The Botteri's Sparrow (Aimophila botterii) is a bird of tall grasslands that temporarily disappeared from Arizona following heavy livestock grazing in the 1890s. Its return was noted first in sacaton (Sporobolus wrightii), an uncommon native floodplain tallgrass often >2 m in height, and subsequently in stands of exotic lovegrasses (Eragrostis spp.) spreading into adjacent uplands that otherwise supported shorter native grasslands. We examined whether the exotic grasslands provided suitable breeding habitat for Botteri's Sparrows, compared to native grasslands. We counted birds for three years on 18 plots, monitored 314 nests on 323 home ranges, banded 583 birds, and measured vegetation on plots and home ranges, and at nests and fledgling locations. Abundance and site fidelity were positively associated with grass height and cover, being greatest in sacaton, intermediate in exotics, and lowest in native upland grasslands. The three habitats did not differ in young fledged per capita. Vegetation cover on Botteri's Sparrow home ranges did not differ from the surrounding available habitat, but locations of flightless recently fledged young included taller and more dense vegetation than either nest sites or random locations, especially in sparsely vegetated native grasslands. These results suggest that fledglings required substantial cover to avoid predation while they completed development. Far from being an ecological trap, the exotic lovegrasses apparently are providing essential cover for the Botteri's Sparrow in Arizona, perhaps allowing it to regain an abundance similar to what existed regionally prior to overgrazing of the late 19th Century.

Degradation of nesting habitat has been proposed as a factor contributing to Greater Sage-Grouse (Centrocercus urophasianus) population declines throughout North America. Delineating suitable nesting habitat across landscapes with relatively contiguous sagebrush cover is difficult but important to identify areas for protection. We used radio-telemetry to locate Greater Sage-Grouse nests in relatively contiguous sagebrush habitats in Wyoming to investigate the spatial arrangement of nests relative to lek and other nest locations. Nest distributions were spatially related to lek location within 3 and 5 km of a lek, and a 5-km buffer included 64% of the nests. There was no relationship between lek size and lek-to-nest distance, suggesting that accurate population trend evaluation might require lek surveys in addition to lek counts. Closest known lek-to-nest distance was greater for successfully hatched compared to destroyed nests, and closely spaced nests tended to experience lower success and have higher probabilities of both nests experiencing the same fate compared to isolated nests, suggesting that a mechanism of enhanced prey detection occurred at higher nest densities. A low probability that a given individual's consecutive-year nest spacing occurred randomly suggested nesting site-area fidelity. Although a grouped pattern of nests occurred within 5 km of a lek, the proportion of nesting females located farther than 5 km could be important for population viability. Managers should limit strategies that negatively influence nesting habitat regardless of lek locations, and preserve adequate amounts of unaltered nesting habitat within treatment boundaries to maintain nest dispersion and provide sites for philopatric individuals.

Hawaiian honeycreepers (Aves: Drepanidinae) evolved in the absence of mosquito-borne diseases such as avian malaria (Plasmodium spp.). Malaria has been largely responsible for the recent wave of extinctions and endangerment among Hawaiian forest birds, which began by the 1920s. Most honeycreepers, especially endangered species, now persist only in forests above 1500 m elevation, where cool temperatures prevent effective malaria development in mosquitoes. We report here that prevalence of malaria in Hawaiian forest birds at 1900 m on the island of Hawai‘i has more than doubled over a decade. This increase was associated with breeding of mosquitoes and warmer summertime air temperatures. We also report direct evidence of tolerance to malaria, and a possible cost of tolerance, in wild native birds. Tolerance is adding to a reservoir of malaria at upper elevations even while vectors are rare and air temperatures are too low for complete development of the parasite in the vector. The data provide a glimpse of how malaria is becoming an emergent infectious disease at upper elevations.

Birds with songs having two or more acoustically distinct elements can arrange them either rigidly (i.e., in the same sequence) or flexibly. Flexible song syntax can be achieved either by varying the number of repetitions of elements or by combining elements in different ways. Combinatorial syntax has been documented only in the songs of oscine passerines and in one nonpasserine, but not in the suboscine passerines. Dawn and day songs of a tyrant flycatcher, the Flammulated Attila (Attila flammulatus), were recorded in Costa Rica. Flexible syntax was noted in both dawn and day song. Attilas not only varied the number of repetitions of their song elements but also combined elements in various ways. This appears to be the first reported case of combinatorial song syntax in a suboscine species.

