Effects of constant and cycling hot environments on mitogen-stimulated proliferation of peripheral blood lymphocytes from sows and litters

1. 1. Lymphocytes from sows maintained in a constant hot environment (32°C) showed reduced proliferative responses to mitogens PHA (P < 0.02) and PWM (P < 0.01) in comparison to sown maintained in a constant cool environment (21°C). In the piglets the hot constant temperature slightly reduced (P < 0.05) proliferative responses of lymphocytes to PHA.

2. 2. No significant effects of a cycling hot environment (27–32°C) were found for any proliferative responses of lymphocytes from sows and litters.

3. 3. In the constant hot environment, serum cortisol concentrations were significantly reduced in the sows (P < 0.0001) while no differences in serum cortisol concentrations were found in the litters.

     

The effects of wind and thermal radiation on thermal responses during rest and exercise in a cold environment

1. 1. The purpose of this study was to investigate the effects of thermal radiation and wind on thermal responses at rest and during exercise in a cold environment.

2. 2. The experimental conditions were radiation and wind (R + W), no radiation and wind (W), radiation and no wind (R), no radiation and no wind (C).

3. 3. The air temperature was −5°C. Thermal radiation was 360 W/m². Air velocities were 0.76, 1.73 and 2.8 m/s. Rectal and skin temperatures, heart rate and oxygen consumption were recorded. Thermal and comfort sensations were questioned.

4. 4. There are no significant effects of thermal radiation and wind on the physiological responses except the mean skin temperature. There are significant effects on the mean skin temperature (P < 0.01) and thermal sensation (P < 0.05).

Infra-red irradiance and set point temperatures in behaviourally thermoregulating lacertid lizards

1. 1. Set point temperatures at which Podarcis muralis and Lacerta vivipara ceased basking (T_move; upper set point) and commenced basking (T_bask; lower set point) increased incrementally with increasing i.r. irradiance; values for all set point temperatures were higher in the former species.

2. 2. Changing the i.r. irradiance during a bask resulted in a shift in the upper set point temperature to a level intermediate between the values expected at constant previous and new irradiances (experiment with L. vivipara only).

3. 3. The changes in set-point temperatures following changes in i.r. irradiance were not due to changes in light intensity.

4. 4. The ability to respond to immediate changes in i.r. irradiance is adaptive for lizards in areas in which rapid changes in amounts of sunshine are a feature of the climate.

     

Thermoregulatory responses to manipulations of photoperiod in wood mice Apodemus sylvaticus from high latitudes (57°N)

1. 1. The thermoregulatory responses to manipulations of photoperiod in wood mice (Apodemus sylvaticus), which were drawn from a population living at a high latitude (57°N) were studied.

2. 2. Mice captured in spring were acclimated to two different photoperiod regimes 16L:8D and 8L:16D at a constant ambient temperature of 24°C, for 3 weeks.

3. 3. Daily rhythms of body temperature, oxygen consumption and body temperature at various ambient temperatures, nonshivering thermogenesis (the response to a noradrenaline injection) and body mass were measured. Minimal overall thermal conductance was calculated for both groups.

4. 4. Acclimation to long photophase increased the thermoregulatory abilities at relatively high ambient temperatures while that of long-scotophase increased thermoregulatory abilities at low ambient temperatures.

5. 5. Changes in photoperiod may therefore be used as cues for seasonal acclimatization of thermoregulatory mechanisms in this population of wood mice.

     

Changes in lipid peroxidation, superoxide dismutase activity, ascorbic acid and phospholipid content in liver of freshwater catfish Heteropneustes fossilis exposed to elevated temperature

1. 1. Lipid peroxidation, superoxide dismutase (SOD) activity, ascorbic acid (AsA) and individual phospholipid contents in liver of fresh water cat fish Heteropneustes fossilis were measured after exposure to different temperatures (25, 27, 32, 37°C) at various times (1–4 h).

2. 2. Lipid peroxidation and superoxide dismutase activity were significantly increased with increases in temperature at various times.

3. 3. Ascorbic acid content was depleted when temperature was increased.

4. 4. After temperature exposure, phosphatidyl inositol was increased while phosphatidyl choline, phosphatidyl serine and phosphatidyl ethanolamine were depleted. Phosphatidic acid level did not change.

5. 5. The findings indicated an increased oxidative stress in liver following increases in temperature at various times. Concurrent with the increase in lipid peroxidation, superoxide dismutase activity and ascorbic acid from the liver of fish varied. It is suggested that depletion of major individual phospholipids following temperature exposure could be due to superoxide created oxidative stress in the liver.

     

A test of the accuracy of operative temperature thermometers for studies of small ectotherms

1. 1. Various devices have been used to estimate the equilibrium body temperature of ectotherms occupying natural environments. We tested the accuracy of such devices under a range of conditions.

