Standard operative temperatures and cost of thermoregulation in the arctic ground squirrel,Spermophilus undulatus

Summary Body temperatures (T _b) and daily activity patterns of free-living arctic ground squirrells (Spermophilus undulatus) were determined via telemetry at a field site in northern Alaska. Simultaneous measurements were made of ambient temperature (T _a), wind speed (V), and incident solar radiation. The operative environmental temperature (T _e) for ground squirrels was obtained from fur-covered, thin metal taxidermic models of the animals. Standard operative temperature (T _es), a comparative index of heat flow, was calculated from T _e, V, and laboratory measurements of thermal conductivity.During the period of the study (August), S. undulatus were active for about 14 h per day (06.00 to 20.00 h). T _b was high throughout the daily cycle, averaging 38–39°C. Circadian variations in T _b were slight; average T _b values dropped <1°C at night. Daytime T _b fluctuations were not closely correlated to activity or to changes in environmental conditions. Air temperatures during the study were low, usually between 10 and 15°C during the day. However, T _es in exposed areas was normally higher, even though skies were generally overcast. During periods of sunshine, T _es may be as high as 34°C. The absence of nocturnal activity may result from increased costs of thermoregulation at night, which sharply reduces foraging efficiency. The high and stable body temperatures of S. undulatus probably result from thermoneutral daytime T _es, low activity levels, and the use of well-insulated nests.     

Thermoregulation in resting and active polar bears

Summary Polar bears (Ursus maritimus) regulate their body temperatures both physiologically and behaviourally proportional to their level of activity while within the thermoneutral zone. Core temperatures (T _c=36.9±0.5°C at rest) varied with the 4^th power of walking speed for the two subadult (220 kg) bears tested, whereas subcutaneous temperatures (T _sk=35.3±2.2°C at rest) were closely correlated withT _c but also varied with wind speed (v _a) and ambient temperature (T _a). Radiative fur temperatures (T _r) were closely correlated withT _a and negligibly withT _sk. Predictive equations for these temperature relationships were derived by regression analysis. Maximum rates of heat storage (S _max) were above that predicted from the literature implying that the polar bear is an energetically costly walker. Radiative heat losses of a resting polar bear amount to between 36–67% of the metabolism and assuming a respiratory heat loss of 7–10%, convective heat losses (by difference) would thus range from 33–64%. When walking, the cooling of the fur surface by forced convection and the pendulum effect of the moving legs of the bear lead to estimated convective heat losses on the order of 75% of the heat production while radiative losses are reduced to 13–22%. Increasing wind speeds enhance further this reciprocal effect.     

Thermoregulatory responses to egg cooling in incubating bantam hens

Summary O₂ consumption, electromyographic activity (EMG), heart rate (HR), cloacal temperature (T _b) and broodpatch temperature (T _sb) were measured in bantam hens incubating eggs of different temperatures (T _e). For comparison, the metabolic response to low ambient temperature (T _a) was measured in non-incubating hens.O₂ consumption increased nearly linearly with decreasingT _e down to 30°C. At this temperature O₂ consumption was about 3.5 x the resting level. Below 30°C O₂ consumption increased non-linearly, and reached 4.6 x the resting consumption at 15°C. Eggs of 10 and 0°C gave no further increase. Pectoral muscle EMG and HR also increased in response to egg cooling. The onset of egg cooling was associated with a decrease inT _b andT _sb. Hens exposed to lowT _a showed a lower critical temperature of about 24°C.It is concluded that heat loss from the brood-patch during incubation of cold eggs is compensated by shivering thermogenesis. AtT _e below 15°C heat production is at a maximum level, corresponding to the expected O₂ consumption at exposure to an ambient temperature of –65°C.Abbrevations EMG electromyography - T _a ambient temperature - T _b cloacal temperature - T _e egg temperature - T _sb brood-patch skin temperature     

Reproduction of Diaeretiella rapae on Russian wheat aphid hosts at different temperatures

