Next Article in Journal
Establishment and Application of a Quantitative PCR Method for E248R Gene of African Swine Fever Virus
Previous Article in Journal
Feeding Thai Native Sheep Molasses Either Alone or in Combination with Urea-Fermented Sugarcane Bagasse: The Effects on Nutrient Digestibility, Rumen Fermentation, and Hematological Parameters
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Predictive Models of Dairy Cow Thermal State: A Review from a Technological Perspective

1
CEFT—Transport Phenomena Research Centre, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal
2
ALiCE—Associate Laboratory in Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal
3
CIISA—Animal Behaviour and Welfare Laboratory, Associate Laboratory for Animal and Veterinary Sciences (AL4AnimalS), Faculty of Veterinary Medicine, University of Lisbon, 1300-477 Lisbon, Portugal
4
ICBAS-UP—Institute of Biomedical Sciences Abel Salazar, University of Porto, Rua Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal
5
CECA/ICETA—Centre for Animal Science Studies, Rua D. Manuel II, Apartado 55142, 4051-401 Porto, Portugal
*
Author to whom correspondence should be addressed.
Vet. Sci. 2022, 9(8), 416; https://doi.org/10.3390/vetsci9080416
Submission received: 30 June 2022 / Revised: 28 July 2022 / Accepted: 4 August 2022 / Published: 8 August 2022
(This article belongs to the Topic Animal Diseases in Agricultural Production Systems)

Abstract

:

Simple Summary

Heat stress in cattle is broadly defined as a physiological condition in which body temperature rises, and the animals are no longer able to adequately dissipate body heat to maintain thermal equilibrium due to environmental factors. Dairy cattle are particularly sensitive to heat stress because of the higher metabolic rate needed for milk production. Due to global warming and the expected growth of milk production in warmer regions, an increase in the occurrence of heat stress can only be avoided with the use of environmental control systems. However, most available systems were developed to take corrective measures or are not accurate enough to effectively prevent heat stress, as there is not yet an automated technological solution that considers all the environmental and animal variables that determine the occurrence of this condition. Further, these systems must be connected in time to prevent this condition in cattle but also disconnected when they are no longer needed, as their use raises major economic and environmental concerns regarding energy and water consumption. This review describes and discusses three types of predictive models that can make these systems more effective in preventing heat stress and more efficient in the use of energy and water.

Abstract

Dairy cattle are particularly sensitive to heat stress due to the higher metabolic rate needed for milk production. In recent decades, global warming and the increase in dairy production in warmer countries have stimulated the development of a wide range of environmental control systems for dairy farms. Despite their proven effectiveness, the associated energy and water consumption can compromise the viability of dairy farms in many regions, due to the cost and scarcity of these resources. To make these systems more efficient, they should be activated in time to prevent thermal stress and switched off when that risk no longer exists, which must consider environmental variables as well as the variables of the animals themselves. Nowadays, there is a wide range of sensors and equipment that support farm routine procedures, and it is possible to measure several variables that, with the aid of algorithms based on predictive models, would allow anticipating animals’ thermal states. This review summarizes three types of approaches as predictive models: bioclimatic indexes, machine learning, and mechanistic models. It also focuses on the application of the current knowledge as algorithms to be used in the management of diverse types of environmental control systems.

Graphical Abstract

1. Introduction

Heat stress in cattle is broadly defined as a physiological condition during which the animal is no longer able to regulate its internal temperature within a comfortable level because of an increase in body heat storage [1]. This physiological condition can lead to impaired health and immunity [2,3], deteriorated living conditions and even mortality during extreme events [4,5], especially in younger cattle [6,7]. Due to global warming, the number of heat stress events is expected to increase (2000 h in Central Europe and Mediterranean regions [8]) causing vast economic losses (e.g., the dairy industry loses approximately USD 900 million/year only in the U. S. [3]). Furthermore, the conventional genetic selection of dairy breeds to increase dry matter intake (DMI) and milk yield [9,10] resulted in cows with elevated internal heat loads (due to high milk production) that may lead to heat stress much earlier than their lower-producing counterparts [11,12,13]. For instance, the loss of milk production due to heat stress is expected to increase at a rate of 174 ± 7 kg/cow/decade in the 21st century [14]. Thus, the impact of this syndrome on animals cannot be neglected in any way as the future dairy industry faces the difficult challenge of increasing milk production in warmer environmental conditions [8], while preserving the welfare of dairy animals.
Several strategies are reported in the literature to mitigate heat stress, from cattle housing design to shifting feeding times to cooler periods and shade seeking [3,15,16], but only cooling and forced ventilation systems are effective above certain temperatures and humidity conditions [16]. Further, these systems must be connected in time to prevent the development of heat stress in cattle but also disconnected when they are no longer needed, as their use raises major concerns regarding energy and water consumption, which may be economically and environmentally unsustainable in the near future [17,18,19].
Presently, as a wide range of sensors and equipment have been developed to support farmer routines, it is possible to measure several variables that, with the aid of algorithms based on predictive models, could allow anticipating the thermal state of the animal. This review summarizes three types of approaches with the potential to be used as predictive models: bioclimatic indexes, machine learning, and mechanistic models. The analyses focused on the application of the current knowledge as algorithms to be used in different types of dairy technology (e.g., fans, sprinklers), considering the several input and output variables of the models as practical issues.

2. Heat Stressed Dairy Cows and the Available Technological Solutions to Detect and Mitigate Heat Load

2.1. Heat Stress Indicators

Heat stress has an enormous impact on animal health, biological functioning, and welfare. One of the most noticeable consequences of heat stress in dairy cows is the reduction of DMI, which causes a drop in milk production by decreasing the availability of nutrients used for milk synthesis [20,21]. Moreover, heat stress compromises cattle welfare by changing or inhibiting social and eating behavior [22], increasing susceptibility to disease [23], and causing stress and discomfort [24]. Under harsh ambient conditions, animals show physiological or behavioral responses or, most often, a combination of both. For instance, in the early stage of heat exposure, the animal body quickly responds to maintain homeostasis. As the amount of heat load increases, the physiological response becomes more evident, triggering an increase in both respiratory (RR; [25,26]) and heart rates (HR; [27,28]). Therefore, cows change their behavior [3,24], e.g., water ingestion, reducing movement and seeking shaded areas to minimize heat load, leading to the subsequent decrease in milk production, and finally a decline in fertility [29]. Although interdependency exists, physiological, behavioral, and production indicators were examined separately to facilitate the analyses [30,31].

2.1.1. Physiological Indicators

The core body temperature in cattle indicates the temperature of the most important organs of the body such as the heart, liver, and brain [32]. It is often used as an indicator of heat stress and typical values of 38.0 to 39.3 °C are observed in non-heat-stressed cattle [27]. Rectal or vaginal temperature is used as a conventional “gold standard” measure of core body temperature [33]. Yan et al. [34] studied the rectal temperature of dairy cows exposed to several heat stress conditions, reporting an increase of 1 °C in rectal temperature (from ~38.5 to ~39.5 °C) from neutral to heat stress conditions. The rectal temperature is the predominant method employed to measure the internal temperature of heat-stressed cows, but other internal regions of the cow body, such as the vagina [35,36], the rumen [16], and the tympanum [37], have also been studied and correlated with typical behavioral and ambient conditions of heat stress. Nordlund et al. [35] monitored the vaginal temperature of 20 high-producing cows, observing a temperature increase during lying bouts and a temperature decrease when the cows were standing in pens (both free stall and milking center holding pens). Another example, reported by Curtis et al. [16], is the delay in the rumen temperature increase of 2 to 5 h when compared to ambient temperature, probably due to the thermal inertia caused by the cow’s substantial body mass. One possible approach to identifying animals affected by heat stress is by monitoring the external temperature of the cow’s body. Several authors have been studying the temperature of eyes, limbs, and udder and have correlated it with core temperature [28,38].
In some situations, the variation of other physiological indicators is more significant than the core body temperature. For example, in moderate heat stress conditions, Vizzoto et al. [27], compared shaded and non-shaded cows at 1300 h (GMT−0200 h) and observed a significant increase in the respiratory and heart rates, but no significant differences in the cow’s body temperature. Cows with access to shade had a lower respiratory rate of 5.9 breaths per minute and a lower heart rate of 20.5 beats per minute when compared with those without access to shade. However, a significant increase in the core temperature of not-shaded cows was observed later at 1700 h. Respiratory rate increase followed by a body temperature increase was also reported by Ferrazza et al. [25] in Holstein cows exposed to intense and prolonged heat stress conditions. Moreover, Brown-Brandl et al. [26] concluded that the respiration rate is a good physiological indicator of heat stress because there was little or no lag associated with it and it was consistently affected in all the categories of the daily maximum temperature–humidity index (THI; i.e., it measures the risk of the animal suffering from heat stress; see Section 3.1).
The endocrine response to heat stress is mainly reflected by elevated glucocorticoids (cortisol), aldosterone, antidiuretic hormone, thyroxine, prolactin, and growth hormone. However, their use as heat stress indicators would imply frequent blood sampling, an invasive procedure that requires the handling of animals. A less invasive measurement is milk cortisol (MC) concentration as it is highly correlated to plasma cortisol concentrations sampled at the same time [39]. Glucocorticoid metabolites (produced by the liver and excreted into the gut via the bile), but not the native glucocorticoids, can be detected in feces [40]. These fecal Cortisol Metabolites (FCM) can thus provide an integrated measure of stress over several hours, whereas MC provides a measure of stress occurring in the previous minutes. Despite being recognized as useful indicators of the occurrence of heat stress in cattle, their use in a heat stress study has several limitations besides laboratory costs. In the case of MC, its measurement as short-term indicators would imply milking cows outside milking hours, which could be a stressful event for the cows.

2.1.2. Behavioural Indicators

Under heat stress conditions, cows tend to adapt their body posture [41,42], spending more time standing to increase the body surface area exposed to air, thus dissipating more heat. Allen et al. [43] showed a direct correlation between the core temperature and the duration of the standing period of lactating dairy cows experiencing mild to moderate heat stress. When a cow’s vaginal temperature exceeded 38.93 °C, there was a 50% likelihood that the cows would be standing. Furthermore, Yan et al. [34] correlated the rectal temperature and temperature–humidity index of cows with different postures (i.e., laying or standing). They observed that recumbent cows showed higher rectal temperature for lower values of THI, which indicates how the laying posture negatively affects the cows’ thermal state.
Heat stress also affects the cow’s disposition to display natural estrous behavior, reducing both the duration and intensity of estrous expression [44,45] and is responsible for a decrease of 20 to 30% in conception rates [46]. Furthermore, the decrease in conception rates during summer is also explained by oocyte quality reduction, early embryonic death, endometrium dysfunction, and reduced spermatogenesis in bulls [47,48].
Although less documented in the literature due to difficult quantification, it is undeniable the important changes in the emotional state, with evident signs of malaise, disorientation and frustration in animals affected by heat stress [3].
Other changes in the social behavior of heat-stressed animals are also reported, such as higher levels of aggression near water drinkers or competition for shade seeking [22,49,50]. Furthermore, the eating and drinking behavior of cows also changes [50]. For example, the increase in heat load is accompanied by an increase in water intake and a significant reduction in dry matter intake (DMI). This reduction in feed intake occurs in all mammalian species under heat stress conditions. However, the extent of this reduction depends not only on environmental conditions but also on the production level [30]. In heat-stressed lactating cows, feed intake may be reduced by as much as 40%, according to the National Research Council of the United States of America [51]. This causes a decline in milk production by decreasing the availability of nutrients used for milk synthesis. Likewise, a change in milk composition is to be expected such as a decline in total protein or fat content [52,53] but also in fat composition [54]. These factors related to the yield and composition of milk are often used as indicators of performance, as described in the following subsection.

