Observations on thermoregulation in the western slender glass lizard, Ophisaurus attenuatus attenuatus (Sauria: Anguidae)

Based upon thermocouple implantation, thermal preferenda and voluntary maxima for the head and body were studied in three individuals of Ophisaurus attenuatus attenuatus collected in Texas. Calculated grouped data for the head and body mean preferred temperature were 31.2°C (range 29.O° -34.7°C) and 31.8°C (range 30.3° -34.5°C) respectively. Gaping or panting were found to be absent in the O. a. attenuatus examined in this study.     

Head-body thermal control, thermal preferenda, and voluntary maxima in the taipan, Oxyuranus scutellatus (Serpentes: Elapidae)

Head-body temperature differences of up to 5.7° and 6.1° C were observed during solar and radiant heating, respectively. Head temperature was more precisely regulated than body temperature and within preferred limits head temperature was significantly lower than body temperature. Higher temperatures were tolerated by the body than the head. Preferred temperatures for both the head and body are higher in the taipan than in other ophidians which have been reported upon, and approximate those temperatures reported for the voluntary maxima in other snakes.     

Thermal effects of dorsal head immersion in cold water on nonshivering humans.

Personal floatation devices maintain either a semirecumbent flotation posture with the head and upper chest out of the water or a horizontal flotation posture with the dorsal head and whole body immersed. The contribution of dorsal head and upper chest immersion to core cooling in cold water was isolated when the confounding effect of shivering heat production was inhibited with meperidine (Demerol, 2.5 mg/kg). Six male volunteers were immersed four times for up to 60 min, or until esophageal temperature = 34 degrees C. An insulated hoodless dry suit or two different personal floatation devices were used to create four conditions: 1) body insulated, head out; 2) body insulated, dorsal head immersed; 3) body exposed, head (and upper chest) out; and 4) body exposed, dorsal head (and upper chest) immersed. When the body was insulated, dorsal head immersion did not affect core cooling rate (1.1 degrees C/h) compared with head-out conditions (0.7 degrees C/h). When the body was exposed, however, the rate of core cooling increased by 40% from 3.6 degrees C/h with the head out to 5.0 degrees C/h with the dorsal head and upper chest immersed (P < 0.01). Heat loss from the dorsal head and upper chest was approximately proportional to the extra surface area that was immersed (approximately 10%). The exaggerated core cooling during dorsal head immersion (40% increase) may result from the extra heat loss affecting a smaller thermal core due to intense thermal stimulation of the body and head and resultant peripheral vasoconstriction. Dorsal head and upper chest immersion in cold water increases the rate of core cooling and decreases potential survival time.     

Temperature-induced changes of early development and yolk utilization in the African catfish Clarias gariepinus

Artificially fertilized eggs and yolk-sac larvae of a freshwater tropical/subtropical fish Clarias gariepinus receiving no external food were incubated at 22, 25 and 28° C until full yolk resorption. Developmental time, size and matter composition (CHNS-O Analyzer and ashing) were assessed at egg fertilization, hatching and yolk resorption; respiration was measured every 4–5 h. The course of acceleration of C. gariepinus embryonic developmental rate with temperature ( Q_{10 dev}) was compared over the temperature range to those of Cyprinus carpio and Oncorhynchus mykiss ; they differed greatly, but were similar when compared on the basis of effective temperatures specific to each fish. Specific growth rates for energy (88, 150 and 183% per day at 22,25 and 28° C, respectively) as well as the conversion efficiencies of egg energy (64, 71 and 68%, respectively) and protein (71, 78 and 76%, respectively) in C. gariepinus larval tissues were higher than those known for the endogenous feeding period of coldwater and temperate fish species. In C. gariepinus at the end of yolk resorption, the carbon percentage and caloric values of dry weight, size (in terms of dry matter, minerals, protein and energy per larva) and transformation efficiencies were lowest at 22° C, highest at 25° C and had slightly decreased at 28° C. A tentative mechanism which leads to the positive or negative response of body size to temperature over the viable temperature range is defined.     

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.     

Thermal effects of whole head submersion in cold water on nonshivering humans.

