Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 99: 1972-1976, 2005. First published July 14, 2005; doi:10.1152/japplphysiol.00329.2005
8750-7587/05 $8.00
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
99/5/1972    most recent
00329.2005v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cheuvront, S. N.
Right arrow Articles by Sawka, M. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cheuvront, S. N.
Right arrow Articles by Sawka, M. N.

Hypohydration impairs endurance exercise performance in temperate but not cold air

Samuel N. Cheuvront, Robert Carter, III, John W. Castellani, and Michael N. Sawka

US Army Research Institute of Environmental Medicine, Natick, Massachusetts

Submitted 22 March 2005 ; accepted in final form 27 June 2005


    ABSTRACT
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 
This study compared the effects of hypohydration (HYP) on endurance exercise performance in temperate and cold air environments. On four occasions, six men and two women (age = 24 ± 6 yr, height = 170 ± 6 cm, weight = 72.9 ± 11.1 kg, peak O2 consumption = 48 ± 9 ml·kg–1·min–1) were exposed to 3 h of passive heat stress (45°C) in the early morning with [euhydration (EUH)] or without (HYP; 3% body mass) fluid replacement. Later in the day, subjects sat in a cold (2°C) or temperate (20°C) environment with minimal clothing for 1 h before performing 30 min of cycle ergometry at 50% peak O2 consumption followed immediately by a 30-min performance time trial. Rectal and mean skin temperatures, heart rate, and ratings of percieved exertion measurements were made at regular intervals. Performance was assessed by the total amount of work (kJ) completed in the 30-min time trial. Skin temperature was significantly lower in the cold compared with the temperate trial, but there was no independent effect of hydration. Rectal temperature in both HYP trials was higher than EUH after 60 min of exercise, but the difference was only significant within the temperate trials (P < 0.05). Heart rate was significantly higher at 30 min within the temperate trial (HYP > EUH) and at 60 min within the cold trial (HYP > EUH) (P < 0.05). Ratings of percieved exertion increased over time with no differences among trials. Total work performed during the 30-min time trial was not influenced by environment but was less (P < 0.05) for HYP than EUH in the temperate trials. The corresponding change in performance (EUH – HYP) was greater for temperate (–8%) than for cold (–3%) (P < 0.05). These data demonstrate that 1) HYP impairs endurance exercise performance in temperate but not cold air but 2) cold stress per se does not.

dehydration; thermoregulation; environment


PERSONS EXERCISING IN COLD WEATHER can incur substantial fluid losses (6) and are commonly advised to maintain hydration to avoid cold injury and sustain performance. Despite these assertions, recent research shows that hypohydration (HYP; reduced body water) does not increase the risk of hypothermia or peripheral cold injury (23, 24). Similarly, HYP in excess of 2% body mass impairs endurance exercise performance in hot and temperate environments with the magnitude of effect largest in the heat (4, 30). The extent to which this is true in cooler environments is unknown, but there is evidence that the mechanisms for HYP-mediated fatigue in warmer environments are blunted in the cold and may therefore have less impact.

Hyperthermia and cardiovascular strain are two major factors implicated in the genesis of HYP-mediated endurance exercise fatigue in hot and temperate environments (4). Both the independent and combined effects of hyperthermia and hypovolemia on cardiovascular strain dynamics in the heat have been elegantly described (911, 28). Recent examination of the same parameters during exercise in cooler environments (3–8°C) indicates that core temperature elevations associated with HYP are significantly reduced (9, 17). Tachycardia is also attenuated and stroke volume and cardiac output better preserved during progressive dehydration up to 4% of body mass during both moderate (50% maximal O2 uptake) (17) and more intense (72% maximal O2 uptake) (9) exercise cold stress. Taken together, cardiovascular strain attributed to hyperthermia and hypovolemia in warm and hot climates is blunted in cooler conditions, which may preserve endurance exercise performance.

