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1.
Influx of Rb+(86Rb+) and Ca2+ (45Ca2+) in roots of intact winter wheat (Triticum aestivum L. cv. Weibulls Starke II) was determined at intervals before, during and after exposure to cold acclimation conditions (2°C and 8 h light period). The plants were grown in nutrient medium of two ionic strengths. During the initial two weeks of growth at 16°C and 16 h light period, Rb+ influx into roots decreased with increasing age, probably as a consequence of a decreasing proportion of metabolically active roots. The presence of 10?4M 2,4-dinitrophenol (DNP) reduced Rb+ influx to a low and constant level, indicating that metabolic influx was the dominant process. In contrast, Ca2+ influx in plants grown in full strength nutrient solution was higher in the presence than in the absence of DNP. This effect may have been due to an active extrusion mechanism mediating re-export of absorbed Ca2+(45Ca2+) during the uptake experiment. With the metabolic uncoupler inhibiting such extrusion the Ca2+(45Ca2+) influx mesured would increase. During cold treatment, Rb+ influx remained at a low level, and was further decreased when DNP was present in the uptake solution. This effect may have been due to inhibition of residual active influx of Rb+ at 2°C by the uncoupler and/or to a decrease in membrane permeability. In contrast to Rb+, Ca2+ influx increased during cold treatment, which could again be explained as inhibition of re-export. The presence of DNP reduced Ca2+ influx at 2°C, indicating decreased membrane permeability by DNP at low temperature. After transfer of plants from cold acclimation conditions to 16°C, Rb+ and Ca2+ influx increased in plants grown at both ionic strengths. Influx levels were independent of the length of the cold acclimation period (1, 6 and 8 weeks), but the patterns were different for the two ions. After each of the cold acclimation periods, Rb+ influx increased during the first week and decreased or remained at the same level during the second week, while Ca2+ influx always decreased during the second week of post-cold treatment.  相似文献   

2.
Abstract— —The influx of glutamic acid in frog sciatic nerve has been studied by monitoring the disappearance of 14C labelled compound from the bathing medium. After 5hr of incubation in 10 −6m non-labelled l -glutamic acid and 0·01, μc/ml labelled isotope, the intracellular concentration of labelled glutamic acid is about 15 times the concentration in the bathing medium; however, there appears to be a net loss of non-labelled compound with incubation. Uptake of L,-glutamic acid is accompanied by conversion of significant amounts of labelled E-glutamic acid to carbon dioxide and glutamine; small amounts of γ-aminobutyric acid and aspartic acid are also formed. The rate of disappearance of labelled l -glutamic acid decreases with increasing concentration of non-labelled isotope in the bathing medium. Construction of a Lineweaver-Burk plot from initial velocities of influx yields an average Vm of 4·02 × 10−9 moles/g/min and an average Km. of 3·23 × 10 −5 moles/l. The influx of glutamic acid is highly specific with regard to molecular structure; of the compounds tested, only l -glutamine, l -glutamic acid, GABA, l -lysine, and l -aspartic acid are taken up, and only l -aspartic acid will compete with l -glutamic acid for uptake.  相似文献   

3.
Evidence for the presence of phosphatide acylhydrolase activity (EC 3.1.1) in centrifuged homogenate supernatants and extracts of squid giant axons and centrifuged homogenate supernatants of frog sciatic nerve bundles is reported. The enzyme was assayed by measurement of the rate of deacylation of [U-14C]phosphatidyl choline. The deacylation activity in the nerve homogenate supernatants exhibits: a pH maximum at 7.2–7.4 (25°C); a calcium ion maximum at 12–13 mM-CaCl2(aq); a Km value of 3.4 × 10?4 M (25°C); and a temperature maximum at 37°C. The activation energy over the range 8–37°C is 5.7 ± 0.2kcal-mol?1.  相似文献   

4.
SUMMARY.
  • 1 We evaluated survival, growth and time to maturation of the fairy shrimp, Streptocephalus seali Ryder, in the laboratory at various combinations of temperature and water hardness.
