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  • 1
    Call number: AWI Bio-24-95742
    Description / Table of Contents: The arctic is warming 2 – 4 times faster than the global average, resulting in a strong feedback on northern ecosystems such as boreal forests, which cover a vast area of the high northern latitudes. With ongoing global warming, the treeline subsequently migrates northwards into tundra areas. The consequences of turning ecosystems are complex: on the one hand, boreal forests are storing large amounts of global terrestrial carbon and act as a carbon sink, dragging carbon dioxide out of the global carbon cycle, suggesting an enhanced carbon uptake with increased tree cover. On the other hand, with the establishment of trees, the albedo effect of tundra decreases, leading to enhanced soil warming. Meanwhile, permafrost thaws, releasing large amounts of previously stored carbon into the atmosphere. So far, mainly vegetation dynamics have been assessed when studying the impact of warming onto ecosystems. Most land plants are living in close symbiosis with bacterial and fungal communities, sustaining their growth in nutrient poor habitats. However, the impact of climate change on these subsoil communities alongside changing vegetation cover remains poorly understood. Therefore, a better understanding of soil community dynamics on multi millennial timescales is inevitable when addressing the development of entire ecosystems. Unravelling long-term cross-kingdom dependencies between plant, fungi, and bacteria is not only a milestone for the assessment of warming on boreal ecosystems. On top, it also is the basis for agriculture strategies to sustain society with sufficient food in a future warming world. The first objective of this thesis was to assess ancient DNA as a proxy for reconstructing the soil microbiome (Manuscripts I, II, III, IV). Research findings across these projects enable a comprehensive new insight into the relationships of soil microorganisms to the surrounding vegetation. First, this was achieved by establishing (Manuscript I) and applying (Manuscript II) a primer pair for the selective amplification of ancient fungal DNA from lake sediment samples with the metabarcoding approach. To assess fungal and plant co-variation, the selected primer combination (ITS67, 5.8S) amplifying the ITS1 region was applied on samples from five boreal and arctic lakes. The obtained data showed that the establishment of fungal communities is impacted by warming as the functional ecological groups are shifting. Yeast and saprotroph dominance during the Late Glacial declined with warming, while the abundance of mycorrhizae and parasites increased with warming. The overall species richness was also alternating. The results were compared to shotgun sequencing data reconstructing fungi and bacteria (Manuscripts III, IV), yielding overall comparable results to the metabarcoding approach. Nonetheless, the comparison also pointed out a bias in the metabarcoding, potentially due to varying ITS lengths or copy numbers per genome. The second objective was to trace fungus-plant interaction changes over time (Manuscripts II, III). To address this, metabarcoding targeting the ITS1 region for fungi and the chloroplast P6 loop for plants for the selective DNA amplification was applied (Manuscript II). Further, shotgun sequencing data was compared to the metabarcoding results (Manuscript III). Overall, the results between the metabarcoding and the shotgun approaches were comparable, though a bias in the metabarcoding was assumed. We demonstrated that fungal shifts were coinciding with changes in the vegetation. Yeast and lichen were mainly dominant during the Late Glacial with tundra vegetation, while warming in the Holocene lead to the expansion of boreal forests with increasing mycorrhizae and parasite abundance. Aside, we highlighted that Pinaceae establishment is dependent on mycorrhizal fungi such as Suillineae, Inocybaceae, or Hyaloscypha species also on long-term scales. The third objective of the thesis was to assess soil community development on a temporal gradient (Manuscripts III, IV). Shotgun sequencing was applied on sediment samples from the northern Siberian lake Lama and the soil microbial community dynamics compared to ecosystem turnover. Alongside, podzolization processes from basaltic bedrock were recovered (Manuscript III). Additionally, the recovered soil microbiome was compared to shotgun data from granite and sandstone catchments (Manuscript IV, Appendix). We assessed if the establishment of the soil microbiome is dependent on the plant taxon and as such comparable between multiple geographic locations or if the community establishment is driven by abiotic soil properties and as such the bedrock area. We showed that the development of soil communities is to a great extent driven by the vegetation changes and temperature variation, while time only plays a minor role. The analyses showed general ecological similarities especially between the granite and basalt locations, while the microbiome on species-level was rather site-specific. A greater number of correlated soil taxa was detected for deep-rooting boreal taxa in comparison to grasses with shallower roots. Additionally, differences between herbaceous taxa of the late Glacial compared to taxa of the Holocene were revealed. With this thesis, I demonstrate the necessity to investigate subsoil community dynamics on millennial time scales as it enables further understanding of long-term ecosystem as well as soil development processes and such plant establishment. Further, I trace long-term processes leading to podzolization which supports the development of applied carbon capture strategies under future global warming.
    Type of Medium: Dissertations
    Pages: xii, 198 Seiten , Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2024 , Table of Contents Summary Deutsche Zusammenfassung 1 Introduction 1.1 Arctic ecosystems under global warming 1.2 The plant-associated microbiome 1.3 Drivers of soil development 1.4 Ancient DNA to unravel past ecosystems 1.4.1 Lake sediments as archives of past community changes 1.4.2 Metabarcoding for targeting specific communities 1.4.3 Shotgun sequencing for broader overview 1.5 Thesis objective 1.6 Thesis outline and author contributions 2 Manuscript I 2.1 Abstract 2.2 Introduction 2.3 Materials and Methods 2.3.1 Primer design and evaluation In silico analyses Evaluation of lake sediment core DNA for analyses of fungal paleoecology 2.4 Results Primer design and evaluation Evaluation of lake sediment core DNA for fungal paleoecology 2.4.1 Taxonomic resolution across the cores 2.4.2 Comprehensiveness: Rarefaction and accumulation curves 2.4.3 Amplicon length and GC content to assess bias through degradation 2.4.4 General taxonomic composition of fungi in Siberian lake sediment cores Diversity of fungal paleocommunities from lake CH12 2.5 Discussion 2.5.1 Preservation biases and potential contamination 2.5.2 Characteristics of the optimized sedaDNA ITS1 metabarcoding assay 2.5.3 Potential of lake sediment fungal DNA for paleoecology 2.6 Author contributions 2.7 Acknowledgements 2.8 Conflict of interest 2.9 References 3 Manuscript II 3.1 Abstract 3.2 Introduction 3.3 Geographic setting and study sites 3.4 Materials and Methods 3.4.1 Sampling 3.4.2 DNA extraction and amplification 3.4.3 Bioinformatic analysis 3.4.4 Assessment of negative controls and contamination 3.4.5 Statistical analysis and visualization 3.5 Results 3.5.1 Fungi: sedaDNA sequencing results and overall patterns of alpha diversity and taxonomic composition 3.5.2 Vegetation: sedaDNA sequencing results and overall patterns of alpha diversity and taxonomic composition 3.5.3 Site-specific plant-fungus covariation 3.5.3.1 Fungus and plant covariation in arctic Siberia from MIS3 to the Holocene 3.5.3.2 Quantitative relationships between fungi and plant richness and composition 3.6 Discussion 3.6.1 Fungus and plant diversity along a spatiotemporal gradient in Siberia 3.6.2 Changes in ecosystem functioning over a spatiotemporal gradient 3.6.3 Implications of our results for ecosystem functioning and future research avenues 3.7 Conclusions Funding Availability of data and material Author contribution Declaration of competing interest Acknowledgements 3.8 References 4 Manuscript III 4.1 Abstract 4.2 Introduction 4.3 Results and Discussion 4.3.1 Compositional changes of plants, fungi, and bacteria in ancient metagenomic datasets 4.3.2 Long-term soil development: a trajectory or environmentally driven processes? 4.3.3 Bioweathering supported by lichens and mycorrhiza 4.3.4 Turnover in carbon, nitrogen, and sulphur cycling 4.3.5 Tracing podzolization 4.4 Implications and conclusions 4.5 Material and methods 4.5.1 Geographical setting and study site 4.5.2 X-ray fluorescence scanning of the sediment core 4.5.3 Core sub-sampling 4.5.4 DNA extraction 4.5.5 Single stranded DNA library build 4.5.6 Bioinformatic pipeline for the analysis of the sequencing results 4.5.7 Data analysis 4.5.8 Analysis of the ancient patterns 4.5.9 Statistical analysis of the dataset Acknowledgements 4.6 References Declarations 5 Discussion and synthesis 5.1 Long-term rhizosphere establishment in tundra and taiga areas 5.1.1 SedaDNA as a proxy for soil microbiome 5.1.1.1 Fungal DNA metabarcoding 5.1.1.2 Targeting soil communities with shotgun sequencing 5.1.1.3 Comparison between metabarcoding and shotgun sequencing for the soil microbiome 5.1.2 Fungi-vegetation interaction changes over time 5.1.3 Soil development on a temporal gradient 5.2 Conclusion and future perspectives 6 References 7 Appendix 7.1 Appendix to manuscript I 7.2 Appendix to manuscript II 7.3 Appendix to manuscript III 7.4 Manuscript IV 7.4.1 Abstract 7.4.2 Introduction 7.4.3 Geographical setting and study sites 7.4.4 Material & Methods 7.4.4.1 Sub-sampling of the sediment cores 7.4.4.2 DNA extraction 7.4.4.3 Single stranded DNA library built 7.4.4.4 Bioinformatic pipeline for the analysis of the sequencing data 7.4.4.5 Data analysis 7.4.4.6 Statistical analysis of the datasets 7.4.5 Results 7.4.5.1 Compositional changes of representative plant taxa alongside dynamics in fungal ecologies and bacterial element cycling in ancient metagenomic datasets 7.4.5.2 Impact of abiotic and biotic drivers on soil establishment across geographical locations 7.4.5.3 Relative positive correlations of functional soil taxa with plants across the locations 7.4.5.4 Assessment of the plant taxon-specific microbiome across the locations 7.4.6 Discussion 7.4.6.1 Site-specific soil development 7.4.6.2 Differences in the bedrock 7.4.6.3 Correlation between the lake biota 7.4.6.3.1 General Trends in positively correlated rhizosphere taxa 7.4.6.3.2 Plant taxa specific microbiome 7.4.7 Implications and future directions 7.4.8 References 7.4.9 Supplement to manuscript IV Acknowledgements Eidesstattliche Erklärung Damage pattern analysis – Auflagen Doktorarbeit Summary Main References
