26 citations as recorded by crossref.

1. Utilisation of mucilage C by microbial communities under drought M. Ahmed et al. https://doi.org/10.1007/s00374-017-1237-6
2. Carbon and nitrogen recycling from microbial necromass to cope with C:N stoichiometric imbalance by priming J. Cui et al. https://doi.org/10.1016/j.soilbio.2020.107720
3. 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
4. Assessing microbial residues in soil as a potential carbon sink and moderator of carbon use efficiency K. Geyer et al. https://doi.org/10.1007/s10533-020-00720-4
5. A sugar biomarker proxy for assessing terrestrial versus aquatic sedimentary input J. Hepp et al. https://doi.org/10.1016/j.orggeochem.2016.05.012
6. Effect of the combined addition of mineral nitrogen and crop residue on soil respiration, organic carbon sequestration, and exogenous nitrogen in stable organic matter Z. Liang et al. https://doi.org/10.1016/j.apsoil.2021.104324
7. Carbon sequestration and turnover in soil under the energy crop Miscanthus: repeated 13C natural abundance approach and literature synthesis H. Zang et al. https://doi.org/10.1111/gcbb.12485
8. Natural 13C abundance reveals age of dietary carbon sources in nematode trophic groups M. Vestergård et al. https://doi.org/10.1016/j.soilbio.2018.11.024
9. The importance of fungal necromass in soil organic carbon: Insights from elevation gradients in arid regions M. Cong et al. https://doi.org/10.1016/j.apsoil.2025.106376
10. Microbial carbon recycling: an underestimated process controlling soil carbon dynamics – Part 2: A C3-C4 vegetation change field labelling experiment A. Basler et al. https://doi.org/10.5194/bg-12-6291-2015
11. Evaluating soil microbial carbon use efficiency explicitly as a function of cellular processes: implications for measurements and models S. Hagerty et al. https://doi.org/10.1007/s10533-018-0489-z
12. 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
13. Testing microbial models with data from a 14C glucose tracer experiment S. Hagerty et al. https://doi.org/10.1016/j.soilbio.2022.108781
14. Divergent accumulation of microbial and plant necromass along paddy soil development in a millennium scale Y. Liu et al. https://doi.org/10.1016/j.still.2023.105769
15. Functional carbon pools and microbial communities in persistent carbon rich erosion buried topsoils M. A.D & H. B.L https://doi.org/10.1016/j.geoderma.2025.117353
16. 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
17. The molecular composition of extractable soil microbial compounds and their contribution to soil organic matter vary with soil depth and tree species M. Lorenz et al. https://doi.org/10.1016/j.scitotenv.2021.146732
18. Soil profile connectivity can impact microbial substrate use, affecting how soil CO2 effluxes are controlled by temperature F. Podrebarac et al. https://doi.org/10.5194/bg-18-4755-2021
19. Nitrogen fertilization modifies organic transformations and coatings on soil biogeochemical interfaces through microbial polysaccharides synthesis X. Huang et al. https://doi.org/10.1038/s41598-019-55174-y
20. Soil organic matter origin and composition along a 3200 m elevation gradient on Mount Kilimanjaro J. Becker et al. https://doi.org/10.1016/j.catena.2025.109319
21. Polyethylene microplastics mineralize slowly in soil but integrate into soil structures and organic matter H. Forsyth et al. https://doi.org/10.1186/s43591-026-00223-3
22. New strategies for submicron characterization the carbon binding of reactive minerals in long-term contrasting fertilized soils: implications for soil carbon storage J. Xiao et al. https://doi.org/10.5194/bg-13-3607-2016
23. Assessing the accumulation efficiency of various microbial carbon components in soils of different minerals Y. Cai et al. https://doi.org/10.1016/j.geoderma.2021.115562
24. Turnover of fungal glucosamine and bacterial muramic acid in comparison with soil organic carbon in two arable soils with distinct fungal communities R. Joergensen & F. Wichern https://doi.org/10.1016/j.soilbio.2025.109889
25. Saccharides of ectomycorrhizal fungal sclerotia as sources of forest soil polysaccharides Y. Sugiura et al. https://doi.org/10.1080/00380768.2017.1381928
26. Different responses of soil bacterial necromass carbon and fungal necromass carbon to nitrogen deposition in meadow steppe N. Jiang et al. https://doi.org/10.1016/j.apsoil.2025.106282