  • 2 Both independent factors affected survival and growth of S. seali. Multiple regression analysis and response surface modelling predict that after 4 days, over 80% survival is obtained at temperatures from 14 to 28°C and water hardnesses from 60 to 130 mg CaCO3 1-?1.
  • 3 Growth rates of larvae were often maximum at physicochemical conditions other than those which had promoted maximum rates of survival. For example, after 12 days mean total body length was almost 12 mm in larvae which had been maintained at 34°C (80 mg CaCO3 1-?1): the maximum survival rate had been obtained at 19°C. Total length was directly correlated with temperature at the lowest hardness tested, but not at the other two hardnesses (100 and 120 mg CaCO3 1-?1). At the latter water hardnesses, total length was significantly less at 34°C than at 32°C on all three sampling occasions (4, 8 and 12 days post-hatch).
  • 4 Similarly, developmental stage of larvae correlated well with temperature but larvae reared at 34°C did not develop more quickly than those reared at 32°C. After 12 days, most larvae at the two highest temperature treatments had developed at least to Stage 14 and many were nearly mature; at 17°C most larvae were still at Stage 10.
  • 5 During our study of maturation rate of females we noted that egg production was initiated after completion of fourteen or fifteen moults. Mean time to maturation at 27°C (17.3±2.8 days) exceeded that at 32°C (12.3±2.6days). The minimum time to maturation of a shrimp was 9 days at 32°C.
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5.
Abstract Effects of temperature on the ionic relations and energy metabolism of Chara corallina were investigated. Measurements were made of the ionic content, tracer ion fluxes, and photosynthetic and dark CO2 fixation in isolated cells, and of O2 exchange in photosynthesis and respiration in isolated shoot apices. The total intracellular concentration of K+, Na+ and Cl? was the same in cells held for 5 days in non-growing medium at 15°C (the growth temperature) as in those held at 25°C or 5°C. The tracer influx in the light of all ions tested (Rb+, Na+, CH3NH3+, Cl? and H2PO4?) was lower at 5°C than at 15°C in experiments in which cells were subjected to 5°C for less than 24 h in toto. The influx at 25°C was greater than that at 15°C for H2PO?4, there was no difference between the two temperatures for Na+, while the influx at 25°C was less than that at 15°C for Cl?, Rb+ and CH3NH3+ For Cl? and H2PO?4 similar results were found in later experiments with cells grown at 20—23°C. Photosynthetic CO2 fixation and O2 evolution, and respiratory O2 uptake, are greater at 25°C, and lower at 5°C, than they are at the growth temperature of 15°C. In longer-term pretreatments at the different temperatures, tracer Cl? influx at 15°C and particularly at 25°C were lower than in short-term experiments, while the influx at 5°C was higher. It was concluded from these experiments, and from previous data on H+ free energy differences across the plasmalemma, that (1) the maintenance of internal ion concentrations involves a close balancing of influx and efflux of K+, Na+ and Cl? at all experimental temperatures; (2) the regulation of the tracer fluxes of the ions is kinetic rather than thermodynamic and (3) that the tracer fluxes at low temperatures are not restricted by the rate at which respiration or photosynthesis can supply energy to them.  相似文献   

6.
  • 1.1. The temperature and water relations of Centruroides hentzi females were investigated. At 12 and 72% relative humidity (RH), the lower and upper Lt50 were -4.5 and 43.7°C, and -4.7 and 45.1°C, respectively. When exposed to high temperature stress, survivorship was significantly greater under mesic conditions.
  • 2.2. Cuticular water loss was higher under xeric conditions (12% RH), ranging from 0.061 mg/cm2/hr at 30°C to 0.211 at 41°C.
  • 3.3. Exposure to dry air (0–5% RH) resulted in a significant increase in hemolymph osmolality: from 441 to 688 mOsm over a 5 day period.
