Evolution of pelagic swells from hardground analysis (Bathonian–Oxfordian, Eastern External Subbetic, southern Spain)

The Middle Bathonian to Middle Oxfordian interval in the Eastern External Subbetic (Betic Cordillera, SE Spain) is characterized by Ammonitico Rosso facies including various stratigraphic breaks. Five hardground-bounded units are recognized in relation to hiatuses in the ammonite record at the following stratigraphic boundaries: Hg1 (Lower–Middle Bathonian), Hg2 (Middle–Upper Bathonian), Hg3 (Lower–Middle Callovian), Hg4 (Middle–Upper Callovian), and Hg5 (Callovian–Oxfordian). Interesting features of these hardgrounds include their microfacies, ferruginous crusts and macro-oncoids, taphonomy of macroinvertebrates, trace fossils, neptunian dykes, and the hiatuses associated with each of them. The main hardgrounds (Hg1, Hg2, and Hg5) contain trace fossils of the Cruziana and Trypanites ichnofacies as well as abundant fossil macroinvertebrates with taphonomic features evidencing corrasion, early diagenesis, and reworking, indicating substrate evolution from softground to hardground. Neptunian dykes affected the trace fossils and ammonoid moulds, and their walls and the hardground surfaces were colonized by ferruginous microbial crusts. These features are characteristic of the External Subbetic pelagic swells, where the absence of sedimentation, sediment bypassing and erosion, and early diagenesis during relative sea-level falls produced hardgrounds. The neptunian dykes are indicative of tectonic activity in the areas of pelagic swells. Ferruginous crusts and macro-oncoids developed only on hardground surfaces and neptunian dykes walls prior to deposition of condensed bioclastic beds, which are interpreted as the first deposits after hardground development and are related to the onset of transgression. The varying ranges of the gaps as well as lateral facies changes are related to different local paleobathymetry controlled by the activity of listric faults.     

Microaerophilic Fe‐oxidizing micro‐organisms in Middle Jurassic ferruginous stromatolites and the paleoenvironmental context of their formation (Southern Carpathians,Romania)

Ferruginous stromatolites occur associated with Middle Jurassic condensed deposits in several Tethyan and peri‐Tethyan areas. The studied ferruginous stromatolites occurring in the Middle Jurassic condensed deposits of Southern Carpathians (Romania) preserve morphological, geochemical, and mineralogical data that suggest microbial iron oxidation. Based on their macrofabrics and accretion patterns, we classified stromatolites: (1) Ferruginous microstromatolites associated with hardground surfaces and forming the cortex of the macro‐oncoids and (2) Domical ferruginous stromatolites developed within the Ammonitico Rosso‐type succession disposed above the ferruginous microstromatolites (type 1). Petrographic and scanning electron microscope (SEM) examinations reveal that different types of filamentous micro‐organisms were the significant framework builders of the ferruginous stromatolitic laminae. The studied stromatolites yield a large range of δ⁵⁶Fe values, from ?0.75‰ to +0.66‰ with predominantly positive values indicating the prevalence of partial ferrous iron oxidation. The lowest negative δ⁵⁶Fe values (up to ?0.75‰) are present only in domical ferruginous stromatolites samples and point to initial iron mobilization where the Fe(II) was produced by dissimilatory Fe(III) reduction of ferric oxides by Fe(III)‐reducing bacteria. Rare‐earth elements and yttrium (REE + Y) are used to decipher the nature of the seawater during the formation of the ferruginous stromatolites. Cerium anomalies display moderate to small negative values for the ferruginous microstromatolites, indicating weakly oxygenated conditions compatible with slowly reducing environments, in contrast to the domical ferruginous stromatolites that show moderate positive Ce anomalies suggesting that they formed in deeper, anoxic–suboxic waters. The positive Eu anomalies from the studied samples suggest a diffuse hydrothermal input on the seawater during the Middle Jurassic on the sites of ferruginous stromatolite accretion. This study presents the first interpretation of REE + Y in the Middle Jurassic ferruginous stromatolites of Southern Carpathians, Romania.     