Avian color ornaments produced by different mechanisms (i.e., melanin, carotenoid, and structural colors) can communicate different sets of information due to differences in their condition or developmental constraints. Although this suggests that different color signals should be analyzed separately, few comparative studies have focused on specific types of coloration. In cardueline finches, interspecific variation in overall plumage brightness (which integrates all types of coloration) was previously shown to be affected by sexual selection and to covary with fecundity and parental care. Using a phylogenetic comparative approach, we extended this line of research and tested whether a specific component of plumage ornamentation, the melanin-based black frontal coloration of finches, showed a similar association with reproductive effort. We found that the extent of male melanization and melanin dichromatism increased in species with reduced clutch sizes, whereas female melanization was negatively correlated with incubation length. These results remained significant when we controlled for the effects of several ecological variables, and were also consistent between two alternative multivariate model-selection approaches. Our results are consistent with the hypothesis that interspecific variation in melanization may be related to fecundity and parental care through trade-offs between investment in sexual signals and parental efforts.

We studied Creamy-bellied Thrush (Turdus amaurochalinus) defenses against brood parasitism by Shiny Cowbirds (Molothrus bonariensis). Shiny Cowbirds decrease the reproductive success of Creamy-bellied Thrushes, and having historical habitats and ranges that overlap, we expected that thrushes possess antiparasitic defenses. We analyzed nest attendance during prelaying, laying and incubation; responses to the presentation of a model of a female cowbird or a control species close to the nest; nest abandonment associated with parasitism; and responses to experimental parasitism with white or spotted cowbird eggs (with or without the simultaneous presentation of a female cowbird model). Nest attendance was 58%–68% during prelaying and 83%–90% during laying and incubation. Thrushes had a shorter latency in returning near the nest and visited nests more frequently when we presented the cowbird model than the control model. The frequency of abandonment of parasitized nests was low and was not temporally associated with parasitism. Thrushes ejected white eggs more frequently than spotted eggs when parasitism was associated with the presentation of the cowbird model, but there were no differences when the model was absent. Our results indicate that Creamy-bellied Thrushes recognize cowbirds as a threat and eject white but not spotted cowbird eggs. We postulate that the low impact of cowbird parasitism on thrush hatching success and chick survival and the likelihood of recognition errors when parasite eggs resemble host eggs may have prevented the evolution of egg ejection in this host.

Adult and juvenile plumage characters were traced onto a well-resolved molecular based phylogeny for Picoides woodpeckers, and a simple phylogenetic test of homology, parallelism, and convergence of plumage characters was performed. Reconstruction of ancestral character states revealed multiple events of independent evolution of derived character states in most characters studied, and a concentrated changes test revealed that some plumage characters evolved in association with habitat type. For example, there was a statistically significant association between loss of dorsal barring and use of densely vegetated habitats among Picoides species. Two analyses indicated that convergence, as opposed to parallel evolution or shared ancestry, underlies the similarity in plumage patterns between the Downy (Picoides pubescens) and Hairy (P. villosus) Woodpeckers. Possible causal explanations for convergence in plumage patterns may include mimicry and interspecific territoriality.

We investigated patterns of seasonal variation in body weight in six populations of five resident species of temperate-zone woodpeckers: Acorn Woodpecker (Melanerpes formicivorus), Red-bellied Woodpecker (M. carolinus), Red-cockaded Woodpecker (Picoides borealis), Downy Woodpecker (P. pubescens), and Great Spotted Woodpecker (Dendrocopos major). After controlling for time of day and overall body size, annual variation in body weight was small and generally not statistically significant. However, analysis revealed evidence of significant “winter fattening,” comparable in magnitude to other temperate-zone resident species, in three of the species. The degree of winter fattening did not correlate with either the size of the acorn crop (for the Acorn Woodpecker) or latitude, two variables potentially related to predictability of food resources. However, the smaller species exhibited significantly greater winter fattening than the larger species, as predicted by the hypothesis that energy storage should be more important for small-bodied species. Furthermore, the food-storing Acorn Woodpecker exhibited considerably less winter fattening than the nonfood-storing species, supporting the hypothesis that food storage provides an ecological alternative to winter fattening.