  • 4.4. Mean oxygen consumption rates increased from 161.7 mm3/g/hr at 34°C to 541.6 at 44°C. ATPase activity was significantly higher in animals acclimated and tested at 35°C.
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7.
  • 1 Growth rates of two dominant Lake Baikal phytoplankton, the winter diatom Aulacoseira baicalensis and the summer cyanobacterium Synechocystis limnetica, were measured in the laboratory under varied temperature and light regimes to determine the potential role of these abiotic factors in seasonal species succession in the lake.
  • 2 Aulacoseira baicalensis grew best at low temperature and not at all above 8 °C. Its maximum instantaneous growth rate was 0.15 d‐1 recorded at 2–3 °C. Cells grew faster as temperature decreased, apparently in contrast to conventional Q10‐based temperature‐growth relationships.
  • 3 The picoplankter Synechocystis limnetica did not grow at 2–3 or 5–6 °C, but grew at a rate of 0.24 d‐1 at the highest incubation temperature of 17 °C. Maximum growth rate was 0.35 d‐1 at 8 °C.
  • 4 Saturation irradiances (Ik) for growth of Aulacoseira baicalensis and Synechocystis limnetica were near pre‐acclimation values of 40 µmol m‐2 s‐1. At temperatures conducive to growth, both phytoplankters grew at all irradiances tested, except for A. baicalensis which would not grow at values above 300 µmol m‐2 s‐1 at 8 °C.
  • 5 We conclude that temperature is a major driving force for the seasonal succession of species in Lake Baikal. Other factors, including vertical mixing of the water column and grazing by zooplankton, may also play important roles.
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8.
9.
  • (1)The preferred temperatures of Macrobrachium acanthurus were determined for prawns acclimated to 20°C, 23°C, 26°C, 29°C and 32°C, and the final preferendum estimate was (29.5°C).
  • (2)The critical thermal minima (CTMin) and maxima (CTMax) were 11.0°C, 12.1°C, 13.0°C and 14.8°C, and 34.2°C, 35.0°C, 36.1°C and 39.8°C, respectively.
  • (3)The zone of thermal tolerance assessed using the CTMin and CTMax boundaries was 644°C2.
  • (4)The acclimation response ratio was between 0.33 and 0.62.
  • (5)To cultivate this species in the southeastern region of México it should be done in not <15°C (CTMin) during the winter and below 38°C in summer (CTMax).
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10.
ABSTRACT.
  • 1 Flight of Melissopus latiferreanus (Walsinghzm), the filbertworm, was influenced by a number of environmental factors including temperature, wind, and rainfall.
  • 2 Few M. latiferreanus moths were trapped in light or suction traps or found in sweep nets samples when air temperatures were above 31°C or below 15°C. Moth captures were optimum when prevailing temperature was between 21 and 26°C.
  • 3 Typically moth flights began at about sunset and continued throughout the night with a peak at 22.00 hours, about an hour after sunset.
  • 4 Very few moths were trapped under showery and gusty conditions when wind velocity was over 16km h?1.
  • 5 More moths were captured in light traps during dark nights than on full moon nights. The pattern of captures indicated that females flew earlier than males.
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11.
12.
13.
