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1.
  • 1.1. The behavioural responses of the freshwater snail Biomphalaria glabrata to chemical gradients of sugars were investigated by means of diffusion olfactometers.
  • 2.2. The snails proved very discriminating in their responses. Thus, only nine (39.1%) of the 23 sugars tested proved to be statistically significant attractants or arrestants. None proved to be statistically significant repellents.
  • 3.3. Of all the sugars tested maltose proved to be the most potent attractant or arrestant. The lower threshold of response to this sugar lies between 5 × 10−6 and 5 × 10−7M.
  • 4.4. The results are compared with those obtained for amino and carboxylic acids and their ecological relevance is discussed.
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2.
  • 1.1.The behavioural responses of two species of freshwater pulmonate snails Bulinus (P.) globosus and Bulinus rohlfsi] to sugar gradients were investigated by means of diffusion olfactometers.
  • 2.2.Both snail species proved to be very discriminating in their responses. Of the 17 sugars tested, 35.3%, namely d(−)glucuronic, maltotriose, maltose, cellobiose, d(−)arabinose, d(+)mannose proved to be statistically significant attractants or arrestants to B. rohlfsi. Only 23.5% of these sugars (maltotriose, maltose), d(+) mannose and d(+) xylose were significant attraetants or arrestants to B. (P.) globosus.
  • 3.3.Glucuronic acid was a significant repellent to B. rohlfsi but none of the sugars was a repellent to B. (P.) globosus.
  • 4.4.The results are compared with those obtained for other snail species and their relevance to the ecology and control of the snails are discussed.
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3.
  • 1.1. The rates at which the pulmonate snail B. glabrata takes up soluble glucose and maltose from a defined medium were evaluated by measuring the buccal mass pulsation rate, the drinking rate, net changes in the concentrations of sugars in the medium and the rate of accumulation of 14C labelled maltose.
  • 2.2. It was demonstrated that B. glabrata was capable of net accumulation of maltose and glucose via the mouth and integument, respectively.
  • 3.3. Some of the maltose in the medium was also hydrolysed to glucose by exogenous snail enzymes.
  • 4.4. The mechanisms involved in the accumulation of the sugars and the relevance of the results to the biochemical ecology of the snails and other aquatic invertebrates are discussed.
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4.
  • 1.1. Myo-inositol is transported in chicken small intestine by a mediated route with an apparent Km of 0.1 mM and by a diffusion mechanism.
  • 2.2. The mediated route is susceptible to inhibition by sugars, though sugars are not transported by this process, nor is myo-inositol transported by the sugar transport system.
  • 3.3. Myo-inositol influx is inhibitable by phlorizin, sulfhydryl reagents, removal of Na+ from the incubation medium, and preloaded sugar; it can be stimulated by theophylline.
  • 4.4. The ability to absorb this nutrient varies greatly between individual animals.
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5.
  • 1.1. A high percentage (53%) of isolated snails injected with prostate gland homogenates lay eggs.
  • 2.2. These egg masses consist of a few eggs which contain many nonviable oocytes.
  • 3.3. Preliminary experiments suggest that an egg-laying factor may be present in prostatic secretions.
  • 4.4. Snails bred in isolation from hatching, whether injected or not, occasionally lay viable eggs.
  • 5.5. This observation shows that self-fertilization or parthenogenesis is, in fact, possible in Helix aspersa Müller.
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6.
  • 1.1. The locomotor-inducting factor of the giant African snail, Achatina fulica, was examined.
  • 2.2. Snails showed nocturnal circadian behavior in relative humidity at least over 50%. Although the rhythmicity was independent of light and darkness, it was disturbed easily by hydration, and hydrated snails continued to locomote throughout the day. For induction of locomotor behavior, relative humidity over 50% was the fundamental factor and water is shown to be the limiting factor for the endogeneous circadian oscillator.
  • 3.3. The integument of snails showed a higher water permeability. Through the integument, hemolymph osmolality changed easily according to hydration and dehydration from about 120 to 400 mOsm/kg H2O. Circadian behavior was induced in snails in which hemolymph osmolality ranged from about 130 to 230 mOsm/kg H2O.
  • 4.4. By hydration, hemolymph osmolality in quiescent and estivated snails which have higher osmolality decreased gradually and then they began to locomote according to the degree of dilution, and vice versa. The induction of behavior in these snails was controlled by low hemolymph osmolality.
  • 5.5. Together with the endogeneous rhythmicity, water environment was shown to be the key factor for the induction of locomotor behavior.
  • 6.6. Based on these results, the mechanisms of the induction of locomotor behavior in terrestrial pulmonates are proposed.
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7.
