60 research outputs found
Permian (Artinskian to Wuchapingian) conodont biostratigraphy in the Tieqiao section, Laibin area, South China
Permian strata from the Tieqiao section (Jiangnan Basin, South China) contain several distinctive conodont assemblages. Early Permian (Cisuralian) assemblages are dominated by the genera Sweetognathus, Pseudosweetognathus and Hindeodus with rare Neostreptognathodus and Gullodus. Gondolellids are absent until the end of the Kungurian stage—in contrast to many parts of the world where gondolellids and Neostreptognathodus are the dominant Kungurian conodonts. A conodont changeover is seen at Tieqiao and coincided with a rise of sea level in the late Kungurian to the early Roadian: the previously dominant sweetognathids were replaced by mesogondolellids. The Middle and Late Permian (Guadalupian and Lopingian Series) witnessed dominance of gondolellids (Jinogondolella and Clarkina), the common presence of Hindeodus and decimation of Sweetognathus. Twenty main and seven subordinate conodont zones are recognised at Tieqiao, spanning the lower Artinskian to the middle Wuchiapingian Stage. The main (first appearance datum) zones are, in ascending order by stage: the Sweetognathus (Sw.) whitei, Sw. toriyamai, and Sw. asymmetrica n. sp. Zones for the Artinskian; the Neostreptognathodus prayi, Sw. guizhouensis, Sw. iranicus, Sw. adjunctus, Sw. subsymmeticus and Sw. hanzhongensis Zones for the Kungurian; the Jinogondolella (J.) nankingensis Zone for the Roadian; the J. aserrata Zone for the Wordian; the J. postserrata, J. shannoni, J. altudaensis, J. prexuanhanensis, J. xuanhanensis, J. granti and Clarkina (C.) hongshuiensis Zones for the Capitanian and the C. postbitteri Zone and C. transcaucasica Zone for the base and middle of the Wuchiapingian. The subordinate (interval) zones are the Pseudosweetognathus (Ps.) costatus, Ps. monocornus, Hindeodus (H.) gulloides, Pseudohindeodus ramovsi, Gullodus (G.) sicilianus, G. duani and H. excavates Zones. In addition, three new species, Gullodus tieqiaoensis n. sp., Pseudohindeodus elliptica n. sp. and Sweetognathus asymmetrica n. sp. are described. Age assignments for less common species (e.g., G. duani, H. catalanoi and Pseudosweetognathus monocornus etc.) are reassessed based on a rich conodont collection
Ichnological record of the Frasnian–Famennian boundary interval: two examples from the Holy Cross Mts (Central Poland)
Disparity Changes in 370 Ma Devonian Fossils: The Signature of Ecological Dynamics?
Early periods in Earth's history have seen a progressive increase in complexity of the ecosystems, but also dramatic crises decimating the biosphere. Such patterns are usually considered as large-scale changes among supra-specific groups, including morphological novelties, radiation, and extinctions. Nevertheless, in the same time, each species evolved by the way of micro-evolutionary processes, extended over millions of years into the evolution of lineages. How these two evolutionary scales interacted is a challenging issue because this requires bridging a gap between scales of observation and processes. The present study aims at transferring a typical macro-evolutionary approach, namely disparity analysis, to the study of fine-scale evolutionary variations in order to decipher what processes actually drove the dynamics of diversity at a micro-evolutionary level. The Late Frasnian to Late Famennian period was selected because it is punctuated by two major macro-evolutionary crises, as well as a progressive diversification of marine ecosystem. Disparity was estimated through this period on conodonts, tooth-like fossil remains of small eel-like predators that were part of the nektonic fauna. The study was focused on the emblematic genus of the period, Palmatolepis. Strikingly, both crises affected an already impoverished Palmatolepis disparity, increasing risks of random extinction. The major disparity signal rather emerged as a cycle of increase and decrease in disparity during the inter-crises period. The diversification shortly followed the first crisis and might correspond to an opportunistic occupation of empty ecological niche. The subsequent oriented shrinking in the morphospace occupation suggests that the ecological space available to Palmatolepis decreased through time, due to a combination of factors: deteriorating climate, expansion of competitors and predators. Disparity changes of Palmatolepis thus reflect changes in the structure of the ecological space itself, which was prone to evolve during this ancient period where modern ecosystems were progressively shaped
Rise of the Earliest Tetrapods: An Early Devonian Origin from Marine Environment
Tetrapod fossil tracks are known from the Middle Devonian (Eifelian at ca. 397 million years ago - MYA), and their earliest bony remains from the Upper Devonian (Frasnian at 375–385 MYA). Tetrapods are now generally considered to have colonized land during the Carboniferous (i.e., after 359 MYA), which is considered to be one of the major events in the history of life. Our analysis on tetrapod evolution was performed using molecular data consisting of 13 proteins from 17 species and different paleontological data. The analysis on the molecular data was performed with the program TreeSAAP and the results were analyzed to see if they had implications on the paleontological data collected. The results have shown that tetrapods evolved from marine environments during times of higher oxygen levels. The change in environmental conditions played a major role in their evolution. According to our analysis this evolution occurred at about 397–416 MYA during the Early Devonian unlike previously thought. This idea is supported by various environmental factors such as sea levels and oxygen rate, and biotic factors such as biodiversity of arthropods and coral reefs. The molecular data also strongly supports lungfish as tetrapod's closest living relative
The Silurian-Devonian Boundary in the Rifugio Lambertenghi Fontana III Section (Wolayer area, Carnic Alps, Italy)
The Silurian-Devonian Boundary in the Rifugio Lambertenghi Fontana III Section (Wolayer area, Carnic Alps, Italy)
Phytoplankton dynamics across the Ordovician/Silurian boundary at low palaeolatitudes: Correlations with carbon isotopic and glacial events
