Mass Extinction in the Cambrian Trilobite Faunas of North America

1990 ◽  
Vol 3 ◽  
pp. 99-115 ◽  
Author(s):  
Stephen R. Westrop

Sepkoski (1981a,b, 1988) has characterized the Cambrian fauna as unique, both in terms of taxonomic composition and in environmental distribution of taxa. Compared with the rest of the Phanerozoic, the frequency of mass extinction in the Cambrian must also rank as a distinctive feature which had a profound impact on macroevolutionary patterns. Three well-documented extinctions occurred in the Upper Cambrian of North America (Figure 1; Palmer, 1979; Westrop and Ludvigsen, 1987) and are best expressed in the trilobite faunas. Possible older extinctions may be present at the top of the Olenellus Zone and near the base of the Bolaspidella Zone (e.g., see Palmer, 1982) but more data are required.

Paleobiology ◽  
1990 ◽  
Vol 16 (2) ◽  
pp. 187-203 ◽  
Author(s):  
Douglas H. Erwin

Paleozoic and post-Paleozoic marine faunas are strikingly different in composition. Paleozoic marine gastropods may be divided into archaic and modern groups based on taxonomic composition, ecological role, and morphology. Paleozoic assemblages were dominated by pleurotomariids (Eotomariidae and Phymatopleuridae), the Pseudozygopleuridae, and, to a lesser extent, the Euomphalidae, while Triassic assemblages were dominated by the Trochiina, Amberleyacea, and new groups of Loxonematoidea and Pleurotomariina. Several new groups of caenogastropods appeared as well. Yet the importance of the end-Permian mass extinction in generating these changes has been questioned. As part of a study of the diversity history of upper Paleozoic and Triassic gastropods, to test the extent to which taxonomic and morphologic trends established in the late Paleozoic are continued after the extinction, and to determine the patterns of selectivity operating during the extinction, I assembled generic and morphologic diversity data for 396 genera in 75 families from the Famennian through the Norian stages. Within this interval, gastropod genera underwent an adaptive radiation during the Visean and Namurian, largely of pleurotomariids, a subsequent period of dynamic stability through the Leonardian, a broad-based decline during the end-Permian mass extinction, and a two-phase post-extinction rebound during the Triassic. The patterns of generic diversity within superfamily-level clades were analyzed using Q-mode factor analysis and detrended correspondence analysis.The results demonstrate that taxonomic affinity, previous clade history, generic age, and gross morphology did not determine survival probability of genera during the end-Permian extinction, with the exception of the bellerophontids, nor did increasing diversity within clades or expansion of particular morphologies prior to the extinction facilitate survival during the extinction or success after it. The pleurotomariids diversified during the Lower Permian, but were heavily hit by the extinction. Similarly, trochiform and turriculate morphologies, among those which Vermeij (1987) has identified as having increased predation resistance, were expanding in the late Paleozoic, but suffered similar extinction rates to other nondiversifying clades. Survival was a consequence of broad geographic and environmental distribution, as was the case during background periods.


Paleobiology ◽  
1989 ◽  
Vol 15 (1) ◽  
pp. 46-52 ◽  
Author(s):  
Stephen R. Westrop

Survival of North American shelf trilobite families during a mass extinction across the upper boundary of the Upper Cambrian Sunwaptan Stage (=“Ptychaspid Biomere”) cannot be predicted from patterns of turnover among their component species: on the shelf, stratigraphic ranges of species belonging to surviving families do not differ significantly from those of eliminated families. Thus, the sorting of families during the extinctions cannot be explained by simple upward causation from the individual level. However, families that ranged from shelf to slope environments before the extinctions (most of which are pandemic) fared significantly better than those confined to shelf settings (which tend to be endemic to North America), indicating that family survival was influenced by geographic and environmental distribution, a property emergent above the individual level. One factor implicated in clade survival during normal background times, high species richness, did not influence the outcome of mass extinction. The results affirm the importance of a hierarchical approach to the interpretation of macroevolutionary patterns and provide some support to the suggestion that sorting processes operating during mass extinctions differ from those of background times.


Geology ◽  
1985 ◽  
Vol 13 (9) ◽  
pp. 667 ◽  
Author(s):  
Rolf Ludvigsen ◽  
Stephen R. Westrop
Keyword(s):  

1873 ◽  
Vol 10 (111) ◽  
pp. 385-395 ◽  
Author(s):  
T. Sterry Hunt

It is proposed in the following pages to give a concise account of the progress of investigation of the lower Palæozoic rocks during the last forty years. The subject may naturally be divided into three parts: 1. The history of Silurian and Upper Cambrian in Great Britain from 1831 to 1854; 2. That of the still more ancient Palæozoic rocks in Scandinavia, Bohemia, and Great Britain up to the present time, including the recognition by Barrande of the so-called primordial Palæozoic; fauna; 3. The history of the lower Palæozoic rocks of North America.


