Influence of climate on heart rate in children: comparison between intermittent and continuous exercise

Heart rate (HR) monitoring is commonly used to assess 24-h energy expenditure (EE) in children but it has been found to overestimate the true values. One reason for this may be the effect of climatic heat stress on HR. An equation has been previously developed to adjust HR measured during continuous exercise for the influence of climate. Since play in children is rarely of a continuous pattern, one objective of this study was to compare the effects of climatic heat stress on the HR response to intermittent and to continuous exercise. A second objective was to determine whether the previously developed equation is suitable for intermittent exercise. A group of 12 boys and 8 girls (aged 8–11 years) cycled in a climatic chamber. The exercise consisted of continuous cycling for 5 min at 35%, 55%, and 75% of peak oxygen up take (random order) followed by alternating cycling at the same resistance and cadence (30 s) and rest (30 s) for 3 additional min. The oxygen uptake (V˙O₂) and HR were determined for 2 min at the end of continuous cycling and for 2 min during intermittent cycling. Climatic conditions (randomly assigned) were dry bulb temperature T _db 22°C, 50% relative humidity (rh); T _db 28°C, 55% rh; T _db 32°C, 52% rh; or T _db 35°C, 58% rh. The difference between HR measured at a given T _db (HR_meas) and HR at 22°C and at the same V˙O₂ was then calculated (ΔHR). The ΔHR increased linearly with increasing temperature but was not related to V˙O₂ or to exercise type. However, a small but significant difference was found if the published equation was used with data from intermittent exercise. The accuracy of the existing equation adjusting HR_meas for the influence of T _db (HR_corr) could be improved to HR_corr= HR_meas · (1.18308−(0.0083218 · T _db)). In conclusion, the effects of climatic heat stress on HR were similar in continuous and intermittent exercise, and HR can be adjusted for the influence of climate in groups of pre- and early pubertal children during rest, intermittent and continuous exercise at ambient temperatures between 22°C and 35°C, thereby reducing the error in predicting EE from HR. Accepted: 13 January 1998     

Changes in exercise and post-exercise core temperature under different clothing conditions

 This study evaluates the effect of different levels of insulation on esophageal (T _es) and rectal (T _re) temperature responses during and following moderate exercise. Seven subjects completed three 18-min bouts of treadmill exercise (75% VO_2max, 22°C ambient temperature) followed by 30 min of recovery wearing either: (1) jogging shoes, T-shirt and shorts (athletic clothing); (2) single-knit commercial coveralls worn over the athletic clothing (coveralls); or (3) a Canadian Armed Forces nuclear, bacteriological and chemical warfare protective overgarment with hood, worn over the athletic clothing (NBCW overgarment). T _es was similar at the start of exercise for each condition and baseline T _re was ∼0.4°C higher than T _es. The hourly equivalent rate of increase in T _es during the final 5 min of exercise was 1.8°C, 3.0°C and 4.2°C for athletic clothing, coveralls and NBCW overgarment respectively (P<0.05). End-exercise T _es was significantly different between conditions [37.7°C (SEM 0.1°C), 38.2°C (SEM 0.2°C and 38.5°C (SEM 0.2°C) for athletic clothing, coveralls and NBCW overgarment respectively)] (P<0.05). No comparable difference in the rate of temperature increase for T _re was demonstrated, except that end-exercise T _re for the NBCW overgarment condition was significantly greater (0.5°C) than that for the athletic clothing condition. There was a drop in T _es during the initial minutes of recovery to sustained plateaus which were significantly (P<0.05) elevated above pre-exercise resting values by 0.6°C, 0.8°C and 1.0°C, for athletic clothing, coveralls, and NBCW overgarment, respectively. Post-exercise T _re decreased very gradually from end-exercise values during the 30-min recovery. Only the NBCW overgarment condition T _re was significantly elevated (0.3°C) above the athletic clothing condition (P<0.05). In conclusion, T _es is far more sensitive in reflecting the heat stress of different levels of insulation during exercise and post-exercise than T _re. Physiological mechanisms are discussed as possible explanations for the differences in response. Received: 30 June 1998 / Accepted: 19 February 1999     

Separate and combined effects of temperature and hypoxia on breathing pattern in the domestic fowl

