Geological and trace element evidence for a marine sedimentary environment of deposition and biogenicity of 3.45 Ga stromatolitic carbonates in the Pilbara Craton, and support for a reducing Archaean ocean

Bedded carbonate rocks from the 3.45 Ga Warrawoona Group, Pilbara Craton, contain structures that have been regarded either as the oldest known stromatolites or as abiotic hydrothermal deposits. We present new field and petrological observations and high‐precision REE + Y data from the carbonates in order to test the origin of the deposits. Trace element geochemistry from a number of laminated stromatolitic dolomite samples of the c. 3.40 Ga Strelley Pool Chert conclusively shows that they precipitated from anoxic seawater, probably in a very shallow environment consistent with previous sedimentological observations. Edge‐wise conglomerates in troughs between stromatolites and widespread cross‐stratification provide additional evidence of stromatolite construction, at least partly, from layers of particulate sediment, rather than solely from rigid crusts. Accumulation of particulate sediment on steep stromatolite sides in a high‐energy environment suggests organic binding of the surface. Relative and absolute REE + Y contents are exactly comparable with Late Archaean microbial carbonates of widely agreed biological origin. Ankerite from a unit of bedded ankerite–chert couplets from near the top of the stratigraphically older (3.49 Ga) Dresser Formation, which immediately underlies wrinkly stromatolites with small, broad, low‐amplitude domes, also precipitated from anoxic seawater. The REE + Y data of carbonates from the Strelley Pool Chert and Dresser Formation contrast strongly with those from siderite layers in a jasper–siderite–Fe‐chlorite banded iron‐formation from the base of the Panorama Formation (3.45 Ga), which is clearly hydrothermal in origin. The geochemical results, together with sedimentological data, strongly support: (1) deposition of Dresser Formation and Strelley Pool Chert carbonates from Archaean seawater, in part as particulate carbonate sediment; (2) biogenicity of the stromatolitic carbonates; (3) a reducing Archaean atmosphere; (4) ongoing extensive terrestrial erosion prior to ～3.45 Ga.     

Early Neoproterozoic well-preserved stromatolites from southern Liaoning,North China: characteristics and paleogeographic implications

We report morphology and microstructure of the stromatolites of the Ganjingzi Formation in southern Liaoning. Sedimentologic and morphologic analyses indicate that the lower stromatolite mounds formed in a transgressive succession, while the stromatolite columns in the more complex upper biostrome changed vertically from dispersed growth to dense clumping. Biostratigraphic analysis shows that the stromatolites in the Ganjingzi Formation are similar to those from coeval strata in the Xuzhou-Huainan Region and in southern Jilin. Comparisons of the morphotype genera of stromatolites and the sedimentary setting between different areas, imply that sea-level was fluctuating in the east of the North China Craton (NCC) during the Ganjingzi interval and that the transgressions were beneficial to stromatolite growth, as indicated by the increased number of stromatolites in the study area.     

Bioclaustration trace fossils in epeiric shallow marine stromatolites: the Cretaceous‐Palaeogene Yacoraite Formation,Northwestern Argentina

The shallow carbonate facies at the top of the Yacoraite Formation (Late Cretaceous–Early Palaeocene) in the Metán sub‐basin, Salta Basin (Cretaceous‐Eocene), northern Argentina, have domal stromatolitic boundstones with peculiar cavities, interpreted here as bioclaustrations. The cavities appear to have been produced by organisms that lived within the microbial mat contemporarily with its growth, producing a distinctive ichnofabric. This is the oldest reported record of bioclaustrations in stromatolites, and the first in shallow marine environments. The interpretation of the facies suggests a stressed shallow, restricted setting with variations in salinity, represented by an intertidal environment with an extensive tidal flat. Bioclaustrations, stromatolites, endobiont Yacoraite Formation (Cretaceous‐Palaeogene), Northwestern Argentina.     

