Biogas slurry substitution regulates soil carbon sequestration by shifting plant- and microbial-derived carbon pathways in a paddy profile

Yulin Wang , Zichuan Li , Yanjun Chai , Zhixi Geng , Ning Zhao , Zhuozhe Wang , JiaJun Wu , Jingyuan Pan , Lifeng Ping , Yan Li , Ming Hung Wong

Soil Ecology Letters ›› 2027, Vol. 9 ›› Issue (2) : 260514

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Soil Ecology Letters ›› 2027, Vol. 9 ›› Issue (2) :260514 DOI: 10.1007/s42832-026-0514-4
RESEARCH ARTICLE
Biogas slurry substitution regulates soil carbon sequestration by shifting plant- and microbial-derived carbon pathways in a paddy profile
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Abstract

Biogas slurry substitution for chemical fertilizers is a key strategy for reducing fertilizer use and recycling agricultural organic waste. However, the mechanisms underlying its impact on the profile distribution of soil organic carbon (SOC) remain unclear. This study compared the effects of different biogas slurry nitrogen substitution ratios (50% and 75%) and application methods (nitrogen-only substitution vs. combined nutrient substitution) on SOC fractions in paddy soils, aiming to elucidate the transformation pathways and stabilization mechanisms of plant- and microbial-derived carbon in the 0−15 cm layer (topsoil) and 15−30 cm layer (subsoil). Results showed that, in the topsoil, biogas slurry substitution enhanced peroxidase (PER) activity while inhibiting phenol oxidase (POX) activity compared with the chemical fertilizer (CF) treatment. This was accompanied by a significant decrease in lignin phenol content by 30.62%−51.78%, whereas the acid/aldehyde (Ad/Al) ratio remained relatively stable. Additionally, biogas slurry application significantly promoted microbial necromass carbon (MNC) accumulation with increases of 33.50%−109.35%, indicating that MNC became a major contributor to the topsoil organic carbon pool. In the subsoil, anaerobic conditions suppressed extracellular enzyme activity, limiting microbial transformation of plant-derived carbon. The 50% nitrogen substitution treatment significantly increased lignin phenol content by 40.26%−69.44%, but significantly reduced MNC by 54.27%−61.15%. This study reveals the stratified SOC stabilization mechanisms driven by biogas slurry: microbial transformation predominates in the topsoil, while physical and chemical stabilization of plant-derived carbon is central in the subsoil. The 50% substitution rate was identified as the optimal strategy for enhancing SOC sequestration efficiency across the entire soil profile.

Graphical abstract

Keywords

biogas slurry substitution / soil organic carbon / lignin phenol / microbial necromass carbon / extracellular enzyme activity

Highlight

● Biogas slurry reshapes vertical SOC pathways in paddy soils.

● Topsoil SOC is dominated by microbial necromass formation under biogas slurry input.

● Subsoil SOC relies on physicochemical preservation of plant-derived carbon.

● 50% substitution enhances lignin shortcut degradation via PER–Fenton processes.

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Yulin Wang, Zichuan Li, Yanjun Chai, Zhixi Geng, Ning Zhao, Zhuozhe Wang, JiaJun Wu, Jingyuan Pan, Lifeng Ping, Yan Li, Ming Hung Wong. Biogas slurry substitution regulates soil carbon sequestration by shifting plant- and microbial-derived carbon pathways in a paddy profile. Soil Ecology Letters, 2027, 9 (2) : 260514 DOI:10.1007/s42832-026-0514-4

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References

[1]

Allison, S.D., 2006. Soil minerals and humic acids alter enzyme stability: Implications for ecosystem processes. Biogeochemistry81, 361–373.

[2]

Angst, G., Mueller, K.E., Nierop, K.G.J., Simpson, M.J., 2021. Plant- or microbial-derived? A review on the molecular composition of stabilized soil organic matter. Soil Biology and Biochemistry156, 108189.

