Microbial regulatory mechanisms involved in groundwater arsenic enrichment: Synergistic interactions between key species and genes in C-N-S metabolism

Jingru Yang , Qiao Li , Ting Chen , Hongfei Tao , Youwei Jiang

Geoscience Frontiers ›› 2025, Vol. 16 ›› Issue (6) : 102132

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Geoscience Frontiers ›› 2025, Vol. 16 ›› Issue (6) :102132 DOI: 10.1016/j.gsf.2025.102132
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Microbial regulatory mechanisms involved in groundwater arsenic enrichment: Synergistic interactions between key species and genes in C-N-S metabolism
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Abstract

Microbially mediated carbon (C), nitrogen (N), and sulfur (S) metabolism are core biogeochemical drivers affecting arsenic (As) mobilization and transformation that regulate the formation of high-arsenic groundwater globally. This study determined the microbial molecular mechanisms driving As mobility via coupled C-N-S cycles in the Kuitun River Basin (Xinjiang, China). Metagenomic and geochemical analyses of high-As (HA; >10 μg/L, n = 5) and low-As (LA; ≤10 μg/L, n = 6) samples revealed significant microbial community divergence (analysis of similarities R = 0.67, P = 0.003). Key differential genera included HA-enriched Candidatus Kuenenia and Sulfuritalea as well as the LA-enriched Sphingobium and Novosphingobium. Key functional genes exhibited contrasting As correlations, with negative correlations (katE, cynT, ncd2, ssuABC, and dmdC) in LA-dominant Rhodopseudomonas/Hydrogenophaga/Acinetobacter promoting As3+ oxidation, competitive inhibition of As5+ reduction, and As2S3 precipitation; positive correlations (ACO, korA, hao, psrA) in HA-associated Candidatus Kuenenia and Thiobacillus enhanced As5+ reduction, Fe/Mn oxide dissolution, and thioarsenate formation. Rhodopseudomonas in unconfined aquifers demonstrated a synergistic C-N-S network (katE-ncd2-ssuABC) for efficient As immobilization. These findings enhance the understanding of microbially driven As biogeochemical cycles and provide a theoretical foundation for developing in situ remediation technologies based on microbial metabolic regulation.

Keywords

High-arsenic groundwater / C-N-S metabolism / Microorganisms / Functional genes

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Jingru Yang, Qiao Li, Ting Chen, Hongfei Tao, Youwei Jiang. Microbial regulatory mechanisms involved in groundwater arsenic enrichment: Synergistic interactions between key species and genes in C-N-S metabolism. Geoscience Frontiers, 2025, 16(6): 102132 DOI:10.1016/j.gsf.2025.102132

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Data availability

The datasets generated and analyzed during the current study are available in the NCBI Sequence Read Archive repository under BioProject ID PRJNA1145651. These data will become publicly accessible on August 1, 2028.

CRediT authorship contribution statement

Jingru Yang: Writing - original draft, Formal analysis, Data curation. Qiao Li: Writing - review & editing, Funding acquisition, Conceptualization. Ting Chen: Methodology, Investigation. Hon-gfei Tao: Supervision, Software, Resources. Youwei Jiang: Visual-ization, Validation.

Declaration of competing interest

The authors declare that they have no known competing finan-cial interests or personal relationships that could have appeared to influence the work reported in this paper.

Acknowledgements

This work was supported by the Natural Science Foundation of Special Project of Key Research and Development Program of Xinjiang Uygur Autonomous Region (2024B03029-2), Xinjiang Uygur Autonomous Region Youth Science Project (2022D01B86), National Natural Science Foundation of China (41762018), Xinjiang Uygur Autonomous Region Graduate Student Innovation Program Project (XJ2025G113) and Xinjiang Water Conservancy Project Safety and Water Disaster Prevention Key Laboratory Research Project (ZDSYS-YJS-2024-05).

Appendix A. Supplementa ry data

Supplementary data to this article can be found online at https://doi.org/10.1016/j.gsf.2025.102132.