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  • 2
    Call number: AWI A5-24-95744
    Description / Table of Contents: The Arctic is the hot spot of the ongoing, global climate change. Over the last decades, near-surface temperatures in the Arctic have been rising almost four times faster than on global average. This amplified warming of the Arctic and the associated rapid changes of its environment are largely influenced by interactions between individual components of the Arctic climate system. On daily to weekly time scales, storms can have major impacts on the Arctic sea-ice cover and are thus an important part of these interactions within the Arctic climate. The sea-ice impacts of storms are related to high wind speeds, which enhance the drift and deformation of sea ice, as well as to changes in the surface energy budget in association with air mass advection, which impact the seasonal sea-ice growth and melt. The occurrence of storms in the Arctic is typically associated with the passage of transient cyclones. Even though the above described mechanisms how storms/cyclones impact the Arctic sea ice are in principal known, there is a lack of statistical quantification of these effects. In accordance with that, the overarching objective of this thesis is to statistically quantify cyclone impacts on sea-ice concentration (SIC) in the Atlantic Arctic Ocean over the last four decades. In order to further advance the understanding of the related mechanisms, an additional objective is to separate dynamic and thermodynamic cyclone impacts on sea ice and assess their relative importance. Finally, this thesis aims to quantify recent changes in cyclone impacts on SIC. These research objectives are tackled utilizing various data sets, including atmospheric and oceanic reanalysis data as well as a coupled model simulation and a cyclone tracking algorithm. Results from this thesis demonstrate that cyclones are significantly impacting SIC in the Atlantic Arctic Ocean from autumn to spring, while there are mostly no significant impacts in summer. The strength and the sign (SIC decreasing or SIC increasing) of the cyclone impacts strongly depends on the considered daily time scale and the region of the Atlantic Arctic Ocean. Specifically, an initial decrease in SIC (day -3 to day 0 relative to the cyclone) is found in the Greenland, Barents and Kara Seas, while SIC increases following cyclones (day 0 to day 5 relative to the cyclone) are mostly limited to the Barents and Kara Seas. For the cold season, this results in a pronounced regional difference between overall (day -3 to day 5 relative to the cyclone) SIC-decreasing cyclone impacts in the Greenland Sea and overall SIC-increasing cyclone impacts in the Barents and Kara Seas. A cyclone case study based on a coupled model simulation indicates that both dynamic and thermodynamic mechanisms contribute to cyclone impacts on sea ice in winter. A typical pattern consisting of an initial dominance of dynamic sea-ice changes followed by enhanced thermodynamic ice growth after the cyclone passage was found. This enhanced ice growth after the cyclone passage most likely also explains the (statistical) overall SIC-increasing effects of cyclones in the Barents and Kara Seas in the cold season. Significant changes in cyclone impacts on SIC over the last four decades have emerged throughout the year. These recent changes are strongly varying from region to region and month to month. The strongest trends in cyclone impacts on SIC are found in autumn in the Barents and Kara Seas. Here, the magnitude of destructive cyclone impacts on SIC has approximately doubled over the last four decades. The SIC-increasing effects following the cyclone passage have particularly weakened in the Barents Sea in autumn. As a consequence, previously existing overall SIC-increasing cyclone impacts in this region in autumn have recently disappeared. Generally, results from this thesis show that changes in the state of the sea-ice cover (decrease in mean sea-ice concentration and thickness) and near-surface air temperature are most important for changed cyclone impacts on SIC, while changes in cyclone properties (i.e. intensity) do not play a significant role.
    Type of Medium: Dissertations
    Pages: VIII, 131 Seiten , Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2024 , Contents 1 Introduction 1.1 The Arctic sea-ice cover 1.1.1 Sea ice in the coupled Arctic climate system 1.1.2 Recent changes of the Arctic sea ice 1.2 The atmosphere as driver of sea-ice variability 1.2.1 Large-scale circulation patterns 1.2.2 Role of cyclones 1.3 Thesis structure and research questions 2 Theory and methods 2.1 Synoptic cyclones 2.1.1 Related fundamentals of atmospheric dynamics 2.1.2 Cyclone activity in the Arctic 2.2 Cyclone tracking and cyclone occurrence mask 2.3 Dynamic and thermodynamic sea-ice variability related to cyclones 3 New insights into cyclone impacts on sea ice in the Atlantic sector of the Arctic Ocean in winter 3.1 Abstract 3.2 Introduction 3.3 Data and methods 3.3.1 Database and cyclone identification 3.3.2 Quantification of cyclone impacts on SIC 3.4 Cyclone impacts on SIC 3.4.1 Effects of different time scales and regions 3.4.2 Effects of SIC conditions and cyclone depth 3.4.3 Spatial variability of SIC response to cyclones 3.4.4 Relation to near-surface wind and surface energy budget 3.5 Signature of ’New Arctic’ conditions 3.6 Conclusions 3.7 Supplementary material 4 Impact of three intense winter cyclones on the sea ice cover in the Barents Sea: A case study with a coupled regional climate model 4.1 Abstract 4.2 Introduction 4.3 Data and methods 4.3.1 HIRHAM–NAOSIM simulation 4.3.2 Supplementary evaluation data 4.3.3 Dynamic and thermodynamic contributions to sea-ice changes 4.4 Results 4.4.1 Cyclone cases 4.4.2 Cyclone impacts on SEB 4.4.3 Cyclone impacts on sea-ice concentration (SIC) 4.4.4 Cyclone impacts on sea-ice thickness (SIT) 4.4.5 Context to other cyclone cases during the MOSAiC winter 4.5 Discussion and conclusions 4.6 Supplementary material 5 Cyclone impacts on sea ice concentration in the Atlantic Arctic Ocean: Annual cycle and recent changes 5.1 Abstract 5.2 Introduction 5.3 Data and methods 5.4 Changes in cyclones and traversed sea ice 5.5 Cyclone impacts on SIC 5.5.1 Annual cycle in the old Arctic 5.5.2 Changes in the new Arctic 5.5.3 Regional changes in autumn 5.6 Conclusions 5.7 Supplementary material 6 Conclusions and Outlook 6.1 What is the statistical impact of cyclone passages on sea-ice concentration (SIC) in the Atlantic Arctic Ocean? 6.2 What are the individual contributions of dynamic and thermodynamic processes to sea-ice changes related to cyclones? 6.3 Do the SIC impacts of cyclones change in a warming Arctic and what are the related mechanisms? 6.4 Ways forward Appendix: Cyclones modulate the control of the North Atlantic Oscillation on transports into the Barents Sea Bibliography
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  • 3
    Call number: AWI Bio-24-95736
    Description / Table of Contents: Moss-microbe associations are often characterised by syntrophic interactions between the microorganisms and their hosts, but the structure of the microbial consortia and their role in peatland development remain unknown. In order to study microbial communities of dominant peatland mosses, Sphagnum and brown mosses, and the respective environmental drivers, four study sites representing different successional stages of natural northern peatlands were chosen on a large geographical scale: two brown moss-dominated, circumneutral peatlands from the Arctic and two Sphagnum-dominated, acidic peat bogs from subarctic and temperate zones. The family Acetobacteraceae represented the dominant bacterial taxon of Sphagnum mosses from various geographical origins and displayed an integral part of the moss core community. This core community was shared among all investigated bryophytes and consisted of few but highly abundant prokaryotes, of which many appear as endophytes of Sphagnum mosses. Moreover, brown mosses and Sphagnum mosses represent habitats for archaea which were not studied in association with peatland mosses so far. Euryarchaeota that are capable of methane production (methanogens) displayed the majority of the moss-associated archaeal communities. Moss-associated methanogenesis was detected for the first time, but it was mostly negligible under laboratory conditions. Contrarily, substantial moss-associated methane oxidation was measured on both, brown mosses and Sphagnum mosses, supporting that methanotrophic bacteria as part of the moss microbiome may contribute to the reduction of methane emissions from pristine and rewetted peatlands of the northern hemisphere. Among the investigated abiotic and biotic environmental parameters, the peatland type and the host moss taxon were identified to have a major impact on the structure of moss-associated bacterial communities, contrarily to archaeal communities whose structures were similar among the investigated bryophytes. For the first time it was shown that different bog development stages harbour distinct bacterial communities, while at the same time a small core community is shared among all investigated bryophytes independent of geography and peatland type. The present thesis displays the first large-scale, systematic assessment of bacterial and archaeal communities associated both with brown mosses and Sphagnum mosses. It suggests that some host-specific moss taxa have the potential to play a key role in host moss establishment and peatland development.
