This article was downloaded by: [Dr Kenneth Shapiro] On: 09 June 2015, At: 06:47 Publisher: Routledge Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Journal of Applied Animal Welfare Science Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/haaw20 Measuring the Heat Loss in Horses in Different Seasons by Infrared Thermography Elena Autio , Riitta Neste , Sanna Airaksinen & Minna-Liisa Heiskanen Published online: 04 Jun 2010. 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Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 Measuring the Heat Loss in Horses in Different Seasons by Infrared Thermography Elena Autio, Riitta Neste, Sanna Airaksinen, and Minna-Liisa Heiskanen Equine Information Centre University of Kuopio It is necessary to consider breed and cold tolerance in the housing and caring of horses. This study demonstrates differences in heat loss between horse types at low temperatures and examines rate of loss in different types during different seasons. Eighteen horses participated. Groups by type were light (L), warmblood (W), coldblood (C), and pony (P). A camera filmed thermographic images at 15° C, 2° C (all types), –8° C (L, W, C), and –12° C (P). The study calculated loss from the neck, trunk, and inner surfaces of front and hind legs. Loss was similar in all types at 15° C. L, W, and C dissipated more heat at 2° C than at 15° C (p < .001) and from neck and trunk at –8° C than at 2° C (p < .05). P dissipated heat similarly at 2° C and –12° C. At 2° C, loss was less from neck and trunk in C and P compared with L (p < .05). At –8° C, loss in L and W was greater than in C (p < .05). A horse’s breed, cold tolerance, plane of nutrition, and the importance of shelter should be noted in the housing and care of horses in different seasons. Ambient temperature, wind, and precipitation affect the rate of heat loss (MacCormack & Bruce, 1991). Therefore, winter weather increases the maintenance energy need of horses kept outside. The most important single climatic stressor is ambient temperature (Cymbaluk & Christison, 1990), which varies between 30° C and –30° C in northern Europe, depending on the season. Long cold periods (–20° C to –30° C) may continue for weeks in winter. The temperature directly influCorrespondence should be sent to Elena Autio, Equine Information Centre, University of Kuopio, P.O. Box 1627, FI–70211 Kuopio, Finland. Email: [email protected] Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 212 AUTIO, NESTE, AIRAKSINEN, HEISKANEN ences the metabolic rate of animals and indirectly influences their health and welfare (Clark & McArthur, 1994). There are limited published data on the cold tolerance of different horse types. The differences between horse types have not usually been taken into account in the construction design of stables, although it is generally thought that coldblood horses are more cold tolerant than warmblood horses (Bender, 1999). The heat production and heat loss of horses have previously been studied by measuring the level of metabolism using indirect calorimetry (Ousey, McArthur, Murgatroyd, Stewart, & Rossdale, 1992) and a hygrometric tent (Morgan, 1997a, 1997b; Morgan, Ehrlemark, & Sällvik, 1997). Respiratory heat loss has been studied by measuring temperature differences across the pulmonary circulation (Hodgson et al., 1993). Kauppinen (2000) examined heat loss in dairy calves and Korhonen and Harri (1986) in farmed raccoon dogs by infrared thermography. The surface temperature of different regions of a horse’s body has also been examined using thermography (Holmes, Gaughan, Gorondy, Hogge, & Spire, 2003; Tunley & Henson, 2004; Verschooten, Desmet, & Verbeeck, 1997); in addition, it is used to a large extent in the diagnosis of muscle, tendon, joint, and hoof injuries (Eddy, Van Hoogmoed, & Snyder, 2001; Lessiter, 1998; Turner, 2001). The aim of this study was to provide information on the cold tolerance of different horse types during different seasons. The rate of heat loss was measured from different body regions using infrared thermography. It was hypothesized that there may be differences in the rate of heat loss between different horse types at low temperatures. In addition, it was assumed that the light and warmblood horse types would dissipate more heat than the coldblood and pony types. MATERIALS AND METHOD Animals The study was carried out between August 1998 and March 2000 in Kiuruvesi, Finland (63°29' N, 26°38' E). Eighteen horses participated in the study. The horses were divided into four groups according