Embryonic development, larval growth and life cycle of Coenagrion puella (Odonata: Zygoptera) from an Austrian pond

SUMMARY. 1. Newly-laid eggs of Coenagrion puella (L.) from a pond near Herzogenburg (Lower Austria) were kept at constant water temperatures (range c .3.5°C to c .28°C)in the laboratory. Hatching success varied with temperature; no eggs hatched below 12°C and nearly all hatched at c .l6°C. Hatching time decreased with increasing temperature and the relationship between the two variables within the range 12–28 °C was well described by a power law. The length of the hatching period was less than 12 days. Hatching times estimated from the power-law equations and those obtained in the field experiments were similar. Therefore both the hatching time and the length of the hatching period in the field could be estimated from the laboratory data for the range 12–28°C.
2. The maximum number of instars from egg to imago was 11; the average body length increment (mm) per moult was proportionately constant at c .26% and Dyar's rule was applicable. The interval between moults decreased with increasing temperature up to the seventh instar and the relationship between the two variables within the range 12–28°C was well described by a power law. The moulting interval for instars 8–11 ranged from 23 to 48 days and was relatively independent of temperature. No moulting occurred at temperatures below 12°C.
3. Larval growth was logistic in the laboratory and variations in mean logistic growth rate (range 0–2.5% length day⁻¹) were related to mean temperature with no growth at temperatures <12°C. Larval growth rates in pond experiments were similar to those estimated from laboratory data, and therefore the regression equations obtained from the laboratory experiments are probably applicable to larval growth in the field.
4. Information on the life cycle of C. puella is briefly reviewed and it is concluded that C. puella from the pond near Herzogenburg has an univoltine life cycle.     

Effect of temperature on the hatching time of eggs of Ephemerella ignita (Poda) (Ephemeroptera:Ephemerellidae)

SUMMARY. Eggs of Ephemerella ignita (Poda) were kept at eight constant temperatures (range 5.9–19.8°C) in the laboratory. Over 85% of the eggs hatched in the temperature range 10.0–14.2°C but the percentage decreased markedly to 39% at 5.9°C and 42% at 19.8°C. Hatching time (days after oviposition) decreased with increasing water temperature over the range 5.9–14.2°C and the relationship between the two variables was well described by a hyperbola. Therefore, the time taken for development was expressed in units of degree-days above a threshold temperature. Mean values (with 95%CL) were 552 (534–573) degree-days above 4.25°C for 10% of the eggs hatched, 862 (725–1064) degree-days above 3.57°C for 50% hatched and 1383 (1294–1486) degree-days above 3.14°C for 90% hatched. These values can be used to predict hatching times at temperatures below 14.68°C for 10% hatched, 14.54°C for 50% hatched and 14.45°C for 90% hatched. At higher temperatures, the hatching time and the number of degree-days required for development both increased with increasing temperature. Equations were developed to estimate the number of degree-days required for development at these higher temperatures.
Eggs were also placed in the Wilfin Beck, a small stony stream in the English Lake District. Maximum and minimum water temperatures were recorded in each week and the summation of degree-days was used to predict the dates on which 10%, 50% and 90% of the eggs should have hatched. There was good agreement between these estimates and the actual hatching times. Only 10–15% of the eggs hatched between October and late February with most of the eggs hatching in March, April and May. Nymphs hatching in October and November probably did not survive the winter.     

Interspecific and intraspecific variations in egg hatching for British populations of Taeniopteryx nebulosa and Brachyptera risi (Plecoptera: Taeniopterygidae)

Adults were obtained from three populations of Taeniopteryx nebulosa and four populations of Brachyptera risi ; their eggs were incubated at seven constant temperatures (range 3.8–22.1°C). There were interspecific, but not intraspecific, differences in adult life-span, mean number of eggs laid per female, hatching success and egg incubation periods. The optimum temperature for hatching success and the range over which at least 50% of the eggs hatched were lower for T. nebulosa (6.5°C, 2.7–15.0°C) than for B. risi (9.0°C, 5.1–15.8°C). No eggs hatched at 22.1°C. The relationship between incubation period (d days) and water temperature (T°C) was given by; d = 326.4 T^−1.015 for T. nebulosa , d = 824.0 T^−0.739 for B. risi . Both equations successfully predicted incubation periods for eggs placed in a stream.
Hatching success and incubation periods were similar to those already published for a Norwegian population of T. nebulosa . The lack of significant intraspecific variation suggests that the genotypes associated with the variables examined in this study have remained remarkably stable in these two species in spite of the geographical isolation of their different populations.     

