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Lamprecht, J. (1992). Variable Leadership in Bar-Headed Geese (Anser Indicus) : an Analysis of Pair and Family Departures. Behaviour, 122(1-2), 105–119.
Abstract: This paper reports quantitative leadership differences in semi-captive bar-headed geese (Anser indicus) at different times of the year, and in different types of groups. Leading is defined here as causing the departure or determining the direction of movement of the whole group. No permanent and exclusive leader of a pair or family group was found, rather relative leading frequencies of male, female and young showed a definite shifting pattern. Females led more often than their mates prior to breeding, and on nest pauses during the incubation period, but less often in summer, autumn and early winter. In families there was no difference between the frequencies of male and female leading. Family females led relatively more often than those of pairs without offspring. This difference was related to the presence, not the number, of young. Goslings led the family about as often as the parents during the rearing period in early summer, less often in autumn, winter and next spring. Such differences and changes are to be expected where competence in particular tasks and dependence on partners vary between group members, and where different situations require different abilities. For the geese, the results can be related to the different options of group members and to the different benefits they derive from leaving (or 'staying put') or following (or waiting for the others) in different situations.
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Lin AC, Bard KA, & Anderson JR. (1992). Development of self-recognition and self-conscious emotions. Child Dev., 106, 120. |
Povinelli DJ, & deBlois S. (1992). Young children's understanding of knowledge information in themselves and others. J. Comp. Psychol., 106, 228. |
Hertsch, B. (1992). [The appearance of stress on the movement apparatus in dressage, jumping and versatility horses]. Dtsch Tierarztl Wochenschr, 99(1), 36–39.
Abstract: Jumping and military (three days events) horses are exposed, during sports activities, to a particularly high stress especially in the region of the extremities (limbs). The genesis of tendon, joint and bone diseases are traced in accordance to the centers of the load during movement sequence. A special statistics on injuries concerning the German competition horses does not exist yet. Out of the available statistics about the German competition horses it is not obvious that as a result of its use as sports horses a particular high loss occur among these horses.
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Kirkpatrick, J. F., Liu, I. M., Turner, J. W. J., Naugle, R., & Keiper, R. (1992). Long-term effects of porcine zonae pellucidae immunocontraception on ovarian function in feral horses (Equus caballus). J Reprod Fertil, 94(2), 437–444.
Abstract: Ten feral mares free-roaming in Maryland, USA, were inoculated with porcine zonae pellucidae (PZP) protein before the breeding season for three consecutive years (1988-90). Ovarian function was monitored for 51 days during the peak of the breeding season after the third annual PZP inoculation, in seven of these mares and in four untreated control mares, by means of urinary oestrone conjugates and nonspecific progesterone metabolites. None of the ten inoculated mares became pregnant in 1990, compared with 55% of 20 control mares, which included two of the four monitored for ovarian function. Three of the untreated mares demonstrated apparent normal ovarian activity, characterized by preovulatory oestrogen peaks, concurrent progesterone nadirs at ovulation, breeding activity, and luteal-phase progesterone increases after ovulation. Two of the seven monitored PZP-treated mares demonstrated ovulatory cycles that did not result in conception. One was pregnant as a result of conception in 1989 and demonstrated a normal, late-gestation, endocrine profile. The remaining four PZP-treated mares revealed no evidence of ovulation, and urinary oestrogen concentrations were significantly depressed. The experiments indicated that (i) a third consecutive annual PZP booster inoculation is greater than 90% effective in preventing pregnancies in mares and (ii) three consecutive years of PZP treatment may interfere with normal ovarian function as shown by markedly depressed oestrogen secretion.
Keywords: Animals; Contraception, Immunologic/*veterinary; *Egg Proteins; Estrogens, Conjugated (USP)/urine; Female; Glycoproteins/*pharmacology; Horses/immunology/*physiology; *Membrane Glycoproteins; Ovary/drug effects/*physiology; Progesterone/metabolism; *Receptors, Cell Surface; Swine/immunology; Time Factors; Zona Pellucida/*immunology
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Harkins, J. D., Kamerling, S. G., & Church, G. (1992). Effect of competition on performance of thoroughbred racehorses. J Appl Physiol, 72(3), 836–841.
Abstract: The effect of competition and the influence of age and sex on performance were examined in a study of 18 Thoroughbred racehorses. The horses performed two solo and two competitive runs at 1,200 and 1,600 m for a total of eight runs. No group ran faster during competition, which may have been a reflection of the quality of horses used for this study and their susceptibility to stress-induced impairment of performance. Males showed no significant difference between competitive and solo run times, whereas females were consistently slower during competition. Males ran significantly faster than females in all runs. There was no difference in run times due to age, which may have been due to the high mean age (5.9 yr) of the group. The slower competitive run times may have occurred because of an earlier onset of fatigue when compared with solo runs. Plasma lactate was significantly greater for the 1,200-m competitive than for the solo runs.
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Mills, M. G. L., & Shenk, M. G. L. (1992). Predator--Prey Relationships: The Impact of Lion Predation on Wildebeest and Zebra Populations. T. J. Anim. Ecol., 61(3), 693–702.
