There were three typographical errors in the second and third paragraphs of the Introduction. Citation: Salamon MA, Niedźwiedzki R, Lach R, Brachaniec T, Gorzelak P (2013) Correction: Ophiuroids ...Discovered in the Middle Triassic Hypersaline Environment.
New 87Sr/86Sr data based on 127 well-preserved and well-dated conodont samples from South China were measured using a new technique (LA-MC-ICPMS) based on single conodont albid crown analysis. These ...reveal a spectacular climb in seawater 87Sr/86Sr ratios during the Early Triassic that was the most rapid of the Phanerozoic. The rapid increase began in Bed 25 of the Meishan section (GSSP of the Permian–Triassic boundary, PTB), and coincided closely with the latest Permian extinction. Modeling results indicate that the accelerated rise of 87Sr/86Sr ratios can be ascribed to a rapid increase (>2.8×) of riverine flux of Sr caused by intensified weathering. This phenomenon could in turn be related to an intensification of warming-driven runoff and vegetation die-off. Continued rise of 87Sr/86Sr ratios in the Early Triassic indicates that continental weathering rates were enhanced >1.9 times compared to those of the Late Permian. Continental weathering rates began to decline in the middle–late Spathian, which may have played a role in the decrease of oceanic anoxia and recovery of marine benthos. The 87Sr/86Sr values decline gradually into the Middle Triassic to an equilibrium values around 1.2 times those of the Late Permian level, suggesting that vegetation coverage did not attain pre-extinction levels thereby allowing higher runoff.
•In situ Sr isotope measurement using LA-MC-ICPMS on single conodont is applied.•Rapid increase of 87Sr/86Sr coincided closely with the latest Permian extinction.•A box model is used to simulate the influence of FR/FM on ocean 87Sr/86Sr values.•The riverine flux of Sr in the PTB increased by >2.8 times.•The riverine flux of Sr in the Early Triassic increased by >1.9 times.
The impact of mass extinctions on biogeographic patterns remains unclear. Analysis of large-scale biogeographic patterns can provide insights into macroevolutionary processes. Here, we aim to trace ...the biogeographic dynamics of bivalves from the Middle Permian to the Early Jurassic based on an updated dataset, including 25,891 bivalve occurrence data, by using biogeographic connectedness (BC) and multiple-site β-diversity measures. The results reveal a significant bivalve cosmopolitanism event following the Permian–Triassic mass extinction (PTME) and a possible cosmopolitanism event after the Triassic–Jurassic mass extinction (TJME). Analysis of the BC of survivors and newcomers in each event reveals that both potential cosmopolitanism events were related to the selective extinction of endemic taxa, suggesting that endemics are more vulnerable during mass extinctions. The geographic expansion of survivors also possibly contributed to the cosmopolitanism in the aftermath of the PTME, supporting the ecological release hypothesis following the PTME. Finally, we found that the spatial sampling heterogeneity can bias biogeographic patterns, for instance, bivalve cosmopolitanism after the TJME.
•A significant bivalve cosmopolitanism occurred after the P-T mass extinction.•A possible bivalve cosmopolitanism occurred after the T-J mass extinction.•Selective extinction of endemics contributed to the bivalve cosmopolitanisms.•The geographic expansion of survivors contributed to the Induan cosmopolitanism.•The heterogeneity in spatial sampling can strongly bias biogeographic patterns.
Birds and mammals are key elements of modern ecosystems, and many biologists explain their great success by their endothermy, or warm-bloodedness. New palaeontological discoveries point to the ...origins of endothermy in the Triassic, and that birds (archosaurs) and mammals (synapsids) likely acquired endothermy in parallel. Here, a further case is made, that the emergence of endothermy in a stepwise manner began in the Late Permian but accelerated in the Early Triassic. The trigger was the profound destruction wrought by the Permian-Triassic mass extinction (PTME). In the oceans, this was the beginning of the Mesozoic Marine Revolution (MMR), and a similar revolution occurred on land, termed here the Triassic Terrestrial Revolution (TTR). Among tetrapods, both synapsids and archosaurs survived into the Triassic, but numbers were heavily depleted. However, the survivors were marked by the acquisition of endothermy, as shown by bone histology, isotopic analyses, and the acquisition of insulating pelage. Both groups before the PTME had been sprawlers; after the event they adopted parasagittal (erect) gait. The new posture and the new physiology enabled both groups to compete in their ecosystems at a faster rate than before the PTME. The new world of the Triassic was characterised by a fast-paced arms race between synapsids and archosauromorphs in which the latter, as both dinosaurs and pterosaurs, initially prevailed.
