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1.
  • 1.1. Fatty acid and lipid class composition were determined in larvae of four marine species: Atlantic halibut (Hippoglossus hippoglossus L.), plaice (Pleuronectes platessa), cod (Gadus morhua) and turbot (Scophthalmus maximus) at hatching and prior to first feeding.
  • 2.2. Total fatty acid content decreased in the four species with up to 50% reduction in one of the halibut groups. Docosahexanaoic acid (22:6 n-3) was especially utilized.
  • 3.3. Low lipid utilization was found in turbot in relation to the other three species.
  • 4.4. Water environmental temperature may explain some of the differences in the fatty acid utilization and the source of metabolic energy between cold water species (halibut, cod, and plaice) and temperate species (turbot), in the period from hatching to prior to first feeding.
  • 5.5. Relative amounts of neutral lipids and phospholipids were similar in plaice, cod and halibut, approximately 25% and 75% of total lipids, respectively, and were approximately constant during the yolk-sac stage. Neutral lipids were dominant for turbot at hatching, accounting for 53–55% of the total lipids, while phospholipids predominated prior to first feeding, being 56–59%.
  • 6.6. Phosphatidylcholine was catabolized in halibut, plaice and cod but not in turbot, while phosphatidylethanolamine tended to be synthesized in all four species.
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2.
  • 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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3.
  • 1.1. Two “en passant” electrodes were implanted around the cerebrobuecal connective (CBC) of Aplysia and used to record the activity, in the unrestrained animal, under three behavioural conditions; (a) absence of feeding behaviour, (b) appetitive feeding behaviour and (c) consummatory feeding behaviour.
  • 2.2. The two simultaneous recordings were subjected to cross-correlation analysis, to subdivide spikes on the basis of their direction and speed of propagation.
  • 3.3. There was virtually no CBC activity in the absence of food and feeding behaviour.
  • 4.4. During appetitive feeding the metacerebral giant cell (MCC) was active and traffic was heaviest in the cerebral-to-buccal direction.
  • 5.5. During consummatory feeding, traffic was also sustained in the buccal-to-cerebral direction; there was a reduction in the activity of the MCC, and a peak in the activity travelling to the cerebral ganglia, in the region of higher conduction velocity, was especially pronounced.
  • 6.6. Further analysis showed this peak to have its largest amplitude during the actual ingestion of food and to be the result of the firing of several different units.
  • 7.7. CBC traffic in both directions was also activated in one case of “spontaneous” biting.
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4.
  • 1.1. Blood, liver, heart, testis, skin, eye, muscle and kidney samples were obtained from elephants (Loxodonta africana) in the Kruger National Park during a culling programme in April 1992.
  • 2.2. Gene products of 25 protein coding loci in L. africana were examined by horizontal starch-gel electrophoresis.
  • 3.3. Eighteen protein coding loci (72%) displayed monomorphic gel banding patterns whereas only seven (28%) displayed polymorphic gel banding patterns.
  • 4.4. Average heterozygosity values for adults, youngsters and the total population are respectively 0.058, 0.024 and 0.047.
  • 5.5. Relative gene diversities within and between populations are 84% and 16% respectively.
  • 6.6. Two population simulation programmes were utilized to predict the duration of the current variability present in this species, based on current genetic variation and gene transfer from one generation to the next.
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5.
  • 1.1. The activities of three lysosomal enzymes (acid phosphatase, β-galactosidase, catepsin D) was observed during metamorphosis in the fat body and midgut cells of two insects (Mamestra brassicae and Pieris brassicae).
  • 2.2. The activities increased slightly during the feeding period and showed a sharp rise at the beginning of the wandering period.
  • 3.3. Subsequently, a decrease was observed during the pre-pupal stage and pupation.
  • 4.4. The activities increased again 2 days after the larval-pupal moult.
  • 5.5. We suggest that an inhibitory mechanism works in the studied cells before pupation to protect the stored proteins from the degradation until the beginning of differentiation of imaginai cells in the pupal stage.
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6.
  • 1.1. Changes in the hemoglobins present in many vertebrates have been observed during development and during anemic episodes.
  • 2.2. A change in the number of hemoglobins present and their relative amounts was observed when adult Triturus cristalus newts were made anemic by injection of acetylphenylhydrazine.
  • 3.3. Hemoglobin IV, which is a minor hemoglobin in healthy adults, was found to be a major component during the subsequent erythropoietic response to hemolytic anemia.
