Index

Abstract

This study aims to assess the impact of time of feeding on the body temperature of West African dwarf (WAD) goats. Twenty-seven goats (15 buck and 12 pregnant does) were used in this experiment. The bucks and gravid does were fed same experimental diet once daily at either, 06:00h, 12:00h or 18:00h in the morning, afternoon or evening, respectively. Rectal temperature (P<0.001) of bucks fed at 18:00h was higher than 12:00h fed bucks which was higher than 06:00h fed bucks. In contrast, pregnant does fed in the evening had lowest (P=0.009) axillary and rectal temperature while afternoon-fed does had the highest. Time of feeding induced increase (P<0.001) in axillary and rectal temperature of the bucks and pregnant does. The excursion ranges of temperature of morning, afternoon and evening-fed bucks was 0.42-0.79, 1.11-1.25, 1.15-1.19oC, respectively, while the excursion range of temperature of morning, afternoon and evening fed bucks was 0.17-0.19, 0.55-0.72, 0.45-0.47oC respectively.  This study shows that time of feeding can entrain body temperature and animal physiological state can affect the temperature rhythm of animals. In conclusion, feeding bucks or pregnant does in the morning or evening may be an effective strategy to manage heat stress in the tropics. Feeding livestock in the afternoon should be avoided. Feeding in the evening may be adopted in the future due to the changing climate that will be accomplished by increased ambient temperature.

Keywords: Body temperature, Diet-Induced thermogenesis, Time of feeding, Pregnant does, Bucks, Tropics.

Received: 27 January 2021 / Revised: 24 February 2021 / Accepted: 22 March 2021/ Published: 13 April 2021

Contribution/ Originality

This study is one of the very few studies that has investigated the impact of time of feeding on the body temperature of livestock specie fed once daily. Feeding in the evening is a good management strategy to reduce body temperature in bucks and pregnant does.


1. INTRODUCTION

Many factors influence the body temperature including food availability and ambient temperature [1, 2]. Naturally, in diurnal animals, body temperature rises from dawn to dusk which coincide with the increase in ambient temperature. Yet, time of feeding has been shown to affect the rhythmicity of expression of body temperature in mammals [3-5]. The rhythm of core body temperature was entrained by feeding time where temperature was phase shifted and amplitude decreased by night feeding in the summer,  indicating alteration of the central clock [6]. Similarly, Salfer and Harvatine [5] reported that night feeding also phase delayed the rhythm of core body temperature, while day-restricted feeding increased its amplitude. The above scenario suggest that time of feeding can be used to manage the time of body temperature peaks.

The climate is continually changing and there is little to nothing farmers can do to put a stop to it. This climate change will induce increases in ambient temperature and humidity, which may result in increased heat-stress in the tropics. Already, climatic conditions are one of the main factors limiting the development of animal production in tropical regions [7] with an ambient temperature as high as (22-32 °C or higher) [8]. This increase in global temperatures is an unsettling factor in livestock production, and elevations of 3-5°C are expected during this century [9]. Feeding cattle at night in hot weather reduced metabolic heat load during daytime when ambient temperature is high while more heat production will be shift to night when the ambient temperature is low [10]. Since farmers cannot stop the climate change-induced increases in temperature, it is plausible to find adaptive techniques to manage it. This study is meant to investigate the impact of time of feeding livestock on the body temperature because it can advance our knowledge of how diet influences thermogenesis in ruminant. Furthermore, it also aims to examine the best time to feed animals in order to reduce the coincidence of high temperature and metabolic heat.

2. MATERIAL AND METHODS

2.1. Experimental procedure

The experiment was carried out at the Goat unit, Teaching and Research farm of the Federal University of Technology, Akure. Twenty-seven goats were used in this study. Experiment 1 consist of fifteen bucks randomly distributed into three treatments of five replicates while in experiment 2, twelve pregnant does were randomly distributed into three treatments of four replicates. The experiment on bucks and pregnant does were carried out concurrently. The buck and gravid does were fed guinea grass (Panicum maximum) and concentrate Table 1 at ratio 50:50 dry matter and fed once daily at 06:00h, 12:00h and 18:00h in the morning, afternoon, and evening, respectively. Fresh water was offered ad libitum.

