典型亚热带河口浮游古生菌的季节动态及环境控制。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Wenya Wei, Penghui Li, Fahui Gong, Cheng Zhang, Kedong Yin, Wei Xie
{"title":"典型亚热带河口浮游古生菌的季节动态及环境控制。","authors":"Wenya Wei, Penghui Li, Fahui Gong, Cheng Zhang, Kedong Yin, Wei Xie","doi":"10.1128/spectrum.00759-25","DOIUrl":null,"url":null,"abstract":"<p><p>Planktonic archaea are pivotal in the biogeochemical cycling across estuaries to coastal seas. A thorough comprehension of their adaptive mechanisms to seasonal environmental fluctuations remains largely unexplored. This study investigates the seasonal dynamics of planktonic archaeal communities and their responses to the biotic and abiotic factors in the Pearl River Estuary (PRE). Thermoproteota and Thermoplasmatota are the two most abundant phyla, and both show a significant difference between summer and winter. As phosphorus is the most limiting nutrient in the PRE, PO<sub>4</sub><sup>3-</sup> is found to have the most significant seasonal variation in random forest, followed by temperature and Chl a. The Mantel test for the abundant archaea showed that the number of phosphate-correlated OTUs was the second highest, following only temperature. The generalized additive modeling (GAM) analysis further reveals that the abundance of Thermoproteota was controlled by PO<sub>4</sub><sup>3-</sup>, temperature, and DO, whereas MGII was controlled by PO<sub>4</sub><sup>3-</sup>, pH, salinity, and Chl a. Our research demonstrates that there is a strong seasonality in coastal archaeal communities and sheds light on revealing their environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.</p><p><strong>Importance: </strong>Archaea not only sustain the equilibrium of elemental cycles but also exhibit remarkable plasticity in responding to and adapting to fluctuating environmental conditions. In particular, the adaptive strategies and ecological impacts of archaea in complex and dynamic settings, such as estuaries, represent a compelling yet unresolved area of scientific inquiry. Our study focused on the seasonal dynamics of planktonic archaeal communities in the Pearl River Estuary (PRE) and their response to biotic and abiotic factors. Our study demonstrates a strong seasonality in the aggregation of these coastal archaeal communities and adaptability to dynamic phosphate concentrations, emphasizing the critical role of phosphate in controlling the distribution of archaea. Our study sheds light on revealing environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0075925"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Seasonal dynamics and environmental controls of planktonic archaea in a typical subtropical estuary.\",\"authors\":\"Wenya Wei, Penghui Li, Fahui Gong, Cheng Zhang, Kedong Yin, Wei Xie\",\"doi\":\"10.1128/spectrum.00759-25\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Planktonic archaea are pivotal in the biogeochemical cycling across estuaries to coastal seas. A thorough comprehension of their adaptive mechanisms to seasonal environmental fluctuations remains largely unexplored. This study investigates the seasonal dynamics of planktonic archaeal communities and their responses to the biotic and abiotic factors in the Pearl River Estuary (PRE). Thermoproteota and Thermoplasmatota are the two most abundant phyla, and both show a significant difference between summer and winter. As phosphorus is the most limiting nutrient in the PRE, PO<sub>4</sub><sup>3-</sup> is found to have the most significant seasonal variation in random forest, followed by temperature and Chl a. The Mantel test for the abundant archaea showed that the number of phosphate-correlated OTUs was the second highest, following only temperature. The generalized additive modeling (GAM) analysis further reveals that the abundance of Thermoproteota was controlled by PO<sub>4</sub><sup>3-</sup>, temperature, and DO, whereas MGII was controlled by PO<sub>4</sub><sup>3-</sup>, pH, salinity, and Chl a. Our research demonstrates that there is a strong seasonality in coastal archaeal communities and sheds light on revealing their environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.</p><p><strong>Importance: </strong>Archaea not only sustain the equilibrium of elemental cycles but also exhibit remarkable plasticity in responding to and adapting to fluctuating environmental conditions. In particular, the adaptive strategies and ecological impacts of archaea in complex and dynamic settings, such as estuaries, represent a compelling yet unresolved area of scientific inquiry. Our study focused on the seasonal dynamics of planktonic archaeal communities in the Pearl River Estuary (PRE) and their response to biotic and abiotic factors. Our study demonstrates a strong seasonality in the aggregation of these coastal archaeal communities and adaptability to dynamic phosphate concentrations, emphasizing the critical role of phosphate in controlling the distribution of archaea. Our study sheds light on revealing environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.</p>\",\"PeriodicalId\":18670,\"journal\":{\"name\":\"Microbiology spectrum\",\"volume\":\" \",\"pages\":\"e0075925\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbiology spectrum\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/spectrum.00759-25\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.00759-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

