Permian–Triassic Osteichthyes (bony fishes): diversity dynamics and body size evolution

The Permian and Triassic were key time intervals in the history of life on Earth. Both periods are marked by a series of biotic crises including the most catastrophic of such events, the end‐Permian mass extinction, which eventually led to a major turnover from typical Palaeozoic faunas and floras to those that are emblematic for the Mesozoic and Cenozoic. Here we review patterns in Permian–Triassic bony fishes, a group whose evolutionary dynamics are understudied. Based on data from primary literature, we analyse changes in their taxonomic diversity and body size (as a proxy for trophic position) and explore their response to Permian–Triassic events. Diversity and body size are investigated separately for different groups of Osteichthyes (Dipnoi, Actinistia, ‘Palaeopterygii’, ‘Subholostei’, Holostei, Teleosteomorpha), within the marine and freshwater realms and on a global scale (total diversity) as well as across palaeolatitudinal belts. Diversity is also measured for different palaeogeographical provinces. Our results suggest a general trend from low osteichthyan diversity in the Permian to higher levels in the Triassic. Diversity dynamics in the Permian are marked by a decline in freshwater taxa during the Cisuralian. An extinction event during the end‐Guadalupian crisis is not evident from our data, but ‘palaeopterygians’ experienced a significant body size increase across the Guadalupian–Lopingian boundary and these fishes upheld their position as large, top predators from the Late Permian to the Late Triassic. Elevated turnover rates are documented at the Permian–Triassic boundary, and two distinct diversification events are noted in the wake of this biotic crisis, a first one during the Early Triassic (dipnoans, actinistians, ‘palaeopterygians’, ‘subholosteans’) and a second one during the Middle Triassic (‘subholosteans’, neopterygians). The origination of new, small taxa predominantly among these groups during the Middle Triassic event caused a significant reduction in osteichthyan body size. Neopterygii, the clade that encompasses the vast majority of extant fishes, underwent another diversification phase in the Late Triassic. The Triassic radiation of Osteichthyes, predominantly of Actinopterygii, which only occurred after severe extinctions among Chondrichthyes during the Middle–Late Permian, resulted in a profound change within global fish communities, from chondrichthyan‐rich faunas of the Permo‐Carboniferous to typical Mesozoic and Cenozoic associations dominated by actinopterygians. This turnover was not sudden but followed a stepwise pattern, with leaps during extinction events.     

Permian reefs re-examined: extrinsic control mechanisms of gradual and abrupt changes during 40 my of reef evolution

The evolution of Permian reefs is characterized by the following sequence of events: (1) Late Carboniferous–Cisuralian radiation, (2) early Late Cisuralian (Artinskian–Kungurian) turnover, (3) Guadalupian radiation, (4) end-Guadalupian crisis, (5) Lopingian radiation, (6) end-Lopingian crisis at the PTB (Permian–Triassic boundary), and (7) the at least 7 my (million years) metazoan reef gap during the Early Triassic. The early Late Cisuralian turnover and the end-Guadalupian reef crisis are gradual changes, while the end-Lopingian reef crisis represents an abrupt event. Lopingian reefs occur in a zone from 40 °N to 15 °S, Guadalupian reefs in an extended equatorial zone from 35 °N to 35 °S, and Lopingian reefs in a narrow equatorial zone of 20 °N and 20 °S. This pattern resulted from a network of global and regional control mechanisms including the assemblage of Pangea, the northward drift of continents, the opening of Neo-Tethys, and second-order sea level changes. The mechanism of the extinction has been intensely debated and a combination of the above mentioned long-term changes and abrupt ocean anoxia or hypercapnia (CO₂-poisoning) for the end-Guadalupian reef crisis is considered.     

