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433 result(s) for "Conodonta"
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Upper Wenlock delta super( 13)C chemostratigraphy, conodont biostratigraphy and palaeoecological dynamics in the Ledai-179 drill core (Eastern Lithuania)
Based on the integrated chemostratigraphic and lithostratigraphic studies, as well as biostratigraphic and palaeoecological analyses of conodonts in the Ledai-179 core, we present a combined model of change in the upper Wenlock and lowermost Ludlow strata of the inner shelf settings in the eastern part of the Baltic Basin. The comparison of the delta super( 13)C trend, and conodont and lithological successions confirms previous suggestions that the Bir?tonas and Neve?is formations correspond to the Homerian. This is quite unexpected, however, that the chronostratigraphic position of the ?irvinta Formation changed from the Gorstian to the upper part of the Homerian. The numerical biostratigraphic changepoint analyses of local conodont richness, per capita immigration and also per capita extirpation rates revealed several episodes of permanent change. These episodes of dynamic states either preceded or postdated the Mulde extinction interval at the beginning of the late Homerian delta super( 13)C excursion, which points to possible transient effects of this extinction event on conodonts.
Untangling a Darriwilian (Middle Ordovician) palaeoecological event in Baltoscandia: conodont faunal changes across the 'Taeljsten' interval
Conodont faunal dynamics and high-resolution biostratigraphy in the lithologically and faunally anomalous 'Taeljsten' succession, which spans the Darriwilian Lenodus variabilis-Yangtzeplacognathus crassus Zone boundary, were investigated in a 2.5 m-thick section on Mt Kinnekulle that includes an interval yielding fossil meteorites and extraterrestrial chromite. The previous interpretation that this interval reflects a regression is consistent with the occurrence and abundance patterns of some conodont taxa. The disappearance of e.g., Periodon, suggests that the regression began prior to the deposition of the grey 'Taeljsten'. The transition from red to grey limestone coincides with a conspicuous faunal re-arrangement. The lower half of the 'Taeljsten' reflects a gradual shallowing favourable for some taxa, such as Lenodus, and the immigration of Microzarkodina cf. ozarkodella and Histiodella holodentata. In the middle of the 'Taeljsten' interval, coinciding with the appearance of abundant cystoids, conditions became less hospitable for conodonts, resulting in a low diversity and low abundance fauna, which occurs to the top of the interval. The overlying red limestone, apparently deposited during a deepening event, marks a return to pre-'Taeljsten' conditions with a re-organised fauna. The close correlation between the lithologic shifts and conodont faunal changes demonstrates the usefulness of conodonts as environmental indicators.
THE OLDEST BRYOZOANS: NEW EVIDENCE FROM THELATE TREMADOCIAN (EARLY ORDOVICIAN) OF EAST YANGTZE GORGES IN CHINA
Previous reports of Cambrian bryozoans have proved not to be bryozoans. No pre-Ordovician bryozoans have been recognized. The oldest unequivocal bryozoans known from North America, Britain, and Russia are evidently of early Arenigian age. New bryozoans recently collected from the Fenxiang Formation in the Daping and Guanzhuangping sections, situated in the area east of the Yangtze Gorges, are described here, including one new genus, Orbiramus, and six new species, Nekhorosheviella nodulifera, N. semisphaerica, Orbiramus normalis, O. ovalis, O. minus, and Prophyllodictya prisca. These are assigned to the Trepostomida, apart from the last species which belongs to the Cryptostomida. The new bryozoans are from the conodont Paltodus deltifer deltifer Zone of the late Tremadocian age, the first three species possibly being present in the P. deltifer pristinus Subzone at the base. Therefore, they are the oldest bryozoans known from anywhere in the world. Extensive reefs resulting from a major regression in the late Tremadocian were dominated by bryozoans in the upper Fenxiang Formation. The bryozoans lived in a shoal environment and accumulated essentially in situ, showing no signs of significant transportation.