References

[1]

Afroz, H., Su, S., Carey, M., Meharg, A., Meharg, C., 2019. Inhibition of microbial methylation via arsM in the rhizosphere: arsenic speciation in the soil to plant continuum. Environ. Sci. Technol. 53 (7), 3451-3463.

[2]

Aldossari, N., Ishii, S., 2021. Fungal denitrification revisited-recent advancements and future opportunities. Soil Biol. Biochem. 157, 108250. https://doi.org/1016/ j.soilbio.2021.108250.

[3]

Anantharaman, K., Brown, C., Hug, L., Sharon, I., Castelle, C., Probst, A., Thomas, B., Singh, A., Wilkins, M., Karaoz, U., Brodie, E., Williams, K., Hubbard, S., Banfield, J., 2016. Thousands of microbial genomes shed light on interconnected biogeochemical processes in an aquifer system. Nat. Commun. 7, 13219. https://doi.org/10.1038/ncomms13219.

[4]

Bauer, M., Blodau, C., 2009. Arsenic distribution in the dissolved, colloidal and particulate size fraction of experimental solutions rich in dissolved organic matter and ferric iron. Geochim. Cosmochim. Acta 73 (3), 529-542.

[5]

Bostick, B.C., Fendorf, S., Brown, G.E., 2005. In situ analysis of thioarsenite complexes in neutral to alkaline arsenic sulphide solutions. Mineral. Mag. 69 (5), 781-795.

[6]

Britta, P., Jacqueline, L., Blaine, M., Kirk, N., Dirk, W., 2007. Thioarsenates in geothermal waters of Yellowstone National Park: determination, preservation, and geochemical importance. Environ. Sci. Technol. 41 (15), 5245-5251.

[7]

Butcher, B.G., Deane, S.M., Rawlings, D.E., 2000. The chromosomal arsenic resistance genes of Thiobacillus ferrooxidans have an unusual arrangement and confer increased arsenic and antimony resistance to Escherichia coli. Appl. Environ. Microbiol. 66 (5), 1826-1833.

[8]

Cai, L., Ding, S., Ma, X., Wang, Y., Sun, Q., Zhong, Z., Chen, M., Fan, X., 2023. Sediment arsenic remediation by submerged macrophytes via root-released O2 and microbe-mediated arsenic biotransformation. J. Hazard. Mater. 449, 131006. https://doi.org/10.1016/j.jhazmat.2023.131006.

[9]

Chafik, A., Essamadi, A., Çelik, S., Mavi, A., 2022. Purification and biochemical characterization of catalase that confers protection against hydrogen peroxide induced by stressful desert environment: the Camelus Dromedarius kidney catalase. Prep. Biochem. Biotechnol. 53, 610-621.

[10]

Chen, T., Shi, Y., Peng, C., Tang, L., Chen, Y., Wang, T., Wang, Z., Wang, S., Li, Z., 2022. Transcriptome analysis on key metabolic pathways in Rhodotorula mucilaginosa under Pb(II) stress. Appl. Environ. Microbiol. 88 (7), e02215- e02221. https://doi.org/10.1128/aem.02215-21.

[11]

Covarrubias, A., Larsson, A., Högbom, M., Lindberg, J., Bergfors, T., Björkelid, C., Mowbray, S., Unge, T., Jones, T., 2005. Structure and function of carbonic anhydrases from Mycobacterium tuberculosis. J. Biol. Chem. 280, 18782-18789.

[12]

Cui, J., Du, J., Tian, H., Chan, T., Jing, C., 2018. Rethinking anaerobic As(III) oxidation in filters: effect of indigenous nitrate respirers. Chemosphere 196, 223-230.

[13]

Eichhorn, E., Ploeg, J., Leisinger, T., 2000. Deletion analysis of the Escherichia coli taurine and alkanesulfonate transport systems. J. Bacteriol. 182 (10), 2687-2695.