Lithostratigraphic analysis of a new stromatolite–thrombolite reef from across the rise of atmospheric oxygen in the Paleoproterozoic Turee Creek Group,Western Australia

This study describes a previously undocumented dolomitic stromatolite–thrombolite reef complex deposited within the upper part (Kazput Formation) of the c. 2.4–2.3 Ga Turee Creek Group, Western Australia, across the rise of atmospheric oxygen. Confused by some as representing a faulted slice of the younger c. 1.8 Ga Duck Creek Dolomite, this study describes the setting and lithostratigraphy of the 350‐m‐thick complex and shows how it differs from its near neighbour. The Kazput reef complex is preserved along 15 km of continuous exposure on the east limb of a faulted, north‐west‐plunging syncline and consists of 5 recognisable facies associations (A–E), which form two part regressions and one transgression. The oldest facies association (A) is characterised by thinly bedded dololutite–dolarenite, with local domical stromatolites. Association B consists of interbedded columnar and stratiform stromatolites deposited under relatively shallow‐water conditions. Association C comprises tightly packed columnar and club‐shaped stromatolites deposited under continuously deepening conditions. Clotted (thrombolite‐like) microbialite, in units up to 40 m thick, dominates Association D, whereas Association E contains bedded dololutite and dolarenite, and some thinly bedded ironstone, shale and black chert units. Carbon and oxygen isotope stratigraphy reveals a narrow range in both δ¹³C_carb values, from ?0.22 to 0.97‰ (VPDB: average = 0.68‰), and δ¹⁸O values, from ?14.8 to ?10.3‰ (VPDB), within the range of elevated fluid temperatures, likely reflecting some isotopic exchange. The Kazput Formation stromatolite–thrombolite reef complex contains features of younger Paleoproterozoic carbonate reefs, yet is 300–500 Ma older than previously described Proterozoic examples worldwide. Significantly, the microbial fabrics are clearly distinct from Archean stromatolitic marine carbonate reefs by way of containing the first appearance of clotted microbialite and large columnar stromatolites with complex branching arrangements. Such structures denote a more complex morphological expression of growth than previously recorded in the geological record and may link to the rise of atmospheric oxygen.     

再论假裸枝叠层石科

概要地介绍了假裸枝科叠层石的特征、分布时限、分类系统、研究方法和形成环境.提出该科叠层石有可能作为我国中元古代乃至蓟县系叠层石标志的意见.     

THE ROLE OF DIATOMS IN STROMATOLITE GROWTH: TWO EXAMPLES FROM MODERN FRESHWATER SETTINGS1

Some modern laminated and calcified stromatolitic structures are partially or completely formed by eukaryotes. Diatom populations in freshwater environments with elevated ionic concentrations contribute to calcite precipitation, and the formation of distinctive mineral-rich stromatolitic laminae. Two types of stromatolite-forming diatom populations were observed. In the first example, in stromatolies growing on a quarry ledge near Laegerdorf, North Germany, calcite crystals with biogenic imprints form around polysaccharide stalks of the diatom Gomphonema olivaceum var. calcarea (Cleve) Cleve-Euler. These individually precipitated crystals eventunally become cemented together in layers, forming rigid, laminated stromatolitic deposits which drape over the quarry ledge. In the second example, in stromatolites forming in a shallow stream near Cuatro Ciénegas, Coahuila, Mexico, diatomaceous laminae also form by the accumulation of carbonate particles in a matrix of diatoms and their extracellular polysaccharide products. These laminae become thick enough to drape over individual stromatolite heads. The diatoms responsible for these deposits are Amphora aff. A. Katii Selva, Nitzschia denticula Grun., and six other species. At Cuatro Ciénegas, in addition to the diatomaceous laminae, carbonate-rich cyanobacterial layers, dominated by two cyanobacterial species with different fabrics and porosities, are also present and contribute substantially to the growth of the stromatolites. In both the Laegerdorf and Cuatro Ciénegas examples, entire stromatolites or thick laminations on stromatolites are built by a small number of diatom species which produce copious amounts of extracellular stalk, gel, and sheath material, a property they share with cyanobacterial stromatolite builders.     

