Soil microbial communities vary in composition and functional strategy across soil aggregate size class regardless of tillage

IF 4.7 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Elementa-Science of the Anthropocene Pub Date : 2022-01-01 DOI:10.1525/elementa.2022.00023
Lukas T. Bernhardt, Richard G. Smith, A. S. Grandy, J. Mackay, Nicholas D. Warren, K. Geyer, J. Ernakovich
{"title":"Soil microbial communities vary in composition and functional strategy across soil aggregate size class regardless of tillage","authors":"Lukas T. Bernhardt, Richard G. Smith, A. S. Grandy, J. Mackay, Nicholas D. Warren, K. Geyer, J. Ernakovich","doi":"10.1525/elementa.2022.00023","DOIUrl":null,"url":null,"abstract":"The physicochemical environment within aggregates controls the distribution of carbon and microbial communities in soils. Agricultural management, such as tillage, can disrupt aggregates and the microscale habitat provided to microorganisms, thus altering microbial community dynamics. Categorizing microbial communities into life history strategies with shared functional traits—as has been done to understand plant community structure for decades—can illuminate how the soil physicochemical environment constrains the membership and activity of microbial communities. We conducted an aggregate scale survey of microbial community composition and function through the lens of the yield–acquisition–stress (Y–A–S) tolerator life history framework. Soils collected from a 7-year tillage experiment were separated into 4 aggregate size classes and enzyme activity, multiple-substrate-induced respiration, and carbon use efficiency were measured to reveal trade-offs in microbial resource allocation. Microbial community structure was interrogated with bacterial and fungal marker gene sequencing, and metagenomic features such as community weighted genome size and traits conferring stress tolerance were predicted using PICRUSt2. Consistent with our hypothesis, aggregates of different size classes harbored distinct microbial communities manifesting distinct life history strategies. Large macroaggregate communities >2 mm were classified as acquisition strategists based on increased enzyme activity relative to other aggregate size classes. Small and medium microaggregate (0.25–2 mm) communities did not show a strong tendency toward any particular life history strategy. Genes conferring stress tolerance were significantly enriched in microaggregates <0.25 mm (indicative of stress tolerators); however, these communities also had the highest carbon use efficiency (indicative of yield strategists). We found trade-offs in resource allocation between communities classified as yield and acquisition strategists consistent with the Y–A–S framework. Tillage did not alter life history strategies within aggregates, suggesting that the aggregate physicochemistry plays a larger role than agricultural management in shaping microbial life history at the scale studied.","PeriodicalId":54279,"journal":{"name":"Elementa-Science of the Anthropocene","volume":null,"pages":null},"PeriodicalIF":4.7000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Elementa-Science of the Anthropocene","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1525/elementa.2022.00023","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 1

Abstract

The physicochemical environment within aggregates controls the distribution of carbon and microbial communities in soils. Agricultural management, such as tillage, can disrupt aggregates and the microscale habitat provided to microorganisms, thus altering microbial community dynamics. Categorizing microbial communities into life history strategies with shared functional traits—as has been done to understand plant community structure for decades—can illuminate how the soil physicochemical environment constrains the membership and activity of microbial communities. We conducted an aggregate scale survey of microbial community composition and function through the lens of the yield–acquisition–stress (Y–A–S) tolerator life history framework. Soils collected from a 7-year tillage experiment were separated into 4 aggregate size classes and enzyme activity, multiple-substrate-induced respiration, and carbon use efficiency were measured to reveal trade-offs in microbial resource allocation. Microbial community structure was interrogated with bacterial and fungal marker gene sequencing, and metagenomic features such as community weighted genome size and traits conferring stress tolerance were predicted using PICRUSt2. Consistent with our hypothesis, aggregates of different size classes harbored distinct microbial communities manifesting distinct life history strategies. Large macroaggregate communities >2 mm were classified as acquisition strategists based on increased enzyme activity relative to other aggregate size classes. Small and medium microaggregate (0.25–2 mm) communities did not show a strong tendency toward any particular life history strategy. Genes conferring stress tolerance were significantly enriched in microaggregates <0.25 mm (indicative of stress tolerators); however, these communities also had the highest carbon use efficiency (indicative of yield strategists). We found trade-offs in resource allocation between communities classified as yield and acquisition strategists consistent with the Y–A–S framework. Tillage did not alter life history strategies within aggregates, suggesting that the aggregate physicochemistry plays a larger role than agricultural management in shaping microbial life history at the scale studied.
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
不同耕作方式的土壤微生物群落在组成和功能策略上存在差异
团聚体内部的物理化学环境控制着土壤中碳和微生物群落的分布。农业管理,如耕作,可以破坏提供给微生物的聚集体和微尺度栖息地,从而改变微生物群落的动态。将微生物群落分类为具有共同功能特征的生活史策略-正如几十年来为了解植物群落结构所做的那样-可以阐明土壤物理化学环境如何限制微生物群落的成员和活动。我们通过产量-获取-应激(Y-A-S)耐受性生命史框架对微生物群落组成和功能进行了总体规模调查。在7年的耕作试验中收集的土壤被分成4个团聚体大小类别,并测量了酶活性、多基质诱导呼吸和碳利用效率,以揭示微生物资源分配的权衡。利用细菌和真菌标记基因测序对微生物群落结构进行了研究,并利用PICRUSt2预测了群落加权基因组大小和耐受性性状等宏基因组特征。与我们的假设一致,不同大小类别的聚集体拥有不同的微生物群落,表现出不同的生活史策略。根据相对于其他聚集体大小类别增加的酶活性,bbb20 mm的大型宏观聚集体群落被归类为收购战略家。中小微聚集体(0.25-2 mm)群落没有表现出强烈的生活史策略倾向。在<0.25 mm的微聚集体中,具有抗逆性的基因显著富集(表明具有抗逆性);然而,这些群落也具有最高的碳利用效率(表明产量战略家)。我们发现在与Y-A-S框架一致的收益和获取策略分类的社区之间的资源分配权衡。耕作并没有改变群落内的生活史策略,这表明在研究的尺度上,群落的物理化学作用比农业管理在塑造微生物生活史方面发挥更大的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Elementa-Science of the Anthropocene
Elementa-Science of the Anthropocene Earth and Planetary Sciences-Atmospheric Science
CiteScore
6.90
自引率
5.10%
发文量
65
审稿时长
16 weeks
期刊介绍: A new open-access scientific journal, Elementa: Science of the Anthropocene publishes original research reporting on new knowledge of the Earth’s physical, chemical, and biological systems; interactions between human and natural systems; and steps that can be taken to mitigate and adapt to global change. Elementa reports on fundamental advancements in research organized initially into six knowledge domains, embracing the concept that basic knowledge can foster sustainable solutions for society. Elementa is published on an open-access, public-good basis—available freely and immediately to the world.
期刊最新文献
Spatiotemporal changes in Iranian rivers’ discharge Structure and function of the western Baffin Bay coastal and shelf ecosystem Agroecological transitions in the mind Temporal evolution of under-ice meltwater layers and false bottoms and their impact on summer Arctic sea ice mass balance Sea ice and snow characteristics from year-long transects at the MOSAiC Central Observatory
×
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