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1.
  • 1.1. The hemolymph osmotic, Na+ K+, Ca++ and Mg++ concentrations were determined for both sexes in crabs from mangrove Ucides cordatus and Goniopsis cruentata and supralittoral Ocypode quadrala after aerial desiccation, for 10 hr.
  • 2.2. There was no difference between sexes in the two mangrove crabs, but in O. quadrata the females were the most significantly affected (P < 0.01).
  • 3.3. Hemolymph osmotic Na+, Ca++ and Mg++ concentrations increased significantly in desiccated ghost crabs, while K + concentration was not significantly changed. In the two mangrove crabs, only hemolymph Ca++ concentration increased significantly, after desiccation.
  • 4.4. The short time desiccation is suggested to be a device to study the steps of osmo-ionic regulation in terrestrial crabs.
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2.
  • 1.1. Hemolymph osmoregulation was examined in Chrysochus auratus, Tetraopes tetrophthalmus and Tenebrio molitor. These beetles differed in their water loss rates and in the availability of free water in their habitats.
  • 2.2. During dehydration at comparable rates, osmotic responses were similar in these species. Osmoregulation after rehydration was better in C. auratus.
  • 3.3. Osmoregulation ability was not significantly affected by the beetle's rate of dehydration.
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3.
  • 1.1. Metabolic rates (ml O2/mg/hr) of three geographically separated populations of the carabid beetle Calathus melanocephalus L. (Finse and Je 10y, Norway and Drenthe, The Netherlands) were measured and compared by ANCOVA.
  • 2.2. No significant relationship (P > 0.05) between metabolic rates and body weight or sex of the animals were found.
  • 3.3. Individuals mostly acclimated to low temperatures by increased metabolic rates and in the opposite direction to higher temperatures. Individuals collected in early summer also showed higher metabolic rates than those caught later in the autumn.
  • 4.4. Contradicting the theory of metabolic cold adaptation, beetles from The Netherlands had the highest metabolic rates, beetles from Finse intermediate rates and beetles from Jeløy the lowest rates.
  • 5.5. No significant relation were found between geographical origin of the beetles and their respective chill-coma temperature.
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4.
  • 1.1. Kidney, oesophagus and gill Na+-K+ ATPase activity and serum Na+, K+ and Cl concentrations are evaluated in European sea bass during experimental acclimation to fresh water.
  • 2.2. Kidney and oesophagus ATPase increase in low salinity and reach a maximum in fresh water.
  • 3.3. Gill ATPase decreases during the acclimation trials and rises again to normal values after a 3-week stay in fresh water.
  • 4.4. Na+ and K+ serum concentrations decrease during the trials and increase back after a 3-week stay in fresh water.
  • 5.5. The correlations between enzymatic activities, serum ion concentrations, morphological changes and environmental salinity are discussed.
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5.
  • 1.1. The effects of alternating current electronarcosis, rectified current electronarcosis and chemical anaesthesia (benzocaine hydrochloride) on plasma electrolytes and on the osmotic pressure of the blood of the freshwater bream Oreochromis mossambicus were evaluated.
  • 2.2. Plasma Ca2+, Na+ and K+ concentrations and the osmotic pressure of the blood were monitored over a period of 7 days.
  • 3.3. The results showed that the different electrolytes respond differently to the different techniques.
  • 4.4. Chemical anaesthesia exhibited the least effects on the parameters studied.
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6.
  • 1.1. In brush border membrane vesicles isolated from eel kidneys, adapted either to sea water or freshwater environments, a Na+/H+ antiporter is present.
  • 2.2. Using a calibration plot it is possible to evaluate the amount of protons that this antiporter can accumulate inside the vesicular space.
  • 3.3. The activity of the antiporter seems to be affected by the salinity of the water; it is higher in animals adapted to seawater.
  • 4.4. This adaptation seems to occur by a Jmax regulation of the antiporter.
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7.
  • 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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8.
  • 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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9.
  • 1.1. Rainbow trout were acclimated to salt water (1.5, 2.0 or 3.0%, which means 40, 60 or 85% concentrated sea-water) and the electrolyte, glucose and cortisol concentrations of the plasma as well as the extra- and intracellular muscle space, the muscle electrolyte concentrations and the ATPase activity were analysed.
  • 2.2. Plasma osmolality, Na+, Ca2+ and Mg2+ concentrations of the plasma had a maximum at 24 hr after the start of acclimation when acclimated to 3.0% salt water. Plasma osmolality, Na+ and Mg2+ concentrations were significantly higher during the whole acclimation time when exposed to 3.0% salt water.
  • 3.3. Variations and regulations of ECS and ICS were clearly demonstrated. The intracellular electrolyte concentrations were also maximal at 24 hr.