Examination of 1622 specimens indicates that North American Falconiformes show a wide variety of remigial (primary and secondary) replacement strategies, detectable throughout the year by evaluation of replacement patterns in the wings. Most Falconidae undergo complete prebasic molts whereas most Accipitridae display retained secondaries or show stepwise molt replacement patterns (“Staffelmäuser”). Among individuals exhibiting Staffelmäuser, minimum age can be inferred up to 5 years (fifth-basic plumage) by the number of “replacement waves” present among the primaries. It may also be able to infer breeding status during the previous summer by “suspension limits,” resulting from the interruption of molt during breeding. Among Accipitridae, Staffelmäuser occurred in species with greater mass, higher wing loading, longer migration distance, and more open rather than wooded foraging habitats: species that experience time constraints on molting and incur greater costs from large gaps in the wing. Thus, this study supports both the “time-constraints hypothesis,” suggesting that Staffelmäuser is a consequence of insufficient time for a complete annual molt, and the “aerodynamic hypothesis,” suggesting that Staffelmäuser reflects an adaptive need to replace as many feathers as possible without inhibiting flight efficiency. Time constraints may have been a proximate cause of Staffelmäuser among Falconiformes, with improvements to flying efficiency being an ultimate adaptive benefit.

Laysan Albatross (Phoebastria immutabilis) and the closely-related Black-footed Albatross (P. nigripes) replace 20%–90% of their 35–41 wing flight feathers every year. Large-scale molt patterns (patterns between rather than within molt series) account for 77% of the variation in the number of flight feathers replaced. We identified four molt series: series A—the five outer primaries; series B—the five inner primaries plus four outer secondaries; series C—the middle secondaries; and series D—the inner secondaries. A fifth molt series may lie between series C and D. Each year, series A and D initiate molt, but series B and C may or may not initiate molt. The result is four “annual molt patterns”: ABCD, ABD, ACD, and AD. Temporally overlapping waves of molt never occur within series A or B, but about one third of the time they occur within series C and D. Multiple, spatially defined waves of molt (replaced feathers separated by unreplaced feathers) never occur within series A, but occur about two thirds of the time within series B, C, and D. The inner primaries and outer secondaries constitute a single molt series, probably to equilibrate between series total feather length, and thus, total molt duration. Studies of foraging range and reproduction in albatrosses would benefit from the development of species-specific indices of molt duration and extent that are biologically as well as statistically defensible. The number of outer primary feathers replaced and the number of molt series that activate molt are two such indices for Laysan and Black-footed Albatrosses.

We examined nest-site selection and nesting success in Saltmarsh Sharp-tailed (Ammodramus caudacutus) and Seaside Sparrows (A. maritimus), at seven sites in Connecticut. We found 160 Saltmarsh Sharp-tailed Sparrow nests and 23 Seaside Sparrow nests, and compared characteristics of their locations to each other and to random locations. We tracked success of all nests, quantified nest productivity and causes of nest losses, and tested for habitat differences between successful and unsuccessful nests. Saltmarsh Sharp-tailed Sparrows nested in higher than average locations, where the vegetation was taller and more dense than at random locations, where there was a deep layer of thatch, and where saltmeadow cordgrass (Spartina patens) dominated the vegetation. There was little evidence that habitat characteristics influenced the success of nesting birds, but the timing of nest initiation relative to spring tides was important. Seaside Sparrow nests occurred in even taller vegetation, that was more sparse than average and dominated by the tall form of smooth cordgrass (S. alterniflora). Habitat influenced the success of Seaside Sparrow nests, but timing did not; on average, successful nests occurred in taller vegetation. Model comparisons suggest that vegetation structure influences site selection more than species composition or inherent differences among marshes. Overall, our results indicate that nest flooding is a major threat to successful reproduction in both species, but they have different strategies to avoid flooding. Saltmarsh Sharp-tailed Sparrows time their reproduction to avoid especially high tides, while Seaside Sparrows avoid flooding spatially by nesting in tall vegetation.