[3]

Bach, C.E., Warnock, D.D., Van Horn, D.J., Weintraub, M.N., Sinsabaugh, R.L., Allison, S.D., German, D.P., 2013. Measuring phenol oxidase and peroxidase activities with pyrogallol, L-DOPA, and ABTS: Effect of assay conditions and soil type. Soil Biology and Biochemistry67, 183–191.

[4]

Balesdent, J., Basile-Doelsch, I., Chadoeuf, J., Cornu, S., Derrien, D., Fekiacova, Z., Hatté, C., 2018. Atmosphere–soil carbon transfer as a function of soil depth. Nature559, 599–602.

[5]

Black, J.E., Wagner, T., Abbott, G.D., 2021. Assessing lignin decomposition and soil organic carbon contents across a tropical savannah-rainforest boundary in Guyana. Frontiers in Forests and Global Change4, 629600.

[6]

Buckeridge, K.M., Creamer, C., Whitaker, J., 2022. Deconstructing the microbial necromass continuum to inform soil carbon sequestration. Functional Ecology36, 1396–1410.

[7]

Buckeridge, K.M., La Rosa, A.F., Mason, K.E., Whitaker, J., McNamara, N.P., Grant, H.K., Ostle, N.J., 2020. Sticky dead microbes: Rapid abiotic retention of microbial necromass in soil. Soil Biology and Biochemistry149, 107929.

[8]

Button, E.S., Pett-Ridge, J., Murphy, D.V., Kuzyakov, Y., Chadwick, D.R., Jones, D.L., 2022. Deep-C storage: Biological, chemical and physical strategies to enhance carbon stocks in agricultural subsoils. Soil Biology and Biochemistry170, 108697.

[9]

Camenzind, T., Mason-Jones, K., Mansour, I., Rillig, M.C., Lehmann, J., 2023. Formation of necromass-derived soil organic carbon determined by microbial death pathways. Nature Geoscience16, 115–122.

[10]

Carter, M.R., Gregorich, E.G., 2007. Soil Sampling and Methods of Analysis. 2nd ed. Boca Raton: CRC Press.

[11]

Chang, X.P., Pei, Z.J., Wang, X.F., Wang, H., Mu, J., Ma, Y.J., Zhang, M.Y., Zhang, K.Q., Du, L.Z., 2025. Divergent responses of plant lignin and microbial necromass to the contribution of soil organic carbon under organic and chemical fertilization. Frontiers in Microbiology16, 1586791.

[12]

Chen, X.B., Hu, Y.J., Xia, Y.H., Zheng, S.M., Ma, C., Rui, Y.C., He, H.B., Huang, D.Y., Zhang, Z.H., Ge, T.D., Wu, J.S., Guggenberger, G., Kuzyakov, Y., Su, Y.R., 2021. Contrasting pathways of carbon sequestration in paddy and upland soils. Global Change Biology27, 2478–2490.

[13]

Chen, Z.M., Ma, J.C., Ma, J.W., Ye, J., Yu, Q.G., Zou, P., Sun, W.C., Lin, H., Wang, F., Zhao, X.L., Wang, Q., 2024. Long-term biogas slurry application increases microbial necromass but not plant lignin contribution to soil organic carbon in paddy soils as regulated by fungal community. Waste Management175, 254–264.

[14]

Cotrufo, M.F., Haddix, M.L., Kroeger, M.E., Stewart, C.E., 2022. The role of plant input physical-chemical properties, and microbial and soil chemical diversity on the formation of particulate and mineral-associated organic matter. Soil Biology and Biochemistry168, 108648.

[15]

Cotrufo, M.F., Wallenstein, M.D., Boot, C.M., Denef, K., Paul, E., 2013. The Microbial Efficiency-Matrix Stabilization (MEMS) framework integrates plant litter decomposition with soil organic matter stabilization: do labile plant inputs form stable soil organic matter. Global Change Biology19, 988–995.

[16]

Datta, R., Kelkar, A., Baraniya, D., Molaei, A., Moulick, A., Meena, R., Formanek, P., 2017. Enzymatic degradation of lignin in soil: a review. Sustainability9, 1163.

