Development, survivorship, and reproduction of Helicoverpa armigera (Lepidoptera: Noctuidae) under constant and alternating temperatures

Laboratory studies were conducted to assess the effect of temperature on the survival, development, fecundity, and longevity of Helicoverpa armigera (Hübner) at 11 constant temperatures ranging from 12.5 to 40 degrees C, as well as at five alternating temperature regimes (25-10, 30-15, 32.5-17.5, 35-20, and 35-27.5 degrees C) and under a photoperiod of 16:8 (L:D) h. H. armigera reared at constant temperatures did not develop from egg to adult (emergence) outside the temperature range of 17.5-32.5 degrees C. The alternating conditions expanded this range from 10 to 35 degrees C. The lowest developmental thresholds of the immature stages were estimated by a linear model and ranged from 10.17 (pupal stage) to 11.95 degrees C (egg stage) at constant temperature regimes and from 1.1 to 5.5 degrees C, respectively at alternating temperatures. The values of developmental thresholds estimated using the nonlinear (Lactin-2) model were lower than those estimated by the linear model for constant and alternating temperature regimes except for larval and pupal stages at constant temperatures. Mean adult longevity fluctuated from 34.4 d at 15 degrees C to 7.6 d at 35 degrees C. Females reared under all alternating temperature regimes laid more eggs than females reared at any, except the 25 degrees C, constant temperature treatment. The intrinsic rate of increase was highest at 27.5 degrees C, at both the constant and the corresponding alternating temperature regimes (0.147 and 0.139, respectively). Extreme temperatures had a negative effect on life table parameters.     

Temperature-dependent development and demography of Scymnus subvillosus (Coleoptera: Coccinellidae) reared on Hyalopterus pruni (Homoptera: Aphididae)

The development, survival, and fecundity of Scymnus subvillosus (Goeze) (Coleoptera: Coccinellidae) were studied at 20, 25, 30, and 35 degrees C, 60 +/- 5% RH, and a photoperiod of 16:8 (L:D) h (5,000 lux) under laboratory conditions. The total developmental time from egg hatch to adult eclosion ranged from 22.6 d at 20 degrees C to 10.6 d at 35 degrees C. The developmental rates of the egg stage, the larval stage, and total preadult stage at different temperatures increased linearly with increasing temperature. The thermal summation of the egg stage, the larval stage, and the total preadult stage was 77.5, 145.8 and 300 degree-days (DD), respectively. The developmental threshold of the egg stage, the larval stage, and the total preadult stage was 7.4, 4.1, and 7.1 degrees C, respectively. The life history raw data were analyzed using the age-stage, two-sex life table. The intrinsic rate of increase was 0.0845, 0.1138, 0.1395, and 0.0668 d(-1) at 20, 25, 30, and 35 degrees C, respectively. The net reproductive rate was highest at 25 degrees C (R0 = 78.7), and lowest at 35 degrees C (R0 = 4.7). The mean generation time was shortest at 35 degrees C (T = 23.9 d). The life table data can be used for the projection of population growth and designing mass rearing programs.     

Effects of temperature and larval diet on development rates and survival of the dengue vector Aedes aegypti in north Queensland, Australia

Immature development times, survival rates and adult size (wing-lengths) of the mosquito Aedes aegypti (L.) (Diptera: Culicidae) were studied in the laboratory at temperatures of 10-40 degrees C. The duration of development from egg eclosion (hatching of the first instar) to adult was inversely related to temperature, ranging from 7.2 +/- 0.2 days at 35 degrees C to 39.7 +/- 2.3 days at 15 degrees C. The minimum temperature threshold for development (t) was determined as 8.3 +/- 3.6 degrees C and the thermal constant (K) was 181.2 +/- 36.1 day-degrees above the threshold. Maximum survival rates of 88-93% were obtained between 20 and 30 degrees C. Wing-length was inversely related to temperature. The sex ratio (female:male) was 1:1 at all temperatures tested (15, 20, 25 and 35 degrees C) except 30 degrees C (4:3). Under field conditions at Townsville and Charters Towers, north Queensland, the duration of immature development varied according to the container position (i.e. shaded or exposed) and the availability of food resources, as well as inversely with temperature. These data indicate that containers with an abundance of organic matter (e.g. those used for striking plant cuttings) or those amongst foliage or under trees (e.g. discarded plastic tubs and tyres) tended to produce the largest adult Ae. aegypti, which had faster development and better immature survival. As such progeny have been linked to a greater risk of dengue transmission, it would seem important to focus on control of such containers.     