Diaeretiella rapae (M'Intosh), a polyphagous and cosmopolitan parasite of aphids, was imported from China to the USA for biological control of Diuraphis noxia (Mordwilko), a pest of small grains. We studied several aspects of its biology on D. noxia hosts in the laboratory at 3 constant temperatures, 10.0, 21.1, and 26.7 °C. Females lived significantly longer than males at all 3 temperatures, and longevity was greatest at 10 °C, followed by 21.1 and 26.7 °C. Fecundity (= number of mummies) did not differ significantly among the 3 temperatures studied. The ovarian egg-load was 129.1 ± 9.3, and was significantly affected by the size of adult females. A pre-oviposition period ± 0.26 days) was detected at 10 °C, but not at the other temperatures. Pre-imaginal survivorship was similar among temperatures, while R _o and T _c decreased with temperature, and r _m increased with temperature. The offspring sex ratio (proportion females) was lowest at 26.7 °C, and similar between 10.0 and 21.1 °C. In addition, the offspring sex ratio significantly declined with the age of the female parent. The suitability of D. rapae for colonization against D. noxia in North America is discussed in relation to its responses to temperature and the climate of its home range.     

The thermal and energetic significance of clustering in the speckled mousebird,Colius striatus

Summary The effect of clustering behaviour on metabolism, body temperature, thermal conductance and evaporative water loss was investigated in speckled mousebirds at temperatures between 5 and 36°C. Within the thermal neutral zone (approximately 30–35 °C) basal metabolic rate of clusters of two birds (32.5 J·g^-1·h^-1) and four birds (28.5 J·g^-1·h^-1) was significantly lower by about 11% and 22%, respectively, than that of individuals (36.4 J·g^-1·h^-1). Similarly, below the lower critical temperature, the metabolism of clusters of two and four birds was about 14% and 31% lower, respectively, than for individual birds as a result of significantly lower total thermal conductance in clustered birds. Body temperature ranged from about 36 to 41°C and was positively correlated with ambient temperature in both individuals and clusters, but was less variable in clusters. Total evaporative water loss was similar in individuals and clusters and averaged 5–6% of body weight per day below 30°C in individuals and below 25°C in clusters. Above these temperatures total evaporative water loss increased and mousebirds could dissipate between 80 and 90% of their metabolic heat production at ambient temperatures between 36 and 39°C. Mousebirds not only clustered to sleep between sunset and sunrise but were also observed to cluster during the day, even at high ambient temperature. Whereas clustering at night and during cold, wet weather serves a thermoregulatory function, in that it allows the brrds to maintain body temperature at a reduced metabolic cost, clustering during the day is probably related to maintenance of social bonds within the flock.Abbreviations BMR basal metabolic rate - bw body weight - C _totab total thermal conductance - EWI evaporative water loss - M metabolism - RH relative humidity - T _a ambient temperature - T _b body temperature - T _ch chamber temperature - T _cl cluster temperature - TEWL total evaporative water loss - LCT lower critical temperature - TNZ thermal neutral zone     

Different thermal conditions of the extremities affect thermoregulation in clothed man

The effects of different types of clothing on human deep body temperature were studied with six healthy male subjects in a supine posture. Two clothing ensembles were employed for the present study: A covered the whole body area with garments except the face (1.97 clo) and B covered only the trunk and the upper half of the extremities with garments (1.53 clo). The experiment was carried out in a climatic chamber at 55% ± 5% relative humidity under cooling and warming temperatures: the temperature was changed from 22°C to 10°C (cooling) and returned to 22°C again (warming). The major findings were: rectal temperature (T _re) continued to decrease gradually in A throughout the experiment, whereas in B it increased during cooling, and returned to previous levels during warming. As a result, Tre and chest skin temperature were maintained at a higher level in B than in A. Internal tissue conductances were greater in A than in B both during cooling and during warming. Thermal comfort appeared to have been influenced more by the rate of skin temperature change than by the level of skin temperature per se. It was concluded that peripheral vasoconstriction in B induced less heat flow from core to shell, and, thus, the core temperature was maintained at a higher level in B than in A.     

