scholarly article | Q13442814 |
P819 | ADS bibcode | 2018JGRE..123.1012M |
P356 | DOI | 10.1029/2017JE005478 |
P932 | PMC publication ID | 6049883 |
P698 | PubMed publication ID | 30034979 |
P50 | author | Derek Briggs | Q530161 |
John P. Grotzinger | Q1701289 | ||
Roger Everett Summons | Q17025799 | ||
Sean McMahon | Q25662830 | ||
Abigail A. Fraeman | Q57895473 | ||
Kenneth H. Williford | Q56424375 | ||
Ralph Milliken | Q59668352 | ||
P2093 | author name string | T Bosak | |
S A Newman | |||
M Daye | |||
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The imprint of atmospheric evolution in the D/H of Hesperian clay minerals on Mars | Q29037858 | ||
Microbial Mats in Terminal Proterozoic Siliciclastics: Ediacaran Death Masks | Q29304364 | ||
Mars methane detection and variability at Gale crater | Q29392167 | ||
Detection of methane in the martian atmosphere: evidence for life? | Q29393231 | ||
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Silica deposits on Mars with features resembling hot spring biosignatures at El Tatio in Chile | Q33807281 | ||
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An early Ediacaran assemblage of macroscopic and morphologically differentiated eukaryotes | Q33823588 | ||
Ichnotaxonomy of microbial trace fossils in volcanic glass | Q58012756 | ||
3.5 billion years of glass bioalteration: Volcanic rocks as a basis for microbial life? | Q58012759 | ||
Insights into cyanobacterial fossilization in Ediacaran siliciclastic environments | Q58041229 | ||
Insights into surface runoff on early Mars from paleolake basin morphology and stratigraphy | Q58041246 | ||
Experimental evidence that clay inhibits bacterial decomposers: Implications for preservation of organic fossils | Q58041360 | ||
Biosignatures link microorganisms to iron mineralization in a paleoaquifer | Q58078595 | ||
Carbon isotope fractionation by circumneutral iron-oxidizing bacteria | Q58078922 | ||
Sulfate availability and the geological record of cold-seep deposits | Q58080674 | ||
A hematite-bearing layer in Gale Crater, Mars: Mapping and implications for past aqueous conditions | Q58083192 | ||
Are the large filamentous microfossils preserved in Messinian gypsum colorless sulfide-oxidizing bacteria? | Q58083291 | ||
Bacteriohopanepolyol signatures of cyanobacterial and methanotrophic bacterial populations recorded in a geothermal vent sinter | Q58098102 | ||
Microbial membrane lipids in active and inactive sinters from Champagne Pool, New Zealand: Elucidating past geothermal chemistry and microbiology | Q58098112 | ||
Opaline silica in young deposits on Mars | Q58211436 | ||
Stratigraphic architectures spotted in southern Melas Chasma, Valles Marineris, Mars | Q58222205 | ||
Ferric oxides in East Candor Chasma, Valles Marineris (Mars) inferred from analysis of OMEGA/Mars Express data: Identification and geological interpretation | Q58355004 | ||
Juvenile chemical sediments and the long term persistence of water at the surface of Mars | Q58365456 | ||
Acid-sulfate weathering of synthetic Martian basalt: The acid fog model revisited | Q58365533 | ||
Iron-oxidizing microbial ecosystems thrived in late Paleoproterozoic redox-stratified oceans | Q58391458 | ||
Suboxic deep seawater in the late Paleoproterozoic: Evidence from hematitic chert and iron formation related to seafloor-hydrothermal sulfide deposits, central Arizona, USA | Q58391492 | ||
Microbiological processes in banded iron formation deposition | Q58417964 | ||
The potential significance of microbial Fe(III) reduction during deposition of Precambrian banded iron formations | Q58418028 | ||
Bacterial clay authigenesis: a common biogeochemical process | Q58418039 | ||
Authigenic mineralization and detrital clay binding by freshwater biofilms: The Brahmani river, India | Q58418040 | ||
In situ silicification of an Icelandic hot spring microbial mat: implications for microfossil formation | Q58418048 | ||
Early Jurassic hydrothermal vent community from the Franciscan Complex, San Rafael Mountains, California | Q58457328 | ||
