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1.
  • 1.1. Osmotic measurements were made on the perivisceral coelomic and water vascular fluids of 4 species of northwest Pacific starfish and their stable sea-water media.
  • 2.2. Mean levels of both fluids were hyperosmotic in every species, often at statistically significant levels.
  • 3.3. For all species combined, mean hyperosmolality (mosmol/kg ± SE) of perivisceral coelomic fluid was 1.49 ± 0.17, and water vascular fluid 6.07 ± 0.74.
  • 4.4. The hyperosmotic nature of these fluids contributes to water balance, working in conjunction with madreporitic inflow and other factors.
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2.
  • 1.1. The glucose and maltose concentrations measured in the thoracic coelomic fluid of Sabella were respectively 0.05 and 0.15mg/ml.
  • 2.2. Maltose transport was observed to be carrier-mediated in the nephridial wall, with a Vmax of 0.03 nmol/min and a Km of 0.24 mmol/l.
  • 3.3. The accumulation rate of maltose in the nephridia was proportional to its reabsorption rate, and exhibited no plateau.
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3.
  • 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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4.
  • 1.1. A novel glycogen phosphorylase inhibitor was partially purified from crayfish hepatopancreas.
  • 2.2. The inhibitor was found only in two species of crayfish examined, and not in lobster, fresh and salt water clams, mussels or cockroaches.
  • 3.3. The inhibitor is a small protein (Mr = 23,000) which did not show proteolytic activity.
  • 4.4. Preliminary kinetic analysis of the inhibitory mechanism indicated that it bound to both glycogen and the glycogen phosphorylase protein.
  • 5.5. Inhibitor binding to glycogen resulted in a competitive inhibition pattern with respect to glycogen phosphorylase (inhibition constant of ca 10 μg/ml).
  • 6.6. The inhibitor also bound glycogen phosphorylase directly with a binding coefficient of 100 μg/ml resulting in a partially non-competitive inhibition pattern with respect to phosphate.
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5.
  • 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.
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6.
  • 1.1. Weight change after submerging the earthworm into water varied remarkably according to the environmental humidity in which animals were placed before submergence.
  • 2.2. Pretreatment with physiological saline solution before submergence in water gave stable values for the ionic concentrations of the body fluid.
  • 3.3. Brain removal caused decrease of both sodium and chloride ion concentrations and increase of potassium ion concentration of the coelomic fluid when animals were submerged in water.
  • 4.4. Although brain replacement failed, action of a brain hormone is suggested to regulate the decrease of both sodium and choride ions and increase of potassium ion of the coelomic fluid to normal level when animals were submerged in water.
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7.
  • 1.1. The specific activity of Na-K ATPase was determined from the microsomal preparation of gills dissected from adult Macrobrachium rosenbergii.
  • 2.2. Maximal ATPase activity was achieved at a substrate concentration of 0.5 mM ATP.
  • 3.3. Optimal enzyme activity was obtained at pH of 7.5.
  • 4.4. The Arrhenius plot of Na-K ATPase activity revealed a marked discontinuity at 30°C. “Mg” ATPase activity did not exhibit a marked discontinuity.
  • 5.5. The Ea for Na-K ATPase and “Mg” ATPase was 14.6 kCal/mole and 9.31 kCal/mole respectively. Q10 values for Na-K ATPase was 2.34 and for “Mg” ATPase 1.65.
  • 6.6. ATPase activity and gill homogenate protein concentration exhibited a linear relationship up to 130 μg protein/ml.
  • 7.7. Na-K ATPase activity was inhibited by 10−3 M ouabain. It was equally inhibited by the removal of K+ from the reaction medium.
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8.
  • 1.1. The midge larva (Chironomus yoshimatsui) exposed to cadmium (10 μg Cd/ml) for 2 days was histochemically stained with benzothiazolylazo-β-naphthol.
  • 2.2. A large portion of cadmium taken up by the larvae was distributed to the digestive tract, epithelial tract and fat bodies.
  • 3.3. Cadmium accumulated in the fat bodies was discharged slowly relative to cadmium in the tract contents when the larvae were placed in control water.
  • 4.4. Glycogen in the fat bodies of cadmium-exposed larvae was insensitive to PAS staining.
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9.
  • 1.1. Hatching Caretta caretta may lose up to 12% of their initial hatched weight from water loss during emergence from the nest.
