Ke. Arnold et Ipf. Owens, COOPERATIVE BREEDING IN BIRDS - A COMPARATIVE TEST OF THE LIFE-HISTORY HYPOTHESIS, Proceedings - Royal Society. Biological Sciences, 265(1398), 1998, pp. 739-745
In approximately 3.2% of bird species individuals regularly forgo the
opportunity to breed independently and instead breed cooperatively wit
h other conspecifics, either as non-reproductive 'helpers' or as co-br
eeders. The traditional explanation for cooperative breeding is that t
he opportunities for breeding independently are limited owing to pecul
iar features of the species' breeding ecology. However, it has proved
remarkably difficult to find any common ecological correlates of coope
rative breeding in birds. This difficulty has led to the 'life history
hypothesis: which suggests that the common feature of cooperatively b
reeding birds is their great longevity, rather than any particular fea
ture of their breeding ecology. Here, we use a comparative method to t
est the life history hypothesis by looking for correlations between li
fe history variation and variation in the frequency of cooperative bre
eding. First, we find that cooperative breeding in birds is not random
ly distributed, but concentrated in certain families, thus supporting
the idea that there may be a common basis to cooperative breeding in b
irds. Second, increases in the level of cooperative breeding are stron
gly associated with decreases in annual adult mortality and modal clut
ch size. Third, the proportion of cooperatively breeding species per f
amily is correlated with a low family-typical value of annual mortalit
y, suggesting that low mortality predisposes cooperative breeding rath
er than vice versa. Finally, the low rate of mortality typically found
in cooperatively breeding species is associated with increasing seden
tariness, lower latitudes, and decreased environmental fluctuation. We
suggest that low annual mortality is the key factor that predisposes
avian lineages to cooperative breeding; then ecological changes, such
as becoming sedentary, further slow population turnover and reduce opp
ortunities far independent breeding. As the traditional explanation su
ggests, the breeding habitat of cooperatively breeding species is satu
rated, but this saturation is not owing to any peculiar feature of the
breeding ecology of cooperative breeders. Rather, the saturation aris
es because the local population turnover in these species is unusually
slow as predicted by the life history hypothesis.