No abstract

Mortality rates are high for most avian species during early life stages, forming a critical source of natural selection that helps shape the diversity of avian life-history traits. We investigated hatching failure (i.e., non-predatory embryonic mortality, excluding abandoned or damaged eggs) and found significant variation among passerine species. Failure rates ranged from 1.0% to 12.7%, and species with cavity nests and larger clutches experienced greater rates of hatching failure. While past research has focused on the direct effects of predation on the nestling and fledgling stages, little is known about how predation may indirectly influence other sources of mortality such as hatching failure. We investigated the influence of nest predation risk and other factors on variation in hatching failure among 14 free-living grassland and shrubland songbird species. Across all species, 7.7% of 1,667 eggs failed to hatch. We found little evidence that variation in nest temperature influenced rates of hatching failure within and among species, although species with larger clutch sizes had more variable nest temperatures. Dissection of failed eggs revealed that most hatching failures occurred before or shortly after the onset of development; however, there was no difference between cavity and open-cup nesters in the rate of early-stage mortality. Our findings suggest there may be tradeoffs to having a large clutch, with a benefit of rearing more young at the cost of greater hatching failure, possibly due to delayed onset of incubation, poor incubation behavior, or inability to incubate large clutches. Additionally, as larger clutches are often laid in cavity nests, which have a relatively low predation risk, this may outweigh the costs of increased hatching failure. More experimental approaches, such as clutch size manipulations and egg-specific incubation behavior are needed to provide greater insight into factors driving variation in hatching failure across species.

Nest‐sharer avian brood parasites do not evict or otherwise kill host chicks, but instead inflict a range of negative effects on their nestmates that are mediated by interactions between the parasite and host life history traits. Although many of the negative fitness effects of avian brood parasitism are well documented across diverse host species, there remains a paucity of studies that have examined the impacts of parasitism across the entirety of host ontogeny (i.e., from when an egg is laid until independence). More specifically, few studies have examined the impact of brood parasitism on the pre‐ and post‐fledging development, physiology, behavior, and survival of host offspring. To help fill this knowledge gap, we assessed the effects of brood parasitism by Brown‐headed Cowbirds (Molothrus ater) across the ontogeny (incubation, nestling, and post‐fledging period) of nine sympatrically breeding host species in central Illinois, USA; due to sample sizes, impacts on the post‐fledging period were only examined in two of the nine species. Specifically, we examined the impact of brood parasitism on ontogenetic markers including the embryonic heart rate, hatching rate, nestling period length, nest survival, and offspring growth and development. Additionally, in species in which we found negative impacts of cowbird parasitism on host nestmate ontogeny, we examined whether the difference in adult size between parasites and their hosts and their hatching asynchrony positively predicted variation in host costs across these focal taxa. We found that costs of cowbird parasitism were most severe during early nesting stages (reduction in the host clutch or brood size) and were predicted negatively by host size and positively by incubation length. In contrast, we only found limited costs of cowbird parasitism on other stages of host ontogeny; critically, post‐fledging survival did not differ between host offspring that fledged alongside cowbirds and those that did not. Our findings (i) highlight the direct costs of cowbird parasitism on host fitness, (ii) provide evidence for when (the stage) those costs are manifested, and (iii) may help to explain why many anti‐cowbird defenses of hosts have evolved for protection from parasitism during the laying and incubation stages.