The study revealed that in the morning, outdoor THI was (P<0.01) higher than indoor THI, whereas, there was no significant difference between the indoor and outdoor THI during evening hours both in winter and in summer season (Table 2). A higher (P<0.01) THI was recorded in the evening of both winter (73.31-73.81) and summer (82.26-82.56) season. The present experiment showed that the average THI ranged from 79.55 to 82.56 during summer and 67.21 to 73.81 during winter season.
Serum cortisol levels in all three treatment groups varied (P<0.01) during the winter (108.89-110.33 nmol/l) and summer (185.60–236.75 nmol/l) seasons (Fig 1). However, no significant differences were found between the two genetic groupings. While there was no discernible difference between the treatment groups in the winter, in the summer, Gr. III pigs had a lower (P<0.01) cortisol concentration (185.60 nmol/l) than the other treatment groups, which included both Hampshire and Hampshire x Local pigs.
The results of the analysis of variance revealed that Hampshire and Hampshire x Local pigs grew more body weight in the winter than in the summer (P<0.01) and that Hampshire pigs gained more body weight than Hampshire × Local pigs (Table 3). Additionally, statistical data analysis showed that the pigs’ body weight gain was influenced (P<0.01) by the energy content of their meal.
Linear body measurements showed no significant difference between the summer and winter seasons in terms of daily changes in height and body length at withers; however, all treatment groups except Grade III showed greater (P<0.01) daily changes in heart girth during the winter. In comparison to Hampshire × Local pigs, Hampshire pigs showed greater daily variations in body length, heart girth and height at withers and there was a significant (P<0.01) difference between the two genetic groups (Table 4, 5 and 6). The average daily changes in body length, heart circumference and height at the withers were larger (P<0.01) in Grade III, followed by Grade I and Grade II, according to the analysis of variance.
According to the current study, the average total feed intake was higher (P<0.01) in the winter than in the summer (Fig 2). The study also found that Hampshire pigs consumed more feed than Hampshire × Local pigs (P<0.05). Statistical data demonstrated that the feed consumption was influenced (P<0.05) by the diet’s energy content. According to the FCR data collected for the study, the winter season had a higher (P<0.05) FCR than the summer. Additionally, the Hampshire x Local pigs had a higher FCR (P<0.05) than the Hampshire pigs (Table 7). The Gr. III animals had a better (P<0.01) FCR, according to dietary energy fluctuation.
Pigs have a dense layer of subcutaneous fat covering their bodies, which prevents heat from escaping and they lack functional sweat glands in their epidermis, making them more susceptible to high ambient temperatures. According to Chakraborty and colleagues (
Chakraborty, 2017), the northeastern Indian states were previously largely immune to heat stress in comparison to the rest of the country. However, as a result of climate change and global warming, these states are now also experiencing high summer temperatures, which causes heat stress in livestock and varying degrees of production losses. The current results are consistent with a previous study (
Nass, 2006) that found that a THI of less than 75 is normal for pigs, while a THI of 75 to 78 indicates that the animals are likely to be experiencing heat stress and a THI of 79 to 83 indicates that the animals would be seriously impacted. When THI exceeds 83, the animal becomes extremely stressed and may eventually perish. According to
Davis and Madder (2002), THI is a dependable tool for managing livestock effectively in a variety of climatic conditions and an appropriate climatic marker to correlate climatic stress on animal physiology and productivity. According to the current study, the average THI for pigs throughout the summer was higher than their comfort level and falls within the danger zone.
Serum cortisol concentration is used as the physiological marker to identify the stresses in animals (
Aggarwal and Singh, 2010). Heat stress exposure in animals activates the hypothalamo-pituitary-adrenal axis
(Abilay et al., 1975), making the estimation of hormone concentrations, particularly cortisol, a significant indicator for assessing heat stress in these animals. The current investigation found that summertime serum cortisol concentrations were noticeably greater than wintertime levels. The study also reveals non-significantly higher concentration of cortisol in Hampshire pigs than the Hampshire × Local pigs during summers. This might be due to more vulnerability of Hampshire pigs to summer stress. In present study, it could be observed that there was no significant difference between the treatment groups during winter season but during the summer season, significantly (P<0.01) higher cortisol level was recorded in Gr.II (LE) followed by Gr.I (NE) and Gr.III (HE).
Sejian et al. (2010) also reported significant increase in serum cortisol concentration in Malpura ewes exposed to thermal and nutritional stress. But they found reduction of cortisol level in nutritionally stressed ewes. This is indicative of differential adaptive capacity of the animals. From the study it was observed that lower level of cortisol in Gr.III (HE) than Gr.I (NE) and Gr.II (LE) might be due to the effect of increasing the concentration of dietary energy through the incorporation of vegetable fat (5%) which might reduce the heat increment of the diet and thus allow pigs to become more heat tolerant
(Velayudhan et al., 2015).
