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1.
  • 1.1. Larvae (first zoeae) of Palaemonetes vulgaris are relatively stenohaline (optimum salinity = 20%.), adults euryhaline (96-hr LD50 values: 0.8 and 51%.).
  • 2.2. The concentration of blood sodium remains nearly constant over the salinity range 5–45%.
  • 3.3. Adult P. vulgaris are less tolerant of dilute (1–20%.) media than sympatric P. pugio but equally tolerant of higher salinities (35–45%.). Palaemonetes vulgaris maintains a slightly more constant and higher (average) sodium concentration in the blood than P. pugio.
  • 4.4. It is suggested that these differences contribute to habitat partitioning of these species and that they reflect the greater affinity of P. vulgaris for a euhaline milieu.
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2.
  • 1.1. A starvation test was conducted in small beakers with stage 1 (S1) and stage 2 (S2) Macrobrachium rosenbergii larvae to determine optimal salinities.
  • 2.2. Experiments were first performed with S2 larvae at 13 ppt to identify a suitable medium made with artificial sea salts.
  • 3.3. A broad-range (0–35 ppt) and a subsequent narrow-range (9–16 ppt) salinity experiment with S2 larvae were used to identify 13 ppt as the optimal salinity, with 12 ppt as the next best; this agrees well with most previous estimates of optimal salinities for rearing larvae.
  • 4.4. S1 larvae were also tested in a narrow-range salinity experiment but were not used further because, unlike starved S2 larvae, they molted during the experiment.
  • 5.5. Identification of the optimal salinity was not affected by 50% daily water exchange or by bright light.
  • 6.6. Exposure of larvae to three different salinities—7, 13 and 19 ppt—during S1 influenced the width of the optimal salinity range for S2 larvae.
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3.
  • 1.1. Activities of Na+-K+ ATPase and carbonic anhydrase were measured through the early post-embryonic development of Penaeusjaponicus. In adults, only the Na+-K+ ATPase activity was measured.
  • 2.2. ATPase activity was variable in the successive development stages. From zero in nauplii, the activity slightly increased in zoeae, and rose sharply in mysis stages 2 and 3.
  • 3.3. A further significant increase in activity was noted at the transition from late mysis to early postlarvae, concomitant with a change from the larval osmoconforming pattern of osmoregulation to the postlarval and adult hyper-hyporegulating pattern.
  • 4.4. The activity of Na+-K+ ATPase, measured in isolated cephalothorax, increased from PL3 to PL4 to its maximum value in PL5; at this stage, osmoregulatory capacity was fully efficient.
  • 5.5. In young stages of P. japonicus, the variations in Na+-K+ ATPase activity appear correlated with the development of osmoregulatory ultrastructures, and with osmoregulation and salinity tolerance.
  • 6.6. These results are discussed with regard to their ecological and physiological implications.
  • 7.7. In adults, the activity of Na+-K+ ATPase was high in gills and epipodites and no activity was detected in branchiostegites. These results are related to the ultrastructure of these organs.
  • 8.8. The activity of carbonic anhydrase did not change significantly in larval and postlarval stages.
  • 9.9. From these results, it is proposed that the effector sites of osmoregulation are located in branchiostegites, pleurae and epipodites in postlarvae, and in epipodites and mainly in gills in adults.
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4.
  • 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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5.
  • 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.
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6.
  • 1.1. Oxygen consumption of low salinity (20‰) acclimated whelks decreases markedly upon acute exposure to hypoxia (PWO2 = 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 (PWO2 = 150 Torr).
  • 4.4. Q10 for oxygen consumption in air is about 1.0 in the temperature range 10–20°C.
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7.
  • 1.1.|Intraspecific variation in the thermal physiology of Rana sylvatica was examined.
  • 2.2.|Heat and cold tolerances of both adult and larval representatives were determined for animals representing populations from New York, Maryland, Kentucky, Ohio, Michigan and Canada.
  • 3.3.|In general, frogs from more northern localities exhibited lower heat tolerances.
  • 4.4.|There was no evidence of interpopulational differences in cold tolerance. Similar trends were revealed by larval testing.
  • 5.5.|Interpopulational differences among laboratory-reared tadpoles suggests a strong genetic component to Rana sylvatica thermal physiology.
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8.
9.
  • 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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10.
  • 1.1. The effect of eyestalk ablation on preadults of Callinectes similis exposed to a constant salinity (30%.) and to simulated tidal changes in salinity (30-11 to 30%.) were measured.
