Cooperative breeding shapes post‐fledging survival in an Afrotropical forest bird

For avian group living to be evolutionary stable, multiple fitness benefits are expected. Yet, the difficulty of tracking fledglings, and thus estimating their survival rates, limits our knowledge on how such benefits may manifest postfledging. We radio‐tagged breeding females of the Afrotropical cooperatively breeding Placid greenbul (Phyllastrephus placidus) during nesting. Tracking these females after fledging permitted us to locate juvenile birds, their parents, and any helpers present and to build individual fledgling resighting datasets without incurring mortality costs or causing premature fledging due to handling or transmitter effects. A Bayesian framework was used to infer age‐specific mortality rates in relation to group size, fledging date, maternal condition, and nestling condition. Postfledging survival was positively related to group size, with fledglings raised in groups with four helpers showing nearly 30% higher survival until independence compared with pair‐only offspring, independent of fledging date, maternal condition or nestling condition. Our results demonstrate the importance of studying the early dependency period just after fledging when assessing presumed benefits of cooperative breeding. While studying small, mobile organisms after they leave the nest remains highly challenging, we argue that the telemetric approach proposed here may be a broadly applicable method to obtain unbiased estimates of postfledging survival.     

Postfledging Survival and Development of Juvenile Lilac-Crowned Parrots

Abstract: We fitted radiotransmitters to 68 lilac-crowned parrot (Amazona finschi) fledglings from 1996 to 2003 to determine the survival and development of juveniles during their first year after leaving the nest. Overall, first-year survival was 73% (CI = 53–94%) and all mortalities occurred within 5 weeks of fledging, with highest mortality in the first week postfledging. Survival varied between years, influencing recruitment of independent young in the population. Nesting lilac-crowned parrots produced 0.70 independent young per egg-laying pair during 1996–2003. Lowest productivity of 0.25 independent young per pair occurred in 2003, with 40% postfledging survival. Juvenile development after fledging was characterized by variations in mobility, distance from the nest, and separation distance between siblings. Mobility and distance of young birds from the nest increased linearly with months postfledging. The first 2–3 weeks after fledging were characterized by low mobility and survival of young parrots, making this the most critical phase postfledging. The dependency period for young parrots extended to 4–5 months postfledging and was characterized by increased mobility and low separation between siblings, as juveniles traveled in family groups. Independence occurred in month 5 and was marked by a significant increase in mobility and separation between siblings, indicating the break-up of family groups. The first weeks after leaving the nest were crucial for survival and highlight the need for secure habitats where fledglings can improve flight and locomotory skills. The 4–5-month dependency of young parrots may be a key period for development, enhancing survival, and establishment in the breeding population. Release programs need to replicate learning and development acquired during the postfledging dependency phase to enhance survival of captive-reared psittacines. Researchers should conduct surveys of parrot group sizes during the dependency period 1–4 months after the end of nesting to provide reliable demographic data on annual recruitment of wild populations.     

Movements and Resource Selection of Fledgling Goshawks in Montane Forests of Southeastern British Columbia

ABSTRACT The northern goshawk (Accipiter gentilis) has been the subject of considerable interest because of the impact of logging on this species' nesting habitat. However, few studies have examined movements of fledgling birds around the nest prior to independence, and even fewer have described resource requirements of young birds during their postfledging period. Over 3 years, we followed 31 radiotagged goshawk fledglings from 15 nests in southeastern British Columbia, Canada. Of these birds, 26 survived to disperse. Between fledging and dispersal 95% of fledgling relocations (n = 1, 148) were within 450 m of the nest. Fledglings primarily remained within 298 m of the nest during the first 21 days postfledging and within 525 m of the nest between 21 days postfledging and dispersal. Fledglings' movements were highly directional, with individual and sibling movements away from any particular nest tending out in one direction. Postfledging areas averaged 36.7 ha in size (median = 23.1, inter-quartile range = 20.8–39.7 ha). Fledglings strongly avoided forest <40 years old and weakly selected young forests (40–80 yr), mature forests (>80 yr), and stands with >40% canopy cover during the first 21 days and after. We suggest forest managers wishing to conserve goshawk postfledging areas in the interior montane forests of British Columbia maintain forests >40 years old with high crown closure covering an area ≥21 ha and preferably >40 ha. This area should contain all identified occupied and alternative nest trees in a nest area. At least half this area should be forest >80 years old and contain existing nests and potential for future nest trees.     