2.1.3. Performance-Related Indicators

Under heat stress conditions, the activation of the cow’s thermoregulatory system can increase metabolic maintenance requirements by 7 to 25% [55], exacerbating both the existing metabolic stress and the reduction of milk production [3,30]. However, the drop in milk production has a time delay associated with it, being clearly noticed a few days after the first day of exposure to a high-temperature environment. For example, Van Laer et al. [56] reported a significant decrease in milk yield after a lag period of two days. Nevertheless, as the heat load decreases to thermoneutral conditions, the milk yield progressively returns to values obtained in thermoneutral cows [30].
Another relevant performance-related indicator that might be affected by heat stress is the milk composition which typically presents a reduction of lactose, protein, and/or fat with increasing values of bioclimatic indexes [53,56]. Nonetheless, the decrease in milk production is not always accompanied by a change in the composition of the milk [30].

2.2. Methods to Detect Heat-Stressed Cows

The complexity of cow physiological mechanisms and their interdependency with its behavior and with environmental conditions recommend the measuring of indicators at various levels: cow’s body, performance, behavior, and environment. The record of the latter is straightforward, and the parameters often studied are the environment temperature, humidity, air velocity, and solar radiation [57,58]. Several types of equipment are available in the market such as temperature and humidity sensors for indoor/outdoor conditions [23,59], anemometers for measuring wind direction and velocity [8,42,60], and solar radiation sensors [57,61]. However, a broader range of methods may be used to assess animal health and welfare [30], from equipment with different frequencies of data acquisition (e.g., real-time vs. hourly measurements) to continuous or scan observations. Thus, to facilitate the analyses of the methods used to study the animal physiological, behavioral, and performance-related indicators, the methods are described in the following sections by these categories: equipment measurement frequency and observations.

2.2.1. Equipment with Low Data Acquisition Frequency

Over the last decades, manual detection has been the most used method for measuring physiological parameters such as heart rate, sweating rate or rectal temperature [57]. However, these methods can be classified as invasive or, at least, disturbing to the animal, since the interaction with the animal, e.g., by touching or inserting portable equipment in the animal body [33], can add extra stress and consequently influence the measurements. These methods are also time-consuming and may involve significant additional labor costs. The advantage of these type of methods is that it often requires cheap and user-friendly equipment, e.g., a thermometer for rectal temperature measurement [1,25] or a stethoscope for heart rate measurement [25,27].
Sensors coupled with data loggers are also often used to record the measurements over discrete time points [2,57,62]. An evaporimeter was used by Rungruang et al. [63] to measure, four times a day, the sweating rate at the skin or hair-end level. In order to avoid the displacement of cattle from their social group for restrainment in a crush, the surface body temperature is often measured with thermal data loggers, e.g., a neck collar attachment for skin temperature measurement [2].
Another rapidly developing promising alternative is infrared thermography [2]. Thermal imaging cameras for Infrared Thermography (IRT) offer a remote, non-contact method for recording surface temperature and have been explored as a proxy for core body temperature measurements [28]. However, the use of such systems presents important operational challenges since the successful determination of IRT of external body surfaces depends on the effective minimization of confounding factors, e.g., the animal skin and hair, or external factors such as ambient temperature, sunlight or wind [2,64]. In a study that used infrared thermographic images to predict heat stress events in feedlot cattle, Unruh et al. [65] concluded that it was an objective method to monitor beef calves for heat stress in research settings, but at the time, they also noted that thermographic data was of little predictive benefit compared, e.g., with forecasted weather conditions. Like Idris et al. [2], these authors refer that the use of infrared thermography as a diagnostic tool to monitor heat stress in cattle requires further research [65].
The research and development of monitoring technology have been accompanying the modernization of the farm sector in the direction of a more efficient and automatized system (i.e., livestock precision farming). To ensure a prompt response, the new monitoring equipment should provide the continuous monitoring of the process (i.e., herd thermal state and environment conditions), ideally in real-time.

2.2.2. Equipment with High Data Acquisition Frequency

Automated temperature monitoring devices can have several applications in livestock, either to monitor animal health or to support scientists and farmers for precision farming and remote monitoring. In 2018, Koltes et al. [66] analyzed different automated body temperature monitoring technologies and discussed their use to develop new strategies to control potential animal health problems. The authors highlighted that the measurement at the animal level would be useful to manage heat stress and disease, despite the associated investment costs. Furthermore, they pointed out a need for developing software for complex data storage and treatments. A similar conclusion was drawn by Sellier et al. [62]. In order to avoid displacement of cattle from their social group and restraint in a crush, thermal data loggers can be used to measure body temperature by, e.g., a neck collar attachment (for skin temperature), a rumen bolus or a vaginal insert, recording temperature at pre-determined time intervals or having a telemetric option to transmit recorded data in real-time to a user-defined receiver [2]. As an alternative, the core body temperature can be monitored in real-time using implantable biosensors [60].
Rumen boluses provide prompt means of measuring rumen (or reticulum) temperature, but measurements may be influenced by the intake of fluids. One of the challenges in using rumen temperature is the acute impact of water intake [58]. Ingestion of large volumes (10 to 15% rumen volume) of cold water (0 to 8 °C) provokes a sudden drop in rumen temperature (up to 10 °C) within 15 min of water consumption and required approximately 2 to 3 h to return to baseline [67]. However, as water intake is directly related to feed intake, it may also be reduced in heat-stressed animals compared to thermoneutral controls [68]. Both feed and water intake can be monitored through several methods: neck-mounted activity collars, ear tags and/or leg data logger, coupled with micro-electro-mechanical accelerometers. This can provide important data regarding feeding behavior as head movements toward the feed bunk are recorded while a ruminal bolus can provide temperature data [69].
Sensors coupled with data loggers have also been used for high-frequency (minutes) measures that can be considered continuous. Polsky et al. [36] used temperature-recording data loggers coupled to an intra-vaginal progesterone implant for vaginal temperature measurement with a 10 min frequency. Respiration sensors coupled with a micro-computer have also been used to record the respiration rate with high incidence [61,70]. On the downside, battery problems or malfunctions (e.g., sensor displacement or removal) are usually only revealed at the end of the trial.

2.2.3. Observations

Respiration rate and panting serve as early indicators of increasing heat stress [24] and provide an easy method for the non-invasive and distant assessment of heat stress response [48,71], unless cattle are more than approximately 30 m away (at this distance it is difficult to visualize the cow’s behavior [72]). The panting score is often assigned on a scale of 0 to 4, in which zero is no panting and four is severe panting [27,28]. The ethogram for panting scoring can be helpful to assess an individual or a group of animals’ response to heat stress [37,72]. However, human observation adds uncertainty to the collected data and the outcomes are extremely dependent on the researcher or farmer’s experience [2]. Additionally, it entails a substantial rise in labor costs.
The major limitation of these animal-based methods is the moment at which the heat stress is detected. The methods identify the signs of heat stress and not the conditions that potentially lead to heat stress (pre-heat stress conditions), so it fails to prevent the deterioration of the animal’s health.

2.3. Cooling Technologies

A wide range of alternative strategies to reduce heat load is used, from shifting feeding times to cooler periods [3] to nutrition adaptation [73]. However, above certain temperature and humidity conditions, only evaporative cooling and forced ventilation systems are effective (e.g., fans [74] and sprinklers [20]). Several environmental control systems for dairy cows exist based on the principles of convection, conduction, radiation, and evaporation and most can mitigate or even avoid heat overload episodes [57,75]. Fan installations, which facilitate air movement and increase convection, can decrease both respiratory rate and rectal temperature and promote DMI [76]. Similar outcomes are achievable with other forms of evaporative cooling systems that make use of high-pressure mist injected into fans or large water droplets from low-pressure sprinkler systems that completely soak the cow’s hair coat [20]. Despite advances in cooling technologies, primary concerns, regarding energy and water consumption, arise with the use of these systems, namely sprinkler systems. Depending on herd size, large volumes of water are needed for cooling, reaching levels of water consumption (215 to 454 L per cow per day) that may become economically and environmentally unsustainable in the near future [17,18]. Furthermore, one should not forget that these systems generate equally large amounts of wastewater that must be managed. Along with drinking water and water needed during the milking routine, water for evaporative cooling is one of the main three uses of potable water in commercial dairies and decreasing water usage and contamination is critical to the sustainability of the industry [19]. Therefore, these cooling systems must be turned on in time to provide immediate thermal relief for dairy cows but also turned off when unnecessary, to avoid wasting energy and water.

3. Predictive Models

Determining the pre-heat stress conditions is essential to make environmental control systems more capable of not only effectively preventing heat stress and related conditions, but also making them more efficient in energy and water usage. Taking into account the above-mentioned limitations of the assessment through animals, trying to determine this condition only with environmental variables is the most logical step, as they are more easily measurable using cheaper equipment. To achieve this objective, it will be necessary first to develop algorithms based on predictive models that integrate all data from the environment and animals, between situations transitioning from thermoneutral conditions to thermal stress conditions and vice versa, and combining all variables that affect the cow’s thermal state. This review summarizes three types of approaches with the potential to be used as predictive models: bioclimatic indexes, machine learning, and mechanistic models.

