Abundances of forest birds in an unfragmented, undisturbed, and relatively mature temperate deciduous forest at the Hubbard Brook Experimental Forest, New Hampshire, changed markedly between 1969 and 1998. Total numbers of birds (all species combined) declined from 210–220 individuals/10 ha in the early 1970s to 70–90/10 ha in the 1990s. Of the 24 regularly occurring species, 12 decreased significantly (four to local extinction), three increased significantly, and nine remained relatively constant in abundance. Nine of the 12 declining species were Neotropical migrants. Most species exhibited similar trends on Breeding Bird Survey (BBS) routes in New Hampshire during the same 30 year period and on three replicate study sites in nearby sections of the White Mountains from 1986–1998. Probable causes of trends were diverse and differed among species. Most could be accounted for by individual species' responses to events occurring primarily in the local breeding area. The most important local factor affecting bird abundance was temporal change in forest vegetation structure, resulting from natural forest succession and local disturbances. Four species that declined markedly and in some cases disappeared completely from the study plot (Least Flycatcher, Empidonax minimus; Wood Thrush, Hylocichla mustelina; Philadelphia Vireo, Vireo philadelphicus; and American Redstart, Setophaga ruticilla) appear to attain peak abundance in early or mid successional forests. Species preferring more mature forests, such as Black-throated Green Warbler (Dendroica virens) and Ovenbird (Seiurus aurocapillus), increased significantly in abundance over the 30 year study. Other important factors influencing bird abundances were food availability and events in the migratory and winter periods. Nest-predation rates, although varying among years, showed no long-term pattern that would account for population declines, and brood parasites were absent from this forest. Findings from this study demonstrate that major changes in bird abundances occur over time even in undisturbed and relatively mature forests, and illustrate the need for considering habitat requirements of individual species and how habitat suitability changes over time when trying to assess the causes of their long-term population trends. The results also imply that any conclusions about the effects of other factors affecting forest bird abundances, such as increased nest predation or brood parasitism associated with habitat fragmentation, must also account for successional changes that may be affecting habitat suitability.

We sequenced the complete mitochondrial cytochrome-b gene (1,143 nucleotides) for representatives of each species in the cardinalid genera Passerina (6 species), Guiraca (1 species), and Cyanocompsa (3 species), and used a variety of phylogenetic methods to address relationships within and among genera. We determined that Passerina, as presently recognized, is paraphyletic. Lazuli Bunting (P. amoena) is sister to the much larger Blue Grosbeak (Guiraca caerulea). Indigo Bunting (P. cyanea) and Lazuli Bunting are not sister taxa as generally thought. In all weighted parsimony trees and for the gamma-corrected HKY tree, Indigo Bunting is the sister of two sister groups, a “blue” (Lazuli Bunting and Blue Grosbeak) and a “painted” (Rosita's Bunting [P. rositae], Orange-breasted Bunting [P. leclancherii], Varied Bunting [P. versicolor], and Painted Bunting [P. ciris]) clade. The latter two species form a highly supported sister pair of relatively more recent origin. Uncorrected (p) distances for ingroup (Passerina and Guiraca) taxa range from 3.0% (P. versicolor–P. ciris) to 7.6% (P. cyanea–P. leclancherii) and average 6.5% overall. Assuming a molecular clock, a bunting “radiation” between 4.1 and 7.3 Mya yielded four lineages. This timing is consistent with fossil evidence and coincides with a late-Miocene cooling during which a variety of western grassland habitats evolved. A reduction in size at that time may have allowed buntings to exploit that new food resource (grass seeds). We speculate that the Blue Grosbeak subsequently gained large size and widespread distribution as a result of ecological character displacement.