    Description / Table of Contents: Während die Beziehungen zwischen Moosen und den mit ihnen assoziierten Mikroorganismen oft durch syntrophische Wechselwirkungen charakterisiert sind, ist die Struktur der Moos-assoziierten mikrobiellen Gemeinschaften sowie deren Rolle bei der Entstehung von Mooren weitgehend unbekannt. Die vorliegende Arbeit befasst sich mit mikrobiellen Gemeinschaften, die mit Moosen nördlicher, naturnaher Moore assoziiert sind, sowie mit den Umweltfaktoren, die sie beeinflussen. Entlang eines groß angelegten geographischen Gradienten, der von der Hocharktis bis zur gemäßigten Klimazone reicht, wurden vier naturbelassene Moore als Probenstandorte ausgesucht, die stellvertretend für verschiedene Stadien der Moorentwicklung stehen: zwei Braunmoos-dominierte Niedermoore mit nahezu neutralem pH-Wert sowie zwei Sphagnum-dominierte Torfmoore mit saurem pH-Wert. Die Ergebnisse der vorliegenden Arbeit machen deutlich, dass die zu den Bakterien zählenden Acetobacteraceae das vorherrschende mikrobielle Taxon der Sphagnum-Moose gleich welchen geographischen Ursprungs darstellen und insbesondere innerhalb des Wirtsmoosgewebes dominieren. Gleichzeitig gehörten die Acetobacteraceae zum wesentlichen Bestandteil der mikrobiellen Kerngemeinschaft aller untersuchten Moose, die sich aus einigen wenigen Arten, dafür zahlreich vorkommenden Prokaryoten zusammensetzt. Die vorliegende Arbeit zeigt zudem erstmals, dass sowohl Braunmoose als auch Torfmoose ein Habitat für Archaeen darstellen. Die Mehrheit der Moos-assoziierten Archaeen gehörte dabei zu den methanbildenden Gruppen, wenngleich die metabolischen Aktivitätsraten unter Laborbedingungen meistens kaum messbar waren. Im Gegensatz hierzu konnte die Bakterien-vermittelte Methanoxidation sowohl an Braunmoosen als auch an Sphagnum-Moosen gemessen werden. Dies zeigt eindrucksvoll, dass Moos-assoziierte Bakterien potenziell zur Minderung von Methanemissionen aus nördlichen, aber auch wiedervernässten Mooren beitragen können. Ein weiteres wichtiges Resultat der vorliegenden Arbeit ist die Bedeutung des Moortyps (Niedermoor oder Torfmoor), aber auch der Wirtsmoosart selbst für die Struktur der Moos-assoziierten Bakteriengemeinschaften, während die archaeellen Gemeinschaftsstrukturen weder vom Moortyp noch von der Wirtsmoosart beeinflusst wurden und sich insgesamt deutlich ähnlicher waren als die der Bakterien. Darüber hinaus konnte erstmalig gezeigt werden, dass sich die bakteriellen Gemeinschaften innerhalb der unterschiedlichen Moorsukzessionsstadien zwar ganz erheblich voneinander unterscheiden, ein kleiner Teil der Bakterien dennoch Kerngemeinschaften bilden, die mit allen untersuchten Moosarten assoziiert waren. Bei der hier präsentierten Arbeit handelt es sich um die erste systematische Studie, die sich auf einer großen geographischen Skala mit den bakteriellen und archaeellen Gemeinschaften von Braunmoosen und Torfmoosen aus naturbelassenen nördlichen Mooren befasst. Die vorliegenden Ergebnisse machen deutlich, dass die untersuchten Moose ein ganz spezifisches mikrobielles Konsortium beherbergen, welches mutmaßlich eine Schlüsselrolle bei der Etablierung der Wirtspflanzen am Anfang der Moorentwicklung spielt und darüber hinaus das Potential hat, die charakteristischen Eigenschaften von Mooren sowie deren weitere Entwicklung zu prägen.
    Type of Medium: Dissertations
    Pages: XX, 139, liv Seiten , Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2024 , Content Preface Acknowledgements Summary Zusammenfassung Abbreviations 1. Introduction 1.1. Peatlands 1.1.1. Peatland development and peat bog succession 1.1.2. Characteristic peatlands of the northern hemisphere 1.1.3. Anthropogenic threats of northern peatlands 1.1.4. Peat bog restoration 1.2. Peatland bryophytes 1.2.1. Brown mosses 1.2.2. Sphagnum mosses 1.3. Moss microbiota 1.3.1. Moss-associated bacteria 1.3.2. Moss-associated archaea 1.3.3. Endophytic prokaryotic communities 1.4. Biotic and abiotic influences on moss-associated microorganisms 1.5. Objectives 1.6. Study sites 1.6.1. High Arctic peatlands of Svalbard (SV) 1.6.2. Polygonal Tundra of Samoylov (SA) 1.6.3. Palsa Bogs of Neiden (NEI) 1.6.4. Kettle Bog Peatlands of Mueritz National Park (MUE) 2. Material and Methods 2.1. Sampling scheme overview 2.2. Sampling of pore water 2.3. Sampling of moss plantlets 2.4. Analysis of pore water chemistry 2.5. Cell wall analysis 2.5.1. Cation exchange capacity (CEC) 2.5.2. Holocellulose (HC) 2.5.3. Lignin and Lignin-like polymers (LLP) 2.5.4. Bulk moss litter analysis 2.6. Moss surface sterilisation and separation of putative epiphytic and endophytic microbial communities 2.7. DNA extraction and sequencing 2.8. Sequence analyses and bioinformatics 2.9. Statistical analyses 2.10. Potential methane production and oxidation assays 2.10.1. Surface sterilisation prior to activity tests 2.10.2. Methane production 2.10.3. Methane oxidation 3. Results 3.1. Peatland bulk and pore water characteristics 3.2. Diversity and structure of natural peatland microbial communities 3.3. Environmental drivers of moss-associated microbial communities 3.4. Microbial taxa associated with brown mosses and Sphagnum mosses 3.4.1. Moss-associated bacteria 3.4.2. Moss-associated archaea 3.4.3. Bacterial and archaeal core communities 3.4.4. Acetobacteraceae as dominant taxon of the bacterial core community 3.5. Sphagnum bacteriomes of disturbed, rewetted and pristine temperate kettle bog 3.6. Potential moss-associated methane production and methane oxidation rates 3.6.1. Moss-associated methane production 3.6.2. Moss-associated methane oxidation 4. Discussion 4.1. Environmental influences on moss-associated bacterial communities 4.2. Moss-associated archaeal communities and their environmental drivers 4.3. Distinct patterns of endophytic bacteria 4.4. The core microbiota and their possible role for peatland succession 4.5. The potential role of Acetobacteraceae for Sphagnum host mosses and bog ecosystems 4.6. Moss-associated microbial communities of the methane cycle and their potential metabolic activity 4.7. Diversity and structure of Sphagnum bacteriomes from pristine, disturbed and rewetted kettle bogs 5. Conclusion 6. Critical remarks and outlook 6.1. Critical remarks 6.2. Outlook Bibliography Supplementary
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  • 4
    Call number: AWI A7-24-95703
    Description / Table of Contents: The icosahedral non-hydrostatic large eddy model (ICON-LEM) was applied around the drift track of the Multidisciplinary Observatory Study of the Arctic (MOSAiC) in 2019 and 2020. The model was set up with horizontal grid-scales between 100m and 800m on areas with radii of 17.5km and 140 km. At its lateral boundaries, the model was driven by analysis data from the German Weather Service (DWD), downscaled by ICON in limited area mode (ICON-LAM) with horizontal grid-scale of 3 km. The aim of this thesis was the investigation of the atmospheric boundary layer near the surface in the central Arctic during polar winter with a high-resolution mesoscale model. The default settings in ICON-LEM prevent the model from representing the exchange processes in the Arctic boundary layer in accordance to the MOSAiC observations. The implemented sea-ice scheme in ICON does not include a snow layer on sea-ice, which causes a too slow response of the sea-ice surface temperature to atmospheric changes. To allow the sea-ice surface to respond faster to changes in the atmosphere, the implemented sea-ice parameterization in ICON was extended with an adapted heat capacity term. The adapted sea-ice parameterization resulted in better agreement with the MOSAiC observations. However, the sea-ice surface temperature in the model is generally lower than observed due to biases in the downwelling long-wave radiation and the lack of complex surface structures, like leads. The large eddy resolving turbulence closure yielded a better representation of the lower boundary layer under strongly stable stratification than the non-eddy-resolving turbulence closure. Furthermore, the integration of leads into the sea-ice surface reduced the overestimation of the sensible heat flux for different weather conditions. The results of this work help to better understand boundary layer processes in the central Arctic during the polar night. High-resolving mesoscale simulations are able to represent temporally and spatially small interactions and help to further develop parameterizations also for the application in regional and global models.
