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Mshelia, W. P., Abdussamad, A. M., Onoja, I. I., Victoria, S.Q., & Richard, E. E. (2012). Husbandry and Management Practices in Domestic horses in Northern Nigeria and their Clinical Implications. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: This study was conducted to identify common husbandry and management practices associated with domestic horses in Northern Nigeria. Fifty (50) of the horse was purposely selected as units of analysis. Primary data was generated by means of a pre-tested, semi-structured questionnaire administered to the sampled respondents. A simple inductive statistics was applied to the primary data. The study revealed that the whole facilities studied 50(100%) had a prior experience with horses. A large number of horses, mostly West African Dongola and West African Barb are kept solely for pleasure or ceremonial purposes (60%). While the other breeds of horses like Argentine (6%) and South Africa polo ponies (2%) are kept for polo. Recently, the Sudan country-bred (4%) and Western Sudan pony (6%) have found a place in West African polo. Other breeds found within the facilities studied are Argentine criollo; Nigerian ponies and various crosses. Only 10% of the facilities had breeding stocks with only 2% carrying out artificial insemination while 8% do natural mating. The housing management system includes stables (40%) and open fields (60%) where horses are tethered. Bedding materials includes straws (50%); sand (20%) and wood shavings (30%). Feed grade provided include a combination of rations-bran; cracked grain and hay (40%), Bran; cracked grain and legumes (48%) and Bran and hay (12%), all feed combination administered along with fresh grass. Watering and feeding practices involves provision of feed and water twice daily (50%) and while others provide it adlib (25%). Feeding horses with various additives accounted for 19% of the studied facilities. The health status as shown by the body condition score ranges from II-IV/V (88%) of the population studied. Routine dental care is regular (30%) with all the facilities while others (70%) are not irregular. Grooming is common in all the facilities especially within the performance horse circle. Routine hoof care including trimming and shoeing is common in 26% of the facilities while hoof trimming without shoeing is a common practice in 74% of the facilities. Orthodox medicine practiced in 80% of the studied area. While ethnoveterinary consist of 10%, while a combination of orthodox and ethnoveterinary medicine was common in 10% of the study area. Vaccination against African horse sickness equine influenza and tetanus is common in the various equine communities.Though 16% of the population do not vaccinate against any known disease. Parasite control program include pasture hygiene (4%); interval dosing (10%); continuous in-feed (4%); selective dosing (40%) and strategic dosing constitute 42%. Exercise is a common practice but intensity and duration is not strictly adhered to especially during tendon injuries. Manure management differs from facility to facility- some dispose manure within the facilities (40%) while others dispose it outside the facilities (60%). A number of clinical signs like limping, coughing, ocular and nasal discharge, swellings on the body, abnormal mucous membrane, fever, ventral oedema and reluctance to move, foul respiratory odour was observed. Clinical cases like laminitis; pigeon fever; bran disease; colic; African horse sickness; exertional rhabdomyolysis; sinusitis; piroplasmosis; dermatomycosis and tumours was observed. KW -
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Novotný, F., Noskovič, ová, J., Valocký, I., Pošivák, J., Boldižár, M., et al. (2012). Differences of biochemical and haematological indices in the aging process in cold-blooded horses Norik Muráň type. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The aim of was to compare of biochemical and haematological parameters in the aging process in a cold-blooded mares breed Norik Muráň type. 27 of breeding mares Norik Muráň type without pathological symptoms in horse breeding farm in Dobšiná (Slovakia) were used in this study. Mares were divided by age into four groups: A (n = 7, 5-8 years), B (n = 6, 9-15), C (n = 7, 16-20) and D (n = 7, 21-23). Blood samples were collected from v. jugularis externa by needles (Vacutainer ® Precision Glide ™, BD Diagnostics, USA) in serum tubes (Serum-SST TM II Advance, BD Diagnostics, USA) in the morning hours, kept at 8 to 10 °C and analyzed as soon as possible. Biochemical parameters of blood serum like aspartate aminotransferase (AST), alkaline phosphatase (ALP), creatinine (CREA), urea (Urea), albumin (ALB) and glucose (Glu) were analyzed using biochemical analyzer Cobas c 111 (Roche, Switzerland). Reference values were determined by Laboratory of Clinical Biochemistry and Haematology (UVMF, Košice). Were used a same nutrition for all mares. The results were statistically processed using Student\'s t-test. The concentrations of AST decreased in mares with aging (A=5.69 ± 1.13 μkat/l; B=5.36 ± 0.9 μkat/l; C=5.13 ± 1.1 μkat/l), but in the oldest mares (D=5.88 ± 1.37 μkat/l). were higher than the youngest age group A. Were found no significant differences between groups (P> 0,05). The concentrations of ALP increased with age (A=2.47 ± 0.3 μkat/l; C=2.66 ± 0.43 μkat/l; D=2.77 ± 1.17 μkat/l), but in the middle age mares were found (B= 2;44 ± 0.46 μkat/l) (P> 0,05). Crea concentrations had a decreasing trend (A=139.1 ± 37.49 μmol/l; B=118.45 ± 23.18 μmol/l; C=119.31 ± 19.85 μmol/l; D=111.59 ± 21.08 μmol/l) (P> 0,05). Urea increased with age (A=7.88 ± 2.04 mmol/l, B= 7.97 ± 0.8 mmol/l, D= 8.29 ± 1.23 mmol/l) except C (7.76 ± 0.85 mmol/l) (P> 0,05). ALB decreased with age (A=31.34 ± 3.24 g/l; B=30.03 ± 2.41 g/l; C=30±2.77 g/l; D=29.67± 2.85 g/l) (P> 0,05). Also glucose concentrations were lower in older mares (A=4.51 ± 0.99 mmol/l; B=4.69 ± 1.05 mmol/l; C= 4.69 ± 1.05 mmol/l; D =4.03 ± 0.64 mmol/l) (P> 0,05). Significantly differences were found in leukocytes between group A =2,76±1,82 g/l versus groups B=6,74±0,56 g/l, C =6,46±1,14 g/l and D =6,13±1,61 g/l (P<0.05), also in neutrophiles between A=2,06±1,26 109/l versus B= 3,47±1,17 109/l, C =3,12±0,9 109/l and D =2,88±0,71 109/l (P<0.05). Were found significantly differences in eosinophiles between group A =0,06±0,09 109/l versus groups B=0,21±0,17 109/l, C=0,19±0,1 109/l and D=0,12±0,11 109/l (P<0.05), also in lymphocytes between A=4,59±1,59109/l versus B =2,95±1,04109/l, C=2,99±1,14109/l and D=2,65±1,87109/l (P<0.05). This research evaluated selected biochemical and haematological parameters of breed mares Norik Muráň type of different ages. We found that age affects these indices in mares Norik Muráň type. Data from this study may enhance our understanding of the biochemical parameters in this species, allowing a veterinarian to fix the interpretation of laboratory data and give these animals the appropriate care. This study was supported by grant from the Ministry of Education VEGA 1/0498/12 of the Slovak Republic.
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Owen, H., Hall, C., Hallam, S., & Smith, E. (2012). The use of GPS to measure feeding behaviour and activity patterns in the horse (Equus caballus). In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The global positioning system (GPS) has been used to record activity and monitor habitat use in many animal species. In the horse (Equus caballus) the monitoring of activity and feeding patterns has been used to assess the impact of environmental factors on behaviour and welfare. In free-ranging animals GPS can provide such information but the accuracy and reliability of these devices has yet to be confirmed. The aim of this study was: 1) to compare the results of visual observation with GPS recordings of the horse’s head and neck position (head up (HU) and down (HD)) used to quantify time spent grazing; 2) to test the use of GPS collars to monitor activity patterns where distance, speed and location paths were recorded. In both studies two animals were fitted with Lotek GPS 3300S collars (with integrated GPS data logger and removable battery pack) round the top of the neck. In study 1 two horses were fitted with collars and turned loose into a 20x40m sand arena for 45 minutes. Feed balls and hay were provided (in nets and on the ground) to encourage movement and feeding behaviour for comparison using the two methods (observation from digital video recordings and GPS). HD was recorded by the GPS collars for a significantly longer time (interpreted as feeding/grazing time) than that recorded by observation (p=0.004). However when the visual observation was split into HU, HD and also head in mid-way position (HMW), where the nose of the horse was level or just above the chest, then no difference between the collar (HU and HD) and visual observation for (HU and HD+HMW) was found. It is likely that when in HMW the GPS collar may not be sufficiently angled to trigger the sensor to record HU or the collar may move on the neck. Conclusions relating to time spent feeding should be treated with caution. In study 2, the collars were fitted to two ponies with access to 2.02 hectares of lowland grazing. Activity (distance travelled and speed) and location was recorded for 2 days. The total distance travelled by the ponies in 24 hours (2.84km) and their average speed (4.04m/minute) was calculated and showed no significant difference between day and night. The total area was split into four equal segments and there was no significant difference in the time the ponies spent in each area although they were found to move at slower speeds and stand for longer in some areas. Movement paths could be identified by inputting the GPS collar data into ArcGIS and viewed on Google Maps. There was a high level of comparability observed between the two ponies confirming behavioural synchronicity. As in other species, the use of GPS collars to monitor the movement and location of horses/ponies was found to be effective, but data relating to head position did not provide a reliable means of recording the time spent feeding.
