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The Upper Cambrian Lower Qiulitag Group in the Tarim Basin, NW China, is overwhelmingly composed of cyclic dolomites. Based on extensive field investigations and facies analysis from four outcrop sections in the Bachu-Keping area, northwestern Tarim Basin, four main types of facies are recognized: open-marine subtidal, restricted shallow subtidal, intertidal, and supratidal facies, and these are further subdivided into ten lithofacies. In general, these facies are vertically arranged into shallowing-upward, metre-scale cycles. These cycles are commonly composed of a thin basal horizon reflecting abrupt deepening, and a thicker upper succession showing gradual shallowing upwards. Based on the vertical facies arrangements and changes across boundary surfaces, two types of cycle: peritidal and shallow subtidal cycle, are further identified. The peritidal cycles, predominating over the lower-middle Lower Qiulitag Group, commence with shallow subtidal to lower intertidal facies and are capped by inter-supratidal facies. In contrast, the shallow subtidal cycles, dominating the upper Lower Qiulitag Group, are capped by shallow-subtidal facies. Based on vertical lithofacies variations, cycle stacking patterns, and accommodation variations revealed by Fischer plots, six larger-scale third-order depositional sequences (Sq1-Sq6) are recognized. These sequences generally consist of a lower transgressive and an upper regressive systems tract. The transgressive tracts are dominated by thicker-than-average cycles, indicating an overall accommodation increase, whereas the regressive tracts are characterized by thinner-than-average peritidal cycles, indicating an overall accommodation decrease. The sequence boundaries are characterized by transitional zones of stacked thinner-than-average cycles, rather than by a single surface. These sequences can further be grouped into lower-order sequence sets: the lower and upper sequence sets. The lower sequence set, including Sq1-Sq3, is characterized by peritidal facies-dominated sequences and a progressive decrease in accommodation space, indicating a longer-term fall in sea level. In contrast, the upper sequence set (Sq4-Sq6) is characterized by subtidal facies-dominated sequences and a progressive increase in accommodation space, indicating a longer-term rise in sea level.
Today, diverse communities of zooxanthellate corals thrive, but do not build reef, under a wide range of environmental conditions. In these settings they inhabit natural bottom communities, sometimes forming patch-reefs, coral carpets and knobs. Episodes in the fossil record, characterized by limited coral-reef development but widespread occurrence of coral-bearing carbonates, may represent the fossil analogs of these non-reef building, zooxanthellate coral communities. If so, the study of these corals could have valuable implications for paleoenvironmental reconstructions. Here we focus on the evolution of early Paleogene corals as a fossil example of coral communities mainly composed by zooxanthellate corals (or likely zooxanthellate), commonly occurring within carbonate biofacies and with relatively high diversity but with a limited bioconstructional potential as testified by the reduced record of coral reefs. We correlate changes of bioconstructional potential and community compositions of these fossil corals with the main ecological/environmental conditions at that time. The early Paleogene greenhouse climate was characterized by relatively short pulses of warming with the most prominent occurring at the Paleocene-Eocene boundary (PETM event), associated with high weathering rates, nutrient fluxes, and pCO(2) levels. A synthesis of coral occurrences integrated with our data from the Adriatic Carbonate Platform (SW Slovenia) and the Minervois region (SW France), provides evidence for temporal changes in the reef-building capacity of corals associated with a shift in community composition toward forms adapted to tolerate deteriorating sea-water conditions. During the middle Paleocene coral-algal patch reefs and barrier reefs occurred from shallow-water settings, locally with reef-crest structures. A first shift can be traced from middle Paleocene to late Paleocene, with small coral-algal patch reefs and coral-bearing mounds development in shallow to intermediate water depths. In these mounds corals were highly subordinated as bioconstructors to other groups tolerant to higher levels of trophic resources (calcareous red algae, encrusting foraminifera, microbes, and sponges). A second shift occurred at the onset of the early Eocene with a further reduction of coral framework-building capacity. These coral communities mainly formed knobs in shallow-water, turbid settings associated with abundant foraminiferal deposits. We suggest that environmental conditions other than high temperature determined a combination of interrelated stressors that limited the coral-reef construction. A continuous enhancement of sediment load/nutrients combined with geochemical changes of ocean waters likely displaced corals as the main bioconstructors during the late Paleocene-early Eocene times. Nonetheless, these conditions did not affect the capacity of some corals to colonize the substrate, maintain biodiversity, and act as locally important carbonate-sediment producers, suggesting broad environmental tolerance limits of various species of corals. The implications of this study include clues as to how both ancient and modern zooxanthellate corals could respond to changing climate.
