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<journal-id journal-id-type="publisher-id">Front. Microbiol.</journal-id>
<journal-title>Frontiers in Microbiology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Microbiol.</abbrev-journal-title>
<issn pub-type="epub">1664-302X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
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<article-meta>
<article-id pub-id-type="doi">10.3389/fmicb.2024.1525521</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Microbiology</subject>
<subj-group>
<subject>Editorial</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Editorial: Microbial involvement in biogeochemical cycling and contaminant transformations at land-water ecotones</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Sheng</surname> <given-names>Yizhi</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x0002A;</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name><surname>Zeng</surname> <given-names>Xiangfeng</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c002"><sup>&#x0002A;</sup></xref>
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<contrib contrib-type="author">
<name><surname>Zhao</surname> <given-names>Linduo</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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<contrib contrib-type="author">
<name><surname>Li</surname> <given-names>Yongbin</given-names></name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>Center for Geomicrobiology and Biogeochemistry Research, State Key Laboratory of Biogeology and Environmental Geology, China University of Geosciences</institution>, <addr-line>Beijing</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Key Laboratory of Pollution Ecology and Environmental Engineering, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang</institution>, <addr-line>Liaoning</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>Prairie Research Institute-Illinois Sustainable Technology Centre/Illinois State Water Survey, University of Illinois at Urbana Champaign</institution>, <addr-line>Champaign, IL</addr-line>, <country>United States</country></aff>
<aff id="aff4"><sup>4</sup><institution>Key Laboratory of Industrial Ecology and Environmental Engineering (Ministry of Education), School of Environmental Science and Technology, Dalian University of Technology</institution>, <addr-line>Dalian</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by"><p>Edited and reviewed by: David Emerson, Bigelow Laboratory for Ocean Sciences, United States</p></fn>
<corresp id="c001">&#x0002A;Correspondence: Yizhi Sheng <email>shengyz&#x00040;cugb.edu.cn</email></corresp>
<corresp id="c002">Xiangfeng Zeng <email>zengxf&#x00040;iae.ac.cn</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>05</day>
<month>12</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1525521</elocation-id>
<history>
<date date-type="received">
<day>09</day>
<month>11</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>21</day>
<month>11</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x000A9; 2024 Sheng, Zeng, Zhao and Li.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Sheng, Zeng, Zhao and Li</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/"><p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p></license>
</permissions>
<related-article id="RA1" related-article-type="commentary-article" xlink:href="https://www.frontiersin.org/research-topics/59854/microbial-involvement-in-biogeochemical-cycling-and-contaminant-transformations-at-land-water-ecotones" ext-link-type="uri">Editorial on the Research Topic <article-title>Microbial involvement in biogeochemical cycling and contaminant transformations at land-water ecotones</article-title></related-article>
<kwd-group>
<kwd>microbial biogeochemistry</kwd>
<kwd>microbial ecology</kwd>
<kwd>contaminant transformation</kwd>
<kwd>land-water ecotones</kwd>
<kwd>bioremediation</kwd>
</kwd-group>
<counts>
<fig-count count="0"/>
<table-count count="0"/>
<equation-count count="0"/>
<ref-count count="14"/>
<page-count count="3"/>
<word-count count="1711"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Microbiological Chemistry and Geomicrobiology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>Microorganisms, including bacteria, archaea, and fungi, play pivotal roles in facilitating energy and matter exchange, promoting mineral weathering, cycling nutrients, and transforming contaminants (Shi et al., <xref ref-type="bibr" rid="B10">2016</xref>; Dong et al., <xref ref-type="bibr" rid="B3">2022</xref>). Land-water ecotones, such as coastal areas, wetlands, riverine zones, and aquifer recharge regions, are characterized by intensive mass and energy exchanges, dynamic redox processes and varying geochemical conditions. These environments serve as critical transitional zones that support complex biogeochemical interactions between terrestrial and aquatic ecosystems. For instance, the complex interactions between organic matter and iron-bearing minerals at redox interfaces across diverse environments can either enhance or inhibit microbial and extracellular enzyme activity, thereby controlling the carbon budget in those transition zones (Dong et al., <xref ref-type="bibr" rid="B4">2023</xref>; Sheng et al., <xref ref-type="bibr" rid="B8">2022</xref>). In wetland transition zones between groundwater and lakes, processes such as dissimilatory nitrate reduction to ammonia are enriched, exhibiting seasonal variations in microbial activity (Chen et al., <xref ref-type="bibr" rid="B1">2024</xref>). In the continental shelf sediments of China, denitrification is the primary pathway for dinitrogen gas production, followed by anaerobic ammonium oxidation (anammox; Sun et al., <xref ref-type="bibr" rid="B12">2021</xref>). In tropical oceans, biological nitrogen fixation is limited by iron-to-nitrogen ratios, with iron primarily sourced from land and mineral dust deposition (Wen et al., <xref ref-type="bibr" rid="B13">2022</xref>). To counteract metal nutrient limitations, microorganisms have evolved strategies such as producing siderophores to acquire essential metals (e.g., Fe, Mo) from minerals for their growth (Sheng et al., <xref ref-type="bibr" rid="B6">2023a</xref>; Zhou et al., <xref ref-type="bibr" rid="B14">2024</xref>). Understanding how microbial communities and biogeochemical processes respond to both natural variations and human-induced disturbances in these environments is crucial.</p>