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Pick, D., & Krueger, K. (2012). Heuristics and complex decisions in man and horses. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Darwin’s claim of differences in mental abilities between man and other animals is a matter of degree rather than of kind and appears to apply nicely to a comparison of choice behaviour in humans and equine. Humans and horses make two kinds of decisions, fast reflexive decisions based on heuristics, and slower more considered decisions that require more complex cognitive processing. Heuristic use is adaptive in that decisions based on them are most often useful in helping an organism to survive while requiring little time and cognitive effort. There is considerable evidence that there is an innate basis to many heuristics in humans as well as horses. A case will be made that the investigation of heuristics specific to horses will lead to an understanding of equine behaviour that has not been possible using traditional learning theories alone. Traditional learning theories are restricted in explaining behaviour to appeals to reinforcement regimes or to the formation of associations between novel stimuli and stimuli that cause innate reflexes, but they are of no use when behaviour is controlled by stimuli that have never been reinforced or been systematically paired with other stimuli that cause reflexive responses. For example, a horse in a two-choice discrimination task may choose a familiar stimulus which has never been reinforced over a new stimulus added to the discrimination task, simply due to the use of an heuristic that usually works -- when in doubt, choose a more familiar object over an unfamiliar one. Conflict resolution strategies provide another good example of heuristic vs. slow decision making. In both humans and horses, conflict resolution strategies are used within, but not typically between social groups. Such groups can be defined as community of interest. Depending on the resource that has to be defended, groups may well be small identities, such as human families or horse harems, or large aggregations such as herds in horses, or religious groups or nations in humans. Fast and simple resolution is possible with stable social identities in simple environments, but more complicated and time consuming deliberative processes are required to resolve conflict over long-term resource acquisition, for decisions in complex conflicts situations and complex social settings.