Post‐fledging survival of altricial birds: ecological determinants and adaptation

For altricial young, fledging is an abrupt step into an unknown environment. Despite increasing numbers of studies addressing the post‐fledging period, our current knowledge of the causes and consequences of post‐fledging survival remains fragmentary. Here, we review the literature on post‐fledging survival of juvenile altricial birds, addressing the following main questions: Is low post‐fledging survival a bottleneck in the altricial reproductive cycle? What is known of proximate and ultimate causal factors such as trophic relations (food and predation), habitat conditions, or abiotic factors acting in the post‐fledging period? We analyzed weekly survival estimates from 123 data series based on studies of 65 species, covering weeks 1–13 post‐fledging. As a general pattern, survival of fledglings was low during the first week post‐fledging (median rate = 0.83), and improved rapidly with time post‐fledging (week 4 median rate = 0.96). For ground‐nesting species, survival immediately after leaving nests was similar to egg‐to‐fledging survival. For species breeding above‐ground, survival during the first week post‐fledging was substantially lower than during both the nestling period and later post‐fledging stages. Thus, the early post‐fledging period is a bottleneck of markedly elevated mortality for most altricial species. Predation was the main proximate cause of mortality. Various factors such as habitat, annual and seasonal variation in the environment, and the physical condition of fledglings have been found to affect post‐fledging survival. Individual survival depended strongly on physical traits such as mass and wing length, which likely influence the ability of fledglings to escape predation. Trophic relationships at various levels are the main ultimate driver of adaptation of traits relevant to survival during the pre‐ and post‐fledging periods. Spatiotemporal dynamics of food resources determine the physical development of juveniles and, in turn, their performance after fledging. However, predators can cause quick and efficient selection for fledgling traits and adult breeding decisions. Parental strategies related to clutch size and timing of breeding, and the age and developmental stage at which young fledge have substantial effects on post‐fledging survival. The intensity and duration of post‐fledging parental investment also influences fledgling survival. Post‐fledging mortality is therefore not a random and inevitable loss. Traits and strategies related to fledging and the post‐fledging stage create large fitness differentials and, therefore, are integral, yet poorly understood, parts of the altricial reproductive strategy.     

Fledgling Bachman’s Sparrows in a longleaf pine ecosystem: survival,movements, and habitat selection

Fledgling ecology remains understudied for many passerine species, yet information about the fledgling life stage is critical for understanding full-annual life cycles and population recruitment. We examined the survival, habitat selection, and movements of fledgling Bachman’s Sparrows (Peucaea aestivalis) in a longleaf pine-wiregrass (Pinus palustris-Aristida stricta) community managed with frequent prescribed fire. We captured and marked 36 fledglings on the day of fledging and used radio-telemetry to relocate them daily until independence during three breeding seasons (2014–2016). We visually confirmed the status of fledglings as live or dead during daily relocations and determined causes of mortality. We measured vegetation characteristics at fledgling locations and compared them to the characteristics of vegetation at the locations of adult males. We used a Known Fates analysis in Program MARK to estimate fledgling survival, and generalized linear mixed effect models to determine habitat selection. Estimated fledgling survival until independence was 0.31 (SE = 0.08), with most mortality during the first 4 d post-fledging. Fledglings with longer wing chords had higher rates of survival than those with shorter wing chords, possibly due to an increased ability to evade predators. Fledgling movements were restricted primarily to natal territories. Fledgling Bachman’s Sparrows were located in areas with greater woody plant, forb, and grass cover and less bare ground than available in natal territories. Similar to fledglings of other songbirds, understory woody and herbaceous plants appear to provide critical cover for fledgling Bachman’s Sparrows, and maintenance of such cover should receive consideration in management plans for longleaf pine communities.     

