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1.
The capacity for increase (Ic) of one laboratory and seven field populations of young adult S. oryzae from different sites in Australia was determined over a thirty-week period at 15°C, a supposedly marginal temperature, in wheat of 14% moisture content. The average value of Ic was 0.0838 ± 0.0017 and the populations comprised three significantly different groups. Variations in the net rate of increase per generation (R0) which averaged 34.7±1.71, had a major effect on the value of rc whereas variation in the cohort generation time (Tc), which averaged 41.6±.23 weeks had only a minor effect. The survivorship of adults of the populations did not differ significantly and 93% of females were alive after thirty weeks. Estimates of rc based on a fifteen-week period and on an amended value of Tc differed little from those over thirty weeks. The capacity for increase at 15°C of a given population was found to be correlated with its fertility at 27°C and with its body-weight rather than with its cold-tolerance, as evidenced by chill-coma temperature, or with its previous temperature-history. The temperature experienced by the immature stages of weevils had a profound effect on rc in that weevils reared at 15 and 27°C had respective values of 0.0350 and 0.0707 when subsequently cultured at 15°C. Because all observed values of rc were higher than expected, possible errors in method were considered. An alternative estimate of R0 agreed closely with that observed and indicated that only 17% of the immature stages survived at 15°C. Metabolic heating due to the higher than expected population density shortened the duration of the immature stages by 7% but did not affect their survival.  相似文献   

2.
The capacity for increase (rc) of three populations of S. oryzae and three populations of S. granarius from Great Britain and Canada was determined over 15 and 24 weeks respectively at 15°C in wheat of 14% moisture content. The fertility of these populations at 27°C, their body weight and chill-coma threshold was also measured. With both S. oryzae and S. granarius, values of rc for the foreign populations fell within the range previously observed when several Australian populations were reared under the same conditions. The cohort generation times (Tc) of the foreign S. oryzae populations were significantly shorter than those of the Australian populations because of the shorter immature development periods (D) of the former. Two of the foreign S. granarius populations had lower values for D than all but one of their Australian counterparts but their values of Tc were within the range previously observed for Australian weevils. When the Australian and foreign populations were considered together, the value of rc was more strongly correlated with fertility at 27°, an optimal temperature, than with body weight in both S. oryzae and S. granarius. With S. oryzae, rc was correlated with the chill-coma threshold of cold-acclimated weevils only. There were no correlations between rc and chill-coma thresholds in S. granarius. It was concluded that the observed differences in rc were related to differences in the vigour of the populations rather than to physiological differences in cold-tolerance. The likelihood of grain weevils becoming cold-tolerant as a result of grain aeration is discussed and the practical significance of differences in rc considered.  相似文献   

3.
The ability of Sitophilus oryzae (L.) and S. granarius (L.) to acclimate when transferred from 27°C, a near optimal temperature, to 15° C, a marginal temperature, was examined in terms of chill-coma temperature, dispersal, oxygen consumption and rate of oviposition. The chill-coma temperature of S. oryzae was higher and the increment of acclimation less than that of S. granarius. Acclimation, although well advanced after 2 weeks after transfer, took more than 4 weeks to complete. Re-acclimation after the reciprocal transfer took only 2 weeks. The dispersal of S. oryzae held at 15 and 27° C prior to testing differed when the weevils were released in wheat at 27°C but not when released at 15°C. Cold-acclimated S. granarius dispersed less than warm-acclimated weevils when released in wheat at both 15 and 27°C. The activity oxygen consumption of cold-acclimated weevils was less than that of warm-acclimated weevils. Inverse-shifts of acutely determined R-T relationships appeared more significant than changes in temperature sensitivity. Acclimation to 15° C took 8–10 days and re-acclimation to 27°C about 6–8 days. S. oryzae consumed less oxygen per unit of weight than S. granarius but was more temperature sensitive. Resting oxygen consumption, which was less temperature sensitive than activity consumption, also exhibited inverse acclimation in both species. S. granarius showed evidence of inverse acclimation of oviposition rate after acclimation at 15°C.  相似文献   

