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.     

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.     

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.     

Effects of husbandry parameters on the life-history traits of the apple snail, Marisa cornuarietis: effects of temperature, photoperiod, and population density

Abstract. These experiments are part of a larger study designed to investigate the influence of husbandry parameters on the life history of the apple snail, Marisa cornuarietis . The overall objective of the program is to identify suitable husbandry conditions for maintaining multi-generation populations of this species in the laboratory for use in ecotoxicological testing. In this article, we focus on the effects of photoperiod, temperature, and population density on adult fecundity and juvenile growth. Increasing photoperiod from 12 to 16 h of light per day had no effect on adult fecundity or egg hatching and relatively minor effects on juvenile growth and development. Rearing snails at temperatures between 22°C and 28°C did not influence the rates of egg production or egg clutch size. However, the rates of growth and development (of eggs and juveniles) increased with increasing temperature in this range, and when temperatures were reduced to 22°C egg-hatching success was impaired. Juvenile growth and development were more sensitive to rearing density than adult fecundity traits. On the basis of the present results, we conclude that rearing individuals of M. cornuarietis at a temperature of 25°C, a photoperiod of 12L:12D, and a density of <0.8 snails L⁻¹ (with lower densities for juvenile snails) should provide favorable husbandry conditions for maintaining multi-generation populations of this species.     

Growth and survival strategy of the Antarctic mite Alaskozetes antarcticus

Growth and mortality rates of three juvenile instars and adults of the oribatid mite Alaskozetes antarcticus were measured over a twelve month period using field enclosures m Its maritime Antarctic habitat A pattern was found of rapid growth during the short summer period (0 2-0 4 μg dry weight increment per day) followed by gradual weight loss overwinter Most individuals completed one instar per year, reaching a premoult resting phase by late summer, with the moult being delayed and relatively synchronised early the next summer A small proportion of proto- and deutonymphs completed two moults within one summer period After the final moult adults overwintered again before commencing oviposition, suggesting that the life cycle (egg-egg) will take at least five years Mortality was not biased towards any instar or time of year Highest individual growth rates were obtained at a constant temperature of 7°C in the laboratory However expenmentai increase of mean field temperature from 2 7 to 4 3°C by use of a plastic cloche led to decreased growth, although no change in moulting frequency or mortality rate Laboratory survival was greatest at 2°C and decreased with increasing temperature
Alaskozetes antarcticus may be descnbed as 'a' (adversity) selected, showing an exceptionally long life cycle of five to six years and extensive physiological investment in survival adaptations Moult synchronisation in early summer, involving entering winter in the inactive premoult phase, will increase overwinter survival by reducing the chance of inoculative freezing from gut contents, and may be advantageous in maximising the time available for feeding during the subsequent summer, or ensuring proximity of the sexes after the final moult     

POPULATION PARAMETERS AND PHOTOSYNTHETIC CAPABILITIES OF CORALLINE RHODOLITHS: BIOGEOGRAPHIC IMPLICATIONS

Rhodoliths are bed forming, unattached coralline algae that incorporate large quantities of carbonate into their thalli in oceans worldwide. Lithophyllum margaritae and Neogoniolithon tricotomun are common Rhodoliths from the Gulf of California, however, little is known about their biogeographic distribution, and their ecological and physiological characteristics. As a consequence, the objective of this study was to define the temporal population dynamics, growth rates and photosynthetic capabilities of L. margaritae and N. tricotomun from the Gulf of California. The Gulf of California is characterized by annual temperature fluctuations that can exceed 20° C. Rhodolith beds exceeding one km in length were observed from the intertidal zone to a depth of approximately 20 m at the southern Gulf. Percent cover estimates for spherical unattached individuals of L. margaritae and N. tricotomun ranged from 10 to 100%. Growth rates were determined by staining the rhodoliths with Alizarine red and evaluating the linear increment of calcium carbonate after an incubation period in the field. Annual growth rates averaged 1.8 mm year⁻¹ in L. margaritae and 3.4 mm year⁻¹ in N. tricotomun , however, growth rates varied seasonally. The photosynthetic response of both species as a function of temperature was evaluated in the laboratory from 10° to 30° C. Maximum net photosynthetic rates peaked at approximately 25 to 30° C in both species, suggesting that maximum growth rates occur during the warmest months of the year. These results lead to a better understanding of the biogeographic ranges of subtidal coralline algae.     