3.1. Bioclimatic Indexes

The bioclimatic index is a measure often used to assess the risk of an animal suffering from heat stress. This type of index was developed to model the combined effect of environment, production, and animal welfare indicators, assuming uniform responses from all the animals. As input variables, the indexes consider a combination of environmental conditions, such as temperature, relative humidity, solar radiation, air velocity, and precipitation [30,57,76,77], that are easily monitored (e.g., with weather stations or indoor/outdoor sensors). Typically, these indexes are based on regression equations, usually with three levels of stress (i.e., mild, moderate, and severe) represented by threshold values [57]. Therefore, the implementation of the indexes as an algorithm is straightforward. The main concerns rely either on the selection of the most adequate index or its feasibility to be integrated into a dairy farm cooling system.
The predominant index incorporates only air temperature and relative humidity, i.e., temperature–humidity index (THI; [30,34,78]). Probably due to the minimum requirement of inputs (meteorological parameters) and the consequent simple application, the THI is a popular approach among farmers and veterinary researchers. Several THI indexes have been developed over the years, considering multiple modifications and refinements based on different breeds and using different parameters to categorize heat stress levels (e.g., respiratory rate, rectal temperature). The input and output variables of some bioclimatic indexes are described in Table 1. In fact, the THI is used to assess the thermal comfort of animals, humans, or others. Thom [79] developed a well-known THI index for the evaluation of human discomfort levels in warm weather using two parameters directly related to sensible and latent heat transfer: dry bulb temperature and wet bulb temperature. For livestock, the THI followed the same rationale to study the discomfort of, e.g., bull calves [80], dairy animals (study cited in [81]), or cattle [7], in this case, considering production (e.g., milk and protein yield; [82,83]) and animal comfort factors (painting scores and rectal temperature [7,80]) as indicators of heat stress.
The THI models have been improved by considering more weather parameters and by fine-tuning the thresholds [7,82,83,84,85]. For example, Mader et al. [7] adjusted a THI model for cattle by including wind velocity and solar radiation in the model, and by assessing the level of heat stress comfort through painting scores. The same model was correlated with the milk yield of Holsteins cows in temperate regions [83], which identified a decline in heat stress thresholds. The same tendency was observed by Gorniak et al. [82] in Germany, for Holstein dairy cows but using a different THI model. Gaughan et al. [37] developed a model that considers ambient temperature, humidity, solar radiation, and wind velocity, but instead of one equation, the model has two. The model is called Heat Load Index (HLI), and the two regression equations are set for different black globe temperature ranges (threshold of 25 °C). Further, the effect of different management strategies (e.g., access to shade) and animal-related factors (e.g., genotype and coat color) are considered through specific heat stress thresholds [37]. Other strategies were used to integrate the effect of wind and solar radiation on the index predictions: indirectly, such as using a black globe temperature (in the dairy heat load index (DHLI) [84]), through multiple non-linear equations (indexes CCI and HLI [37,86]) or even considering the weather parameters interaction (equivalent temperature index for cattle (ETIC) [85]).
The thermal state of a heat-stressed animal strongly depends on the intensity and duration of heat-stress conditions, as well as the heat accumulated from previous exposures, both time-related factors, that are often neglected by the broader bioclimatic indexes. Nevertheless, Ji et al. [87] adjusted bioclimatic indexes to simultaneously quantify the intensity and duration of heat stress, considering both short- and long-term effects. Multiple linear regressions were correlated between DMY and the developed indexes considering the animal’s age, body mass and days in milk. Following a different approach, Gaughan et al. [37] developed a model (i.e., accumulated heat load (AHL)) to predict the body heat load balance over time, considering the total hours above a threshold HLI. For HLI values above the threshold, the animal accumulates heat, and the opposite occurs if below the threshold value. The AHL index showed a high correlation with the panting score for different beef cattle genotypes.
Several more advanced indexes have been studied. However, they were developed for different geographic locations, on varied diets, and farm systems. For that reason, numerous studies comparing the performance of bioclimatic indexes under specific conditions [11,88,89], have been drawing distinct conclusions. For example, Van Laer et al. [11] likened six bioclimatic indices and found that the HLI was the best predictor of cow thermal discomfort. The authors evaluated the summer conditions and shade availability for two herds (i.e., Holstein dairy cows and Belgian Blue beef cows) kept on pasture in a temperate area. However, in another study of lactating cows, in this case, housed in a naturally ventilated barn [88], it was concluded that the HLI underestimate the degree of heat stress (originally developed for unshaded animals [37]) while the CCI was indicated as a promising index to estimate heat stress of housed dairy cows. Ji et al. [57] showed a straightforward comparison of bioclimatic indices under several ambient conditions, i.e., temperature (20 to ~35 °C), humidity (~50 to ~86%), wind velocity (0 to ~7 m·s−1), and solar radiation (0 to ~1100 W·m−2). According to Ji et al. (2020, [57]), it is clear that the use of different bioclimatic indexes can lead to opposing conclusions: from neutral conditions, with one index, to moderate heat stress conditions, with another one, or even odd outcomes. For example, for critical hot-wet conditions, only a maximum level of moderate heat stress was obtained with one of the indexes evaluated (HLI1 [57]), in opposition to the level of severe heat stress predicted by the remaining indexes. This emphasizes the need to study the index accuracy and possibly adjust the thresholds to both local farm features and cattle traits.
In order to build an algorithm based on the mentioned indexes, the values above which the animal starts feeling uncomfortable need to be defined. However, the threshold values that define if the animal is in mild, moderate, or severe heat stress, are very dependent on the index selected. For instance, as an indicator of a mild level of heat stress, values around 25 (to 30), 65 (to 74), and 70 (to 80) are, respectively, reported in studies based on CCI [86,88], THI [7,34,78], and HLI indexes [11,37]. Additionally, it is unrealistic to assume uniform thresholds for categorizing the level of heat stress of all animals on a farm as the animals have varied biological attributes (age, genotype, and production level), and the animal thermal state is highly dependent on the specific environmental conditions each animal is exposed to. As an example, Ji et al. [90] adjusted the thresholds, by using a machine learning technique to obtain accurate levels of heat stress for individual cows, although uniform thresholds were found adequate to predict the decline of daily milk yield of the herd in a previous study [76].
The effect of animal individual characteristics on heat load threshold has been recently studied [7,34,78,90]. For example, Pinto et al. [78] determined the heat load thresholds of THI based on respiration rate for different postures (standing or laying) of Holstein-Friesian lactating cows. More cow-related factors were considered by Yan et al. [34], namely milk yield, days in milk, and parity, in a study with Chinese Holstein lactating cows. In both studies, the heat load thresholds were significantly affected by the animal physiological and behavior indicators. Though, under a daily farm routine, it is not feasible to monitor the mentioned indicators. For instance, the continuum tracking of an individual cow’s physiological and behavior indicators can be compromised due to technical issues (sensors displacement or total removal), requiring significant expenses on human and equipment resources (e.g., a high number of measurements were reported in studies evaluating painting scores; in Table 1). Under this perspective, it seems reasonable to disregard individual indicators (physiological and behavioral), focusing instead on the measurement of parameters already monitored by the farm system (e.g., milk production) and relying more on relatively inexpensive equipment, such as environmental sensors. Nevertheless, the animal individual response can be considered through mechanistic models as proposed by Berman [91]. The author developed an index based on data simulation of a mechanistic model considering the variety of animal-specific data (e.g., metabolic heat production, skin water loss, coat thickness, tissue and coat insulation). A correlation between respiratory heat loss (HER, [91]), air temperature, velocity and humidity was expressed by two regression equations. Furthermore, a similar mechanistic model was used to evaluate the accuracy of two indexes (THI and CCI) to predict the cow thermal status considering different cooling methods (e.g., fans and sprinklers; [89]). Devoe et al. [89] concluded that the index that accounted for the airspeed (CCI) was the most suitable to predict heat stress level of shaded cows regarding mitigation methods. As already mentioned, another possibility for adjusting the heat stress threshold is the use of machine learning. Ji et al. [90] calculated the thresholds considering the individual variance of body mass, age, and days in milk, as described in the following section.
The predictions of the mentioned bioclimatic indexes are estimations, always associated with a certain degree of uncertainty, that can be minimized by testing and validation of the indexes for the farm conditions, considering the management strategies (e.g., shade and cooling methods), and the animals’ physiological variables. Nowadays, research and development of full extended indexes can benefit from the available technological solutions and techniques to create a virtual environment for testing and refinement, e.g., through machine learning algorithms (Section 3.2) and/or by using mechanistic models (Section 3.3).
Table 1. Example of bioclimatic indexes and the corresponding input and output variables.
Table 1. Example of bioclimatic indexes and the corresponding input and output variables.
Study GoalPopulationInputsOutputsObservationsRef.
Temperature-humidity index (THI) developed for bull calvesFour Ayrshire bull calves (9 months old)Dry-bulb temperature; Wet-bulb temperature.Rectal temperatureOne equation. For five hours, each animal was kept inside a climate chamber. The trials were repeated 3 times per animal.[80]
Correlation between milk production and ambient temperature and humidity56 Holstein cows (with several stages of lactation and production levels ranging from 6 to 70 lb per day)Dry-bulb temperature; Wet-bulb temperature; Normal production level.Production levelOne equation. A good relationship between a THI index and milk production was obtained. A new equation was proposed considering besides air temperature and humidity also the normal production level. [92]
Adjusted THI for cattle, considering wind and solar radiationThree experiments with a varied number of animals (from 72 to 192) Air temperature; Relative humidity; Wind velocity; Solar radiation.Panting scoreOne equation. Required more than 2000 individual panting score assessments derived from ~12 d of observations.[7]
Linear regression equation to estimate respiration rate of no-shade feedlot cattleEight crossbred steersDry-bulb temperature; Relative humidity; Wind velocity; Solar radiation.Respiration rateTwo equations. Responses were studied during eight periods within 4-months. Animals randomly assigned to concrete surfaced pens with shade or no-shade option. [61]
Respiratory heat loss (HER)Simulation dataAir temperature; Relative humidity; Wind velocity; Animal-related factors (e.g., coat insulation and thickness)Respiratory heat lossLumped model. Outputs of simulations were used to produce estimates of thresholds of maximal respiratory response as a function of ambient conditions for different cows-related factors. [91]
Heat load index (HLI) Feedlot cattle for seven genotypes (more than 10,000 animals)Air temperature; Relative humidity; Wind velocity; Solar radiation; Animal-related factors (e.g., genotype, coat color, health status).Panting scoreTwo equations. Responses were studied for eight summers. Approximately 162 observations were made per animal (3 times per day for 54 days).[37]
Comprehensive climate index (CCI) for application under a wide range of environmental conditions (hot and cold)Livestock cattle (number not defined)Air temperature; Relative humidity; Wind velocity; Solar radiation.Dry Matter IntakeMultiple non-linear equations. Based on experimental results reported in the literature. Responses were studied for nine summers and six winters. The model performance was compared with wind-chill and heat indexes.[86]

3.2. Machine Learning

Most of the developed bioclimatic indexes assume either linear relationships between environmental factors and the physiological responses, or relationships with a specific form, which are still relatively simple representations of the heat stress on dairy cows. In recent years, several technologies have been developed allowing the collection of a large amount of data about these animals from a generalized use of sensors to automatic milking systems. With the increase in available data, it is also important to use methods that allow a better understanding as well as the treatment of large quantities of data to help a farmer run operations more efficiently. These methods leverage data to go beyond linear relationships and other simple models. Among them, are the machine learning (ML) tools [93].

3.2.1. Fundamentals of Machine Learning (ML)

Machine learning is a powerful concept, part of Artificial Intelligence, that enables systems to learn complex non-linear relationships in data without being explicitly programmed to do so [94,95]. By learning by themselves, machine learning systems also minimize bias regarding the expected relationships, such as between environmental factors and physiological responses [96]. Machine learning has been used in different areas from petroleum reservoir characterization [97] to predictions in the stock market [98]. ML has also been applied to assess dairy cow behavior as well as milk production [99,100], and ultimately the effect of heat stress on the cow’s body response [101].
Machine learning has three main categories: supervised, unsupervised, and reinforcement learning. Most studies dedicated to predicting dairy cow behavior are supported by supervised learning methods, thus, a brief description of these methods is provided.
Supervised learning means that the model is fed with a set of inputs for which the outputs are known. The program already knows the result for an initial set of conditions. The algorithm will then learn the necessary steps that allow it to go from the inputs to the outputs. This type of machine learning is one of the most prevalent and it tackles different scenarios: regression (outputs are real numbers) or classification (the outputs are categorical; [102]). Supervised learning algorithms include linear regression, logistic regression [103], naïve Bayes, Support-Vector machines [104], decision trees [105], and Artificial Neural Networks (ANN) as well as several variations of these and other entirely separate algorithms altogether. These algorithms can also be combined with different methods to improve their functionality.
These systems are data-driven so the right quality/quantity of data points is essential to have a reliable tool to attend to the problem. As such, the first requirement to implement this type of method is to have an adequate dataset. A part of this data (60% to 80%) will be used to train the algorithm. Once a model is trained, the ability of the model to predict new results is tested against new values that were not part of the training data set. The approach can be iterated upon and changed until the model shows a good prediction performance. At this point, the model can be used for new inputs for which the outputs are not known. Figure 1 shows a schematic representation of how the ML can be used to predict a heat stress event and help the farmer in choosing when to turn on or off the cooling techniques.
Building a highly accurate prediction model comes with multiple challenges such as which data and features to use, which algorithm to choose, how to deal with large amounts of data, as well as how to guarantee the performance of the model in a real-world context.