The Paleocene-Eocene thermal maximum represents one of the most rapid and extreme warming events in the Cenozoic. Shallow-water stratigraphic sections from the Adriatic carbonate platform offer a rare opportunity to learn about the nature of Paleocene-Eocene thermal maximum and the effects on shallow-water ecosystems. We use carbon and oxygen isotope stratigraphy, in conjunction with detailed larger benthic foraminiferal biostratigraphy, to establish a high-resolution paleoclimatic record for the Paleocene-Eocene thermal maximum. A prominent negative excursion in delta C-13 curves of bulk-rock (similar to 1 parts per thousand-3 parts per thousand), matrix (similar to 4 parts per thousand), and foraminifera (similar to 6 parts per thousand) is interpreted as the carbon isotope excursion during the Paleocene-Eocene thermal maximum. The strongly C-13-depleted delta(1)d(3)C record of our shallow-marine carbonates compared to open-marine records could result from organic matter oxidation, suggesting intensified weathering, runoff, and organic matter flux.
The Ilerdian larger benthie foraminiferal turnover is documented in detail based on high-resolution correlation with the carbon isotopic excursion. The turnover is described as a two-step process, with the first step (early Ilerdian) marked by a rapid diversification of small alveolinids and nummulitids with weak adult dimorphism, possibly as adaptations to fluctuating Paleocene-Eocene thermal maximum nutrient levels, and a second step (middle Ilerdian) characterized by a further specific diversification, increase of shell size, and well-developed adult dimorphism. Within an evolutionary scheme controlled by long-term biological processes, we argue that high seawater temperatures could have stimulated the early Ilerdian rapid specific diversification. Together, these data help elucidate the effects of global warming and associated feedbacks in shallow-water ecosystems, and by inference, could serve as an assessment analog for future changes.
Upper Thanetian microbialite-coral mounds from the Adriatic Carbonate Platform (SW Slovenia) are described herein for the first time, representing an important case study of extensively microbially-cemented boundstones in the Early Paleogene. The mounds are constructed primarily by microbialites associated to small-sized coral colonies, forming metric bioconstructions in a mid-ramp setting. Detailed macroscopic and microscopic studies show that microbes are the major framework builders, playing a prominent role in the stabilization and growth of the mounds, with corals being the second most important component. Microbial carbonates represent up to 70% of the mounds, forming centimetric-thick crusts alternating with coral colonies. The microbial nature of the crusts is demonstrated by their growth form and internal microfabrics, showing accretionary, binding, and encrusting growth fabrics, often with gravity-defying geometries. Thin sections and polished slabs reveal a broad range of mesofabrics, with dense, structureless micrite (leiolite), laminated crusts (stromatolites), and clotted micritic masses (thrombolites). A first layer of micro- encrusters, including leiolites and thrombolites, occurs in cryptic habitats, whereas discontinuous stromatolites encrust the upper surface of corals. A second encrustation, the major mound construction phase, follows and is dominated by thrombolites, encrusting corals and other micro-encrusters. This sequence represents the basic constructional unit horizontally and vertically interlocked, in an irregular pattern, to form the mounds. The processes, which favored the deposition of these microbial carbonates, were mainly related to in situ precipitation, with minor evidences for grain agglutination and trapping processes. Scleractinian corals comprise moderately diversified community of small (centimetric) colonial, massive, platy encrusting, and branching forms. Coral colonies are distributed uniformly throughout the mounds without developing any ecological zonation. These features indicate that coral development remained at the pioneer stage throughout the mound growth. The spatial relationships between corals and microbialites, as well as the characteristics of microbial crusts and coral colonies, indicate a strong ecological competition between corals and microbes. A model for the evolution of the trophic structures during the mound growth is proposed, with changes in the paleoecology of the main bioconstructors triggered by frequent environmental perturbations. Turbidity and nutrient pressure, interpreted here as related to frequent recurrences of wet phases during the warm, humid climate of the Uppermost Thanetian, might have promoted temporary dominance of microbes over corals, causing rapid environmentally- driven "phase shifts" in the dominant biota.
