Whether they are big or small, species geographic ranges can be divided into core and edge populations. Verbal models from macroecology and population genetics predict that patterns of population abundance, individual fitness, and genetic diversity should differ across core and edge populations (Brown, 1984;Sagarin & Gaines, 2002), which can then contribute to the formation of range limits (García-Ramos & Kirkpatrick, 1997;Gaston, 2003).At the centre of their range, species are hypothesized to be optimally adapted for the habitat, allowing them to maintain large, interconnected populations characterized by high local abundance (Brown, 1984;Sagarin & Gaines, 2002). Moving away from the centre, the habitat becomes more marginal, leading to decreased reproductive output (Angert, 2006;Gaston, 2009;Pigott & Huntley, 1981). Or, favourable habitat may become increasingly patchy towards the range edge, leading to depression of regional abundance relative to range centres. Populations towards