Seasonal reproductive cycle in relation to tolerance to high temperatures in the terrestrial slug Lehmannia valentiana

Abstract. Seasonal maturation of the gonad (hermaphrodic gland) was examined in the terrestrial slug Lehmannia valentiana in Osaka, Japan. The ratio of the gonad weight to body weight was low in June–September, rapidly increased in October, and gradually decreased thereafter. In May–September, most slugs had only spermatogonia and spermatocytes, and all slugs had mature sperms in October–April. The oocyte size increased in September and large oocytes were observed in late October–April. Under natural temperature and photoperiodic conditions in Osaka, slugs laid eggs in early November–May. Therefore, this species reproduces from late autumn to spring, in contrast to many terrestrial slugs. In January–early February, however, the number of laid eggs was small and oviposition activity showed a bimodal seasonal pattern. In contrast, the hatching pattern was unimodal and most hatching was observed in spring. After a 1-h exposure to 33°C, the survival rate was 100% in juvenile slugs but 0% in eggs. Although hatching success was >85% at 15°–20°C, no eggs hatched when they were maintained at 25°C. The heat susceptibility of eggs in this species may be one of the key factors restricting oviposition from late autumn to spring.     

Ectoparasitic Argulus coregoni (Crustacea: Branchiura) hedge their bets – studies on egg hatching dynamics

Unpredictability in the temporal availability of susceptible hosts is likely to act as a selection pressure affecting the life history strategies of parasites. In highly variable environments the future of the lineage can be secured by spreading the risk, for example, by producing descendants that differ in their timing of emergence. Counter to this, in predictable environments a single "best-adapted" phenotype is expected. We asked whether ectoparasitic Argulus coregoni egg hatching pattern can be explained as a genetically canalized individual trait; an instance of phenotypic plasticity or bet-hedging. We collected egg clutches laid by individual A. coregoni females in early and late reproductive period of the lice population and randomized the clutches within 3 treatments. Intra- and inter-clutch variability in the hatching dynamics of A. coregoni eggs was monitored and the reproductive potential assessed. On average A. coregoni females laid 317 (SD±176.6) eggs. We found that the plasticity in the hatching dynamics among A. coregoni eggs was remarkable. Noticeable peaks in hatching were followed each of the repeated artificial "winter treatments" in 1°C. Repeated 2 weeks cold treatments induced relatively bigger hatching peaks than 2 days cold treatments compared to controls at room temperature. However, in all treatments, egg clutches hatched through an extended period of 7 months on average and the total hatching percentages were similar. We found that intra-clutch variability in hatching among eggs laid by single A. coregoni females was greater than inter-clutch variability. Our data support the predictions of the adaptive bet-hedging strategy in relation to egg-hatching dynamics. Response to cooling and bet-hedging may be adaptive for such species like A. coregoni since by synchronizing the life-cycle with the seasonal environment will assist transmission and parasite fitness.     

Interspecific and intraspecific variations in egg hatching for British populations of the stoneflies Siphonoperla torrentium and Chloroperia tripunctata (Plecoptera: Chloroperiidae)

SUMMARY 1. The objective was to compare variations in egg hatching between the two species (interspecific variations) and between populations of the same species (intraspecific variations). There were significant interspecific, but not intraspecific, differences in female size, adult life-span, egg production, hatching success, incubation periods and hatching periods.
2. The optimum temperature for hatching success within the range 3.8–22.1°C in the laboratory and the range over which at least 50% of the eggs hatched were lower for Chloroperia tripunctata (Scopoli) (8.5°C, 4.2–17.3°C) than for Siphonoperla torrentium (Pictet) (12.8°C, 6.1–19.4°C). Few eggs hatched at 22.r°C.
3. The relationship between incubation period (d days) and water temperature (T°C) was given by: d=1219/T^1.368 for S. torrentium , d=253/T^0.459 for C. tripunctata . Both equations successfully predicted incubation periods for eggs placed in a stream. The period over which eggs hatched was much longer for C. tripunctata than for S. torrentium at all temperatures.
4. The shorter incubation period (at r>5.6°C) and shorter hatching period for S. torrentium ensure that larvae of this species are already growing when eggs of C. tripunctata start to hatch, but the prolonged hatching period of the latter species ensures a long period of larval recruitment to the population. These differences in egg hatching may reduce competition between the two closely-related species.     

