Abstract: The ability of horses to learn through social observation may ease the implementation of new management systems, because the use of automatic feeders etc. by naive horses could be facilitated by observation of experienced horses. However, previous studies found no documentation for observational learning abilities in horses. This study aimed to investigate the ability of horses to learn an instrumental task from a familiar conspecific when social interaction was allowed during the demonstration. Two similar experiments were performed. In the first experiment, Observer horses (n=11) participated in ten successive demonstrations, where a trained Demonstrator opened an operant device by pushing a sliding lid aside with the muzzle in order to obtain a food reward. Immediately after the demonstrations the Observer horses were given the opportunity to operate the device alone. Control horses (n=11) were aware that the device contained food but were presented to the operant device without demonstration of the task. The learning criterion was at least two openings. Accomplishment of and latency to accomplish the learning criterion, and investigative behaviour towards the operant device were recorded. Five Observers and one Control, out of the eleven horses in each treatment group, accomplished the learning criterion. Even though this presents a high odds ratio (OR) in favour of the Observer treatment (OR=7.6), there was no significant difference between the treatment groups (P=0.15). Analysis of investigative behaviour showed, however, that the demonstrations increased the motivation of the Observer horses to investigate the device. Subsequently, a similar experiment was performed in a practical setting with 44 test horses (mixed age, gender and breed). We used the same operant device and the same number and type of demonstrations, although the horses were held on a loose rope to minimise aggression. In this second experiment, six of 23 Observer horses and five of 21 Control horses learned the instrumental task, representing no influence of the demonstration. Thus, this study did not demonstrate an ability of horses to learn an instrumental task through observation.

Abstract: The aim of the study was to evaluate the Hungarian Sporthorse population based on eventing competition performance. The database contained the results of 792 horses and 449 riders between 1996 and 2006. The eventing results were gathered from Hungary and other European countries. Blom transformed ranks were used to measure competition performance. Sporthorses competed in fourteen categories but only the easiest category (category ’A’) contained enough result to handle it as a single category (model I.). The other 13 categories were handled together based on professional reasons in a different model (model II.). In model III., all records were analysed together and the results were weighted according to the difficulty of the category. The competition results were classified into eight groups, each group had a weight (0-7) and it was multiplied by a constant 3, and the result of this formula was added to the original Blom score. The linear mixed models included fixed effects for age, sex, breeder, owner, location, year and random effects for animal and rider. The model II. contained one more fix effect for difficulty of the competition level. The distribution of number of horses and number of starts by sex were heterogeneous (P<0.05). For category ’A’ mares and geldings appeared in higher proportion, despite this fact ratio of stallions is greater in higher competition levels. Considering the goodness of fit in each model, model fitting to the weighted Blom scores was the best R2=0.82. In model III. every fix effects (age, sex, breeder, owner, location, year) were significant. Random effects for animal and rider were not significant, but form professional point of view they need to be included in the model. The variance components estimated for the weighted Blom scores were the highest also (0.52 rider effect, 0.09 animal effect), the animal x rider interaction effect was zero. The variance proportion of rider effect exceeded the variance proportion of animal effect in each model. Breeding values of eventing performance were predicted using model III. The reliability of the estimated breeding values was acceptable for only a few stallions. To improve the reliability of breeding values, more progenies should be used in eventing competitions (as a kind of progeny test) and more competition records needed (as a kind of own performance test).

Abstract: The aim of was to compare of biochemical and haematological parameters in the aging process in a cold-blooded mares breed Norik Murá&#328; type. 27 of breeding mares Norik Murá&#328; 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 &#956;kat/l; B=5.36 ± 0.9 &#956;kat/l; C=5.13 ± 1.1 &#956;kat/l), but in the oldest mares (D=5.88 ± 1.37 &#956;kat/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 &#956;kat/l; C=2.66 ± 0.43 &#956;kat/l; D=2.77 ± 1.17 &#956;kat/l), but in the middle age mares were found (B= 2;44 ± 0.46 &#956;kat/l) (P> 0,05). Crea concentrations had a decreasing trend (A=139.1 ± 37.49 &#956;mol/l; B=118.45 ± 23.18 &#956;mol/l; C=119.31 ± 19.85 &#956;mol/l; D=111.59 ± 21.08 &#956;mol/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 Murá&#328; type of different ages. We found that age affects these indices in mares Norik Murá&#328; 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.

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.

Abstract: The living equids display a variety of different forms of social organisation; plains (Equus quagga) and mountain zebra (Equus zebra) associate in small, closed harems, whereas the asses and Grevy’s zebra (Equus grevyi) are found in looser, more ephemeral associations. Feral domestic horses appear to be somewhat intermediate: although stallions generally maintain harems, there is some movement of individuals between groups. This talk will use several statistical approached to explore evolutionary explanations for these differences. Firstly, we will explore the relationship between brain architecture and social organisation both among the equids and across all Perissodactyls. Equids have larger relative neocortices than other Perissodactyls; within the equids, species typically found in more stable groups have larger neocortices than equids in more unstable ephemeral groups. The strong relationship between group stability and brain size and architecture mirrors that found in other mammals, including primates. Thus, living in stable social groups consistently appears to impose cognitive demands across species. In order to understand the historical trajectory resulting in the relatively large, social brains found in some species, we then reconstruct the evolutionary pathway of social living in the equids. Finally, we discuss how we can use network theory to measure social structure and how these differences may impose different cognitive demands on individuals.