The majority of thermoregulatory research available focuses on males rather than females and emphasizes core temperature and whole body sweat loss. Limited research is available on females, with a sparsity of information on regional sweat rates (RSR). Historically, RSR has been measured over a very limited number of sites or studies have used qualitative methods to assess sweating over large surface areas (28,29). More recently, several studies have measured RSR on multiple body regions (12,31–33,40,41,43); however, these studies used only males or reported combined data from both sexes. The only data currently available on females were limited to torso sweat rates (22), which identified significant regional variation between zones. The first study measuring RSR over almost the whole body surface area in males was recently published by Smith and Havenith (39), identifying both significant inter- and intraregional variation in sweating. To the knowledge of the authors, no study has attempted to measure RSR simultaneously over large skin surface areas for females.
Considerable debate surrounds sex differences in thermoregulation. Traditionally, women (testing a population average) are considered less effective in regulating body temperature than males in dry heat (37), with maintenance of a significantly lower sweat rate compared with men, and a substantially higher rectal temperature (7,13,14,37,38). A more pronounced delay in sweat onset has also been noted in women, attributed in part to a lower body water content (20) and potential effects of menstruation (25). Observations of sex-related differences in sweat rate, sweat thresholds (25), sweat gland size, and distribution (4,5,25) have contributed to the opinion that females generally sweat less than males. Conversely, several studies have observed that sex differences in thermoregulation cease to be significant upon matching subjects or correcting for anthropometric, acclimatization, and fitness parameters (2,3,14,15,23,24). Such disagreement in the literature must be viewed with careful consideration of the experimental design, measurement technique, and subject characteristics. Individual characteristics play a major role in thermoregulatory responses to heat stress (23,24) and are thought to explain a substantial part of response variation observed (17). More recently, however, studies supporting the existence of sex differences per se in thermoregulation have emerged; Madeira et al. (34) have demonstrated a greater pilocarpine-induced sweating responses in males compared with females when groups were matched for V˙O2peak. Aerobic capacity is known to enhance sudomotor response to pilocarpine in males (8), which may partially explain sex differences in local sweating in studies using unmatched groups. In addition, Gagnon and Kenny (19) observed lower evaporative heat loss and thermosensitivity in females despite a fixed absolute metabolic heat production and matching of physical characteristics between sexes.
This is of particular importance when considering fixed absolute versus relative work rates, whereby sex differences may be artificially created. During absolute work rate protocols, results may be confounded between groups if unmatched for V˙O2max and/or body composition. Alternatively, when relative work rates are used, differences in absolute work rates and thus metabolic heat production may arise between sexes (18,21). Group “matching” is therefore important to consider, and in doing so, either comparing “average” individuals from each population or, to match V˙O2max, accepting that this is an unrepresentative sample from one population. With this in mind, the present study has taken an applied approach in comparing thermoregulatory responses between sexes in which the groups were selected for similar training and athletic performance levels (elite to subelite athletes) and were therefore not matched for physical characteristics. For exercise load, it was decided to use relative work rates that represent training and competition practice.
The aims of the present study were 1) to produce a whole body sweat map of aerobically trained females during mild exercise-induced hyperthermia and 2) compare these data to previously published body maps of sweating in aerobically trained males produced in our laboratory under the same experimental conditions (39). It was hypothesized that, similar to males, significant regional variation in sweat rate would be observed within the female group, with consistent patterns of variation between participants. It was further hypothesized that females would sweat significantly less than males because of a lower absolute metabolic heat production when exercising at a fixed relative workload, arising from a lower absolute aerobic capacity. Similar patterns of distribution of sweating were expected between sexes.
Thirteen female unacclimated, aerobically trained, elite to subelite runners participated in whole body sweat mapping. All experimental procedures were approved by the Loughborough University Ethical Committee and were fully explained to the participants before obtaining informed written consent and completion of a healthscreen questionnaire.
