Inherited geochemical diversity of 3.4 Ga organic films from the Buck Reef Chert, South Africa

International audienceArchean rocks contain crucial information about the earliest life forms on Earth, but documenting these early stages of biological evolution remains challenging. The main issue lies in the geochemical transformations experienced by Archean organic matter through its multibillion-year geological history. Here we present spatially resolved chemical investigations conducted on 3.4 Ga organic films from the Buck Reef Chert, South Africa which indicate that they possess significantly different chemical compositions. Since these organic films allunderwent the same post-depositional geological history, this geochemical diversity is most likely inherited, reflecting original chemical differences which were not completely obliterated by subsequent burial-induced degradation processes. These results demonstrate that earlyArchean organic films carry chemical information directly related to their original molecular compositions. This paves the way for the reconstruction of the initial chemical nature of organic microfossils found in ancient rocks, provided that the geologically-induced chemicaltransformations they underwent are properly constrained

External controls on the distribution, fabrics and mineralization of modern microbial mats in a coastal hypersaline lagoon, Cayo Coco (Cuba).

45 pagesInternational audienceActive, carbonate-mineralizing microbial mats flourish in a tropical, highly evaporative, marine-fed lagoonal network to the south of Cayo Coco Island (Cuba). Hypersaline conditions support the development of a complex sedimentary microbial ecosystem with diverse morphologies, a variable intensity of mineralization and a potential for preservation. In this study, the role of intrinsic (i.e. microbial) and extrinsic (i.e. physicochemical) controls on microbial mat development, mineralization and preservation was investigated. The network consists of lagoons, forming in the interdune depressions of a Pleistocene aeolian substratum; they developed due to a progressive increase in sea-level since the Holocene. The hydrological budget in the Cayo Coco lagoonal network changes from west to east, increasing the salinity. This change progressively excludes grazers and increases the saturation index of carbonate minerals, favouring the development and mineralization of microbial mats in the easternmost lagoons. Detailed mapping of the easternmost lagoon shows four zones with different flooding regimes. The microbial activity in the mats was recorded using light–dark shifts in conjunction with microelectrode O2 and HS− profiles. High rates of O2 production and consumption, in addition to substantial amounts of exopolymeric substances, are indicative of a potentially strong intrinsic control on mineralization. Seasonal, climate-driven water fluctuations are key for mat development, mineralization, morphology and distribution. Microbial mats show no mineralization in the permanently submersed zone, and moderate mineralization in zones with alternating immersion and exposure. It is suggested that mineralization is also driven by water-level fluctuations and evaporation. Mineralized mats are laminated and consist of alternating trapping and binding of grains and microbially induced magnesium calcite and dolomite precipitation. The macrofabrics of the mats evolve from early colonizing Flat mats to complex Cerebroid or Terrace structures. The macrofabrics are influenced by the hydrodynamic regime: wind-driven waves inducing relief terraces in windward areas and flat morphologies on the leeward side of the lagoon. Other external drivers include: (i) storm events that either promote (for example, by bioclasts covering) or prevent (for example, by causing erosion) microbial mat preservation; and (ii) subsurface degassing, through mangrove roots and desiccation cracks covered by Flat mats (i.e. forming Hemispheroids and Cerebroidal structures). These findings provide in-depth insights into understanding fossil microbialite morphologies that formed in lagoonal settings

Intense biogeochemical iron cycling revealed in Neoarchean micropyrites from stromatolites

