103 citations as recorded by crossref.

1. Amino sugars as specific indices for fungal and bacterial residues in soil R. Joergensen https://doi.org/10.1007/s00374-018-1288-3
2. Distinct regulation of microbial processes in the immobilization of labile carbon in different soils X. Wang et al. https://doi.org/10.1016/j.soilbio.2020.107723
3. Metagenomic highlight contrasting elevational pattern of bacteria- and fungi-derived compound decompositions in forest soils L. Chen et al. https://doi.org/10.1007/s11104-023-06104-5
4. Land use types affect soil microbial NO3− immobilization through changed fungal and bacterial contribution in alkaline soils of a subtropical montane agricultural landscape X. Wang et al. https://doi.org/10.1007/s00374-023-01787-5
5. Turnover of gram-negative bacterial biomass-derived carbon through the microbial food web of an agricultural soil T. Zheng et al. https://doi.org/10.1016/j.soilbio.2020.108070
6. Resource Legacies of Organic and Conventional Management Differentiate Soil Microbial Carbon Use M. Arcand et al. https://doi.org/10.3389/fmicb.2017.02293
7. Microbial metabolic potential to transform plant residual carbon Z. Bai et al. https://doi.org/10.1016/j.apsoil.2020.103726
8. Metagenomic insights into the characteristics of soil microbial communities in the decomposing biomass of Moso bamboo forests under different management practices X. Zhang et al. https://doi.org/10.3389/fmicb.2022.1051721
9. Metagenomics and stable isotope probing reveal the complementary contribution of fungal and bacterial communities in the recycling of dead biomass in forest soil R. López-Mondéjar et al. https://doi.org/10.1016/j.soilbio.2020.107875
10. Turnover of bacterial biomass to soil organic matter via fungal biomass and its metabolic implications T. Zheng et al. https://doi.org/10.1016/j.soilbio.2023.108995
11. Microbial necromass carbon and nitrogen persistence are decoupled in agricultural grassland soils K. Buckeridge et al. https://doi.org/10.1038/s43247-022-00439-0
12. Contribution of rhizodeposit associated microbial groups to SOC varies with maize growth stages S. Zhang et al. https://doi.org/10.1016/j.geoderma.2022.115947
13. Disentangling immobilization of nitrate by fungi and bacteria in soil to plant residue amendment X. Li et al. https://doi.org/10.1016/j.geoderma.2020.114450
14. Saprotrophic-mycorrhizal divide in stable isotope composition throughout the whole fungus: from mycelium to hymenophore A. Zuev et al. https://doi.org/10.1007/s00572-025-01203-w
15. Bacterial necromass determines the response of mineral-associated organic matter to elevated CO2 Y. Li et al. https://doi.org/10.1007/s00374-024-01803-2
16. Untargeted Metabolomics Reveals Distinct Soil Metabolic Profiles Across Land Management Practices Z. Vickery et al. https://doi.org/10.3390/metabo15120783
17. Integrated soil–crop system management stabilizes soil organic carbon in saline soils via calcium-mediated synergy between microbial and mineral carbon pumps L. Liu et al. https://doi.org/10.1016/j.catena.2026.109947
18. Decomposer food web in a deciduous forest shows high share of generalist microorganisms and importance of microbial biomass recycling R. López-Mondéjar et al. https://doi.org/10.1038/s41396-018-0084-2
19. Plant-Associated Microbiomes: Crosstalk and Engineering to Improve Nutrient Use Efficiency (NUE) in Crops of Global Importance P. Tiwari & K. Park https://doi.org/10.3390/plants15081265
20. Earthworms negate the adverse effect of arbuscular mycorrhizae on living bacterial biomass and bacterial necromass accumulation in a subtropical soil X. He et al. https://doi.org/10.1016/j.soilbio.2020.108052
21. Variations in Soil Organic Carbon Fractions and Microbial Community in Rice Fields under an Integrated Cropping System C. Wang et al. https://doi.org/10.3390/agronomy14010081
22. Proactive monitoring of changes in the microbial community structure in wastewater treatment bioreactors using phospholipid fatty acid analysis L. Mensah et al. https://doi.org/10.1016/j.engmic.2024.100177
23. Altered microbial CAZyme families indicated dead biomass decomposition following afforestation C. Ren et al. https://doi.org/10.1016/j.soilbio.2021.108362
24. In-situ 13CO2 labeling to trace carbon fluxes in plant-soil-microorganism systems: Review and methodological guideline R. Pang et al. https://doi.org/10.1016/j.rhisph.2021.100441
25. Divergent mineralization of hydrophilic and hydrophobic organic substrates and their priming effect in soils depending on their preferential utilization by bacteria and fungi S. Deng et al. https://doi.org/10.1007/s00374-020-01503-7
26. Dynamics of soil respiration and microbial communities: Interactive controls of temperature and substrate quality R. Ali et al. https://doi.org/10.1016/j.soilbio.2018.09.010
