Number Of Estrous Females Research Articles

Environmental factors influencing the seasonality of estrus in chimpanzees

Although the energetics of the estrous cycle in primates is not well understood, evidence suggests that energy and nutrient acquisition influence ovulation and the timing of conception. Energy for estrus has to compete with energy allocated for cellular maintenance, thermoregulation, movement for food, and predation avoidance. While some chimpanzee (Pan troglodytes) populations do not have a seasonal birth period, evidence suggests that there is seasonality in the number of estrous females. Similarly, the onset of postpartum cycles has been reported to be seasonal. We used 33 months of data from the Taï National Park, Côte d'Ivoire, to examine how the number of estrous females in a given month was influenced by the abundance and distribution of food, diet, rainfall and temperature. In a second analysis, we examined if there was a seasonal effect on first estrous swellings in adolescent females and postpartum adult females. Results demonstrated that the number of females in estrous in a given month was positively related to food abundance and percent foraging time spent eating insects, and negatively related to mean rainfall in the two preceding months and the mean high temperature. The timing of first estrous swellings of postpartum females and prepartum young females was positively related to the food abundance, and negatively related to mean high temperature. These results showed that environmental conditions can seasonally limit the energetically demanding estrus cycle. The presence of estrous females increases gregariousness in chimpanzee communities, and this study identified environmental factors that affect estrus directly and hence social grouping indirectly.

Influence of fluctuation in the operational sex ratio to mating of troop and non-troop male Japanese macaques for four years on Kinkazan Island, Japan

Taking advantage of a marked yearly fluctuation in the number of estrous females, I studied the differences in mating success between troop males and non-troop males in an unprovisioned group of Japanese macaques. Fluctuation in the defendability of estrous females by troop males, as predicted by the operational sex ratio (the number of estrous females per troop male), strongly affected the mating with ejaculation (successful mating) per observation day of both troop and non-troop males. When operational sex ratio was low, troop males monopolized successful mating inside the troop. No successful mating of non-troop males was observed inside the troop. In contrast, both troop and non-troop males were able to mate often inside the troop when operational sex ratio was high. These findings suggest that troop males obtained the benefit of secured successful mating in the troop because troop males could mate successfully even in mating seasons with a low operational sex ratio, and the chance of successful mating for non-troop males will increase as the ability of troop males to monopolize estrous females decreases.

What Factors Affect the Size of Chimpanzee Parties in the Kalinzu Forest, Uganda? Examination of Fruit Abundance and Number of Estrous Females

We examined factors affecting the size of chimpanzee parties in the Kalinzu Forest, Uganda. We found that the number of individuals in a party increased with observation time. Therefore, we employed two methods to reduce this bias: (1) we evaluated party size via the mean number of individuals observed in each 1-h period during the observation of a party (1-h party size), and (2) we used the number of all individuals observed in a party (1-day party size) and performed an analysis of covariance, with observation time of the party as the covariant. We examined factors that might affect party size: fruit abundance, fruit distribution, and number of estrous females. There was no relationship between party size and fruit abundance or distribution. Conversely, the number of males has a significant positive correlation with the number of estrous females, though there is no correlation with the number of anestrous females. These results suggest that males tended to join parties with more females in estrous, irrespective of differences in fruit availability.

Correlates of Intergroup Transfer in Male Grey-cheeked Mangabeys

We studied factors influencing intergroup transfer in male mangabeys (Lophocebus albigena) inhabiting 7 social groups in Kibale National Park over a 2-year period. The sample consisted of 40 males including 36 that we captured and marked during the study. Intergroup transfers are movements between groups that culminate in either long-term (dispersal) or short-term (visits) residency by males in the new groups. Both dispersers and visitors had a greater tendency to move into groups that contained higher numbers of estrous females than their prior group. Using averages of weekly group counts, we found a significant positive relationship between the number of estrous females in a group and the number of adult males in a group, but not between the number of nonestrous females and the number of adult males in the 7 study groups. There is no evidence that dispersal events were released by aggression. For a sample of males followed ≥2 mo before emigration, aggression did not increase just before emigration. Results suggest that spatiotemporal availability of estrous females is a major proximate factor influencing intergroup transfer in mangabeys. The results also suggest that dispersing males are more sensitive to relative numbers of estrous females than to measures of female availability such as operational sex ratio, socionomic ratio, and the number of excess females that take into account the potential for male-male competition.

MOVEMENTS, HOME RANGE, AND TERRITORIES OF MALE SEA OTTERS OFF CENTRAL CALIFORNIA

AbstractSixty male sea otters (Enhydra lutris) were tagged on the rear flippers with colored tags. Of these, 46 (77%) were resighted. Movements of 127 km were documented for adults and 187 km for subadults. Adults maintained breeding territories that averaged 40.3 ha (n= 10, SE = 4.0). They returned to the same territory seasonally for up to seven consecutive years. Territorial males moved from areas of high male abundance to areas of high female abundance on a seasonal basis. During the winter, 74% of adult males left breeding areas and joined concentrations of males located near the ends of the range. Thirty percent of the subadult males were observed in male groups near the extremities of the range. During the summer and fall, the density of adult males (15/1,000 ha) and adult male to independent otter (non‐pup) ratio (1:5) in female areas was highest. The number of adult males in areas of female abundance was inversely related to the number of dependent pups, perhaps because when pup numbers are low (late summer and fall) the number of estrous females is high. Subadult males may remain in female areas on a year round basis until their second or third year. However, they were not generally associated with adult females.

Male-male Competition and Reproductive Success in Elephant Seals

Male-male competition and reproductive success of northern elephant seals, Mirounga augustirostris, was studied for six consecutive breeding seasons at Año Nuevo Island, California. The conclusions were as follows: (i) Less than one third of the males in residence copulate during a breeding season. A few males are responsible for the majority of copulations, (ii) The number and age of males copulating varies with: (a) harem location and topography, (b) the number of estrous females in the harem, and (c) the number of males competing for females, (iii) Copulation frequency is related directly to success in male-male competition, i.e., social rank. (iv) The same individuals may dominate breeding for three consecutive breeding seasons. (v) Successful males die within a year or two after their reproductive peak. (vi) The reproductive success of most males is nil or low because many die before reaching breeding age and some of those that reach maturity are prevented from mating by the highest ranking males. (vii) Individual strategies have important consequences for reproductive success, (viii) Male-male competition is a major cause of pup mortality prior to weaning. The potential reproductive success of males is much greater than that of females. Changes in colony number and composition affect the reproductive success of males as well as females.