Thermal sensations during simultaneous warming and cooling at theh forearm: A human psychophysical study

1. 1.The forearm of 5 female subjects ws thermally stimulated by 2 sets of interposed servo-thermodes that respectively drove skin temperature at ±0.1°C.s⁻¹ for 25 s and then held it constant. Mean skin temperature remained constant. The sequence was repeated at adapting temperatures between 22.5 and 37.5°C.

2. 2.Thermal sensations, continuously reported by the position of a dial, were warmer for heterogeneous thermal stimuli than for homogeneous stimuli when mean skin temperature was greater than 30°C and cooler when less than 27.5°C.

3. 3.This phenomenon is inconsistent with a single additive contribution of “warm” and “cold” information to thermal sensations.

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”.

Cheek skin temperature and thermal resistance in active and inactive individuals during exposure to cold wind

1. The present study examined the effect of the thermal state of the body (as reflected by rectal temperature) on cheek skin temperature and thermal resistance in active and inactive subjects.

2. Active subjects were exposed to a 30 min conditioning period (CP) (0 °C air with a 2 m/s wind), followed immediately by a 30 min experimental period (EP) (0 °C with a 5 m/s wind). Inactive subjects were exposed to a 30 min CP (22 °C air with no wind), followed immediately by a 45 min EP (0 °C air with a 4.5 m/s wind). The CP period was used to establish a core temperature difference between the active and inactive subjects prior to the start of EP. The 0 °C exposure was replaced with a −10 °C ambient air exposure and the experiment was repeated on a separate day. Subjects were comfortably dressed for each ambient condition.

3. Cheek skin temperature was not significantly higher in active subjects when compared to inactive subjects, but thermal resistance was higher in active subjects.

4. Cheek skin temperature and thermal resistance both decreased as ambient temperature decreased from 0 to −10 °C. The lower cheek thermal resistance at −10 °C may have been due to a greater cheek blood flow as a result of cold-induced vasodilation.

Increased hand blood flow limits other skin vasodilation

1. 1. To examine whether the increased hand blood flow (BF), mainly arteriovenous anastomoses (AVA) flow, limits an increase in other skin BF during thermal load, 7 healthy male subjects were exercised for 25 min and then rested for 20 min in wrist occlusion (OCCL) and control experiments (CONT), respectively.

2. 2. In OCCL, both wrists were occluded at pressure of 250 mmHg from the 15th min of exercise.

3. 3. In CONT, the wrists were free throughout the experiment. Finger and forearm skin temperature greatly increased in CONT, but did not rise in OCCL.

4. 4. Suppressed hand BF in OCCL induced compensatory increases of skin BF and sweat rate in the chest at least.

5. 5. However, wrist occlusion induced a significant rise in esophageal temperature and a significant fall in mean arterial pressure (MAP).

6. 6. These results suggest that the rising hand BF greatly contributes to limit the increase in other skin BFs without any fall of MAP during thermal load.

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.

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.

Thermoregulatory effects of central injection of noradrenaline in the new-born columbian ground squirrel (Spermophilus columbianus)

1. 1.Effects of centrally injected noradrenaline (NA) into new-born (12–300 h. post-partum) Columbian ground squirrels (Spermophilus columbianus) were studied to provide comparative data on ontogeny of the thermoregulatory pathways in a hibernating species.

2. 2.At warm ambient temperatures (32–34°C, similar to nest temperature), NA increased heat production (47–92%). rectal temperature (0.27–1.73°C), and axillary temperature (0.59–1.92°C). Peak magnitudes of heat production increased with increasing age on a per unit weight basis.

3. 3.At lower temperatures (28–31°C), NA had no effect on heat production.

4. 4.The data indicate that metabolic and thermal responses to NA in neonates of hibernating species are comparable (e.g. rabbit. guinea pig) or different (e.g. lamb) from those observed in neonates of non-hibernating species.

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.

Physiological and psychological thermal response to local cooling of human body

1. 1. In order to investigate the thermoregulatory responses to the non-uniform thermal environment of the human body, the effects of cooling 10 different body regions were compared by circulating cool water to the neck, breast, back, loin, upper-arms, lower-arms, hands, thighs, legs and feet, respectively. Tympanic temperature, regional (11 sites) and mean skin temperature, and the thermal sensations were measured during experiment in which 30 min local coolings were applied on 5 female students in a climatic chamber controlled at 30°C and 50% r.h.

2. 2. The skin temperature beneath the cooling pad decreased in the order of arms, legs, hands and feet, and trunk.

3. 3. The temperature drop was significantly correlated with the thermal sensation of the region itself.

4. 4. On the other hand, the tympanic temperature increased once by any local cooling. The increase of it was correlated with the change of the general thermal sensation.

5. 5. Results of principal component analysis of skin temperature showed that the peripheral cooling affected the skin temperature in the limited peripheral regions, while the effects of cooling of the breast and the back extended to both the central and peripheral.

Thermoregulatory responses of old men to gradual changes in ambient temperature

1. 1. Thermoregulatory respones to gradual rise and fall in the ambient temperature (T_a) were compared between 8 old (68–78 years) and 8 younger (20–25 years) male subjects.

2. 2. Starting at T_a of 31.5°C (r.h. 40%), T_a was raised to 39.5°C, then lowered to 21.5°C, and raised back to 31.5°C at a constant rate of 0.3°C/min.

