冰川表面活跃和休眠的微生物

IF 2.7 2区 地球科学 Q2 BIOLOGY Geobiology Pub Date : 2022-11-30 DOI:10.1111/gbi.12535
James A. Bradley, Christopher B. Trivedi, Matthias Winkel, Rey Mourot, Stefanie Lutz, Catherine Larose, Christoph Keuschnig, Eva Doting, Laura Halbach, Athanasios Zervas, Alexandre M. Anesio, Liane G. Benning
{"title":"冰川表面活跃和休眠的微生物","authors":"James A. Bradley,&nbsp;Christopher B. Trivedi,&nbsp;Matthias Winkel,&nbsp;Rey Mourot,&nbsp;Stefanie Lutz,&nbsp;Catherine Larose,&nbsp;Christoph Keuschnig,&nbsp;Eva Doting,&nbsp;Laura Halbach,&nbsp;Athanasios Zervas,&nbsp;Alexandre M. Anesio,&nbsp;Liane G. Benning","doi":"10.1111/gbi.12535","DOIUrl":null,"url":null,"abstract":"<p>Glacier and ice sheet surfaces host diverse communities of microorganisms whose activity (or inactivity) influences biogeochemical cycles and ice melting. Supraglacial microbes endure various environmental extremes including resource scarcity, frequent temperature fluctuations above and below the freezing point of water, and high UV irradiance during summer followed by months of total darkness during winter. One strategy that enables microbial life to persist through environmental extremes is dormancy, which despite being prevalent among microbial communities in natural settings, has not been directly measured and quantified in glacier surface ecosystems. Here, we use a combination of metabarcoding and metatranscriptomic analyses, as well as cell-specific activity (BONCAT) incubations to assess the diversity and activity of microbial communities from glacial surfaces in Iceland and Greenland. We also present a new ecological model for glacier microorganisms and simulate physiological state-changes in the glacial microbial community under idealized (i) freezing, (ii) thawing, and (iii) freeze–thaw conditions. We show that a high proportion (&gt;50%) of bacterial cells are translationally active in-situ on snow and ice surfaces, with Actinomycetota, Pseudomonadota, and Planctomycetota dominating the total and active community compositions, and that glacier microorganisms, even when frozen, could resume translational activity within 24 h after thawing. Our data suggest that glacial microorganisms respond rapidly to dynamic and changing conditions typical of their natural environment. We deduce that the biology and biogeochemistry of glacier surfaces are shaped by processes occurring over short (i.e., daily) timescales, and thus are susceptible to change following the expected alterations to the melt-regime of glaciers driven by climate change. A better understanding of the activity of microorganisms on glacier surfaces is critical in addressing the growing concern of climate change in Polar regions, as well as for their use as analogues to life in potentially habitable icy worlds.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 2","pages":"244-261"},"PeriodicalIF":2.7000,"publicationDate":"2022-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12535","citationCount":"4","resultStr":"{\"title\":\"Active and dormant microorganisms on glacier surfaces\",\"authors\":\"James A. Bradley,&nbsp;Christopher B. Trivedi,&nbsp;Matthias Winkel,&nbsp;Rey Mourot,&nbsp;Stefanie Lutz,&nbsp;Catherine Larose,&nbsp;Christoph Keuschnig,&nbsp;Eva Doting,&nbsp;Laura Halbach,&nbsp;Athanasios Zervas,&nbsp;Alexandre M. Anesio,&nbsp;Liane G. Benning\",\"doi\":\"10.1111/gbi.12535\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Glacier and ice sheet surfaces host diverse communities of microorganisms whose activity (or inactivity) influences biogeochemical cycles and ice melting. Supraglacial microbes endure various environmental extremes including resource scarcity, frequent temperature fluctuations above and below the freezing point of water, and high UV irradiance during summer followed by months of total darkness during winter. One strategy that enables microbial life to persist through environmental extremes is dormancy, which despite being prevalent among microbial communities in natural settings, has not been directly measured and quantified in glacier surface ecosystems. Here, we use a combination of metabarcoding and metatranscriptomic analyses, as well as cell-specific activity (BONCAT) incubations to assess the diversity and activity of microbial communities from glacial surfaces in Iceland and Greenland. We also present a new ecological model for glacier microorganisms and simulate physiological state-changes in the glacial microbial community under idealized (i) freezing, (ii) thawing, and (iii) freeze–thaw conditions. We show that a high proportion (&gt;50%) of bacterial cells are translationally active in-situ on snow and ice surfaces, with Actinomycetota, Pseudomonadota, and Planctomycetota dominating the total and active community compositions, and that glacier microorganisms, even when frozen, could resume translational activity within 24 h after thawing. Our data suggest that glacial microorganisms respond rapidly to dynamic and changing conditions typical of their natural environment. We deduce that the biology and biogeochemistry of glacier surfaces are shaped by processes occurring over short (i.e., daily) timescales, and thus are susceptible to change following the expected alterations to the melt-regime of glaciers driven by climate change. A better understanding of the activity of microorganisms on glacier surfaces is critical in addressing the growing concern of climate change in Polar regions, as well as for their use as analogues to life in potentially habitable icy worlds.</p>\",\"PeriodicalId\":173,\"journal\":{\"name\":\"Geobiology\",\"volume\":\"21 2\",\"pages\":\"244-261\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2022-11-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12535\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geobiology\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/gbi.12535\",\"RegionNum\":2,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geobiology","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbi.12535","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 4

