Effect of salinity on the osmotic,chloride, total protein and calcium concentrations in the hemolymph of the prawn Peneaus monodon (fabricius)

• 1.1. Osmolality and chloride concentrations in the hemolymph of Penaeus monodon became stable 1 day after molting in 32 ppt, while total protein and calcium concentrations remained stable throughout the molting cycle. When intermolt (≥ 36 hr postmolt) animals were transferred from control (32 ppt) to experimental (8–40 ppt) salinities, osmolality, chloride and total protein, but not calcium, concentrations in the hemolymph achieved steady state values 24–48 hr after transfer.
• 2.2. The hemolymph osmolality was a linear function (slope = 0.28) of medium osmolality at salinities between 8 and 40 ppt. It was isosmotic to seawater at 698 mOsm (10 g prawns) and 752 mOsm (30 g), and was hyperosmotic to the medium below isosmotic concentrations, and hypoosmotic to those above.
• 3.3. Hemolymph chloride concentration was isoionic to seawater at 334 mM, and was hyperregulated below isoionic concentrations, and hyporegulated to those above.
• 4.4. P. monodon maintained its hemolymph calcium concentration between 6.4 and 10 mM when medium salinities increased from 8 to 40 ppt.
• 5.5. Total protein concentration in the hemolymph was independent of medium salinity (8–40 ppt) and hemolymph osmolality (540–850 mOsm).

     

Salinity tolerance of adult and juvenile red king crabs Paralithodes camtschatica

• 1.1. Juvenile king crabs were more tolerant of reduced salinities than adult crab; juvenile crab were better volume regulators at reduced salinities than adult crab.
• 2.2. Adult female king crab hemolymph was hyperosmotic to full seawater (30 ppt) and isosmotic to dilute seawater. Juvenile king crab (2 years old) were hypoosmotic at the same concentrations.
• 3.3. Lower osmotic concentration of juvenile hemolymph is at least partially due to lower sodium concentration.
• 4.4. Juvenile king crab can tolerate some dilution and survive for short periods in the reduced salinity of the lower intertidal zone.

     

The effect of salinity on the osmotic,sodium and chloride concentrations in the hemolymph of euryhaline shrimp of the genus Penaeus

• 1.1. The hemolymph is isosmotic to seawater at 745 mOs/kg in P. aztecus, 768 mOs/kg in P. duorarum, 680 mOs/kg in P. setiferus, 699 mOs/kg in P. stylirostris, and 718 mOs/kg in P. vannamei.
• 2.2. The hemolymph is hyperosmotic to seawater at salinities below the isosmotic concentrations and hypoosmotic to those above.
• 3.3. With respect to sodium and chloride, the hemolymph is hyperionic to seawater at low salinities and hypoionic to seawater at high salinities.
• 4.4. P. aztecus and P. duorarum are weaker osmotic and ionic regulators at low salinities than P. setiferus, P. stylirostris, and P. vannamei.
• 5.5. There are no significant differences in the osmotic and ionic regulatory capabilities of all five species at high salinities.

     

Anaerobic metabolism in sublittoral living Mytilus galloprovincialis in the mediterranean—IV. Role of amino acids in adaptation to low salinities during anaerobiosis and aerobiosis

• 1.1. When Mytilus galloprovincialis were transferred from 38 to 19%. sea water (S), the metabolism became anaerobic for at least 8 hr. After 24 hr the animals were entirely aerobic again.
• 2.2. Upon transfer to 19%. S, the total free amino acid concentration in haemolymph doubled within 4 hr, remaining nearly constant thereafter, up to 48 hr.
• 3.3. In the posterior adductor muscle a strong decrease of alanine and glycine occurred at 48 hr exposure to 19%. S, and a smaller decrease of glutamate; taurine remained relatively constant. When transferred again to 38%. S after 14 days, a strong overcompensation occurred in the concentrations of alanine and proline, and a smaller overcompensation in those of threonine and serine.
• 4.4. In the gill no distinct change in the amino acid pool occurred during 14 days of exposure, with the exception of a decrease in serine. When transferred again to 38%. S, a strong overcompensation occurred in alanine, proline, glycine and serine, and a smaller in glutamate and threonine.
• 5.5. No evidence for anaerobic metabolism in the decrease of the amino acid pool was found.
• 6.6. M. galloprovincialis is less able to adapt to low salinities than the more euryhaline M. edulis.