Summary Minute ventilation (V _E), tidal volume (V _T), respiratory frequency (f) and clavicular air sac gas composition were measured in conscious domestic fowl breathing air and hypoxic gas mixtures at neutral (18±1°C) and raised (33±1°C) air temperatures. Increases inV _E caused by inhalation of 10%, 8% or 6.5% O₂ in N₂, respectively, were independent of temperature although at each level the absoluteV _E was ca. 21·min⁻¹ greater in the panting birds. Changes in respiratory pattern during hypoxia were markedly dependent on temperature. At 18°C almost all of the increasedV _E resulted from increasedf. At 33°C hypoxia led to a strong suppression off and increase inV _T. It is concluded that hyperthermia and hypoxia are additive and non-interactive in their effects on ventilatory drive, in agreement with previously reported effects of hypercapnia and physical exercise on breathing in panting fowl.     

Factors influencing the radiative surface temperature of grey seal (<Emphasis Type="Italic">Halichoerus grypus</Emphasis>) pups during early and late lactation

The aim of this study was to examine the variation in body surface temperature of grey seal (Halichoerus grypus) pups throughout lactation in response to different environmental conditions. Radiative surface temperatures (T _r, °C) of pups were measured on the Isle of May (56°11′N, 02°33′W), southeast Scotland from 29 October to 25 November 2003. Records were obtained from a total of 60 pups (32 female and 28 male) from three different pupping sites during early and late lactation. Pups were sheltered from high wind speeds but air temperature, humidity and solar radiation at pupping sites were similar to general meteorological conditions. The mean T _r of all pups was 15.8°C (range 7.7–29.7°C) at an average air temperature of 10.2°C (range 6.5–13.8°C). There was no difference in the mean T _r of pups between early and late lactation. However, the T _r varied between different regions of the body with hind flippers on average 2–6°C warmer than all other areas measured. There was no difference in mean T _r of male and female pups and pup body mass did not account for the variation in T _r during early or late lactation. Throughout the day there was an increase in the T _r of pups and this explained 20–28% of the variation in T _r depending on stage of lactation. There was no difference in the mean T _r of pups between pupping sites or associated with different substrate types. Wind speed and substrate temperature had no effect on the T _r of pups. However, solar radiation, air temperature and relative humidity accounted for 48% of the variation in mean T _r of pups during early lactation. During late lactation air temperature and solar radiation alone accounted for 43% of the variation in T _r. These results indicate that environmental conditions explain only some of the variation in T _r of grey seal pups in natural conditions. Differences in T _r however indicate that the cost of thermoregulation for pups will vary throughout lactation. Further studies examining intrinsic factors such as blubber thickness and activity levels are necessary before developing reliable biophysical models for grey seals.     

The effect of body temperature on the hunting response of the middle finger skin temperature

The relationship between body temperature and the hunting response (intermittent supply of warm blood to cold exposed extremities) was quantified for nine subjects by immersing one hand in 8°C water while their body was either warm, cool or comfortable. Core and skin temperatures were manipulated by exposing the subjects to different ambient temperatures (30, 22, or 15°C), by adjusting their clothing insulation (moderate, light, or none), and by drinking beverages at different temperatures (43, 37 and 0°C). The middle finger temperature (T _fi) response was recorded, together with ear canal (T _ear), rectal (T _re), and mean skin temperature (Tˉ _sk). The induced mean T _ear changes were −0.34 (0.08) and +0.29 (0.03)°C following consumption of the cold and hot beverage, respectively. Tˉ _sk ranged from 26.7 to 34.5°C during the tests. In the warm environment after a hot drink, the initial finger temperature (T _fi,base) was 35.3 (0.4)°C, the minimum finger temperature during immersion (T _fi,min) was 11.3 (0.5)°C, and 2.6 (0.4) hunting waves occurred in the 30-min immersion period. In the neutral condition (thermoneutral room and beverage) T _fi,base was 32.1 (1.0)°C, T _fi,min was 9.6 (0.3)°C, and 1.6 (0.2) waves occurred. In the cold environment after a cold drink, these values were 19.3 (0.9)°C, 8.7 (0.2)°C, and 0.8 (0.2) waves, respectively. A colder body induced a decrease in the magnitude and frequency of the hunting response. The total heat transferred from the hand to the water, as estimated by the area under the middle finger temperature curve, was also dependent upon the induced increase or decrease in T _ear and Tˉ _sk. We conclude that the characteristics of the hunting temperature response curve of the finger are in part determined by core temperature and Tˉ _sk. Both T _fi,min and the maximal finger temperature during immersion were higher when the core temperature was elevated; Tˉ _sk seemed to be an important determinant of the onset time of the cold-induced vasodilation response. Accepted: 29 April 1997     