We used data from Northern Spotted Owl (Strix occidentalis caurina) territories to model the effects of habitat (particularly intermediate-aged forest stand types), climate, and nonhabitat covariates (i.e., age, sex) on owl reproductive rate and apparent survival in southwestern Oregon. Our best model for reproductive rate included an interaction between a cyclic, annual time trend and male breeding experience, with higher reproductive rates in even years compared to odd, particularly for males with previous breeding experience. Reproductive rate was also negatively related to the amount of winter precipitation and positively related to the proportion of old-growth forest near the owl territory center. Apparent survival was not associated with age, sex, climate or any of the intermediate-aged forest types, but was positively associated with the proportion of older forest near the territory center in a pseudothreshold pattern. The quadratic structure of the proportion of nonhabitat farther from the nest or primary roost site was also part of our best survival model. Survival decreased dramatically when the amount of nonhabitat exceeded ∼50%. Habitat fitness potential estimates (λ̂_h) for 97 owl territories ranged from 0.29–1.09, with a mean of 0.86 ± 0.02. Owl territories with habitat fitness potentials <1.0 were generally characterized by <40%–50% old forest habitat near the territory center. Our results indicate that both apparent survival and reproductive rate are positively associated with older forest types close to the nest or primary roost site. We found no support for either a positive or negative direct effect of intermediate-aged forests on either survival or reproductive rate.

We studied the foraging behavior of insectivorous songbirds during the breeding season at four sites in Illinois, each with restored open-canopy savanna habitat (65% mean canopy closure) and closed-canopy forests (89% mean canopy closure). We sampled and compared apparent tree species preference, foliage layer preference, and proportional use of different prey-attack maneuvers in the two habitats. In closed-canopy forests, three of nine songbird species foraged in black oak (Quercus velutina) and white oak (Q. alba) more than expected based on availability, and foraged less than expected in shade-tolerant trees such as sugar maple (Acer saccharum) and red elm (Ulmus rubra). Four species also displayed apparent preferences for black locust (Robinia pseudoacacia) and hackberry (Celtis occidentalis). In contrast, songbirds used tree species according to availability in open-canopy habitat. We observed apparent preferences for the shrub and subcanopy vegetation layers (0–5 m and 6–10 m) in open-canopy habitat and apparent preferences for the subcanopy and lower canopy vegetation layers (6–10 m and 11–15 m) in closed-canopy forests. Relative use of prey-attack maneuvers in open versus closed-canopy habitat was significantly different for the Eastern Wood-Pewee (Contopus virens) and the Great Crested Flycatcher (Myiarchus crinitus), but not for foliage-gleaning species. These results suggest that restoration of oak savannas has important effects on the habitat use and foraging ecology of selected insectivorous birds.

To evaluate the contribution of simultaneous clutches to breeding success in female Mountain Quail (Oreortyx pictus), we located nests of radio-marked male and female Mountain Quail in west-central Idaho from 1992 to 1995 and estimated rates and parameters of nesting success. In our sample, 29 females, 19 males, and 4 quail of unknown sex, including 12 apparently monogamous pairs, incubated nests. Using logistic regression, we found that constant survival and sex were the best-supported models to explain nest success for 45 nests of known age. Odds of success for male-incubated nests were 1.7-times (95% CI: 0.4–7.9) greater than for female-incubated nests. Mean clutch size for first nests was 11.8 (range: 6–16) and clutches incubated by males (12.6 ± 0.3 eggs) were significantly larger than female-incubated clutches (11.4 ± 0.4 eggs). Mean hatching date for all nests was 2 July (range: 10 June–23 July). Two of six females whose nests were depredated renested. Paired females produced an average of 24 eggs (range: 20–28). Mean hatching date for nine paired males was 30 June ± 3 days and 3 July ± 3 days for females. The estimated average number of days spent on nesting activities for nine successfully hatched pairs was 59 (range: 54–64). All 12 paired females hatched at least eight chicks from both clutches. Our findings indicate that simultaneous clutches in Mountain Quail ensures breeding success in females under conditions that may not be amenable to other forms of multiple brooding.