This study isolated the effect of whole head submersion in cold water, on surface heat loss and body core cooling, when the confounding effect of shivering heat production was pharmacologically eliminated. Eight healthy male subjects were studied in 17 degrees C water under four conditions: the body was either insulated or uninsulated, with the head either above the water or completely submersed in each body-insulation subcondition. Shivering was abolished with buspirone (30 mg) and meperidine (2.5 mg/kg), and subjects breathed compressed air throughout all trials. Over the first 30 min of immersion, exposure of the head increased core cooling both in the body-insulated conditions (head out: 0.47 +/- 0.2 degrees C, head in: 0.77 +/- 0.2 degrees C; P < 0.05) and the body-exposed conditions (head out: 0.84 +/- 0.2 degrees C and head in: 1.17 +/- 0.5 degrees C; P < 0.02). Submersion of the head (7% of the body surface area) in the body-exposed conditions increased total heat loss by only 10%. In both body-exposed and body-insulated conditions, head submersion increased core cooling rate much more (average of 42%) than it increased total heat loss. This may be explained by a redistribution of blood flow in response to stimulation of thermosensitive and/or trigeminal receptors in the scalp, neck and face, where a given amount of heat loss would have a greater cooling effect on a smaller perfused body mass. In 17 degrees C water, the head does not contribute relatively more than the rest of the body to surface heat loss; however, a cold-induced reduction of perfused body mass may allow this small increase in heat loss to cause a relatively larger cooling of the body core.     

The critical swimming speed of the sand smelt (Atherina presbyter Cuvier) in relation to capture at a power station cooling water intake

Critical swimming speeds (CSS) of sand smelt, Atherina presbyter , were measured in a laboratory flume. Individuals of all age classes (0+ to III +) found in the vicinity of Fawley power station, Hampshire, were tested at temperatures covering the seasonal range. The median CSS was 2.7 body lengths per second (bl s⁻¹) at 5.8 °C, rising to 5.7 bl s⁻¹ at 18.5°C.
A two-variable (water temperature and body length) regression model was fitted to the data, and this was used to assess escape potential of fish coming into contact with the power station cooling water intake currents and the extent of possible bias in fish length data collected from this source. It is concluded that the sand smelt remains vulnerable to entrainment at the power station over its whole length range and over the full range of seasonal temperatures and that size-dependent swimming performance will not lead to significant bias in sample length distributions.     

Freezing and desiccation tolerance of imbibed canola seed

Depending on the environmental conditions, imbibed seeds survive subzero temperatures either by supercooling or by tolerating freezing-induced desiccation. We investigated what the predominant survival mechanism is in freezing canola ( Brassica napus cv. Quest) and concluded that it depends on the cooling rate. Seeds cooled at 3°C h⁻¹ or faster supercooled, whereas seeds cooled over a 4-day period to −12°C and then cooled at 3°C h⁻¹ to−40°C did not display low temperature exotherms. Both differential thermal analysis and nuclear magnetic resonance (NMR) spectroscopy confirmed that imbibed canola seeds undergo freezing-induced desiccation at slow cooling rates. The freezing tolerance of imbibed canola seed (LT₅₀) was determined by slowly cooling to −12°C for 48 h, followed with cooling at 3°C h⁻¹ to −40°C, or by holding at a constant −6°C (LD₅₀). For both tests, the loss in freezing tolerance of imbibed seeds was a function of time and temperature of imbibition. Freezing tolerance was rapidly lost after radicle emergence. Seeds imbibed in 100 μ M abscisic acid (ABA), particularly at 2°C, lost freezing tolerance at a slower rate compared with water-imbibed seeds. Seeds imbibed in water either at 23°C for 16 h, or 8°C for 6 days, or 2°C for 6 days were not germinable after storage at −6°C for 10 days. Seeds imbibed in ABA at 23°C for 24 h, or 8°C for 8 days, or 2°C for 15 days were highly germinable after 40 days at a constant −6°C. Desiccation injury induced at a high temperature (60°C), as with injury induced by freezing, was found to be a function of imbibition temperature and time.     