Rectal and esophageal temperatures during upper- and lower-body exercise

This study investigated the question: is core temperature measurement influenced by whether exercise involves predominantly upper- or lower-body musculature? Healthy men were allocated to three groups: treadmill ergometry (T) n=4, cycle ergometry (C) n=6 and arm crank ergometry (AC) n=5. Subjects underwent an incremental exercise test to exhaustion on an exercise-specific ergometer to determine maximum/peak oxygen consumption (V˙O_2max). One week later subjects exercised for 36 min on the same ergometer at approximately 65% V˙O_2max while temperatures at the rectum (T _re) and esophagus (T _es) were simultaneously measured. The V˙O_2max (l · min⁻¹) for groups T [4.76 (0.50)] and C [4.35 (0.30)] was significantly higher than that for the AC group [2.61 (0.24)]. At rest, T _re was significantly higher than T _es in all groups (P<0.05). At the end of submaximal exercise in the C group, T _re [38.32 (0.11)°C] was significantly higher than T _es [38.02 (0.12)°C, P<0.05]. No significant differences between T _re and T _es at the end of exercise were noted for AC and T groups. The temperature difference (T _diff) between T _re and T _es was dissimilar at rest in the three groups; however, by the end of exercise T _diff was approximately 0.2°C for each of the groups, suggesting that at the end of steady-state exercise T _re can validly be used to estimate core temperature. Accepted: 3 November 1997     

Respiratory responses to intermittent and prolonged exercise in a hot-dry environment

Ventilatory gas exchange ratio (R), V?O₂, ventilation (V?_E), respiration rate (RR), rectal temperature (T_re), and heart rate (HR) were determined for four acclimatized subjects during intermittent and prolonged exercise on a treadmill at 24° and 45°C (dry) as follows: 1) 8 cycles (10 min. exercise and 5 min. rest), and 2) prolonged exercise lasting for 90 min. While during intermittent and prolonged exercise, V?O₂ and V?_E did not differ in the heat, RR, T_re, HR and the respiratory dead space were higher in the hot ambient environment. After steady-state attainment, exercise R was higher in the initial as compared to the last cycles with higher values in neutral as compared to the hot ambient condition. It was concluded that heat was more effective than time in lowering the R, probably with a greater dependence on fat oxidation in the latter exercise cycles which seemed to be more pronounced in the heat.     

Behavioral responses of Colorado potato beetle larvae to combinations of temperature and insolation, under field conditions

In short-term field trials at combinations of ambient temperature (°C) and insolation (W·m⁻²), larval Colorado potato beetles (Leptinotarsa decemlineata [Say] [Coleoptera: Chrysomelidae]) were observed after their release on the adaxial surface of leaflets on potato plants (Solanum tuberosum L. Solanaceae). The larvae either began feeding or moved under the leaflet; mean interval from release to expression of these behaviors (2.9±0.05 min [n =358]) was independent of air temperature and insolation. Proportion of larvae moving under the leaflet increased logistically with both air temperature and insolation. A 1 W·m⁻² change in insolation (P) evoked the same effect on this proportion as a 0.0838 °C change in air temperature (T _a ), so the two quantities were combined as T^*=T _a +P·0.0838 °C/(W·m⁻²), which has units of °C. The proportion of larvae moving under the leaflet increased logistically with T^*. In 1-day field trials we monitored air temperature, insolation and proportion of larvae under the leaflet, and compared the latter to predictions from the logistic regression derived from the short-term trials. Consistently more larvae occurred under leaflets than predicted from the logistic regression; this bias diminished as T^* increased until at T^*≥40 °C, observed and predicted proportions were equal. This pattern of deviation from the predictions of the logistic regression is consistent with a thermoregulatory strategy in which larvae move away from hostile conditions, rather than seek optimal conditions.     