3.2.2. Prediction of Heat-Stressed Cows

As previously mentioned, the use of ML in the domain of cattle has already been reported in the literature. This chapter focuses on the use of these technologies to predict events or possible indicators of heat stress on cattle. A robust tool able to predict the conditions in which the animal will face heat stress is the desired output. This will provide a non-invasive method to prevent the animal from being exposed to extreme conditions while allowing more efficient management of the resources (water/energy) to cool down the animal.
In several studies, ML is used to predict physiological responses (outputs), from the environmental variables as well as other easy-to-measure inputs. Table 2 shows a summary of some machine learning studies and the corresponding input and output variables.
One of the first studies aiming to evaluate heat stress on heifers was presented by Brown-Brandl et al. [106]. This study considered different techniques to predict the physiological response (in the form of respiration rate) to evaluate if the animal was under heat stress. As inputs, several environmental parameters were considered (dry bulb temperature, dew point temperature, solar radiation, and wind speed) as well as the breed of the animal (average temperatures of hair coat surface in the afternoon; animal color). The authors concluded that different breeds are affected differently by environmental conditions, and as such, taking into account the breed is necessary to predict the effect of the different factors on thermal stress. In terms of models, it is shown that ANN is slightly better at predicting respiration rate than regressions. However, if more information is desired, other than simply the value of the physiological response, fuzzy inference systems (data-dependent) may be more useful. The authors also pointed out that even though these techniques are promising, the available data was not yet enough to lead to accurate predictions. Furthermore, they suggested that a factor accounting for heat accumulation could be a method for improving these models.
The work of Hernandez-Julio [101] also uses different ML tools to predict the physiological response of dairy cows (rectal temperature and respiratory rate) based on dry-bulb air temperature and relative humidity as inputs. Two ANNs are proposed to obtain the physiological response of the animal (one for each output), based on both experimental data and data from the literature. The latter avoids carrying out further experiments, hence minimizing the costs related to equipment and human resources.
Another example of using ML to predict the physiological response of the animal is the work presented by Gorczyca and Gebremedhina [96]. This study evaluated how the environmental factors (air temperature, relative humidity, solar radiation, and wind speed) influenced physiological responses (respiration rate, skin temperature, and vaginal temperature) and it also tried to rank the environmental factors according to their “contribution” on heat stress events. This study, once again, showed the usefulness of ML algorithms in predicting the physiological response of the animal. Besides, it indicated air temperature as the factor that had the highest impact on the physiological response, while wind speed had the lowest.
Sousa [107] performed a study to predict the rectal temperature (an indicator of heat stress) of feedlot cattle using the head surface temperature of the animal (IRT), dry bulb temperature, and wet bulb temperature. The predicted and measured rectal temperatures were classified on levels of thermal stress and compared with the classification based on traditional THI (temperature–humidity index). An ANN and a linear regression model were compared. The ANN led to models that are better at predicting the rectal temperature than standard correlations, in addition to allowing individual assessments.
Hempel [8] showed a different approach to the heat stress prediction problem. The goal was to infer the conditions inside the barn at any moment just by assessing the environmental conditions near it. Using the conditions inside the barn, the authors used empirical models to evaluate the comfort and discomfort of the animals—THI and ETIC (equivalent temperature index for cattle). Economic and environmental impacts were also estimated based on the heat stress events (heat stress risk).
Table 2. Example of machine learning studies and the corresponding input and output variables.
Table 2. Example of machine learning studies and the corresponding input and output variables.
Study GoalPopulationInputsOutputsAlgorithmsRef.
Evaluate the heat stress of cattle128 heifersEnvironmental data: dry bulb temperature, dew point temperature, solar radiation, wind speed. Animal related parameter: temperature of the hair coat color.Respiration rate.Regression models; Fuzzy inference systems; ANN.[106]
Predict the physiological response of dairy cowsHolstein dairy cows (experimental + literature data)Environmental data: dry-bulb air temperature, relative humidity.Rectal temperature; respiratory rate.Regression; ANN; Neurofuzzy networks.[101]
Effect of the environmental factors on physiological responses 19 dairy cowsEnvironmental data: air temperature; relative humidity, solar radiation, and wind speed.Respiration rate; Skin temperature; Vaginal temperature.Penalized linear regression; random forests; Gradient boosted machines; ANN.[96]
Predicting the heat stress for feedlot cattle26 Nellore steersEnvironmental data: dry and wet bulb temperature.
Physiological parameter: temperature of head surface.
Rectal temperature.Correlations; ANN.[107]
Evaluate the heat stress in naturally ventilated barns for dairy cows Outdoor conditions: temperature, relative humidity, zonal and meridional wind, sea level pressure, and global radiation;Conditions inside the husbandries: temperature, relative humidity, and wind components.Linear regression with and without regularization; random forest; ANN; Support-vector models.[8]
Definition of dynamic thresholds for heat stress alerts126 cowsEnvironmental data: minimum and mean ambient temperature. Body mass, days in milk, daily milk yields, and milk temperature.Heat stress thresholds were redefined for the herd taking into consideration the daily milk yield and milk temperature.Decision tree[90]
Evaluate the milk yield under different thermal conditionsHolstein-Friesian cowsAir temperature around cowsheds. Milk yieldANN[99]
Best cow treatment to improve the milk yielddairy cows in IndonesiaEnvironmental data: temperature, wind speed, and relative humidity. Physiological parameters: heart rate, body temperature.Milk yieldANN[108]
Prediction of the milk yield91 dairy cowsBarn environmental data: relative humidity and temperature. Days in milk of the cow.Daily milk yieldRandom forest [100]
Ji et al. [90] also used ML techniques to define dynamic thresholds for heat stress alerts with auto-calibration. Data to be used was collected from a robotic farm: body mass, days in milk, daily milk yields, and milk temperature, as well as ambient temperature (minimum and mean value). Heat stress thresholds were redefined for the herd taking into consideration the daily milk yield as well as the milk temperature. Then, at an individual scale, a decision tree (machine learning model) was used to artificially define new thresholds where specific groups were summarized as classification factors (age, body mass, and days in milk). Taking the minimum (representing night-time cooling conditions) and the mean temperature (daily thermal conditions), these models were able to predict new heat stress thresholds. The authors also stated that while a large quantity of data was used, it all came from a single farm. Therefore, data from other sources are desirable to generalize these conclusions.
Some studies do not deal with heat stress directly but report other parameters (like milk quality) that can be an indicator that the cow is under thermal stress. One example is the work of Bonieck et al. [99]. In this research, the authors used air temperature around cowsheds (maximum temperature of the day) to build an ANN capable of predicting milk yield under different thermal conditions.
Sugiono et al. [108] also used ML to develop a model for the selection of the best cow management to improve milk yield. Once again, the main goal was not to evaluate the heat stress, but it did take into consideration environmental data (temperature, wind speed, and relative humidity) and physiological aspects (heart rate and body temperature) to correlate with milk yield. A sensitive analysis was also performed, and it pointed to relative humidity, heart rate, environment temperature, and cow body temperature as the factors that had a higher effect on milk production. The authors still recommended the improvement of this model by adding more points, testing different learning algorithms, and including other factors such as age and weight, among others.
Bovo et al. [100] used a random forest algorithm to evaluate the daily milk yield of a single cow. The authors used data from dairy cows collected by automatic milking systems (AMSs) as well as the environmental conditions of the barn (relative humidity and temperature) that were incorporated in the form of THI. This algorithm considered the THI on the test day and on the previous five days. It was tested for the data set available and the authors reported that it could predict the daily milk yield with a relative error of just 18%.
Overall, these studies showed that machine learning can be very useful to help predict/monitor heat stress to which the animals are exposed. However, as some of these works have pointed out, much remains to be done. More data are necessary, as well as a better understanding of the critical factors (like accounting for heat accumulation) to predict heat stress. Once reliable tools to predict heat stress are available, it will be possible to trigger the cooling systems only when necessary and minimize the use of invasive techniques to obtain information from the animals. As mentioned by Gorczyca [96], even though this is a powerful set of tools it does not mean that these algorithms/models will be consistently the best option to predict heat stress. This is in part because computational and large amounts of data resources are necessary to train and optimize these methods but may not always be available. As an option, alternative mathematical models (mechanistic models) can be used to generate the necessary numerical data to feed the machine learning models. Different types of input variables can be assumed from environmental and animal data to numerical results obtained through mechanistic models.

3.3. Mechanistic Models

A mechanistic model can be defined as a mathematical model that correlates physical phenomena in a deterministic way. The mathematical models used to predict animals’ thermal responses are few and extremely restricted to the considered scenario (e.g., neglecting body region characteristics [109,110,111]). Even fewer models consider cattle thermoregulation mechanisms (e.g., panting, sweating; [112,113,114]). Nevertheless, the latter model [114] has the potential to simulate the dynamic thermal balance of the cow. As the main assumption, the animal body is assumed as one horizontal cylinder with closed ends, and the model has three layers: core, skin, and coat (model 1, Figure 2). As a lumped element model, the calculated loads at every time step assume a quasi-steady state. Furthermore, the model allows the study of a wide combination of environmental conditions (temperature, humidity, air velocity, and solar radiation). However, only one asymmetrical environment condition option is considered (i.e., exposed area to shadow or direct sunlight) and, for that reason, it is not possible to analyze the effect of non-uniform distribution of environmental conditions on cow thermal state (e.g., it is not possible to simulate the heat transfer between the body region of a laying cow and the ground). To approximate realistic scenarios, it is necessary to determine proper boundary conditions by body region. Additionally, another relevant requirement is the reference values used to characterize the neutral conditions (e.g., temperature by body layers) according to the cow’s physical conditions (e.g., age, days in milk).
The McGovern and Bruce model [114] could not be used to predict the cow thermal balance at low temperatures since cold-induced thermogenesis is neglected. This simplification can put at stake the accuracy of the analyses of cooling technologies’ performance, or, in some cases, the prediction of cow cooling during the night. Furthermore, proper cutaneous and respiratory evaporation rates must be considered [91,116], since the original model set some correlations (e.g., tidal volume of the respiratory system) and animal parameters (e.g., tissue thermal resistance) based on the available literature on different breeds [114], and, consequently, only the qualitative behavior of the numerical results were assessed. Berman [91] adjusted seven animal parameters in the model, specifically for the Holstein cow breed. The author concluded that this modification increased the accuracy of total skin and respiratory heat loss predictions. However, the described validation assumptions do not allow us to infer the accuracy of the cow thermal state predictions during highly transient ambient conditions. Nevertheless, these mechanistic models were used to develop a bioclimatic index considering animal-related factors [91] and to create contour maps with optimal cooling system recommendations throughout the United States [89].
At the surface of the cow body, the sensible and latent heat losses are generally ruled by convection (heat and mass) and radiation phenomena. For that reason, and to reduce the effect of thermal stress on dairy cattle, the main cooling technologies are shade structures to diminish incoming radiation, forced convection to increase heat/mass removal or water to remove heat by evaporation. To predict the evaporative and convective heat loss from a cow body, Gebremedhin and Wu [117] developed a one-dimensional model, considering the heat and mass transfer model along with the hair coat of a cow, in steady-state conditions. Several parameters can be studied as different levels of wetness, air velocity, ambient temperature, relative humidity, and hair properties. As a practical application, the model can provide insights into the effectiveness of evaporative cooling such as, for example, ventilated spaces [118] or water sprays coupled with fans [110]. Gebremedhin and Wu [118] studied the (sensible and latent) heat loss from cattle in a ventilated space occupied by 10 cows. It should be noted that the fluid flow around each cow is highly dependent on the air inlet velocity and the geometric features of the surrounding obstacles (i.e., chamber dimensions and other cows). Therefore, numerical simulations were conducted to characterize the fluid flow around the cattle using Computation Fluid Dynamics software. Therefore, the numerical results of fluid flow were used as inputs of the coupled model of heat and mass transfer through cow fur. The total heat loss from the cows changed from 215 to 710 W due to the different characteristics of the flow field surrounding the animals. A similar one-dimensional model was used by Chen et al. [110] to study the transient behavior of wetted fur (model 2, Figure 2). The authors estimated the drying time and heat removal as a function of ambient conditions (air temperature, air speed, humidity, and mean radiant temperature). Furthermore, the numerical results were used to develop a correlation for a control algorithm of a sprinkler–fan system. The equipment frequency was related to cooling load thresholds obtained for outdoor conditions. Moreover, the use of the control algorithm was estimated to reduce electricity and water consumption by 25% and 50%, respectively. This highlights the potential ability of mechanistic models to improve the performance of cooling systems while contributing to a more sustainable dairy industry.
An often-used mechanistic model to simulate heat transfer in human tissues is the Pennes’ bioheat model [119,120], which was the same used by Gebremedhin and Wu [115] to predict the udder heat loss in cows under different conditions of ambient temperature. At the udder skin (model 3, Figure 2), the heat was transferred to the environment by convection and eliminated by evaporation. At the core of the udder, a fixed temperature was assumed. The model quantifies the total heat loss, which can be useful to estimate the performance of cooling technologies that promote convection and/or evaporation [115]. Furthermore, this model can be used to study the thermal behavior of different body regions under different scenarios of air velocity and temperature.
The potential of artificial cooling methods to alleviate the heat stress of dairy cattle has been proven. However, the economic benefits of a particular cooling method depend on farm features and geographical location. Thus, the benefits/limitations should be assessed prior to the installation of any equipment [74,89]. For example, Herzog et al. [121] concluded that the advantage of using basket fans for heat abatement is slightly higher than the environmental costs associated with fan production and operation, highlighting the necessity of studies based on primary data regarding the effectiveness of fan cooling to improve cow productivity. Mechanistic models can also be used as a support tool to analyze the environmental impact of the equipment’s implementation. Based on numerical data, Devoe et al. [89] obtained multiple maps of the U.S. that help producers determine which cooling strategy is the most economical in their region.
The complexity of the mechanistic models (several input variables and equations) makes them difficult to be used by an ordinary end-user without a background in transfer phenomena [58]. However, and to overcome this problem, the mechanistic models can be integrated as predictive algorithms for controlling systems, running in the background, and being automatically fed by input variables measured through emergent monitoring technologies (e.g., sensors/wireless/cloud-based).
Table 3 shows a summary of some studies that used mechanistic models and the corresponding input and output variables.