  • 2.2. After subsequent osmotic and excretory water loss in sea water, hatchlings will drink sea water (166 μl 100 g−1 hr−1) and return to their initial weight within 10–15 days, without feeding.
  • 3.3. There were no significant changes in plasma osmolarity or sodium levels over this period.
  • 4.4. This osmoregulatory strategy is in marked contrast to that seen in the estuarine crocodile, Crocodylus porosus.
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10.
  • 1.1. American crocodiles (C. acutus) weighing less than 200 g are unable to grow when kept in 35 ppt sea water in the laboratory. Yet paradoxically there are some highly saline areas in south Florida where rapid growth occurs. It is possible that these conflicting observations can be reconciled by behavioral osmoregulation of young crocodiles.
  • 2.2. Hatching occurs during the rainy season and small crocodiles may drink from the brackish “lens” available during and after rainfall.
  • 3.3. Using a weekly regime of alternating exposure to 35 ppt (6 days) and 4 ppt (12–24 hr), it has been demonstrated that growth of small crocodiles occurs. Feeding takes place primarily when brackish water is available. Salinities as high as 18 ppt were drunk when crocodiles were dehydrated by 15–20% of initial mass.
  • 4.4. C. acutus and Alligator have a rather low rate of water efflux in sea water (0.2ml/100g-hr).
  • 5.5. Sodium influx in sea water of C. acutus is low, but higher than efflux. Thus there is no evidence yet for a significant role of the lingual salt glands in sodium excretion.
  • 6.6. The major adaptations to saline water of hatchling C. acutus are a low intake of sodium, an ability to selectively drink water of lower salinities, and to grow very rapidly (within 3–4 months) to a size much more tolerant of immersion in 35 ppt sea water.
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11.
  • 1.1. The oxygen affinity of Urechis caupo coelomic cells is the same in normoxic and in hypoxic animals. There is no Bohr effect between pH 6.8 and 8.0.
  • 2.2. The oxygen affinity of intact coelomic cells is the same as that of extracted, stripped hemoglobin. The oxygen binding properties of stripped hemoglobin are not affected by 1 mM ATP, IMP, or hydrogen ions between pH 6.8 and 8.0, nor do they clearly show cooperativity. The heat of oxygenation. ΔH, = −13.1 kcal/mol between 10 and 25 C.
  • 3.3. Although U. caupo coelomic cell hemoglobin is tetrameric and intracellular, it apparently exhibits neither heterotropic nor homotropic interactions.
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12.
  • 1.1. Recombinant salmon growth hormone at doses of 0.8 and 2.1 μg/g significantly enhanced linear growth in hypophysectomized male killifish, Fundulus heteroclitus, over that of controls and a significant regression was found between growth and the logarithm of dose.
  • 2.2. Bovine growth hormone elicited significant growth enhancement at all three dosages tested (1,4 and 10 μg/g) and a significant log/dose relationship was also observed.
  • 3.3. Observations on the relative weight of the gonads indicate that whole salmon pituitary extract (25 μg/g) possesses strong gonadotropic activity and that both bGH and rsGH had smaller but significant effects on the gonads.
  • 4.4. It is suggested that growth hormone may play a subsidiary synergistic role to other pituitary hormones in gonadal development.
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13.
  • 1.1. A specific and sensitive sandwich enzyme-linked immunosorbent assay (ELISA) was developed for the measurement of low levels of serum immunoglobulin M (IgM) of chum salmon Oncorhynchus keta.
  • 2.2. In this assay, 5 μl serum was enough to measure the concentration of IgM and the minimum detectable concentration of serum IgM was about 5 ng/ml.
  • 3.3. Coefficients of variation within and between assays ranged from 2.90 to 9.61%.
  • 4.4. IgM concentrations remained at low level (< 300 ng/ml) until 40 days after hatching and then increased rapidly at the period of emergence (48 days after hatching).
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14.
  • 1.1. The sialic acid content of newborn calf serum (4.8 μmol/ml) is approx. 3-fold higher than that of mature animals (1.4 μmol/ml) and decreases to 2.4 μmol/ml at 20 days of age. Colostrum-fed and colostrum-deprived calves have similar levels of sialic acid from birth to 14 days of age.
