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Dormant microbes dominate soils across China and are regulated by water and resource availability
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  • Published: 12 March 2026

Dormant microbes dominate soils across China and are regulated by water and resource availability

  • Xue Zhao1,2 na1,
  • Liyuan He  ORCID: orcid.org/0000-0003-3326-92603 na1,
  • Gangsheng Wang  ORCID: orcid.org/0000-0002-8117-50344,
  • Jun Wang1,2,5,6,7,8,
  • Zhenghu Zhou  ORCID: orcid.org/0000-0003-2226-42619,
  • Chengjie Ren  ORCID: orcid.org/0000-0003-4959-312910,
  • Sha Zhou11,
  • Jieying Wang1,2,12 na2 &
  • …
  • Fazhu Zhao  ORCID: orcid.org/0000-0003-4758-32771,2,5,6,8 na2 

Communications Earth & Environment , Article number:  (2026) Cite this article

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Subjects

  • Biogeography
  • Microbial ecology

Abstract

Dormancy, as a microbial survival strategy, plays a crucial role in sustaining microbial diversity. However, the large-scale distribution patterns of microbial dormancy and drivers remain poorly understood. Here, we analyzed 591 soil samples from 197 field sites across China, spanning deserts, croplands, grasslands, and forests, to quantify the proportion of dormant microbial cells (Dormancy%). On average, 95.48% of soil microbial cells were dormant, with the lowest Dormancy% in forests (93.84%) and the highest in deserts (96.81%). This regulation followed a regular mechanism: soil water-holding capacity and β−1,4-glucosidase activity acted as immediate triggers, while mineral-associated organic carbon, dissolved organic carbon and microbial biomass carbon indirectly governed the process. Overall, this study provides evidence at the China scale for the dominance of dormant microorganisms in terrestrial ecosystems and reveals the environmental regulatory mechanism of dormancy, highlighting its ecological importance for maintaining microbial diversity and ecosystem stability.

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Data availability

Data supporting the findings of this study are available in figshare (https://doi.org/10.6084/m9.figshare.31419065).

Code availability

The R code we used in this study were put into https://github.com/FEBC-lab.

References

  1. McDonald, M. D. et al. What is microbial dormancy? Trends Microbiol. 32, 142–150 (2024).

    Google Scholar 

  2. Jones, S. E. & Lennon, J. T. Dormancy contributes to the maintenance of microbial diversity. Proc. Natl. Acad. Sci. 107, 5881–5886 (2010).

    Google Scholar 

  3. Lennon, J. T. & Jones, S. E. Microbial seed banks: the ecological and evolutionary implications of dormancy. Nat. Rev. Microbiol. 9, 119–130 (2011).

    Google Scholar 

  4. Mestre, M. & Höfer, J. The microbial conveyor belt: connecting the globe through dispersion and dormancy. Trends Microbiol. 29, 482–492 (2021).

    Google Scholar 

  5. Chesson, P. Mechanisms of maintenance of species diversity. Annu. Rev. Ecol. Evol. Syst. 31, 343–366 (2000).

    Google Scholar 

  6. Kuzyakov, Y., Ling, N., Pietramellara, G. & Nannipieri, P. Some new grand questions in soil biology and biochemistry. Soil Biol. Biochem. 212, 109996 (2026).

    Google Scholar 

  7. Kearns, P. J. et al. Nutrient enrichment induces dormancy and decreases diversity of active bacteria in salt marsh sediments. Nat. Commun. 7, 12881 (2016).

  8. Wang, G., Li, W., Wang, K. & Huang, W. Uncertainty quantification of the soil moisture response functions for microbial dormancy and resuscitation. Soil Biol. Biochem. 160, 108337 (2021).

    Google Scholar 

  9. Georgiou, K., Abramoff, R. Z., Harte, J., Riley, W. J. & Torn, M. S. Microbial community-level regulation explains soil carbon responses to long-term litter manipulations. Nat. Commun. 8, 1223 (2017).