We examined the influence of female age, male age, and pair-bond duration on start of egg-laying, clutch size, and number of young fledged in the Lesser Spotted Woodpecker (Dendrocopos minor). We also attempted to disentangle the relative influence of individual age and pair-bond duration on reproduction, because the effect of those factors may be confounded. Breeding performance improved with age in that old females started egg-laying earlier and old males raised more young than yearlings, and old pairs both started egg-laying earlier and raised more young than new pairs. Clutch size was not affected by age, but showed a strong negative relation with laying date. Late-laying yearling females experienced a lower survival, and the survival of yearling males showed a positive relation with fledgling production. That differential survival was a likely mechanism explaining the differences in reproductive performance between yearling and old birds. Several analyses suggested that pair-bond duration had independent positive effects on reproduction. Benefit of long-term pair-bonds appeared to depend upon repeated breeding with a particular partner. The mechanisms behind the benefit of remating with a particular partner remain unclear, however. We postulate that much of the patterns of age effects on reproduction in the Lesser Spotted Woodpecker may be caused by constraints posed by the territorial system and effects of territory quality, although effects of individual quality can not be excluded.

Black-legged Kittiwakes (Rissa tridactyla) nest at 25 distinct colonies located throughout Prince William Sound that range in size from <20 to >7,000 pairs. Dramatic changes have occurred in the distribution of breeding birds among those colonies during the past few decades (1972–1997). Reproductive success data collected since 1985 confirm that individual colonies are habitat patches of varying quality in space and time. Even with such variation, predictability of habitat quality did occur in short- and long-term (≥3 year) intervals as indicated by significant (P < 0.05) relationships between current (t) and previous year's (t−1, t−2, etc.) reproductive success. Those circumstances provided suitable conditions for testing hypotheses concerning dispersal and recruitment strategies of a long-lived species. Breeding birds responded to both short- and long-term cues and, in general, recruited to the most successful colonies. An apparently lower dispersal propensity and the importance of long-term cues was in contrast to a similar study of kittiwake colonies in France (Danchin et al. 1998). Differences between these studies may be attributed to primary factors controlling habitat quality in Prince William Sound operating in the long-term versus the short-term and the magnitude of scale. Colonies in our study covered a much larger geographic area and therefore, factors such as foraging-site faithfulness, mate retention, and natal philopatry may also have influenced dispersal decisions. Nonetheless, recruitment of kittiwakes in Prince William Sound supported the performance-based conspecific attraction hypothesis, which, in turn, led to an ideal free distribution of breeding birds. Those short-term mechanisms for dispersal and recruitment manifested in a long-term redistribution of nesting kittiwakes from poor breeding conditions in southern Prince William Sound to favorable conditions in northern Prince William Sound. Favorable conditions in northern Prince William Sound were apparently supported by stable or increasing populations of juvenile herring. In contrast, reproductive failures and population declines in southern Prince William Sound were concordant with colonies in the Gulf of Alaska where diets were similar, consisting of primarily capelin (Mallotus villosus) and Pacific sand lance (Ammodytes hexapterus). Those trends corresponded with the influence of Gulf of Alaska waters in southern Prince William Sound and may have been associated with a reported decline in the abundance of key forage species related to a late 1970s regime shift in the Gulf of Alaska.

Due to extensive clearing of bottomland forest in the southeastern United States, Swainson's Warbler (Limnothlypis swainsonii) is restricted in many drainages to seasonally inundated buffer zones bordering rivers and swamps. This migratory species is especially vulnerable to flooding because of its ground foraging ecology, but little is known about patterns of habitat occupancy at wetland ecotones. I investigated the physiognomic and floristic correlates of habitat use along a subtle hydrological gradient in the Great Dismal Swamp, southeastern Virginia. Hydrology is the driving force influencing vegetation and the distribution of Swainson's Warbler in that habitat. Foraging and singing stations of territorial males were significantly drier and more floristically diverse than unoccupied habitat. There was scant evidence that the distribution and abundance of particular plant species, including giant cane (Arundinaria gigantea), influenced habitat selection. Instead, Swainson's Warbler seems to evaluate potential territories on the basis of multiscale physiognomic, hydrological, and edaphic characteristics. Territories were characterized by extensive understory thickets (median = 36,220 small woody stems and cane culms per hectare; range, 14,000–81,400/ha), frequent greenbriar tangles, deep shade at ground level, and an abundance of leaf litter overlying moist organic soils. Those sites occurred most frequently in relatively well-drained tracts of broad-leaf forest that had suffered extensive canopy damage and windthrow. Data suggest a preference for early successional forest in the current landscape or disturbance gaps in primeval forest. Because territories in otherwise optimal habitat are abandoned when flooding extends into the breeding season, it is recommended that the water table be maintained at subsurface levels from late March through September in natural areas managed primarily for this species. Direct and indirect environmental factors that influence the breeding biology of the warbler are summarized in an envirogram.