4.
L. Smith  D. A. Rutz 《BioControl》1987,32(4):315-327
Urolepis rufipes Ashmead, a recently discovered parasitoid of house flies at New York dairies, was reared at 15, 20, 25, 30 and 34°C to measure daily fertility, fecundity and adult survivorship. Little reproduction occurred at 15°C, and only a few ♀ successfully emerged at 34°C. The intrinsic rate of growth was fastest at 30°C (0.282 ♀/day), but fecundity was highest at 25°C (165.5 hosts attacked, producing 124.5 progeny). Some reproductive statistics at 25°C were: net reproductive rate (R0=72.1 ♀/♀, generation time =18.7 days, intrinsic rate of increase (rm)=0.228, finite rate of increase (λ)=1.26, daily birth rate =0.302, daily death rate =0.021 and Fisher's reproductive value =418. Sex ratio (average =75.9%) did not vary significantly with temperature (between 20–30°C) nor with mother's age.   相似文献   

5.
The development, survivorship, longevity, reproduction, and life table parameters of the Asian citrus psyllid, Diaphorina citri Kuwayama were evaluated at 10°C, 15°C, 20°C, 25°C, 28°C, 30°C and 33°C. The populations reared at 10°C and 33°C failed to develop. Between 15°C and 30°C, mean developmental period from egg to adult varied from 49.3 days at 15°C to 14.1 days at 28°C. The low‐temperature developmental thresholds for 1st through 5th instars were estimated at 11.7°C, 10.7°C, 10.1°C, 10.5°C and 10.9°C, respectively. A modified Logan model was used to describe the relationship between developmental rate and temperature. The survival of the 3rd through 5th nymphal instars at 15–28°C was essentially the same. The mean longevity of females increased with decreasing temperature within 15–30°C. The maximal longevity of individual females was recorded 117, 60, 56, 52 and 51 days at 15°C, 20°C, 25°C, 28°C and 30°C, respectively. The average number of eggs produced per female significantly increased with increasing temperature and reached a maximum of 748.3 eggs at 28°C (P<0.001). The population reared at 28°C had the highest intrinsic rate of increased (0.199) and net reproductive rate (292.2); and the shortest population doubling time (3.5 days) and mean generation time (28.6 days) compared with populations reared at 15–25°C. The optimum range of temperatures for D. citri population growth was 25–28°C.  相似文献   

6.
Development time, reproduction, survival and sex ratio were determined for the omnivorous mite Amblyseius swirskii at nine constant temperatures (13, 15, 18, 20, 25, 30, 32, 34 and 36°C) on pepper leaf disks with cattail, Typha latifolia, pollen for food. These data were used to derive life table parameters at these constant temperatures. No development was observed at 13°C. The lower development threshold, based on the fit to the linear portion of the development curve, was 11.3°C. The upper development threshold was 37.4 ± 1.12°C, and the optimum temperature was calculated to be 31.5°C. Average lifetime fecundity ranged from a low of 1.3 ± 0.24 eggs/female at 15°C to a high of 16.1 ± 0.34 eggs/female at 25°C, and r m was greatest at 32°C. Non-linear regression of the relationship between temperature and r m produced an estimate of 15.49 ± 0.905°C for the lower threshold for population growth and 36.99 ± 0.816°C for the upper threshold for population growth, and an optimum temperature of 30.1°C. These values suggest that A. swiskii populations should grow quickly in response to food availability (pollen or prey) between 20 and 32°C, but that, especially below 20°C, population growth could be slow and impacts on prey populations should be monitored carefully.  相似文献   