Table-1. Gross composition (g/100g) of the concentrate diet.

Ingredient
Diet
Cassava peel
40.00
Palm kernel cake
26.00
Wheat offals
14.00
Brewer dried grains
15.00
Bone meal
2.0
Urea
1.0
Premix
1.0
Salt
1.00
Total
100
Calculated crude protein (%)
10.73
Calculated crude fibre (%)
9.82

2.2. Body Temperature Measurement

The axillary and rectal temperature of the bucks and pregnant does was carried out for 8 weeks between March and May 2020. The pregnant does were in mid-gestation stage. The temperature reading for all morning, afternoon and evening-fed goats were carried out three time daily between 06:00-07:00h, 12:00-13:00h and 18:00-19:00h and three times in a week. The readings were taken using a clinical digital thermometer (SKU:WA904SE1ICXF2NAFAMZ and Bio-check). For the rectum, the thermometer was inserted 2cm deep into the rectum and the reading were taken once the thermometer beeps. The skin temperature was taken through the axillary point. The ambient temperature and relative humidity records were taken between 06:00-06:15h, 12:00-12:15h, and 18:00-18:15h, respectively, using a digital hygro-thermometer (Thermopro TP50). The average of the recordings taken three times a week were used as weekly value. The temperature humidity index (THI) was calculated from the recorded daily relative humidity and ambient temperature according to Marai, et al. [11];
THI = dboC - {(0.31 - 0.31 RH) (dboC – 14.4)
Where:
THI = Temperature – humidity index
dboC = Dry bulb temperature oC
RH = Relative humidity (RH %)/100
THI was rated as follows:
ahs = absence of heat stress (values < 22.2).
mhs = moderate heat stress (values between 22.2 to < 23.3).
shs = severe heat stress (values between 23.3 to < 25.6).
ehs = extreme heat stress (values from 25.6 and more).

2.3. Statistical Analysis

A factorial design with the following model: Yijk = µ + ai + bk + abik + eijk was used. Where Yij= any of the response variables; µ = the overall mean; ai= effect of the ith time of feeding, bk= effect of time of measurement, abik= interaction of time of feeding and time of measurement and eij= random error due to experimentation. All data collected were subjected to analysis of variance (ANOVA) using SPSS version 23.0 [12]. The differences between treatment means were examined by Duncan multiple range test of the same package. 

3. RESULTS

3.1. Overall Axillary and Rectal Temperature of Bucks

Trends of overall axillary and rectal temperature of bucks animal fed under different feeding regime and at different time are shown in Figure 1, Figure 2. Time of feeding had no impact (P>0.05) on the axillary temperature of bucks fed in the morning, afternoon or evening Table 2. Rectal temperature of bucks fed in the evening was higher (P<0.001) than those fed afternoon, while morning-fed bucks had the lowest rectal temperature. Regardless of feeding time, axillary and rectal temperature (P<0.001) increased from dawn to dusk. Time of feeding and time of measurement interaction, showed that irrespective of feeding time, buck axillary and rectal temperature increased (P<0.001) from dawn to dusk. Furthermore, for axillary temperature, at 06:00h, the temperature of bucks fed in the morning was similar to bucks fed in the evening but higher (P<0.001) than those fed in the afternoon. At 12:00h, axillary temperature of bucks fed in the afternoon was higher (P<0.001) than bucks fed in the morning while the evening-fed bucks had the lowest axillary temperature.

Table-2. Body Temperature (oC) of WAD bucks under different feeding regimes.