    Type of Medium: Dissertations
    Pages: xii, 110 Seiten , Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2023 , Contents 1. Introduction 2. Boundary Layers Types of the Atmosphere 2.1. The Convective Boundary Layer (CBL) 2.2. The Neutral Boundary Layer (NBL) 2.3. The Stable Boundary Layer (SBL) 3. The Closure problem 4. Model description 4.1. Applied model versions 4.2. Governing equations 4.3. Horizontal grid 4.4. Vertical grid 4.5. Lateral boundaries 4.6. Parametrizations 4.6.1. Radiation scheme 4.6.2. Microphysics 4.6.3. Mellor-Yamada scheme 4.6.4. Smagorinsky scheme 4.6.5. Sea ice scheme 4.7. Difference to classical LES Models 5. Experimental Setup 6. MOSAiC Measurements 6.1. ARM Meteorological tower 6.2. Radiosondes 7. Model evaluation for the central Arctic 7.1. Impact of the horizontal resolution 7.1.1. Under cold, light wind conditions 7.1.2. Under stormy conditions 7.2. Impact of the sea-ice scheme 7.3. Impact of the lower boundary conditions 7.4. Impact of the parametrization schemes under cold, light wind conditions 7.4.1. Near-surface variables 7.4.2. Vertical profiles 7.4.3. Surface fluxes 7.4.4. Boundary Layer Height 7.5. Impact of the parametrization schemes under stormy conditions 7.5.1. Near-surface variables 7.5.2. Vertical profiles 7.5.3. Surface fluxes 7.5.4. Boundary Layer height 8. Discussion and Summary Acknowledgements Appendix
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  • 5
    Call number: AWI G3-24-95700
    Description / Table of Contents: With Arctic ground as a huge and temperature-sensitive carbon reservoir, maintaining low ground temperatures and frozen conditions to prevent further carbon emissions that contrib-ute to global climate warming is a key element in humankind’s fight to maintain habitable con-ditions on earth. Former studies showed that during the late Pleistocene, Arctic ground condi-tions were generally colder and more stable as the result of an ecosystem dominated by large herbivorous mammals and vast extents of graminoid vegetation – the mammoth steppe. Characterised by high plant productivity (grassland) and low ground insulation due to animal-caused compression and removal of snow, this ecosystem enabled deep permafrost aggrad-ation. Now, with tundra and shrub vegetation common in the terrestrial Arctic, these effects are not in place anymore. However, it appears to be possible to recreate this ecosystem local-ly by artificially increasing animal numbers, and hence keep Arctic ground cold to reduce or-ganic matter decomposition and carbon release into the atmosphere. By measuring thaw depth, total organic carbon and total nitrogen content, stable carbon iso-tope ratio, radiocarbon age, n-alkane and alcohol characteristics and assessing dominant vegetation types along grazing intensity transects in two contrasting Arctic areas, it was found that recreating conditions locally, similar to the mammoth steppe, seems to be possible. For permafrost-affected soil, it was shown that intensive grazing in direct comparison to non-grazed areas reduces active layer depth and leads to higher TOC contents in the active layer soil. For soil only frozen on top in winter, an increase of TOC with grazing intensity could not be found, most likely because of confounding factors such as vertical water and carbon movement, which is not possible with an impermeable layer in permafrost. In both areas, high animal activity led to a vegetation transformation towards species-poor graminoid-dominated landscapes with less shrubs. Lipid biomarker analysis revealed that, even though the available organic material is different between the study areas, in both permafrost-affected and sea-sonally frozen soils the organic material in sites affected by high animal activity was less de-composed than under less intensive grazing pressure. In conclusion, high animal activity af-fects decomposition processes in Arctic soils and the ground thermal regime, visible from reduced active layer depth in permafrost areas. Therefore, grazing management might be utilised to locally stabilise permafrost and reduce Arctic carbon emissions in the future, but is likely not scalable to the entire permafrost region.
    Type of Medium: Dissertations
    Pages: X, 104, A-57 Seiten , Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2024 , Table of contents ABSTRACT ZUSAMMENFASSUNG ABBREVIATIONS AND NOMENCLATURE CHAPTER 1: INTRODUCTION 1.1 SCIENTIFIC BACKGROUND 1.1.1 ARCTIC GROUND 1.1.2 THE PHENOMENON OF PERMAFROST 1.1.3 ARCTIC NON - PERMAFROST AREAS 1.1.4 HYPOTHESIS 1.2 AIMS AND OBJECTIVES 1.3 METHODS 1.3.1 FIELD METHODS AND SAMPLING APPROACH 1.3.2 STUDY AREA SELECTION 1.3.3 LABORATORY METHODS 1.4 THESIS ORGANISATION CHAPTER 2: LARGE HERBIVORES ON PERMAFROST – A PILOT STUDY OF GRAZING IMPACTS ON PERMAFROST SOIL CARBON STORAGE IN NORTHEASTERN SIBERIA 2.1 ABSTRACT 2.2 I NTRODUCTION 2.3 STUDY AREA 2.4 METHODS 2.4.1 FIELD SAMPLING APPROACH 2.4.2 LABORATORY WORK 2.4.3 DATA ANALYSIS AND EXTERNAL DATA 2.5 RESULTS 2.5.1 VEGETATION ASSESSMENT 2.5.2 SEASONAL THAW DEPTH 2.5.3 CARBON PARAMETERS (TOC, TOC/TN RATIOS , AND Δ13 C RATIOS ) 2.5.4 GRAIN SIZE DISTRIBUTION AND WATER CONTENT 2.5.5 STATISTICS AND CORRELATION ANALYSIS 2.6 DISCUSSION 2.6.1 EFFECTS OF GRAZING ON VEGETATION STRUCTURE AND PERMAFROST THAW 2.6.2 CARBON ACCUMULATION UNDER GRAZING IMPACT 2.6.3 METHODOLOGICAL LIMITATIONS OF THE PILOT STUDY 2.7 CONCLUSION 2.8 DATA AVAILABILITY STATEMENT 2.9 AUTHOR CONTRIBUTIONS 2.10 FUNDING 2.11 ACKNOWLEDGEMENTS 2.12 CONFLICT OF INTERESTS CHAPTER 3: IMPACTS OF REINDEER ON SOIL CARBON STORAGE IN THE SEASONALLY FROZEN GROUND OF NORTHERN FINLAND: A PILOT STUDY 3.1 ABSTRACT 3.2 I NTRODUCTION 3.3 STUDY AREA 3.4 METHODS 3.4.1 FIELD WORK 3.4.2 LABORATORY ANALYSIS 3.4.3 DATA ANALYSIS AND CALCULATIONS 3.5 RESULTS 3.5.1 CORE DESCRIPTIONS 3.5.2 VEGETATION 3.5.3 CARBON PARAMETERS 3.5.6 COMPARATIVE DATA ANALYSIS 3.6 DISCUSSION 3.6.1 REINDEER IMPACT ON SOIL CARBON STORAGE 3.6.2 REINDEER IMPACT ON VEGETATION 3.6.3 REINDEER IMPACT ON GROUND CHARACTERISTICS 3.6.4 SOC DENSITY AND STOCKS ACROSS THE KUTUHARJU STATION AREA 3.6.5 METHODOLOGICAL LIMITATIONS OF THE PILOT STUDY DESIGN 3.6.6 IMPLICATIONS OF THE PILOT STUDY FOR FUTURE RESEARCH 3.7 CONCLUSION 3.8 DATA AVAILABILITY 3.9 AUTHOR CONTRIBUTION 3.10 COMPETING INTERESTS 3.11 ACKNOWLEDGEMENTS 3.12 FUNDING TABLE 3-1 TABLE 3-2 TABLE 3-3 CHAPTER 4: LIPID BIOMARKER SCREENING TO TRACE RECENT LARGE HERBIVORE INFLUENCE ON SOIL CARBON IN PERMAFROST AND SEASONALLY FROZEN ARCTIC GROUND 4.1 ABSTRACT 4.2 I NTRODUCTION 4.3 STUDY AREA 4.4 METHODS 4.4.1 SAMPLING APPROACH 4.4.2 LABORATORY ANALYSIS 4.4.3 LIPID BIOMARKER INDICES 4.4.4 STATISTICS 4.5 RESULTS 4.5.1 TOC 4.5.2 C/N RATIO 4.5.3 STABLE CARBON ISOTOPE RATIO 4.5.4 ABSOLUTE N- ALKANE CONCENTRATION 4.5.5 AVERAGE CHAIN LENGTH 4.5.6 CARBON PREFERENCE INDEX 4.5.7 HIGHER - PLANT ALCOHOL INDEX 4.5.8 STATISTICAL RESULTS 4.6 DISCUSSION 4.6.1 EFFECTS OF GRAZING INTENSITY ON BIOMARKER SIGNALS 4.6.2 EFFECTS OF GROUND THERMAL REGIME ON SOIL OM DEGRADATION 4.6.3 I MPACT OF HERBIVORY ON PERMAFROST OM STORAGE 4.7 CONCLUSION 4.8 ACKNOWLEDGEMENTS 4.9 COMPETING INTERESTS 4.10 AUTHOR CONTRIBUTION 4.11 FUNDING 4.12 DATA AVAILABILITY CHAPTER 5: SYNTHESIS 5.1 ECOSYSTEM CHANGES UNDER THE IMPACT OF LARGE HERBIVORES 5.2 GRAZING EFFECTS ON SOIL ORGANIC MATTER DECOMPOSITION 5.3 F EASIBILITY OF UTILISING HERBIVORY IN THE ARCTIC 5.4 RESEARCH IMPLICATIONS FOR SUCCESSFUL PLANNING AND USE OF ARCTIC HERBIVORY REFERENCES 93 FINANCIAL AND TECHNICAL SUPPORT APPENDIX 1 APPENDIX I ORGANIC CARBON CHARACTERISTICS IN ICE - RICH PERMAFROST IN ALAS AND YEDOMA DEPOSITS , CENTRAL YAKUTIA, SIBERIA APPENDIX II WHAT ARE THE EFFECTS OF HERBIVORE DIVERSITY ON TUNDRA ECOSYSTEMS ? A SYSTEMATIC REVIEW (ABSTRACT) APPENDIX III SUPPLEMENTARY MATERIAL TO CHAPTER 2: LARGE HERBIVORES ON PERMAFROST – A PILOT STUDY OF GRAZING IMPACTS ON PERMAFROST SOIL CARBON STORAGE IN NORTHEASTERN SIBERIA APPENDIX IV SUPPLEMENTARY MATERIAL TO CHAPTER 3: IMPACTS OF REINDEER ON SOIL CARBON STORAGE IN THE SEASONALLY FROZEN GROUND OF NORTHERN FINLAND : A PILOT STUDY APPENDIX V SUPPLEMENTARY MATERIAL TO CHAPTER 4: A PILOT STUDY OF LIPID BIOMARKERS TO TRACE RECENT LARGE HERBIVORE INFLUENCE ON SOIL CARBON IN PERMAFROST AND SEASONALLY ROZEN ARCTIC GROUND APPENDIX VI SUPPLEMENTARY MATERIAL TO APPENDIX IV: ORGANIC CARBON CHARACTERISTICS IN ICE - RICH PERMAFROST IN ALAS AND YEDOMA DEPOSITS , CENTRAL YAKUTIA, SIBERIA ACKNOWLEDGEMENTS - DANKSAGUNG
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  • 6
    Call number: AWI A4-23-95497
    Description / Table of Contents: Extreme weather and climate events are one of the greatest dangers for present-day society. Therefore, it is important to provide reliable statements on what changes in extreme events can be expected along with future global climate change. However, the projected overall response to future climate change is generally a result of a complex interplay between individual physical mechanisms originated within the different climate subsystems. Hence, a profound understanding of these individual contributions is required in order to provide meaningful assessments of future changes in extreme events. One aspect of climate change is the recently observed phenomenon of Arctic Amplification and the related dramatic Arctic sea ice decline, which is expected to continue over the next decades. The question to what extent Arctic sea ice loss is able to affect atmospheric dynamics and extreme events over mid-latitudes has received a lot of attention over recent years and still remains a highly debated topic. In this respect, the objective of ...