  • 4.4. The plasma glucose level was just slightly elevated, but the cortisol level clearly indicated a stress response at 24 hr.
  • 5.5. The activity of gill Na-K-ATPase increased during the acclimation time.
  • 6.6. The regulatory processes in trout during acclimation to salt water are compared with those occurring in tilapia and carp.
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10.
  • 1.1. Blood volume and plasma biochemical changes and feed and water consumption in response to a hemorrhage by phlebotomy of 30% of the calculated total blood volume with and without replacement of blood volume with physiological saline were determined in juvenile male Coturnix coturnix japonica.
  • 2.2. Plasma protein and osmolality decreased rapidly posthemorrhage and did not recover by 72 hr posthemorrhage.
  • 3.3. Plasma glucose, Na+ and K+ increased within Ihr postphlebotomy. Plasma Na+ returned to nonphlebotomized levels within 6 hr postphlebotomy.
  • 4.4. Saline replacement of blood volume resulted in hypervolemia within 3–5 min postphlebotomy.
  • 5.5. Phlebotomized quail receiving no saline recovered blood volume to 0 hr (nonphlebotomized) levels within l hr postphlebotomy.
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11.
  • 1.1. Gains in the water content of the Fundulus heteroclitus follicle account for over 90% of the total wet weight increase, and consequentially most of the size increase, associated with meiotic maturation.
  • 2.2. Increases in intracellular Na+ and K+ actually exceed the accompanying increases in oocyte water, resulting in net gains in the concentration of these solutes. Changes in oocyte osmolality during maturation are mostly closely paralleled by variations in the concentration of K+.
  • 3.3. Concentrations of various free amino acids, including taurine, remain constant or decline during maturation.
  • 4.4. Taken together, these results suggest that an influx of K+, followed by osmotically-obliged water, is a primary cause of water uptake during oocyte maturation in F. heteroclitus.
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12.
  • 1.1. Changes in urine and plasma concentrations (sodium, potassium, magnesium, calcium and total osmotic) and urine production were determined in fish exposed to various concentrations of an ionically active substance, sodium chloride, and a non-electrolyte, mannitol, as well as freshwater.
  • 2.2. Responses occurred for the most part over a short crisis period preceeding establishment of new stable conditions.
  • 3.3. It was shown that plasma homeostasis was not maintained in response to changing ion-osmotic and osmotic gradients.
  • 4.4. Urinary osmotic and ionic concentrations were unaffected and urine production was shown to be inversely related to the external concentration.
  • 5.5. It is suggested that ionic shifts between body compartments are an important aspect of ion-osmotic adaptation.
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13.
  • 1.1. Developing eggs of whitefish (Coregonus lavaretus L.) and vendace (Coregonus albula L.) were kept at 1–2°C and some eggs taken gradually up to 8°C to provoke mass hatching of embryos.
  • 2.2. Wet weight, dry matter and the contents of lipid, protein and ash were measured in fish during the course of experiment.
  • 3.3. Dry matter content decreased gradually in whitefish eggs from 15.64 to 11.95% during 1 month at 1–2°C, whereas vendace eggs showed only a slight decrease from 16.27 to 15.53%.
  • 4.4. In both species protein content decreased but lipid increased when approaching the natural time of hatching.
  • 5.5. During delayed hatching at low water temperatures protein contributes to catabolism, whereas lipid content decreased only in the later phase of the experiment.
  • 6.6. Larvae starved for 10 days after hatching lost increasing amounts of dry matter (from 26.1 to 50.3% of body weight) and protein (from 18.7 to 45.9% of body weight) as they remained longer in cold water as embryos.
  • 7.7. A correspondence was found between assessment of metabolic utilization of body stores based on chemical analysis of fish body and previous work on oxygen consumption and nitrogen excretion.
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14.
  • 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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15.
  • 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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16.
  • 1.1. Behavioural observations and haemolymphatic measurements of Na+ K+ and Ca+ were performed in Chasmagnalhus granulata during emersion.
  • 2.2. Activity levels were found to be higher during voluntary emersion periods than when the animals were submerged. A lt50 of 39.45 hr was observed when no access to water was allowed.
  • 3.3. The Na+ and K+ and Ca+ levels increased during aerial exposure. The Na+ and K+ levels were restored prior the end of the experimental period. Mechanisms for such regulation are therefore discussed. The Ca2+ levels, remaining high during emersion, are probably a result of acid-base balance adjustments.
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17.
  • 1.1. Gilthead sea breams (Sparus aurata L.) adapted to sea water (SW, 39‰ salinity) and brackish water (BW, 7‰) were submitted to abrupt osmotic stress by transferring the specimens to 7‰ and 39‰, respectively.
