Microclimate variables
Variation of microclimatic to varying air speed treatments during the hot dry (HD) and hot humid (HH) season are presented in Fig 1A and 1B, with the corresponding physiological responses (RT and RR) summarized in Table 1 and the peripheral surface temperature measurements and representative thermogram of hot dry cooling, control, hot humid cooling, hot humid control detailed in Table 2 and Fig 2 respectively, providing a comprehensive overview of the immediate thermal and physiological adjustments under the different airflow treatments. THI values showed clear seasonal and airflow dependent differences, ranging from approximately 74-85 in the hot dry period and increasing to 76-89 under hot humid conditions, indicating a greater thermal load during humid conditions, especially in the afternoon. CO
2 concentrations similarly varied with airflow, declining from 720-760 ppm at 0 h to 310-340 ppm at 6 h as air speed increased (ASc-AS3), reflecting improved ventilation efficiency. Statistical analysis showed that air speed and time point significantly affect both THI and CO‚ (p<0.001) in each season.
Rectal temperature (RT) and respiration rate (RR) responses to air-speed treatments
Rectal temperature and respiration rate exhibited a clear diurnal pattern across seasons and air-speed treatments (Table 1), with lower values in the morning, a pronounced increase during the afternoon and partial recovery during the evening. In the hot-dry season, morning rectal temperature ranged from 38.45-38.57°C, whereas under hot-humid conditions it was consistently higher (38.81-38.93°C, p<0.001). Rectal temperature peaked during the afternoon, reaching 39.59°C in hot-dry control animals and 39.98°C in hot-humid control animals, before declining in the evening to 39.09°C and 39.57°C, respectively. Increasing air speed significantly reduced rectal temperature across all times of day (p<0.001), with the lowest afternoon values observed at 3.6 m/s (
e.
g., 39.30°C vs 39.59°C in hot-dry conditions and 39.63°C vs 39.98°C in hot-humid conditions). Respiration rate showed a similar diurnal pattern, increasing from morning to afternoon and declining during the evening. Morning respiration rate was higher under hot-humid conditions (25.58 breaths/min) compared with hot-dry conditions (23.58 breaths/min). Afternoon respiration rate reached 33.50 and 37.33 breaths/min in hot-dry and hot-humid control animals, respectively and was markedly reduced with increasing air speed, declining to 27.42-26.00 breaths/min at 3.6 m/s (p<0.001). Evening respiration rate also decreased progressively with increasing air speed, from 30.25 to 22.33 breaths/min in hot-dry conditions and from 34.17 to 22.08 breaths/min in hot-humid conditions.
Peripheral surface temperature responses to air-speed treatments
Peripheral surface temperature at different body regions was significantly influenced by season, air speed and their interaction (Table 2). Across all regions, surface temperatures were consistently higher under hot-humid conditions than hot-dry conditions, indicating greater peripheral heat load during humid heat stress. At the forehead, surface temperature under hot-dry conditions ranged from 35.49 to 36.00°C, whereas under hot-humid conditions it increased markedly to 35.60-37.73°C, of season (p<0.001), air speed (p<0.001). Increasing air speed, particularly 3.6-4.8 m/s, significantly reduced forehead temperature in both seasons, with the lowest values observed at 3.6 m/s.
A similar response pattern was observed at the head region, where hot-humid animals exhibited higher surface temperatures (38.4838.85°C) compared with hot-dry animals (37.49-37.75°C). Both season (p<0.001) and air speed (p<0.001) exerted strong effects, indicated enhanced cooling efficiency of higher air speeds under humid conditions. At the eye region, surface temperature showed pronounced sensitivity to air movement, declining from 39.79 to 39.20°C in hot-dry conditions and from 40.18 to 38.78°C in hot-humid conditions as air speed increased, with highly significant effects of season (p<0.001), air speed (p<0.001) similarly Surface temperature at the flank followed comparable trends, with hot-humid values (36.41-37.63°C) remaining higher than hot-dry values (36.01-36.83°C). Increasing air speed significantly reduced flank temperature in both seasons (p<0.001), In contrast, leg surface temperature was less sensitive to seasonal differences, showing a modest season effect (p = 0.001) and a significant air speed effect (p<0.001). skin temperature gradient (ST gradient) also increased significantly with rising air speed in both seasons, reflecting enhanced peripheral heat dissipation. Under hot-dry conditions, the ST gradient increased from 2.76 to 3.34°C, while under hot-humid conditions it increased from 2.36 to 3.25°C, with significant effects of season (p = 0.002), air speed (p<0.001). Overall, higher air speeds, particularly 3.6-4.8 m/s, effectively reduced peripheral surface temperatures and increased thermal gradients, with more pronounced benefits observed under hot-humid conditions.
