Formation and calcification of modern gypsum-dominated stromatolites,EMISAL, Fayium,Egypt

Recent gypsum stromatolites are forming along the margin as well as on the pond floor of the EMISAL saltworks, Fayium, Egypt. Gypsum precipitates are classified according to their morphology, fabrics, and crystal size into (1) subaqueous bottom gypsum crusts, (2) selenitic gypsum facies, (3) stromatolitic gypsum dome facies, and (4) gypsolite facies. Two types of microbial mats, lithifying and non-lithifying, can be identified. The lithifying mat is shallow and composed of an alternation of gypsum and microbial layers that are seasonally controlled. The non-lithifying mat, formed in the deeper part of the pond, is a greenish-brown slime-rich layer that exhibits a frothy macro texture and produces a firm gelatinous film covering the sediment surface. Calcium carbonate (mostly aragonite) particles, identified by light and scanning electron microscopy, and X-ray diffraction occur within the deeper part of the lithified mat and are associated with living and degrading biofilm. Precipitation of aragonite is associated with the dissolution of gypsum, which may have resulted from bacterial sulphate reduction. The latter process increases alkalinity and ultimately results in the replacement of gypsum by aragonite.     

Geospatial insights into the controls of microbialite formation at Laguna Negra,Argentina

Microbialites provide a record of the interaction of microorganisms with their environment constituting a record of microbial life and environments through geologic time. Our capacity to interpret this record is limited by an incomplete understanding of the microbial, geochemical, and physical processes that influence microbialite formation and morphogenesis. The modern system Laguna Negra in Catamarca Province, Argentina contains microbialites in a zone of carbonate precipitation associated with physico-chemical gradients and variable microbial community structure, making it an ideal location to study how these processes interact to drive microbialite formation. In this study, we investigated the geospatial relationships between carbonate morphology, geochemistry, and microbial community at the macro- (decimeter) to mega- (meter) scale by combining high-resolution imagery with field observations. We mapped the distribution of carbonate morphologies and allochtonously-derived volcaniclasts and correlated these with sedimentary matrices and geochemical parameters. Our work shows that the macroscale distribution of different carbonate morphologies spatially correlates with microbial mat distributions—a result consistent with previous microscale observations. Specifically, microbialitic carbonate morphologies more commonly occur associated with microbial mats while abiotically derived carbonate morphologies were less commonly associated with microbial mats. Spatial variability in the size and abundance of mineralized structures was also observed, however, the processes controlling this variability remains unclear and likely represent a combination of microbial, geochemical, and physical processes. Likewise, the processes controlling the spatial distribution of microbial mats at Laguna Negra are also unresolved. Our results suggest that in addition to the physical drivers observed in other modern environments, variability in the spatial distribution of microbialites and other carbonate morphologies at the macro- to megascale can be controlled by microbial processes. Overall, this study provides insight into the interpretation of microbialite occurrence and distributions in the geologic record and highlights the utility of geospatial statistics to probe the controls of microbialite formation in other environments.     

Lacustrine Nostoc (Nostocales) and associated microbiome generate a new type of modern clotted microbialite

Microbialites are mineral formations formed by microbial communities that are often dominated by cyanobacteria. Carbonate microbialites, known from Proterozoic times through the present, are recognized for sequestering globally significant amounts of inorganic carbon. Recent ecological work has focused on microbial communities dominated by cyanobacteria that produce microbial mats and laminate microbialites (stromatolites). However, the taxonomic composition and functions of microbial communities that generate distinctive clotted microbialites (thrombolites) are less well understood. Here, microscopy and deep shotgun sequencing were used to characterize the microbiome (microbial taxa and their genomes) associated with a single cyanobacterial host linked by 16S sequences to Nostoc commune Vaucher ex Bornet & Flahault, which dominates abundant littoral clotted microbialites in shallow, subpolar, freshwater Laguna Larga in southern Chile. Microscopy and energy‐dispersive X‐ray spectroscopy suggested the hypothesis that adherent hollow carbonate spheres typical of the clotted microbialite begin development on the rigid curved outer surfaces of the Nostoc balls. A surface biofilm included >50 nonoxygenic bacterial genera (taxa other than Nostoc) that indicate diverse ecological functions. The Laguna Larga Nostoc microbiome included the sulfate reducers Desulfomicrobium and Sulfospirillum and genes encoding all known proteins specific to sulfate reduction, a process known to facilitate carbonate deposition by increasing pH. Sequences indicating presence of nostocalean and other types of nifH, nostocalean sulfide:ferredoxin oxidoreductase (indicating anoxygenic photosynthesis), and biosynthetic pathways for the secondary products scytonemin, mycosporine, and microviridin toxin were identified. These results allow comparisons with microbiota and microbiomes of other algae and illuminate biogeochemical roles of ancient microbialites.     