4. Future Considerations

As a predictive algorithm, the mechanistic models have more degrees of freedom and flexibility to be easily adapted to ever-changing situations (e.g., days in milk of the cows) or to assess several types of cooling technologies (e.g., basket fans, sprinklers) than the bioclimatic indexes and machine learning algorithms.
The next step in the development of more robust mechanistic models is the incremental improvement of the thermal model complexity by considering a virtual cow with different body segments, following the approach often used in human thermoregulation models: fitting the physiological dimensions to a suitable geometry [115]. Furthermore, more layers can be considered in each body segment (i.e., core, muscle, fat, and skin), and a central core to which the heat of each body layer is transferred by blood flow [122]. Therefore, it is necessary to determine the distribution of the heat generated along body segments and layers due to different mechanisms (e.g., heat generated by external work occurs only in the muscle layer). Another relevant requirement is the definition of reference values of parameters/properties obtained in neutral conditions, such as the temperature of body layers, or local heat produced (metabolic heat), according to the cow’s physical conditions (e.g., age, days in milk).
The simulation of a countless number of scenarios with precise outcomes entails the definition of proper boundary conditions of heat and mass transfer phenomena. For instance, the fluid flow around the animal body is dependent on the animal posture (laying or standing), the location (inside/outside the barn), and the surrounding obstacles (trees or other cows), and it will be significantly different between body regions (e.g., due to geometry considerations, and hair coat density). This affects the net of heat and mass exchange between the cow skin and the environment and further studies should be carried out to assess realistic heat and mass transfer coefficients. Radiation is another relevant heat transfer phenomenon, which is significantly constrained by the surrounding surfaces’ thermal state (e.g., region–region, body–environment, and cow–cow body exchange). Representative boundary conditions of radiation should be studied, consisting, e.g., in the determination of suitable radiative coefficients distribution along the different body regions.
Additionally, the results of these mechanistic models combined with data collected from real case scenarios can be used as inputs to develop new and more robust machine learning models (as proposed in Figure 1). Machine learning can be a useful tool to predict heat stress conditions, but it requires significant quantities of data to make reliable predictions about any phenomena. Mechanistic models, as well as the generalized use of sensors, can be useful to obtain a great volume of important information on heat stress conditions, which may help to overcome the actual problems associated with the use of machine learning models. Besides, the continuous monitoring of several features associated with animal well-being and productivity (in a robotic farm, for example), may also be useful to monitor and improve the performance of these tools.

5. Conclusions

Under certain environmental conditions, only cooling systems are efficient to mitigate dairy cattle heat stress. The integration of predictive algorithms in the operation of these systems is a possible method of efficiently regulating environmental conditions while reducing the associated energy and water consumption. Three potential approaches to be used as predictive models were analyzed in this review.
Bioclimatic indexes have been studied for several years, and they were developed for different geographic locations, on varying diets and farm systems. From a practical perspective, the selection of a suitable bioclimate index for a farm implies carrying out a local study, which is time-consuming and can also be expensive. Furthermore, the typical bioclimatic indexes are based on average daily measurements, presenting direct relationships between the environmental factors. Additionally, they consider the general physiological conditions of the herd, rather than the individual or herd-specific characteristics. In a complementary way, machine learning and mechanistic models are two methods capable of predicting individual and herd responses, assuming more complex relationships between factors.
The application of machine learning to predict the cow’s discomfort level is a recent trend, with several studies using ML to predict physiological responses. The application of these models can provide a non-invasive tool that predicts the conditions that lead to heat stress in animals, providing information on when and for how long to use cooling types of equipment. Nevertheless, one must consider important limitations such as the apparent inability to understand the fundamental aspects of heat stress in dairy cattle and the need for large amounts of data, with more efficient and comprehensive models implying the acquisition of data from more sources. The use of an ML model in a specific farm implies, at least, the validation of the results and, in the worst-case scenario, carrying out a new set of experiments to fine-tune the model. As an alternative, mathematical models (mechanistic models) can be used to generate numerical data to feed machine learning models.
Mechanistic models are a less popular approach than bioclimatic indexes and machine learning but they are the most transversal ones. Their capacity to simulate the individual cow’s thermal state, exposed to countless dynamic ambient conditions, offers an advanced tool for research, development of new bioclimatic indexes, and training of machine learning algorithms. Currently, there are several mechanistic models that allow us to study at different scales (e.g., considering only the animal hair coat or the entire body of the cow), with the potential to evaluate the efficiency of cooling technologies or management strategies (e.g., early access to pasture).
We believe that the integration of suitable predictive models will be a step forward for dairy industry productivity, animal welfare, and the research and development of more efficient technologies for the sustainable use of water and energy.