  • 2.2. The high level of sialic acid in newborn calf serum is due predominantly to N-acetylneuraminic acid, since this sialic acid accounts for 93% of the total and since <5% of the sialic acid is O-acetylated.
  • 3.3. Comparison of day 0 and day 20 serum by gel filtration and by SDS polyacrylamide gel electrophoresis demonstrates that the increase in sialic acid is associated with increased production and/or sialylation of components with MW of 45–60 kDa.
  • 4.4. A high percentage (64%) of the sialic acid in newborn calf serum is detected with the lipid-linked sialic acid assay, relative to 20 day old (25%) or mature (18%) animals.
  • 5.5. This indicates that the glycoproteins of newborn calf serum are more efficiently extracted under the conditions of this assay than glycoproteins of mature serum.
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15.
  • 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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16.
  • 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
  • 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
  • 3.3. The specific mass exponent (dimension: μg O2/g/hr) is temperature independent and ranges from 0.27–0.29.
  • 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
  • 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
  • 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
  • 7.7. The results obtained are generally in agreement with those recorded for other teleosts.
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17.
  • 1.1. Free amino acids were analysed in the haemolymph of Galleria mellonella larvae by HPLC chromatography with o-phthaldialdehyde (OPA)-l-thio-β-d-glucose as derivatization agent.
  • 2.2. Fourteen primary amino acids were detected among which glutamine, alanine, γ-aminobutyric acid (GABA) and glycine predominated and constituted 67.7% of the amino acids found.
  • 3.3. The concentration of GABA increased significantly with the age of larvae entering the wandering phase and reached a maximum during metamorphosis.
  • 4.4. Analysis of cold-acclimated larvae revealed a net increase of free primary amino acids from 96 to 151.8 μmol/ml during consecutive acclimation to 0°C within 20 days and to 205.4μmol/ml during cold shock injury at 0°C (3 hr).
  • 5.5. The bulk of this increase was accounted for by alanine, glycine, phenylalanine and lysine.
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18.
  • 1.1. Accumulation and distribution of dietary Se in relation to mortality was investigated in adult house flies.
  • 2.2. The midgut preferentially accumulated Se and thereby limited toxicity.
  • 3.3. Midgut Se concentrations were from 6- to 107-fold higher than in carcass, and from 15 to 71% of the total Se was associated with midgut.
  • 4.4. When dietary levels of Se were raised the midgut saturated at 15 μg Se/g tissue, followed by a rise in carcass levels to greater than 0.5 μg Se/g tissue and increased mortality.
  • 5.5. Se levels in lysosomal fractions were from 3- to 50-fold higher than in other subcellular fractions, suggesting that Se is sequestered in lysosomes.
  • 6.6. Se added to drinking water was toxic at 4–8 ppm.
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19.
  • 1.1. Immature Atlantic salmon post-smolts weighting approximately 150 g were transferred abruptly to fresh water (FW) after 5 months in sea water (SW).
  • 2.2. Losses of ions and gain of body water are reversed after 3 days with about 10–12 days taken for complete FW adaptation.
  • 3.3. Immediately on transfer from SW to FW, immature salmon take up sodium at 45 μmol/kg/hr, about one-third the rate observed in maturing salmon on their spawning migration.
  • 4.4. The sodium uptake rate increases to that of maturing salmon after 2 days in freshwater. Differences in the osmoregulatory ability of immature and maturing salmon are discussed.
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20.
  • 1.1. At 37 stations in the English Channel and the southern North Sea concentrations of four brominated phenols in Lanice conchilega were determined using ECD equipped capillary gas chromatography: 2,4-dibromophenol, 2,6-dibromo-4-methylphenol, 2,4,6-tribromophenol, 3,5-dibromo-4-hydroxybenzaldehyde.
  • 2.2. Concentrations in worms of the southern North Sea were generally below 1 μg/g wet wt.
  • 3.3. Levels were slightly raised in worms of sheltered shores, those of 3,5-dibromo-4-hydroxybenzaldehyde were increased in subtidal populations.
  • 4.4. Concentrations in L. conchilega of Brittany were considerably higher than those in worms of the Frisian Islands, North Sea; they deviated from the latter by factors of 3, 16, 4, 4, respectively.
  • 5.5. The reasons for the conspicuous differences are hitherto unknown; three explanations are suggested.
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