Effect of thermoperiod on diapause intensity in Pyrrhocoris apterus (Heteroptera Pyrrhocoridae)

The intensity of adult diapause in Pyrrhocoris apterus was measured in two series of experiments as the duration of pre-oviposition period at a constant temperature of 25 degrees C after transfer from short (12L:12D) to long day conditions (18L:6D). Higher diapause intensity was induced with a thermoperiod than at constant temperatures. After the induction throughout larval instars 3-5 and during 4 weeks of adult life at short days and a thermoperiod of 25/15 degrees C the pre-oviposition period was 30+/-4 and 26+/-3 days. After induction at constant 25 degrees C the pre-oviposition period was 22+/-3 and 23+/-4 days, while after induction at constant 20 degrees C it was 17+/-4 and 19+/-4 days. Induction at a lower constant temperature of 20 degrees C was thus followed by a less intense diapause than the induction at a higher constant temperature of 25 degrees C. These counterintuitive results are discussed. The oxygen consumption rate measured at experimental temperatures prior to transfer from short to long days was higher at thermoperiodic conditions than at constant temperatures and it was similar at constant 20 and 25 degrees C. Thus, the oxygen consumption rate measured prior to the transfer was highest (indication of the least intense diapause) in the insects that showed later, after the transfer to long days, the longest pre-oviposition period (indication of the most intense diapause). Within the first two days after transfer to constant 25 degrees C, oxygen consumption rate measured at 25 degrees C decreased in the thermoperiodic insects, while it transiently increased in insects from constant 20 degrees C. Two days and later after the transfer, oxygen consumption rate was similar in all groups. Cold hardiness was not correlated with diapause intensity. The low lethal temperature in diapausing insects was correlated with the night temperature during diapause induction.     

The development and mortality of the free-living stages of Haemonchus contortus in laboratory culture.

Haemonchus contortus eggs were cultured in intact fecal pellets at various temperatures (5-35 degrees C) for 22 days. Temperature and relative humidity were kept constant throughout the incubation period. Nl larval development occurred at 5 degrees C; peak third-stage larval recovery occurred at 20 degrees C. Egg mortality was an age-dependent phenomenon, whereas larval mortality remained constant irrespective of larval age. Development was characterized by a minimum development time followed by a transition to the next stage which occurred at a constant rate. All rates were temperature dependent. The minimum development times reported here are much less than those previously reported. Based on these results a mathematical model was used to describe the demography of the free-living stages of H. contortus at various temperatures.     

Effects of photoperiod and temperature on the rhythm and free‐running of adult eclosion in the Indian meal moth Plodia interpunctella

The rhythm of adult eclosion in the Indian meal moth Plodia interpunctella Hübner (Lepidoptera: Pyralidae) is investigated under various photoperiods and temperatures aiming to determine the nature of the temperature compensation and the free‐running period. Insects that are committed to a nondiapause larval development show diel rhythms of adult eclosion at 30, 25 and 20 °C. At 30 °C, the eclosion peak (i.e. the mean time of eclosion) occurs approximately 20 h after lights off under an LD 4 : 20 h photocycle, and at approximately 15 h under an LD 20 : 4 h photocycle. At 25 °C, the peak of eclosion occurs approximately 19 h after lights off under an LD 2 : 20 h photocycle and at approximately 16 h under an LD 20 : 4 h photocycle. At 20 °C, the eclosion peak is significantly advanced under long days of >12 h (i.e. approximately 20 h after lights off under an LD 4 : 20 h photocycle and approximately 9 h under an LD 20 : 4 h photocycle), indicating an effect of both lights‐off and lights‐on signals on the timing of the adult eclosion. To determine the involvement of a self‐sustained oscillator, the rhythm of adult eclosion is examined under darkness at different temperatures (30 to 21 °C). The mean free‐running periods are 22.4, 22.8, 22.0 and 22.5 h at 30, 24, 23 and 22 °C, respectively, indicating that the eclosion rhythm is temperature‐compensated. However, this rhythm does not free‐run under constant darkness at 21 °C. Because a clear diel rhythm is observed under 24‐h photocycles at 20 °C, the oscillator might be damped out within 24 h at the lower temperature.     