ToF
Axillary
Rectal
ToM
Axillary
Rectal
THI
AT (oC)
RH (%)
Morning
38.41
38.24c
6:00
37.96c
38.05c
24.72c
24.99c
91.63a
Afternoon
38.47
38.44b
12:00
38.54b
38.44b
30.02a
31.93a
65.83b
Evening
38.50
38.56a
18:00
38.87a
39.20a
28.88b
30.60b
66.25b
SEM
0.040
0.041
SEM
0.040
0.041
0.319
0.415
1.649
P-Value
0.243
<0.001
P-Value
<0.001
<0.001
<0.001
<0.001
<0.001
ToF x ToM
6:00
12:00
18:00
SEM
P-value
Excursion
 
Axillary
Morning
38.13aB
38.55bA
38.54cA
0.047
<0.001
0.42
 
 
Afternoon
37.77bB
38.78aA
38.88bA
0.079
 
1.11
 
 
Evening
38.00aC
38.30cB
39.19aA
0.076
 
1.19
 
Rectal
Morning
37.72bB
38.48bA
38.51cA
0.062
<0.001
0.79
 
 
Afternoon
37.71bC
38.64aB
38.96bA
0.078
 
1.25
 
 
Evening
38.05aC
38.44bB
39.20aA
0.070
 
1.15
 

Note: abc=  Means within the same column but with different superscripts are statistically (P<0.05) significant. ABC= Means along the same row but with different superscripts are statistically (P<0.05) significant; ToF: Time of feeding; ToM: Time of temperature measurement; THI: Temperature humidity Index; AT: Ambient Temperature; RH: Relative humidity.

At 18:00h, evening-fed bucks (P<0.001) had the highest body temperature, followed by afternoon-fed bucks while morning-fed bucks had the lowest. At 06:00h, rectal temperature of evening-fed bucks was higher than morning and afternoon-fed bucks which were similar. At 12:00h, rectal temperature of afternoon-fed bucks was the higher than morning and evening-fed bucks which were similar. Furthermore, rectal temperature (P<0.001) in evening-fed bucks at 18:00h was higher than afternoon-fed bucks while the rectal temperature of morning-fed bucks was the lowest. Ambient temperature and THI at 12:00h, was higher (P<0.001) than 18:00 and 06:00h, while RH was higher at 06:00h than at 12:00h and 18:00h Table 2.  

Figure-1. Overall axillary temperature for bucks under different feeding regimes. The M depicts 06:00h measuring time, the A depicts 12:00h measuring time while the E represents 18:00h measuring time.  This shows the rhythm of axillary temperature at each measuring time for the three times measurement per week. It shows that the time bucks were fed actually entrained the pattern of distribution of their temperature. The axillary temperature of morning fed bucks was controlled in a tight excursion range resulting in less fluctuation compared to other feeding time.

Figure-2. Overall rectal temperature for bucks under different feeding regimes. The M depicts 06:00h measuring time, the A depicts 12:00h measuring time while the E represents 18:00h measuring time. This shows the rhythm of rectal temperature at each measuring time for the three times measurement per week. It shows that the time bucks were fed actually entrained the pattern of distribution of their temperature.

3.2. Overall Axillary and Rectal Temperature of Gravid WAD Does

Figure 3, Figure 4 shows the overall axillary and rectal temperature of pregnant does fed at different times of the day. Axillary and rectal temperature of gravid does fed in the morning and afternoon were similar but higher (P=0.009) than does fed in evening Table 3. Axillary (P<0.001) and rectal (P<0.002) temperature at each time of measurement simultaneously increased from dawn to dusk Table 3.  Interaction between the period of feeding and Time of measurement of axillary and rectal temperature of gravid does in all feeding regimes increased from dawn to dusk. At 06:00h, axillary temperature (P<0.001) in morning-fed does was higher than evening-fed does while axillary temperature in afternoon-fed does was the lowest. At 12:00h, axillary temperature (P<0.001) of afternoon-fed gravid does was higher than temperature of morning-fed does while evening-fed does have the lowest temperature. Axillary temperature of afternoon and evening-fed gravid does were similar but higher than in morning-fed does at 18:00h. Rectal temperature (P<0.001) of morning-fed does increased compared to afternoon and evening-fed does at 06:00h. At 12:00h, rectal temperature (P<0.001) of does fed in the afternoon increased compared to morning and evening-fed does which were similar. At 18:00h, rectal temperature (P<0.001) of afternoon-fed does was higher than morning-fed does while the temperature of evening-fed does was.

Table-3Body Temperature of gravid WAD under different feeding regimes.

