Heat flow of the paraplegic and able-bodied lower limb during resting heat exposure

1. The heat flow of paraplegic (PA) and able-bodied (AB) subjects were determined at rest in cool and warm conditions.

2. During heat exposure upper body sites for both groups showed heat loss, whereas the lower body sites of the PA groups showed heat gain.

3. During heat exposure, a systematic difference between groups in the relationship between heat flow and calf-skin temperature existed.

4. In conclusion, heat storage appears to be localised in PA subjects at rest and centralised for AB subjects.

Selected body temperatures in the lizard Lacerta vivipara: Variation within and between populations

1. 1.|Selected body temperatures (SBT) of adult male, female and subadult Lacerta vivipara from a Belgian population, were measured monthly in a laboratory thermogradient.

2. 2.|Monthly mean SBTs varied between 29.9 and 34.0°C and differed significantly among months in all three lizard groups, and among lizard groups in 4 out of 6 months.

3. 3.|Evidence for a positive relationship between monthly SBT and air temperature was found in the subadults, but not in the adult lizards.

4. 4.|Monthly mean SBTs measured in this study were consistently higher (mean difference = 2.0°C) than those obtained by Patterson and Davies (1978) in a similar study on Lacerta vivipara from southern England.

Development of autonomic and behavioural thermoregulation in turkeys (Meleagris gallopavo)

1. 1.|Heat production (HP) and body temperature (T_b) measurements were conducted at ambient temperatures (T_a) between 10 and 40°C. In addition preference temperatures (PT) were determined in a temperature channel and T_b was measured at preferred T_a

2. 2.|The influence of age on T_b at constant, as well as at PT, was proved. Increasing age was accompanied by an elevation of T_b whereas HP remained constant in the mid-range of T_a

3. 3.|The lower T_b in the first days of life is suggested to result from a lower thermoregulatory set point during the postnatal period.

4. 4.|The PT were different for the observed types of behaviour. The PT at rest was higher than the PT during locomotion, food intake and drinking.

TLV in cold environments

1. 1. The risks encountered during cold exposure are general body cooling or local cooling of parts of th body.

2. 2. Measures of cold stress must account for the effects of climate, clothing and metabolic heat production on heat balance.

3. 3. The combinaed effect of air temperature, mean radiant temperature, humidity and air velocity determines the cooling power of the environment.

4. 4. The cooling power can be easily converted into a required insulation value (IREQ) for whole body heat balance.

5. 5. Extensive cooling of hands and feet may be a limiting factor, even when sufficient total insulation is provided. In addition the cooling effect of wind on unprotected skin must be considered.

6. 6. Recommendation regarding acceptable exposures can be expressed as lowest ambient temperatures and time limits as function of available protection and activity level, with due attention to both general and local effects.

Temperature-mediated morphology changes during metamorphic climax in the African clawed frog, Xenopus laevis

(1) Investigations of the effect of temperature on body size are largely limited to the larval phase, with our understanding of the effect of temperature during metamorphic climax entirely restricted to the insects.

(2) Environmental temperature was manipulated only during metamorphosis in the aquatic amphibian Xenopus laevis.

(3) Lower temperatures during metamorphosis resulted in individuals with greater mass, head width and snout–vent length on the completion of metamorphosis.

(4) This suggests that temperatures experienced during the relatively short metamorphic phase will play an important part in determining the temperature–size relationship in amphibians.

Thermal responses of the fresh water turtle Mauremys caspica to step-function changes in the ambient temperature

1. 1.|The turtle Mauremys caspica cools significantly faster than it heats in air. The heating/cooling ratio is 0.49.

2. 2.|The variation of body temperature in relation to time-course in response to a step-function change of environmental temperature, fitted to a second-order system improves that of a first-order system.

3. 3.|The gradient between ambient temperature (T_a) and equilibrium body temperature (T_b) increases significantly and progressively when ambient temperature rises over 25°C.

4. 4.|At 40°C thermoregulatory hyperventilation was detected, implying an increase in air convection requirement (ventilation relative to O₂ consumption, ).

Bed climate of Korean using ondol heating system

1. 1. To examine the influence of different bed conditions (ondol sleep, bed sleep on ondol with same bedding) of the Korean ondol traditional heating system on human response during sleep, bed climates and physiological responses such as skin and rectal temperatures, weight loss, body movement and subjective sensation were measured with 4 grown-up females as subjects while they were sleeping for 7 h.