台湾地区上下第三系界线划分的孢粉学证据

通过对台湾中部南投县国姓地区北港溪剖面的孢粉样品分析,结合已有的台湾北部基隆地区万里－大武仑露头剖面的孢粉资料,认为台湾地区上下第三系界线置于炭寮地层与十四股层（南投）或公馆凝灰岩与木山层（基隆）之间较为合理。其孢粉组合特征,反映出古气候由晚渐新世经含桤木粉－松粉孢粉组合为特征的寒冷潮湿的北亚热带型向早中新世以含榆科、栎属孢粉组合为特征的温暖湿润的南亚热带型过渡趋势。由于南海北部大陆架北坡的珠海组     

THE ROLE OF DIATOMS IN STROMATOLITE GROWTH: TWO EXAMPLES FORM MODERN FRESHWATER SETTINGS1

Some modern laminated find calcified stromatolitic structures are partially or completely formed by eukaryotes. Diatom populations in freshwater environments with elevated ionic concentrations contribute to calcite precipitation, and the formation of distinctive mineral-rich stromatolitic laminae. Two types of stromatolite-forming diatom populations were observed. In the first example, in stromatolites growing on a quarry ledge near Laegerdorf, North Germany, calcite crystals with biogenic imprints form around polysaccharide stalks of the diatom Gomphonema olivaceum var. calcarea (Cleve) Cleve-Euler. These individually precipitated crystals eventually become cemented together in layers, forming rigid, laminated stromatolitic deposits which drape over the quarry ledge. In the second example, in stromatolites forming in a shallow stream near Cuatro Ciénegas, Coahuila, Mexico, diatomaceous laminae also form by the accumulation of carbonate particles in a matrix of diatoms and their extracellular polysaccharide products. These laminae become thick enough to drape over individual stromatolite heads. The diatoms responsible for these deposits are Amphora aff. A. katii Selva, Nitzschia denticula Grun., and six other species. At Cuatro Ciénegas, in addition to the diatomaceous laminae, carbonate-rich cyanobacterial layers, dominated by two cyanobacterial species with different fabrics and porosities, are also present and contribute substantially to the growth of the stromatolites. In both the Laegerdorf and Cuatro Ciénegas examples, entire stromatolites or thick laminations on stromatolites are built by a small number of diatom species which produce copious amounts of extracellular stalk, gel, and sheath material, a propertuy they share with cyanobacterial stromatolite builders.     

Algal stromatolites from the Late Precambrian of Sweden

Stromatolitic structures from the Late Precambrian Visingö Beds are described. The mode of development of these sedimentary-biogenic structures and the problems related to their characterization in a system of formulas are discussed. The study of the stromatolitic structures and their associated sediments proved that the stromatolitic structures LLH (vertically arranged, lateral-linked hemispher-oids) and SH (discrete, vertically stacked hemispheroids) could develop together on the same stromatolite dome, depending on different degrees of exposure to the action of water currents in an intertidal environment. Superimposed LLH and SH structures in the Visingsö Beds may indicate periodical changes in current activity depending on repeated periodic events such as tidal and/or storm waves.     

皖南石台下奥陶统仑山组的叠层石

扬子区东南台缘下奥陶统特马道克阶仑山组上段多见厚层碳酸盐岩,其中的叠层石礁出露厚度23m,穹窿状叠层石密集生长序列厚度20m,往上部的3m叠层石变得稀少。微相特征显示叠层石的纹层多不清晰,存在不同程度的生物、物理及化学营力的干扰现象,可识别数种成因。生物对藻席表面的啃食和内部的栖居钻孔可破坏纹层;高能水流时常带入的生屑、砂屑堆积能点断叠层石纹层的正常生长;部分叠层石中常见压溶缝合线和白云岩化。区域海退过程抑制了叠层石礁的连续生长。     

Formation of micro‐spherulitic barite in association with organic matter within sulfidized stromatolites of the 3.48 billion‐year‐old Dresser Formation,Pilbara Craton