Temperature-dependent development and immature survival of an aphidophagous ladybeetle, Propylea dissecta (Mulsant)

Development and survival of the immature stages of an aphidophagous ladybeetle, Propylea dissecta (Mulsant) was investigated at five constant temperatures, viz. 20, 25, 27, 30 and 35°C, using Aphis gossypii Glover as prey. Developmental period of all the life stages were significantly affected with change in constant temperature and developmental rate increased with increase in temperature. Theoretical lower thermal threshold for complete development and thermal constant was 10.39°C and 465.11 Day‐degrees, respectively. Of the various life stages, first instar larvae were most susceptible to mortality at temperatures between 20 and 30°C, whilst pre‐pupae suffered least mortality. Egg‐mortality was maximum at 35°C. Female biased sex ratios were obtained at all five temperatures tested with higher proportion of females at the extremes of temperature, thus suggesting that females are more thermal‐tolerant. Lowest mortality of immature stages with maximum larval survival and adult emergence was recorded at 27°C, while reverse was the case at 35°C. Thus, 27°C may be considered best for the laboratory rearing of P. dissecta.     

温度对棉大卷叶螟生长发育和繁殖的影响

本文利用生命表方法评价了温度对棉大卷叶螟生长发育和繁殖的影响.结果表明：在17 ℃～26 ℃温度范围内,棉大卷叶螟的发育历期随温度升高而显著缩短;当温度超过32 ℃时,其发育历期延长.棉大卷叶螟的世代起点发育温度为12.08 ℃,有效积温为436.2日·度.在17 ℃～35 ℃温度范围内,棉大卷叶螟的存活率在26 ℃下最高,其他温度下的存活率随温度的升高或降低而降低.在17 ℃～35 ℃之间,棉大卷叶螟实验种群的内禀增长率、世代净增殖率、周限增长率分别在29、26和32 ℃下最大,其值分别为0.1268、415.65和1.185.世代平均历期随着温度的升高而缩短,在17 ℃下最长,为89.11 d;在35 ℃下最短,为28.68 d.     

Temperature tolerance of the diamondback moth, Plutella xylostella (Lepidoptera: Yponomeutidae) in tropical and temperate regions of Asia

Temperature tolerance was investigated in nine populations of Plutella xylostella Linnaeus from tropical and temperate regions of Asia. At all rearing temperatures between 15 and 35 degrees C, no clear differences were observed in female egg production or larval development between tropical and temperate populations. Thus, tropical populations did not show a high-temperature tolerance superior to that of the temperate populations. In all populations, the net reproductive rate (number of new females born per female) largely depended on the number of eggs laid per female, and egg production significantly decreased with increasing temperature (P < 0.001). Larval developmental rate also showed a significant positive correlation with temperature (P < 0.001). Per cent hatch of eggs and larval survival did not show a significant correlation with temperature: hatching was constant between 15 and 32.5 degrees C, but considerably lower at 35 degrees C. Larval survival was similar between 15 and 30 degrees C, appreciably lower at 32.5 degrees C and declined to 0% at 35 degrees C. Based on these results, environmental conditions under which P. xylostella can maintain a high population density throughout the year in tropical and subtropical regions are discussed.     

Oviposition and eclosion periods of Ixodes didelphidis Fonseca and Aragão, 1951 (Acari: Ixodidae) under laboratory conditions

Oviposition and eclosion periods for Ixodes didelphidis were observed under two temperatures (25 degrees C and 27 degrees C) and 90-95% humidity. Although there was a significant increase in the eclosion period (p<0.05) and a tendency to increase the oviposition period at 25 degrees C, there was neither significant differences in the interval (days), until maximum peak of eclosion nor in the number of emerging larvae during the peak nor the total number of emerged larvae. These temperature values are not critical for embryological development of the species. Because at 27 degrees C and under high humidity the oviposition and eclosion periods are shorter, and the percentage of emerged larvae is higher, we consider this to be the ideal temperature for laboratory studies.     