Whilst sophisticated multiphase fluid flow models are routinely employed to understand behaviour of oil and gas reservoirs, high-resolution data describing the three-dimensional (3D) distribution of rock characteristics is rarely available to populate models. We present a new approach to developing a quantitative understanding of the effect of individual controls on the distribution of petrophysical properties and their impact on fluid flow. This involves simulating flow through high-detail permeability architectures generated by forward modelling of the coupled depositional-diagenetic evolution of isolated platforms using CARB3D(+). This workflow is exemplified by an investigation of interactions between subsidence and climate, and their expression in spatial variations in reservoir quality in an isolated carbonate platform of similar size and subsidence history to the Triassic Latemar Platform.
Dissolutional lowering during subaerial exposure controls platform-top graininess via platform top hydrodynamics during the subsequent transgression. Dissolved carbonate is reprecipitated as cements by percolating meteoric waters. However, associated subsurface meteoric dissolution generates significant secondary porosity under a more humid climate. Slower subsidence enhances diagenetic overprinting during repeated exposure events. Single-phase streamline simulations show how early diagenesis develops more permeable fairways within the finer-grained condensed units that can act as thief zones for flow from the grainier but less diagenetically altered cyclic units.
Following the Middle Permian (Capitanian) mass extinction there was a global ‘reef eclipse’, and this event had an important role in the Paleozoic-Mesozoic transition of reef ecosystems. Furthermore, the recovery pattern of reef ecosystems in the Wuchiapingian of South China, before the radiation of Changhsingian reefs, is poorly understood. Here, we present a detailed sedimentological account of the Tieqiao section, South China, which records the only known Wuchiapingian reef setting from South China. Six reef growing phases were identified within six transgressive-regressive cycles. The cycles represent changes of deposition in a shallow basin to a subtidal outer platform setting, and the reefal build-ups are recorded in the shallowest part of the cycles above wave base in the euphotic zone. Our results show that the initial reef recovery started from the shallowing up part of the 1st cycle, within the Clarkina leveni conodont zone, which is two conodont zones earlier than previously recognized. In addition, even though metazoans, such as sponges, do become important in the development of the reef bodies, they are not a major component until later in the Wuchiapingian in the 5th and 6th transgressive-regressive cycles. This suggests a delayed recovery of metazoan reef ecosystems following the Middle Permian extinction. Furthermore, even though sponges do become abundant within the reefs, it is the presence and growth of the encrusters Archaeolithoporella and Tubiphytes and abundance of microbial micrites that play an important role in stabilizing the reef structures that form topographic highs.
The occurrence of mounds dominated by siliceous sponges and microbialites is often related to distal, deep settings of middle ramps and shelves. This paper presents evidence for Bajocian (Garanliana garantiana Zone) microbial-siliceous sponge mounds formed in open marine but relatively shallow settings of a ramp from the Iberian Basin of eastern Spain. Marked differences in mound spacing, morphology, and composition of the related intermound facies are observed from distal to more proximal settings. The distal (below storm wave base) settings are characterized by alternating tabular-bedded marls and limestones rich in pelagic fossils (ammonites, belemnites), open-marine thin-shelled bivalves (Bositra-like), as well as peloids, which include widely or randomly spaced isolated, small (up to 0.4 m high) and larger (up to 2.5 m high) mounds with upward accretion. The intermediate (near to above storm wave base) settings show tabular, thickened beds of peloidal and/or intraclastic limestones with closely spaced mounds (similar to 1 m high), which often coalesce laterally, forming extensive lenticular structures (up to 10 m wide). The proximal (above storm wave base) depositional settings consist of tabular to irregular beds of intraclastic limestones with widely spaced small (up to 0.4 m high) mounds with mainly tabular geometries. The mound framework contains variable proportions of microbialites (dense to clotted peloidal thrombolitic fabrics) and siliceous sponges (hexactinellids and lithistids in similar proportion) ranging from planar to conic shapes. These morphological and compositional changes allow characterizing three shallowing-upward sequences (sequences 1-3) developed in the overall regressive trend of a basin-wide, upper Bajocian T-R cycle. Episodic wave reworking of the early-cemented mounds resulted in the formation of peloids, small rounded intraclasts, and large, rounded or subangular intraclasts. These nonskeletal micritic grains show internal fabrics related to those of the mound and/or microbialites. A progressive textural gradation towards greater size and lesser roundness of the nonskeletal grains in the areas in the vicinity of the main mound factory is documented (i.e., from large, subangular intraclasts in the areas close to the main mound factory to peloids in the areas that are far from it). We discuss the alternative model of internal waves (instead of storm-induced waves) as the hydrodynamic agent providing the high-energy events needed to explain the origin of the peloidal-intraclastic intermound facies and, likely, also the nutrients needed by the microbialites and siliceous sponges to grow.
