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3 The New York Years (1931–1953)

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Zoogeography 165<br />

members of such groups colonized other continents or islands where they radiated<br />

conspicuously (e.g., meliphagids in <strong>New</strong> Zealand, drepanidids in Hawaii); (3)<br />

faunas are built up by waves of colonization from outside sources superimposed<br />

on original stocks; (4) geographical speciation occurs in populations separated by<br />

physical barriers (due to continental movements and climatic-vegetational fluctuations);<br />

(5) secondary range expansion from the areas of origin led to sympatry of<br />

representatives of different faunas.<br />

Mayr (1982h) severely criticized an exclusive explanation of zoogeographic<br />

patterns by the vicariance paradigm but agreed (1983e) that it is no longer sufficient<br />

simply to develop an explanatory scenario. Hypotheses and predictions should be<br />

tested. On the other hand, he pointed out that not all problems can be settled in this<br />

manner, e.g., the placement of borders between biogeographical regions (Wallace’s<br />

or Weber’s lines versus “Wallacea” in the Malay Archipelago). In quantitative<br />

studies one must avoid treating all species of certain animal groups as exhibiting<br />

uniform biogeographical characteristics. Island birds are not a random sample of<br />

mainland birds with equal dispersal facilities. Among all kinds of animals there<br />

are good and poor dispersers. Mayr (1983f) emphasized again that the elements of<br />

faunas have had different histories and mean values are often meaningless. Mayr<br />

and Diamond (2001g) discussed these aspects in great detail with respect to the<br />

avifauna of northern Melanesia.<br />

To explain discontinuous ranges, many authors favored an “either-or” choice,<br />

either secondary (vicariance) or primary (dispersal across a barrier). However, it<br />

is becoming clearer that in poor dispersers many if not most discontinuities are<br />

secondary, while in good dispersers they are primary. Also, the extant pattern of<br />

distribution was, at least in part, established in that geological period in which<br />

a group had its major evolutionary development, hence earthworms or mayflies<br />

have other patterns than mammals and birds. Single-track explanations are unable<br />

to cope with this pluralism and are, therefore, bound to be misleading.<br />

Summarizing, spatial events and climatic-vegetational fluctuations shape faunas<br />

and species from their early history. Separation of populations through dispersal<br />

and vicariance, secondary contact and overlap led to speciation and faunal differentiation.<br />

<strong>The</strong> early history of faunal lineages was influenced by continental drift,<br />

i.e., the break-up and contact of continental blocks–processes which had more<br />

pronounced effects on some groups, like freshwater fishes, than others like birds.<br />

First Steps<br />

<strong>The</strong> ecology and distribution of birds fascinated Mayr already as a student (see<br />

pp. 28, 35). In his dissertation prepared under Erwin Stresemann as thesis advisor,<br />

Mayr analyzed a zoogeographical problem, the range expansion of the Serin<br />

(Serinus serinus), a small greenish yellow finch which, spreading northward from<br />

the Mediterranean region, had colonized large portions of Europe since the early<br />

19th century (Mayr 1926e; see Vuilleumier 2005b). He described the process of<br />

range expansion and discussed the ecology of this and other expanding species

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