Participants attended the Environmental Ergonomics Research Center for anthropometric measurements of height, mass, and body dimensions used for the calculation of body surface area (9) and absorbent pad sizes. Skinfolds were taken using a four-point calliper method (26) specific to female athletes for calculation of body fat percentage. Aerobic fitness level, expressed as maximal oxygen uptake (V˙O2max), was calculated from a submaximal fitness test based on the Åstrand–Ryhming method (1). The test was conducted at an ambient temperature of 18°C to prevent thermal stress and composed of four exercise intensities running on a treadmill (h/p/cosmos mercury 4.0 h/p/cosmos sports & medical gmbh, Nussdorf-Traunstein, Germany) each lasting 5 min. Estimation of V˙O2max was based upon the linear relationship between HR and work rate (work rate based upon treadmill speed and angle) (10).
Sweat pad preparation and application.
RSR was determined using the method developed in our laboratory (12,22,39,40) by applying absorbent material directly to the skin for a short, predefined period (5 min). Two sets of absorbent pads were produced for each participant based on the anthropometric data (see online text, Supplemental Digital Content 1; http://links.lww.com/MSS/A171 for details of pad sizing). Pads were weighed (Sartorius YACOILA, Sartorius AG, Goettingen, Germany. Precision 0.01 g) inside individually labeled airtight bags, in which they were stored until testing. A total of 78 pads were used to produce a whole body sweat map for each exercise intensity (see Fig. 1 of online Supplemental Digital Content 2 (http://links.lww.com/MSS/A172) for sweat map pad locations). Pads were attached to custom-sized plastic sheeting for fast application to the body and to prevent the evaporation of sweat during the test periods. The pads were kept in place against the skin using a stretch long sleeve T-shirt and trousers. For the breast area, pads were attached inside a sports bra. On the feet, pads were secured in place on the ankles and dorsal surface of the foot inside 100% cotton socks, which were also used to collect sweat from the top of the foot. Plastic stretch socks were worn on top to prevent evaporation of sweat from the cotton socks during the measurement period. Similarly, 100% cotton gloves were worn to collect sweat on the hands, with small incisions made at the base of each finger to prevent the migration of sweat between regions, while maintaining their structural integrity during the test. Latex gloves were worn over the cotton gloves during the measurement period to secure the gloves in place against the skin and prevent sweat evaporation.
Experimental sessions were conducted in a climate-controlled room at 25.7°C ± 0.4°C, 45% ± 7% relative humidity, and a 2 m·s−1 frontal air velocity. Data were obtained in three identical experimental sessions per participant, with approximately one third of the skin surface area covered in each test, thus allowing enough exposed skin for thermoregulation. The three sessions focused on 1) torso/upper body (UB), 2) legs, and 3) arms, hands, buttocks, and feet (AHBF). Testing sequence was balanced to prevent any order effect and performed at the same time of day to minimize circadian variation. Menstrual cycle phase was not controlled for during experimental sessions; participants were tested over a wide range of the menstrual cycle, providing a representative sample of menses state in the results.
On arrival to the laboratory, participants were provided with shorts and T-shirt and then weighed. Infrared images (Thermacam B2; FLIR Systems Ltd., West Malling, Kent, UK) of the nude, dried skin were taken before testing, before and after each pad application, and immediately after testing to monitor skin temperature (Tsk). Resting HR was recorded before participants warmed up, with HR monitored throughout the experiment at 15-s intervals. Tcore was measured using a VitalSense Integrated Physiological Monitoring System (Mini Mitter Company, Inc., Bend, OR). Participants swallowed a CorTemp™ ingestible temperature pill 5 h before testing. Throughout the experiment, the VitalSense monitor wirelessly tracked and recorded Tcore four times per minute. Participants ran for a total of 60 min involving two exercise intensities of 30 min each on the treadmill with an incline of 1%. The target HR was 125–135 and 150–160 bpm for intensity 1 (I1) and intensity 2 (I2), respectively, to control workload at the targets of 60% and 75% of V˙O2max. Exercise intensities were not separated by a break; however, subjects were required to step off the treadmill for all measurements and pad application/removal (approximately 3 min). Participants removed their clothing and toweled their skin dry immediately before pad application to ensure only sweat produced during the sample period was collected. All of the pads had an impermeable backing to prevent evaporation. Sweat samples were taken during the last 5 min of each exercise intensity at 30 and 60 min, during which time the participants returned to the treadmill donning the absorbent pads. Immediately after the sample periods, the pads were quickly returned to their airtight bags and sealed. The participants could drink water freely during the experiment, which was recorded, to prevent dehydration. After the 60-min run, final measurements of core temperature, skin temperature, and body weight were recorded. All pads were reweighed inside their sealed bags. The cotton glove and sock segments could not be individually weighed before testing because they were not yet separated from each other. Immediately after sweat collection, specific sections of the gloves and socks were dissected and placed in individually labeled airtight bags. The posttest wet weight of each sample was recorded before being dried out in a thermal chamber at 30°C, 50% relative humidity, for 24 h then reweighed to obtain the “dry” (pretest) weight. The surface area of each pad was calculated from the dry weight of each pad and the weight per unit of surface area of the material. Local sweat rate was calculated in grams per meter square of body surface area per hour (g·m−2·h−1) using the weight change of the pad, the pad surface area, and duration of application to the skin.
