Orgasm in female primates

The major genital responses of arousal in women are vasocongestion, resulting in tumescence of the vaginal walls, and vaginal lubrication, facilitating penile intromission and thrusting. During orgasm, several involuntary muscular reactions occur, the most adaptive being in the outer third of the vagina and the uterus. Uterine suction of the ejaculate seems to occur when the reproductive apparatus is functioning at full efficiency. Coitus may result in reflex ovulation. Indices of female nonhuman primate orgasm thus far proposed include rhythmic vaginal and anal contractions, hyperventilation, involuntary muscle tension, arm and leg spasms, grimacing, and uterine contractions. Orgasm in our species may exist as a result of phylogenetic inertia, not as a novel response selected during protohominid or hominid evolution. A theory for the evolutionary nature of orgasm in women states that the orgasmic vaginal contractions stimulate ejaculation. Reasons for the common asynchrony of this adaptive pattern are the usually lowered ejaculatory threshold because of non-species-typical orgasmic frequency in the male, and the frequently delayed female orgasm because of psychological inhibition and/or inadequate control and development of the pubococcygeus.     

Effects of egg-production and of exposure to males on female survival in Drosophila melanogaster

Female Drosophila melanogaster whose rate of egg-laying was lowered by removal of a suitable substrate or additionally by reduction in protein intake had longer lifespans than control females. The association between lifespan and egg-laying rate could not be accounted for in terms of variation in either exposure to males or nutritional status. Females continuously exposed to males lived less long than intermittently exposed females, and this longevety difference could not be explained in terms of differences in either rate of egg-production or egg-hatchability.     

Postcanine tooth size in female primates

The results of many allometric studies of postcanine tooth size in mammals have not corresponded to expectations of tooth size based on energy requirements and dental function. The purpose of this study is to investigate the relationship between postcanine occlusal surface area, body size, and the metabolic demands of pregnancy and lactation in female primates. Tooth and body sizes from 38 primate species were taken from the literature to test two hypotheses: 1) females should have relatively larger teeth than males in order to masticate additional food for the energetic costs of reproduction; 2) taxa with the largest neonatal size (a measure of average metabolic costs of pregnancy and lactation) should have females with a greater degree of relative dental enlargement. The results show that relatively large female teeth are not found consistently in primate species. Females have less occlusal surface area than expected on the basis of the male tooth and body size regression in 21% of the species, and there is no correlation between relative female tooth size and relative newborn size across higher primate taxa. The degree of female dental enlargement is most closely related to degree of sexual dimorphism in body weight. The correlation between degree of body weight dimorphism and relatively larger postcanine teeth in females than in males is 0.87 in the 38 species. Species that are monomorphic in weight tend to be monomorphic in tooth size even though females apparently require more food than males.(ABSTRACT TRUNCATED AT 250 WORDS)     

Adolescent exaggeration in female catarrhine primates

Adolescent females of 11 primate species display exaggerated versions of the cues to sexual cycle state or fertility which are displayed by adult females: anubis baboons; geladas; Assamese, Barbary, crab-eating, Japanese, and stump-tailed macaques; patas monkeys; gorillas; and humans. These cases are briefly described and a variety of hypotheses is presented and evaluated to account for the adolescent exaggeration. Such exaggeration may be a super-normal sexual stimulus, a barrier to cross-species hybridization, a helpful prop in female:female competition, a passport for transfers, an insurance policy where unpredictable changes of circumstance are likely, or a non-adaptive side-effect of some other phenomenon. The transfer and unpredictability hypotheses seem to apply to the largest number of species, including humans.     

