Massive cryptic microbe-sponge deposits in a Devonian fore-reef slope (Elbingerode Reef Complex, Harz Mts., Germany)

A massive occurrence of microbial carbonates, including abundant sponge remains, within the Devonian Elbingerode Reef Complex was likely deposited in a former cavity of the fore-reef slope during the early Frasnian. It is suggested that the formation of microbial carbonate was to a large part favored by the activity of heterotrophic, i.e., sulfate-reducing bacteria, in analogy to Quaternary coral reef microbialites. The Elbingerode Reef Complex is an example of an oceanic or Darwinian barrier reef system. In modern barrier reef settings, microbialite formation is commonly further facilitated by weathering products from the central volcanic islands. The Devonian microbialites of the Elbingerode Reef Complex occur in the form of reticulate and laminated frameworks. Reticulate framework is rich in hexactinellid glass sponges, the tissue decay of which led to the formation of abundant micrite as well as peloidal and stromatactis textures. Supposed calcimicrobes such as Angusticellularia (formerly Angulocellularia) and Frutexites, also known from cryptic habitats, were part of the microbial association. The microbial degradation of sponge tissue likely also contributed to the laminated framework accretion as evidenced by the occurrence of remains of so-called “keratose” demosponges. Further typical textures in the microbialite of the Elbingerode Reef Complex include zebra limestone, i.e., the more or less regular intercalation of microbial carbonate and cement. Elevated concentrations of magnesium in the microbialite as compared to the surrounding metazoan (stromatoporoid-coral) reef limestone suggests that the microbialite of the Elbingerode Reef Complex was initially rich in high-magnesium calcite, which would be yet another parallel to modern, cryptic coral reef microbial carbonates. Deposition and accretion of the microbialite largely occurred in oxygenated seawater with suboxic episodes as indicated by the trace element (REE + Y) data.

Possible poriferan body fossils in early Neoproterozoic microbial reefs

Molecular phylogeny indicates that metazoans (animals) emerged early in the Neoproterozoic era1, but physical evidence is lacking. The search for animal fossils from the Proterozoic eon is hampered by uncertainty about what physical characteristics to expect. Sponges are the most basic known animal type2,3; it is possible that body fossils of hitherto-undiscovered Proterozoic metazoans might resemble aspect(s) of Phanerozoic fossil sponges. Vermiform microstructure4,5, a complex petrographic feature in Phanerozoic reefal and microbial carbonates, is now known to be the body fossil of nonspicular keratosan demosponges6–10. This Article presents petrographically identical vermiform microstructure from approximately 890-million-year-old reefs. The millimetric-to-centimetric vermiform-microstructured organism lived only on, in and immediately beside reefs built by calcifying cyanobacteria (photosynthesizers), and occupied microniches in which these calcimicrobes could not live. If vermiform microstructure is in fact the fossilized tissue of keratose sponges, the material described here would represent the oldest body-fossil evidence of animals known to date, and would provide the first physical evidence that animals emerged before the Neoproterozoic oxygenation event and survived through the glacial episodes of the Cryogenian period.

Microfabric features of microbial carbonates: experimental and natural evidence of mold holes and crusts

Results of our study based on examination of induced precipitation of carbonate by a cyanobacterium, Lyngbya in the laboratory, and the analyses of microphotographs of both modern and ancient microbial carbonates, demonstrated the importance of recognition of mold holes and carbonate crusts in understanding microbial carbonates. In the experiment, only cyanobacteria Lyngbya can induce precipitation of carbonate, forming scattered grains on the surface of Lyngbya filaments. Carbonate crusts enclosing the old parts of the filaments were formed through aggregation of these scatter grains while mold holes were formed after decay of the filaments. Mainly based on the experiment, six different ways of microbial carbonate formation were recognized: (1) trapping without mold holes, (2) trapping with mold holes, (3) particle-forming induced-precipitation of carbonate, (4) discrete crust-forming induced-precipitation of carbonate, (5) induced precipitation, forming tangled crusts that build a porous construction, and (6) induced precipitation, forming a dense construction. And mold holes and crusts can form in ways (4), (5), and (6). Examination of both modern microbial carbonates from the Shark Bay of Australia, Highborne Cay of Bahamas and the atoll of Kiritimati and the microbialites from the Cambrian dolostone sequence in Tarim, Xinjiang, China all demonstrated the limitation of recognizing only mesofabric features and importance of examining microfabric features for understanding of the genesis of the microbial carbonates and their proper classification. The shape, size and arrangement of the mold holes, crusts, and the features of the minerals filling in pores between the crusts, which are referred as the microfabric features here, are keys to better understand the formation and environments of both modern and ancient microbial carbonates.

Depositional system and lake-stage control on microbialite morphology, Green River Formation, eastern Uinta Basin, Colorado and Utah, U.S.A.