Because data from the different experimental sessions were to be combined in a whole body sweat map, and because sweat rates may differ, even between identical sessions for an individual, it was decided to correct individual session data in line with the session’s gross sweat loss (GSL) value. Data for each individual were standardized toward the mean GSL over all three sessions for that individual. All corrections work on the assumption that within each workload, there is a relation between regional and GSL for an individual.
GSL was calculated based on the weight change of each participant across each test period, adjusted for fluid intake. Corrections were made for respiratory and metabolic mass losses. Evaporative loss from respiration (Eres (W)) was calculated using equation 1, based upon the work described by Livingstone et al. (30):
and converted into mass loss (g):
where Eres is the evaporative loss from respiration (W); M, metabolic rate (W); Ta, air temperature (°C); t, time: duration of intensity or experiment (s); and 2430, latent heat of evaporation of 1 g of water (J·g−1).
Metabolic mass loss (g) was calculated based upon Kerslake (27):
where V˙O2 is rate of oxygen consumption (L·min−1); RQ, respiratory quotient (ND); t, time (s).
The RQ was taken as 0.85 for intensity 1 and 1.00 for intensity 2 (35).
Sweating sensitivity for each segment (i) was calculated as follows:
Finally, overall sweat sensitivity was calculated for comparison with literature (31–33,43) as follows:
Paired sample t-tests were performed both with and without Bonferroni correction to analyze right–left differences in sweat rate and changes with exercise intensity. A one-way repeated-measures ANOVA was performed to analyze regional differences within each intensity, presented both with and without Bonferroni correction for post hoc comparisons. Both values are presented first because of the exploratory nature of the study and second because of the large number of zones studied compared with any earlier study (6,36). This makes the Bonferroni correction very stringent, and zones that would show significance in a smaller study will struggle to reach significance here. For RSR comparison between sexes, a two-way repeated-measures ANOVA was performed with sex (between-subject factor), region, and sex–region interaction as factors. To allow direct comparison of the upper chest between sexes despite the use of differing pads, the upper chest (three pads) in the males and the upper chest and bra pads (11 pads) in the females were area weighted to produce a single “upper chest” sweat rate value for each sex.
To allow standardization of sweat data over participants and for the easy identification of “higher” and “lower than average” sweat regions regardless of absolute sweat rates, RSR was normalized for the area-weighted sweat rate of all zones. The same analysis was performed on the normalized regional sweat data as described above for the absolute data. Pearson correlation coefficient was calculated to assess correlations between RSR and regional Tsk and RSR and GSL. Finally, it was decided that it would be more relevant to graphically show results for the “average sweater” (the median) rather than the “average amount of sweat produced” (the mean) because the latter can be affected more easily by outliers, i.e., extreme sweaters. In tables, both values are presented to provide insight into the data distribution.
Male data presented in the present article have been reported previously (39) and are in part included here to allow comparison with the female data.
