72 research outputs found
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Comment on: Lehrmann, D. J., Bentz, J.M., Wood, T., Goers, A., Dhillon, R., Akin, S., Li, X., Payne, J.L., Kelley, B.M., Meyer, K. M., Schaal, E.K., Suarez, M. B., Yu, M., Qin, Y., Li, R., Minzoni, M., Henderson, C.M., 2015, environmental controls on the gensis of marine microbialites and dissolution surface associated with the end-permian mass extinction: New sctions and observations from the nanpanjiang basin, South Chaina. Palaios
Ostracodes Tournaisiens du massif de la Tombe (Synclinorium de Namur - Belgique)
70 benthic Ostracode species have been discovered in Lower Tournaisian (Tn1b?) and Middle Tournaisian (Tn2) limestones of «Massif de la Tombe» (South part of Namur Synclinorium). A table gives the faunal inventory. Two new species are described: Shishaella hastierensis n. sp. and Bairdia (B.) raoulti n. sp. Paleoecological affinities and variations in the Ostracode assemblage are discussed. Comparison is made with Dinant Synclinorium
Geochemistry of post-extinction microbialites as a powerful tool to assess the oxygenation of shallow marine water in the immediate aftermath of the end-Permian mass extinction
Rapid and profound changes in earth surface environments and biota across the Permian–Triassic boundary are well known and relate to the end-Permian mass extinction event. This major crisis is demonstrated by abrupt facies change and the development of microbialite carbonates on the shallow marine shelves around Palaeo-Tethys and western Panthalassa. Microbialites have been described from a range of sites in end-Permian and basal Triassic marine sedimentary rocks, immediately following the end-Permian mass extinction. Here, we present geochemical data primarily focused on microbialites. Our geochemical analysis shows that U, V, Mo and REE (Ce anomaly) may be used as robust redox proxies so that the microbialites record the chemistry of the ancient ambient sea water. Among the three trace metals reputed to be reliable redox proxies, one (V) is correlated here with terrigenous supply, the other two elements (U and Mo) do not show any significant authigenic enrichment, thereby indicating that oxic conditions prevailed during the growth of microbialites. REE profiles show a prominent negative Ce anomaly, also showing that the shallow marine waters were oxic. Our geochemical data are consistent with the presence of some benthic organisms (ostracods, scattered microgastropods, microbrachiopods and foraminifers) in shallow marine waters that survived the mass extinction event.A. Lethiers, F. Delbès, A. Michel and B. Villemant, Q. Feng, J. Haas, K. Hips and Erdal Kosu
Diverse earliest Triassic ostracod fauna of the non-microbialite-bearing shallow marine carbonates of the Yangou section, South China
Earliest Triassic microbialites in the South China Block and other areas; controls on their growth and distribution
Earliest Triassic microbialites (ETMs) and inorganic carbonate crystal fans formed after the end-Permian mass extinction (ca. 251.4 Ma) within the basal Triassic Hindeodus parvus conodont zone. ETMs are distinguished from rarer, and more regional, subsequent Triassic microbialites. Large differences in ETMs between northern and southern areas of the South China block suggest geographic provinces, and ETMs are most abundant throughout the equatorial Tethys Ocean with further geographic variation. ETMs occur in shallow-marine shelves in a superanoxic stratified ocean and form the only widespread Phanerozoic microbialites with structures similar to those of the Cambro-Ordovician, and briefly after the latest Ordovician, Late Silurian and Late Devonian extinctions. ETMs disappeared long before the mid-Triassic biotic recovery, but it is not clear why, if they are interpreted as disaster taxa. In general, ETM occurrence suggests that microbially mediated calcification occurred where upwelled carbonate-rich anoxic waters mixed with warm aerated surface waters, forming regional dysoxia, so that extreme carbonate supersaturation and dysoxic conditions were both required for their growth. Long-term oceanic and atmospheric changes may have contributed to a trigger for ETM formation. In equatorial western Pangea, the earliest microbialites are late Early Triassic, but it is possible that ETMs could exist in western Pangea, if well-preserved earliest Triassic facies are discovered in future work
New data on the Silurian-Devonian paleontology and biostratigraphy of Bolivia
P. 269-314In order to precisely establish the bio- and chronostratigraphic position of several levels of the Silurian–Devonian succession
of Bolivia, with respect to the International Time Scale, additional Silurian and Devonian localities belonging to
the Eastern Cordillera and the Interandean Zone areas have been recently revised and sampled, both for macrofossils and
palynomorphs. Specifically, the localities are Ñuñumayani, and Muruhuta from the late Silurian–early Devonian time
interval. Correlations with other fossiliferous localities are discussed, namely Huacallani and Rumicorral.S
The Ordovician caryocaridid phyllocarids (Crustacea): diversity and evolutionary tendencies
International audienc
Microbialites and environmental change at the Permian-Triassic boundary: An overview
International audienc
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