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•Birds and mammals likely acquired endothermy (warm-bloodedness) at the same time•This time was the Early Triassic, as suggested by phylogenetic macroevolutionary studies of both archosaurs and synapsids•Life remodelled itself most significantly in the aftermath of the devastating end-Permian mass extinction•The switchover happened in parallel with a shift in posture from sprawling to parasagittal in both major lineages•Cynodonts and avemetatarsalian archosaurs engaged in arms races through the Triassic, as their metabolic rates speeded up
•High-resolution conodont, foraminifer, biostratigraphy.•Magnetic reversal, magnetic susceptibility, chemical stratigraphy, and geochronology.•Upper Permian–Upper Triassic.•Guandao section, south ...China.
The chronostratigraphy of Guandao section has served as the foundation for numerous studies of the end-Permian extinction and biotic recovery in south China. Guandao section is continuous from the Permian–Triassic boundary to the Upper Triassic.
Conodonts enable broad delineation of stage and substage boundaries and calibration of foraminifer biostratigraphy as follows. Changhsingian–Griesbachian: first Hindeodus parvus, and first appearance of foraminifers Postcladella kalhori and Earlandia sp. Griesbachian–Dienerian: first Neospathodus dieneri, and last appearance of foraminifer P. grandis. Dienerian–Smithian: first Novispathodus waageni and late Dienerian first appearance of foraminifer Hoyenella ex gr. sinensis. Smithian–Spathian: first Nv? crassatus and last appearance of foraminifers Arenovidalina n. sp. and Glomospirella cf. vulgaris. Spathian–Aegean: first Chiosella timorensis and first appearance of foraminifer Meandrospira dinarica. Aegean–Bithynian: first Nicoraella germanica and first appearance of foraminifer Pilammina densa. Bithynian–Pelsonian: after last Neogondolella regalis, prior to first Paragondolella bulgarica and first appearance of foraminifer Aulotortus eotriasicus. Pelsonian–Illyrian: first Pg. excelsa and last appearance of foraminifers Meandrospira? deformata and Pilamminella grandis. Illyrian–Fassanian: first Budurovignathus truempyi, and first appearance of foraminifers Abriolina mediterranea and Paleolituonella meridionalis. Fassanian–Longobardian: first Bv. mungoensis and last appearance of foraminifer A. mediterranea. Longobardian–Cordevolian: first Quadralella polygnathiformis and last appearance of foraminifers Turriglomina mesotriasica and Endotriadella wirzi.
The section contains primary magnetic signature with frequent reversals occurring around the Permian–Triassic, Olenekian–Anisian, and Anisian–Ladinian boundaries. Predominantly normal polarity occurs in the lower Smithian, Bithynian, and Longobardian–Cordevolian. Predominantly reversed polarity occurs in the upper Griesbachian, Induan–Olenekian, Pelsonian and lower Illyrian. Reversals match well with the GPTS. Large amplitude carbon isotope excursions, attaining values as low as −2.9‰ δ13C and high as +5.7‰ δ13C, characterize the Lower Triassic and basal Anisian. Values stabilize around +2‰ δ13C through the Anisian to Carnian. Similar signatures have been reported globally. Magnetic susceptibility and synthetic gamma ray logs show large fluctuations in the Lower Triassic and an overall decline in magnitude of fluctuation through the Middle and Upper Triassic. The largest spikes in magnetic susceptibility and gamma ray, indicating greater terrestrial lithogenic flux, correspond to positive δ13C excursions. High precision U–Pb analysis of zircons from volcanic ash beds provide a robust age of 247.28±0.12Ma for the Olenekian–Anisian boundary at Guandao and an age of 251.985±0.097Ma for the Permian–Triassic boundary at Taiping. Together, the new U–Pb geochronology from the Guandao and Taiping sections suggest an estimated duration of 4.71±0.15Ma for the Early Triassic Epoch.