to horse type: light (L), warmblood (W), coldblood (C), and pony (P) (Table 1). The same people were not caregivers (owners) of the horses, but the horses were working similarly and fed for moderate work scaled to body weight (Tuori et al., 1996). The mean age of the horses was 9.5 years (SD = 4.8 years) at the beginning of the study. The horses were housed in a stable and kept in a paddock 10 hr a day between September and May. In the summer, the horses were kept in a pasture for 24 hr a day. Rugs were not used; thus, the horses were able to acclimatize to seasonal environmental conditions. MEASURING HEAT LOSS IN HORSES 213 TABLE 1 Characteristics of the Horse Types Used in the Study Breed n Gender Weighta Body Condition Score 1. Light Type (L) Standardbred 4 Gelding 458.5 ± 68.8 3.3 ± 0.5 2. Warmblood type (W) Danish Warmblood Polish Warmblood 3 Gelding 604.0 ± 25.4 5.0 ± 1.6 1 Gelding 3. Coldblood type (C) Finnish horse 4 Gelding 547.5 ± 20.6 5.0 ± 1.2 4. Pony type (P) Connemara Pony New Forest Pony 2 1 1 2 Gelding Mare Gelding Mare 323.3 ± 26.8 5.0 ± 1.7 Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 Horse Type Origin /Description A light horse breed of North American originb Warmblood breeds were developed by crossing draft horses with light horses.b A light-heavy horse breed originating from Finland.c Irelandb Southern England aGiven in kg. b Definition by Wagoner (1999). cSuomen Hippos, the national body of trotting and breeding in Finland. The body condition of the horses was evaluated using a scale of 1 to 9 (Henneke, Potter, Kreider, & Yeates, 1983) before the thermographic examination (Table 1). The body condition of the horses did not change during the study. In addition, hair samples were taken from the midneck about 5 cm below the base of the mane using a coat clipper (Oster Golden A5®, Oster Professional Products, McMinnville, TN). The sample area was determined, and the samples were oven-dried at 40° C for 12 hr and weighed. The hair weight per area unit was calculated. The following hair sample was taken from an area next to the previous sampling area. Care was taken in subsequent samplings not to overlap with the previous sampling area. Thermographic Examination The thermographic examination was carried out in August (15° C) and October (2° C) in 1998 with all the horse types; in March 1999 (–12° C) with type P; and in March 2000 (–8° C) with types L, W, and C. The thermographic examination of types L, W, and C failed in March 1999, which is why the examination was repeated with the same horses 1 year later at the same time of the year. The temperatures given in parentheses are the temperatures in the riding arena at the time of the thermographic examination. Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 214 AUTIO, NESTE, AIRAKSINEN, HEISKANEN The circumstances were standardized by taking the horses to a cold, indoor riding arena that protected them from wind, sun, and rain. The temperature in the riding arena was the same as the outside temperature (difference < 0.5° C), to which the horses were acclimatized. The horses were paired and kept in small pens inside the riding arena. The horses were fed in the morning at 6:00 and brought to the riding arena after feeding, 3 hr before the thermal examination. The recommended period required for a horse to equilibrate fully to its environment prior to taking thermographic images is between 39 and 60 min (Tunley & Henson, 2004). The temperature in the arena was measured every 30 min during the 3 hr and was 14.7 ± 0.6° C in August, 2.0 ± 0.5° C in October, and –8.2 ± 0.2° C and –11.3 ± 0.6° C in March. The horses were not fed during the examination. Thermal images were taken with an Inframetrics 600 camera (FLIR Systems, Inc., Portland, OR), which is a thermographic system with 256 × 200 pixels per frame. The camera has a 15 × 20° field of view and is capable of distinguishing a temperature difference of 0.1° C. A general view was taken from the nonmane side of the horse at a distance of 8 m and the images of the legs at a distance of 1 m. The rate of emissivity used was 0.95. A thermographic camera detects surface heat emitted as infrared radiation and produces a picture that is a map of temperature differences across the target (Dereniak & Boreman, 1996). In a cold environment, heat is mainly dissipated as nonevaporative heat loss (McArthur, 1991). Heat loss is expressed in watts per square meter (W/m2) of surface area of the animal (MacCormack & Bruce, 1991). The images were analyzed at Satakunta Polytechnic