Post-fledging survival of individual great tits: the effect of hatching date and fledging mass

Pre-breeeding survival is one of the major sources of individual variation in lifetime reproductive success. However, very little is known about the reasons for differences in survival among individuals during this important phase of the life cycle. Some studies, using local return rates as indices of survival, have shown a relationship between post-fledging survival and fledging date and mass in birds, most of them suggesting directional selection towards heavy masses and early fledging dates. Recent development of capture-recapture models allows the separate estimate of survival and recapture probabilities, as well as the inclusion of individual covariates into the modelling process. We used here these models to explore the relative effects of fledging date and fledging mass on local recruitment of individual great tit Parus major fledglings. Individual capture-recapture histories of 2051 fledglings (cohorts 1992–1999), 184 of which were recaptured as breeding birds during 1993–2000, were used in the analyses. Hatching date, offspring mass at day 15, their squared terms, and interactions between mass and date, were included as covariates into the modelling process. Models with age (fledglings and adults) and time (year) dependence were used. The probability of local recruitment increased with fledging mass in each of the years studied. Fledging date also affected recruitment but, against what is commonly thought, fledgling early is not the best option every year. Either early, intermediate or late fledglings were favoured in different years. This between-year variation in the optimum fledging date offers an alternative explanation to the lack of evolution towards earlier breeding dates, in spite of the advantages of early breeding some years.     

Fledgling survival increases with development time and adult survival across north and south temperate zones

Slow life histories are characterized by high adult survival and few offspring, which are thought to allow increased investment per offspring to increase juvenile survival. Consistent with this pattern, south temperate zone birds are commonly longer‐lived and have fewer young than north temperate zone species. However, comparative analyses of juvenile survival, including during the first few weeks of the post‐fledging period when most juvenile mortality occurs, are largely lacking. We combined our measurements of fledgling survival for eight passerines in South Africa with estimates from published studies of 57 north and south temperate zone songbird species to test three predictions: (1) fledgling survival increases with length of development time in the nest; (2) fledgling survival increases with adult survival and reduced brood size controlled for development time; and (3) south temperate zone species, with their higher adult survival and smaller brood sizes, exhibit higher fledgling survival than north temperate zone species controlled for development time. We found that fledgling survival was higher among south temperate zone species and generally increased with development time and adult survival within and between latitudinal regions. Clutch size did not explain additional variation, but was confounded with adult survival. Given the importance of age‐specific mortality to life history evolution, understanding the causes of these geographical patterns of mortality is important.     

The effects of force‐fledging and premature fledging on the survival of nestling songbirds

Despite the broad consensus that force‐fledging of nestling songbirds lowers their probability of survival and therefore should be generally avoided by researchers, that presumption has not been tested. We used radiotelemetry to monitor the survival of fledglings of Ovenbirds Seiurus aurocapilla and Golden‐winged Warblers Vermivora chrysoptera that we unintentionally force‐fledged (i.e. nestlings left the nest in response to our research activities at typical fledging age), that fledged prematurely (i.e. nestlings left the nest earlier than typical fledging age), and that fledged independently of our activities. Force‐fledged Ovenbirds experienced significantly higher survival than those that fledged independent of our activities, and prematurely fledged Ovenbirds had a similarly high survival to those that force‐fledged at typical fledging age. We observed a similar, though not statistically significant, pattern in Golden‐winged Warbler fledgling survival. Our results suggest that investigator‐induced force‐fledging of nestlings, even when deemed premature, does not necessarily result in reduced fledgling survival in these species. Instead, our results suggest that a propensity or ability to fledge in response to disturbance may be a predictor of a higher probability of fledgling survival.     