Cryopreservation of entrapped monoxenically produced spores of an arbuscular mycorrhizal fungus

A study was conducted to quantify the ability of entrapped, monoxenically produced spores of an arbuscular mycorrhizal fungus to germinate and reproduce the fungal life cycle after cryopreservation. No germination was obtained after incubation of entrapped spores in glycerol and mannitol and subsequent cryopreservation at −70 °C, regardless of the concentration of cryoprotectants and duration of incubation. Incubation for 1 d in 0.5 M sucrose, and for 1 and 2 d in 0.5 M trehalose, led to spore germination after cryopreservation at −70 °C. Lower cryopreservation temperatures were tested with entrapped spores incubated for 1 d in 0.5 M trehalose. The highest germination rate, estimated by the percentage of potentially infective beads (%PIB), was obtained at −100 °C. A %PIB of 95% (water agar medium) to 100% (Strullu–Romand medium) was obtained at this temperature. Thereafter, %PIB rapidly decreased at −140 and −180 °C. Heavy sporulation and high internal root colonization were obtained after re-association of the entrapped spores, incubated for 1 d in 0.5 M trehalose and subsequently cryopreserved at −100 °C, with transformed carrot roots. This demonstrates the ability of entrapped spores to reproduce the fungal life cycle following cold treatment.     

Octopus joubini (Mollusca: Cephalopoda): a detailed study of growth through the full life cycle in a closed seawater system

Twenty individual pygmy octopuses, Octopus joubini , were reared at 25°C from hatching to maturity on a quantified diet of live crabs in closed (recirculating) natural seawater systems. At 24 week intervals the animals were narcotized, weighed and measured. There was 85% survival to sexual maturity.
Growth rates were highest during the first four weeks of exponential growth. Beyond four weeks, growth rates steadily declined and growth became logarithmic in form. Female octopuses grew slightly faster than males and attained a larger size at maturity. The length-weight relationship showed male Octopus joubini to weigh more than females at a given mantle length. This species displays slight allometric growth resulting in changing body proportions through the life cycle. Relative food intake is highest at hatching and decreases with age. Mean gross growth efficiency over the life span was approximately 40%.     

Thermal effects on growth and time to starvation during the yolk-sac larval period of Atlantic mackerel Scomber scombrus L.

The effect of incubation temperature (8·6, 11·1, 13·2, 15·1 and 16·8° C) on north-east Atlantic mackerel Scomber scombrus development, growth and age at starvation during the yolk-sac larval period was investigated. Standard length at hatch was found to be inversely proportional to incubation temperatures within the natural thermal ranges of this species; it ranged from 3·76 mm at 11·1° C to 3·30 mm at 17·8° C. Following hatch, however, larval growth rate was positively related to temperature. Individual logistic models, as a function of temperature and age, were fitted to the development processes of gape, eye pigmentation, jaw mobility and yolk exhaustion. Thereafter, development was classified into different ordered stages and an extended continuation model was fitted to the multinomial ordered stage classification. In all cases, there was a difference of >23 h between the first and the last individual developing in certain stage. The probability of survival decreased with age and was inversely related to temperature. Yolk utilization varied from 4·5 to 8·6 days and individuals died between 7·9 and 12·2 days from 17·8 to 11·1° C. The study demonstrated the significant impact that temperature has on development, growth and survival rates, during the early life history.     

Growth responses of planktonic desmid species in a temperature—light gradient

SUMMARY. 1. Isolates of twelve planktonic desmid species were tested for their growth response in batch culture, using an apparatus that generates crossed gradients of temperature and light intensity.
2. Up to 15°C, growth was mainly temperature-limited. At higher temperatures, there was an increasing effect of light limitation. Optimal growth temperatures were in the range 25–30°C.
3. Highest specific growth rates varied from 0.28 to 1.34 day⁻¹. Species with lowest growth rates originated from oligo-mesotrophic habitats, those with highest growth rates from eutrophic ones.
4. Ecophysiological aspects are discussed in some detail, as well as the significance of the experimental data for distributions in the field.     

Hatching time and growth of Nemurellapictetii (Plecoptera: Nemouridae) in the laboratory and a Lake District stream

