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Shelly communities and reef ecosystems represent the pinnacle of generic diversity and organizational complexity in marine environments. These systems are sensitive to climatic, tectonic, eustatic, and catastrophic changes, and their [...]

Abstract: The Early Silurian carbonate succession of Anticosti Island, eastern Canada, contains a rich and diverse pentameride brachiopod fauna. Multivariate analyses of 91 samples (total 17 230 specimens) confirm a [...]

Abstract: Brachiopods from the lower Tonggao Formation (Floian, late Early Ordovician) of Sandu, southeastern Guizhou Province, represent a deep-water benthic shelly fauna from the Jiangnan Slope facies of the South [...]

Abstract: Systematic and statistical study of brachiopods from the Dawan Formation of the Yichang area, western Hubei Province, central China, indicates that, at generic and specific levels, the α diversity [...]

Abstract: Primary δ[sup.18]O signals of 97 brachiopod shells from the Lower Silurian (Llandovery) carbonate succession of Anticosti Island were used to test the hypothesis of water-depth and water-temperature gradient for [...]

Restudy of two Early Silurian (Aeronian) stricklandioid species, Stricklandinia transversa Grabau, 1925 and Stricklandiella robusta Rong and Yang, 1981 from the Yichang area of South China, leads to the recognition of two new genera, Sinokulumbella and Sinostricklandiella. Two types of spondylia and four types of cardinalia are recognized for the Stricklandioidea and can be used for classification of the superfamily at the generic or even familial level. On the basis of these characters, five groups (typified by Stricklandia, Stricklandiella, Kulumbella, Microcardinalia, and Aenigmastrophia) can be recognized within the superfamily. Sinokulumbella n. gen., with a small, shallow, bowl-shaped spondylium and a pair of outer hinge plates that are discrete from the crura, is regarded to be affiliated with the Kulumbella group. Sinostricklandiella n. gen. has superimposed plicae and costae, although its internal structures are similar to the Stricklandiella group. A revised classification of stricklandioids implies that the Chinese pentamerides were characterized by strong provincialism during the early and middle Llandovery. This interpretation is supported further by the complete lack of true Stricklandia and Microcardinalia lineages in South China. Different stocks of stricklandioids in Baltica, Laurentia, South China, Siberia, and Kazakhstan may have experienced allopatric evolution, punctuated by several pulses of faunal migration or exchange between these paleoplates during the Llandovery. Evolution of the Stricklandia lineage is significantly different from that of Kulumbella and Sinokulumbella, particularly in that the outer plates disappeared earlier in the kulumbellids than in the stricklandiids.

A newly discovered Late Ordovician (early Ashgill) brachiopod assemblage from the Linhsiang Formation in the middle part of the Yangtze Platform, South China, bridges the paleobiogeographical gap between the early Ashgill Foliomena-bearing associations known previously from the upper and the lower parts of the Yangtze Platform. Characterized by minute shells in calcareous to siliciclastic mudstones, the fauna contains 13 brachiopod genera, of which two plectambonitoids are new: Hadroskolos and Jingshanella. Cluster and principal component analyses, based on 29 global occurrences of the Foliomena fauna in Laurentia, Avalonia, Kazakhstan, Baltica, Sardinia, Bohemia, Sibumasu, North China, and South China, revealed broad trends of spatial and temporal faunal differentiation in terms of taxonomic compositions. The analyses demonstrate for the first time that early Foliomena-bearing associations of Caradoc age occupied primarily deepwater (distal shelf) environments with a siliciclastic or calcareous mud substrate. The fauna attained its widest paleogeographical distribution and paleoecological range (midshelf to shelf margin settings) during the early Ashgill.

Holorhynchus giganteus Kiaer, 1902, a common Late Ordovician (mid-Ashgill) pentameride brachiopod in the Baltic region, Kazakhstan, and southern Tien Shah, is documented for the first time from the Badanjilin Formation (mid-Ashgill) of western Inner Mongolia (Alxa block), North China. Serial sections of the Chinese material confirm the presence of a vestigial ventral median septum in the early growth stage of H. giganteus, but the septum becomes embedded in the secondary shell thickening at the adult growth stage. A survey of the type material from Norway and additional material from other regions indicates that the incipient ventral median septum is a much more commonly developed structure than was previously believed. The presence of a well-developed pseudodeltidium in the Tien Shah material of H. giganteus and the absence of such a structure in conspecific material from many other regions require a systematic revision of the generic group. Holorhynchus has rodlike crurn (=brachial processes) that do not form flanges at their junctions with the inner hinge plates (=outer plates = crural plates) and outer hinge plates (inner plates). This, together with the development of a crude spondylial comb structure, points to its affinity to the Virgianidae rather than to the Stricklandiidae. Holorhynchus can be regarded as a Lazarus taxon because of its absence during the crisis (Hirnantian) and survival (early-middle Rhuddanian) intervals associated with the Late Ordovician mass extinction and its reappearance in Kazakhstan and North China during the Early Silurian (late Rhuddanian-early Aeronian). The mid-Ashgill Holorhynchus fauna, typified by a number of large-shelled pentamerides, was common in the Baltic region, the Urals, Kazakhstan, Tien Shah, Alxa, Qaidam, Kolyma, and east-central Alaska, but largely absent from Laurentia and Siberia (except for Taimyr) in the ancient tropical-subtropical regions. This paleobiogeographic pattern agrees with the general pattern of the Late Ordovician brachiopod provincialism.