New evidence for 250 Ma age of halotolerant bacterium from a Permian salt crystal | Q58458056 | ||
Processes of carbonate precipitation in modern microbial mats | Q58866997 | ||
A mineralogical signature for Burgess Shale–type fossilization | Q57585282 | ||
Reply to comment on the paper by Davies et al. “Resolving MISS conceptions and misconceptions: A geological approach to sedimentary surface textures generated by microbial and abiotic processes” (Earth Science Reviews, 154 (2016), 210–246) | Q57660863 | ||
Resolving MISS conceptions and misconceptions: A geological approach to sedimentary surface textures generated by microbial and abiotic processes | Q57660870 | ||
Curiosity's Mission of Exploration at Gale Crater, Mars | Q57727553 | ||
Primary silica precipitate at the Precambrian/Cambrian boundary in the South Oman Salt Basin, Sultanate of Oman | Q57846095 | ||
Mineralogy of an ancient lacustrine mudstone succession from the Murray formation, Gale crater, Mars | Q57852716 | ||
Multiple stages of aqueous alteration along fractures in mudstone and sandstone strata in Gale Crater, Mars | Q57852721 | ||
Fossilization potential of iron-bearing minerals in acidic environments of Rio Tinto, Spain: Implications for Mars exploration | Q57859280 | ||
Diagenetic silica enrichment and late-stage groundwater activity in Gale crater, Mars | Q57867905 | ||
Detection of crystalline hematite mineralization on Mars by the Thermal Emission Spectrometer: Evidence for near-surface water | Q57874334 | ||
Archean (3.33 Ga) microbe-sediment systems were diverse and flourished in a hydrothermal context | Q57884145 | ||
Defining biominerals and organominerals: Direct and indirect indicators of life | Q57884322 | ||
Hydrocarbon seep and hydrothermal vent paleoenvironments and paleontology: Past developments and future research directions | Q57884346 | ||
Biomineralization mediated by anaerobic methane-consuming cell consortia | Q33907176 | ||
Evidence for early life in Earth's oldest hydrothermal vent precipitates | Q34048025 | ||
Preservation of biological information in thermal spring deposits: developing a strategy for the search for fossil life on Mars | Q34089431 | ||
On the possibility of chemosynthetic ecosystems in subsurface habitats on Mars | Q34089648 | ||
Stromatolites in Precambrian carbonates: evolutionary mileposts or environmental dipsticks? | Q34089995 | ||
Natural transfer of viable microbes in space | Q34090049 | ||
Organic-walled microfossils in 3.2-billion-year-old shallow-marine siliciclastic deposits | Q34097462 | ||
Iron-oxidizing bacteria: an environmental and genomic perspective. | Q34121849 | ||
Preservation of martian organic and environmental records: final report of the Mars biosignature working group | Q34171765 | ||
Desulfotomaculum and Methanobacterium spp. dominate a 4- to 5-kilometer-deep fault | Q34232256 | ||
Global distribution of microbial abundance and biomass in subseafloor sediment | Q34296356 | ||
Gypsum-permineralized microfossils and their relevance to the search for life on Mars. | Q34337098 | ||
Deep fracture fluids isolated in the crust since the Precambrian era. | Q34344887 | ||
Martian fluvial conglomerates at Gale crater | Q34347765 | ||
In situ evidence for an ancient aqueous environment at Meridiani Planum, Mars | Q34373014 | ||
Mineralogy of a mudstone at Yellowknife Bay, Gale crater, Mars | Q34390861 | ||
In situ radiometric and exposure age dating of the martian surface | Q34390874 | ||
Mars' surface radiation environment measured with the Mars Science Laboratory's Curiosity rover | Q34390889 | ||
Volatile and organic compositions of sedimentary rocks in Yellowknife Bay, Gale crater, Mars | Q34390894 | ||
Sulfates in Martian layered terrains: the OMEGA/Mars Express view | Q34395598 | ||
Ancient aqueous environments at Endeavour crater, Mars | Q34399846 | ||
Trajectories of martian habitability | Q34403029 | ||
The Rhynie cherts: an early Devonian ecosystem preserved by hydrothermal activity | Q34434267 | ||