SUMMARY. 1. Nemurella pictetii Klapæplek took 2 years to complete its life cycle in both the laboratory and a small stream in the English Lake District.
2. Hatching time (days after oviposition for 10%. 50% and 90% of the eggs to hatch) and hatching period (days between dates for 10% and 90% hatched) decreased with increasing water temperature in the laboratory, and the relationships were well described by a power-law. Estimates of the mean time for 50% hatching in the stream varied between 16 and 31 days after oviposition. depending on temperature.
3. Larval instars numbered fifteen for males and seventeen for females with a constant ratio of 1.18 between successive instars (conformed with Dyar's rule). Larval growth was exponential at four constant temperatures in the laboratory; mean instantaneous growth rates were 0.40±0.01% day⁻¹ at 5.9°C, 0.43±0.01% day⁻¹ at 8.2°C, 0.46±0.01% day⁻¹ at 12. 1°C. 0.56±0.02%day⁻¹ at 19.8°C. No larvae survived after instar XI at 19.8°C.
4. Larval growth was exponential in the stream and was scarcely affected by variations in water temperature (range 4.2 -14.0°C); mean growth rates for three year-classes were 0.41±0.02, 0.43±0.08, 0.54±0.05% day⁻¹. Their similarity to laboratory growth rates under optimum conditions suggests that the availability of resources, such as food and space, was not restricting growth in the stream.     

Morphological dormancy in seeds of the autumn-germinating shrub Lonicera caerulea var. emphyllocalyx (Caprifoliaceae)

To better understand the germination ecophysiology of the genus Lonicera , the dormancy class, temperature requirements for embryo growth and radicle emergence and phenology of seedling emergence were determined for Lonicera caerulea var. emphyllocalyx . At maturity, seeds have an underdeveloped embryo (approximately 28% of the length of full-grown embryos). Embryos in fresh seeds grew to full length at 15, 20, 20/10 and 25/15°C within 3 weeks, but failed to grow at ≤ 10°C and at 30°C. Radicles emerged from 86–100% of freshly matured seeds in light at 15, 20, 20/10 and 25/15°C within 28 days, but failed to emerge at 10°C. Radicles emerged equally well in a 12 h photoperiod and in continuous darkness at 25/15°C. Rapid embryo growth and germination over a range of conditions indicate that seeds of this taxon have morphological dormancy (MD); this is the first report of MD in a species of Lonicera . Seeds are dispersed in summer, at which time high temperatures promote embryo growth. Embryos grow to the critical length for germination in approximately 1 month; the peak of seedling emergence occurs in early autumn. Radicles emerged within 2 months from 98% of seeds buried at soil depths of 2 cm and 10 cm in the field in August in Sapporo, Japan; thus, seeds have no potential to form a persistent soil seed bank. However, seeds sown too late in autumn for embryos to grow remained viable and germinated the following summer when temperatures were high enough to promote embryo growth.     

Population growth in some Mesostoma species (Turbellaria) predatory on mosquitoes

SUMMARY 1. Turbellarian predators of the genus Mesostoma prey on the aquatic stages of mosquitoes. In order to evaluate their potential as control agents, a comparison of population parameters has been made on three species from Australia, Africa and Papua New Guinea: M. appinum , M. zariae and M. timbunke.
2. The life cycle of these species is relatively short at higher temperature ranges (22–30°C) and varies from 12 to 35 days, depending on the temperature. M. appinum does not increase in numbers at 30°C, white M. timbunke is unable to reach sexual maturity at 15°C. M. appinum , but not M. zariae , multiplies slowly at 15°C, although both species survive at this temperature. The fastest population growth was obtained for M. appinum at 22°C, and for M. zariae and M. timbunke at 30°C. The doubling time for the population is about 6–7 days in the multivoltine species, M. appinum and M. zariae , and about 18.5 days in univoltine M. timbunke .
3. A significant part of the growing population is composed of immature individuals, which corresponds to the high values of the reproductive parameters R_o and r_m. In M. appinum and M. zariae , individuals rarely produce dormant resting eggs except under deteriorating conditions. M. timbunke produces only dormant eggs, and in this respect resembles arctic and subarctic species. A convergence of the reproductive modes between this equatorial species and the high latitude species might be interpreted as adaptation to harsh environments.
4. The overall population growth of all Mesostoma spp. is several times faster than in Dugesia dorotocephala and D. trigrina , other flatworms studied as potential biological control agents of mosquitoes     

Growth at sub-zero temperatures of black spot fungi from meat

Glycerol can prevent both freezing and desiccation of micro-organisms growing at sub-zero temperatures. On media containing glycerol, at concentrations readily tolerated by the organisms at ambient temperatures, three species of fungi isolated from black spot spoilt meat failed to grow at temperatures much below -5°C. This would, therefore, seem to be the minimum possible growth temperature of these organisms. Although the fungi could grow on frozen media, their rates of growth were such that, on frozen meat, several months would be required for colonies to become barely visible. It therefore seems that significant black spot spoilage will only develop on frozen meat if it is held at temperatures within 2–3° below the freezing point for prolonged periods, or if the meat surface reaches higher temperatures with surface drying inhibiting bacterial growth. There has been little study during the last 50 years of mould spoilage of meat, although it is still of importance in the international trade in frozen meats. Because moulds grow relatively slowly, they only spoil meat if the storage conditions prevent bacterial growth, but there are few firm data on the time and temperature requirements for visible mould growth to develop in the absence of bacterial spoilage. Such data are necessary if the causes of particular outbreaks of fungal spoilage are to be assessed correctly.     