Comparison of the circadian eclosion rhythm between non-diapause and diapause pupae in the onion fly, Delia antiqua: the change of rhythmicity

When pupae of Delia antiqua were transferred to constant darkness (DD) from light-dark (LD) cycles or constant light (LL), the sensitivity to light of the circadian clock controlling eclosion increased with age. The daily rhythm of eclosion appeared in both non-diapause and diapause pupae only when this transfer was made during late pharate adult development. When transferred from LL to DD in the early pupal stage, the adult eclosion was weakly rhythmic in non-diapause pupae but arrhythmic in diapause pupae. However, the sensitivity of the circadian clock to temperature cycles or steps was higher in diapause pupae than in non-diapause pupae; in the transfer to a constant 20 degrees C from a thermoperiod of 25 degrees C (12 h)/20 degrees C (12 h) on day 10 after pupation or from chilling (7.5 degrees C) in DD, the adult eclosion from diapause pupae was rhythmic but that from non-diapause pupae arrhythmic. In a transfer to 20 degrees C from the thermoperiod after the initiation of eclosion, rhythmicity was observed in both types of pupae. The larval stage was insensitive to the effect of LD cycle initiating the eclosion rhythm. In D. antiqua pupae in the soil under natural conditions, therefore, the thermoperiod in the late pupal stage would be the most important 'Zeitgeber' for the determination of eclosion timing.     

Temperature-related duration of aquatic stages of the Afrotropical malaria vector mosquito Anopheles gambiae in the laboratory

Vector abundance is an important factor governing disease risk and is often employed when modelling disease transmission. The longevity of the aquatic stages of mosquitoes (Diptera: Culicidae) dictates the rate of production of adults and hence the intensity of disease transmission. We examined how temperature influences the survival of larval stages (larvae and pupae) of Anopheles gambiae Giles sensu stricto and subsequent adult production of this most efficient malaria vector. Groups of 30 mosquitoes were reared at constant temperatures (from 10 to 40 degrees C) from the first instar and observed until death or metamorphosis of the last individual. Larvae developed into adults at temperatures ranging from 16 to 34 degrees C. Larval survival was shortest (< 7 days) at 10-12 degrees C and 38-40 degrees C, and longest (> 30 days) at 14-20 degrees C. Within the temperature range at which adults were produced, larval mortality was highest at the upper range 30-32 degrees C, with death (rather than adult emergence) representing over 70% of the terminal events. The optimal survival temperatures were lower than the temperatures at which development was quickest, suggesting a critical relationship between temperature and the life cycle of the insect. These data provide fundamental information about An. gambiae s.s. adult productivity at different temperatures, which may facilitate the construction of process-based models of malaria risk in Africa and the development of early warning systems for epidemics.     

Temperature-related development of the parasitoid wasp Nasonia vitripennis as forensic indicator

Development times of the forensically significant parasitic wasp Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae) from oviposition to pupation, and from oviposition to adult emergence, were studied in the laboratory at temperatures of 15-35 degrees C using host pupae of the blowfly Protophormia terraenovae (Robineau-Desvoidy) (Diptera: Calliphoridae). Total developmental time of N. vitripennis from oviposition to adult emergence (mean+/-SD) was 43.5+/-2.4, 22.5+/-1.1, 14.8+/-1.7 and 11.3+/-0.9 days when reared at 15, 20, 25 and 30 degrees C, respectively. At 35 degrees C, N. vitripennis did not develop successfully. The rate of total immature development (1/days) increased with temperature. From linear regression of development rates, it was determined that the minimum threshold (tL) for total immature development was 9.8 degrees C (approximately 10 degrees C). Above this threshold, the overall thermal constant (K) for N. vitripennis was found to be 224.3+/-1.7 degree-days.     