巴基斯坦盐岭地区二叠纪生物地层研究的新进展

近30年来,巴基斯坦盐岭地区的Wargal组和Chhidru组以及在喜马拉雅地区相当地层的地质时代被许多学者视为中二叠世(瓜达鲁普世)。根据华南与盐岭地区瓜达鲁普统和乐平统的牙形类化石带对比,可以确定Amb组和Wargal组底部的时代为瓜达鲁普世晚期,瓜达鲁普统与乐平统的界线位于Wargal组下部,吴家坪阶与长兴阶的界线位于Chhidru组的下部,而二叠与三叠系的界线位于Mianwali组下部的Kathwai段之内。我国西藏南部色龙群及相当地层含有与巴基斯坦盐岭地区Kalabagh段和Chhidru组可对比的乐平世腕足动物群以及二叠系—三叠系界线附近连续的牙形类化石带,由此可以推定色龙群的时代应为乐平世。     

Late Paleozoic–early Mesozoic continental biostratigraphy — Links to the Standard Global Chronostratigraphic Scale

Nonmarine biostratigraphic/biochronologic schemes have been created for all or parts of the late Carboniferous–Middle Triassic using palynomorphs, megafossil plants, conchostracans, blattoid insects, tetrapod footprints and tetrapod body fossils, and these provide varied temporal resolution. Cross correlation of the nonmarine biochronologies to the Standard Global Chronostratigraphic Scale has been achieved in some parts of the late Carboniferous–Middle Triassic in locations where nonmarine and marine strata are intercalated, the nonmarine strata produce biochronologically significant fossils and the marine strata yield fusulinids, conodonts and/or ammonoids. Other cross correlations have been aided by magnetostratigraphy, chemostratigraphy and a growing database of radioisotopic ages. A synthetic nonmarine biochronology for the late Carboniferous–Middle Triassic based on all available nonmarine index fossils, integrated with the Standard Global Chronostratigraphic Scale, is presented here. The focus is on the nonmarine biostratigraphy/biochronology of blattoid insects, conchostracans, branchiosaurid amphibians, tetrapod footprints and tetrapod body fossils within the biochronological framework of land-vertebrate faunachrons. Correlation to the Standard Global Chronostratigraphic Scale presented here is divided into seven time intervals: Pennsylvanian, Carboniferous–Permian boundary, Cisuralian, Guadalupian, Lopingian, Permian–Triassic boundary and Early to Middle Triassic. The insects, conchostracans and branchiosaurs provide robust nonmarine correlations in the Pennsylvanian–Cisuralian, and the footprints and tetrapod body fossils provide robust correlations of varied precision within the entire Pennsylvanian–Middle Triassic. Radioisotopic ages are currently the strongest basis for cross correlation of the nonmarine biostratigraphy/biochronology to the Standard Global Chronostratigraphic Scale, particularly for the Pennsylvanian–Cisuralian. Chemostratigraphy and magnetostratigraphy thus far provide only limited links of nomarine and marine chronologies. Improvements in the nonmarine-marine correlations of late Paleozoic–Triassic Pangea require better alpha taxonomy and stratigraphic precision for the nonmarine fossil record integrated with more reliable radioisotopic ages and more extensive chemostratigraphic and magnetostratigraphic datasets.     

Palaeobiogeographic distribution patterns and processes of Neochonetes and Fusichonetes (Brachiopoda) in the late Palaeozoic and earliest Mesozoic

The global palaeobiogeographic distributions of two resembling genera, Neochonetes and Fusichonetes (Brachiopoda), from the Carboniferous to Griesbachian are analysed. This analysis provides insight into the biotic response of two related genera to changing palaeoclimate, regional tectonics, and environmental crises. Neochonetes originated in the equatorial area in the Mississippian, and it mostly retained this position during the peak of the glaciation in the Carboniferous–Permian ice age (namely in the Pennsylvanian). Neochonetes then dispersed globally during the Cisuralian when the climate became warmer and the ice sheet started to retreat. In the Guadalupian and Lopingian, following the closure of the Ural seaway at the end of the Cisuralian and the regression at the end-Guadalupian, Neochonetes almost disappeared in the western part of Gondwana. Subsequently during the Lopingian the genus retracted to the middle- and low-latitude Palaeo-Tethys and Tethys. In comparison, Fusichonetes originated in the equatorial area in the late Guadalupian and was still present in that area in the Lopingian. Both genera occurred only in South China in the Griesbachian. It is inferred that this could be related, not only to the deteriorated palaeoenvironmental conditions (e.g., anoxia, global warming) leading up to the extinction of most of the Neochonetes and Fusichonetes species in other areas, but also to the better physiological adaptation of the smaller shells of Neochonetes and Fusichonetes species in South China.     

