Thermal effects on the biological parameters of the predatory mirid Pilophorus gallicus (Hemiptera: Miridae)

Pilophorus gallicus Remane (Hemiptera: Miridae) is a predatory mirid reported in deciduous trees in the western Mediterranean area. This work aimed to determine the biological and demographic parameters for this species at different temperatures (15, 20, 25 and 30°C). Egg hatching times shortened from 57.8 days at 15°C to 9.2 days at 30°C, and nymphal development times declined from 62.8 days at 15°C to 11.1 days at 30°C. The hatching and nymphal survival rates were low at 15 and 30°C. The lower thermal thresholds for the egg and nymphal development were 12.4 and 12.0°C, respectively. These high thermal thresholds could be a safety mechanism to avoid the emergence of nymphs in the unfavorable winter period. Female weight increased between 15 and 25°C and decreased at 30°C. The fecundity increased from 70.2 eggs per female at 15°C to 212.4 eggs per female at 25°C, and decreased to 88.5 eggs per female at 30°C. Fertility ranged from 9.4% at 15°C to 40.9% at 25°C, being 24.9% at 30°C. The intrinsic rate of natural increase (r_m) rose from 0.001 to 0.081 between 15 and 25°C and decreased to 0.05 at 30°C. In summary, this species performs poorly at low temperatures and has a relative tolerance of high temperatures (30°C); its performance was best at 25°C. Knowledge of the variation in the biological parameters with temperature may be very useful for the understanding of its ecology and population dynamics.     

Life history parameters for Nesidiocoris tenuis (Reuter) (Het., Miridae) under different temperature regimes

The development time for eggs and nymphs and female fertility were determined for Nesidiocoris tenuis Reuter (Het., Miridae: Dicyphini) at 15, 20, 25, 30, 35 and 40 ± 1°C, using tomato, Solanum esculentum (Miller), as substrate and eggs of Ephestia kuehniella Zeller as substitute prey. At 40°C, N. tenuis was unable to develop and barely reproduced. Egg development ranged from 30.8 days at 15°C to 6.3 days at 35°C. The cumulative thermal requirements for the eggs were 148.6 degree days (°d) and the lower thermal threshold, 10.3°C. The duration of the nymphal instar decreased from 55.9 days at 15°C to 8.6 days at 35°C. The thermal constant for the nymphs was 182.3 °d and the lower thermal threshold 11.7°C. No nymphs survived at 40°C, and the highest mortalities were at extreme temperatures (15 and 35°C). Female and male weights were influenced significantly by temperature. The fertility of N. tenuis females was reduced greatly at 15 and 40°C. The highest fertility during an observation period of 18 days following female emergence (79.5–60.0 nymphs per female) was within the temperature range of 20 to 35°C. Fertility was related directly to female weight and temperature (r² = 0.932). Based on development, reproduction data and thermal requirements, the optimum temperature range for N. tenuis was established as being between 20 and 30°C. Overall, N. tenuis is the most thermophilous of all dicyphines from vegetable crops in the Mediterranean area studied so far.     

Early warning of egg hatching in pea moth (Cydia nigricana)

Female pea moths (Cydia nigricana) kept at 23 ^oC began to lay eggs 2–3 days after emergence, lived for 16–21 days and laid on average 71 eggs. Individuals kept in field cages lived for slightly longer and laid on average 91 eggs. About 85% of eggs were laid during the first 11 days of the oviposition period, usually in the late afternoon and early evening. The relationship between the rate of egg development and temperature was defined. The estimated developmental zero was 9-4 ^oC at constant temperatures and 8-5 ^oC at fluctuating temperatures. Above 28 ^oC mortality increased and above 31 ^oC development was apparently retarded. Development at constant temperatures took 6–16% longer than at fluctuating temperatures with the same mean. Estimates of hatching dates in the field made from temperature data recorded at several sites in and near a pea crop, and 8 km distant, were usually within a day of the observed date. In warm weather, estimated and observed dates usually coincided; in cooler weather hatching was 2–3 days later than expected. Hatching dates predicted from temperature data after only 80% of development had occurred were correct on 28 out of 36 occasions. An example is given to show how the method could be used eventually with a sex attractant trapping system to provide early warning of first hatching and spraying dates.     