2. 2. Bed climate: Temperatures under the mattress and inside the quilt were higher on ondol while temperatures on the mattress and humidity inside the quilt were higher on the bed.

3. 3. Rectal temperature was significantly higher on ondol; skin temperature showed no major differences in relation to bed conditions. The frequency of body movements had the highest correlation with bed climate of the parameters measured.

4. 4. Mattress weight decreased on ondol and increased on the bed.

5. 5. The frequency of body movements was significantly higher in ondol sleep.

6. 6. The subjects sensation showed difference on cushion sensation between the two types of bed condition.

7. 7. To obtain the same level of comfort on both ondol and bed sleeping conditions less thermal insulating value is needed for ondol sleep.

A simple moder for estimating the ice content of freezing ectotherms

1. 1.Although body ice content is an important variable affecting freeze tolerance, present calorimetric methods for its measurement necessarily require the termination of a freezing protocol.

2. 2.A simple iterative model, based on the colligative properties of solutions and requiring precise measurements of only equilibrium freezing point (of the unfrozen organism) and of core body temperature, allows estimation of the percentage of body water frozen at any time during a freezing episode.

3. 3.This model can also predict the lethal temperature for a freezing ectotherm, assuming that death occurs due to osmotic dehydration when 67% (of any other known lethal fraction) of the body water is frozen.

4. 4.The basic model is easily extended to evaluate the effects of variables such as: body mass, initial body water content, initial osmotic concentration, and test chamber microenvironment.

5. 5.This model is not intended to supplant existing more exact biophysical models of freezing kinetics. Rather it is proposed as a first approximation which is generally supported by published data and which should be of significant practical value for investigators of freeze tolerant organisms.

Comparison of thermal responses with and without cold protective clothing in a warm environment after severe cold exposures

1. 1. Ten male students remained in a severely cold room (-25°C) for 20 min. thereafter, they transferred in a warm room (25°C) for 20 min.

2. 2. This pattern was repeated three times, total cold exposure time amounting to 60 min.

3. 3. In the warm room, the subjects removed their cold-protective jackets, or wore them continously.

4. 4. Rectal temperature, skin temperatures, manual performance and thermal comfort were measured during the experiment.

5. 5. Removing cold-protective jackets after severe cold exposure increased peripheral skin temperatures and reduced the discomfort in the warm room.

6. 6. However, these results were accompanied by a greater decrease in rectal temperature and manual performance.

7. 7. It is recommended that workers continue to wear cold-protective clothing in the warm areas outside of the cold storage to prevent decreases in deep body temperature and work efficiency caused by repated cold exposures.

Mismatch between temperature preferences and morphology in F1 hybrid newts (Triturus carnifex×T. dobrogicus)

1. The influence of interspecific hybridization on temperature preferences and morphology was examined in newts, Triturus carnifex and Triturus dobrogicus, before and after metamorphosis.

2. Thermoregulatory behavior was measured in an aquatic thermal gradient (5–32.5 °C) during 24 h.

3. Hybrid temperature preferences were similar to preferences of maternal species in both premetamorphic larvae and recently metamorphosed individuals.

4. Hybrid morphology (i.e., forelimb length and axilla–groin distance) was intermediate relative to parental species.

5. The mismatch between morphology and thermal preference in hybrid phenotypes indicates potential hybrid disadvantage in both intermediate and parental habitats.

Thermal gradients in the oesophagus of man during exercise and passive warming

1. 1.|Oesophageal temperature (T_es) has been recorded at four vertical levels in the oesophagus of human subjects during exercise and during passive body heating.

2. 2.|The temperature increased with depth.

3. 3.|The rate of increase in T_es during exercise was greatest at the level of the diaphragm.

4. 4.|During passive heating of the body T_es increased most rapidly, and with shortest latency time, at the level adjacent to the left atrium of the heart.

5. 5.|During exercise, when breathing is deeper than at rest, T_es should be measured at a deeper level than that which is used during passive heating.

The effect of acclimation temperature and the removal of peripheral temperature receptors on body temperature preference in the cockroach, Periplaneta americana

1. 1.|Body temperature preferences were compared between cockroaches acclimated to different ambient temperatures and between 25°C acclimated cockroaches and cockroaches deprived of their peripheral temperature receptors.

2. 2.|Acclimation to 35°C resulted in a significantly higher mean body temperature and low body temperature selected compared with 25°C acclimated cockroaches.

3. 3.|Cockroaches deprived of their peripheral temperature receptors showed a significantly higher mean high body temperature selected when compared to normal 25°C acclimated cockroaches.