  • 4.4. No new hemoglobin not already present in the non-anemic state was detected during the response to induced anemia.
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7.
  • 1.1. Changes in the glycogen content, condition, stomach content and acetic acid concentration of mussels Mytilus edulis and cockles Cerastoderma edule were followed during periods of up to 14 days of exposure (to air) at temperatures of 5 and 20°C.
  • 2.2. In animals with a high glycogen content the glycogen is not used during the first 3 to 7 days, at high and low temperature respectively.
  • 3.3. After this latent period the glycogen concentration often decreased, coinciding with a high mortality and an increase of the concentration of acetic acid.
  • 4.4. In cockles with a low glycogen content, and kept at a high temperature, glycogen can be used from the beginning of the stress period.
  • 5.5. Between species no clear differences were found.
  • 6.6. The stomach content decreased during exposure; however, the stomach content amounted to only 0.5 to 0.7% of the body weight, and is thought to be of minor importance as an energy source during the stress period.
  • 7.7. Especially at the higher temperatures glycogen finally is transformed into acetic acid.
  • 8.8. It is concluded that during exposure, the animals do not die because of a lack of energy reserves, but because of a high accumulation of acids.
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8.
  • 1.1. The energy contributions of aerobic metabolism, phosphoarginine, ATP and octopine in the adductor muscles of P. magellanicus were examined during swimming and recovery.
  • 2.2. A linear relationship was observed between the size of the phosphoarginine pool and the number of valve snaps. A linear increase in arginine occurred during the same period.
  • 3.3. Octopine was formed during the first few hours of recovery, particularly in the phasic muscle.
  • 4.4. The restoration of the phosphoarginine pool appeared to be by aerobic metabolism.
  • 5.5. It is concluded that the role of octopine formation is to supply energy when the tissues are anoxic and to operate at such a rate as to maintain the basal rate of energy production.
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9.
  • 1.1. Chemical feeding stimulants for an herbivorous fish, Tilapia zillii have been determined by fractionation and bioassay of substances derived from a model food plant.
  • 2.2. Stimulation was produced by amino acids; glutamic acid, aspartic acid, serine, lysine and alanine produced the bulk of stimulatory activity.
  • 3.3. These amino acids are among the most abundant in the test plant, and are markedly different from the amino acids found to stimulate feeding in carnivorous fish.
  • 4.4. On the basis of these results, a chemically-mediated mechanism of feeding niche separation is postulated.
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10.
  • 1.1. Oxygen uptake attributable to Specific Dynamic Action (SDA) was measured in common carp, Cyprinus carpio L. (63.6–84.0 g) fed on 20, 35 and 50% dietary protein at 0.40 to 1.00% ration levels at 28°C.
  • 2.2. After feeding both SDA magnitude and mean peak oxygen consumption increased directly with dietary protein and ration levels. SDA duration was not significantly related to dietary protein but significantly increased with ration levels.
  • 3.3. SDA coefficients were 8.99, 13.51 and 15.94% with 20, 35 and 50% dietary protein showing a direction relationship to the protein content. The SDA coefficient did not change with ration size.
  • 4.4. SDA models resulting from this work are of great interest for the aquaculturist, as post-feeding oxygen requirements in an intensive fish culture can be predicted where dietary protein and ration levels are known.
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11.
  • 1.1. A significant diurnal rhythm of net sodium flux was demonstrated in the freshwater clam Corbicula fluminea entrained to either a 12L:12D or 24L photoperiod.
  • 2.2. Highest net flux occurred during the dark hours on 12L: 12D. The overall mean net flux over 24 hr was not significantly different from a steady state condition.
  • 3.3. Net flux values of clams on a 24L photoperiod were negative and significantly lower than the net flux on a 12L:12D photoperiod.
  • 4.4. The 12L: 12D net sodium flux rhythm pattern is similar to rhythmic patterns of other physiological processes in another freshwater clam.
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12.
  • 1.1. Crossbred Yorkshire (Yorkshire × Landrace) pigs were fed butter oil, cream, low erucic acid rapeseed oil, sunflower oil and partially hydrogenated sunflower oil in amounts representing 30% of energy for periods of up to 13 weeks.
  • 2.2. After 13 wk of feeding serum total cholesterol levels of pigs fed milk fat were significantly higher than of pigs fed vegetable oils.