The effect of temperature on the egg incubation period and nymphal growth of two Nemoura species (Plecoptera) from subarctic fennoscandia

Field studies of Nemoura arctica and N. viki showed that the two species preferred different biotopes and indicated differences in their life‐cycles. N. arctica seemed to have a semivoltine life‐cycle, at least in some years, this was not the case for N. viki.

Laboratory studies showed that the temperature tolerance of the eggs of N. arctica was wider than for those of N. viki. The length of the egg incubation period of both species was influenced by the ambient temperature, but no significant interspecific difference existed between the regression lines of the relationship between the temperature (T°C) and egg incubation period (Y days), as given by the regression equation Y = aT^?b for the log values. Reared at constant food supply, nymphal growth occurred in two periods. Firstly a rapid growth to about 4 mm, followed by a period of slow growth until emergence. During the first period growth (G)at (D) days was linear, according to the simple linear regression equation G = a+bD . The temperature tolerance of the nymphs of N. arctica was wider than for those of N. viki and significant interspecific differences between the species in growth were recorded at relatively high rearing temperatures, such as 12° and 16°C, but not at low temperatures. At constant food supply, nymphal growth was greatly influenced by the rearing temperature. At a mean temperature of 16°C N. arctica nymphs grew rapidly and emerged after 120 days; whereas at a mean temperature of 4°C growt h was slow and the nymphs did not even manage to reach the emergence stage after 700 days.     

Development times and fecundity of three important arthropod pests of strawberry in the United Kingdom

The development rates and fecundity of three important pests of strawberry in the UK were determined over a range of temperatures. Development time of the strawberry tarsonemid mite, Phytonemus pallidus, from egg lay to adult, ranged from a mean of 28.4 days at 12.5°C to 8.8 days at 25°C. No nymphs developed to adult at 10°C. Females lived for up to 45 days and laid a mean of 24.3 and 28.5 eggs at 20°C and 25°C respectively. Total development time from egg lay to adult for the strawberry blossom weevil, Anthonomus rubi, ranged from a mean of 95.7 days at 10°C to 18.2 days at 25°C. Mean fecundity at 20°C was 157.6 eggs, and the oviposition period averaged 71.6 days. When nymphs were reared on strawberry, development of the European tarnished plant bug, Lygus rugulipennis, from egg lay to adult, ranged from 83.8 days at 15°C to 28.8 days at 25°C. Development times on groundsel were shorter and ranged from 65.6 to 22.2 days at 15°C and 25°C. Only two nymphs developed to adults at 10°C; no eggs hatched at that temperature. Mean fecundity at 20°C was 75.4 eggs, but ranged from 23 to 179. Under a fluctuating temperature regime of 10°C for 12 h:20°C for 12 h, nymphs of L. rugulipennis took 40.3 days to become adult on strawberry, and 33.4 days on groundsel. Simple linear models fitted the developmental rate ‐ constant temperature relationship well for all species, accounting for 95–98% of the total variation in observed developmental rates. Development under fluctuating temperatures illustrated the potential problem of extrapolating linear models beyond the conditions of the experiment.     

The effect of temperature on the behaviour and development of Triatoma brasiliensis

Abstract. The effects of temperature on the development of early stages and the thermopreference of nymphs and adults were analysed in the haematophagous bug Triatoma brasiliensis Neiva, 1911 (Hemiptera, Reduviidae). Egg hatching, mortality of nymphs, feeding and moulting success of the early stages of T. brasiliensis were all affected by temperature. While high rates of egg hatching were observed between 25 and 27 °C, no hatching occurred at 12, 19 and 38 °C. The mortality of first‐instar nymphs was highest at 38 °C, at which no insects survived after 10 days of exposure. Feeding success was only affected at the lowest temperature (12 °C). No ecdysis was observed in the groups exposed to 12, 19 and 21 °C. Recently fed fourth‐instar nymphs preferred to stay at a temperature of approximately 30 °C. The preferred temperature began to decline gradually to approximately 27 °C during ecdysis, reaching 26 °C at 30 days after ecdysis. After a second blood meal, the insects' preferred temperature was again approximately 30 °C. The thermopreference pattern of females was similar to that of nymphs. Nymphs and females showed a daily fluctuation in their preferred temperature, moving towards higher values at the beginning of the dark phase, and choosing lower ones after this time interval, at which they remained until the end of the light phase. The females laid their eggs in all sectors of the arena, although the largest numbers of eggs were found between 28 and 32 °C.     

