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1.
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  1. 1.The Root effect was measured in hemolysates from representatives of 56 genera of Amazonianfishes.
  2. 2.Hemolysates from several species of air-breathing fishes were found to have Root effects, contraryto published hypotheses.
  3. 3.Hemolysates from Potamotrygon, a freshwater ray, exhibit a Root effect under our experimental conditions.
  4. 4.The pattern of Root effect distribution correlates positively with the distribution of choroid retiamirabile and swimbladders, but not with the distribution of swimbladder retia mirabile; it is proposed that the former is the more primitive structure which is associated with the origin of Root effect hemoglobins
  5. 5.Some of the fish hemoglobins differ spectrally from one another. The positions of the absorptionmaxima of the deoxyhemoglobins range from 553 nm (Lepidosiren paradoxa and Potamotrygon sp.) to 560 nm (Plagioscion)
  6. 6.Occurrence of Root effects is not correlated with the complexity of the hemoglobin electrophoreticpattern, although several species are found to have multiple hemoglobin systems in which the Root effect is restricted to certain components.
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2.
  • 1.1. The Root effect was evaluated in hemolysates from 26 species of bony fish and 20 species of cartilaginous fish found on the Brazilian southeastern coast.
  • 2.2. Teleost Root shifts, with a single exception, are correlated with the presence of the choroid rete mirabile but not with its counterpart in the swimbladder.
  • 3.3. Five ray species displayed weak and moderate Root effects despite the absence of choroid and swimbladder rete.
  • 4.4. The presence and intensity of the Root effect is probably primarily related to the high oxygen demand of the retina and with the importance of visual perception in fish.
  • 5.5. In marine teleosts the magnitude of the Root effect seems to be associated with the presence and size of both the choroid rete and the pseudobranch.
  • 6.6. An antioxidant protection of the fish eyes can be advocated for the pseudobranch.
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3.
  • 1.1. To date, only a few authors have assayed the agglutinic activity of marine algae against fish erythrocytes, and in these cases, mainly against freshwater fish.
  • 2.2. For the first time, the hemagglutinic activity of 70 seaweeds (29 brown, 37 red and four green algae) against erythrocytes of 16 seaflsh species is reported.
  • 3.3. The presence of agglutinins was demonstrated in 100% of algae assayed, against at least one of the different types of erythrocytes tested.
  • 4.4. The results obtained confirm the presence of receptors for algae agglutinins on the surface of the erythrocytes of the fish studied.
  • 5.5. This could be useful in establishing the origins of fish populations, as these serological differences could distinguish between populations of cultivated and wild fish.
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4.
  • 1.1. Size and composition of sagittal otoliths from red drum, Sciaenops ocellatus (Sciaenidae), reared at various constant temperatures were compared with otoliths from wild-caught fish.
  • 2.2. Uncoupling of otolith growth and somatic growth in laboratory-reared fish was evident in otolith length, area, volume, weight, density, and organic fraction.
  • 3.3. Fish grown at low temperatures had significantly smaller and less dense otoliths having a greater organic content than fish of the same size grown at higher temperatures.
  • 4.4. Changes in inorganic elements were poorly related to temperature in laboratory-reared fish.
  • 5.5. The effect of temperature on otolith elemental composition was small relative to the effects of age and its associated physiological changes.
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5.
  • 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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6.
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Highlights
  • •Quantitative proteomes and epigenetic regulation of T. gondii.
  • •Protein crotonylation and 2-hydroxyisobutylation in phenotypically different T. gondii parasites.
  • •Regulation of invasion regulation of T. gondii by protein modification.
  • •Lysine crotonylation and 2-hydroxyisobutylation regulated in multiple biological processes in phenotypically different T. gondii parasites.
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7.
  • 1.1. Eggs of wild cod, and of farmed cod fed (a) a diet supplemented with astaxanthin and (b) a diet supplemented with both astaxanthin and canthaxanthin, were analysed with respect to carotenoids.
  • 2.2. The total carotenoid contents in eggs were 0.7 ppm for wild cod and 0.5 ppm for farmed cod.
  • 3.3. Cod, having white flesh, deposit ketocarotenoids in the eggs, preferably astaxanthin.
  • 4.4. Canthaxanthin can replace astaxanthin in the eggs, but astaxanthin appears to be deposited preferentially when both carotenoids are present in the diet.
  • 5.5. The isomer distribution of (3S, 3′S):(3R, 3′S, meso):(3R, 3′R) astaxanthin in the eggs reflected the isomer composition of the diet.