Water temperature fluctuations and territoriality in the intertidal zone: two possible explanations for the elevational distribution of body size in Graus nigra

On the central coast of Chile, distribution of body size in Graus nigra varied with tidal pool height. With the objective of determining whether environmental temperature is one of the possible causes which explains the observed distribution pattern, two behavioural responses were analysed during an experimental period of increasing water temperature: number of opercular movements (an indirect measure of energy expenditure) and activity levels. The interactions of temperature × time and body size × time had a significant effect on the number of opercular movements. At low temperatures (13–15° C), large fish reached a maximum number of opercular movements, while small fish reached a maximum only at high temperatures (23–25° C). The interaction temperature × time had a significant effect on activity levels of different body sizes. In general, large fish appeared to be less active than small fish, however, at very high temperatures (24–26° C) all individuals increased their activity levels. These data indicate that small fish are acclimatized to live in a wider range of temperatures (13–23° C), and, for fish of all body sizes, the highest temperatures (23–26° C) probably constitute a suboptimal microhabitat. Strong territoriality was observed, with large individuals displacing smaller individuals. These data suggest that temperature is an important factor in explaining why large individuals are not present in high tidal pools (high temperatures), whereas territoriality explains why small individuals are not in low tidal pools (habitat of large individuals).     

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.     

Influence of ambient and thoracic temperatures upon sexual behaviour of the gypsy moth, Lymantria dispar

ABSTRACT. In an ambient temperature ( T _a) range of 18–28°C, thoracic temperatures ( T _th) of individual male Lymantria dispar (L.), caught at flight in the field, ranged from 21 to 36.5°C, with a correlation coefficient of 0.63 between T _th and ambient temperature ( T _a). Ambient temperature (and insolation) altered the insect's body temperature and the probabilities, latencies, and durations of preflight responses to pheromone. In a wind tunnel at 16 and 20°C, quiescent males exposed to pheromone raised their T _th by sustained wing fanning from 17 and 21°C, respectively, to c. 24°C before takeoff. At 24 and 28°C ambient, T _th rose by takeoff to 28 and 31°C, respectively. The latencies of male wing fanning in response to pheromone decreased from 1.44 min at 16°C ambient, to 0.58 min at 20°C, to 0.26 min at 24°C, and to 0.16min at 28°C. The components of behaviour (antennal twitch, body jerk, step and wing tremor) that occurred between quiescence and wing fanning were more frequent at ambients of 16 and 20°C than at 24 and 28°C.     

Supercooling ability in apple seeds as affected by temperature-induced modifications in water relations in the seed parts

Prolonged storage of apple fruits ( Pyrus malus L. cv. Golden Delicious) at different temperatures (0, 12 and 35°C) decreased the water content in seed coats and endosperms, higher temperatures being much more effective than the lower (0°C) one. No effect of the temperature on the embryo hydration was found. However, a pronounced decrease in water potential in the embryos was observed during the first 9 weeks. The decrease was much faster and the water potential reached lower levels in embryos isolated from seeds pretreated with higher temperatures (12 or 35°C) than from cold-pretreated (0°C) material. Higher temperatures of fruit storage also resulted in a decreased permeability of the embryo membranes to electrolytes and sugars. At the same time, membrane permeability to water was not modified. It is proposed that the previously observed occurrence of the discontinuous type of freezing in apple seeds (Nguyen and Kacperska, Physiologia Plantarum (X): 000-000, 1989) is associated with the temperature-induced dehydration of seed coat and endosperm, whereas a higher super cooling ability of the high-temperature-pretreated embryos is due to a decrease in the free energy of water in the system, and to the effective protection of embryo cells against heterogenous ice nucleation. The changes in water potential showed a high negative correlation with the embryo phospholipid content determined in the other work (Nguyen et al. Plant Physiol. Bio chem. 25: 697–703, 1987). Therefore, it is proposed that changes in matrix potential play an important role in the regulation of the water potential in the embryo cells.     

Effect of springtime water temperature on the time of emergence and size of Pteronarcys californica in the Henry's Fork catchment, Idaho, U.S.A.