Survival of young in waterfowl is poorly understood, particularly in regions outside of the traditional prairie breeding areas. Further, traditional methods of survival estimation lack the ability to statistically characterize between the extremes of random and catastrophic mortality events. We estimated Mallard (Anas platyrhynchos) duckling survival rates for 121 broods at nine study sites across the Great Lakes region from 2001–2003, using a novel statistical method that allows for the partitioning of random and correlated mortality processes. Results indicated that survival increased rapidly with age, did not change with hatching dates, did not differ among years, but varied across site-by-year replicates. Rates of random mortality were found to vary among site-years, while rates of correlated mortality varied little across site-years. In contrast to most studies of Mallard duckling survival, seasonal increases in duckling survival were not detected. We speculate that the observed patterns in survival rates with hatching date are related to productivity in Great Lakes brood-rearing wetlands and temperate regional climate.

The historical relationships of ground antbirds and their relatives have long been unresolved. Here, I present a phylogenetic analysis of ground antbird (Formicariidae) relationships based on DNA sequence data from the cytochrome-b and ND2 genes. Results support novel hypotheses of historical relationships, including two revisions of suboscine taxonomy: (1) paraphyly of the Formicariidae with the tentative inclusion of at least some rhinocryptids (Liosceles, Rhinocrypta, and Scytalopus) in the ground antbird lineage, and (2) placement of Pittasoma with Conopophaga in the Conopophagidae.

I investigated the relationship of plumage to age and sex in the Lance-tailed Manakin (Pipridae, Chiroxiphia lanceolata) in the lowlands of western Panama from 1999–2004. I captured birds in mist nets, categorized their plumages, examined them for molt, and followed them for several years to document plumage changes. Male Lance-tailed Manakins exhibited three distinct postjuvenal plumages. Males achieved definitive adult plumage through sequential changes that occurred in the same order as in other Chiroxiphia manakins. Definitive male plumage developed over the same time span as reported for C. caudata but one year faster than C. linearis. Juvenal male plumage was similar to that of females, and 5% of 226 females had plumage similar to formative male plumage. Genetic sexing verified that changes observed late in the formative male plumage unambiguously identified sex and age of individual birds. This information can be used in behavioral studies to identify the age of male Lance-tailed Manakins captured in any of the predefinitive plumage stages.

We investigated patterns and consequences of intraclutch egg-size variation in Magellanic Penguins (Spheniscus magellanicus). First-laid eggs were significantly larger than second-laid eggs, although the mean difference represented only 2% of an average egg's volume. The degree of intraclutch egg-size variation was similar among years and females of different ages. Intraclutch egg-size variation did not affect intraclutch differences in chick hatching weights or fledging success. We found no selective advantage for laying eggs of different sizes. Because both eggs have an equal probability of being lost, chance favors equal provisioning of eggs. Egg volume explained 35% of the variation in hatching weight but did not determine fledging success. Laying order, year, and female age were better predictors of fledging success than egg size. Factors such as laying and hatching order, parental quality, oceanographic conditions, fights, and predation are more important in determining chick survival than are differences in egg size.

We collected unincubated eggs from wild Mallard (Anas platyrhynchos), Gadwall (A. strepera), Blue-winged Teal (A. discors), and Northern Shoveler (A. clypeata) nests and artificially incubated them at 37.5°C. Average incubation lengths of Mallard, Gadwall, and Northern Shoveler eggs did not differ from their wild-nesting counterparts, but artificially incubated Blue-winged Teal eggs required an additional 1.7 days to hatch, suggesting that wild-nesting teal incubated more effectively. A small sample of Mallard, Gadwall, and Northern Shoveler eggs artificially incubated at 38.3°C hatched 1 day sooner, indicating that incubation temperature affected incubation length. Mean incubation length of Blue-winged Teal declined by 1 day for each 11-day delay in nesting, but we found no such seasonal decline among Mallards, Gadwalls, or Northern Shovelers. There is no obvious explanation for the seasonal reduction in incubation length for Blue-winged Teal eggs incubated in a constant environment, and the phenomenon deserves further study.

In previous studies, bones from archeological midden deposits on Kodiak and Amchitka Islands, Aleutians, were erroneously identified as belonging to Great Cormorant (Phalacrocorax carbo), Pallas's Cormorant (P. perspicillatus), and Japanese Cormorant (P. capillatus), none of which is otherwise known from Alaska. These specimens are all re-identified as having come from the Double-crested Cormorant (P. auritus), which is much larger in Alaska than in middle and southern latitudes in North America.