Lipids are the dominant fuel source during migratory flight, but the factors controlling the relative importance of lipid, protein, and carbohydrate to flight metabolism remain unclear. I tested the nonexclusive hypotheses that diet, migration distance, or endogenous lipid reserves mediate variation in the fuels birds catabolize during migration. Blood plasma metabolite concentrations were significantly different among species, and indicated clear differences in protein and lipid utilization among three turdid chat and five sylviid warbler species caught during spring migration in the Negev Desert, Israel. Fruit-eating species (omnivores) catabolized less protein and more lipid during migration than insectivores. Metabolite concentrations of omnivorous Blackcaps (Sylvia atricapilla), Garden Warblers (S. borin), and Lesser Whitethroats (S. curruca) were consistent with low rates of proteolysis (low uric acid), and high rates of lipolysis (high free-fatty acid and β-hydroxybutyrate). On the other hand, metabolite concentrations of insectivorous Redstarts (Phoenicurus phoenicurus), Nightingales (Luscinia megarhynchos), Thrush Nightingales (L. luscinia), Barred Warblers (S. nisoria), and Orphean Warblers (S. hortensis) indicated increased proteolysis and decreased lipolysis. Blood metabolite concentrations, however, were not correlated with migration distance, and the results do not support the hypothesis that long-distance migrants use fuel differently than short-distance migrants. Triacylglycerol mobilization was positively correlated with the amount of visible subcutaneous fat, but blood metabolite composition was more strongly affected by diet. Omnivores and insectivores exhibit different fuel-use strategies to overcome the physiological challenges of migration.

The response of passerine birds to forest edge was examined in old-growth and mature second-growth coast redwood (Sequoia sempivirens) forest in northern California. The study objectives were to determine which common passerine species are sensitive to edges during the breeding season and to estimate edge width for forest interior species. Response to edge was measured along twelve 100 × 400 m plots extending from the edge into the forest interior to obtain relative density of birds. Plots were surveyed 4 to 5 times in 1996 and 8 to10 times in 1997. We found that 14 common passerines showed a gradient of edge sensitivity. Steller's Jay (Cyanocitta stelleri) and Swainson's Thrush (Catharus ustulatus) had higher relative densities near edges than in the forest interior (P < 0.05) and were categorized as edge species. Brown Creeper (Certhia americana), Winter Wren (Troglodytes troglodytes), Pacific-slope Flycatcher (Empidonax difficilis), and Varied Thrush (Ixoreus naevius) had lower relative densities near edges (P < 0.05) and were categorized as interior birds. Based on exponential regression models, estimated edge widths were 140 m for Varied Thrushes, 85 m for Brown Creepers, 120 m for Winter Wrens, and 125 m for Pacific-slope Flycatchers. Creation of edges would probably benefit Steller's Jays (which may be a nest predator), may not benefit Swainson's Thrushes, and may be detrimental to species that avoid edges. We recommend that edge effects be taken into consideration when planning for the conservation of bird species in the region.

