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1.
  • 1.1. The characteristics of both, motor and electroretinographic circadian rhythms in the crayfish Procambarus bouvieri, were examined.
  • 2.2. The correlation between both rhythms in intact and brainless crayfish, was obtained.
  • 3.3. The presence of at least two different but coupled oscillators responsible for the circadian variations in crayfish, is proposed.
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2.
  • 1.1. In order to investigate the function of the dorsal tricorn-type sensilla on Ligia exotica, the morphology and distribution of the setae and neural responses to certain stimulus modalities were studied.
  • 2.2. These foraminate sensilla are found to occur over the body surface, except for several appendages and the ventral carapace (sternite); the dorsal carapace (tergite) is covered by only this type of sensilla.
  • 3.3. The tricorn-type sensilla located on the dorsal carapace responded to mechanical, gustatory and olfactory stimulation.
  • 4.4. The function of the tricorn-type sensilla on the dorsal carapace was discussed.
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3.
  • 1.1. The critical thermal minima (CTMin) and maxima (CTMax) were determined for field-acclimatized and laboratory-acclimated crayfish (Orconectes rusticus) throughout 1984.
  • 2.2. The CTMin and CTMax of field-acclimatized crayfish were seasonally adjusted by 9.7 C and 14.7 C respectively.
  • 3.3. Seasonal variation in both tolerance regimes persisted in crayfish acclimated in the laboratory at 5 and 25°C for one week; however, no diel variation existed in either the CTMin or CTMax of laboratory-acclimated crayfish.
  • 4.4. Integration of thermal acclimation of the CTMin and CTMax with seasonal conditioning may influence the functional capacities of this species when considered in relation to the seasonal ranges in stream temperature.
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4.
  • 1.1. A blue carotenoprotein (λmax = 634 nm) containing astaxanthin as prosthetic group, was extracted and purified from the carapace of the crayfish Astacus leptodactylus.
  • 2.2. The blue carotenoprotein contained (3S,3′S)-astaxanthin, (3R,3′S, meso)-astaxanthin and (3R,3′R)-astaxanthin in relative ratio 38:41:21.
  • 3.3. The blue carotenoprotein had an approximate mol. wt of 440,000 (gel filtration) and 437,000 (gradient gel electrophoresis).
  • 4.4. Sodium dodecyl sulphate polyacrylamide gel electrophoresis indicated the presence of two polypeptides of 19,600 and 18,600 daltons, with different mobility in polyacrylamide gel electrophoresis in the presence of 6 M urea.
  • 5.5. At low ionic strength and in the presence of denaturing agents such as SDS, urea, extreme pH and heat, the blue complex showed a greater stability than most of the carotenoproteins studied to date.
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5.
  • 1.1. Mitochondrial malic enzyme (l-Malate: NADP oxidoreductase (oxaloacetate decarboxylating) EC 1.1.1.40) has been isolated from abdomen muscle of crayfish Orconectes limosus by chromatography on Sepharose 6B and DEAE cellulose. Specific activity of the purified enzyme was about 5 μmols per min per mg protein, which corresponds to about 30-fold purification.
  • 2.2. This enzyme showed extremely small reversiblity, since the reaction in the direction of decarboxylation is at least 37, 190 and 760 times that for the carboxylation at pH 7.0, 7.5 and 8.0 respectively.
  • 3.3. Purified enzyme showed allosteric properties, which was more accentuated at more alkaline pH (Hill coefficients were 1.1, 1.7 and 1.8 at pH 7.0, 7.5 and 8.0 respectively). The activity of malic enzyme was increased considerably in the presence of succinate and fumarate.
  • 4.4. Mitochondira isolated from abdomen muscle of Orconectes limosus incubated in the presence of malate, fumate and succinate catalysed pyruvate production which was stimulated by ADP and inhibited by respiratory chain inhibitors.
  • 5.5. NADH but not NADPH oxidation was catalysed by broken mitochondria or sonic particles. When NADPH and NAD were added simultaneously the rate of oxidation. This suggests the presence of active NADPH:NAD transhydrogenase in mitochondria isolated from the crayfish abdomen muscle.
  • 6.6. A possible metabolic role for NADP-linked malic enzyme/transhydrogenase couple in abdomen muscle of crayfish Orconectes limosus is proposed.
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6.
  • 1.1. A bioassay for octopus saliva, based on detachment of crab dactylopodite flexor muscle under standard conditions, has been developed.
  • 2.2. There is a direct relationship between increasing caseinolytic activity of saliva from Eledone cirrhosa and decreasing muscle detachment time.
