| Q117428287 | A 1500-year multiproxy record of coastal hypoxia from the northern Baltic Sea indicates unprecedented deoxygenation over the 20th century |
| Q114604860 | A Lacustrine Biomarker Record From Rebun Island Reveals a Warm Summer Climate in Northern Japan During the Early Middle Holocene Due to a Stronger North Pacific High |
| Q63971584 | A Late Quaternary climate record based on long-chain diol proxies from the Chilean margin |
| Q28648028 | A TEX₈₆ surface sediment database and extended Bayesian calibration |
| Q120434443 | A climatic chamber experiment to test the short term effect of increasing temperature on branched GDGT distribution in Sphagnum peat |
| Q58097783 | A diagnostic GDGT signature for the impact of hydrothermal activity on surface deposits at the Southwest Indian Ridge |
| Q123167214 | A downcore calibration of theTEX |
| Q63971638 | A four-year record of U K′ 37 - and TEX 86 -derived sea surface temperature estimates from sinking particles in the filamentous upwelling region off Cape Blanc, Mauritania |
| Q59485617 | A high resolution record of sea surface temperature in southern Okinawa Trough for the past 15,000 years |
| Q110015256 | A multiproxy analysis of sedimentary organic carbon in the Changjiang Estuary and adjacent shelf |
| Q58074261 | A new Fossil-Lagerstätte from the Lower Eocene of Lessini Mountains (northern Italy): A multidisciplinary approach |
| Q59895911 | A new paleoclimate classification for deep time |
| Q39109419 | A progressively wetter climate in southern East Africa over the past 1.3 million years. |
| Q57978578 | A rapid lake-shallowing event terminated preservation of the Miocene Clarkia Fossil Konservat-Lagerstätte (Idaho, USA) |
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| Q59791177 | An assessment of latest Cretaceous Pycnodonte vesicularis (Lamarck, 1806) shells as records for palaeoseasonality: a multi-proxy investigation |
| Q57881020 | An interlaboratory study of TEX86and BIT analysis of sediments, extracts, and standard mixtures |
| Q57940057 | An offset in TEX86 values between interbedded lithologies: Implications for sea-surface temperature reconstructions |
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| Q114868500 | Analytical and Computational Advances, Opportunities, and Challenges in Marine Organic Biogeochemistry in an Era of “Omics” |
| Q58087680 | Appraisal of TEX86 and TEX 86 L thermometries in subpolar and polar regions |
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| Q108162471 | Archaeal and bacterial H-GDGTs are abundant in peat and their relative abundance is positively correlated with temperature |
| Q108162474 | Archaeal and bacterial glycerol dialkyl glycerol tetraether (GDGT) lipids in environmental samples by high temperature-gas chromatography with flame ionisation and time-of-flight mass spectrometry detection |
| Q64448582 | Archaeal cell surface biogenesis |
| Q58311127 | Archaeal community changes in Lateglacial lake sediments: Evidence from ancient DNA |
| Q117426086 | Archaeal intact polar lipids in polar waters: a comparison between the Amundsen and Scotia seas |
| Q114175906 | Archaeal lipids in soils and sediments: Water impact and consequences for microbial carbon sequestration |
| Q114215785 | Archaeal lipids reveal climate‐driven changes in microbial ecology at Lake El'gygytgyn (Far East Russia) during the Plio‐Pleistocene |
| Q117804880 | Archaeal tetraether lipids and their biphytane carbon isotope composition in sediments along an estuarine biogeochemical gradient |
| Q90653684 | Arctic shrub colonization lagged peak postglacial warmth: Molecular evidence in lake sediment from Arctic Canada |
| Q63964907 | Assessing Mechanisms and Uncertainty in Modeled Climatic Change at the Eocene-Oligocene Transition |