Bateman revisited: the reproductive tactics of female primates

The breeding system of an animal population is thought to depend on the ability of one sex (usually the male) to acquire mates, either directly through association with females or indirectly through defense of the resources desired by females. The sex that contributes most to infant care (usually the female) is constrained by parental involvement and thereby limits reproduction of the opposite sex. Accordingly, males, but not females, enhance their reproductive success by acquiring additional mates. This classical view has emphasized the role of male-male competition in sexual selection, at the expense of fully exploring the potential for female choice. A more recent shift in focus has revealed substantial variation in female reproductive success and increasingly accentuates the importance of female intrasexual competition and male mate choice. A comparative review of primate reproduction, therefore, challenges expectations of male control and female compliance, and calls for a comprehensive treatment of costs and benefits that extends beyond conventional mention of heavy female investment versus male negligence or absenteeism. For individuals that manipulate their social environment or reproductive output, consideration of more subtle, even cryptic, aspects of female behavior and physiology (e.g., social strategizing, sexual solicitation or rejection, sexual advertisement or concealed ovulation, multiple mating, and reproductive failure) raises the question of whether females can be effectively 'monopolized.' Widespread patterns that counter Bateman's paradigm call for a reexamination of the predictions generated by dichotomizing gametes into 'expensive eggs' and 'cheap sperm,' and encourage continued mechanistic research focused on conception quality rather than quantity.     

The value of grooming to female primates

Current socioecological models suggest that the structure of female-bonded primate groups is predicated on the need for coalitionary support in competitive interactions. Social grooming is thought to be the means by which females ensure support from other individuals, either by the direct exchange of grooming for aid or by using grooming as a means of strengthening social bonds. Since these relationships are valuable, they must be regularly serviced and must be repaired if they become damaged. We question this position and show that empirical evidence to support these theoretical arguments is lacking. We then go on to present a new framework in which the inconsistencies regarding grooming and relationship negotiation are interpreted in the context of individual decision-making processes. In this framework, primate groups represent biological markets in which individuals either trade grooming in a reciprocal manner for the direct benefits that grooming itself offers, or exchange it for tolerance by more powerful animals. A number of testable predictions are derived from this hypotheses. The need for socioecological studies to focus on the dynamics of individual relationships rather than using summary measures is emphasized since only a detailed knowledge of serial interaction will provide the key to understanding the complexities of individual decision-making processes.     

Two further males with female karyotypes

Summary Two males with the karyotype 46,XX are reported. In both individuals, the karyotype was determined in over 400 cells from lymphocyte, skin, and testis cultures.Case 1, a man born in 1935, had a normal male appearance. The Xg blood group distribution in his family was: father Xg(a+), mother Xg(a-), and propositus xg(a-). Case 2, a boy born in 1964, had penoscrotal hypospadias, and a small penis and scrotum, but otherwise appeared normal.Results of clinical, histological, genetical and blood group investigations are given.     

Evolution of female preference for younger males

Previous theoretical work has suggested that females should prefer to mate with older males, as older males should have higher fitness than the average fitness of the cohort into which they were born. However, studies in humans and model organisms have shown that as males age, they accumulate deleterious mutations in their germ-line at an ever-increasing rate, thereby reducing the quality of genes passed on to the next generation. Thus, older males may produce relatively poor-quality offspring. To better understand how male age influences female mate preference and offspring quality, we used a genetic algorithm model to study the effect of age-related increases in male genetic load on female mate preference. When we incorporate age-related increases in mutation load in males into our model, we find that females evolve a preference for younger males. Females in this model could determine a male's age, but not his inherited genotype nor his mutation load. Nevertheless, females evolved age-preferences that led them to mate with males that had low mutation loads, but showed no preference for males with respect to their somatic quality. These results suggest that germ-line quality, rather than somatic quality, should be the focus of female preference in good genes models.     