    Google Scholar 

  10. Zhou, Z. et al. The biogeography of soil microbiome potential growth rates. Nat. Commun. 15, 9472 (2024).

    Google Scholar 

  11. Blagodatskaya, E. & Kuzyakov, Y. Active microorganisms in soil: critical review of estimation criteria and approaches. Soil Biol. Biochem. 67, 192–211 (2013).

    Google Scholar 

  12. Bradley, J. A. Microbial dormancy as an ecological and biogeochemical regulator on Earth. Nat. Commun. 16, 3909 (2025).

    Google Scholar 

  13. Loeppmann, S., Semenov, M., Kuzyakov, Y. & Blagodatskaya, E. Shift from dormancy to microbial growth revealed by RNA:DNA ratio. Ecol. Indic. 85, 603–612 (2018).

    Google Scholar 

  14. Tripathi, B. M. et al. Trends in taxonomic and functional composition of soil microbiome along a precipitation gradient in Israel. Microb. Ecol. 74, 168–176 (2017).

    Google Scholar 

  15. Wang, G. et al. Microbial dormancy improves development and experimental validation of ecosystem model. ISME J. 9, 226–237 (2014).

    Google Scholar 

  16. Ren, C. et al. Temporal variation in soil enzyme activities after afforestation in the Loess Plateau, China. Geoderma 282, 103–111 (2016).

    Google Scholar 

  17. Joergensen, R. G. & Wichern, F. Alive and kicking: why dormant soil microorganisms matter. Soil Biol. Biochem. 116, 419–430 (2018).

    Google Scholar 

  18. Versele, M., Lemaire, K. & Thevelein, J. M. Sex and sugar in yeast: two distinct GPCR systems. EMBO Rep. 2, 574–579 (2001).

    Google Scholar 

  19. Lennon, J. T., den Hollander, F., Wilke-Berenguer, M. & Blath, J. Principles of seed banks and the emergence of complexity from dormancy. Nat. Commun. 12, 4807 (2021).

    Google Scholar 

  20. López-Amorós, R., Castel, S., Comas-Riu, J. & Vives-Rego, J. Assessment of E. coli and Salmonella viability and starvation by confocal laser microscopy and flow cytometry using rhodamine 123, DiBAC4(3), propidium iodide, and CTC. Cytometry 29, 298–305 (1997).

    Google Scholar 

  21. Sokol, N. W. et al. Life and death in the soil microbiome: how ecological processes influence biogeochemistry. Nat. Rev. Microbiol. 20, 415–430 (2022).

    Google Scholar 

  22. Winding, A., Binnerup, S. J. & Sørensen, J. Viability of indigenous soil bacteria assayed by respiratory activity and growth. Appl. Environ. Microbiol. 60, 2869–2875 (1994).

    Google Scholar 

  23. Kasahara, Y. & Hattori, T. Analysis of bacterial populations in a grassland soil according to rates of development on solid media. FEMS Microbiol. Lett. 86, 95–101 (1991).

    Google Scholar 

  24. He, P., Zhang, Y., Shen, Q., Ling, N. & Nan, Z. Microbial carbon use efficiency in different ecosystems: a meta-analysis based on a biogeochemical equilibrium model. Glob. Change Biol. 29, 4758–4774 (2023).

    Google Scholar 

  25. Jordaan, K. et al. Hydrogen-oxidizing bacteria are abundant in desert soils and strongly stimulated by hydration. mSystems 5, https://doi.org/10.1128/msystems.01131-01120 (2020).

  26. You, Y. et al. Growth in agricultural water demand aggravates water supply-demand risk in arid Northwest China: more a result of anthropogenic activities than climate change. Hydrol. Earth Syst. Sci. 29, 6373–6392 (2025).

    Google Scholar 

  27. Shen, C., Zhang, J., Yang, X., Liu, J. & Han, G. Effects of grazing on temperate grassland ecosystems: a meta-analysis. Agric. Ecosyst. Environ. 381, 109452 (2025).