Although multiple meteorological variables can influence endurance exercise success (32), performances typically improve as air temperatures decline (32, 33). Laboratory (7) and field data (32, 33) support an "optimal" air temperature threshold near 12°C; above or below this temperature, performance is relatively impaired (7). Endurance performance limitations in hot environments are well documented (21, 31), but evidence during exercise cold stress is complicated by the comparison reference temperature (7), wearing heavily insulated clothing (25), and possibly the choice of an open-ended endurance exercise task (1, 7, 25). The best explanation for fatigue offered by cold performance studies also implicates factors other than cardiovascular strain or O2 uptake as performance limiting. Competitive endurance athletes appear to perform at a high level coincident with significant body water losses in cool environments (4), but few studies have manipulated hydration state to experimentally compare the impact of HYP on performance in cold vs. more temperate conditions. Those that have are difficult to interpret due to the absence of true control conditions (18) or wearing heavily insulated clothing (27).

The purpose of this study was to compare the effects of HYP on endurance exercise performance in temperate and cold air. Our hypothesis was that cold air would mitigate the decrement in performance attributable to HYP in a temperate environment. A combination of air motion and low air temperatures was used to induce cold stress beyond previous studies but without exceeding cold injury thresholds. In addition, a close-ended exercise task was selected to reduce the influence of cold-stress tolerance on performance.


    METHODS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 
Subjects

Eight healthy volunteers (age = 24 ± 6 yr, height = 170 ± 6 cm, weight = 72.9 ± 11.1 kg, body fat 22 ± 6%) participated in this study and completed all phases of experimentation. Subjects (6 men, 2 women) were physically active and moderately fit [peak O2 consumption (O2 peak) = 48 ± 9 ml·kg–1·min–1]. Subjects were provided informational briefings and gave voluntary and informed written consent to participate. Investigators adhered to AR 70-25 and U.S. Army Medical Research and Materiel Command Regulation 70-25 on the use of volunteers in research and the appropriate Institutional Review Boards approved this study.

Preliminary Procedures

Each subject's O2 peak was measured using an incremental cycle ergometer protocol with continuous gas-exchange measurements (TrueMax, ParvoMedics, Sandy, UT). The calculated workload at 50% O2 peak was validated during 30 min of steady-state cycling 1 day later. The ergometer used (Lode Excalibur Sport, Lode, Groningen, The Netherlands) allows pedal rate-independent (hyperbolic) and -dependent (linear) modes of cycling. Individual linear factors (LF) were calculated [W = LF x (rpm)2] for each subject to reflect a 50% O2 peak exercise intensity at a pedal cadence of 60 rpm. The linear factor setting provided room to increase work output during the time trial before reaching maximal sustainable workloads, which were estimated from O2 peak testing at ~100 rpm. Practice trials included 30 min of steady-state cycling (50% O2 peak), followed immediately by a 30-min performance time trial. Three practice sessions were used to reduce training and learning effects (8, 13). Elapsed time was displayed, and the total work (kJ) completed in 30 min was given as feedback for motivation to improve with each subsequent practice ride. Experimental test scenarios were the same as those used in practice except that subjects were blinded to all test parameters but elapsed time. Semi-nude body mass (shorts only) was measured after voiding and before breakfast each morning for 10-days to establish a normal individual baseline body mass for euhydration (EUH) assessment on test days. All experimentation began within 3 days of completing preliminary procedures.

Experimental Procedures

A counterbalanced 2 x 2 (hydration x environment) experimental design was employed. Each was separated by at least 48 h. Experiments were conducted at the same time of day, and women were tested in the follicular phase of their menstrual cycle to control for circadian and ovulatory fluctuations in body temperature. On the morning of each trial, body mass was measured with an electronic precision balance scale (Toledo 1D1 accuracy ±20 g, Worthington, OH) for comparison against within-subject 10-day averages, and a 10-ml venous blood sample was collected for serum osmolality determination. A standardized breakfast was provided, after which subjects rested in a seated position for ~1 h before moving to a hot room (45°C, 50% relative humidity, 1 m/s air speed) for 3 h of passive heat exposure with (EUH) or without (HYP) fluid replacement. A 2-h recovery period followed in which a shower was permitted and a small snack was provided (200 ml of water and 250 kcal). The precise fluid deficit incurred was calculated from the acute change in body mass from pre- to post-heat exposure, corrected for snack, and expressed as a percentage of preexercise body mass.