     

The effect of salinity on coelomic fluid osmolyte concentration and intracellular water content in Luidia clathrata (Say) (Echinodermata: Asteroidea)

• 1.1. The concentrations (mM) of osmolytes in the coelomic fluid of Luidia clathrata kept at 25‰S seawater (control individuals) were: 345, Na⁺; 10, K⁺; 10, Ca²⁺; 44, Mg²⁺; 387, Cl⁻; 0.67, amino acids; 0.09, NH₄⁺.
• 2.2. When individuals were transferred from 25‰S to 15‰S or 35‰S, the concentrations of inorganic ions in the coelomic fluid usually equilibrated within 24hr and became the same as those in the medium.
• 3.3. The intracellular water content (g intracellular H₂O/g solute-free dry tissue) of the pyloric caeca and tube feet of control individuals throughout the experiment was 2.13 and 5.40, respectively.
• 4.4. In tissues of individuals transferred to 15‰S, the intracellular water content increased by an average 50% in 12 hr but returned to 19% above control levels during 1 week.
• 5.5. In tissues of individuals transferred to 35‰S, the intracellular water content decreased by an average 17% in 12 hr and did not change during 1 week.
• 6.6. Luidia clathrata is an osmoconformer and partial cell volume regulator within the seasonal salinity range it encounters.

     

Effects of salinity and temperature on oxygen consumption in a freshwater population of Palaemonetes antennarius (Crustacea,decapoda)

• 1.1. After step-like increases in salinity the shrimps exhibit the smallest increase in oxygen consumption in the lower salinity range. At higher salinities the shrimps show longer recovery times and greater increases in the metabolic rate after salinity shock.
• 2.2. In steady-state experiments, the shrimps display the lowest oxygen consumption rates near the isosmotic point. The lowest metabolic rates occur at salinities of 3‰ and 10‰ At salinities of 20‰ and above the rate of metabolism increases by 20–30%.
• 3.3. The calculated osmoregulatory work for animals in fresh water amounts to only 2.7% of routine metabolism and drops to 1.1% for shrimps in 3‰ and 0.7% in 5‰ salinity.
• 4.4. Locomotory activity in the form of position change was not responsible for the increased oxygen consumption of the animals after salinity shocks. A “tentative swimming activity” by fast and frequent beating of the pleopods without position change may be an important factor in the increase of metabolic rates.
• 5.5. In its temperature response, the brackish water population has a higher metabolic rate than the freshwater one. Between 5 and 35°C Q ₁₀-values range from 4.01 to 1.37.

     

The relationship between osmoregulation and nitrogen metabolism in the intertidal prawn,Palaemon elegans (Rathke)

• 1.1. The relationship between nitrogen metabolism and osmoregulation has been studied in the prawn Palaemon elegans (Rathke) following sudden exposure to hyper- and hyposaline conditions.
• 2.2. Animals acclimated to a salinity of 30‰ showed a pronounced increase in the rates of ammonia excretion during the first 2 hr after transfer to lower salinities. These gradually declined during the next 6 hr to rates that were significantly higher than that of control animals (30‰) and were maintained throughout the rest of the experiment.
• 3.3. Rates of ammonia excretion in animals transferred to hypersaline conditions (40‰) fluctuated considerably during the experiment. It was consistently observed, however, that there were two periods during the experiments when ammonia excretion rates had negative values indicating that NH⁺₄ ions were being taken up by the prawns.
• 4.4. Experiments in which small quantities of (NH₄)₂SO₄ containing the stable isotope ¹⁵N were added to the sea-water confirmed that P. elegans was able to take NH⁺₄ ions from the sea-water.
• 5.5. Changes in the Na⁺ ion concentration in the blood and the changes in free amino acid concentration in the blood and in the muscle after exposure to differing salinities were also determined. Their significance and relationship to the observed changes in the rates of ammonia excretion are discussed.

     

Organ specific changes in energy metabolism due to anaerobiosis in the sea mussel Mytilus edulis (L.)

• 1.1. Anaerobic energy metabolism was investigated in different organs of Mytilus edulis and the whole animal.
• 2.2. Succinate accumulates to high levels in most organs but remains low in the hemolymph.
• 3.3. After 16 hours propionate accumulation is observed in all organs. Experimental evidence is not sufficient yet to point out organs that produce more propionate than others.
• 4.4. Acetate is a minor end product.
• 5.5. Acetate and propionate are found in the hemolymph in amounts equal to those in the organs.
• 6.6. Animals incubated in oxygen-free seawater accumulate more end products than animals exposed to air, in the form of volatile fatty acids that are excreted into the incubation water.
• 7.7. Alanine and glutamine increase in the posterior adductor muscle. Aspartate decreases in the total animal, posterior adductor muscle and gills, while in the hemolymph decrease in alanine, asparagine, serine, threonine and proline are observed.

