Overwintering survivorship of pupae of the mimosa web worm, Homadaula anisocentra (Lepidoptera: Plutellidae), in an urban landscape

ABSTRACT. 1. Overwintering survivorship of pupae of the mimosa webworm, Homadaula anisocentra Meyrick (Lepidoptera: Plutellidae), was examined in several urban habitats in central Iowa during the winters of 1981–82, 1982–83 and 1983–84.
2. Survivorship and supercooling point temperatures were determined throughout the winters. Corroborative laboratory studies were conducted during the winter of 1982–83.
3. Minimum ambient temperatures that equalled or were below the supercooling point of the insect, at any time, were lethal.
4. Prolonged cold exposure below 0°C and above the supercooling point resulted in high mortality levels. To quantify this relationship, a concept of minimum-temperature exposure was developed by tabulating the number of degrees that the daily minimum temperature was below 0°C for a given sampling period.
5. Some mimosa webworm pupae were found to overwinter in highly protected sites (2.5–5.0°C warmer than the ambient air temperatures) in the urban environment, resulting in less minimum-temperature exposure and reducing the probability of reaching the lethal supercooling point temperature.     

Habitat temperature and the temporal scaling of cold hardening in the high Arctic collembolan, Hypogastrura tullbergi (Schäffer)

Abstract.  1. Cold tolerance is a fundamental adaptation of insects to high latitudes. Flexibility in the cold hardening process, in turn, provides a useful indicator of the extent to which polar insects can respond to spatial and temporal variability in habitat temperature.
2. A scaling approach was adopted to investigate flexibility in the cold tolerance of the high Arctic collembolan, Hypogastrura tullbergi , over different time-scales. The cold hardiness of animals was compared from diurnal warming and cooling phases in the field, and controlled acclimation and cooling treatments in the laboratory. Plasticity in acclimation responses was examined using three parameters: low temperature survival, cold shock survival, and supercooling points (SCPs).
3. Over time-scales of 24–48 h, both field animals from warm diurnal phases and laboratory cultures from a 'warm' acclimation regime (18 °C) consistently showed greater or equivalent cold hardiness to animals from cool diurnal phases and acclimation regimes (3 °C).
4. No significant evidence was found of low temperature acclimation after either hours or days of low temperature exposure. The cold hardiness of H. tullbergi remained 'seasonal' in character and mortality throughout was indicative of the summer state of acclimatization.
5. These data suggest that H. tullbergi employs an 'all or nothing' cryoprotective strategy, cold hardening at seasonal but not diel-temporal scales.
6. It is hypothesised that rapid cold hardening offers little advantage to these high Arctic arthropods because sub-zero habitat temperatures during the summer on West Spitsbergen are rare and behavioural migration into soil profiles offers sufficient buffering against low summer temperatures.     

Seasonal variation in freezing tolerance of the New Zealand alpine cockroach Celatoblatta quinquemaculata

1. The cold hardiness of the alpine cockroach Celatoblatta quinquemaculata was investigated. This species is found at 1360 m a.s.l. beneath schist slabs on the Rock and Pillar Range (Central Otago, New Zealand). Cockroaches were collected monthly from January to December 1996, and their LT₅₀ and supercooling points determined.
2. Celatoblatta quinquemaculata was freezing tolerant throughout the year, with a lower lethal temperature in winter of – 8.9 °C. Celatoblatta quinquemaculata was also found frozen under rocks in the field when the under-rock temperature was below – 3 °C, and could survive being frozen at – 5 °C for 4 days in the laboratory.
3. There was a marked decrease in LT₅₀ temperature from – 5.5 °C in April to – 7.5 °C in May. This coincides with decreasing temperatures from summer through autumn to winter, during which temperatures beneath snow-covered rocks may reach – 7.3 °C.
4. Supercooling points fluctuated during the year, with an increase from – 4.2 °C in autumn to – 3.4 °C in winter. Supercooling point was highest in spring, and changes in supercooling point do not appear to be related to changes in LT₅₀.
5. Recordings of environmental temperatures from the Rock and Pillar Range suggest that cockroaches may undergo up to twenty-three freeze–thaw cycles in the coldest month of the year, and that they may remain frozen for periods of up to 21 h. Maximum cooling rates recorded in the field (0.01 °C min^–1) were 100-fold slower than laboratory cooling rates, so survival estimates from laboratory experiments may be underestimates.     