Low substrate temperature imposes higher limitation to photosynthesis of orange plants as compared to atmospheric chilling

The aim of this study was to evaluate the effects of low air temperature during nocturnal (T_N) and diurnal (T_D) periods as well as the substrate temperature (T_S) on photosynthesis of ‘Valencia’ orange tree grafted on Rangpur lime rootstock. The experiment was carried out in a growth chamber with seven-month-old plants. The plants were exposed to the following temperature regimes: low substrate temperature (LTS, with: T_D = 28°C, T_N = 20°C, T_S = 10°C); low air temperature during night (LT_N, with: T_D = 28°C, T_N = 10°C, T_S = 26°C); low temperature during nighttime and also low substrate temperature (LT_SN, with: T_D = 28°C, T_N = 10°C, T_S = 10°C); low air temperature during both diurnal and nocturnal periods (LT_ND, with: T_D = 17°C, T_N = 10°C, T_S = 26°C); and finally to low air temperature (night and day) and low substrate temperature (LT_SND, with: T_D = 17°C, T_N = 10°C, T_S = 10°C). As reference (control), plants were subjected to T_D = 28°C, T_N = 20°C, and T_S = 26°C. Measurements of leaf gas exchange, photochemical activity and carbohydrate concentrations were performed after six days of exposure to each thermal treatment. Compared to the control, all thermal regimes caused reductions in photosynthesis due to diffusive and metabolic limitations. The photoinhibition was transient in plants exposed to night and substrate low temperatures, whereas it was severe and chronic in plants subjected to chilling during the diurnal period. However, the lowest photosynthesis was observed in plants with low substrate temperature of 10°C (in LT_S, LT_SND and LT_SN treatments), regardless of air temperature. The occurrence of cold night and/or its combination with low substrate temperature caused accumulation of starch in leaves. When considering carbohydrate concentrations in stems and roots, it was not possible to establish a clear response pattern to chilling. In conclusion, the low substrate temperature causes a greater reduction of CO₂ assimilation in citrus plants as compared to the occurrence of low air temperature, being such response a consequence of diffusive and biochemical limitations.     

Diurnal variation in repeated sprint performance cannot be offset when rectal and muscle temperatures are at optimal levels (38.5°C)

The present study investigated whether increasing morning rectal temperatures (T_rec) to evening levels, or increasing morning and evening T_rec to an “optimal” level (38.5°C), resulting in increased muscle temperatures (T_m), would offset diurnal variation in repeated sprint (RS) performance in a causal manner. Twelve trained males underwent five sessions [age (mean ± SD) 21.0 ± 2.3 years, maximal oxygen consumption (V?O₂max) 60.0 ± 4.4 mL.kg^–1 min^–1, height 1.79 ± 0.06 m, body mass 78.2 ± 11.8 kg]. These included control morning (M, 07:30 h) and evening (E, 17:30 h) sessions (5-min warm-up), and three further sessions consisting of a warm-up morning trial (M_E, in 39–40°C water) until T_rec reached evening levels; two “optimal” trials in the morning and evening (M_38.5 and E_38.5, in 39–40°C water) respectively, until T_rec reached 38.5°C. All sessions included 3 × 3-s task-specific warm-up sprints, thereafter 10 × 3-s RS with 30-s recoveries were performed a non-motorised treadmill. T_rec and T_m measurements were taken at the start of the protocol and following the warm-up periods. Values for T_rec and T_m at rest were higher in the evening compared to morning values (0.48°C and 0.69°C, p < 0.0005). RS performance was lower (7.8–8.3%) in the M for distance covered (DC; p = 0.002), average power (AP; p = 0.029) and average velocity (AV; p = 0.002). Increasing T_rec in the morning to evening values or optimal values (38.5°C) did not increase RS performance to evening levels (p = 1.000). However, increasing T_rec in the evening to “optimal” level through a passive warm-up significantly reduced DC (p = 0.008), AP (p < 0.0005) and AV (p = 0.007) to values found in the M condition (6.0–6.9%). Diurnal variation in T_rec and T_m is not wholly accountable for time-of-day oscillations in RS performance on a non-motorised treadmill; the exact mechanism(s) for a causal link between central temperature and human performance are still unclear and require more research.     

