Oecologia Roles of spatial partitioning, competition, and predation in the North American invasion of an exotic mosquito T. Z. Freed and P. T. Leisnham* Department of Environmental Science and Technology, University of Maryland, College Park, MD 20742-2315, USA. *corresponding author, leisnham@umd.edu ESM 1: Calculation of finite rate of population increase λ' Calculation ln 1 / N 0 Axf wx x ' exp xAxf wx x D Axf wx x Where N0 is the initial number of females (assumed to be 50%), x is the median days to eclosion, Ax is the mean number of females eclosing on day x, and wx is the mean wing length on day x. The function f(wx) is the species-specific relationship between fecundity and female wing length. For A. albopictus, f(wx)=0.5 * (78.02 * wx – 121.24) (Lounibos 2002). For A. japonicus, f(wx)= (53.078* wx) – 113.91 (Armistead et al. 2008). D is the time from eclosion to reproduction, which is estimated to be 14 days for A. albopictus (Lounibos 2002) and 12 days for A. japonicus (Armistead et al. 2008). References Armistead JS, Arias JR, Nishimura N, Lounibos LP (2008) Interspecific larval competition between Aedes albopictus and Aedes japonicus (Diptera : Culicidae) in northern Virginia. J. Med. Entomol. 45:629-637 Lounibos LP (2002) Invasions by insect vectors of human disease. Annu. Rev. Entomol. 47:233266 ESM 2: Calculation of the aggregation indices. Calculation of the index of intraspecific aggregation, J; the index of interspecific calculation, C; and the index of relative aggregation T: 𝐽1 = V1 1 2−m m1 1 where m1 is the mean and V1 is the variance of species 1 per patch. At J = 0, species 1 is randomly distributed among patches, and at J > 0 species 1 is aggregated. 𝐶12 = Cov12 (m1 ∗ m2 ) where Cov12 is the covariance between species 1 and species 2. At C = 0 the two species are independently distributed, at C > 0 the two species are positively associated, and at C < 0 the two species are negatively associated. 𝑇12 = (𝐶12 + 1) (𝐽2 + 1) where the inferior competitor is aggregated independently of the superior competitor at T < 1. T12 is considered to be a necessary and sufficient condition for coexistence between competitors (Sevenster 1996). References Sevenster JG (1996) Aggregation and coexistence .1. Theory and analysis. Journal of Animal Ecology 65:297-307 ESM 3: Site and site type trends of physiochemical characteristics. Figure 1 Bivariate plots of (A) detritus (g dry mass) and volume (mL), and (B) total nitrogen (mg L-1) and total phosphorus (mg L-1) among tree hole (filled) and tire (open) sites. Least squares means are ± SE.