  • 3.3. Fractionation of saliva, using preparative isoelectric focusing, shows that muscle releasing activity is restricted to fractions containing proteins with high isoelectric points and maximum caseinase activity.
  • 4.4. It is concluded that proteolytic enzyme(s) in octopus saliva selectively release crab muscle from attachment to the carapace.
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7.
  • 1.1. Six of eight life-history traits related to growth and reproduction were significantly affected by temperature-photoperiod regimes.
  • 2.2. A temperature-photoperiod interaction was the most significant factor affecting life-history traits.
  • 3.3. Temperature probably significantly affected length of life, age at first brood, mean carapace length at first brood, length of time between broods, and number of young per day of adult life independent of the temperature-photoperiod interactions.
  • 4.4. Photoperiod probably did not significantly affect any of the life-history traits independent of the temperature-photoperiod interactions.
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8.
  • 1.1.|The high-energy phosphorylation metabolism in crayfish, Procambarus clarkii eggs during brooding and juvenile crayfish after hatching was studied by in vivo31P nuclear magnetic resonance (31P NMR) spectroscopy.
  • 2.2.|Inorganic phosphoric acid (Pi) and adenosine-5′-triphosphate ATP(γ-,α-,β-) were detected in the dark brownish red eggs after oviposition.
  • 3.3.|In orange unhatched eggs, only sugar phosphate (SP), Pi and resolved phosphometabolite from ATP were observed.
  • 4.4.|Peaks of SP, Pi, arginine phosphate (Arg-P), and ATP (γ,α,β) appeared in larvae of crayfish after hatching (nauplius, zoea and juvenile crayfish).
  • 5.5.|The high-energy phosphorylation metabolism changed to an anaerobic condition along with a decrease in the concentration of dissolved oxygen in fresh water.
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9.
  • 1.1. The objective of the present work was to study the ontogeny of the ERG circadian rhythm in crayfish.
  • 2.2. Long-term recordings of ERG and shielding retinal pigments position measured from the instar, the second instar, the third instar and the adult crayfish were obtained.
  • 3.3. In the youngest animals (1–8 days old) an ultradian rhythm (15min-4hr periods) in the ERG amplitude was detected.
  • 4.4. Older animals showed a progressive increment in the period length before they exhibited a circadian pattern. This last appeared, the first time, in 30-day-old animals and showed noticeable differences in the adult crayfish. At the same time, the crayfish began to show photomotor reflex. Later on (140-day-old crayfish) the circadian rhythm attained its final parameters.
  • 5.5. The SD was used as a measure of lability in periods. The 4 hr ultradian rhythm and the 22.4 hr circadian rhythm showed the lowest SD indicating that they are the most precise period values.
  • 6.6. Our results support the idea that the ERG circadian rhythm results from the coupling among high frequency (ultradian) oscillators, particularly those of 4 hr periods and that the coupling depends on the action of neurosecretions released from the sinus gland.
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10.
  • 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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11.
  • 1.1. Membrane modifications and junctional structures involved in neuron-glia exchange in crustaceans are reviewed, including some new observations on the crayfish Procambarus clarkii.
  • 2.2. Neuron cell bodies and associated glia interact through trans-glial channels, modified neuronal endocytosis and gap-like junctions.
  • 3.3. Tubular lattices, trans-glial channels, endocytosis and capitate projections give support to axo-glial relationships.
  • 4.4. Unidentified neuron-glia membrane appositions have been also found in neuropile.
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12.
  • 1.1. In vitro yolk synthesis was measured in fragments of the ovary of developing shrimp, Penaeus vannamei.
  • 2.2. Progesterone and estradiol stimulated yolk synthesis in vitro, while ecdysterone, testosterone and estrogen had no effect.
  • 3.3. A peptide factor from the eyestalks of crayfish stimulated yolk synthesis in vitro. A peptide factor from shrimp eyestalks inhibited yolk synthesis in vitro.
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13.
  • 1.1. Muscle proteins from the chelae of six crayfish species and ten species of Uca were compared through disc electrophoresis (split gel technique).
  • 2.2. No intraspecies variation of the electrophoretic pattern was found.
  • 3.3. In interspecies comparisons all components (bands) were weighted individually and specified as ancestral or derived characters.
  • 4.4. In the crayfishes the phylogenetic trees constructed from electrophoretic and classical data were found to be congruent. In Uca some branches of either tree remained undefined. Each tree, however, helped complete the other one.
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14.
  • 1.1. The locust vitellogenin (VTG) receptor which is embedded in oocyte plasma membranes is a glycoprotein.