[17]

DeForest, J.L., 2009. The influence of time, storage temperature, and substrate age on potential soil enzyme activity in acidic forest soils using MUB-linked substrates and l-DOPA. Soil Biology and Biochemistry41, 1180–1186.

[18]

Deng, J., Feng, X.Q., Wang, D.Y., Lu, J., Chong, H.T., Shang, C., Liu, K., Huang, L.Y., Tian, X.H., Zhang, Y.B., 2020. Root morphological traits and distribution in direct-seeded rice under dense planting with reduced nitrogen. PLoS One15, e0238362.

[19]

Dubeux, J.C.B., Lira Junior, M.D.A., Simili, F.F., Bretas, I.L., Trumpp, K.R., Bizzuti, B.E., Garcia, L., Oduor, K.T., Queiroz, L.M.D., Acuña, J.P., Mendes, C.T.E., 2024. Deep soil organic carbon: A review. CABI Reviews19, 1.

[20]

Falade, A.O., Nwodo, U.U., Iweriebor, B.C., Green, E., Mabinya, L.V., Okoh, A.I., 2017. Lignin peroxidase functionalities and prospective applications. MicrobiologyOpen6, e00394.

[21]

Feng, G.Y., Hao, F.X., He, W., Ran, Q.F., Nie, G., Huang, L.K., Wang, X., Yuan, S.H., Xu, W.Z., Zhang, X.Q., 2024. Effect of biogas slurry on the soil properties and microbial composition in an annual ryegrass-silage maize rotation system over a five-year period. Microorganisms12, 716.

[22]

Fenner, N., Freeman, C., 2011. Drought-induced carbon loss in peatlands. Nature Geoscience4, 895–900.

[23]

Frenzel, P., Rothfuss, F., Conrad, R., 1992. Oxygen profiles and methane turnover in a flooded rice microcosm. Biology and Fertility of Soils14, 84–89.

[24]

Gunina, A., Kuzyakov, Y., 2015. Sugars in soil and sweets for microorganisms: review of origin, content, composition and fate. Soil Biology and Biochemistry90, 87–100.

[25]

Hao, J.J., Chai, Y.N., Lopes, L.D., Ordóñez, R.A., Wright, E.E., Archontoulis, S., Schachtman, D.P., 2021. The effects of soil depth on the structure of microbial communities in agricultural soils in Iowa (United States). Applied and Environmental Microbiology87, e02673–20.

[26]

Hicks Pries, C.E., Ryals, R., Zhu, B., Min, K., Cooper, A., Goldsmith, S., Pett-Ridge, J., Torn, M., Berhe, A.A., 2023. The deep soil organic carbon response to global change. Annual Review of Ecology, Evolution, and Systematics54, 375–401.

[27]

Hicks Pries, C.E., Sulman, B.N., West, C., O’Neill, C., Poppleton, E., Porras, R.C., Castanha, C., Zhu, B., Wiedemeier, D.B., Torn, M.S., 2018. Root litter decomposition slows with soil depth. Soil Biology and Biochemistry125, 103–114.

[28]

Hu, J.X., Huang, C.D., Zhou, S.X., Liu, X., Dijkstra, F.A., 2022. Nitrogen addition increases microbial necromass in croplands and bacterial necromass in forests: A global meta-analysis. Soil Biology and Biochemistry165, 108500.

[29]

Huang, W.G., Kuzyakov, Y., Niu, S.L., Luo, Y., Sun, B., Zhang, J.B., Liang, Y.T., 2023. Drivers of microbially and plant-derived carbon in topsoil and subsoil. Global Change Biology29, 6188–6200.

[30]

Jain, S., Jain, S., Wolf, I.T., Lee, J., Tong, Y.W., 2015. A comprehensive review on operating parameters and different pretreatment methodologies for anaerobic digestion of municipal solid waste. Renewable and Sustainable Energy Reviews52, 142–154.

[31]

Jandl, G., Horn, R., Schroeder, R., Eckhardt, K.U., Leinweber, P., 2023. Influence of biogas digestates on the composition of soil organic matter. Journal of Energy and Power Technology5, 1–32.