International audienceIron isotope compositions of sedimentary pyrites (FeS2) are used to constrain the redox evolution of the Precambrian ocean and early Fe-based metabolisms such as Dissimilatory Iron Reduction (DIR). Sedimentary pyrites can record biotic and abiotic iron reduction, which have similar ranges of Fe isotopic fractionation, as well as post-depositional histories and metamorphic overprints that can modify Fe isotope compositions. However, some exceptionally well-preserved sedimentary records, such as the stromatolite-bearing Tumbiana Formation (ca. 2.7 Ga, Western Australia) have been proven to retain primary information on Early Neoarchean microbial ecosystems and associated metabolic pathways. Here, we present in situ Fe isotope measurements of micropyrites included in four stromatolites from the Tumbiana Formation in order to assess iron respiration metabolism using Fe isotope signatures. A set of 142 micropyrites has been analyzed in three lamina types, i.e. micritic, organic-rich and fenestral laminae, by Secondary Ion Mass Spectrometry (SIMS), using a Hyperion radio-frequency plasma source. The diversity of laminae is attributed to specific depositional environments, leading to the formation of Type 1 (micritic laminae) and Type 2 (organic-rich laminae) and early diagenetic effects (Type 3, fenestral laminae). Type 1 and 2 laminae preserved comparable δ56Fe ranges, respectively from −1.76‰ to +4.15‰ and from −1.54‰ to +4.44‰. Type 3 laminae recorded a similar range, although slightly more negative δ56Fe values between −2.20‰ and +2.65‰. Globally, our data show a large range of δ56Fe values, from −2.20‰ to +4.44‰, with a unimodal distribution that differs from the bimodal distribution previously reported in the Tumbiana stromatolites. Such a large range and unimodal distribution cannot be explained by a unique process (e.g., biotic/abiotic Fe reduction or pyrite formation only controlled by the precipitation rate). It rather could reflect a two-step iron cycling process in the sediment pore water including i) partial Fe oxidation forming Fe(OH)3 with positive δ56Fe values followed by ii) partial, possibly microbially induced, Fe reduction leading to Fe2+ availability for pyrite formation by sulfate reducers carrying both negative δ56Fe and δ34S signatures. In this model, the buildup and subsequent reduction through time of a residual Fe(OH)3 reservoir arising from the activity of methanotrophs, can explain the strongly positive δ56FeFe(OH)3 values up to 4‰. These results indicate that Archean microbial mats have been the site of the interaction of several closely linked biogeochemical cycles involving Fe, S and C

Multiple Sulfur Isotope Records of the 3.22 Ga Moodies Group, Barberton Greenstone Belt

Co-auteur étrangerInternational audienceThe Moodies Group, the uppermost unit in the Barberton Greenstone Belt (BGB) in SouthAfrica, is a ~3.7-km-thick coarse clastic succession accumulated on terrestrial-to-shallow marinesettings at around 3.22 Ga. The multiple sulfur isotopic composition of pyrite of Moodies intervalswas newly obtained to examine the influence of these depositional settings on the sulfur isotope record.Conglomerate and sandstone rocks were collected from three synclines north of the Inyoka Fault of thecentral BGB, namely, the Eureka, Dycedale, and Saddleback synclines. The sulfur isotopic compositionof pyrite was analyzed by Secondary Ion Mass Spectrometry (SIMS) for 6 samples from the threesynclines and by Isotope Ratio Mass Spectrometry (IR-MS) for 17 samples from a stratigraphic sectionin the Saddleback Syncline. The present results show a signal of mass-independent fractionation ofsulfur isotopes (S-MIF), although t-tests statistically demonstrated that the Moodies S-MIF signals(mostly 0% < D33S < +0.5%) are significantly small compared to the signal of the older Paleoarchean(3.6–3.2 Ga) records. These peculiar signatures might be related to initial deposition of detrital pyriteof juvenile origin from the surrounding intrusive (tonalite–trondhjemite–granodiorite; TTG) andfelsic volcanic rocks, and/or to secondary addition of hydrothermal sulfur during late metasomatism.Moreover, fast accumulation (~0.1–1 mm/year) of the Moodies sediments might have led to a reducedaccumulation of sulfur derived from an atmospheric source during their deposition. As a result, thesulfur isotopic composition of the sediments may have become susceptible to the secondary additionof metasomatic sulfur on a mass balance point of view. The sulfur isotopic composition of Moodiespyrite is similar to the composition of sulfides from nearby gold mines. It suggests that, after theMoodies deposition, metasomatic pyrite formation commonly occurred north of the Inyoka Fault inthe central BGB at 3.1–3.0 Ga