Evolution of Permian conodont provincialism and its significance in global correlation and paleoclimate implication

The main components of Asselian through Artinskian conodont faunas found around the world are basically the same, and the provincialism is indicated only by less common endemic elements such as Gondolelloides and New Genus A Henderson in North Pangea, Sweetognathus bucaramangus around the equator and Vjalovognathus in eastern Gondwana. Provincialism is marked by differences at the species level of Mesogondolella, Neostreptognathodus and Sweetognathus during the Kungurian, and becomes very distinct with differences at the genus level during the Guadalupian and Lopingian. Three provinces of Permian conodonts, referred to as the North Cool Water Province (NCWP), the Equatorial Warm Water Province (EWWP) and the peri-Gondwana Cool Water Province (GCWP), are recognized. The NCWP is marked by Gondolelloides in the early Cisuralian, dominance of Neostreptognathodus and no or rare Sweetognathus in the late Cisuralian, dominance of Merrillina and Mesogondolella and absence of Sweetognathus in the Guadalupian, and dominance of Merrillina and Mesogondolella and absence of Iranognathus in the Lopingian. The EWWP is characterized by the absence of Gondolelloides and Vjalovognathus in the Cisuralian, abundance of Sweetognathus and Pseudosweetognathus in the Kungurian (late Cisuralian), Jinogondolella and Sweetognathus in the Guadalupian, and Clarkina and Iranognathus in the Lopingian. The GCWP is marked by Vjalovognathus, Merrillina in the Cisuralian, Vjalovognathus, Merrillina and Mesogondolella in the Guadalupian, and Vjalovognathus and Merrillina in the Lopingian. Mixed faunas are recognized in regions bordering between the EWWP and GCWP including Western Timor during the Artinskian, Pamirs during the Kungurian and the Salt Range during the Guadalupian and Lopingian.

Three different conodont zonations are proposed, one for each of the three conodont provinces. Four potential horizons for inter-provincial correlation of Permian conodonts are recognized. They are in ascending order: (1) the first appearance of Sweetognathus whitei, which is closely related to the last occurrence of Carboniferous-type conodonts such as Streptognathodus and Adetognathus; (2) the first appearance of Neostreptognathodus pequopensis; (3) the base of the Jinogondolella nankingensis Zone; and (4) the base of the Clarkina postbitteri–Iranognathus erwini Zone.

The spatial and temporal distribution pattern of Permian conodonts suggests that temperature is the primary controlling factor. Evolution of Permian conodont provincialism reveals a glaciation during the Asselian and Sakmarian, a global warming during the Artinskian, a climate cooling in North Pangea during the Kungurian, a continuation of Kungurian climate trends in the Guadalupian, a relatively minor warming during the Wuchiapingian, a returned cooling in the Changhsingian and Lower and Middle Griesbachian, and a global warming in the Late Griesbachian, which ended the Permian conodont lineage.     

Amniotes through major biological crises: faunal turnover among Parareptiles and the end‐Permian mass extinction

Abstract: The Parareptilia are a small but ecologically and morphologically diverse clade of Permian and Triassic crown amniotes generally considered to be phylogenetically more proximal to eureptiles (diapsids and their kin) than to synapsids (mammals and their kin). A recent supertree provides impetus for an analysis of parareptile diversity through time and for examining the influence of the end‐Permian mass extinction on the clade’s origination and extinction rates. Phylogeny‐corrected measures of diversity have a significant impact on both rates and the distribution of origination and extinction intensities. Time calibration generally results in a closer correspondence between origination and extinction rate values than in the case of no time correction. Near the end‐Permian event, extinction levels are not significantly higher than origination levels, particularly when time calibration is introduced. Finally, regardless of time calibration and/or phylogenetic correction, the distribution of rates does not differ significantly from unimodal. The curves of rate values are discussed in the light of the numbers and distributions of both range extensions and ghost lineages. The disjoint time distributions of major parareptile clades (e.g. procolophonoids and nycteroleterids‐pareiasaurs) are mostly responsible for the occurrence of long‐range extensions throughout the Permian. Available data are not consistent with a model of sudden decline at the end‐Permian but rather suggest a rapid alternation of originations and extinctions in a number of parareptile groups, both before and after the Permian/Triassic boundary.     