Oncoidal granular iron formation in the Mesoarchaean Pongola Supergroup,southern Africa: Textural and geochemical evidence for biological activity during iron deposition

We document the discovery of the first granular iron formation (GIF) of Archaean age and present textural and geochemical results that suggest these formed through microbial iron oxidation. The GIF occurs in the Nconga Formation of the ca. 3.0–2.8 Ga Pongola Supergroup in South Africa and Swaziland. It is interbedded with oxide and silicate facies micritic iron formation (MIF). There is a strong textural control on iron mineralization in the GIF not observed in the associated MIF. The GIF is marked by oncoids with chert cores surrounded by magnetite and calcite rims. These rims show laminated domal textures, similar in appearance to microstromatolites. The GIF is enriched in silica and depleted in Fe relative to the interbedded MIF. Very low Al and trace element contents in the GIF indicate that chemically precipitated chert was reworked above wave base into granules in an environment devoid of siliciclastic input. Microbially mediated iron precipitation resulted in the formation of irregular, domal rims around the chert granules. During storm surges, oncoids were transported and deposited in deeper water environments. Textural features, along with positive δ⁵⁶Fe values in magnetite, suggest that iron precipitation occurred through incomplete oxidation of hydrothermal Fe²⁺ by iron‐oxidizing bacteria. The initial Fe³⁺‐oxyhydroxide precipitates were then post‐depositionally transformed to magnetite. Comparison of the Fe isotope compositions of the oncoidal GIF with those reported for the interbedded deeper water iron formation (IF) illustrates that the Fe²⁺ pathways and sources for these units were distinct. It is suggested that the deeper water IF was deposited from the evolved margin of a buoyant Fe²⁺_aq‐rich hydrothermal plume distal to its source. In contrast, oncolitic magnetite rims of chert granules were sourced from ambient Fe²⁺_aq‐depleted shallow ocean water beyond the plume.     

Brachiopods from the Cisuralian–Guadalupian of Darvaz,Tajikistan and implications for Permian stratigraphic correlations

In this paper, we describe the upper Cisuralian Safetdara and Gundara formations of the Darvaz mountains, North Pamir, which were part of the Kunlun Arc, developed along the active Eurasian margin. The Safetdara Formation comprises massive limestones (mainly cyanobacterial, Tubiphytes and Archaeolithoporella boundstones) alternating with well-bedded bioclastic and oncoidal limestones and an interval of recessive shales. The formation crops out above the Chelamchi Formation consisting of turbiditic siltstones and sandstones with bioclastic silty limestones yielding massive limestone olistoliths. The Gundara Formation consists of fine sandstones at the base, followed by well-bedded marly bioclastic, oncoidal and microbial limestones, bearing a rich silicified brachiopod fauna in life-position. Two new taxa have been identified in this association: the cemented coralliform Gundaria insolita n. gen. n. sp. and the pedicle attached Hemileurus politus n. sp. The inferred environmental setting is that of shoal deposits of warm, shallow, high energy, clear marine waters for the Safetdara Formation. The agglutinated microbial reefs to cluster reefs of the Gundara Formation were probably growing in a muddier, quieter and probably slightly deeper setting.The foraminifers of the Brevaxina Zone suggest a Bolorian age for the top of the Chelamchi Formation, the Safetdara Formation and the base of the Gundara Formation. Kungurian conodonts have been found in the lower part of the Safetdara Formation. The biostratigraphic data from the sedimentary succession of North Pamir, integrated with those already obtained from Southeast Pamir, allow to refine the correlations between the Tethyan regional scale and the International Time Scale. In particular, it seems now clear that the Bolorian and the lower part of the Kubergandian correlate to the Kungurian.     