    Google Scholar 

  28. Potts, M. Desiccation tolerance of prokaryotes. Microbiol. Rev. 58, 755–805 (1994).

    Google Scholar 

  29. Schimel, J. & Schaeffer, S. M. Microbial control over carbon cycling in soil. Sec. Terrestrial Microbiol. 3, 2012 (2012).

  30. Manzoni, S., Schimel, J. P. & Porporato, A. Responses of soil microbial communities to water stress: results from a meta-analysis. Ecology 93, 930–938 (2012).

    Google Scholar 

  31. Cordero, I., Leizeaga, A., Hicks, L. C., Rousk, J. & Bardgett, R. D. High intensity perturbations induce an abrupt shift in soil microbial state. ISME J. 17, 2190–2199 (2023).

    Google Scholar 

  32. Xue, R., Shen, Y. & Marschner, P. Low soil water content during plant growth influences soil respiration and microbial biomass after plant removal and rewetting. J. Soil Sci. Plant Nutr. 16, 955–966 (2016).

  33. Manzoni, S., Schaeffer, S. M., Katul, G., Porporato, A. & Schimel, J. P. A theoretical analysis of microbial eco-physiological and diffusion limitations to carbon cycling in drying soils. Soil Biol. Biochem. 73, 69–83 (2014).

    Google Scholar 

  34. Li, K. et al. Achieving high-concentration lignocellulosic sugars by using the Trichoderma reesei strain with high β-glucosidase activity for inducer synthesis and cellulase production. Chem. Eng. J. 522, 167764 (2025).

    Google Scholar 

  35. Zhou, J. et al. Labile substrate input weakens the memory effect of soil microbial functions under global warming. CATENA 232, 107381 (2023).

    Google Scholar 

  36. Laugier, J. The “comfort timing” strategy: a potential pathway for the cultivation of uncultured microorganisms and a possible adaptation for environmental colonisation. FEMS Microbiol. Ecol. 99, fiad026 (2023).

  37. Bodor, A. et al. Challenges of unculturable bacteria: environmental perspectives. Rev. Environ. Sci. Bio/Technol. 19, 1–22 (2020).

    Google Scholar 

  38. Kim, S. B., Lyou, E. S., Kim, M. S. & Lee, T. K. Bacterial resuscitation from starvation-induced dormancy results in phenotypic diversity coupled with translational activity depending on carbon substrate availability. Microb. Ecol. 86, 325–336 (2023).

    Google Scholar 

  39. Stenström, J., Svensson, K. & Johansson, M. Reversible transition between active and dormant microbial states in soil. FEMS Microbiol. Ecol. 36, 93–104 (2001).

    Google Scholar 

  40. Papp, K., Hungate, B. A. & Schwartz, E. Glucose triggers strong taxon-specific responses in microbial growth and activity: insights from DNA and RNA qSIP. Ecology 101, e02887 (2020).

  41. Blagodatskaya, E. V., Blagodatsky, S. A., Anderson, T.-H. & Kuzyakov, Y. Contrasting effects of glucose, living roots and maize straw on microbial growth kinetics and substrate availability in soil. Eur. J. Soil Sci. 60, 186–197 (2009).

  42. Behera, B. & Wagner, G. H. Microbial growth rate in glucose-amended. Soil Sci. Soc.Am. J. 38, 591–594 (1974).

    Google Scholar 

  43. Gilmullina, A. Microbial biomass activation induced by glucose added at different concentrations. In: EGU General Assembly Conference Abstracts (EGU, 2018).

  44. Chen, S. et al. Deciphering the active bacteria involving glucose-triggered priming effect in soils with gradient N inputs. Soil Biol. Biochem. 199, 109612 (2024).

    Google Scholar 

  45. Fu, Y. et al. Microbial metabolisms determine soil priming effect induced by organic inputs. Soil Biol. Biochem. 209, 109885 (2025).

    Google Scholar 

  46. Chen, R. et al. Mineral-associated organic carbon predicts the variations in microbial biomass and specific enzyme activities in a subtropical forest. Geoderma 439, 116671 (2023).