Survival and development of different life stages of three Ceratitis spp. (Diptera: Tephritidae) reared at five constant temperatures

Fruit flies (Diptera: Tephritidae) are the most damaging pests on fruit crops on Réunion Island, near Madagascar. Survival and development of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann), the Natal fruit fly, C. rosa Karsch and the Mascarenes fruit fly, C. catoirii Guérin-Mèneville were compared at five constant temperatures spanning 15 to 35 degrees C. Durations of the immature stages of C. capitata, C. rosa and C. catoirii ranged from 14.5-63.8, 18.8-65.7 and 16.8-65.8 days, respectively, at 30-15 degrees C. The lower developmental threshold and thermal constant were calculated using the temperature summation model. The thermal constant for total development of the immature stages of C. capitata, C. rosa and C. catoirii were 260, 405 and 356 DD, respectively. Species differed mainly during the larval stages and ovarian maturation period, with smaller differences in the egg stage. Ceratitis rosa appeared to be better adapted to low temperatures than the two other species as it showed a lower larval developmental threshold of 3.1 degrees C compared to 10.2 degrees C for C. capitata and 8.9 degrees C for C. catoirii. Overall, C. catoirii had a low survival rate within the range of temperatures studied. The different responses of the three Ceratitis species to various temperatures explain to some extent their distribution on the island. The results obtained will be used for optimizing laboratory rearing procedures and for constructing computer simulation models to predict fruit fly population dynamics.     

Temperature-dependent development of Chilocorus bipustulatus (Coleoptera: Coccinellidae)

The effect of temperature on development and survival of Chilocorus bipustulatus L. (Coleoptera: Coccinellidae), a predator of many scale insects, was studied under laboratory conditions. The duration of development of egg, first, second, third, and fourth larval instars, pupa, and preovioposition period at seven constant temperatures (15, 17.5, 20, 25, 30, 32.5, and 35°C) was measured. Development time decreased significantly with increasing temperature within the range 15-30°C. Survival was higher at medium temperatures (17.5-30(ο)C) in comparison with that at more extreme temperature regimens (15 and >30(ο)C). Egg and first larval instars were the stages where C. bipustulatus suffered the highest mortality levels at all temperatures. The highest survival was recorded when experimental individuals were older than the third larval instar. Thermal requirements of development (developmental thresholds, thermal constant, optimum temperature) of C. bipustulatus were estimated with application of linear and one nonlinear models (Logan I). Upper and lower developmental thresholds ranged between 35.2-37.9 and 11.1-13.0°C, respectively. The optimum temperature for development (where maximum rate of development occurs) was estimated at between 33.6 and 34.7°C. The thermal constant for total development was estimated 474.7 degree-days.     

Heat and cold-induced male sterility in Drosophila buzzatii: genetic variation among populations for the duration of sterility

Here we studied three phenotypic traits in Drosophila buzzatii that are strongly effected by temperature, and are expected to be closely associated with fitness in nature. The traits measured were thermal threshold of male sterility, time for males to gain fertility when reared at a sterility-inducing temperature and transferred to 25 degrees C on eclosion and survival after development. The last two traits were measured under four temperature regimes, constant 12 degrees C, 25 degrees C, 31 degrees C, and fluctuating 25 degrees C (18 h) and 38 degrees C (6 h). We looked for genetic variation in these traits and relations among them in four lines of D. buzzatii originating from Argentina and Tenerife. The thermal threshold of heat-induced male sterility was found to lie within the range of 30.0-31.0 degrees C. When measuring the time for males to gain fertility, males reared at a nonstressful temperature (25 degrees C) were fertile 58-67 h after emergence with only minor differences among lines. When reared constant 31 degrees C, males were fertile 174-225 h after hatching. The Argentinean lines were significantly faster in recovering from sterility than were the lines from Tenerife. When reared in a fluctuating temperature regime, differences among lines increased, dividing the lines into three significantly different groups, with a sterility period of 135-215 h. When reared at 12 degrees C from the pupal stage, males were fertile after 106-130 h with significant difference in the variance but not in the mean duration of sterility. Significant differences in viability were found among development temperatures, but not among lines, and viability and the duration of sterility seem to be genetically independent.     