Climatic and biotic upheavals following the end-Permian mass extinction
The recovery from the end-Permian mass extinction was slow and prolonged. A temperature reconstruction shows that further biotic crises during the recovery were associated with extreme warmth. Recovery from the end-Permian mass extinction is frequently described as delayed 1 , 2 , 3 , with complex ecological communities typically not found in the fossil record until the Middle Triassic epoch. However, the taxonomic diversity of a number of marine groups, ranging from ammonoids to benthic foraminifera, peaked rapidly in the Early Triassic 4 , 5 , 6 , 7 , 8 , 9 , 10 . These variations in biodiversity occur amidst pronounced excursions in the carbon isotope record, which are compatible with episodes of massive CO 2 outgassing from the Siberian Large Igneous Province 4 , 11 , 12 , 13 . Here we present a high-resolution Early Triassic temperature record based on the oxygen isotope composition of pristine apatite from fossil conodonts. Our reconstruction shows that the beginning of the Smithian substage of the Early Triassic was marked by a cooler climate, followed by an interval of warmth lasting until the Spathian substage boundary. Cooler conditions resumed in the Spathian. We find the greatest increases in taxonomic diversity during the cooler phases of the early Smithian and early Spathian. In contrast, a period of extreme warmth in the middle and late Smithian was associated with floral ecological change and high faunal taxonomic turnover in the ocean. We suggest that climate upheaval and carbon-cycle perturbations due to volcanic outgassing were important drivers of Early Triassic biotic recovery.
Bivalved arthropods from the Middle Ordovician Winneshiek Lagerstaette, Iowa, USA
The Middle Ordovician (Darriwilian) Winneshiek Lagerstaette of northeast Iowa is preserved in a meteorite crater. Besides conodonts, the fossils are dominated by arthropods, particularly eurypterids and phyllocarids. Here we describe the bivalved forms, which include at least seven different taxa. The small phyllocarid Ceratiocaris winneshiekensis, new species, is the most abundant; it is the oldest representative of the Ceratiocarididae. A single incomplete abdomen and telson bearing furcal rami is reminiscent of notostracan branchiopods but its affinities are unknown. Decoracaris hildebrandi, new genus and species, is a rare form with a shield that extends anteriorly into a swollen horn and reaches lengths of 9 cm: it may represent a thylacocephalan crustacean but this cannot be confirmed without soft parts. Iosuperstes collisionis, new genus and species, is represented by suboval valves 10-25 mm long: its affinities are unknown. A probable leperditicopid, which ranges in length from 8 to 18 mm, is commonly preserved in a 'butterflied' configuration. It does not preserve the scars and sinuses characteristic of three-dimensionally preserved leperditicopids from elsewhere. Finally the fauna includes at least three ostracods, including a palaeocope with a granular surface and relief similar to Lomatopisthia, and a smooth ?podocope. The Winneshiek fauna differs from those of other Ordovician Lagerstaetten from restricted settings such as Airport Cove and William Lake in Manitoba (Katian) where, apart from ostracods, bivalved arthropods are absent, and Silurian examples such as Brandon Bridge (Telychian), which lacks eurypterids, and the Williamsville Member of the Bertie Formation (Pridoli) where conodont assemblages are absent.
Frasnian Late Devonian conodont biostratigraphy in New York: graphic correlation and taxonomy
Two regional composite sections in the Frasnian, Upper Devonian, of New York State result from graphic correlation of conodont species. The first extends from Frasnian conodont zones 3 to 7, the second from Frasnian zones 11 to 13c (we prefer this terminology to “Montagne Noire” or “MN” zonation as the zone-defining species occur throughout the Devonian tropics). Key beds, widely traceable bases of prominent black shales, have been used with only a few exceptions to position the lines of correlation (LOC) in the graphs. Other key beds, not used for positioning, fall exactly on the LOC supporting the hypothesis of their synchrony. Fifty-five conodont species in the New York regional composites are compared with their ranges in the global Frasnian Composite Standard proving no major discrepancies. The taxonomy of Ancyrodella nodosa Ulrich and Bassler, widely misidentified in the past, has been clarified through restudy of the type specimens, resulting in its distinction from A. hamata Ulrich and Bassler (= A. buckeyensis Stauffer). A new species of Polygnathellus Bassler, which is restricted to Frasnian Zone 4, is kept in open nomenclature because the rarity of specimens is insufficient to determine the extent of intraspecifc variation and whether one or two species are represented in our New York and Western Australian collections.
