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1.
  • 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.
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2.
  • 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).
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3.
  • 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.
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4.
  • 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.
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5.
  • 1.1. Phascolopsis gouldi, the commonly studied sipunculan of the Woods Hole area, Massachusetts, can tolerate a salinity range from about 45% seawater to at least 100% SW, with literature records extending to about 160% SW. There was no survival at 40% SW.
  • 2.2. Over this salinity range, P. gouldi is an osmotic and ionic conformer.
  • 3.3. The osmotic and sodium concentrations of the coelomic fluid are the same as that of the medium; the chloride concentration is about 9% less than that of the medium; the potassium concentration is about 30% higher.
  • 4.4. Analysis of water content regulation by two different approaches shows that P. gouldi does have a limited ability for volume regulation, restricted to salinities higher than 58% SW.
  • 5.5. P. gouldi is not a “simple osmometer”.
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6.
  • 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.
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7.
  • 1.1. Soluble proteins extracted from male and female Penaeus vannamei tissues such as eyes, eyestalks, brain, nerve cord, hemolymph, heart, muscle, hepatopancreas, hepatopancreas membrane and cuticular epidermis were analyzed and compared by high-resolution mini-two-dimensional polyacrylamide gel electrophoresis (mini-2D-PAGE).
  • 2.2. In each shrimp tissue a large number of discrete polypeptides was observed.
  • 3.3. The polypeptide patterns from the same tissue of female and male shrimp were mostly similar but both qualitative and quantitative differences were noted, suggesting the presence of sex-specific gene products in various shrimp tissues.
  • 4.4. Future applications of these results are discussed.
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8.
  • 1.1. The locomotor-inducting factor of the giant African snail, Achatina fulica, was examined.
  • 2.2. Snails showed nocturnal circadian behavior in relative humidity at least over 50%. Although the rhythmicity was independent of light and darkness, it was disturbed easily by hydration, and hydrated snails continued to locomote throughout the day. For induction of locomotor behavior, relative humidity over 50% was the fundamental factor and water is shown to be the limiting factor for the endogeneous circadian oscillator.
  • 3.3. The integument of snails showed a higher water permeability. Through the integument, hemolymph osmolality changed easily according to hydration and dehydration from about 120 to 400 mOsm/kg H2O. Circadian behavior was induced in snails in which hemolymph osmolality ranged from about 130 to 230 mOsm/kg H2O.
  • 4.4. By hydration, hemolymph osmolality in quiescent and estivated snails which have higher osmolality decreased gradually and then they began to locomote according to the degree of dilution, and vice versa. The induction of behavior in these snails was controlled by low hemolymph osmolality.
  • 5.5. Together with the endogeneous rhythmicity, water environment was shown to be the key factor for the induction of locomotor behavior.
  • 6.6. Based on these results, the mechanisms of the induction of locomotor behavior in terrestrial pulmonates are proposed.
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9.
  • 1.1. Glycine, proline, and taurine are the quantitatively most important amino acid osmolytes in Penaeus aztecus postlarvae.
  • 2.2. Taurine dominates the amino acid pool in low salinity, while proline dominates the amino acid pool at higher salinities.
  • 3.3. Although not major contributors to the pool, glutamate and alanine are constitutively synthesized from [14C]glucose and [14C]glutamate under constant salinity and under hyperosmotic stress treatments.
  • 4.4. Proline synthesis from [14C]-precursors is apparent under constant high (but not low) salinity and is significantly induced by hyperosmotic stress.
  • 5.5. No appreciable glycine synthesis was observed from [14C]glucose or [14C]glutamate under any experimental conditions.
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10.
  • 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.
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11.
  • 1.1. Water efflux and urine production rates were measured in blue crabs acclimated to several salinities.
  • 2.2. In 100% seawater the mean rate of water efflux (31.3 ml/100g hr−1) was significantly greater than that in 50% seawater (18.9 ml/100 g hr−1.
  • 3.3. Water efflux was directly related to body weight.
  • 4.4. The mean urine production rate was significantly greater in crabs acclimated to 50% and 30% seawater (0.17 and 0.18 ml/100g hr−1) than in animals conditioned to 100% seawater (0.09 ml/100 g hr−1).
  • 5.5. The difference between theoretical net water fluxes for crabs exposed to 100% seawater and 50% seawater was similar to the difference in urine output in the same salinities, demonstrating the importance of the antennal gland in volume regulation.
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12.
  • 1.1. The mean concentration of total hemolymph iron was 3060μg/100 ml in Patella peronii and 2950μg/100 ml in Patelloida alticostata.
  • 2.2. Ferritin was found to act as a major iron-binding protein in the hemolymph of both P. peronii and P. alticostata.
  • 3.3. P. alticostata ferritin has a molecular weight of approximately 505,000, while that of P. peronii has a mol wt. of approximately 520,000.