ToF
Axillary
Rectal
ToM
Axillary
Rectal
THI
AT (oC)
RH (%)
Morning
38.51ab
38.80a
6:00
38.26c
38.57c
24.72c
24.99c
91.63a
Afternoon
38.56a
38.82a
12:00
38.56b
38.81b
30.02a
31.93a
65.83b
Evening
38.45b
38.60b
18:00
38.72a
38.96a
28.88b
30.60b
66.25b
SEM
0.023
0.018
SEM
0.023
0.018
0.319
0.415
1.649
P-Value
0.009
0.009
P-Value
<0.001
<0.002
<0.001
<0.001
<0.001
ToF x ToM
6:00
12:00
18:00
SEM
P-value
Excursion
 
Axillary
Morning
38.41aB
38.54bA
38.60bA
0.026
<0.001
0.19
 
 
Afternoon
38.08cB
38.81aA
38.80aA
0.022
 
0.72
 
 
Evening
38.28bB
38.33cB
38.75aA
0.049
 
0.47
 
Rectal
Morning
38.74aB
38.75bB
38.91bA
0.038
<0.001
0.17
 
 
Afternoon
38.46bB
38.99aA
39.01aA
0.038
 
0.55
 
 
Evening
38.52bC
38.70bB
38.97abA
0.030
 
0.45
 

Note: abc= Means within the same column but with different superscripts are statistically (P<0.05) significant. ABC= Means along the same row but with different superscripts are statistically (P<0.05) significant; ToF: Time of feeding; ToM: Time of temperature measurement; THI: Temperature humidity Index; AT: Ambient Temperature; RH: Relative humidity.

Figure-3. Overall axillary temperature for gravid WAD does under different feeding regimes. The M depicts 06:00h measuring time, the A depicts 12:00h measuring time while the E represents 18:00h measuring time. This showed the rhythm of axillary temperature at each measuring time for the three times measurement per week. It shows that the time does were fed actually entrained the pattern of distribution of their temperature.  In the morning-fed does, the temperature rhythms were fairly consistent throughout the day for each week. In evening and afternoon-fed does, the temperature rhythms greatly fluctuate.   

Figure-4. Overall rectal temperature for gravid WAD does under different feeding regimes. The M depicts 06:00h measuring time, the A depicts 12:00h measuring time while the E represents 18:00h measuring time.  This showed the rhythm of axillary temperature at each measuring time for the three times measurement per week. It showed that the time pregnant does were fed actually entrained the pattern of distribution of their temperature.  In the morning-fed does, the temperature rhythms were fairly consistent throughout the day for each week. In evening and afternoon-fed does, the temperature rhythms greatly fluctuate.    