Author Contributions

Conceptualization: S.F.N., M.C.F.S. and P.P.C.; Writing—Original Draft Preparation: S.F.N., M.C.F.S. and P.P.C.; Writing—Review and Editing: S.F.N., M.C.F.S., J.M.M., G.S. and P.P.C. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by LA/P/0045/2020 (ALiCE), UIDB/00532/2020 and UIDP/00532/2020 (CEFT), funded by national funds through FCT/MCTES (PIDDAC).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Dikmen, S.; Hansen, P.J. Is the temperature-humidity index the best indicator of heat stress in lactating dairy cows in a sub-tropical environment? J. Dairy Sci. 2009, 92, 109–116. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Idris, M.; Uddin, J.; Sullivan, M.; McNeill, D.M.; Phillips, C.J.C. Non-invasive physiological indicators of heat stress in cattle. Animals 2021, 11, 71. [Google Scholar] [CrossRef] [PubMed]
  3. Polsky, L.; von Keyserlingk, M.A.G. Invited review: Effects of heat stress on dairy cattle welfare. J. Dairy Sci. 2017, 100, 8645–8657. [Google Scholar] [CrossRef] [Green Version]
  4. Lacetera, N.; Bernabucci, U.; Scalia, D.; Basiricò, L.; Morera, P.; Nardone, A. Heat stress elicits different responses in peripheral blood mononuclear cells from brown swiss and holstein cows. J. Dairy Sci. 2006, 89, 4606–4612. [Google Scholar] [CrossRef] [Green Version]
  5. Lacerda, T.F.; Loureiro, B. Selecting thermotolerant animals as a strategy to improve fertility in holstein cows. Glob. J. Anim. Sci. Res. 2014, 3, 119–127. [Google Scholar]
  6. Belhadj Slimen, I.; Najar, T.; Ghram, A.; Abdrrabba, M. Heat stress effects on livestock: Molecular, cellular and metabolic aspects, a review. J. Anim. Physiol. Anim. Nutr. 2016, 100, 401–412. [Google Scholar] [CrossRef] [Green Version]
  7. Mader, T.L.; Davis, M.S.; Brown-Brandl, T. Environmental factors influencing heat stress in feedlot cattle. J. Anim. Sci. 2006, 84, 712–719. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Hempel, S.; Menz, C.; Pinto, S.; Galán, E.; Janke, D.; Estellés, F.; Müschner-Siemens, T.; Wang, X.; Heinicke, J.; Zhang, G.; et al. Heat stress risk in European dairy cattle husbandry under different climate change scenarios—Uncertainties and potential impacts. Earth Syst. Dyn. 2019, 10, 859–884. [Google Scholar] [CrossRef] [Green Version]
  9. Nguyen, T.T.; Bowman, P.J.; Haile-Mariam, M.; Pryce, J.E.; Hayes, B.J. Genomic selection for tolerance to heat stress in Australian dairy cattle. J. Dairy Sci. 2016, 99, 2849–2862. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. de Haas, Y.; Calus, M.; Veerkamp, R.; Wall, E.; Coffey, M.; Daetwyler, H.; Hayes, B.; Pryce, J. Improved accuracy of genomic prediction for dry matter intake of dairy cattle from combined European and Australian data sets. J. Dairy Sci. 2012, 95, 6103–6112. [Google Scholar] [CrossRef] [Green Version]
  11. Van Laer, E.; Moons, C.P.H.; Ampe, B.; Sonck, B.; Vandaele, L.; De Campeneere, S.; Tuyttens, F.A.M. Effect of summer conditions and shade on behavioural indicators of thermal discomfort in Holstein dairy and Belgian Blue beef cattle on pasture. Animal 2015, 9, 1536–1546. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Purwanto, B.P.; Abo, Y.; Sakamoto, R.; Furumoto, F.; Yamamoto, S. Diurnal patterns of heat production and heart rate under thermoneutral conditions in Holstein Friesian cows differing in milk production. J. Agric. Sci. 1990, 114, 139–142. [Google Scholar] [CrossRef]
  13. Peyraud, J.; Macleod, M. Study on Future of EU Livestock: How to Contribute to a Sustainable Agricultural Sector? Final Report. Available online: https://ec.europa.eu/info/food-farming-fisheries/key-policies/common-agricultural-policy/cmef/farmers-and-farming/future-eu-livestock-how-contribute-sustainable-agricultural-sector_en (accessed on 1 December 2020).
  14. Gunn, K.M.; Holly, M.A.; Veith, T.L.; Buda, A.R.; Prasad, R.; Rotz, C.A.; Soder, K.J.; Stoner, A.M.K. Projected heat stress challenges and abatement opportunities for U.S. milk production. PLoS ONE 2019, 14, e0214665. [Google Scholar] [CrossRef] [Green Version]
  15. Al-Qaisi, M.; Horst, E.; Kvidera, S.; Mayorga, E.; Timms, L.; Baumgard, L. Technical note: Developing a heat stress model in dairy cows using an electric heat blanket. J. Dairy Sci. 2019, 102, 684–689. [Google Scholar] [CrossRef] [Green Version]
  16. Curtis, A.; Scharf, B.; Eichen, P.; Spiers, D. Relationships between ambient conditions, thermal status, and feed intake of cattle during summer heat stress with access to shade. J. Therm. Biol. 2017, 63, 104–111. [Google Scholar] [CrossRef]
  17. Strickland, J.T.; Bucklin, R.A.; Nordstedt, R.A.; Beede, D.K.; Bray, D.R. Sprinkler and Fan Cooling System for Dairy Cows in Hot, Humid Climates. Appl. Eng. Agric. 1989, 5, 231–236. [Google Scholar] [CrossRef]
  18. Means, S.L.; Bucklin, R.A.; Nordstedt, R.A.; Beede, D.K.; Bray, D.R.; Wilcox, C.J.; Sanchez, W.K. Water Application Rates for a Sprinkler and Fan Dairy Cooling System in Hot, Humid Climates. Appl. Eng. Agric. 1992, 8, 375–379. [Google Scholar] [CrossRef]
  19. Chen, J.M.; Schütz, K.E.; Tucker, C.B.; Van Os, J. Cooling cows efficiently with sprinklers: Physiological responses to water spray. J. Dairy Sci. 2015, 98, 6925–6938. [Google Scholar] [CrossRef] [PubMed]
  20. West, J.W. Effects of Heat-Stress on Production in Dairy Cattle. J. Dairy Sci. 2003, 86, 2131–2144. [Google Scholar] [CrossRef]
  21. Rhoads, M.L.; Rhoads, R.P.; VanBaale, M.J.; Collier, R.J.; Sanders, S.R.; Weber, W.J.; Crooker, B.A.; Baumgard, L.H. Effects of heat stress and plane of nutrition on lactating Holstein cows: I. Production, metabolism, and aspects of circulating somatotropin. J. Dairy Sci. 2009, 92, 1986–1997. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Heinicke, J.; Hoffmann, G.; Ammon, C.; Amon, B.; Amon, T. Effects of the daily heat load duration exceeding determined heat load thresholds on activity traits of lactating dairy cows. J. Therm. Biol. 2018, 77, 67–74. [Google Scholar] [CrossRef] [PubMed]
  23. Heinicke, J.; Ibscher, S.; Belik, V.; Amon, T. Cow individual activity response to the accumulation of heat load duration. J. Therm. Biol. 2019, 82, 23–32. [Google Scholar] [CrossRef]
  24. Nienaber, J.; Hahn, G. Livestock production system management responses to thermal challenges. Int. J. Biometeorol. 2007, 52, 149–157. [Google Scholar] [CrossRef] [Green Version]
  25. Ferrazza, R.D.A.; Garcia, H.D.M.; Aristizábal, V.H.V.; Nogueira, C.D.S.; Veríssimo, C.J.; Sartori, J.R.; Sartori, R.; Ferreira, J.C.P. Thermoregulatory responses of Holstein cows exposed to experimentally induced heat stress. J. Therm. Biol. 2017, 66, 68–80. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Brown-Brandl, T.M.; Eigenberg, R.A.; Nienaber, J.A.; Hahn, G.L. Dynamic Response Indicators of Heat Stress in Shaded and Non- shaded Feedlot Cattle, Part 1: Analyses of Indicators. Biosyst. Eng. 2005, 90, 451–462. [Google Scholar] [CrossRef] [Green Version]
  27. Vizzotto, E.; Fischer, V.; Neto, A.T.; Abreu, A.; Stumpf, M.; Werncke, D.; Schmidt, F.; McManus, C. Access to shade changes behavioral and physiological attributes of dairy cows during the hot season in the subtropics. Animal 2015, 9, 1559–1566. [Google Scholar] [CrossRef] [Green Version]
  28. Daltro, D.D.S.; Fischer, V.; Alfonzo, E.P.M.; Dalcin, V.C.; Stumpf, M.T.; Kolling, G.J.; Da Silva, M.V.G.B.; McManus, C. Infrared thermography as a method for evaluating the heat tolerance in dairy cows. Rev. Bras. Zootec. 2017, 46, 374–383. [Google Scholar] [CrossRef] [Green Version]
  29. De Rensis, F.; Lopez-Gatius, F.; García-Ispierto, I.; Morini, G.; Scaramuzzi, R. Causes of declining fertility in dairy cows during the warm season. Theriogenology 2016, 91, 145–153. [Google Scholar] [CrossRef]
  30. Hoffmann, G.; Herbut, P.; Pinto, S.; Heinicke, J.; Kuhla, B.; Amon, T. Animal-related, non-invasive indicators for determining heat stress in dairy cows. Biosyst. Eng. 2019, 199, 83–96. [Google Scholar] [CrossRef]
  31. Can, E.; Vieira, A.; Battini, M.; Mattiello, S.; Stilwell, G. Consistency over time of animal-based welfare indicators as a further step for developing a welfare assessment monitoring scheme: The case of the Animal Welfare Indicators protocol for dairy goats. J. Dairy Sci. 2017, 100, 9194–9204. [Google Scholar] [CrossRef] [Green Version]
  32. Farooq, U.; Samad, H.A.; Shehzad, F.; Qayyum, A. Physiological responses of cattle to heat stress. World Appl. Sci. J. 2010, 8, 38–43. [Google Scholar]
  33. Vickers, L.; Burfeind, O.; von Keyserlingk, M.; Veira, D.; Weary, D.; Heuwieser, W. Technical note: Comparison of rectal and vaginal temperatures in lactating dairy cows. J. Dairy Sci. 2010, 93, 5246–5251. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Yan, G.; Liu, K.; Hao, Z.; Shi, Z.; Li, H. The effects of cow-related factors on rectal temperature, respiration rate, and temper-ature-humidity index thresholds for lactating cows exposed to heat stress. J. Therm. Biol. 2021, 100, 103041. [Google Scholar] [CrossRef] [PubMed]
  35. Nordlund, K.; Strassburg, P.; Bennett, T.; Oetzel, G.; Cook, N. Thermodynamics of standing and lying behavior in lactating dairy cows in freestall and parlor holding pens during conditions of heat stress. J. Dairy Sci. 2019, 102, 6495–6507. [Google Scholar] [CrossRef]
  36. Polsky, L.B.; Madureira, A.M.; Filho, E.L.D.; Soriano, S.; Sica, A.F.; Vasconcelos, J.L.; Cerri, R.L. Association between ambient temperature and humidity, vaginal temperature, and automatic activity monitoring on induced estrus in lactating cows. J. Dairy Sci. 2017, 100, 8590–8601. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Gaughan, J.B.; Mader, T.L.; Holt, S.M.; Lisle, A. A new heat load index for feedlot cattle1. J. Anim. Sci. 2008, 86, 226–234. [Google Scholar] [CrossRef] [Green Version]
  38. Yadav, B.; Singh, G.; Wankar, A. The use of infrared skin temperature measurements for monitoring heat stress and welfare of crossbred cattle. Indian J. Dairy Sci. 2017, 70, 127–131. [Google Scholar]
  39. Mormède, P.; Andanson, S.; Aupérin, B.; Beerda, B.; Guémené, D.; Malmkvist, J.; Manteca, X.; Manteuffel, G.; Prunet, P.; van Reenen, C.G.; et al. Exploration of the hypothalamic–pituitary–adrenal function as a tool to evaluate animal welfare. Physiol. Behav. 2007, 92, 317–339. [Google Scholar] [CrossRef] [PubMed]
  40. Möstl, E.; Palme, R. Hormones as indicators of stress. Domest. Anim. Endocrinol. 2002, 23, 67–74. [Google Scholar] [CrossRef]
  41. Herbut, P.; Angrecka, S. Relationship between THI level and dairy cows’ behaviour during summer period. Ital. J. Anim. Sci. 2017, 17, 226–233. [Google Scholar] [CrossRef] [Green Version]
  42. Pilatti, J.A.; Vieira, F.M.C.; Rankrape, F.; Vismara, E.S. Diurnal behaviors and herd characteristics of dairy cows housed in a compost-bedded pack barn system under hot and humid conditions. Animal 2019, 13, 399–406. [Google Scholar] [CrossRef] [Green Version]
  43. Allen, J.; Hall, L.; Collier, R.; Smith, J. Effect of core body temperature, time of day, and climate conditions on behavioral patterns of lactating dairy cows experiencing mild to moderate heat stress. J. Dairy Sci. 2015, 98, 118–127. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Orihuela, A. Some factors affecting the behavioural manifestation of oestrus in cattle: A review. Appl. Anim. Behav. Sci. 2000, 70, 1–16. [Google Scholar] [CrossRef]