Relationships between temperature, development and survival of different life stages of the tomato fruit fly, Neoceratitis cyanescens

The development and survival of female Neoceratitis cyanescens (Bezzi) (Diptera: Tephritidae) from egg to complete ovarian maturation were studied in the laboratory at five different constant temperatures: 15, 20, 25, 30, and 35 °C. The aim of this study was to get information on the influence of temperature on pre-mature stages, as a prerequisite to optimise rearing procedures and to understand temporal and geographical patterns of fruit fly occurrence. The developmental rate of the different life stages increased linearly with increasing temperatures up to 30 °C. The fastest development of pre-mature stages was recorded at 30 °C (22±1 days) and the slowest at 15 °C (98±3 days). The day-degrees requirements (K) to complete total development were 432.6 day-degrees. Lower temperature thresholds were 11.4, 11.9, 10.0, and 11.1 °C for egg, larval, pupal stages and ovarian maturation, respectively. The number of adults obtained from an initial batch of 100 eggs reached a maximum (64) at 25 °C. At 35 °C, no adults emerged. Larval developmental time was significantly shorter in green tomato fruits than in potato tubers at 15, 20, and 25 °C. Mortality rate of larvae was higher in green tomato fruits than in potato tubers at 25 and 30 °C.     

Development, survival and reproduction of black citrus aphid, Toxoptera aurantii (Hemiptera: Aphididae), as a function of temperature

The development, survival, and reproduction of the black citrus aphid Toxoptera aurantii (Boyer de Fonscolombe) were evaluated at ten constant temperatures (4, 7, 10, 15, 20, 25, 28, 30, 32 and 35 degrees C). Development was limited at 4 and 35 degrees C. Between 7 and 32 degrees C, developmental periods of immature stages varied from 44.2 days at 7 degrees C to 5.3 days at 28 degrees C. Overall immature development required 129.9 degree-days above 3.8 degrees C. The upper temperature thresholds of 32.3, 28.6, 29.3, 27.2, and 28.6 degrees C were determined from a non-linear biophysical model for the development of instars 1-4 and overall immature stages, respectively. Immature survivorship varied from 82.1 to 97.7% within the temperature range of 10-30 degrees C. However, immature survivorship was reduced to 26.3% at 7 degrees C and 33.1% at 32 degrees C. Mean adult longevity was the longest (44.2 days) at 15 degrees C and the shortest (6.2 days) at 32 degrees C. The predicted upper temperature limit for adult survivorship was at 32.3 degrees C. Total nymph production increased from 16.3 nymphs per female at 10 degrees C to 58.7 nymphs per female at 20 degrees C, declining to 6.1 nymphs per female at 32 degrees C. The estimation of lower and upper temperature limits for reproduction was at 8.2 and 32.5 degrees C, respectively. The population reared at 28 degrees C had the highest intrinsic rate of increase (0.394), the shortest population doubling time (1.8 days), and shortest mean generation time (9.5 days) compared with the populations reared at six other temperatures. The population reared at 20 degrees C had the highest net reproductive rate (54.6). The theoretical lower and upper temperature limits for population development, survival and reproduction were estimated at 9.4 and 30.4 degrees C, respectively. The biology of T. aurantii was also compared with three other citrus aphid species.     

Effect of temperature on development rate and fecundity of apterous Aphis gossypii Glover (Hom., Aphididae) reared on Gossypium hirsutum L.

The developmental time, survival and reproduction of the cotton aphid, Aphis gossypii Glover (Hom., Aphididae), were evaluated on detached cotton leaves at five constant and two alternating temperatures (15, 20, 25, 30, 35, 25/30, and 30/35°C). The developmental periods of the immature stages ranged from 12.0 days at 15°C to 4.5 days at 30°C. A constant temperature of 35°C was lethal to the immature stages of A. gossypii. The lower developmental threshold for the cotton aphid was estimated at 6.2°C and it required 108.9 degree-days for a first instar to become adult. The average longevity of adult females was reduced from 39.7 days at 15°C to 12.6 days at 30/35°C. The average reproduction rate per female was 51.5 at 25/30°C and 20.9 at 30/35°C. Mean generation time of the population ranged from 10.4 days at 30°C to 24.5 days at 15°C. The largest per capita growth rate ( r _m = 0.413) occurred at 30°C, the smallest at 15°C ( r _m = 0.177). It was evident that temperatures over 30°C prolonged development, increased the mortality of the immature stages, shortened adult longevity, and reduced fecundity. The optimal range of temperature for population growth of A. gossypii on cotton was 25/30–30°C.