Polar bear thermoregulation: Effect of oil on the insulative properties of fur

1. 1.|Oil caused a substantial decrease in the insulative value of polar bear (Ursus maritimus) pelts measured in vitro.

2. 2.|Following oil contamination the calm air heat transfer coefficient increased by a factor of 2 to 5: the wind coefficient averaged 290% greater and the solar utilization increased by 55%.

3. 3.|Conductance through oil-covered furs remained high at winter temperatures (T_a = 0.6°C) but decreased with time at summer temperatures (T_a = 24.7°C).

4. 4.|The most viscous of the three oils tested had a more consistently negative effect on insulation.

Direct heat injury of roots of woody swamp species

1. 1.Three month-old seedlings of Taxodium distichum, Nyssa aquatica, Cephalanthus occidentalis and cuttings of Salix nigra were acclimated to simulated natural swamp conditions (ambient temperature, saturated soil) and then used to assess direct high temperature injury of root tissue.

2. 2.Electrolyte leakage from excised root tissue exposed for 30 min to temperatures ranging from 30 to 66°C was used to assess cellular injury.

3. 3.The relationship between leakage and temperature was sigmoidal for each species.

4. 4.Inflection point temperatures on the response curves, ranged from 45.4 to 51.0°C, were species-specific, and indicated differences in thermal tolerance of root membranes.

5. 5.Root of C. occidentalis and N. aquatica were more heat tolerant than roots of T. distichum and S. nigra.

Thermal acclimation and hardening in tadpoles of the bullfrog, Rana catesbeiana

1. 1.|Critical thermal maxima (CTMax) and minima (CTMin) were measured to evalute thermal hardening in Rana catesbeiana.

2. 2.|Tadpoles show heat hardening and CTMax acclimation, and both responses are influenced by developmental stage.

3. 3.|The first evidence of cold hardening in vertebrates is reported here.

4. 4.|Heat hardening significantly reduces cold tolerance, but there is otherwise no evidence of a cross-hardening effect.

Thermal parameters of four species of Gerbillurus

1. 1.Thermal parameter of the four Gerbillurus species measured in the laboratory were examined in relation to their micro-environments in a xeric habitat.

2. 2.Basal metabolic rates (BMR) were lower than predicted, while thermoneutral zonds (TNZ) were narrow and exceeded burrow temperatures.

3. 3.Body temperatures (T_b) were regulated over a range of ambient temperatures (T_a). Evaporative water loss was used as a short-term cooling mechanism to reduce hyperthermia above the TNZ.

4. 4.Conductance was low below the TNZ to reduce heat loss.

5. 5.Adaptation to low temperatures is important for gerbils when active at night.

6. 6.The adaptive significance of the thermal biology of Gerbillurus is discussed in relation to phylogeny, distribution, food availability and nocturnal activity.

Functions of fat in hibernators: Thermal aspects

1. 1.|A numerical, distributed parameter model of heat exchange is used to evaluate the thermal significance of the presence and placement of subcutaneous fat in hibernating marmots. The model is most sensitive to changes in conductivity and metabolic rate of muscle tissue, parameters which are known to greater precision than are others in the model.

2. 2.|Alternative models are developed for animals with fat located dorsally and with no fat at all.

3. 3.|A comparison of these three models shown that there is no difference in the metabolic output required to maintain body temperature among the three alternatives. Therefore, neither the presence nor the location of fat serves an insulative role in hibernators.

Circadian change of heat loss in response to change in core temperature in rats

1. 1.|Circadian changes in heat production (M), heat loss (H), core temperature (T_c) and feeding activity (FA) of ad-lib fed rats were observed by direct and indirect calorimetry.

2. 2.|M, H and T_c showed a clear nocturnal increase associated with several discrete increases.

3. 3.|Whereas the slope of M vs T_c relation did not change appreciably within a day, the slope of H vs T_c or thermal conductance vs T_c relation tended to decrease at night, implying that the correlation between heat loss and body temperature is also a function of time of day in rats.

Tolerances of Nauplii of Balanus balanoides (L.) and Elminius modestus (Darwin) exposed to cyclical temperature fluctuations

1. 1.|Newly-released larvae of both E. modestus and B. balanoides show similar tolerances to steady temperature levels.

2. 2.|Both species show an ability to withstand a wider range of temperatures when subjected to cyclic thermal shocks.

3. 3.|E. modestus shows a greater tolerance to short-term thermal shocks than B. balanoides.

Acute adjustment of thermal tolerance in vertebrate ectotherms following exposure to critical thermal maxima

1. 1.|Heat hardening in a transitory increase in heat tolerance following a sublethal exposure to lethal high temperatures.

2. 2.|Within 1–2 h of an initial exposure to the critical thermal maximum (CTM), the CTM of two species of amphibians and two species of fish had increased significantly above the initial level and then decreased to the initial level within 24 h.