We collected eggs, neonates, and adults of Canada Geese (Branta canadensis interior) and Lesser Snow Geese (Chen caerulescens caerulescens) from Akimiski Island, Nunavut, during the 1996 breeding season. This was done to assess interspecific differences in egg composition, egg-nutrient catabolism, developmental maturity, tissue maturity, and body reserves, and to relate observed differences in those variables to ecological conditions historically experienced by Canada Geese and Lesser Snow Geese. Eggs of both species had identical proportional compositions, but Canada Goose embryos catabolized 13% more of their egg protein, whereas Lesser Snow Goose embryos catabolized 9% more of their egg lipid. Neonate Canada Geese and Lesser Snow Geese had similar protein reserves, relative to body size, but Lesser Snow Geese had relatively smaller lipid reserves than did Canada Geese. Relative to conspecific adults, Lesser Snow Goose goslings generally were structurally larger at hatch than were Canada Goose goslings. Neonate Lesser Snow Geese had more developmentally mature keels, wings, and breast muscles, and larger gizzards and caeca for their body size, than did neonate Canada Geese. Despite hatching from smaller eggs and having a shorter period of embryonic growth, skeletal muscles and gizzard tissues of Lesser Snow Geese were more functionally mature than those of Canada Geese. Increased lipid use during embryonic development could account for how Lesser Snow Geese hatched in a more developmentally and functionally mature state. In turn, differences in developmental and functional maturity of Lesser Snow Geese, as compared to Canada Geese, likely are adaptations that offset metabolic costs associated with their small body size, or to selection pressures associated with high arctic environmental conditions and colonial nesting and brood rearing.

For various reasons, migrating birds may not refuel and gain mass immediately after they have arrived at a stopover site. That led to the concept of a search-settling time after arrival with a low or negative initial refueling rate, but its existence has not been clearly demonstrated in field studies. Body-mass changes resulting from capture–recapture data can be misleading if used for the estimation of a natural low initial refueling rate because (1) it is usually unknown whether the day of first capture is also the first day of stopover, and (2) handling at first capture may have an adverse effect on subsequent body-mass development. To circumvent those problems we increased probability of catching birds shortly after arrival by inducing landfall by tape-luring, and we estimated body-mass change without previous handling effects from concentration of two metabolites in blood plasma. In the Eurasian Reed-Warbler (Acrocephalus scirpaceus) studied at a stopover site in Switzerland, there was no difference in plasma-metabolite concentrations between a group of mostly newly arrived individuals and a group with few newly arrived birds. Similarly, there was no difference in those parameters between birds that had been handled before and birds at first capture. However, the analysis of capture–recapture data from two other Swiss stopover sites with longer handling times indicated that mean body mass of Eurasian Reed-Warblers and European Robins (Erithacus rubecula) dropped after capture and reached initial values only after one to several days. We concluded that mass loss after capture depended mainly on lost foraging time and that natural low initial refueling rate after arrival at a stopover site is not detectable under the conditions of this study.

Patterns of abundance of the seabird tick Amblyomma loculosum and their effects on Roseate Tern (Sterna dougallii) nestling growth, fledging age, and survival are described on Aride Island, Seychelles, in 1997–1999. Female ticks attached to nestlings from 4 to 14 days (to engorge) whereas male ticks attached for 1–3 days. The linear growth rate of birds carrying female ticks (0.24 g/day) was significantly different from that of nonparasitized nestlings of the same age and similar (or even lower) hatching weight (4.07 g/day). Parasitized nestlings that fledged did so 5.2 days later than nonparasitized nestlings of similar age. Only 37.5% of the nestlings infested with female ticks fledged compared with 83.3% of the noninfested nestlings. During the successful 1998 breeding season, around 100 nestlings died from tick infestation (24.3% of the nestling deaths). Ticks appeared to accelerate nestling mortality during periods of food shortage. Despite an annual difference of two weeks in the timing of breeding of the Roseate Terns between 1997 and 1998, adult ticks parasitized nestlings in July, with an infestation peak occurring between 8–12 July in both years. However, in 1997, nestlings were parasitized at a younger age, suggesting that ticks (nymph stage) must attach to Roseate Tern adults as soon as they make a nest scrape (usually in May). Ironically, the frequent breeding failures of the Roseate Terns will result in lower infestation levels in subsequent years, which will benefit the birds.