The significant effect of thermal stress during summer season on body weight gain of pigs in the present study was in agreement with the findings of
Das et al., (2001). Pigs generally attempt to reduce the impacts of summer heat stress in two main ways since they are homeostatic animals. These include a decrease in heat generated by bodily metabolism and an improvement in heat dissipation. Pigs will expand their body surface area by sprawling out to make more contact with a cool surface, such as a floor. Pigs will also raise their respiration rate (RR) in order to dissipate more heat. By consuming less feed, the pig can lower its metabolic heat output since heat is produced during the eating, digestion and nutrient absorption processes (the heat increment of feeding). In order to reduce the heat increase caused by feeding and, consequently, the quantity of heat that must be released into the environment, the pig voluntarily reduces the amount of feed that it consumes
(Velayudhan et al., 2015). A reduction in feed intake results in reduced growth which affects the body weight gain and this might be the primary reason of significantly (P<0.01) lower average daily body weight gain in summer season than the winter season.
In the present study, it was found that Hampshire breed gained higher (P<0.01) average daily body weight than Hampshire x Local pigs, but it was further observed that Hampshire pigs comparatively gain less average daily body weight in summer than the winter season as compared to Hampshire x Local pigs. This might be due to the less tolerance of Hampshire pigs to thermal stress (THI >75) during summer season, as the recorded THI ranged from 79.55±0.28 to 84.20±0.30 in inside the sty. The findings support earlier observations of
Thornton et al., (2009).
Animals utilise dietary energy for maintenance and productive performance. Basal metabolism and involuntary processes including muscle tone, feed digestion, blood circulation and tissue renewal are also considered maintenance functions (
Verstegen et al., 1987). After maintenance energy needs are met, the pig can focus its energy on developing lean and fatty body tissues and increase in size. Furthermore, metabolisable energy is used to meet the pig’s various energy needs, including growth, maintenance, protein or lipid gain, milk production, etc.
(Noblet et al., 1994a). A significant difference in the average efficiency of ME utilisation for these several functions has been shown in the past: roughly 80% for fat accumulation or maintenance, 60% for protein deposition, 75% for weight gain during growth and 70% for milk
(Noblet et al., 1994a). According to
Sirohi and Michaelowa, (2007), our research further supports earlier results that livestock may experience heat stress due to hot and muggy weather, which can result in behavioural and metabolic changes, such as decreased feed intake and a drop in production. Changing the energy levels of the feed formulation could help overcome this lower production (
Sailo, 2011), which is what we attempted in our study as well. The average daily body weight gain in Gr. III (HE) was then found to have decreased the least amount in the summer compared to the winter when 10% more energy (
NRC, 1998 recommendation) was added to the diet in the form of vegetable oil. This could be attributed to nutritional adjustments that reduce the influence of a hot and humid environment on swine development performance throughout the summer season. These results are consistent with previous studies by
Velayudhan et al., (2015).
In the present study, daily changes in body length and height at withers had no significant difference between winter and summer season but recorded higher value during winter than summer season in all experimental groups. In case of heart girth, analysis of variance revealed (P<0.01) higher measurement in winter in all experimental groups except Gr.III (HE) in both the genetic groups. It was observed that Hampshire pigs had (P<0.01) higher measurement of body length, heart girth and height at withers than the Hampshire x Local pigs which was in accordance with the findings of
Dash and Mishra (1986). A significant (P<0.01) effect of dietary energy levels (Table 4, 5 and 6) on the average daily changes in the linear body measurements of the present study might be attributed to the higher growth rate of pigs that were fed with HE ration as compared to the LE ration. The higher daily changes in body length; heart girth and height at withers of pigs fed with HE diets had been well documented by
Sailo (2011). However, in contrast to the present finding,
Das (2000) had reported non-significant effect of dietary energy levels on the body measurements.
Exposure to high ambient temperature has been shown to affect daily feed intake
(Black et al., 1993; McGlone, 1999) which finally results in lower body weights. The average total feed intake was higher (P<0.01) during winter season than the summer season which might be due to the lower THI during winter season providing thermal comfort to the animals. The less intake of feed during summer season might be an effort of animal to lower heat increment due to feed metabolism which was in agreement with the findings of
(Velayudhan et al., 2015). Although the average total feed intake was significantly (P<0.01) higher in Hampshire pigs, a significantly (P<0.01) lower feed intake could be seen in high energy incorporated group (Gr.III) as compared to the others which may be attributed to the increase energy density of the diet.
The recorded better (P<0.01) FCR value during winter as compared to summer season might be due to the favourable environmental temperature during winter (THI: 67.21 to 73.81) that helped to maintained feed intake and body metabolism (
Mayer and Bucklin, 2001). According to
Tokach et al., (2010), the HE integrated group had a reduced feed intake and a superior (P<0.01) FCR when there was dietary energy-wise variation. This could be because the Gr. III group’s feed was energy-rich and deficient in fibre.