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Mating behavior of the Hog-badger (Arctonyx collaris) was recorded on 463 videos (totally 8053 s) taken with auto-trigger cameras between March 13 and May 13, 2017 in Jiangxi Wuyishan. Males followed and guarded the females for several hours before mating. One mounting behavior, and three mating behaviors were observed from 01:55 to 08:49 on April 18. The durations of mating behaviors lasted for 731s, 1690s and 1494s, respectively. Based on these observations, we found: 1) mating behavior was controlled by the female, including obvious sexual solicitations; 2) females can mate more than one time within one estrous cycle; 3) quickly and repeatedly pumping and inserting behavior was observed in male during mating.  相似文献   
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灵长类交配模式是灵长类社群结构和婚配制度的重要表征之一,其研究有助于了解灵长类社群结构和两性交配策略。2013年11月至2014年10月,我们对云南白马雪山国家级自然保护区一人工辅助投食滇金丝猴群进行了观察研究,采用焦点动物取样法和全事件记录法收集了雌雄个体的交配相关的行为数据,主要包括邀配对象、交配过程、持续时间和回合数,以及参与交配的雌雄对在交配结束后的相互理毛的持续时间和回合数。研究结果表明:研究群滇金丝猴全年均有交配行为,交配高峰期在7-9月,两性参与交配的积极性和对季节变化的响应不同;交配主要由雌性通过邀配发动(76%),交配高峰期也是雌性邀配的高峰期;雄性爬跨频次(年均0.43次/月,n=5)和射精爬跨比(年均19%,n=5)则在全年无显著变化。交配行为发生的典型表现为:雌性通过小跑或跳跃进入雄性视线范围内,爬伏呈臀向雄性邀配;雌猴爬伏时离雄猴的远近距离不同(<1m vs. 2-5m : 69% vs. 31%)会影响其邀配成功率(<1 m vs. 2-5 m :68% vs. 40%);若一次邀配失败,雌猴可能会连续爬伏邀配(最多4次),连续多次邀配的成功率显著高于单次邀配(79% vs. 52%)。交配结束后雌性会主动为雄性理毛,但雌性主动理毛与交配是否射精无关。  相似文献   
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Previous research has demonstrated that female behaviors toward men or sexual interest are different across the menstrual cycle. However, women's receptivity to an explicit courtship solicitation still remained in question. In a field experiment, 20-year-old women were approached by 20-year-old male confederates in nightclubs and solicited to dance during the period when slow songs were played. A survey was administered to the women in order to obtain information about the number of days since the onset of previous menses. It was found that women in their fertile phase agreed more favorably to the dance request than women in their luteal phase or in their menstrual phase.  相似文献   
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Parental care involves elaborate behavioural interactions between parents and their offspring, with offspring stimulating their parents via begging to provision resources. Thus, begging has direct fitness benefits as it enhances offspring growth and survival. It is nevertheless subject to a complex evolutionary trajectory, because begging may serve as a means for the offspring to manipulate parents in the context of evolutionary conflicts of interest. Furthermore, it has been hypothesized that begging is coadapted and potentially genetically correlated with parental care traits as a result of social selection. Further experiments on the causal processes that shape the evolution of begging are therefore essential. We applied bidirectional artificial selection on begging behaviour, using canaries (Serinus canaria) as a model species. We measured the response to selection, the consequences for offspring development, changes in parental care traits, here the rate of parental provisioning, as well as the effects on reproductive success. After three generations of selection, offspring differed in begging behaviour according to our artificial selection regime: nestlings of the high begging line begged significantly more than nestlings of the low begging line. Intriguingly, begging less benefitted the nestlings, as reflected by on average significantly higher growth rates, and increased reproductive success in terms of a higher number of fledglings in the low selected line. Begging could thus represent an exaggerated trait, possibly because parent–offspring conflict enhanced the selection on begging. We did not find evidence that we co‐selected on parental provisioning, which may be due to the lack of power, but may also suggest that the evolution of begging is probably not constrained by a genetic correlation between parental provisioning and offspring begging.  相似文献   
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The mating behaviors of the proboscis monkey were observed in a riverine forest along a tributary of the Kinabatangan River, Sabah, Malaysia, for a period of 30 months. Solicitation for copulation was initiated frequently by males and occasionally by females. Most copulations involved only one mount; however, some multiple-mount copulations were observed and a maximum of six mounts per copulation were recorded. The mean duration of mounts was about 27 sec. Nonsexual mounts (female-female, female-juvenile/infant, juvenile-juvenile, and juvenile-infant) were also observed. Female-female mounts occurred shortly after failed solicitations toward males were observed. Harassment by juveniles and/or infants was observed during copulation; however, these harassments apparently did not interfere with copulation. Sexual swelling was evident in 77.4% of copulating females, with copulating subadult females showing the most distinct swelling.  相似文献   
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That repeated copulation with the same partner within a singlefertile period is beneficial to the male is generally accepted,but why it should be adaptive to the female is controversialand clear evidence supporting any hypothesis is lacking. Hunteret al. (1993) presented seven hypotheses explaining repeatedmating from the female perspective. Four of them are consistentwith the occurrence of male refusal to copulate: females mighttrade copulations for (1) immediate and or (2) future materialbenefits, or use mating as a mechanism for (3) mate-guardingand or (4) mate-assessment. To test these hypotheses in a populationof crested tits Parus cristatus, we collected data on variationin female solicitation rate, proportion of male refusal, andextra-pair paternity. We found that (1) female solicitationrate was independent of male condition, (2) the proportion ofmale refusal was higher in poor-condition males and (3) femalespaired to poor-condition males sought extra pair paternity.These findings agree with predictions stemming from the mateassessment hypothesis. Therefore, it is suggested that, in crestedtits, male response to female copulation solicitation reflectsmale condition and is used by females to assess male quality  相似文献   
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Virgin females of the subtropical pierid butterfly Eurema daira were observed to actively solicit male courtship. The resulting interactions involved both aggressive contact with male individuals and elaborate female posturing. Cage-based trials showed that there was a direct relationship between the frequency of courtship solicitation attempts and female age. Virgin females under 3 days old showed little or no interest in initiating courtship. By contrast, 23.2 percent of the virgin females over three days old actively solicited available males with peak solicitation behavior exhibited from five day old individuals.  相似文献   
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