Female subjects were significantly shorter (female, 165 ± 8 cm, vs male, 179 ± 4 cm, P < 0.001), were lighter (59 ± 7 vs 74 ± 5 kg, P < 0.001), had a smaller surface area (1.64 ± 0.10 vs 1.92 ± 0.10 m2, P < 0.001), and showed a higher body fat percentage than males (18% ± 4% vs 11% ± 5%, P < 0.01). Although age was significantly different between groups (female, 21 ± 1 yr, vs male, 23 ± 3 yr, P = 0.047), this was not biologically relevant. Females had a significantly lower V˙O2max (59.5 ± 10 vs 70.2 ± 13 mL·kg−1·min−1, P < 0.05) with a value 85% that of the trained males. When based on fat-free mass, females had a V˙O2max 92% that of males (female, 78.9 mL·kg−1·min−1, vs male, 72.6 mL·kg−1·min−1).
Core Temperature, Work Rate, and HR
Baseline data (BL) were taken as the temperature and HR recorded immediately before commencing I1. Reported I1 and I2 data were the mean values over the final 5 min of each intensity. Tcore increased significantly from 37.29°C ± 0.29°C at baseline to 37.83°C ± 0.19°C at I1 (BL to I1 ΔTcore = 0.54°C ± 0.21°C, P < 0.001) and to 38.06°C ± 0.24°C at I2 (ΔTcore; BL to I2 = 0.77°C ± 0.35°C, P < 0.001, I1 to I2 = 0.23°C ± 0.25°C, P < 0.01). HR increased significantly from 66 ± 13 bpm at baseline to 134 ± 3 at I1 (P < 0.001) and to 157 ± 3 (P < 0.001) at I2, reflecting relative work rates of 61% ± 7% and 72% ± 11% V˙O2max for I1 and I2, respectively.
No differences in HR were present between groups for either exercise intensity; however, running speed (km·h−1) was significantly higher in males compared with females (I1, 10.4 ± 2.0 vs 8.5 ± 1.7, P < 0.05; I2, 13.6 ± 2.2 vs 10.5 ± 1.7, P < 0.01). Males showed a lower resting Tcore than females (male, 36.93°C ± 0.39°C, P < 0.05), but no sex difference was present at the end of either exercise intensity (male I1 = 37.68°C ± 0.45°C, I2 = 38.06°C ± 0.44°C). ΔTcore was significant over both exercise intensities (male ΔTcore; BL to I1 = 0.76°C ± 0.18°C, I1 to I2 = 0.45°C ± 0.30°C, P < 0.001) in both sexes, with the rise being significantly greater in males from BL to I1, reflecting the lower resting Tcore (P < 0.05).
Substantial variation in GSL was observed both within (between sessions) and between participants. The mean GSL of all sweat mapping experiments was 272 ± 103 g·m−2·h−1, with mean values for UB/torso, legs, and AHBF sessions of 300 ± 113, 268 ± 95, and 246 ± 101 g·m−2·h−1, respectively. The mean surface areas covered in each experiment were 0.49, 0.45, and 0.33 m2 for the AHBF, legs, and UB experiments, respectively, totaling 1.28 m2. The percentage of body coverage was 30.1%, 27.7%, and 20.2% over the three experiments, totaling 78% of the whole body. GSL increased significantly with exercise intensity (P < 0.001) from 168 ± 81 to 410 ± 144 g·m−2·h−1 and correlated positively with V˙O2max (r = 0.71, P < 0.01), and for individual work intensities (Fig. 1), GSL (g·h−1) correlated positively with metabolic rate (W; I1 r = 0.89, P < 0.001; I2 r = 0.87, P < 0.05) with no significant difference present between the gradient of regression lines for each exercise intensity.
Males showed significantly higher GSL compared with females both during each exercise intensity and overall (male GSL: I1, 364 ± 84 g·m−2·h−1; I2, 657 ± 119 g·m−2·h−1; overall, 458 ± 115 g·m−2·h−1; male vs female GSL all P < 0.001). When GSL was plotted against V˙O2max, no significant differences between the gradient of the regression lines or the intercepts were present between sexes. Metabolic heat production was significantly greater in males than females expressed in absolute terms (Fig. 1: male I1, 993 ± 185 W; I2, 1335 ± 259 W; both P < 0.001), but only at I2 when expressed as a function of surface area (male I1, 519 ± 103 W·m−2, P = 0.081; I2, 697 ± 137 W·m−2, P < 0.01).