The depositional geometry and facies distribution of an Early Miocene (Burdigalian) carbonate system in the Perfugas Basin (NW Sardinia) comprise a well-exposed example of a transition from a ramp to a steep-flanked platform. The carbonate succession (Sedini Limestone Unit) is composed of two depositional sequences separated by a major erosional unconformity. The lower (sequence 1) records a ramp dominated by heterozoan producers and the upper (sequence 2) is dominated by photozoan producers and displays a gradual steepening of the depositional profile into a steep- flanked platform. This paper shows the process of creating a digital outcrop model including a facies model. This process consists of combining field data sets, including 17 sedimentary logs, and a spatial dataset consisting of differential global positioning system data points measured along key stratigraphic surfaces and sedimentary logs, with the goal of locking traditional field observations into a 3D spatial model. Establishing a precise geometrical framework and visualizing the overall change in the platform geometry and the related vertical and lateral facies variations of the Sedini carbonate platform, allows us to better understand the sedimentary processes leading to the geometrical turn- over of the platform. Furthermore, a detailed facies modeling helps us to gain insight into the detailed depositional dynamics. The final model reproduces faithfully the depositional geometries observed in the outcrops and helps in understanding the relationships between facies and architectural framework at the basin scale. Moreover, it provides the basis to characterize semiquantitatively regional sedimentological features and to make further reservoir and subsurface analogue studies.
The occurrence of neritic microbial carbonates is often related to ecological refuges, where grazers and other competitors are reduced by environmental conditions, or to post-extinction events (e.g. in the Late Devonian, Early Triassic). Here, we present evidence for Middle Jurassic (Bajocian) microbial mounds formed in the normal marine, shallow neritic setting of an inner, ramp system from the High Atlas of Morocco. The microbial mounds are embedded in cross-bedded oolitic facies. Individual mounds show low relief domal geometries (up to 3 m high and 4.5 m across), but occasionally a second generation of mounds exhibits tabular geometries (<1 m high). The domes are circular in plan view and have intact tops, lacking evidence of current influence on mound preferred growth direction or distribution patterns, or truncation. The mound fades consists almost entirely of non-laminated, micritic thrombolites with branching morphologies and fine-grained, clotted and peloidal fabrics. Normal marine biota are present but infrequent. Several lines of evidence document that microbial mound growth alternates with time intervals of active ooid shoal deposition. This notion is of general significance when compared with modern Bahamian microbialites that co-exist with active sub-aquatic dunes. Furthermore, the lack of detailed studies of Middle Jurassic, normal marine shallow neritic microbial mounds adds a strong motivation for the present study. Specifically, Bajocian mounds formed on a firmground substratum during transgressive phases under condensed sedimentation. Furthermore, a transient increase in nutrient supply in the prevailing mesotrophic setting, as suggested by the heterotrophic-dominated biota, may have controlled microbial mound stages.
The recognition and understanding of vegetated habitats in the fossil record are of crucial importance in order to investigate paleoecological responses and indirectly infer climate and sea-level changes. However, the low preservation potential of plants and macroalgae hampers a direct identification of these environments in the geological past. Here we present sedimentological and paleontological evidences as tool to identify the presence of different seagrass-vegetated environments in the shallow marine settings of the lower Eocene jafnayn platform of Oman and their responses to paleoenvironmental changes. The studied lower Eocene deposits consist of well bedded, nodular pacicstones dominated by encrusting acervulinid and alveolinid foraminifera passing upward to an alternance of packstones with echinoids and quartz grains and grainstones rich in Orbitolites, smaller miliolid foraminifera and quartz grains. The presence of seagrass is inferred by the occurrence of encrusting acervulinids and soritid Orbitolites, as well as by their test morphologies together with further sedimentological criteria. The clear shift observed in the faunal assemblages and sedimentary features may be related to a major reorganization of the carbonate system passing from a carbonate platform to a ramp-like platform with increased terrigenous sedimentation. Heterotroph tubular acervulinids and oligotroph alveolinids of the carbonate platform were replaced upward by more heterotroph organisms such as large, discoidal Orbitolites and smaller miliolids, most likely due to enhanced nutrient levels which would have led to a change of phytal substrate, from cylindrical-leaf dominated grasses into flat-leafed ones. (C) 2016 Elsevier B.V. All rights reserved.