The present study reveals that air speed is a decisive factor in moderating heat stress responses and our findings clearly show that targeted airflow within the resting area can substantially improve both thermal and respiratory stability in animals exposed to tropical summer conditions. The observed diurnal variation from our findings in rectal temperature and respiration rate highlights the influence of circadian rhythm on thermoregulatory responses under heat stress. Afternoon and evening values were consistently higher, with rectal temperature peaking at 39.98±0.03°C and respiration rate reaching 37.33±0.39 breaths/min under hot-humid control conditions, reflecting the cumulative thermal load during peak ambient exposure. Increasing air speed significantly attenuated these responses, with reductions of up to 0.68°C in rectal temperature and 11 breaths/min in respiration rate at 3.6 m/s, indicating effective cooling even during circadian peaks. These findings suggest that optimized air speed delivery, particularly during afternoon and evening hours can modulate physiological rhythms and maintain core temperature and respiratory stability within acceptable thresholds, despite elevated external temperatures. Recent studies support that mechanical airflow interventions aligned with circadian heat stress profiles enhance animal comfort, reduce metabolic strain and mitigate heat stress behaviour in young bulls
(Magrin et al., 2017; Slayi and Jaja et al., 2025). In addition to thermal benefits, targeted airflow in the resting area also contributed to lower THI and CO
2 accumulation, improving air quality within the animal microclimate. Such microclimate enrichment is known to reduce respiratory irritation and support healthier breathing patterns under heat stress
(Jeppsson et al., 2021; Jannat et al., 2025). These combined effects indicate that airflow can buffer both thermal and respiratory load during circadian heat stress peaks. Increasing air speed produced a clear and consistent cooling response across all peripheral regions, with surface temperatures declining steadily as airflow intensified. Under hot humid conditions, Forehead temperature dropped from 37.73±0.09°C in the control to 35.60±0.08°C at 3.6 m/s, while Eye temperature decreased from 40.18±0.03°C to 38.78±0.04°C, demonstrating strong convective heat removal. Comparable reductions were evident in the Flank (37.63±0.03°C to 36.41±0.03°C) and Leg (39.09±0.09°C to 38.40±0.05°C). The corresponding rise in ST Gradient from 2.36±0.05 to 3.34±0.06 at 3.6 m/s further confirms enhanced heat dissipation under increased airflow. However, at the highest air speed (4.8 m/s), animals exhibited a slight rebound in physiological responses and greater peripheral temperature variability, particularly during dry summer conditions
(Sinha et al., 2018; Ahirwar et al., 2019), which may reflect the added thermal load associated with excessive dry heat exposure. These findings align with recent reports showing that higher air velocity improves boundary layer disruption, increases skin heat transfer and reduces peripheral thermal load in cattle (
Kleinjan-Elazary et al., 2020;
Bah et al., 2021). Studies using forced ventilation systems similarly demonstrate that air speeds above 2-3/ m/s substantially enhance convective cooling efficiency, particularly under humid conditions where evaporative heat loss is limited
(Reuscher et al., 2023). Overall, the present results confirm that elevated air movement is an effective strategy for reducing peripheral heat stress, especially in environments with high humidity. A distinctive strength of the present study is its focused evaluation of targeted cooling within the animal resting area, a micro zone often overlooked in conventional heat stress mitigation research. Unlike whole barn ventilation approaches, directing optimized air speed (3.6 m/s) specifically over the animal-occupied resting zone enriched the microclimate by reducing CO
2 accumulation and particulate concentration, thereby improving both thermal and respiratory comfort. This is particularly relevant because animals spend prolonged periods in the resting area, where stagnant air pockets and elevated humidity typically intensify heat load and respiratory irritation. Recent studies emphasize that microclimate level interventions can substantially improve welfare and physiological stability under tropical conditions
(Andrade et al., 2022). Our finding shows that targeted airflow in the resting area provides both immediate circadian stabilization and sustained physiological resilience, integrating thermal relief, respiratory comfort.