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Pierard, M. (2012). Agonistic and affiliative interactions in group housed riding horses (Equus caballus). In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Group housed horses at a stud farm/riding stable in Belgium were observed on 17 days between 21 February and 25 April 2008, totalling 54hr25min of detailed data. The original group consisted of 8 Irish Cob mares, 1 Warmblood mare, 1 Arabian gelding and 2 Arabian mares. The group had been established in December 2007. During the course of the study 5 horses were removed from the group and 2 foals were born. 3 highly pregnant mares were housed adjacent to the group for part of the period. Horses were regularly used for lessons. Available surface area differed with the group on pasture at the end. Continuous all occurrence sampling of 10 agonistic and 2 affiliative behaviours was carried out for all group members present. Overall the group showed a frequency of 44.75 agonistic interactions per hour and 11.25 affiliative per hour. Of those agonistic interactions 46.3% were threats while 47% were less active interactions (displacement, being avoided), leaving only 6.7% more aggressive interactions ( mainly biting, some kicking and chasing). The effect on acting agonistically was not significant for age (p=0.1591) and borderline significant for density (p=0.0627). The analysis of the frequency of affiliative interactions showed there is no significant effect of age (p=0.1865) or density (p=0.7923). Agonistic and affiliative interactions were not significantly correlated (p=0.72). Affiliative behaviour a horse received showed a borderline effect (p=0.0787) on agonistic behaviour, as did the interaction between received agonistic and affiliative interactions (p=0.0725). Received agonistic interactions had a borderline negative effect (p=0.0656) on affiliative behaviour. A dominance hierarchy was calculated based on agonistic interactions using Empirical Bayes’ estimates based on Poisson regression with random effects. Agonistic behaviour expressed to other horses was significantly effected by relative rank (p=0.0243). Overall horses tended to be 3.7 times more aggressive towards lower ranking horses compared to higher ranking horses. Affiliative behaviour shown to other horses was not significantly influenced by the rank of the social partner (p=0.7915). Some individuals did show a significant effect whereby they showed more affiliative behaviour towards lower ranking individuals. This study was a small project to look at a practical situation of riding horses being kept in group housing. The frequent changes in group composition and available surface made it possible to look at agonistic and affiliative interactions in such circumstances. This is useful as instability in group composition is often used as main reason not to keep horses in social groups. The results from this study showed a borderline effect of density on agonistic behaviour. In reality it was also influenced by practical details, like a narrow paddock with only 2 hay crates on the smallest surface. Rank in a dominance hierarchy, based on agonistic behaviour, had a significant effect on the agonistic behaviour expressed towards higher or lower ranking horses. No injuries or escalating fights were observed. This study shows it is possible to keep a group of riding horses in a social context without excessive aggression.
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Pokorná, M., & Bartošová, J. (2012). Social learning in horses. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Social observational learning is one of learning abilities expected in domestic horses (Equus caballus) because of their ecological and evolutional history. However, a few studies on this type of learning in horses failed to provide clear evidence of observational learning and/or could not distinguished it from other types of learning. We tested interspecific observational learning abilities using the spatial task and a human demonstrator. We hypothesised that 1) horses with possibility of observing a human demonstrator will complete the task in shorter time than control horses without any demonstrator, and 2) horses observing a familiar demonstrator will carry out the task in shorter time than horses with an unfamiliar demonstrator due to established positive human-horse relationship. We randomly allocated 24 riding horses of mixed age and breed to three groups per 8 and started the task either with observing a familiar demonstrator, unfamiliar demonstrator or without demonstrator (control group). Each horse was released individually at the starting point in the experimental paddock and the latency to pass the task was recorded. A horse completed the task once it walked 25 m from the starting point to the squared area (4x4 m) fenced by a tape, went into it through the entrance on the opposite side and touched the bucket with food. Eight people served as demonstrators, each for one familiar and one unfamiliar horse. Horses from groups with a demonstrator, either familiar or unfamiliar, reached the food bucket significantly faster than control horses during the first trial (mean±SE: 29.1±3.13 s with familiar, 28.9±3.13 s unfamiliar and 41.5 ± 3.13 s without demonstrator, P<0.02, GLMM, PROC MIXED, SAS). Horses did not differ in time needed to reach the fence of the squared area, but in “solving time”, i.e. time from reaching the fence of the squared area and touching the bucket (14.6±2.34, 14.3±2.34 and 27.6±2.34 s in horses with familiar, unfamiliar or without demonstrator, P<0.001). Despite our presumption, the horses observing a familiar demonstrator finished the task in comparable time as horses with an unfamiliar demonstrator (P=0.85) which indicated little effect of long lasting positive relationship between a horse and a particular human. We found, however, large individual variability in performance of individual demonstrators. Further, horses did not differ in time needed to pass the same task without a demonstrator repeated either shortly or 7 days after the first test which supported that interspecific observational learning rather than social facilitation occurred. In conclusion, horses with a human demonstrator, regardless familiar or unfamiliar, were able to solve the task in shorter time compared to control horses but they did not differ in performing repeated task if they learned it by individual or social learning process. This indicates that interspecific observational learning does occur in horses. Supported by AWIN, EU FP7 project No. 266213.
