Paleoecology of Pamlico Formation (Late Pleistocene), Horry County, South Carolina: ABSTRACT

AAPG Bulletin ◽  
1962 ◽  
Vol 46 ◽  
Author(s):  
Jules R. Du Bar, James R. Chaplin,
2000 ◽  
Vol 66 (1) ◽  
pp. 109
Author(s):  
G. Wayne King ◽  
Catherine H. Lewis
Keyword(s):  

2010 ◽  
Vol 33 (2) ◽  
pp. 121-173 ◽  
Author(s):  
Thomas M. Cronin

Upper Pleistocene deposits from 21 localities in Maryland, Virginia, South Carolina, North Carolina, and northern Florida yielded 77 ostracode species; virtually all are living today in brackish and marine water. Five late Pleistocene ostracode biofacies signifying lagoonal, oyster bank, estuarine, open sound, and inner sublittoral environments were delineated using Principal Coordinate Analysis. During the late Pleistocene, the Lagoonal and Oyster Bank Biofacies predominated in the Chesapeake Bay area, whereas east-central North Carolina was characterized by an Open Sound Biofacies similar to that in Pamlico Sound today. The Inner Sublittoral Biofacies was present in southeastern Virginia and along the South Carolina coast. The Estuarine Biofacies was found only in the Chesapeake Bay region. Paleoclimates were inferred by a comparison of Holocene and late Pleistocene ostracode zoogeography; apparently the climate during the late Pleistocene was as warm as, and in some areas warmer than at the same latitudes today. Ostracode species are illustrated by scanning electron photomicrographs Cyprideis margarita, Neocaudites atlan-tica, and Microcytherura norfolkensis are described as new species.


1980 ◽  
Vol 13 (2) ◽  
pp. 213-229 ◽  
Author(s):  
Thomas M. Cronin

AbstractMarine ostracodes from 50 localities were studied to determine the age and elevation of Pleistocene sea levels in the Atlantic coastal plain from Maryland to northern Florida. Using ostracode taxon and concurrent ranges, published planktic biostratigraphic, paleomagnetic, and radiometric data, ostracode assemblage zones representing early (1.8-1.0 my), middle (0.7-0.4 my), and late (0.3-0.01 my) Pleistocene deposition were recognized and used as a basis for correlation. Ostracode biofacies signifying lagoonal, oyster bank, estuarine, open sound, and inner sublittoral environments provided estimated ranges of paleodepths for each locality. From these data the following minimum and maximum Pleistocene sea-level estimates were determined for the southeastern coastal plain: late Pleistocene, 2–10 m from Maryland to northern Florida; middle Pleistocene, 6–15 m in northern South Carolina; early Pleistocene, 4–22 m in central North Carolina, 13–35 m in southern North Carolina, and 6–27 m in South Carolina. Climatically induced glacio-eustatic sea-level fluctuations adequately account for the late Pleistocene sea-level data, but other factors, possibly differential crustal uplift, may have complicated the early Pleistocene record.


1950 ◽  
Vol 15 (3) ◽  
pp. 254-258 ◽  
Author(s):  
Carl F. Miller

In 1946 and 1947 Dr. C.L. Glenn of Vanderbilt University gathered a collection of sherds from nine sites in the vicinity of Myrtle Beach, Horry County, South Carolina. These sherds were presented to the Smithsonian Institution. Some of the sherds were obtained to the north of Myrtle Beach, others in the immediate vicinity, and still others to the south of the city. The sites consist of small sandy ridges, 20 to 30 feet above mean sea level and overlooking Long Bay.Dr. Glenn reports that the sites contained ashes, sherds, and a few scattered oyster shells of the “racoon” type, which is the common type found in this vicinity. No bone, antler, or stone material was found in the debris deposit. He states that no local stones are present from which to fashion implements and that the very few which are found are crude and made from imported stones. In the entire collection, only two stone artifacts are included—one projectile point and one scraper.


Author(s):  
J. T. Ellzey ◽  
D. Borunda ◽  
B. P. Stewart

Genetically alcohol deficient deer mice (ADHN/ADHN) (obtained from the Peromyscus Genetic Stock Center, Univ. of South Carolina) lack hepatic cytosolic alcohol dehydrogenase. In order to determine if these deer mice would provide a model system for an ultrastructural study of the effects of ethanol on hepatocyte organelles, 75 micrographs of ADH+ adult male deer mice (n=5) were compared with 75 micrographs of ADH− adult male deer mice (n=5). A morphometric analysis of mitochondrial and peroxisomal parameters was undertaken.The livers were perfused with 0.1M HEPES buffer followed by 0.25% glutaraldehyde and 2% sucrose in 0.1M HEPES buffer (4C), removed, weighed and fixed by immersion in 2.5% glutaraldehyde in 0.1M HEPES buffer, pH 7.4, followed by a 3,3’ diaminobenzidine (DAB) incubation, postfixation with 2% OsO4, en bloc staining with 1% uranyl acetate in 0.025M maleate-NaOH buffer, dehydrated, embedded in Poly/Bed 812-BDMA epon resin, sectioned and poststained with uranyl acetate and lead citrate. Photographs were taken on a Zeiss EM-10 transmission electron microscope, scanned with a Howtek personal color scanner, analyzed with OPTIMAS 4.02 software on a Gateway2000 4DX2-66V personal computer and stored in Excel 4.0.


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