<p>The 10 published articles in this Research Topic provide valuable insights into two main themes: (1) microbial community distribution responses to environmental variations, and (2) the impacts of anthropogenic activities on microbial processes, along with potential bioremediation and sustainable development strategies.</p>
<p>The assembly of microbial communities demonstrates remarkable adaptability to fluctuating environmental conditions, including changes in temperature, pH, salinity, oxygen levels, nutrient availability, moisture, hydrodynamic disturbances, and contaminant stress (Sheng et al., <xref ref-type="bibr" rid="B7">2016</xref>; Ruff et al., <xref ref-type="bibr" rid="B5">2023</xref>; Chen et al., <xref ref-type="bibr" rid="B2">2022</xref>; Shu and Huang, <xref ref-type="bibr" rid="B11">2022</xref>). <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2023.1261079">Liu et al.</ext-link> investigated bacterial community dynamics in oligosaline lakes, revealing that temporal succession was the primary driver of community assembly, with temperature, pH, and nitrate significantly influencing microbial structure and function across seasons. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2023.1305345">Shi et al.</ext-link> explored the effects of environmental gradients on microbial diversity and co-occurrence networks at various depths in Hulun lake, providing insights into nitrogen-cycling taxa and their habitat-specific adaptations in grassland lakes. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1367062">Xian et al.</ext-link> highlighted the significant impact of water masses, identifiable body of water with a common formation history which has physical properties distinct from surrounding water, on the bacterial composition, topological characteristics and assembly process in the Yangtze River Estuary. These findings offer a theoretical foundation for predicting alterations in microbial communities within estuarine ecosystems under the influence of water masses. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1388973">Brooks and Field</ext-link> studied responses of microbial communities in freshwater iron mats to hydrocarbon exposure and found that hydrocarbon pollution affects diversity, community structure, and resilience in contaminated ecotones. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1463665">Guo et al.</ext-link> examined the effects of mining-induced soil fissures on microbial communities, showing that varying fissure conditions impacted soil moisture, pH, and nutrient availability, with rare species playing critical roles in maintaining microbial network stability.</p>
<p>Nutrient and contaminant transformation through microbial degradation, redox reactions, and related processes can either intensify or mitigate their ecological effects. As mobile contaminants cross ecosystem boundaries, the role of microbial communities in detoxification and stabilization becomes crucial for sustaining ecological balance (Sheng et al., <xref ref-type="bibr" rid="B9">2023b</xref>). <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1389954">Li et al.</ext-link> examined the hydrocarbon degradation capabilities of a facultative anaerobic bacterium <italic>Shewanella putrefaciens</italic> CN32 under both aerobic (using O<sub>2</sub> as an electron acceptor) and anaerobic [using Fe (III) as an electron acceptor] conditions, emphasizing its potential for bioremediation in fluctuating redox environments. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1383360">Zhan et al.</ext-link> identified the zinc resilience of <italic>Chlamydomonas</italic> sp. 1710, with the half-maximal inhibitory concentration (IC50) values of 225.4 mg/L, suggesting its potential in phytoremediation for metal-contaminated waters. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1423741">Ak&#x000E9; et al.</ext-link> identified microbial strains with high Cr (VI) adsorption capacities, offering insights for Cr-laden wastewater treatment or similar contaminated environments. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2023.1320853">Feng et al.</ext-link> explored the application of phosphate-solubilizing microorganisms (PSMs) to enhance soil fertility and plant resilience in urban areas, offering a sustainable alternative to chemical fertilizers. <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fmicb.2024.1430498">Wang et al.</ext-link> reviewed microbial biosorption techniques for radioactive nuclides, highlighting microbial approaches as sustainable alternatives for nuclear waste management in geological environments.</p>
<p>Taken together, this Research Topic advances our understanding of microbial metabolism, distribution, and the key underlying drivers of microbial functions in both pristine and contaminated ecotones and similar environments. By integrating these findings, we will gain a better understanding of global nutrient cycles, contaminant bioremediation, and microbial-environment interactions.</p>
</body>
<back>
<sec sec-type="author-contributions" id="s1">
<title>Author contributions</title>
<p>YS: Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing. XZ: Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing. LZ: Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing. YL: Writing &#x02013; original draft, Writing &#x02013; review &#x00026; editing.</p>
</sec>
<ack><p>We would like to extend our sincere gratitude to all the authors, reviewers, and editorial team for their distinguished contributions to our Research Topic in Frontiers in Microbiology.</p>
</ack>
<sec sec-type="COI-statement" id="conf1">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
<p>The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
</sec>
<sec sec-type="disclaimer" id="s2">
<title>Publisher&#x00027;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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