The design of artificial nestboxes for the study of secondary hole-nesting birds: a review of methodological inconsistencies and potential biases. Acta Ornithol. 45: 1-26.

Measures of body condition, immune function, and hematological health are widely used in ecological studies of vertebrate populations, predicated on the assumption that these traits are linked to fitness. However, compelling evidence that these traits actually predict long-term survival and reproductive success among individuals in the wild is lacking. Here, we show that body condition (i.e., size-adjusted body mass) and cutaneous immune responsiveness to phytohaemagglutinin (PHA) injection among neonates positively predict recruitment and subsequent longevity in a wild, migratory population of house wrens (Troglodytes aedon). However, neonates with intermediate hematocrit had the highest recruitment and longevity. Neonates with the highest PHA responsiveness and intermediate hematocrit prior to independence eventually produced the most offspring during their lifetime breeding on the study site. Importantly, the effects of PHA responsiveness and hematocrit were revealed while controlling for variation in body condition, sex, and environmental variation. Thus, our data demonstrate that body condition, cutaneous immune responsiveness, and hematocrit as a neonate are associated with individual fitness. Although hematocrit's effect is more complex than traditionally thought, our results suggest a previously underappreciated role for this trait in influencing survival in the wild.

The ¢tness-related consequences of egg mass, independent of confounding in£uences associated with parental quality, remain poorly understood for wild birds in general and for passerines in particular. We performed cross-fostering experiments to test the hypothesis that egg mass, independent of parental quality, is the primary determinant of ¢tness-related traits in nestling house wrens (Troglodytes aedon), an insectivorous passerine. Nestling mass was signi¢cantly correlated with the mass of the eggs from which nestlings hatched early but not late in the nestling period in early-season broods. In contrast, in lateseason broods, nestling mass was correlated with egg mass until nestlings achieved asymptotic mass. Neither nestling growth nor survival to nest leaving was related to egg mass in either early-or late-season broods; however, nestlings in late-season broods grew more slowly than did nestlings in early-season broods. We propose that nestling mass and egg mass remained correlated throughout the nestling period in late-season broods because decreased arthropod food resources late in the breeding season constrain parents' ability to provision nestlings. We conclude that female house wrens in this population trade-o¡ clutch size for greater egg mass to maximize reproductive success in late-season broods.

We studied the natal and breeding dispersal of yearling and adult House Wrens (Troglodytes aedon) for 7 yr in central Illinois. The forested study areas contained 910 identical nest boxes placed in a grid pattern. On average 38.1% (n = 643) of the adult males and 23.3% (n = 1,468) of the adult females present in one year returned the next; 2.8% (n = 6,299) of the nestlings that survived to leave the nest returned each year. Adult male (median distance = 67 m) and adult female (median = 134 m) breeding dispersal was less than yearling male (median = 607.5 m) and yearling female (median = 674 m) natal dispersal. Females that returned had produced more offspring the previous season than had nonreturning females, and females that successfully produced at least one chick in their last nesting attempt of the previous season moved shorter distances than did unsuccessful females. There were, however, no consistent differences between returning and nonreturning females in two other measures of reproductive success. Females that were unsuccessful in their last breeding attempt of the previous year were more likely to be successful in their next attempt if they moved two or more territories than if they did not move. Reproductive success did not affect the likelihood that a male would return nor the distance that he moved. The success of subsequent nesting attempts by males was also not related to the distance moved. Inbreeding avoidance may explain differences between breeding and natal dispersal, but it does not explain the lack of difference in dispersal of yearling females and males. Differences between adult and yearling dispersal are best explained by advantages accruing to adults that remain near former breeding sites and by the necessity for yearlings to move farther because of their late return from the wintering grounds. The advantages for adults to reoccupy previous breeding sites are counterbalanced, especially in females, by advantages associated with moving after breeding failure.

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