Planktonic marine iron oxidizers drive iron mineralization under low‐oxygen conditions

Observations of modern microbes have led to several hypotheses on how microbes precipitated the extensive iron formations in the geologic record, but we have yet to resolve the exact microbial contributions. An initial hypothesis was that cyanobacteria produced oxygen which oxidized iron abiotically; however, in modern environments such as microbial mats, where Fe(II) and O₂ coexist, we commonly find microaerophilic chemolithotrophic iron‐oxidizing bacteria producing Fe(III) oxyhydroxides. This suggests that such iron oxidizers could have inhabited niches in ancient coastal oceans where Fe(II) and O₂ coexisted, and therefore contributed to banded iron formations (BIFs) and other ferruginous deposits. However, there is currently little evidence for planktonic marine iron oxidizers in modern analogs. Here, we demonstrate successful cultivation of planktonic microaerophilic iron‐oxidizing Zetaproteobacteria from the Chesapeake Bay during seasonal stratification. Iron oxidizers were associated with low oxygen concentrations and active iron redox cycling in the oxic–anoxic transition zone (<3 μm O₂, <0.2 μm H₂S). While cyanobacteria were also detected in this transition zone, oxygen concentrations were too low to support significant rates of abiotic iron oxidation. Cyanobacteria may be providing oxygen for microaerophilic iron oxidation through a symbiotic relationship; at high Fe(II) levels, cyanobacteria would gain protection against Fe(II) toxicity. A Zetaproteobacteria isolate from this site oxidized iron at rates sufficient to account for deposition of geologic iron formations. In sum, our results suggest that once oxygenic photosynthesis evolved, microaerophilic chemolithotrophic iron oxidizers were likely important drivers of iron mineralization in ancient oceans.     

Mineral evolution and processes of ferruginous microbialite accretion – an example from the Middle Eocene stromatolitic and ooidal ironstones of the Bahariya Depression,Western Desert,Egypt

Peritidal ferruginous microbialites form the main bulk of the Middle Eocene ironstone deposits of the Bahariya Depression, Western Desert, Egypt. They include ferruginous stromatolites and microbially coated grains (ferruginous oncoids and ooids). Their internal structures reveal repeated cycles of microbial and Fe oxyhydroxide laminae. The microbial laminae consist of fossilised neutrophilic filamentous iron‐oxidising bacteria. These bacteria oxidised the Fe(II)‐rich acidic groundwater upon meeting the marine water at an approximately neutral pH. The iron oxyhydroxide laminae were initially precipitated as amorphous iron oxhydroxides and subsequently recrystallised into nanocrystalline goethite during early diagenesis. Organic remains such as proteinaceous compounds, lipids, carbohydrates and carotenoids are preserved and can be identified by Raman spectroscopy. The ferruginous microbialites were subjected to post‐depositional subaerial weathering associated with sea‐level retreat and subsurface alteration by continued ascent of the Fe(II)‐rich acidic groundwater. At this stage, another iron‐oxidising bacterial generation prevailed in the acidic environment. The acidity of the groundwater was caused by oxidation of pyrite in the underlying Cenomanian Bahariya formation. The positive iron isotopic ratios and presence of ferrous and ferric iron sulphates may result from partial iron oxidation along the redox boundary in an oxygen‐depleted environment.     

Facies control on lower Cambrian wrinkle structure development and paleoenvironmental distribution, southern Great Basin, United States

Assessing the role that physical processes play in restricting microbial mat distribution has been difficult due to the primary control of bioturbation in the modern ocean. To isolate and determine the physical controls on microbial mat distribution and preservation, a time in Earth’s history must be examined when bioturbation was not the primary control. This restricts the window of observation primarily to the Precambrian and Cambrian, which precede the development of typical Phanerozoic and modern levels of bioturbation. Lower Cambrian strata of the southern Great Basin, United States, record the widespread development of seafloor microbial mats in shallow shelf and nearshore settings. These microbial mats are recorded by wrinkle structures, which consist of millimeter-scale ridges and sinuous troughs that represent the former presence of a surface microbial mat. Wrinkle structures within these strata occur exclusively within heterolithic deposits of the offshore transition, i.e., between fair-weather wave base and storm wave base, and within heterolithic tidal-flat deposits. Wrinkle structures are not preserved in siltstone-dominated offshore deposits or amalgamated shoreface sandstones. The preservation of wrinkle structures within these environments is due to: (1) the development of microbial mats atop clean quartz-rich sands for growth and casting of the structures; and (2) the draping of the microbial mat by finer-grained sediment to inhibit erosion. The exclusion from offshore deposits may be due to a lack of sufficient sunlight, whereas the restriction from the shoreface is likely due to the amalgamation of proximal tempestites, resulting in the erosion of any incipient microbial mat development.     