4. 4.|It is concluded that cockroach temperature regulation is more precise than expected and that central temperature receptors are the primary sensing elements for cockroach thermoregulation.

A relationship between heat load and plasma enzyme concentration

1. 1. The sensitivity of serum enzyme levels as indicators of tissue damage is less well established in the prodromal period of heatstroke, especially for sub-lethal stress conditions.

2. 2. Anaesthetized rats were exposed to two different sets of thermal conditions.

3. 3. Plasma levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), creatine kinase (CK) and lactate dehydrogenase (LD) were assayed in each group upon termination of stress, 6 h post-stress and 24 h post-stress.

4. 4. The tissue “damage” sustained was mild to moderate and completely reversible.

5. 5. The rate of rise in body temperature may constitute an important factor in the ultimate pathology.

6. 6. CK proved to be the most sensitive parameter of tissue “damage”.

Field surveys on cooling effects of vegetation in an urban area

1. 1. Three kinds of field survey on different scales were carried out in Fukuoka City in summer to examine the relationship between the quantity of vegetation and air temperature.

2. 2. The field of the largerst scale measurement is across the city.

3. 3. Several parks and shrines of various sizes in the city were selected as other measurement areas.

4. 4. The most detailed measurements are carried out in a park with an area of 1.25 ha located in a down town area of the city.

5. 5. Though the amount of vegetation is expressed in a unique way in each survey, it is clearly found that the greener it is, the lower is the air temperature.

Effect of warm rearing on temperature regulation in resting and exercising rats

1. 1.|Hypothalamic and rectal temperatures were recorded in 8 warm-reared (wr) and in 12 warm-acclimated control rats during resting in the heat and during 30 min running under thermoneutral conditions.

2. 2.|Brain and body temperatures of wr rats were significantly higher (P < 0.001) than control rats, both in normothermia as well as in hyperthermia; at rest, and also during exercise.

3. 3.|Warm-reared rats were more tolerant to heat.

4. 4.|During normothermia a weak selective brain cooling was present in control but absent in wr rats. During hyperthermia, however, the cooling intensified in control and occurred in wr rats.

5. 5.|The main strategy of adaptation to heat in wr rats is an upward resetting of the temperature set-point and increased passivity.

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.

Muscle potentials and temperature acclimation and acclimatization in flight muscles of workers and drones of Apis mellifera

1. 1.Muscle potentials in fibrillar flight muscles of worker and drone honeybees were recorded extracellularly at thoracic temperatures from 30 to 10°C.

2. 2.Extinction temperatures for muscle potentials were higher in drones for all treatments.

3. 3.Cold acclimation (15°C) lowered extinction temperatures significantly in workers and drones. Acclimitization changed extinction temperatures significantly only in drones.

4. 4.Cold acclimitization had a bigger effect on the rate of muscle potential amplitude decline with decreasing temperature than acclimation.

5. 5.Acclimation and acclimitization had no effect on the increase of muscle potential duration with falling temperature.

6. 6.Muscle potential frequency during shivering was not much different between cold and warm treated bees.

Cellular mechanisms of neuronal thermosensitivity

1. There are differences between warm sensitive and temperature insensitive neurons in the rostral hypothalamus.

2. In warm sensitive neurons, temperature affects the rate of depolarization in prepotentials that precede action potentials. Warming increases the depolarization rate, which shortens the interspike interval and increases firing rate.

3. Inactivation of the potassium A current is temperature sensitive and contributes to the depolarizing prepotential.

4. In addition to intrinsic mechanisms, neuronal warm-sensitivity is affected by inhibitory synaptic input. Since cooling increases neuronal resistance, temperature affects the amplitude of postsynaptic inhibitory potentials, and this enhances neuronal thermosensitivity.

A new device for measurement of the thermal conductivity of fur and blubber

1. 1. A new and simple device for measurements of thermal conductivity of fur and blubber is described.

2. 2. The device measures temperature differences across the sample and across a polyethylene plate with known conductivity which is placed in series with the sample.

3. 3. The conductivity of the polyethylene was determined from the steady state temperature difference and heat flux through the wall of a polyethylene pipe with a central heat source.

4. 4. The accuracy of the device is ±4.0%.

5. 5. The thermal conductivity of harp seal (Phoca groenlandica) and minke whale (Balaenoptera acutorostrata) blubber, as determined by use of this device, is very close to previously reported values.