| Q58410269 | Assessment and calibration of TEX86 paleothermometry in the Sea of Okhotsk and sub-polar North Pacific region: Implications for paleoceanography |
| Q56296554 | Bacteriohopanepolyol distribution in Yenisei River and Kara Sea suspended particulate matter and sediments traces terrigenous organic matter input |
| Q63489443 | Bacteriohopanepolyols in tropical soils and sediments from the Congo River catchment area |
| Q88782957 | Bathyarchaeota: globally distributed metabolic generalists in anoxic environments |
| Q63971589 | Benthic archaea as potential sources of tetraether membrane lipids in sediments across an oxygen minimum zone |
| Q117428082 | Biogeochemical evidence of anaerobic methane oxidation on active submarine mud volcanoes on the continental slope of the Canadian Beaufort Sea |
| Q57698911 | Biogeochemical formation of calyx-shaped carbonate crystal fans in the subsurface of the Early Triassic seafloor |
| Q117808966 | Biogeochemistry of hadal trenches: Recent developments and future perspectives |
| Q58097764 | Biogeochemistry of intertidal microbial mats from Qatar: New insights from organic matter characterisation |
| Q59486986 | Biological source and provenance of deep-water derived isoprenoid tetraether lipids along the Portuguese continental margin |
| Q123233595 | Biomarker and Pollen Evidence for Late Pleistocene Pluvials in the Mojave Desert |
| Q59839998 | Biomarkers in Lake Van sediments reveal dry conditions in eastern Anatolia during 110.000-10.000 years B.P |
| Q35128457 | Biosignatures in chimney structures and sediment from the Loki's Castle low-temperature hydrothermal vent field at the Arctic Mid-Ocean Ridge |
| Q109318170 | Black Sea rivers capture significant change in catchment-wide mean annual temperature and soil pH during the Miocene-to-Pliocene transition |
| Q59840002 | Branched GDGT signals in fluvial sediments of the Danube River basin: Method comparison and longitudinal evolution |
| Q110273891 | Branched GDGT-based paleotemperature reconstruction of the last 30,000 years in humid monsoon region of Southeast China |
| Q59840031 | Branched glycerol dialkyl glycerol tetraethers in Arctic lake sediments: Sources and implications for paleothermometry at high latitudes |
| Q99418573 | Bridging the membrane lipid divide: bacteria of the FCB group superphylum have the potential to synthesize archaeal ether lipids |
| Q116953306 | Burial and Origin of Permafrost‐Derived Carbon in the Nearshore Zone of the Southern Canadian Beaufort Sea |
| Q121008287 | CO2-dependent carbon isotope fractionation in Archaea, Part I: Modeling the 3HP/4HB pathway |
| Q90176545 | Carbon Oxidation State in Microbial Polar Lipids Suggests Adaptation to Hot Spring Temperature and Redox Gradients |
| Q110252895 | Carbon isotope excursions during the late Miocene recorded by lipids of marine Thaumarchaeota, Piedmont Basin, Mediterranean Sea |
| Q46857432 | Changes in the ratio of tetraether to diether lipids in cattle feces in response to altered dietary ratio of grass silage and concentrates |
| Q38112288 | Chemical markers for rumen methanogens and methanogenesis. |
| Q114828809 | Climate and sea-level changes across a shallow marine Cretaceous-Palaeogene boundary succession in Patagonia, Argentina |
| Q109542313 | Climate and the Evolution of the Ocean: The Paleoceanographic Data |
| Q53100238 | Climate model and proxy data constraints on ocean warming across the Paleocene–Eocene Thermal Maximum |
| Q59786252 | Climate of the Late Cretaceous North American Gulf and Atlantic Coasts |
| Q63071773 | Climate- and gateway-driven cooling of Late Eocene to earliest Oligocene sea surface temperatures in the North Sea Basin |
| Q61360184 | Climatic history of the northeastern United States during the past 3000 years |
| Q30681318 | Collapsed bipolar glycolipids at the air/water interface: effect of the stereochemistry on the stretched/bent conformations. |