in Pori, Finland. The rate of heat loss (W/m2) was calculated from the neck (the area between the ear, withers, elbow, and throatlatch), trunk (the area from the withers and the point of the elbow to the buttock), and inner surfaces of the front and hind legs (the area of the armpit or groin) using a Microsoft Excel® based computer program developed at Satakunta Polytechnic (Figure 1). The neck and trunk were chosen as measuring points for a practical reason: Heat loss from these areas can be reduced with a rug. The front and hind legs were chosen to represent special regions of the body. The program calculated the heat radiated from a particular area of the horse by the calculation method derived from Stefan–Boltzmann’s Law (Dereniak & Boreman, 1996): P = εσ(Ts4 – Ta4 ) P = emitted power (W / m 2 ) ε = emissivity 0.95 σ = Stefan–Boltzmann constant 5.67 × 10 –8Wm –2 K –4 Ts = surface temperature (K ) Ta = air temperature (K ) — = average of measuring points. Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 MEASURING HEAT LOSS IN HORSES 215 FIGURE 1 A thermographic image of a standardbred horse (light horse type) at a temperature of 2° C. The areas of the neck, trunk, front leg, and hind leg where the rate of heat loss was determined are outlined. Statistical Analyses The statistical analyses were made using nonparametric tests in SPSS 10.0 for Windows. The effect of horse type and environmental temperature on heat loss was tested using the Kruskal–Wallis and Mann–Whitney U tests. The differences in heat loss from the various body regions were tested using the Friedman and Wilcoxon signed-rank tests. The differences in hair weight were tested using the Kruskal–Wallis and Mann–Whitney U tests. Nonparametric statistical tests were chosen because they are suitable for statistical analysis of data with a small number of samples and an abnormal distribution. RESULTS Effect of Environmental Temperature on Heat Loss The L, W, and C horse types dissipated more heat from the trunk, neck, front, and hind legs at 2° C than at 15° C (p < .001; Table 2). Heat loss from the P type was similar at 2° C and –12° C. In Type P, heat loss from the front and hind legs was greater at –12° C than at 15° C (p < .05). There were no differences between the neck and trunk in Type P at 15° C and –12° C. The change in temperature from 2° C to –8° C increased heat loss from the trunk and neck in Types L, TABLE 2 The Rates of Heat Loss in Light, Warmblood, and Coldblood Horse Types and Pony Type From the Trunk, Neck, Front Leg, and Hind Leg at Different Temperatures Horse Type La,b Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 Body Region 15° C T N FL HL 2° C T N FL HL –8° C T N FL HL –12° C T N FL HL Wa,b M SD 39.5 43.5 28.0 19.0 2.4 1.3 14.1 14.2 77.5d 83.0d 113.5g 134.0f 96.5h 108.0h 123.0i 158.5i M Ca,b SD M 37.3 38.8 30.8 32.5 13.3 15.7 5.0 12.0 40.5 44.8 25.8 23.5 1.3 4.3 8.1 11.4 70.8 76.5e 100.8g 102.8 12.1 12.1 8.5 5.4 8.3 10.0 12.4 20.0 97.0h 112.0h 101.5 142.2i 22.9 22.3 16.8 16.9 Pc SD M SD 13.1 14.2 3.3 14.2 38.3 43.3 34.8 28.3 9.8 9.9 19.6 3.7 55.8 62.0 88.0g 105.0 5.0 5.0 18.0 8.7 51.7 58.2 66.8 89.3 11.1 14.0 5.8 15.2 68.2 81.7 90.2 111.6 7.9 11.8 6.8 16.6 48.7 58.8 62.2 97.5 5.9 8.7 15.6 40.2 Note. Light: n = 4; warmblood: n = 4; coldblood: n = 4; pony: n = 6. Heat loss measured in w/m2. Asymptotic significance (two-tailed); Mann–Whitney U test. L = light; W = warmblood; C = coldblood; P = pony; T = trunk; N = neck; FL = front leg; HL = hind leg. aDifference in heat loss from T, N, FL, and HL in horse type between 15° C and 2° C (p < .001). bDifference in heat loss from T and N in horse type between 2° C and –8° C (p < .05). cDifference in heat loss from FL and HL in horse type between 15° C and –12° C (p < .05). dDifference in heat loss from body region when compared with Types C and P at 2° C (p < .05). eDifference in heat loss from body region when compared with Type C at 2° C (p < .05). fDifference in heat loss from body region when compared with Types W, C, and P at 2° C (p < .05). gDifference in heat loss from body region when compared with Type P at 2° C (p < .05). hDifference in heat loss from body region when compared with Type C at –8° C (p < .05). iDifference in heat loss from body region when compared with Type C at –8° C (p < .01). 216 217 MEASURING HEAT LOSS IN HORSES W, and C (p < .05). That change in temperature did not influence the rate of heat loss from the front and hind legs. Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 Effect of Horse Type on Heat Loss There were no differences between the horse types in the rate of heat loss from different regions at 15° C (Table 2). Type L dissipated more heat from the trunk and neck than Types C and P at 2° C (p < .05). Type W also dissipated more heat from the neck than Type C at 2° C (p < .05). Type L lost more heat from the hind legs than Types W, C, and P at 2° C (p < .05). Type P dissipated less heat from the front legs than Types L, W, and C at 2° C (p < .05). Type L dissipated more heat from the trunk, neck (p < .05), and front and hind legs (p < .01) than Type C at –8° C (Table 2). Type W lost more heat from the trunk, neck (p < .05), and hind legs (p < .01) than Type C at –8° C. There were no differences in heat loss between Types L and W at –8° C. Hair Weight Hair weight increased in all the horse types between August and March (p < .001; Table 3). Type L had less hair than types W, C, and P in August and October (p < .05). Types W and C also had less hair than type P in October (p < .05). The hair weight of Types L and W was lower than that of types C and P in March (p < .05). TABLE 3 Hair Weight of Light, Warmblood, and Coldblood Horse Types and Pony Type From the Neck in August, October, March, and April Horse Type L Month Augusta October Marchd April W C P M SD M SD M SD M SD 2.4b 6.5b 16.1c 8.0 1.3 0.7 4.3 5.0 8.2 11.3c 15.6e 8.7f 3.2 5.2 3.0 2.0 9.8 16.5c 42.0 13.2 5.2 4.8 8.0 2.0 9.1 33.3 36.9 15.4 2.2 5.7 13.3 2.0 Note. Light (L): n = 4; warmblood (W): n = 4; coldblood (C): n = 4; pony (P): n = 6. Dry weight measured in mg/cm2. Asymptotic significance (two-tailed), Mann–Whitney U test. aDifference in all horse types compared with March (p < .001). bDifference compared with Types W, C, and P in August and October (p < .05). cDifference compared with Type P in October (p < .05). dDifference in all horse types compared with April (p < .05). eDifference compared with Types C and P in March (p < .05). fDifference compared with Type P in April (p < .05). 218 AUTIO, NESTE, AIRAKSINEN, HEISKANEN Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 DISCUSSION The temperature of 15° C is within the thermoneutral zone of horses (Lewis, 1995). In this study, the rate of heat loss was lowest at 15° C. All the horse types also dissipated heat equally from the neck, trunk, and between the legs at this temperature. In a warm environment, the temperature difference between the surface of the horse and the environment is small, which limits nonevaporative heat loss (Morgan, 1997a). Heat loss occurs mainly by evaporation associated with the loss of water vapor from the body surface and respiratory system (Clark & McArthur, 1994). The rate of nonevaporative heat loss increases almost linearly as the temperature decreases (Clark & McArthur, 1994). At a temperature of 2° C, differences in heat loss started to occur. The L horse type dissipated more heat from the neck and trunk than the C and P types. The body resistance affects the rate of heat loss (Ousey et al., 1992). The total insulation between an animal’s body core and the animal’s environment is provided by three thermal insulation layers acting in series: the peripheral body tissue, the coat, and the boundary layer of air (McArthur, 1991). The tissue resistance acts between the body core and skin surface (Ousey et al., 1992). It depends on the thickness of the skin, the amount of subcutaneous fat, and the peripheral blood flow. Reduction in peripheral blood flow in a cold environment decreases heat loss (Mogg & Pollitt, 1992). Subcutaneous fat is three times more insulating than other tissues (Guyton, 1991). Thus, the lower body condition score of Type L may have increased heat loss compared with the other horse types. The thermal insulation of the coat varies with the length and density of the hair (Morgan, 1997b). In a cold environment, piloerection may also increase the insulating value of the coat because the amount of insulating air in the coat increases (McArthur, 1991). Thus, it would have been interesting to measure the piloerection of the hair at different temperatures. The lower hair coat weight of horse type L versus C and P may have enhanced heat loss. In addition, Type W horses have relatively thin skin compared with Type C horses (Talukdar, Calhoun, & Stinson, 1972). It should be noted that the winter coat of the horses was still growing in October, which may also explain the differences in the rates of heat loss between the horse types. The rate of heat loss of Types L, W, and C increased as the temperature dropped from 2° C to –8° C. It