[32]

Jin, K.M., Shen, J.B., Ashton, R.W., White, R.P., Dodd, I.C., Parry, M.A.J., Whalley, W.R., 2015. Wheat root growth responses to horizontal stratification of fertiliser in a water-limited environment. Plant and Soil386, 77–88.

[33]

Kallenbach, C.M., Frey, S.D., Grandy, A.S., 2016. Direct evidence for microbial-derived soil organic matter formation and its ecophysiological controls. Nature Communications7, 13630.

[34]

Kasmerchak, C.S., Daughtridge, R.C., Margenot, A.J., 2025. Differential response of chitinolytic and proteolytic depolymerization-mineralization pathways to organic nitrogen substrates. Biology and Fertility of Soils61, 1215–1234.

[35]

Khan, M.Z., Chabbi, A., Felbacq, A., Piton, G., Bertrand, I., Maron, P.A., Rumpel, C., 2025. Whole soil warming promotes surface soil carbon loss but deep soil carbon gain, depending on land management practices in temperate climate. Soil Biology and Biochemistry207, 109832.

[36]

Lal, R., Monger, C., Nave, L., Smith, P., 2021. The role of soil in regulation of climate. Philosophical Transactions of the Royal Society B376, 20210084.

[37]

Lehmann, J., Kleber, M., 2015. The contentious nature of soil organic matter. Nature528, 60–68.

[38]

Li, Y., Zhang, W., Li, J., Zhou, F., Liang, X.N., Zhu, X.F., He, H.B., Zhang, X.D., 2023. Complementation between microbial necromass and plant debris governs the long-term build-up of the soil organic carbon pool in conservation agriculture. Soil Biology and Biochemistry178, 108963.

[39]

Liang, C., Amelung, W., Lehmann, J., Kästner, M., 2019. Quantitative assessment of microbial necromass contribution to soil organic matter. Global Change Biology25, 3578–3590.

[40]

Liang, L., Ding, Q.S., Zhang, H.Y., Liu, Q., 2025. Disturbance characteristics of subsoiling in paddy soil based on smoothed particle hydrodynamics (SPH). Agronomy15, 2695.

[41]

Liang, X.Y., Wang, H., Wang, C.J., Wang, H.T., Yao, Z.L., Qiu, X.F., Ju, H., Wang, J.D., 2024. Unraveling the relationship between soil carbon-degrading enzyme activity and carbon fraction under biogas slurry topdressing. Journal of Environmental Management356, 120641.

[42]

Ling, J., Dungait, J.A.J., Delgado-Baquerizo, M., Cui, Z.L., Zhou, R.R., Zhang, W.S., Gao, Q., Chen, Y.X., Yue, S.C., Kuzyakov, Y., Zhang, F.S., Chen, X.P., Tian, J., 2025. Soil organic carbon thresholds control fertilizer effects on carbon accrual in croplands worldwide. Nature Communications16, 3009.

[43]

Liu, L., Cheng, M., Yang, L., Gu, X.Y., Jin, J.Y., Fu, M.J., 2023. Regulation of straw decomposition and its effect on soil function by the amount of returned straw in a cool zone rice crop system. Scientific Reports13, 15673.

[44]

Liu, X., Bol, R., An, T.T., Liu, Y.C., Xu, Y.D., Li, S.Y., Wang, J.K., 2024. Divergent accumulation of microbial necromass and plant lignin phenol induced by adding maize straw to fertilized soils. Soil and Tillage Research243, 106177.

[45]

Liu, X.J.A., Finley, B.K., Mau, R.L., Schwartz, E., Dijkstra, P., Bowker, M.A., Hungate, B.A., 2020. The soil priming effect: Consistent across ecosystems, elusive mechanisms. Soil Biology and Biochemistry140, 107617.

[46]

Liu, Z.W., Liu, X.X., Wu, X.L., Bian, R.J., Liu, X.Y., Zheng, J.F., Zhang, X.H., Cheng, K., Li, L.Q., Pan, G.X., 2021. Long-term elevated CO2 and warming enhance microbial necromass carbon accumulation in a paddy soil. Biology and Fertility of Soils57, 673–684.