General palaeontology (Palaeobiochemistry) Biological activity and the Earth&apos;s surface evolution: Insights from carbon, sulfur, nitrogen and iron stable isotopes in the rock record

Abstract The search for early Earth biological activity is hindered by the scarcity of the rock record. The very few exposed sedimentary rocks have all been affected by secondary processes such as metamorphism and weathering, which might have distorted morphological microfossils and biogenic minerals beyond recognition and have altered organic matter to kerogen. The search for biological activity in such rocks therefore relies entirely on chemical, molecular or isotopic indicators. A powerful tool used for this purpose is the stable isotope signature of elements related to life (C, N, S, Fe). It provides key informations not only on the metabolic pathways operating at the time of the sediment deposition, but more globally on the biogeochemical cycling of these elements and thus on the Earth&apos;s surface evolution. Here, we review the basis of stable isotope biogeochemistry for these isotopic systems. Rather than an exhaustive approach, we address some examples to illustrate how they can be used as biosignatures of early life and as proxies for its environment, while keeping in mind what their limitations are. We then focus on the covariations among these isotopic systems during the Archean time period to show that they convey important information both on the evolution of the redox state of the terrestrial surface reservoirs and on co-occurring ecosystems in the Archean. Résumé Apport des isotopes stables (C, N, S, Fe) à l&apos;étude des interrelations entre activités biologiques et conditions physicochimiques de surface de la terre primitive. La recherche et la caractérisation des écosystèmes à la surface de la Terre primitive sont un défi, étant donné le faible degré de préservation des roches archéennes. Les quelques formations sédimentaires disponibles ont, en effet, été modifiées par de nombreux processus secondaires (métamorphisme, altération) qui excluent toute diagnose morphologique robuste des microfossiles et des minéraux associés. La recherche de traces de vie fossile et la caractérisation des environnements contemporains du dépôt reposent ainsi sur des indices chimiques dont les plus robustes sont les isotopes stables. Dans ce manuscrit, nous tenterons de résumer les bases de la biogéochimie des isotopes stables et nous illustrerons comment cette discipline peut permettre d&apos;apporter des contraintes sur la vie primitive et son environnement. Quelques exemples choisis dans différents systèmes isotopiques pertinents pour l&apos;étude de la vie (C, N, S, Fe) et pour l&apos;étude des conditions d&apos;oxydation de surface de la Terre primitiv

Biological Soil Crusts as Modern Analogues for the Archean Continental Biosphere: Insights from Carbon and Nitrogen Isotopes

5 pagesInternational audienceStable isotope signatures of elements related to life such as carbon and nitrogen can be powerful biomarkers that provide key information on the biological origin of organic remains and their paleoenvironments. Marked advances have been achieved in the last decade in our understanding of the coupled evolution of biological carbon and nitrogen cycling and the chemical evolution of the early Earth thanks, in part, to isotopic signatures preserved in fossilized microbial mats and organic matter of marine origin. However, the geologic record of the early continental biosphere, as well as its evolution and biosignatures, is still poorly constrained. Following a recent report of direct fossil evidence of life on land at 3.22 Ga, we compare here the carbon and nitrogen isotopic signals of this continental Archean biosphere with biosignatures of cyanobacteria biological soil crusts (cyanoBSCs) colonizing modern arid environments. We report the first extended δ13C and δ15N data set from modern cyanoBSCs and show that these modern communities harbor specific isotopic biosignatures that compare well with continental Archean organic remains. We therefore suggest that cyanoBSCs are likely relevant analogs for the earliest continental ecosystems. As such, they can provide key information on the timing, extent, and possibly mechanism of colonization of the early Earth's emergent landmasses

General palaeontology (Palaeobiochemistry) Biological activity and the Earth&apos;s surface evolution: Insights from carbon, sulfur, nitrogen and iron stable isotopes in the rock record