AMMONOIDS ACROSS THE PERMIAN/TRIASSIC BOUNDARY: A CLADISTIC PERSPECTIVE

Abstract:  The rapid diversification of ceratitid ammonoids during the earliest Mesozoic has been taken at face value as an example of explosive radiation following the Permian/Triassic mass extinction. However, the validity of this interpretation has never been tested within a phylogenetic framework. A total evidence cladistic analysis of Mid–Late Permian and Induan (earliest Triassic) ammonoids confirms the monophyly of the Ceratitida. Partitioned phylogenetic analysis of suture line characters vs. shell shape and ornament characters confirms the importance of suture-line characters for resolving the higher taxonomy of ammonoids. When the cladogram is compared with the observed fossil record, the resultant tree implies that the divergence of a number of early Triassic lineages actually occurred during the latest Permian. If these range extensions are taken into account the ammonoid per-genus extinction rate across the Permian/Triassic boundary drops from c. 85 per cent to c. 60 per cent.     

Permian and early Triassic isotopic records of carbon and strontium in Australia and a scenario of events about the Permian‐Triassic boundary

The negative shift in δ¹³C values of carbonate carbon at the Permian/Triassic boundary is one of the better documented geochemical signatures of a mass extinction event. The similar negative shift in δ¹³C values in organic carbon from Permian/Triassic boundary marine sediments in Austria and Canada is shown to occur also in marine and non‐marine sediments from Australian sedimentary basins. This negative shift in δ¹³C values is used to calibrate Australian sections lacking diagnostic faunal elements identifying the Permian/Triassic boundary. The minimum in the carbonate ⁸⁷Sr/⁸⁶Sr seawater curve from carbonates across the Guadalupian/Ochoan Stage boundary, mainly from North America, is shown to occur also in brachiopod calcite mainly from the Bowen Basin of eastern Australia, hence providing a second calibration point in the Australian sedimentary record. These two geochemical events support a model of a runaway greenhouse developing about the Permian/Triassic boundary; this is inferred to have contributed to the end‐Permian mass extinction.     

New insights into the diversity dynamics of Triassic conodonts

In this paper, we examine the diversity trends and the evolutionary patterns of Triassic conodonts through a newly powered large-scale data-set compiled directly from the primary literature. Paleodiversity dynamics analyses have been undertaken by working at the species level and using a system of time units based on biozone subdivisions for a fine temporal level resolution. The role of heterogeneous duration of taxa in diversity estimates has been evaluated through the probabilistic profiles. Results reveal three different stages in the diversity behaviour of Triassic conodonts from standing metrics delimited by two inflections at the mid-Anisian and mid-Carnian. Survivorship analysis supports this pattern. Origination–extinction metrics report a diversification pattern characterised by important fluctuations during the Lopingian–Induan (earliest Triassic), the early-middle Olenekian (Early Triassic) and the Anisian–Ladinian transitions (Middle Triassic), as well as in the early Late Triassic. In addition, two clear diversification peaks are observed in the late Carnian and in the end-Norian. Reported patterns are interpreted in the context of deep extinction and environmental instability by documenting the biological signal of the main diversification and turnover patterns observed from such records. This study emphasises the singularity behaviour of diversity trends derived from the conodont record.     

EXTINCTION SPACE—A METHOD FOR THE QUANTIFICATION AND CLASSIFICATION OF CHANGES IN MORPHOSPACE ACROSS EXTINCTION BOUNDARIES

Three main modes of extinction are responsible for reductions in morphological disparity: (1) random (caused by a nonselective extinction event); (2) marginal (a symmetric, selective extinction event trimming the margin of morphospace); and (3) lateral (an asymmetric, selective extinction event eliminating one side of the morphospace). These three types of extinction event can be distinguished from one another by comparing changes in three measures of morphospace occupation: (1) the sum of range along the main axes; (2) the sum of variance; and (3) the position of the centroid. Computer simulations of various extinction events demonstrate that the pre‐extinction distribution of taxa (random or normal) in the morphospace has little influence on the quantification of disparity changes, whereas the modes of the extinction events play the major role. Together, the three disparity metrics define an “extinction‐space” in which different extinction events can be directly compared with one another. Application of this method to selected extinction events (Frasnian‐Famennian, Devonian‐Carboniferous, and Permian‐Triassic) of the Ammonoidea demonstrate the similarity of the Devonian events (selective extinctions) but the striking difference from the end‐Permian event (nonselective extinction). These events differ in their mode of extinction despite decreases in taxonomic diversity of similar magnitude.     

