Cockrem J F
Department of Physiology and Anatomy, Massey University, Palmerston North, New Zealand.
Reprod Fertil Dev. 1995;7(1):1-19. doi: 10.1071/rd9950001.
A model to explain the timing of seasonal breeding in birds is presented. It is assumed that, despite the wide range in egg-laying seasons, there are common physiological mechanisms which underlie seasonality in birds and that most, if not all, birds are photoperiodic. Birds are considered to possess an internal rhythm of reproduction which is synchronized with seasonal changes in the environment by external factors, particularly the annual cycle of daylength. The rhythm consists, at least in part, of regular changes in the photoperiodic response between states of photosensitivity and photorefractoriness. Avian breeding seasons effectively start in autumn when birds become photosensitive, regardless of when egg-laying occurs. The timing of breeding is then influenced by the rate of increase of hypothalamic 'drive' and by the sensitivity of the hypothalamus and pituitary gland to inhibitory feedback from gonadal steroids. If sensitivity is high, gonadal growth will not occur until the threshold daylength for photostimulation is exceeded after the winter solstice. Egg-laying then starts in late winter, spring or summer. Alternatively, steroid feedback may be relatively low and gonadal growth may be sufficiently rapid once the birds become photosensitive that breeding occurs in late autumn or winter. The time of egg-laying in birds may also be strongly influenced by supplementary information, such as social cues, food availability, temperature and rainfall and, in some species, this information is more important than daylength in determining the timing of breeding. The review also includes the first summary of the breeding seasons of New Zealand birds. The pattern of egg-laying is exactly the same in native birds, in birds introduced to New Zealand and in other Southern hemisphere birds from similar latitudes, with a broad peak of egg-laying occurring from September to December. In addition, annual cycles of steroid hormone concentrations in the North Island brown kiwi, the yellow-eyed penguin and the kakapo are consistent with results from many studies on Northern hemisphere birds. This model for the timing of breeding in birds can be applied to New Zealand birds and it is concluded that the physiological control mechanisms for the timing of seasonal breeding in New Zealand birds are similar to those of other birds.
本文提出了一个解释鸟类季节性繁殖时间的模型。假定尽管鸟类的产卵季节范围广泛,但存在共同的生理机制作为鸟类季节性的基础,并且大多数(即便不是全部)鸟类具有光周期现象。鸟类被认为拥有一个内部繁殖节律,该节律通过外部因素,特别是日长的年度周期,与环境的季节性变化同步。这种节律至少部分地由光敏状态和光不应状态之间光周期反应的规律性变化组成。无论产卵发生在何时,鸟类的繁殖季节实际上始于秋季,此时鸟类开始具有光敏性。繁殖时间随后受下丘脑“驱动力”的增加速率以及下丘脑和垂体对性腺类固醇抑制性反馈的敏感性影响。如果敏感性高,性腺生长直到冬至后超过光刺激的临界日长才会发生。然后产卵在冬末、春季或夏季开始。或者,类固醇反馈可能相对较低,一旦鸟类具有光敏性,性腺生长可能足够迅速,以至于繁殖在深秋或冬季发生。鸟类的产卵时间也可能受到补充信息的强烈影响,如社会线索、食物可获得性、温度和降雨,并且在某些物种中,这些信息在确定繁殖时间方面比日长更重要。该综述还首次总结了新西兰鸟类的繁殖季节。本地鸟类、引入新西兰的鸟类以及来自类似纬度的其他南半球鸟类的产卵模式完全相同,产卵高峰大致出现在9月至12月。此外,北岛褐几维鸟、黄眼企鹅和鸮鹦鹉体内类固醇激素浓度的年度周期与许多关于北半球鸟类的研究结果一致。这个鸟类繁殖时间模型可以应用于新西兰鸟类,并且得出结论,新西兰鸟类季节性繁殖时间的生理控制机制与其他鸟类相似。