Brood parasitism occurs disproportionately in birds with precocial young and is particularly common in Anseriformes. In part, that pattern may result because precocial hosts, relative to altricial species, incur relatively few costs when caring for precocial eggs. Empirical data do not consistently support that hypothesis, and some parameters have not been adequately compared between parasitized and nonparasitized nests or females. We used a combination of experimentation (egg and duckling additions) and analysis of a larger observational data set to compare reproductive parameters, recruitment, and adult survival between parasitized and nonparasitized female Common Pochard (Aythya ferina) and Tufted Ducks (A. fuligula). Addition of three eggs to nests during the host's laying cycle had no effect on host clutch size, host egg hatch success, or nest success for either species. Nest success was not affected by parasitism intensity for pochards, but we did detect a small drop in nest success for Tufted Duck nests parasitized with >6 eggs. Recruitment probability did not differ between parasitized and nonparasitized nests for either species, and parasitism had no negative effect on adult survival. Between-year nest initiation dates were later for parasitized Tufted Ducks, although the biological consequences of that difference (3.8 days) seem negligible. Moderate levels of parasitism do not negatively affect hosts for these two species.

We examined habitat selection by breeding Cerulean Warblers (Dendroica cerulea) at three spatial scales in eastern Ontario over three years (1997–1999). Territories were characterized by well-spaced large trees, with high canopies and dense foliage cover at heights between 12–18 m. Nesting habitat additionally was characterized by dense foliage cover above 18 m. The results of our nest-patch (0.04 ha circle around nest) and nest-site (0.01 ha circle) analyses indicate that male Cerulean Warblers may take active roles in nest-site selection when selecting territories. We conclude from our nest-patch and nest-site selection analyses that territories likely contain multiple nest patches and sites and that male Cerulean Warblers may defend areas with multiple nest patches or sites, which may attract females to settle with them. Whether or not Cerulean Warbler females use nest-site availability as a mate- or territory-choice cue remains unknown. We also tested the validity of a commonly made assumption that a random sampling of habitat by researchers is representative of the habitat actually available to birds and found that, in our study area, the assumption was invalid. Taken together, our results point toward the need to maintain sizeable stands of mature, deciduous forest to ensure the persistence of Cerulean Warblers in eastern Ontario. Population characteristics such as lower minimum area requirements and a resilience to habitat disturbance may make that an easier job in eastern Ontario than elsewhere in this species' breeding range.

We manipulated nestbox choices in Eastern Bluebirds (Sialia sialis) to assess (1) whether the presence of a previously used (and presumably parasite-ridden) nest cavity increases or decreases the likelihood of within-season nestbox reuse and (2) whether birds prefer previously successful cavities. Initially, birds were presented with two clean identical nestboxes erected 1 m apart. After the first nesting, we removed nest material from half of the successful box pairs and recorded subsequent nesting choices. Given a choice between a used and an unused box, bluebirds chose the unused but parasite-free cavity significantly more often. Presented with a cleaned successful box and an identical unused one, bluebirds opted to reuse the former significantly more often. Those results suggest that (1) bluebirds recognize a cost of within-season nest reuse and are willing to switch nest sites to minimize parasitism, (2) bluebirds prefer successful cavities, but only if they are clean, and (3) in our population, in which cost of nest switching was minimized, the aversion to parasites was stronger than the preference for successful cavities.

We investigated sex-related differences in habitat use in wintering American Kestrels (Falco sparverius) at two scales: within a 10 m radius and within a 100 m radius of perch sites. Female kestrels used areas containing a higher percentage of short vegetation (<0.25 m high) suitable for foraging than did males at both scales (100 m radius females 80%, males 69%; 10 m radius females 80%, males 73%). At both scales, females had more pasture (a high-quality foraging substrate) available than did males; areas within a 100 m radius of male perch sites contained more woodlot than did female perch sites. Logistic regression models indicated greater overlap between male and female habitat use on a 10 m radius scale than on a 100 m radius scale, suggesting that males may preferentially select smaller areas devoid of woody vegetation relative to what is available within 100 m radius of perch sites. Our results suggest that males may be constrained to winter in areas with lower overall foraging opportunities and possibly higher predation risk than areas used by females. Our work supports the hypothesis that males and female kestrels prefer open areas as wintering habitat.

We report association between female blood parasite prevalence (percentage of infected birds) just after egg laying and reproductive success in two successive breeding seasons, in a breeding population of Pied Flycatcher Ficedula hypoleuca in central Spain. Females infected with Trypanosoma spp. had a higher probability of deserting their clutches during the incubation period than noninfected females. Females infected with Haemoproteus balmorali hatched proportionally fewer eggs than noninfected females. Female infected with H. balmorali during the incubation period may have a decreased ability to thermoregulate which may affect their incubation capacity. Fledging success, breeding success, fledgling mass, and tarsus length were not associated with infection of the mother by blood parasites during the incubation period, suggesting that females and their mates may compensate during the nestling period for the negative effect of blood parasites during the incubation period.