  • 1.1. Final urine is intermittently released from the pneumostome of the pulmonate freshwater snail Lymnaea slagnalis. A technique is described to sample this fluid.
  • 2.2. The ionic composition of final urine greatly differs from that of haemolymph; Na+ and Cl are reabsorbed to a considerable degree. In lettuce fed snails K+ is excreted.
  • 3.3. The urine Na+ and Cl concentrations are about 38 and 31 mM lower, respectively, than the haemolymph concentrations, also when the latter concentrations vary.
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8.
  • 1.1. Kinetic aspects of the enzyme UDP-galactose 4-epimerase in crude homogenates of the albumen gland of the snail Lymnae stagnalis were estimated. The mean values of the Km for UDP-galactose and for NAD are 0.343 and 0.097 mM, respectively. The enzyme is inhibited by NADH. It is inactivated by freezing and raised temperature (25°C), but it can be reactivated by NAD.
  • 2.2. In the albumen gland the epimerase activity is 10–100 times higher than in other tissues, reflecting the high turnover of glucose to galactose, essential for the synthesis of galactogen in this organ.
  • 3.3. In fed snails long day conditions stimulates albumen gland epimerase activity, coinciding with high egg production.
  • 4.4. In starved snails a fairly high residual activity of the enzyme is maintained, irrespective of photoperiod or egg production.
  • 5.5. Trematode infection leads to a considerable reduction of the epimerase activity.
  • 6.6. The results indicate that the epimerase activity in fed snails, when the gland shows a regular release, reflects long-term adaptations (photoperiod). In starved and parasitized snails, when no regular release or product occurs, a basic epimerase activity is maintained. This might be important for a rapid restoration of egg production after the termination of adverse conditions.
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9.
  • 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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10.
  • 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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11.
  • 1.1. The ECG of aquatic Amhystoma tigrinum from the Colorado Rocky Mountains was recorded while the animals submerged and emerged in water. Older larvae and metamorphosed adults were compared.
  • 2.2. Free-swimming animals of both types showed slight emergence tachycardia when taking a “gulp” of air.
  • 3.3. Preventing access to air for 30 min or more resulted in a slight bradycardia in larvae. Some adults responded with increased, others with decreased, heart rate depending on their level of excitement.
  • 4.4. Restraining the animals before forced submergence caused a greater bradycardia than when unrestrained.
  • 5.5. Low dissolved oxygen accentuated the cardiac responses of larvae to submergence but not in adults.
  • 6.6. Atropine only partially blocked the diving responses of both forms.
  • 7.7. The degree of submergence bradycardia seems to be a function of the ability to extract oxygen from water. It probably is not an adaptation to diving in these forms. Instead the submerged heart rate in these predominantly aquatic salamanders may be the “normal” rate with emergence tachycardias for breaths of air.
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12.
  • 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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13.
  • 1.1. Sulphated and etherified sterols were isolated from the far eastern holothurian Stichopus japonicus S. The sterol composition of both fractions was determined using gas-liquid chromatography and mass-spectroscopic methods. The structures of individual sterols were proved on the basis of mass-spectrometry and 1H-NMR-spectroscopy data.
  • 2.2. The structures of 29 sterols were established.
  • 3.3. Sterols (22E, 24R)-23,24-dimethyl-5α-cholest-22-en-3β-ol, 23,24-dimethyl-cholesta-5,22-dien-3β-ol, 24-methyl-cholesta-5,24(28)-dien-3β-ol, (24Z)-24-ethyl-cholesta-5,24(28)-dien-3β-ol, 24-nor-cholesta-5,22-dien-3β-ol, 24-ethyl-cholesta-5,25-dien-3β-ol were described for holothurians for the first time.
  • 4.4. Δ5-sterols were shown to be the main components of the sulphated alcohol fractions (67.61%), while the saturated and Δ7-sterols were there in less quantities (14.72 and 9.52%, respectively).
  • 5.5. The etherified sterols were represented, mainly, by saturated and Δ7-sterols (37.82% and 33.95%, respectively). Δ5-sterols were 19%.
  • 6.6. The sensitivity of liposomal membranes, containing steroid metabolites of the holothurian St. japonicus (Δ7-, sulphated and glycosilated sterols) to the action of endotoxin-stichoposide A, was studied.
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14.
  • 1.1. The addition of cAMP to stimulating solutions of NaCl, fructose (furanose sugar), sucrose, or glucose (pyranose sugars) decreases the responsiveness of labellar chemosensilla in Phormia.
  • 2.2. The addition of ATP, while decreasing the responsiveness to NaCl or fructose enhances the responsiveness to glucose and sucrose.
  • 3.3. The inhibiting effect of ATP on NaCl or fructose responses is suppressed by GDPßS, an inhibitor of adenylate cyclase (and thus of cAMP synthesis); moreover GDPßS further enhances the increase in response due to ATP when added to the sucrose or glucose solutions.