Common origins of RNA, protein and lipid precursors in a cyanosulfidic protometabolism | Q34468399 | ||
Evidence for indigenous nitrogen in sedimentary and aeolian deposits from the Curiosity rover investigations at Gale crater, Mars | Q34469772 | ||
Bacillus subtilis spores on artificial meteorites survive hypervelocity atmospheric entry: implications for Lithopanspermia | Q34479770 | ||
Deposition, exhumation, and paleoclimate of an ancient lake deposit, Gale crater, Mars | Q34497447 | ||
Reconstructing the transport history of pebbles on Mars | Q34497799 | ||
The changing view of eukaryogenesis - fossils, cells, lineages and how they all come together | Q34541216 | ||
Water activity and the challenge for life on early Mars | Q34782710 | ||
Morphogenesis of self-assembled nanocrystalline materials of barium carbonate and silica. | Q34924040 | ||
Detection of perchlorate and the soluble chemistry of martian soil at the Phoenix lander site | Q34990418 | ||
Record of archaeal activity at the serpentinite-hosted Lost City Hydrothermal Field | Q35015710 | ||
Organic molecules in the Sheepbed Mudstone, Gale Crater, Mars | Q36355274 | ||
Redox stratification of an ancient lake in Gale crater, Mars. | Q36390087 | ||
Unearthing the Antibacterial Mechanism of Medicinal Clay: A Geochemical Approach to Combating Antibiotic Resistance | Q36443563 | ||
Experimental simulation of evaporation-driven silica sinter formation and microbial silicification in hot spring systems | Q36638577 | ||
Accommodating the load: The transposable element content of very large genomes | Q37619228 | ||
Iron minerals within specific microfossil morphospecies of the 1.88 Ga Gunflint Formation | Q37733808 | ||
Subsurface water and clay mineral formation during the early history of Mars | Q37952501 | ||
Perchlorates on Mars enhance the bacteriocidal effects of UV light | Q38430051 | ||
Taphonomy of Microbial Biosignatures in Spring Deposits: A Comparison of Modern, Quaternary, and Jurassic Examples | Q38432536 | ||
Ancient sedimentary structures in the <3.7 Ga Gillespie Lake Member, Mars, that resemble macroscopic morphology, spatial associations, and temporal succession in terrestrial microbialites | Q38446376 | ||
Morphological biosignatures in gypsum: diverse formation processes of Messinian (∼6.0 Ma) gypsum stromatolites | Q38452813 | ||
Potential fossil endoliths in vesicular pillow basalt, Coral Patch Seamount, eastern North Atlantic Ocean | Q38462192 | ||
The preservation and degradation of filamentous bacteria and biomolecules within iron oxide deposits at Rio Tinto, Spain | Q38464468 | ||
Experimental silicification of the extremophilic Archaea Pyrococcus abyssi and Methanocaldococcus jannaschii: applications in the search for evidence of life in early Earth and extraterrestrial rocks | Q38471861 | ||
Hydrogeologic controls on episodic H2 release from precambrian fractured rocks--energy for deep subsurface life on earth and mars. | Q38478353 | ||
Coupled ferric oxides and sulfates on the Martian surface | Q38479917 | ||
Spectral properties of Lake Superior banded iron formation: application to Martian hematite deposits | Q38483219 | ||
Exploring for a record of ancient Martian life | Q38497460 | ||
A low temperature transfer of ALH84001 from Mars to Earth | Q38498989 | ||
Earth analogs for Martian life. Microbes in evaporites, a new model system for life on Mars | Q38510083 | ||
Buried Alive: Microbes from Ancient Halite. | Q38706563 | ||
Paleoecology and paleoceanography of the Athel silicilyte, Ediacaran-Cambrian boundary, Sultanate of Oman | Q38848571 | ||
Growth of synthetic stromatolites and wrinkle structures in the absence of microbes - implications for the early fossil record | Q39236974 | ||
Discovery of a new chert-permineralized microbiota in the Proterozoic Buxa Formation of the Ranjit window, Sikkim, northeast India, and its astrobiological implications | Q40037729 | ||