In the afternoon, subjects sat in a cold (2°C, 50% relative humidity, 2.2 m/s air speed) or temperate (20°C, 50% relative humidity, 1 m/s air speed) environment with minimal clothing (t-shirt, shorts, socks, shoes, cotton gloves, and head band) for 1 h before performing 30 min of cycle ergometry at 50% O2 peak followed immediately by a 30-min performance time trial. No motivation was provided during the time trial, and subjects performed without distraction from any data-collection measurements. Time trial performance was assessed by the total amount of work (kJ) completed in 30 min. Rectal (Tre) and mean skin temperatures (26) and heart rate (HR) were collected remotely at regular intervals throughout testing. Rating of perceived exertion was assessed at 30 min and again immediately after the completion of exercise. Gas-exchange measurements were made once in the initial 10 min of exercise using an automated system, and workloads were adjusted to reflect a 50% O2 peak intensity.

Statistical Analysis

Following tests for normality of distribution and equality of variances, treatment effects were analyzed using a paired t-test and one- or two-way ANOVA for repeated measurements. A one-sample t-test was also used to compare performance effects against a hypothetical value of importance (20). When appropriate, Tukey's honestly significant difference procedure was used to identify pairwise differences among means following significant main and/or interaction effects. The primary outcome variable of interest in this experiment was time trial performance. An analysis selecting conventional {alpha} (0.05) and {beta} (0.20) parameters showed that eight subjects would provide sufficient power to detect a 5% change in time trial performance (~15 kJ) using the mean total work (295 kJ) and coefficient of variation (CV; 2.5%) calculated from trials of negligible difference (i.e., practice trials 2 and 3; P > 0.05) during 2 wk of time trial practice. The desire to detect a twofold change from the %CV was chosen based on the likelihood of experimental perturbations producing unique performance infidelity (12, 13, 15), thus increasing variability. A sample size of eight allows detection of said differences with a CV up to 4.5%. The practical importance of hydration effects on performance within environments was also interpreted using 95% confidence limits of the true effect for % change in performance to include comparison against an a priori zone of indifference (2.5% CV) using a one-sample t-test, which affords evaluation against an evidentiary standard other than zero (5, 14, 20). The spirit of this approach, most closely related to equivalence testing in the clinical sciences (5), has recently been championed as a performance interpretation tool for the exercise sciences (14). Graphical data are presented with unidirectional error bars and may be slightly juxtaposed for presentation clarity. All data are presented as means ± SD except where indicated.


    RESULTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 
Hydration

EUH was estimated on the morning of each trial by a body mass within 1% of the average 10-day baseline (3). Two subjects >1% lower than 10-day baseline were given additional water with breakfast. Serum osmolality (289 ± 1 mosmol/kgH2O) confirmed EUH (16). The fluid deficit achieved before the start of each HYP trial was –2.9 ± 0.7 and –3.0 ± 0.8% of body mass for cold and temperate, respectively. Values for EUH trials were –0.3 ± 0.6 (cold) and –0.4 ± 0.7% (temperate) of starting baseline. Differences were significant (P < 0.05) between hydration levels (HYP vs. EUH) but not between environments (cold vs. temperate). Thus subjects were adequately matched for preexercise hydration status in EUH and HYP trials.

Exercise Performance

Table 1 presents individual and mean time trial performance data. Total work in temperate HYP was lower than temperate EUH (P = 0.012). There was no effect of hydration in the cold (cold EUH vs. cold HYP) and no independent effect of environment on performance (cold EUH vs. temperate EUH). Associated mean power outputs from Table 1 were 140 ± 30 (temp HYP), 152 ± 30 (temp EUH), 154 ± 36 (cold EUH), and 150 ± 35 W (cold HYP). Viewed individually, all eight subjects performed worse when hypohydrated in temperate air, whereas only five of eight experienced the same from HYP in the cold. Figure 1 presents the % change in performance from EUH to HYP in temperate and cold environments. The change was significantly larger for temperate (–7.6 ± 5.9%) than cold (–2.7 ± 4.9%) (P = 0.021). The means and 95% confidence limits for performance (–12.6 to –2.7% temperate; –6.8 to 1.4% cold) provide the likely range of the true change effects and illustrate why there is a difference between HYP and EUH within temperate but not within cold (i.e., confidence interval crosses zero for cold). In addition, only the range of the confidence interval for temperate falls entirely outside the a priori zone of indifference (P = 0.04, 1-sample t-test), which provides evidence that the negative effect of HYP on performance in temperate air is also of practical importance.


