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kobvindex_GFZ20210601135455
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This thesis investigates how the permafrost microbiota responds to global warming. In detail, the constraints behind methane production in thawing permafrost were linked to methanogenic activity, abundance and composition. Furthermore, this thesis offers new insights into microbial adaptions to the changing environmental conditions during global warming. This was assesed by investigating the potential ecological relevant functions encoded by plasmid DNA within the permafrost microbiota. Permafrost of both interglacial and glacial origin spanning the Holocene to the late Pleistocene, including Eemian, were studied during long-term thaw incubations. Furthermore, several permafrost cores of different stratigraphy, soil type and vegetation cover were used to target the main constraints behind methane production during short-term thaw simulations. Short- and long-term incubations simulating thaw with and without the addition of substrate were combined with activity measurements, amplicon and metagenomic sequencing of permanently frozen and seasonally thawed active layer. Combined, it allowed to address the following questions. i) What constraints methane production when permafrost thaws and how is this linked to methanogenic activity, abundance and composition? ii) How does the methanogenic community composition change during long-term thawing conditions? iii) Which potential ecological relevant functions are encoded by plasmid DNA in active layer soils?
The major outcomes of this thesis are as follows. i) Methane production from permafrost after long-term thaw simulation was found to be constrained mainly by the abundance of methanogens and the archaeal community composition. Deposits formed during periods of warmer temperatures and increased precipitation, (here represented by deposits from the Late Pleistocene of both interstadial and interglacial periods) were found to respond strongest to thawing conditions and to contain an archaeal community dominated by methanogenic archaea (40% and 100% of all detected archaea). Methanogenic population size and carbon density were identified as main predictors for potential methane production in thawing permafrost in short-term incubations when substrate was sufficiently available.
ii) Besides determining the methanogenic activity after long-term thaw, the paleoenvironmental conditions were also found to influence the response of the methanogenic community composition. Substantial shifts within methanogenic community structure and a drop in diversity were observed in deposits formed during warmer periods, but not in deposits from stadials, when colder and drier conditions occurred. Overall, a shift towards a dominance of hydrogenotrophic methanogens was observed in all samples, except for the oldest interglacial deposits from the Eemian, which displayed a potential dominance of acetoclastic methanogens. The Eemian, which is discussed to serve as an analogue to current climate conditions, contained highly active methanogenic communities. However, all potential limitation of methane production after permafrost thaw, it means methanogenic community structure, methanogenic population size, and substrate pool might be overcome after permafrost had thawed on the long-term. iii) Enrichments with soil from the seasonally thawed active layer revealed that its plasmid DNA (‘metaplasmidome’) carries stress-response genes. In particular it encoded antibiotic resistance genes, heavy metal resistance genes, cold shock proteins and genes encoding UV-protection. Those are functions that are directly involved in the adaptation of microbial communities to stresses in polar environments. It was further found that metaplasmidomes from the Siberian active layer originate mainly from Gammaproteobacteria. By applying enrichment cultures followed by plasmid DNA extraction it was possible to obtain a higher average contigs length and significantly higher recovery of plasmid sequences than from extracting plasmid sequences from metagenomes. The approach of analyzing ‘metaplasmidomes’ established in this thesis is therefore suitable for studying the ecological role of plasmids in polar environments in general.
This thesis emphasizes that including microbial community dynamics have the potential to improve permafrost-carbon projections. Microbially mediated methane release from permafrost environments may significantly impact future climate change. This thesis identified drivers of methanogenic composition, abundance and activity in thawing permafrost landscapes. Finally, this thesis underlines the importance to study how the current warming Arctic affects microbial communities in order to gain more insight into microbial response and adaptation strategies.
Note:
Kumulative Dissertation
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Dissertation, Universität Potsdam, 2020
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Contents
Preface
Acknowledgements
Contents
Summary
Zusammenfassung
List of abbreviations
Chapter 1. Introduction
1.1 Motivation
1.2 Carbon storage in Arctic permafrost environments and the permafrost carbon
feedback (PCF)
1.3 Methane cycling microorganisms
1.4 The microbial ecology of permafrost
1.5 Plasmids and their potential role in stress tolerance
1.6 Objectives
Chapter 2. Study sites
2.1 Regional settings
2.2 Kurungnakh and Samoylov Island
2.3 Bol'shoy Lyakhovsky Island
2.4 Herschel Island
Chapter 3. Manuscripts
3.1 Overview of manuscripts, including contribution of co-authors.
3.2 Manuscript I
Methanogenic response to long-term permafrost thaw is determined by
paleoenvironment
3.3 Manuscript II
Methane production in thawing permafrost is constrained by methanogenic
population size and carbon density
3.4 Manuscript III
Metaplasmidome-encoded functional potential of permafrost active layer soils
Chapter 4. Synthesis
4.1 Introduction
4.2 Constraints behind methane production from thawing permafrost
4.3 The methanogenic community response to long-term permafrost thaw
4.4 The adaptive potential of the permafrost micro biota to cope with stress
factors during global warming
4.5 Conclusion
Chapter 5. Future research directions and perspectives
Chapter 6. References
Chapter 7. Appendix
7.1 Supporting information for manuscript I
7.2 Supporting information for manuscript II
7.3 Supporting information for manuscript III
7.4 ESR collaboration, manuscript IV
Language:
English
Keywords:
Hochschulschrift
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