The effect of irradiance and temperature on the photosynthesis of the red alga, Pyropia tenera, was determined for maricultured gametophytes and sporophytes collected from a region that is known as one of the southern limits of its distribution in Japan. Macroscopic gametophytes were examined using both pulse‐amplitude modulated fluorometry and/or dissolved oxygen sensors. A model of the net photosynthesis–irradiance (P‐E) relationship of the gametophytes at 12°C revealed that the net photosynthetic rate quickly increased at irradiances below the estimated saturation irradiance of 46 μmol photons m?2 s?1, and the compensation irradiance was 9 μmol photons m?2 s?1. Gross photosynthesis and dark respiration for the gametophytes were also determined over a range of temperatures (8–34°C), revealing that the gross photosynthetic rates of 46.3 μmol O2 mgchl‐a?1 min?1 was highest at 9.3 (95% Bayesian credible interval (BCI): 2.3–14.5)°C, and the dark respiration rate increased at a rate of 0.93 μmol O2 mgchl‐a?1 min?1°C?1. The measured dark respiration rates ranged from ?0.06 μmol O2 mgchl‐a?1 min?1 at 6°C to ?25.2 μmol O2 mgchl‐a?1 min?1 at 34°C. The highest value of the maximum quantum yield (Fv/Fm) for the gametophytes occurred at 22.4 (BCI: 21.5–23.3) °C and was 0.48 (BCI: 0.475–0.486), although those of the sporophyte occurred at 12.9 (BCI: 7.4–15.1) °C and was 0.52 (BCI: 0.506–0.544). This species may be considered well‐adapted to the current range of seawater temperatures in this region. However, since the gametophytes have such a low temperature requirement, they are most likely close to their tolerable temperatures in the natural environment.  相似文献   

14.
SUMMARY.
  • 1 A fifth-order section of the Grabia River was investigated over two years: 1984/85 (low water level) and 1985/86 (high spate). Chironomidae (thirty-nine species) dominated the macrobenthos in both years.
  • 2 In 1984/85 (mean annual water temperature 10.2°C), the number of Chironomidae species in coarse sediment was highest in spring (thirty-three species) while in sand it was highest in summer (fifteen species). A decrease in species richness was recorded in autumn and winter at each of the established sites. The estimated Chironomidae production for the whole river section was 5.37 g dry wt m?2 yr?1, but it differed widely amongst the study sites, ranging from 3.75 to 12.07 g m?2 yr?l.
  • 3 In 1984/85 (mean annual temperature 8.1°C) there occurred a summer spate which was more intense than any recorded over the previous 20 years. This substantially reduced the number of species, the greatest reduction being in the coarse sediment, which was buried with sand during the spate. Production for the whole section decreased to 1.17 g m?2 yr?1, and the variability amongst sites ranged from 1.04 to 1.45 g m?2 yr?1.
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15.
16.
  • 1.1. Freshwater-resident Arctic charr acclimated for 2 months at 8°C, 15% were divided into four experimental groups in July and exposed to 1 and 8°C in 15 and 34% salinity.
  • 2.2. Only slight changes in gill Na-K-ATPase activity, blood plasma osmolality and blood plasma concentrations of Cl and Mg2+ were found for the fish exposed to 1 or 8°C in brackish water.
  • 3.3. When exposed to sea-water at 8°C, an increase in osmolality and in concentrations of Cl and Mg2+ took place during the first 2–3 days, after which it levelled off.
  • 4.4. If exposed to sea-water at 1°C, however, marked increases were found for all parameters measured and all the fish were dead within 5 days of exposure.
  • 5.5. These results show that freshwater-resident Arctic charr—if acclimated to brackish water—can survive in sea-water during summer if the environmental temperature is not too low.
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17.
This study was undertaken to evaluate the effects of various metabolic blockers on the Na-K-pump activity and ATP content of frog erythrocytes. To eliminate K-C1 cotransport, the frog erythrocytes were incubated in nitrate media at 20 °C. Incubation of the red cells in a glucose-free medium for 2 h had no effect on cell ATP content and K+ influx measured as 86Rb uptake for 60 min. The Na+-K+-pump activity was also unchanged in the frog erythrocytes incubated in a glucose-free medium containing 10 mM 2-deoxy-D-glucose or adenosine. Unexpectedly, the treatment of red cells with 1–2 mM glycolytic blocker iodoacetate produced a 2-fold increase in the ouabain-sensitive K+ influx. The cell ATP content declined by 9.4% after 2 h of cell incubation with iodoacetate. Incubation of the red cells for 90 min in the presence of 2 mM cyanide, 0.01 mM antimycin A or 5 mM azide resulted in a significant reduction in K+ influx by about 50%, 45% and 32%, respectively. The cell ATP content diminished over 60 min and 120 min of cell incubation with 2 mM cyanide by 15.6% and 31.7% of control levels, respectively. In time-course experiments, a 50% reduction in the K+ influx was observed when the frog erythrocytes were incubated for only 30 min in the presence of 2 mM cyanide. In contrast, 0.01–0.10 mM rotenone, a site I inhibitor, and 0.01 mM carbonyl cyanide m-chlorophenylhydrazone, an uncoupler of oxidative phosphorylation were without effect on K+ influx into frog erythrocytes. These results indicate that about one-half of the Na+ -K+-pump activity in frog erythrocytes is tightly functionally coupled to cytochromes via a separate “membrane-associated” ATP pool. Accepted: 12 July 1997  相似文献   

18.