浮游古菌在河口到近海的生物地球化学循环中起着关键作用。对它们对季节性环境波动的适应机制的透彻理解在很大程度上仍未得到探索。研究了珠江口浮游古细菌群落的季节动态及其对生物和非生物因子的响应。热变形门和热原藻门是最丰富的两个门,在夏季和冬季都表现出显著的差异。由于磷是PRE中最具限制性的养分,PO43-在随机森林中具有最显著的季节变化,其次是温度和Chl a。对丰富的古菌进行Mantel测试表明,与磷酸盐相关的otu数量仅次于温度。广义加性模型(GAM)进一步揭示了热变形菌的丰度受PO43-、温度和DO的控制,而MGII受PO43-、pH、盐度和Chl a的控制。研究结果表明,沿海古菌群落存在较强的季节性,有助于揭示其环境适应性和预测生物地球化学功能对区域和全球环境变化的响应。重要性:古细菌不仅维持元素循环的平衡,而且在响应和适应波动的环境条件方面表现出显著的可塑性。特别是,古细菌在复杂和动态环境中的适应策略和生态影响,如河口,代表了一个令人信服但尚未解决的科学探索领域。研究了珠江口浮游古细菌群落的季节动态及其对生物和非生物因子的响应。我们的研究表明,这些沿海古菌群落的聚集具有很强的季节性和对动态磷酸盐浓度的适应性,强调了磷酸盐在控制古菌分布中的关键作用。我们的研究揭示了环境适应和预测生物地球化学功能对区域和全球环境变化的响应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Seasonal dynamics and environmental controls of planktonic archaea in a typical subtropical estuary.

Planktonic archaea are pivotal in the biogeochemical cycling across estuaries to coastal seas. A thorough comprehension of their adaptive mechanisms to seasonal environmental fluctuations remains largely unexplored. This study investigates the seasonal dynamics of planktonic archaeal communities and their responses to the biotic and abiotic factors in the Pearl River Estuary (PRE). Thermoproteota and Thermoplasmatota are the two most abundant phyla, and both show a significant difference between summer and winter. As phosphorus is the most limiting nutrient in the PRE, PO43- is found to have the most significant seasonal variation in random forest, followed by temperature and Chl a. The Mantel test for the abundant archaea showed that the number of phosphate-correlated OTUs was the second highest, following only temperature. The generalized additive modeling (GAM) analysis further reveals that the abundance of Thermoproteota was controlled by PO43-, temperature, and DO, whereas MGII was controlled by PO43-, pH, salinity, and Chl a. Our research demonstrates that there is a strong seasonality in coastal archaeal communities and sheds light on revealing their environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.

Importance: Archaea not only sustain the equilibrium of elemental cycles but also exhibit remarkable plasticity in responding to and adapting to fluctuating environmental conditions. In particular, the adaptive strategies and ecological impacts of archaea in complex and dynamic settings, such as estuaries, represent a compelling yet unresolved area of scientific inquiry. Our study focused on the seasonal dynamics of planktonic archaeal communities in the Pearl River Estuary (PRE) and their response to biotic and abiotic factors. Our study demonstrates a strong seasonality in the aggregation of these coastal archaeal communities and adaptability to dynamic phosphate concentrations, emphasizing the critical role of phosphate in controlling the distribution of archaea. Our study sheds light on revealing environmental adaptation and predicting biogeochemical function alterations in response to regional and global environmental changes.

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
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信