The Occurrence of Pelecypods in Early Paleozoic Epeiric-Sea Environments, Late Ordovician of the Cincinnati, Ohio Area

Palaios ◽  
1987 ◽  
Vol 2 (1) ◽  
pp. 3 ◽  
Author(s):  
Robert C. Frey
2020 ◽  
pp. SP503-2020-89 ◽  
Author(s):  
J. Javier Álvaro ◽  
Josep Maria Casas ◽  
Cecilio Quesada

AbstractA Cambro-Ordovician palaeogeographical restoration of the southwestern European margin of Gondwana is proposed based on the relative positions of Variscan tectonostratigraphic units. Four palaeogeographical proximal–distal transects are recognized and comprise: (i) the Cantabrian, West Asturian-Leonese, Central Iberian/Central Armorican and Ossa-Morena/North Armorican zones and domains of the Iberian and Armorican massifs, respectively; (ii) the South Armorican Domain and its lateral prolongation into the Thiviers-Payzac unit and the Occitan Domain, including the transect from the Axial, southern and northern Montagne Noire, and the Albigeois-southern Cévennes unit; (iii) the southern and northern sides of the Canigó Massif in the Eastern Pyrenees; and (iv) the External Zone and the External and Internal nappes of Sardinia. Two geodynamic scenarios are recognized controlled by the presence/absence of: (i) the Furongian–Early Ordovician (Toledanian or ‘lacaune normande’) break-up unconformity across the Ossa-Morena/North Armorican and Central Iberian/Central Armorican belts; (ii) the Early–Late Ordovician (Sardic) Phase across the Occitan and Pyrenean domains and SW Sardinia; and (iii) the migration of peaks in trilobite and cinctan (echinoderm) diversity. Other similar palaeogeographical shifts are recognized in zircon provenance patterns, the occurrence of climatically sensitive subtropical facies and mineral indicators across platform–basinal transects along the Gondwana margin. This multidisciplinary framework is proposed as a preliminary step in the quest to produce more tightly constrained Early Paleozoic reconstructions along southwestern Europe.


1987 ◽  
Vol 61 (2) ◽  
pp. 242-267 ◽  
Author(s):  
Robert C. Frey

The Treptoceras duseri shale unit within the Waynesville Formation of Late Ordovician (early Richmondian) age in southwest Ohio and the equivalent Trilobite shale unit in the same formation exposed in adjacent portions of Indiana represent an Ordovician shallow marine mud-bottom epeiric sea facies. These fine-grained elastics contain a moderately diverse mollusk-trilobite assemblage dominated by vagrant epifaunal detritus-feeding calymenid and asaphid trilobites, large endobyssate and infaunal filter-feeding pelecypods, and nektonic nautiloids. Articulate brachiopods, ectoprocts, and pelmatozoan echinoderms form only minor elements of this fauna.This mollusk-trilobite assemblage was common in Late Ordovician shallow marine clastic environments where mobility was an asset and there was an abundance of oxygen and food resources. Such assemblages are characteristic of the Lorraine Fauna of Late Ordovician (Edenian to Richmondian) age that occurs from the Ohio Valley north and east into New York, Ontario, Quebec, and Ireland. These early Paleozoic mud-bottom assemblages were considerably modified by the Late Ordovician extinction event and were replaced in the Silurian and Devonian by distinctly different assemblages dominated by large epifaunal strophomenid and spiriferid brachiopods, crinoids, and phacopid trilobites.


1987 ◽  
Vol 2 (2) ◽  
pp. 165-176 ◽  
Author(s):  
R. L. Anstey ◽  
S. F. Rabbio ◽  
M. E. Tuckey
Keyword(s):  

2019 ◽  
Vol 116 (15) ◽  
pp. 7207-7213 ◽  
Author(s):  
Christian M. Ø. Rasmussen ◽  
Björn Kröger ◽  
Morten L. Nielsen ◽  
Jorge Colmenar

The greatest relative changes in marine biodiversity accumulation occurred during the Early Paleozoic. The precision of temporal constraints on these changes is crude, hampering our understanding of their timing, duration, and links to causal mechanisms. We match fossil occurrence data to their lithostratigraphical ranges in the Paleobiology Database and correlate this inferred taxon range to a constructed set of biostratigraphically defined high-resolution time slices. In addition, we apply capture–recapture modeling approaches to calculate a biodiversity curve that also considers taphonomy and sampling biases with four times better resolution of previous estimates. Our method reveals a stepwise biodiversity increase with distinct Cambrian and Ordovician radiation events that are clearly separated by a 50-million-year-long period of slow biodiversity accumulation. The Ordovician Radiation is confined to a 15-million-year phase after which the Late Ordovician extinctions lowered generic richness and further delayed a biodiversity rebound by at least 35 million years. Based on a first-differences approach on potential abiotic drivers controlling richness, we find an overall correlation with oxygen levels, with temperature also exhibiting a coordinated trend once equatorial sea surface temperatures fell to present-day levels during the Middle Ordovician Darriwilian Age. Contrary to the traditional view of the Late Ordovician extinctions, our study suggests a protracted crisis interval linked to intense volcanism during the middle Late Ordovician Katian Age. As richness levels did not return to prior levels during the Silurian—a time of continental amalgamation—we further argue that plate tectonics exerted an overarching control on biodiversity accumulation.


