| Global marine redox changes drove the rise and fall of the Ediacara biota |
19 |
| What the similar to 1.4 Ga Xiamaling Formation can and cannot tell us about the mid-Proterozoic ocean |
14 |
| A morphogram for silica-witherite biomorphs and its application to microfossil identification in the early earth rock record |
14 |
| Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesis |
14 |
| Oxygen, animals and aquatic bioturbation: An updated account |
14 |
| Slime travelers: Early evidence of animal mobility and feeding in an organic mat world |
13 |
| A sluggish mid-Proterozoic biosphere and its effect on Earth's redox balance |
13 |
| A combined lipidomic and 16S rRNA gene amplicon sequencing approach reveals archaeal sources of intact polar lipids in the stratified Black Sea water column |
11 |
| Unprecedented S-34-enrichment of pyrite formed following microbial sulfate reduction in fractured crystalline rocks |
11 |
| Nitrous oxide from chemodenitrification: A possible missing link in the Proterozoic greenhouse and the evolution of aerobic respiration |
10 |
| Tracking the rise of eukaryotes to ecological dominance with zinc isotopes |
10 |
| Survival of the fewest: Microbial dormancy and maintenance in marine sediments through deep time |
10 |
| Early Archean origin of Photosystem II |
10 |
| Evidence of oxygenic phototrophy in ancient phosphatic stromatolites from the Paleoproterozoic Vindhyan and Aravalli Supergroups, India |
10 |
| Oxygen isotope analysis of bacterial and fungal manganese oxidation |
9 |
| A small marine biosphere in the Proterozoic |
9 |
| Absence of biomarker evidence for early eukaryotic life from the Mesoproterozoic Roper Group: Searching across a marine redox gradient in mid-Proterozoic habitability |
9 |
| Cyanobacterial formation of intracellular Ca-carbonates in undersaturated solutions |
8 |
| Mineralisation of filamentous cyanobacteria in Lake Thetis stromatolites, Western Australia |
8 |
| Heterogeneity and incorporation of chromium isotopes in recent marine molluscs (Mytilus) |
7 |
| Paleoenvironmental proxies and what the Xiamaling Formation tells us about the mid-Proterozoic ocean |
6 |
| Holocene paleodepositional changes reflected in the sedimentary microbiome of the Black Sea |
6 |
| Mineralized microbialites as archives of environmental evolution, Laguna Negra, Catamarca Province, Argentina |
6 |
| Dating phototrophic microbial lineages with reticulate gene histories |
6 |
| Environmental insights from high-resolution (SIMS) sulfur isotope analyses of sulfides in Proterozoic microbialites with diverse mat textures |
5 |
| Facies selectivity of benthic invertebrates in a Permian/Triassic boundary microbialite succession: Implications for the microbialite refuge hypothesis |
5 |
| A stable and productive marine microbial community was sustained through the end-Devonian Hangenberg Crisis within the Cleveland Shale of the Appalachian Basin, United States |
5 |
| The Sirius Passet Lagerstatte of North Greenland-A geochemical window on early Cambrian low-oxygen environments and ecosystems |
5 |
| Subsurface processes influence oxidant availability and chemoautotrophic hydrogen metabolism in Yellowstone hot springs |
5 |
| Stable isotope fractionation of strontium in coccolithophore calcite: Influence of temperature and carbonate chemistry |
5 |
| Phylogenetic diversity in freshwater-dwelling Isochrysidales haptophytes with implications for alkenone production |
5 |
| Bioturbation and directionality in Earth's carbon isotope record across the Neoproterozoic-Cambrian transition |
4 |
| Microbial diversity and biomarker analysis of modern freshwater microbialites from Laguna Bacalar, Mexico |
4 |
| Rates and pathways of CH4 oxidation in ferruginous Lake Matano, Indonesia |
4 |
| Microbial assemblage and palaeoenvironmental reconstruction of the 1.38 Ga Velkerri Formation, McArthur Basin, northern Australia |
4 |
| The late-stage ferruginization of the Ediacara Member (Rawnsley Quartzite, South Australia): Insights from uranium isotopes |
4 |
| Morphological and isotopic changes of heterocystous cyanobacteria in response to N-2 partial pressure |
4 |
| Pigment carbon and nitrogen isotopic signatures in euxinic basins |
3 |
| Cr isotopic insights into ca. 1.9 Ga oxidative weathering of the continents using the Beaverlodge Lake paleosol, Northwest Territories, Canada |
3 |
| The importance of groundwater flow to the formation of modern thrombolitic microbialites |
3 |
| Influence of pH on the balance between methanogenesis and iron reduction |
3 |
| Unusual microbial mat-related structural diversity 2.1 billion years ago and implications for the Francevillian biota |
3 |
| Sulfur isotope's signal of nanopyrites enclosed in 2.7 Ga stromatolitic organic remains reveal microbial sulfate reduction |
3 |
| From microbial eukaryotes to metazoan vertebrates: Wide spectrum paleo-diversity in sedimentary ancient DNA over the last similar to 500years |
3 |
| The kinetics of siderophore-mediated olivine dissolution |
3 |
| Tracing the fate of steroids through a hypersaline microbial mat (Kiritimati, Kiribati/Central Pacific) |
3 |
| The taphonomic fate of isorenieratene in Lower Jurassic shales-controlled by iron? |
2 |
| Evidence for the development of local anoxia during the Cambrian SPICE event in eastern North America |
2 |
| Carbon isotopic heterogeneity of coenzyme F430 and membrane lipids in methane-oxidizing archaea |
2 |
| A paleosol record of the evolution of Cr redox cycling and evidence for an increase in atmospheric oxygen during the Neoproterozoic |
2 |