Temperature-Dependent Sex Determination in Gekko japonicus (Gekkonidae, Reptilia)

The effects of temperature on sexual differentiation in early development of the gekkonid lizard, Gekko japonicus were studied. The eggs were collected within 24 hr after the oviposition and were incubated at 20, 24, 28 and 32°C. The number of eggs hatched was 14 at 24°C, 20 at 28°C and 21 at 32°C. Hatching never occurred at 20°C. The hatched lizards without Müllerian ducts were judged as males. The sex of all lizards with Müllerian ducts were identified histologically. The sex ratios, male/(male+female), were 0.07 at 24°C, 0.75 at 28°C and 0.24 at 32°C. The disparities of the sex ratio from 1/2 were statistically significant and differences in the sex ratio with various incubation temperatures were also significant. These sex ratios can probably be best interpreted by a temperature-dependent sex determination. The different sex ratios do not seem to be related to a predetermination of sex with a differential mortality.     

The effect of temperature on development and hatching of scad, Trachurus trachurus L., eggs

The effect of temperature on the rates of development and hatching of artificially fertilized eggs of the scad, Trachurus trachurus L., was studied using a thermal gradient incubator. Development of eggs through to hatching occurred within the temperature range 10.5–21.2° C, with greatest survival between 12.2 and 15.8° C. The mean egg diameter was 0.94 mm and mean length of larvae on hatching 2.46 mm. Regressions of development time on mean incubation temperature are presented. The data are compared with those reported in the literature and related to sea temperatures in scad spawning grounds.     

Muscle growth in yolk-sac larvae of the Atlantic halibut as influenced by temperature in the egg and yolk-sac stage

Atlantic halibut eggs and yolk-sac larvae were incubated at 1, 5 and 8° C. Eggs incubated at 8° C gave slightly shorter larvae at hatching with a significantly smaller total cross-sectional area of white muscle fibres than eggs incubated at 5° C. Transport of eggs 2 days prior to hatching gave significantly longer larvae at hatching with a significantly larger red fibre cross-sectional area than when eggs were transported shortly after the blastopore closure. A higher survival until 230 degree days after hatching was also observed in the former group. All eggs incubated at 1° C died before hatching and all larvae incubated at 1° C died before 45 degree days after hatching. From hatching until 230 degree days the total white cross-sectional area increased threefold in all temperature groups. The increase in white cross-sectional area was entirely due to hypertrophy between hatching and 150 degree days (10 mm L _S). Recruitment of new white fibres increased in germinal zones at the dorsal, ventral and lateral borders of the myotome from 150 degree days onwards, but at 230 degree days (12–13 mm L _S) the recruitment fibre zone constituted <10% of the total white cross-sectional area. Larval incubation at 8° C gave slightly longer larvae with a significantly larger cross-sectional area of recruitment fibres at 230 degree days than incubation at 5° C. The larval group incubated at 8° C also had a significantly lower survival until 230 degree days than did the 5° C group. Incubation temperature regimes did not affect the volume density of myofibrils in the axial muscle fibres at 230 degree days. Thus hypertrophy is the predominant mechanism of axial white muscle growth in Atlantic halibut yolk-sac larvae and an increased rearing temperature during the yolk-sac stage increases white muscle fibre hyperplasia.     