View this table:
[in this window]
[in a new window]
 
Table 1. Time trial work performance

 


View larger version (17K):
[in this window]
[in a new window]
 
Fig. 1. Percent change in performance from euhydration (EUH) to hypohydration (HYP) in temperate and cold trials. Data are means; bars are 95% confidence intervals. Shaded area represents zone of indifference (±2.5%) based on the typical performance variability measured during practice sessions (see text for detailed explanation). *Significant difference between trials (paired t-test, P = 0.021) and significant difference from zone of indifference (1-sample t-test, P = 0.044).

 
Physiological Responses

Metabolic rate.   Metabolic rates during the initial 30 min of cycling were calculated from a 2-min gas sample made 5 min into exercise and adjusted to reflect ~50% of O2 peak. All measurements were similar (P > 0.05) at 49 ± 6 (cold EUH), 51 ± 5 (cold HYP), 47 ± 2 (temperate EUH) and 48 ± 3% (temperate HYP) O2 peak. Subjects were therefore matched among trials for exercise intensity preceding the cycling time trial.

Cardiovascular strain and thermoregulatory strain.   Figure 2, A and B, represents HR and perceived exertion responses to exercise at 30 and 60 min of exercise. Data collected at rest were unreliable due to extreme shivering in the cold trials and were therefore excluded from the analysis. All 60-min HR exceeded 30-min values (P < 0.05). HR for temperate HYP at 30 min was higher than for temperate EUH and cold HYP. Both temperate HYP and cold HYP were higher than temperate EUH (~5 beats/min; P > 0.05) and cold EUH (~11 beats/min; P < 0.05) at 60 min. Rating of perceived exertion increased over time with no differences among trials (60 min > 30 min; P < 0.05). Tre increased significantly over time in all trials (Fig. 3A). At rest, Tre was higher in both cold compared with temperate trials due to rigorous shivering. No differences among trials were seen at 30 min, but temperate HYP was higher than cold EUH (0.4°C; P < 0.05) and temperate EUH (0.3°C; P < 0.05) at exercise cessation. Skin temperature was significantly lower in the cold (Fig. 3B) and was independent of hydration status.



View larger version (14K):
[in this window]
[in a new window]
 
Fig. 2. Effect of hydration and environment on heart rate (HR; A) and ratings of perceived exertion (RPE; B). Values are means ± SD. a,b,c,dSignificant differences (P < 0.05) from corresponding values from temperate EUH, cold EUH, temperate HYP, and cold HYP, respectively. *Significant effect of time (60 > 30 min; P < 0.05).

 


View larger version (16K):
[in this window]
[in a new window]
 
Fig. 3. Effect of hydration and environment on rectal (A) and mean skin temperatures (B). Values are means ± SD. Significance by letter designation as indicated in Fig. 2. Significant effects of time (P < 0.05): * 30 > 0 min; **60 > 30 and 0 min.

 

    DISCUSSION
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 
This study determined the effects of HYP on endurance exercise performance in temperate and cold air. In accordance with our hypothesis, the principal finding of this study is that HYP by –3% body mass impaired cycling time trial performance in a temperate, but not a cold, environment. In addition, we found that cold stress per se did not reduce performance.