| Q109318176 | Comparing Seawater Temperature Proxy Records for the Past 90 Myrs From the Shallow Shelf Record Bass River, New Jersey |
| Q59335137 | Comparison of , and LDI temperature proxies for reconstruction of south-east Australian ocean temperatures |
| Q59139288 | Comparison of soil derived tetraether membrane lipid distributions and plant-wax δD compositions for reconstruction of Canadian Arctic temperatures |
| Q117427420 | Comparison of the U<sub>37</sub><sup>K<sup>′</sup></sup>, LDI, TEX<sub>86</sub><sup>H</sup>, and RI-OH temper |
| Q117744340 | Compositional Characteristics of Fluvial Particulate Organic Matter Exported From the World's Largest Alpine Wetland |
| Q59839961 | Constraining Instantaneous Fluxes and Integrated Compositions of Fluvially Discharged Organic Matter |
| Q89503300 | Constraining the formation of authigenic carbonates in a seepage-affected cold-water coral mound by lipid biomarkers |
| Q63971642 | Constraints on the applicability of the organic temperature proxies UK'37, TEX86 and LDI in the subpolar region around Iceland |
| Q63971621 | Constraints on the application of long chain diol proxies in the Iberian Atlantic margin |
| Q63971660 | Constraints on the sources of branched tetraether membrane lipids in distal marine sediments |
| Q57891816 | Contribution of Marine Group II Euryarchaeota to cyclopentyl tetraethers in the Pearl River estuary and coastal South China Sea: impact on the TEX86 paleothermometer |
| Q110565307 | Controlling factors and environmental significance of BIT and δ13C of sedimentary GDGTs from the Pearl River Estuary, China over recent decades |
| Q114647822 | Coupled Southern Ocean cooling and Antarctic ice sheet expansion during the middle Miocene |
| Q57933825 | Cretaceous sea-surface temperature evolution: Constraints from TEX 86 and planktonic foraminiferal oxygen isotopes |
| Q116287068 | Cyclisation degree of tetramethylated brGDGTs in marine environments and its implication for source identification |
| Q113227536 | DYNAMICS OF DEPOSITION AND FOSSIL PRESERVATION AT THE EARLY EOCENE OKANAGAN HIGHLANDS OF BRITISH COLUMBIA, CANADA: INSIGHTS FROM ORGANIC GEOCHEMISTRY |
| Q58492456 | Data report: distribution and sources of tetraether lipids in Oligocene deposits from the western North Atlantic, IODP Sites U1406 and U1411 |
| Q100233452 | Deglacial temperature controls on no-analog community establishment in the Great Lakes Region |
| Q57887358 | Dependence of the cyclization of branched tetraethers on soil moisture in alkaline soils from arid–subhumid China: implications for palaeorainfall reconstructions on the Chinese Loess Plateau |
| Q120434427 | Depth-dependent variation of archaeal ether lipids along soil and peat profiles from southern China: Implications for the use of isoprenoidal GDGTs as environmental tracers |
| Q48004580 | Depth-related distribution of a key gene of the tetraether lipid biosynthetic pathway in marine Thaumarchaeota |
| Q58053955 | Descent toward the Icehouse: Eocene sea surface cooling inferred from GDGT distributions |
| Q100695372 | Determination of the δ2 H values of high molecular weight lipids by high temperature GC coupled to isotope ratio mass spectrometry |
| Q92574318 | Determining stoichiometry and kinetics of two thermophilic nitrifying communities as a crucial step in the development of thermophilic nitrogen removal |
| Q117426026 | Development of global temperature and pH calibrations based on bacterial 3-hydroxy fatty acids in soils |
| Q48109747 | Did Photosymbiont Bleaching Lead to the Demise of Planktic Foraminifer Morozovella at the Early Eocene Climatic Optimum? |
| Q59487076 | Different seasonality of pelagic and benthic Thaumarchaeota in the North Sea |
| Q63971699 | Differential degradation of intact polar and core glycerol dialkyl glycerol tetraether lipids upon post-depositional oxidation |