    Google Scholar 

  47. Kleber, M. et al. Dynamic interactions at the mineral–organic matter interface. Nat. Rev. Earth Environ. 2, 402–421 (2021).

    Google Scholar 

  48. Chen, X. et al. Global patterns and drivers of soil extracellular enzyme activities in response to plant invasion: a meta-analysis. Glob. Ecol. Biogeogr. 34, e70084 (2025).

    Google Scholar 

  49. German, D. P. et al. Optimization of hydrolytic and oxidative enzyme methods for ecosystem studies. Soil Biol. Biochem. 43, 1387–1397 (2011).

    Google Scholar 

  50. Dalai, R. C., Sahrawat, K. L. & Myers, R. J. K. Inclusion of nitrate and nitrite in the Kjeldahl nitrogen determination of soils and plant materials using sodium thiosulphate. Commun. Soil Sci. Plant Anal. 15, 1453–1461 (1984).

    Google Scholar 

  51. Koide, R. T., Petprakob, K. & Peoples, M. Quantitative analysis of biochar in field soil. Soil Biol. Biochem. 43, 1563–1568 (2011).

    Google Scholar 

  52. Shi, J. et al. Recalcitrant organic carbon plays a key role in soil carbon sequestration along a long-term vegetation succession on the Loess Plateau. CATENA 233, 107528 (2023).

    Google Scholar 

  53. Wang, J. et al. Linkage between microbial functional genes and net N mineralisation in forest soils along an elevational gradient. Eur. J. Soil Sci. 73, 13276 (2022).

  54. Feyissa, A., Raza, S. T., Gomez-Casanovas, N., Timilsina, A. & Cheng, X. Linking extracellular enzyme activities in soil aggregates to carbon stabilization along an elevational gradient in alpine forest and grassland ecosystems. CATENA 250, 108702 (2025).

    Google Scholar 

  55. Kirchman, D. L. Microbial Ecology of the Oceans (Wiley, 2008).

  56. Maraha, N., Backman, A. & Jansson, J. K. Monitoring physiological status of GFP-tagged Pseudomonas fluorescens SBW25 under different nutrient conditions and in soil by flow cytometry. FEMS Microbiol. Ecol. 51, 123–132 (2004).

    Google Scholar 

  57. Servais, P., Agogué, H., Courties, C., Joux, F. & Lebaron, P. Are the actively respiring cells (CTC+) those responsible for bacterial production in aquatic environments? FEMS Microbiol. Ecol. 35, 171–179 (2001).

    Google Scholar 

  58. Manini, E. & Danovaro, R. Synoptic determination of living/dead and active/dormant bacterial fractions in marine sediments. FEMS Microbiol. Ecol. 55, 416–423 (2006).

    Google Scholar 

  59. Williams, S. C. et al. Distinguishing between living and nonliving bacteria: evaluation of the vital stain propidium iodide and its combined use with molecular probes in aquatic samples. J. Microbiol. Methods 32, 225–236 (1998).

    Google Scholar 

  60. Deng, Y., Wang, L., Chen, Y. & Long, Y. Optimization of staining with SYTO 9/propidium iodide: interplay, kinetics and impact on Brevibacillus brevis. Biotechniques 69, 88–98 (2020).

    Google Scholar 

  61. Nescerecka, A., Hammes, F. & Juhna, T. A pipeline for developing and testing staining protocols for flow cytometry, demonstrated with SYBR Green I and propidium iodide viability staining. J. Microbiol. Methods 131, 172–180 (2016).

    Google Scholar 

  62. Osborne, J. Notes on the use of data transformations. Practical Assess. Res. Eval. 8, 1–7 (2002).

    Google Scholar 

  63. Wright, M. N. & Ziegler, A. ranger: A fast implementation of random forests for high dimensional data in C++ and R. J. Stat. Softw. 77, 1–17 (2017).