4. DISCUSSION

4.1. Axillary and Rectal Temperature of WAD Bucks

The physiological state of domestic livestock is key to their productivity [13]. West African dwarf does are adapted to the tropical humid condition, but could be stressed by the high ambient temperature [14]. Heat stress as a prevailing challenge in the tropics compromises livestock welfare. Consumption of nutrient at inappropriate time has the potential to cause misalignment of thermoregulatory mechanism in the body [5]. Diet-induced thermogenesis is associated with food ingestion which causes acute rise in body temperature in various species due to increase energy expenditures [4]. Food anticipatory behavior is often accompanied by increases in body temperature [15]. The increase in temperature in evening-fed bucks may be due to the additive effects of rhythmically increasing body temperature, increased activity due to food anticipation behavior and diet-induced metabolic heat. In morning-fed bucks, the lower rectal temperature despite metabolic heat may be due to lower morning ambient temperature. Body temperature is usually low in the morning and high in the evening [16]. Thus, lower rectal temperature in afternoon-fed bucks compared to evening-fed bucks might be because the core body temperature had not peaked at the time of feeding. The rise in both axillary and rectal temperature from dawn to dusk in bucks fed at the different times of the day shows that body temperature exists in circadian rhythm with lower temperature in the morning and high temperature in the evening. This is because body temperature rises with increasing environmental temperature [17] . Interaction of time of feeding and time of measurement showed that feeding time induced body temperature changes. This agrees with Salfer and Harvatine [5]  who reported that body temperature can be entrained by feeding time, resulting in a shift in the rhythm of core body temperature. The high rectal temperature in evening-fed bucks and its similarity with axillary temperature in morning-fed buck at 06:00h suggests that the rate of elimination of metabolic heat overnight was slower due to high relative humidity. High relative humidity reduces the rate of dissipation of body heat due to decline in efficiency of evaporative cooling [18]. Feeding cattle at night in hot weather reduced metabolic heat during daytime when ambient temperature is high, while more heat production will be shifted to night when the ambient temperature is low [10]. Temperature range in this study for axillary and rectal temperature was 37.77-39.19oC and 37.71-39.20oC, respectively. This is lower than the skin and rectal temperatures range reported as 37.52-39.76oC and 38.13-40.88oC, respectively [19]. This excursing range in this study falls between 0.4-1.90oC reported by Ayo, et al. [20]; Piccione, et al. [21].  The AT in this study was similar to 25.50-37.75oC reported by Minka and Ayo [22]; Aro, et al. [23]. The THI in this study shows that the bucks were heat stressed. The range observed in morning-fed bucks was tightly regulated by the SCN, whereas the feeding of other bucks at “wrong time” of the day disrupted the temperature rhythm, causing fluctuations in the body temperature Figure 1, Figure 2. This depicts that feeding time can entrain body temperature rhythms. Thus, to manage heat stress in bucks fed once a day, feeding in the morning or evening could be the best strategy.

4.2. Axillary and Rectal Temperature of Gravid Does

Average axillary and rectal temperature of gravid does fed in the evening was lower than WAD does fed in the morning and afternoon. This may be due to increased ability of evening-fed does to transfer heat load from the visceral part to the skin surface area resulting in increased level of heat dissipation. This result is similar to Niu and Harvatine [6] that reported decreased temperature in evening-fed cattle which is an indication of alteration in central clock. The result of this study agrees with the report that the thermal effect from food during the morning was higher than in the evening [3]. Increasing temperature from dawn to dusk throughout the measuring time shows that body temperature exists in a rhythm which occur repeatedly. Interaction of time of feeding and time of measurement showed that axillary and rectal temperature progressively increases in all feeding regimes. Meal timing is an important factor affecting the thermal effect of foods [4]. The increased axillary and rectal temperature at 06:00h and 12:00h in gravid does fed at this time compared to 18:00h is an indication of diet-induced thermogenesis. This increase is a result of the feed consumed, increasing ambient temperature and increased food anticipatory activity around the usual time of feeding. Feeding in the morning increased the heat load during the late morning to early afternoon while feeding in the afternoon increased heat load in the cooler hours of the day when heat losses from the animal through conduction and radiation were more efficient [24]. At 18:00h, similarity between the axillary and rectal temperature of afternoon and evening-fed pregnant does indicate that the heat load in afternoon-fed does was not quickly dissipated. The axillary and rectal temperature range was 38.08-38.80oC and 38.46-39.01oC respectively with an excursion range of 0.17-0.72 oC. The morning-fed does had a tight excursion in axillary and rectal temperature compared other feeding time. This indicate the regulatory mechanism of morning-fed does has not be disrupted compared to pregnant does in other feeding regimes which fluctuated greatly Figure 3, Figure 4. The temperature in this study is in the range reported for skin temperature and rectal temperature as 37.52-39.76oC and 38.13-40.88oC respectively [19]. The excursion range in our study is lower than 0.4-1.90oC reported in Ayo, et al. [20]; Piccione, et al. [21]. This may be due to the different physiological state of the goats used. The goats in our study were pregnant. Circulating hormone during pregnancy can influence the body temperature of animals causing 0.5–1°C reduction in maternal temperature during pregnancy [25, 26]. However, the rectal temperature in our study is similar to 38.80-39.28oC reported by Shittu, et al. [8] for WAD does from the third to fifth month of pregnancy. In contrast, it is lower than the 40.84-41.22oC reported for rectal temperature in WAD does at 3-5 months of gestation [27]. Thus, feeding does in the evening can be a feeding strategy to manage heat stress in pregnant goat.

5. CONCLUSION

The time of feeding of a goat can affect the daily average axillary and rectal body temperature range of the goat. Feeding bucks or pregnant goat does once daily in the afternoon or evening, causes change in the rhythm of body temperature compared to those fed in the morning. Farmers should avoid feeding their goats in the afternoon period. This study shows that feeding goat early in the morning or late in the evening is a good adaptive strategy to manage heat stress in bucks. Feeding in the evening is a good adaptive strategy to manage heat stress in pregnant does.

Funding: This study received no specific financial support.  

Competing Interests: The authors declare that they have no competing interests.

Acknowledgement: All authors contributed equally to the conception and design of the study.

REFERENCE

[1]          S. Masri and P. Sassone-Corsi, "The emerging link between cancer, metabolism, and circadian rhythms," Nature Medicine, vol. 24, pp. 1795-1803, 2018.Available at: https://doi.org/10.1038/s41591-018-0271-8.

[2]          D. J. Stenvers, F. A. Scheer, P. Schrauwen, S. E. la Fleur, and A. Kalsbeek, "Circadian clocks and insulin resistance," Nature Reviews Endocrinology, vol. 15, pp. 75-89, 2019.

[3]          C. J. Morris, J. I. Garcia, S. Myers, J. N. Yang, N. Trienekens, and F. A. Scheer, "The human circadian system has a dominating role in causing the morning/evening difference in diet-induced thermogenesis," Obesity, vol. 23, pp. 2053-2058, 2015.Available at: https://doi.org/10.1002/oby.21189.

[4]          Y. Serin and N. A. Tek, "Effect of circadian rhythm on metabolic processes and the regulation of energy balance," Annals of Nutrition and Metabolism, vol. 74, pp. 322-330, 2019.Available at: https://doi.org/10.1159/000500071.

[5]          I. J. Salfer and K. J. Harvatine, "Night-restricted feeding of dairy cows modifies daily rhythms of feed intake, milk synthesis and plasma metabolites compared with day-restricted feeding," The British Journal of Nutrition, vol. 123, pp. 849-858, 2020.Available at: https://doi.org/10.1017/s0007114520000057.

[6]          M. Niu and K. Harvatine, "The effects of morning compared with evening feed delivery in lactating dairy cows during the summer," Journal of Nairy Science, vol. 101, pp. 396-400, 2018.Available at: https://doi.org/10.3168/jds.2017-13635.

[7]          P. BV., S. NB., L. SB., N. JA., and P. CC., "Differential expression of heat shock protein genes associated with heat stress in Nelore and Caracu beef cattle," Livest. Science, vol. 230, p. 103839, 2019.Available at: https://doi.org/10.1016/j.livsci.2019.103839.

[8]          O. Shittu, N. Okwelum, S. Famakinde, J. Odeyemi, D. Toviesi, M. Yussuff, and O. Oluwatosin, "Original research article physiological changes at different stages of gestation in west african dwarf goats in the humid tropics," Journal of Agriculture and Food Environment, vol. 5, pp. 32-39, 2018.

[9]          WMO, "World meteorology organization. World Meteorological Day. Retrieved from: https://worldmetday.wmo.int/en/secretary-generals-message. [Accessed 2 May 2019]," 2019.

[10]        Y. Aharoni, A. Brosh, and Y. Harari, "Night feeding for high-yielding dairy cows in hot weather: Effects on intake, milk yield and energy expenditure," Livestock Production Science, vol. 92, pp. 207-219, 2005.

[11]        I. Marai, M. Ayyat, and U. Abd El-Monem, "Growth performance and reproductive traits at first parity of New Zealand White female rabbits as affected by heat stress and its alleviation under Egyptian conditions," Tropical Animal Health and Production, vol. 33, pp. 451-462, 2001.

[12]        SPSS, IBM SPSS Scientist Statistics for windows, Version 23.0. USA Armonk: IBM SPSS Corp, 2015.

[13]        B. Fuchs, K. M. Sørheim, M. Chincarini, E. Brunberg, S. M. Stubsjøen, K. Bratbergsengen, S. O. Hvasshov, B. Zimmermann, U. S. Land, and L. Grøv, "Heart rate sensor validation and seasonal and diurnal variation of body temperature and heart rate in domestic sheep," Veterinary and Animal Science, vol. 8, p. 100075, 2019.