Microbial diversity and biomarker analysis of modern freshwater microbialites from Laguna Bacalar,Mexico

Laguna Bacalar is a sulfate‐rich freshwater lake on the Yucatan Peninsula that hosts large microbialites. High sulfate concentrations distinguish Laguna Bacalar from other freshwater microbialite sites such as Pavilion Lake and Alchichica, Mexico, as well as from other aqueous features on the Yucatan Peninsula. While cyanobacterial populations have been described here previously, this study offers a more complete characterization of the microbial populations and corresponding biogeochemical cycling using a three‐pronged geobiological approach of microscopy, high‐throughput DNA sequencing, and lipid biomarker analyses. We identify and compare diverse microbial communities of Alphaproteobacteria, Deltaproteobacteria, and Gammaproteobacteria that vary with location along a bank‐to‐bank transect across the lake, within microbialites, and within a neighboring mangrove root agglomeration. In particular, sulfate‐reducing bacteria are extremely common and diverse, constituting 7%–19% of phylogenetic diversity within the microbialites, and are hypothesized to significantly influence carbonate precipitation. In contrast, Cyanobacteria account for less than 1% of phylogenetic diversity. The distribution of lipid biomarkers reflects these changes in microbial ecology, providing meaningful biosignatures for the microbes in this system. Polysaturated short‐chain fatty acids characteristic of cyanobacteria account for <3% of total abundance in Laguna Bacalar microbialites. By contrast, even short‐chain and monounsaturated short‐chain fatty acids attributable to both Cyanobacteria and many other organisms including types of Alphaproteobacteria and Gammaproteobacteria constitute 43%–69% and 17%–25%, respectively, of total abundance in microbialites. While cyanobacteria are the largest and most visible microbes within these microbialites and dominate the mangrove root agglomeration, it is clear that their smaller, metabolically diverse associates are responsible for significant biogeochemical cycling in this microbialite system.     

Recent evaporite deposition associated with microbial mats,Al-Kharrar supratidal–intertidal sabkha,Rabigh area,Red Sea coastal plain of Saudi Arabia

The supratidal–intertidal sabkha of the Al-Kharrar area, Red Sea coast, Saudi Arabia, contains the evaporite minerals gypsum, anhydrite, and halite. Microbial mats flourish adjacent to the sabkha evaporites in tidal flats and pools of the Al Kharrar lagoon. Desiccation and decay of some microbial mats in tidal flat areas have led to precipitation of gypsum and halite there. The evaporite minerals have been precipitated through displacive, inclusive, and replacive growth within mud, sand, gravelly sand, and bioclastic sediment of the sabkha. Gypsum occurs as lenticular and tabular crystals whereas anhydrite occurs as nodular (individual, mosaic, and enterolithic) and pseudomorphs of lenticular gypsum crystals that grew displacively and replacively near the surface of the sabkha. Halite exists as a diagenetic cement within the sabkha sediment, or as primary rafts and skeletal crystals in desiccated tidal pools with salinity over 220‰. Microbial mats are growing on the surface of the upper tidal flat areas and in pools at a salinity range of 80–110‰, and they lead to biostabilization of the sediment. They have induced a range of sedimentary surface structures (MISS) including gas domes, reticulate patterns, tufts, pinnacles, wrinkles, and microbial shrinkage cracks. The occurrence, abundance, and association of evaporite minerals and MISS are controlled by local environmental factors such topography of the sabkha, emergence or submergence of tidal areas, surface area of the evaporite basin, contribution of meteoric water from floods from the adjoining Red Sea Mountains, and water salinity. These factors promote the growth of the microbial mats in the winter months, and deposition of evaporite minerals during summer months. Field and petrographic data indicate that the main recharge to the sabkha area is from tidal flow and water seepage from the Al-Kharrar lagoon. The results of this study indicate that within a small sabkha area of Al-Kharrar (3?×?17 km), a large variation in evaporite mineral types and morphologies grade into and are associated with MISS due to local environmental parameters. The interpretation of this association of evaporite minerals and MISS provides useful data for understanding the mechanisms responsible for precipitation of evaporite minerals and formation of MISS.     