Iron microbial communities in Belgian Frasnians carbonate mounds

Summary The Belgian Frasnian carbonate mounds occur in three stratigraphic levels in an overall backstepping succession. Petit-Mont and Arche Members form the famous red and grey “marble” exploited for ornamental stone since Roman times. The evolution and distribution of the facies in the mounds is thought to be associated with ecologic evolution and relative sea-level fluctuations. Iron oxides exist in five forms in the Frasnian mounds; four are undoubtedly endobiotic organized structures: (1) microstromatolites and associated forms (blisters, veils...), possibly organized in “endostromatolites”; (2) hematitic coccoids and (3) non dichotomic filaments. The filaments resemble iron bacteria of theSphaerotilus-Leptothrix “group”; (4) networks of dichotomic filaments ascribable to fungi; (5) a red ferruginous pigment dispersed in the calcareous matrix whose distribution is related to the mound facies type. The endobiotic forms developed during the edification of the mounds, before cementation by fibrous calcite. The microbial precipitation of iron took place as long as the developing mounds were bathed by water impoverished in oxygen.     

A modern-type Kimmeridgian reef (Ota Limestone,Portugal): Implications for Jurassic reef models

Upper Jurassic reefs rich in microbial crusts generally appear in deeper (sponge—‘algal’ crust reefs) or in very shallow but protected settings (coral or coral-coralline sponge meadows with ‘algal’ crusts). Upper Jurassic high-energy reefs (coral reefs and coral-stromatoporoid reefs) normally lack major participation of microbial crusts but rather represent huge bioclastic piles with only minor framestone patches preserved. An exception to this rule is represented by the high-energy, coral-‘algal’ Ota Reef from the Kimmeridgian of the Lusitanian Basin (Portugal). The narrow Ota Reef tract rims a small intra-basinal carbonate platform exhibiting perfect facies zonation (from W to E: Reef tract, back reef sands, peritidal belt, low-energy shallow lagoon). The reef is dominated by massive corals (Thamnasteria, Microsolena, Stylina). Complete preservation of coral framework is rare: like other Upper Jurassic high-energy reefs, the Ota Reef is very rich in debris; however, this debris is largely stabilized by algal and microbial crusts, what contrasts the other examples and gives the Ota Reef the appearance of a typical modern high-energy coral-melobesioid algal reef. Further similarities to modern reefs are the likely existence of a spur-and-groove system, the perfect sheltering of inner platform areas and the occurrence of small islands, as indicated by local blackenings and early vadose and karstic features.     

Phototrophs in High-Iron-Concentration Microbial Mats: Physiological Ecology of Phototrophs in an Iron-Depositing Hot Spring

At Chocolate Pots Hot Springs in Yellowstone National Park the source waters have a pH near neutral, contain high concentrations of reduced iron, and lack sulfide. An iron formation that is associated with cyanobacterial mats is actively deposited. The uptake of [¹⁴C]bicarbonate was used to assess the impact of ferrous iron on photosynthesis in this environment. Photoautotrophy in some of the mats was stimulated by ferrous iron (1.0 mM). Microelectrodes were used to determine the impact of photosynthetic activity on the oxygen content and the pH in the mat and sediment microenvironments. Photosynthesis increased the oxygen concentration to 200% of air saturation levels in the top millimeter of the mats. The oxygen concentration decreased with depth and in the dark. Light-dependent increases in pH were observed. The penetration of light in the mats and in the sediments was determined. Visible radiation was rapidly attenuated in the top 2 mm of the iron-rich mats. Near-infrared radiation penetrated deeper. Iron was totally oxidized in the top few millimeters, but reduced iron was detected at greater depths. By increasing the pH and the oxygen concentration in the surface sediments, the cyanobacteria could potentially increase the rate of iron oxidation in situ. This high-iron-content hot spring provides a suitable model for studying the interactions of microbial photosynthesis and iron deposition and the role of photosynthesis in microbial iron cycling. This model may help clarify the potential role of photosynthesis in the deposition of Precambrian banded iron formations.     