27. D2O labelling reveals synthesis of small, water-soluble metabolites in soil C. Warren https://doi.org/10.1016/j.soilbio.2021.108543
28. Functional trait diversity in overstorey and understorey increases microbial carbon use efficiency in a forest plantation soil R. Wan et al. https://doi.org/10.1016/j.soilbio.2026.110119
29. Manure application accumulates more nitrogen in paddy soils than rice straw but less from fungal necromass Y. Xia et al. https://doi.org/10.1016/j.agee.2021.107575
30. Decreased rhizodeposition, but increased microbial carbon stabilization with soil depth down to 3.6 m L. Peixoto et al. https://doi.org/10.1016/j.soilbio.2020.108008
31. Manufacturing triple-isotopically labeled microbial necromass to track C, N and P cycles in terrestrial ecosystems M. Schmitt et al. https://doi.org/10.1016/j.apsoil.2021.104322
32. Differential effects of forest-floor litter and roots on soil organic carbon formation in a temperate oak forest Y. Zhang et al. https://doi.org/10.1016/j.soilbio.2023.109017
33. Effect of nitrogen fertilization on the fate of rice residue-C in paddy soil depending on depth: 13C amino sugar analysis X. Chen et al. https://doi.org/10.1007/s00374-018-1278-5
34. Soil aggregate carbon accrual via the microbial life footprint with nutrient management in worldwide croplands Y. Wang et al. https://doi.org/10.1016/j.jclepro.2025.144717
35. Lipids represent a dynamic, yet stable pool of microbially-derived soil carbon K. Rempfert et al. https://doi.org/10.1016/j.soilbio.2025.110013
36. Mechanisms for Retention of Low Molecular Weight Organic Carbon Varies with Soil Depth at a Coastal Prairie Ecosystem J. McFarland et al. https://doi.org/10.2139/ssrn.3955839
37. Living and Dead Microorganisms in Mediating Soil Carbon Stocks Under Long-Term Fertilization in a Rice-Wheat Rotation J. Chen et al. https://doi.org/10.3389/fmicb.2022.854216
38. Effects of microbial groups on soil organic carbon accrual and mineralization during high- and low-quality litter decomposition X. Bai et al. https://doi.org/10.1016/j.catena.2024.108051
39. Management extensification in oil palm plantations reduces SOC decomposition N. Hennings et al. https://doi.org/10.1016/j.soilbio.2021.108535
40. Soil enzyme activities in heavily manured and waterlogged soil cultivated with ryegrass (Lolium multiflorum) T. Rupngam et al. https://doi.org/10.1139/cjss-2023-0097
41. Changes of microbial residues after wetland cultivation and restoration X. Ding et al. https://doi.org/10.1007/s00374-019-01341-2
42. Nitrogen addition decreases the soil cumulative priming effect and favours soil net carbon gains in Robinia pseudoacacia plantation soil Z. Su & Z. Shangguan https://doi.org/10.1016/j.geoderma.2023.116444
43. Impact of single and binary mixtures of phenanthrene and N-PAHs on microbial utilization of 14C-glucose in soil I. Anyanwu & K. Semple https://doi.org/10.1016/j.soilbio.2018.02.009
44. Variations and controls of soil microbial necromass carbon in grasslands along aridity gradients Y. Xue et al. https://doi.org/10.1016/j.ecolind.2023.111188
45. Functional Genes Highlight Contrasting Elevational Pattern of Bacteria- and Fungi-Derived Compound Decompositions in Forest Soils L. Chen et al. https://doi.org/10.2139/ssrn.4066274
46. Glucose and ribose stabilization in soil: Convergence and divergence of carbon pathways assessed by position-specific labeling E. Bore et al. https://doi.org/10.1016/j.soilbio.2018.12.027
47. Phosphorus drives adaptive shifts in membrane lipid pools and synthesis between soils C. Warren & O. Butler https://doi.org/10.1016/j.soilbio.2024.109387
48. Microbial necromass as the source of soil organic carbon in global ecosystems B. Wang et al. https://doi.org/10.1016/j.soilbio.2021.108422
49. Harnessing plant–microbe interactions: strategies for enhancing resilience and nutrient acquisition for sustainable agriculture A. Yusuf et al. https://doi.org/10.3389/fpls.2025.1503730
50. Differences in straw derived hydrophilic and hydrophobic carbon incorporation into soil microbial necromass J. Zhang et al. https://doi.org/10.1016/j.soilbio.2025.109901
51. Litter quality controls the contribution of microbial carbon to main microbial groups and soil organic carbon during its decomposition X. Bai et al. https://doi.org/10.1007/s00374-023-01792-8
52. Forests have a higher soil C sequestration benefit due to lower C mineralization efficiency: Evidence from the central loess plateau case L. Dong et al. https://doi.org/10.1016/j.agee.2022.108144
53. Karst biogeochemistry in China: past, present and future Y. Huang & Q. Li https://doi.org/10.1007/s12665-019-8400-3
54. Divergent accumulation of microbial necromass and plant lignin components in grassland soils T. Ma et al. https://doi.org/10.1038/s41467-018-05891-1