Development and feeding of <Emphasis Type="Italic">Tetraphleps galchanoides</Emphasis>, a predator of the hemlock woolly adelgid

Tetraphleps galchanoides Ghauri (Hemiptera: Anthocoridae) nymphs were collected from hemlock woolly adelgid (HWA) Adelges tsugae Annand (Hemiptera: Adelgidae) infested Tsuga sp. in Baoxing, Sichuan, China. First and second stage nymphs collected from foliage shipped from China; were reared to adults and tested for feeding rates and host preferences. They were reared at 5, 8, 12, and 15 ± 1 °C from November to December, January to March, April, and May to June, respectively, in the quarantine laboratory at Virginia Polytechnic Institute and State University. At 8 °C, development time was 15, 20, and 40 days for the N-III, IV, and V nymphal stages, respectively. Adult males lived 83 days with a range of 21–147 days. A single adult female lived for 21 days. At 5 °C, second stage T. galchanoides nymphs consumed 0.8 HWA nymphs per day, and 2.0 HWA nymphs per day at the N-V stage. At 8 °C, consumption of HWA nymphs ranged from 1.3 to 3.4 nymphs per day for the N-III to N-V stages, respectively. Adult T. galchanoides consumed more HWA eggs than HWA adults, pine bark adelgid (PBA) Pineus strobi (Hartig) (Hemiptera: Adelgidae) adults, and eggs in no-choice tests. In choice tests with HWA eggs and PBA eggs, more HWA eggs were eaten. Adult and nymph body measurements are presented for determination of nymphal instars.     

Temperature effects on development ofOrius tantillus (Het.: Anthocoridae), A predator ofThrips palmi (Thys.: Thripidae)

To explore the possibility of usingOrius tantillus (Motschulsky) as a control agent againstThrips palmi Karny in greenhouses in Japan during the winter months, the effects of temperature on the development of eggs and nymphs of this predator were determined by rearing individuals under eight constant temperatures ranging from 17.5–35.0°C. Estimates of lower developmental threshold temperatures for eggs, male nymphs and female nymphs were 13.7°C, 11.9°C and 13.4°C, respectively. These estimates were lower than the average winter temperature at night in greenhouses in Japan, suggesting thatO. tantillus could possibly be used for the control ofT. palmi in such greenhouses. Thermal constants were estimated at 52.6, 185.2 and 153.8 degree days for eggs, male nymphs and female nymphs, respectively. Egg survival at temperatures between 20°C and 30°C was higher (p=0.05) than at 17.5°C.     

Zur fortpflanzungsbiologie von mesostoma ehrenbergii (Focke, 1836) (Turbellaria)

1. At temperature levels from 10 to 25°C animals from resting eggs produce subitaneous eggs independent on temperature. In contrast animals from subitaneous eggs produce subitaneous eggs dependent on temperature. At a high rate subitaneous eggs are only formed at temperature levels above 20°C.
2. Below 10°C no development occurs in the juveniles. At temperatures of 30/22°C (24.7°C) the first subitaneous eggs are formed after 6–9 days, at 14/9°C (10.7°C) they are formed after 34 days. At different temperature levels the developmental rate of the young is from 10.5 to 42 days. One generation extends over 16.5 (30/22°C) to 75 days (14/9°C). The average egg production is 10–20 subitaneous eggs or 30–60 resting eggs. The maximum egg production of one individual is 50 subitaneous eggs or 84 resting eggs. 50% of the animals have just formed resting eggs, before the juveniles are hatched. Resting eggs in the first egg-batch are formed 6–20 days later than subitaneous eggs. The duration of life is between 65 (30/22°C) and 140 days (19/13°C).
3. Young worms in resting eggs have a dormance period of at least 15–30 days.