[47]

Lu, Z., Li, H., Sayer, E.J., Liu, Z.F., Li, L.H., Chen, Y., Qin, G.M., Li, J.T., Zhou, J.G., Huang, X.Y., Zhang, J.F., Wu, J.T., Thapa, P., Wang, F.M., 2023. Enhanced abundance of generalist and litter saprotrophs explain increased tropical forest soil carbon with long-term nitrogen deposition. Functional Ecology37, 2282–2296.

[48]

Mazzon, M., Cavani, L., Margon, A., Sorrenti, G., Ciavatta, C., Marzadori, C., 2018. Changes in soil phenol oxidase activities due to long-term application of compost and mineral N in a walnut orchard. Geoderma316, 70–77.

[49]

Mehmood, I., Qiao, L., Chen, H.Q., Tang, Q.Y., Woolf, D., Fan, M.S., 2020. Biochar addition leads to more soil organic carbon sequestration under a maize-rice cropping system than continuous flooded rice. Agriculture, Ecosystems & Environment298, 106965.

[50]

Min, K., Freeman, C., Kang, H., Choi, S.U., 2015. The regulation by phenolic compounds of soil organic matter dynamics under a changing environment. BioMed Research International2015, 825098.

[51]

Otto, A., Simpson, M.J., 2006. Evaluation of CuO oxidation parameters for determining the source and stage of lignin degradation in soil. Biogeochemistry80, 121–142.

[52]

Pei, Z.F., Shen, Q.G., Shang, X.L., Hong, M., 2024. Different responses of lipids and lignin phenols to nitrogen addition in meadow grassland soil. Journal of Soils and Sediments24, 1887–1898.

[53]

Pham, L.T.M., Kim, S.J., Kim, Y.H., 2016. Improvement of catalytic performance of lignin peroxidase for the enhanced degradation of lignocellulose biomass based on the imbedded electron-relay in long-range electron transfer route. Biotechnology for Biofuels9, 247.

[54]

Prommer, J., Walker, T.W.N., Wanek, W., Braun, J., Zezula, D., Hu, Y.T., Hofhansl, F., Richter, A., 2020. Increased microbial growth, biomass, and turnover drive soil organic carbon accumulation at higher plant diversity. Global Change Biology26, 669–681.

[55]

Pu, R.F., Wang, P.P., Guo, L.P., Li, M.H., Cui, X.M., Wang, C.X., Liu, Y., Yang, Y., 2022. The remediation effects of microbial organic fertilizer on soil microorganisms after chloropicrin fumigation. Ecotoxicology and Environmental Safety231, 113188.

[56]

Qin, G.M., He, W.J., Sanders, C.J., Zhang, J.F., Zhou, J.G., Wu, J.T., Lu, Z., Yu, M.X., Li, Y.W., Li, Y.X., Lambers, H., Li, Z.A., Wang, F.M., 2024. Contributions of plant- and microbial-derived residuals to mangrove soil carbon stocks: Implications for blue carbon sequestration. Functional Ecology38, 573–585.

[57]

Reda, A., Hailu, A.H., 2017. Extensive utilization of inorganic fertilizers in Ethiopian agriculture and its possible consequences on soil quality. World Journal of Agricultural Sciences13, 155–171.

[58]

Ren, B.H., Li, H.Y., Li, D.Y., Meng, M., Li, J.H., Bai, L., Feng, Y.L., 2025. Nitrogen addition changes the nitrogen conversion process in forest steppe ecotone by increasing enzyme activity. Ecological Processes14, 38.

[59]

Roberts, P., Jones, D.L., 2012. Microbial and plant uptake of free amino sugars in grassland soils. Soil Biology and Biochemistry49, 139–149.

[60]

Saidy, A.R., Smernik, R.J., Baldock, J.A., Kaiser, K., Sanderman, J., 2015. Microbial degradation of organic carbon sorbed to phyllosilicate clays with and without hydrous iron oxide coating. European Journal of Soil Science66, 83–94.