    Google Scholar 

  64. Jones, Z. & Linder, F. edarf: Exploratory data analysis using random forests. J. Open Source Softw. 1, 92 (2016).

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Acknowledgements

This work was supported by the National Natural Science Foundation of China (Grant No. 42277284), Central Government to Guide Local Science & Technology Development in Qinghai Province (2025ZY007), Qinling Hundred Talents Project of Shaanxi Academy of Science (2024K-31). The soil sampling conducted in this study did not require any specific permits or permissions.

Author information

Author notes
  1. These authors contributed equally: Xue Zhao, Liyuan He.

  2. These authors jointly supervised this work: Fazhu Zhao, Jieying Wang.

Authors and Affiliations

  1. Shaanxi Key Laboratory of Earth Surface System and Environmental Carrying Capacity, Northwest University, Xi’an, China

    Xue Zhao, Jun Wang, Jieying Wang & Fazhu Zhao

  2. College of Urban and Environmental Sciences, Northwest University, Xi’an, China

    Xue Zhao, Jun Wang, Jieying Wang & Fazhu Zhao

  3. Environmental Sciences Division and Climate Change Science Institute, Oak Ridge National Laboratory, Oak Ridge, TN, USA

    Liyuan He

  4. State Key Laboratory of Water Resources Engineering and Management, and Institute for Water-Carbon Cycles and Carbon Neutrality, Wuhan University, Wuhan, China

    Gangsheng Wang

  5. Carbon Neutrality College (Yulin), Northwest University, Xi’an, China

    Jun Wang & Fazhu Zhao

  6. Shaanxi Xi’an Urban Ecosystem National Observation and Research Station, National Forestry and Grassland Administration, Xi’an, China

    Jun Wang & Fazhu Zhao

  7. State Key Laboratory of Soil Erosion and Dryland Farming on the Loess Plateau, Institute of Soil and Water Conservation, Chinese Academy of Sciences and Ministry of Water Resources, Yangling, China

    Jun Wang

  8. Shaanxi Key Laboratory for Carbon Neutral Technology, Northwest University, Xi’an, China

    Jun Wang & Fazhu Zhao

  9. School of Ecology, Northeast Asia Biodiversity Research Center, Northeast Forestry University, Harbin, China

    Zhenghu Zhou

  10. College of Agronomy, Northwest A&F University, Yangling, China

    Chengjie Ren

  11. Xi’an Botanical Garden of Shaanxi Province (Institute of Botany of Shaanxi Province), Xi’an, China

    Sha Zhou

  12. Laboratorio de Biodiversidad y Funcionamiento Ecosistémico, Instituto de Recursos Naturales y Agrobiología de Sevilla (IRNAS), Consejo Superior de Investigaciones Científicas (CSIC), Sevilla, Spain

    Jieying Wang

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  1. Xue Zhao
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Contributions

F.Z.Z. and J.Y.W. designed the work and led the formal analyses. F.Z.Z., L.Y.H., and X.Z. wrote the first draft of the manuscript. X.Z. and J.Y.W. analyzed the data. F.Z.Z., L.Y.H., G.S.W., J.W., Z.H.Z., C.J.R. and S.Z. substantively revised the draft. F.Z.Z. acquired funding for it. All other authors acquired and interpreted the data and edited the drafts.

Corresponding authors

Correspondence to Jieying Wang or Fazhu Zhao.

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The authors declare no competing interests.

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Communications Earth and Environment thanks the anonymous reviewers for their contribution to the peer review of this work. Primary Handling Editors: Leiyi Chen, Marisa McDonald, Mengjie Wang. A peer review file is available.

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Zhao, X., He, L., Wang, G. et al. Dormant microbes dominate soils across China and are regulated by water and resource availability. Commun Earth Environ (2026). https://doi.org/10.1038/s43247-026-03377-3

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  • Received: 18 August 2025

  • Accepted: 26 February 2026

  • Published: 12 March 2026

  • DOI: https://doi.org/10.1038/s43247-026-03377-3

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