Abstract: 1. The role of lion Panthera leo predation in the dynamics of blue wildebeest Connochaetes taurinus and zebra Equus burchelli populations was investigated through simulation models. The data used in the models were from intensive observations over 4 years in the south-east of the Kruger National Park. 2. Population estimates of wildebeest and zebra were made from aerial surveys, sex and age ratios from ground counts. Lion numbers were determined from observations of marked and radio-collared animals. Predation was studied by following lions for continuous periods of up to 336 h. 3. Two models were constructed. Model 1 ascertained the number of killing lions (adult females) that could be supported by each prey population while remaining stable. A single model was constructed for the sedentary wildebeest population. A summer and winter model was constructed for the semi-migratory zebra population. The sensitivity of the parameters in the model was tested by changing their value by 10%. In model 2, the kill age structure for each species was changed to determine the number of killing lions the altered prey selection parameters could support. 4. There was no difference in the vulnerability of either species to predation. Zebra foals (<1 year) were killed more frequently than expected. No selection for sex or by season could be found for either species. 5. Model 1 predicted that the wildebeest population stabilizes with 7.7 killing lions, close to the number in the study area. The winter zebra population stabilizes with 6.8 killing lions and the summer zebra population with 19.4. Manipulation of kill rate followed by adult fecundity rate had the greatest effect on population size of both species. In model 2, wildebeest predation was made selective towards calves and zebra predation was made non-selective for sex and age. With these parameters the wildebeest population stabilizes with 10.7 killing lions and the zebra population with 5.4 in winter and 15.1 in summer. 6. The models suggest that lion predation affected wildebeest more severely than zebra during the study. This was through the way in which lions selected their prey, and because of the sedentary behaviour of the wildebeest, as opposed to the semi-migratory behaviour of the zebra.
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Brunner, D., Kacelnik, A., & Gibbon, J. (1992). Optimal foraging and timing processes in the starling, Sturnus vulgaris: effect of inter-capture interval. Anim. Behav., 44(4), 597–613.
Abstract: Laboratory experiments with starlings, Sturnus vulgaris, were conducted to investigate the interaction between timing and cost-benefit considerations. The design simulated an environment in which food was distributed in patches. Patches contained a random number of food items (N=0-4) separated by a fixed inter-capture interval or fixed interval. All patches ended with sudden depletion. The time elapsed since the last prey capture was the only way to detect the depletion of the patch. Once the patch was depleted a new patch could be reached by travelling between two perches. Three measures of timing were taken: (1) rate of working for food as function of `waiting' time in a patch, (2) the time of the last response in a patch or `giving-in' time, and (3) the time at which travel was initiated or `moving-on' time. The fixed interval that characterized patches was varied between conditions. The mean time of the peak in working rate was consistently centred around the fixed interval, while the other two measures of timing kept a roughly linear relation to the fixed interval, with slope greater than one. In accordance with Scalar Expectancy Theory, variability in the three forms of timing was proportional to the magnitude of the fixed interval. The birds seemed to take account of this increase in variability as shown by the mean value of their giving-up criterion. These results imply that information-processing constraints are important for modelling behavioural optimality.
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Caraco, T., Kacelnik, A., Mesnick, N., & Smulewitz, M. (1992). Short-term rate maximization when rewards and delays covary. Anim. Behav., 44(Part 3), 441–447.
Abstract: In nature foragers must exploit resources that vary randomly in both the energy acquired per item (reward) and the time required to pursue, capture and process an item (delay). Furthermore, rewards and delays associated with particular resources may often covary significantly. An analytical model asks how variance-covariance levels for rewards and delays could influence choice of resources when lack of information or cognitive limitation implies that a consumer attempts to maximize its short-term rate of energy gain. Both greater expected reward and reduced expected delay clearly should enhance preference for a resource. The model predicts that increased delay variance and reduced reward-delay covariance should increase a forager's preference for a resource. A forager should be risk-averse towards reward variance when the reward-delay covariance is positive, but should become risk-prone towards reward variance when the reward-delay covariance is negative.
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Aureli, F., Cossolino, R., Cordischi, C., & Scucchi, S. (1992). Kin-oriented redirection among Japanese macaques: an expression of a revenge system? Anim. Behav., 44(2), 283–291.
Abstract: The ability to recognize the close associates of other group members may permit the display of redirected aggression against the relatives of the former aggressor. However, the dominance structure and the kin-based alliance system of macaque society are expected not to favour the occurrence of this kin-oriented redirection. Nevertheless, within 1 h of being the victim of an attack, Japanese macaques, Macaca fuscata, were more likely to attack the former aggressor's kin than without such a conflict. The conditions under which the victim redirected against the former aggressor's kin were investigated. This kin-oriented redirection did not occur preferentially either after conflicts between individuals with unstable and/or uncertain dominance relationships or after conflicts with individuals that were unlikely to intervene in favour of their kin. Victims redirected against individuals that were younger than the former aggressor and often subordinate to the victim. They also redirected in an opportunistic way by joining polyadic interactions against the former aggressor's kin. The possibility that this kin-oriented redirection may have a long-term function in changing the aggressive attitude of the aggressor towards the victim is also discussed. In addition, the victim's kin also displayed a form of kin-oriented redirection. They were more likely to attack the kin of an individual after it had attacked their own kin.
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