| Q91473842 | Discriminative biogeochemical signatures of methanotrophs in different chemosynthetic habitats at an active mud volcano in the Canadian Beaufort Sea |
| Q31136899 | Disentangling interactions between microbial communities and roots in deep subsoil. |
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| Q117429054 | Distribution of branched glycerol dialkyl glycerol tetraethers in surface soils of the Qinghai–Tibetan Plateau: implications of brGDGTs-based proxies in cold and dry regions |
| Q108162536 | Distribution of branched tetraether lipids in ponds from Inner Mongolia, NE China: Insight into the source of brGDGTs |
| Q58097779 | Distribution of glycerol dialkyl glycerol tetraether (GDGT) lipids in a hypersaline lake system |
| Q104776769 | Distribution of glycerol dialkyl glycerol tetraethers in soils from two environmental transects in the USA |
| Q59920795 | Distribution of glycerol ether lipids in the oxygen minimum zone of the Eastern Tropical North Pacific Ocean |
| Q59920797 | Distribution of intact and core tetraether lipids in water column profiles of suspended particulate matter off Cape Blanc, NW Africa |
| Q117428834 | Distribution of tetraether lipids in agricultural soils – differentiation between paddy and upland management |
| Q117745080 | Distributions and Sources of Glycerol Dialkyl Glycerol Tetraethers in Sediment Cores From the Mariana Subduction Zone |
| Q58878226 | Distributions of bacterial and archaeal membrane lipids in surface sediments reflect differences in input and loss of terrestrial organic carbon along a cross-shelf Arctic transect |
| Q58097895 | Distributions of isoprenoid and branched glycerol dialkanol diethers in Chinese surface soils and a loess–paleosol sequence: Implications for the degradation of tetraether lipids |
| Q64103175 | Distributions of soil branched glycerol dialkyl glycerol tetraethers from different climate regions of China |
| Q56296597 | Drastic changes in the distribution of branched tetraether lipids in suspended matter and sediments from the Yenisei River and Kara Sea (Siberia): Implications for the use of brGDGT-based proxies in coastal marine sediments |
| Q114108458 | Early Cretaceous sea surface temperature evolution in subtropical shallow seas |
| Q63964860 | Early Jurassic North Atlantic sea‐surface temperatures from TEX 86 palaeothermometry |
| Q57235711 | Effects of growth phase on the membrane lipid composition of the thaumarchaeon Nitrosopumilus maritimus and their implications for archaeal lipid distributions in the marine environment |
| Q108162317 | Effects of temperature and pH on archaeal membrane lipid distributions in freshwater wetlands |
| Q56610332 | Environmental conditions in the South Atlantic (Angola Basin) during the Early Cretaceous |
| Q47380950 | Environmental factors shaping the archaeal community structure and ether lipid distribution in a subtropic river and estuary, China |
| Q28681372 | Eocene cooling linked to early flow across the Tasmanian Gateway |
| Q28654493 | Ether- and ester-bound iso-diabolic acid and other lipids in members of acidobacteria subdivision 4 |
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| Q117427259 | Evaluation of bacterial glycerol dialkyl glycerol tetraether and <sup>2</sup>H–<sup>18</sup>O biomarker proxies along a central European topsoil transect |
| Q110682978 | Evaluation of branched GDGTs and leaf wax n-alkane δ2H as (paleo) environmental proxies in East Africa |
| Q110685539 | Evaluation of leaf wax δD and soil brGDGTs as tools for paleoaltimetry on the southeastern Tibetan Plateau |
| Q112764579 | Evaluation of lipid biomarkers as proxies for sea ice and ocean temperatures along the Antarctic continental margin |
| Q58041067 | Evidence for Cretaceous-Paleogene boundary bolide “impact winter” conditions from New Jersey, USA |