RSR data were grouped for corresponding right and left zones because only one zone showed a bilateral difference. Median grouped data for all participants are illustrated for both exercise intensities in Figure 2. The pads illustrated in gray, located below the anterior and posterior neck and at the axilla, acted to absorb excess sweat, which might otherwise have dripped from these areas and thus preventing it from being absorbed by adjacent pads. These extra pads were discarded after sweat collection and were not used in sweat mapping calculations. The highest sweat rates observed at I1 were at the central upper back, heels, and dorsal foot and between the breasts, with values of 223, 161, 139, and 139 g·m−2·h−1, respectively. Sweat rate increased at all regions with increasing exercise intensity, with exception of the feet, ankles, and the lateral lower breast (Table 1). At I2, the central upper back and the area between the breasts showed the highest sweat rates with values of 723 and 470 g·m−2·h−1 compared with significantly lower values on the breasts and toward the extremities. Detailed comparisons of all absolute RSR within each exercise intensity may be viewed in the Supplemental Digital Content 3 (http://links.lww.com/MSS/A173) (Tables 1–4). “Higher” and “lower than average” sweat rates may easily be identified using normalized RSR data, illustrated in Figure 3. Regions with sweat rate ratios significantly different from average (=1) are denoted in Table 1 by gray shading in the ratio column. A comparison of normalized ratio data between exercise intensities indicated little change in distribution between I1 and I2, with exception to a significant decrease in distribution toward the feet and shoulders and an increase toward the breasts at the higher exercise intensity.
Regional absolute and normalized sweat data for male athletes (adapted from Smith and Havenith ) are presented in Figure 4. Absolute and normalized data comparisons between sexes are presented both with and without Bonferroni correction in Table 2. As expected, males showed significantly greater absolute local sweat rates compared with females at both exercise intensities, with exception of areas of the hands and feet at I1 and only the thumbs and dorsal hand at I2. Both sexes did exhibit similarities in RSR, showing 1) greater sweat rates on the anterior compared with the posterior torso, 2) a medial to lateral decrease in sweat rates across the torso, 3) the greatest sweat rates on the central and lower back (with exception to the bra triangle in females at I2), and 4) the lowest sweat rates toward the extremities. Normalized ratio data (Fig. 3. vs Fig. 4B) indicated a significantly higher distribution of sweat toward the torso in males, and females showing a significantly higher distribution toward the hands and feet compared with males at both exercise intensities.
Because no significant difference in absolute metabolic rate was present between sexes for male I1 compared with female I2, a comparison of absolute and normalized data between sexes was performed for these data (Table 2). GSL did not differ significantly between males at I1 compared with females I2 when compared in absolute terms (male, 699 ± 157 g·h−1, vs female, 685 ± 260 g·h−1, P = 0.887), nor when normalized for body surface area (365 ± 84 vs 410 ± 131 g·m−2·h−1, P = 0.379). Absolute RSR remained significantly higher in males compared with females on the torso, legs, and areas of the feet, representing 17 of the 34 regions compared. Despite significantly greater sweat rates in males, regions of high and low sweating were similar between sexes. A significant region–sex interaction for both I1 and I2 normalized data (P < 0.001) did however indicate some differences in distribution. Fewer differences were present in relative sweat distribution compared with absolute data, with the main exception being significantly greater ratio values for the arms and hands in females compared with males, with significance present at 9 of the 34 regions compared.
Regional Tsk data were right and left grouped because only 5 of the 48 regions measured showed significant bilateral differences, and no significant differences after Bonferroni correction. Tsk increased from baseline to I1 at only the feet and ankles (uncorrected: heels, soles, and dorsal foot, P < 0.001, ankles, P < 0.05; corrected: heels and soles, P < 0.001, dorsal foot, P < 0.01), reflecting their low baseline temperatures. The lowest baseline Tsk of 26.5°C was observed at the heels compared with the highest value of 34.0°C at the anterior upper chest and medial upper back. Interestingly, the mean increase in Tsk of all regions from pre- to postpad application was 1.1°C for both I1 and I2, reflecting the effect of the measurement technique itself on Tsk.