Experimental food supplementation affects the physical development,behaviour and survival of Little Owl Athene noctua nestlings

In birds, energy supply during growth is a major predictor of the fledglings' physical condition and survival prospects. Differential quantity and quality of fledglings produced under varying nestling food supplies are likely to affect the number of offspring that recruit into the breeding population. However, the underlying mechanisms and associated consequences are still poorly known. Using a partial cross‐fostering and food supplementation experiment, we estimated the effect of variation in food supply during growth on nestling survival and fledgling phenotypic traits of Little Owls Athene noctua. Survival to fledging was much higher in food‐supplemented nestlings (98.6%) than in control nestlings (82.4%). Furthermore, supplemented nestlings were on average 8.9 g heavier and were more likely to develop subcutaneous fat deposits (99.4 vs. 73.7% of treatment and control nestlings, respectively). Supplemented nestlings also had on average longer wings than control nestlings, but tarsi and culmen did not differ significantly. Furthermore, experimentally supplemented fledglings struggled more when handled and emerged sooner from tonic immobility than control fledglings. The irises of supplemented fledglings were less intensely coloured. The experimentally induced changes in nestling development probably affect individual performance beyond fledging. Nestlings from orchard‐dominated habitats were larger than those from habitats dominated by arable land. As nestling food supply is largely determined by natural food availability, we conclude that habitat quality affects Little Owl productivity and offspring quality, and ultimately, population dynamics.     

Testing common assumptions in studies of songbird nest success

We studied Ovenbird Seiurus aurocapilla and Golden‐winged Warbler Vermivora chrysoptera populations in northern Minnesota, USA, to test two common assumptions in studies of songbird nest success: (1) that the condition of an empty nest on or near its expected fledge date is an indicator of nest fate; and (2) that the presence of a fledgling or family group within a territory confirms a successful nest in that territory. We monitored the condition of nests and used radiotelemetry to monitor juveniles through the expected fledging date and early post‐fledging period. Of nests that contained nestlings 1–2 days before the expected fledge date, fates were misidentified using nest condition alone for 9.5% of Ovenbird nests, but those misidentifications were made in both directions (succeeded or failed), yielding only a small bias in estimated nest success. However, 20% of Golden‐winged Warbler nests were misidentified as successful using nest condition during the final visit interval, biasing the nest success estimate upward by 21–28% depending on the treatment of uncertain nest fates. Fledgling Ovenbirds from 58% of nests travelled beyond their natal territory within 24 h, rising to 98% after 5 days, and those fledglings travelled up to 390 m from nests within 10 days of fledging. Fledgling Golden‐winged Warblers from 13% of nests travelled beyond their natal territory within 24 h, rising to 85% after 5 days, and those fledglings travelled up to 510 m from nests within 10 days of fledging. We conclude that nest condition and fledgling presence can be misleading indicators of nest fate, probably commonly biasing nest success estimates upward, and we recommend that these assumptions should be tested in additional species.     

Habitat selection of nesting and fledgling salt marsh songbirds in northeast Florida

Understanding habitat selection by breeding birds and their newly fledged young can be an essential aspect of the conservation of vulnerable species. During 2015–2017, we examined nest site selection of Worthington's marsh wren (Cistothorus palustris griseus) and MacGillivray's seaside sparrow (Ammospiza maritima macgillivraii), and fledgling habitat use by Worthington's marsh wren, 2 imperiled species in northeast Florida, USA. We compared vegetation at unused points to vegetation at nests of both subspecies and at locations used by radio-tagged marsh wren fledglings. Vegetation was taller and stem counts were greater at nest sites compared to unused points. Worthington's marsh wrens also used nest sites with a greater proportion of tall-form smooth cordgrass (Spartina alterniflora) than was observed at unused points. Worthington's marsh wren fledglings also used locations with taller, denser vegetation, but vegetation use changed with fledgling age and tidal stage; older fledglings more frequently used areas with short-form smooth cordgrass and bare ground (and more so during low tides). In contrast, so few nests and nestlings were in black needlerush (Juncus roemerianus) that we could not consider it in our analysis despite its prevalence within our study sites. Our results indicate that tall, dense cordgrass is an important habitat component for these subspecies during the nesting and fledgling life stages in southeastern Atlantic salt marshes.     

