“…Since the generalized N-mixture model was introduced (Dail & Madsen, 2011), studies focused on developing population estimators that incorporate density dependence, intrinsic population growth rates, and environmental stochasticity into modelling (Bellier, Kéry, & Schaub, 2016;Hostetler & Chandler, 2015;Zipkin, Thorson, See, et al, 2014). Empirical application of generalized N-mixture models has been made to estimate population changes across generations (Bruggeman, Swem, Andersen, Kennedy, & Nigro, 2015;Hocking et al, 2013;McCaffery, Nowak, & Lukacs, 2016; Thorson, Scheuerell, Semmens, & Pattengill-Semmens, 2014;Zipkin, Sillett, Grant, et al, 2014), to test environmental effects on local abundances of an elusive bird species (Chandler & King, 2011), or to estimate the emergence timing of bivoltine butterflies (Matechou, Dennis, Freeman, & Brereton, 2014). To our knowledge, however, this approach has not been used to estimate a population size that is subject to extreme temporal changes, as occurring in migratory populations at staging sites.…”