INFLUENCE OF ENVIRONMENTAL TEMPERATURE ON THE CALCULATIONS OF MEAN SKIN TEMPERATURE

2001 ◽  
Vol 33 (5) ◽  
pp. S222 ◽  
Author(s):  
D D. Pascoe ◽  
J Llanos ◽  
J M. Molloy ◽  
J W. Smith ◽  
W A. Kramer
1991 ◽  
Vol 77 (1) ◽  
pp. 41-47
Author(s):  
A. J. Allsopp ◽  
Kerry A. Poole

AbstractThe effects of hand immersion on body temperature have been investigated in men wearing impermeable NBC clothing. Six men worked continuously at a rate of approximately 490 J.sec−1 in an environmental temperature of 30°C. Each subject was permitted to rest for a period of 20 minutes when their aural temperature reached 37.5°C, and again on reaching 38°C, and for a third time on reaching 38.5°C (three rest periods in total). Each subject completed three experimental conditions whereby, during the rest periods they either: a.Did not immerse their hands (control).b.Immersed both hands in a water bath set at 25°c.c.Immersed both hands in water at 10°C.Physiological measures of core temperature, skin temperature and heart rate were recorded at intervals throughout the experiment.Measures of mean aural temperature and mean skin temperature were significantly (P<0.05) reduced if hands were immersed during these rest periods, compared to non immersion. As a result, the total work time of subjects was extended when in the immersed conditions by some 10–20 minutes within the confines of the protocol.It is concluded that this technique of simple hand immersion may be effective in reducing heat stress where normal routes to heat loss are compromised.


1994 ◽  
Vol 81 (SUPPLEMENT) ◽  
pp. A252
Author(s):  
C. Cheng ◽  
T. Matsukawa ◽  
A. Kurz ◽  
D. I. Sessler ◽  
B. Merrifield

1977 ◽  
Vol 42 (6) ◽  
pp. 909-914 ◽  
Author(s):  
M. B. Maron ◽  
J. A. Wagner ◽  
S. M. Horvath

To assess thermoregulatory responses occuring under actual marathon racing conditions, rectal (Tre) and five skin temperatures were measured in two runners approximately every 9 min of a competitive marathon run under cool conditions. Race times and total water losses were: runner 1 = 162.7 min, 3.02 kg; runner 2 = 164.6 min, 2.43 kg. Mean skin temperature was similar throughout the race in the two runners, although they exhibited a marked disparity in temperature at individual skin sites. Tre plateaued after 35--45 min (runner 1 = 40.0--40.1, runner 2 = 38.9--39.2 degrees C). While runner 2 maintained a relatively constant level for the remainder of the race, runner 1 exhibited a secondary increase in Tre. Between 113 and 119 min there was a precipitous rise in Tre from 40.9 to 41.9 degrees C. Partitional calorimetric calculations suggested that a decrease in sweating was responsible for this increment. However, runner 1's ability to maintain his high Tre and running pace for the remaining 44 min of the race and exhibit no signs of heat illness indicated thermoregulation was intact.


2019 ◽  
Vol 44 (1) ◽  
pp. 22-30 ◽  
Author(s):  
Keiji Hayashi ◽  
Nozomi Ito ◽  
Yoko Ichikawa ◽  
Yuichi Suzuki

Food intake increases metabolism and body temperature, which may in turn influence ventilatory responses. Our aim was to assess the effect of food intake on ventilatory sensitivity to rising core temperature during exercise. Nine healthy male subjects exercised on a cycle ergometer at 50% of peak oxygen uptake in sessions with and without prior food intake. Ventilatory sensitivity to rising core temperature was defined by the slopes of regression lines relating ventilatory parameters to core temperature. Mean skin temperature, mean body temperature (calculated from esophageal temperature and mean skin temperature), oxygen uptake, carbon dioxide elimination, minute ventilation, alveolar ventilation, and tidal volume (VT) were all significantly higher at baseline in sessions with food intake than without food intake. During exercise, esophageal temperature, mean skin temperature, mean body temperature, carbon dioxide elimination, and end-tidal CO2 pressure were all significantly higher in sessions with food intake than without it. By contrast, ventilatory parameters did not differ between sessions with and without food intake, with the exception of VT during the first 5 min of exercise. The ventilatory sensitivities to rising core temperature also did not differ, with the exception of an early transient effect on VT. Food intake increases body temperature before and during exercise. Other than during the first 5 min of exercise, food intake does not affect ventilatory parameters during exercise, despite elevation of both body temperature and metabolism. Thus, with the exception of an early transient effect on VT, ventilatory sensitivity to rising core temperature is not affected by food intake.


Development ◽  
1970 ◽  
Vol 24 (2) ◽  
pp. 405-410
Author(s):  
Janet F. Noel ◽  
E. A. Wright

C3H mice were bred at 30°C and 22°C. At 28 days of age the lengths of the sacral and caudal vertebrae were measured from radiographs and related to the local skin temperature. Growth of the sacral and proximal caudal vertebrae was slightly retarded in the hot environment, but the distal caudal vertebrae showed increased growth which could be quantitatively related to an increase in skin temperature. This suggests that in hot climates the increased growth of peripheral organs of some mammals is due to local increases in tissue temperature.


1962 ◽  
Vol 17 (1) ◽  
pp. 103-106 ◽  
Author(s):  
H. S. Belding ◽  
B. A. Hertig

Human subjects were transferred between environments imposing different levels of heat stress. Analyses of measurements obtained after a reasonably steady state had been achieved in each of several environments revealed equally good correlation between a) sweat rate and ear temperature (tympanic membrane), and b) sweat rate and calculated deep skin temperature (hypothetical). The correlations are consistent with adjustment of sweating in response to either hypothalamic temperature or temperature of skin receptors or some combination of the two. However, during the first 20 min after transfer, changes in sweat rate and skin temperature occurred together and in the same direction, but were not accompanied by any consistent change in ear temperature. Thus, to the extent that ear temperature represents hypothalamic temperature, an hypothesis of control of sweating based on hypothalamic temperature alone is not tenable. Alternative physiological explanations are given for data developed elsewhere and used in support of an hypothesis of sweat control solely from the hypothalamus. Submitted on August 14, 1961


1974 ◽  
Vol 36 (5) ◽  
pp. 625-628 ◽  
Author(s):  
D. D. Lund ◽  
C. V. Gisolfi

1981 ◽  
Vol 25 (1) ◽  
pp. 774-778
Author(s):  
Alex Loewenthal ◽  
David J. Cochran ◽  
Michael W. Riley

Nine fully acclimatized men falling in the lean, medium and obese categories of body composition were observed during heat exposure periods for four days following acclimatization decay periods of various lengths in order to determine the effects of body composition on the decay and reinduction of acclimatization. The physiological variables taken into consideration were core temperature, “DuBois” mean skin temperature, heart rate, weight loss due to perspiration and the temperature differential between the core and surface. All of the men were subjected to an acclimatization schedule of twelve daily sessions in order to insure that they were all fully acclimatized. Three decay, or non-exposure, periods of four, eight and twelve days were each followed by four days of reinduction. It was determined that body composition does not affect the rate of decay or reinduction of acclimatization, although this parameter as well as the extent of decay and the duration of the reinduction period does affect the physiological variables monitored in this study.


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