     

Metabolic responses of the mussels Perna viridis and Perna indica to declining oxygen tension at different salinities

• 1.1. Oxygen uptake and ammonia loss were monitored during responses to reductions of both salinity and oxygen tension (PO₂) in the marine mussels Perna viridis and Perna indica from southern India.
• 2.2. The proportional contribution of protein to total catabolic substrates under natural environmental conditions was as much as 96% in P. viridis, relative to only 19% in P. indica.
• 3.3. Normoxic oxygen consumption remained statistically unchanged in P. viridis conditioned to salinities between 32 and 15‰, with no obvious signs of distress. Although equally unaffected at salinities between 32 and 20‰, P. indica showed significantly reduced oxygen uptake following transfer from 32 to 15‰, and had died within the next 7 days.
• 4.4. At salinities greater than 20‰, P. viridis was better able than P. indica to regulate oxygen consumption independent of PO₂.
• 5.5. P. indica showed a compensatory increase in oxyregulatory capacity at 15‰. This exceeded unstressed abilities, helping to maintain albeit reduced oxygen uptake throughout wider ranges of PO₂.
• 6.6. Different responses recorded in each of these tropical and often intertidal species were in accordance with their natural distributions. Nevertheless, the oxyregulatory capacity in both species was higher than in bivalves from temperate and/or subtidally restricted habitats.

     

The dependence of oxygen consumption of the common whelk (Buccinum undatum) on hypoxia,salinity and air exposure

• 1.1. Oxygen consumption of low salinity (20‰) acclimated whelks decreases markedly upon acute exposure to hypoxia (P_WO₂ = 35 Torr), but almost regenerates its original level within 48 hr exposure to the hypoxic condition.
• 2.2. This ability to regain the original level of oxygen consumption is not seen in high salinity (35‰) acclimated whelks.
• 3.3. Oxygen consumption in air at 10°C is more than twice the rate shown by low salinity acclimated whelks in normoxic water (P_WO₂ = 150 Torr).
• 4.4. Q₁₀ for oxygen consumption in air is about 1.0 in the temperature range 10–20°C.

     

The sterol constituents and Δ5,7-sterol content of some bivalve molluscs

• 1.1. The bivalve molluscs Cerastoderma edula, Chlamys opercularis, Ensis soliqua, Modiolus modiolus, Mya arenaria, Mytilus edulis and Pecten maximus contained mixtures of C₂₆-, C₂₇-, C₂₈- and C₂₉-sterols. Cholesterol, 24-methylcholesta-5,22-dien-3β-ol and 24-methylene-cholesterol were the major sterols.
• 2.2. The sterols of Cerastoderma edula, Mya arenaria and Mytilus edulis contained 6–16% of cholesta-5,24-dien-3β-ol.
• 3.3. All the molluscs contained Δ^5,7-sterols in amounts ranging from 2 to 21% of the total sterols.
• 4.4. Cholesta-5,7-dien-3β-ol and 24-methylcholesta-5,7,22-trien-3β-ol were identified in Mytilus edulis. 25-Norcholesta-5,7,22-trien-3β-ol was detected in Modiolus modiolus.

     

Temperature and salinity tolerance of the mole crab,Emerita talpoida (Say) (Crustacea,Anomura)

• 1.1. Adult Emerita talpoida were subjected to 25 temperature-salinity combinations within the range of 5–35°C and 15–65‰.
• 2.2. E. talpoida tolerated 15–65‰ salinity at 20°C and below.
• 3.3. Optimum salinity for survival at stressful temperatures was 40‰.
• 4.4. Crabs transferred directly from one salinity to another experienced changes in osmoconcentration toward that of the new salinity.
• 5.5. Temperature modified the rate of change toward the experimental salinity. Q values averaged 1.2.

     

Variations of respiratory rate of Tisbe holothuriae humes (copepoda,harpacticoida) in relation to temperature,salinity and food type

• 1.1. The influence of temperature (14,19, 24°C), salinity (26,32, 38,44%.) and food type (artificial diets: Fryfood, Mytilus, Soya, Yeast, Spirulina) on the respiratory rate of Tisbe holothuriae has been studied.
• 2.2. Oxygen consumption decreased with decreasing temperature, but with a greater rate at supra- or subnormal salinities.
• 3.3. Multiple-regression analysis showed the quadratic effect of temperature and the linear effect of salinity to be the more important factors affecting respiration.
• 4.4. The food type also seems to exert an important effect on oxygen consumption.
• 5.5. A significant lowering of respiration was observed for all food tested when the animals were starved.

     

Effect of temperature and salinity on the oxygen consumption of laboratory produced Penaeus californiensis postlarvae

• 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
• 2.2. The O₂ in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O₂ concentration down to 1.6 mg/l.
• 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q₁₀) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
• 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.

     

Potassium contracture of anterior byssus retractor muscle of Mytilus edulis

• 1.1. The potassium contracture in the anterior byssus retractor muscle of Mytilus edulis relaxed spontaneously, and the relaxation was accelerated by 5-HT (10⁻⁶ M), but the contractile activation and inactivation was not affected significantly.
• 2.2. By reducing [Ca]₀, the “activation curve” was shifted downward at higher [K]₀, and the “inactivation curve” was shifted toward lower [K]₀ and the rate of inactivation was increased.
• 3.3. The steady-state inactivation was maintained for at least 2 hr without complete inactivation.
• 4.4. The half-inactivation time was dependent on [K]₀, while the half-relaxation time in the contracture induced by conditioning K solutions was not.