Body temperatures and behavioural thermoregulation strategies of threePieris butterflies in relation to solar radiation

Behavioural thermoregulation of 3Pieris butterfly species,P. rapae, P. melete andP. napi, was examined in relation to the intensity of solar radiation. To evaluate solar radiation intensity, the temperature (T_wr) was measured with a mercury thermometer whose bulb was covered with white cloth and exposed to direct sunlight. On clear days, the diurnal air temperature was between 16 and 28°C. The T_wt varied between 18 and 45°C, while the temperature in the shade was under 25°C. When the T_wt was under 28°C, the body temperatures (T_h) of butterflies closely coincided with it. Butterflies with T_b's under 26°C were resting, while those with T_b's between 26 and 28°C were basking. When T_wr was between 28 and 40°C, the butterflies were active and their T_b's were always lower than T_wr, never exceeding 36°C, though body temperatures could be artificially elevated easily up to the level of T_wr. When T_wr exceeded 40°C, butterflies showed species-specific heat-avoiding behaviour.P. rapae, whose habitat resources exist in the sun, intercepted solar radiation by closing the wings over the body.P. melete andP. napi, however, whose main habitat resources exist in the shade, moved into the shade. Strictly speaking, it is concluded that both butterflies, in many cases, leave shaded habitats for sunny habitats to elevate their T_b rather than enter the shaded habitats for heat-avoiding.     

Conventional and novel body temperature measurement during rest and exercise induced hyperthermia

Despite technological advances in thermal sensory equipment, few core temperature (T_CORE) measurement techniques have met the established validity criteria in exercise science. Additionally, there is debate as to what method serves as the most practically viable, yet upholds the proposed measurement accuracy. This study assessed the accuracy of current and novel T_CORE measurement techniques in comparison to rectal temperature (T_REC) as a reference standard. Fifteen well-trained subjects (11 male, 4 female) completed 60 min of exercise at an intensity equating to the lactate threshold; measured via a discontinuous exercise test. T_REC was significantly elevated from resting values (37.2±0.3 °C) at the end of moderate intensity exercise (39.6±0.04 °C; P=0.001). Intestinal telemetric pill (T_PILL) temperature and temporal artery temperature (T_TEM) did not differ significantly from T_REC at rest or during exercise (P>0.05). However, aural canal temperature (T_AUR) and thermal imaging temperature (T_IMA) were both significantly lower than T_REC (P<0.05). Bland Altman analysis revealed only T_PILL was within acceptable limits of agreement (mean bias; 0.04 °C), while T_TEM, T_AUR and T_IMA demonstrated mean bias values outside of the acceptable range (>0.27 °C). Against T_REC, these results support the use of T_PILL over all other techniques as a valid measure of T_CORE at rest and during exercise induced hyperthermia. Novel findings illustrate that T_IMA (when measured at the inner eye canthus) shows poor agreement to T_REC during rest and exercise, which is similar to other ‘surface’ measures.     

Regional differences in sweat rate response of steers to short-term heat stress

Six Angus steers (319 ± 8.5 kg) were assigned to one of two groups (hot or cold exposure) of three steers each, and placed into two environmental chambers initially maintained at 16.5–18.8°C air temperature (T _a). Cold chamber T _a was lowered to 8.4°C, while T _a within the hot chamber was increased to 32.7°C over a 24-h time period. Measurements included respiration rate, and air and body (rectal and skin) temperatures. Skin temperature was measured at shoulder and rump locations, with determination of sweat rate using a calibrated moisture sensor. Rectal temperature did not change in cold or hot chambers. However, respiration rate nearly doubled in the heat (P < 0.05), increasing when T _a was above 24°C. Skin temperatures at the two locations were highly correlated (P < 0.05) with each other and with T _a. In contrast, sweat rate showed differences at rump and shoulder sites. Sweat rate of the rump exhibited only a small increase with T _a. However, sweat rate at the shoulder increased more than four-fold with increasing T _a. Increased sweat rate in this region is supported by an earlier report of a higher density of sweat glands in the shoulder compared to rump regions. Sweat rate was correlated with several thermal measurements to determine the best predictor. Fourth-order polynomial expressions of short-term rectal and skin temperature responses to hot and cold exposures produced r values of 0.60, 0.84, and 0.98, respectively. These results suggest that thermal inputs other than just rectal or skin temperature drive the sweat response in cattle.     