Nest‐site selection and demography of Wilson's Plovers on a North Carolina barrier island

Despite concerns about their population status, information about the habitat preferences, population size, and vital statistics of Wilson's Plovers (Charadrius wilsonia) is currently lacking. We compared habitat characteristics of nest sites and unused sites and examined factors affecting nest success on a barrier island in North Carolina in 2010 and 2011. We monitored 83 nests with cameras and added heart‐rate monitors in artificial eggs to 36 of these nests for a concurrent study of the effects of jet overflights; predator exclosures were placed around 17 of the nests with cameras. Wilson's Plovers used interdune areas, flats, and isolated dunelets on flats more than expected based on availability, and nests were located closer to dense vegetation than unused sites. Nests in interdune areas had higher daily survival rates than nests on flats, but distance to dense vegetation did not affect nest survival. Nests without cameras, heart‐rate monitors, or exclosures had a 35% predicted probability of hatching at least one egg. Exclosed nests had higher daily survival rates than nests without exclosures, but daily survival rates were lower for nests with cameras or heart‐rate monitors and for nests initiated later in the season. Daily survival rates also declined as nests aged. The predicted probability of fledging was 74%, resulting in a reproductive output of 0.78 fledglings/pair. Apparent annual adult survival was 77%, and the apparent annual survival rate for birds banded as chicks was 42%. Additional research is needed throughout the range of Wilson's Plovers to determine if populations are stable or decreasing, and to predict the productivity rates needed to maintain current populations. However, our results suggest that in our study area, predator removal and protection of sparsely vegetated overwash habitats will likely have the greatest impact on reproductive output.     

Not for Parents Only: Begging Calls Allow Nest‐Mate Discrimination in Juvenile Zebra Finches

The benefits of recognition of family members may range from inbreeding avoidance to cooperative and coordinated behaviors within the family group. In birds, recognition of family members has almost exclusively been studied between parents and offspring or within cooperatively breeding societies. Yet, recognition of nest‐mates could be of special importance in recently fledged birds of colonial species by helping in locating the nest, maintaining family group cohesion, or allowing detection of feeding opportunities by recognizing the begging calls nest‐mates produced on the return of a parent. Here we study nest‐mate discrimination based on begging calls in fledglings of domesticated zebra finches (Taeniopygia guttata), a gregarious songbird living in loose colonies in which juveniles may gather in crèches and are fed by parents up to 20 d after fledging. Using playback tests, we show that fledglings called more and spent more time near the loudspeaker in response to the begging calls of their nest‐mates than to the calls of other familiar individuals. Because each fledgling was exposed to the repeated association of the begging calls of its nest‐mates and the subsequent feeding of its parents, this preferential response to the nest‐mates' calls could be a conditioned response to the food reward. Whereas fledglings answered more to male fledgling calls than to female fledgling calls, response to playback was influenced neither by the sex of the subject nor by its brood size. Discriminant function analysis based on acoustic parameters showed that begging calls carried an individual signature as well as a brood signature which might account for such nest‐mate discrimination. Begging signals are major study systems of the evolution of communication in the face of conflicts of interest between signalers and receivers. Our results suggest that eavesdropping and communication networks may be other informative frameworks to understand the design of offspring solicitation signals.     

Comparing food limitation among three stages of nesting: supplementation experiments with the burrowing owl

Food availability is an important limiting factor for avian reproduction. In altricial birds, food limitation is assumed to be more severe during the nestling stage than during laying or incubation, but this has yet to be adequately tested. Using food‐supplementation experiments over a 5‐year period, we determined the degree and timing of food limitation for burrowing owls (Athene cunicularia) breeding in Canada. Burrowing owls are an endangered species and food limitation during the nestling stage could influence reproductive performance of this species at the northern extent of their range. Supplemented pairs fledged on average 47% more owlets than unfed pairs, except during a year when natural food was not limiting (i.e., a prey irruption year). The difference in fledgling production resulted from high nestling mortality in unfed broods, with 96% of all nestling deaths being attributed to food shortage. Supplemental feeding during the nestling period also increased fledgling structural size. Pairs fed from the start of laying produced the same number of hatchlings as pairs that received no supplemental food before hatch. Furthermore, pairs supplemented from egg laying to fledging and pairs supplemented during the nestling period alone had the same patterns of nestling survival, equal numbers of fledglings, and similar fledgling mass and structural size. Our results provide empirical support for the hypothesis that the nestling period is the most food‐limited phase of the breeding cycle. The experimental design we introduce here could be used with other altricial species to examine how the timing of food limitation differs among birds with a variety of life‐history strategies. For burrowing owls, and other species with similar life histories, long‐term, large‐scale, and appropriately timed habitat management increasing prey abundance or availability is critical for conservation.     