2000 ◽  
Vol 6 ◽  
pp. 21-46 ◽  
Author(s):  
Gregory J. Retallack

Many Paleontologists share the opinion of McGhee (1996), who wrote “Prior to the Devonian, there was no terrestrial ecosystem to speak of. Some primitive plants precariously establishing a beachhead in protected coastal areas was about it. The interiors of the continents of the planet Earth were as barren as the rocky landscapes of Mars.” Thus, it was with trepidation that I reported paleosols containing trace fossils of early land animals in the late Ordovician, Juniata Formation, of Pennsylvania (Retallack and Feakes, 1987; Retallack, 1992a, 1992b, 1993). My late colleague, Jane Gray, engendered considerable debate by reporting Ordovician and Early Silurian spores like those of liverworts (Gray and Boucot, 1977; Gray, 1985). This spore, trace fossil and paleosol evidence for life on land in the Ordovician has remained controversial (Buatois et al., 1998; Shear, 1998), but evidence for Ordovician life on land has continued to accumulate. Especially important was discovery of myriapod trackways from mid-Ordovician (Llandeilian-Caradocian) Borrowdale Volcanics of the Lake District, England (Johnson et al., 1994). Abundant arthropod burrows and tracks, and a single body fossil of an euthycarcinoid in the fluvial-eolian Tumblagooda Sandstone of Western Australia (White 1990; McNamara and Trewin, 1993; Trewin and McNamara, 1995) are now thought to be late Ordovician in age (Iaksy et al., 1998). An enigmatic assemblage of arthropods and plants from a mid-Ordovician paleokarst in Tennessee (Caster and Brooks, 1956) is now thought to have been lacustrine (Gray, 1988a). The fossil record of Ordovician land plants also has improved with the discovery of possible megafossil mosses (Snigirevskaya et al. 1992), and possible late Ordovician trilete spores (Nøhr-Hansen and Koppelhus, 1998; Richardson 1988; Strother, 1991; Strother et al., 1996). But the most abundant evidence for Ordovician life on land remains fossil soils, now exploited by increasingly thorough and sophisticated studies (Retallack, 1985, 1992a, 1992b, 1993; Feakes et al., 1989; Driese and Foreman 1991, 1992a, 1992b; Driese et al., 1992, 1997; Mora et al., 1991, 1996; Mora and Driese, 1993; Yapp and Poths, 1992, 1994, 1996; Yapp, 1993, 1996). Mounting evidence from fossils and paleosols now presents an increasingly detailed view of Ordovician ecosystems on land.


2010 ◽  
Vol 47 (10) ◽  
pp. 1347-1366 ◽  
Author(s):  
E. H. Brown ◽  
G. E. Gehrels ◽  
V. A. Valencia

The Chilliwack composite terrane in northwest Washington is part of an assemblage of mid-Paleozoic arc terranes extending from California to Alaska. Some terranes bear evidence of exotic origin, whereas others apparently formed proximal to western Laurentia, posing a complex problem in unraveling the Paleozoic accretionary history of the Cordillera. In our proposed broader definition, the Chilliwack composite terrane includes the volcanic and sedimentary East Sound and Chilliwack groups, and the plutonic and metamorphic Turtleback and Yellow Aster complexes. New zircon ages indicate that the plutonic and volcanic rocks are mutually related as parts of the same arc complex and that its inception was as old as Late Ordovician to Silurian, older than most other parts of the mid-Paleozoic terrane assemblage. Basement to the arc complex is a passive margin assemblage of metamorphosed quartzose sandstone and calc-silicate rock of the Yellow Aster Complex, bracketed in age by ca. 1000 Ma detrital zircons and 418 Ma intrusive rocks. This association of paragneiss basement and overlying and (or) intruding arc resembles that of older parts of the extensive Yukon–Tanana terrane in the northern Cordillera. Detrital zircon ages support a western Laurentian pericratonic origin for the paragneiss basement and the overlying arc. However, an early to mid-Paleozoic connection of this assemblage to the exotic outboard Alexander terrane is also indicated, based on (1) Mesoproterozoic and early Paleozoic detrital zircons in Devonian sedimentary rocks of the arc, and also in certain other pericratonic Devonian terranes and strata of the miogeocline; (2) Late Ordovician – Silurian igneous ages; and (3) an earliest Devonian or older metamorphic age of the basement paragneiss.


2020 ◽  
Vol 11 (1) ◽  
pp. 89-106
Author(s):  
R. O. Ovchinnikov ◽  
A. A. Sorokin ◽  
N. M. Kudryashov ◽  
V. P. Kovach ◽  
J. V. Plotkina ◽  
...  

The article presents new age data on the ‘key’ Early Paleozoic igneous complexes located in the central part of the Bureya continental massif of the Central Asian Fold Belt. Porphyroblastic quartz monzonites of the Kivili complex are dated to 453±2 Ma. The age of gneissic granites of the Sularin complex is ~481 Ma. The Sm-Nd isotope stu­dies show that Late Ordovician quartz monzonites were formed mainly from crustal sources with Paleoproterozoic Nd model isotopic ages. Both ancient (Paleoproterozoic?) and younger sources were involved in the formation of Cambrian granites. Our data, as well as previously published materials, suggest several stages of the Early Paleozoic magmatism in the evolution of the Bureya continental massif: ~541, ~504–500, ~487, ~474 and ~453 Ma. Early Paleozoic magmatism developed under a similar scenario in the Jiamusi continental massif. In addition to the synchronism of Neoproterozoic magmatism within these continental massifs, this feature testifies to their common geological history.


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