Heterothermy in an Australian passerine, the Dusky Woodswallow (Artamus cyanopterus)

Information regarding passerine heterothermy and torpor is scant, although many species are small and must cope with a fluctuating food supply and presumably would benefit from energy savings afforded by torpor. We studied whether insectivorous Dusky Woodswallows (Artamus cyanopterus; ∼35 g) enter spontaneous torpor (food ad libitum) when held outdoors as a pair in autumn/winter. Woodswallows displayed pronounced and regular daily fluctuations in body temperature (T _b) over the entire study period. The mean T _b ranged from ∼39°C to 40°C (photophase, day time) and ∼33°C to 36°C (scotophase, night time). However, on 88% of bird nights, nocturnal T _b minima fell to < 35°C. The lowest T _b observed in air was 29.2°C. However, when a bird fell into water its T _b dropped further to ∼22°C; this T _b was regulated for several hours and the bird survived. Our observations suggest that heterothermy is a normal part of the daily thermal regime for woodswallows to minimise energy expenditure. Spontaneous nocturnal torpor in captive woodswallows suggests that torpor in the wild may be more pronounced than recorded here because free-living birds are likely challenged by both low food availability and adverse weather.     

Thermal comfort modelling of body temperature and psychological variations of a human exercising in an outdoor environment

Human thermal comfort assessments pertaining to exercise while in outdoor environments can improve urban and recreational planning. The current study applied a simple four-segment skin temperature approach to the COMFA (COMfort FormulA) outdoor energy balance model. Comparative results of measured mean skin temperature ( [`(T)]\nolimits<sub>Msk</sub> \mathop{{\bar{T}}}\nolimits_{{Msk}} ) with predicted [`(T)]\nolimits_sk \mathop{{\bar{T}}}\nolimits_{{sk}} indicate that the model accurately predicted [`(T)]\nolimits<sub>sk</sub> \mathop{{\bar{T}}}\nolimits_{{sk}} , showing significantly strong agreement (r = 0.859, P < 0.01) during outdoor exercise (cycling and running). The combined 5-min mean variation of the [`(T)]\nolimits_sk \mathop{{\bar{T}}}\nolimits_{{sk}} RMSE was 1.5°C, with separate cycling and running giving RMSE of 1.4°C and 1.6°C, respectively, and no significant difference in residuals. Subjects’ actual thermal sensation (ATS) votes displayed significant strong rank correlation with budget scores calculated using both measured and predicted [`(T)]\nolimits<sub>sk</sub> \mathop{{\bar{T}}}\nolimits_{{sk}} (r <sub>s</sub>  = 0.507 and 0.517, respectively, P < 0.01). These results show improved predictive strength of ATS of subjects as compared to the original and updated COMFA models. This psychological improvement, plus [`(T)]\nolimits_sk \mathop{{\bar{T}}}\nolimits_{{sk}} and T _c validations, enables better application to a variety of outdoor spaces. This model can be used in future research studying linkages between thermal discomfort, subsequent decreases in physical activity, and negative health trends.     

Heat acclimation does not modify autonomic responses to core cooling and the skin thermal comfort zone

Exercise heat acclimation (HA) is known to magnify the sweating response by virtue of a lower threshold as well as increased gain and maximal capacity of sweating. However, HA has been shown to potentiate the shivering response in a cold-air environment. We investigated whether HA would alter heat loss and heat production responses during water immersion. Twelve healthy male participants underwent a 10-day HA protocol comprising daily 90-min controlled-hyperthermia (target rectal temperature, T_re 38.5 °C) exercise sessions. Preceding and following HA, the participants performed a maximal exercise test in thermoneutral conditions (ambient temperature 23 °C, relative humidity 50%) and were, following exercise, immersed in 28 °C water for 60 min. Thermal comfort zone (TCZ) was also assessed with participants regulating the temperature of a water-perfused suit during heating and cooling. Baseline pre-immersion T_re was similar pre- and post-HA (pre: 38.33 ± 0.33 °C vs post: 38.12 ± 0.36 °C, p = 0.092). The T_re cooling rate was identical pre-to post-HA (−0.03 ± 0.01 °C·min⁻¹, p = 0.31), as was the vasomotor response reflected in the forearm-fingertip temperature difference. Shivering thresholds (p = 0.43) and gains (p = 0.61) were not affected by HA. TCZ was established at similar temperatures, with the magnitude in regulated water temperature being 7.6 (16.3) °C pre-HA and 5.1 (24.7) °C post-HA (p = 0.65). The present findings suggest that heat production and heat loss responses during whole body cooling as well as the skin thermal comfort zone remained unaltered by a controlled-hyperthermia HA protocol.     