High-precision U-Pb zircon age calibration of the global Carboniferous time scale and Milankovitch band cyclicity in the Donets Basin, eastern Ukraine
High‐precision ID‐TIMS U‐Pb zircon ages for 12 interstratified tuffs and tonsteins are used to radiometrically calibrate the detailed lithostratigraphic, cyclostratigraphic, and biostratigraphic framework of the Carboniferous Donets Basin of eastern Europe. Chemical abrasion of zircons, use of the internationally calibrated EARTHTIME mixed U‐Pb isotope dilution tracer, and improved mass spectrometry guided by detailed error analysis have resulted in an age resolution of <0.05%, or ∼100 ka, for these Carboniferous volcanics. This precision allows the resolution of time in the Milankovitch band and confirms the long‐standing hypothesis that individual high‐frequency Pennsylvanian cyclothems and bundles of cyclothems into fourth‐order sequences are the eustatic response to orbital eccentricity (∼100 and 400 ka) forcing. Tuning of the fourth‐order sequences in the Donets Basin to the long‐period eccentricity cycle results in a continuous age model for the Middle to Late Pennsylvanian (Moscovian‐Kasimovian‐Ghzelian) strata of the basin and their record of biological and climatic changes through the latter portion of the late Paleozoic Ice Age. Detailed fusulinid and conodont zonations allow the export of this age model to sections throughout Euramerica. Additional ages for Mississippian strata provide among the first robust radiometric calibration points within this subperiod and result in variable lowering of the base ages of its constituent stages compared to recent global time scale compilations.
Middle Cambrian through lowermost Ordovician conodonts from Hunan, South China
Since 1986, samples with a total mass of more than 14,000 kg, mainly from three key sections in western Hunan, South China, have been processed for conodonts. Previous work mainly focused on biostratigraphy, but the taxonomy has been performed only on the faunas of the middle Cambrian. Described herein are conodonts of the upper Cambrian (Furongian Series) through lowermost Ordovician from Hunan, South China. Conodonts of the middle Cambrian are redescribed, based on material that has been recovered for more than three decades. The fauna consists of 82 species belonging to 36 genera. Newly established genera are Lugnathus n. gen., Miaognathus n. gen., Millerodontus n. gen., Tujiagnathus n. gen., Wangcunella n. gen. and Wangcunognathus n. gen. New species are Coelocerodontus hunanensis n. sp., Furnishina wangcunensis n. sp., Laiwugnathus hunanensis n. sp., Laiwugnathus transitans n. sp., Lugnathus hunanensis n. gen. n. sp., Miaognathus multicostatus n. gen. n. sp., Millerodontus intermedius n. gen. n. sp., Prosagittodontus compressus n. sp., Tujiagnathus gracilis n. gen. n. sp., Wangcunella conicus n. gen. n. sp., Wangcunognathus elegans n. gen. n. sp., Westergaardodina dimorpha n. sp., Westergaardodina gigantea n. sp., and Westergaardodina sola n. sp. The taxonomy of some conodont genera is revised. In the light of histological investigation, genera are assigned to euconodonts, paraconodonts, or protoconodonts. The 13 conodont zones previously proposed in the middle Cambrian through lowermost Ordovician remain the same, but taxa within these conodont zones are documented more clearly because of the revised taxonomy proposed herein.
The Role of Temporal Abundance Structure and Habitat Preferences in the Survival of Conodonts during the Mid-Early Silurian Ireviken Mass Extinction Event: e0124146
The Ireviken event was one of the most intense extinction episodes that occurred during the mid-Paleozoic era. It had a strong global effect on a range of clades, with conodonts, graptolites and chitinozoans affected most. Using geophysical proxies and conodont species parameters of their temporal abundance structure we investigate how they affected the selectivity of conodont species survival during this calamity. After performing bivariate logistic analyses on 34 species of conodonts, we find three variables that were statistically significantly associated with their odds of survival. These namely include spectral exponents that describe degrees of autocorrelation in a time series, the skewness of species abundance distribution, and average environmental preferences, which are mostly determined by ancient water depths at sampling sites. Model selection of multivariate logistic models found the best model includes species local abundance skewness and substrate preference. A similar pattern is revealed through the regression tree analysis. The apparent extinction selectivity points to a possible causes of environmental deterioration during the Ireviken event. The significant positive relationship between extinction risk and preferential existence in deeper environments suggests the open ocean causal mechanisms of biotic stress that occurred during the Ireviken event. Marine regressions, which were previously suggested as a causal factor in this extinction episode, on theoretical grounds should have had higher impact on species living in near-shore environments, through the processes of habitat loss which are associated with decreases of shelfal areas. In addition, the significant positive correlations found between skewness of abundance distributions and spectral exponent values and the probability of species survival suggest that community and ecosystem processes (which controlled species abundance fluctuation patterns) were significantly related to selectivity processes of this smaller mass extinction event.