Metabolic potential of lithifying cyanobacteria-dominated thrombolitic mats

Thrombolites are unlaminated carbonate deposits formed by the metabolic activities of microbial mats and can serve as potential models for understanding the molecular mechanisms underlying the formation of lithifying communities. To assess the metabolic complexity of these ecosystems, high throughput DNA sequencing of a thrombolitic mat metagenome was coupled with phenotypic microarray analysis. Functional protein analysis of the thrombolite community metagenome delineated several of the major metabolic pathways that influence carbonate mineralization including cyanobacterial photosynthesis, sulfate reduction, sulfide oxidation, and aerobic heterotrophy. Spatial profiling of metabolite utilization within the thrombolite-forming microbial mats suggested that the top 5 mm contained a more metabolically diverse and active community than the deeper within the mat. This study provides evidence that despite the lack of mineral layering within the clotted thrombolite structure there is a vertical gradient of metabolic activity within the thrombolitic mat community. This metagenomic profiling also serves as a foundation for examining the active role individual functional groups of microbes play in coordinating metabolisms that lead to mineralization.     

Deep‐water microbialites of the Mesoproterozoic Dismal Lakes Group: microbial growth,lithification, and implications for coniform stromatolites

Offshore facies of the Mesoproterozoic Sulky Formation, Dismal Lakes Group, arctic Canada, preserve microbialites with unusual morphology. These microbialites grew in water depths greater than several tens of meters and correlate with high‐relief conical stromatolites of the more proximal September Lake reef complex. The gross morphology of these microbial facies consists of ridge‐like vertical supports draped by concave‐upward, subhorizontal elements, resulting in tent‐shaped cuspate microbialites with substantial primary void space. Morphological and petrographic analyses suggest a model wherein penecontemporaneous upward growth of ridge elements and development of subhorizontal draping elements initially resulted in a buoyantly supported, unlithified microbial form. Lithification began via precipitation within organic elements during microbialite growth. Mineralization either stabilized or facilitated collapse of initially neutrally buoyant microbialite forms. Microbial structures and breccias were then further stabilized by precipitation of marine herringbone cement. During late‐stage diagenesis, remaining void space was occluded by ferroan dolomite cement. Cuspate microbialites are most similar to those found in offshore facies of Neoarchean carbonate platforms and to unlithified, buoyantly supported microbial mats in modern ice‐covered Antarctic lakes. We suggest that such unusual microbialite morphologies are a product of the interaction between motile and non‐motile communities under nutrient‐limiting conditions, followed by early lithification, which served to preserve the resultant microbial form. The presence of marine herringbone cement, commonly associated with high dissolved inorganic carbon (DIC), low O₂ conditions, also suggests growth in association with reducing environments at or near the seafloor or in conjunction with a geochemical interface. Predominance of coniform stromatolite forms in the Proterozoic—across a variety of depositional environments—may thus reflect a combination of heterogeneous nutrient distribution, potentially driven by variable redox conditions, and an elevated carbonate saturation state, which permits preservation of these unusual microbialite forms.     

Mineralized microbialites as archives of environmental evolution,Laguna Negra,Catamarca Province,Argentina

Environmental fluctuations are recorded in a variety of sedimentary archives of lacustrine depositional systems. Geochemical signals recovered from bottom sediments in closed‐basin lakes are among the most sensitive paleoenvironmental indicators and are commonly used in reconstructing lake evolution. Microbialites (i.e., organosedimentary deposits accreted through microbial trapping and binding of detrital sediment or in situ mineral precipitation on organics [Palaios, 2, 1987, 241]), however, have been largely overlooked as paleoenvironmental repositories. Here, we investigate concentrically laminated mineralized microbialites from Laguna Negra, a high‐altitude (4,100 m above sea level) hypersaline, closed‐basin lake in northwestern Argentina, and explore the potential for recovery of environmental signals from these unique sedimentary archives. Spatial heterogeneity in hydrological regime helps define zones inside Laguna Negra, each with their own morphologically distinct microbialite type. Most notably, platey microbialites (in Zone 3A) are precipitated by evaporative concentration processes, while discoidal oncolites (in Zone 3C) are interpreted result from fluid mixing and biologically mediated nucleation. This spatial heterogeneity is reflected in petrographically distinct carbonate fabrics: micritic, botryoidal, and isopachous. Fabric type is interpreted to reflect a combination of physical and biological influences during mineralization, and paired C‐isotope measurement of carbonate and organic matter supports ecological differences as a dominant control on C‐isotopic evolution between zones. Laminae of Laguna Negra microbialites preserve a range of δ¹³C_carb from +5.75‰ to +18.25‰ and δ¹⁸O_carb from ?2.04‰ to +9.28‰. Temporal trends of lower carbon and oxygen isotopic compositions suggest that the influence of CO₂ degassing associated with evaporation has decreased over time. Combined, these results indicate that microbialite archives can provide data that aid in interpretation of both lake paleohydrology and paleoenvironmental change.     