The shallow marine and subaerial sedimentary and hydrothermal rocks of the ~3.48 billion‐year‐old Dresser Formation are host to some of Earth's oldest stromatolites and microbial remains. This study reports on texturally distinctive, spherulitic barite micro‐mineralization that occur in association with primary, autochthonous organic matter within exceptionally preserved, strongly sulfidized stromatolite samples obtained from drill cores. Spherulitic barite micro‐mineralization within the sulfidized stromatolites generally forms submicron‐scale aggregates that show gradations from hollow to densely crystallized, irregular to partially radiating crystalline interiors. Several barite micro‐spherulites show thin outer shells. Within stromatolites, barite micro‐spherulites are intimately associated with petrographically earliest dolomite and nano‐porous pyrite enriched in organic matter, the latter of which is a possible biosignature assemblage that hosts microbial remains. Barite spherulites are also observed within layered barite in proximity to stromatolite layers, where they are overgrown by compositionally distinct (Sr‐rich), coarsely crystalline barite that may have been sourced from hydrothermal veins at depth. Micro‐spherulitic barite, such as reported here, is not known from hydrothermal systems that exceed the upper temperature limit for life. Rather, barite with near‐identical morphology and micro‐texture is known from zones of high bio‐productivity under low‐temperature conditions in the modern oceans, where microbial activity and/or organic matter of degrading biomass controls the formation of spherulitic aggregates. Hence, the presence of micro‐spherulitic barite in the organic matter‐bearing Dresser Formation sulfidized stromatolites lend further support for a biogenic origin of these unusual, exceptionally well‐preserved, and very ancient microbialites.     

Subtidal stromatolites from the Sinemurian of the Lusitanian Basin (Portugal)

Well-preserved dome-shaped carbonate stromatolites occur in the lowermost part of the Sinemurian of the Lusitanian Basin (Portugal), at S. Pedro de Moel region (W of the basin). Deposition in the region took place on a westward-dipping carbonate ramp. The stromatolitic mounds are not found anywhere else in the Sinemurian of the basin and therefore are regarded as specific bioevents. In contrast to marginal-marine stromatolitic crusts, subtidal carbonate mounds other than sponge-mounds have been seldom reported in the Lower Jurassic, in particular in the Sinemurian, either from Europe or North-Africa. Therefore, the case documented here contributes to enhance the knowledge on stromatolites of this age in the Peri-Tethyan and Proto-Atlantic regions. The depositional setting of the studied succession is interpreted as a mainly low-energy, restricted marine one, punctuated by higher-energy episodes and, locally, subjected to more open marine influence. The existence of a topographic high and detached shoals at a more distal location of the ramp is likely, considering regional seismic evidence, the record in offshore (to the W) wells of peloidal/ooid wacke-packstones with detrital quartz and occurrence of a few ooid grainstones in the studied section. The inferred positive relief would act as a physical constraint that, coupled with the low-gradient of the ramp, defined an embayment-like environment in which the prevailing ecological conditions must have been, for the part of the succession bearing the stromatolites, unfavorable for many benthic organisms, favoring the microbial community. The upper part of the succession suggests stepwise environmental openness to more marine influence alternating with frequent environmental restriction.     

Stromatolite biostromes and associated facies in the late precambrian porsanger dolomite formation of Finnmark,Arctic Norway