[14]        L. Jaber, A. Habre, N. Rawda, M. Abi Said, E. Barbour, and S. Hamadeh, "The effect of water restriction on certain physiological parameters in Awassi sheep," Small Ruminant Research, vol. 54, pp. 115-120, 2004.

[15]        J. Bass and J. S. Takahashi, "Circadian integration of metabolism and energetics," Science, vol. 330, pp. 1349-1354, 2010.

[16]        R. Refinetti, "Entrainment of circadian rhythm by ambient temperature cycles in mice," Journal of Biological Rhythms, vol. 25, pp. 247-256, 2010.

[17]        B. Scharf, J. Carroll, D. Riley, C. Chase Jr, S. Coleman, D. Keisler, R. Weaber, and D. Spiers, "Evaluation of physiological and blood serum differences in heat-tolerant (Romosinuano) and heat-susceptible (Angus) Bos taurus cattle during controlled heat challenge," Journal of Animal Science, vol. 88, pp. 2321-2336, 2010.Available at: https://doi.org/10.2527/jas.2009-2551.

[18]        S. Indu and A. Pareek, "A review: Growth and physiological adaptability of sheep to heat stress under semi–arid environment," International Journal of Emerging Trends in Science and Technology, vol. 2, pp. 3188-3198, 2015.

[19]        M. Alam, M. Hashem, M. Rahman, M. Hossain, M. Haque, Z. Sobhan, and M. Islam, "Effect of heat stress on behavior, physiological and blood parameters of goat," Progressive Agriculture, vol. 22, pp. 37-45, 2011.

[20]        J. Ayo, S. Oladese, S. Ngam, A. Fayomi, and S. Afolayan, "Diurnal fluctuations in rectal temperature of the Red Sokoto goat during the Harmattan season," Res. Vet. Science, vol. 66, pp. 7-9, 1998.Available at: https://doi.org/10.1053/rvsc.1998.0231.

[21]        G. Piccione, G. Caola, and R. Refinetti, "Circadian rhythms of body temperature and liver function in fed and food-deprived goats," Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, vol. 134, pp. 563-572, 2003.

[22]        N. Minka and J. Ayo, "Effects of cold-dry (harmattan) and hot-dry seasons on daily rhythms of rectal and body surface temperatures in sheep goats in a natural tropical environment," J. Circa. Rhy, vol. 14, pp. 1-11, 2016.

[23]        S. O. Aro, I. B. Osho, and O. O. Awoneye, "Comparison of rectal and axillary temperatures of Isa brown and Harco black layers fed different levels of dietary acetylsalicylic acid," Animal Research International, vol. 14, pp. 2691-2696, 2017.

[24]        A. Brosh, Y. Aharoni, A. Degen, D. Wright, and B. Young, "Effects of solar radiation, dietary energy, and time of feeding on thermoregulatory responses and energy balance in cattle in a hot environment," Journal of Animal Science, vol. 76, pp. 2671-2677, 1998.Available at: https://doi.org/10.2527/1998.76102671x.

[25]        H. P. Laburn, D. Mitchell, and K. Goelst, "Fetal and maternal body temperatures measured by radiotelemetry in near-term sheep during thermal stress," Journal of Applied Physiology, vol. 72, pp. 894-900, 1992.Available at: https://doi.org/10.1152/jappl.1992.72.3.894.

[26]        J. E. Fewell, "Body temperature regulation in rats near term of pregnancy," Canadian Journal of Physiology and Pharmacology, vol. 73, pp. 364-368, 1995.

[27]        J. Imasuen and C. Aloamaka, "An assessment of pregnancy induced physiological changes in West African Dwarf (WAD) does at different stages of gestation," Annual Review & Research in Biology, vol. 2, pp. 53-57, 2012.

Views and opinions expressed in this article are the views and opinions of the author(s), Animal Review shall not be responsible or answerable for any loss, damage or liability etc. caused in relation to/arising out of the use of the content.