[61]

Saiya-Cork, K.R., Sinsabaugh, R.L., Zak, D.R., 2002. The effects of long term nitrogen deposition on extracellular enzyme activity in an Acer saccharum forest soil. Soil Biology and Biochemistry34, 1309–1315.

[62]

Shao, P.S., Liang, C., Lynch, L., Xie, H.T., Bao, X.L., 2019. Reforestation accelerates soil organic carbon accumulation: Evidence from microbial biomarkers. Soil Biology and Biochemistry131, 182–190.

[63]

Si, Y.T., Xiong, L., Chen, Y., Zhu, J.M., Xie, J.S., Gao, R., Yang, Y.S., 2018. Contribution of the vertical movement of dissolved organic carbon to carbon allocation in two distinct soil types under Castanopsis fargesii Franch. and C. carlesii (Hemsl.) Hayata forests. Annals of Forest Science75, 79.

[64]

Sinsabaugh, R.L., 2010. Phenol oxidase, peroxidase and organic matter dynamics of soil. Soil Biology and Biochemistry42, 391–404.

[65]

Sinsabaugh, R.L., Follstad Shah, J.J., 2012. Ecoenzymatic Stoichiometry and Ecological Theory. Annual Review of Ecology, Evolution, and Systematics43, 313–343.

[66]

Sinsabaugh, R.L., Hill, B.H., Follstad Shah, J.J., 2009. Ecoenzymatic stoichiometry of microbial organic nutrient acquisition in soil and sediment. Nature462, 795–798.

[67]

Sinsabaugh, R.L., Moorhead, D.L., 1994. Resource allocation to extracellular enzyme production: a model for nitrogen and phosphorus control of litter decomposition. Soil Biology and Biochemistry26, 1305–1311.

[68]

Su, R.L., Wu, X., Hu, J.L., Li, H.B., Xiao, H.B., Zhao, J.S., Hu, R.G., 2024. Carbon availability and microbial activity manipulate the temperature sensitivity of anaerobic degradation in a paddy soil profile. Environmental Research252, 118453.

[69]

Tamura, M., Suseela, V., 2021. Warming and labile substrate addition alter enzyme activities and composition of soil organic carbon. Frontiers in Forests and Global Change4, 691302.

[70]

Tang, Y.F., Luo, L.M., Carswell, A., Misselbrook, T., Shen, J.H., Han, J.G., 2021. Changes in soil organic carbon status and microbial community structure following biogas slurry application in a wheat-rice rotation. Science of the Total Environment757, 143786.

[71]

Thevenot, M., Dignac, M.F., Rumpel, C., 2010. Fate of lignins in soils: a review. Soil Biology and Biochemistry42, 1200–1211.

[72]

Thirunavukkarasu, A., Hedenström, M., Sparrman, T., Nilsson, M.B., Schleucher, J., Öquist, M., 2025. Unraveling the dynamics of lignin chemistry on decomposition to understand its contribution to soil organic matter accumulation. Plant and Soil511, 1485–1502.

[73]

Vance, E.D., Brookes, P.C., Jenkinson, D.S., 1987. An extraction method for measuring soil microbial biomass C. Soil Biology and Biochemistry19, 703–707.

[74]

Wang, B.R., An, S.S., Liang, C., Liu, Y., Kuzyakov, Y., 2021. Microbial necromass as the source of soil organic carbon in global ecosystems. Soil Biology and Biochemistry162, 108422.

[75]

Wang, C., Shi, Z.Y., Li, A.G., Geng, T.Y., Liu, L.L., Liu, W.X., 2024a. Long-term nitrogen input reduces soil bacterial network complexity by shifts in life history strategy in temperate grassland. iMeta3, e194.

[76]

Wang, H.T., Qiu, X.F., Liang, X.Y., Wang, H., Wang, J.D., 2024b. Biogas slurry change the transport and distribution of soil water under drip irrigation. Agricultural Water Management294, 108719.

[77]

Wang, N.N., Zheng, T., Zhang, G.S., Wang, P., 2016. A review on Fenton-like processes for organic wastewater treatment. Journal of Environmental Chemical Engineering4, 762–787.

