Jf. Cockrem, TIMING OF SEASONAL BREEDING IN BIRDS, WITH PARTICULAR REFERENCE TO NEW-ZEALAND BIRDS, Reproduction, fertility and development, 7(1), 1995, pp. 1-19
A model to explain the timing of seasonal breeding in birds is present
ed. It is assumed that, despite the wide range in egg-laying seasons,
there are common physiological mechanisms which underlie seasonality i
n birds and that most, if not all, birds are photoperiodic. Birds are
considered to possess an internal rhythm of reproduction which is sync
hronized with seasonal changes in the environment by external factors,
particularly the annual cycle of daylength. The rhythm consists, at l
east in part, of regular changes in the photoperiodic response between
states of photosensitivity and photorefractoriness. Avian breeding se
asons effectively start in autumn when birds become photosensitive, re
gardless of when egg-laying occurs. The timing of breeding is then inf
luenced by the rate of increase of hypothalamic 'drive' and by the sen
sitivity of the hypothalamus and pituitary gland to inhibitory feedbac
k from gonadal steroids. If sensitivity is high, gonadal growth will n
ot occur until the threshold daylength for photostimulation is exceede
d after the winter solstice. Egg-laying then starts in late winter, sp
ring or summer. Alternatively, steroid feedback may be relatively low
and gonadal growth may be sufficiently rapid once the birds become pho
tosensitive 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 r
ainfall and, in some species, this information is more important than
daylength in determining the timing of breeding. The review also inclu
des the first summary of the breeding seasons of New Zealand birds. Th
e 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 Sept
ember to December. In addition, annual cycles of steroid hormone conce
ntrations in the North Island brown kiwi, the yellow-eyed penguin and
the kakapo are consistent with results from many studies on Northern h
emisphere birds. This model for the timing of breeding in birds can be
applied to New Zealand birds and it is concluded that the physiologic
al control mechanisms for the timing of seasonal breeding in New Zeala
nd birds are similar to those of other birds.