THE EFFECT OF TEMPERATURE ON EGGS AND IMMATURE STAGES OF CULEX ANNULIROSTRIS SKUSE (DIPTERA: CULICIDAE)

Abstract
No immature stages of Culex annulirostris were found during field sampling in 1979–1980 when the average water temperature was < 17 °C; they reappeared when the average water temperature was 19 °C and reached the peak density (mean 107 immatures/cylinder) at 26.5 °C.
The effect of 6 temperatures (15–40°C) on egg hatching, development and survival of the immature stages of Cx annulirostris in the laboratory showed that at 15 and 40°C, eggs failed to hatch and larvae died in the first instars. The optimum temperatures for egg hatching and the survival of immature stages were 25 and 30°C. At these temperatures, 85 and 82% respectively of egg rafts hatched, the mean number of larvae per raft was 258 ± 9.8 and 260 ± 11.4 with immature survival of 83.5 and 79.0% respectively. Mean time to hatch at 20–35°C ranged from 1.2 d (35°C) to 2.9 d (20 °C). Developmental times from first instar to adult ranged from 7.1 d (35 °C) to 25.2 d (20 °C). The threshold for development of the immatures was 15.6 ± 2.5°C and the thermal constant was 142.9 ± 26.5 day—degrees (incubation temperatures 20–35°C). At less suitable temperatures of 20 and 35 °C, hatching (57.5 and 45%), number larvae per raft (mean 139.8 ± 9.8 and 102.6 ± 14.2) and survival were low.     

Incubation of eggs of tuatara, Sphenodon punctatus

Eggs of the tuatara, Sphenodon punctatus , were incubated either buried or half buried in vermiculite at constant temperatures of 15, 18, 20, 22 and 25 °C and constant water potentials between —90 and —400 kPa. Many clutches failed completely, possibly because they had been taken from females prior to proper shell development. Failed eggs were significantly smaller than successful eggs. Incubation is unsuccessful at 15 °C. Hatching success is high between 18 and 22 °C but low at 25 °C, but equally successful between 18 and 22°C. Incubation is strongly influenced by temperature, with mean incubation periods of 328 days at 18 °C, 259 days at 20 °C, 169 days at 22 °C and 150 days at 25 °C. Water potential generally has little influence on incubation time at a given temperature. Buried eggs hatch sooner than partially buried eggs at 20 °C but the large range makes significance dubious.
Eggs on the driest substrata at 18 and 20 °C lose water initially but then gain water through the rest of incubation. Eggs in all other conditions gain water throughout incubation, with the rate of i water absorption being maintained or increasing late in incubation. The suggestion that increasing rate of water absorption late in incubation facilitates explosive hatching is not supported. Egg mass at the time of hatching varies from 132 to 398% of initial values, depending on incubation conditions. Final egg mass is not affected significantly by incubation temperature. Hence, rates of absorption increase with temperature.
Water potential has no influence on hatchling size. However, hatchlings from buried eggs generally are significantly larger than those from partially buried eggs.     

Resting eggs of lake- Daphnia I. Distribution, abundance and hatching of eggs collected from various depths in lake sediments

SUMMARY. 1. Resting eggs (ephippia) of Daphnia galeata, D. hyalina, D. cucullata and D. galeata X D. hyalina hybrids were collected from the upper 8 cm of sediments at various water depths from two glacial lakes in the Northern Federal Republic of Germany.
2. The horizontal distribution of 'intact' ephippia (i.e. those containing two apparently healthy eggs) was extremely patchy, with mean densities in the upper 8 cm ranging from 1325 to 113,907 m⁻² (coefficient of variation, C=65.5%; Schöhsee, Holstein) and 25,343–159,143 m⁻² (C=58.5%; Kel-lersee. Holstein). Ephippial densities were greatest in sediments from deep waters. The highest densities of intact ephippia were in the upper 4 cm of sediment, with progressively fewer with increasing depth.
3. A proportion of eggs obtained from sediments during autumn (September-November 1985) and spring (March-May 1986) were exposed to continuous light (approximately 18 W m⁻²) at three temperatures (6, 12, 20°C), and the incidence of hatches recorded.
4. Hatching success was consistently low (maximum 14.4%), with most hatching occurring at 12°C. There was no significant difference between the hatching success of ephippia collected during autumn and spring. Decapsulation of ephippial eggs inhibited hatching. Hatching was highly synchronous within each treatment, and the pattern did not differ significantly with sediment depth, though hatching success was lower in deep sediments. A huge reservoir of ephippia is present in lake sediments, of which a proportion may remain viable for many years. Periodic recruitment of hatchlings to the pelagic population may provide an important mechanism for the maintenance of genetic diversity in Daphnia populations, as well as affecting rates of evolutionary change.     