Daily and seasonal cycles of body temperature and aspects of heterothermy in the hedgehog Erinaceus europaeus

Summary Intra-abdominal temperature-sensitive radio transmitters were used to collect more than 350 sets of body temperature (T _b ) data from 23 captive adult hedgehogs over a 3-year period. Each data set comprised measurements made every 1/2 h for 24-h periods. Between 20 and 60 such data sets were recorded every calendar month, and a total of 17400 measurements of T _b were collected. The hedgehogs were exposed to natural environmental conditions at 57°N in NE Scotland. Hedgehogs showed seasonal changes in mean daily euthermic T _b ,with a July maximum of 35.9±0.2°C, a September minimum of 34.7±0.9°C, and a marked circadian T _b cycle that correlates closely with photoperiod. Maximal T _b occurred within 2 h of midnight and this pattern of nocturnal maximum and diurnal minimum T _b was most marked between April and September. The circadian T _b cycle was least correlated with photoperiod during winter. Hibernal T _b during winter correlated with ambient temperature (T _a ),it was maximal in September (17.7±1.0°C) and minimal in December (5.2±0.9°C). Apart from the tracking of T _a and T _b during hibernal bouts, with a time-lag of 4–6 h, circadian rhythmicity of hibernal T _b was not evident. However, the T _b of hibernating hedgehogs rose significantly when T _a fell below — 5°C, although the animals did not neccessarily arouse. Although hibernal bouts occurred between September and April, 89.5% of such bouts were recorded between November and February. The mean time of entry into hibernation was 01:45±5.1 h GMT while the mean time of the start of spontaneous arousal from hibernation was 11:53±4.8 h GMT. Therefore, during hibernation hedgehogs were either fully aroused at night, when euthermic hedgehogs have maximalT _b ,or in deep hibernation around midday, when euthermic hedgehogs have minimal T _b .Since wild hedgehogs will feed during spontaneous arousal from hibernation, these timings are probably adaptive, and suggest that entry into, and arousal from, hibernation may be extensions of circadian cyclicity. Spontaneous bouts of transient shallow torpor (TST) were recorded throughout the year, with nearly 80% of observations occurring during August and September, at the start of the hibernal period. TST bouts lasted for 4.9±2.9 h, with T _b falling to 25.8±3.1 °C. Only 20% of TST bouts immediately preceded hibernation and their duration did not correlate with T _a or body mass. TST bouts started at 06:51±4.7 h GMT, significantly later than entry into hibernation, and ended at 13:04±5.4 h GMT. The function of TST bouts is unclear, but they may be preparation for the hibernation season or a further energy conservation strategy. When arousing from hibernation hedgehogs warmed at a rate of 1.9±0.4°C·h^-1, and when entering hibernation cooled at 7.9±1.9°C·h^-1. Warming rates were slightly higher during mid-winter when T _b and body mass were minimal, but cooling rates were 44% higher at the end of the hibernal period compared to the start. Cooling and warming rates were strikingly similar to those measured in hedgehogs at 31°N. These results demonstrate that thermoregulation in the hedgehog is closely regulated and changes on a seasonal basis, in meeting with requirements of surviving food shortages and low temperature during winter.Abbreviations T _a ambient temperature - T _b body temperature - CSD circular standard deviation - SWS slow wave sleep - TST transient shallow torpor     

Pigeon flight in a wind tunnel

Summary Core temperatureT _c, breast temperatureT _s–br and leg temperatureT _s–1 were measured simultaneously in pigeons during rest and flight in a wind tunnel, using thermistors.MeanT _c at rest is 39.8±0.7°C and is independent of ambient temperatureT _a (10–30°C). In the first minutes of flight,T _c increases to 1.5–3.0°C above resting level and remains at this higher level. This hyperthermia increases withT _a (v=const.). It is±constant in the lowT _a range (10.6–13.9°C) at flight speeds v ranging from 10–18 m s^–1 and normal body mass, but increases with v and elevated body mass in the highT _a range (23.7–28.8°C). T _s–1 is adapted toT _a at rest and increases in flight up to 3–4°C belowT _c. This increase inT _s–1 is linear toT _a. T _s–br is always lower thanT _c, in extreme cases reaching restingT _c in flight.Supported by the Deutsche Forschungsgemeinschaft     

Respiration of individual honeybee larvae in relation to age and ambient temperature