  • 4.4. The lateral radula teeth of both species are mineralized by deposits of silica (SiO2) and iron in the form of goethite (α-FeOOH).
  • 5.5. Hemolymph ferritin is suggested to act as a high capacity transport system to supply iron to the mineralizing front of the radula.
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13.
  • 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.
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14.
  • 1.1. Yolk proteins were isolated from ovaries of the shrimp Penaeus vannamei and used as an antigen for antibody production in rabbits.
  • 2.2. Protein synthesis was measured for both the hepatopancreas and the ovary in vitro, and proteins present in both tissues were immunoreactive with the antibodies.
  • 3.3. Extracts of shrimp eyestalks inhibited in vitro protein synthesis by both tissues. The inhibitory factor from the eyestalks was heat stable and had a molecular weight of 3300 daltons.
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15.
  • 1.1. Patterns of osmoregulation were studied in three species of Swan river atherinids (Leptatherina presbyteroides, lower estuarine and marine; Craterocephalus mugiloides, mid estuarine; Leptatherina wallacei, upper estuarine) over a wide range of salinities.
  • 2.2. The plasma Na+ concentration was elevated with an increase in salinity.
  • 3.3. Haematocrit and body water content decreased with acclimation to higher salinity.
  • 4.4. All three species of atherinids osmotically regulated over a salinity range greater than that which these fish are reported to occur in.
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16.
  • 1.1. In vitro yolk synthesis was measured in fragments of the ovary of developing shrimp, Penaeus vannamei.
  • 2.2. Progesterone and estradiol stimulated yolk synthesis in vitro, while ecdysterone, testosterone and estrogen had no effect.
  • 3.3. A peptide factor from the eyestalks of crayfish stimulated yolk synthesis in vitro. A peptide factor from shrimp eyestalks inhibited yolk synthesis in vitro.
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17.
  • 1.1. The dietary and inter-organ cholesterol transport in the hemolymph of the bivalve mollusc Diplodon delodontus, was studied. Plasma and hemocytes were obtained after feeding labeled cholesterol to animals or injecting it into the posterior adductor muscle.
  • 2.2. In both cases, cholesterol was incorporated either into plasma or hematic cells.
  • 3.3. Two plasmatic fractions differing in their hydrated densities were recognized as cholesterol carriers and were isolated. They have characteristics of high density (HDL) and very high density (VHDL) lipoproteins, respectively.
  • 4.4. The major lipids in the different classes of lipoproteins were free sterols in HDL and phospholipids in VHDL.
  • 5.5. Neither low nor very low density lipoprotein transporting cholesterol was detected.
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18.
  • 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.
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19.
  • 1.1. The distribution of different phospholipids and the repartition of fatty acids extracted from hemolymph of crab Carcinus maenas are analysed.
  • 2.2. The action of the temperature on the lipid composition is also determined: an increase of content of PE and a slight rise of the degree of unsaturation of fatty acids are found at lower temperatures.
  • 3.3. The specific radioactivity of total phospholipids, phosphatidyl-choline and phosphatidylethanolamine from hemolymph of Carcinus maenas is studied from two radioactive precursors (32Phosphorus and 3H]ethanolamine). Results suggested that the conversion of PE into PC by methylation could take place in hepatopancreas of Carcinus maenas.
  • 4.4. The specific radioactivity of phospholipids from these two same radioactive compounds is increased following a variation in the environmental temperature.
  • 5.5. The composition of hemolymph lipids could be a direct reflection of the lipid metabolism of the hepatopancreas and that the temperature alters the rate of the phospholipid exchange between hepatopancreas and hemolymph.
  • 6.6. It is suggested that these lipid alterations occur in order to permit crab Carcinus maenas to support large changes in environmental temperatures.
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20.
  • 1.1. The phenoloxidase activity, protein and carbohydrate levels were studied for 24 hr in the hemolymph of the migratory grasshopper, Melanoplus sanguinipes after artificial wounding of the insect cuticle or the injection of Beauveria bassiana conidia.
  • 2.2. Injection or wounding induced a primary response and phenoloxidase activity was found to increase within 10–60 min. The values for phenoloxidase activity in viable B. bassiana-injected insects exhibited a secondary response, i.e., an increase 24 hr after injection.
  • 3.3. In wounded insects and those injected with inactivated conidia, the phenoloxidase activity receded after the initial increase and remained at low levels.
  • 4.4. Protein concentrations in the hemolymph increased immediately after infection and wounding and returned to basal levels during the course of the experiment.
  • 5.5. Injection of viable B. bassiana resulted in a gradual increase in the protein concentrations between 12 and 24 hr.
  • 6.6. There was no apparent change in the carbohydrate levels in either B. bassiana-infected or wounded insects.
  • 7.7. These results are discussed in relation to their possible role(s) and interrelationships in the immune response to infection or wounding. Furthermore, we suggest that a “factor” is released after mechanical injury of the integument.
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