The roles of temperature and diapause in the life history of a temperate-zone dragonfly: Argia vivida (Odonata: Coenagrionidae)

Abstract. 1. The life cycle of Argia vivida Hagen generally took longer to complete in the field than was predicted on the basis of the thermal sum accumulated in laboratory rearing.
2. The prediction of a bivoltine life-cycle from geothermal sites with either a constant annual temperature of 26°C or thermal range of 11–31°C was not borne out because the intervention of short-day induced developmental delays in later larval instars extended the life cycle to 1 year.
3. This diapause, which synchronizes adult emergence with favourable summer temperatures, was also present in larvae from sites with annual temperature ranges of 0–33°C and 5–20°C.
4. At these colder sites completion of the life cycle takes 2 and 3 years respectively and dragonflies must be in cold-resistant stages during the winter. A long-day diapause, principally affecting late-instar larvae below a certain size during the summer, achieves this.
5. Large diurnal temperature fluctuations at the 0–33°C site markedly increase the useful thermal energy available to larvae for growth over that predicted by the thermal sum equation.
6. The interaction between the effects of temperatures favourable for growth and day-length-governed diapause, synchronize the emergence of the low-temperature sensitive adult stage of this tropical dragonfly with northern-latitude summers at a variety of habitats.     

Changes in the ovaries of olive flies (Dacus oleae (Gmelin)) during the summer, and their relationship to temperature, humidity and fruit availability

Abstract. 1. Examination of the ovaries of female olive flies ( Dacus oleae ) from wild populations on Corfu during the summer months of 1975 indicated that all were non-gravid for a period of several weeks during June and July and the terminal follicles were resorbed.
2. Experiments in outdoor cages indicated that olive fruits could stimulate ovarian development during the summer months.
3. Experiments in constant temperature cabinets indicated that high temperatures (i. e. 26–29°C) in conjunction with a low humidity (45 ± 5°%) inhibited ovarian maturation.
4. Whereas the presence of olive fruits offset the effects of temperature and humidity on ovarian development at 26°C in all flies, at 29°C very few were able to mature their ovaries.
5. It is suggested that it is the interaction of temperature, humidity and access to fruit which determine when ovarian maturation ceases and recommences during the summer months.     

Late autumn eclosion in the winter moth Operophtera brumata: compromise of selective forces in life-cycle timing

Abstract. 1. In eclosion experiments at constant temperatures (6, 9, 12, 15, 18, 21, and 25 °C), Operophtera brumata (L.) pupae were found to respond nonlinearly to temperature, with 9 °C giving the highest developmental rate.
2. Pupal development rate decreased and mortality increased at the highest and lowest temperatures. No pupae eclosed at 6, 21, or 25 °C.
3. Exposing pupae to periods of cold did not enhance their rate of development consistently, indicating that no pupal diapause occurred. Light did not affect the length of the pupal period significantly.
4. Variation in mean developmental rates across temperatures was modelled both for data in the present study (northern Norway) and for a previously published German study (20° further south). The German population had a longer pupal period at all temperatures than the northern population (mean difference of 88 days). The difference is assumed to be genetically based, and hence an adaption to (and not a consequence of) differences in phenology between the two sites.
5. The diversity of the life cycle of O. brumata is discussed. Timing of eclosion can be explained by the selective forces of predation by birds on the one hand and mortality due to early snowfall on the other.     

Alterations of gene expression in potato (Solanum commersonii) during cold acclimation

Plantlets of Solanum commersonii stem-culture were acclimated at 5°C day/night temperature for 14 days. Cold hardiness increased from – 3.5°C to – 8.6°C. During the course of acclimation, the synthesis of polypeptides was investigated and poly (A⁺) RNA was isolated. Translation products of poly(A⁺) RNA in a rabbit rcticulocyte lysate system were then analyzed. During the 14 days of acclimation, 23 cold-induced polypeptides were identified. Most of them disappeared following 1 day of de-acclimation at a 20/15°C day/night regime. The synthesis of one group of polypeptides is prominent and stable throughout the acclimation period. The other group is transient. The most prominent and stable polypeptides have molecular weights of 21, 22, 31 and 83 kDa.
Acclimation alters translatable mRNA population during the development of cold hardiness. Two mRNAs encoding in vitro translation products at 26 and 27 kDa were identified during the course of acclimation. These proteins may play important roles in the overall programming for the development of cold hardiness in tuber-bearing S. commersonii.     

Contact with the host plant enhances aphid survival at low temperatures

1. The hypothesis, suggested by previous studies, that host plant contact reduces the cold tolerance of anholocyclic aphids was tested under laboratory conditions. Adult and first-instar Rhopalosiphum padi (L.) were exposed to temperatures of 0, –5 and –10 °C on intact plants, excised leaves and in the absence of contact with plant material.
2. Median lethal time (LT₅₀) values at all three temperatures indicate that aphids exposed in association with plant material survive longer than aphids that have no contact with their host plant. The difference in survival was most pronounced at –10 °C. Therefore, the above hypothesis is rejected for aphids on cereals because host plant contact apparently enhances cold tolerance.
3. Exposure on excised leaves also enhanced aphid survival at low temperature but was less effective than the intact plant. This suggests that plant quality as well as the presence or absence of plants is important in the cold tolerance of aphids on cereals.     

Interspecific variation in the response to low temperature storage in different aphid parasitoids

Cold storage of natural enemies usually involves placing insects under constant subambient temperatures. Even at non-freezing temperatures, a reduction in survival is the norm. Using fluctuating thermal regimes (FTR) instead of constant low temperature (CLT) has shown that mortality due to accumulation of chilling injuries was significantly reduced in Aphidius colemani . Whether this phenomenon can be generalised to other parasitoid species is not known. The aim of this study was to analyse interspecific variation in the ability to tolerate cold storage under CLT (continuous 2°C) versus FTR (daily cycle: 2°C for 22 h and 20°C for 2 h) for various durations (0–20 days). Survival, sex ratio and development of five different Aphidiine parasitoids were analysed: A. colemani , Aphidius ervi , Aphidius matricariae , Ephedrus cerasicola and Praon volucre. A marked interspecific variation in the ability to tolerate cold storage was observed: A. matricariae and A. ervi were most chill tolerant, P. volucre and E. cerasicola had an intermediate chill sensitivity and A. colemani was most chill sensitive. In all species tested, FTR significantly reduced cold-induced mortality. This phenomenon was manifested more in chill-sensitive species as they probably accumulate chilling injuries more rapidly. The sex ratio remained unaffected in all the species. Interspecific variation was also observed in developmental responses to cold storage. Under CLT, time to adult emergence of A. matricariae, A. colemani, A. ervi and P. volucre was temporarily stopped and in E. cerasicola it increased. Under FTR, the short daily intervals at 20°C for 2 h allowed parasitoids to continue development in all the species. Interspecific differences are discussed. This study suggests that positive impact of FTR may apply to a wide range of species.     

Intra- and inter-specific variations in egg survival and brood development time for Austrian populations of Gammarus fossarum and G. roeseli (Crustacea: Amphipoda)

SUMMARY. 1. Egg survival (ES, percentage of eggs hatched in vitro ), reproductive success (RS, percentage of live young released from the brood pouch) and brood development lime ( d , days) in four populations of Gammarus fossarum and two populations of Gammarus roeseli were studied, in the laboratory at water temperatures of 2.0–26.1°C. Intraspecific differences between populations were not significant, but interspecific differences were found between the two species.
2. In natural stream populations, the reproductive period of G. fossarum lasted from December to September, that of G. roeseli from March to September.
3. In the experimental temperature range 2–26°C, 73% of the total number (771) of G. fossarum females and 69% of 469 G. roeseli females were ovigerous. Of these, 45% of G. fossarum and 43% of G. roeseli females successfully released live young from their brood pouches.
4. For G. fossarum , the optimum temperatures were 11.4°C for ES, where 76% of the eggs hatched, and 11.8°C for RS, where 77% of the females released live young from their brood pouches. For G. roseli , the optimum temperatures were 13.5°C for ES (51% hatched) and 14.0°C for RS (76% released). Over 50% of eggs hatched at temperatures of 3.6–19.2°C in G. fossarum and at 1 1.9–15.1°C in G. roeseli . Development time increased from 12 days at 21.9°C to 251 days at 2.0°C in G. fossarum , and from 10 days at 24.1°C to 212 days at 4.1°C in G. roeseli .
5. interspecific differences between the effects of water temperature on ES, RS and d are used to explain the different distributional patterns of G. fossarum and G. roeseli in central European running water systems. assuming that other physico-chemical variables are suitable for both species.     

Long‐term after‐effects of cold exposure in adult Alphitobius diaperinus (Tenebrionidae): the need to link survival ability with subsequent reproductive success

1. The effects of cold acclimation and cold exposure on the survival and reproductive capabilities of Alphitobius diaperinus (Tenebrionidae) adult beetles are examined. 2. First, the impact of temperature on survival duration was assessed by placing beetles in a range of cool temperature treatments. Second, the importance of acclimation duration was assessed. Third, the impact of thermal stress on subsequent reproductive ability was examined for beetles that had no previous cold exposure, and for beetles that had been subjected to previous cold exposure (i.e. acclimated) at various conditions, including fluctuating temperatures. 3. In all groups, the number of recorded survivors was strongly impacted by recovery period duration (i.e. 2 vs. 10 days). Survival of non‐acclimated and 3‐day acclimated beetles, expressed as lethal time for 50% of the samples, was reduced significantly when the insects were re‐assessed for survival at 10 days after being returned to optimal growth conditions (7.9 ± 0.4 vs. 5.1 ± 0.6 days and 8.8 ± 0.5 vs. 6.8 ± 0.6 days, respectively). 4. Insects that had been subject to cold acclimation expressed better subsequent reproduction success than non‐acclimated beetles. This beneficial impact increased when the acclimation period was prolonged, but some longer acclimation periods had no significant impact on survival. 5. Our results indicate that cold exposure has the capacity to irreversibly damage the reproductive system and that insect survival depends on the duration of the recovery period. Both the survival ability and subsequent reproductive output have to be examined to objectively determine insect cold resistance.     

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.     

Behavioural thermoregulation by subyearling fall (autumn) Chinook salmon Oncorhynchus tshawytscha in a reservoir

This study investigated behavioural thermoregulation by subyearling fall (autumn) Chinook salmon Oncorhynchus tshawytscha in a reservoir on the Snake River, Washington, U.S.A. During the summer, temperatures in the reservoir varied from 23° C on the surface to 11° C at 14 m depth. Subyearlings implanted with temperature-sensing radio transmitters were released at the surface at temperatures >20° C during three blocks of time in summer 2004. Vertical profiles were taken to measure temperature and depth use as the fish moved downstream over an average of 5·6–7·2 h and 6·0–13·8 km. The majority of the subyearlings maintained average body temperatures that differed from average vertical profile temperatures during most of the time they were tracked. The mean proportion of the time subyearlings tracked within the 16–20° C temperature range was larger than the proportion of time this range was available, which confirmed temperature selection opposed to random use. The subyearlings selected a depth and temperature combination that allowed them to increase their exposure to temperatures of 16–20° C when temperatures <16 and >20° C were available at lower and higher positions in the water column. A portion of the subyearlings that selected a temperature c. 17·0° C during the day, moved into warmer water at night coincident with an increase in downstream movement rate. Though subyearlings used temperatures outside of the 16–20° C range part of the time, behavioural thermoregulation probably reduced the effects of intermittent exposure to suboptimal temperatures. By doing so, it might enhance growth opportunity and life-history diversity in the population of subyearlings studied.     

Patterns of metamorphosis in summer flounder, Paralichthys dentatus

Summer flounder, Paralichthys dentatus , spawn over the continental shelf off the east coast of the United States from September to January with the peak in October–November. Based on plankton collections, mid-metamorphic larvae (stages G-H; mean s.l . 13.1 mm) enter Great Bay–Little Egg Harbor estuary in southern New Jersey as early as October with continued ingress through April. In the laboratory, mortality during metamorphosis ranged from 17 to 83% among treatment groups, and was significantly greater in flounder maintained at approximately 4°C relative to those maintained at ambient temperatures (daily average temperature 10.l°C). Laboratory-reared summer flounder averaged 24.5 days (range 20 to 32 days) to complete metamorphosis (from Stage F– to Stage I) at ambient spring temperatures (daily average temperature =16.6° C). The time to completion of metamorphosis in wild-caught flounder maintained in the laboratory was clearly temperature dependent. Both cold and ambient temperature treatments resulted in delayed metamorphosis such that, at ambient winter temperatures (daily average=6.6°C), partial metamorphosis (from Stage H – to Stage I) required as much as 92.9 days (range 67 to 99 days). There was no apparent effect of starvation on either mortality or time to completion of metamorphosis at cool water temperatures (< 10° C). It appears that prevailing temperature conditions influence the duration of metamorphosis in summer flounder, and that mortality during metamorphosis may play a significant role in the population dynamics of this species.     

The effects of temperature acclimation on organ/tissue mass and cytochrome c oxidase activity in juvenile cod (Gadus morhua)

Cod were acclimated to 5 and 15° C (cold and warm acclimation, respectively) for at least 43 days after which tissue-somatic indices, tissue protein, DNA content, and cytochrome c oxidase (CCO) activity were measured. Liver, stomach, intestine, total heart and ventricle-somatic indices were all increased significantly in the cold acclimated animals compared with their warm acclimated counterparts. There were no differences in gill or white muscle-somatic indices between the acclimation temperatures. Tissue protein concentration (mg protein g tissue⁻¹) was generally unaffected by temperature acclimation. Cold acclimation resulted in higher white muscle and lower ventricle CCO specific activities(μmol cytochrome c oxidized min⁻¹· g tissue⁻¹) compared with the respective warm acclimated tissues. No significant differences in CCO specific activity were observed in the remaining tissues (when measured at an intermediate temperature of 10° C). Total tissue CCO activity (measured at an intermediate temperature of 10° C) did not differ significantly between the cold and warm acclimated fish.     

The relative importance of temperature and diet to larval development and adult size of the winter stonefly, Soyedina carolinensis (Piecoptera: Nemouridae)

SUMMARY. 1. Soyedina carolinensis Claassen, a leaf shredding stonefly, was reared in a series of three laboratory experiments from early instar to adult on different species of deciduous leaves and at various constant and fluctuating temperature regimes.
2. Experiment 1, which involved rearing larvae on fourteen different leaf diets at ambient stream temperatures, showed that diet significantly affected larval growth and adult size but did not affect overall developmental time.
3. Experiment 2, which involved rearing larvae on five different leaf diets at each of three fluctuating temperature regimes (viz ambient White Clay Creek (WCC), ambient WCC+3°C, and ambient WCC+6°C), showed that: (i) adding 6°C to the normal temperature regime of WCC was lethal to 99% of the larvae regardless of diet; and (ii) warming WCC by 3°C did not affect developmental time but did significantly reduce adult size relative to adults reared at WCC temperatures on certain diets.
4. Experiment 3, which involved rearing larvae on five different leaf diets at each of five constant temperatures (viz 5, 10, 15, 20, 25°C), showed that: (i) temperature significantly affected the mortality, growth, and development time of larvae whereas diet only affected larval growth and mortality; (ii) temperatures at or near 10°C yielded maximum larval growth and survival for most diets; (iii) at 5°C, larval mortality was high and growth was low resulting in a few small adults for most diets; (iv) larval mortality was at or near 100% at 15°C regardless of diet; and (v) no larvae survived at 20 and 25°C.     

