JOHNSTON: CAYMAN ISLAND AVIFAUNA A GENERAL ASSESSMENT OF FEEDING ECOLOGIES AND HABITAT DISTRIBUTIONS It is instructive now to generalize and summarize data on feeding ecologies or feeding niches of the resident terrestrial avifauna. As shown in Table 17, most of the bird species (57% ) are arboreal foragers, either on arthropods or fruits. Furthermore, with the expected exception of pastures and cultivated areas, these same species are each widely dis- tributed in the seven upland formations and have comparable frequency of occurrence and relative abundance therein. Conversely, ground-feed- ing forms (21'i ) are relatively less common as a whole in the Caymans and are virtually restricted to the non-forested formations. The latter distribution strongly suggests the scarcity of insects and seeds on the ground in the several forest formations. Indeed, ground cover is notice- ably scarce in the several forest formations due to a combination of factors (edaphic karst topography, light penetration). The relatively high proportion of arboreal insectivores and frugivores, augmented by the timber-probing and -gleaning woodpeckers would be expected on islands, such as the Caymans, where forest formations of several types predominate in areal extent (see Figs. 1-3). Bird species diversity is a known function of habitat or plant species diversity. Although plant species diversity was not determined quantita- tively in the present study, it is nonetheless empirically true that in the comparisons of avifaunal compositions of the several ecological forma- tions, bird species diversity does attain its peak in those forest formations with the greatest plant diversity. Complexity of floristic composition (presence of many codominant trees vs. one or two dominants, height of vegetation, some semblance of stratification, etc.) may be sequentially arranged in descending order (number of bird species in parentheses) as follows: towns and house sites (20), limestone forests (17), logwood- thatch palm-red birch forest (15), sea grape-almond woodland (16), mangrove swamps (11), pure logwood forests (11), and pastures and cultivated areas (11). A relationship between number of terrestrial bird species and habitat complexity is implied by these data. TAXON CYCLES A subject of recent interest to some island biogeographers is that of taxon cycles, and for the West Indian avifauna these have been explored generally and in detail by Ricklefs and Cox (1972). Whether an anal- ysis of taxon cycles for individual small islands or archipelagos is mean- ingful (see Ricklefs 1970, for Jamaica) is a moot point because of great areal and relief differences in large island groupings, but an attempt at