  45. Santos, V.; Carvalho, P.; Maia, C.; Carneiro, B.; Valenza, A.; Fricke, P. Fertility of lactating Holstein cows submitted to a Double-Ovsynch protocol and timed artificial insemination versus artificial insemination after synchronization of estrus at a similar day in milk range. J. Dairy Sci. 2017, 100, 8507–8517. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. De Rensis, F.; Scaramuzzi, R.J. Heat stress and seasonal effects on reproduction in the dairy cow—A review. Theriogenology 2003, 60, 1139–1151. [Google Scholar] [CrossRef]
  47. Roth, Z.; Arav, A.; Bor, A.; Zeron, Y.; Braw-Tal, R.; Wolfenson, D. Improvement of quality of oocytes collected in the autumn by enhanced removal of impaired follicles from previously heat-stressed cows. Reproduction 2001, 122, 737–744. [Google Scholar] [CrossRef] [PubMed]
  48. Silanikove, N. Effects of heat stress on the welfare of extensively managed domestic ruminants. Livest. Prod. Sci. 2000, 67, 1–18. [Google Scholar] [CrossRef]
  49. Kovács, L.; Kézér, F.L.; Bakony, M.; Jurkovich, V.; Szenci, O. Lying down frequency as a discomfort index in heat stressed Holstein bull calves. Sci. Rep. 2018, 8, 15065. [Google Scholar] [CrossRef]
  50. Ammer, S.; Lambertz, C.; Gauly, M. Is reticular temperature a useful indicator of heat stress in dairy cattle? J. Dairy Sci. 2016, 99, 10067–10076. [Google Scholar] [CrossRef] [Green Version]
  51. National Research Council. Effect of Environment on Nutrient Requirements of Domestic Animals; National Academies Press: Washington, DC, USA, 1981; p. 78. ISBN 0-309-53374-0. [Google Scholar] [CrossRef]
  52. Bernabucci, U.; Basiricò, L.; Morera, P.; DiPasquale, D.; Vitali, A.; Cappelli, F.P.; Calamari, L. Effect of summer season on milk protein fractions in Holstein cows. J. Dairy Sci. 2015, 98, 1815–1827. [Google Scholar] [CrossRef] [Green Version]
  53. Hill, D.; Wall, E. Dairy cattle in a temperate climate: The effects of weather on milk yield and composition depend on management. Animal 2015, 9, 138–149. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Liu, Z.; Ezernieks, V.; Wang, J.; Arachchillage, N.W.; Garner, J.B.; Wales, W.J.; Cocks, B.G.; Rochfort, S. Heat Stress in Dairy Cattle Alters Lipid Composition of Milk. Sci. Rep. 2017, 7, 961. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. National Research Council. Nutrient Requirements of Dairy Cattle; National Academies Press: Washington, DC, USA, 2001; p. 138. ISBN 978-0-309-06997-7. [Google Scholar] [CrossRef] [Green Version]
  56. Van Laer, E.; Tuyttens, F.; Ampe, B.; Sonck, B.; Moons, C.P.H.; Vandaele, L. Effect of summer conditions and shade on the production and metabolism of Holstein dairy cows on pasture in temperate climate. Animal 2015, 9, 1547–1558. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Ji, B.; Banhazi, T.; Perano, K.; Ghahramani, A.; Bowtell, L.; Wang, C.; Li, B. A review of measuring, assessing and mitigating heat stress in dairy cattle. Biosyst. Eng. 2020, 199, 4–26. [Google Scholar] [CrossRef]
  58. Rashamol, V.P.; Sejian, V.; Pragna, P.; Lees, A.M.; Bagath, M.; Krishnan, G.; Gaughan, J.B. Prediction models, assessment methodologies and biotechnological tools to quantify heat stress response in ruminant livestock. Int. J. Biometeorol. 2019, 63, 1265–1281. [Google Scholar] [CrossRef] [Green Version]
  59. Müschner-Siemens, T.; Hoffmann, G.; Ammon, C.; Amon, T. Daily rumination time of lactating dairy cows under heat stress conditions. J. Therm. Biol. 2020, 88, 102484. [Google Scholar] [CrossRef]
  60. Chung, H.; Li, J.; Kim, Y.; Van Os, J.M.; Brounts, S.H.; Choi, C.Y. Using implantable biosensors and wearable scanners to monitor dairy cattle’s core body temperature in re-al-time. Comput. Electron. Agric. 2020, 174, 105453. [Google Scholar] [CrossRef]
  61. Eigenberg, R.A.; Nienaber, J.A.; Hahn, G.L. Dynamic response indicators of heat stress in shaded and non-shadedfeedlot cattle, Part 2: Predictive Relationships. Biosyst. Eng. 2005, 91, 111–118. [Google Scholar] [CrossRef] [Green Version]
  62. Sellier, N.; Guettier, E.; Staub, C. A Review of Methods to Measure Animal Body Temperature in Precision Farming. Am. J. Agric. Sci. Technol. 2014, 2, 74–99. [Google Scholar] [CrossRef]
  63. Rungruang, S.; Collier, J.; Rhoads, R.; Baumgard, L.; De Veth, M.; Collier, R. A dose-response evaluation of rumen-protected niacin in thermoneutral or heat-stressed lactating Holstein cows. J. Dairy Sci. 2014, 97, 5023–5034. [Google Scholar] [CrossRef] [Green Version]
  64. Kunc, P.; Knizkova, I. The use of infrared thermography in livestock production and veterinary field. In Infrared Thermog-Raphy: Recent Advances and Future Trends; Bentham Science Publisher: Sharjah, United Arab Emirates, 2012; pp. 85–101. [Google Scholar]
  65. Unruh, E.M.; Theurer, M.E.; White, B.J.; Larson, R.L.; Drouillard, J.S.; Schrag, N. Evaluation of infrared thermography as a diagnostic tool to predict heat stress events in feedlot cattle. Am. J. Veter-Res. 2017, 78, 771–777. [Google Scholar] [CrossRef]
  66. Koltes, J.E.; Koltes, D.A.; Mote, B.E.; Tucker, J.; Hubbell, D.S. Automated collection of heat stress data in livestock: New technologies and opportunities. Transl. Anim. Sci. 2018, 2, 319–323. [Google Scholar] [CrossRef] [Green Version]
  67. Cantor, M.C.; Costa, J.H.C.; Bewley, J.M. Impact of Observed and Controlled Water Intake on Reticulorumen Temperature in Lactating Dairy Cattle. Animals 2018, 8, 194. [Google Scholar] [CrossRef] [Green Version]
  68. Eslamizad, M.; Lamp, O.; Derno, M.; Kuhla, B. The control of short-term feed intake by metabolic oxidation in late-pregnant and early lactating dairy cows exposed to high ambient temperatures. Physiol. Behav. 2015, 145, 64–70. [Google Scholar] [CrossRef]
  69. Borchers, M.R.; Chang, Y.M.; Proudfoot, K.L.; Wadsworth, B.A.; Stone, A.E.; Bewley, J.M. Machine-learning-based calving prediction from activity, lying, and ruminating behaviors in dairy cattle. J. Dairy Sci. 2017, 100, 5664–5674. [Google Scholar] [CrossRef] [PubMed]
  70. Eigenberg, R.A.; Hahn, G.L.; Nienaber, J.A.; Brown-Brandl, T.M.; Spiers, D.E. Development of a new respiration rate monitor for cattle. Trans. ASAE 2000, 43, 723–728. [Google Scholar] [CrossRef]
  71. Gaughan, J.B.; Mader, T.L. Body temperature and respiratory dynamics in un-shaded beef cattle. Int. J. Biometeorol. 2014, 58, 1443–1450. [Google Scholar] [CrossRef] [PubMed]
  72. Gaughan, J.B.; Mader, T.L.; Holt, S.M.; Sullivan, M.L.; Hahn, G.L. Assessing the heat tolerance of 17 beef cattle genotypes. Int. J. Biometeorol. 2010, 54, 617–627. [Google Scholar] [CrossRef]
  73. Min, L.; Li, D.; Tong, X.; Nan, X.; Ding, D.; Xu, B.; Wang, G. Nutritional strategies for alleviating the detrimental effects of heat stress in dairy cows: A review. Int. J. Biometeorol. 2019, 63, 1283–1302. [Google Scholar] [CrossRef] [PubMed]
  74. Armstrong, D. Heat Stress Interaction with Shade and Cooling. J. Dairy Sci. 1994, 77, 2044–2050. [Google Scholar] [CrossRef]
  75. Drwencke, A.M.; Tresoldi, G.; Stevens, M.M.; Narayanan, V.; Carrazco, A.V.; Mitloehner, F.M.; Pistochini, T.; Tucker, C.B. Innovative cooling strategies: Dairy cow responses and water and energy use. J. Dairy Sci. 2020, 103, 5440–5454. [Google Scholar] [CrossRef] [PubMed]
  76. Ji, B.; Banhazi, T.; Ghahramani, A.; Bowtell, L.; Wang, C.; Li, B. Modelling of heat stress in a robotic dairy farm. Part 1: Thermal comfort indices as the indicators of production loss. Biosyst. Eng. 2019, 199, 27–42. [Google Scholar] [CrossRef]
  77. Wijffels, G.; Sullivan, M.; Gaughan, J. Methods to quantify heat stress in ruminants: Current status and future prospects. Methods 2020, 186, 3–13. [Google Scholar] [CrossRef] [PubMed]
  78. Pinto, S.; Hoffmann, G.; Ammon, C.; Amon, T. Critical THI thresholds based on the physiological parameters of lactating dairy cows. J. Therm. Biol. 2020, 88, 102523. [Google Scholar] [CrossRef]
  79. Thom, E.C. The Discomfort Index. Weatherwise 1959, 12, 57–61. [Google Scholar] [CrossRef]
  80. Bianca, W. Relative Importance of Dry- and Wet-Bulb Temperatures in Causing Heat Stress in Cattle. Nature 1962, 195, 251–252. [Google Scholar] [CrossRef]
  81. Johnson, H.D. Environmental temperature and lactation (with special reference to cattle). Int. J. Biometeorol. 1965, 9, 103–116. [Google Scholar] [CrossRef]
  82. Gorniak, T.; Meyer, U.; Südekum, K.-H.; Dänicke, S. Impact of mild heat stress on dry matter intake, milk yield and milk composition in mid-lactation Holstein dairy cows in a temperate climate. Arch. Anim. Nutr. 2014, 68, 358–369. [Google Scholar] [CrossRef]
  83. Hammami, H.; Bormann, J.; M’Hamdi, N.; Montaldo, H.; Gengler, N. Evaluation of heat stress effects on production traits and somatic cell score of Holsteins in a temperate environment. J. Dairy Sci. 2013, 96, 1844–1855. [Google Scholar] [CrossRef] [Green Version]
  84. Lees, J.C.; Lees, A.; Gaughan, J. Developing a heat load index for lactating dairy cows. Anim. Prod. Sci. 2018, 58, 1387. [Google Scholar] [CrossRef]
  85. Wang, X.; Gao, H.; Gebremedhin, K.G.; Bjerg, B.; Van Os, J.; Tucker, C.; Zhang, G. A predictive model of equivalent temperature index for dairy cattle (ETIC). J. Therm. Biol. 2018, 76, 165–170. [Google Scholar] [CrossRef] [PubMed]
  86. Mader, T.L.; Johnson, L.J.; Gaughan, J. A comprehensive index for assessing environmental stress in animals1. J. Anim. Sci. 2010, 88, 2153–2165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Ji, B.; Banhazi, T.; Ghahramani, A.; Bowtell, L.; Wang, C.; Li, B. Modelling of heat stress in a robotic dairy farm. Part 4: Time constant and cumulative effects of heat stress. Biosyst. Eng. 2020, 199, 73–82. [Google Scholar] [CrossRef]
  88. Yan, G.; Li, H.; Zhao, W.; Shi, Z. Evaluation of thermal indices based on their relationships with some physiological responses of housed lactating cows under heat stress. Int. J. Biometeorol. 2020, 64, 2077–2091. [Google Scholar] [CrossRef]
  89. DeVoe, K.R.; Hoff, S.J.; Ramirez, B.C.; Baumgard, L.H. Climate Dependent Heat Stress Mitigation Modeling for Dairy Cattle Housing. In Proceedings of the 2017 ASABE Annual International Meeting, Spokane, WA, USA, 16–19 July 2017. [Google Scholar]
  90. Ji, B.; Banhazi, T.; Ghahramani, A.; Bowtell, L.; Wang, C.; Li, B. Modelling of heat stress in a robotic dairy farm. Part 2: Identifying the specific thresholds with production factors. Biosyst. Eng. 2019, 199, 43–57. [Google Scholar] [CrossRef]
  91. Berman, A. Estimates of heat stress relief needs for Holstein dairy cows1. J. Anim. Sci. 2005, 83, 1377–1384. [Google Scholar] [CrossRef]
  92. Berry, I.L.; Shanklin, M.D.; Johnson, A.H.D. Dairy Shelter Design Based on Milk Production Decline as Affected by Temperature and Humidity. Trans. ASAE 1964, 7, 0329–0331. [Google Scholar] [CrossRef]
  93. Hudson, C.; Kaler, J.; Down, P. Use of big data in cattle practice. Practice 2018, 40, 396–410. [Google Scholar] [CrossRef]