Growth and food choice by two species of limnephilid caddis larvae given natural and artiflcial foods

SUMMARY 1. Larvae of the caddisfly Limnephilus externus grew faster than those of Nemotaulius hostilis in a permanent pond in southern Alberta.
2. We investigated whether this was due to more efficient food processing by L. externus , whether their growth coincided with high environmental temperatures, or whether they had the ability to choose and exploit higher quality food.
3. Of five foods used, protein content was highest in wheat flakes, similar in alder, bur-reed and willow leaves, and lowest in the moss Leptodictyum .
4. Both species grew faster and survived better on the wheat flakes, but there was no statistically significant difference between species on the same food when reared at 4 or 8°C in the laboratory.
5. At 16°C L. externus grew better than N. hostilis when fed wheat, but N. hostilis survived better on alder. Both species had higher survival and growth rates per day-degree at 8 and 4 than at 16°C.
6. Thus, faster growth rates of L. externtus in the field appear to be due simply to higher temperatures during the larval growth period. Indeed, N. hostilis had a significantly higher growth rate per day-degree in a field experiment.
7. In food preference experiments, L. externus chose wheat first, moss second, alder third, and willow last; N. hostilis chose alder first, bur-reed second, moss third, and wheat last.
8. Protein content, leaf texture, microbial conditioning, and an interaction between larval behaviours selecting for food quality and case materials, are potential factors that influence'food preference'results.     

Temperature-induced changes in the life cycle of Leuctra nigra(Plecoptera: Leuctridae) from a Lake District stream

1. The life cycle of Leuctra nigra (Olivier) took 2 years in a small stream in the English Lake District and the exponential growth of the larvae was scarcely affected by variations in water temperature (range 4.2-14.0°C). Mean growth rates for three year-classes were 0.43±0.01, 0.42±0.01, 0.39±0.05% body length day^?1. There were thirteen or fourteen larval instars for males and fourteen or fifteen for females. The ratio between successive instars was a constant 1.20 (conformed with Dyar's rule). 2. Larval growth and mortality were exponential at six constant temperatures (5.9, 8.2, 12.1, 15.8, 18.2, 19.8°C) in the laboratory. Mean growth rates (% body length day^?1) increased directly with temperature from 0.37 (5.9°C) to 0.55 (19.8°C). Mean mortality rates (% day^?1) increased directly with temperature from 0.20 (5.9°C) to 0.26 (12.1°C) and then markedly increased to 0.54-0.58 at the three higher temperatures. Only 7-10% of animals completed their life cycle at the three higher temperatures compared with 23–27% at the three lower temperatures. Egg production also decreased considerably at the higher temperatures. 3. As growth rates in the stream and laboratory were similar at similar temperatures (<14°C), the optimum conditions for growth in the laboratory were probably similar to those in the stream; therefore resources such as food and space were not restricting growth in the stream. 4. The implications of the temperature-induced changes in growth and mortality are discussed and it is concluded that although the life cycle can change from semivoltine to univoltine with increasing temperature, the costs of a univoltine life cycle are high in terms of survival and egg production, both of which decreased markedly between 12.1 and 15.8°C. Therefore the optimum habitat for this species appears to be a summer cool stream (maximum temperature <14°C) and the optimal life cycle appears to be about 2 years from egg to adult.     

Effect of temperature on sulphate reduction, growth rate and growth yield in five psychrophilic sulphate-reducing bacteria from Arctic sediments

Five psychrophilic sulphate-reducing bacteria (strains ASv26, LSv21, PSv29, LSv54 and LSv514) isolated from Arctic sediments were examined for their adaptation to permanently low temperatures. All strains grew at −1.8°C, the freezing point of sea water, but their optimum temperature for growth ( T _opt) were 7°C (PSv29), 10°C (ASv26, LSv54) and 18°C (LSv21, LSv514). Although T _opt was considerably above the in situ temperatures of their habitats (−1.7°C and 2.6°C), relative growth rates were still high at 0°C, accounting for 25–41% of those at T _opt. Short-term incubations of exponentially growing cultures showed that the highest sulphate reduction rates occurred 2–9°C above T _opt. In contrast to growth and sulphate reduction rates, growth yields of strains ASv26, LSv54 and PSv29 were almost constant between −1.8°C and T _opt. For strains LSv21 and LSv514, however, growth yields were highest at the lowest temperatures, around 0°C. The results indicate that psychrophilic sulphate-reducing bacteria are specially adapted to permanently low temperatures by high relative growth rates and high growth yields at in situ conditions.     