Abstract The search for early Earth biological activity is hindered by the scarcity of the rock record. The very few exposed sedimentary rocks have all been affected by secondary processes such as metamorphism and weathering, which might have distorted morphological microfossils and biogenic minerals beyond recognition and have altered organic matter to kerogen. The search for biological activity in such rocks therefore relies entirely on chemical, molecular or isotopic indicators. A powerful tool used for this purpose is the stable isotope signature of elements related to life (C, N, S, Fe). It provides key informations not only on the metabolic pathways operating at the time of the sediment deposition, but more globally on the biogeochemical cycling of these elements and thus on the Earth&apos;s surface evolution. Here, we review the basis of stable isotope biogeochemistry for these isotopic systems. Rather than an exhaustive approach, we address some examples to illustrate how they can be used as biosignatures of early life and as proxies for its environment, while keeping in mind what their limitations are. We then focus on the covariations among these isotopic systems during the Archean time period to show that they convey important information both on the evolution of the redox state of the terrestrial surface reservoirs and on co-occurring ecosystems in the Archean. Résumé Apport des isotopes stables (C, N, S, Fe) à l&apos;étude des interrelations entre activités biologiques et conditions physicochimiques de surface de la terre primitive. La recherche et la caractérisation des écosystèmes à la surface de la Terre primitive sont un défi, étant donné le faible degré de préservation des roches archéennes. Les quelques formations sédimentaires disponibles ont, en effet, été modifiées par de nombreux processus secondaires (métamorphisme, altération) qui excluent toute diagnose morphologique robuste des microfossiles et des minéraux associés. La recherche de traces de vie fossile et la caractérisation des environnements contemporains du dépôt reposent ainsi sur des indices chimiques dont les plus robustes sont les isotopes stables. Dans ce manuscrit, nous tenterons de résumer les bases de la biogéochimie des isotopes stables et nous illustrerons comment cette discipline peut permettre d&apos;apporter des contraintes sur la vie primitive et son environnement. Quelques exemples choisis dans différents systèmes isotopiques pertinents pour l&apos;étude de la vie (C, N, S, Fe) et pour l&apos;étude des conditions d&apos;oxydation de surface de la Terre primitiv

Microbial and diagenetic steps leading to the mineralisation of Great Salt Lake microbialites.

12 pagesInternational audienceMicrobialites are widespread in modern and fossil hypersaline environments, where they provide a unique sedimentary archive. Authigenic mineral precipitation in modern microbialites results from a complex interplay between microbial metabolisms, organic matrices and environmental parameters. Here, we combined mineralogical and microscopic analyses with measurements of metabolic activity in order to characterise the mineralisation of microbial mats forming microbialites in the Great Salt Lake (Utah, USA). Our results show that the mineralisation process takes place in three steps progressing along geochemical gradients produced through microbial activity. First, a poorly crystallized Mg-Si phase precipitates on alveolar extracellular organic matrix due to a rise of the pH in the zone of active oxygenic photosynthesis. Second, aragonite patches nucleate in close proximity to sulfate reduction hotspots, as a result of the degradation of cyanobacteria and extracellular organic matrix mediated by, among others, sulfate reducing bacteria. A final step consists of partial replacement of aragonite by dolomite, possibly in neutral to slightly acidic porewater. This might occur due to dissolution-precipitation reactions when the most recalcitrant part of the organic matrix is degraded. The mineralisation pathways proposed here provide pivotal insight for the interpretation of microbial processes in past hypersaline environments

New thylacocephalans from the Early Triassic Paris Biota (Bear Lake County, Idaho, USA).

International audienceTwo new genera and species of thylacocephalans (Arthropoda, Thylacocephala), Parisicaris triassica Charbonnier and Ligulacaris parisiana Charbonnier, are described from the early Spathian Paris Biota. These new occurrences are the first reports of thylacocephalans from Triassic rocks in North America. They considerably enlarge the spatiotemporal distribution of these enigmatic arthropods and highlight their relatively high generic richness during the Early Triassic. It also confirms that the Triassic was the taxonomically richest period for Thylacocephala