ABSTRACT Lake-margin lacustrine carbonates of the Green River Formation, in the eastern Uinta basin of Colorado and Utah, occur interbedded with fluvial and shoreline-parallel sandstone and shale. Microbial bindstones were deposited in a saline-alkaline lake during and after the Early Eocene Climate Optimum (EECO) (52–50 million years ago) that is characterized by global hot-house conditions, elevated atmospheric CO2, and highly fluctuating climate conditions. The stratigraphic architecture, chemostratigraphy, and morphology of the microbialites and other associated carbonate beds can be related to these climatic conditions. Three facies associations are recognized in the carbonate units across the lake margin from upper littoral to lower sublittoral environments: facies association 1, delta proximal non-microbial carbonates, characterized by quartzose bioclastic, peloidal, intraclastic packstones and grainstones–rudstones, quartose peloid wackestones and sandy oil shale; facies association 2, microbialite associated non-microbial carbonates, composed of ostracod, ooilitic, peloidal packstones–grainstones and intraclastic packstones, grainstones and rudstones; and facies association 3, microbial carbonates, consisting of diverse forms of stromatolitic and thrombolitic lithofacies. Multiple scales of carbonate cyclicity are suggested by shifts of δ18O and δ13C stable isotopes and deepening-upward microbialite facies. High-frequency cycles, on the order of 1 to 5 m thickness, are characterized by positive shifts in stable isotopes and interpreted deepening trends from littoral to lower sublittoral conditions. Large-scale trends, on the order of tens to hundreds of meters thickness record long-term lake changes, including: 1) sparse microbialite deposition during initial fresh conditions in lake stage 1, with low macro-structure diversity and light δ18O and δ13C isotope values; 2) transitional lake stage 2 corresponding to moderate macro-structural diversity, large meter-scale biostromal and biohermal buildups, and a positive shift in δ18O and δ13C isotope values that suggest increasing saline and alkaline conditions; 3) a highly fluctuating lake stage 3 that contains the highest microbialite macro-structural diversity and marks the interval of heaviest δ18O and δ13C isotope values, suggesting the greatest lake restriction, and the highest salinity and alkalinity conditions; and 4) a rising lake stage 4 that marks the lowest microbialite macro-structure diversity and a reversal in trend of δ18O and δ13C isotope values, that indicate deepening and freshening conditions.

Chromium Isotope Systematics in Modern and Ancient Microbialites

Changes in stable chromium isotopes (denoted as δ53Cr) in ancient carbonate sediments are increasingly used to reconstruct the oxygenation history in Earth’s atmosphere and oceans through time. As a significant proportion of marine carbonate older than the Cambrian is microbially-mediated, the utility of δ53Cr values in ancient carbonates hinges on whether these sediments accurately capture the isotope composition of their environment. We report Cr concentrations (Cr) and δ53Cr values of modern marginal marine and non-marine microbial carbonates. These data are supported by stable C and O isotope compositions, as well as rare earth elements and yttrium (REY) concentrations. In addition, we present data on ancient analogs from Precambrian strata. Microbial carbonates from Marion Lake (Australia, δ53Cr ≈ 0.99‰) and Mono Lake (USA, ≈0.78‰) display significantly higher δ53Cr values compared with ancient microbialites from the Andrée Land Group in Greenland (720 Ma, ≈0.36‰) and the Bitter Springs Formation in Australia (800 Ma, ≈−0.12‰). The δ53Cr values are homogenous within microbialite specimens and within individual study sites. This indicates that biological parameters, such as vital effects, causing highly variable δ53Cr values in skeletal carbonates, do not induce variability in δ53Cr values in microbialites. Together with stable C and O isotope compositions and REY patterns, δ53Cr values in microbialites seem to be driven by environmental parameters such as background lithology and salinity. In support, our Cr and δ53Cr results of ancient microbial carbonates agree well with data of abiotically precipitated carbonates of the Proterozoic. If detrital contamination is carefully assessed, microbialites have the potential to record the δ53Cr values of the waters from which they precipitated. However, it remains unclear if these δ53Cr values record (paleo-) redox conditions or rather result from other physico-chemical parameters.

Sedimentary and Diagenetic Features and Their Impacts on Microbial Carbonate Reservoirs in the Fourth Member of the Middle Triassic Leikoupo Formation, Western Sichuan Basin, China

In recent years, the discovery of two gas fields in the fourth member of the Leikoupo Formation in the Western Sichuan Basin of SW China confirmed the exploration potential of microbial carbonates. The aim of the present study is to clarify the formation mechanism of the microbial reservoirs in the Leikoupo Formation. For this purpose, lithofacies, depositional environments, and diagenesis analyses were performed in samples collected from cores of 12 wells. The climate of study area was arid during Anisian time, and the water body was restricted. In such a climate, an evaporitic environment was developed, where ten types of lithofacies, dominated by microbial carbonates and gypsum rocks, were recognized. Thrombolites and stromatolites are the main high-quality reservoirs rock types in the fourth member of the Leikoupo Formation in the Western Sichuan Basin of SW China, which developed as microbial mounds, with reservoir space of microbial inter-clot pores, intra-clot pores, fenestral pores, inter-crystalline pores, and cracks. The microbial inter-clot pores are the main reservoir space, formed by trapping and binding of marls by benthic microbial communities. These pores were partially filled with evaporites because of the arid climate, which were subsequently dissolved (mainly gypsum) in the syn-depositional period, thus greatly improving the quality of reservoirs. Although some pores were occluded by multi-stage cements during the burial stage, major pores were well preserved own to the early dolomitization, rapid burial of the Leikoupo Formation, and early charging of hydrocarbon. The early dolomitization enhanced the anti-compaction ability of microbial carbonates during the burial stage. Rapid burial of the Leikoupo succession slowed down early cementation, and it also accelerated the maturation and expulsion process source rock to promote early charging of hydrocarbon in pores, which created a closed system, inhibiting strong burial cementation.