1. The emergence time of Pteronarcys californica in streams in the Henry's Fork catchment, Idaho, U.S.A. was negatively correlated with mean April water temperature. Emergence was in mid- to late May at sites influenced by groundwater, where April water temperature averaged 7.9 °C. Adults emerged in mid-June in streams receiving run-off from snowmelt (mean April water temperature 5.4 °C). Intermediate emergence times were observed in a regulated section of river where water temperature was influenced, on one bank, by dam release (mean April water temperature 4.5 °C) and, on the other, by a spring-fed tributary stream (mean April water temperature 6.3 °C).
2. During each of the three study years, emergence was earlier on the bank of the regulated section that was warmer during April and May. The mean body length of P. californica exuviae, collected from the warm side of the river, averaged 1.2 mm longer than those collected from the cold side.
3. We tested the effect on emergence of altering springtime water temperature by translocating P. californica in cages from one location to another during April. Individuals moved to sites with higher April water temperature emerged earlier than individuals that remained at the site from which they were collected.     

BODY TEMPERATURE IN THE NEWBORN SOUTHERN ELEPHANT SEAL, MIROUNGA LEONINA, AT MACQUARIE ISLAND

Newborn southern elephant seal pups were reported by Laws (1953) to be "to some extent poikilothermic at birth." Rectal temperatures of known age southern elephant seal pups were recorded during the 1985 pupping season at Macquarie Island. The mean pup rectal temperature was found to be 381°C ± 0.1°C SEM ( n = 131, range = 36.5°-39.1°C). Pups at two hours, six hours, and one day after birth had significantly higher rectal temperatures than pups two, three, or four days of age. Rectal temperatures of neonatal southern elephant seals were within the range observed for other pinnipeds, (but never as low as the 31°C previously observed for southern elephant seals at Signy Island in 1953). A significant though weak positive correlation was found between pup temperature and body weight. However, no correlation between pup temperature and age or any environmental factor was found. These observations demonstrated that southern elephant seal pups at Macquarie Island are homeothermic, rather than heterothermic from birth.     

Using infrared thermography to assess seasonal trends in dorsal fin surface temperatures of free-swimming bottlenose dolphins (Tursiops truncatus) in Sarasota Bay, Florida

The temperature differential (Δ T ) between a body surface and the environment influences an organism's heat balance. In Sarasota Bay, FL, where ambient water temperature ( T _w) ranges annually from 11° to 33°C, Δ T was investigated in a resident community of bottlenose dolphins ( Tursiops truncatus ). Dorsal fin surface temperatures ( T _dfin) were measured on wild, free-swimming dolphins using infrared thermography. Field and laboratory calibration studies were also undertaken to assess the efficacy of this non-invasive technology in the marine environment. The portability of infrared thermography permitted measurements of T _dfin across the entire range of environmental temperatures experienced by animals in this region. Results indicated a positive, linear relationship between T _dfin and T _w ( r ²= 0.978, P < 0.001). On average, T _dfin was 0.9°C warmer than T _w across seasons, despite the 22°C annual range in T _w. Changes in integumentary and vascular insulation likely account for the stability of Δ T _{dfin − w} and the protection of core temperature ( T _core) across seasons. The high thermal conductivity of water may also influence this Δ T . The use of infrared thermography is an effective, non-invasive method of assessing dorsal fin skin surface temperatures (±1°C) across large numbers of wild, free-swimming dolphins throughout their thermally dynamic aquatic environment.     

Deep body and surface temperature responses to hot and cold environments in the zebra finch

Global warming increasingly challenges thermoregulation in endothermic animals, particularly in hot and dry environments where low water availability and high temperature increase the risk of hyperthermia. In birds, un-feathered body parts such as the head and bill work as ‘thermal windows’, because heat flux is higher compared to more insulated body regions. We studied how such structures were used in different thermal environments, and if heat flux properties change with time in a given temperature. We acclimated zebra finches (Taeniopygia guttata) to two different ambient temperatures, ‘cold’ (5 °C) and ‘hot’ (35 °C), and measured the response in core body temperature using a thermometer, and head surface temperature using thermal imaging. Birds in the hot treatment had 10.3 °C higher head temperature than those in the cold treatment. Thermal acclimation also resulted in heat storage in the hot group: core body temperature was 1.1 °C higher in the 35 °C group compared to the 5 °C group. Hence, the thermal gradient from core to shell was 9.03 °C smaller in the hot treatment. Dry heat transfer rate from the head was significantly lower in the hot compared to the cold treatment after four weeks of thermal acclimation. This reflects constraints on changes to peripheral circulation and maximum body temperature. Heat dissipation capacity from the head region increased with acclimation time in the hot treatment, perhaps because angiogenesis was required to reach peak heat transfer rate. We have shown that zebra finches meet high environmental temperature by heat storage, which saves water and energy, and by peripheral vasodilation in the head, which facilitates dry heat loss. These responses will not exclude the need for evaporative cooling, but will lessen the amount of energy expend on body temperature reduction in hot environments.     