The Permian-Triassic mass extinction (PTME, ca. 252 Mya) was one of the most severe biotic crises of the Phanerozoic, eliminating >90% of marine and terrestrial species. This was followed by a long ...period of recovery in the Early and Middle Triassic which revolutionised the structure of both marine and terrestrial ecosystems, triggering the new ecosystem structure of the Mesozoic and Cenozoic. Entire new clades emerged after the mass extinction, including decapods and marine reptiles in the oceans and new tetrapods on land. In both marine and terrestrial ecosystems, the recovery is interpreted as stepwise and slow, from a combination of continuing environmental perturbations and complex multilevel interaction between species in the new environments as ecosystems reconstructed themselves. Here, we present a review of Early Triassic terrestrial tetrapod faunas, geological formations and outcrops around the world, and provide a semi-quantitative analysis of a data set of Early Triassic terrestrial tetrapods. We identify a marked regionalisation of Early Triassic terrestrial tetrapods, with faunas varying in both taxonomic composition and relative abundance according to palaeolatitudinal belt. We reject the alleged uniformity of faunas around Pangaea suggested in the literature as a result of the hot-house climate. In addition, we can restrict the “tetrapod gap” of terrestrial life in the Early Triassic to palaeolatitudes between 15°N and about 31°S, in contrast to the earlier suggestion of total absence of tetrapod taxa between 30°N and 40°S. There was fairly strong provincialism following the PTME, according to cluster analysis of a taxon presence matrix, entirely consistent with Early Triassic palaeobiogeography. Unexpectedly, the overall pattern for Early Triassic terrestrial tetrapod faunas largely reflects that of the Late Permian, suggesting that the recovery faunas in the Early Triassic retained some kind of imprint of tetrapod distributions according to palaeogeography and palaeoclimate, despite the near-total extinction of life through the PTME.
The Meishan section, South China is the Global Stratotype Section and Point (GSSP) for the Permian–Triassic boundary (PTB), and is also well known for the best record demonstrating the ...Permian–Triassic mass extinction (PTME) all over the world. This section has also been studied using multidisciplinary approaches to reveal the possible causes for the greatest Phanerozoic biocrisis of life on Earth; many important scenarios interpreting the great dying have been proposed on the basis of data from Meishan. Nevertheless, debates on biotic extinction patterns and possible killers still continue. This paper reviews all fossil and sedimentary records from the Permo-Triassic (P–Tr) transition, based on previously published data and our newly obtained data from Meishan, and assesses ecologically the PTME and its aftermath to determine the biotic response to climatic and environmental extremes associated with the biocrisis. Eight updated conodont zones: Clarkina yini, Clarkina meishanensis, Hindeodus changxingensis, Clarkina taylorae, Hindeodus parvus, Isarcicella staeschei, Isarcicella isarcica, and Clarkina planata zones are proposed for the PTB beds at Meishan. Major turnover in fossil fragment contents and ichnodiversity occurs across the boundary between Bed 24e-5 and Bed 24e-6, suggesting an extinction horizon in a thin stratigraphic interval. The irregular surface in the middle of Bed 27 is re-interpreted as a firmground of Glossifungites ichnofacies rather than the previously proposed submarine dissolution surface or hardground surface. Both fossil fragment contents and ichnodiversity underwent dramatic declines in Beds 25–26a, coinciding with metazoan mass extinction. Fossil fragment content, ichnodiversity and all ichnofabric proxies (including burrow size, tiering level, bioturbation level) indicate that the P–Tr ecologic crisis comprises two discrete stages, coinciding with the first and second phases of the PTME in Meishan. Ecologic crisis lagged behind biodiversity decline during the PTME. Pyrite framboid size variations suggest that depositional redox condition was anoxic to euxinic in the latest Changhsingian, became euxinic in Beds 25–26a, turned dysoxic in Bed 27, then varied from euxinic to anoxic through most of the Griesbachian. The ~9°C increase in seawater surface temperature from Bed 24e to Bed 27 at Meishan seems to result in dramatic declines in biodiversity and fossil fragment contents in Beds 25–26a, but had little effect on all ecologic proxies. Both metazoans and infauna seem not to have been affected by the pre-extinction anoxic–euxinic condition. The anoxic event associated with the PTME may have occurred in a much shorter period than previously thought and is only recorded in Beds 25–26a at Meishan. Fossil fragment contents, ichnofaunas, ichnofabrics and pyrite framboid size all show that no signs of oceanic acidification and anoxia existed in Bed 27. The early Griesbachian anoxia may have resulted in rarity of ichnofauna and metazoans in the lower Yinkeng Formation, in which the ichnofauna is characterized by small, simple horizontal burrows of Planolites, and metazoan faunas are characterized by low diversity, high abundance, opportunist-dominated communities. The rapid increase of ~9°C in sea-surface temperature and a short anoxia or acidification coincided with the first-pulse biocrisis, while a prolonged and widespread anoxia probably due to a long period of high seawater temperate condition may be crucial in mortality of most organisms in the second-pulse PTME. Marine ecosystems started to recover, coupled with environmental amelioration, in the late Griesbachian.
