Abstract: The tendency in primate groups for two opponents to affiliate shortly after a fight has been described as dyadic reconciliation. The response has been shown to restore disrupted relationships and curtail ongoing aggression. Rates of self-directed behaviour (e.g. scratching) are positively correlated with anxiety in primates and the rates decline after reconciliation, indicating that the response also functions to reduce postconflict tension. Third parties not involved in an aggressive interaction are also likely to affiliate with one of the combatants subsequent to a fight. Such `triadic' interactions may also promote conflict resolution when, for instance, the relatives of a victim affiliate with their relative's aggressor. Because aggression in a group influences a bystander's behaviour with combatants, we hypothesized that aggression between two animals would also influence a bystander's behaviour with other bystanders. Such `quadratic' postconflict interactions might also function to reduce postconflict tension or occur in patterns among kin subgroups to resolve conflict. We tested for quadratic interactions in an 18-member group of captive hamadryas baboons, Papio hamadryas hamadryas. Immediately following a fight, an uninvolved bystander was randomly selected for observation and its affiliative interactions with other bystanders and its displacement activities were recorded for 3 min. Rates of behaviour during these postconflict periods were compared to rates during 3-min baseline periods not preceded by aggression. Bystanders engaged in quadratic interactions by increasing affiliation with other bystanders following aggression. Bystanders directed affiliation to nonkin bystanders that were their preferred social partners. Displacement activities of bystanders were significantly higher during postconflict intervals compared to baseline intervals, and bystander displacement activity levels before affiliative contact with other bystanders were significantly higher than after contact. Apparently, bystanders become tense or anxious after witnessing aggression and affiliate with preferred partners to reduce the arousal.

Abstract: The ideals of equestrian technique combine art and science. Therefore students of equitation
encounter measurable variables such as rhythm, tempo and impulsion alongside more ethereal ones
such as outline and harmony. This mixture accounts for many of the idiosyncrasies of equestrianism
including the subjective scoring of performance in dressage tests, the elusiveness of perfection even at
an elite level of competition and the difficulty of expressing equestrian technique in empirical terms
(Roberts, 1992).
This chapter will describe and offer examples of the unwelcome behavioural responses horses
produce under saddle. Two broad sections are then proposed to allow the reader to consider
unwelcome behavioural responses caused directly by humans as distinct from those attributable more
to the horse than the rider. Ultimately the responsibility for problems in the ridden horse lies with
humans since we have undertaken the domestication and exploitation of equids. Therefore it is
accepted that the dichotomy is not absolute. The chapter closes with a

Abstract: Fourteen riding horses of mixed age and breed were randomly allocated to observer and control treatments. An additional horse was pre-trained as a demonstrator to walk the 13.8 m length of the test arena and select one of two food buckets using colour and pattern cues. Observer horses were exposed to correct performances of the task by the trained demonstrator, for 20 trials held over 2 days. Control horses were subjected to the same handling and placement procedures as the observer horses but without exposure to the behaviour of the demonstrator. The third day for all subjects was designated as a test day. Each subject was released individually in a predetermined place in the arena, and the latency to walk the length of the test arena to the food buckets, the latency to feed, the identity of the bucket approached and the identity of the bucket selected were recorded on ten consecutive trials. During tests both food buckets contained food to minimize the possibility of individual trial and error learning. On the first trial the mean latency to approach the goal area was 18 s for observer horses, compared with 119 s for control horses (t = 2.8, d.f. = 12, P < 0.01) and the mean latency to eat was 35 s for observer horses, compared with 181 s for control horses (t = 4.86, d.f. = 11, P < 0.001). However, observer horses were no more likely to choose the demonstrated bucket than control horses on the first trial. Twelve of the 14 horses decreased their latency to approach the goal area during the series of ten trials, but there were no significant changes in the buckets selected.

Abstract: Dogs' (Canis familiaris) and cats' (Felis catus) interspecific communicative behavior toward humans was investigated. In Experiment 1, the ability of dogs and cats to use human pointing gestures in an object-choice task was compared using 4 types of pointing cues differing in distance between the signaled object and the end of the fingertip and in visibility duration of the given signal. Using these gestures, both dogs and cats were able to find the hidden food; there was no significant difference in their performance. In Experiment 2, the hidden food was made inaccessible to the subjects to determine whether they could indicate the place of the hidden food to a naive owner. Cats lacked some components of attention-getting behavior compared with dogs. The results suggest that individual familiarization with pointing gestures ensures high-level performance in the presence of such gestures; however, species-specific differences could cause differences in signaling toward the human.