Sur l’origine bactérienne et fongique de la pigmentation de l’Ammonitico Rosso (Jurassique, région de Vérone, Italie du nord)

Fourteen sections in the Ammonitico Rosso Veronese (Callovian to Tithonian, Trento altipiano) disclose the presence of diverse facies ranging from pelagic to outer platform. In spite of this diversity, red limestones are present at different levels. Many microfacies are similar to those observed in other Paleozoic and Mesozoic red carbonates with an abundance of hematitic bioconstructions. We therefore postulate that the origin of the pigmentation is similar in all the studied cases and due to the activity of iron-oxidizing bacteria. Nevertheless, 2 notable differences are observed: the presence in the Ammonitico Rosso of manganese and the existence of in situ bacterial-fungal mats in the matrix. These “algal” mats can represent up to 20% of the sediment. Their excellent preservation (absence of packing down or crushing) is due to the slow sedimentation rate of the pelagic sediments or of the hardgrounds.     

Morphology and ultrastructure of epilithic versus cryptic,microbial growth in lower Cambrian phosphorites from the Montagne Noire,France

The lower Cambrian grainy phosphorites of the northern Montagne Noire occur interbedded with grey to black, laminated to massive shales and limestones deposited along the edge of a continental shelf, associated with slope‐related facies and unstable substrates. The concentration of phosphate took place by repeated alternations of low sedimentation rates and condensation (hardgrounds), in situ early‐diagenetic precipitation of fluorapatite, winnowing and polyphase reworking of previously phosphatized skeletons and hardground‐derived clasts. The succession of repeated cycles of sedimentation, phosphate concentration, and reworking led to multi‐event phosphate deposits rich in allochthonous particles. Phosphogenesis was primarily mediated by microbial activity, which is evidenced by the abundance of phosphatized putative microbial remains. These occur as smooth and segmented filaments, sheaths, and ovoid‐shaped coccoids. These simple morphologies commonly form composite frameworks as a result of their aggregation and entanglement, leading to the record of biofilms, microbial mats, and complex networks. These infested the calcitic skeletonized microfossils that littered the substrate. Microbial activity evidences epilithic (anisotropic coatings on skeletons), euendolithic (perforating skeletal walls), and cryptoendolithic (lining inter‐ and intraparticulate pores) strategies, the latter dominated by bundles of filaments and globular clusters that grew along the cavities of helcionellids and hyoliths. According to their epilithic versus cryptic strategies, microbial populations that penetrated and dwelled inside hard skeletal substrates show different network and colonial morphologies. These early Cambrian shell concentrations were the loci of a stepwise colonization made by saprophytic to mutualistic, cyanobacterial–fungal consortia. Their euendolithic and cryptoendolithic ecological niches provided microbial refugia to manage the grazing impact mainly led by metazoans.     

Coral biostromes of the Middle Jurassic from the Subbetic (Betic Cordillera,southern Spain): facies,coral taxonomy,taphonomy, and palaeoecology

Coral biostromes from the Camarena Formation (External Subbetic, Betic Cordillera) are reviewed under palaeoecologic, taphonomic, and palaeontologic aspects. The biostromes are dominated by phaceloid forms and are characterized by a typical shallow-marine microencruster assemblage with photophilic microencrusters and scarce microbial crusts. The abundance of stylinid corals and light-dependant microencrusters suggests oligotrophic conditions. Coral colonies were located among oolitic shoals that were unfavorable for coral growth. The corals were developed in phases without oolitic production alternating with phases of oolitic production, forming metric-scale sequences. A relative sea-level fall would have reduced the ooidal production and led to the deposition of thin layers of micritic facies in intertidal areas. The cementation and hardening of the bottom resulted in a hardground that was colonized by corals after a subsequent relative sea-level rise. The progressive increase of the energetic conditions induced an increasing production of ooids and the migration of oolitic shoals, which covered and finished the coral biostromes. Repetition of this process gave rise to sequences reflecting small pulses of oscillations in the relative sea level.     