Contribution of microbial mats to sedimentary surface structures

Summary This paper summarizes studies of sedimentary surface structures in which microbial mats play a role. Intertidal/supratidal transitions of tidal flats of the North Sea coast, and shallow hypersaline water bodies of salterns (Bretagne, Canary and Balearic Islands), and Gavish Sabkha (Sinai) reveal a multitude of sedimentary surface structures which can be grouped and primary biologically controlled structures. Physically controlled surface structures include shrinkage cracks, erosion marks, deformation structures caused by water friction, gas pressure and mineral encrustation. Shrinkage cracks in microbial mats reveal the following features: (i) horizontally arranged cauliflower pattern that differs from the usually orthogonally regular crack morphology in clay, (ii) rounded edges and pillow-like thickening along the crack edges, caused by the growth of mats into the cracks. Criteria of erosion are pocket-like depressions and ripple marks on the thus exposed non-stabilized sand, and residual stacks of microbial mats. Deformation structures are due to water friction causing flotation of loosely attached microbial mats which fold and tear. Gas migration from deeper layers causes domal upheaval, protuberance structures, folds and “fairy rings”. Protuberance structures are caused by the rupture of gas domes and rapid escape of the enclosed gas. The sudden drop of pressure forces sediment to well up from below through the gas channels and to fill the internal hollow spaces of the domes. “Fairy rings” are horizontal ringshaped structures. Their center is the exit point of gas bubbles which escape from the substrate into the shallow water. The bubbles generate concentric waves which cause displacement of fine muddy sediments at the sediment-water interface Such gradual displacement guides mat-constructing microbes to grow concentrically. The “fairy rings” are crowned by pinnacle structures of bacterial and diatom origin. Pinnacles, “fairy rings” and pillow-like coatings of crack margins are biogenic structures which have to be genetically separated from purely physically controlled structures.     

Microbial influence in the Messinian sedimentation: Example of Cap Bon (NE Tunisia)

Messinian sedimentation in Tunisia is characterized by the absence of large carbonate platforms known in many Mediterranean marginal basins. As a result, correlations are not easy to establish in order to integrate it into a general pattern of development at the regional level. However, the discovery of microbial constructions of metric scale makes it possible to precise uncertain points. Thus in the sector of Cap Bon in the northeast of Tunisia, stromatolitic constructions can form, over distances of several hundred meters, domes containing columnar structures at different scales as well as carbonate beds showing sedimentary ripples also of microbialite nature. The highlighting of an assemblage of microbialites, associated with oolitic deposits, allows linking these formations to the Terminal Carbonate Complex which finds its place at a part of the so-called Messinian Salinity Crisis.     

Modern carbonate microbialites from an asbestos open pit pond, Yukon, Canada

Microbialites were discovered in an open pit pond at an abandoned asbestos mine near Clinton Creek, Yukon, Canada. These microbialites are extremely young and presumably began forming soon after the mine closed in 1978. Detailed characterization of the periphyton and microbialites using light and scanning electron microscopy was coupled with mineralogical and isotopic analyses to investigate the mechanisms by which these microbialites formed. The microbialites are columnar in form (cm scale), have an internal spherulitic fabric (mm scale), and are mostly made of aragonite, which is supersaturated in the subsaline pond water. Initial precipitation is seen as acicular aragonite crystals nucleating onto microbial biomass and detrital particles. Continued precipitation entombs benthic diatoms (e.g. Brachysira vitrea), filamentous algae (e.g. Oedogonium sp.), dinoflagellates, and cyanobacteria. The presence of phototrophs at spherulite centers strongly suggests that these microbes play an important initial role in aragonite precipitation. Substantial growth of individual spherulites occurs abiotically through periodic precipitation of aragonite that forms concentric laminations around spherulite centers while pauses in spherulite growth allow for colonization by microbes. Aragonite associated with biomass (δ(13)C = -4.6‰ VPDB) showed a (13)C-enrichment of 0.8‰ relative to aragonite exhibiting no biomass (δ(13)C = -5.4‰ VPDB), which suggests a modest removal of isotopically light dissolved inorganic carbon by phototrophs. The combination of a low sedimentation rate, high calcification rate, and low microbial growth rate appears to result in the formation of these microbialites. The formation of microbialites at an historic mine site demonstrates that an anthropogenically constructed environment can foster microbial carbonate formation.     