2. 2. We measured body temperatures of lizards (Sceloporus magister) exposed to short-wave radiation under varying convective conditions and compared these to temperatures of hollow metal casts duplicating the animal's shape and reflectivity, as well as to the temperatures of cylinders similar to those used by other workers.

3. 3. Casts equilibrated within 2–3°C of live animals, yielding errors of 14–37% of the radiation-produced elevation of body temperature.

4. 4. Various cylinders differed from animal body temperature more than lizard casts did, producing errors equally 33–53% of the radiation-produced elevation.

5. 5. It is imperative that workers using operative-temperature thermometers experimentally confirm the adequacy of the devices they use for the range of conditions encountered within a specific analysis.

     

Thermoregulatory behavior and critical thermal limits of the angelfish Pterophyllum scalare (Lichtenstein) (Pisces: Cichlidae)

(1)Final temperature preferendum of juvenile (0.9–1.9 g) and adult (5.2–12.5 g) angelfish Pterophyllum scalare were determined with acute and gravitation methods. The final preferenda were similar, independent of the method and development stage (29.0–31.1°C).

(2)The critical thermal maxima (CTMax) for juveniles were 36.9°C, 37.6°C, 40.6°C, 40.8°C and for adults 38.4°C, 38.6°C, 41.0°C, 42.1°C. Adult angelfish CTMax was slightly higher than in juveniles (1°C; P<0.05); the endpoint of CTMax was the onset of spasms.

(3)The acclimation response ratio for both stages had an interval of 0.33–0.44; these values are in agreement with results for subtropical and tropical fishes.

(4)Therefore it is recommended that angelfish cultivation should be consistent with temperatures that do not change abruptly throughout the year and temperature maximum does not exceed 30°C.

     

Behavioral thermoregulation of Bulla gouldiana (Gastropoda: Opisthobranchia: Cephalaspidea)

1. 1. The preferred temperature of Bulla gouldiana is 26.7–28.7°C.

2. 2. In constant scotophase, photophase, and light and dark photoperiod the organisms do not have a diel cycle of thermoregulation.

3. 3. It takes the animal 6–16 h to reach the preferred temperature.

4. 4. The lowest and highest temperatures visited were 11 and 33°C.

5. 5. Spawning of the species occurred in the thermal gradient between 27 and 28.5°C.

     

Response of brown mussel, Perna indica, to elevated temperatures in relation to power plant biofouling control

1. 1. Results of a study on lethal and sublethal responses of different size groups of the tropical brown mussel, Perna indica, when exposed to different temperatures are presented.

2. 2. Exposure to a temperature of 38°C showed 100% mortality of 9 mm size group mussels in 120 min.

3. 3. Mortality was dependent on age (size) of the mussels, young ones being more susceptible than older ones.

4. 4. All size groups showed a progressive reduction in physiological activities such as filtration rate, foot activity and byssus thread production when temperature was increased from 30°C.

5. 5. This study suggests that heat treatment is an attractive alternative to chlorination for mussel fouling control in tropical power stations.

     

Electrical skin resistance and rectal temperature changes in resting human subjects exposed to heat

1. 1.|Fourteen male volunteers were examined under passive heating.

2. 2.|Electrical skin resistance (ESR) and rectal temperature (T_re) were measured during the whole period of exposure.

3. 3.|It was found that:

• —|ESR decreases rapidly with increasing air temperature. Assuming an exponential curve yields a mean time constant of 14 min.

• —|There is a correlation between the individual ESR time constants and T_re increases (r = 0.695, P < 0.005).

• —|Additional changes of ESR were noted in 8 subjects at a constant air temperature of 42°C.

4. 4.|It is concluded that ESR may be a useful indicator of the sweating response of the human thermoregulatory system during exogenous heat load.

Interactions of environmental temperature with photoperiod in determining age at maturity in a semelparous polychaete Nereis (neanthes) virens sars

1. 1. Larger members of the Polychacta exhibit two contrasting life cycles: semelparous in the Nereidae, iteroparous in most others.

2. 2. In semelparous forms environmental interaction determines age at reproduction and fecundity in the single spawning event whereas in iteroparous forms such interaction influences the variable age specific reproductive effort.

3. 3. Development of aquaculture has created conditions where organisms are grown under conditions of optimum temperature for growth and unlimited food.

4. 4. We present data on the life history responses (reaction norms) of the semelparous Nereis virens in which age at death in natural populations varies between 3 to 8+ years.

5. 5. In Nereis virens minimum life span (= generation time) in culture is one year but the lifespan remains modular 12 months without manipulation of photoperiod.

6. 6. Environmental temperature plays two roles: i) in conjunction with energy availability to determine “age at first/only reproduction” and secondly as an element (with photoperiod) in the control of gametogenic processes imposing seasonality on the life cycle.