should be noted that the –8° C examination of the horses was carried out 1 year later, which dilutes the comparability of these results. The heat loss in Type P did not increase greatly as the temperature dropped. The reason may have been that these horses had a very thick winter coat in March when the thermal images were taken at a temperature of –12° C. The thermal images at 2° C were taken in October when the winter coat was still growing. A similar rate of heat loss at 2° C and –12° C may indicate that the lower limit of the thermoneutral zone of Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 MEASURING HEAT LOSS IN HORSES 219 Type P was at least –12° C and not –8° C as Lewis (1995) stated. A temperature of –12° C is not yet very cold for cold-adapted horses because they tolerate temperatures down to near –18° C in the absence of wind and moisture (Lewis, 1995). However, for a confident conclusion, thermoneutrality should be studied further. The size of the horse is an important factor in determining heat loss (MacCormack & Bruce, 1991). The heat loss is directly proportional to the effective surface area involved in heat exchange. In addition, the mass of the animal has an influence. For example, the surface area in proportion to the body weight is larger in calves than in adult animals, which enhances heat loss (Pyykkönen, 1991). In this study, Type P differed from the other horse types; they were the smallest in size and the only group with mares. In many cases, however, Type P horses dissipated significantly less heat than the other horse types. This may have been a consequence of the good body insulation (hair weight) of the ponies. Because of the different rates of heat loss from the different body regions, it is important to measure heat loss at least from the neck and trunk. The inner surfaces of the legs are special regions because of their thin skin and small surface area compared with the neck and trunk. Therefore, these regions are not very representative in evaluating the general heat loss of horses. In the thermographic images the head exhibited the hottest body temperature. Thus, it would be meaningful to also measure the rate of heat loss from the head when estimating the thermoregulation of a horse. Infrared thermography usually provides a two-dimensional temperature field of an object surface (Wolfe & Zissis, 1989). A profile was taken from the vertical side of the horses and consequently there were not very steep curvatures in the body regions where the radiated heat was calculated. A curvature of a surface has an effect on the precision of radiated temperature measurements when the angle of view exceeds 60° compared with the vertical view (Wolfe & Zissis, 1989). In this study, this can be seen when examining the outer edges of the horse where the surface temperature seems colder (Figure 1). These areas were not included in the calculations of radiated heat. In northern Europe, long cold periods (–20° C to –30° C) may continue for weeks in winter. Heat loss in horses should be studied further at even lower temperatures than those in this study. Another interesting factor is the effect of wind and humidity on the rate of heat loss. A combination of cold and wind, especially in wet weather, is very stressful for a horse; if the coat gets wet, its insulating capacity is lost (Lewis, 1995). It has been previously reported that a wind speed of 8 m/sec increases the heat flow from the coat two- to threefold compared with still air (Morgan, 1994). On the basis of this study, there are differences in the rate of heat loss at cold temperatures between different horse types. In cold winter weather, L and W horse types may benefit from extra feed or shelter more than C and P types. The rate of 220 AUTIO, NESTE, AIRAKSINEN, HEISKANEN heat loss can be reduced with a rug, thereby lessening the need for extra energy in cold weather (MacCormack & Bruce, 1991). Downloaded by [Dr Kenneth Shapiro] at 06:47 09 June 2015 ACKNOWLEDGMENTS We thank the State Provincial Office of Eastern Finland (European Social Fund) and the Employment and Economic Development Centre of Northern Savo (European Agricultural Guidance and Guarantee Fund) for providing financial support for this study. We also thank the personnel of the Vocational Institute of Ylä-Savo, P. Mäenpää, A. Lehmuskero, and T. Stjernberg from Infradex Oy for their help. REFERENCES Bender, I. (1999). Praxishandbuch Pferdehaltung [The practical handbook of horse management]. 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