机构地区:[1]Department of Life Sciences, Kingston Lane, Brunel University [2]State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University [3]CAS Key Laboratory of Economic Stratigraphy and Palaeogeography, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences [4]CASP, Department of Earth Sciences, University of Cambridge
出 处:《Journal of Palaeogeography》2018年第1期32-47,共16页古地理学报(英文版)
基 金:support in Southwest Petroleum University;National Scientific and Technology Major Project (Grant No. 2016ZX05004002-001);National Natural Science Foundation of China (Grant No. 41602166)
摘 要:Carbonate sediments deposited in normally-oxygenated shallow ocean waters of the latest Permian period, immediately prior to the end-Permian mass extinction, contain well-developed diverse shelly faunas. After the extinction of these skeletal metazoans, the sediments commonly comprise microbialites(regarded by most authors as benthic) and associated facies bearing evidence interpreted by many authors to indicate reduced oxygenation of the shallow ocean waters. However, the evidence of oxygenation state is inconsistent and the sequences have gaps, indicated in the following 5 points:1) Shelly fossils occur commonly in post-extinction shallow marine limestones, and likely to have been aerated in contact with the atmosphere. Nevertheless, although the largest mass extinction in Earth history may have caused reduced body size in shelly organisms, such reduction is arguably due to environmental stress of lowered oxygenation. Discriminating between these controls remains a challenge.2) Abundant pyrite framboids in many post-extinction limestones are interpreted by several authors as indicating dysoxic contemporaneous waters, so the organisms that lived there, now shelly fossils, were dysaerobic. However, verification is problematic because pyrite framboids scattered amongst shelly fossils cannot have formed amongst living organisms, which need at least some oxygen; synsedimentary framboid formation requires anoxic conditions in the redox boundary where sulphate-reducing processes work. Thus, framboids and shelly fossils found together means taphonomic mixing of sediments, destroying original depositional relationships so that it is not possible to determine whether the shells were aerobic or dysaerobic prior to sediment mixing. Furthermore, diagenetic growth of framboids is possible, as is import of previously-formed framboids from deeper water during upwelling. Thus, there is no proof of an environmental link between framboid size and occurrence, and contemporaneous oxygenation in these post-extinction shallow water fCarbonate sediments deposited in normally-oxygenated shallow ocean waters of the latest Permian period, immediately prior to the end-Permian mass extinction, contain well-developed diverse shelly faunas. After the extinction of these skeletal metazoans, the sediments commonly comprise microbialites(regarded by most authors as benthic) and associated facies bearing evidence interpreted by many authors to indicate reduced oxygenation of the shallow ocean waters. However, the evidence of oxygenation state is inconsistent and the sequences have gaps, indicated in the following 5 points:1) Shelly fossils occur commonly in post-extinction shallow marine limestones, and likely to have been aerated in contact with the atmosphere. Nevertheless, although the largest mass extinction in Earth history may have caused reduced body size in shelly organisms, such reduction is arguably due to environmental stress of lowered oxygenation. Discriminating between these controls remains a challenge.2) Abundant pyrite framboids in many post-extinction limestones are interpreted by several authors as indicating dysoxic contemporaneous waters, so the organisms that lived there, now shelly fossils, were dysaerobic. However, verification is problematic because pyrite framboids scattered amongst shelly fossils cannot have formed amongst living organisms, which need at least some oxygen; synsedimentary framboid formation requires anoxic conditions in the redox boundary where sulphate-reducing processes work. Thus, framboids and shelly fossils found together means taphonomic mixing of sediments, destroying original depositional relationships so that it is not possible to determine whether the shells were aerobic or dysaerobic prior to sediment mixing. Furthermore, diagenetic growth of framboids is possible, as is import of previously-formed framboids from deeper water during upwelling. Thus, there is no proof of an environmental link between framboid size and occurrence, and contemporaneous oxygenation in these post-extinction shallow water f
关 键 词:STROMATOLITE Thrombolite MICROBIALITE Permian-Triassic boundary Pyrite ANOXIA
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