A within-participant analysis of the correlation between RSR and corresponding regional Tsk was performed to avoid the potentially confounding effects of between-participant factors on Tsk and RSR (particularly absolute work rate affecting SR). RSR and regional Tsk were not correlated in any participant at either exercise intensity or across measurement periods (mean ± SD Pearson r correlation: I1, 0.14 ± 0.34; I2, 0.06 ± 0.17).
No significant differences in regional Tsk were present between sexes at any measurement period with exception to baseline. Similar to the females, the lowest regional Tsk for males at baseline of 25.8°C was at the heels, compared with the highest of 32.5°C observed on the anterior upper arm. Tsk at baseline was significantly higher in females at all regions of the UB (torso: posterior medial upper, posterior lateral upper, P < 0.05; anterior upper, anterior medial lower, anterior lateral lower, posterior medial lower, posterior lateral lower, P < 0.01; sides, P < 0.001). The posterior medial upper, posterior lateral upper, anterior medial lower, and posterior lateral lower regions did not show significance after Bonferroni correction. Absolute regional Tsk increased significantly at only the feet and ankles during I1, with most sites on the torso and the anterior arms increasing from I1 to I2. The mean increase in Tsk over all regions during pad application was 0.9°C during I1 and 0.8°C during I2, reflecting the effect of the procedure on Tsk (for complete regional Tsk data, see Supplemental Digital Content 4 (http://links.lww.com/MSS/A174)). No correlation between RSR and regional Tsk was observed in males (Pearson r correlation: I1, 0.17 ± 0.23; I2, −0.11 ± 0.19).
The present study aimed to produce a whole body sweat map of aerobically trained white females at two exercise intensities in a temperate environment. A secondary aim of the study was to compare these data with whole body sweat maps of aerobically trained white males tested under the same experimental conditions (39). The data have clearly illustrated significant intra- and interregional variation in sweat rate in aerobically trained females, similar to that observed in males, and have shown large variation in absolute sweat rates between individuals. Regardless of the variation in absolute quantities of sweat produced, differences in distribution were observed between sexes, despite similarities in high and low sweat regions. Such differences should be considered in sex-specific application of clothing design, clothing evaluation with thermal manikins, and thermal modeling.
It is clear from the present data that absolute gross sweat rates were significantly higher in males compared with females exercising at the same relative work rate and unmatched for physical characteristics. This approach elicited a greater metabolic heat production in males (18) because of a higher absolute work rate compared with females and a greater body mass. This is largely reflected in the absolute regional sweat data in which 28 of the 34 regions measured were significantly higher in males than females at I1 and 32 of the 34 regions at I2. When considering distribution, at both exercise intensities, the males had a significantly higher distribution of sweat toward the torso, whereas the females had a significantly higher distribution toward the hands and feet in comparison with males. Comparing absolute sweat rates between sexes when exercising at similar rates of metabolic heat production (male I1 vs female I2), still, 17 of the 34 regions measured were significantly higher in males, mostly on the torso and legs, despite the similarity in GSL. Although the distribution of sweat was approximately similar between sexes, females did show a significantly higher distribution toward the arms (anterior and posterior) and hands (fingers, thumbs and dorsal hand) than the males, compared with a small number of regions showing a higher distribution of sweat on the torso in males compared with females. These data are consistent with previous UB sweat mapping data produced by our laboratory using males and females of equal aerobic fitness (22). These data observed no overall effect of sex but a significant zone and sex interaction, which showed that certain regions sweated more in males, whereas other regions sweated more in females. Similarly to the present data, the highest normalized sweat rates were observed on the midcentral back in both sexes (with exception only to the area between the breasts in females), sweating to be greater on the posterior compared with anterior torso, and lowest on the extremities.