7.
Culex quinquefasciatus plays a major role in the transmission of important parasites and viruses throughout the world. Because temperature is an important limiting factor on growth and longevity of all mosquito species, estimating the reaction norms provides very important basic information for understanding both plasticity and individual variations of the population. In the present study, Cx. quinquefasciatus were maintained at five different constant temperatures (15°, 20°, 23°, 27°, and 30°C) for two subsequent generations. Reproductive population parameters in blood‐fed mated females and longevities of virgin and blood‐fed mated adults reared at different temperatures were compared for the two generations. Longevity increased as temperature decreased within a range of 15° to 30°C for the unmated adults, and 15° to 27°C for the mated and blood‐fed adults. Generation times were as long as 124.07 and 106.76 days for two subsequent generations reared at 15°C, and the highest intrinsic rate of increase (rm) values were estimated at 0.22 and 0.18, respectively, from the cohorts reared at 27°C. For survival rates, reproductive rates (R0), and rm values, 30°C was found to be a critical temperature for this species. These cohorts produced the smallest amount of eggs (R0= 5.06), rm values decreasing across generations (from 0.11 to 0.06), and the survival rates from egg to adult were found to be insufficient (16.1 and 10.8%). Additionally, the rate of exponential increase with age and age specific mortalities (b) were calculated for the virgin cohorts. Age specific mortality rates increased as temperature decreased. The increase in mortality rates started to accelerate at 27°C and was more pronounced at 30°C, for both females and males. We estimated the coefficients of variation for the b values in which females have smaller coefficients than those of the males at all temperatures.  相似文献   

8.
It is widely known that water temperature affects the swimming capacity of fish. But the effect of the rearing temperature on the swimming ability of the fish at later stages, has not had similar attention. In this study, four populations of zebrafish, were reared in different water temperatures (22, 25, 28 and 31°C) and after being acclimatized in a common temperature (26.5°C) for over a month, they were subjected to swimming trials in order to evaluate the maximum relative critical velocity (RU crit ) in each case. Fish that were reared in 22°C showed statistically significant lower performance than the ones reared in 31°C (7.72 ± 0.17 vs. 8.79 ± 0.28, means ± S.E.). Possible explanations for the observed differentiation could be the effect of early life temperature on fish muscle ontogeny or on body shape.  相似文献   

9.
In this study, we developed an oviposition model of Neoseiulus californicus (McGregor) with Tetranychus urticae Koch as prey. To obtain data for the model, we investigated the longevity, fecundity and survivorship of adult female N. californicus at six constant temperatures (16, 20, 24, 28, 32 and 36°C), 60–70% RH and a photoperiod of 16 : 8 (L : D) h. Longevity (average ± SE) decreased as temperature increased and was longest at 16°C (46.7 ± 5.25 days) and shortest at 36°C (12.8 ± 0.75 days). Adult developmental rate (1/average longevity) was described by the Lactin 1 model (r2 = 0.95). The oviposition period (average±SE) was also longest at 16°C (29.8 ± 2.93 days) and shortest at 36°C (6.7 ± 0.54 days). Fecundity (average±SE) was greatest at 24°C (43.8 ± 3.23 eggs) and lowest at 36°C (15.9 ± 1.50 eggs). The oviposition model comprised temperature‐dependent fecundity, age‐specific cumulative oviposition rate and age‐specific survival rate functions. The temperature‐dependent fecundity was best described by an exponential equation (r2 = 0.81). The age‐specific cumulative oviposition rate was best described by the three‐parameter Weibull function (r2 = 0.96). The age‐specific survival rate was best described by a reverse sigmoid function (r2 = 0.85).  相似文献   

10.
Fertility life table parameters were assessed for five populations (strains) of two Trichogramma species, T. embryophagum Hartig and T. principium Sugonyaev & Sorokina, collected from eggs of the carob moth Ectomyelois ceratoniae (Zeller) in Iranian pomegranate orchards. Four combinations of two constant temperatures (25°C, 30°C) and two relative humidity levels (50% RH, 70% RH) were used. The overall intrinsic rate of natural increase (rm) was significantly decreased with decreased relative humidity but was uninfluenced by temperature. The highest and lowest rm values were observed in T. embryophagum from Qum (0.34 ± 0.004) and T. embryophagum from Varamin (0.13 ± 0.01), respectively. Two‐way interaction analyses revealed that the strains had significantly different responses in their rm values at different temperatures and relative humidities. In general, rm values were significantly higher at 25°C and 70% RH than at 30°C and 50% RH. The Qum strain of T. embryophagum was the most promising candidate to be considered as a biocontrol agent against E. ceratoniae due to its high reproductive rate (0.27 ± 0.01) at conditions (30°C and 50% RH) similar to the actual climatic conditions in Iranian pomegranate orchards during the major part of the growing season.  相似文献   