The Late Ordovician culminated in a major glacial period that has been related to one of the strongest mass extinctions recorded during the Phanerozoic. During this interval, Anticosti Island (Quebec, eastern Canada) was located at low to intermediate palaeolatitudes (15-30 degrees S) on the eastern margin of Laurentia. It displays a relatively complete section across the Ordovician-Silurian (O/S) boundary. Upper Ordovician to Lower Silurian strata of Anticosti studied here comprise the Vaureal (Katian), Ellis Bay (Hirnantian) and Becscie (latest Hirnantian-Rhuddanian) formations. Phytoplankton dynamics inferred from the acritarch content of these strata are locally compared with new geochemical environmental proxies (delta(13)C), with recent palynological data from Baltica and also with phytoplankton dynamics as described from near-polar, high latitude localities of the Gondwana region. Two positive excursions of the carbon isotope record have been identified in the lower and upper Ellis Bay Formation. Overall, phytoplankton trends are as follows: (1) as with chitinozoans, conodonts, brachiopods and corals, acritarchs from Anticosti display a major turn-over during the early Hirnantian (uppermost Vaureal Formation-lower Ellis Bay Formation), with the appearance of taxa that exhibit Silurian affinities (e.g.. Tylotopalla sp., Ammonidium sp., Oppilatala sp., Evittia sp., Dilatisphaera spp.). High polymorphism for some common taxa is observed in the interval corresponding to the first delta(13)C positive excursion. Using sequence stratigraphy, this period may be related to a first glacially driven sea-level drawdown corresponding to terrestrial ice-sheet growth on Gondwana, such as recorded in Morocco. (2) Subsequently, during the late Himantian of Anticosti (uppermost Ellis Bay Formation), phytoplanktic communities suffered a crisis, exemplified by the disappearance of several typical, large Late Ordovician taxa (i.e., Orthosphaeridium spp., Peteinosphaeridium spp., large Baltisphaeridum spp., Sacculidium sp.). The lower Becscie strata, corresponding to the time of deglaciation at the O/S boundary interval, only contain a low diversity assemblage dominated by large acritarchs of the genus Hoegklintia and other morphologically related forms, and a few tolerant and long-ranging taxa (e.g., Evittia remota, Micrhystridium spp., leiospheres). Despite a possible taphonomic bias in the uppermost Ellis Bay Formation, the major crisis in the late Himantian coincides with the second delta(13)C excursion and a second, stronger glacially-driven sea-level fall corresponding to the time of the maximum extend of the ice sheets on Gondwana. (3) Such phytoplankton events have also been detected in Gondwanan ice-center area, but with "typical Ordovician taxa crises" occurring apparently later when plotted against positive carbon isotope excursions, as also observed in Baltica. This time-lag may be linked to a basin configuration of the studied areas, where environmental stress consequently differed or linked to the presence of omission surfaces coupled with preservation bias of acritarch assemblages in the uppermost Ordovician strata of Anticosti. In addition to their biostratigraphic and palaeobiogeographic utility, acritarchs turn out to be more specific in highlighting palaeoenvironmental conditions. (C) 2011 Elsevier B.V. All rights reserved
Lethally hot temperatures during the Early Triassic greenhouse.
Global warming is widely regarded to have played a contributing role in numerous past biotic crises. Here, we show that the end-Permian mass extinction coincided with a rapid temperature rise to exceptionally high values in the Early Triassic that were inimical to life in equatorial latitudes and suppressed ecosystem recovery. This was manifested in the loss of calcareous algae, the near-absence of fish in equatorial Tethys, and the dominance of small taxa of invertebrates during the thermal maxima. High temperatures drove most Early Triassic plants and animals out of equatorial terrestrial ecosystems and probably were a major cause of the end-Smithian crisis
Devonian paleoclimate and its drivers: A reassessment based on a new conodont δ18O record from South China
A new Devonian oxygen isotope record based on 180 measurements of conodont apatite is reported from South China. The comparison with published Devonian δ18Oapatite data shows a considerable offset between records from different paleocontinents. This difference can be interpreted by regional variations in salinity, with the epicontinental seas having a distinctly lower salinity and δ18Oseawater than the open ocean due to the influence of fresh-water runoff. Our findings suggest that the oxygen isotope record from open ocean settings is the preferred archive for reconstructing the history of ocean temperature and/or ice volume over the Phanerozoic.
Despite regional differences, the South China and European records show similar long-term trends characterized by a pronounced cooling during the Pragian to Eifelian followed by significant warming over the Eifelian/Givetian to Frasnian, and a further cooling starting in the Famennian, accelerating in the earliest Carboniferous. The Early Devonian cooling coincided with early vascular plant root − soil interactions and a significant diversity increase in both spores and megaplant fossils, suggesting that the rise of rooted vascular plants may have played a key role in triggering climate cooling. Subsequent climatic warming over the Middle to Late Devonian transition may have been linked to metamorphic CO2 input from the Acadian Orogeny, while Famennian cooling occurred in a context of exposure and weathering of basalts and ophiolites and coincided with the advent of seed plants. We conclude that climate changes during the Devonian were likely driven by a combination of plant evolutionary advances and changes in tectonics.
We further test these interpretations by running the COPSE (Carbon, Oxygen, Phosphorus, Sulfur and Evolution) biogeochemical model. The model prediction is capable of reproducing the pCO2 record under these scenarios, although the model is not capable of reproducing the degree of temperature variation, likely due to its simplicity
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