Explaining the observed differences in sweat distribution both within and between sexes requires further investigation. They cannot be explained by Tsk in the present data, and high versus low heat-activated sweat gland distributions are reported to be similar in both males and females (28). Despite a higher heat-activated sweat gland density in females, there are no differences in total numbers of glands between sexes because of a greater surface area in males. Notably, a lower output per gland in females for a given thermal or pharmacological stimulus (5,25,34) may help explain the lower absolute RSRs in females compared with males, although not the regional differences, nor the effect on the heat balance this may have. In both sexes, regional sweat gland densities vary considerably over the body, with the greatest densities (glands per square centimeter) reported on the soles (620 ± 120), forehead (360 ± 60), and cheeks (320 ± 60), compared with the lowest values on the back, buttocks, arms, and legs (ranging from 160 ± 30 to 120 ± 10, respectively) (42). Notably, these data used a small cadaver sample in which the type of sweat gland and its status as active or inactive was not discernible. A comprehensive review of torso sweat gland densities (inactive and active) is available from Machado-Moreira et al. (32), providing more reliable values. Regional glandular densities on the torso were relatively uniform (range: 115–81 glands per square centimeter on the abdomen and the chest and abdomen (umbilicus), respectively), failing to explain the regional sweating variation observed in the present study. Alternative explanations include the number of active sweat glands, output per gland, and sudomotor sensitivity. Segmental sudomotor sensitivity calculated by Machado-Moreira et al. (32) closely matched RSR variation observed in the current data, supporting this factor as a likely explanation.
Applications for the current data can be found in some areas. First, in models of human thermophysiology, these have moved over the last five decades from relatively simple two-node models (a core and a skin compartment) (16) to highly detailed multinode models that represent the whole body shape and calculate heat exchanges separately for many individual compartments (e.g., 63 body surface segments for Fiala et al. ). This means that heat transfer is calculated differently for a chest section than for an arm section, for example. Until the current data were available, this difference was only in the heat transfer coefficients (difference in movements), but now, also different sweat production levels for different areas can be included (11), providing an additional level of realism. The second application area is in clothing design. The body mapping data provided from the present and earlier work (12,39) have been used by sportswear designers to target areas of high sweat generation with additional ventilation openings and with fabrics with different absorption and wicking properties, thereby improving heat loss (38). Third, the obtained data feed directly into the design of sweating thermal manikins, used for the evaluation of clothing and environments; being able to provide a more realistic sweat distribution adds an extra level of realism.
During exercise in a temperate environment, aerobically trained white females demonstrated large regional variation in absolute RSR over the body but a consistent pattern of distribution. When compared with aerobically trained white males working at the same relative work rates, males showed a greater GSL compared with females, owing to a greater metabolic heat production. Despite this, males and females showed similar “high” and “low” sweat distributions; however, slightly different overall patterns of distribution were present between sexes. Males had a relatively higher distribution of sweat toward the torso compared with females, where the arms, hands, and feet contributed relatively more to total sweat loss in the females. Regional variation in sweat rate cannot be explained by regional skin temperature in the present study and does not correspond with regional sweat gland densities reported in the literature.
Limitations and Future Research
The present research has provided novel regional sweating data in white females and a comparison with white males under the same experimental conditions. It is difficult to dissociate the contributions of physical characteristics to the core temperature responses, requiring further studies using groups matched for physical characteristics to elucidate sex differences. Because of the applied and largely descriptive approach of this work, it is beyond the scope of the article to explain both the regional sweating variation and sex differences from a mechanistic viewpoint. Future work is needed to investigate regional differences in active eccrine sweat gland densities, gland sensitivity, and sudomotor innervation.
The authors acknowledge the continued support from the Adidas Innovation Team during this study, with special thanks to Berthold Krabbe, Brady Anderson, Jean Piere Roy, and James Lamont. The research presented was cofunded by the Adidas Innovation Team, Germany, and the Environmental Ergonomics Research Center, Loughborough University.
The authors are fully responsible for conducting the trial and for the data.
The authors declare that there are no conflicts of interest.
The results from the present study do not constitute endorsement by the American College of Sports Medicine.
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SWEATING; METABOLIC RATE; SEX; SWEAT MAPPING; REGIONAL
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