[78]

Wei, L., Ge, T.D., Zhu, Z.K., Luo, Y., Yang, Y.H., Xiao, M.L., Yan, Z.F., Li, Y.H., Wu, J.S., Kuzyakov, Y., 2021. Comparing carbon and nitrogen stocks in paddy and upland soils: Accumulation, stabilization mechanisms, and environmental drivers. Geoderma398, 115121.

[79]

Wordell-Dietrich, P., Don, A., Helfrich, M., 2017. Controlling factors for the stability of subsoil carbon in a Dystric Cambisol. Geoderma304, 40–48.

[80]

Yang, Y., Dou, Y.X., Wang, B.R., Wang, Y.Q., Liang, C., An, S.S., Soromotin, A., Kuzyakov, Y., 2022. Increasing contribution of microbial residues to soil organic carbon in grassland restoration chronosequence. Soil Biology and Biochemistry170, 108688.

[81]

Ye, G.P., Lin, Y.X., Kuzyakov, Y., Liu, D.Y., Luo, J.F., Lindsey, S., Wang, W.J., Fan, J.B., Ding, W.X., 2019. Manure over crop residues increases soil organic matter but decreases microbial necromass relative contribution in upland Ultisols: Results of a 27-year field experiment. Soil Biology and Biochemistry134, 15–24.

[82]

Yuan, Y., Li, Y., Mou, Z.J., Kuang, L.H., Wu, W.J., Zhang, J., Wang, F.M., Hui, D.F., Peñuelas, J., Sardans, J., Lambers, H., Wang, J., Kuang, Y.W., Li, Z., Liu, Z.F., 2021. Phosphorus addition decreases microbial residual contribution to soil organic carbon pool in a tropical coastal forest. Global Change Biology27, 454–466.

[83]

Zhang, L.G., Chen, X., Xu, Y.J., Jin, M.C., Ye, X.X., Gao, H.J., Chu, W.Y., Mao, J.D., Thompson, M.L., 2020. Soil labile organic carbon fractions and soil enzyme activities after 10 years of continuous fertilization and wheat residue incorporation. Scientific Reports10, 11318.

[84]

Zhang, M.Y., Cui, J.T., Mi, M., Jin, Z.W., Wong, M.H., Shan, S.D., Ping, L.F., 2024. Persistent effects of swine manure biochar and biogas slurry application on soil nitrogen content and quality of lotus root. Frontiers in Plant Science15, 1359911.

[85]

Zhang, X.D., Amelung, W., 1996. Gas chromatographic determination of muramic acid, glucosamine, mannosamine, and galactosamine in soils. Soil Biology and Biochemistry28, 1201–1206.

[86]

Zhang, Y.J., Gao, W., Huang, S.W., Li, C.Y., Tang, J.W., Zhang, Q., Li, M.Y., Wang, Y.L., Ai, C., 2025. Long-term manure and straw addition enhance protistan diversity and stimulate soil microbial interactions and nutrient mineralization in vegetable field. Applied Soil Ecology212, 106170.

[87]

Zhao, W.T., Wei, C.L., Cui, Y.D., Ye, J.Q., He, B., Liu, X.M., Sun, J., 2022. Efficient demethylation of lignin for polyphenol production enabled by low-cost bifunctional protic ionic liquid under mild and halogen-free conditions. Chemical Engineering Journal443, 136486.

[88]

Zhou, L.H., Liu, S.S., Shen, H.H., Zhao, M.Y., Xu, L.C., Xing, A.J., Fang, J.Y., 2020. Soil extracellular enzyme activity and stoichiometry in China’s forests. Functional Ecology34, 1461–1471.

[89]

Zhou, R.R., Liu, Y., Dungait, J.A.J., Kumar, A., Wang, J.S., Tiemann, L.K., Zhang, F.S., Kuzyakov, Y., Tian, J., 2023. Microbial necromass in cropland soils: A global meta-analysis of management effects. Global Change Biology29, 1998–2014.

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