Carbonate fabrics in the modern microbialites of Pavilion Lake: two suites of microfabrics that reflect variation in microbial community morphology,growth habit,and lithification

Modern microbialites in Pavilion Lake, BC, provide an analog for ancient non‐stromatolitic microbialites that formed from in situ mineralization. Because Pavilion microbialites are mineralizing under the influence of microbial communities, they provide insights into how biological processes influence microbialite microfabrics and mesostructures. Hemispherical nodules and micrite–microbial crusts are two mesostructures within Pavilion microbialites that are directly associated with photosynthetic communities. Both filamentous cyanobacteria in hemispherical nodules and branching filamentous green algae in micrite–microbial crusts were associated with calcite precipitation at microbialite surfaces and with characteristic microfabrics in the lithified microbialite. Hemispherical nodules formed at microbialite surfaces when calcite precipitated around filamentous cyanobacteria with a radial growth habit. The radial filament pattern was preserved within the microbialite to varying degrees. Some subsurface nodules contained well‐defined filaments, whereas others contained only dispersed organic inclusions. Variation in filament preservation is interpreted to reflect differences in timing and amount of carbonate precipitation relative to heterotrophic decay, with more defined filaments reflecting greater lithification prior to degradation than more diffuse filaments. Micrite–microbial crusts produce the second suite of microfabrics and form in association with filamentous green algae oriented perpendicular to the microbialite surface. Some crusts include calcified filaments, whereas others contained voids that reflect the filamentous community in shape, size, and distribution. Pavilion microbialites demonstrate that microfabric variation can reflect differences in lithification processes and microbial metabolisms as well as microbial community morphology and organization. Even when the morphology of individual filaments or cells is not well preserved, the microbial growth habit can be captured in mesoscale microbialite structures. These results suggest that when petrographic preservation is extremely good, ancient microbialite growth structures and microfabrics can be interpreted in the context of variation in community organization, community composition, and lithification history. Even in the absence of distinct microbial microfabrics, mesostructures can capture microbial community morphology.     

Photosynthesis versus Exopolymer Degradation in the Formation of Microbialites on the Atoll of Kiritimati,Republic of Kiribati,Central Pacific

Aragonitic microbialites, characterized by a reticulate fabric, were discovered beneath lacustrine microbial mats on the atoll of Kiritimati, Republic of Kiribati, Central Pacific. The microbial mats, with cyanobacteria as major primary producers, grow in evaporated seawater modified by calcium carbonate and gypsum precipitation and calcium influx via surface and/or groundwaters. Despite the high aragonite supersaturation and a high photosynthetic activity, only minor aragonite precipitates are observed in the top parts of the microbial mats. Instead, major aragonite precipitation takes place in lower mat parts at the transition to the anoxic zone. The prokaryotic community shows a high number of phylotypes closely related to halotolerant taxa and/or taxa with preference to oligotrophic habitats. Soil- and plant- inhabiting bacteria underline a potential surface or subsurface influx from terrestrial areas, while chitinase-producing representatives coincide with the occurrence of insect remains in the mats. Strikingly, many of the clones have their closest relatives in microorganisms either involved in methane production or consumption of methane or methyl compounds. Methanogens, represented by the methylotrophic genus Methanohalophilus, appear to be one of the dominant organisms in anaerobic mat parts. All this points to a significant role of methane and methyl components in the carbon cycle of the mats. Nonetheless, thin sections and physicochemical gradients through the mats, as well as the ¹²C-depleted carbon isotope signatures of carbonates indicate that spherulitic components of the microbialites initiate in the photosynthesis-dominated orange mat top layer, and further grow in the green and purple layer below. Therefore, these spherulites are considered as product of an extraordinary high photosynthesis effect simultaneous to a high inhibition by pristine exopolymers. Then, successive heterotrophic bacterial activity leads to a condensation of the exopolymer framework, and finally to the formation of crevice-like zones of partly degraded exopolymers. Here initiation of horizontal aragonite layers and vertical aragonite sheets of the microbialite occurs, which are considered as a product of high photosynthesis at decreasing degree of inhibition. Finally, at low supersaturation and almost lack of inhibition, syntaxial growth of aragonite crystals at lamellae surfaces leads to thin fibrous aragonite veneers. While sulfate reduction, methylotrophy, methanogenesis and ammonification play an important role in element cycling of the mat, there is currently no evidence for a crucial role of them in CaCO₃ precipitation. Instead, photosynthesis and exopolymer degradation sufficiently explain the observed pattern and fabric of microbialite formation.     

