Foraging by captive individuals of three species of towhees (Pipilo:Emberizinae) was investigated to determine if patch choice was associated with critical threshold levels of foraging success. Birds were offered a choice of feeding in three litter types. Once individual preferences for litter type were determined, I reduced the amount of food (millet seed) under a preferred litter each day, while maintaining high levels under a non-preferred litter. Thus, birds experienced a declining resource gradient under their preferred litter. During the bird's initial foraging period each day, I noted number of seeds taken and number of double-scratches made in each litter type, until the bird abandoned its preferred litter and shifted to the other patch. Foraging theory assumes that patch choice is made when foraging success declines as resources decline to some threshold level. I estimated success using information potentially available for decision-making by the birds. One of four success variables, mean seeds/scratch, best conformed to the expected pattern, providing supportive evidence for the threshold assumption. The three species changed patches at species-specific thresholds. Pipilo fuscus, a foraging generalist, switched to its non-preferred litter when food levels under the preferred litter were high. Pipilo aberti and P. erythrophthalmus, two foraging specialists, foraged in their preferred litters until food levels were much lower. Optimal Foraging Theory predicts that shifts in patch use are determined by between-patch comparisons of foraging success. Timing of towhee patch changes was not consistent with between-patch comparisons. An alternative expectation theory, Status-quo Foraging, which emphasizes comparisons of within-patch success, was more consistent with observed results. The rapid patch switching shown by P. fuscus may reflect greater flexibility of this species' foraging repertoire in its natural habitat. This result suggests that foragers with imperfect knowledge may use recent past experience to make foraging decisions. Optimal Foraging Theory provided a useful null model for comparing foraging theories. Deviations from predictions indicated how more realistic hypotheses can be constructed. The nature of available information plays an increasingly important role in modeling decision-making by imperfect foragers.

Studies of vocalizations in a montane population of Green-Tailed Towhees were conducted during the summer months of 1971 and 1972 in Cache County, Utah. The song and call repertoiries of 10 breeding pairs were recorded and analyzed on a sound spectograph. Males averaged 8.7 different song and 18.2 different not types. Song variation on the population level is high (58 different songs) but the sharing of these songs among the males is low (22.4) . Populational note structure is equally diverse but reveals a greater degree of sharing (75%). Both males and females used three calss, the meow, tick, and poitt, whereas at least three more, the rattle, tst-tst-tst, and skee-skee-skee, are used only by the female. Recoginition of the songs of conspecifies apparently is promoted by the distinctive introductory note, the duration of the song and the abruptness of changes within it.

Habitat fragmentation, and the resulting increase in edge habitat, has important effects on birds, including the increased probability of nest predation, changes in habitat structure, and the increased presence of non-native plant species. It is critical to understand the effects of fragmentation at all stages of the avian life cycle, including the often overlooked postfledging period. Because much of juvenile mortality occurs during the immediate postfledging period, and juvenile mortality contributes substantially to population dynamics, it is necessary to understand if fledgling survival is reduced in edge habitats and if fledglings' survival is influenced by their habitat use. During 2008 and 2009 I radio-tracked 52 fledgling Spotted Towhees (Pipilo maculatus) during the 30-day postfledging period in a 24-ha urban park near Portland, Oregon. Thirty-six fledglings (69%) survived the 27-day tracking period (an estimated 62.1% survived the entire 30-day postfledging period). At least 9 of 16 predation events were attributable to domestic cats (Felis domesticus) or Western Screech-owls (Megascops kennicottii). Although fledglings were more likely to be found near edges than the park interior, fledglings located closer to park edges had a higher probability of dying. However, I found that towhee nests were more likely to be found near edges, nests near edges produced more fledglings, and nestlings near edges were heavier. I used a STELLA-based stochastic model of nest success and fledgling survival to show that the benefits initially gained by nesting near edges were reversed during the postfledging period. The number of fledglings per nest that survived to the end of the 30-day postfledging period was significantly lower near edges than in the park interior. This apparent preference for nesting near edges, paired with higher fledgling mortality near edges, is consistent with the idea that edges are ecological traps. Fledgling habitat was significantly more structurally dense and had a greater abundance of non-native plant species, particularly Himalayan Blackberry (Rubus armeniacus), than nest habitat. Towhees avoided English Ivy (Hedera helix) for both nesting and care of fledglings. However, fledgling survival was not related to vegetation characteristics, which suggests that increased fledgling mortality near edges was a direct result of increased predator abundance or predation near edges, and was not an artifact of changes in habitat near edges. My results help to establish that fledgling survival and the unique habitat requirements of fledglings should be considered along with nest success and nest habitat when examining the effects of habitat fragmentation on bird populations. More broadly, this study has important implications for conservation, as it exemplifies how phenomena such as ecological traps created by anthropogenic changes in the environment can be overlooked if only one life history stage is studied.

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