[14]

Fan, X., Nie, L., Chen, Z., Zheng, Y., Wang, G., Shi, K., 2023. Simultaneous removal of nitrogen and arsenite by heterotrophic nitrification and aerobic denitrification bacterium Hydrogenophaga sp. H7. Front. Microbiol. 13, 1103913. https://doi.org/10.3389/fmicb.2022.1103913.

[15]

Fang, Y., Du, Y., Hu, L., Xu, J., Long, Y., Shen, D., 2016. Effects of sulfur-metabolizing bacterial community diversity on H2S emission behavior in landfills with different operation modes. Biodegradation 27 (4-6), 237-246.

[16]

Gadda, G., Francis, K., 2010. Nitronate monooxygenase, a model for anionic flavin semiquinone intermediates in oxidative catalysis. Arch. Biochem. Biophys. 493, 53-61.

[17]

Gao, Z., Jia, Y., Guo, H., Zhang, D., Zhao, B., 2020. Quantifying geochemical processes of arsenic mobility in groundwater from an inland basin using a reactive transport model. Water Resour. Res. 56 (2), e2019WR025492. https://doi.org/ 10.1029/2019wr025492.

[18]

Geen, A., 2011. International drilling to recover aquifer sands (IDRAs) and arsenic contaminated groundwater in Asia. Sci. Drill. 12, 49-52.

[19]

Glodowska, M., Stopelli, E., Schneider, M., Rathi, B., Straub, D., Lightfoot, A., Kipfer, R., Berg, M., Jetten, M., Kleindienst, S., Kappler, A., Glodowska, M., Kappler, A., Kleindienst, S., Cirpka, O., Rathi, B., Lightfoot, A., Stopelli, E., Berg, M., Kipfer, R., Winkel, L., Schneider, M., Eiche, E., Kontny, A., Neumann, T., Viet, P., Pham, T., Vu, D., Lan, V., Tran, M., Nga, V., Prommer, H., 2020. Arsenic mobilization by anaerobic iron-dependent methane oxidation. Commun. Earth Environ. 1, 42. https://doi.org/10.1038/s43247-020-00037-y.

[20]

Glodowska, M., Stopelli, E., Straub, D., Thi, D., Trang, P., Viet, P., Members, A., Berg, M., Kappler, A., Kleindienst, S., 2021. Arsenic behavior in groundwater in Hanoi (Vietnam) influenced by a complex biogeochemical network of iron, methane, and sulfur cycling. J. Hazard. Mater. 407, 124398. https://doi.org/10.1016/j. jhazmat.2020.124398.

[21]

Griebler, C., Lueders, T., 2009. Microbial biodiversity in groundwater ecosystems. Freshw. Biol. 54 (4), 649-677.

[22]

Guo, H., Zhou, Y., Jia, Y., Tang, X., Li, X., Shen, M., Lu, H., Han, S., Wei, C., Norra, S., Zhang, F., 2016. Sulfur cycling-related biogeochemical processes of arsenic mobilization in the western Hetao Basin, China: evidence from multiple isotope approaches. Environ. Sci. Technol. 50 (23), 12650-12659.

[23]

Hassan, Z., Sultana, M., Westerhoff, H., Khan, S., Röling, W., 2016. Iron cycling potentials of arsenic contaminated groundwater in Bangladesh as revealed by enrichment cultivation. Geomicrobiol. J. 33 (9), 779-792.

[24]

He, X., Li, P., Ji, Y., Wang, Y., Su, Z., Elumalai, V., 2020. Groundwater arsenic and fluoride and associated arsenicosis and fluorosis in China: Occurrence, distribution and management. Expo. Health. 12, 355-368.

[25]

Huang, Y., Wen, L., Zhang, L., Xu, J., Wang, W., Hu, H., Xu, P., Li, Z., Tang, H., 2022. Community-integrated multi-omics facilitates the isolation of an organohalide dehalogenation microorganism. Innovation 4 (1), 100355. https://doi.org/ 10.1016/j.xinn.2022.100355.

[26]

Humbert, S., Tarnawski, S., Fromin, N., Mallet, M., Aragno, M., Zopfi, J., 2010. Molecular detection of anammox bacteria in terrestrial ecosystems: distribution and diversity. ISME J. 4 (3), 450-454.

[27]

Islam, F., Gault, A., Boothman, C., Polya, D., Charnock, J., Chatterjee, D., Lloyd, J., 2004. Role of metal-reducing bacteria in arsenic release from Bengal delta sediments. Nature 430 (6995), 68-71.

[28]

Jia, Y., Huang, H., Zhong, M., Wang, F., Zhang, L., Zhu, Y., 2013. Microbial arsenic methylation in soil and rice rhizosphere. Environ. Sci. Technol. 47 (7), 3141-3148.

[29]

Ke, T., Zhang, D., Guo, H., Xiu, W., Zhao, Y., 2022. Geogenic arsenic and arsenotrophic microbiome in groundwater from the Hetao Basin. Sci. Total Environ. 852, 158549. https://doi.org/10.1016/j.scitotenv.2022.158549.

[30]

Kondratyeva, T., Muntyan, L., Karavaiko, G., 1995. Zinc- and arsenic-resistant strains of Thiobacillus ferrooxidans have increased copy numbers of chromosomal resistance genes. Microbiology 141 (5), 1157-1162.

[31]

Kumar, M., Goswami, R., Patel, A., Srivastava, M., Das, N., 2020a. Scenario, perspectives and mechanism of arsenic and fluoride Co-occurrence in the groundwater: a review. Chemosphere 249, 126126. https://doi.org/10.1016/j. chemosphere.2020.126126.

[32]

Kumar, N., Noël, V., Planer-friedrich, B., Besold, J., Lezama-pacheco, J., Bargar, J., Brown, G., Fendorf, S., Boye, K., 2020b. Redox heterogeneities promote thioarsenate formation and release into groundwater from low arsenic sediments. Environ. Sci. Technol. 54 (6), 3237-3244.

[33]

Kuypers, M., Marchant, H., Kartal, B., 2018. The microbial nitrogen-cycling network. Nat. Rev. Microbiol. 16 (5), 263-276.

[34]

Lerm, S., Alawi, M., Miethling-Graff, R., Wolfgramm, M., Rauppach, K., Seibt, A., Würdemann, H., 2011. Influence of microbial processes on the operation of a cold store in a shallow aquifer: impact on well injectivity and filter lifetime. Grundwasser 16 (2), 93-104.

[35]

Lett, M., Muller, D., Lièvremont, D., Silver, S., Santini, J., 2012. Unified nomenclature for genes involved in prokaryotic aerobic arsenite oxidation. J. Bacteriol. 194 (2), 207-208.

[36]

Li, Q., Jiang, J., Tao, H., Jiang, Y., 2021. Effect of sediment characteristics on arsenic in aquifer of Kuitun River Basin. In: Proc. 2021 Annual Conference of Science and Technology, Chinese Society of Environmental Sciences, pp. 574-580.

[37]

Li, S., Jiang, Z., Ji, G., 2022. Effect of sulfur sources on the competition between denitrification and DNRA. Environ. Pollut. 305, 119322. https://doi.org/10.1016/ j.envpol.2022.119322.

[38]

Li, W., Liu, J., Hudson-edwards, K., 2020. Seasonal variations in arsenic mobility and bacterial diversity: the case study of Huangshui Creek, Shimen Realgar Mine, Hunan Province, China. Sci. Total Environ. 749, 142353. https://doi.org/10.1016/ j.scitotenv.2020.142353.

[39]

Li, Y., Guo, H., Hao, C., 2014. Arsenic release from shallow aquifers of the Hetao basin, Inner Mongolia: evidence from bacterial community in aquifer sediments and groundwater. Ecotoxicology 23 (10), 1900-1914.

[40]

Liu, X., Li, P., Wang, H., Han, L., Yang, K., Wang, Y., Jiang, Z., Cui, L., Kao, S., 2023. Nitrogen fixation and diazotroph diversity in groundwater systems. ISME J. 17 (11), 2023-2034.

[41]

Luo, Y., Li, J., Jiang, P., Xing, Y., 2017. Distribution, classification and cause analysis of geogenic high-arsenic groundwater in Kuitun, Xinjiang. Acta Sci. Circumst. 37 (08), 2897-2903 (in Chinese with English abstract).

[42]

Lv, C., Zhang, Y., Zhao, C., Guo, S., Yang, S., Chen, S., 2012. Arsenic resistance mechanisms in Rhodopseudomonas palustris under anaerobic and light conditions. Acta Sci. Circumst. 32 (10), 2375-2383 (in Chinese with English abstract).

[43]

Ma, B., Chu, M., Zhang, H., Chen, K., Li, F., Liu, X., Kosolapov, D., Zhi, W., Chen, Z., Yang, J., Deng, Y., Sekar, R., Liu, T., Liu, X., Huang, T., 2024. Mixotrophic aerobic denitrification facilitated by denitrifying bacterial-fungal communities assisted with iron in micro-polluted water: Performance, metabolic activity, functional genes abundance, and community co-occurrence. J. Hazard. Mater. 476, 135057. https://doi.org/10.1016/j.jhazmat.2024.135057.

[44]

Malasarn, D., Saltikov, C., Campbell, K., Santini, J., Hering, J., Newman, D., 2004. arrA is a reliable marker for As(V) respiration. Science 306 (5695), 455.

[45]

Mohammadian, M., Farzampanah, L., Behtash-oskouie, A., Majdi, S., Mohseni, G., Imandar, M., Shirzad, M., Soleimani, R., Negahdary, M., 2013. A Biosensor for detect nitrite (NO- ) and hydroxylamine (NH OH) by using of hydroxylamine oxidase and modified electrode with ZnO nanoparticles. Int. J. Electrochem. Sci. 8, 11215-11227.2 2

[46]

Mosley, O., Gios, E., Close, M., Weaver, L., Daughney, C., Handley, K., 2022. Nitrogen cycling and microbial cooperation in the terrestrial subsurface. ISME J. 16, 2561-2573.

[47]

Naujokas, M., Anderson, B., Ahsan, H., Aposhian, H., Graziano, J., Thompson, C., Suk, W., 2013. The broad scope of health effects from chronic arsenic exposure: Update on a worldwide public health problem. Environ. Health Perspect. 121 (3), 295-302.

[48]

Neutzling, O., Trüper, H.G., 1982. Assimilatory sulfur metabolism in rhodopseudomonas sulfoviridis. Arch. Microbiol. 133 (2), 145-148.

[49]

Pedersen, H., Postma, D., Jakobsen, R., 2006. Release of arsenic associated with the reduction and transformation of iron oxides. Geochim. Cosmochim. Acta 70 (16), 4116-4129.

[50]

Poulton, S., Krom, M., Raiswell, R., 2004. A revised scheme for the reactivity of iron (oxyhydr)oxide minerals towards dissolved sulfide. Geochim. Cosmochim. Acta 68, 3703-3715.

[51]

Probst, A.J., Ladd, B., Jarett, J.K., Geller-mcgrath, D.E., Sieber, C.M.K., Emerson, J.B., Anantharaman, K., Thomas, B.C., Malmstrom, R.R., Stieglmeier, M., Klingl, A., Woyke, T., Ryan, M.C., Banfield, J.F., 2018. Differential depth distribution of microbial function and putative symbionts through sediment-hosted aquifers in the deep terrestrial subsurface. Nat. Microbiol. 3 (3), 328-336.

[52]

Rodríguez-lado, L., Sun, G., Berg, M., Zhang, Q., Xue, H., Zheng, Q., Johnson, C.A., 2013. Groundwater arsenic contamination throughout China. Science 341 (6148), 866-868.

[53]

Schütz, M., Maldener, I., Griesbeck, C., Hauska, G., 1999. Sulfide-Quinone reductase from Rhodobacter capsulatus: Requirement for growth, periplasmic localization, and extension of gene sequence analysis. J. Bacteriol. 181 (20), 6516-6523.

[54]

Shao, X., Cao, H., Zhao, F., Peng, M., Wang, P., Li, C., Shi, W., Wei, T., Yuan, Z., Zhang, X., Chen, X., Todd, J.D., Zhang, Y., 2019. Mechanistic insight into 3- methylmercaptopropionate metabolism and kinetical regulation of demethylation pathway in marine dimethylsulfoniopropionate-catabolizing bacteria. Mol. Microbiol. 111 (4), 1057-1073.

[55]

Shi, L., Guo, T., Lv, P., Niu, Z., Zhou, Y., Tang, X., Zheng, P., Zhu, L., Zhu, Y., Kappler, A., Zhao, H., 2020. Coupled anaerobic methane oxidation and reductive arsenic mobilization in wetland soils. Nat. Geosci. 13 (12), 799-805.

[56]

Shrestha, J., Rich, J.J., Ehrenfeld, J.G., Jaffe, P.R., 2009. Oxidation of ammonium to nitrite under iron-reducing conditions in wetland soils: Laboratory, field demonstrations, and push-pull rate determination. Soil Sci. 174 (3), 156-164.

[57]

Smith, R.L., Kent, D.B., Repert, D.A., Böhlke, J., 2017. Anoxic nitrate reduction coupled with iron oxidation and attenuation of dissolved arsenic and phosphate in a sand and gravel aquifer. Geochim. Cosmochim. Acta 196, 102-120.

[58]

Speth, D.R., Hu, B., Bosch, N., Keltjens, J.T., Stunnenberg, H.G., Jetten, M.S.M., 2012. Comparative genomics of two independently enriched ‘‘Candidatus Kuenenia Stuttgartiensis” anammox bacteria. Front. Microbiol. 3, 307. https://doi.org/ 10.3389/fmicb.2012.00307.

[59]

Stauder, S., Raue, B., Sacher, F., 2005. Thioarsenates in sulfidic waters. Environ. Sci. Technol. 39 (16), 5933-5939.

[60]

Su, Y., Li, Q., Tao, H., He, Y., Li, X., Aihemaiti, M., 2022a. Causes of excessive arsenic in groundwater of Kuitun river basin in Xinjiang. J. CRSRI. 39 (3), 54-59 (in Chinese with English abstract).

[61]

Su, Y., Li, Q., Tao, H., He, Y., Li, X., Aihemaiti, M., Jiang, Y., Xian, H., 2022b. Factors influencing the abnormal spatial distribution of arsenic content in groundwater in Kuitun river basin. J. CRSRI. 39 (2), 43-49 (in Chinese with English abstract).

[62]

Sultan, M.W., Qureshi, F., Ahmed, S., Kamyab, H., Rajendran, S., Ibrahim, H., Yusuf, M., 2025. A comprehensive review on arsenic contamination in groundwater: sources, detection, mitigation strategies and cost analysis. Environ. Res. 265, 120457.

[63]

Sun, A., Liu, X., Zhang, S., Yang, Q., Huang, S., Zhang, N., 2023. Enhancing nitrogen removal efficiency and anammox metabolism in microbial electrolysis cell coupled anammox through different voltage application. Bioresour. Technol. 384, 129283. https://doi.org/10.1016/j.biortech.2023.129283.

[64]

Then, J., Trüper, H.G., 1981. The role of thiosulfate in sulfur metabolism of Rhodopseudomonas globiformis. Arch. Microbiol. 130 (2), 143-146.

[65]

Varghese, S., Tang, Y., Imlay, J.A., 2003. Contrasting sensitivities of escherichia coli aconitases a and B to oxidation and iron depletion. J. Bacteriol. 185 (1), 221-230.

[66]

Wang, H., Fu, B., Xi, J., Hu, H., Liang, P., Huang, X., Zhang, X., 2019. Remediation of simulated malodorous surface water by columnar air-cathode microbial fuel cells. Sci. Total Environ. 687, 287-296.

[67]

Wang, X., 2021. Mobilization Processes of arsenic in groundwater of Kuitun river downstream. M.S. thesis, Xinjiang Agricultural University, pp. 1-46 (in Chinese with English abstract).

[68]

Wang, Y., Gu, J., 2012. Higher diversity of ammonia/ammonium-oxidizing prokaryotes in constructed freshwater wetland than natural coastal marine wetland. Appl. Microbiol. Biotechnol. 97, 7015-7033.

[69]

Wang, Y., Xie, X., Johnson, T.M., Lundstrom, C.C., Ellis, A., Wang, X., Duan, M., Li, J., 2014. Coupled iron, sulfur and carbon isotope evidences for arsenic enrichment in groundwater. J. Hydrol. 519, 414-422.

[70]

Weng, T., Liu, C., Kao, Y., Hsiao, S.S., 2017. Isotopic evidence of nitrogen sources and nitrogen transformation in arsenic-contaminated groundwater. Sci. Total Environ. 578, 167-185.

[71]

Wu, Y., Xu, L., Wang, Z., Cheng, J., Lu, J., You, H., Zhang, X., 2022. Microbially mediated Fe-N coupled cycling at different hydrological regimes in riparian wetland. Sci. Total Environ. 851, 158237. https://doi.org/10.1016/j. scitotenv.2022.158237.

[72]

Xiu, W., Ke, T., Lloyd, J.R., Shen, J., Bassil, N.M., Song, H., Polya, D.A., Zhao, Y., Guo, H., 2021. Understanding microbial arsenic-mobilization in multiple aquifers: Insight from DNA and RNA analyses. Environ. Sci. Technol. 55, 15181-15195.

[73]

Xiu, W., Lloyd, J., Guo, H., Dai, W., Nixon, S., Bassil, N.M., Ren, C., Zhang, C., Ke, T., Polya, D., 2020. Linking microbial community composition to hydrogeochemistry in the western Hetao Basin: potential importance of ammonium as an electron donor during arsenic mobilization. Environ. Int. 136, 105489. https://doi.org/10.1016/j.envint.2020.105489.

[74]

Xiu, W., Wu, M., Nixon, S.L., Lloyd, J.R., Bassil, N.M., Gai, R., Zhang, T., Su, Z., Guo, H., 2022. Genome-resolved metagenomic analysis of groundwater: Insights into arsenic mobilization in biogeochemical interaction networks. Environ. Sci. Technol. 56, 10105-10119.

[75]

Yan, L., Xie, X., Wang, Y., Qian, K., Chi, Z., Li, J., Deng, Y., Gan, Y., 2020. Organic-matter composition and microbial communities as key indicators for arsenic mobility in groundwater aquifers: evidence from PLFA and 3D fluorescence. J. Hydrol. 591, 125308. https://doi.org/10.1016/j.jhydrol.2020.125308.

[76]

Yang, J., Li, Q., Tao, H., Jiang, Y., Zhang, Y., Aihemaiti, M., Yang, W., 2023a. Sediment biogeochemistry and relationship with arsenic in the Kuitun River Basin, Xinjiang, China: influences of microbial community structure and characteristics on arsenic migration. Environ. Res. Commun. 5 (10), 105004. https://doi.org/10.1088/2515-7620/ace615.

[77]

Yang, J., Lv, S., Li, Q., Su, Y., Tao, H., Jiang, Y., MaHemujiang, A., 2023b. Analysis of Microbial diversity and community structure underground-source arsenic stress. Chin. J. Appl. Environ. Biol. 30 (2), 309-316 (in Chinese with English abstract).

[78]

Yang, W.H., Weber, K.A., Silver, W.L., 2012. Nitrogen loss from soil through anaerobic ammonium oxidation coupled to iron reduction. Nat. Geosci. 5 (8), 538-541.

[79]

Yokota, A., Kitaoka, S., Miura, K., 1985. Reactivity of glyoxylate with hydrogen perioxide and simulation of the glycolate pathway of C 3 plants and Euglena. Planta 165, 59-67.

[80]

Zeng, Q., Sun, J., Bai, X., Xu, Z., 2023a. Immobilization of phototroph-derived extracellular polymer for simultaneous removal of antibiotics and heavy metals: a sustainable approach for advanced treatment of secondary effluent. J. Clean. Prod. 396, 136495. https://doi.org/10.1016/j.jclepro.2023.136495.

[81]

Zeng, X., Xu, Y., Lu, H., Xiong, J., Xu, H., Wu, W., 2023b. Contradictory impacts of nitrate on the dissimilatory arsenate-respiring prokaryotes-induced reductive mobilization of arsenic from contaminated sediments: Mechanism insight from metagenomic and functional analyses. Environ. Sci. Technol. 57 (36), 13473-13486.

[82]

Zhai, W., Guo, T., Yang, S., Gustave, W., Hashmi, M.Z., Tang, X., Ma, L.Q., Xu, J., 2021. Increase in arsenic methylation and volatilization during manure composting with biochar amendment in an aeration bioreactor. J. Hazard. Mater. 411, 125123. https://doi.org/10.1016/j.jhazmat.2021.125123.

[83]

Zhang, F., 2021. Vulnerability assessment and functional zoning of groundwater in Kuitun river basin plain. M.S. thesis, Xinjiang Agricultural University, p. 6.

[84]

Zhang, F., Wu, B., Gao, F., Du, M., Xu, L., 2021. Hydrochemical characterization and cause of groundwater in plain area of Kuitun river basin. Environ. Sci. Technol. 34 (7), 1663-1671.

[85]

Zhang, L., Xing, S., Huang, F., Xiu, W., Rensing, C., Zhao, Y., Guo, H., 2024a. Metabolic coupling of arsenic, carbon, nitrogen, and sulfur in high arsenic geothermal groundwater: evidence from molecular mechanisms to community ecology. Water Res. 249, 120953. https://doi.org/10.1016/j.watres.2023.120953.

[86]

Zhang, M., Xiong, Y., Sun, H., Xiao, T., Xiao, E., Sun, X., Li, B., Sun, W., 2024b. Selective pressure of arsenic and antimony co-contamination on microbial community in alkaline sediments. J. Hazard. Mater. 464, 132948. https://doi.org/10.1016/j. jhazmat.2023.132948.

[87]

Zhang, S., Su, J., Sun, G., Yang, Y., Zhao, Y., Ding, J., Chen, Y., Shen, Y., Zhu, G., Rensing, C., Zhu, Y., 2017. Land scale biogeography of arsenic biotransformation genes in estuarine wetland. Environ. Microbiol. 19, 2468-2482.

[88]

Zhang, S., Zhang, Z., Xia, S., Ding, N., Long, X., Wang, J., Chen, M., Ye, C., Chen, S., 2020. Combined genome-centric metagenomics and stable isotope probing unveils the microbial pathways of aerobic methane oxidation coupled to denitrification process under hypoxic conditions. Bioresour. Technol. 318, 124043. https://doi. org/10.1016/j.biortech.2020.124043.

[89]

Zhang, S., Zhao, F., Sun, G., Su, J., Yang, X., Li, H., Zhu, Y., 2015. Diversity and abundance of arsenic biotransformation genes in paddy soils from southern China. Environ. Sci. Technol. 49, 4138-4146.

[90]

Zhou, W., Zhu, H., Hu, S., Zhang, B., Gao, K., Dang, Z., Liu, C., 2024. Dynamic coupling of ferrihydrite transformation and associated arsenic desorption/redistribution mediated by sulfate-reducing bacteria. J. Environ. Sci. 135, 39-50.

[91]

Zhou, Z., Tran, P.Q., Cowley, E.S., Trembath-reichert, E., Anantharaman, K., 2025. Diversity and ecology of microbial sulfur metabolism. Nat. Rev. Microbiol. 23, 122-140.

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