Maximum diving depths were measured for shearwaters breeding on Cousin Island, Seychelles. Eighty-three percent of 23 Wedge-tailed Shearwaters (Puffinus pacificus) dived, and their mean maximum depth was 14 m (SD = 23 m, range 1–66 m, N = 19). All Audubon's Shearwaters (P. lherminieri) dived, and their mean maximum depth was 15 m (SD = 12 m, range 6–35 m, N = 7). These data contradict the hypothesis that tropical shearwaters should not specialize in underwater foraging. They are capable of exploiting deep prey unavailable to most other tropical seabirds. Five Puffinus species (temperate and tropical) attained allometrically scaled maximum depths comparable to those of penguins and alcids.

Breeding male Ruffs (Philomachus pugnax) appear to communicate individual identity through extreme variation in coloration and pattern of their plumages. If plumage variation evolved to provide sufficient information to signal individual identity, we might expect different plumage components to vary independently. We find that variation in four plumage characteristics is largely independent. Previous studies produced conflicting answers about plumage-component independence, perhaps because they failed to separate two genetically distinct behavioral categories of males, which differ in plumage types, in their analysis. We propose that using plumage variation to signal individual identity, rather than voice (used by most other bird species) was favored by lengthy daytime male display in open habitats in close proximity to receivers. However, signaling associated with the unique dimorphism in this species' male mating behavior might also have influenced the evolution of extraordinary plumage diversity in this species.

Researchers have suggested that Brown-headed Cowbirds (Molothrus ater) destroy nest contents of potential hosts to induce renesting and thus enhance future opportunities for parasitism. Although cowbird destruction of passerine nests has been witnessed and surmised, few data are available on frequency of those events. We used miniature video-cameras at nests of grassland passerines and documented partial or complete destruction of eggs or nestlings by cowbirds at 7 of 132 nests monitored with cameras. At least three of the seven cases appeared to be attempts to totally destroy the nest contents; those cowbirds did not appear to be motivated by food or an intent to parasitize the nest. Three cases probably were associated with parasitism, but two involved egg removal late in incubation and the third was unusually destructive. Cowbirds were responsible for 24% of egg losses and 5% of nestling losses caused by predators. The importance of cowbirds as an agent of egg and nestling loss undoubtedly varies among sites and years, but it should not be overlooked.

In this study, Field Sparrows (Spizella pusilla) deserted 46% of nests, parasitized by Brown-headed Cowbirds (Molothrus ater) and only 1% of unparasitized nests suggesting that desertion functions primarily as an antiparasite defense. Sparrows did not desert nests following various clutch manipulations that are often associated with parasitism, indicating that desertion was not in response to the presence of cowbird eggs. Sparrows often deserted nests following encounters with real or mounted cowbirds, suggesting that nest desertion is a response to adult cowbirds. Sparrows deserted nests only in stages most vulnerable to the effects of parasitism. That finding is consistent with the possibility that desertion is a parasite-specific response. Sparrows arrived at nests earlier in the day at our Illinois site, where parasitism was greater, than in Missouri. Our findings confirm that host vigilance can prevent successful parasitism, and we provide the first direct evidence that encounters with cowbirds may cause hosts to desert nests. Our findings may help explain why cowbirds parasitize nests extremely early in the morning and lay rapidly. We suggest that consideration be given to host response following interactions with adult brood parasites because those interactions may have implications for both the ecology and evolution of both the parasite and host.

We conducted aggression experiments using model cowbirds on nesting Field Sparrows (Spizella pusilla) in heavily, moderately, and rarely parasitized populations. We also documented Field Sparrow morning nest arrival times during the laying period, because Field Sparrows appear to desert nests in response to encounters with laying female cowbirds. Field Sparrows responded most aggressively to cowbird models and arrived the earliest in Illinois, where they were most heavily parasitized. Field Sparrows responded the least to models in Pennsylvania, where they are almost never parasitized. Our results suggest that those host behaviors result from some aspect of host–cowbird interactions, but the extent to which such behaviors are genetic or learned needs further study.