Fossilization processes in siliceous thermal springs: trends in preservation along thermal gradients | Q41550382 | ||
Putative cryptoendolithic life in Devonian pillow basalt, Rheinisches Schiefergebirge, Germany | Q42004038 | ||
Weighing the deep continental biosphere | Q43777568 | ||
Mineral surface control of organic carbon in black shale | Q44084891 | ||
Reassessing the evidence for the earliest traces of life | Q44094626 | ||
Self-assembled silica-carbonate structures and detection of ancient microfossils. | Q44654401 | ||
Carbon and sulfur isotopic signatures of ancient life and environment at the microbial scale: Neoarchean shales and carbonates | Q46220673 | ||
Experimental fossilization of mat-forming cyanobacteria in coarse-grained siliciclastic sediments | Q46419275 | ||
Hematite-coated microfossils: primary ecological fingerprint or taphonomic oddity of the Paleoproterozoic? | Q46779324 | ||
Habitability on Early Mars and the Search for Biosignatures with the ExoMars Rover. | Q47140722 | ||
Evidence from fluid inclusions for microbial methanogenesis in the early Archaean era. | Q47297315 | ||
Archean microfossils and abiomorphs | Q47329606 | ||
Carbonate petrography, kerogen distribution, and carbon and oxygen isotope variations in an early Proterozoic transition from limestone to iron-formation deposition, Transvaal Supergroup, South Africa. | Q47339834 | ||
The simulated silicification of bacteria--new clues to the modes and timing of bacterial preservation and implications for the search for extraterrestrial microfossils | Q47418091 | ||
The role of microbes in accretion, lamination and early lithification of modern marine stromatolites | Q47660973 | ||
Microorganisms from the Gunflint Chert | Q47795957 | ||
Dating phototropic microbial lineages with reticulate gene histories | Q48042909 | ||
Large alluvial fans on Mars | Q54196752 | ||
Ancient ocean on Mars supported by global distribution of deltas and valleys | Q55870266 | ||
Mars Reconnaissance Orbiter observations of light-toned layered deposits and associated fluvial landforms on the plateaus adjacent to Valles Marineris | Q55879909 | ||
Fungus-like mycelial fossils in 2.4-billion-year-old vesicular basalt | Q55882648 | ||
Sequence and timing of conditions on early Mars | Q55884346 | ||
Valley network-fed, open-basin lakes on Mars: Distribution and implications for Noachian surface and subsurface hydrology | Q55884458 | ||
Micropaleontology of the lower Mesoproterozoic Roper Group, Australia, and implications for early eukaryotic evolution | Q55884616 | ||
Geologic and mineralogic mapping of Aram Chaos: Evidence for a water-rich history | Q55888270 | ||
Groundwater activity on Mars and implications for a deep biosphere | Q55896714 | ||
Evidence for the origin of layered deposits in Candor Chasma, Mars, from mineral composition and hydrologic modeling | Q55919717 | ||
An abiotic model for stromatolite morphogenesis | Q55922589 | ||
Alteration assemblages in the nakhlites: Variation with depth on Mars | Q55933033 | ||
The early environment and its evolution on Mars: Implication for life | Q55934496 | ||
Modelling the surface and subsurface Martian radiation environment: Implications for astrobiology | Q55934497 | ||
Reanalysis of the Viking results suggests perchlorate and organics at midlatitudes on Mars | Q55934502 | ||
Exceptional preservation of soft-bodied Ediacara Biota promoted by silica-rich oceans | Q56001443 | ||
Advanced Oxidation Processes for Organic Contaminant Destruction Based on the Fenton Reaction and Related Chemistry | Q56049490 | ||
Cambrian Burgess Shale–type deposits share a common mode of fossilization | Q56115275 | ||
Silica deposits in the Nili Patera caldera on the Syrtis Major volcanic complex on Mars | Q56227225 | ||
Physical and hydraulic properties of modern sinter deposits: El Tatio, Atacama | Q56270172 | ||
Simulation of the environmental climate conditions on martian surface and its effect on Deinococcus radiodurans | Q56286419 | ||
The origins of perchlorate in the Martian soil | Q56385129 | ||
Unravelling abiogenic and biogenic sources of methane in the Earth's deep subsurface | Q56386952 | ||
Molecular evidence for life in the 3.5 billion year old Warrawoona chert | Q56431902 | ||
Secular distribution of Burgess-Shale-type preservation | Q56460317 | ||
Microbial biofilms and the preservation of the Ediacara biota | Q56460544 | ||
An assessment of the meteoritic contribution to the Martian soil | Q56475066 | ||
Geologic setting of serpentine deposits on Mars | Q56552131 | ||
Carbonaceous and siliceous Neoproterozoic vase-shaped microfossils (Urucum Formation, Brazil) and the question of early protistan biomineralization | Q56553174 | ||
Rates and mechanisms of chemical weathering of ferromagnesian silicate minerals on Mars | Q56565536 | ||
Global mapping of Martian hematite mineral deposits: Remnants of water-driven processes on early Mars | Q56568420 | ||
Gray hematite distribution and formation in Ophir and Candor chasmata | Q56568421 | ||
HiRISE imaging of impact megabreccia and sub-meter aqueous strata in Holden Crater, Mars | Q56568424 | ||
Columbus crater and other possible groundwater-fed paleolakes of Terra Sirenum, Mars | Q56568434 | ||
The Role of Decay and Mineralization in the Preservation of Soft-Bodied Fossils | Q56592815 | ||
The Weng'an biota and the Ediacaran radiation of multicellular eukaryotes | Q56636716 | ||
Microfossils of sulphur-metabolizing cells in 3.4-billion-year-old rocks of Western Australia | Q56672579 | ||
Composition and implications of diverse lipids in New Zealand Geothermal sinters | Q56682505 | ||
The effect of cyanobacteria on silica precipitation at neutral pH: implications for bacterial silicification in geothermal hot springs | Q56687251 | ||
The effect of ionizing radiation on the preservation of amino acids on Mars | Q56698040 | ||
Textured organic surfaces associated with the Ediacara biota in South Australia | Q56766788 | ||
Remarkable preservation of microbial mats in Neoproterozoic siliciclastic settings: Implications for Ediacaran taphonomic models | Q56766790 | ||
Sublacustrine depositional fans in southwest Melas Chasma | Q56835279 | ||
Microbially Induced Sedimentary Structures: A New Category within the Classification of Primary Sedimentary Structures | Q56907925 | ||
Oxygen-Dependent Morphogenesis of Modern Clumped Photosynthetic Mats and Implications for the Archean Stromatolite Record | Q57541892 | ||
Carbonates in the Martian meteorite Allan Hills 84001 formed at 18 +/- 4 degrees C in a near-surface aqueous environment | Q35345809 | ||
Selective stabilization of aliphatic organic carbon by iron oxide | Q35659709 | ||
Ultrastructural Heterogeneity of Carbonaceous Material in Ancient Cherts: Investigating Biosignature Origin and Preservation. | Q35819140 | ||
Tracing Biosignature Preservation of Geothermally Silicified Microbial Textures into the Geological Record | Q35819146 | ||
Evidence for methane in Martian meteorites. | Q35905931 | ||
The microbial role in hot spring silicification | Q36018155 | ||
Impact-generated hydrothermal systems on Earth and Mars | Q59153057 | ||
The igneous oceanic crust – Earth's largest fungal habitat? | Q59267266 | ||
Identification of hydrated silicate minerals on Mars using MRO-CRISM: Geologic context near Nili Fossae and implications for aqueous alteration | Q59700291 | ||
Light and variable 37 Cl/ 35 Cl ratios in rocks from Gale Crater, Mars: Possible signature of perchlorate | Q59770459 | ||
Poor preservation potential of organics in Meridiani Planum hematite-bearing sedimentary rocks | Q59781690 | ||
Late Archean Calcite-Microbe Interactions: Two Morphologically Distinct Microbial Communities That Affected Calcite Nucleation Differently | Q59781697 | ||
INFLUENCE OF GAS PRODUCTION AND FILAMENT ORIENTATION ON STROMATOLITE MICROFABRIC | Q59829123 | ||
Geological context of water-altered minerals in Valles Marineris, Mars | Q59835678 | ||
Discovery of alunite in Cross crater, Terra Sirenum, Mars: Evidence for acidic, sulfurous waters | Q59835706 | ||
Evaluating the role of microbial sulfate reduction in the early Archean using quadruple isotope systematics | Q59842425 | ||
Most Mars minerals in a nutshell: Various alteration phases formed in a single environment in Noctis Labyrinthus | Q59896720 | ||
Diagenetic haematite and sulfate assemblages in Valles Marineris | Q59896818 | ||
Stratigraphy of hydrated sulfates in the sedimentary deposits of Aram Chaos, Mars | Q59896877 | ||
First detection of fluorine on Mars: Implications for Gale Crater's geochemistry | Q59926114 | ||
Structure and stratigraphy of Home Plate from the Spirit Mars Exploration Rover | Q59935848 | ||
The origin and occurrence of subaqueous sedimentary cracks | Q59947041 | ||
The role of experiments in investigating the taphonomy of exceptional preservation | Q59947068 | ||
Salinity Influences the Response ofHalomonas hydrothermalisto Artificial Fossilization by Evaporative Silicification | Q60038033 | ||
Light-toned strata and inverted channels adjacent to Juventae and Ganges chasmata, Mars | Q60154056 | ||
LXXIII.—Oxidation of tartaric acid in presence of iron | Q60304014 | ||
Feedbacks between flow, sediment motion and microbial growth on sand bars initiate and shape elongated stromatolite mounds | Q60508271 | ||
Microbial shaping of sedimentary wrinkle structures | Q60508273 | ||
Microbial biofacies in hot-spring sinters; a model based on Ohaaki Pool, North Island, New Zealand | Q60682930 | ||
Limitations to a microbial iron cycle on Mars | Q61043906 | ||
Mineralogy of the Martian Surface | Q66363715 | ||
Water on Mars and the prospect of Martian life | Q66364390 | ||
Paleoclimate of Mars as captured by the stratigraphic record in Gale Crater | Q66371318 | ||
Deep crustal carbonate rocks exposed by meteor impact on Mars | Q68981096 | ||
The silica cycle in the Precambrian | Q70941452 | ||
Brazilian Analog for Ancient Marine Environments on Mars | Q70941904 | ||
Environmental control on diverse stromatolite morphologies in the 3000 Myr Pongola Supergroup, South Africa | Q71066538 | ||
Examining Archean methanotrophy | Q73892332 | ||
Spatially-resolved isotopic study of carbon trapped in ∼3.43 Ga Strelley Pool Formation stromatolites | Q73894905 | ||
The origin and evolution of oxygenic photosynthesis | Q74530080 | ||
Formation and stability of oxygen-rich bubbles that shape photosynthetic mats | Q82426350 | ||
Calculated fractionation factors for carbon and hydrogen isotope exchange in the system calcite-carbon dioxide-graphite-methane-hydrogen-water vapor | Q95496895 | ||
EARLY JURASSIC HYDROTHERMAL VENT COMMUNITY FROM THE FRANCISCAN COMPLEX, CALIFORNIA | Q99659808 | ||
Distribution, Classification, and Ages of Martian Impact Crater Lakes | Q101248627 | ||
Wind-blown sandstones cemented by sulfate and clay minerals in Gale Crater, Mars | Q102362276 | ||
Depth of the Martian cryosphere: Revised estimates and implications for the existence and detection of subpermafrost groundwater | Q105244130 | ||
Iron oxyhydroxide mineralization on microbial extracellular polysaccharides | Q105726535 | ||
Distribution and formation of chlorides and phyllosilicates in Terra Sirenum, Mars | Q105737747 | ||
Extended survival of several organisms and amino acids under simulated martian surface conditions | Q106533516 | ||
Radiolytic H2in continental crust: Nuclear power for deep subsurface microbial communities | Q106533573 | ||
Dating ultra-deep mine waters with noble gases and 36Cl, Witwatersrand Basin, South Africa | Q106533579 | ||
Geochemistry and sedimentology of a facies transition from limestone to iron-formation deposition in the early Proterozoic Transvaal Supergroup, South Africa | Q107369164 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1012-1040 | |
P577 | publication date | 2018-05-24 | |
P1433 | published in | Journal of Geophysical Research. Planets | Q27726640 |
P1476 | title | A Field Guide to Finding Fossils on Mars | |
P478 | volume | 123 |
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