Effect of estrogen deprivation on the reproductive physiology of male and female primates

The availability of CGS 16949A, CGS 20267 and CGP 47645, a series of aromatase inhibitors (AIs) having high specific activity and specificity, made possible this study wherein the need for estrogen (E) for regulating (a) follicular maturation/ovulation, luteal function and pregnancy establishment, and (b) testicular function of the bonnet monkey (Macaca radiata) has been examined. Generally these compounds, used in the range of 500 μg to 2.5 mg/day did not inhibit follicular maturation although they did reduce E levels. Although low doses had no effect on ovulation it appears that relatively high doses of CGS 20267 and CGP 47645 could be inhibiting it. Three oral doses of letrozole (CGS 20267, each dose of 2 mg) during the follicular phase resulted in the formation of multiple follicles in cycling females, and these could be ovulated by exogenous hCG (1000 IU) treatment. Although administration of AI during the early luteal phase had no effect on progesterone (P) production, it prevented pregnancy establishment. Whereas AI administration in the female had no significant effect on luteinizing hormone (LH) and follicle stimulating hormone (FSH) levels (except at high drug dosages), it significantly increased serum testosterone (T) levels in the male. Sustained high levels of T (30–50 ng/ml) could be maintained for 100 days by administering 2.5 mg of CGP 47465 orally once in 5 days. Blockade of E synthesis in the male led to the disruption of testicular germ cell transformation, which in turn resulted in a significant reduction in sperm production. These studies with aromatase inhibitors in the monkey suggest that these compounds have a potential for use as fertility regulating agents in both the male and female primate.     

The evolution of social philopatry in female primates

The transition from solitary life to sociality is considered one of the major transitions in evolution. In primates, this transition is currently not well understood. Traditional verbal models appear insufficient to unravel the complex interplay of environmental and demographic factors involved in the evolution of primate sociality, and recent phylogenetic reconstructions have produced conflicting results. We therefore analyze a theoretical model for the evolution of female social philopatry that sheds new light on the question why most primates live in groups. In individual-based simulations, we study the evolution of dispersal strategies of both resident females and their offspring. The model reveals that social philopatry can evolve through kin selection, even if retention of offspring is costly in terms of within-group resource competition and provides no direct benefits. Our model supports the role of predator avoidance as a selective pressure for group-living in primates, but it also suggests that a second benefit of group-living, communal resource defense, might be required to trigger the evolution of sizable groups. Lastly, our model reveals that seemingly small differences in demographic parameters can have profound effects on primate social evolution.     

The number of males in a primate troop

Primate species in which the breeding group contains more than one adult female may typically live in ‘harems’, with one male, or multi-male troops. This paper shows, in a review of the published evidence for 33 species, that that variable is associated with the duration of the breeding season: harems are commoner when the breeding season is long, multi-male troops when it is short. The sex ratio of adults in a troop is likewise correlated with the length of the breeding season.     

样地数量对气候变化背景下树种分布预测的影响

基于不同景观破碎化程度下的中性景观,探讨了气候变化背景下样地数量对景观尺度树种分布预测的影响.采用模型耦合的方法进行树种分布预测,设置了3个样地数量预案与1个参考预案.分别在每一破碎化程度下检验3种样地数量预案的预测结果与参考预案之间的差异.结果表明:样地数量会影响树种分布预测结果,具有不同生活史属性的树种对样地数量的需求不同,对普适性树种进行分布预测需要的样地数量较多;除极度特异种外,景观的破碎化程度也会影响样地数量对树种分布预测的影响;随着模拟时间的增加,样地数量对景观尺度树种分布预测的作用会发生变化,对于一些普适种树种来说,长期模拟需要较多的样地.     

Responsiveness of Pseudaletia unipuncta males to the female sex pheromone

ABSTRACT. In wind tunnel experiments male response to different concentrations of synthetic pheromone varied with age. At 25°C responsiveness increased up to day 5 and then declined slightly on day 7. For any given age the level of response generally increased with an increase in pheromone concentration. Males held at 15°C (since emergence) showed a continual increase in responsiveness with age; however, overall response levels were less than at 25°C. At 25°C male response to low concentrations of pheromone (10 and 30 μg) varied markedly over a 24 h period but no differences were observed at higher concentrations (100 and 300 μg).