The Late Precambrian Porsanger Dolomite Formation, occurring beneath the Varanger tillite in Arctic Norway, consists of various dolomitic lithofacies of subtidal, intertidal and supratidal environments. The lithofacies belong to three facies associations, A, B and C, which are repeated several times in the sequence. Facies association A comprises cryptalgal laminites, dolomicrites and thin-bedded grainstones and flakestones. The environment represented by this facies is broadly intertidal (locally supratidal) flat, with the interbedded carbonate sands representing storm deposits. Facies association B, of shallow subtidal to low intertidal origin, comprises cross-bedded carbonate sands (flakestones, grainstones and oolites) forming units up to 10 m thick. Small stromatolite bioherms (5 m wide, 2 m high) are locally developed within these “high-energy” deposits. Facies association C formed in a subtidal environment consists of laterally extensive (over 20 km) uniformly developed stromatolite biostromes, up to 16 m thick. The biostromes, locally divided by channels filled with grainstones and intraformational conglomerates, are composed of cylindrical and turbinate columnar (SH-V and SH-C) and digitate stromatolites (Gymnosolen, Inseria and Tungussia) in their lower parts. Larger, bulbous (SH-C and LLH-C) and conical (Conophyton) stromatolites occur in the upper parts, as well as the branching conophyte, Jacutophyton.All of the biostromes are always developed above cross-bedded carbonate sands (facies association B). A broadly symmetrical cyclic pattern, A B C B A, of tidal flat deposits (facies association A) passing up into carbonate sands (B), into biostrome (C), overlain by carbonate sands (B) and then tidal flat deposits (A), is repeated four times in the Porsanger Dolomite sequence. The pattern is interpreted in terms of two controls on sedimentation: (1) a slow transgressive phase followed by (2) depositional regression. The former (1) took place either through eustatic sea-level rise or more likely through accelerated subsidence because of tectonic instability and compaction of underlying sediments. This resulted in the sequence: tidal flat sediments, low intertidal/shallow subtidal carbonate sands, subtidal biostrome (A, B, C). Depositional regression through prograding tidal flats, generated the shoaling upward part of the cycle: biostrome, carbonate sands, tidal flat sediments (C, B, A).     

Biomineralization at hot springs and mineral springs, and their significance in relation to the Earth's history]

Recently, there is strong interest on microbe-mineral interactions. This is related also to recent expanded knowledges on extremely severe environments in which microbes live. Interaction between microbes and minerals contains biomineralization processes. Varieties of biomineralization products are found not only in various geologic materials and processes in the earth's history but also in present surface environments. Some hot springs represent such environments similar to those of unique and extremely severe environments for life. In this short review, the author briefly shows some examples of biomineralizations at some hot springs and mineral springs, Japan. In such environments, iron ore was formed and some varieties of growing stromatolites were found. The varieties of stromatolite are siliceous, calcic and manganese types. Cyanobacteria and the other bacteria are related to form the stromatolite structure. In the Gunma iron ore, sedimentary iron ores were mineralogically described in order to evaluate the role of microorganisms and plants in ore formation. The iron ore is composed of nanocrystalline goethite. Algal fossils are clearly preserved in some ores. Various products of biomineralization are found in the present pH 2-3, Fe2(+)- and SO4(2-)-rich streams. Bacterial precipitation had variations from amorphous Fe-P-(S) precipitates near the outlet of mineral spring, to Fe-P-S precipitates and to Fe-S-(P) precipitates. Mosses and green algae are also collecting Fe precipitates in and around the living and dead cells. The Gunma Iron Ore can be said as Biologically Induced Iron Ore. At Onikobe and Akakura hot springs, growing stromatolites of siliceous and calcareous types, were found, respectively. At Onikobe, The stromatolites grow especially near the geyser. Cyanobacterial filaments in stromatolite were well preserved in the siliceous and calcic stromatolites. The filaments oriented in two directions which form the layered structures were found. At Yunokoya hot spring, black and brittle stromatolitic structures which were composed of amorphous Mn minerals are growing. The form of these structures are hemispherical. Many bacteria that were coated with amorphous Mn minerals were found on these structures. Furthermore, Precambrian (Proterozoic : Wittenoom-Chichester region, western Australia) manganese stromatolite was briefly shown in comparison. The black stromatolite has been clarified to be composed of todorokite. Small spotty and donuts-like shaped todorokite aggregates which are very similar to biologically induced Mn-precipitates were found in massive dolomite layers.     