The % change in performance (EUH – HYP) within cold (–2.7 ± 4.9%) and temperate (–7.6 ± 5.9%) environments was statistically different (Fig. 1). The 95% confidence limits were plotted about the mean to provide insight into the likely range of the true change value (Fig. 1). These limits were also applied in the traditional sense to examine the importance of the change relative to an evidentiary standard other than zero (5, 14, 20). This standard is the zone of indifference selected a priori as any value within the typical noise of the performance measurement (i.e., 2.5% CV) (5, 14). Although the choice of 95% confidence limits for this integrated analytic approach is admittedly conservative (14, 15), the fact that the entire temperate confidence interval lies outside this zone (Fig. 1) strongly supports the conclusion that the performance impairment due to HYP in temperate environments is both statistically significant and of practical importance (5, 14, 20). No statistical difference in performance was observed between EUH and HYP in cold air, but since one-half of the cold interval lies outside the zone of indifference, the meaning of this effect is ambiguous at best (5, 14, 20).

The preservation of endurance performance in cold air when hypohydrated may be explained by differences in cardiovascular and oxygen uptake dynamics. Although the present experiment was not designed to assess the mechanisms behind performance changes, reasonable explanations can be gleaned from our observations when combined with the work of others. For example, Gonzalez-Alonso et al. (9–11) demonstrated that tachycardia (via hyperthermia) and hypovolemia explain most of the reduction in cardiac output between EUH and HYP in hot environments, with similar effects of lesser magnitude in the cold (9). In addition, hypovolemia reduces maximal O2 uptake and endurance capacity even in the presence of normothermia and cool skin (22). It is conceivable that hypovolemia and a higher Tre (~0.30°C) and HR (~5 beats/min) in temperate HYP (Fig. 2A) reduced stroke volume, cardiac output, and oxygen uptake enough to reduce performance (253 kJ) relative to temperate EUH (273 kJ) despite similar efforts (Fig. 2B). However, the preservation of performance in cold HYP (270 kJ) vs. cold EUH (277 kJ) occurred with similar Tre differences and a larger HR disparity (11 beats/min) between HYP and EUH (Fig. 2A). It therefore remains possible that cold skin in cold HYP (Fig. 3B) maintained a larger central blood volume and better preserved stroke volume and cardiac output (9, 17, 19, 22, 29). Similar Tre and HR at exhaustion between cold HYP and temperate HYP also seem to support this conclusion since performance in temperate HYP, but not cold HYP, was less than cold and temperate EUH (Table 1).

The finding that cold stress per se did not reduce performance (temperate EUH vs. cold EUH) (Table 1) is in opposition to others (1, 7, 25), but comparisons are made difficult by several methodological factors. For example, Galloway and Maughan (7) found that time to fatigue at 4°C was reduced compared with 11°C, but no different from 20°C, or improved relative to 31°C. Patton and Vogel (25) compared –20 and 20°C, but wearing heavily insulated clothing at –20°C limits the interpretation of reduced performance at the latter temperature. Both of these studies and that of Adolph and Molnar (1) also used open-ended endurance exercise tasks. Adolph and Molnar (1) suggested that the most important predictor of performance in the cold using this kind of task was exposure time and cold tolerance. Indeed, Cabanac and Leblanc (2) demonstrated that simultaneous exposure to cold and exercise fatigue produces a sensory conflict resolved by compromise toward the least displeasing input signal, but others (7, 25) implicate local muscle effects for accelerated fatigue under similar circumstances. Exposure time in this experiment was fixed, which may have alleviated motivation issues related to cold tolerance. Postexperiment interviews even suggest that total work in cold EUH and cold HYP may have actually been augmented by cold avoidance (2). It is inconclusive whether using time to exhaustion, rather than a time trial, would (1, 25) or would not (7) have altered the performance outcomes observed herein between 2 and 20°C.

We conclude that moderate HYP impairs endurance performance in temperate, but not cold, air. Cold stress per se had no effect. Application of these findings to competitive endurance exercise contested in environments similar to those described herein is logical (13, 14) but tentative given the subject population tested. These findings are nonetheless of phenomenological importance.


    ACKNOWLEDGMENTS
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 
The authors thank Carrie Vernieuw, Lou Stephenson, Scott Robinson, Lenny Elliott, Walida Leammukda, Leslie Levine, Kaye Brownlee, Laurie Bronson, Lenny Souza, Eric Lammi, Mike Durkot, and Erik Lloyd for expert technical assistance.