    Type of Medium: Dissertations
    Pages: xi, 126 Seiten , Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2023 , CONTENTS 1 SCIENTIFIC BACKGROUND AND RESEARCH QUESTIONS 1.1 Extreme events and attribution 1.2 Arctic climate change and mid-latitude linkages 1.3 Research questions 2 FOUNDATIONS 2.1 Atmospheric basics 2.1.1 Governing equations 2.1.2 Zonal wind and temperature profiles 2.1.3 Atmospheric waves and instabilities 2.1.4 Large-scale variability patterns and blocking 2.2 Atmospheric circulation regimes 2.2.1 Dynamical concepts 2.2.2 Regime computation 2.2.3 Regime number 2.3 Arctic climate change 2.3.1 Recent trends in Arctic sea ice and temperatures 2.3.2 Surface fluxes and energy balance in Arctic regions 2.3.3 Polar amplification mechanisms 2.3.4 Arctic-mid-latitude linkages 2.4 Weather and climate extremes 2.4.1 Recent trends 2.4.2 Dynamical driver of temperature extremes 3 DATA AND METHODS 3.1 ERA5 reanalysis 3.2 Model experiments 3.2.1 The atmospheric general circulation model ECHAM6 3.2.2 Polar Amplification Intercomparison Project data 3.3 Methods 3.3.1 Statistical significance 3.3.2 Extreme definition 4 RESULTS AND DISCUSSION 4.1 Mean circulation in ERA5 and ECHAM6 experiments 4.1.1 Climatological mean states in ERA5 and the reference simulation 4.1.2 Climatological responses in ECHAM6 sensitivity experiments 4.2 Circulation regimes and sea ice-induced frequency changes 4.2.1 Regime structures in ERA5 and ECHAM6 experiments 4.2.2 Regime frequency changes in ERA 4.2.3 Regime frequency changes in ECHAM6 experiments 4.3 Changes in Northern Hemispheric temperature extremes induced by sea ice loss 4.3.1 Extreme occurrence frequency changes 4.3.2 Temperature return level changes 4.4 Links between circulation regimes and extremes over Europe 4.4.1 Winter temperature extremes 4.4.2 Summer heat extremes 4.4.3 Winter wind extremes 4.5 Decomposition of sea ice-induced frequency changes in European winter extremes 4.5.1 Midwinter cold extremes along a SCAN storyline 4.5.2 January warm extremes along a ATl- storyline 4.5.3 February warm extremes along a NAO+ storyline 4.5.4 Comparison with futSST 4.5.5 January wind extremes along a ATL- storyline 4.6 Circulation Analogue-based approach for summer season 4.6.1 ERA5 event definitions 4.6.2 Reference flows and analogues in ERA5 4.6.3 Circulation analogues in ECHAM6 experiments 4.6.4 Decomposition of sea ice-induced changes in European heat extremes 5 CONCLUSION 5.1 Summary 5.2 Final discussion and outlook Appendix A METHODS A.1 Principal Component Analysis A.2 𝑘-Means clustering A.2.1 Algorithm A.2.2 Computation of circulation regimes A.3 Taylor diagram A.4 Regression model for describing ERA5 regime frequency changes A.4.1 General setup A.4.2 Multinomial Logistic Regression A.4.3 Linear predictor A.5 Definition and calculation of return levels A.5.1 Block maxima approach and Generalized Extreme Value distribution A.5.2 Return level estimation A.6 Framework for conditional extreme event attribution Appendix B ADDITIONAL FIGURES B.1 Circulation regimes and sea ice-induced frequency changes B.2 Changes in Northern Hemispheric temperature extremes induced by sea ice loss B.3 Links between circulation regimes and extremes over Europe B.3.1 Conditioned vs. unconditioned ERA5 and wind extreme probabilities B.3.2 Wind and synoptic-scale activity anomalies B.4 Decomposition of sea ice-induced frequency changes in European winter extremes B.5 Circulation Analogue-based approach for summer season B.6 Miscellaneous B.6.1 Recent Arctic sea ice trends B.6.2 futSST forcing field B.6.3 Fluxes over sea ice and ocean surfaces in ECHAM6 BIBLIOGRAPHY
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  • 7
    Call number: AWI Bio-23-95302
    Description / Table of Contents: Climate change of anthropogenic origin is affecting Earth’s biodiversity and therefore ecosystems and their services. High latitude ecosystems are even more impacted than the rest of Northern Hemisphere because of the amplified polar warming. Still, it is challenging to predict the dynamics of high latitude ecosystems because of complex interaction between abiotic and biotic components. As the past is the key to the future, the interpretation of past ecological changes to better understand ongoing processes is possible. In the Quaternary, the Pleistocene experienced several glacial and interglacial stages that affected past ecosystems. During the last Glacial, the Pleistocene steppe-tundra was covering most of unglaciated northern hemisphere and disappeared in parallel to the megafauna’s extinction at the transition to the Holocene (~11,700 years ago). The origin of the steppe-tundra decline is not well understood and knowledge on the mechanisms, which caused shifts in past communities and ecosystems, is of high priority as they are likely comparable to those affecting modern ecosystems. Lake or permafrost core sediments can be retrieved to investigate past biodiversity at transitions between glacial and interglacial stages. Siberia and Beringia were the origin of dispersal of the steppe-tundra, which make investigation this area of high priority. Until recently, macrofossils and pollen were the most common approaches. They are designed to reconstruct past composition changes but have limit and biases. Since the end of the 20th century, sedimentary ancient DNA (sedaDNA) can also be investigated. My main objectives were, by using sedaDNA approaches to provide scientific evidence of compositional and diversity changes in the Northern Hemisphere ecosystems at the transition between Quaternary glacial and interglacial stages. In this thesis, I provide snapshots of entire ancient ecosystems and describe compositional changes between Quaternary glacial and interglacial stages, and confirm the vegetation composition and the spatial and temporal boundaries of the Pleistocene steppe-tundra. I identify a general loss of plant diversity with extinction events happening in parallel of megafauna’ extinction. I demonstrate how loss of biotic resilience led to the collapse of a previously well-established system and discuss my results in regards to the ongoing climate change. With further work to constrain biases and limits, sedaDNA can be used in parallel or even replace the more established macrofossils and pollen approaches as my results support the robustness and potential of sedaDNA to answer new palaeoecological questions such as plant diversity changes, loss and provide snapshots of entire ancient biota.