Microatoll microbialites of Lake Clifton,Western Australia: Morphological analogues ofCryptozoön proliferum Hall,the first formally-named stromatolite

Summary The Linnaean nameCryptozo?n proliferum Hall was proposed in 1883 for a previously undescribed life-form preserved in spectacular exposures of Cambrian limestones in New York State, USA. It is now recognised that these are exposures of stromatolitic microbialites, laminated organosedimentary structures formed from interaction between a benthic microbial community (BMC) and the environment. Microbialites are neither fossil organisms nor trace fossils. These complex structures are the products of dissipative, self-organising systems involving a BMC, the external environment and the accreting microbialite. Functionally analogous BMCs of different species compositions may build similar structures in similar environments in quite separate periods. The type exposures ofCryptozo?n proliferum show objects composed of complex, concentric rings, up to a metre in diameter, that have grown laterally without any restriction other than that provided by neighbouring structures. They are not the relicts of domes truncated by penecontemporaneous erosion or Pleistocene glaciation, but depositional forms in which upward growth was restricted. Analogous modern structures occur on a reef platform along the north east shore of hyposaline Lake Clifton, Western Australia. These are tabular thrombolitic microbialites that vary lakeward across the reef platform from low, compound structures to discrete, concentric structures up to 50 cm high. The Lake Clifton forms are, in turn, morphological analogues of microatolls found on coral reef platforms. Coral microatolls are coral colonies with flat, dead tops and living perimeters in which upward growth is constrained by the sea surface. In shallow water they form circular rims of laterally growing coral around a dead centre. In deeper water they form coral heads that develop flat tops on reaching sea level. It is concluded that both the tabular microbialites of Lake Clifton and the type exposures ofCryptozo?n proliferum are analogous to coral microatolls in both form and origin-structures that have been able to grow laterally, but in which upward growth is restricted by subaerial exposure. Similar microatoll microbialites have been described from other modern environments, including Great Salt Lake, Utah, USA and Stocking Island, Exuma Cays, Bahamas. Ancient examples may include some of the “tufa” deposits of the Basal Purbeck Formation in Dorset, UK, as well as the coalesced domal bioherms of the Upper Cambrian Arrinthrunga Formation of the Georgina Basin, Central Australia, and the “washbowl” structures described from the B?tsfjord Formation of the Varanger Peninsula, north Norway. Progress towards a reliable interpretation of ancient microbialites depends on an understanding of modern environments in which analogous structures are forming. This study of microatolls has demonstrated that other sessile life forms may create colonial ecomorphs that, used cautiously, can serve as analogues for understanding the factors controlling the growth and form of microbialites. The surprising lack of pre-Pleistocene examples of microatolls recorded to date has simply been due to their lack of recognition in the geological record. They occur in sequences from the Proterozoic onwards, and provide powerful environmental indicators of ancient reef platforms on which biological growth was adjusted to contemporary sea level.     

Field- and Lab-Based Potentiometric Titrations of Microbial Mats from the Fairmont Hot Spring,Canada

Potentiometric titrations are an effective tool to constrain the protonation constants and site concentrations for microbial surface ligands. Protonation models developed from these experiments are often coupled with data from metal adsorption experiments to calculate microbial ligand-metal binding constants. Ultimately, the resulting surface complexation models can be used to predict metal immobilization behavior across diverse chemical conditions. However, most protonation and metal-ligand thermodynamic constants have been generated in laboratory experiments that use cultured microbes which may differ in their chemical reactivity from environmental samples. In this study, we investigate the use of in situ field potentiometric titrations of microbial mats at a carbonate hot spring located at Fairmont Hot Springs, British Columbia, with the aim to study microbial reactivities in a natural field system. We found that authigenic carbonate minerals complicated the potentiometric titration process due to a “carbonate spike” introduced by the contribution of inorganic carbonate mineral dissolution and subsequent carbonate speciation changes during the transition from low to high pH. This inhibits the determination of microbial surface ligand variety and concentrations. Our preliminary study also highlights the need for developing novel probes to quantify in situ microbial mat reactivity in future field investigations.     