The main aim of this paper is to review Middle Permian through Middle Triassic continental successions in European. Secondly, areas of Middle–Late Permian sedimentation, the Permian–Triassic Boundary ...(PTB) and the onset of Triassic sedimentation at the scale of the westernmost peri-Tethyan domain are defined in order to construct palaeogeographic maps of the area and to discuss the impact of tectonics, climate and sediment supply on the preservation of continental sediment.
At the scale of the western European peri-Tethyan basins, the Upper Permian is characterised by a general progradational pattern from playa-lake or floodplain to fluvial environments. In the northern Variscan Belt domain, areas of sedimentation were either isolated or connected to the large basin, which was occupied by the Zechstein Sea. In the southern Variscan Belt, during the Late Permian, either isolated endoreic basins occurred, with palaeocurrent directions indicating local sources, or basins underwent erosion and/or there was no deposition. These basins were not connected with the Tethys Ocean, which could be explained by a high border formed by Corsica–Sardinia palaeorelief and even parts of the Kabilia microplate. The palaeoflora and sedimentary environments suggest warm and semi-arid climatic conditions.
At the scale of the whole study area, an unconformity (more or less angular) is observed almost everywhere between deposits of the Upper Permian and Triassic, except in the central part of the Germanic Basin. The sedimentation gap is more developed in the southern area where, in some basins, Upper Permian sediment does not occur. The large sedimentary supply, erosion and/or lack of deposition during the Late Permian, as well as the variable palaeocurrent direction pattern between the Middle–Late Permian and the Early Triassic indicate a period of relief rejuvenation during the Late Permian. During the Induan, all the intra-belt basins were under erosion and sediment was only preserved in the extra-belt domains (the northern and extreme southern domains). In the northern domain (the central part of the Germanic Basin), sediment was preserved under the same climatic conditions as during the latest Permian, whereas in the extreme southern domain, it was probably preserved in the Tethys Ocean, implying a large amount of detrital components entering the marine waters. Mesozoic sedimentation began in the early Olenekian; the ephemeral fluvial systems indicate arid climatic conditions during this period. Three distinct areas of sedimentation occur: a northern and southern domain, separated by an intra-belt domain. The latter accumulated sediments during the Early–Middle Permian and experienced erosion and/or no-deposition conditions between the Middle–Late Permian and the beginning of Mesozoic sedimentation, dated as Anisian to Hettangian. At the top of the Lower Triassic, another tectonically induced, more or less angular unconformity is observed: the Hardegsen unconformity, which is dated as intra-Spathian and is especially found in the North European basins. This tectonic activity created new source areas and a new fluvial style, with marine influences at the distal part of the systems. During the Anisian and Ladinian, continental sedimentation was characterised by a retrogradational trend. In other words, the fluvial system evolved into fluvio-marine environments, attesting to a direct influence of the Tethys Ocean in the southern and northern domains. Both at the end of the Olenekian (Spathian) and during the Anisian, the presence of palaeosols, micro- and macrofloras indicate less arid conditions throughout this domain.
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