    Description / Table of Contents: Der vom Menschen verursachte Klimawandel wirkt sich auf die biologische Vielfalt der Erde und damit auf die Ökosysteme und ihre Leistungen aus. Die Ökosysteme in den hohen Breitengraden sind aufgrund der verstärkten Erwärmung an den Polen noch stärker betroffen als der Rest der nördlichen Hemisphäre. Dennoch ist es schwierig, die Dynamik von Ökosystemen in den hohen Breitengraden vorherzusagen, da die Wechselwirkungen zwischen abiotischen und biotischen Komponenten sehr komplex sind. Da die Vergangenheit der Schlüssel zur Zukunft ist, ist die Interpretation vergangener ökologischer Veränderungen möglich, um laufende Prozesse besser zu verstehen. Im Quartär durchlief das Pleistozän mehrere glaziale und interglaziale Phasen, welche die Ökosysteme der Vergangenheit beeinflussten. Während des letzten Glazials bedeckte die pleistozäne Steppentundra den größten Teil der unvergletscherten nördlichen Hemisphäre und verschwand parallel zum Aussterben der Megafauna am Übergang zum Holozän (vor etwa 11 700 Jahren). Der Ursprung des Rückgangs der Steppentundra ist nicht gut erforscht, und die Kenntnis über die Mechanismen, die zu den Veränderungen in den vergangenen Lebensgemeinschaften und Ökosystemen geführt haben, ist von hoher Priorität, da sie wahrscheinlich mit denen vergleichbar sind, die sich auf moderne Ökosysteme auswirken. Durch die Entnahme von See- oder Permafrostkernsedimenten kann die vergangene Artenvielfalt an den Übergängen zwischen Eis- und Zwischeneiszeiten untersucht werden. Sibirien und Beringia waren der Ursprung der Ausbreitung der Steppentundra, weshalb die Untersuchung dieses Gebiets hohe Priorität hat. Bis vor kurzem waren Makrofossilien und Pollen die gängigsten Methoden. Sie dienen der Rekonstruktion vergangener Veränderungen in der Zusammensetzung der Bevölkerung, haben aber ihre Grenzen und Schwächen. Seit Ende des 20. Jahrhunderts kann auch sedimentäre alte DNA (sedaDNA) untersucht werden. Mein Hauptziel war es, durch den Einsatz von sedaDNA-Ansätzen wissenschaftliche Beweise für Veränderungen in der Zusammensetzung und Vielfalt der Ökosysteme der nördlichen Hemisphäre am Übergang zwischen den quartären Eiszeiten und Zwischeneiszeiten zu liefern. In dieser Arbeit liefere ich Momentaufnahmen ganzer alter Ökosysteme und beschreibe die Veränderungen in der Zusammensetzung zwischen Quartärglazialen und Interglazialen und bestätige die Vegetationszusammensetzung sowie die räumlichen und zeitlichen Grenzen der pleistozänen Steppentundra. Ich stelle einen allgemeinen Verlust der Pflanzenvielfalt fest, wobei das Aussterben der Pflanzen parallel zum Aussterben der Megafauna verlief. Ich zeige auf, wie der Verlust der biotischen Widerstandsfähigkeit zum Zusammenbruch eines zuvor gut etablierten Systems führte, und diskutiere meine Ergebnisse im Hinblick auf den laufenden Klimawandel. Mit weiteren Arbeiten zur Eingrenzung von Verzerrungen und Grenzen kann sedaDNA parallel zu den etablierteren Makrofossilien- und Pollenansätzen verwendet werden oder diese sogar ersetzen, da meine Ergebnisse die Robustheit und das Potenzial von sedaDNA zur Beantwortung neuer paläoökologischer Fragen wie Veränderungen der Pflanzenvielfalt und -verluste belegen und Momentaufnahmen ganzer alter Biota liefern.
    Type of Medium: Dissertations
    Pages: vi, 217 Seiten , Illustrationen, Diagramme, Karten
    Language: English
    Note: Dissertation, Universität Potsdam, 2023 , TABLE OF CONTENTS Acknowledgements Summary Zusammenfassung 1 General introduction 1.1 A changing world 1.1.1 Global changes of anthropogenic origin 1.1.2 Amplified crisis in the high latitudes 1.2 The past is the key to the future 1.2.1 The Quaternary glacial and interglacial stages 1.2.2 The Beringia study case 1.3 Investigating past biodiversity 1.3.1 Traditional tools 1.3.2 Newest sedaDNA proxies 1.4 Motivation and aims of the thesis 1.5 Structure of the thesis 1.6 Author’s contributions 2 Manuscript I 2.1 Abstract 2.2 Introduction 2.3 Materials and Methods 2.3.1 Geographical settings 2.3.2 Fieldwork and subsampling 2.3.3 Core splicing and dating 2.3.4 Sediment-geochemical analyses 2.3.5 Pollen analysis 2.3.6 Molecular genetic preparation 2.3.7 Processing of sedaDNA data 2.3.8 Statistical analysis and visualization 2.4 Results 2.4.1 Age model 2.4.2 Sediment-geochemical core composition 2.4.3 Pollen stratigraphy 2.4.4 sedaDNA composition 2.4.5 Comparison between pollen and sedaDNA 2.4.6 Taxa richness investigation 2.5 Discussion 2.5.1 Proxy validation 2.5.2 Vegetation compositional changes in response to climate inferred from pollen and sedaDNA records 2.5.3 The steppe-tundra of the Late Pleistocene 2.5.4 The disrupted Pleistocene-Holocene transition 2.5.5 The boreal forest of the Holocene 2.5.6 Changes in vegetation richness through the Pleistocene/Holocene transition inferred from the sedaDNA record 2.6 Conclusion Data availability statement Funding References 3 Manuscript II 3.1 Abstract 3.2 Introduction 3.3 Material and Method 3.3.1 Site description and timeframe 3.3.2 Sampling, DNA extraction and PCR 3.3.3 Filtering and cleaning dataset 3.3.4 Identification of taxa – species signal 3.3.5 Resampling 3.3.6 Assessment of the species pool stability 3.3.7 Quantification of extinct and extirpated taxa 3.3.8 Characterisation of species and candidate species 3.4 Results 3.4.1 Changes in the composition and species pool at the Pleistocene - Holocene transition 3.4.2 Decrease in the regional plant species richness between the Pleistocene and the Holocene 3.4.3 Identification of loss taxa events 3.4.4 Characterisation of lost taxa 3.5 Discussion 3.5.1 Biotic and abiotic changes in the ecosystem - a cocktail for extinction 3.5.2 Identification and quantification of potential plant taxa loss 3.5.3 Characterisation of potential taxa loss 3.5.4 Limits of the method 3.5.5 Conclusions and perspectives Funding References 4 Manuscript III 4.1 Abstract 4.2 Introduction 4.3 Material & Methods 4.3.1 Fieldwork and subsampling 4.3.2 Chronology 4.3.3 Pollen analysis 4.3.4 Isolation of sedimentary ancient DNA 4.3.5 Metabarcoding approach 4.3.6 Shotgun approach 4.3.7 Bioinformatic processing 4.4 Results 4.4.1 General results of the three approaches: pollen, metabarcoding and shotgun sequencing 4.4.2 Plants (Viridiplantae) 4.4.3 Fungi 4.4.4 Mammals (Mammalia) 4.4.5 Birds (Aves) 4.4.6 Insects (Insecta) 4.4.7 Prokaryotes (Bacteria, Archaea) and Viruses 4.5 Discussion 4.5.1 Interglacial communities 4.5.2 Glacial communities 4.5.3 Potential and limitations of the sedaDNA shotgun approach applied to ancient permafrost sediments 4.6 Conclusions Data availability statement Funding References 5 Synthesis 5.1 Ecological changes between glacial and interglacial stages 5.1.1 Changes in the compositional structure 5.1.2 Loss of plant diversity 5.1.3 Potential drivers of change 5.2 High potential of sedaDNA for past biodiversity reconstruction 5.3 Conclusions and future perspectives Bibliography Appendices Appendix 1: Supplementary material for Manuscript I Appendix 2: Supplementary material for Manuscript II Appendix 3: Supplementary material for Manuscript III Appendix 4: Manuscript IV Eidesstattliche Erklärung
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    Call number: AWI G5-23-95172
    Description / Table of Contents: Throughout the last ~3 million years, the Earth's climate system was characterised by cycles of glacial and interglacial periods. The current warm period, the Holocene, is comparably stable and stands out from this long-term cyclicality. However, since the industrial revolution, the climate has been increasingly affected by a human-induced increase in greenhouse gas concentrations. While instrumental observations are used to describe changes over the past ~200 years, indirect observations via proxy data are the main source of information beyond this instrumental era. These data are indicators of past climatic conditions, stored in palaeoclimate archives around the Earth. The proxy signal is affected by processes independent of the prevailing climatic conditions. In particular, for sedimentary archives such as marine sediments and polar ice sheets, material may be redistributed during or after the initial deposition and subsequent formation of the archive. This leads to noise in the records challenging reliable reconstructions on local or short time scales. This dissertation characterises the initial deposition of the climatic signal and quantifies the resulting archive-internal heterogeneity and its influence on the observed proxy signal to improve the representativity and interpretation of climate reconstructions from marine sediments and ice cores. To this end, the horizontal and vertical variation in radiocarbon content of a box-core from the South China Sea is investigated. The three-dimensional resolution is used to quantify the true uncertainty in radiocarbon age estimates from planktonic foraminifera with an extensive sampling scheme, including different sample volumes and replicated measurements of batches of small and large numbers of specimen. An assessment on the variability stemming from sediment mixing by benthic organisms reveals strong internal heterogeneity. Hence, sediment mixing leads to substantial time uncertainty of proxy-based reconstructions with error terms two to five times larger than previously assumed. A second three-dimensional analysis of the upper snowpack provides insights into the heterogeneous signal deposition and imprint in snow and firn. A new study design which combines a structure-from-motion photogrammetry approach with two-dimensional isotopic data is performed at a study site in the accumulation zone of the Greenland Ice Sheet. The photogrammetry method reveals an intermittent character of snowfall, a layer-wise snow deposition with substantial contributions by wind-driven erosion and redistribution to the final spatially variable accumulation and illustrated the evolution of stratigraphic noise at the surface. The isotopic data show the preservation of stratigraphic noise within the upper firn column, leading to a spatially variable climate signal imprint and heterogeneous layer thicknesses. Additional post-depositional modifications due to snow-air exchange are also investigated, but without a conclusive quantification of the contribution to the final isotopic signature. Finally, this characterisation and quantification of the complex signal formation in marine sediments and polar ice contributes to a better understanding of the signal content in proxy data which is needed to assess the natural climate variability during the Holocene.
