Hinge modifications and musculature of strophomenoid brachiopods: examples across the Ordovician-Silurian boundary, Anticosti Island, Quebec

2001 ◽  
Vol 38 (2) ◽  
pp. 125-141 ◽  
Author(s):  
Keith Dewing

Six modifications to the hinge occur in strophomenoid brachiopods from Anticosti Island: (1) overhanging socket ridges; (2) posterolateral socket ridges along the interarea articulate with grooves on the posterior of teeth; (3) anteromedian dental notches articulate with the crests of socket ridges; (4) dental crenulations on the surfaces of teeth mesh with socket ridges; (5) denticles extend laterally to the cardinal extremities; and (6) the margin of the ventral interarea fits into a long socket along the dorsal interarea forming a lateral tooth. Denticulate hinges and dental notches that typify Silurian and Devonian strophomenids begin in the fauna of the Ellis Bay Formation. Thus the most important interval of strophomenid faunal turnover was at the base of the Gamachian (the base of the Hirnantian) and not at the Ordovician–Silurian boundary. Muscle attachment pads in the delthyrial cavity do not correspond to the positions of either the adductor or diductor muscle scars. Pedicle adjustor muscles in modern brachiopods occupy this position. The round gap between the median fold of the pseudodeltidium and groove on chilidium is proposed as the point of emergence of the pedicle muscle. The tiny foramen, commonly sealed early in growth, is suggested to be part of a neanic water-intake system, active before the growth of the cardinal process in ephebic shells. Once the cardinal process appeared, the foramen was blocked. Recurring types of strophomenid ornamentation, such as posteriorly steepened rugae and checkerboard ornamentation, may have served as a plow to redistribute sediment as the shell was pulled backwards along the pedicle.


2019 ◽  
Vol 20 (5) ◽  
pp. 375-384
Author(s):  
Dae-Hung Kang ◽  
Yeongseok Kim ◽  
Sun-Joon Park ◽  
Ikjoong Kim
Keyword(s):  






1962 ◽  
Vol 5 (1) ◽  
pp. 135-160
Author(s):  
Yutaka Inai ◽  
Akira Seyama ◽  
Toshio Togashi


1995 ◽  
Vol 32 (4) ◽  
pp. 359-367 ◽  
Author(s):  
K. Wang ◽  
B. D. E. Chatterton ◽  
C. J. Orth ◽  
M. Attrep Jr

Geochemical analysis of the Ordovocian–Silurian boundary interval on Anticosti Island, Quebec, has revealed low Ir abundances for the lower Becscie Formation (0.005–0.039 ppb), comparable to those reported for the upper Ellis Bay Formation (0.005–0.058 ppb). When normalized as CaCO3-free values and ratioed to Al, a small amount of excess Ir (over background Ir levels) was observed in and on the upper surface of an oncolite platform bed in Member 7 (Laframboise) of the Ellis Bay Formation. Except for this bed, the abundances of Ir and other elements are relatively uniform throughout the section, but small enrichments are apparent in a few clay layers. As in other areas previously studied (South China, northwestern Canada, Scotland), the Ir maxima on Anticosti Island occur near the base of the graptolite persculptus Zone, and are attributable to condensation and slower sedimentation rates associated with the hardgrounds found within and on the upper surface of the oncolite platform bed. Although we cannot preclude a large extraterrestrial impact as the source for the Ir abundance maxima near the end of the Ordovician, which appear to be stratigraphically coeval and geographically widespread in the world, all of them are found to be associated with sedimentary condensation that may have resulted from glacio-eustatic sea-level fluctuations at the end of the Ordovician. From our data, we note that certain elements (e.g., Th, La, Lu, Sc, Cr, Ir, Fe, Al, Ca) show distinct abundance patterns in limestones, calcareous shales, and clays, apparently a result of increasing clay mineral contents.