     

A comparison of the capabilities of juvenile and adult Penaeus setiferus and Penaeus stylirostris to regulate the osmotic,sodium, and chloride concentrations in the hemolymph

• 1.1. The capabilities of juvenile and mature adult Penaeus setiferus and P. stylirostris to regulate the osmotic, sodium, and chloride concentrations in the hemolymph are compared.
• 2.2. In P. setiferus and P. stylirostris acclimated to salinities of 9.8 and 10.8%. respectively, juvenile shrimp are stronger hyperosmotic and hyperionic regulators than adults. However, the reduced regulatory capabilities of adult shrimp are not sufficient to require migration to offshore waters for survival.
• 3.3. At 40.4%. juvenile P. setiferus are more effective hypoosmotic and hypoionic regulators than adults. However, there is no difference between the regulatory capabilities of juvenile and adult P. stylirostris at 36.2%.
• 4.4. Differences in hemolymph concentration between juvenile and adult P. setiferus at 23.5%. indicate that the isosmotic and isoionic crossover concentrations are elevated with maturation.

     

Time related changes in the free amino acid pool of the sea anemone,Bunodosoma cavernata,during salinity stress

• 1.1. The sea anemone, Bunodosoma cavernata, is a relatively eurybaline cnidarian tolerating salinities from 12 to 40%.
• 2.2. Taurine, glutamic acid and aspartic acid all showed some increases with increased salinity.
• 3.3. The amino acid showing the greatest accumulation under high salinity conditions was β-alanine which increased 28-fold from 1.5 to 41.9 μmol/g dry weight when salinity was raised from 26 to 40%.
• 4.4. When B. cavernata was subjected to increased salinity, β-alanine was rapidly accumulated and reached maximum levels within 4 days.
• 5.5. When salinity was dropped from 36 to 26%0, β-alanine concentrations dropped from 15 to 2 μmol/g dry weight in 2 days.

     

Osmoregulation in the estuarine mysid,Mysidopsis bahia molenock: comparison with other mysid species

• 1.1. The estuarine mysid, Mysidopsis bahia Molenock hypo- and hyper-osmoregulates at salinities from 5 to 37%. and exhibits an isosmotic point of 24%.
• 2.2. Hemolymph osmolality attained steady-state condition by 95 min post-transfer to high (32%.) and low (6%.) salinity water. Transfer from 25%. to the high salinity medium resulted in an initial overshoot in hemolymph concentration followed by rapid recovery. Transfer from 25%. to the lower salinity did not result in an undershoot.
• 3.3. The osmoregulatory capacity of M. bahia is similar to that reported for other estuarine mysids, all of which differ from both freshwater and polystenohaline species.

     

Genetic variation at the Lap locus and ammonia excretion following salinity transfer in an estuarine snail

• 1.1. Thais haemastoma were transferred from 30 to 15‰ and 15 to 30‰ S and ammonia excretion was measured for 72 hr.
• 2.2. Increased ammonia excretion following transfer from high to low salinity was significantly greater in snails with the rare Lap allele, Lap⁹⁴.
• 3.3. Increased rates of nitrogen loss induced by salinity reductions could be responsible for maintaining the Lap⁹⁴ allele at low frequency in estuarine populations of T. haemastoma.

     

The effect of a toxic dinoflagellate (Alexandrium tamarense) on the oxygen uptake of juvenile filter-feeding bivalve molluscs

• 1.1. Oxygen uptake and grazing rates of juvenile bivalve molluscs Mytilus edulis, Mya arenaria, Geukensia demissa, Placopecten magellanicus and Crassostrea virginica were measured following 1 hr exposure to bloom concentrations (10⁶ cells/1) of the toxic dinoflagellate Alexandrium tamarense (GT429) using a non-toxic clone of the same species (PLY 173) as control.
• 2.2. For all bivalves, prefeeding estimates of V̇O₂ were similar to postfeeding values and values recorded 24 hr after exposure to bloom conditions.
• 3.3. V̇O₂ was similar for bivalves fed on both the toxic and non-toxic strains of A. tamarense suggesting that there were no adverse effects on V̇O₂ following 1 hr exposure to toxic GT429.
• 4.4. Bivalves differed in their rates of grazing between toxic GT429 and non-toxic PLY 173. Similar grazing rates were recorded for M. edulis and G. demissa. For P. magellanicus and M. arenaria reduced rates of clearance were recorded in GT429 compared with the non-toxic strain.