Search USGS⌕ Search

Geology topics

T.D. Singer

Publications and source records attributed to T.D. Singer.

2 recordsLinked to original sources

Interactive effects of cortisol treatment and ambient seawater challenge on gill Na+,K+-ATPase and CFTR expression in two strains of Atlantic salmon smolts

During peak smoltification, the interactive effects of cortisol and ambient seawater challenge were compared in two strains of Atlantic salmon (Salmo salar) smolts: a domesticated strain, AquaGen and a native River Imsa strain. Tissue and blood samples were taken from untreated fish on 20 May. Fish were then transferred to experimental tanks, allowed to recover for 24 h and cortisol (50 mg kg body mass-1), dissolved in vegetable oil, or vegetable oil alone (sham) was implanted. Samples were taken 5 days post implantation. Fish were then exposed to 24 h ambient seawater challenge (FW-SW) or freshwater to freshwater replacement (FW-FW) and sampled as before. Sham implantation had no significant impact on any of the measured parameters. Cortisol implantation significantly elevated plasma cortisol in FW-FW Imsa smolts, while no effect was observed in FW-SW Imsa smolts. Cortisol implantation had no effect on the plasma cortisol levels of AquaGen smolts regardless of FW-SW challenge. Increased plasma cortisol corresponded with significantly higher plasma glucose levels in FW-FW Imsa smolts. Plasma Na+ and Cl- levels were not affected by cortisol implantation but were significantly increased in FW-SW smolts of both strains. Gill Na+,K+-ATPase activity increased in response to cortisol implantation in only FW-FW smolts but not FW-SW smolts. Gill Na+,K+-ATPase ??-subunit mRNA levels were not affected by strain, cortisol injection or transfer protocol, while both CFTR I and CFTR II mRNA levels were significantly higher in AquaGen versus Imsa smolts regardless of treatment. CFTR I mRNA was elevated following cortisol implantation in FW-FW smolts from both strains suggesting CFTR I expression is under the control of cortisol. These findings also suggest that plasma cortisol levels are regulated differently between strains and that cortisol implantation and ambient FW-SW challenge interact, interfering with the individual effects of each of these factors. ?? 2003 Published by Elsevier Science B.V.

Aquaculture↗

Time course of salinity adaptation a strongly euryhaline estuarine teleost, Fundulus Heteroclitus: A multivariable approach

Freshwater-adapted killifish ( Fundulus heteroclitus ) were transferred directly from soft fresh water to full-strength sea water for periods of 1 h, 3 h, 8 h and 1, 2, 7, 14 and 30 days. Controls were transferred to fresh water for 24 h. Measured variables included: blood [Na + ], osmolality, glucose and cortisol levels, basal and stimulated rates of ion transport and permeability of in vitro opercular epithelium, gill Na + /K + -ATPase and citrate synthase activity and chloride cell ultrastructure. These data were compared with previously published killifish cystic fibrosis transmembrane conductance regulator (kfCFTR) expression in the gills measured over a similar time course. Plasma cortisol levels peaked at 1 h, coincident with a rise in plasma [Na + ]. At 8 h after transfer to sea water, a time at which previous work has shown kfCFTR expression to be elevated, blood osmolality and [Na + ] were high, and cortisol levels and opercular membrane short-circuit current ( I sc ; a measure of Cl − secretion rate) were low. The 24 h group, which showed the highest level of kfCFTR expression, had the highest plasma [Na + ] and osmolality, elevated plasma cortisol levels, significantly lower opercular membrane resistance, an increased opercular membrane ion secretion rate and collapsed tubule inclusions in mitochondria-rich cells, but no change in gill Na + /K + -ATPase and citrate synthase activity or plasma glucose levels. Apparently, killifish have a rapid (<1 h) cortisol response to salinity coupled to subsequent (8–48 h) expression of kfCFTR anion channel proteins in existing mitochondria-rich cells that convert transport from ion uptake to ion secretion.

Journal of Experimental Biology↗