Division of Tropical Environments and Societies, James Cook University, Townsville, Australia.
Fenner School of Environment and Society, Australian National University, Canberra, Australia.
Oecologia. 2022 Dec;200(3-4):285-294. doi: 10.1007/s00442-022-05232-6. Epub 2022 Aug 12.
Male and female reproductive behaviour is typically synchronised. In species such as those in the family Cervidae, reproductive timing is often cued by photoperiod, although in females, it can be dependent on body condition. When a species is introduced to a novel environment, the environment changes, or responses of the sexes to such cues differ, asynchronous reproductive behaviour between males and females may occur. We investigated the seasonality of reproductive behaviour in introduced chital deer in northern Queensland by examining male antler phase in relation to female conception rates. We then analysed the influence of different variables likely to affect the timing of male and female reproductive physiology. The lowest percentage of chital in hard antler in any 1 month in this study was 35% (Fig. 1), but the average value was closer to 50%, thus there was a seasonal peak in antler phase linked with photoperiod. Females conceived at any time of year, but were strongly influenced by the amount of rainfall 3 months prior to conception. This resulted in varying conception peaks year-to-year that often did not correspond to the male's peak in hard antler. In this system, a proportion of males and females were physiologically and behaviourally ready to mate at any time of the year. We predict that differences in the timing of the peaks between the males and females will lead to increased reproductive skew (variation in reproductive success among individual males). This pattern may select for different mating strategies or physiological mechanisms to increase reproductive success. Fig. 1 The average percentage of male chital deer in hard antler by month from 2014 to 2019 in north Queensland. Values above the bars indicate the total number of males that were sampled in each month and the error bars indicate the standard error. In the month with the lowest % males in hard antler in the entire study (November, 2017), 35% of males were in hard antler.
雄性和雌性的繁殖行为通常是同步的。在像鹿科这样的物种中,繁殖时间通常由光周期 cues 决定,尽管在雌性中,它可能依赖于身体状况。当一个物种被引入到一个新的环境中时,环境发生了变化,或者雌雄对这些 cues 的反应不同,雄性和雌性之间可能会出现异步的繁殖行为。我们通过检查雄性鹿角阶段与雌性受孕率的关系,研究了北昆士兰州引入的印度梅花鹿的繁殖季节性。然后,我们分析了可能影响雌雄繁殖生理 timing 的不同变量的影响。在这项研究中,任何一个月 chital 处于硬角状态的比例最低为 35%(图 1),但平均值更接近 50%,因此鹿角阶段与光周期有一个季节性高峰。雌性可以在一年中的任何时候受孕,但强烈受到受孕前 3 个月降雨量的影响。这导致了每年受孕高峰期的变化,这些高峰期通常与雄性硬角高峰期不一致。在这个系统中,一部分雄性和雌性在一年中的任何时候都有生理和行为上的交配准备。我们预测,雌雄之间高峰期的时间差异将导致繁殖偏斜(个体雄性之间繁殖成功率的差异)增加。这种模式可能会选择不同的交配策略或生理机制来提高繁殖成功率。图 1 2014 年至 2019 年北昆士兰州雄性印度梅花鹿每月硬角的平均比例。棒上的值表示每个月采样的雄性总数,误差线表示标准误差。在整个研究中雄性硬角比例最低的月份(2017 年 11 月),35%的雄性处于硬角状态。