Evolution of the Permian and Triassic tetrapod communities of Eastern Europe

The Permo-Triassic terrestrial and freshwater tetrapod communities of Eastern Europe are reconstructed as food-webs. The Late Permian theriodont-dinocephalian community (Ocher, Mezen, Isheyevo) changes to a latest Permian theriodont-pareiasaur community (North Dvina, Vyazniki). After a major extinction, the Triassic thecodontian-dicynodont communities appear, a lystrosaurid one in the Early Triassic (Lower and ?Upper Vetluga), and a kannemeyerid one in the later Early Triassic (?Yarenga) and the Mid Triassic (Donguz, Bukobay). Similar stages are represented in the evolution of aquatic communities: the Late Permian temnospondyl community (Ocher, Isheyevo), the latest Permian chroniosuchian one (North Dvina, Vyazniki), the Lower and Middle Triassic new temnospondyl one (from Vetluga to Bukobay). The faunal changes in Eastern Europe are mirrored in other parts of the world, although there are some endemic Russian forms.     

Timing and progression of the end-Guadalupian crisis in the Fars province (Dalan Formation, Kuh-e Gakhum, Iran) constrained by foraminifers and other carbonate microfossils

The Middle-to-Upper Permian in the Kuh-e Gakhum anticline (southeastern Iran) has rarely been studied due to its structural complexity and the difficult access. Rich Permian fusulinid assemblages varying in age from Wordian to Changhsingian were found in a thick carbonate succession corresponding to the Dalan Formation. Three new species of foraminifers are described and a new biostratigraphic framework including five biozones is proposed. One of these, described and defined for the first time in the Dalan Formation, is based on the presence of Praedunbarula simplicissima n. gen. n. sp. When compared to the fossil content of existing bioprovinces, the floro-faunal biota of the Dalan Formation shows an affinity with Central and Western Tethys. A mass extinction of fusulinids and small foraminifers (70%) occurred concomitantly with the onset of a relative sea-level fall. This event led to a change in the carbonate factories from biologically induced carbonate production to ooid-rich chemically induced precipitation. The morphology of the platform at the Guadalupian/Lopingian transition evolves from a bioclastic ramp to a shelf. This transition is also characterized by a major sequence boundary and morphological anomalies in foraminifers. Therefore, as the regression and the changes in floro-faunal contents have been observed at the Guadalupian/Lopingian boundary, the extinction event is considered as end-Guadalupian. It is followed by a Lopingian transgression yielding renewed foraminiferal assemblages.     

Trends and patterns in the evolution of vascular plants: macroevolutionary implications of a multilevel taxonomic analysis

Cascales‐Miñana, B., Muñoz‐Bertomeu, J., Ros, R., Segura, J. 2010: Trends and patterns in the evolution of vascular plants: macroevolutionary implications of a multilevel taxonomic analysis. Lethaia, 10.1111/j.1502‐3931.2009.00212.x Studying the macroevolutionary patterns of vascular plants from the Silurian to the present‐day provides a global record of plant life history. Evolutionary rates (origination, extinction and diversification) for families, orders, classes and divisions were analysed, as was abundance and richness for 21 time intervals. An accumulative analysis, based on the total plant fossil record, the accumulated extinctions and relative diversity, was also carried out. The diversification rate shows a uniquely constant and progressive reduction from the end of the Carboniferous to the Permian when the lowest values are registered. Very small peaks seem to reflect Cretaceous extinction for families. At family level, only two time intervals present higher extinctions, than originations. Richness and accumulative analyses reveal that only 32% of the families analysed became extinct, and that approximately 90% of them disappeared at the end of the Palaeozoic. Our results indicate that plants did not undergo mass extinction events in the ‘big five’ sense, but rather, mass ecological reorganization the absence of important extinction events or evolutionary innovations producing diversification patterns without abrupt changes. □Diversification, evolutionary, extinction, fossil record, innovations, radiation, vascular plants.     

Diversity and extinction patterns of Permian coral faunas of China

Coral diversity and extinction patterns in the Permian of China are revealed through statistical analyses of 56 coral families, 263 genera and 2100 species from five consecutive time intervals. The highest coral diversity is in the Chuanshanian, with 753 species, 167 genera and 39 families. In contrast, the lowest diversity is in the Changhsingian, with only 68 species, 20 genera and 10 families. Two decreases in diversity can be recognized during the Permian. The first occurred at the end of the Maokouan (end-Guadalupian) and is marked by the loss of 75.6% of coral families, 77.8% of coral genera and 82.2% of coral species. The second major diversity drop took place at the end of the Changhsingian, when all rugose and tabulate corals became extinct. The extinction at the end of the Guadalupian in Pangea may be related to the middle Permian global regression. However, in South China the end-Maokouan extinction may be related to the eruption of the Omeishan Basalt. A triple-zoned palaeobiogeographical pattern is well expressed by coral diversity.     