Isotope and microelement systematics of <Emphasis Type="Italic">Gallionella</Emphasis> sp.-containing bacterial mats from the northwest of the East European Platform

Microelement composition of Gallionella sp.-containing bacterial mats from the environs of St. Petersburg and isotope composition of organic carbon, strontium, and neodymium from these mats have been determined. Isotope and microelement systematics of iron oxides of bacterial origin characterize the geochemistry of aquafacies that contain ferrobacteria. Certain pre-Cambrian ferruginous quartzites have a similar composition; therefore, one may assume that bacterial oxidation of iron under continental conditions had occurred upon the formation of ironstone during the Precambrian.     

Phototrophs in high-iron-concentration microbial mats: physiological ecology of phototrophs in an iron-depositing hot spring

At Chocolate Pots Hot Springs in Yellowstone National Park the source waters have a pH near neutral, contain high concentrations of reduced iron, and lack sulfide. An iron formation that is associated with cyanobacterial mats is actively deposited. The uptake of [(14)C]bicarbonate was used to assess the impact of ferrous iron on photosynthesis in this environment. Photoautotrophy in some of the mats was stimulated by ferrous iron (1.0 mM). Microelectrodes were used to determine the impact of photosynthetic activity on the oxygen content and the pH in the mat and sediment microenvironments. Photosynthesis increased the oxygen concentration to 200% of air saturation levels in the top millimeter of the mats. The oxygen concentration decreased with depth and in the dark. Light-dependent increases in pH were observed. The penetration of light in the mats and in the sediments was determined. Visible radiation was rapidly attenuated in the top 2 mm of the iron-rich mats. Near-infrared radiation penetrated deeper. Iron was totally oxidized in the top few millimeters, but reduced iron was detected at greater depths. By increasing the pH and the oxygen concentration in the surface sediments, the cyanobacteria could potentially increase the rate of iron oxidation in situ. This high-iron-content hot spring provides a suitable model for studying the interactions of microbial photosynthesis and iron deposition and the role of photosynthesis in microbial iron cycling. This model may help clarify the potential role of photosynthesis in the deposition of Precambrian banded iron formations.     

Jelly-like Microbial Mats over Subsurface Fields of Gas Hydrates at the St. Petersburg Methane Seep (Central Baikal)

Jelly-like microbial mat samples were collected from benthic surfaces at the St. Petersburg methane seep located in Central Baikal. The concentrations of certain ions, specifically chloride, bromide, sulphate, acetate, iron, calcium, and magnesium, were 2–40 times higher in the microbial mats than those in the pore and bottom water. A large number of diatom valves, cyanobacteria, and filamentous, rod-shaped and coccal microorganisms were found in the samples of bacterial mats using light, epifluorescence and scanning microscopy.Comparative analysis of a 16S rRNA gene fragment demonstrated the presence of bacteria and archaea belonging to the following classes and phyla: Betaproteobacteria, Gammaproteobacteria, Deltaproteobacteria, Verrucomicrobia, Cytophaga-Flavobacteria-Bacteroidetes, Cyanobacteria, and Euryarchaeota. The chemical composition and phylogenetic structure of the microbial community showed that the life activity of the mat occurs due to methane and its derivatives involved. Values of δ¹³C for the microbial mats varied from ?73.6‰ to ?65.8‰ and for animals from ?68.9‰ to ?36.6‰. Functional genes of the sequential methane oxidation (pmoA and mxaF) and different species of methanotrophic bacteria inhabiting cold ecosystems were recorded in the total DNA. Like in other psychroactive communities, the destruction of organic substances forming formed as a result of methanotrophy, terminates at the stage of acetate formation in the microbial mats of Lake Baikal (1,400 m depth). Its further transformation is limited by hydrogen content and carried out in the subsurface layers of sediments.     