The CO₂ production of individual larvae of Apis mellifera carnica, which were incubated within their cells at a natural air humidity of 60–80%, was determined by an open-flow gas analyzer in relation to larval age and ambient temperature. In larvae incubated at 34 °C the amount of CO₂ produced appeared to fall only moderately from 3.89±1.57 µl mg^–1 h^–1 in 0.5-day-old larvae to 2.98±0.57 µl mg^–1 h^–1 in 3.5-day-old larvae. The decline was steeper up to an age of 5.5 days (0.95±1.15 µl mg^–1 h^–1). Our measurements show that the respiration and energy turnover of larvae younger than about 80 h is considerably lower (up to 35%) than expected from extrapolations of data determined in older larvae. The temperature dependency of CO₂ production was determined in 3.5-day-old larvae, which were incubated at temperatures varying from 18 to 38 °C in steps of 4 °C. The larvae generated 0.48±0.03 µl mg^–1 h^–1 CO₂ at 18 °C, and 3.97±0.50 µl mg^–1 h^–1 CO₂ at 38 °C. The temperature-dependent respiration rate was fitted to a logistic curve. We found that the inflection point of this curve (32.5 °C) is below the normal brood nest temperature (33–36 °C). The average Q₁₀ was 3.13, which is higher than in freshly emerged resting honeybees but similar to adult bees. This strong temperature dependency enables the bees to speed up brood development by achieving high temperatures. On the other hand, the results suggest that the strong temperature dependency forces the bees to maintain thermal homeostasis of the brood nest to avoid delayed brood development during periods of low temperature.Abbreviations m body mass - R rate of development or respiration - T_I inflexion point of a logistic (sigmoid) curve - T_L lethal temperature - T_O temperature of optimum (maximum) developmentCommunicated by G. Heldmaier     

Seasonal and daily rhythms of body temperature in the European hamster (Cricetus cricetus) under semi-natural conditions

Body temperature of five European hamsters exposed to semi-natural environmental conditions at 47° N in Southern Germany was recorded over a 1.5-year period using intraperitoneal temperature-sensitive radio transmitters. The animals showed pronounced seasonal changes in body weight and reproductive status. Euthermic body temperature changed significantly throughout the year reaching its maximum of 37.9±0.2°C in April and its minimum of 36.1±0.4°C in December. Between November and March the hamsters showed regular bouts of hibernation and a few bouts of shallow torpor. During hibernation body temperature correlated with ambient temperature. Monthly means of body temperature during hibernation were highest in November (7.9±0.8°C) and March (8.2±0.5°C) and lowest in January (4.4±0.7°C). Using periodogram analysis methods, a clear diurnal rhythm of euthermic body temperature could be detected between March and August, whereas no such rhythm could be found during fall and winter. During hibernation bouts, no circadian rhythmicity was evident for body temperature apart from body temperature following ambient temperature with a time lag of 3–5 h. On average, hibernation bouts lasted 104.2±23.8 h with body temperature falling to 6.0±1.7°C. When entering hibernation the animals cooled at a rate of -0.8±0.2°C·h^-1; when arousing from hibernation they warmed at a rate of 9.9±2.4°C·h^-1. Warming rates were significantly lower in November and December than in January and February, and correlated with ambient temperature (r=-0.46, P<0.01) and hibernating body temperature (r=-0.47, P<0.01). Entry into hibrnation occured mostly in the middle of the night (mean time of day 0148 hours ±3.4 h), while spontaneous arousals were widely scattered across day and night. For all animals regression analysis revealed free-running circadian rhythms for the timing of arousal. These results suggest that entry into hibernation is either induced by environmental effects or by a circadian clock with a period of 24 h, whereas arousal from hibernation is controlled by an endogenous rhythm with a period different from 24 h.Abbreviations bw body weight - CET central European time - T _a ambient temperature - T _b body temperature - TTL transistor-transistor logic     

The effect of temperature on digestive and assimilation efficiency,gut passage time and appetite in an ambush foraging lizard,<Emphasis Type="Italic"> Cordylus melanotus melanotus</Emphasis>

In ectotherms, an increase in body temperature increases metabolic rate and may increase rates of digestive processes. We measured the thermal dependence of the apparent digestive and apparent assimilation efficiencies (ADE and AAE), gut passage time (GP) and appetite in Cordylus melanotus melanotus, a medium sized Crag Lizard, which is endemic to South Africa. Trials were conducted at 20, 22, 25, 30, 32 and 35 °C under controlled conditions. Trials lasted 14 days, during which, lizards were fed ca. 1 g mealworms per day. Glass beads were used as markers to determine GP at the beginning and end of trials. Faeces and urates were collected daily and oven dried at 50 °C. The energy content of egested matter was then measured using bomb calorimetry. ADE and AAE were not affected by temperature for either males or females. The mean±SE ADE and AAE were 94.4±0.3% and 87.2±0.6%, respectively. GP was not significantly different between males and females at any temperature, but decreased significantly with increasing temperature. Appetite was significantly different between the different temperatures measured. The decrease of gut passage time with increasing temperature was expected, since the digestive and assimilation efficiencies are similar over the range of temperatures tested. Lizards are thus assimilating a similar proportion of ingested energy, but at faster rates at higher temperatures. The results indicate that the digestive physiology of this species results in maximum energy gain per meal in environments where food is scarce.Abbreviations AAE apparent assimilation efficiency - ADE apparent digestive efficiency - AE assimilation efficiency - DE digestive efficiency - GP gut passage rate - NEA net energy absorbed through gut - NER net usable energy retained - SVL snout-vent length - T _b body temperature Communicated by G. Heldmaier     

