Abstract: A split-plot experiment evaluated the effect of handling and reserpine on the autonomic heart-rate response of yearling horses to various stimuli. The emotionality levels of 32 Quarter-Horse yearlings were rated by 4 experienced horsemen on a scale from 1 to 4 (1 = most nervous and erratic disposition; 4=quiet disposition). The yearlings were subsequently classified and penned based on their emotionality level; normal or nervous. Within each emotionality group, one-half the yearlings were handled daily for 14 days and the other one-half remained free in the pens. Following the handling treatment, every yearling was individually exposed to a series of stimuli, while the heart rate was monitored via a radio-telemetry system. A second treatment, reserpine, was subsequently given intramuscularly (0.005 mg/kg body weight) to one-half the yearlings of each treatment combination of emotionality and handling. The heart rate of the yearlings to the same series of stimuli previously employed was determined at 24 and 120 h and 16 days following the reserpine injection. Summarizing the results, the handled yearlings tended to exhibit lower heart rates with the handling stimulus, but the heart rate with a more novel stimulus was not affected by the previous handling treatment. Reserpine tended to suppress the heart rate of the unhandled group during the presence of a handler, but the permanency of this effect was not evident 16 days after the drug was administered. The reserpine-treated groups tended to exhibit the lowest heart-rate response to stimuli during the 120-h test-day following the administration of the drug. Heart-rate responses to the stimuli were not different between the normal and nervous yearlings.

Abstract: Thirty-six mares, blocked by age and temperament score, were assigned to one of three treatment groups: pasture (P); confinement stalls (C), allowing social contact; isolation stalls (ISS), allowing no contact with conspecifics. After 48 h on treatment, the mares were observed in situ for 1 h. Medium temperament and highly reactive ISS mares spent more time eating grain (P<0.01) and exhibited more grain-eating bouts (P<0.03) than P and C mares. Calm P mares had longer forage-eating bouts than C and ISS mares (P<0.02). During a 15 min open-field test in a 23 m x 23 m pen after 72 h on treatment, ISS mares traveled farther (P<0.005) than C and P mares, spent more total time trotting (P<0.01) than C and P mares, and exhibited a greater number of trotting bouts (P<0.01) than both C and P mares. Isolated mares spent less total time standing during the open-field test than C (P<0.05) and P (P<0.01) mares, but exhibited a greater number of standing bouts than C (P<0.05) and P (P<0.01) mares. Isolated mares also exhibited a greater number of total activity bouts (P<0.01) during the open-field test than both C and P mares; P mares also exhibited fewer activity bouts than C mares (P<0.1). Results indicate that mares kept in confined and isolated environments showed greater motivation for movement and performance of a greater number of activities than those maintained on pasture with conspecifics.

Abstract: Summary Four geldings and four mares of primarily Thoroughbred and Quarter Horse breeding were used in simultaneous 4x4 Latin square experiments to test the effects of dietary cation-anion balance (DCAB), defined as meq ((Na+K)-C1)/kg diet dry matter, on blood pH, blood gases, acid-base status and plasma glucose in horses at rest and following anaerobic exercise. Four diets, consisting of a base concentrate of corn, soybean meal and cottonseed hulls fed in a 60:40 ratio with Bermudagrass hay, were formulated to provide a DCAB of 5 (L=Low), 107 (ML=Medium Low), 201 (MH=Medium High) and 327 (H=High) meq ((Na+K)-C1)/kg diet dry matter. Calcium chloride and ammonium chloride were added to treatment L and ML and sodium bicarbonate and potassium citrate were added to treatment H to achieve the desired cation-anion balance. Treatment MH was not supplemented and served as the control treatment. Prior to the experiment, horses performed six weeks of long, slow, distance (LSD) work. During the experimental periods, horses were subjected to an exercise regimen alternating LSD with an interval training protocol 6 days/week. Venous blood pH, pCO2 and bicarbonate levels were significantly lower in horses at rest consuming diet L versus diets MH and H. Blood pH and acid-base parameters decreased with decreasing DCAB. There were no significant differences in blood pH or acid-base parameters between treatments, after anaerobic exercise. Plasma glucose concentrations for treatment L were significantly lower than treatment H at 10, 20, and 30 minutes post-exercise. These data suggest that DCAB has significant effect on acid-base status and indicate that horses consuming diets with low DCAB may experience a metabolic acidosis.

Abstract: Gaze following is a behavior that draws the human infant into perceptual contact with objects or events in the world to which others are attending One interpretation of the development of this phenomenon is that it signals the emergence of joint or shared attention, which may be critical to the development of theory of mind An alternative interpretation is that gaze following is a noncognitive mechanism that exploits social stimuli in order to orient the infant (or adult) to important events in the world We report experimental results that chimpanzees display the effect in response to both movement of the head and eyes in concert and eve movement alone Additional tests indicate that chimpanzees appear able to (a) project an imaginary line of sight through invisible space and (b) understand How that line of sight can be impeded by solid, opaque objects This capacity may have arisen because of its reproductive payoffs in the context of social competition with conspecifics, predation avoidance, or both.

Abstract: Two studies are reported in which chimpanzees attempted to use social cues to locate hidden food in one of two possible hiding places. In the first study four chimpanzees were exposed to a local enhancement cue (the informant approached and looked to the location where food was hidden and then remained beside it) and a gaze/point cue (the informant gazed and manually pointed towards the location where the food was hidden). Each cue was given by both a human informant and a chimpanzee informant. In the second study 12 chimpanzees were exposed to a gaze direction cue in combination with a vocal cue (the human informant gazed to the hiding location and produced one of two different vocalizations – a 'food-bark' or a human word-form). The results were – (i) all subjects were quite skillful with the local enhancement cue, no matter who produced it; (ii) few subjects were skillful with the gaze/point cue, no matter who produced it (most of these being individuals who had been raised in infancy by humans); and (iii) most subjects were skillful when the human gazed and vocalized at the hiding place, with little difference between the two types of vocal cue. Findings are discussed in terms of chimpanzees' apparent need for additional cues, over and above gaze direction cues, to indicate the presence of food.