| Q42230663 | Evidence for global cooling in the Late Cretaceous |
| Q58097776 | Evidence of moisture control on the methylation of branched glycerol dialkyl glycerol tetraethers in semi-arid and arid soils |
| Q59839982 | Evolution of biomolecular loadings along a major river system |
| Q108162302 | Exploring the Influences of Temperature on “H-Shaped” Glycerol Dialkyl Glycerol Tetraethers in a Stratigraphic Context: Evidence From Two Peat Cores Across the Late Quaternary |
| Q58390230 | Flat meridional temperature gradient in the early Eocene in the subsurface rather than surface ocean |
| Q46921737 | Fossilization and degradation of archaeal intact polar tetraether lipids in deeply buried marine sediments (Peru Margin). |
| Q57890886 | Freshwater discharge controlled deposition of Cenomanian–Turonian black shales on the NW European epicontinental shelf (Wunstorf, northern Germany) |
| Q57235708 | From ether to acid: A plausible degradation pathway of glycerol dialkyl glycerol tetraethers |
| Q58271404 | GDGT and alkenone flux in the northern Gulf of Mexico: Implications for the TEX86and UK'37paleothermometers |
| Q90573464 | GDGT cyclization proteins identify the dominant archaeal sources of tetraether lipids in the ocean |
| Q37303438 | GDGT distribution in a stratified lake and implications for the application of TEX86 in paleoenvironmental reconstructions |
| Q113873114 | General Holocene warming trend in arid Central Asia indicated by soil isoprenoid tetraethers |
| Q108162490 | Geochemical impacts of hydrothermal activity on surface deposits at the Southwest Indian Ridge |
| Q104415840 | Geophysical and geochemical analysis of shallow gas and an associated pockmark field in Bantry Bay, Co. Cork, Ireland |
| Q91329765 | Glacial Indonesian Throughflow weakening across the Mid-Pleistocene Climatic Transition |
| Q58390237 | Glacial cooling as inferred from marine temperature proxies TEX H 86 and U K′ 37 |
| Q114667806 | Global scale production of brGDGTs by benthic marine bacteria: Implication for developing ocean bottom environmental proxies |
| Q33466739 | Glycerol monoalkanediol diethers: a novel series of archaeal lipids detected in hydrothermal environments |
| Q53100164 | Gradual and sustained carbon dioxide release during Aptian Oceanic Anoxic Event 1a |
| Q112724033 | Gulf Stream intensification after the early Pliocene shoaling of the Central American Seaway |
| Q41525318 | Heat Stress Dictates Microbial Lipid Composition along a Thermal Gradient in Marine Sediments |
| Q56673682 | High temperatures in the terrestrial mid-latitudes during the early Palaeogene |
| Q111283517 | Holocene environmental history in high‐Arctic North Greenland revealed by a combined biomarker and macrofossil approach |
| Q57556579 | Holocene surface hydroclimate changes in the Indo-Pacific warm pool |
| Q57556594 | Hydrographic variability in the northern South China Sea over the past 45,000 years: New insights based on temperature reconstructions by U k’ 37 and TEX H 86 proxies from a marine sediment core (MD972146) |
| Q57880959 | Hydrologic controls on seasonal and inter-annual variability of Congo River particulate organic matter source and reservoir age |
| Q59920764 | Hydroxylated isoprenoid GDGTs in Chinese coastal seas and their potential as a paleotemperature proxy for mid-to-low latitude marginal seas |
| Q59920815 | Hypersaline conditions during deposition of the Calcare di Base revealed from archaeal di- and tetraether inventories |
| Q117427573 | Ice formation on lake surfaces in winter causes warm-season bias of lacustrine brGDGT temperature estimates |
| Q56296576 | Identification and carbon isotope composition of a novel branched GDGT isomer in lake sediments: Evidence for lacustrine branched GDGT production |
| Q56935667 | Identification of novel 7-methyl and cyclopentanyl branched glycerol dialkyl glycerol tetraethers in lake sediments |