Effects of temperature on growth rates of fungi from subantarctic Macquarie Island and Casey,Antarctica

Summary The linear growth rates of fungal isolates were measured on agar plates at temperatures ranging from 4° to 35°C. Fungi tested included the major fungal colonizers of leaves and litter of the three dominant plant species on subantarctic Macquarie Island, and major fungal species associated with plant and soil communities near Australia's Casey Station on the Antarctic Continent. All fungi grew at 4°C and were classified as psychrotrophs. Maximum growth rates were recorded at temperatures of 10° to 20°C for 13 of the 15 isolates from Macquarie Island and for all six isolates from Casey. Most of the leaf colonizing fungi from Macquarie Island had optimum growth temperatures of 15°C whereas all litter fungi from Macquarie Island and Casey fungi except Thelebolus microsporus had optimum growth temperatures of 20°C or above. Maximum growth of all species was at temperatures above those normally prevailing in their natural environments, with most species growing at 4°C at between 10% and 30% of their maximum rates. However, microclimatic effects may have resulted at times in temperatures near their growth optima. The highest growth rates at 4°C were recorded for Phoma spp. 1 and 2, Phoma exigua and Mortierella gamsii from Macquarie Island and Mortierella sp. 1 from Casey. Thelebolus microsporus and sterile sp. G from Casey also grew relatively fast at 4°C, and these species, and Phoma sp. 3 and Phoma exigua from Macquarie Island had the lowest Q-₁₀ values for the temperature range 4° to 15°C.     

Adaptation of soil microbial communities to temperature: comparison of fungi and bacteria in a laboratory experiment

Temperature not only has direct effects on microbial activity, but can also affect activity indirectly by changing the temperature dependency of the community. This would result in communities performing better over time in response to increased temperatures. We have for the first time studied the effect of soil temperature (5–50 °C) on the community adaptation of both bacterial (leucine incorporation) and fungal growth (acetate-in-ergosterol incorporation). Growth at different temperatures was estimated after about a month using a short-term assay to avoid confounding the effects of temperature on substrate availability. Before the experiment started, fungal and bacterial growth was optimal around 30 °C. Increasing soil temperature above this resulted in an increase in the optimum for bacterial growth, correlated to soil temperature, with parallel shifts in the total response curve. Below the optimum, soil temperature had only minor effects, although lower temperatures selected for communities growing better at the lowest temperature. Fungi were affected in the same way as bacteria, with large shifts in temperature tolerance at soil temperatures above that of optimum for growth. A simplified technique, only comparing growth at two contrasting temperatures, gave similar results as using a complete temperature curve, allowing for large scale measurements also in field situations with small differences in temperature.     

Rapid cold-hardening of Drosophila melanogaster in a field setting

Abstract.  Although laboratory studies demonstrate that cooling to ecologically relevant temperatures and/or at ecologically relevant rates induces rapid cold-hardening (RCH) in a variety of insects, little is known of the induction of RCH in nature. In the present study, caged Drosophila melanogaster (1–2 days posteclosion) from a colony established with flies collected locally are placed in a field setting (i.e. in approximately 4-cm deep leaf litter beneath an apple tree in Mount Pleasant, Michigan) during late afternoon (18.00 h EST; 05.00 h GMT). As the cage temperature falls from 22.1 ± 0.8 to 10.1 ± 0.1 °C between 18.00 and 06.00 h, the proportion of flies surviving a transfer to –6 °C for 1 h increases from 10.0 ± 6.2% to 68.1 ± 7.2%. When obtained from field cages, and then cooled from 23 °C at approximately 0.33 °C min⁻¹, more female flies remain behaviourally responsive (clinging to surfaces, exhibiting an active righting response, and/or climbing) at temperatures of 8–12 °C (24.00 h samples) or 7–12 °C (06.00 h samples), than do those sampled from cages kept in an incubator (23 °C). Field cooling reduces chill coma temperature from 8.7 ± 0.2 °C at 06.00 h to 7.1 ± 0.2 °C at 24.00 h, and to 6.6 ± 0.2 °C at 06.00 h. These data demonstrate that, in a recently collected culture of D. melanogaster , natural changes in microenvironmental temperature induce RCH that can benefit the organism at temperatures encountered in nature.