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The purpose of this research was to test how, why, and when social power influences victims’ revenge seeking, grudge holding, and forgiveness. Based on Keltner, Gruenfeld, and Anderson’s (2003) power approach theory and McCullough, Kurzban, and Tabak’s (2013) theorizing about revenge and forgiveness systems, we tested (a) the associations between victims’ social power and revenge, grudge, and forgiveness; (b) the mediational role of approach/inhibition motivation in explaining why the associations exist; and (c) the moderating role of whether the transgressor apologizes or not in explaining the associations. Five studies (Ns = 279, 181, 154, 131, and 81) that varied in sample (undergraduate, community), research method (nonexperimental, experimental), context (laboratory, online), measures (self-reported, behavioral), and statistical method (regression, ANOVA), supported our predictions and the systematic generalizability of the effects. Applied implications are discussed.

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The variable start and duration of the Grey seal breeding season makes the estimation of total pup production from a single census very difficult. Classifying the count into morphological age classes enables the form and timing of the birth rate curve and estimates of pup mortality rates to be elucidated. A simulation technique is described which enables the duration of each morphological stage to be determined from a series of such classified counts taken over one season. A further statistical technique uses these estimates to calculate the mean timing and duration of the breeding season from a single classified count taken from similar populations in subsequent years. This information allows total pup production to be calculated for any appropriate breeding colony. Some guidance is given as to the optimal timing of that single census which would yield the best estimate of production, although the precise date is not critical to the success of the technique. Results from single census estimates obtained in this way are compared with known production data from more detailed surveys for a number of different colonies.

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Patterns of colonisation and breeding behaviour were observed in part of the Grey seal rookery at North Rona during the entire breeding season in 1972. Bulls came ashore when pupping started and joined cows grouped around pools. Numbers of cows and bulls increased to maxima in three and five weeks respectively. Limited access to the rookery and the presence of pools and waterlogged ground influenced site selection by cows. In the study area the breeding season lasted for 74 days, with individual bulls staying for periods varying from 6–57 days. Daily ratios of bulls to cows varied, but the average ratio was 1:7‐5. It was estimated that 275 cows participated in mating, compared with 37 bulls, during the entire breeding season. The interval of 18 days between peak numbers of cows and bulls ashore corresponded closely with the average time that cows spent ashore. The aggressive responses of cows in mating behaviour were noted during observations of 114 copulations. It was concluded that a bull requires a very strong sexual drive in order to overcome a cow's aggressive responses, and this reinforces the selective advantage of aggressive dominance in bulls. The stimulus inducing a bull to attempt mating seemed to be the presence of oestrous cows in the rookery rather than an individual cow being in oestrus, because the number of attempted copulations increased even when the number of cows in oestrus temporarily declined during the season. Direct observations and calculations using an index of copulation suggested that the copulation frequency for individual cows ranged from 2.5‐3.6. A bull's participation in mating, and therefore, its genetic influence, was related to the length of its stay in the rookery, and from this evidence it was deduced that a social hierarchy existed amongst the bulls. Appraisal of the results led to the conclusion that the Grey seal bull maintains a high level of sexual activity so as to mate with as many cows as possible, rather than ensuring exclusive access to cows through territorial fighting and boundary display.

The Grey seal breeding assembly on North Rona was studied throughout autumn 1972. Weekly censuses provided data on birth rate and mortality. It is estimated that 1736 pups were born in 1972. This is about 500 less than the mean production estimate for this assembly during the period 1959–71, possibly a result of disturbance of the breeding site by the expedition. About 600 of the pups died before putting to sea. The mean date of birth and the duration of the pupping season agree closely with earlier work on North Rona, although the mean daily birth rate curve is somewhat irregular, perhaps because there was an unusually dry spell of weather at a critical time in the pupping season. An improved estimate of mortality at this assembly showed a relationship with pup density similar to that observed at the Fame Islands. Techniques for estimating pup production (and consequently total population), though not reliable for determining absolute values, are useful for indicating trends and they suggest a stable population of 8000–9000 animals at North Rona. Such estimates might be improved by the use of better methods of aerial photography.