pathways, Biogeochemistry, 104, 365, 10.1007/s10533-010-9510-x · DOI
  68. Willers, 2015, Phospholipid fatty acid profiling of microbial communities-a review of interpretations and recent applications, J. Appl. Microbiol., 119, 1207, 10.1111/jam.12902 · DOI
  69. Williams, 2006, Carbon flow from 13 C-labeled straw and root residues into the phospholipid fatty acids of a soil microbial community under field conditions, Soil Biol. Biochem., 38, 759, 10.1016/j.soilbio.2005.07.001 · DOI
  70. Yao, 2015, 13C PLFAs: a key to open the soil microbial black box?, Plant Soil, 392, 3, 10.1007/s11104-014-2300-9 · DOI
  71. Zelles, 1999, Fatty acid patterns of phospholipids and lipopolysaccharides in the characterisation of microbial communities in soil: a review, Biol. Fert. Soils, 29, 111, 10.1007/s003740050533 · DOI
  72. Zentner, 2011, Effects of input management and crop diversity on non-renewable energy use efficiency of cropping systems in the Canadian Prairie, Eur. J. Agron., 34, 113, 10.1016/j.eja.2010.11.004 · DOI

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Metadata

Authors
Arcand, M. M., Helgason, B. L., & Lemke, R. L.
Affiliations
  • University of Saskatchewan (CA)
  • Agriculture and Agri-Food Canada (CA)
Corresponding author
Helgason, Bobbi L.
Venue
Applied Soil Ecology
Publisher
Elsevier BV
Published
2016-11
Volume
107
Pages
347-359
ISSN
0929-1393 (ISSN-L)
OpenAlex
W2487535923
Cited by
97
References
1
Citations by year
2026: 6 · 2025: 10 · 2024: 15 · 2023: 6 · 2022: 9 · 2021: 16 · 2020: 11 · 2019: 9 · 2018: 12 · 2017: 3
FWCI
9.37
Type
journal article
Language
en
Open access
closed
Locations
Applied Soil Ecology (publishedVersion)
Funders
Agriculture and Agri-Food Canada
Topics
  • Life Sciences › Agricultural and Biological Sciences › Soil Science › Soil Carbon and Nitrogen Dynamics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Mycorrhizal Fungi and Plant Interactions
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
Keywords
crop residue decomposition, organic management, conventional management, soil microbial communities, extracellular enzyme activity, phospholipid fatty acids, microbial succession, fungi, actinobacteria, soil organic carbon, soil carbon quality, long-term cropping systems, soil fertility

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CoChat. (2026). Citation check: Microbial crop residue decomposition dynamics in organic and conventionally managed soils. https://app.cochat.ai/papers/10.1016/j.apsoil.2016.07.001
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Arcand, M. M., Helgason, B. L., & Lemke, R. L. (2016). Microbial crop residue decomposition dynamics in organic and conventionally managed soils. Applied Soil Ecology. https://doi.org/10.1016/j.apsoil.2016.07.001