11.
Summary A model was developed to describe interactive effects of exposure time and treatment on thermostability of excisedIllicium parviflorum Michx. root cell membranes using electrolyte leakage (Lc) procedures. Roots were moved from 25°C to treatment temperatures between 35°C and 60°C for 30 to 300 min. A sigmoidal response described Lc increases with increasing temperature at selected time exposures and the lethal exposure time decreased exponentially as temperature increased. The lethal temperature (52.0±1.1°C) for a 15 min exposure using this technique was comparable to the critical temperature (52.2±1.2°C) when roots were exposed to gradually increasing temperatures (4°C per h). Total protein content of roots began to decrease as temperatures increased from 35 to 40°C and the temperature corresponding to 50% reduction in total proteins was 49.1±2.2°C.  相似文献   

12.
Development, survival, fecundity, progeny sex ratio (PSR) and age-specific life-table parameters of the parasitoid Campoletis chlorideae Uchida (Hymenoptera: Ichneumonidae) were examined at six different constant temperatures (12, 17, 22, 27, 32 and 37°C) in the laboratory [70 ± 10% RH and 10:14 h (light:dark) photoperiod]. Second instar larvae of Helicoverpa armigera (Hübner) (Lepidoptera: Noctuidae) were reared on chickpea (Cicer arietinum L.) and used as the host. Development times shortened as the temperature increased from 12 to 37°C. The estimated lower developmental threshold (tL) was 3.4°C. The thermal summation for total immature stages was 379.97 degree-days. A reciprocal relationship between temperature and longevity was observed in the range of 12–17°C. The maximum mortality of pupae (71.8%) occurred at 37°C. At 22°C, the yield of a female parasitoid averaged 137.3 ± 14.7 (mean ± SD) progeny, of which 89.6 ± 7.6 were daughters. The number of daughters produced decreased when the females were kept either above or below 22°C, although the PSR was female biased in the range of 17–27°C. The analyses of life-table parameters, developmental rates, reproduction, mortality and PSR suggest that maximum population growth (r m ) is near 27°C. There was little variation observed in most of the desired qualities of C. chlorideae in the range of 17–27°C, and it appears that the parasitoid is adapted to a wide range of temperatures. We suggest that for maximum production the parasitoid should be reared at 22 ± 4°C and be released in areas where the temperature ranges between 17° and 27°C, as in the plains of northern India.  相似文献   

13.
The thermotropic properties of bovine blood coagulation Factors IX and X, as well as the activation intermediates and products of these proteins, have been investigated by differential scanning microcalorimetry in the presence and absence of Ca2+. Bovine Factor IX displays a single thermal-denaturation transition characterized by a temperature midpoint (TM) of 54.5 ± 0.5 °C and a calorimetric enthalpy (ΔHc) of 105 ± 15 kcal/mol, in the absence of Ca2+. In the presence of Ca2+ concentrations sufficient to saturate its sites on Factor IX, the Tm value is increased to 57.0 ± 0.5 °C and the ΔHc is virtually unchanged. When the activation intermediate, Factor IXα, is similarly analyzed in the absence of Ca2+, a broad, diffuse thermogram was obtained which did not lend itself to calculation of thermodynamic parameters. In the presence of Ca2+, Factor IXα displayed thermograms characterized by a TM of 51.0 ± 0.5 °C and a ΔHc of 109 ± 10 kcal/mol. The activated product, Factor IXaα, in the absence of Ca2+ (the values in the presence of saturating Ca2+ are given in parentheses), undergoes thermal denaturation with a TM of 54.5 ± 0.5 °C (57.0 ± 0.5 °C) and a ΔHc of 158 ±10 kcal/mol (156 ± 10 kcal/mol). Similarly, the terminal-activation product, Factor IXaβ, displays a TM of 51.5 ± 0.5 °C (54.0 ± 0.5 °C) and a ΔHc of 85 ± 5 kcal/mol (126 ± 10 kcal/mol). Bovine blood coagulation Factor X has been analyzed in this same fashion, and shows very similar thermal properties to Factor IX. The thermal denaturation of Factor X is represented by a TM of 54.0 ± 0.5 °C (55.0 ± 0.5 °C) and a ΔHc of 102 ± 10 kcal/mol (118 ± 10 kcal/mol), whereas its activated form, Factor Xaβ, possesses a TM of 55.0 ± 0.5 °C (55.0 ± 0.5 °C) and a ΔHc of 92.0 ± 5 kcal/mol (136 ± 10 kcal/mol). These studies indicate that, for many of these proteins, Ca2+ induces a conformational alteration to a more thermally stable form, which also requires the absorption of greater amounts of heat for thermal denaturation.  相似文献   