Mortality of Apatania fimbriata (Insecta: Trichoptera) during embryonic, larval and adult life stages

1. Egg masses, oviposition site preferences, and abiotic and biotic factors causing mortality during embryonic, larval and adult life stages of Apatania fimbriata were studied. Laboratory investigations provided information on the temperature dependence of embryonic development, measured as an increase in egg volume.
2. A. fimbriata laid hemispherical egg masses, consisting of a transparent matrix containing a mean of 208 eggs. Egg masses were laid on stones situated just above the water surface in dark cavities in the stream bank.
3. Two hundred egg masses were mapped and individually monitored during embryonic development. There was no significant correlation between mortality during embryonic development and any of the abiotic parameters measured. First-instar larvae of Osmylus fulvicephalus consumed developing eggs, and chironomids preyed on newly hatched larvae.
4. A mean of seventy-two females emerged per metre of stream. Mortality during the 1993/94 life cycle was measured as a percentage of the potential number of eggs laid. Female mortality between emergence and oviposition was ≈ 80%. Eight per cent of individuals were lost during embryonic development. Larval mortality to emergence in 1994 was 11.3%. This indicates that the terrestrial life stage is probably decisive in the regulation of A. fimbriata populations.
5. Duration of embryogenesis at constant temperatures (4–20 °C) in the laboratory was described best by a negative exponential function. This species is cold stenothermal and there was no hatching success at 20 °C.
6. Egg volumes during embryonic development increased sigmoidally over time.     

Mortality of Apatania fimbriata (Insecta: Trichoptera) during embryonic, larval and adult life stages

1. Egg masses, oviposition site preferences, and abiotic and biotic factors causing mortality during embryonic, larval and adult life stages of Apatania fimbriata were studied. Laboratory investigations provided information on the temperature dependence of embryonic development, measured as an increase in egg volume.
2. A. fimbriata laid hemispherical egg masses, consisting of a transparent matrix containing a mean of 208 eggs. Egg masses were laid on stones situated just above the water surface in dark cavities in the stream bank.
3. Two hundred egg masses were mapped and individually monitored during embryonic development. There was no significant correlation between mortality during embryonic development and any of the abiotic parameters measured. First-instar larvae of Osmylus fulvicephalus consumed developing eggs, and chironomids preyed on newly hatched larvae.
4. A mean of seventy-two females emerged per metre of stream. Mortality during the 1993/94 life cycle was measured as a percentage of the potential number of eggs laid. Female mortality between emergence and oviposition was ≈ 80%. Eight per cent of individuals were lost during embryonic development. Larval mortality to emergence in 1994 was 11.3%. This indicates that the terrestrial life stage is probably decisive in the regulation of A. fimbriata populations.
5. Duration of embryogenesis at constant temperatures (4–20 °C) in the laboratory was described best by a negative exponential function. This species is cold stenothermal and there was no hatching success at 20 °C.
6. Egg volumes during embryonic development increased sigmoidally over time.     

Reproductive behaviour and early development of the Drysdale hardyhead, Craterocephalus sp. nov. (Pisces: Atherinidae), from the Alligator Rivers System, Northern Territory, Australia

Craterocephalus sp. nov. showed sexual dimorphism in body shape during the breeding season. Pairing occurred during daylight with a single release of eggs amongst submerged vegetation between sunrise and the early afternoon on the same day. The eggs were demersal, adhesive, spherical (0.87–0.96 mm diameter) and had 12 adhesive filaments (0.5–1.5 mm long) at the animal pole. Approximately 24 oil droplets (0.02–0.08 mm diameter) persisted throughout egg and larval development. Hatching occurred 155–160 h after spawning at 25–27° C.
The yolk-sac larvae were 3.85–3.95 mm notochord length at hatching and began feeding at the surface after absorption of the yolk (3–12 h after hatching). All fin rays were developed in 9.4 mm standard length fry, which moved from midwater to feed on the substrate. Aquarium reared fish first spawned at 30 mm s.L. when 165 days of age.
Features of Craterocephalus reproduction, as they relate to a specific survival strategy, are briefly discussed.     