| Q117843044 | Identifying marine and freshwater overprints on soil-derived branched GDGT temperature signals in Pliocene Mississippi and Amazon River fan sediments |
| Q92526909 | Identifying novel treeline biomarkers in lake sediments using an untargeted screening approach |
| Q114167107 | Impact of Eurasian Ice Sheet and North Atlantic Climate Dynamics on Black Sea Temperature Variability During the Penultimate Glacial (MIS 6, 130–184 ka BP) |
| Q63971668 | Impact of river channel shifts on tetraether lipids in the Rhône prodelta (NW Mediterranean): Implication for the BIT index as an indicator of palaeoflood events |
| Q56296623 | In situ produced branched glycerol dialkyl glycerol tetraethers in suspended particulate matter from the Yenisei River, Eastern Siberia |
| Q117378203 | In situ production of core and intact bacterial and archaeal tetraether lipids in groundwater |
| Q114143894 | In-situ provenance of brGDGTs in peat sediments: A case study from southern China and a comparison of global results |
| Q114215619 | Increased petrogenic and biospheric organic carbon burial in sub‐Antarctic fjord sediments in response to recent glacier retreat |
| Q38603090 | Inference on Paleoclimate Change Using Microbial Habitat Preference in Arctic Holocene Sediments |
| Q37102418 | Influence of ammonia oxidation rate on thaumarchaeal lipid composition and the TEX86 temperature proxy |
| Q58062846 | Influence of deep-water derived isoprenoid tetraether lipids on the TEX86H paleothermometer in the Mediterranean Sea |
| Q28083652 | Innovative methods in soil phosphorus research: A review |
| Q58097819 | Insoluble prokaryotic membrane lipids in a Sphagnum peat: Implications for organic matter preservation |
| Q106728107 | Intact polar lipid and core lipid inventory of the hydrothermal vent methanogens Methanocaldococcus villosus and Methanothermococcus okinawensis |
| Q63971629 | Interannual and (multi-)decadal variability in the sedimentary BIT index of Lake Challa, East Africa, over the past 2200 years: assessment of the precipitation proxy |
| Q57935108 | Introducing global peat-specific temperature and pH calibrations based on brGDGT bacterial lipids |
| Q63647644 | Investigating the Origins of Membrane Phospholipid Biosynthesis Genes Using Outgroup-Free Rooting |
| Q58825308 | Isolation and compound specific radiocarbon dating of terrigenous branched glycerol dialkyl glycerol tetraethers (brGDGTs) |
| Q63971636 | Isoprenoid and branched GDGT-based proxies for surface sediments from marine, fjord and lake environments in Chile |
| Q63971671 | Lack of 13C-label incorporation suggests low turnover rates of thaumarchaeal intact polar tetraether lipids in sediments from the Iceland shelf |
| Q106957633 | Lacustrine brGDGT response to microcosm and mesocosm incubations |
| Q108162395 | Late Cretaceous Temperature Evolution of the Southern High Latitudes: A TEX86 Perspective |
| Q114660527 | Late Cretaceous climate in the Canadian Arctic: Multi-proxy constraints from Devon Island |
| Q114018612 | Late Paleocene–early Eocene Arctic Ocean sea surface temperatures: reassessing biomarker paleothermometry at Lomonosov Ridge |
| Q63884675 | Late Quaternary vegetation, climate, and fire history of the Southeast Atlantic Coastal Plain based on a 30,000-yr multi-proxy record from White Pond, South Carolina, USA |
| Q58055782 | Latest Cretaceous climatic and environmental change in the South Atlantic region |
| Q109542314 | Latitudinal Migrations of the Subtropical Front at the Agulhas Plateau Through the Mid‐Pleistocene Transition |
| Q103864412 | Life and death in the Chicxulub impact crater: a record of the Paleocene–Eocene Thermal Maximum |
| Q117801766 | Limits of our knowledge, part 2: Selected frontiers in marine organic biogeochemistry |