  • 1.Lower and upper temperature tolerances of 240 goldfish, Carassius auratus, were measured at constant acclimation temperatures of 5, 15, 25 and 35 °C via critical thermal methodology.
  • 2.Mean critical thermal minima and maxima ranged from 0.3 to12.6 °C and 30.8 to 43.6 ° C, respectively, and were significantly linearly related to acclimation temperature. Acclimation temperature accounted for approximately 90% of the variance in temperature tolerance. Ultimate critical thermal minimum and maximum equaled 0.3 and 43.6 °C, respectively.
  • 3.Integrating the temperature tolerance polygon yielded an area of temperature tolerance of 1429 °C2, which is approximately 17% larger than the polygon measured via the incipient lethal temperature approach. This difference is explained by methodological differences in these two techniques to quantify temperature tolerance.
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19.
Nitzschia seriata Cleve, a common member of marine bottom ice communities in the Arctic, was grown in unialgal batch cultures to test for compensatory mechanisms for the low temperatures (?1.8° C) typical of its natural habitat. The upper lethal limit for growth was between 12° and 15°C, and the optimum was between 6° and 12° C. The Arrhenius function adequately (R2= 73%) fitted the relationship between growth rate and temperature from – 1.6° up to 10° C, with an average Q10 of 1.9 over the entire range. Light-saturated and light-limited rates of photosynthesis (normalized to chlorophyll a or cell carbon) showed complete compensation from 12° to 4° C. Photosynthetic rates, especially at light saturation, declined rapidly at temperatures below 4° C. Susceptibility to photoinhibition was greatest at the lowest growth temperatures. Cellular composition (chlorophyll a, protein, polysaccharide, and lipid contents) was not systematically related to temperature in any simple way, although cell size (carbon per cell) was maximal at the lowest growth temperature. Dark respiration was unmeasurably low (<0.015 day?1) at all growth temperatures. The strategy of adaptation in N. seriata may be characterized as optimizing efficiency and compensation, rather than maximization, of growth rate.  相似文献   

20.
Cotton leaf curl virus disease reduces the cotton yield significantly every year and is transmitted by Bemisia tabaci. The study was designed to evaluate 15 varieties/lines against the disease. Multiple regression analysis was performed based on a-biotic environmental variables (maximum air temperature, minimum air temperature, relative humidity and rainfall) to predict disease incidence and its vector (Bemisia tabaci). Two bio-products were evaluated against the whitefly population to control the disease. Out of 15 cotton varieties/lines, no one was found highly resistant against the disease. Five varieties/lines (BT BT-980, BT-457, KIRAN, BT-666 and SLH-BT-6) exhibited moderately resistant response. Maximum air temperature (34–35.5 °C), minimum temperature (25.75–26.25 °C), relative humidity (64.14–66%), rainfall (1–2 mm) and wind speed (5.50–5.75 Kmh?1) favoured the disease development. Maximum whitefly population was favoured by maximum air temperature from 34–35.5 °C, 25.8–26.2 °C minimum air temperature, 64.14–66% relative humidity, 1–2 mm from rainfall and 5.50–5.75 Kmh?1 wind speed. Datura stramonium was found more effective as compared to Aviara (Homoeopathic) but not from the positive control (Acetamiprid).  相似文献   

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