Habitat loss, fragmentation, and degradation are the leading causes of faunal population declines.Substantial effort has been invested in identifying how these landscape changes are related to population parameters. However, to effectively mitigate declines, we must understand the underlying mechanisms impacted by landscape change. Woodland-dependent avian insectivores seem particularly vulnerable, and decline at rates disproportionately greater than other foraging guilds. This pattern suggests that reduced food availability in less-wooded landscapes may be a contributing factor. However, the evidence supporting this hypothesis is sparse. I adopted a multidisciplinary approach to investigate the mechanisms driving population changes of an avian insectivore in highly-modified landscapes by integrating physiological indices with measures of prey availability and landscape structure. First, I presented a framework for conceptualising how the spatiotemporal scale of fragmentation influences the mechanisms impacting populations. I then used the eastern yellow robin (Eopsaltria australis) in the Brigalow Belt South bioregion of southern Queensland to test the importance of local and landscape factors on robin site occupancy, prey density, and robin condition. I also investigated whether an index of chronic stress could be used to predict changes to robin occurrence and identify potential threats to the population. I concluded this work by conducting a supplementary feeding experiment to determine whether food availability was causing the variation in robin condition. A pilot study conducted in the study region four years earlier found that robins were more physiologically stressed (had higher heterophil:lymphocyte ratios) in sites with less woodland in the surrounding landscape, but site occupancy was unrelated to woodland cover. Re-examining the same study system, I established that woodland cover was now the strongest predictor of iii occupancy. While woodland cover at a local scale (within 500 m) was important for robin persistence, woodland cover at a broader scale relevant to dispersal movements (within 5 km) was not. While my stress index could not accurately predict the precise locations of future extirpations, patterns of stress indices (birds were more stressed where woodland cover was lower) did foreshadow a change to the pattern of occurrence. Extirpations from sites with low levels of woodland cover were balanced by colonisations of more-wooded sites. Surprisingly, I found that arthropod prey density was greater at sites that had less surrounding woodland. This result was primarily driven by a large number of Formicidae (ants). However, Formicidae have low nutritional value and once they were excluded from the results, soil moisture, not woodland cover, became the primary determinant of arthropod density. I predicted that robin condition would be strongly associated with arthropod density, but this was not the case. Instead, robins had elevated stress levels at sites with apparently more-favourable...