Desalination ◽  
2007 ◽  
Vol 203 (1-3) ◽  
pp. 199-217 ◽  
Author(s):  
Manuel Fariñas ◽  
Luis Ángel López


2002 ◽  
Vol 2 ◽  
pp. 58-80 ◽  
Author(s):  
Elgin Perry ◽  
Greg Seegert ◽  
Joe Vondruska ◽  
Timothy Lohner ◽  
Randy Lewis

To assess the possible impacts caused by cooling-water intake system entrainment and impingement losses, populations of six target fish species near power plants on the Ohio River were modeled. A Leslie matrix model was constructed to allow an evaluation of bluegill, freshwater drum, emerald shiner, gizzard shad, sauger, and white bass populations within five river pools. Site-specific information on fish abundance and length-frequency distribution was obtained from long-term Ohio River Ecological Research Program and Ohio River Sanitation Commission (ORSANCO) electrofishing monitoring programs. Entrainment and impingement data were obtained from 316(b) demonstrations previously completed at eight Ohio River power plants. The model was first run under a scenario representative of current conditions, which included fish losses due to entrainment and impingement. The model was then rerun with these losses added back into the populations, representative of what would happen if all entrainment and impingement losses were eliminated. The model was run to represent a 50-year time period, which is a typical life span for an Ohio River coal-fired power plant. Percent changes between populations modeled with and without entrainment and impingement losses in each pool were compared to the mean interannual coefficient of variation (CV), a measure of normal fish population variability. In 6 of the 22 scenarios of fish species and river pools that were evaluated (6 species × 5 river pools, minus 8 species/river pool combinations that could not be evaluated due to insufficient fish data), the projected fish population change was greater than the expected variability of the existing fish population, indicating a possible adverse environmental impact. Given the number of other variables affecting fish populations and the conservative modeling approach, which assumed 100% mortality for all entrained fish and eggs, it was concluded that the likelihood of impact was by no means assured, even in these six cases. It was concluded that in most cases, current entrainment and impingement losses at six Ohio River power plants have little or no effect at the population level.



1992 ◽  
Vol 6 ◽  
pp. 84-84
Author(s):  
Keith Dewing ◽  
W.G.E. Caldwell

A combination of shape and form, mode of preservation, and degree of variation makes the strophomenoids one of the more difficult groups of brachiopods to study taxonomically. In turn, taxonomic confusion may explain why the strophomenoids have not been used to the same extent as other groups of brachiopods as a basis for biostratigraphic classification and correlation, and for elucidating biogeographic provincialism. Such conclusions certainly seem warranted following a detailed investigation of the strophomenoids present in the Late Ordovician-Early Silurian carbonate sequence of Anticosti Island, Quebec.The abundance and superb preservation of Anticosti strophomenoids permit a thorough analysis of external and internal features and the high degree of variation that some of these exhibit. Serial sections are critical to reconstructing the interiors of articulated specimens, establishing taxonomic relationships among discrete valves, and exposing developmental changes in shell structure. When subject to such detailed treatment, at least seventeen genera and twenty-seven species of strophomenoids can be securely identified. Variation among these taxa is such that some features - shape, convexity, ornamentation, and outline of muscle field - hitherto depended upon for taxonomic purposes, have little value in this respect. Other features - pattern of pseudopuncta, form of foramen, pseudodeltidium, chilidium, cardinal process, teeth, dental plates, and socket plates, and presence of ridges and septa bounding and dividing the muscle field - are demonstrably more reliable.The Ordovician-Silurian boundary in the Anticosti sequence is broadly characterized by change from a plectambonitid-rafinesquinid-strophomenid fauna in the Vaureal Formation (Ashgill), through a plectambonitid-leptaenid-stropheodontid-Fardenia fauna in the Ellis Bay Formation (uppermost Ashgill), to a leptaenid-stropheodontid-Fardenia fauna in the Becscie to Chicotte formations (Llandovery). Considerable overlap occurs between Ordovician and Silurian taxa. The oldest known chonetid and the oldest stropheodontid on Anticosti Island occur in the Vaureal Formation. Plectambonitids and strophomenids are rare in the late Llandovery Jupiter Formation.Taking a more rigorous biostratigraphical approach, however, distribution of the twenty-seven well-constrained species allows numerous sequential biozones of different type (assemblage, range, overlapping range) to be recognized, up to six of them in the Ashgill section alone. Some zones are distinguished by cosmopolitan species, others by species known from basins well removed from the Anticosti Basin, others again by species seemingly endemic to the Anticosti Basin. These replacements point to a changing pattern of faunal provincialism as Late Ordovician gave way to Early Silurian time. In the Ordovician portion of the section in particular, the biostratigraphic refinement of the potential strophomenoid zones exceeds that of such other brachiopod groups as rhynchonellids or of conodonts.





1998 ◽  
Vol 13 (2) ◽  
pp. 165-169 ◽  
Author(s):  
J. Savitz ◽  
L. G. Bardygula-Nonn ◽  
R. A. Nonn ◽  
G. Wojtowicz


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