  • 2.2. In constant salinity, crabs showed a persistent respiratory rhythm, with a maximum oxygen consumption during the day. Under these conditions, ablation significantly increased the respiratory rate but not the rhythm.
  • 3.3. In variable salinities, the highest respiratory rates occurred in salinities of 11 and 16%. during the night. In these crabs, ablation of eyestalks and subsequent injection of eyestalk extracts did not alter the respiration rate rhythm.
  • 4.4. The circadian rhythm is controlled by the periodicity of environmental changes instead of the influence of eyestalk hormones.
  • 5.5. Regulation of metabolism in C. similis associated with osmoregulation involves other neurosecretory organs.
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11.
  • 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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12.
  • 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.
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13.
  • 1.1. Cells of tentacles and body wall of the sea anemone Condylactis gigantea behaved as simple osmometers during 5hr exposure to 50, 67, 83, 100 and 125% sea-water.
  • 2.2. All intracellular water appeared to be osmotically active.
  • 3.3. Cell sodium, chloride and total osmolyte content remained invariable, with taurine decreasing and potassium increasing as sea-water concentration was reduced.
  • 4.4. Tissues, as a whole, exhibited a pseudoregulatory response to changes in salinity as the large and osmotically inert extracellular space buffered volume changes to a considerable extent.
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14.
  • 1.1. Embryos and larvae of the asteroid Echinaster spinulosus were exposed to high salinity stress at various stages during early development.
  • 2.2. Highest percentages of three-rayed (9.7%) and four-rayed (29%) individuals occurred when individuals which had developed for 48 hr (appearance of pre-oral lobe) at ambient salinity (30%o) were exposed to high salinity (39%o).
  • 3.3. The percentage of ray-number aberrancies increased with increasing salinity.
  • 4.4. The ontogenetic events associated with the formation of the hydrocoelic rudiments at the pre-oral lobe stage may be sensitive to salinity and influence the development of ray number.
  • 5.5. The ability to induce variations of ray number in asteroids with salinity stress may yield an experimental approach for the determination of the adaptive significance of ray number in asteroids.
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15.
  • 1.1. Daphnia magna were exposed for 24 hr to 14C-labelled pentachlorophenol (PCP) at an initial concentration of 20μg/l in the incubation water. Occurrence of free PCP and its metabolites were measured both from the animals and the water.
  • 2.2. Hydrophilic metabolites excreted into water were analysed, after acid or enzymatic hydrolyses, with a liquid-liquid extraction and TLC.
  • 3.3. PCP was metabolized and excreted, perhaps solely, via the sulphate conjugation. The average excretion rate, 2.65nmol/g/hr, accounted for 35% of the absorption rate measured at the start of exposure.
  • 4.4. Neonate daphnids had an equal ability to metabolize PCP as the older animals. Bioconcentration in young animals was, however, only 23% of that in adult ones.
  • 5.5. Effect of naturally humic water on metabolization and excretion of PCP was negligible.
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16.
  • 1.1. Inductively coupled plasma atomic emission spectroscopy (ICP-AES) was used to measure iron concentration in several body tissues throughout the life cycle of the lamprey, Petromyzon marinus L.
  • 2.2. Iron concentration in the liver rises sharply during metamorphosis, decreases in parasitic adults, and falls to the lowest value in upstream migrants.
  • 3.3. In the intestine, the concentration of this metal is highest in the larval stage, but values decline steadily through transformation to their lowest levels in parasitic adults.
  • 4.4. Dorsal skin has, on average, three times the iron content of ventral skin and it is only in upstream migrants that the levels of both regions increase significantly over those of other stages.
  • 5.5. Differences in iron concentration in tissues of larval and adult lampreys reflect changes which take place at metamorphosis.
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17.
  • 1.1. Levels of progesterone, pregnenolone, testosterone, 5α-dihydrotestosterone, estrone and estradiol were measured by radioimmunoassay in purified gonadal extracts of larval and adult male and female Locusta migratoria.
  • 2.2. The average steroid contents varied between less than 1 ng to more than 160 ng/g tissue.
  • 3.3. Young adults were treated with precocene or ketoconazole in an attempt to influence the steroid contents in gonads.
  • 4.4. Ketoconazole treatment had no effect on the steroid contents in gonads whereas precocene treatment resulted in higher contents of androgens.
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18.
  • 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.
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19.
  • 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.
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20.
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