The effect of temperature on the pattern of torpor in a marsupial hibernator

Physiological variables of torpor are strongly temperature dependent in placental hibernators. This study investigated how changes in air temperature affect the duration of torpor bouts, metabolic rate, body temperature and weight loss of the marsupial hibernator Burramys parvus (50 g) in comparison to a control group held at a constant air temperature of 2°C. The duration of torpor bouts was longest (14.0±1.0 days) and metabolic rate was lowest (0.033±0.001 ml O₂·g^-1·h^-1) at2°C. At higher air temperatures torpor bouts were significantly shorter and the metabolic rate was higher. When air temperature was reduced to 0°C, torpor bouts also shortened to 6.4±2.9 days, metabolic rate increased to about eight-fold the values at 2°C, and body temperature was maintained at the regulated minimum of 2.1±0.2°C. Because air temperature had such a strong effect on hibernation, and in particular energy expenditure, a change in climate would most likely increase winter mortality of this endangered species.Abbreviationst STP standard temperature and pressure - T _a air temperature - T _b body temperature - VO₂ rate of oxygen consumption     

Bioenergetics and thermal physiology of American water shrews (<Emphasis Type="Italic">Sorex palustris</Emphasis>)

Rates of O₂ consumption and CO₂ production, telemetered body temperature (T_b) and activity level were recorded from adult and subadult water shrews (Sorex palustris) over an air temperature (T_a) range of 3–32°C. Digesta passage rate trials were conducted before metabolic testing to estimate the minimum fasting time required for water shrews to achieve a postabsorptive state. Of the 228 metabolic trials conducted on 15 water shrews, 146 (64%) were discarded because the criteria for inactivity were not met. Abdominal T_b of S. palustris was independent of T_a and averaged 38.64±0.07°C. The thermoneutral zone extended from 21.2°C to at least 32°C. Our estimate of the basal metabolic rate for resting, postabsorptive water shrews (96.88±2.93 J g^–1 h^–1 or 4.84±0.14 ml O₂ g^–1 h^–1) was three times the mass-predicted value, while their minimum thermal conductance in air (0.282±0.013 ml O₂ g^–1 h^–1) concurred with allometric predictions. The mean digesta throughput time of water shrews fed mealworms (Tenebrio molitor) or ground meat was 50–55 min. The digestibility coefficients for metabolizable energy (ME) of water shrews fed stickleback minnows (Culaea inconstans) and dragonfly nymphs (Anax spp. and Libellula spp.) were 85.4±1.3% and 82.8±1.1%, respectively. The average metabolic rate (AMR) calculated from the gas exchange of six water shrews at 19–22°C (208.0±17.0 J g^–1 h^–1) was nearly identical to the estimate of energy intake (202.9±12.9 J g^–1 h^–1) measured for these same animals during digestibility trials (20°C). Based on 24-h activity trials and our derived ME coefficients, the minimum daily energy requirement of an adult (14.4 g) water shrew at T_a = 20°C is 54.0 kJ, or the energetic equivalent of 14.7 stickleback minnows.     