    Type of Medium: Dissertations
    Pages: xx, 167 Seiten : Illustrationen, Diagramme
    Language: English
    Note: Dissertation, Universität Potsdam, 2023 (publikationsbasierte Dissertation) , CONTENTS 1 Introduction 1.1 Introduction to climate reconstructions 1.1.1 Radiocarbon as a tracer of time 1.1.2 Environmental information stored in snow 1.2 Challenges of climate reconstructions 1.2.1 The particle flux 1.2.2 Modifications after the initial deposition 1.2.3 Sampling and measurement uncertainty 1.3 Objectives and overview of the thesis 1.4 Author contributions to the Manuscripts 2 Age-heterogeneity in marine sediments revealed by three-dimensional high-resolution radio-carbon measurements 2.1 Introduction 2.2 Methods 2.2.1 Study approach 2.2.2 Core setup and sampling 2.2.3 Estimation of the sediment accumulation rate 2.2.4 Estimation of the sediment mixing strength 2.2.5 Estimation of the net sediment displacement 2.2.6 Visual assessment of mixing 2.3 Results 2.3.1 Radiocarbon measurements 2.3.2 Sediment accumulation rate 2.3.3 Sediment mixing estimates 2.3.4 Spatial structure of sediment mixing 2.3.5 Components of age uncertainty 2.4 Discussion 2.4.1 Spatial scale of sediment heterogeneity 2.4.2 Potential implications for palaeo-reconstructions 2.4.3 Suggested 14C measurement strategy 2.5 Conclusions 2.6 Supplementary Material 2.6.1 Supplementary figures and tables 2.6.2 Supplementary table 3 Local-scale deposition of surface snow on the Greenland ice sheet 3.1 Introduction 3.2 Data and methods 3.2.1 Study site 3.2.2 SfM photogrammetry 3.2.3 Additional snow height and snowfall data 3.2.4 Estimation of surface roughness 3.3 Results 3.3.1 Relative snow heights from DEMs 3.3.2 Temporal snow height evolution 3.3.3 Day-to-day variations of snowfall 3.3.4 Changes in surface roughness 3.3.5 Implied internal structure of the snowpack 3.4 Discussion 3.4.1 Changes of surface structures 3.4.2 Implications for proxy data 3.4.3 Implications for snow accumulation 3.4.4 SfM as an efficient monitoring tool 3.5 Conclusions 3.6 Appendix 3.6.1 Additional information 3.6.2 Accuracy estimates and validation 3.6.3 Validation 3.6.4 Overall snow height evolution 3.6.5 Surface roughness 4 A snapshot on the buildup of the stable water isotopic signal in the upper snowpack at east-grip, Geenland ice sheet 4.1 Introduction 4.2 Methods and data 4.2.1 Study site 4.2.2 DEM generation 4.2.3 Isotope measurements 4.2.4 Simulation of the snowpack layering 4.2.5 Expected uncertainty 4.3 Results 4.3.1 Snow height evolution 4.3.2 Mean isotopic records 4.3.3 Combining isotopic data with snow height information 4.3.4 Observed vs. simulated composition 4.3.5 Changes in the isotope signal over time 4.4 Discussion 4.4.1 Evolution of the snow surface 4.4.2 Two-dimensional view of isotopes in snow 4.4.3 Buildup of the snowpack isotopic signal 4.5 Conclusion 5 General discussion and conclusions 5.1 Heterogeneity in sedimentary archives 5.1.1 Quantifying archive-internal heterogeneity 5.1.2 Relation between signal and heterogeneity 5.2 Methods to improve climate reconstructions 5.3 Implications for climate reconstructions 5.4 Concluding remarks Bibliography A the role of sublimation as a driver of climate signals in the water isotope content of surface snow: laboratory and field experimental results A.1 Introduction A.2 Methods A.2.1 Laboratory experimental methods A.2.2 Field experimental methods A.3 Results A.3.1 Laboratory experiments A.3.2 Field experiments A.4 Discussion A.5 Conclusions B Atmosphere-snow exchange explains surface snow isotope variability Acknowledgments Eidesstattliche Erklärung
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  • 9
    Call number: AWI G8-23-95167
    Description / Table of Contents: The Arctic nearshore zone plays a key role in the carbon cycle. Organic-rich sediments get eroded off permafrost affected coastlines and can be directly transferred to the nearshore zone. Permafrost in the Arctic stores a high amount of organic matter and is vulnerable to thermo-erosion, which is expected to increase due to climate change. This will likely result in higher sediment loads in nearshore waters and has the potential to alter local ecosystems by limiting light transmission into the water column, thus limiting primary production to the top-most part of it, and increasing nutrient export from coastal erosion. Greater organic matter input could result in the release of greenhouse gases to the atmosphere. Climate change also acts upon the fluvial system, leading to greater discharge to the nearshore zone. It leads to decreasing sea-ice cover as well, which will both increase wave energy and lengthen the open-water season. Yet, knowledge on these processes and the resulting impact on the nearshore zone is scarce, because access to and instrument deployment in the nearshore zone is challenging. Remote sensing can alleviate these issues in providing rapid data delivery in otherwise non-accessible areas. However, the waters in the Arctic nearshore zone are optically complex, with multiple influencing factors, such as organic rich suspended sediments, colored dissolved organic matter (cDOM), and phytoplankton. The goal of this dissertation was to use remotely sensed imagery to monitor processes related to turbidity caused by suspended sediments in the Arctic nearshore zone. In-situ measurements of water-leaving reflectance and surface water turbidity were used to calibrate a semi-empirical algorithm which relates turbidity from satellite imagery. Based on this algorithm and ancillary ocean and climate variables, the mechanisms underpinning nearshore turbidity in the Arctic were identified at a resolution not achieved before. The calibration of the Arctic Nearshore Turbidity Algorithm (ANTA) was based on in-situ measurements from the coastal and inner-shelf waters around Herschel Island Qikiqtaruk (HIQ) in the western Canadian Arctic from the summer seasons 2018 and 2019. It performed better than existing algorithms, developed for global applications, in relating turbidity from remotely sensed imagery. These existing algorithms were lacking validation data from permafrost affected waters, and were thus not able to reflect the complexity of Arctic nearshore waters. The ANTA has a higher sensitivity towards the lowest turbidity values, which is an asset for identifying sediment pathways in the nearshore zone. Its transferability to areas beyond HIQ was successfully demonstrated using turbidity measurements matching satellite image recordings from Adventfjorden, Svalbard. The ANTA is a powerful tool that provides robust turbidity estimations in a variety of Arctic nearshore environments. Drivers of nearshore turbidity in the Arctic were analyzed by combining ANTA results from the summer season 2019 from HIQ with ocean and climate variables obtained from the weather station at HIQ, the ERA5 reanalysis database, and the Mackenzie River discharge. ERA5 reanalysis data were obtained as domain averages over the Canadian Beaufort Shelf. Nearshore turbidity was linearly correlated to wind speed, significant wave height and wave period. Interestingly, nearshore turbidity was only correlated to wind speed at the shelf, but not to the in-situ measurements from the weather station at HIQ. This shows that nearshore turbidity, albeit being of limited spatial extent, gets influenced by the weather conditions multiple kilometers away, rather than in its direct vicinity. The large influence of wave energy on nearshore turbidity indicates that freshly eroded material off the coast is a major contributor to the nearshore sediment load. This contrasts results from the temperate and tropical oceans, where tides and currents are the major drivers of nearshore turbidity. The Mackenzie River discharge was not identified as a driver of nearshore turbidity in 2019, however, the analysis of 30 years of Landsat archive imagery from 1986 to 2016 suggests a direct link between the prevailing wind direction, which heavily influences the Mackenzie River plume extent, and nearshore turbidity around HIQ. This discrepancy could be caused by the abnormal discharge behavior of the Mackenzie River in 2019. This dissertation has substantially advanced the understanding of suspended sediment processes in the Arctic nearshore zone and provided new monitoring tools for future studies. The presented results will help to understand the role of the Arctic nearshore zone in the carbon cycle under a changing climate.