  • 2.2. Plasma osmolality, Na,+ Cl, K, + Ca, 2+ cortisol and glucose were measured before and after the transfers.
  • 3.3. The transfer from SW to BW led to transitory hypomineralization and hyperglycemia. In long-term adapted fish cortisol level increased, and osmolality slightly decreased.
  • 4.4. Conversely, the transfer from BW to SW provoked transitory hypermineralization. In adapted fish, cortisol levels strongly decreased, and osmolality slightly increased.
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18.
  • 1.1. Chelodina rugosa dug from aestivation sites at the end of the dry season were immediately alert and well coordinated.
  • 2.2. Compared with non-aestivating animals, aestivating turtles had 20% higher plasma osmotic pressure and 7% higher sodium. Coupled with a small, but significant weight gain upon return to the water, this suggested the occurrence of minor dehydration in aestivating animals.
  • 3.3. Plasma lactate levels of aestivating animals were low, averaging 1.99 mmol/l, consistent with aerobic rather than anaerobic metabolism having sustained their long period under ground.
  • 4.4. No evidence was seen of dramatic physiological specialization. Aestivation in this species is interpreted as a primarily behavioural adaptation, made possible by typically reptilian abilities to tolerate a wide range in plasma electrolytes and to survive long periods without feeding.
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19.
  • 1.1. Rainbow trout maintained in fresh water or Actapted to sea-water for 24 hr were fed casein-based dry diet. After feeding, fish were kept in fresh water (FW) or transferred to artificial sea-water (SW) and sacrificed after 10 or 20 hr.
  • 2.2. The digestive tract was separated into five parts: stomach, pyloric caeca region, middle intestine and two equal lengths of rectum.
  • 3.3. The content of these parts was analysed for ions Na+, K+, Cl, Mg2+ and for free, peptide and total amino acids.
  • 4.4. In the fish stomach all ions, with the exception of Ca2+, indicate drinking of sea-water. In the pyloric caeca region Na+ appears to be efficiently absorbed in SW fish but influxed in FW fish. In the rectum of SW fish K+ appears to be reabsorbed but Na+ concentrated in faeces.
  • 5.5. Free amino acid concentrations were always higher in gut lumen of SW than in FW fish in respect to time after feeding and portion of intestinal content. Free amino acids constitute at most 7.4–8.7% of total amino acids in the content of pyloric caeca region.
  • 6.6. Peptide amino acids, being mostly di-, tri- and tetra-peptides, increased in stomach content from 14.7 to 28.4% of the total, from 6 to 10 hr after a meal in SW fish. Peptide amino acids constituted 80.3–89.0% of total amino acids in intestinal content of the pyloric caeca region. These peptide portions decreased in the mid-intestine (47.5–52.5%) and increased again in the rectum (73.6–76.0%).
  • 7.7. It was concluded that in rainbow trout fed in both sea- or fresh water, ion concentrations do not seem to interfere with protein digestion and nutrient absorption in alimentary tract.
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20.
  • 1.1. Brook trout (Salvelinus fontinalis) of a single genetic stock, and hatched at the same time, were raised under two photoperiod and two feeding regimes to obtain fish of the same age but with different sizes and photoperiod experiences. In 11 experiments over 1.5 firs, fish were gradually exposed to 32 ppt seawater for 20 days to investigate the ontogeny of salinity tolerance.
  • 2.2. Daily changes in plasma osmolarity, [Na+], [Cl], [K+], [Mg2+], thyroxine, hematocrit and gill Na+,K+-ATPase during adaptation to 10, 20 and 32 ppt were examined in one experiment.
  • 3.3. Size was the primary determinant of seawater survival (r2 = 0.77) the effect of size on seawater survival slowed after fish reached a fork length of 14 cm. The effect of age on seawater survival (r2 = 0.65) was through its covariance with size.
  • 4.4. Photoperiod affected seawater survival only through its influence on the timing of male maturation, which decreased salinity tolerance.
  • 5.5. Regulation of plasma osmolarity, [Na+], [Cl], [K2+], [Mg2+] and hematocrit in sea water increased linearly with size over the entire range of sizes (6–32 em).
  • 6.6. Gill Na+,K+-ATPase activity after 20 days in seawater decreased with increasing size of brook trout, possibly reflecting decreased demand for active ion transport in larger fish.
  • 7.7. Plasma thyroxine concentrations declined in seawater, but no definitive role of this hormone in seawater adaptation was found.
  • 8.8. Size dependent survival and osmoregulatory ability of brook trout is compared to other salmonids and a conceptual model is developed.
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