Precocious sexual dimorphism and the Lilliput effect in Neo‐Tethyan Ostracoda (Crustacea) through the Permian–Triassic boundary

The Elikah River section spanning the Lopingian (Late Permian) to the Griesbachian (Early Triassic) time interval in the Central Alborz Mountains (north Iran) was sampled for ostracod analysis. We report 79 species distributed among 38 genera. Four new species are described: Acratia? pervagata Forel sp. nov., Microcheilinella alborzella Forel sp. nov., Basslerella superarella Crasquin sp. nov. and Cavellina nesenensis Crasquin sp. nov. The ontogeny of 13 species is described and sexual dimorphism in the genus Microcheilinella is here undoubtedly recognized for the first time. Six species show precocious sexual dimorphism of their carapace as early as A‐5 juvenile. The Lilliput effect is for the first time recorded and quantified for two species. Rare long‐time span Palaeocopida species, known throughout the entire Permian, document relatively long‐term evolution, including the size and growth rate modifications associated with the earlier appearance of carapace sexual dimorphism through time. These patterns might be related to the Guadalupian–Lopingian events and/or to climatic modifications occurring during the Permian interval.     

Callistophytalean pteridosperms from Permian aged floras of China

Abstract: Recent investigations into Permian aged floras from China have highlighted the widespread occurrence of callistophytalean pteridosperms that challenge previous understanding of their spatial and temporal distribution and diversity. In China, the group spans the Permian period and constitutes a distinctive but rare component in many peat‐forming environments. The stratigraphically earliest callistophytalean occurs in the Asselian‐Sakmarian stages with fossils from the Taiyuan Formation of northern China including ovules of Callospermarion undulatum in coal ball assemblages, and ovulate fronds of Norinosperma shanxiensis and synangiate fronds of Norinotheca shanxiensis in adpression assemblages. More abundant in the fossil records are adpression remains from the Roadian‐Wordian stages with the Lower Shihhotse Formation preserving abundant vegetative and ovulate remains of Emplectopteris triangularis that is now considered to represent a callistophytalean. The youngest callistophytalean recognised is from the Wuchaipingian‐Changhsingian stages with the Xuanwei Formation of southern China containing a single stem of Callistophyton boyssetii that provides indisputable evidence of the group in the lead up to the end‐Permian mass extinction. These accounts are augmented by analysis of pollen records that demonstrate the callistophytalean pollen genus Vesicaspora to be widespread through palynological assemblages from the Permian period in both North and South China, including the Upper Shihhotse Formation, Shihchienfeng Group, Xuanwei Formation, and possibly also in the mid‐Pennsylvanian Benxi Formation. Although macrofossil specimens are uncommon elements in the assemblages that contain them, they demonstrate the continuity of callistophytalean pteridosperms from the Pennsylvanian sub‐period into the early Guadalupian epoch of the Permian in North China and into the Lopingian epoch of the Permian in South China. Of the species present, both Callistophyton boyssetii and Callospermarion undulatum are known from the Pennsylvanian–earliest Permian age floras of Euramerica, whereas Norinosperma, Norinotheca and Emplectopteris appear to represent endemic Cathaysian elements. Results imply that callistophytalean pteridosperms can no longer be excluded from theories of post‐Carboniferous plant evolution and floristics, appearing to have played an important role in both Permian and Carboniferous aged plant communities. The presence of Vesicaspora in several formations from which macro‐remains have not been identified is a hopeful indicator that further callistophytalean pteridosperms are yet to be found.     