14.
The fecundity and life table parameters of Campoletis sonorensis females were measured using thirty 4-day-old Trichoplusia ni larvae daily at 24°C, 60% RH and a photoperiod of 12 h L:12 h D. The mean longevity was 34.5±2.8 days, the mean oviposition period was 22.7±1.9 days, and the mean constant oviposition period and the mean post-oviposition period were 15.9±1.3 and 11.9±2.2 days, respectively. The mean realised fecundity and the mean fertility differed significantly at 66.9±7.8 and 60.4±7.8 parasitoids per female, respectively. The mean sex ratio for the mean oviposition period (23 days) was 0.13±0.07, indicating a highly female biased ratio. The life table parameters were: intrinsic rate of natural increase (r m), 0.135 female/day; gross reproductive rate (GRR), 50.30; net reproductive rate (R o), 49.96; finite capacity for increase (λ), 1.14 female/day; mean generation time (T), 28.97 days; doubling time (DT), 5.13; capacity for increase (r c), 0.33; and cohort generation time (T c), 11.69. Campoletis sonorensis may be a suitable candidate for a biocontrol program of T. ni populations mostly because the primary selection criterion, rm , obtained for this parasitoid can be similar to or larger than the rate obtained for T. ni.  相似文献   

15.
  1. Neochetina eichhorniae is the most widely established biocontrol agent on water hyacinth populations around South Africa. However, some N. eichhorniae populations have failed to adequately control their host population, specifically those exposed to cold conditions.
  2. The aim of this study was to determine whether two climatically distinct populations of N. eichhorniae in South Africa differ in their low‐temperature physiology, which tests whether local‐climate adaptation has occurred.
  3. We estimated weevil CTmin, LLT50, SCP, and SCP mortality using standard approaches. Contrary to expectation based on climatic thermal profiles at the two sites, weevils from the warm locality ((mean ± SE) CTmin = 5.0 °C ± 0.2, LLT50 = ?11.3 °C ± 0.03, SCP = ?15.8 °C ± 0.6) were able to maintain activity and tolerate colder temperatures than the weevils from the colder site (CTmin = 6.0 °C ± 0.5, LLT50 = ?10.1 °C ± 0.1, SCP = ?12.9 °C ± 0.8).
  4. These contradictory outcomes are likely explained by the poor nutrient quality of the plants at the cold site, driving low‐temperature performance variation that overrode any macroclimate variation among sites. The cold site weevils may also have adapted to survive wide‐temperature variability, rather than perform well under very cold conditions. In contrast, the mass‐reared population of insects from the warm site has likely adapted to the consistent conditions that they experience over many years in confinement.
  相似文献   

16.
Peristenus spretus Chen et van Achterberg (Hymenoptera: Braconidae), a parasitoid of the plant bug Apolygus lucorum (Hemiptera: Miridae), has been studied for use in augmentative biological control in China. Under laboratory conditions, we explored the development, survival, age-specific and potential lifetime fecundity, oviposition period and progeny sex ratio of P. spretus reared at six constant temperatures (15°C, 19°C, 23°C, 27°C, 31°C, 35°C) on the second instar nymphs of A. lucorum. At 15°C, male and female P. spretus took 48.7 ± 0.3 and 52.5 ± 0.3 days to complete their immature development, while developmental time was reduced by more than half at 23°C and 27°C. The parasitoid can only develop to the larval stage at 31°C and neither larva nor pupa survived at 35°C. The estimated lower developmental threshold of the immature stage was 7.3°C. When parasitoid adults were exposed at 15°C, females laid 90% of their eggs at first 19 days of oviposition and had an extended reproductive life. In contrast, females held at 27°C laid most of their eggs (90%) in their first of 10 days of oviposition and had shorter longevity. The highest potential lifetime fecundity of P. spretus was 671.2 ± 34.7 SE eggs produced over 23.4 ± 1.4 SE days at 23°C. At 15°C, 19°C and 23°C, sex ratios of reared parasitoids were male-biased, but at 27°C there was no male bias.  相似文献   