The opinions or assertions contained herein are the private views of the authors and should not to be construed as official or reflecting the views of the Army or the Department of Defense. Approved for public release: distribution is unlimited.


    FOOTNOTES
 

Address for reprint requests and other correspondence: S. N. Cheuvront, US Army Research Institute of Environmental Medicine, Thermal and Mountain Medicine Division, Kansas St., Natick, MA 01760-5007 (e-mail: samuel.cheuvront{at}na.amedd.army.mil)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


    REFERENCES
 TOP
 ABSTRACT
 METHODS
 RESULTS
 DISCUSSION
 ACKNOWLEDGMENTS
 REFERENCES
 

  1. Adolph EF and Molnar GW. Exchange of heat and tolerances to cold in men exposed to outdoor weather. Am J Physiol 146: 507–537, 1946.[Free Full Text]
  2. Cabanac M and Leblanc J. Physiological conflict in humans: fatigue vs. cold discomfort. Am J Physiol Regul Integr Comp Physiol 244: R621–R628, 1983.[Abstract/Free Full Text]
  3. Cheuvront SN, Carter, R III, Montain SJ, and Sawka MN. Daily body mass variability and stability in active men undergoing exercise-heat stress. Int J Sport Nutr Exerc Metab 14: 532–540, 2004.[ISI][Medline]
  4. Cheuvront SN, Carter R III, and Sawka MN. Fluid balance and endurance exercise performance. Curr Sports Med Rep 2: 202–208, 2003.[Medline]
  5. Ebbutt AF and Frith L. Practical issues in equivalence trials. Stat Med 17: 1691–1701, 1998.[CrossRef][ISI][Medline]
  6. Freund BJ and Sawka MN. Influence of cold stress on human fluid balance. In: Nutrient Requirements for Work in Cold and High Altitudes, edited by Marriott BM. Washington, DC: Natl. Acad. Sci., 1995, p. 161–180.
  7. Galloway SD and Maughan RJ. Effects of ambient temperature on the capacity to perform prolonged cycle exercise in man. Med Sci Sports Exerc 29: 1240–1249, 1997.[ISI][Medline]
  8. Gleser MA and Vogel JA. Endurance exercise: effect of work-rest schedules and repeated testing. J Appl Physiol 31: 735–739, 1971.[Free Full Text]
  9. Gonzalez-Alonso J, Mora-Rodrigueuz R, and Coyle EF. Stroke volume during exercise: interaction of environment and hydration. Am J Physiol Heart Circ Physiol 278: H321–H330, 2000.[Abstract/Free Full Text]
  10. Gonzalez-Alonso J, Mora-Rodrigueuz R, and Coyle EF. Supine exercise restores arterial blood pressure and skin blood flow despite dehydration and hyperthermia. Am J Physiol Heart Circ Physiol 277: H576–H583, 1999.[Abstract/Free Full Text]
  11. Gonzalez-Alonso J, Mora-Rodrigueuz R, Below PR, and Coyle EF. Dehydration markedly impairs cardiovascular function in hyperthermic endurance athletes during exercise. J Appl Physiol 82: 1229–1236, 1997.[Abstract/Free Full Text]
  12. Hopkins WG, Hawley JA, and Burke LM. Design and analysis of research on sport performance enhancement. Med Sci Sports Exerc 31: 472–485, 1999.[ISI][Medline]
  13. Hopkins WG, Schabort EJ, and Hawley JA. Reliability of power in physical performance tests. Sports Med 31: 211–234, 2001.[CrossRef][ISI][Medline]
  14. Hopkins WG. How to interpret changes in an athletic performance test. Sportscience 8: 1–7, 2004.
  15. Hopkins WG. Measures of reliability in sports medicine and science. Sports Med 30: 1–5, 2000.[CrossRef][ISI][Medline]
  16. Institute of Medicine. Dietary Reference Intakes: Water, Potassium, Sodium, Chloride, and Sulfate. Washington, DC: National Academy Press, 2005, p. 73–185.
  17. Kenefick RW, Mahood NV, Hazzard MP, Quinn TJ, and Castellani JW. Hypohydration effects on thermoregulation during moderate exercise in the cold. Eur J Appl Physiol 92: 565–570, 2004.[ISI][Medline]