3. 3.|Experiments with exposure to sub-CTM temperatures and multiple exposures to the CTM indicated that hardening requires exposure to the CTM and may be the maximum CTM attainable by the animal.

4. 4.|Diel and seasonal variation had significant effects on hardening ability.

5. 5.|Field evidence suggests that heat hardening is adaptive in that it provides an acute means of adjustment to extreme fluctuations in diurnal temperatures.

Thermal conductivity and H2O content in rabbit kidney cortex and medulla

1. 1.|H₂O content and local-tissue thermal conductivity were measured in cortex and medulla of 7 freshly-excised rabbit kidneys.

2. 2.|Tissue H₂O content and thermal conductivity k (83.4% and 0.516 W m^−t K⁻¹, respectively) in the medulla were significantly higher than those (77.7% and 0.475 W m⁻¹ K⁻¹, respectively) measured in the cortex.

3. 3.|Correlations between the measured parameters are made, and the variability of previously-reported measurements of kidney-tissue thermal conductivity is discussed.

Thermosensitivity during embryonic development of Lymnaea stagnalis (Mollusca)

1. 1.|The percentage of survival after 1 hr at 40.0°C is lowest at the larval trochophore stage and at hatching of the young snail.

2. 2.|Heat resistance depends on the stage of development.

3. 3.|From the early cleavage stage onwards a higher percentage of embryos can withstand high temperature after a previous heat treatment than without it.

4. 4.|The pattern of thermosensitivity is discussed in relation to the organizational level of the stage of development.

5. 5.|It is concluded that the developing Lymnaea is a suitable system to study heat resistance and thermotolerance at the level of cells, organs and organism.

Effect of hygroscopic fabrics on wear comfort in the fluctuating microclimate of clothing

1. 1. A new type of simulator for clothing microclimate was designed and constructed.

2. 2. The simulator was designed to simulate the humidity fluctuation of clothing microclimate as observed under light working conditions and to measure the surface temperature of sample fabrics against the skin by means of a radiation thermometer.

3. 3. Knitted fabrics of cotton and polyester, and polyethylene films were used as specimens with different hygroscopicities.

4. 4. The quick rise and fall in the surface temperature of cotton fabric was observed under rapid fluctuations of the microclimate humidity.

5. 5. Under the same humidity fluctuations, the temperature of polyester fabric rose and fell more moderately than that of cotton fabrics, and the temperature of the polyethylene film did not change. When the rate of change in stimulus temperature is higher, the threshold temperature of warm sensation of the skin comes closer to a given adaption temperature.

6. 6. Therefore, the rapid and large changes in the fabric temperature against the skin, which were observed especially for hygroscopic cotton fabric, must affect the thermal comfort of clothing.

Diel thermoregulation of the crawfish Procambarus Clarkii (crustacea, cambaridae)

1. 1. In a diel cycle Procambarus clarkii has two preferred temperatures: 24.0 ± 0.15 SEM °C during the day and 26.7 ± 0.13 SEM °C at night.

2. 2. The preferred temperatures are independent from the weight of the organisms.

3. 3. In the photophase the animals are dispersed, in the scotophase they congregate.

4. 4. The crawfish seem to feed during the thermal interphases.

5. 5. Animals in a constantly dark condition maintain a diel preferendum of temperature.

Strategies of social wasps for thermal homeostasis in light paper nests

1. With the derived free-run temperature of light paper nests the influence of the thermal capacity of the nest or the nest site, respectively, on thermal homeostasis is quantified.

2. Gravimetric information from the continuous investigation of the nest weight coupled with temperature and humidity measurement allows the correlation of the colonies’ foraging behavior with their heat production inside the nest.

3. Wasps (Vespa crabro) do not regulate their nest environment towards a specific and constant temperature but rather build nests adapted to their foraging behavior and general energy budget.

Two types of heat tolerance in FHM-cells. Induction by heat-shock versus elevated culturing temperature

1. 1.Increased heat tolerance in FHM-cells from Pimephales promelas (Pisces) can be induced by culturing the cells at elevated temperatures (heat resistant acclimation) as well as by heat shock (heat hardening).

2. 2.After shift of culturing temperature (CT) from 16 to 32°C both effects are detectable with different temporal patterns.

3. 3.Cellular concentrations of heat-shock proteins correlate with the hardening effect but not with heat resistance acclimation.

4. 4.Several culturing temperature specific proteins were detected. The patterns of some enzymes are also altered by culturing temperature.

5. 5.Heat resistance acclimation is not caused by selection of a thermoresistant subpopulation of cells.

6. 6.Heat hardening and heat resistance acclimation must be distinguished as different phenomena in FHM-cells.