ABSTRACT Middle Ordovician iron ooids in the Upper Yangtze region of South China are composed mainly of hematite and/or chamosite, found in mixed siliciclastic and carbonate successions, with hematitic ooids occurring in the west, and predominantly chamositic ooids in the east of the study area. In the three iron ooid‐bearing Middle–Upper Ordovician successions, 19 microfacies are recognized and grouped into eight facies associations, representing a shallow‐water mosaic comprising restricted and semi‐restricted lagoons, and open marine subtidal deposits interfingering with tidal flat and shoal facies. Hematitic ooids with well‐sorted and well‐rounded quartz grains formed in the transgressive shoal setting when the depositional environments changed from restricted lagoon to bioclast–quartz shoal and open marine subtidal. Episodic stasis and erosional intervals during transgression controlled the formation of hematite‐rich and mixed hematite–chamosite laminae within the cortices of hematitic ooids. In contrast, chamositic ooids formed in a semi‐restricted lagoonal environment, under long‐term transgressive condensation. Alternating episodes of relatively oxic conditions with thriving organisms and eutrophication‐driven anoxia resulted in the alternation of porous and dense laminae consisting mainly of chamosite in chamositic ooids. The stromatolite‐like cauliflower structures associated with chamositic ooids suggest microbial activity that promoted iron concentration, similar to the origin of approximately coeval iron‐rich oncoids in South China. Various iron ooid types demonstrate that these coated grains could form in a range of depositional setting and palaeooceanographic conditions on a generally shallow‐marine platform during the Ordovician. [ABSTRACT FROM AUTHOR]

While it is well established that the shapes and sizes of shells are strongly phylogenetically controlled, little is known about the phylogenetic constraints on shell thickness. Yet, shell thickness is likely to be sensitive to environmental fluctuations and has the potential to illuminate environmental perturbations through deep time. Here we systematically quantify the thickness of the anterior brachiopod shell which protects the filtration chamber and is thus considered functionally homologous across higher taxa of brachiopods. Our data come from 66 genera and 10 different orders and shows well‐defined upper and lower boundaries of anterior shell thickness. For Ordovician and Silurian brachiopods we find significant order‐level differences and a trend of increasing shell thickness with water depth. Modern (Cenozoic) brachiopods, by comparison, fall into the lower half of observed shell thicknesses. Among Ordovician–Silurian brachiopods, older stocks commonly have thicker shells, and thick‐shelled taxa contributed more prominently to the Great Ordovician Biodiversification but suffered more severely during the Late Ordovician Mass Extinction. Our data highlight a significant reduction in maximum and minimum shell thickness following the Late Ordovician mass extinction. This points towards stronger selection pressure for energy‐efficient shell secretion during times of crisis. [ABSTRACT FROM AUTHOR]

The Late Ordovician marks an epoch of substantial change during Earth’s geologic history. It documents the first mass extinction event of the Phanerozoic, which wiped out a plethora of marine genera. Though signatures of the extinction event are quite evident on the species level, there are many underlying uncertainties as to which factors drove the near destruction of Ordovician marine life. The exact causes and contributing factors of the Late Ordovician Mass Extinction (LOME) are highly debated. Previous studies propose processes such as redox shifts, volcanism, deep-water anoxia, low atmospheric oxygen, or excess CO2 as significant influencers. In this study, we utilized a multi-archive/proxy approach in reconstructing paleoenvironmental, stratigraphic, chronologic, and diagenetic signatures of halite and carbonate sequences from two localities containing the Ordovician–Silurian boundary. Our preliminary findings suggest that an abrupt, multi-pulsed glaciation was probably the main driver of the LOME. However, the exact duration, intensity, and number of cooling pulses are still up to interpretation and will require additional geochemical work to paint the entire picture. Samples were obtained from two localities of similar low paleo-latitudes. Marine halite and carbonate were obtained from the upper Ordovician Red Head Rapids Formation, Hudson Bay Basin, Canada. Another suite of halite was collected from the Ordovician/Silurian Mallowa Salt Formation, Canning Basin, Western Australia. The diagenetic integrity of Red Head Rapids halite and carbonate were assessed through strontium isotope analysis. Since the strontium isotope remains in equilibrium with seawater, we can cross-analyse the preservation potentials of both marine archives. All sample results lay within the ± 0.00006 ‰ natural variation of 87Sr/86Sr measured in modern marine counterparts, providing evidence of primary material and accurate paleo-interpretations. Trace element chemistry study was conducted on halite samples from both localities. Previous studies suggested that the spikes of Hg, Mo, and U concentrations signify the aftermath of a greenhouse event that triggered the expansion of deep-water anoxia. Furthermore, heightened volcanic activity led to significant greenhouse gas emissions and produced a period of warming. Instead, our halite Hg, Mo and U concentrations are extremely low, many below detection limits, which correspond to glacial signatures of an icehouse. Interpretation of the sedimentary cerium anomaly of the Red Head Rapids and Mallowa salts also revealed characteristics of an oxygenated marine environment, with all calculated values below the threshold, typical of anoxia. Rigorous halite fluid inclusion analysis was conducted to qualitatively distinguish between primary and secondary material based on size, shape, orientation, and multiple growth pat­terns. Microthermometry homogenization temperatures derived quantitative distinctions between primary and secondary fluid inclusions of preserved and altered material, respectively. Paleotemperatures of primary fluid inclusions exhibited oscillations that were evident of daily/seasonal variation of inter- and/or glacial times, averaging approximately 24.2°C ± 0.5°C for the latest-Ordovician–earliest-Silurian. Apart from minor fluctuations, we noticed up to four major cool­ing pulses associated with the major glaciation characterizing the latest-Ordovician–earliest-Silurian time. [ABSTRACT FROM AUTHOR]

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Canadian Journal of Earth Sciences is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)