At room temperatures (20°C) no juvenile in resting eggs hatches from water. By combining room and refrigerator (3.5°C) temperatures the hatching rate increases to a maximum of 85%. To reach a hatching rate of 50–65% the influence of low temperatures must be at least 30 days. At room temperatures 60% of the young in resting eggs hatch from mud covered with water. Combining high and low temperatures the hatching success is between 67 and 81%, where the highest percentage of the young may hatch at room temperature. Up to 90 days low temperatures cause a maximum hatching rate of 79%. It decreases to approximately 30% after 180 days. At high temperatures resting eggs preserved in 100% moist mud, survive for two months. By adding a period of low temperatures the hatching rate increases to a maximum of 52%. Low temperatures are survived for more than 6 months. Up to 30 days preservation at 3.5°C causes a maximum hatching rate of 61%, up to 12o days it decreases to 30%. At room temperature the young in resting eggs are not resistant against air-dried mud (30–40% rel. air moisture). Combining high and low temperatures air-dried mud is endured 1 month (hatching rate 5–14%). Preservation of 30–120 days at 3.5°C and 70% rel. air moisture result in a hatching rate of 43–61%. li]4. In the open air in Middle-Europe there occur 5–6 generations of M. ehrenbergii per life-cycle. The first generation hatches from resting eggs in May, where the production of subitaneous eggs is independent on temperature. All other generations up to October hatch from subitaneous eggs. The egg-production of those worms is dependent on environmental factors. In summer subitaneous egg production prevails, in autumn resting egg production. The abundance during the life-cycle is dependent on the number of animals which produce subitaneous eggs. Resting eggs are predestinated to endure periods of dryness and cold. The life-cycles of the species M. lingua and M. productum are different from those of M. ehrenbergii in length and in the number of generations. In both species 7 generations occur over 8 to 8.5 respectively 5.5 months. M. nigrirostrum only forms resting eggs. The life-cycle consists of one generation from February/March to May/June.     

Effect of temperature on reproduction and embryonic development of the cabbage stem flea beetle,Psylliodes chrysocephala L., (Coleoptera: Chrysomelidae)

The cabbage stem flea beetle, Psylliodes chrysocephala (L.) (Coleoptera: Chrysomelidae), is a major pest of winter oilseed rape. Despite the importance of this pest, detailed information on reproduction to predict risk of crop damage is lacking. This study investigates the effect of temperature on parameters of reproduction, egg development and viability at five constant temperatures. Significant temperature effects were found on the pre‐oviposition period, total number of eggs laid, daily oviposition rate, female longevity, egg‐development rate and viability. The mean length of the pre‐oviposition period ranged from 93.1 days at 4°C to 14.6 days at 20°C. Analysis of total number of eggs laid and daily oviposition rate during female lifespan estimated the highest total number of eggs laid (696 eggs/female) at 16°C and the highest oviposition rate (6.8 eggs/female and day) at 20°C. The daily oviposition rate at 20°C was not significantly higher than 5.4 eggs/female and day at 16°C. Female longevity was significantly longer at 4°C, shorter at 20°C and not significantly different between 8, 12 and 16°C. Estimated 50% survival time of females was 239, 153, 195, 186 and 78 days at 4, 8, 12, 16 and 20°C, respectively. A linear model of egg development at 8–20°C estimated the lower developmental threshold to be 5.1°C and the thermal constant for development 184.9 degree‐days. The percentage of eggs hatching was significantly lower at 4°C than at all other temperatures tested. The estimated mean hatching percentages were 47.3%, 70.0%, 72.4%, 66.2% and 67.9% at 4, 8, 12, 16 and 20°C, respectively. These results can be used to predict the start and intensity of egg‐laying in the autumn and the appearance of larvae in the field from knowledge about time of field invasion and from monitoring the weather.     