  • 2.2. With various lectins oligosaccharide units have been identified, among them neuraminic acid linked to Gal or GalNAc, mannose chains, Gal linked to GalNAc or GlcNAc and fucose linked to GlcNAc.
  • 3.3. With specific enzymes it could be shown that mannose and most other oligosaccharides are O-linked while others like fucose are N-linked.
  • 4.4. Enzymatic removal of all O-linked carbohydrates resulted in a drop of the molecular mass of the receptor protein from 200,000 to 110,000.
  • 5.5. A total of N- and O-linked oligosaccharides of 54% was calculated.
  • 6.6. The isoelectric point of the receptor was found to be at pH 3.4 increasing slightly after removal of neuraminic acid.
  • 7.7. Removal of neuraminic acids destroyed the binding ability for VTG.
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15.
  • 1.1. Some aspects of the gas exchange system of a diving lizard, Physignathus lesuewii were studied.
  • 2.2. Breathing patterns were analysed.
  • 3.3. Breathing rate increases logarithmically with temperature and Q10 = 1.8. LogBR = −0.237 + 0.0256 T.
  • 4.4. Gas tensions in lung air and arterial and venous blood were measured. Arterial pH declines with increasing temperature.
  • 5.5. Temperature has a marked effect on oxygen affinity of the blood (ΔH = −10.1 kcal mol). A Bohr effect was also noted.
  • 6.6. CO2 equilibrium curves were drawn.
  • 7.7. The results are considered with a view to anticipating the efficiency of the gas exchange system of this species under conditions of variable temperature and during diving.
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16.
  • 1.1. The pathway and distribution of motor neurons in the uropod muscles of the crayfish, Procambarus clarkii, was investigated electrophysiologically and histologically.
  • 2.2. There were three crossing points of motor neurons between the peripheral motor bundle originating from the second and third roots of the sixth abdominal ganglion.
  • 3.3. It seems that there are no anatomical and functional regularity in the innervation pattern of the uropod muscles.
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17.
18.
  • 1.1. The fiber types of uropod muscles of the crayfish, Procambarus clarkii, were determined by the myofibrillar ATP-ase histochemistry and electrophysiology.
  • 2.2. The ATP-ase histochemistry was carried out on the sections of the whole tailfan and the slow muscles were identified as being of the slow type on the basis of their low staining intensities.
  • 3.3. The location of slow bundles in the mixed type muscles i.e. the dorsal rotator (DRT), the ventral rotator (VRT), and the telson-uropodalis posterior (TUP) was confirmed.
  • 4.4. TUP was newly revealed in this study to be a mixed muscle.
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19.
  • 1.1. Total chromophore contents as well as the contributions made by 11-cis retinal were determined by high pressure liquid chromatography in light- and dark-adapted eyes of Orchomene plebs and Glyptonotus antarcticus (Amphipoda and Isopoda, respectively).
  • 2.2. In O. plebs the highest amount of total chromophore in pmol/eye was found to be 18.5 in 36 hr dark-adapted animals. The lowest amount (11.6 pmol/eye) was recorded in 24 hr light-adapted individuals.
  • 3.3. In dark-adapted O. plebs, irrespective of whether dark-adapted for 36 or 60 hr, the percentage of 11-cis retinal was maximally 96.6%. In the light-adapted material it reached 71.2%
  • 4.4. In eyes of 20 hr dark-adapted Glyptonotous antarcticus, possibly because of insufficient dark adaptation, a total chromophore content of only 3.2 pmol/eye was found. The percentage of 11-cis retinal was 55.8.
  • 5.5. Porphyropsin with its testable 3-dehydroretinal (vitamin A2-aldehyde) was not encountered in any of our samples.
  • 6.6. Calculations of photopigment per gram body weight and a comparison with data from freshwater crayfish show that dark-adapted O. plebs possess approximately 20 times the relative photopigment amount of the crayfish. Absolute sensitivity of the eye of O. plebs is, therefore, expected to be very high.
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20.
  • 1.1. Eight ornate box turtles, Terrapene ornata, were heated and cooled in water at 35 and 15°C respectively.
  • 2.2. Thermal time constants were calculated and no significant differences were found (t-test; 0.05 level) between warming and cooling rates.
  • 3.3. Heart-rate data indicated slightly higher, but non-significant, mean values during warming.
  • 4.4. It was concluded that T. ornata is not able to physiologically alter rates of heat exchange in water significantly and must rely on behavioral mechanisms to maintain body temperature.
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