Latest Guadalupian brachiopods from the Guadalupian/Lopingian boundary GSSP section at Penglaitan in Laibin, Guangxi, South China and implications for the timing of the pre-Lopingian crisis

A brachiopod fauna comprising nine species in eight genera from three closely spaced stratigraphic horizons of the same stratigraphic section is described for the first time from the Laibin Limestone in the uppermost part of the Maokou Formation in the Guadalupian/Lopingian (G/L) GSSP section at Penglaitan, Guangxi Autonomous Region, South China. The brachiopod assemblages are bracketed between two conodont zones: Jinogondolella xuanhanensis Zone below and Jinogondolella granti Zone above and, therefore, they can be safely assigned to the latest Capitanian in age. However, all but one of the nine brachiopod species from the Laibin Limestone carry strong early Lopingian (Wuchiapingian) aspect. Thus, the discovery of this brachiopod fauna not only suggests that some Lopingian brachiopod species had already appeared in the late Guadalupian (Capitanian); more importantly, it has also highlighted the fact that both the previously noted pre-Lopingian life crisis (or end-Guadalupian or Middle Permian mass extinction) and Lopingian recovery/radiation actually occurred in late Capitanian times, sometime before the G/L chronostratigraphic boundary. So far, the Penglaitan GSSP section provides the highest-resolution disappearance patterns of different fossil groups around the G/L boundary.     

Organism activity levels predict marine invertebrate survival during ancient global change extinctions

Multistressor global change, the combined influence of ocean warming, acidification, and deoxygenation, poses a serious threat to marine organisms. Experimental studies imply that organisms with higher levels of activity should be more resilient, but testing this prediction and understanding organism vulnerability at a global scale, over evolutionary timescales, and in natural ecosystems remain challenging. The fossil record, which contains multiple extinctions triggered by multistressor global change, is ideally suited for testing hypotheses at broad geographic, taxonomic, and temporal scales. Here, I assess the importance of activity level for survival of well‐skeletonized benthic marine invertebrates over a 100‐million‐year‐long interval (Permian to Jurassic periods) containing four global change extinctions, including the end‐Permian and end‐Triassic mass extinctions. More active organisms, based on a semiquantitative score incorporating feeding and motility, were significantly more likely to survive during three of the four extinction events (Guadalupian, end‐Permian, and end‐Triassic). In contrast, activity was not an important control on survival during nonextinction intervals. Both the end‐Permian and end‐Triassic mass extinctions also triggered abrupt shifts to increased dominance by more active organisms. Although mean activity gradually returned toward pre‐extinction values, the net result was a permanent ratcheting of ecosystem‐wide activity to higher levels. Selectivity patterns during ancient global change extinctions confirm the hypothesis that higher activity, a proxy for respiratory physiology, is a fundamental control on survival, although the roles of specific physiological traits (such as extracellular pCO₂ or aerobic scope) cannot be distinguished. Modern marine ecosystems are dominated by more active organisms, in part because of selectivity ratcheting during these ancient extinctions, so on average may be less vulnerable to global change stressors than ancient counterparts. However, ancient extinctions demonstrate that even active organisms can suffer major extinction when the intensity of environmental disruption is intense.     

Global Taxonomic Diversity of Anomodonts (Tetrapoda,Therapsida) and the Terrestrial Rock Record Across the Permian-Triassic Boundary

The end-Permian biotic crisis (∼252.5 Ma) represents the most severe extinction event in Earth''s history. This paper investigates diversity patterns in Anomodontia, an extinct group of therapsid synapsids (‘mammal-like reptiles’), through time and in particular across this event. As herbivores and the dominant terrestrial tetrapods of their time, anomodonts play a central role in assessing the impact of the end-Permian extinction on terrestrial ecosystems. Taxonomic diversity analysis reveals that anomodonts experienced three distinct phases of diversification interrupted by the same number of extinctions, i.e. an end-Guadalupian, an end-Permian, and a mid-Triassic extinction. A positive correlation between the number of taxa and the number of formations per time interval shows that anomodont diversity is biased by the Permian-Triassic terrestrial rock record. Normalized diversity curves indicate that anomodont richness continuously declines from the Middle Permian to the Late Triassic, but also reveals all three extinction events. Taxonomic rates (origination and extinction) indicate that the end-Guadalupian and end-Permian extinctions were driven by increased rates of extinction as well as low origination rates. However, this pattern is not evident at the final decline of anomodont diversity during the Middle Triassic. Therefore, it remains unclear whether the Middle Triassic extinction represents a gradual or abrupt event that is unique to anomodonts or more common among terrestrial tetrapods. The end-Permian extinction represents the most distinct event in terms of decline in anomodont richness and turnover rates.