Effect of temperature on survival and immature development of Arma chinensis

Arma chinensis (Fallou) is a predaceous pentatomid with the potential to control a wide range of insect pests. In this study, the stage-specific temperature-dependent development and survival of A. chinensis was investigated under seven constant temperatures (range 18–35 °C) when fed with yellow mealworm (Tenebrio molitor L.). Developmental times (in days) for the immature stage, entire nymphal stage, and egg-to-adult development were inversely proportional to temperatures between 18 and 33 °C (30 °C for eggs and 1st instar nymphs). The lowest survival rate of A. chinensis was observed at 18 °C (6.7%), whereas it was the highest (80–93.3%) at temperatures ranging from 21 to 24 °C. The low temperature thresholds for the egg, entire nymph stage, and egg-to-adult development were 14.3, 12.28, and 12.8 °C, respectively, while the thermal constants for these stages were estimated to be 85.47, 334.9, and 423.8° days. Among the three non-linear models examined, the Taylor model showed the best fit for the egg data, the Briére1 model was the best fit for the 1st instar nymph stage, and the Lactin1 model was more approprate for all the other instar stages, the entire nymphal stage, and overall development. The upper temperature thresholds estimated using the Lactin1 model for eggs, overall nymphal stage, and egg-to-adult development were 38.57, 38.9, and 40.0 °C. The optimal temperature for the overall egg-to-adult period was estimated to be 33.5 °C. The results of this study can be used for the mass rearing of this natural pest enemy and development of phenology models of its seasonal progress.     

Effect of temperature on the biology of Creontiades dilutus (Stål) (Heteroptera: Miridae)

The egg and nymphal development, fecundity and survival of the green mirid, Creontiades dilutus were examined at a range of temperatures and a modified day-degree model fitted to the data. Day degree (DD) requirements for egg and nymphal development, and threshold temperatures were calculated from the fitted lines. Female fecundity and longevity, egg and nymphal development, and survival of C. dilutus were significantly influenced by temperature. Eggs and nymphs failed to complete development at temperatures below 17 and at 38°C. Females also failed to produce any eggs at 11 and 38°C. The optimum temperature range for female fecundity was found to be 26–32°C. The optimum temperature for the development of eggs was calculated from the model as 30.5°C and for nymphs as 31.5°C. The threshold temperature for development was 15.8°C for egg and 15.1°C for nymph; 69.4 and 156.7 DD were required for completing the egg and the nymphal development, respectively. At the optimum temperature, it was estimated that development from egg to adult took 15 days. Survival was highest at 26°C for eggs and at 30–32°C for nymphs.     

Biology of Triatoma flavida Neiva, 1911 (Hemiptera: Reduviidae) under laboratory conditions

The complete life cycle of Triatoma flavida, weekly fed on hens, was studied at 28+/-2 degrees C and 80+/-10% RH. Aspects related to hatching, life span, mortality and feeding behavior for each stage of its life cycle were evaluated. The hatching rate observed for 100 eggs was 93% with an average incubation period of 27.2 days. Sixty-two nymphs completed the cycle and the mean egg to adult development time was 230.4 days. Mean duration of 1st, 2nd, 3rd, 4th and 5th instar nymphs was 22.1, 25.3, 36.7, 49.7 and 69.4 days, respectively. The number of blood meals on each nymphal stage varied from 1 to 7. The mortality rate was 6.5% for NI, 23% for NIII and 7.5% for NV nymphs. Mean number of laid eggs per female was 283.1. Adult survival rates were 344.8 +/- 256.4 days for males and 285.3 +/- 201.8 days for females.     

Etude expérimentale de Tincubation des oeufs de Baetis rhodani Pictet

The eggs of Baetis rhodani were collected from natural conditions just after laying and incubated at different constant temperatures (from 7-5°C to 27-5°C) with a constant photoperiod. The incubation period was shorter at higher temperatures up to 25°C (8 days); above this eggs no longer hatched. The slowest development (determined by extrapolation) was at about 3°C (theoretically 130 days). The hatching period was always very short (about 3-5 days). Fewer eggs hatched at higher temperatures.     

Field and laboratory studies on the effects of temperature on the development of the carrot fly (Psila rosae F.)

The thermal requirements for the pre-oviposition period, egg, larval, pupal and adult stages of the carrot fly were measured under field conditions and at a range of constant temperatures in the laboratory. In the laboratory, the pre-oviposition period lasted from 4 days at 24^oC to 28 days at 9^oC. In general, female carrot flies laid about 20–40 eggs in each batch. Once the first eggs had been laid, subsequent batches were laid after an average of 3 days at 24^oC to 7 days at 11.5^oC. The numbers of days required for egg, larval and pupal development ranged from 5, 31 and 24 days respectively at 21.5^oC to 25, 145 and 84 days respectively at 9^oC. Under laboratory conditions, complete development from egg to adult required from 60 days at 21.5^oC to 254 days at 9^oC. Newly-formed carrot fly pupae were exposed to temperatures of 22–30^oC for various 5–10 day periods during pupal development. Exposure to temperatures of 24^oC and 26^oC caused some, and exposure to 28^oC and 30^oC caused all, of the pupae to delay development. Pupae were sensitive to high temperatures only for approximately 4–10 days after pupation. Under field conditions between mid-May and early September, full carrot fly development (egg-adult) took 84–100 days. The numbers of day-degrees required (base temperatures of 2^oC and 4^oC) for carrot fly development in the laboratory and in the field were similar for egg hatching but not for the pre-oviposition period or for egg-adult development. The thermal requirement for fly development in the field varied between inoculation dates, fewest day-degrees being required when development was rapid.     