Biogeochemistry of a gypsum-encrusted microbial ecosystem

Gypsum crusts containing multicolored stratified microbial populations grow in the evaporation ponds of a commercial saltern in Eilat, Israel. These crusts contain two prominent cyanobacterial layers, a bright purple layer of anoxygenic phototrophs, and a lower black layer with active sulphate reduction. We explored the diel dynamics of oxygen and sulphide within the crust using specially constructed microelectrodes, and further explored the crust biogeochemistry by measuring rates of sulphate reduction, stable sulphur isotope composition, and oxygen exchange rates across the crust–brine interface. We explored crusts from ponds with two different salinities, and found that the crust in the highest salinity was the less active. Overall, these crusts exhibited much lower rates of oxygen production than typical organic‐rich microbial mats. However, this was mainly due to much lower cell densities within the crusts. Surprisingly, on a per cell‐volume basis, rates of photosynthesis were similar to organic‐rich microbial mats. Due to relatively low rates of oxygen production and deep photic zones extending from 1.5 to 3 cm depth, a large percentage of the oxygen produced during the day accumulated into the crusts. Indeed, only between 16% to 34% of the O₂ produced in the crust escaped, and the remainder was internally recycled, used mainly in O₂ respiration. We view these crusts as potential homologs to ancient salt‐encrusted microbial ecosystems, and we compared them to the 3.45 billion‐year‐old quartz barite deposits from North Pole, Australia, which originally precipitated gypsum.     

Phototrophs in high iron microbial mats: microstructure of mats in iron-depositing hot springs

Chocolate Pots Hot Springs in Yellowstone National Park are high in ferrous iron, silica and bicarbonate. The springs are contributing to the active development of an iron formation. The microstructure of photosynthetic microbial mats in these springs was studied with conventional optical microscopy, confocal laser scanning microscopy and transmission electron microscopy. The dominant mats at the highest temperatures (48-54 degrees C) were composed of Synechococcus and Chloroflexus or Pseudanabaena and Mastigocladus. At lower temperatures (36-45 degrees C), a narrow Oscillatoria dominated olive green cyanobacterial mats covering most of the iron deposit. Vertically oriented cyanobacterial filaments were abundant in the top 0.5 mm of the mats. Mineral deposits accumulated beneath this surface layer. The filamentous microstructure and gliding motility may contribute to binding the iron minerals. These activities and heavy mineral encrustation of cyanobacteria may contribute to the growth of the iron deposit. Chocolate Pots Hot Springs provide a model for studying the potential role of photosynthetic prokaryotes in the origin of Precambrian iron formations.     

Serpulid-bryozoan-foraminiferal biostromes controlled by temperate climate and reduced salinity: Middle miocene of the Styrian Basin,Austria

Summary Reduced salintiy and a temperate climate prevailed during the Sarmatian in the Styrian Basin, the westernmost embayment of the Central Paratethys. At its northern margin (in the study area) tectonic processes initiated a transgression causing the incision of a cliff into the metamorphic basement and the formation of a carbonate buildup in the latest Sarmatian. The buildup consists of two serpulid-bryozoan-foraminiferal biostromes separated by a microbialite. Serpulids, bryozoa and the encrusting foraminifer Sinzowella caespitosa (Steinmann) as well as microbial mats formed a rigid framework, in which biogenic debris and siliciclastics were baffled. The different biota show complex growth relationships. Stromatolitic crusts and laminated micritic microbial crusts with birdseyes grew in a small sheltered lagoon. The upper biostrome is truncated by a ravinement surface of eustatic orgin and is overlain by ooid grainstone. The buildup drowned during maximum sea-level rise.