Water balance in developing eggs of the codGadus morhua L.

Measurements of yolk osmolality from the embryo of codGadus morhua L. revealed significant variations in the hyposmolality during the embryonic development. The embryo proved to have an extremely low water permeability, protecting it from dehydration in the hyperosmotic seawater. The effect of temperature on the water permeability is high, expressed by an exceptionally high activation energy for water transfer. The agreement between embryonic volume decrease and diffusion permeability during the first 8-10 days after fertilization indicates that no water uptake mechanism is present at this time, thus leaving the embryo fully dependent on internal water stores. The cod egg is buoyant in seawater throughout development. The mechanism for providing hydrostatic lift is the large volume of diluted tissue water located in the yolk and subdermal spaces.

Drinking activity of the newly hatched larvae of codGadus morhua L.

The drinking rate of cod larvae 1-7 days post hatching was measured from the uptake of(3)H-labelled dextran (MW = 70000) admixed in the incubation seawater (34 ppt 5°C). The drinking rate increased gradually from 0.15% to 0.59% of the larval body weight on day 1 and day 7 respectively. This increase in drinking rate correlated with an observed decrease in the volume of the yolk sac and its water store. Autoradiographs showed the labelled dextran to be confined to the intestine. Electron micrographs showed an open mouth communicating with the oesophagus and the intestine in cod larvae at the time of hatching. Chloride cells were present on the opercular folds but not on the vestigial, developing gills. The data indicate that the water acquisition mechanism of larval cod is similar to that of adult marine fish.

Effects of A23187 and Ca2+ on volume- and thiol-stimulated, ouabain-resistant K+C1- fluxes in low K+ fluxes in low K+ sheep erythrocytes.

Ouabain-resistant (OR), C1- -dependent K+ (K+C1-) transport measured by Rb+ influx in isosmotic and anisosmotic media was stimulated by the Ca2+ ionophore A23187 and EGTA (ethylene-glycol-tetracetic acid) in low K+ (LK) but not in high K+ (HK) sheep red cells. Increasing external Ca2+ concentrations, [Ca2+]o, from about 10(-7) to 10(-3)M in presence of A23187 and in absence of EGTA inhibited OR Rb+ influx, in LK red cells osmotically shrunken or swollen as well as treated with the thiol reagent N-ethylmaleimide (NEM). Hence the volume- and the NEM-stimulated K+C1- transport system in LK cells can be experimentally modulated by cellular Ca2+ or other Me2+, which may interact with sites on the K+C1- transporter under the control of membrane sulfhydryl (SH) groups.

Contractility and 45Ca fluxes in heart muscle of flounder at a lowered extracellular NaCl concentration.

The twitch force of isolated electrically paced ventricular strips of flounder, Platichthys flesus L., increased after lowering the extracellular sodium chloride concentration by 50 mmol l-1. This response was markedly reduced by replacing the sodium chloride with either Tris-HCl or sucrose, so that osmolarity was unchanged. The 45Ca efflux decreased and the 45Ca influx increased when the extracellular sodium concentration Nao+ was lowered. In contrast, changing only the osmolarity had no observable effect on these fluxes. An increased resting tension appeared in strips exposed to a Na+-, Ca2+-free solution. This was transient at an unchanged osmolarity but became permanent at an osmolarity lowered by 100 mosmol l-1. These results suggest that both a lowered Nao and a lowered osmolarity have a positive inotropic effect, due respectively to an increased cellular uptake of Ca2+ and a redistribution of cellular Ca2+.