Comparative study of temperature‐dependent life histories of three economically important Adelphocoris spp.

Subsequent to the widespread adoption of Bt transgenic cotton in China and an associated reduction in pesticide use, Adelphocoris spp. (Hemiptera: Miridae) are the key pests of this crop. Three species (Adelphocoris suturalis, Adelphocoris fasciaticollis and Adelphocoris lineolatus) are found in Chinese Bt cotton fields, each with a distinct geographic distribution and phenology. In the present study, the development and fecundity of the three species are compared in the laboratory at various temperatures in the range 10–35 °C. Although nymphal development and adult moulting occurs under all temperature regimes, egg eclosion is not observed at 10 °C. In general, egg and nymphal development periods decrease with increasing temperature up to 30 °C. The lower and upper development thresholds are, respectively, 5.6 and 40.1 °C for A. suturalis eggs; 5.0 and 38.4 °C for nymphs; 6.3 and 39.0 °C for A. fasciaticollis eggs, 3.0 and 41.9 °C for nymphs; 5.6 and 41.3 °C for A. lineolatus eggs; and 6.2 and 38.8 °C for nymphs. Thermal constants are 189.9 degree days (DD) (egg) and 308.8 DD (nymph) for A. suturalis, 188.8 DD (egg) and 366.7 DD (nymph) for A. fasciaticollis, and 231.7 DD (egg) and 291.6 DD (nymph) for A. lineolatus. Temperatures above 30 °C affect egg development of A. fasciaticollis and A. lineolatus adversely, but not that of A. suturalis. At the same time, nymphal survival of A. suturalis is reduced at 10 °C. Longevity of all species declines with increasing temperature, whereas extremes of temperature (i.e. 10 and 35 °C) interfere with oviposition. The estimated optimum range for oviposition is 23–25 °C, irrespective of species. In general, development and fecundity of the three Adelphocoris spp. is consistent with their respective distribution and seasonal dynamics. The present study provides insight into the distribution and phenology of Adelphocoris spp., and contributes to the modelling of their population dynamics.     

Establishment potential of the predatory mirid <Emphasis Type="Italic">Dicyphus hesperus</Emphasis> in northern Europe

The predatory mirid Dicyphus hesperus Knight (Hemiptera: Miridae) is native to North America. The species has been used for the control of glasshouse whitefly on aubergine in the Netherlands, and is currently being evaluated for continued and wider release in Europe. Field and laboratory studies were conducted on a population collected from southern California, USA, to assess the cold tolerance and potential for outdoor establishment under prevailing northern European climates. The supercooling points (whole animal freezing temperatures) of nymphal and adult insects were around −20°C. The lethal temperatures (LTemp₅₀) of non-diapausing nymphs and adults and diapausing adults were close to their respective freezing temperatures at −17.6, −17.6 and −19.2°C. At 5°C, the LTime₅₀ was 54, 101.7 and 117.5 days for fed nymphs, non-diapausing and diapausing adults respectively. When first instar nymphs were placed in the field in winter, starved samples died out after 70 days, but 5% of the fed nymphs survived until the end of winter (140 days) and developed to adult on return to the laboratory. After a similar 5-month field exposure, 50% of fed diapausing adults and 15% of fed non-diapausing adults were still alive at the end of winter, whereas starved diapausing adults died after 140 days. On return to the laboratory after 5 months in the field, both diapausing and non-diapausing adults mated and laid eggs, forming viable populations. Overall, the field and laboratory experiments indicate that this population of D. hesperus is able to enter diapause and that winter temperatures are not a barrier to establishment in northern Europe.     