SURVIVAL COST OF AN EARLY IMMUNE SOLICITING IN NATURE

If immune functions confer obvious benefits to hosts, life-history theory assumes that they also induce costs, leading to trade-offs between immunity and other fitness components. However, whether substantial fitness costs are associated with immune systems in the wild is debatable, as numerous factors may influence the costs and benefits associated with immune activation. Here, we explore the survival cost of immune deployment in postfledging birds. We injected Eurasian collared dove nestlings ( Streptopelia decaocto ) with antigens from Escherichia coli , and examined whether this immune challenge affected survival after fledging. To assess survival, birds were fitted with radiotags and the fate of each individual was monitored regularly. Our results show that mimicking a bacterial infection in nestlings lowered their survival prospects after fledging, in comparison to controls. The main identified cause of mortality (by examination of dead birds) was presumed to be predation. This study provides experimental evidence that immune activation may entail dramatic survival costs in a free-ranging vertebrate, and emphasizes the potential role that environmental factors such as predation may play in this interaction.     

Prolonged offspring dependence and cooperative breeding in birds

It has been suggested that the evolution of cooperative breedingin birds is associated with unusually long periods of offspringdependence ; this appears paradoxical because cooperative breedersoften produce more broods than their noncooperatively breedingrelatives. I compared the duration of parental care betweencooperatively and noncooperatively breeding species using phylogeneticallyindependent contrasts and matched pairs. The incubation andnestling periods did not differ between the two parental caresystems, but the duration of postfledging offspring care wassignificantly longer in species that regularly breed cooperatively.This relationship remained when other factors that are thoughtto affect the duration of fledgling care (breeding habitat,body size, latitude of breeding, diet) were controlled statistically.Cooperative breeders appear to provide more prolonged postfledgingcare because additional care providers reduce the costs of parenting, offspring have less incentive to become independent,and a division of labor can develop during reproduction—helperscontinue to feed fledglings while breeders initiate the nextnesting attempt.     

Ectoparasitism and the role of green nesting material in the European starling

Summary The use of green nesting material is widespred among birds. Recent evidence suggests that birds use secondary chemicals contained in green plants to control ectoparasites. We manipulated green nesting material and ectoparasites of European starlings (Sturnus vulgaris) to test two hypotheses: (1) ectoparasites adversely affect prefledging survival and morphometrics or postfledging survival, and (2) green nesting material ameliorates the effects of ectoparasites. We recorded fat score, numbers of scabs, tarsal length, body mass, and hematocrit level on each nestling 17 days after hatching. We also fitted each nestling with unique patagial tags and resighted the starlings for 6–8 weeks after fledging to estimate survival and sighting rates. Nests devoid of green nesting material and dusted with the insecticide, carbaryl, had fewer high ectoparasite infestations, and nestlings had significantly lower scab scores, and significantly higher body masses than nestlings in undusted boxes. However, there was no difference in postfledging survival between birds from carbaryl-treated and undusted nests. There also was no difference in prefledging survival and morphometrics or postfledging survival between nestlings from boxes with and without green nesting material. These results do not support the hypothesis that starlings use green nesting material to control nest ectoparasites. We suggest an alternative hypothesis; green nesting material is used for mate selection or pairbonding in the starling.     