Short-term warming does not affect intrinsic thermotolerance but induces strong sustaining photoprotection in tropical evergreen citrus genotypes

Consequences of warming and postwarming events on photosynthetic thermotolerance (P_T) and photoprotective responses in tropical evergreen species remain elusive. We chose Citrus to answer some of the emerging questions related to tropical evergreen species' P_T behaviour including (i) how wide is the genotypic variation in P_T? (ii) how does P_T respond to short-term warming and (iii) how do photosynthesis and photoprotective functions respond over short-term warming and postwarming events? A study on 21 genotypes revealed significant genotypic differences in P_T, though these were not large. We selected five genotypes with divergent P_T and simulated warming events: T_max 26/20°C (day-time highest maximum/night-time lowest maximum) (Week 1) < T_max 33/30°C (Week 2) < T_max 36/32°C (Week 3) followed by T_max 26/16°C (Week 4, recovery). The P_T of all genotypes remained unaltered despite strong leaf megathermy (leaf temperature > air temperature) during warming events. Though moderate warming showed genotype-specific stimulation in photosynthesis, higher warming unequivocally led to severe loss in net photosynthesis and induced higher nonphotochemical quenching. Even after a week of postwarming, photoprotective mechanisms strongly persisted. Our study points towards a conservative P_T in evergreen citrus genotypes and their need for sustaining higher photoprotection during warming as well as postwarming recovery conditions.     

Temperature dependence of two parameters in a photosynthesis model

The temperature dependence of the photosynthetic parameters V_cmax, the maximum catalytic rate of the enzyme Rubisco, and J_max, the maximum electron transport rate, were examined using published datasets. An Arrehenius equation, modified to account for decreases in each parameter at high temperatures, satisfactorily described the temperature response for both parameters. There was remarkable conformity in V_cmax and J_max between all plants at T_leaf < 25 °C, when each parameter was normalized by their respective values at 25 °C (V_cmax0 and J_max0), but showed a high degree of variability between and within species at T_leaf > 30 °C. For both normalized V_cmax and J_max, the maximum fractional error introduced by assuming a common temperature response function is < ± 0·1 for most plants and < ± 0·22 for all plants when T_leaf < 25 °C. Fractional errors are typically < ± 0·45 in the temperature range 25–30 °C, but very large errors occur when a common function is used to estimate the photosynthetic parameters at temperatures > 30 °C. The ratio J_max/V_cmax varies with temperature, but analysis of the ratio at T_leaf = 25 °C using the fitted mean temperature response functions results in J_max0/V_cmax0 = 2·00 ± 0·60 (SD, n = 43).     

Comparison of heat dissipation response between Malaysian and Japanese males during exercise in humid heat stress

This study investigated the differences in heat dissipation response to intense heat stress during exercise in hot and humid environments between tropical and temperate indigenes with matched physical characteristics. Ten Japanese (JP) and ten Malaysian (MY) males participated in this study. Subjects performed exercise for 60 min at 55% peak oxygen uptake in 32°C air with 70% relative humidity, followed by 30 min recovery. The increase in rectal temperature (T _re) was smaller in MY during exercise compared to JP. The local sweat rate and total body mass loss were similar in both groups. Both skin blood flow and mean skin temperature was lower in MY compared to JP. A significantly greater increase in hand skin temperature was observed in MY during exercise, which is attributable to heat loss due to the greater surface area to mass ratio and large number of arteriovenous anastomoses. Also, the smaller increase in T _re in MY may be explained by the presence of a significantly greater core–skin temperature gradient in MY than JP. The thermal gradient is also a major factor in increasing the convective heat transfer from core to skin as well as skin blood flow. It is concluded that the greater core–skin temperature gradient observed in MY is responsible for the smaller increase in T _re.