  18. Lennquist S, Grangberg PO, and Wedin B. Fluid balance and physical work capacity in humans exposed to cold. Arch Environ Health 29: 241–250, 1974.[ISI][Medline]
  19. Maw GJ, Mackenzie IL, and Taylor NA. Human body-fluid distribution during exercise in hot, temperate, and cool environments. Acta Physiol Scand 163: 297–304, 1998.[CrossRef][ISI][Medline]
  20. Motulsky HJ. Prism 4 Statistics Guide: Statistical Analyses for Laboratory and Clinical Researchers. San Diego, CA: GraphPad Software, 2003, p. 35–39.
  21. Nielsen B. Olympics in Atlanta: a fight against physics. Med Sci Sports Exerc 28: 665–668, 1996.[ISI][Medline]
  22. Nybo L, Jensen T, Nielsen B, and Gonzalez-Alonso J. Effects of marked hyperthermia with and without dehydration on O2 kinetics during intense exercise. J Appl Physiol 90: 1057–1064, 2001.[Abstract/Free Full Text]
  23. O'Brien C, Young AJ, and Sawka MN. Hypohydration and thermoregulation in cold air. J Appl Physiol 84: 185–189, 1998.[Abstract/Free Full Text]
  24. O'Brien C and Montain SJ. Hypohydration effect on finger skin temperature and blood flow during cold-water finger immersion. J Appl Physiol 94: 598–603, 2003.[Abstract/Free Full Text]
  25. Patton JF and Vogel JA. Effects of acute cold exposure on submaximal endurance performance. Med Sci Sports Exerc 16: 494–497, 1984.[CrossRef][ISI][Medline]
  26. Ramanathan ML. A new weighting system for mean surface temperature of the human body. J Appl Physiol 19: 531–533, 1964.[Abstract/Free Full Text]
  27. Roberts DE, Patton JF, Pennycook JW, Jacey MJ, Tappan DV, Gray P, and Heyder E. Effects of Restricted Water Intake on Performance in a Cold Environment. Natick, MA: US Army Research Institute of Environmental Medicine, 1984, p. 1–19. (Tech. Rept. T2-84)
  28. Rowell LB, Marx HJ, Bruce RA, Conn RD, and Kusumi F. Reductions in cardiac output, central blood volume, and stroke volume with thermal stress in normal men during exercise. J Clin Invest 45: 1801–1816, 1966.[ISI][Medline]
  29. Rowell LB, Murray JA, Brengelmann GL, and Kraning KK. Human cardiovascular adjustments to rapid changes in skin temperature during exercise. Circ Res 24: 711–724, 1969.[Abstract/Free Full Text]
  30. Sawka MN. Physiological consequences of hypohydration: exercise performance and thermoregulation. Med Sci Sports Exerc 24: 657–670, 1992.[ISI][Medline]
  31. Sawka MN and Pandolf KB. Physical exercise in hot climates: physiology, performance, and biomedical issues. In: Textbooks of Military Medicine: Medical Aspects of Harsh Environments, edited by Pandolf KB and Burr RE. Bethesda, MD: Office of the Surgeon General, 2001, p. 87–133.
  32. Trapasso LM and Cooper JD. Record performances at the Boston Marathon: biometeorological factors. Int J Biometeorol 33: 233–237, 1989.[CrossRef][ISI][Medline]
  33. Zhang S, Meng G, Wang Y, and Li J. Study of the relationships between weather conditions and the marathon race, and of meteorotropic effects on distance runners. Int J Biometeorol 36: 63–68, 1992.[CrossRef][ISI][Medline]



This article has been cited by other articles:


Home page
J. Am. Coll. Nutr.Home page
B. Murray
Hydration and Physical Performance
J. Am. Coll. Nutr., October 1, 2007; 26(suppl_5): 542S - 548S.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
99/5/1972    most recent
00329.2005v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cheuvront, S. N.
Right arrow Articles by Sawka, M. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cheuvront, S. N.
Right arrow Articles by Sawka, M. N.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2005 by the American Physiological Society.