Diversity in amylopectin structure, thermal and pasting properties of starches from wheat varieties/lines

Structural, thermal and pasting diversity of starches from Indian and exotic lines of wheat was studied. Majority of the starches showed amylose content ranging between 22% and 28%. Endotherm temperatures (T_o, T_p and T_c) of the starches showed a range between 56–57, 60 –61 and 65.5–66.5 °C, respectively. Exotherms with T_p between 87.0 and 88.2 °C were observed during cooling of heated starches, indicating the presence of amylose–lipid complexes. Exotherm temperatures were negatively correlated to swelling power. Amylopectin unit chains with different degree of polymerization (DP) were observed to be associated with pasting temperature, setback and thermal (endothermic T_o, T_p, and T_c) parameters. Amylopectin unit chains of DP 13–24 showed positive relationship with endothermic T_o, T_p and T_c. Pasting temperature showed positive correlation with short chains (DP 6–12) while negative correlation with medium chain (DP 13–24) amylopectins. Setback was positively correlated to DP 16–18 and negatively to DSC amylose–lipid parameters.     

Thermoregulation as a limit to habitat use in alpine marmots (Marmota marmota)

Summary The body temperature (T _b) of free-living alpine marmots rose with activity; the higher the effective environmental temperature (T _e), the higher the rise. Maximum T _bof 40° C was reached at the time of greatest activity in late afternoon or evening. The activity pattern was strongly influenced by the microclimate. Up to an T _eof 25° C the animals spent more time above ground and were more active the higher T _ewas, but above 25° C this trend was reversed, and the animals withdrew increasingly into their burrows. On warm days the activity pattern was therefore bimodal and above ground presence was reduced, in contrast to cool days. Hence behavioural thermoregulation limits the available time for above ground activity on days with high T _ein this strictly diurnal species. We suggest that the alpine marmots' preference for south oriented slopes is due to the better conditions for hibernation there, the microclimate during summer is more favourable on northerly slopes. Thermoregulatory constraints could also keep alpine marmots away from lower elevations.     

Energy relations of winter roost-site utilization by American goldfinches (Carduelis tristis)

Summary American goldfinches (Carduelis tristis) were observed roosting in Colorado blue spruce (Picea pungens), which comprised part of a mixed stand of conifers. Their winter roost-sites were distally situated among the most densely-needled branches on the leeward sides of these trees. Heated and unheated taxidermic goldfinch mounts were placed within these sites and at the same height in an adjacent clearing. The radiative and convective characteristics of these locations were monitored simultaneously and compared to predicted power requirements of live goldfinches (based on laboratory calibration of heated mounts) and operative temperatures (T _e ; based on body temperatures of unheated mounts). The winter roost-sites significantly reduced radiative and convective heat exchanges between goldfinches and the environment. Based on body composition data for winter goldfinches, all but two birds sampled could endure a 15-h roost period at average overnight T _e 's as low as-40°C. In contrast, if these birds were prevented from feeding the following day, only 30% could survive the imposition of a 39-h fast at average T _e 's of-2°C. Winter roost-site selection may be more constrained by thermoregulatory considerations in small birds than in larger species.     

Life history of Euseius scutalis feeding on citrus red mite Panonychus citri at various temperatures

The aim of this study was todetermine the biology and reproductivepotential of Euseius scutalis(Athias-Henriot) (Acari: Phytoseiidae) atvarious temperatures. These data are of valuein relation to mass rearing and the developmentof population dynamics models. The developmenttime, survival and fecundity of E.scutalis were determined at 20, 25 and30 ± 1 °C, 65 ± 10% RH and 16:8photoperiod. Total development times of E.scutalis were 6.7, 4.9 and 4.2 days at 20, 25and 30 ± 1 °C, respectively, using adiet of all life stages of the spider mite Panonychus citri (McGregor) (Acari:Tetranychidae). In general, preoviposition andpostoviposition periods of E. scutaliswere shortened as temperature increased, butthe oviposition period was longer at 25 °C than at 20 and 30 °C. Theshortest survival time of E. scutalis, at30 °C, was 10.1 days, followed by 23.7days and 28.6 days at 20 and 25 °C,respectively. Mated females laid on average1.1, 1.4 and 1.7 eggs per female per day and21.5, 39.7 and 17.1 eggs over their entire lifetime at 20, 25 and 30 °C, respectively.The sex ratios of E. scutalis were2.11/1, 2.24/1 and 2.11/1 female/male at 20, 25and 30 °C, respectively. The intrinsicrate of natural increase (r _m) increasedwith rising temperatures from 0.166 at 20 °C to 0.295 females/female/day at 30 °C. The net reproductive rate (R ₀)was highest at 25 °C (26.03females/female) and lowest at 30 °C(12.95 females/female). Mean generation time(T ₀) was longest at 25 °C (17.50days) and shortest (9.53 days) at 30 °C.     