Water temperature in a stream gravel bed and implications for salmonid incubation

SUMMARY. 1. Water temperatures were recorded at hourly intervals in the gravel of a trout spawning area in a small stony stream at depths of 0–20 cm in 1985–86 and 0– 40 cm in 1987.
2. As depth within gravel increased, the size of the daily fluctuations reduced and their time of occurrence was delayed by about 12 min cm⁻¹' in 1985–86 and about 6 min cm⁻¹ in 1987.
3. From October to February mean temperatures at 20 cm depth were, on average, 0.5°C higher than those at the gravel surface. This reflected elevated daily minima more than it reflected elevated daily maxima.
4. From March to July daily minima were lower and daily maxima were higher in the stream than in the gravel. Consequences were: (a) an appreciable increase in mean daily range at all depths in the gravel during the summer, (b) higher daily means (by an average of about 0.4°C) in the water than in the gravel in May to August.
5. Some implications for the early development of salmonid fish are considered.     

Cold tolerance of the aphid predator Episyrphus balteatus (DeGeer) (Diptera, Syrphidae)

Abstract. Larvae of the hoverfiy Episyrphus balteatus (DeGeer) are important predators of aphids in the U.K. A large proportion of the U.K. population migrates south to warmer climes at the end of summer, but a small number are thought to overwinter in the U.K., with the mated female being the overwintering morph. The cold tolerance of adult flies was investigated to assess the overwintering potential of E. balteatus in the U.K. The high supercooling point (SCP) of -8.3 ± 0.7°C, and lethal temperature (LTemp₃₀) of -9.1°C for acclimated females suggest that E. balteatus has limited cold hardiness. This was confirmed by experiments where, despite a strong acclimation response in both males and females, there was no long-term survival at 5, 0 or - 5°C. At 5°C, 90% of females had died after 10 days. The weak cold hardiness of adult E. balteatus was corroborated by field experiments which demonstrated a 100% mortality after 10 weeks' exposure to U.K. winter conditions. The ecological significance of this limited cold hardiness is discussed in relation to the overwintering abilities of E. balteatus in the U.K.     

Temperature-related fluctuations in the timing of emergence and pupation of Windermere alder-flies over 30 years

1. From 1966 to 1995, dates were recorded when adult alder-flies, Sialis lutaria L., were first seen (30-year range: 23 April – 25 May), 50% of the maximum density occurred (4 May – 4 June), and maximum density occurred (11 May – 17 June) along 200 m of Windermere shore. These emergence dates occurred at similar temperatures, estimated by mean values for both the emergence date and the week prior to emergence. The latter was the least variable at 10.1 °C (95% CL ± 0.37) for start of emergence, 11.2 °C (± 0.49) for 50% maximum density, 14.2 °C (± 0.51) for maximum density.
2. Final-instar larvae pupated in damp soil just above the water line. As laboratory temperatures were increased slowly from an initial 5 °C, the cumulative number of larvae leaving the water to pupate increased. A quadratic equation described this relationship from a threshold temperature of 7.2 °C to completion at 14.0 °C (50% point, 9.3 °C). The relationship between successful pupations and constant temperatures in the laboratory was well described by a quadratic equation with an optimum 14.9 °C (over 90% success) and no success outside the range 7–23 °C. A negative power-function described the relationship between days required for pupation and temperature, ranging from c . 28 days at 8.2 °C to c . 4 days at 22.1 °C.
3. Dates for larvae leaving the lake to pupate were back-calculated from dates for adult emergence, using the power-function for pupation time. Mean temperatures for estimated dates on which larvae left the lake to pupate were less variable than those for adult emergence, being 7.5 °C (± 0.20) for the start of pupation, 9.4 °C (± 0.16) for 50% maximum density, 13.7 °C (± 0.16) for maximum density. These values are similar to those obtained in the laboratory and can be used to predict pupation and adult emergence for different temperature regimes.     

Effects of temperature on the growth and survival of the European eel, Anguilla anguilla L.

Experiments to determine the growth rate of eels ( Anguilla anguilla L.) at different temperatures are described and show the optimum temperature for growth to be 22–23° C. The ultimate upper lethal temperature was found to be 38° C and the critical thermal maximum varied from 33 to 39° C for fish acclimated at 14 to 29° C. An attempt was also made to determine lower lethal temperatures. Eels enter a state of torpor at temperatures varying from 3° C for fish acclimated at 29° C to less than 1° C for fish acclimated at 23° C or below. The results have been used to estimate the growth rates expected from eels cultured in power station cooling water using different types of temperature control.