7. 7. The observations suggest that long generation time in natural populations of N. virens is associated with reduced growth rate and that low growth rate is associated with reproduction at a larger size.

     

Diurnal activity, temperature responses and endothermy in three South American cicadas (Homoptera: Cicadidae: Dorisiana bonaerensis, Quesada gigas and Fidicina mannifera)

1. 1. Measurements of body temperature (T_b) in the field demonstrated that endothermic cicadas regulate T_b by behavioral mechanisms as well as by endogenous heat production.

2. 2. The T_b of endothermically active cicadas without access to exogenous heat is approximately the same as the T_b of basking cicadas.

3. 3. Dorisiana bonaerensis (Berg) and Quesada gigas (Olivier) raise T_b in the field with the heat produced in flight.

4. 4. The thermal responses of a particular species are related to its activity patterns and habitat.

5. 5. Endothermy in cicadas may serve to uncouple reproductive behavior from environmental constraints; to circumvent possible thermoregulatory problems; to permit the utilization of habitats unavailable to strictly ectothermic cicadas; to reduce predation; and to optimize broadcast coverage and sound transmission.

     

Temperature regulation by evaporative cooling in a desert grasshopper, Calliptamus barbarus (Ramme, 1951)

1. 1. We examined the desert-dwelling grasshopper, Calliptamus barbarus, to determine whether it used evaporative cooling, and if differences existed in the use of evaporative cooling between the small males and larger females. Male C. barbarus are the smallest grasshoppers tested for their use of evaporative cooling.

2. 2. Calliptamus barbarus use evaporative cooling at high ambient temperatures to keep their body temperature below lethal levels. This has been shown in insects such as cicadas, bees and other grasshoppers. Maximal water loss rates for C. barbarus are similar (8–10% of body mass per hour) to those of other grasshoppers.

3. 3. Male C. barbarus weigh 370 mg on average, and are 20% of the females' mass. At low ambient temperatures males evaporated 13.31 ± 1.14 mg water/h (n = 12), a similar rate to that in females, who evaporated 17.53 ± 2.03 mg water/h (n = 29), but a considerably greater fraction of body mass per unit time. At high ambient temperatures, the males lost less in absolute terms, but a similar amount relative to body mass. The differences are partially accounted for by scaling effects, but for the most part, the reasons for these differences are unclear. They may be linked to differences in ventilatory patterns between males and females or differences in cuticular permeability, the two major pathways of water loss in insects.

     

Reproductive status and torpor of the marsupial Sminthopsis crassicaudata: Effect of photoperiod

1. 1. We investigated the effects of photoperiod on the reproductive state and the occurrence and pattern of torpor in male Sminthopsis crassicaudata.

2. 2. Testes regressed when animals were exposed to a short photoperiod (L:D 8:16) and recrudesced under a long photoperiod (L:D 16:8).

3. 3. Animals entered torpor under both photoperiods and no significant differences were observed in the frequency or physiological variables of torpor of S. crassicaudata between the short and long photoperiods.

4. 4. The differences in the response to photoperiod in thermal physiology and reproduction suggest that, unlike in many rodent species, torpor and reproduction in S. crassicaudata are controlled by separate environmental cues and mechanisms.

     

The effect of shielding the parietal eye of Podarcis muralis on behavioral thermoregulation

1. 1. Body temperatures (T_bs) and thermoregulatory precision of 7 sham shielded and 7 parietal eye shielded Podarcis muralis were measured in a linear thigmothermal gradient over a 24 h period.

2. 2. Shielding the parietal eye did not alter the mean T_b selected over the 24 h period.

3. 3. Both groups selected T_bs that did not differ between photophase and scotophase.

4. 4. Shielding the parietal eye did not influence thermoregulatory precision when measured over the 12 h of photophase, but from 0600–1200 h EST parietal eye shielded lizards thermoregulated more precisely than sham shielded lizards.

     

A simple index of standard operative temperature for mule deer and cattle in winter

1. 1. Scientists often use ambient temperature, relative humidity, or windspeed alone to describe an animal's thermal environment. Standard operative temperature (T_es) incorporates solar and thermal radiation, ambient temperature, and windspeed with a species' resistance to heat loss; thus it more accurately represents an animal's thermal environment. Standard operative temperature is not often recorded in the field because of instruments needed to measure short- and long-wave radiation.

2. 2. Our objective was to determine if regression equations could relate simple micrometeorological measurements to T_es for mule deer and cattle in winter.

3. 3. Blackglobe and ambient temperatures, windspeed, net radiation, total radiation, albedo, and ground surface temperature were recorded during one winter in a field in Bozeman, Montana. We used species specific resistance values for mule deer and cattle in winter to calculate T_es for both species. Then, we regressed T_es with blackglobe and ambient temperatures, and windspeed. The mule deer regression model was applied to an independent data set to determine if it worked well under varying weather conditions.