| Q34656612 | Linking isoprenoidal GDGT membrane lipid distributions with gene abundances of ammonia-oxidizing Thaumarchaeota and uncultured crenarchaeotal groups in the water column of a tropical lake (Lake Challa, East Africa). |
| Q63971674 | Lipid biomarkers for anaerobic oxidation of methane and sulphate reduction in cold seep sediments of Nyegga pockmarks (Norwegian margin): discrepancies in contents and carbon isotope signatures |
| Q108162403 | Lipid biomarkers in lacustrine sediments of subtropical northeastern Mexico and inferred ecosystem changes during the late Pleistocene and Holocene |
| Q114583258 | Lipidomics of Environmental Microbial Communities. I: Visualization of Component Distributions Using Untargeted Analysis of High-Resolution Mass Spectrometry Data |
| Q38763695 | Lipids as paleomarkers to constrain the marine nitrogen cycle |
| Q63971573 | Long-chain diols in settling particles in tropical oceans: insights into sources, seasonality and proxies |
| Q113350998 | Long-term hydroclimate variability in the sub-tropical North Atlantic and anthropogenic impacts on lake ecosystems: A case study from Flores Island, the Azores |
| Q114018582 | Maastrichtian–Rupelian paleoclimates in the southwest Pacific – a critical re-evaluation of biomarker paleothermometry and dinoflagellate cyst paleoecology at Ocean Drilling Program Site 1172 |
| Q26777218 | Marine Group II Archaea, potentially important players in the global ocean carbon cycle |
| Q96685772 | Marine Group II Euryarchaeota Contribute to the Archaeal Lipid Pool in Northwestern Pacific Ocean Surface Waters |
| Q123241453 | Meltwater events and the Mediterranean reconnection at the Saalian–Eemian transition in the Black Sea |
| Q91325295 | Membrane Lipid Composition and Amino Acid Excretion Patterns of Methanothermococcus okinawensis Grown in the Presence of Inhibitors Detected in the Enceladian Plume |
| Q92667415 | Membrane Lipid Composition of the Moderately Thermophilic Ammonia-Oxidizing Archaeon "Candidatus Nitrosotenuis uzonensis" at Different Growth Temperatures |
| Q114174588 | Metabolic and ecological controls on the stable carbon isotopic composition of archaeal (isoGDGT and BDGT) and bacterial (brGDGT) lipids in wetlands and lignites |
| Q59888046 | Methane seepage in a Cretaceous greenhouse world recorded by an unusual carbonate deposit from the Tarfaya Basin, Morocco |
| Q59901673 | Methane seepage intensities traced by biomarker patterns in authigenic carbonates from the South China Sea |
| Q116210113 | Methods and future directions for paleoclimatology in the Maya Lowlands |
| Q118071945 | Microbial Community Responses to Modern Environmental and Past Climatic Conditions in Omongwa Pan, Western Kalahari: A Paired 16S rRNA Gene Profiling and Lipid Biomarker Approach |
| Q104680504 | Microbial Signatures in Deep CO2-Saturated Miocene Sediments of the Active Hartoušov Mofette System (NW Czech Republic) |
| Q28083033 | Microbial Surface Colonization and Biofilm Development in Marine Environments |
| Q110015653 | Microbial lipid signatures and substrate potential of organic matter in permafrost deposits: Implications for future greenhouse gas production |
| Q114143900 | Microbial lipid signatures in Arctic deltaic sediments – Insights into methane cycling and climate variability |
| Q34498225 | Microbial methane turnover at Marmara Sea cold seeps: a combined 16S rRNA and lipid biomarker investigation. |
| Q58410259 | Mid-latitude continental temperatures through the early Eocene in western Europe |
| Q117426600 | Millennial-age glycerol dialkyl glycerol tetraethers (GDGTs) in forested mineral soils: <sup>14</sup>C-based evidence for stabilization of microbial necromass |
| Q29994852 | Miocene flooding events of western Amazonia |
| Q40149841 | Model for a novel membrane envelope in a filamentous hyperthermophilic virus |