  • 6.6. Echinenone, 4′-hydroxyechinenone, adonixanthin and zeaxanthin encountered in cod eggs may represent reductive metabolites of canthaxanthin and astaxanthin.
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8.
  • 1.1. The carnitine-responsive mutant yeast, Candida pintolopesii ATCC 26014 and the wild type strain (ATCC 22987) were used to investigate the role of carnitine and the carnitine acetyltransferase system.
  • 2.2. [3H]l-Carnitine, supplied to the cells, was incorporated into acetylcamitine and [14C]pantothenate was incorporated into CoA and its derivatives.
  • 3.3. Both bioautography and quantitative assays indicated that the relative amounts of CoA and acetylCoA were very different in the mutant and wild type cells.
  • 4.4. The wild type yeast maintained an acetylCoA/CoA ratio of 0.33 ± 0.09 indicating that most of the CoA in the cell is in the free CoA form. Carnitine was not required to establish this ratio nor did its presence lower it further.
  • 5.5. In contrast, the mutant cells contained a high acetylCoA/CoA ratio (12.8 ± 3.0).
  • 6.6. In the mutant cells, carnitine lowered the ratio by decreasing the intracellular acetylCoA concentration and releasing free CoA.
  • 7.7. These data indicated that wild type yeast possess an effective mechanism that is not related to the CAT system for regulating the acetylCoA/CoA ratio.
  • 8.8. This mechanism appears to be lacking in the mutant. The CAT system decreased the acetylCoA/CoA ratio in the mutant cells but not to the value which is found in the wild type strain.
  • 9.9. In both stains of Candida pintolopesii, in the presence of carnitine, an acetylcamitine pool can be created whose concentration exceeds that of acetylCoA.
  • 10.10. The intracellular apparent equilibrium constant (Kapp) for carnitine acetyltransferase for wild type Candida pintolopesii ATCC 22987 was 0.73 ± 0.12, close to the established value of 0.6, indicating that the CAT system ran close to equilibrium.
  • 11.11. The Kapp for the CAT system of the carnitine-responsive mutant yeast was 7.7 ± 1.7 indicating that this reaction was not at equilibrium.
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9.
  • 1.1. Unlike common fishes and as its Latin name implies, the upside-down catfish, Synodontis nigriventris, possesses dark ventral skin. Microscopic observation reveals that melanophores are present on both the ventral and the dorsal skin but differ in size and density of distribution.
  • 2.2. The darkness of both sides of the fish changes in accordance with that of the background.
  • 3.3. At night, the fish are very active and the body becomes pale. The change in color is more noticeable in the dorsal than the ventral skin.
  • 4.4. When melatonin was added to the bathing water, the fish became pale and swam restlessly even when they were exposed to the black background.
  • 5.5. It was found that the catfish preferred the black background to the white one.
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10.
  • 1.1. The effect of regular handling on fear reactions was investigated in mallard (Anas platyrhynchos) by exposing six hand-reared and four wild ducks to an approaching human being and recording heart rates with an external ECG device.
  • 2.2. All ducks reacted to the approach with tachycardia, but the response was significantly less in tame birds.
  • 3.3. Hand-reared females showed less response than males. No sex-linked differences were apparent in the wild ducks.
  • 4.4. Decreasing responses throughout the experiments were only found in tame birds.
  • 5.5. Fear or stress reactions can apparently be diminished through habituation induced by regular handling.
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11.
  • 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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12.
  • 1.1. Seasonal acclimatization effects on oxygen consumption, body temperature, and body weight were evaluated in three different experimental groups of Dipodomys panamintinus.
  • 2.2. Body weights of wild field as well as captive animals housed in outdoor sand cages were maximum in winter and lowest in summer for both sexes.
  • 3.3. Mean oxygen consumption was maximum in winter and lowest during spring in both sexes of the wild field and captive exposed groups.
  • 4.4. Neither weight nor oxygen consumption of indoor control animals varied with the seasons.
  • 5.5. No significant differences in body temperatures were observed during either the fall or winter seasons.
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13.
  • 1.1. A comparative study of the proteolytic activity in four different sections of the digestive tracts of the European sea bass (Dicentrarchus labrax) and hybrid striped bass (Morone chrysops × M. saxatilis) reared in freshwater revealed minor differences between these fish.
  • 2.2. Tryptic activity plays a major role in the proteolytic process in both fish.
  • 3.3. The activity of seven intestinal proteolytic enzymes was detected utilizing a combination of specific substrates and inhibitors.
  • 4.4. High levels of proteolytic activity were detected in both the proximal and distal sections of the fish intestine at a high pH range (9–10).
  • 5.5. In situ monitoring of pH levels revealed a lower pH level in the intestinal proximal section of hybrid striped bass compared with the distal section.
  • 6.6. In contrast, higher pH levels were detected at the proximal compared with the distal sections of D. labrax intestine.
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14.
  • 1.1. A potentiometric method for the assay of cholinesterase has been proposed and compared with a colorimetric assay.
  • 2.2. Main kinetic parameters of cholinesterase from Hypostomus punctatus brain were determined indicating that true acetylcholinesterase is by far the predominant enzyme in the brain of this fish.
  • 3.3. We have compared our data with published results described from other fish species.
  • 4.4. The enzyme inhibition achieved after 3 hr incubation of brain homogenates with ethyl-parathion have indicated that this enzyme shows a characteristic organophosphorous sensitive behavior.
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15.
  • 1.1. Growth rates and body condition factors for native wild and captive-raised juvenile alligators (Alligator mississippiensis) that had been released to the wild were studied using tag-recapture methods for 274 alligators over a 4-year period. Alligators were grouped by sex, size class, source (farm-released vs native wild) and as to whether they had overwintered or not.
  • 2.2. In most groups, the farm-released alligators grew significantly better than wild alligators matched for sex and size; in the remaining groups the post-release alligators grew as well as their counterparts, though not better.
  • 3.3. Overwintering tended to slow growth rates in both groups, but farm-released alligators still demonstrated superior growth over native wild alligators even after overwintering.
  • 4.4. Males tended to grow faster than females, though this trend was not always significantly greater. In no matched group did females grow faster than males.
  • 5.5. Growth rates diminished with increasing size in native wild alligators (smaller alligators grew faster), but growth rates of farm-released alligators remained accelerated even at the larger size classes.
  • 6.6. Growth curves were constructed using known recapture data with three growth models (von Bertlanffy, Gompertz and logistic); the calculated maximum attainable length and growth parameters were significantly larger (P < 0.01) for farm-released alligators than wild using all three models.
  • 7.7. Body condition factors were not different in captive-raised post-released alligators than native wild alligators.
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16.
  • 1.1. External and internal examinations of otoliths in fishes for macrostructure and microstructure has demonstated yearly, daily and population rhythmic patterns.
  • 2.2. Chemical analyses (atomic absorption) of otolith carbonate from reared Fundulus heteroclitus for strontium-calcium concentration ratios demonstrated changes in chemistry related to temperature.
  • 3.3. Microprobe analyses made it feasible to interpret almost daily changes in temperature to provide the temperature history of an individual fish.
  • 4.4. A combination of microprobe analyses and daily increment analyses of otoliths can provide a life history profile for individual fish and can provide information on the environmental history of each fish.
  • 5.5. Such information is vital to our understanding of the processes underlying recruitment and growth rates, and would make it possible to link growth and mortality rates to environmental occurrences.
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17.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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18.
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Highlights
  • •Atlantic salmon O-glycome expanded to 169 structures in three epithelia.
  • •Low interindividual variation amongst all populations and geographical regions.
  • •Small variations in glycosylation between geographical locations and fish size.
  • •Prominent fucosylation in gastrointestinal mucins from Tasmanian fish.
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19.
  • 1.1. The effects of thermal acclimatization at 10 and 24°C on heart rate were investigated on unrestrained soles (Solea vulgaris).
  • 2.2. The sensitivity of heart rate to temperature changes induced by temperature acclimatization was higher in cold-acclimatized than in warm-acclimatized soles.
  • 3.3. Heart rate of cold-acclimatized fish to temperature changes was not affected by blocking the vagal tone with atropine.
  • 4.4. After atropine treatment the ability of heart rate to show thermal compensation decreased in warm-acclimatized soles.
  • 5.5. It is suggested that the vagus nerve can function differently at different temperatures.
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20.
  • 1.1. The transcellular movement of chloride was measured in the red blood cells of the fish Tilapia mossambica utilizing 36-chloride.
  • 2.2. Tilapia red cells possess an efficient anion carrier which is totally blocked by SITS.
  • 3.3. Although a factor in tilapia plasma inhibits the dehydration of extracellular bicarbonate by the red cells, it was without effect on the transcellular movement of chloride.
  • 4.4. It is concluded that the inability of fish whole blood to dehydrate extracellular bicarbonate is not explained by a general anion impermeability as was suggested by Haswell & Randall (1976).
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