Stromatolitic communities in Mediterranean streams: adaptations to a changing environment

A stromatolitic microbial mat extensively covers La Solana streambed, a calcareous Mediterranean stream. This stromatolite shows remarkable biological and physiological diversity. It is mainly composed by cyanobacteria, with Rivularia and Schizothrix as the most abundant taxa. The stromatolite is photosynthetically adaptated to the high irradiances reaching the streambed. Photosynthetically active chlorophyll is present even in the lowest layers of the stromatolite, indicating the presence of well-preserved cyanobacteria in that part. Diffusion of gases and nutrients within the stromatolite can be possible because of the high porosity of the crust. It has been experimentally established that the stromatolite recovers heterotrophic and autotrophic activities in a few hours, after being desiccated for long periods. Recovery after desiccation is indicative of the high resilience of this community to environmental extremes, which are common in Mediterranean climatic regimes. The stromatolitic community is adapted to nutrient limitation, both to low availability of inorganic phosphorus and nitrogen (that constrain growth of primary producers), and to low dissolved organic carbon (mainly affecting heterotrophs). Stromatolitic heterotrophs mainly rely on the organic carbon stored in the crust as the main organic carbon source. These strategies are the direct response of the stromatolite to oligotrophy, and justify the restricted occurrence in stream systems affected by organic pollution.     

Analysis of growth directions of columnar stromatolites from Walker Lake, western Nevada

Samples of digitate, branching, columnar stromatolites were collected from the steep sides and near horizontal top of four in situ boulders located on the southwestern side of Walker Lake, Nevada, to test the widely held assumption that stromatolite column formation represents a phototropic response. We would predict that the columns on the steeply dipping sides of the boulder would bend upwards toward the light during growth if phototropism was significant during stromatolite morphogenesis. Angle of growth measurements on >300 stromatolites demonstrate that the stromatolites grew nearly normal to their growth surface, regardless of the inclination of their growth surface. No significant differences in the distribution of growth angles between north-, south-, east-, or west-facing samples were observed, and stromatolite lamina thickness did not systematically vary with position on the boulder. The lack of a strong phototropic response does not rule out a biological origin for the Walker Lake structures, but it does suggest that phototropic growth was not a dominant factor controlling stromatolite morphogenesis in these stromatolites and that column formation cannot be uniquely attributed as a phototropic response in stromatolites. It is interesting to note that the morphology of the stromatolites on the top of the boulder is identical to stromatolites on the steep sides. Stromatolite morphogenetic models that predict branching typically require a vertically directed sedimentary component, a feature that would have likely affected the stromatolites on the tops of the boulders, but not the sides, suggesting that other factors may be important in stromatolite morphogenesis.     

Late Paleozoic stromatolites: new insights from the Lower Permian of Kansas

Carboniferous to Permian marine stromatolites are widely dispersed across the Pangaean margins and embayments and are typified by the ‘Ottonosia-grade stromatolite’ (designated herein). This stromatolite type consists of a well-laminated oncoid or domical stromatoid that developed into branching, laminated columns in the upper reaches. To develop a model for the global pattern, we investigated Lower Permian stromatolites from Kansas (Howe Limestone Member, Red Eagle Limestone). Stromatoids from the Lyon County locality typify the Ottonosia-grade stromatolites. The laminae are sharp throughout the stromatoid and are defined by an increase in cornuspirid foraminfera and algal filaments. The upper zone of the stromatoid is composed of well-laminated branching and brecciated columns (‘pseudo-thrombolitic’). Coeval stromatolites from a new exposure at the Tuttle Creek Dam spillway possess a more massive mesostructure. These stromatolites are composed of a turbinate stromatoid or oncoid base and an overlying domical stromatoid, and are rimmed by smaller meandering columns. Only the basal stromatoid, oncoids, and upper columns are well laminated. In both localities, the microbial-constructing ecosystem is dominated by cornuspirids and calcifying filamentous algae (?Girvanella). The mesostructural differences of the stromatolites are due to different environments of formation. The Tuttle Creek stromatolites formed in a shallow-subtidal to intertidal open marine setting. The coeval Lyon County stromatolites formed in a semi-restricted, marginal marine environment such as a lagoon or supratidal zone. Based on this information and independent sedimentological data, we conclude that lagoonal or supratidal zones were common features in the late Paleozoic intracratonal zones of the Pangaean supercontinent and account for Ottonosia-grade stromatolites occurring in the Laurentian mid-continent, the Zechstein Basin, Japan, Brazil, and Tunisia.     