Physiological adaptation to aridity in the bushveld gerbil, Tatera leucogaster

Oxygen consumption, rectal temperature, thermal conductance, and evaporative water loss (EWL) were determined in resting captive Tatera leucogaster at ambient temperatures of between 14 and 38 °C. Basal metabolic rate (BMR) was 0.86 ml O₂. min⁻¹ (S.D.=0.15, n = 6), 45% of that expected for a rodent of the same body mass (106.2 g). Minimum wet thermal conductance was 0.21 ml O₂. min⁻¹, °C⁻¹ (S.D. = 0.01, n = 6), 113% of that expected for a mammal of the same body mass. Wet thermal conductance increased exponentially at temperatures greater than 32 °C. Mean rectal temperature was 35.3 °C below 35 °C (S.D. = 0.5, n = 6) and 39.3 (S.D. = 0.6, n = 5) at 38 °C. Mean resting EWL was 1.43 mg. min⁻¹ (S.D. = 0.14, n = 6) between 15 and 32 °C and increased dramatically at temperatures above 32 °C. Combining our data with data from the literature suggests that gerbils (Family Muridae; subfamily Gerbillinae) have, on average, low BMR and average minimum wet thermal conductance when compared to other rodents and other mammals, respectively, of the same body mass. Similarly, rodents (including gerbils) from arid habitats have, on average, lower rates of EWL when at rest below thermoneutrality than do other rodents of the same body mass from mesic habitats.     

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.     

Gestation temperature affects sexual phenotype, morphology, locomotor performance, and growth of neonatal brown forest skinks, Sphenomorphus indicus

We maintained pregnant Sphenomorphus indicus under four thermal conditions for the whole gestation period to assess the effects of gestation temperature on offspring phenotypes. Parturition occurred between late June and early August, with females at high body temperatures giving birth earlier than those maintained at low body temperatures. Litter size, litter mass, and postpartum body mass did not differ among treatments, and females with relatively higher fecundity produced smaller offspring. Females gave birth to predominantly female offspring (85.7% of the 14 sexed offspring were females) at 24 °C and to predominantly male offspring (76.5% of the 17 sexed offspring were males) at 28 °C. Females with the opportunity to regulate body temperature produced a mix of sexes that did not differ from equality. Offspring produced in different treatments differed in head size, hind-limb length, and tympanum length, but not in snout-vent length, tail length, body mass, fore-limb length, and eye length. Offspring produced at 28 °C were not only smaller in head size, but also shorter in hind-limb length and tympanum length than those offspring produced at lower temperatures. Offspring produced at 28 °C performed more poorly in the racetrack and grew more slowly than offspring produced in the other three treatments. Taken together, our results show that S. indicus might be a temperature-dependent sex determination species and that offspring phenotypes are impaired at high gestation temperatures but maximized at relatively low gestation temperatures.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 88 , 453–463.     

Spontaneous and gonadotropin-induced ovulation in the goldfish, Carassius auratus L: effects of external factors

Spontaneous ovulation in goldfish is synchronized with photoperiod and influenced by water temperature and aquatic vegetation. As the latency to ovulation from injection of HCG is highly temperature dependent, the finding that ovulation occurs at approximately the same time of day at temperatures from 12° to 26° C suggests the time of the endogenous preovulatory gonadotropin surge may change with the temperature. The time of spontaneous ovulation adjusts to a reversed light:dark cycle within 2 weeks; some 4–6 h shifts in a single light:dark cycle modify the time of ovulation.
Few sexually mature females kept under long photoperiod (16L:8D) and transferred from cold (13 ± 1°C) to warm (21 ± 1°C) water ovulated spontaneously. Exposure to artificial aquatic vegetation for as little as one light phase significantly increases the proportion offish ovulating in warm water. Fish kept in cold water without vegetation do not ovulate; the addition of vegetation induces ovulation, although the response latency is longer than in warm water. Aquatic vegetation may be an effective stimulus for ovulation in other teleosts which spawn on this substrate.