Termite gas emissions select for hydrogenotrophic microbial communities in termite mounds

Author:

Chiri Eleonora12,Nauer Philipp A.23ORCID,Lappan Rachael1ORCID,Jirapanjawat Thanavit1,Waite David W.45ORCID,Handley Kim M.4ORCID,Hugenholtz Philip5,Cook Perran L. M.3,Arndt Stefan K.2,Greening Chris1ORCID

Affiliation:

1. Department of Microbiology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia;

2. School of Ecosystem and Forest Sciences, University of Melbourne, Richmond, VIC 3121, Australia;

3. School of Chemistry, Monash University, Clayton, VIC 3800, Australia;

4. School of Biological Sciences, University of Auckland, Auckland, New Zealand;

5. Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia

Abstract

SignificanceTermites are textbook examples of the “extended phenotype” given their ability to construct complex mounds and regulate environments. Here, we show that termites also control microbial composition and biogeochemical cycling in their mounds through their emissions of hydrogen. These emissions drive remarkable enrichments of mound bacteria that use hydrogen to drive aerobic respiration and sometimes carbon fixation (i.e., lithoautotrophs). Such mound communities efficiently consume all termite-produced hydrogen and even mediate atmospheric uptake, while termite-produced methane escapes to the atmosphere. This provides further evidence that hydrogen is a major substrate for aerobic bacteria and that the terrestrial hydrogen sink is highly responsive to elevated emissions.

Funder

Swiss National Science Foundation

Australian Research Council

Department of Health | National Health and Medical Research Council

Publisher

Proceedings of the National Academy of Sciences

Reference79 articles.

1. Embracing the unknown: disentangling the complexities of the soil microbiome

2. Trace gas oxidizers are widespread and active members of soil microbial communities

3. A Hydrogen-Rich Early Earth Atmosphere

4. Hydrothermal vents and the origin of life

5. R. Conrad, “Capacity of aerobic microorganisms to utilize and grow on atmospheric trace gases (H2, CO, CH4)” in Current Perspectives in Microbial Ecology, M. G. Klug, C. A. Reddy, Eds. (American Society for Microbiology, 1984), pp. 461–467.

Cited by 24 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.7亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2025 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3