Abstract: We tested untrained horses (foals and breeding mares) in 3 different breeding centres. Horses were kept in a pasture during daytime in bigger groups (median 12, min: 6, max 35 / pasture) according to age, gender and breed (hungarian halfbred, hucul, arabian and thoroughbred). To measure their reactions to an unfamiliar person we conducted an active and a passive human test. In the active human test the test person (TP) approached a focal animal in the group from a predetermined direction: from their front, from their side (left or right) or from the rear. As TP reached the horse (of app. 0.5 m distance), she tried to pet the animal’s head. The TP always chose and approached a standing or a grazing horse (ie. those that were not walking, galloping, playing etc.). The horse’s reaction to the approaching human was scored 1-5. Score 1: the horse moved away and the TP could not even approach it within 0.5 m; Score 2: the horse made max. 2 steps away, but could be reached and petted; Score 3 and Score 4: the horse stood in its place but showed different signs of discomfort (head turn – Score 3; backing ears, tail slash – Score 4); Score 5: the horse stood and did not show any sign of discomfort or actively approached the TP. There was no significant difference in the horses’ reaction between approaching from their left or right side. Approaching from their front or from their side (left or right) did not differ significantly either. However, the odds of walking away from the TP (score 1 or 2) was 2.7 (Fisher-test, p=0.039) and 3.3 (p=0.012) times higher when TP approached from the rear compared to approaching from their front or from their side (left or right), respectively. In the passive human test the TP stood immobile for 4 minutes in 5 or 10 m far from the horses during their active (grazing) or inactive (standing idle during noon) period. Horses approached TP significantly sooner (general linear model, p=0.017) when she stood 5m distance (38 ±63 s) compared to 10m (97 ±52 s). The arrival of a second horse after the first horse approached the TP showed significant high correlation with the latency of the first horse arrival (Pearson correlation, r=0.96, p<0.001). The horses were less keen (p=0.008) to approach the human when they were tested in an inactive period (177 ±110 s) compare to active period (38 ±63 s).

Abstract: This study investigated drinking behaviour of unhandled, semi-feral Dartmoor ponies. Aspects studied were drinking behaviour, latency to drink from novel unfamiliar drinkers after transport, preferences for different types of artificial water drinkers, effects of mixing with unfamiliar ponies and group size, on drinking behaviour, and the effect of a simulated market on the latency to drink. Ponies were tested in groups of three or six animals, or as individuals in test pens that were equipped with three water drinkers: bucket, automatic drinking bowl, flowing water trough. Behaviour was recorded using time-lapse video. An individual pony drank on average 10 l per day. Ponies also drank, but at a lower rate, during the night. The latencies to drink after 4.5 h of transport showed large variation, but most ponies drank within the first hour after being transported (all groups 80.5 ± 32.94 min, mean ± SEM). In the individual choice tests, the preferred drinkers were the bucket and the flowing water trough, but not the automatic drinking bowl (drinking time 25.2 ± 4.66, 11.5 ± 4.26, 2.4 ± 2.23 min for bucket, trough and bowl respectively, mean ± SEM; paired t-tests, bowl versus other drinkers, all tests p < 0.02). A possible reason for the avoidance of the automatic bowl was the noise it made when filling. After mixing a group of three ponies with a group of three unfamiliar animals, the ponies did not express their individual drinker preferences anymore. The use of the previously preferred bucket decreased significantly and the use of the initially, non-preferred, bowl increased significantly. This was likely caused by the fact that ponies were either intentionally or accidentally obstructing drinkers in certain areas of the pen and unfamiliar ponies did not want to push past them. In the simulated market, the differences in latencies to drink between ponies in the home pen and market groups did not reach significance. No significant effect of group size (groups of three versus six ponies) on drinking behaviour was detected. The results have implications for situations where only automatic water bowls are provided, such as during pony sales at livestock markets. Preventing ponies from expressing their drinking choice, either by offering non-preferred drinkers or by mixing with unfamiliar animals, could adversely affect their welfare especially if this happens in conjunction with other stressful events such as transport and markets, and potentially weaning.

Abstract: Facial features appear to be a prominent kinship cue for ascribing relatedness among human individuals. Although there is evidence that adults can detect kinship in unrelated and unfamiliar individual’s faces, it remains to be seen whether people already possess the ability when they are young. To further understand the development of this skill, we explored children’s ability to detect parent-offspring resemblance in unrelated and unfamiliar faces. To this end, we tested approximately 140 children, aged 5–11, in two photo-matching tasks. We used a procedure that asked them to match one neonate’s face to one of three adults’ faces (Task 1), or to match one adult’s face to one of three neonate’s faces (Task 2). Our findings reveal asymmetrical performance, depending on the tasks assigned (performance of Task 2 is stronger than for Task 1), and on the sex of individuals who made up the parent-offspring pair (male parents are better matched with neonates than female parents, and boys are better matched than girls). The picture that emerges from our study is, on one hand, that the ability to detect kinship is already present at the age of five but continues to improve as one gets older, and on the other, that perception of parent-offspring facial resemblance varies according to the appraisers’ characteristics.

Abstract: Rinder und Pferde werden in den Abruzzen das ganze Jahr auf großen Weiden gehalten. Dies fördert nachweislich den Artenreichtum, verbessert die Bodenqualität und trägt durch Kohlenstoffbindung zum Klimaschutz bei.

Abstract: It has recently been shown that some non-human animals can cross-modally recognize members of their own taxon. What is unclear is just how plastic this recognition system can be. In this study, we investigate whether an animal, the domestic horse, is capable of spontaneous cross-modal recognition of individuals from a morphologically very different species. We also provide the first insights into how cross-modal identity information is processed by examining whether there are hemispheric biases in this important social skill. In our preferential looking paradigm, subjects were presented with two people and playbacks of their voices to determine whether they were able to match the voice with the person. When presented with familiar handlers subjects could match the specific familiar person with the correct familiar voice. Horses were significantly better at performing the matching task when the congruent person was standing on their right, indicating marked hemispheric specialization (left hemisphere bias) in this ability. These results are the first to demonstrate that cross-modal recognition in animals can extend to individuals from phylogenetically very distant species. They also indicate that processes governed by the left hemisphere are central to the cross-modal matching of visual and auditory information from familiar individuals in a naturalistic setting.