17.
Determining the capacity of organisms to acclimate and adapt to increased temperatures is key to understand how populations and communities will respond to global warming. Although there is evidence that elevated water temperature affects metabolism, growth and condition of tropical marine fish, it is unknown whether they have the potential to acclimate, given adequate time. We reared the tropical reef fish Acanthochromis polyacanthus through its entire life cycle at present day and elevated (+1.5 and+3.0 °C) water temperatures to test its ability to thermally acclimate to ocean temperatures predicted to occur over the next 50–100 years. Fish reared at 3.0 °C greater than the present day average reduced their resting oxygen consumption (RMR) during summer compared with fish reared at present day temperatures and tested at the elevated temperature. The reduction in RMR of up to 69 mg O2 kg?1 h?1 in acclimated fish could represent a significant benefit to daily energy expenditure. In contrast, there was no acclimation to summer temperatures exhibited by fish reared at 1.5 °C above present day temperatures. Fish acclimated to +3.0 °C were smaller and in poorer condition than fish reared at present day temperatures, suggesting that even with acclimation there will be significant consequences for future populations of tropical fishes caused by global warming.  相似文献   

18.
19.
Aphids are a good model to study insect reaction to habitat change. Temperature is one of the main factors that influences insects. This paper examines the influence of temperature on developmental stages, fecundity, survival rate and demographic parameters of Cinara tujafilina (Hemiptera: Aphidoidea, Lachnidae), connected with decorative plants of the Cupressaceae family. C. tujafilina was reared in a laboratory on T. orientalis at five constant temperatures of 10, 15, 20, 25 and 28°C, 70% humidity and 14L:10D. The pre-reproduction stage varied from 7 at 25°C to 19 days at 10°C. Developmental threshold was assigned at 3.5°C. The longest reproduction stage for the aphids developing was recorded at 25°C, namely 33 days, while the shortest, at the temperature of 10°C, lasted 8 days. At 25°C this species is characterised by the shortest pre-reproduction stage, the highest fecundity, the highest survival rate and the highest demographic parameters, particularly rm (0.17). The results suggest that the optimal temperature for the species is 25°C, and indicate that climatic change will favourably influence its development and increase its role as a pest of decorative plants.  相似文献   

20.
The effect of temperature on the life table of Acyrthosiphon pisum reared on Pisum sativum was evaluated under laboratory conditions using temperatures of 10, 15, 20, 25, 30, and 35°C. The development time of juvenile A. pisum decreased with increasing temperature (from 21.3 days at 10°C to 4.7 days at 35°C). Adult longevity also decreased with increasing temperature (from 53.2 days at 10°C to 2.3 days at 35°C). Interestingly, 70% and 25% of A. pisum nymphs reared at 30°C and 35°C, respectively, successfully developed into adults. These temperatures have previously been considered unsuitable for A. pisum development. However, adult aphids reared at 30°C and 35°C failed to reproduce. Linear regression analysis revealed that the lower development threshold of A. pisum was 153.1 degree‐days above 1.9°C. Maximal average reproductive capability was observed at 10°C for A. pisum adults, with each adult producing more than 120 nymphs. The intrinsic rate of increase (rm) of A. pisum increased from 0.124/day at 10°C to 0.337/day at 25°C, whereas opposite trends were observed for the net reproductive rate (R0) and the mean generation time (GT). At 20°C and 25°C, the intrinsic rate of increase of A. pisum was significantly higher than at 10°C and 15°C (P < 0.0001), indicating that 20°C and 25°C are within the optimal range for the growth of A. pisum, and that 30°C is beyond the upper threshold limit for reproduction, which involves a temperature range that is narrower than that of the survival range (upper limit is unknown, but above 35°C).  相似文献   

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