Hatching of Daphnia sexual eggs. II. The effect of age and a second stimulus

• 1 We examined the effect of age on the hatching response of Daphnia magna sexual eggs of specific families. For old eggs (>2 years), hatching characteristics were compared at two storage temperatures (4°C and 20°C). Also, the hatching response after a second dark incubation and subsequent incubation under conditions favourable for hatching was compared with that after the first stimulus.
• 2 Daphnia sexual eggs were found to remain viable for several (at least 4.5) years. The effect of age on the hatching rate was family dependent. At least in some families, hatching rate was higher for old (>2 years) than for young (<5 months) eggs. Low temperature (4°C) during dark incubation resulted in a higher hatching rate compared with incubation at 20°C.
• 3 The application of a second hatching stimulus resulted in a renewed hatching response. The overall hatching rate after the second stimulus was, however, lower than that of the first stimulus.
• 4 More than 80% of the hatchlings of young eggs appeared on Day 3 or 4, with minor between-family differences in time distribution of hatching. The timing of the response to hatching stimuli was more variable in old than in young eggs, with the average time at hatching being 6.4 instead of 4.0 days. The response to the application of hatching stimuli was also slower after the second stimulus compared with the first stimulus.

     

The effects of temperature on development of the large narcissus fly (Merodon equestris)

Eggs, larvae, pupae and adults of the large narcissus fly (Merodon equestris) were reared at a series of constant temperatures between 9–24°C. Egg development required from 37 days at 9°C to 7 days at 21.5°C. The low-temperature threshold for development was 6.7°C. Larvae reared at 1424°C were fully-grown after 18 weeks, but it took much longer for such insects to pupate, and adult flies emerged only after about 45 weeks of development. Large narcissus flies enter diapause during the larval stage and overwinter as fully-fed larvae, forming pupae in the following spring. Post-winter pupation and pupal development took from 169 days at 10°C to 36 days at 21.5°C. Of this, pupal development required from 91 days at 10°C to 19 days at 21.5°C. The low-temperature threshold for post-winter pupation and pupal development was 7.1°C, and for pupal development alone, 7.2°C. Females maintained at or below 19°C laid few eggs, whereas some females kept at or above 21.5°C laid more than 100 eggs (mean 69 ± 36). Approximately 50% of females maintained at or above 21.5°C laid less than 10 eggs during their lifetime. The mean egg-laying time was 6 to 9 days. Although temperatures at or below 19°C inhibited mating, once a female had mated, such temperatures did not prevent oviposition.     

How incubation temperature influences the physiology and growth of embryonic lizards

Eggs of two small Australian lizards, Lampropholis guichenoti and Bassiana duperreyi, were incubated to hatching at 25 °C and 30 °C. Incubation periods were significantly longer at 25 °C in both species, and temperature had a greater effect on the incubation period of B. duperreyi (41.0 days at 25 °C; 23.1 days at 30 °C) than L. guichenoti (40.1 days at 25 °C; 27.7 days at 30 °C). Patterns of oxygen consumption were similar in both species at both temperatures, being sigmoidal in shape with a fall in the rate of oxygen consumption just prior to hatching. The higher incubation temperature resulted in higher peak and higher pre-hatch rates of oxygen consumption in both species. Total amount of oxygen consumed during incubation was independent of temperature in B. duperreyi, in which approximately 50 ml oxygen was consumed at both temperatures, but eggs of L. guichenoti incubated at 30 °C consumed significantly more (32.6 ml) than eggs incubated at 25 °C (28.5 ml). Hatchling mass was unaffected by either incubation temperature or the amount of water absorbed by eggs during incubation in both species. The energetic production cost of hatchling B. duperreyi (3.52 kJ · g⁻¹) was independent of incubation temperature, whereas in L. guichenoti the production cost was greater at 30 °C (4.00 kJ · g⁻¹) than at 25 °C (3.47 kJ · g⁻¹). Snout-vent lengths and mass of hatchlings were unaffected by incubation temperature in both species, but hatchling B. duperreyi incubated at 30 °C had longer tails (29.3 mm) than those from eggs incubated at 25 °C (26.2 mm). These results indicate that incubation temperature can affect the quality of hatchling lizards in terms of embryonic energy consumption and hatchling morphology. Accepted: 27 January 2000