55. Mechanisms and implications of bacterial–fungal competition for soil resources C. Wang & Y. Kuzyakov https://doi.org/10.1093/ismejo/wrae073
56. Tibetan Plateau grasslands might increase sequestration of microbial necromass carbon under future warming Q. Zhang et al. https://doi.org/10.1038/s42003-024-06396-y
57. Stabilization of microbial residues in soil organic matter after two years of decomposition C. Wang et al. https://doi.org/10.1016/j.soilbio.2019.107687
58. Temporal dynamics of soil dissolved organic carbon in temperate forest managed by prescribed burning in Northeast China X. Dou et al. https://doi.org/10.1016/j.envres.2023.117065
59. Pore‐scale view of microbial turnover: Combining 14C imaging, μCT and zymography after adding soluble carbon to soil pores of specific sizes A. Kravchenko et al. https://doi.org/10.1111/ejss.13001
60. Unraveling the influence of microbial necromass on subsurface microbiomes: metabolite utilization and community dynamics B. Finley et al. https://doi.org/10.1093/ismeco/ycaf006
61. Soil stoichiometric C/N and nitrogen availability jointly shape fungal and bacterial necromass carbon accumulation across ecosystems B. Wang et al. https://doi.org/10.1016/j.still.2025.107042
62. Elevation shapes the biogeography and assembly of soil microbial carbon-cycling functions in mountain ecosystems X. Liu et al. https://doi.org/10.1007/s42832-026-0431-6
63. High turnover rate of free phospholipids in soil confirms the classic hypothesis of PLFA methodology Y. Zhang et al. https://doi.org/10.1016/j.soilbio.2019.05.023
64. Fate and stabilization of labile carbon in a sandy boreal forest soil – A question of nitrogen availability? N. Meyer et al. https://doi.org/10.1016/j.apsoil.2023.105052
65. Distinct responses of soil fungal and bacterial nitrate immobilization to land conversion from forest to agriculture X. Li et al. https://doi.org/10.1016/j.soilbio.2019.03.023
66. Mechanisms for retention of low molecular weight organic carbon varies with soil depth at a coastal prairie ecosystem J. McFarland et al. https://doi.org/10.1016/j.soilbio.2022.108601
67. Fungal key players of cellulose utilization: Microbial networks in aggregates of long-term fertilized soils disentangled using 13C-DNA-stable isotope probing Y. Miao et al. https://doi.org/10.1016/j.scitotenv.2022.155051
68. Soil Properties Control Microbial Carbon Assimilation and Its Mean Residence Time R. Ali et al. https://doi.org/10.3389/fenvs.2020.00033
69. In vitro Evaluation of Biofilm Biomass Dynamics M. Gryndler et al. https://doi.org/10.1134/S0026261721050064
70. Soil bacterial and fungal communities beneath different forest types differentially and promptly respond to non-catastrophic typhoon disturbance Z. Wang et al. https://doi.org/10.1007/s00374-025-01913-5
71. The extent and pathways of nitrogen loss in turfgrass systems: Age impacts H. Chen et al. https://doi.org/10.1016/j.scitotenv.2018.05.053
72. Enhancing soil carbon in arid regions: key role of dissolved organic matter in straw-amended systems J. Zhang et al. https://doi.org/10.1007/s00374-026-01997-7
73. Paddy soils have a much higher microbial biomass content than upland soils: A review of the origin, mechanisms, and drivers L. Wei et al. https://doi.org/10.1016/j.agee.2021.107798
74. Microbial Carbon Use Efficiency and Growth Rates in Soil: Global Patterns and Drivers J. Hu et al. https://doi.org/10.1111/gcb.70036
75. Shifts in microbial- and plant-derived biomass degradation genes with afforestation promoting carbon accumulation M. Cong et al. https://doi.org/10.1016/j.jenvman.2025.126417
76. Methylation procedures affect PLFA results more than selected extraction parameters C. Zosso & G. Wiesenberg https://doi.org/10.1016/j.mimet.2021.106164
77. The vulnerability of microbial necromass carbon: Loss pathways, microbial mechanisms, and factors of its destabilization J. Liu et al. https://doi.org/10.1007/s00374-026-01977-x
78. Metabolic tracing unravels pathways of fungal and bacterial amino sugar formation in soil M. Dippold et al. https://doi.org/10.1111/ejss.12736
79. Microbial biomass estimation by fumigation extraction and ATP – A review in memoriam of Phil Brookes R. Joergensen https://doi.org/10.1007/s00374-025-01939-9
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82. Different Response of Plant- and Microbial-Derived Carbon Decomposition Potential between Alpine Steppes and Meadows on the Tibetan Plateau Y. Yuan et al. https://doi.org/10.3390/f14081580
83. A water stress-adapted inoculum affects rhizosphere fungi, but not bacteria nor wheat C. Giard-Laliberté et al. https://doi.org/10.1093/femsec/fiz080
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