  • 4.4. Results suggest a possible involvement of cAMP and ATP in the taste reception mechanism in the blowfly.
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15.
  • 1.1. The effects of Ba2+ and K+ ions on the membrane currents of Paramecium tetraurelia under a voltage clamp were investigated.
  • 2.2. External Ba2+ suppresses the inward-going K-current and the Ca-induced K-outward current and changes the activation and inactivation kinetics of transient inward current through the Ca-channel.
  • 3.3. K+ increases the Ca-induced K-conductances but little affects the leakage conductance.
  • 4.4. The resting potentials by changing those ionic concentrations shift the voltage sensitivities of all voltage sensitive channels, simultaneously.
  • 5.5. The competition between ions to the channel responses was discussed.
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16.
  • 1.1. The nDNA of carrion crow Corvus corone L., hooded crow C. cornix L., their hybrids, as well as magpie Pica pica L., were digested by the tetranucleotide recognizing restriction enzymes Sau3a, AluI, BspRI and then analysed using electrophoresis with microdensitometry.
  • 2.2. The distribution patterns of restriction DNA fragments proved to be nuclease- and taxon specific.
  • 3.3. The observed families of repeated sequences are characterized by different length (from 30 bp to 23 tbp), number of copies in genome (approximately 103 and 106) and supposedly different types of organization and evolutionary age.
  • 4.4. The total DNA amount identified in the form of discrete fragments is 16 and 19–21% for magpie and crows, respectively.
  • 5.5. The DNA restriction patterns of hybrid forms do not differ from the parental species.
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17.
  • 1.1. Various tissues of the porcupine Hystrix hodgesoni including liver, intestine, stomach, spleen, kidney, brain and lung were examined for the presence of growth hormone binding sites.
  • 2.2. Membranes were prepared from the aforementioned tissues and tested for binding to 125I-bovine growth hormone (125I-bGH).
  • 3.3. Porcupine kidney membranes yielded 1.3 and 2.7% specific binding when tested at 1000 and 2500 μg protein, respectively. Porcupine liver membranes demonstrated approximately 1% specific binding at 3000 μg protein. The other tissues gave low specific binding. The results indicate that porcupine kidney contained binding sites for growth hormone.
  • 4.4. Various tissues of two teleosts, the snakehead Channa maculata and the winter founder Pleuronectes americanus, were similarly processed and tested for binding to 125I-bGH. It was found that among the different tissues studied, the liver membranes of Channa maculata and the gonad membranes of Pleuronectes americanus gave the highest specific binding of 125I-bGH.
  • 5.5. Liver and intestine membranes of the lamprey Petromyzon marinus did not bind 125I-bGH.
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18.
  • 1.1. Serum urea, ammonia concentrations in the blood and excretion were measured in tadpoles of different stages and juveniles of Xenopus laevis.
  • 2.2. The urea excretion rate was determined with the help of injected 14C-urea.
  • 3.3. Urea concentrations are higher during metamorphic climax and at the end of metamorphosis than during prometamorphosis.
  • 4.4. Blood ammonia levels remain rather constant throughout metamorphosis.
  • 5.5. Coincidentally, the relative amount of urea in the blood increases.
  • 6.6. The 14C-urea excretion rates slow down from very high values (48%/hr) at the beginning of prometamorphosis to low rates (5%/hr) in newly metamorphosed animals.
  • 7.7. This means that during metamorphosis not only is the possibility of urea production established. but there is a capacity to retard and store urea to some extent.
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19.
  • 1.1. Decreased staining intensity with the Alcian Blue-Alcian Yellow technique for neurosecretory material led to a reduction in the visible numbers of Yellow Cells and Yellow-green Cells in brains from snails exposed to deionized water for more than 2 days. compared with snails from standard tapwater.
  • 2.2. A significant drop in blood Na+ and Cl concentrations preceded the histological change in Yellow Cell and Yellow-green Cell appearance.
  • 3.3. A significant drop in blood volume only occurred after 4 days exposure to deionized water, rather delayed with respect to the above histological and physiological changes.
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20.
  • 1.1. Acid mucopolysaccharide (AMPS) of the body wall of Aplysia has been isolated by papain digestion and selective precipitation with cetylpyridinium chloride (CPC).
  • 2.2. Chemical analysis of the AMPS preparation revealed the presence of hexosamine, hexuronic acid, neutral sugars and protein.
  • 3.3. Electrophoretically three types of AMPS were observed: one unsulphated and two sulphated.
  • 4.4. Functional aspects of AMPS as well as association of AMPS to collagen in invertebrates is briefly discussed.
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