We studied the standard and comparative energetics of the Rufous-tailed Plancutter (Phytotoma rara), one of the smallest avian herbivores. The Rufous-tailed Plancutter had basal metabolic rate (BMR) values that so far are the highest mass-independent values observed in avian herbivores. Probably the BMR values attained by P. rara reflect its geographic distribution in temperate environments. Using a comparative analysis, we observed that herbivorous birds from temperate geographic areas tend to have higher BMR than tropical ones.

We analyze the use and functionality of ossuaries by the Bearded Vulture (Gypaetus barbatus) in the Pyrenees during the nestling period. In 71% of cases, the ossuary was used to prepare food for chicks, in 11% for storing food, and only in 18% for preparing the adults' own food. Pairs used an average of two ossuaries at a mean distance from the nest of 789 m (SE ± 377). The average time dedicate to breaking bone was 5.3 min (SE ± 4.2) and 4.5 throws (SE ± 5.8) for each session in the ossuarie (n = 86). The temporal variation found in the use of the ossuaries, with maximum frequencies between 31–90 days of age of chicks, may be due to a possible qualitative variation in chicks' diets. Ossuaries are also used to store food, this being a differentiating and advantageous trait with respect to feeding behavior developed by other meat scavengers.

The cloacal protuberance (CP) of passerines functions primarily to store spermatozoa. When gently squeezed, the CP of male Tree Swallows (Tachycineta bicolor) everts to expose a small papilla from which semen can be expressed. From 1994 to 1999, I examined individual and seasonal variation in CP dimensions and papilla length of mated male Tree Swallows in western Michigan. Male CP volumes were greatest when their mates were laying eggs and declined to the nestling period. Papilla lengths did not vary over the course of the breeding season. Cloacal protuberance dimensions and papilla length were not associated with the age class of a male's mate, the date she started laying eggs, or number of eggs she laid. The decrease in CP size over the course of the breeding season is consistent with the steady decrease in reproductive opportunities for male swallows. Although it seems likely, whether or not the papilla of Tree Swallows functions as an intromittent organ awaits further study of the anatomical mechanics of copulation in these birds.

Migratory hummingbirds forage on diverse assemblages of flowers varying in shape, color, and accessibility. Do hummingbirds learn to feed from flowers by observing other hummingbirds? Learning abilities of Ruby-throated (Archilochus colubris), Broad-tailed (Selasphorus platycercus), and Rufous (S. rufus) hummingbirds were studied in the presence or absence of a knowledgeable tutor. In two sequential trials hummingbirds learned to feed from artificial feeders of increasing complexity. Feeders in the first trial had easy access and were colored red at the nectar spout. In this initial trial, hummingbirds attempted to feed from the artificial feeder regardless of tutor presence, but tutored birds learn to feed more quickly. Feeders in the second trial were uncolored and the nectar spout was surrounded by a long artificial corolla. Tutored birds again learned to feed more quickly than their solitary counterparts. However, both untutored and tutored hummingbirds learned to feed more quickly in the second trial than the first, suggesting that the initial task of identifying a novel feeding resource is more difficult than learning how to access an identified resource.

A novel nuclear marker, the avian ovomucoid intron G (OVOG) was sequenced from 19 galliform taxa. Results of the phylogenetic analyses using OVOG were compared to those obtained using the mitochondrial cytochrome b (cytb) gene to determine the phylogenetic utility of OVOG. OVOG appeared to have strong phylogenetic signal for reconstructing relationships among genera and families, and the only difference between OVOG and cytb was in the placement of the New World quail (Odontophoridae). Genetic distances estimated using OVOG are approximately half of those estimated using cytb, although that relationship was not linear. OVOG exhibited patterns of nucleotide substitution very different from cytb, with OVOG having little base compositional bias, a relatively low transition–transversion ratio, and little among-site rate heterogeneity.