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K.J. Kroll

Publications and source records attributed to K.J. Kroll.

2 recordsLinked to original sources

Evaluation of reproductive status in Atlantic Tripletail by traditional and nonlethal approaches

Reproductive biology information is an important tool for fishery management actions such as the identification of spawning areas and the development of protective size limits, bag limits, and seasons. Such information for the management of Atlantic Tripletail Lobotes surinamensis is currently limited, particularly in the western Atlantic Ocean, as information regarding the reproductive biology of this species is sparse in the published literature. To this end, we determined the reproductive status of tripletail and compared the results of a nonlethal sampling method, plasma vitellogenin (VTG) analysis, with those of two traditional (lethal) methods, gonadosomatic index (GSI) and gonad histology. A total of 223 (122 male and 101 female) tripletail were sampled over 2 years near Jekyll Island, Georgia. Gonad histology indicated that 107 (94%) of the male tripletail were in the spawning-capable reproductive phase. Female tripletail were found in all reproductive phases, but only nine (8.9%) were in the spawning-capable phase. Plasma VTG was strongly related to GSI in females ( R 2 = 0.832, n = 77), and female GSI differed significantly among reproductive phases ( p < 0.0001). The estimated length at which 50% (L50) of female tripletail reached maturity was 463 mm; however, the L50 for male tripletail could not be determined because of the lack of immature fish within the study sample. Our study provides valuable information for the management of tripletail and indicates that a nonlethal approach (plasma VTG) may be useful for differentiating developing and spawning-capable females from males and from females in other reproductive phases.

Georgia

Estradiol-induced gene expression in largemouth bass (Micropterus salmoides)

Vitellogenin (Vtg) and estrogen receptor (ER) gene expression levels were measured in largemouth bass to evaluate the activation of the ER-mediated pathway by estradiol (E2). Single injections of E2 ranging from 0.0005 to 5 mg/kg up-regulated plasma Vtg in a dose-dependent manner. Vtg and ER mRNAs were measured using partial cDNA sequences corresponding to the C-terminal domain for Vtg and the ligand-binding domain of ER?? sequences. After acute E2-exposures (2 mg/kg), Vtg and ER mRNAs and plasma Vtg levels peaked after 2 days. The rate of ER mRNA accumulation peaked 36-42 h earlier than Vtg mRNA. The expression window for ER defines the primary response to E2 in largemouth bass and that for Vtg a delayed primary response. The specific effect of E2 on other estrogen-regulated genes was tested during these same time windows using differential display RT-PCR. Specific up-regulated genes that are expressed in the same time window as Vtg were ERp72 (a membrane-bound disulfide isomerase) and a gene with homology to an expressed gene identified in zebrafish. Genes that were expressed in a pattern that mimics the ER include the gene for zona radiata protein ZP2, and a gene with homology to an expressed gene found in winter flounder. One gene for fibrinogen ?? was down-regulated and an unidentified gene was transiently up-regulated after 12 h of exposure and returned to basal levels by 48 h. Taken together these studies indicate that the acute molecular response to E2 involves a complex network of responses over time. ?? 2002 Elsevier Science Ireland Ltd. All rights reserved.

Molecular and Cellular Endocrinology