A radio-telemetric study of the thermoregulation of free living water monitor lizards,Varanus S. salvator

Eight water monitor lizards, Varanus s. salvator, were captured; four individuals from an oil palm estate on the Malayan peninsula, and four from fresh water-deficient Tulai island 65 km off-shore in the South China Sea. They were fitted with a radio transmitter attached to a thermistor which was inserted into the cloaca of the animals and released. The heating rate during basking was measured as 0.117 and 0.118 °C·min^-1 while the daily cloacal temperature fluctuated between 29.5–37.3 °C. Cloacal temperature was measured on other individuals caught at random times during the day, which revealed a considerable daily and individual variation. The average cloacal temperature during activity was 30.4 °C. The peak activity appeared when body temperature was 31 °C. Thermoregulation by behavioural means included cooling in water and reducing heat loss at night by sleeping in burrows. The cooling rate for two individuals when submerged in 29 °C water was 0.308 and 0.340 °C·min^-1. There appeared to be a strong correlation between ambient temperature and cloacal temperature.Abbreviations bw body weight - T _a ambient temperature - T _a body temperature - T _c cloacal temperature - TOP Timor Oil Palm Estate - TUL Tulai Island     

Synchronous Crepuscular Flight of Female Asian Gypsy Moths: Relationships of Light Intensity and Ambient and Body Temperatures

Female gypsy moths (Lymantria dispar) of Asian heritage studied in central Siberia and Germany exhibit a highly synchronous flight at dusk, after light intensity falls to about 2 lux. This critical light intensity sets the timing of flight behaviors independent of ambient temperature. Flight follows several minutes of preflight wing fanning during which females in Germany and those from a laboratory colony (derived from Siberian stock) raised their thoracic temperatures to 32–33°C at ambient temperatures of 19–22°C. Thoracic temperature of females in free flight exceeded the air temperature (19–22°C) by approximately 11–13°C. The duration of wing fanning was strongly dependent on ambient temperature. In Germany, where ambient temperatures at dusk ranged between 21 and 25°C, females wing fanned for only 2.1 ± 0.2 (SE) min; in the much colder temperatures prevalent at dusk in Bellyk, central Siberia (11–13°C), females spent 11.2 ± 0.6 min in preflight wing fanning. The majority (80%) of mated and even virgin females initiated flight during the evening of the day they eclosed. However, in Bellyk, a small proportion (12%) of females wing fanned for an extended time but then stopped, whereas others (8%) never wing fanned and, therefore, did not take flight. Females also were capable of flight when disturbed during the daylight hours in Germany where the maximal temperature was high (27–30°C), but not in Siberia, where temperatures peaked at only 17–19°C. However, Siberian females were able to propel themselves off the tree on which they were perched by executing several vigorous wing flicks when approached by the predaceous tettigoniid, Tettigonia caudata.     

Weather,microclimate, and energy costs of thermoregulation for breeding Adélie Penguins

Summary We measured meteorological conditions and estimated the energy costs of thermoregulation for young and adult Adélie Penguins (Pygoscelis adeliae) at a breeding colony near the Antarctic Peninsula. Air temperatures averaged < 5°C and strong winds were frequent. Operative temperatures (T_e) for adults ranged from –8 to 28°C, averaging 5–6°C, for the period from courtship to fledging of chicks. The average energy cost of thermoregulation (C_th) for adult penguins was equivalent to 10–16% of basal metabolism. C_th comprised about 15% of the estimated daily energy budget (DEB) of incubating adults, but only about 1% of the DEB of adults feeding chicks. The T_e's for chicks older than 14 days ranged from 0 to 31°C, averaging 8.0 C. The C_th for downy chicks ranged from about 31% of minimal metabolic rate (MMR) in 1 kg chicks to about 10% of MMR in 3 kg chicks. Between initial thermal independence (age 12–14 days) and the cessation of parental feeding (age 35–40 days), chicks use about 10–11% of assimilated energy for thermoregulation. C_th is equivalent to about 17% of the MMR of fledglings during their 2–3 week fast. We observed no indication of thermal stress (i.e., conditions in which birds cannot maintain stable T_b) in adults and no indication of cold stress in any age class. However, on clear, calm days when air temperature exceeds 7–10°C for several hours, downy chicks are vulnerable to lethal hyperthermia.