Methods for the activation of the resting eggs of Daphnia

SUMMARY. 1. The conditions required to initiate development of resting eggs of thirty-six clones of Daphnia representing seven species were investigated.
2. The temperature of both dark incubation and subsequent light treatment are shown to affect hatch success. By varying these parameters the majority of resting eggs from each test clone were stimulated to develop. Arctic clones required a low hatching temperature (7°C), whereas clones from warmer climates hatched best at 14–21°C.
3. Variation in hatching cues existed between conspecific individuals from different collection sites. These differences suggest that research determining macro- and microgeographic patterns in hatching phenology would be fruitful.     

Effects of temperature of adults and eggs on the induction of embryonic diapause in the band-legged ground cricket, Dianemobius nigrofasciatus

Abstract.  Eggs laid by adult female Dianemobius nigrofasciatus , reared under long-day (LD 16 : 8 h, 25 °C) or short-day (LD 12 : 12 h, 25 °C) conditions from the nymphal stage, are kept at several constant temperatures. At 22.5–30.0 °C, eggs laid by long-day adults show lower incidences of diapause than those laid by short-day adults. In both eggs laid by adults under long-day conditions and those under short-day conditions, the higher the temperature at which the eggs are kept, the lower the incidence of diapause. When eggs of long-day adults are exposed to a low-temperature pulse (10 °C, 24 h) on the day of deposition (day 0), the incidence of diapause increases. The low-temperature pulse on day 1 does not increase the incidence of diapause. By contrast, when the eggs of short-day adults are exposed to a high-temperature pulse (35 °C, 24 h) on day 0 or day 1, the incidence of diapause decreases. The temperature pulses on day 0 are more effective at diapause prevention. Staining of diapause eggs by the Feulgen–Rossenbeck method shows that the eggs enter diapause at the blastoderm stage, which is on day 1 or day 2 at 25 °C. The exposure of adults to long days and higher temperatures prevents the eggs from entering diapause. In D. nigrofasciatus , embryonic diapause is controlled by maternal effects, adult photoperiod and temperature, and egg temperature before or at diapause.     

Development of eggs and larvae of the flounders Rhombosolea tapirina and Ammotretis rostratus (Pisces: Pleuronectidae)

The stages of development of laboratory-reared eggs and larvae of Rhombosolea tapirina and Ammotrelis rostratus are described. They both exhibited á typical pleuronectid pattern of development. At ambient seawater temperature of 11.1–13.8° C R. tapirina eggs hatched 83–93 h after fertilization and larvae metamorphosed c. 65 days later at mean length of 8.83 mm. Hatching of A. rostratus eggs occurred 93–105 h after fertilization and larvae metamorphosed after c. 69 days (mean length 11.21 mm) at 12.7–16.5° C. The two species can be readily separated by their morphology, meristics and pigmentation. In particular, the eggs differ in diameter, only R. tapirina larvae possess a pair of spines in the otic region, and juvenile A. rostratus have only a left pelvic fin.     

Influence of temperature on egg hatching, growth and survival of larvae of Heterobranchus longifilis Val. 1840 (Teleostei: Clariidae)

Eggs of Heterobranchus longifilis Val. 1840 were artificially fertilized and incubated at a range of temperatures (20, 23, 25, 27, 29 and 32°C). The time from fertilization to hatching decreased with increasing temperature. No eggs survived to hatch at 20 and 32°C incubation temperatures, while at 23 and 29°C hatching was only minimal. Optimum hatching was obtained at 25 and 27°C, which corresponds to the ambient temperature range during the breeding season. Larvae of H. longifilis were reared for 11 days post-hatching at 20, 25, 27, 29 and 32°C. Growth increased with temperature (P < 0.05), whereas survival depicted an inverse relationship. Growth was minimal at 20°C and larvae rarely survived to the end of the experiment. Optimum temperature for the primary nursing of H. longifilis larvae was within the 25–27°C temperature range.     

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.