摘要

冰川和冰盖表面有多种微生物群落,它们的活动(或不活动)影响生物地球化学循环和冰融化。冰川上的微生物忍受各种极端环境,包括资源短缺、温度在水的冰点上下波动频繁、夏季紫外线照射强、冬季数月完全黑暗。使微生物生命能够在极端环境中持续存在的一种策略是休眠,尽管在自然环境中微生物群落中普遍存在,但在冰川表面生态系统中尚未直接测量和量化。在这里,我们结合使用元条形码和元转录组学分析,以及细胞特异性活性(BONCAT)孵育来评估冰岛和格陵兰冰川表面微生物群落的多样性和活性。我们还提出了一个新的冰川微生物生态模型,并模拟了理想(i)冻结、(ii)融化和(iii)冻融条件下冰川微生物群落的生理状态变化。我们发现,在冰雪表面上,有很高比例(50%)的细菌细胞具有原位翻译活性,其中放线菌门、假单胞菌门和植菌门在总群落组成和活跃群落组成中占主导地位,冰川微生物即使在冷冻状态下,也能在解冻后24小时内恢复翻译活性。我们的数据表明,冰川微生物对其自然环境典型的动态和变化条件反应迅速。我们推断,冰川表面的生物和生物地球化学是由短期(即每天)时间尺度上发生的过程形成的,因此很容易受到气候变化驱动的冰川融化状态预期变化的影响。更好地了解冰川表面微生物的活动,对于解决人们对极地地区气候变化日益关注的问题至关重要,对于它们在可能适合居住的冰雪世界中作为生命的类比物也至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Active and dormant microorganisms on glacier surfaces

Glacier and ice sheet surfaces host diverse communities of microorganisms whose activity (or inactivity) influences biogeochemical cycles and ice melting. Supraglacial microbes endure various environmental extremes including resource scarcity, frequent temperature fluctuations above and below the freezing point of water, and high UV irradiance during summer followed by months of total darkness during winter. One strategy that enables microbial life to persist through environmental extremes is dormancy, which despite being prevalent among microbial communities in natural settings, has not been directly measured and quantified in glacier surface ecosystems. Here, we use a combination of metabarcoding and metatranscriptomic analyses, as well as cell-specific activity (BONCAT) incubations to assess the diversity and activity of microbial communities from glacial surfaces in Iceland and Greenland. We also present a new ecological model for glacier microorganisms and simulate physiological state-changes in the glacial microbial community under idealized (i) freezing, (ii) thawing, and (iii) freeze–thaw conditions. We show that a high proportion (>50%) of bacterial cells are translationally active in-situ on snow and ice surfaces, with Actinomycetota, Pseudomonadota, and Planctomycetota dominating the total and active community compositions, and that glacier microorganisms, even when frozen, could resume translational activity within 24 h after thawing. Our data suggest that glacial microorganisms respond rapidly to dynamic and changing conditions typical of their natural environment. We deduce that the biology and biogeochemistry of glacier surfaces are shaped by processes occurring over short (i.e., daily) timescales, and thus are susceptible to change following the expected alterations to the melt-regime of glaciers driven by climate change. A better understanding of the activity of microorganisms on glacier surfaces is critical in addressing the growing concern of climate change in Polar regions, as well as for their use as analogues to life in potentially habitable icy worlds.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Geobiology
Geobiology 生物-地球科学综合
CiteScore
6.80
自引率
5.40%
发文量
56
审稿时长
3 months
期刊介绍: The field of geobiology explores the relationship between life and the Earth''s physical and chemical environment. Geobiology, launched in 2003, aims to provide a natural home for geobiological research, allowing the cross-fertilization of critical ideas, and promoting cooperation and advancement in this emerging field. We also aim to provide you with a forum for the rapid publication of your results in an international journal of high standing. We are particularly interested in papers crossing disciplines and containing both geological and biological elements, emphasizing the co-evolutionary interactions between life and its physical environment over geological time. Geobiology invites submission of high-quality articles in the following areas: Origins and evolution of life Co-evolution of the atmosphere, hydrosphere and biosphere The sedimentary rock record and geobiology of critical intervals Paleobiology and evolutionary ecology Biogeochemistry and global elemental cycles Microbe-mineral interactions Biomarkers Molecular ecology and phylogenetics.
期刊最新文献
Redox Gradient Shapes the Chemical Composition of Peatland Microbial Communities Ultrastructural Perspectives on the Biology and Taphonomy of Tonian Microfossils From the Draken Formation, Spitsbergen Issue Information Featured Cover A Biofilm Channel Origin for Vermiform Microstructure in Carbonate Microbialites
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1