Divergence in allopatry provides a simple null model of speciation (Mayr, 1947). Following geographic isolation and given enough time, reproductive isolation is inevitable as incompatibilities will eventually become fixed as a result of genetic drift and/or selection (Bateson, 1909;Dobzhansky, 1937;Muller, 1942). Taxa that evolved partial reproductive isolation in allopatry may come into secondary contact as a result of range shifts and-depending on their degree of reproductive isolation and niche overlap-either form a contact zone or invade each other's range (Barton, 1985;Pigot, 2013). If allopatric divergence dominates speciation, then local alpha diversity for a given clade cannot accrue until secondary sympatry is achieved (Weir & Price, 2011). Thus, the forces that facilitate or hamper secondary sympatry and the timescale over which this occurs have profound consequences both for speciation and for the spatial distribution of species diversity. While modern ranges only provide a snapshot of the dynamic history of range shifts, understanding the