  • 3.3. The difference in cholesterol was mainly due to an increase in the density range of 1.063–1.125 g/ml containing pig LDL2 and some HDL.
  • 4.4. A shift towards smaller LDL particle size was apparent in pigs fed milk fat.
  • 5.5. The effects of dietary trans fatty acids did not differ from cis polyunsaturated or monounsaturated fatty acids.
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13.
  • 1.1. The extent of anaerobic energy production of Arenicola marina during low tide is dependent on the season and on the locality in the intertidal.
  • 2.2. Anaerobic energy production was only found: (a) in animals from sediments, which fall dry for several hours; (b) in summer and autumn, but not in winter and spring.
  • 3.3. A correlation between the extent of anaerobic energy production and the development of gametes was demonstrated.
  • 4.4. The process of spawning represents a great stress to the animals. At this time the ability of Arenicola marina to survive anaerobic conditions was reduced drastically.
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14.
  • 1.1. Lipid, glucose and glycogen concentrations were measured in different tissues of the crab Chasmagnathus granulata during emersion.
  • 2.2. After 6 hr of emersion no reduction in the total amount of carbohydrates was found to occur, suggesting that a general metabolic arrest was taking place.
  • 3.3. A transitory increase in haemolymphatic glucose and lipid levels was observed. Possible causes are therefore discussed in relation to changes in the flux of substrates for energy production.
  • 4.4. The mobilization of carbohydrates and lipids to the gills, observed only during summer, may be concerned with energy supplying for ionic regulation.
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15.
16.
  • 1.1. The effect of sonication on reconstituted freeze-dried bovine and porcine blood was examined by analysis of particle size and by feeding to Glossina palpalis palpalis.
  • 2.2. Sonication reduced the particle size of both reconstituted blood products.
  • 3.3. Tsetse flies feeding on both sonicated blood products performed significantly better than flies feeding on non-sonicated blood products with respect to total pupae produced and fecundity, and for porcine blood, pupal weights were higher.
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17.
  • 1.1. The haematology of tame racing pigeons (Columba livia) and wild guinea-fowl (Numida meéagris) was investigated immediately after transportation to the laboratory and during subsequent acclimatization.
  • 2.2. Significant changes were observed in many of the parameters studied and both experimental groups showed similar variations.
  • 3.3. The results are discussed in relation to the factors which may be responsible for incorrect haematological values being obtained in birds.
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18.
  • 1.1. Seasonal variation in total lipids was examined in several body components of the turtle Sternotherus odoratus.
  • 2.2. Carcass fat stores in both sexes were depleted during winter. Additionally, a decline in carcass lipids was associated with increases in gonadal mass.
  • 3.3. Concentrations of liver lipids were maximal during August and minimal during winter.
  • 4.4. Males showed little seasonal change in plasma lipid levels, whereas females had seasonal peaks temporally associated with ovarian development and carcass fat storage.
  • 5.5. Ovarian concentrations of lipids were minimal after nesting and increased during fall.
  • 6.6. Results suggest that S. odoratus uses stored fats both for reproduction and maintenance during winter.
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19.
  • 1.1. Drosophila mettleri have been found feeding but not breeding on decaying stems of senita cactus, the normal host for Drosophila pachea.
  • 2.2. Alkaloids were extracted from senita stems and used in tests of egg-to-adult viability, developmental rate, and adult longevity.
  • 3.3. The results show that developmental rate is not appreciably affected by senita alkaloids.
  • 4.4. In general, D. mettleri was less affected by the alkaloids with respect to egg-to-adult viability and adult longevity than D. pachea at concentrations which are fatal to other desert Drosophila.
  • 5.5. Tolerance to alkaloids gives D. mettleri an ecological advantage.
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20.
  • 1.1. A single neuron is found in each buccal ganglion of the giant garden slug, Limax maximus, which is autoactive and has an axon in both the ipsilateral and contralateral salivary nerve.
  • 2.2. This neuron, the bilateral salivary neuron (BSN), is a slow bursting neuron and is presynaptic to some of the secretory acinar cells of the salivary gland.
  • 3.3. Increases in BSN action potential frequency and saliva flow during the generation of feeding motor program are shown, as is the relationship of BSN activity to that of other salivary neurons.
  • 4.4. BSN is affected synaptically by the serotonergic metacerebral giant cell.
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