    Type of Medium: Dissertations
    Pages: xv, ii, 85, xvii Seiten , Illustrationen, Diagramme, Karten
    Language: English
    Note: Dissertation, Universität Potsdam, 2022 (kumulative Dissertation) , TABLE OF CONTENTS Abstract Zusammenfassung Allgemeinverständliche Zusammenfassung List of Figures List of Tables Funding Chapter 1 Introduction 1.1 Scientific Background 1.1.1 Arctic Climate Change 1.1.2 The Arctic Nearshore Zone 1.1.3 Ocean Color Remote Sensing 1.2 Objectives 1.3 Study Area 1.4 Methods 1.4.1 Field Sampling 1.4.2 Data Processing 1.4.3 Satellite Imagery Processing 1.5 Thesis Structure 1.6 Author Contributions Chapter 2 Long-Term High-Resolution Sediment and Sea Surface Temperature Spatial Patterns in Arctic Nearshore Waters retrived using 30-year Landsat Archive Imagery 2.1 Abstract 2.2 Introduction 2.3 Material and Methods 2.3.1 Regional Setting 2.3.2 Landsat Images Acquisition and Processing 2.3.3 Landsat Turbidity Retrieval 2.3.4 Transects in the nearshore zone 2.3.5 Wind Data 2.4 Results 2.4.1 Brightness Temperature 2.4.2 Surface Reflectance and Turbidity Mapping 2.4.3 Gradients in the nearshore zone 2.5 Discussion 2.6 Conclusion Appendix A Chapter 3 The Arctic Nearshore Turbidity Algorithm (ANTA) - A Multi Sensor Turbidity Algorithm for Arctic Nearshore Environments 3.1 Abstract 3.2 Introduction 3.3 Methods 3.3.1 Regional setting 3.3.2 In-situ sampling 3.3.3 Optical data processing 3.3.4 Algorithm tuning 3.3.5 Satellite imagery processing 3.4 Results and Discussion 3.4.1 Turbidity and SPM 3.4.2 ANTA performance 3.4.3 Comparison with the Dogliotti et al., (2015) algorithm 3.4.4 Test and transfer of the ANTA 3.5 Conclusion Chapter 4 Drivers of Turbidity and its Seasonal Variability in the Nearshore Zone of Herschel Island Qikiqtaruk (western Canadian Arctic) 4.1 Abstract 4.2 Introduction 4.3 Methods 4.3.1 Study Area 4.3.2 Satellite Imagery 4.3.3 In-situ data 4.3.4 Reanalysis data 4.4 Results and Discussion 4.4.1 Time Series Analysis 4.4.2 Drivers of turbidity 4.5 Conclusion Chapter 5 Synthesis 5.1 Applicability of Remote Sensing Algorithms in the Arctic Nearshore Zone 5.2 Drivers of Nearshore Turbidity 5.3 Spatial Variations of Nearshore Turbidity 5.4 Challenges and Outlook List of Acronyms Bibliography Danksagung
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  • 10
    Call number: AWI G3-23-95073
    Description / Table of Contents: The Arctic is changing rapidly and permafrost is thawing. Especially ice-rich permafrost, such as the late Pleistocene Yedoma, is vulnerable to rapid and deep thaw processes such as surface subsidence after the melting of ground ice. Due to permafrost thaw, the permafrost carbon pool is becoming increasingly accessible to microbes, leading to increased greenhouse gas emissions, which enhances the climate warming. The assessment of the molecular structure and biodegradability of permafrost organic matter (OM) is highly needed. My research revolves around the question “how does permafrost thaw affect its OM storage?” More specifically, I assessed (1) how molecular biomarkers can be applied to characterize permafrost OM, (2) greenhouse gas production rates from thawing permafrost, and (3) the quality of OM of frozen and (previously) thawed sediments. I studied deep (max. 55 m) Yedoma and thawed Yedoma permafrost sediments from Yakutia (Sakha Republic). I analyzed sediment cores taken below thermokarst lakes on the Bykovsky Peninsula (southeast of the Lena Delta) and in the Yukechi Alas (Central Yakutia), and headwall samples from the permafrost cliff Sobo-Sise (Lena Delta) and the retrogressive thaw slump Batagay (Yana Uplands). I measured biomarker concentrations of all sediment samples. Furthermore, I carried out incubation experiments to quantify greenhouse gas production in thawing permafrost. I showed that the biomarker proxies are useful to assess the source of the OM and to distinguish between OM derived from terrestrial higher plants, aquatic plants and microbial activity. In addition, I showed that some proxies help to assess the degree of degradation of permafrost OM, especially when combined with sedimentological data in a multi-proxy approach. The OM of Yedoma is generally better preserved than that of thawed Yedoma sediments. The greenhouse gas production was highest in the permafrost sediments that thawed for the first time, meaning that the frozen Yedoma sediments contained most labile OM. Furthermore, I showed that the methanogenic communities had established in the recently thawed sediments, but not yet in the still-frozen sediments. My research provided the first molecular biomarker distributions and organic carbon turnover data as well as insights in the state and processes in deep frozen and thawed Yedoma sediments. These findings show the relevance of studying OM in deep permafrost sediments.
    Type of Medium: Dissertations
    Pages: xxiii, 178 Seiten , Illustrationen, Diagramme, Karten
    Language: English
    Note: Table of Contents Abstract Zusammenfassung Samenvatting Acknowledgements List of Figures List of Tables List of Abbreviations 1 Introduction 1.1 Motivation 1.2 Aims and research questions 1.3 Scientific background 1.3.1 The Arctic in a changing climate 1.3.2 Northern Hemisphere permafrost region 1.3.3 Permafrost degradation 1.3.3.1 Thermokarst development 1.3.3.2 Retrogressive thaw slumps 1.3.4 Organic matter in permafrost deposits 1.4 Material and methods 1.4.1 Study sites 1.4.2 Main laboratory methods 1.5 Thesis structure 1.6 Overview of publications 1.6.1 Publication “n-Alkane Characteristics of Thawed Permafrost Deposits Below a Thermokarst Lake on Bykovsky Peninsula, Northeastern Siberia” 1.6.2 Publication “Greenhouse gas production and lipid biomarker distribution in Yedoma and Alas thermokarst lake sediments in Eastern Siberia” 1.6.3 Publication “Organic matter characteristics of a rapidly eroding permafrost cliff in NE Siberia (Lena Delta, Laptev Sea region)” 1.6.4 Publication “Molecular biomarkers in Batagay megaslump permafrost deposits reveal clear differences in organic matter preservation between glacial and interglacial periods” 1.6.5 Contributions to complementary research 2 Bykovsky Peninsula 2.1 Abstract 2.2 Introduction 2.3 Study area 2.4 Material and methods 2.4.1 Field work 2.4.2 Laboratory analyses 2.4.2.1 Biomarker analysis 2.4.2.2 Biomarker indices 2.5 Results 2.5.1 Bulk sediment 2.5.1.1 Long core PG2412 2.5.1.2 Short core PG2420 2.5.2 Hydrochemistry 2.5.3 n-Alkane distributions 2.6 Discussion 2.6.1 Depositional history at the study site 2.6.1.1 Unit I - Early Weichselian fluvial sedimentation 2.6.1.2 Unit II – Yedoma deposition in wetland landscapes dominated by low-centered polygons 2.6.1.3 Unit III/Unit A – Yedoma deposition under cold-dry conditions during the Late Weichselian 2.6.1.4 Unit IV/Unit B – Holocene thermokarst lake formation and lacustrine sedimentation 2.6.2 Organic matter degradation 2.7 Conclusion 2.8 Acknowledgements 3 Yukechi Alas 3.1 Abstract 3.2 Introduction 3.3 Methods and materials 3.3.1 Study area 3.3.2 Field work 3.3.3 Laboratory analyses 3.3.3.1 Organic carbon content 3.3.3.2 Lipid biomarkers 3.3.4 Incubations 3.3.5 Statistical analysis 3.4 Results 3.4.1 Organic matter characteristics 3.4.1.1 Alas lake sediment core YU-L7 3.4.1.2 Yedoma lake sediment core YU-L15 3.4.2 Greenhouse gas production 3.4.2.1 Alas lake sediment core YU-L7 3.4.2.2 Yedoma lake sediment core YU-L15 3.4.2.3 Carbon mineralization 3.4.3 Statistical correlation and regression 3.5 Discussion 3.5.1 Organic matter degradation potential 3.5.1.1 Organic carbon quantity 3.5.1.2 Organic matter preservation and talik formation 3.5.1.3 Presence of methanogenic communities 3.5.2 Greenhouse gas production 3.5.2.1 Carbon dioxide production 3.5.2.2 Methane production 3.5.3 GHG links with other parameters and outlook 3.6 Conclusion 3.7 Acknowledgements 4 Sobo-Sise cliff 4.1 Abstract 4.2 Introduction 4.3 Study area 4.4 Methods 4.4.1 Fieldwork 4.4.2 Sedimentological organic matter parameters 4.4.3 Lipid biomarkers 4.4.3.1 Extraction and fraction separation 4.4.3.2 GC-MS measurements and compound quantification 4.4.4 Biomarker indices 4.4.4.1 Average Chain Length 4.4.4.2 Carbon Preference Index 4.4.4.3 Higher Plant Fatty Acids 4.4.5 Data analysis 4.5 Results 4.5.1 Sedimentological organic matter parameters 4.5.2 Biomarkers 4.5.2.1 n-Alkanes 4.5.2.2 Fatty acids 4.5.3 Clustering 4.6 Discussion 4.6.1 Terrestrial depositional environment 4.6.1.1 Organic matter source 4.6.1.2 Organic matter quality 4.6.2 Implications and outlook 4.7 Conclusion 4.8 Acknowledgements 5 Batagay thaw slump 5.1 Abstract 5.2 Introduction 5.3 Study site 5.4 Methods 5.4.1 Sample collection 5.4.2 Laboratory analyses 5.5 Results 5.5.1 Detected biomolecules 5.5.2 Lower Ice Complex 5.5.3 Lower Sand Unit 5.5.4 Woody Layer 5.5.5 Upper Ice Complex - Yedoma 5.5.6 Holocene Cover 5.6 Discussion 5.6.1 Biogeochemical legacy of glacial periods 5.6.2 Biogeochemical legacy of interglacial periods 5.6.3 Modern organic matter mobilization in the Batagay megaslump 5.7 Conclusion 5.8 Acknowledgements 6 Synthesis 6.1 Lipid biomarkers to characterize permafrost organic matter 6.1.1 Organic matter source 6.1.2 Organic matter quality 6.2 Mobilization of organic matter in thawing permafrost 6.2.1 Methane production vs. emission 6.2.2 Using the data in models 6.2.3 Transport of OM into aquatic systems 6.3 Recommendations for future research References Appendix A Supporting information for Chapter 2 Appendix B Supporting information for Chapter 3 Appendix C Supporting information for Chapter 4 Appendix D Supporting information for Chapter 5
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