No effect of habitat fragmentation on post-fledging, first-year and adult survival in the middle spotted woodpecker

Despite its relevance for the dynamics of populations, the ecological mechanisms underlying juvenile and adult survival are poorly known in most bird species. This study focuses on the effect of habitat fragmentation on early post-fledging, first-year and adult survival of the middle spotted woodpecker Dendrocopus medius by combining data of radio-tagged and ringed birds. Among juveniles, most deaths occurred during the first three weeks after fledging (survival rate: 0.359±0.077) and were mainly caused by predation. After independence, birds faced another critical period during their first autumn-winter that lowered first-year survival further (0.255±0.044), whereas adult mortality was considerably lower (annual survival rate: 0.786±0.074). We did not find any significant effect of habitat fragmentation (measured as patch size and connectivity) on juvenile or adult survival. Sex ratio at fledging did not differ significantly from parity (proportion of females: 0.513) and was not correlated to patch size. Regardless of age, survival did not differ between the sexes, suggesting that a female-biased mortality was not the mechanism behind the presence of unpaired territorial males in this population. Lighter nestlings underwent significantly higher post-fledging mortality, indicating that conditions in the nest may substantially affect survival later in life.     

Breeding success and chronology of Wood Storks Mycteria americana in northern and central Florida, U.S.A.

The breeding success and chronology of Wood Storks Mycteria americana were studied at eight colonies in northern and central Florida during 1981–1985. Mean ± s.d. clutch size for all colony-years was 3.07 ± 0.56 (n = 2694 nests), with three-egg clutches (72%) most frequent. Mean clutch size among all colonies and years ranged from 2.73 ± 0.55 to 3.41 ± 0.61. Many colonies exhibited significant negative trends in clutch size with, hatching date because of a proportional decrease in four-egg clutches later in the season. Mean colony clutch size was not correlated with nest numbers, nesting density or mean hatching date within most years. Mean ± s.d. number of fledglings for all colonies and years was 1.29 ± 1.16 fledglings per nest (n = 2812 nests). Mean annual fledging rates in colonies ranged from 0 (colony failed) to 2.66 fledglings per nest. Most breeding failure occurred prior to egg hatching, and the second highest mortality occurred between hatching and 2 weeks of age. Four-egg clutches fledged more storks than three-egg clutches, which in turn were more successful than two-egg clutches. However, all clutch sizes showed similar fledgling per egg rates. The seasonal decline in productivity was associated proportionally with smaller clutch sizes later in the breeding season. An increase in mean hatching date was correlated with an increase in latitude. There was greater within-year breeding synchrony among colonies than interyear breeding synchrony within each colony. Breeding synchrony was not correlated with mean hatching date, latitude, longitude, nest numbers or nesting density.     

Post‐independence mortality of juveniles is driven by anthropogenic hazards for two passerines in an urban landscape

Urban environments impose novel selection pressures with varying impacts across species and life history stages. The post‐fledging stage for migratory passerines, defined as the period of time from when hatch‐year birds fledge until their first migration, is a poorly understood component of annual productivity that potentially limits population growth. We studied two migratory passerines with positive and negative population responses to urbanization, respectively: gray catbird Dumetella carolinensis and wood thrush Hylocichla mustelina. Our goals were to estimate post‐fledging survival rates for urban bird populations and determine which features of the urban landscape impact mortality risk during the post‐fledging stage. From 2012–2014, we tracked 127 fledglings (60 gray catbirds and 67 wood thrushes). Over 55 d after fledging, cumulative survival of gray catbirds (0.32 [95% CI: 0.22–0.47]) was approximately half that of wood thrushes (0.63 [95% CI: 0.52–0.75]). Thus, survival rates during the post‐fledging stage, taken in isolation, do not explain differential trajectories of gray catbird and wood thrush populations in urban environments. Most mortality (86%) for both species was due to predation. However, after reaching independence from parental care, 6 birds (9.4% of mortalities) died of anthropogenic causes (e.g. building, car strikes). Crossing roads significantly increased mortality risk, but increasing daily movement distance decreased mortality risk. Our results raise the question of whether anthropogenic sources of mortality are compensatory or additive to natural mortality; we emphasize the need to monitor fledgling survival beyond the parental‐dependence stage in order to fully understand the impacts of anthropogenic hazards on juvenile birds.