Molecular and lipid biomarker analysis of a gypsum‐hosted endoevaporitic microbial community

Modern evaporitic microbial ecosystems are important analogs for understanding the record of earliest life on Earth. Although mineral‐depositing shallow‐marine environments were prevalent during the Precambrian, few such environments are now available today for study. We investigated the molecular and lipid biomarker composition of an endoevaporitic gypsarenite microbial mat community in Guerrero Negro, Mexico. The 16S ribosomal RNA gene‐based phylogenetic analyses of this mat corroborate prior observations indicating that characteristic layered microbial communities colonize gypsum deposits world‐wide despite considerable textural and morphological variability. Membrane fatty acid analysis of the surface tan/orange and lower green mat crust layers indicated cell densities of 1.6 × 10⁹ and 4.2 × 10⁹ cells cm^?3, respectively. Several biomarker fatty acids, ?7,10‐hexadecadienoic, iso‐heptadecenoic, 10‐methylhexadecanoic, and a ?12‐methyloctadecenoic, correlated well with distributions of Euhalothece, Stenotrophomonas, Desulfohalobium, and Rhodobacterales, respectively, revealed by the phylogenetic analyses. Chlorophyll (Chl) a and cyanobacterial phylotypes were present at all depths in the mat. Bacteriochlorophyl (Bchl) a and Bchl c were first detected in the oxic‐anoxic transition zone and increased with depth. A series of monomethylalkanes (MMA), 8‐methylhexadecane, 8‐methylheptadecane, and 9‐methyloctadecane were present in the surface crust but increased in abundance in the lower anoxic layers. The MMA structures are similar to those identified previously in cultures of the marine Chloroflexus‐like organism ‘Candidatus Chlorothrix halophila’ gen. nov., sp. nov., and may represent the Bchl c community. Novel 3‐methylhopanoids were identified in cultures of marine purple non‐sulfur bacteria and serve as a probable biomarker for this group in the lower anoxic purple and olive‐black layers. Together microbial culture and environmental analyses support novel sources for lipid biomarkers in gypsum crust mats.     

‘Stromatolites’ built by sponges and microbes – a new type of Phanerozoic bioconstruction

Two ‘stromatolites’ from Carboniferous and Triassic carbonates previously regarded as microbial bioconstructions are analysed and reinterpreted as sponge‐microbial build‐ups. The automicritic aggregations in these build‐ups are similar to the previously reported fossils of keratose demosponges in showing moulded anastomosing filamentous structures. All the studied columnar or domal constructions were formed in turbulent water with high sedimentation rate. The Carboniferous build‐ups were constructed in the shallow subtidal zone of an open shelf or a ramp. The laminations within the stromatolite‐like columns are composed of alternating dark micritic laminae of sponge fossils and pale laminae of neomorphic microspars. The accretion of these columns is probably related to the repeated cycles of sponge growth, rapid lithification after burial, re‐exposure and erosion, and settlement of new generations. The Triassic rocks are presumed to have been precipitated in a slightly evaporitic environment based on lithological features. They show a transition from planar laminae, which were formed under the influence of microbial mats, to stromatolitic columnar or domal build‐ups, which are dominated by stacked micritic clumps of probable sponge fossils. The sponge–microbe alternation may have been controlled by variation of salinity. Comparable with a recent study, this work shows that sponge‐related bioconstructions can be morphologically similar to microbialites in the level of mega‐ and mesostructures.     