3. 3. Noticeable differences in responses between the age groups were as follows: decline of sweating rate and reduction of acral blood flow during room cooling were retarded in the aged group, with wider variations among individuals, compared with those in the younger group; the tympanic and oesophageal temperatures fell considerably during cooling in the elderly group, failing to return to the level at start during the rewarming of the room, in contrast to the younger group.

4. 4. Such sluggish responses may be attributed largely to reduced cutaneous thermal perception with advancing age.

Energy budget of the chicken foot

1. 1.|A mathematical model predicts the energy loss from a chicken foot provided the following variables are known: body temperature, air temperature, wind velocity, blood flow to the foot, and the relative partitioning of blood flow via two distinct venous returns.

2. 2.|Chickens are capable of keeping their feet from freezing at temperatures as low as −30°C ambient, but at a high energy cost.

3. 3.|Chickens can modulate blood flow to their feet at thermoneutral temperatures enough to vary heat loss to environment by about one-fourth metabolic heat production.

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.

Transient response of the human-clothing system

1. 1. A transient clothing model which considers the effects of adsorption and thermal capacitance on the dynamic thermal response of clothing was developed.

2. 2. Moisture adsorption and desorption by the fabric are the major factors that affect the transient response of clothing.

3. 3. This moisture can come from evaporated sweat or from the environment.

4. 4. The clothing model was combined with a modified version of the two-node thermal model of the human body.

5. 5. The combined model shows that, during transients, the mix of latent and sensible heat flow from the skin may differ considerably from the corresponding heat flows from the clothing surface to the environment.

6. 6. The alteration of the heat flows can have a significant impact on the thermal response of the body by changing the sweat rate required to achieve the heat loss necessary to maintain thermal balance.

The combined effects of ambient temperature and enforced sustained swimming activity on body temperatures of arctic charr (Salvelinus alpinus L.)

1. 1.|The difference between tissue temperatures and ambient water temperatures (ΔT) of the ectothermic Arctic charr (Salvelinus alpinus L.) ranged between 0.2 and 0.6°C.

2. 2.|For fish held at 5.7°C there were no significant differences in ΔT of exercising fish and those of controls.

3. 3.|By contrast, for fish held at 1.7°C sustained exercise led to a significant increase in ΔT of all body compartments compared with fish held in standing water (controls).

4. 4.|It is suggested that Arctic charr are capable of a limited control of metabolic heat exchange between body compartments and surrounding water when subjected to sustained exercise and ambient temperatures <2°C.

Characteristics of wettedness under constant average skin temperature

1. 1. Experiments were carried out concerning the characteristics of wettedness revealed under constant average skin temperature using sitting-resting nude subjects. From the basic measurements of both environmental parameters and human physiological responses, the conclusions detailed below were proposed regarding the changes of wettedness under constant average skin temperature.

2. 2. There is positive correlation between the wettedness and environmental humidity, and negative correlation between the wettedness and air temperature.

3. 3. There is positive correlation between the evaporative heat loss from the skin surface and air temperature, and negative correlation between the evaporative heat loss and environmental humidity.

4. 4. There is negative correlation between the wettedness and evaporative heat loss.

5. 5. Wettedness is not constant but takes varying values, that is, corresponding to each average skin temperature both the maximum and the minimum wettedness values occur.

6. 6. Deriving from the items mentioned above, the theoretical locus of equal average skin temperature is not a straight line, but is a curved line plotted on the psychrometric chart.

Effect of fiber type and fabric moisture content on the hydration state of human stratum corneum

1. 1. The purpose of this study was to determine the effect of fiber type and fabric moisture content on SC hydration.

2. 2. Using three similarly constructed fabrics, six fabric type/moisture content combinations were selected.

3. 3. Fabric swatches were placed on both “normal” and “hydrated” volar forearm skin of five subjects for a specified period, then removed.

4. 4. Two minutes after removal, evaporative water loss (EWL) and skin temperature were measured.

5. 5. Data were analyzed using analyses of variance and Bonferroni t-tests.

6. 6. For normal skin, SC hydration generally increased as fabric moisture content increased. SC was significantly drier after being in contact with cotton swatches at regain than at the two moisture content levels above regain, and also under polyester swatches.

7. 7. For hydrated skin, hydration state was significantly lower under the cotton swatch at regain than at 38.6% moisture content or at saturation, but was not significantly different under the polyester swatch at regain or at saturation.

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.

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.

Responses of human skin temperature and thermal sensation to step change of air temperature

1. 1. The purpose of this paper is to clarify the non-linearity of the human physiological and psychological responses to step change of air temperature by impulse response analysis using Discrete Fourier Transformation.

2. 2. Experiments were conducted to investigate the effect of thermal transients on human responses.

3. 3. Experimental conditions were as follows: lowering air temperature from 30 to 20°C and raising air temperature from 20 to 30°C.

4. 4. The responses of local skin temperature on lowering air temperature from 30 to 20°C are not necessarily opposite to the responses found on raising air temperature from 20 to 30°C.

5. 5. From impulse response analysis using Discrete Fourier Transformation, skin temperature responses to the opposite air temperature change do not necessarily coincide with each other whenever the same temperature stimulus is occurred.