1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky

Concepts of the family Hyolithidae Nicholson fide Fisher and the genera Hyolithes Eichwald and Orthotheca Novak have been expanded through time to encompass a variety of morphologically dissimilar shells. The Hyolithidae is here considered to include only those hyolithid species which have a rounded (convex) dorsum; slopes on the dorsum are inflated, and the venter may be flat or slightly inflated. Hyolithes encompasses species which possess a low dorsum and a prominent longitudinal sulcus along each edge of the dorsum; the ligula is short and the apertural rim is flared. The emended concept of Orthotheca includes only those species of orthothecid hyoliths which have a subtriangular transverse outline and longitudinal lirae covering the shell on both dorsum and venter.Eighteen species of Hyolithes and one species of Orthotheca from the Appalachian region and Western Interior were reexamined in light of more modern taxonomic concepts and standards of quality for type material. Reexamination of type specimens of H. similis Walcott from the Lower Cambrian of Newfoundland, H. whitei Resser from the Lower Cambrian of Nevada, H. billingsi Walcott from the Lower Cambrian of Nevada, H. gallatinensis Resser from the Upper Cambrian of Wyoming, and H. partitus Resser from the Middle Cambrian of Alabama indicates that none of these species represents Hyolithes. Hyolithes similis is here included under the new genus Similotheca, in the new family Similothecidae. Hyolithes whitei is designated as the type species of the new genus Nevadotheca, to which H. billingsi may also belong. Hyolithes gallatinensis is referred to Burithes Missarzhevsky with question, and H. partitus may represent Joachimilites Marek. The type or types of H. attenuatus Walcott, H. cecrops Walcott, H. comptus Howell, H. cowanensis Resser, H. curticei Resser, H. idahoensis Resser, H. prolixus Resser, H. resseri Howell, H. shaleri Walcott, H. terranovicus Walcott, and H. wanneri Resser and Howell lack shells and/or other taxonomically important features such as a complete aperture, rendering the diagnoses of these species incomplete. Their names should only be used for the type specimens until better preserved topotypes become available for study. Morphology of the types of H.? corrugatus Walcott and “Orthotheca” sola Resser does not support placement in the Hyolitha; the affinities of these species are uncertain.


2008 ◽  
Vol 70 (3) ◽  
pp. 426-432 ◽  
Author(s):  
R. Lee Lyman

AbstractFor more than fifty years it has been known that mammalian faunas of late-Pleistocene age are taxonomically unique and lack modern analogs. It has long been thought that nonanalog mammalian faunas are limited in North America to areas east of the Rocky Mountains and that late-Pleistocene mammalian faunas in the west were modern in taxonomic composition. A late-Pleistocene fauna from Marmes Rockshelter in southeastern Washington State has no modern analog and defines an area of maximum sympatry that indicates significantly cooler summers than are found in the area today. An earliest Holocene fauna from Marmes Rockshelter defines an area of maximum sympatry, including the site area, but contains a single tentatively identified taxon that may indicate slightly cooler than modern summers.


Paleobiology ◽  
2007 ◽  
Vol 33 (3) ◽  
pp. 397-413 ◽  
Author(s):  
Margaret L. Fraiser ◽  
David J. Bottjer

AbstractThe end-Permian mass extinction is commonly portrayed not only as a massive biodiversity crisis but also as the time when marine benthic faunas changed from the Paleozoic Fauna, dominated by rhynchonelliform brachiopod taxa, to the Modern Fauna, dominated by gastropod and bivalve taxa. After the end-Permian mass extinction, scenarios involving the Mesozoic Marine Revolution portray a steady increase in numerical dominance by these benthic molluscs as largely due to the evolutionary effects of an “arms race.” We report here a new global paleoecological database from study of shell beds that shows a dramatic geologically sudden earliest Triassic takeover by bivalves as numerical dominants in level-bottom benthic marine communities, which continued through the Early Triassic. Three bivalve genera were responsible for this switch, none of which has any particular morphological features to distinguish it from many typical Paleozoic bivalve genera. The numerical success of these Early Triassic bivalves cannot be attributed to any of the well-known morphological evolutionary innovations of post-Paleozoic bivalves that characterize the Mesozoic Marine Revolution. Rather, their ability to mount this takeover most likely was due to the large extinction of rhynchonelliform brachiopods during the end-Permian mass extinction and aided by their environmental distribution and physiological characteristics that enabled them to thrive during periods of oceanic and atmospheric stress during the Permian/Triassic transition.


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