Abstract: A feral horse population inhabiting the Vodnyi Isl, Manych-Ghudilo Lake, on the territory of Rostov Region, S Russia, has been established in 1950s according to questionnaire data (Paklina, Klimov, 1990). It is a sole permanent grouping of feral horse known to exist in European Russia (Spasskaya, Spasskyi, 2007; Spasskaya, 2008). Range of this group is part of Federal Reserve “Rostovsky” established in 1995, and its monitoring has being been conducted since 2006. The principal aim of monitoring includes gathering data on demographic, spatial, and ethological structure of the island horse population, along with investigation of its phenotypic and ethological patterns. Analysis of previously published (Paklina, Klimov, 1990) and recently obtained data on the color patterns of the island horse indicate that they have become isolated supposedly about 18–20 years ago. Some trends in variation of several phenotypic traits indicate slight rising of inbreeding level in this population, including decrease in the horse withers height, changes in body proportions, increase of heterogeneity in body color patterns (size and number of head and leg spots), and increase of frequency of dental malformations, especially of false polydonty of P1 (Spasskaya et al., 2010). Principal demographic parameters of this population are similar in general to those known for other feral horse studied by now. However, several peculiar features of this population were revealed: its age structure appeared to be of steadily fading type judging by high proportion of mature individuals (64–72 %); high mortality rate of individuals of the first year of life (16–25 %); predominance of males among newborns with increase of population size. Ethological structure of the population included standard harem bands and bachelor groups, with few solitary animals (usually old or sick stallion). The most of individuals (58.2–84.3 %) were the part of harem bands, which appeared to be the most stable groupings. The harems were small in their numbers with predominatingly 3–8 individuals. The bachelor groups were inconstant in composition, their portion in population being not high (7.7–15.4 % of the total number). A lot of “mixed” groupings of various composition were recorded in the population during its high number phase: harem bands with several mature stallions; associations consisting of several harem bands; youth groupings consisting of approximately coeval stallions and mares. These “mixed” groupings appeared to be rather stable, with their total number reaching up to 25.8 % of the population. They however used to disappear with population number decrease. The Rostov population is characterized by absence of conspicuous home range of social groupings (Spasskaya, Shcherbakova, 2007; Spasskaya, 2009), so the latter form a united herd with minimal intergroup distances. This phenomenon is probably not related to population density or to the island size, but is rather caused by some other factors to be revealed.

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.

Abstract: Solving horse nutrition challenges require contributions from Psychology, Biology, Agriculture, and Veterinary Medicine because these are biological challenges of an anthropological nature. The domesticated horse has shifted from an animal of war, transportation, and farmwork, to a companion enjoyed for sport, leisure and recreation. The first realization and responsibility must lie in the fact that it is the owners and managers which are the source of many of the horses’ challenges. Nutritional challenges include: defining requirements and absorption of nutrients, improving feed efficiencies for performance, improving feeding management and eating behaviors, and preventing or treating clinical problems. These challenges can be addressed through science, horse management, and education. Many of today’s challenges in horse nutrition can be related to the equine genome and genetics. Those that can be addressed with nutritional consequences include Polysaccharide Storage Myopathy, Equine Metabolic Syndrome, Recurrent Exertional Rhabdomyolysis, Glycogen Branching Enzyme Deficiency, Hyperkalemic Periodic Paralysis, and Development Orthopedic Disorders. It is the scientific understanding of cellular processes in relation to nutrients which address the symptoms associated with these diseases. Consequently, feeding management can be changed to actually treat the disease. The most recent advances in equine nutrition implement the use of molecular and cellular based techniques to understand how nutrients are needed during times of stress, feed withdrawal and to maintain gut health. For example, the absorptive capacity and transporter gene expression and localization, are now being quantified. We are also now assessing the impact of the loss of reproductive endocrines on calcium and phosphorus homeostasis in the horse. Additionally, bioluminescent pathogenic bacteria have been utilized to view attachment rates in the gastrointestinal tract of the horse. These are merely examples of the approaches of science to these nutritional challenges. Science is of little use unless it is incorporated into improved management of horses. Every type of horse requires different management and good husbandry. In our country, 70+% of the horses are kept in small herds, on limited acreage, and used for recreation and sport. Since we have taken the horse out of its natural environment and subjected it to these roles, we now seek to determine ways to feed the horse in our environments; i.e. obesity, inconsistent exercise, confinement, surgery, competition, diseases. Private horse feed agribusinesses have aggressively positioned excellent products with claims to improve health, reproduction, performance, and even horse happiness. Owners and managers seek unbiased science upon which they ultimately make their own decisions. General challenge categories seem to be feeding geriatric horses, active performance horses, and idle horses with secondary metabolic problems. Thus, feeding recommendations include the determination of specific horse nutrient requirements, maximization of available forages, providing other nutrients, and exercise to manage horses more as horses. Private and public companies and Extension systems exist to provide online and other sources of information. As more and more people own horses as a hobby and for recreation, they share responsibility to inform themselves on how to best feed and care for their horses.