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Posta, J., Mezei, A., & Mihók, S. (2012). Genetic evaluation of competition years, as a kind of measurement of durability in Hungarian show-jumping horses. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The aim of the study was to investigate the possibilities to use “number of years in competition” as a measure of durability in the genetic evaluation of Hungarian show-jumping horses. Competition results recorder between 1996 and 2009 in show-jumping competitions were used to estimate genetic parameters for number of years in competition. The results were collected by the Show-jumping Group of the Hungarian Horse Breeder’s Society. For estimation of genetic parameters for number of years in competition different linear mixed models were tested. In the first model, sex and birth year were taken into account as fixed effects. In the second model, an adjustment was made for age at first result in competition. The model fit was compared based on their determination coefficient. Variance components were estimated with VCE-6 software package. The determination coefficients of the models were 0.09 and 0.20, while the estimated heritability for number of years in competition was 0.27 and 0.23, respectively.
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Ramnath, D., Ralston, S., & Anderson, H. (2012). Trainability and reactivity of Mustang Horses (Equus Equus) fed Forage-Based Total Mixed (TMR) rations with or without added grain. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The relationship between ration and behavior in horses has not been extensively studied, though it is widely thought that the type of feed fed can influence how a horse behaves. For example rations high in sugar and starch have been documented to increase young horses' reactivity to novel stimuli. Since the temperament of a horse has been linked to the ease with which it can be trained, documenting if a horse’s behavior can be altered by its ration would be of interest to the equine industry. We hypothesized that increasing the starch intake of young mustangs by addition of corn or oats to a forage-based total mixed ration (TMR) would alter their reactivity to stimuli and responsiveness to learned commands. To test this hypothesis 8 recently tamed mustangs (4 geldings and 4 fillies, one and two years of age) were used. The mustangs were divided into two groups based on age, sex and temperament. In a series of three experiments they were fed TMR cubes with or without 10% added corn free choice (Exp. 1, Fall, 2010), or a basal ration of TMR cubes free choice with morning meals of 1kg TMR cubes versus an equicaloric amount of corn (exp. 2, Spring, 2011) or oats (Exp. 3, Spring 2011) in a simple crossover design with 2 to 2.5 week adaptation periods for each trial. The horses’ trainability and reactivity to stimuli were evaluated before the treatments were initiated and after each adaptation period 60 to 90 minutes after the morning meals were fed. In the tests the horses were asked to perform a standardized series of commands (ie: walk on, turn, stop and stand still, back up), and were then confronted with a novel stimulus, which varied with each trial. A single handler (SLR) led each horse through the tests, which was then repeated on the next day using a student handler instead. Treatments were then switched and the horses were re-tested, so that each horse was tested on each feed type in all 3 experiments. Each horse’s performance was scored by 2 judges, who were both professional trainers who had been assigned 4 horses to train throughout the study. These judges scored the horses' performances as the tests were done. Each test was videotaped for further evaluation by a third judge (D. Ramnath) who was not familiar with the horses and who was blind to the ration being fed. The performances were scored using a numerical scale of 0-5, with 0=total noncompliance and 5=perfect execution of the tasks asked of the horse. There were no differences (p>0.1) in responses to commands or reactivity to stimuli between rations in any of the trials or with respect to which trainer had trained the horse. There were, however, differences (P<0.05) among horses, handlers and judges with respect to the scores. It appears that addition of a moderate amount of starchy feed to a horse's ration has less influence on the horse's trainability and reactivity than the animal's natural temperament and handler ability. KW -
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Reuber, W., & Reuber, K. (2012). Kennen Pferde ihren Namen? In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Abstract Missing KW -
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Rubenstein, D. (2012). Wild Equid Movements: Impacts of Habitat Quality, Predation Pressure and Leadership. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Animals spend much of their lives on the move searching for food, shelter and mates. As long-legged, large bodied species, equids are well suited for traveling long distances. Understanding where free-ranging equids go, why they choose particular locations, some near and some far, and what impact such movements have on patterns of sociality, demography and human livelihoods are only now coming into focus. This talk will explore how bottom-up factors, such as the abundance and distribution of key resources, and top-down factors, such as the type and location of predators, interact to shape overall movement patterns of equids, how leadership roles develop and what outcomes such movements are likely to have on human activities.
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