Geobiology

Papers
(The TQCC of Geobiology is 6. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Production of diverse brGDGTs by Acidobacterium Solibacter usitatus in response to temperature, pH, and O2 provides a culturing perspective on brGDGT proxies an50
The Sedimentary Geochemistry and Paleoenvironments Project31
Carbon cycle inverse modeling suggests large changes in fractional organic burial are consistent with the carbon isotope record and may have contributed to the rise of oxygen28
A new constraint on the antiquity of ancient haloalkaliphilic green algae that flourished in a ca. 300 Ma Paleozoic lake27
A late Paleoproterozoic (1.74 Ga) deep‐sea, low‐temperature, iron‐oxidizing microbial hydrothermal vent community from Arizona, USA26
The ‘classic stromatolite’ Cryptozoön is a keratose sponge‐microbial consortium22
A new model for silicification of cyanobacteria in Proterozoic tidal flats20
The gammaproteobacterium Achromatium forms intracellular amorphous calcium carbonate and not (crystalline) calcite20
The occurrence of 2‐methylhopanoids in modern bacteria and the geological record17
Cryptogamic ground covers as analogues for early terrestrial biospheres: Initiation and evolution of biologically mediated proto‐soils16
A sedimentary record of the evolution of the global marine phosphorus cycle16
Microbial succession and dynamics in meromictic Mono Lake, California15
Isotopic analyses of Ordovician–Silurian siliceous skeletons indicate silica‐depleted Paleozoic oceans13
Metagenomic analysis of microbial communities across a transect from low to highly hydrocarbon‐contaminated soils in King George Island, Maritime Antarctica13
Neoproterozoic syn‐glacial carbonate precipitation and implications for a snowball Earth13
Ediacaran–Cambrianbioturbation did not extensively oxygenate sediments in shallow marine ecosystems13
Volcanic controls on the microbial habitability of Mars‐analogue hydrothermal environments13
Morphogenesis of digitate structures in hot spring silica sinters of the El Tatio geothermal field, Chile12
Microbially induced chromium isotope fractionation and trace elements behavior in lower Cambrian microbialites from the Jaíba Member, Bambuí Basin, Brazil12
Inter‐domain horizontal gene transfer of nickel‐binding superoxide dismutase12
The biogeochemical cycling of chlorine11
Phosphatic scales in vase‐shaped microfossil assemblages from Death Valley, Grand Canyon, Tasmania, and Svalbard11
Inverse hydrogen isotope fractionation indicates heterotrophic microbial production of long‐chain n‐alkyl lipids in desolate Antarctic ponds11
Anoxygenic photosynthesis linked to Neoarchean iron formations in Carajás (Brazil)11
Hematite‐promoted nitrate‐reducing Fe(II) oxidation by Acidovorax sp. strain BoFeN1: Roles of mineral catalysis and cell encrustation11
Evaporative silicification in floating microbial mats: patterns of oxygen production and preservation potential in silica‐undersaturated streams, El Tatio, Chile11
Messinian bottom‐grown selenitic gypsum: An archive of microbial life10
Influences of pH and substrate supply on the ratio of iron to sulfate reduction10
Electrochemical evidence for in situ microbial activity at the Deep Mine Microbial Observatory (DeMMO), South Dakota, USA10
Dubiofossils from a Mars‐analogue subsurface palaeoenvironment: The limits of biogenicity criteria10
Widespread mineralization of soft‐bodied insects in Cretaceous amber10
Nitrogen‐based symbioses, phosphorus availability, and accounting for a modern world more productive than the Paleozoic10
Active and dormant microorganisms on glacier surfaces10
Widespread seafloor anoxia during generation of the Ediacaran Shuram carbon isotope excursion10
In search of the RNA world on Mars9
Iron‐mediated anaerobic ammonium oxidation recorded in the early Archean ferruginous ocean9
Detection of the deep biosphere in metamorphic rocks from the Chinese continental scientific drilling9
Marine and terrestrial nitrifying bacteria are sources of diverse bacteriohopanepolyols9
The influence of elevated SiO2(aq) on intracellular silica uptake and microbial metabolism8
Carbon reservoir perturbations induced by Deccan volcanism: Stable isotope and biomolecular perspectives from shallow marine environment in Eastern India8
Mesoproterozoic surface oxygenation accompanied major sedimentary manganese deposition at 1.4 and 1.1 Ga8
Silicate minerals as a direct source of limiting nutrients: Siderophore synthesis and uptake promote ferric iron bioavailability from olivine and microbial growth8
The Dziani Dzaha Lake: A long‐awaited modern analogue for superheavy pyrites8
Builders, tenants, and squatters: the origins of genetic material in modern stromatolites8
Minimum levels of atmospheric oxygen from fossil tree roots imply new plant−oxygen feedback7
The interplay of environmental constraints and bioturbation on matground development along the marine depositional profile during the Ordovician Radiation7
Exploring the secondary mineral products generated by microbial iron respiration in Archean ocean simulations7
Bacterial and archaeal lipids trace chemo(auto)trophy along the redoxcline in Vancouver Island fjords7
Copper mobilisation from Cu sulphide minerals by methanobactin: Effect of pH, oxygen and natural organic matter7
Subseafloor Archaea reflect 139 kyrs of paleodepositional changes in the northern Red Sea7
Endospores associated with deep seabed geofluid features in the eastern Gulf of Mexico7
Contrasting nutrient availability between marine and brackish waters in the late Mesoproterozoic: Evidence from the Paranoá Group, Brazil7
Sedimentary pyrite sulfur isotope compositions preserve signatures of the surface microbial mat environment in sediments underlying low‐oxygen cyanobacterial mats6
The deposition and significance of an Ediacaran non‐glacial iron formation6
A review of microbial‐environmental interactions recorded in Proterozoic carbonate‐hosted chert6
Potential role for microbial ureolysis in the rapid formation of carbonate tufa mounds6
Influence of aphotic haloclines and euxinia on organic biomarkers and microbial communities in a thalassohaline and alkaline volcanic crater lake6
Biogeochemical transformations after the emergence of oxygenic photosynthesis and conditions for the first rise of atmospheric oxygen6
New geochemical tools for investigating resource and energy functions at deep‐sea cold seeps using amino acid δ15N in chemosymbiotic mussels (Bathymodiolus childressi)6
The diagenetic fate of collagen as revealed by analytical pyrolysis of fossil fish scales from deep time6
Using thermodynamics to obtain geochemical information from genomes6
A re‐examination of the mechanism of whiting events: A new role for diatoms in Fayetteville Green Lake (New York, USA)6
Structure and function of Shark Bay microbial communities following tropical cyclone Olwyn: A metatranscriptomic and organic geochemical perspective6
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