4. 4. The mule deer and cattle regression models represented T_es for both species well (adjusted R² 0.96 and 0.94, respectively). The mule deer regression model also represented the independent data set well. Standard operative temperatures predicted by our model and those predicted by the independent data set were highly correlated (r > 0.96 for four different comparisons). Our simple micrometeorological measurements are suitable predictors of T_es for mule deer and cattle in winter.

     

How to measure the thermal death of Daphnia? A comparison of different heat tests and effects of heat injury

1. 1. The thermal death point of the water flea Daphnia magna (age < 24 h, cultured at 20°C) varied considerably depending on the method used. The median lethal dose (LD₅₀), induced by an acute 24 h heat exposure was 34.8°C. It was 37.8°C following a thermal shock for 15 min, and it was 39.4°C when a continuous temperature increase (0.2°C/min) was used.

2. 2. Heat death temperature of daphnids was related to the acute heating rate.

3. 3. The logarithm of median lethal time (Lt₅₀) of daphnids, kept at a constant high temperature, had a linear relationship to temperature (°C) within the range of 28.0–38.5°C.

4. 4. The mortality after heat exposure increased with recovery time at 20°C for up to 3 days.

5. 5. The animals which survived the heat exposure produced eggs and offspring. Furthermore, no time lag in development between the control and heat exposure group was observed.

6. 6. The comparison of the results made by different heat tests categorized to Methods 1 and 2 by Precht (1973), for use in the determination of lethal limits of ectotherms, has been discussed.

     

Body temperature in arboreal and nonarboreal anuran amphibians: Differential effects of a small change in water vapor density

1. 1.|Body temperatures (T_b) and contaneous evaporative water loss rates (CWL) were measured in tree frogs (Hyla cinerea) and toads (Bufo valliceps) exposed to cyclical ramp changes in water vapor density (WVD) between 7.5 and 9.8 gm⁻³ (1 cycle h⁻¹ at an air temperature of 27.0°C.

2. 2.|CWL was 3.3 times greater in toads than in tree frogs.

3. 3.|T_b in toads cycled directly with WVd; WVD accounted for 98% of the variation in toad T_b.

4. 4.|T_b in tree frogs was independent of WVD, probably due to changes in skin resistance to water loss.

Some effects of thyroidectomy on growth, heat production and the thermoregulatory ability of the immature fowl (Gallus domesticus)

1. 1.|The effect of thyroidectomy at 12 days of age on weight gain, and on heat production and thermoregulatory ability of 4- to 5-week-old chickens at temperatures within and below the thermo-neutral zone was investigated.

2. 2.|Despit the absence of thyroid tissue, as demonstrated with radioiodine, a small amount of thyroxine was found in the plasma of some thyroidectomized (TX) birds.

3. 3.|Thyroidectomy depressed weight gain; pair-fed controls grew significantly faster than TX birds.

4. 4.|Resting heat production of TX birds at thermoneutrality (30°C) was depressed by 18% (P < 0.001) and body temperature by 0.4°C (P < 0.001).

5. 5.|At 12°C heat production of TX birds was similar to that of controls but the body temperature of TX birds was 0.7°C lower (P < 0.001).

6. 6.|Thyroidectomized birds were unable to regulate body temperature at 5°C even if thyroxine was provided on the day before and at the time of cold-exposure. This inability to thermoregulate was probably due to inadequate insulation and poor nutritional status.

Synthesis and problematic crystal structures of [Al(CH3CN)6][MCl6]3(CH3CN)3 (M=Ta, Nb or Sb)

Compounds of formula [Al(CH₃CN)₆][MCl₆]₃(CH₃CN)₃ (M=Ta (1); Nb (2); Sb (3)) have been synthesized from the reactions of MCl₅ and AlCl₃ in acetonitrile and characterized by X-ray crystallography. Complex 1 crystallizes in the tetragonal space group P4/mbm with a = B = 10.408(2), C = 7.670(3) Å, V = 830.9(4) ų and Z = 2/3. Complex 2 crystallizes in the tetragonal space group P4/mnc with a = B = 330(a), C = 15.320(3) ų V = 1634.8(4) ų and Z = 4/3. Complex 3 also crystallizes in the tetragonal space group P4/mnc with a = B = 10.313(1), C = 15.238(2) Å, V = 1621.0(1) ų and Z = 4/3. The non-integer Z values for complexes 1–3 result unusual problems of disorder and/or twinning in these crystal structures due to their high symmetry. The M---Cl distances range from 2.329(3) Å in the Ta complex to 2.355(1) Å in the Sb complex, while the Al---N distances are similar in all three complexes, ranging from 1.92(1) to 1.97(1) Å, respectively. Complexes 1–3 are the first structurally characterized complexes that contain a (hexaacetonitrile)aluminum(III) cation.