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| Q43029728 | Molecular dynamics simulation study of the effect of glycerol dialkyl glycerol tetraether hydroxylation on membrane thermostability |
| Q43026306 | Mono-, di- and trimethylated homologues of isoprenoid tetraether lipid cores in archaea and environmental samples: mass spectrometric identification and significance |
| Q92380978 | Mountain biodiversity and ecosystem functions: interplay between geology and contemporary environments |
| Q114556493 | Multiple crises preceded the Mediterranean Salinity Crisis: Aridification and vegetation changes revealed by biomarkers and stable isotopes |
| Q108162413 | Multiple environmental and ecological controls on archaeal ether lipid distributions in saline ponds |
| Q98387437 | Multiple environmental parameters impact lipid cyclization in Sulfolobus acidocaldarius |
| Q64102350 | New Insights Into the Polar Lipid Composition of Extremely Halo(alkali)philic Euryarchaea From Hypersaline Lakes |
| Q56296615 | Occurrence and abundance of 6-methyl branched glycerol dialkyl glycerol tetraethers in soils: Implications for palaeoclimate reconstruction |
| Q120434438 | Occurrence and distribution of glycerol dialkanol diethers and glycerol dialkyl glycerol tetraethers in a peat core from SW Tanzania |
| Q117801618 | Organic biogeochemistry in the oxygen-deficient ocean: A review |
| Q63970817 | Organic geochemical and palynological evidence for Holocene natural and anthropogenic environmental change at Lake Dojran (Macedonia/Greece) |
| Q57873127 | Organic proxies in speleothems – New developments, advantages and limitations |
| Q58097871 | Organic-rich sedimentation in the South Pacific Ocean associated with Late Paleocene climatic cooling |
| Q60180598 | Origin of lipid biomarkers in mud volcanoes from the Alboran Sea, western Mediterranean |
| Q59839957 | Paleoceanography and ice sheet variability offshore Wilkes Land, Antarctica – Part 3: Insights from Oligocene–Miocene TEX86-based sea surface temperature reconstructions |
| Q60180591 | Paleoclimate and paleoceanography over the past 20,000 yr in the Mediterranean Sea Basins as indicated by sediment elemental proxies |
| Q111304706 | Paleoclimate reconstruction of the last 36 kyr based on branched glycerol dialkyl glycerol tetraethers in the Padul palaeolake record (Sierra Nevada, southern Iberian Peninsula) |
| Q104777032 | Paleoelevation records from lipid biomarkers: Application to the tropical Andes |
| Q113874756 | Paleoenvironmental evolution during the Early Eocene Climate Optimum in the Chicxulub impact crater |
| Q63971648 | Palynological evidence for prolonged cooling along the Tunisian continental shelf following the K–Pg boundary impact |
| Q58097849 | Peatland GDGT records of Holocene climatic and biogeochemical responses to the Asian Monsoon |
| Q111981782 | Planetary Mass Spectrometry for Agnostic Life Detection in the Solar System |
| Q28655550 | Planktonic Euryarchaeota are a significant source of archaeal tetraether lipids in the ocean |
| Q59920775 | Possible roles of uncultured archaea in carbon cycling in methane-seep sediments |
| Q117801621 | Potential recycling of thaumarchaeotal lipids by DPANN Archaea in seasonally hypoxic surface marine sediments |
| Q58097753 | Precession driven changes in terrestrial organic matter input to the Eastern Mediterranean leading up to the Messinian Salinity Crisis |
| Q117427615 | Predominance of hexamethylated 6-methyl branched glycerol dialkyl glycerol tetraethers in the Mariana Trench: source and environmental implication |
| Q57235706 | Production rates of bacterial tetraether lipids and fatty acids in peatland under varying oxygen concentrations |
| Q28657375 | Pronounced zonal heterogeneity in Eocene southern high-latitude sea surface temperatures |
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