Day-night variation of thermoregulatory responses to intraperitoneal electric heating in rats

1. 1.Hypothalamic temperature (T_hy), nonevaporative heat loss (R + C + K), evaporative heat loss (E), thermal conductance (k), metabolic heat production (M) and heat storage (S) of rats were simultaneously measured by direct and indirect calorimetry during internal heat loading (2 W per rat) with an intraperitoneal electric heater.

2. 2.The tests were made twice a day; once during the day (1000–1200 h) and once at night (2200–2400 h) at an ambient temperature of 24°C.

3. 3.The resting values of T_hy, colonic temperature, (R + C + K), E, M and heart rate, and the T_hy threshold for tail skin vasodilation (T_th) during internal heat load were significantly higher at night than during the day.

4. 4.The slopes showing the relationshiop between (R + C + K), k or M and T_hy were significantly steeper during the day than at night after T_hy exceeded T_th.

5. 5.The slopes showing the relationship between E or S and T_hy were not different during the day and at night.

6. 6.These results indicate that the responses of nonevaporative heat loss and heat production to internal heat load vary with the time of day in rats.

Temperature gradients in the nasal cavity of the rabbit

1. 1.|Temperatures at four sites along the ventral nasal concha were recorded in four unrestrained rabbits exposed to ambient temperatures from 0 to 35°C.

2. 2.|The nasal temperatures decreased and temperature gradients from proximal to distal parts of the concha increased in cold-exposed rabbits.

3. 3.|The temperature gradients increased also during panting in heat-stressed rabbits.

4. 4.|The ventral nasal concha is suggested to be an efficacious heat exchanger both in cold and hot ambient, due to its geometry and vascularization.

Thermal responses and temperature tolerance of a dessert ant-lion larva

1. 1.Cueta trivirgata larvae construct pits in the dry Kuiseb River bed in the Namib Desert.

2. 2.An art, Ocymyrmex robustior comprises 65.4% of the biomass of prey consumed by the ant-lions.

3. 3.O. robustior is active between surface temperatures of 27–68°C.

4. 4.Ant-lions tolerate high body temperatures (LD₅₀ = 53.4°C).

5. 5.By exploiting the pit microclimate and by digging below the surface during extreme thermal loads, ant-lions can capture prey at surface temperatures of 13–63°C.

6. 6.These behavioural and physiological adaptations enable ant-lions to maximize the duration of vigilance and hence prey capture success.

Morphological and root carbohydrate responses of bald cypress to water level and water temperature regimes

1. 1. Reduced carbohydrate reserves have been suggested as a factor in the decline of bald cypress in swamp areas impacted by thermal effluents.

2. 2. Morphological characteristics and root carbohydrate concentrations were examined for bald cypress seedlings subjected to three temperature regimes (ambient, mid, and high) and three water levels (drained, saturated and flooded).

3. 3. Although few differences in total root carbohydrate concentrations existed after 3 weeks, the proportion of starch to sugar decreased with increasing temperature treatment.

4. 4. After senescence, mid saturated seedlings had the greatest aboveground and belowground biomass, whereas high flooded seedlings had the lowest concentration of root carbohydrates.

Thermal resistance of the ciliary activity in the gills of the fresh water mussel Anodonta anatina

1. 1.|The thermal resistance of the activity of frontal cilia in the median gills of the fresh water mussel Anodonta anatina was studied.

2. 2.|The resistance acclimation appeared in 2 days in the gills of intact animals, but not in the isolated gills kept at 4, 14 and 24°C, for between 1 to 3 days.

3. 3.|Warm-acclimation increased the ACh sensitivity of the gills of intact mussels.

4. 4.|Isolation of the gills enhanced the thermal resistance.

5. 5.|ACh, choline and tetramethylammonium enhanced the thermal resistance in the isolated gills. whereas atropine and physostigmine diminished it.

6. 6.|It is concluded that in A. anatina the control if the thermal resistance is probably neural.

Thermal acclimation, hydroperoxide detoxifying enzymes and oxidative stress in the lung and liver of Rana perezi

1. 1.Rana perezi adult frogs were acclimated to cold (10 ± 2°C) and warm (29 ± 1°C) temperatures for 4 months.

2. 2.After acclimation, a partial compensation of the oxygen consumption of the animals was found because of a reduction of its thermal sensitivity.

3. 3.Activities of liver and lung catalase, selenium (Se)-dependent and Se-independent glutathione peroxidases were not changed by thermal acclimation.

4. 4.Tissue peroxidation (TBA-RS) increased in the liver of heat acclimated animals.

5. 5.Hydroperoxide detoxifying enzyme activities did not show inverse compensation of temperature during acclimation. It is proposed that the pattern of thermal compensation shown by these enzymes in different species depends on a variety of factors including: (a) the thermal sensitivities of hydroperoxide producing and scavenging systems; (b) the changes induced by acclimation in the rate of hydroperoxide generation.