A Mediterranean Holocene restricted coastal lagoon under arid climate: Case of the sedimentary record of Sabkha Boujmel (SE Tunisia)

The Holocene sedimentary record of Sabkha Boujmel (SE Tunisia) is expressed by a shallowing-upward carbonate lagoon-tidal flat cycle (2.3 m thick) unconformably overlying continental silt-sandy sediment, Late Würmian in age. The sedimentary package of this cycle starts with transgressive marginal shallow marine (intertidal to subtidal) bioclastic sands grading upwards to black mudstone, rich in organic matter (T.O.C. up to 1.3%) deposited within a lagoon protected from the sea by Upper Pleistocene lithified sand spits.The uppermost part of the cycle is represented by oobioclastic carbonate sands covered with dead biodegraded microbial mats and/or reddish sands of aeolian origin deposited in intertidal to supratidal environments. The facies arrangement, particularly the spatial distribution of the ancient and the more recent microbial mats, records the progressive infilling of the lagoon as well as the progradation of the shoreline during the last 2000 years. The organic-rich facies which provide an age varying between 4130 and 6800 yr B.P. were deposited when the Boujmel lagoon started to be progressively separated from the Mediterranean Sea.The main factors controlling the facies and the thickness variation are the local topographic sea-floor irregularities most likely controlled by the inheritance morphology resulting from an important fluviatile digging that occurred during the last glacial maximum, the relative sea-level fluctuations, the hydro-isostatic rebound and the climate.     

Prokaryote populations of extant microbialites along a depth gradient in Pavilion Lake,British Columbia,Canada

Pavilion Lake in British Columbia, Canada, is home to modern‐day microbialites that are actively growing at multiple depths within the lake. While microbialite morphology changes with depth and previous isotopic investigations suggested a biological role in the formation of these carbonate structures, little is known about their microbial communities. Microbialite samples acquired through the Pavilion Lake Research Project (PLRP) were first investigated for phototrophic populations using Cyanobacteria‐specific primers and 16S rRNA gene cloning. These data were expounded on by high‐throughput tagged sequencing analyses of the general bacteria population. These molecular analyses show that the microbial communities of Pavilion Lake microbialites are diverse compared to non‐lithifying microbial mats also found in the lake. Phototrophs and heterotrophs were detected, including species from the recently described Chloroacidobacteria genus, a photoheterotroph that has not been previously observed in microbialite systems. Phototrophs were shown as the most influential contributors to community differences above and below 25 meters, and corresponding shifts in heterotrophic populations were observed at this interface as well. The isotopic composition of carbonate also mirrored this shift in community states. Comparisons to previous studies indicated this population shift may be a consequence of changes in lake chemistry at this depth. Microbial community composition did not correlate with changing microbialite morphology with depth, suggesting something other than community changes may be a key to observed variations in microbialite structure.     

Evidence of oxygenic phototrophy in ancient phosphatic stromatolites from the Paleoproterozoic Vindhyan and Aravalli Supergroups,India

Fossil microbiotas are rare in the early rock record, limiting the type of ecological information extractable from ancient microbialites. In the absence of body fossils, emphasis may instead be given to microbially derived features, such as microbialite growth patterns, microbial mat morphologies, and the presence of fossilized gas bubbles in lithified mats. The metabolic affinity of micro‐organisms associated with phosphatization may reveal important clues to the nature and accretion of apatite‐rich microbialites. Stromatolites from the 1.6 Ga Chitrakoot Formation (Semri Group, Vindhyan Supergroup) in central India contain abundant fossilized bubbles interspersed within fine‐grained in situ‐precipitated apatite mats with average δ¹³C_org indicative of carbon fixation by the Calvin cycle. In addition, the mats hold a synsedimentary fossil biota characteristic of cyanobacterial and rhodophyte morphotypes. Phosphatic oncoid cone‐like stromatolites from the Paleoproterozoic Aravalli Supergroup (Jhamarkotra Formation) comprise abundant mineralized bubbles enmeshed within tufted filamentous mat fabrics. Construction of these tufts is considered to be the result of filamentous bacteria gliding within microbial mats, and as fossilized bubbles within pristine mat laminae can be used as a proxy for oxygenic phototrophy, this provides a strong indication for cyanobacterial activity in the Aravalli mounds. We suggest that the activity of oxygenic phototrophs may have been significant for the formation of apatite in both Vindhyan and Aravalli stromatolites, mainly by concentrating phosphate and creating steep diurnal redox gradients within mat pore spaces, promoting apatite precipitation. The presence in the Indian stromatolites of alternating apatite‐carbonate lamina may result from local variations in pH and oxygen levels caused by photosynthesis–respiration in the mats. Altogether, this study presents new insights into the ecology of ancient phosphatic stromatolites and warrants further exploration into the role of oxygen‐producing biotas in the formation of Paleoproterozoic shallow‐basin phosphorites.