Abstract: Temperament is an important factor when working with horses. Behavioral tests have been developed to measure certain dimensions in horses. Relations between temperament and ability to riding activity have been highlighted (Lansade 2008a). The aims of this study were 1) to evaluate the effect of age on temperament, 2) to verify that temperament are related to breeds 3) to check if the ease to be ridden is in relation with temperament, on a first set of data. Five dimensions of temperament have been measured in 98 field stallions (Table 1). They were tested as described by Lansade (2008 a,b): fearfulness/curiosity (tests: crossing a novel aera, suddenly opening an umbrella, novel object), gregariousness (test: isolation), locomotor activity (during the other tests), reactivity/curiosity to a non familiar human (tests: passive and active human), tactile (Von Frey filament) and auditory sensitivities. Table 1: Number of stallions according to breed (or group of breeds) and age. Breeds or groups of breeds Young (<13 years) Old (>=13 <20 years) Merens 1 15 10 Leasure horse breeds 2 13 10 Jumping pony breeds 3 / 20 Jumping horse breeds4 9 10 Arabians / 11 Total 37 61 (1) Merens : french mountain horse breed (2) Appaloosa, Barbe, Lusitanian, Polish, Paint (3) French Saddle Pony, Connemara, New Forest, Welsh (4) French Saddle Horse, Anglo-Arab, KWPN, Foreign breeds Effect of age. Due to imbalanced data, only stallions from 3 breed groups were compared (29 young ones selected at random and 30 old ones). Young stallions presented a higher emotivity (more elevated distance/intensity of the flight after umbrella opening (P=0.001)) and curiosity (more sniffings/nibblings the passive human (P=0.04) and the novel object (P<0.0001)) compared to old ones. Relation with breed groups. In young stallions, differences were noted : in the number of trots during social isolation (P=0.001) and in the tactile sensitivity (P=0.005). Merens had smaller values than Jumping horses for these 2 variables. In older stallions, differences were also noted: in the number of sniffings/nibblings the novel object (P=0.04), in the manner to cross the novel aera (P=0.03), in the distance and intensity of the flight after umbrella opening (P=0.04), in the number of trots during isolation (P=0.02) and in the tactile sensitivity (P=0.03). Merens had lower reactivity compared: 1) to Arabians (for novel aera) and 2) compared to Jumping ponies and Jumping horses (for isolation and tactile sensitivity). Minimal level of rider. Stallions of all ages and breeds were divided into 3 groups according to the level of riders able to ride them safely, according to a questionnaire: beginners, intermediate level and pre-national competition level. Stallions adapted to beginners showed lower values in the number of trots during isolation (P=0.02) and in the tactile sensitivity (P=0.03) than stallions rode by pre-competition level riders. Conclusion : The intensity of fear reactions to suddenness decreased with age. Differences between breeds and eases of use have been related to temperament measurements.

Abstract: Horses kept in small enclosures move very little in comparison to horses living in an unconfined environment. There are health consequences of this sedentary lifestyle. The use of GPS allows the accurate quantification of distance travelled by horses. Methods: Ten horses (5 pairs) were alternated between a control paddock and a research paddock, both measuring 20 x 30m. Grass hay was fed from a novel feeding system in the research paddock, while the same hay was fed from a standard hay feeder in the control paddock. In the research paddock access to hay was alternated at 5 min intervals between either side of a fence, forcing horses to walk around a walkway to access feed continuously. The interactive behavior of horses was observed and movement was monitored using GPS. Results: All 10 horses learnt to use the feeding system quickly. Dominance behavior in some horses was modified by competition for feed. On average, horses in the research paddock travelled 5.4 times more distance than in the control paddock. Conclusion: The dynamic feeding system was successful in encouraging horses to exercise in a small paddock. However, due to the exaggeration of dominance behavior in some horses, horses should be well matched if housed in pairs. This system may have application in the management of equine obesity and insulin resistance in horses. KW -