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<journal-id journal-id-type="publisher-id">Front. Environ. Sci.</journal-id>
<journal-title>Frontiers in Environmental Science</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Environ. Sci.</abbrev-journal-title>
<issn pub-type="epub">2296-665X</issn>
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<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1610193</article-id>
<article-id pub-id-type="doi">10.3389/fenvs.2025.1610193</article-id>
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<subj-group subj-group-type="heading">
<subject>Environmental Science</subject>
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<subject>Review</subject>
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<title-group>
<article-title>A review of research progress on the application of bryophytes in the ecological restoration of mining areas of China</article-title>
<alt-title alt-title-type="left-running-head">Qiao et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fenvs.2025.1610193">10.3389/fenvs.2025.1610193</ext-link>
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<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Qiao</surname>
<given-names>Zhanrui</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
</xref>
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</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Lin</surname>
<given-names>Xiaoai</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
</xref>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Tao</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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<role content-type="https://credit.niso.org/contributor-roles/investigation/"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Luo</surname>
<given-names>Shuigen</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
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<role content-type="https://credit.niso.org/contributor-roles/Writing - review &#x26; editing/"/>
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<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Cunbao</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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</contrib>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Zhou</surname>
<given-names>Wei</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Luo</surname>
<given-names>Longzao</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
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<aff id="aff1">
<sup>1</sup>Technology Innovation Center for Land Spatial Ecological Protection and Restoration in Great Lakes Basin, <institution>Ministry of Natural Resources of the People&#x2019;s Republic of China</institution>, <addr-line>Nanchang</addr-line>, <addr-line>Jiangxi</addr-line>, <country>China</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>The Eight Geological Team of Jiangxi Geological Bureau Shangrao</institution>, <addr-line>Shangrao</addr-line>, <addr-line>Jiangxi</addr-line>, <country>China</country>
</aff>
<aff id="aff3">
<sup>3</sup>College of Life Science, <institution>Shangrao Normal University</institution>, <addr-line>Shangrao</addr-line>, <country>China</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Jiangxi Provincial Institute of Land and Space Survey and Planning</institution>, <addr-line>Nanchang</addr-line>, <addr-line>Jiangxi</addr-line>, <country>China</country>
</aff>
<aff id="aff5">
<sup>5</sup>School of Chemistry and Environmental Science, <institution>Shangrao Normal University</institution>, <addr-line>Shangrao</addr-line>, <addr-line>Jiangxi</addr-line>, <country>China</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/2754495/overview">Can Wang</ext-link>, Southwest Jiaotong University, China</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3078859/overview">Chen Zhang</ext-link>, Institute of Loess Plateau, Shanxi University, China</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3079396/overview">Qiming Mao</ext-link>, Central South University, China</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Wei Zhou, <email>46752711@qq.com</email>; Longzao Luo, <email>luolongzao@sru.edu.cn</email>
</corresp>
<fn fn-type="equal" id="fn001">
<label>
<sup>&#x2020;</sup>
</label>
<p>These authors have contributed equally to this work and share first authorship</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>18</day>
<month>07</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>13</volume>
<elocation-id>1610193</elocation-id>
<history>
<date date-type="received">
<day>11</day>
<month>04</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Qiao, Lin, Zhang, Luo, Wang, Zhou and Luo.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Qiao, Lin, Zhang, Luo, Wang, Zhou and Luo</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>
<abstract>
<p>The process of mining is invariably associated with ecological and environmental challenges within the mining region, making ecological restoration efforts in these areas especially crucial. Bryophytes, acting as key pioneer species, exhibit distinctive advantages and potential for application in the ecological restoration of mining sites. This study offered a concise overview of the fundamental traits of bryophytes, as well as their classification and distribution in mining regions across China using literature synthesis and field surveys. It primarily explored the role bryophytes played in the ecological restoration of such areas, the selection of appropriate bryophyte species, and cultivation techniques through systematic analysis. Additionally, the case studies of bryophytes&#x2019; applications in ecological restoration within mining regions were analyzed. Results indicated that bryophytes in China&#x2019;s mining areas were diverse and widely distributed. Notably, bryophytes contributed to soil improvement, vegetation recovery, and the monitoring and indication of heavy metal pollution, with most demonstrating a robust tolerance to these contaminants. Future research should focus on screening suitable bryophytes, refining cultivation methods, and investigating their interactions with soil microorganisms.</p>
</abstract>
<kwd-group>
<kwd>bryophyte</kwd>
<kwd>mining area</kwd>
<kwd>ecological restoration</kwd>
<kwd>bryophyte ecological restoration</kwd>
<kwd>rapid cultivation</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Ecosystem Restoration</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec id="s1">
<title>1 Introduction</title>
<p>Mining activities have significantly contributed to the economic development of mining regions and adjacent areas, but the detrimental impacts on the ecological environment cannot be underestimated. Prolonged mineral extraction has led to the destruction of surface vegetation, exacserbating soil erosion and degradation (<xref ref-type="fig" rid="F1">Figure 1</xref>). These processes have reduced soil fertility and hinder vegetation recovery and growth (<xref ref-type="bibr" rid="B6">Chen et al., 2023</xref>). Furthermore, waste residues and effluents generated during mining operations have caused severe contamination of soil and water resources, posing threats to both the local ecosystem and public health (<xref ref-type="bibr" rid="B12">Feng et al., 2025</xref>). The resulting environmental degradation has also triggered a decline in biodiversity, disrupted ecological equilibrium, and destabilized the broader ecosystem (<xref ref-type="bibr" rid="B6">Chen et al., 2023</xref>). To mitigate these challenges, ecological restoration in mining areas is imperative. Effective strategies include vegetation rehabilitation, soil amelioration, water resource conservation, and heavy metal pollution remediation. These measures enhance environmental quality, conserve biodiversity, create sustainable economic opportunities, and ultimately advance the goals of ecological civilization and long-term sustainability (<xref ref-type="bibr" rid="B12">Feng et al., 2025</xref>). Given the severe ecological damage caused by mining activities, exploring effective ecological restoration strategies is imperative. Among these strategies, bryophytes offer unique advantages and potential, as detailed in the following sections.</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Impacts of mining activities on the ecological environment.</p>
</caption>
<graphic xlink:href="fenvs-13-1610193-g001.tif">
<alt-text content-type="machine-generated">Diagram showing the environmental impact of mining activities. Central image of an excavator symbolizes mining. Arrows point to three main consequences: direct destruction (soil erosion, mine pits/tailings, groundwater damage), pollution diffusion (water, soil, air pollution), and biodiversity loss (habitat fragmentation, extinction, food chain disruption).</alt-text>
</graphic>
</fig>
<p>Bryophytes act as pioneer species in ecological restoration, contributing to soil improvement and vegetation recovery through strong adaptability and tolerance to harsh environments. Although bryophytes possess a simple structure without true roots, stems, or leaves, these organisms thrive in harsh environments and are therefore regarded as pioneer species in vegetation restoration. Bryophytes demonstrate extraordinary vitality, capable of surviving in extreme environments such as barrenness, drought, and acidity. Additionally, these plants exhibit excellent soil-binding and water-retaining abilities, which effectively control soil erosion and improve soil structure (<xref ref-type="bibr" rid="B5">Cao et al., 2020</xref>). Unlike conventional methods (e.g., vascular plant seeding, chemical stabilization), bryophytes establish on degraded slopes without soil replacement/amendment, reducing long-term maintenance costs through minimized reseeding or chemical applications. Furthermore, bryophytes can absorb carbon dioxide and release oxygen through photosynthesis, improving air quality and creating favorable conditions for the growth of other organisms. Bryophytes assimilate atmospheric carbon dioxide via photosynthesis and convert it into organic carbon stored within biomass, thereby contributing to long-term carbon sequestration. This process holds substantial relevance for advancing China&#x2019;s &#x201c;dual carbon&#x201d; goals. Bryophytes regulate net carbon dioxide emissions via litter input, photosynthesis, and respiration (<xref ref-type="bibr" rid="B9">Elbert et al., 2012</xref>). For example, <italic>Sphagnum</italic> contributes more than half of the world&#x2019;s peat, accounting for 10%&#x2013;15% of terrestrial carbon storage (<xref ref-type="bibr" rid="B51">Zhu, 2022</xref>). Therefore, bryophytes are ideal materials for ecological restoration and have shown great potential in the ecological restoration of mining areas.</p>
<p>In recent years, extensive research has been conducted globally on the application of bryophytes in ecological restoration of mining areas. Internationally, universities and research institutions have validated the efficacy of bryophytes under diverse environmental conditions through experimental studies. Notable examples include investigations in Ukraine (<xref ref-type="bibr" rid="B30">Lobachevska et al., 2019</xref>), Canada (<xref ref-type="bibr" rid="B29">Liu et al., 2024</xref>), Slovakia (<xref ref-type="bibr" rid="B39">&#x160;irka et al., 2018</xref>), the United States (<xref ref-type="bibr" rid="B42">Stern et al., 2016</xref>), Turkey (<xref ref-type="bibr" rid="B21">Karakaya et al., 2015</xref>), Portugal (<xref ref-type="bibr" rid="B1">Anawar et al., 2013</xref>), Poland (<xref ref-type="bibr" rid="B36">Rola and Osyczka, 2018</xref>), and Japan (<xref ref-type="bibr" rid="B44">Suzuki et al., 2016</xref>), which collectively highlight the adaptability of bryophytes in varying mining contexts. In China, significant advancements have also been achieved. For example, researchers from Sichuan University showed that bryophyte mats not only significantly reduced rainfall-induced heavy metal migration (particularly Cd and Cu) but also improved critical soil characteristics including pH regulation, cation exchange capacity, and bulk density optimization. These improvements further stimulated microbial community diversity and abundance in pyritic tailings (<xref ref-type="bibr" rid="B27">Lin K. K. et al., 2024</xref>). Investigations by research groups from Wuhan City and Guizhou Province characterized bryophyte assemblages in mining areas through community architecture (<xref ref-type="bibr" rid="B33">Pengpeng et al., 2023</xref>; <xref ref-type="bibr" rid="B15">Han et al., 2022</xref>; <xref ref-type="bibr" rid="B16">Huang and Zhang, 2017</xref>; <xref ref-type="bibr" rid="B19">Ji and Zhang, 2015</xref>; <xref ref-type="bibr" rid="B20">Jiang and Zhang, 2012</xref>; <xref ref-type="bibr" rid="B32">Pan and Zhang, 2011</xref>), metallophyte adaptation (<xref ref-type="bibr" rid="B33">Pengpeng et al., 2023</xref>; <xref ref-type="bibr" rid="B31">Ma et al., 2023</xref>), life history strategies (<xref ref-type="bibr" rid="B26">Liao et al., 2024</xref>), and restoration ecology applications (<xref ref-type="bibr" rid="B34">Ren et al., 2021</xref>). Furthermore, scholars explored bryophyte community dynamics and artificial cultivation techniques in rare earth mining regions of southern Jiangxi Province, providing critical insights for region-specific restoration practices (<xref ref-type="bibr" rid="B22">Kong et al., 2023</xref>; <xref ref-type="bibr" rid="B37">Shen et al., 2022</xref>).</p>
<p>Despite the significant potential of bryophytes in ecological restoration of mining areas, practical application of bryophytes in ecological restoration faces persistent challenges. Key issues include the selection of species adapted to site-specific environmental conditions, optimization of planting techniques and management protocols, and the development of robust evaluation frameworks to assess restoration efficacy. These challenges demand immediate attention, as unresolved limitations may hinder the scalability and long-term success of bryophyte-based restoration strategies. Consequently, advancing research on the mechanistic roles of bryophytes and refining technical methodologies is critical for enhancing restoration technologies and accelerating ecological recovery. Through a systematic review and meta-analysis of global case studies, this work evaluated the practical viability of bryophytes in mining area restoration, aiming to bridge knowledge gaps and inform future scientific and engineering endeavors.</p>
</sec>
<sec id="s2">
<title>2 Biological characteristics and ecological functions of bryophytes</title>
<sec id="s2-1">
<title>2.1 Morphological characteristics and adaptive traits</title>
<p>Bryophytes, classified as non-vascular plants, lack true roots and vascular tissues. The morphology is typically characterized by small stature, green leaf-like structures, and simple thalloid or foliose gametophytes, accompanied by distinct reproductive organs (<xref ref-type="table" rid="T1">Table 1</xref>). Reproduction occurs through sexual (spore dispersal) and asexual strategies (vegetative fragmentation, stem segment regeneration, and clonal colonization via specialized structures like gemmae) (<xref ref-type="bibr" rid="B45">Wang et al., 2022</xref>). Notably, bryophytes exhibit exceptional environmental adaptability, thriving under extreme conditions such as drought, low temperatures, nutrient-poor substrates, and limited light availability (<xref ref-type="bibr" rid="B45">Wang et al., 2022</xref>). Additionally, bryophytes demonstrate remarkable tolerance to abiotic stressors, including high salinity, acidic pH, and elevated heavy metal concentrations (<xref ref-type="bibr" rid="B28">Lin X. et al., 2024</xref>; <xref ref-type="bibr" rid="B14">Guan and Zhang, 2020</xref>). These adaptive traits underpin their ecological resilience in mining areas, where harsh environments (e.g., metal-contaminated soils, unstable substrates) necessitate robust survival mechanisms. Consequently, bryophytes serve as pivotal agents in mining area restoration by stabilizing substrates, enhancing microhabitat conditions, and facilitating secondary succession.</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Morphological and structural characteristics of bryophytes.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Characteristic</th>
<th align="center">Specific manifestation</th>
<th align="center">Ecological significance</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">Morphological structure</td>
<td align="center">Absence of vascular tissues, rhizoids composed of uniseriate cells (not unicellular)</td>
<td align="center">Reduced metabolic consumption; adaptation to nutrient-poor substrates</td>
</tr>
<tr>
<td align="center">Water metabolism</td>
<td align="center">Direct water absorption through leaves, low transpiration rate (0.5&#x2013;2.0&#xa0;mmol&#xa0;m<sup>-2</sup>&#xa0;s<sup>&#x2212;1</sup>)</td>
<td align="center">Drought tolerance, maintenance of microhabitat humidity</td>
</tr>
<tr>
<td align="center">Reproductive strategy</td>
<td align="center">High spore production (&#x3e;10<sup>6</sup> per plant), regenerative capacity of vegetative propagules (&#x3c;2&#xa0;mm)</td>
<td align="center">Rapid colonization, facilitation of community succession</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="s2-2">
<title>2.2 Role of bryophytes in ecological restoration in mining areas</title>
<p>Bryophytes play a pivotal role in ecological restoration within mining areas, particularly through capacity to rehabilitate degraded soils (<xref ref-type="fig" rid="F2">Figure 2</xref>). During growth, bryophytes accumulate substantial organic matter, which enhances soil structure and fertility, thereby establishing a nutrient-rich foundation for subsequent vegetation recovery (<xref ref-type="bibr" rid="B8">Chun et al., 2021</xref>). The water absorption capability of bryophytes reduce soil moisture evaporation, improving water-holding capacity and creating optimal hydration conditions for plant regeneration (<xref ref-type="bibr" rid="B8">Chun et al., 2021</xref>). Furthermore, bryophytes secrete organic acids that chelate mineral ions, forming insoluble complexes. These complexes, combined with bryophyte detritus, facilitate the accumulation of soil organic matter, ultimately elevating nutrient availability and promoting vascular plant establishment (<xref ref-type="bibr" rid="B11">Feng et al., 2022</xref>). Empirical validation from the Shengli Coal Mine reclamation project in Inner Mongolia confirmed fundamental bryophyte-soil synergies, with statistical analyses demonstrating significant positive correlations between bryophyte colonization density and critical soil nutrient parameters including total nitrogen content and phosphorus availability across rehabilitation chrono sequences. Bryophyte distribution patterns further aligned with microscale improvements in organic matter stabilization and biogeochemical cycling efficiency, establishing these non-vascular plants as both biomarkers and active mediators of pedogenic recovery in post-mining ecosystems (<xref ref-type="bibr" rid="B8">Chun et al., 2021</xref>). Similarly, long-term studies on a potassium-magnesium salt tailings pond in Sweden revealed that natural succession over decades led to the formation of resilient biological soil crusts dominated by bryophytes, lichens, and cyanobacteria. These crusts demonstrated high tolerance to heavy metals (e.g., Cd, Pb) and effectively restored soil functionality by stabilizing substrates and enhancing microbial activity (<xref ref-type="bibr" rid="B30">Lobachevska et al., 2019</xref>). Complementary research by Ren et al. in manganese slag areas further highlighted the role of bryophytes in enriching bioavailable nutrients and diversifying soil microbial communities, which collectively primed the environment for vascular plant colonization (<xref ref-type="bibr" rid="B34">Ren et al., 2021</xref>). These findings underscore the pivotal role of bryophytes in initiating ecological succession, which is further explored in the following section on species screening.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Ecological functions of bryophytes.</p>
</caption>
<graphic xlink:href="fenvs-13-1610193-g002.tif">
<alt-text content-type="machine-generated">Four-section circular diagram with each section labeled: &#x22;Soil and Water Conservation&#x22; includes intercepting precipitation, root system stabilization, increasing soil porosity; &#x22;Pollution Control&#x22; involves heavy metal adsorption, organic pollutants decomposition, air particulate capture; &#x22;Micro-ecological Reconstruction&#x22; provides microbial habitats, pioneers vascular plants, secretes organic acids; &#x22;Carbon Sink and Climate Regulation&#x22; focuses on carbon fixation, oxygen release, surface temperature regulation. Arrows indicate interaction among sections.</alt-text>
</graphic>
</fig>
<p>As pioneer species in mining area restoration, bryophytes colonize exposed slag surfaces, creating foundational soil and moisture conditions for subsequent vegetation establishment (<xref ref-type="bibr" rid="B8">Chun et al., 2021</xref>). The collaborative interactions with algae, lichens, bacteria, and fungi drive the formation of biological soil crusts (BSCs). BSCs stabilize substrates, mitigate erosion, and shield emerging plant communities during early succession (<xref ref-type="bibr" rid="B41">Song et al., 2018</xref>). Beyond physical protection, bryophytes regulate soil microenvironments by modulating temperature fluctuations and enhancing moisture retention, thereby optimizing conditions for vascular plant recruitment (<xref ref-type="bibr" rid="B13">Gao et al., 2017</xref>). Field investigations in rare earth tailing ecosystems revealed the crucial ecological functions of bryophytes. Shen et al. recognized T<italic>richostomum brachydontium</italic>, <italic>T. involutum</italic>, <italic>Anoectangium stracheyanum</italic>, and <italic>Brachymenium exile</italic> as stress-adapted bryophyte species that can expedite revegetation via rapid substrate stabilization (<xref ref-type="bibr" rid="B37">Shen et al., 2022</xref>). Similarly, &#x160;irka et al. measured the contributions of bryophytes to biodiversity restoration in Central Slovakian mercury and copper slag heaps. Total of 83 and 76 bryophyte taxa were reported respectively. These bryophytes together increased species richness and promoted successional paths (<xref ref-type="bibr" rid="B39">&#x160;irka et al., 2018</xref>).</p>
<p>Bryophytes act as potent bioindicators in mining areas due to high heavy metal capability. Quantifying metal concentrations in bryophyte tissues (e.g., Cu, Pb, Cd) provides a reliable proxy for assessing soil pollution levels, with elevated values directly correlating to anthropogenic mining impacts (<xref ref-type="bibr" rid="B35">Ren et al., 2020</xref>). Moreover, changes in bryophyte communities, particularly increases in the number of species and their diversity, can be used to measure the success of ecological restoration. This is because a greater variety of species often indicates better habitat conditions (<xref ref-type="bibr" rid="B11">Feng et al., 2022</xref>). Field investigations in Wanshan mercury mining district in Guizhou Province demonstrated that mercury speciation analysis (total Hg and methyl-Hg concentrations) in seven bryophyte species effectively tracked atmospheric Hg pollution sources and quantified spatiotemporal dispersion gradients. This biomonitoring approach revealed distinct species-specific accumulation patterns correlated with industrial emission profiles and microclimatic deposition dynamics (<xref ref-type="bibr" rid="B4">Cao et al., 2016</xref>). Although lichens and bryophytes are well-known for indicating air quality, their potential for diagnosing soil pollution is not fully used. Notably, Rola and Osyczka documented that lichen-bryophyte consortia in southern Poland&#x2019;s Zn-Pb mining zones exhibited high sensitivity to soil metal gradients, enabling quantitative estimation of contamination severity (<xref ref-type="bibr" rid="B36">Rola and Osyczka, 2018</xref>). Similarly, in Turkey&#x2019;s Giresun sulfide deposits, <italic>Rhabdoweisia crispata</italic>, <italic>Pohlia nutans</italic>, and <italic>Pohlia elongata</italic> showed remarkable metal accumulation capabilities, which could be ascribed to the absence of cuticles and cation-exchangeable cell walls (<xref ref-type="bibr" rid="B21">Karakaya et al., 2015</xref>). Japanese researchers further identified <italic>Scopelophila cataractae</italic> as a dual Cu-As hyperaccumulator in aquatic systems near copper tailings, demonstrating bryophytes&#x2019; niche-specific adaptation to polymetallic stress (<xref ref-type="bibr" rid="B44">Suzuki et al., 2016</xref>).</p>
</sec>
<sec id="s2-3">
<title>2.3 Distribution characteristics of bryophytes in mining areas of China</title>
<p>There are approximately 3,108 bryophyte species spanning 160 families and 632 genera in mining areas of China, demonstrating exceptional diversity and stress adaptation (<xref ref-type="bibr" rid="B52">Zhu et al., 2022</xref>). Recent research prioritizes the spatial heterogeneity and metal hyperaccumulation capacities, particularly regarding bioremediation mechanisms in post-mining ecosystems. <xref ref-type="fig" rid="F3">Figure 3</xref>; <xref ref-type="table" rid="T2">Table 2</xref> systematically presented the bryophyte species and the heavy metal enrichment characteristics in copper, gold, manganese, rare earth, and coal mining areas in China.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Distribution of bryophyte species in different types of mines in China.</p>
</caption>
<graphic xlink:href="fenvs-13-1610193-g003.tif">
<alt-text content-type="machine-generated">Map of China showing locations where bryophytes were found in mining areas. Labels indicate the number of families, genera, and species at each site. Highlights include: Shengli coal mine in Inner Mongolia (4 families, 6 genera, 7 species), Lamingou gold mine in Gansu (15 families, 37 genera, 81 species), Tangdan copper mine in Yunnan (6 families, 16 genera, 22 species), Zhangjiawanzi gold mine in Guizhou (9 families, 16 genera, 23 species), Wanshan mercury mine in Guizhou (21 families, 52 genera, 95 species), and a rare earth mine in Jiangxi (36 families, 66 genera, 118 species).</alt-text>
</graphic>
</fig>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Comparison of species diversity and heavy metal enrichment characteristics of bryophytes in Chinese mining areas.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="center">Mine type</th>
<th align="center">Representative mine</th>
<th align="center">Number of moss species</th>
<th align="center">Dominant families</th>
<th align="center">Heavy metal enrichment ability</th>
<th align="center">Typical data source</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="center">Copper mine</td>
<td align="center">Tangdan Copper Mine in Yunnan Province</td>
<td align="center">22 species</td>
<td align="center">
<italic>Pottiaceae</italic>
</td>
<td align="center">68% of species inhabited patinated cupreous rocks and 32% cupreous soil</td>
<td align="center">
<xref ref-type="bibr" rid="B50">Zhou and Zhang (2007)</xref>
</td>
</tr>
<tr>
<td align="center">Gold mine</td>
<td align="center">Guizhou Zhangjiawanzi Gold Mine</td>
<td align="center">23 species</td>
<td align="center">
<italic>Pottiaceae</italic> and <italic>Bryaceae</italic>
</td>
<td align="center">Gymnostomum subrigidulum has a strong ability to enrich Cd, with an enrichment coefficient of 5.58 for Cd</td>
<td align="center">
<xref ref-type="bibr" rid="B2">Bing and Zhaohui (2008)</xref>
</td>
</tr>
<tr>
<td align="center">Mercury Mine</td>
<td align="center">Guizhou Wanshan Mercury Mining Area</td>
<td align="center">95 species</td>
<td align="center">
<italic>Hypnaceae</italic>, <italic>Thuidiaceae</italic> and <italic>Brachytheciaceae</italic>
</td>
<td align="center">With total mercury contents of 120&#x2013;450&#xa0;mg&#xa0;kg<sup>&#x2212;1</sup>, methylmercury contents of 0.8&#x2013;3.2&#xa0;mg&#xa0;kg<sup>&#x2212;1</sup>
</td>
<td align="center">(<xref ref-type="bibr" rid="B32">Pan and Zhang (2011)</xref>, <xref ref-type="bibr" rid="B4">Cao et al. (2016)</xref>
</td>
</tr>
<tr>
<td align="center">Manganese Mine</td>
<td align="center">Guizhou Yinjiang Manganese Slag Area</td>
<td align="center">24 species</td>
<td align="center">
<italic>Pottiaceae</italic> and <italic>Bryaceae</italic>
</td>
<td align="center">Mn enrichment coefficient of 0.009&#x2013;0.212, Cd enrichment coefficient of 0.754&#x2013;5.360</td>
<td align="center">
<xref ref-type="bibr" rid="B34">Ren et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="center">Rare Earth Mine</td>
<td align="center">Jiangxi South rare earth ion-type mine</td>
<td align="center">118 species</td>
<td align="center">
<italic>Polytrichaceae, Dicranales, Fissidentales</italic> and <italic>Pottiales</italic>
</td>
<td align="center">&#x2014;</td>
<td align="center">
<xref ref-type="bibr" rid="B22">Kong et al. (2023)</xref>, <xref ref-type="bibr" rid="B3">Cai et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="center">Coal Mine</td>
<td align="center">Inner Mongolia Shengli Coal Mine</td>
<td align="center">7 species</td>
<td align="center">
<italic>Ditrichaceae</italic>, <italic>Bryaceae</italic>, <italic>Funariaceae</italic> and <italic>Pottiaceae</italic>
</td>
<td align="center">&#x2014;</td>
<td align="center">
<xref ref-type="bibr" rid="B11">Feng et al. (2022)</xref>
</td>
</tr>
</tbody>
</table>
</table-wrap>
<sec id="s2-3-1">
<title>2.3.1 Copper mines</title>
<p>The Tangdan Copper Mine in Yunnan Province&#x2019;s metallogenic belt exemplified extreme edaphic constraints on bryophyte colonization, sustaining merely six families (e.g., <italic>Pottiaceae</italic>, <italic>Mniaceae</italic>) with 68% of observed species selectively inhabiting Cu-oxide encrustations rather than Cu-saturated soils. This niche partitioning showed specialized substrate optimization. Protonemal attachment and exocellular metal exclusion strategies allowed survival in Cu-rich environments (<xref ref-type="bibr" rid="B50">Zhou and Zhang, 2007</xref>).</p>
</sec>
<sec id="s2-3-2">
<title>2.3.2 Gold mines</title>
<p>The Zhangjiawanzi and Lanni Gou gold mines in Guizhou Province exhibited striking bryophyte community contrasts driven by microenvironmental heterogeneity. At Zhangjiawanzi, 23 species (16 genera, 9 families) demonstrated extreme oligotrophic adaptation. The families <italic>Polytrichaceae</italic> and <italic>Bryaceae</italic> were particularly dominant, indicating a preference for the nutrient-poor, acidic soils often found in gold mine environments. In contrast, the nearby Lanni Gou Gold Mine boasted a richer bryophyte community, with 81 species spread across 37 genera and 15 families, pointing to a greater ecological complexity and a higher level of biodiversity in this area (<xref ref-type="bibr" rid="B2">Bing and Zhaohui, 2008</xref>).</p>
</sec>
<sec id="s2-3-3">
<title>2.3.3 Mercury mines</title>
<p>The Wanshan Mercury Mine in Guizhou Province presented a striking contrast to typical mining environments, with a notable diversity of 95 bryophyte species spanning 52 genera and 27 families. This remarkable biodiversity might stem from the unique ecological niches formed by mercury extraction activities, which created heterogeneous microhabitats. A parallel example from Yunchangping Town, also in Guizhou Province, documented 62 bryophyte species over a 1-year period. These findings underscored the resilience and adaptability of bryophyte communities in heavily contaminated environments, suggesting high dynamic capacity to colonize and thrive under persistent heavy metal stress (<xref ref-type="bibr" rid="B32">Pan and Zhang, 2011</xref>).</p>
</sec>
<sec id="s2-3-4">
<title>2.3.4 Manganese mines</title>
<p>A 50-year-old manganese slag heap in Guizhou Province has developed into a distinct bryophyte refuge, supporting 20 taxa dominated by the structurally resilient families <italic>Bryaceae</italic> and <italic>Polytrichaceae</italic>. In the manganese slag area of Yinjiang County, 24 bryophyte species were found. <italic>Gymnostomum subrigidulum</italic>, <italic>Pohlia gedeana</italic>, and <italic>Bryum atrovirens</italic> were the most common, probably because they can tolerate high levels of metals. By contrast, the electrolytic manganese slag area in Songtao County hosted a depauperate bryophyte community of just six species, reflecting harsher edaphic or microclimatic conditions. Strikingly, <italic>B. atrovirens</italic> populations in both regions exhibit dual hyperaccumulation of manganese and cadmium. This remarkable ability of <italic>B. atrovirens</italic> to bind metals makes it a prime candidate for phytostabilization efforts in ecosystems contaminated with heavy metals (<xref ref-type="bibr" rid="B34">Ren et al., 2021</xref>).</p>
</sec>
<sec id="s2-3-5">
<title>2.3.5 Rare earth mines</title>
<p>In Jiangxi Province, ion-adsorption rare earth mines presented a unique ecological scenario where bryophyte biocrusts played a crucial role in shaping microbial community diversity and structure. Land-use intensity and anthropogenic disturbances strongly mediated bryophyte distribution patterns, with soil moisture regimes and substrate stability identified as key determinants of habitat suitability. Erect-growing forms were the most common in these groups, a trait that likely helps them retain moisture and stabilize soil in damaged areas. This ecological specialization positioned bryophytes as pivotal agents for post-mining revegetation, offering a natural template for restoring biogeochemical cycles in leached soils (<xref ref-type="bibr" rid="B22">Kong et al., 2023</xref>). Building on this, Cai et al. demonstrated that targeted bryophyte cultivation could accelerate ecosystem recovery pathways, leveraging dual role in microbial habitat provisioning and physical substrate rehabilitation (<xref ref-type="bibr" rid="B3">Cai et al., 2023</xref>).</p>
</sec>
<sec id="s2-3-6">
<title>2.3.6 Coal mines</title>
<p>In the semi-arid steppes of Inner Mongolia Autonomous Region, the Shengli Coal Mine was a key test site for studying how bryophytes adapt to post-industrial environments. Bryophyte assemblages here were tightly mediated by soil edaphic filters, particularly pH gradients and silt content, which served as deterministic forces structuring community composition. Only 7 bryophyte species were observed in the Shengli Coal Mine, likely due to aridity and alkaline soils limiting diversity. These findings revealed that the physical and chemical characteristics of the soil play a pivotal role in determining the species composition and distribution of bryophytes in coal mine environments (<xref ref-type="bibr" rid="B11">Feng et al., 2022</xref>).</p>
<p>Together, these studies delineated bryophytes as biodiversity hotspots within China&#x2019;s mining regions, showcasing not only wide biogeographic range but also evolutionarily refined heavy metal detoxification pathways. The capacity to dominate oligotrophic, metal-laden substrates underscored the dual ecological role as pioneers in primary succession and engineers of microhabitat amelioration. This dominance is further underpinned by critical interactions with soil microbiomes, including the secretion of organic acids (e.g., oxalate) for nutrient solubilization and metal bioavailability control, as well as stress-alleviating fungal symbioses that form nutrient-sharing networks analogous to mycorrhizae. Crucially, this functional resilience positioned bryophytes as keystone species for phytostabilization protocols and bioindicator frameworks. These distribution patterns further exemplify niche partitioning theory, with species like <italic>B</italic>. <italic>atrovirens</italic> (Mn-Cd hyperaccumulator) and <italic>G. subrigidulum</italic> occupying distinct ecological niches. Metal toxicity and edaphic filters shape these niches, driving community assembly through resource-use differentiation (<xref ref-type="table" rid="T2">Table 2</xref>).</p>
</sec>
</sec>
</sec>
<sec id="s3">
<title>3 Mine-adapted bryophytes screening</title>
<p>Screening aimed to identify bryophyte species with high adaptability to the harsh environmental conditions of mining areas, such as heavy metal contamination, soil erosion, and extreme pH levels. The selection of bryophyte species suitable for mining ecosystem rehabilitation was guided by a multi-criteria screening framework that integrates environmental tolerance, functional performance, and ecological benefits (<xref ref-type="fig" rid="F4">Figure 4</xref>). The screening criteria encompassed five key parameters: (1) Tolerance to Heavy Metals, defined as the ability to survive and proliferate in soils contaminated with elevated concentrations of toxic elements, (2) Soil Adaptation, reflecting the capacity to establish in nutrient-poor substrates characterized by low organic matter and extreme pH ranges, (3) Drought Resistance, quantified through survival rates under prolonged water scarcity and post-dehydration recovery efficiency, (4) Growth Rate, prioritizing species with rapid colonization and high biomass accumulation, and (5) Ecosystem Benefits, including soil stabilization via rhizoid networks, enhanced water infiltration capacity, and facilitation of microbial symbionts.</p>
<fig id="F4" position="float">
<label>FIGURE 4</label>
<caption>
<p>screening criteria and process for mining-adapted.</p>
</caption>
<graphic xlink:href="fenvs-13-1610193-g004.tif">
<alt-text content-type="machine-generated">Screening criteria and process diagram for mining-adapted bryophytes. Environmental tolerance includes heavy metal tolerance, soil adaptation, and drought resistance. Functional performance involves growth rate and ecosystem benefits. The screening process involves field collection, laboratory cultivation, heavy metal exposure test, soil adaptation test, drought simulation, and field trials.</alt-text>
</graphic>
</fig>
<p>The screening process followed a sequential experimental protocol (<xref ref-type="fig" rid="F4">Figure 4</xref>). Initially, bryophyte samples were collected from naturally occurring populations in mining-impacted zones or analogous degraded ecosystems. These specimens underwent laboratory cultivation under controlled light, temperature, and humidity to assess baseline growth dynamics and stress resilience. Subsequent heavy metal exposure tests employed dose-response assays to evaluate metal tolerance thresholds and bioaccumulation potential. Concurrently, soil adaptation tests measure establishment succussed in mining-derived substrates, with performance metrics including shoot elongation rate and biomass partitioning. Drought simulation experiments utilized osmotic stress gradients to quantify desiccation tolerance and rehydration recovery kinetics. Finally, candidate species demonstrating robust laboratory performance were subjected to field trials involving transplantation to target mining sites, where long-term viability, ecological integration, and functional efficacy were monitored over &#x2265;2 growing seasons. This systematic approach ensured the identification of bryophyte species that align with site-specific rehabilitation goals while minimizing ecological risks.</p>
<p>Researchers systematically evaluated bryophyte species to identify candidates with high adaptability, rapid growth rates, and multifunctional ecological benefits for mining area restoration. Selected species exhibited exceptional survival rates and restoration efficacy under harsh mining conditions. Early research emphasized the pioneering role of bryophytes in ecological restoration, particularly the drought tolerance (xerophytic adaptation), resilience to nutrient-poor substrates, and prolific reproductive strategies, which collectively prime degraded sites for subsequent vegetation recovery (<xref ref-type="bibr" rid="B43">Sun et al., 2004</xref>; <xref ref-type="bibr" rid="B53">Zuo et al., 2006</xref>). For instance, Sun et al. assessed the feasibility of bryophyte-mediated restoration in Jiuzhaigou Valley&#x2019;s post-disaster landscapes, identifying key constraints (e.g., substrate instability) requiring mitigation in practical applications (<xref ref-type="bibr" rid="B43">Sun et al., 2004</xref>). Subsequent studies shifted focus to drought resistance screening. Through controlled drought simulations, Li et al. identified three hyper-tolerant bryophyte species (e.g., <italic>Bryum argenteum</italic>) in northern Hebei Province and optimized the cultivation protocols for slope stabilization (<xref ref-type="bibr" rid="B25">Li, 2017</xref>). Following the Jiuzhaigou earthquake, Xia et al. developed an Analytic Hierarchy Process (AHP)-based evaluation framework to prioritize bryophyte species for revegetating exposed slopes. Criteria included stress tolerance, propagule availability, ecological functionality, reproductive capacity, biomass yield, and aesthetic value. This approach selected five species&#x2014;<italic>Racomitrium japonicum</italic>, <italic>Hypnum plumaeforme</italic>, <italic>Eurohypnum leptothallum</italic>, <italic>Plagiomnium acutum</italic>, and <italic>Brachythecium rutabulum</italic>&#x2014;for targeted slope greening (<xref ref-type="bibr" rid="B46">Xia et al., 2023</xref>).</p>
</sec>
<sec id="s4">
<title>4 Cultivation of bryophytes</title>
<p>
<xref ref-type="fig" rid="F5">Figure 5</xref> outlined a standardized <italic>in vitro</italic> protocol for bryophyte rapid propagation, integrating surface sterilization, hormone-regulated differentiation, and cyclic subcultures to achieve high-efficiency biomass production while maintaining genetic uniformity and pathogen-free status. This optimized protocol enabled rapid clonal propagation of bryophyte species (e.g., <italic>Physcomitrium</italic> patens) through surface-sterilized gametophyte explants cultured on hormone-supplemented media (MS/B5) under controlled light and temperature. Protonema induction, cytokinin-mediated gametophore differentiation, and cyclic subcultures ensured scalable biomass production, followed by acclimatization on low-nutrient substrates. Genetic fidelity and contamination-free status were validated via molecular assays, supporting applications in research and ecological restoration.</p>
<fig id="F5" position="float">
<label>FIGURE 5</label>
<caption>
<p>Rapid propagation scheme for bryophytes.</p>
</caption>
<graphic xlink:href="fenvs-13-1610193-g005.tif">
<alt-text content-type="machine-generated">Flowchart illustrating moss propagation process: Explant Selection, Surface Sterilization, Culture Medium Preparation, Inoculation, Protonema Induction, Gametophore Differentiation, Multiplication Phase, Rooting &#x26; Acclimatization, Transplanting, and Quality Control. Steps involve sterilization, culture vessel conditions, hormonal adjustments, shoot formation, subculture, rhizoid development, and genetic fidelity testing.</alt-text>
</graphic>
</fig>
<p>Common methods for bryophyte cultivation include stem cutting propagation and tissue culture rapid propagation. Stem cutting propagation technology can rapidly propagate certain bryophyte species and adapt to artificial environmental control. For example, Chen et al. successfully identified the suitable environmental conditions and propagation factors for the feather bryophyte in artificial culture through stem cutting propagation experiments, providing an efficient rapid propagation method for stone slope greening and ecological restoration (<xref ref-type="bibr" rid="B7">Chen et al., 2022</xref>). Additionally, the application of tissue culture technology has made rapid propagation of bryophytes possible while ensuring the genetic stability of the seed sources (<xref ref-type="bibr" rid="B48">Zhang X. et al., 2023</xref>). Taking Yue&#x2019;s research as an example, rapid propagation of bryophytes was achieved by inducing callus formation, adventitious buds, and adventitious roots (<xref ref-type="bibr" rid="B18">Huanli, 2009</xref>). Huang et al. used four wild bryophyte species from a uranium tailings area as materials to explore the effects of different pH, temperature, cultivation substrates, and plant growth regulators on bryophyte growth and established the rapid propagation techniques for the grey bryophyte, large grey bryophyte, sharp-leafed creeping light bryophyte, and scale bryophyte (<xref ref-type="bibr" rid="B17">Huang et al., 2019</xref>). Although bryophyte cultivation techniques have made some progress, there are still some challenges. The application scalability of bryophytes is compromised by poikilohydric constraints, particularly slow biomass accrual rates and multi-year reproductive maturation periods, requiring targeted culturing innovations to overcome these physiological barriers. Spore propagation is greatly influenced by environmental factors, and its germination rate and survival rate are usually low. Moreover, bryophytes have strict requirements for the growth environment, necessitating precise control of light, water, temperature, and other conditions, which can lead to relatively high cultivation costs.</p>
<p>In recent years, important research achievements have been made in the field of bryophyte cultivation techniques. Studies indicate that bryophyte species possess different preferences for cultivation substrates. Common cultivation substrates like peat, perlite, and vermiculite demonstrate high compatibility with multiple bryophyte species. This was exemplified by a Canadian case study on lithium mine waste rock revegetation in Quebec, where bryophyte regeneration success rates showed significant variation depending on substrate composition and microenvironmental conditions (<xref ref-type="bibr" rid="B29">Liu et al., 2024</xref>). Meanwhile, special substrates such as volcanic rock and forest humus have a significant promotional effect on the growth of certain bryophyte species (<xref ref-type="bibr" rid="B38">Shi et al., 2022</xref>). Through proportional experiments with different substrates, researchers can select the most suitable ratio for the growth of specific bryophytes. For example, a volume ratio of peat to vermiculite of 2:1 is most beneficial for the growth of short-toothed bryophyte (<xref ref-type="bibr" rid="B47">Yu et al., 2024</xref>). In terms of environmental factors, light intensity is a key factor affecting bryophyte growth. Studies have shown that moderate shading helps the growth of certain bryophyte species (<xref ref-type="bibr" rid="B10">Fazan et al., 2022</xref>). Water and temperature are also limiting factors for bryophyte growth. Appropriate watering and a suitable temperature range can promote bryophyte growth, while excessive watering or extreme temperatures can inhibit bryophyte growth (<xref ref-type="bibr" rid="B40">Slate et al., 2024</xref>; <xref ref-type="bibr" rid="B49">Zhang Y. et al., 2023</xref>).</p>
</sec>
<sec id="s5">
<title>5 Application cases of bryophytes in mine ecological restoration</title>
<sec id="s5-1">
<title>5.1 Application of bryophytes in ecological restoration of limestone mine slopes in northern Guangxi Province</title>
<p>Guangxi Province is one of China&#x2019;s representative regions for karst landscapes, rich in limestone resources. In the past, simple open-pit mining methods severely damaged the landforms and vegetation in mining areas, making ecological restoration research critical. Li conducted a case study at the Tieshan Quarry (Qixing District, Guilin City, Guangxi Province) to investigate bryophyte-based ecological restoration on limestone mine slopes. The mining area located in a subtropical monsoon climate zone with brown-gray limestone soil. Open-pit mining has damaged the land, vegetation, mountain structures, and rock and soil exposures. By integrating drone surveys with ground-based observations, a 3D terrain model was developed and six bryophyte species across five families and six genera were identified, with <italic>Barbula unguiculata</italic> as the dominant taxon. The study revealed that climatic temperature-humidity fluctuations critically regulate bryophyte colonization, while an optimized protocol combining crushed bark inoculation, Hoagland solution application, and intermittent misting achieved a coverage of 7.18% within 20 days, which was much higher than the control treatment (0.17%) (<xref ref-type="bibr" rid="B24">Li, 2023</xref>).</p>
</sec>
<sec id="s5-2">
<title>5.2 Application of bryophytes in semi-underground space ecological restoration of a 100-m deep mining pit</title>
<p>In karst areas, abandoned mining pits often have complex geological conditions due to post-mining changes like increased karstification and more fissures in rock walls. This makes it hard for plants to grow and difficult to redevelop the land. In the ecological restoration of Xinsheng Cement Plant&#x2019;s abandoned mining pit (Changsha City, Hunan Province), a novel rapid greening technology was developed using cold-tolerant bryophytes and biodegradable bio-glue for concrete and rock wall stabilization (<xref ref-type="bibr" rid="B23">Li et al., 2021</xref>). Through rigorous species screening, xerophytic mosses with 99.5% survival rates under high solar irradiance and drought stress were selected. This approach significantly accelerated plant community succession, transforming the degraded site into the &#x201c;Joyful Paradise&#x201d; landscape within 12&#xa0;months. This ecological engineering approach created synergistic value chains where bryophyte-mediated slope stabilization enhanced biodiversity, which in turn attracted nature-based tourism while empowering local stakeholders through hands-on restoration workshops.</p>
<p>These applications operationalize ecological succession theory. Bryophytes act as early-successional engineers that accelerate trajectory shifts from degraded to functional states. Bryophyte restoration helps achieve UN Sustainable Development Goals by naturally repairing damaged land. Bryophytes act as pioneer species that form erosion-proof living crusts on degraded sites like mines, supporting SDG 15 for terrestrial ecosystems. These organisms capture carbon three to five times more effectively than regular plants, directly advancing climate action under SDG 13, with peat mosses alone locking away 10%&#x2013;15% of the world&#x2019;s land-based carbon. Dense mats of bryophytes also filter toxic metals from runoff, protecting water quality for SDG 6. Unlike traditional methods that often need chemicals or repeated planting, bryophyte solutions eliminate pollution while cutting long-term costs. By creating self-sustaining microhabitats that boost biodiversity, bryophytes offer a practical nature-based path to meet global sustainability targets in challenging environments.</p>
</sec>
</sec>
<sec sec-type="conclusion" id="s6">
<title>6 Conclusion</title>
<p>Bryophytes are emerging as pivotal agents in mining ecosystem restoration, bridging applied remediation needs with fundamental ecological research due to strong adaptability, soil-binding ability, and heavy metal enrichment capacity. While substantial progress has been made in laboratory settings, field implementation challenges persist, particularly regarding scaling propagation protocols and ensuring survivability in oligotrophic substrates or metal-contaminated environments. Notably, tolerant species immobilize contaminants through exclusion/detoxification mechanisms, enabling phytostabilization, whereas hyperaccumulators actively concentrate metals in harvestable tissues for phytoextraction, which requires distinct deployment strategies to avoid ecological risks. Moreover, overcoming key practical barriers, notably high propagation costs, slow growth rates, and the logistical complexity of large-scale deployment, remains critical for enhancing the scalability and economic feasibility of bryophyte-based restoration as a transformative ecological strategy. Future research should prioritize three interconnected fronts: 1) conducting long-term monitoring studies on bryophyte-based restoration projects, 2) exploring the combined use of bryophytes with other plant species for enhanced restoration outcomes, and 3) refining species-specific cultivation matrices through machine learning optimization, deciphering bryophyte-microbiome synergies governing metal (loid) sequestration, and mapping epigenetic adaptation pathways under climate fluctuation scenarios. These investigations will catalyze next-generation phytostabilization technologies while advancing ecological theory on pioneer species&#x2019; roles in anthropogenic landscape rehabilitation.</p>
</sec>
</body>
<back>
<sec sec-type="author-contributions" id="s7">
<title>Author contributions</title>
<p>ZQ: Conceptualization, Writing &#x2013; original draft, Data curation, Methodology. XL: Formal Analysis, Writing &#x2013; original draft. TZ: Writing &#x2013; original draft, Methodology, Validation, Investigation. SL: Writing &#x2013; review and editing, Conceptualization, Resources. CW: Writing &#x2013; review and editing, Writing &#x2013; original draft, Formal Analysis. WZ: Formal Analysis, Writing &#x2013; review and editing. LL: Supervision, Writing &#x2013; review and editing, Investigation, Project administration.</p>
</sec>
<sec sec-type="funding-information" id="s8">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This work was funded by the Open Project of Technology Innovation Center for Land Spatial Ecological Protection and Restoration in Great Lakes Basin, MNR, grant number No. JXCXZX2024007.</p>
</sec>
<sec sec-type="COI-statement" id="s9">
<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>
</sec>
<sec sec-type="ai-statement" id="s10">
<title>Generative AI statement</title>
<p>The author(s) declare that Generative AI was used in the creation of this manuscript. Generative AI was used to grammar, spelling errors, etc.</p>
</sec>
<sec sec-type="disclaimer" id="s11">
<title>Publisher&#x2019;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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</ref-list>
</back>
</article>