Biotic and Abiotic Imprints on Mg-Rich Stromatolites: Lessons from Lake Salda,SW Turkey

Abstract

Modern hydrated Mg rich stromatolites are actively growing along the shallow shorelines of Lake Salda (SW Turkey). An integrated approach involving isotopic, mineralogical, microscopic, and organic/geochemical techniques along with culture-independent molecular methods were applied to various lake samples to assess the role of microbial processes on stromatolite formation. This study further explores the biosignature preservation potential of fossil stromatolites by comparing with textures, lipid profiles and isotopic composition of the modern stromatolites. Similar lipid profile and δ¹³C isotope values in active and fossil stromatolites argue that CO₂ cycling delicately balanced between photosynthetic and heterotrophic (aerobic) activity as in the active ones may have regulated stromatolite formation in the lake. A decrease in the exopolymeric substances (EPS) profile of the mat and concurrent hydromagnesite precipitation imply a critical role for EPS in the formation of stromatolite. Consistently, a discrete, discontinuous lamination and clotted micropeloidal textures with cyanobacterial remnants in the fossil stromatolites likely refer to partial degradation of EPS, creating local nucleation sites and allowing precipitation of hydrated Mg minerals and provide a link to the active microbial mat in the modern stromatolites. Our results for the first time provide strong evidence for close coupling of cyanobacterial photosynthesis and aerobic heterotrophic respiration on hydromagnesite textures involved in the stromatolite formation of Lake Salda. The creation of photosynthesis induced high-pH conditions combined with a change in the amount and properties of the EPS and the repetition of these processes over time seems to be a possible pathway for stromatolite growth in the lake. Understanding these microbial symbioses and their mineralized records may provide new insights on the formation mechanism of Mg-rich carbonates not only for terrestrial geological records but also for planetary bodies like Mars, where hydrated Mg-carbonate deposits have been identified in possible paleolake deposits at Jezero crater, the landing site of the NASA Mars 2020 rover.     

Nanoscale petrographic and geochemical insights on the origin of the Palaeoproterozoic stromatolitic phosphorites from Aravalli Supergroup,India

Stromatolites composed of apatite occur in post‐Lomagundi–Jatuli successions (late Palaeoproterozoic) and suggest the emergence of novel types of biomineralization at that time. The microscopic and nanoscopic petrology of organic matter in stromatolitic phosphorites might provide insights into the suite of diagenetic processes that formed these types of stromatolites. Correlated geochemical micro‐analyses of the organic matter could also yield molecular, elemental and isotopic compositions and thus insights into the role of specific micro‐organisms among these communities. Here, we report on the occurrence of nanoscopic disseminated organic matter in the Palaeoproterozoic stromatolitic phosphorite from the Aravalli Supergroup of north‐west India. Organic petrography by micro‐Raman and Transmission Electron Microscopy demonstrates syngeneity of the organic matter. Total organic carbon contents of these stromatolitic phosphorite columns are between 0.05 and 3.0 wt% and have a large range of δ¹³C_org values with an average of ?18.5‰ (1σ = 4.5‰). δ¹⁵N values of decarbonated rock powders are between ?1.2 and +2.7‰. These isotopic compositions point to the important role of biological N₂‐fixation and CO₂‐fixation by the pentose phosphate pathway consistent with a population of cyanobacteria. Microscopic spheroidal grains of apatite (MSGA) occur in association with calcite microspar in microbial mats from stromatolite columns and with chert in the core of diagenetic apatite rosettes. Organic matter extracted from the stromatolitic phosphorites contains a range of molecular functional group (e.g. carboxylic acid, alcohol, and aliphatic hydrocarbons) as well as nitrile and nitro groups as determined from C‐ and N‐XANES spectra. The presence of organic nitrogen was independently confirmed by a CN^? peak detected by ToF‐SIMS. Nanoscale petrography and geochemistry allow for a refinement of the formation model for the accretion and phototrophic growth of stromatolites. The original microbial biomass is inferred to have been dominated by cyanobacteria, which might be an important contributor of organic matter in shallow‐marine phosphorites.