  94. Frank, M.; Drikakis, D.; Charissis, V. Machine-learning methods for computational science and engineering. Computation 2020, 8, 15. [Google Scholar] [CrossRef] [Green Version]
  95. Kotsiantis, S.B.; Zaharakis, I.D.; Pintelas, P.E. Machine learning: A review of classification and combining techniques. Artif. Intell. Rev. 2006, 26, 159–190. [Google Scholar] [CrossRef]
  96. Gorczyca, M.T.; Gebremedhin, K.G. Ranking of environmental heat stressors for dairy cows using machine learning algo-rithms. Comput. Electron. Agric. 2020, 168, 105124. [Google Scholar] [CrossRef]
  97. Anifowose, F.A.; Labadin, J.; Abdulraheem, A. Ensemble machine learning: An untapped modeling paradigm for petro-leum reservoir characterization. J. Pet. Sci. Eng. 2017, 151, 480–487. [Google Scholar] [CrossRef]
  98. Krollner, B.; Vanstone, B.; Finnie, G. Financial Time Series Forecasting with Machine Learning Techniques: A Survey; Computational and machine learning; European Symposium on Artificialneural Networks: Bruges, Belgium, 2010; pp. 25–30. [Google Scholar]
  99. Boniecki, P.; Lipiński, M.; Koszela, K.; Przybył, J. Neural prediction of cows milk yield according to environment tem-perature. Afr. J. Biotechnol. 2013, 12, 4707–4712. [Google Scholar] [CrossRef] [Green Version]
  100. Bovo, M.; Agrusti, M.; Benni, S.; Torreggiani, D.; Tassinari, P. Random Forest Modelling of Milk Yield of Dairy Cows under Heat Stress Conditions. Animals 2021, 11, 1305. [Google Scholar] [CrossRef]
  101. Hernández-Julio, Y.F.; Yanagi, T., Jr.; Pires, M.D.F.; Lopes, M.A.; De Lima, R.R. Models for Prediction of Physiological Responses of Holstein Dairy Cows. Appl. Artif. Intell. 2014, 28, 766–792. [Google Scholar] [CrossRef]
  102. Jain, V.K. Machine Learning; Khanna Publishing House: Delhi, India, 1990; pp. 1–108. [Google Scholar]
  103. Ruczinski, I.; Kooperberg, C.; Leblanc, M. Logic Regression. J. Comput. Graph. Stat. 2003, 12, 475–511. [Google Scholar] [CrossRef]
  104. Maimon, O.; Rokach, L. Data Mining and Knowledge Discovery Handbook; Springer: New York, NY, USA, 2005; pp. 149–164. [Google Scholar] [CrossRef]
  105. Gehrke, J.; Ramakrishnan, R.; Ganti, V. Rainforest—A framework for fast decision tree construction of large datasets. Data Min. Knowl. Discov. 2000, 4, 127–162. [Google Scholar] [CrossRef]
  106. Brown-Brandl, T.; Jones, D.; Woldt, W. Evaluating modelling techniques for cattle heat stress prediction. Biosyst. Eng. 2005, 91, 513–524. [Google Scholar] [CrossRef]
  107. de Sousa, R.V.; Rodrigues, A.V.D.S.; de Abreu, M.G.; Tabile, R.A.; Martello, L.S. Predictive model based on artificial neural network for assessing beef cattle thermal stress using weather and physiological variables. Comput. Electron. Agric. 2018, 144, 37–43. [Google Scholar] [CrossRef]
  108. Sugiono, S.; Soenoko, R.; Andriani, D.P. Analysis the relationship of physiological, environmental, and cow milk productivity using AI. In Proceedings of the 2016 International Conference on Data and Software Engineering (ICoDSE), Denpasar, Indonesia, 26–27 May 2016. [Google Scholar]
  109. Turnpenny, J.; Wathes, C.; Clark, J.; McArthur, A. Thermal balance of livestock: 2. Applications of a parsimonious model. Agric. For. Meteorol. 2000, 101, 29–52. [Google Scholar] [CrossRef]
  110. Chen, E.; Narayanan, V.; Pistochini, T.; Rasouli, E. Transient simultaneous heat and mass transfer model to estimate drying time in a wetted fur of a cow. Biosyst. Eng. 2020, 195, 116–135. [Google Scholar] [CrossRef]
  111. Gebremedhin, K.G.; Wu, B.; Perano, K. Modeling conductive cooling for thermally stressed dairy cows. J. Therm. Biol. 2016, 56, 91–99. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  112. McArthur, A. Thermal interaction between animal and microclimate: A comprehensive model. J. Theor. Biol. 1987, 126, 203–238. [Google Scholar] [CrossRef]
  113. Thompson, V.A.; Sainz, R.D.; Strathe, A.B.; Rumsey, T.R.; Fadel, J.G. The evaluation of a dynamic, mechanistic, thermal balance model for Bos indicus and Bos taurus. J. Agric. Sci. 2013, 152, 483–496. [Google Scholar] [CrossRef] [Green Version]
  114. McGovern, R.; Bruce, J. AP—Animal Production Technology: A Model of the Thermal Balance for Cattle in Hot Conditions. J. Agric. Eng. Res. 2000, 77, 81–92. [Google Scholar] [CrossRef]
  115. Gebremedhin, K.G.; Wu, B. Modeling heat loss from the udder of a dairy cow. J. Therm. Biol. 2016, 59, 34–38. [Google Scholar] [CrossRef] [Green Version]
  116. Maia, A.S.C.; Da Silva, R.G.; Loureiro, C.M.B. Latent heat loss of Holstein cows in a tropical environment: A prediction model. Rev. Bras. Zootec. 2008, 37, 1837–1843. [Google Scholar] [CrossRef] [Green Version]
  117. Gebremedhin, K.G.; Wu, B. A model of evaporative cooling of wet skin surface and fur layer. J. Therm. Biol. 2001, 26, 537–545. [Google Scholar] [CrossRef]
  118. Gebremedhin, K.; Wu, B. Characterization of flow field in a ventilated space and simulation of heat exchange between cows and their environment. J. Therm. Biol. 2003, 28, 301–319. [Google Scholar] [CrossRef]
  119. Malaquias, A.F.; Neves, S.; Campos, J.M. The impact of water on firefighter protective clothing thermal performance and steam burn occurrence in firefighters. Fire Saf. J. 2022, 127, 103506. [Google Scholar] [CrossRef]
  120. Das, K.; Mishra, S.C. Study of thermal behavior of a biological tissue: An equivalence of Pennes bioheat equation and Wulff continuum model. J. Therm. Biol. 2014, 45, 103–109. [Google Scholar] [CrossRef]
  121. Herzog, A.; Winckler, C.; Hörtenhuber, S.; Zollitsch, W. Environmental impacts of implementing basket fans for heat abatement in dairy farms. Animal 2021, 15, 100274. [Google Scholar] [CrossRef]
  122. Stolwijk, J.A.J. A Mathematical Model of Physiological Temperature Regulation in Man; Report number: NASA-CR-1855; NASA: Washington, DC, USA, 1971.
Figure 1. General tasks associated with the implementation of ML techniques to predict the herd thermal state.
Figure 1. General tasks associated with the implementation of ML techniques to predict the herd thermal state.
Vetsci 09 00416 g001
Figure 2. Representation of three independent mechanistic models developed for different zones of the cow: entire body (model 1, [114]), coat (model 2, [110]), and udder (model 3, [115]).
Figure 2. Representation of three independent mechanistic models developed for different zones of the cow: entire body (model 1, [114]), coat (model 2, [110]), and udder (model 3, [115]).
Vetsci 09 00416 g002
Table 3. Example of mechanistic model studies and the corresponding input and output variables.
Table 3. Example of mechanistic model studies and the corresponding input and output variables.
Model DescriptionMain Mathematical AssumptionsInputsOutputsObservationsRef.
Thermal balance for cattle in hot conditions.Three node model: core, skin, and coat. Main transfer phenomena at the cow surface (skin + hair): heat transfer by convection and radiation, and mass transfer by convection. Main thermoregulation mechanisms: panting and sweating.Environmental conditions: temperature, humidity, air velocity, solar radiation.
Animal-related parameters: e.g., weight, metabolic heat, body-specific heat, coat reflection coefficient and thickness.
Core, skin, and coat temperature. Sensible and heat loss from respiration. Stored heat. Latent heat loss from the skin.Only qualitative behavior of the numerical results was assessed.[114]
Thermal balance for Holstein cows in hot conditions.Based on [118]. Additionally, the author adjusted several animal-related parameters.Based on [118].Based on [118].Improvement of the accuracy of total skin and respiratory heat loss prediction.[91]
Thermal balance of livestock.Three node model: core, skin, and coat. Main transfer phenomena at the cow surface: convection, evaporation, radiation, and solar radiation gain (for animals outdoors). Furthermore, considers the rain effect. Physiological responses: vasomotor action, sweating and panting.Environmental conditions: temperature, humidity, air velocity, precipitation, direct and diffuse solar radiation. Animal-related parameters: e.g., tissues thermal resistance. Skin and coat temperature
Sensible and latent heat loss.
Simplification of the physical and physiological mechanisms to simulate long data sets for climate change impact analysis.[109]
Simulation of udder heat loss.One dimensional approach (heat transfer through skin; from core to ambient). Main phenomena at the skin surface: convection and sweat evaporation. Main phenomena through the skin: conduction, convection (heating by infused blood flow), and metabolic heat production.Environmental conditions: air temperature and velocity. Animal-related factors: e.g., tissue density and specific heat, metabolic heat production.Udder skin temperature. Evaporative heat loss from the udder skin. Convective heat loss from the udder skin.The approach can be used to study the heat loss of other body zones and the performance of cooling technologies (e.g., fans).[115]
Heat and mass transfer model to estimate drying time of a wetted fur.One dimensional approach. Simulation domain: hair coat. Main phenomena: heat conduction, diffusion of water vapor, and evaporation.Environmental conditions: air temperature, humidity and velocity. Animal-related factors: e.g., tissue thermal resistance, fur thermal conductivity, coat thickness.Skin temperature. Total heat flux at the skin and coat surfaces. Water mass fraction.It can be used to study the efficiency of water sprays coupled with fan-induced air flow.[110]
Heat loss from cattle randomly distributed along a ventilated barn.Domain: ventilated space occupied by 10 cows.
Fluid flow fields characterized through 3-dimensional simulation. Cows thermal balance calculated through a coupled heat and mass transfer model (based on [114,121]).
Environmental conditions: air temperature, humidity, and air velocity. Animal-related factors: e.g., tissue thermal resistance, fur thermal conductivity, coat thickness, and animal position inside the barn.Fluid field around each cow. Skin temperature. Total heat loss for each cow convective and radiant heat losses, sensible and latent heat components).The approach can be used to obtain realistic convective heat and mass transfer coefficients, assuming different cows’ dimensions and spatial distribution.[118]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Neves, S.F.; Silva, M.C.F.; Miranda, J.M.; Stilwell, G.; Cortez, P.P. Predictive Models of Dairy Cow Thermal State: A Review from a Technological Perspective. Vet. Sci. 2022, 9, 416. https://doi.org/10.3390/vetsci9080416

AMA Style

Neves SF, Silva MCF, Miranda JM, Stilwell G, Cortez PP. Predictive Models of Dairy Cow Thermal State: A Review from a Technological Perspective. Veterinary Sciences. 2022; 9(8):416. https://doi.org/10.3390/vetsci9080416

Chicago/Turabian Style

Neves, Soraia F., Mónica C. F. Silva, João M. Miranda, George Stilwell, and Paulo P. Cortez. 2022. "Predictive Models of Dairy Cow Thermal State: A Review from a Technological Perspective" Veterinary Sciences 9, no. 8: 416. https://doi.org/10.3390/vetsci9080416

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop