| scholarly article | Q13442814 |
| P2093 | author name string | Hall AJ | |
| Russell MJ | |||
| P2860 | cites work | Origin of life: The RNA world | Q22122409 |
| P433 | issue | 3 | |
| P921 | main subject | iron | Q677 |
| P304 | page(s) | 377-402 | |
| P577 | publication date | 1997-05-01 | |
| P1433 | published in | Journal of the Geological Society | Q3186960 |
| P1476 | title | The emergence of life from iron monosulphide bubbles at a submarine hydrothermal redox and pH front | |
| P478 | volume | 154 |
| Q28596840 | A Field Trip to the Archaean in Search of Darwin's Warm Little Pond |
| Q52681612 | A Hydrothermal-Sedimentary Context for the Origin of Life. |
| Q28598274 | A Hypothesis: Life Initiated from Two Genes, as Deduced from the RNA World Hypothesis and the Characteristics of Life-Like Systems |
| Q21145705 | A bioenergetic basis for membrane divergence in archaea and bacteria |
| Q89983868 | A hydrogen-dependent geochemical analogue of primordial carbon and energy metabolism |
| Q57781707 | A novel iron sulphide mineral switch and its implications for Earth and planetary science |
| Q34065403 | A possible evolutionary origin for the Mn4 cluster of the photosynthetic water oxidation complex from natural MnO2 precipitates in the early ocean |
| Q47381396 | A suggested pioneer organism for the Wächtershäuser origin of life hypothesis |
| Q57006255 | Acetyl Phosphate as a Primordial Energy Currency at the Origin of Life |
| Q46673919 | Activation and dissociation of CO2 on the (001), (011), and (111) surfaces of mackinawite (FeS): A dispersion-corrected DFT study. |
| Q63487381 | Activation of diatomic and triatomic molecules for the synthesis of organic compounds: Metal catalysis at the subseafloor biosphere |
| Q88633814 | Amphiphilic Compounds Assemble into Membranous Vesicles in Hydrothermal Hot Spring Water but Not in Seawater |
| Q44644980 | Amplification of diverse catalytic properties of evolving molecules in a simulated hydrothermal environment |
| Q28757602 | An RNA-making reactor for the origin of life |
| Q57382868 | An all-inorganic polyoxometalate–polyoxocation chemical garden |
| Q28651014 | An origin-of-life reactor to simulate alkaline hydrothermal vents |
| Q34107198 | An overview of endosymbiotic models for the origins of eukaryotes, their ATP-producing organelles (mitochondria and hydrogenosomes), and their heterotrophic lifestyle |
| Q41666512 | Ancient Living Organisms Escaping from, or Imprisoned in, the Vents? |
| Q28078616 | AstRoMap European Astrobiology Roadmap |
| Q28647655 | Autocatalytic sets in E. coli metabolism |
| Q36937103 | Beating the acetyl coenzyme A-pathway to the origin of life. |
| Q84854706 | Behavior of a hammerhead ribozyme in aqueous solution at medium to high temperatures |
| Q57178934 | Big questions and skepsis: Review of “In Search of Cell History |
| Q34469977 | Bio-inspired CO2 conversion by iron sulfide catalysts under sustainable conditions |
| Q28776341 | Biochemical evolution II: origin of life in tubular microstructures on weathered feldspar surfaces |
| Q34994987 | Biochemistry and molecular biology of lithotrophic sulfur oxidation by taxonomically and ecologically diverse bacteria and archaea. |
| Q38208795 | Bioenergetic constraints on the evolution of complex life |
| Q28601441 | Biogenesis of reactive sulfur species for signaling by hydrogen sulfide oxidation pathways |
| Q28607185 | Biosignatures on Mars: What, Where, and How? Implications for the Search for Martian Life |
| Q37249795 | Calculation of the aqueous thermodynamic properties of citric acid cycle intermediates and precursors and the estimation of high temperature and pressure equation of state parameters |
| Q38430071 | Can Life Begin on Enceladus? A Perspective from Hydrothermal Chemistry |
| Q70643141 | Carbon dioxide cycling and implications for climate on ancient Earth |
| Q47610461 | Chance, necessity and the origins of life: a physical sciences perspective. |
| Q57478708 | Chemical Diversity of Metal Sulfide Minerals and Its Implications for the Origin of Life |
| Q38440681 | Chemical Gardens as Flow-through Reactors Simulating Natural Hydrothermal Systems |
| Q27335088 | Conditional iron and pH-dependent activity of a non-enzymatic glycolysis and pentose phosphate pathway |
| Q41775480 | Conjecture and hypothesis: The importance of reality checks |
| Q28085556 | Current Ideas about Prebiological Compartmentalization |
| Q35218019 | Cyclic growth of hierarchical structures in the aluminum-silicate system |
| Q46316484 | Darwin's prescient guess |
| Q45774235 | Density functional theory simulations of the structure, stability and dynamics of iron sulphide clusters in water. |
| Q56048096 | Early Archean fossil bacteria and biofilms in hydrothermally-influenced sediments from the Barberton greenstone belt, South Africa |
| Q38673754 | Early Microbial Evolution: The Age of Anaerobes |
| Q35121801 | Early assembly of cellular life |
| Q27011350 | Early bioenergetic evolution |
| Q28741296 | Early evolution without a tree of life |
| Q54559213 | Earth as a Tool for Astrobiology—A European Perspective |
| Q92274910 | Earth's Impact Events Through Geologic Time: A List of Recommended Ages for Terrestrial Impact Structures and Deposits |
| Q49344321 | Effects of salinity on the adsorption of nucleotides onto phyllosilicates. |
| Q21708375 | Electronic and magnetic structure of Fe 3 S 4 : GGA + U investigation |
| Q46595901 | Enantiomeric excess of amino acids in hydrothermal environments |
| Q41183776 | Energetics of Amino Acid Synthesis in Alkaline Hydrothermal Environments |
| Q43110849 | Energy, genes and evolution: introduction to an evolutionary synthesis |
| Q47200953 | Enhanced photocatalytic performance of ZnS for reversible amination of α-oxo acids by hydrothermal treatment |
| Q48163167 | Environmental Adaptation from the Origin of Life to the Last Universal Common Ancestor |
| Q60060341 | Evidence of bacterial activity from micrometer-scale layer analyses of black-smoker sulfide structures (Pito Seamount Site, Easter microplate) |
| Q53504447 | Evolution of cell division in bacteria. |
| Q36953192 | Evolution of enzymes and pathways for the biosynthesis of cofactors |
| Q47635785 | Evolution. Energy at life's origin |
| Q89557416 | Experimental and Simulation Efforts in the Astrobiological Exploration of Exooceans |
| Q35839592 | Extreme accumulation of nucleotides in simulated hydrothermal pore systems |
| Q57781582 | FeS-Induced Radical Formation and Its Effect on Plasmid DNA |
| Q28727326 | Field-Control, Phase-Transitions, and Life's Emergence |
| Q43027706 | Filamentous microfossils in a 3,235-million-year-old volcanogenic massive sulphide deposit |
| Q92419669 | Formation and loss of metastable brucite: does Fe(II)-bearing brucite support microbial activity in serpentinizing ecosystems? |
| Q58586582 | Formation of Proton Motive Force Under Low-Aeration Alkaline Conditions in Alkaliphilic Bacteria |
| Q24678275 | From volcanic origins of chemoautotrophic life to Bacteria, Archaea and Eukarya |
| Q92320860 | Functional analyses of ancestral thioredoxins provide insights into their evolutionary history |
| Q28658952 | Functional capabilities of the earliest peptides and the emergence of life |
| Q34280277 | Genetics first or metabolism first? The formamide clue |
| Q33477246 | Genome beginnings: rooting the tree of life |
| Q91631486 | Geochemistry and the Origin of Life: From Extraterrestrial Processes, Chemical Evolution on Earth, Fossilized Life's Records, to Natures of the Extant Life |
| Q52597436 | Geoelectrochemical CO production: Implications for the autotrophic origin of life. |
| Q58700184 | Green Rust: The Simple Organizing 'Seed' of All Life? |
| Q57086684 | Greigite nanocrystals produced by hyperthermophilic archaea of Thermococcales order |
| Q47140722 | Habitability on Early Mars and the Search for Biosignatures with the ExoMars Rover. |
| Q38497711 | High-temperature life without photosynthesis as a model for Mars |
| Q27006000 | Hydrogen, metals, bifurcating electrons, and proton gradients: the early evolution of biological energy conservation |
| Q57664518 | Hydrolysis of glucose-6-phosphate in aged, acid-forced hydrolysed nanomolar inorganic iron solutions—an inorganic biocatalyst? |
| Q47639635 | Hydrothermal circulation of seawater through hot vents and contribution of interface chemistry to prebiotic synthesis. |
| Q43242951 | Hydrothermal focusing of chemical and chemiosmotic energy, supported by delivery of catalytic Fe, Ni, Mo/W, Co, S and Se, forced life to emerge |
| Q38502708 | Hydrothermal hydration of Martian crust: illustration via geochemical model calculations |
| Q47830228 | Hydrothermal reactions of pyruvic acid: synthesis, selection, and self-assembly of amphiphilic molecules. |
| Q34838951 | Hydrothermal vents and the origin of life |
| Q47344814 | In Praise of Error |
| Q35961930 | In vitro evolution of distinct self-cleaving ribozymes in diverse environments |
| Q28283707 | Inhibition of carbonate synthesis in acidic oceans on early Mars |
| Q47216711 | Iron catalysis at the origin of life. |
| Q52567096 | Lack of Microbial Diversity in an Extreme Mars Analog Setting: Poás Volcano, Costa Rica. |
| Q33983766 | Life with carbon monoxide |
| Q42025219 | Life's Order, Complexity, Organization, and Its Thermodynamic-Holistic Imperatives |
| Q28744658 | Links between hydrothermal environments, pyrophosphate, na(+), and early evolution |
| Q58818430 | Magnetic ordering in tetragonal FeS: Evidence for strong itinerant spin fluctuations |
| Q57083963 | Magnetic properties of sedimentary greigite (Fe3S4): An update |
| Q37103945 | Mapping metabolism onto the prebiotic organic chemistry of hydrothermal vents |
| Q41983003 | Metalloproteins and the pyrite-based origin of life: a critical assessment |
| Q57154374 | Methane on Mars and Habitability: Challenges and Responses |
| Q43032688 | Methane: Fuel or Exhaust at the Emergence of Life? |
| Q54989376 | Mimicking the surface and prebiotic chemistry of early Earth using flow chemistry. |
| Q28752520 | Mineral surfaces, geochemical complexities, and the origins of life |
| Q35785644 | Modelling evolution on design-by-contract predicts an origin of life through an abiotic double-stranded RNA world. |
| Q36337118 | Molecules into cells: specifying spatial architecture |
| Q51730944 | NADPH-dependent and -independent Disulfide Reductase Systems. |
| Q28076481 | Natural pH Gradients in Hydrothermal Alkali Vents Were Unlikely to Have Played a Role in the Origin of Life |
| Q28654998 | Natural pyrrhotite as a catalyst in prebiotic chemical evolution |
| Q46647385 | Nucleic acids bind to nanoparticulate iron (II) monosulphide in aqueous solutions |
| Q97521025 | Older Than Genes: The Acetyl CoA Pathway and Origins |
| Q43020809 | On an early gene for membrane-integral inorganic pyrophosphatase in the genome of an apparently pre-luca extremophile, the archaeon Candidatus Korarchaeum cryptofilum |
| Q57086913 | On the differing growth mechanisms of black-smoker and Lost City-type hydrothermal vents |
| Q24648668 | On the origin of biochemistry at an alkaline hydrothermal vent |
| Q33511648 | On the origin of cells and viruses: primordial virus world scenario |
| Q33225133 | On the origin of genomes and cells within inorganic compartments |
| Q27498817 | On the origin of life in the Zinc world. 2. Validation of the hypothesis on the photosynthesizing zinc sulfide edifices as cradles of life on Earth |
| Q21093195 | On the origin of life in the zinc world: 1. Photosynthesizing, porous edifices built of hydrothermally precipitated zinc sulfide as cradles of life on Earth |
| Q33286326 | On the origin of the translation system and the genetic code in the RNA world by means of natural selection, exaptation, and subfunctionalization |
| Q24675851 | On the origins of cells: a hypothesis for the evolutionary transitions from abiotic geochemistry to chemoautotrophic prokaryotes, and from prokaryotes to nucleated cells |
| Q36405407 | Organic compounds in fluid inclusions of Archean quartz-Analogues of prebiotic chemistry on early Earth. |
| Q47838537 | Origin of self-replicating biopolymers: autocatalytic feedback can jump-start the RNA world |
| Q47103307 | Origin of the Reductive Tricarboxylic Acid (rTCA) Cycle-Type CO2 Fixation: A Perspective. |
| Q47605873 | Origins and emergent evolution of life: the colloid microsphere hypothesis revisited |
| Q43670470 | Origins of life: a route to nanotechnology |
| Q58288495 | Palaeontology of Devonian thermal spring deposits, Drummond Basin, Australia |
| Q55898622 | Panspermia in the context of the timing of the origin of life and microbial phylogeny |
| Q44923251 | Peptide and RNA contributions to iron-sulphur chemical gardens as life's first inorganic compartments, catalysts, capacitors and condensers. |
| Q24793636 | Phylogenetic analysis of bacterial and archaeal arsC gene sequences suggests an ancient, common origin for arsenate reductase |
| Q34183627 | Prebiological evolution and the metabolic origins of life |
| Q41058413 | Prebiotic selection for motifs in a model of template-free elongation of polymers within compartments. |
| Q55053676 | Prebiotic synthesis of protobiopolymers under alkaline ocean conditions. |
| Q21203798 | Predicting the conformations of peptides and proteins in early evolution. A review article submitted to Biology Direct |
| Q79864155 | Pressure effects on the abiotic polymerization of glycine |
| Q28655007 | Primal eukaryogenesis: on the communal nature of precellular States, ancestral to modern life |
| Q34722099 | Primary producing prokaryotic communities of brine, interface and seawater above the halocline of deep anoxic lake L'Atalante, Eastern Mediterranean Sea. |
| Q36025633 | Primordial soup or vinaigrette: did the RNA world evolve at acidic pH? |
| Q91106656 | Promotion of protocell self-assembly from mixed amphiphiles at the origin of life |
| Q28829212 | Proteomic indicators of oxidation and hydration state in colorectal cancer |
| Q46481071 | Pyrite surface environment drives molecular adsorption: cystine on pyrite(100) investigated by X-ray photoemission spectroscopy and low energy electron diffraction |
| Q57794083 | Quantum chemistry reveals thermodynamic principles of redox biochemistry |
| Q47596971 | Reactivity of CO2 on the surfaces of magnetite (Fe3O4), greigite (Fe3S4) and mackinawite (FeS). |
| Q92929539 | Realtime Observation of Diffusing Elements in a Chemical Garden |
| Q44354889 | Reduction of nitrite and nitrate on nano-dimensioned FeS. |
| Q47802338 | Reduction of nitrite and nitrate to ammonium on pyrite |
| Q43029132 | Reply to 'Is LUCA a thermophilic progenote?' |
| Q36474674 | Role of pK(a) of nucleobases in the origins of chemical evolution |
| Q47686436 | Scanning tunnelling microscopy and molecular modelling of xanthine monolayers self-assembled at the solid-liquid interface: relevance to the origin of life |
| Q41855895 | Selective orbital reconstruction in tetragonal FeS: A density functional dynamical mean-field theory study |
| Q91694895 | Serpentinization: Connecting Geochemistry, Ancient Metabolism and Industrial Hydrogenation |
| Q58246502 | Session 5 – Origin and evolution of life: evidence from ancient mineral deposits |
| Q28740456 | Single-molecule paleoenzymology probes the chemistry of resurrected enzymes |
| Q46486851 | Sites for phosphates and iron-sulfur thiolates in the first membranes: 3 to 6 residue anion-binding motifs (nests). |
| Q58913446 | Softening the “Crystal Scaffold” for Life’s Emergence |
| Q34708811 | Spiral precipitation patterns in confined chemical gardens. |
| Q50891934 | Spontaneous formation of complex structures made from elastic membranes in an aluminum-hydroxide-carbonate system. |
| Q47610499 | Subsumed complexity: abiogenesis as a by-product of complex energy transduction |
| Q64028842 | Surfactant Assemblies and their Various Possible Roles for the Origin(S) of Life |
| Q34297826 | Systems biology perspectives on minimal and simpler cells |
| Q47200239 | The "Origin-of-Life Reactor" and Reduction of CO2 by H2 in Inorganic Precipitates |
| Q28596454 | The Astrobiology Primer v2.0 |
| Q73306024 | The Birthplace of Proto-Life: Role of Secondary Minerals in Forming Metallo-Proteins through Water-Rock Interaction of Hadean Rocks |
| Q41990546 | The Fe-rich clay microsystems in basalt-komatiite lavas: importance of Fe-smectites for pre-biotic molecule catalysis during the Hadean eon. |
| Q92005339 | The Hot Spring Hypothesis for an Origin of Life |
| Q39428730 | The Hypothesis that the Genetic Code Originated in Coupled Synthesis of Proteins and the Evolutionary Predecessors of Nucleic Acids in Primitive Cells |
| Q46289813 | The Possible Emergence of Life and Differentiation of a Shallow Biosphere on Irradiated Icy Worlds: The Example of Europa |
| Q24614775 | The RNA world hypothesis: the worst theory of the early evolution of life (except for all the others)(a) |
| Q38671099 | The Role of Hydrogen Sulfide in Evolution and the Evolution of Hydrogen Sulfide in Metabolism and Signaling |
| Q28647611 | The Significance of Microbe-Mineral-Biomarker Interactions in the Detection of Life on Mars and Beyond |
| Q34317225 | The algorithmic origins of life |
| Q24672194 | The cosmological model of eternal inflation and the transition from chance to biological evolution in the history of life |
| Q28658605 | The drive to life on wet and icy worlds |
| Q46978783 | The effects of ferrous and other ions on the abiotic formation of biomolecules using aqueous aerosols and spark discharges. |
| Q41130504 | The energetics of anabolism in natural settings |
| Q57859248 | The environment of early Mars and the missing carbonates |
| Q37827251 | The evolution of organic matter in space |
| Q35752527 | The ineluctable requirement for the trans-iron elements molybdenum and/or tungsten in the origin of life. |
| Q28681335 | The inevitable journey to being |
| Q58775339 | The last universal common ancestor between ancient Earth chemistry and the onset of genetics |
| Q92342005 | The microbiomes of deep-sea hydrothermal vents: distributed globally, shaped locally |
| Q35172166 | The origin and emergence of life under impact bombardment |
| Q46276794 | The origin of heredity in protocells. |
| Q28755444 | The origin of modern terrestrial life |
| Q57134882 | The origins of cellular life |
| Q29391568 | The physiology and habitat of the last universal common ancestor |
| Q42048347 | The possible role of volcanic aquifers in prebiologic genesis of organic compounds and RNA. |
| Q28081004 | The production of methane, hydrogen, and organic compounds in ultramafic-hosted hydrothermal vents of the Mid-Atlantic Ridge |
| Q36325067 | The progene hypothesis: the nucleoprotein world and how life began |
| Q40874762 | The redox protein construction kit: pre-last universal common ancestor evolution of energy-conserving enzymes |
| Q37734958 | The role of natural selection in the origin of life |
| Q28710471 | The significance of Mg in prebiotic geochemistry |
| Q24672457 | The stability of the RNA bases: implications for the origin of life |
| Q33241702 | The versatile epsilon-proteobacteria: key players in sulphidic habitats |
| Q28236859 | Thermal energy and the origin of life |
| Q43457644 | Thermodynamics, Disequilibrium, Evolution: Far-From-Equilibrium Geological and Chemical Considerations for Origin-Of-Life Research |
| Q36798085 | Third-generation synchrotron x-ray diffraction of 6-microm crystal of raite, approximately Na3Mn3Ti0.25Si8O20(OH)2.10H2O, opens up new chemistry and physics of low-temperature minerals |
| Q47097852 | Toy trains, loaded dice and the origin of life: dimerization on mineral surfaces under periodic drive with Gaussian inputs |
| Q28770147 | Tubular precipitation and redox gradients on a bubbling template |
| Q51365259 | Tubular precipitation structures: materials synthesis under non-equilibrium conditions. |
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