Crosswise migration by Yellow Warblers,Nearctic‐Neotropical passerine migrants

Yellow Warblers (Setophaga petechia) are abundant breeding birds in North America, but their migratory and non‐breeding biology remain poorly understood. Studies where genetic and isotopic techniques were used identified parallel migration systems and longitudinal segregation among eastern‐ and western‐breeding populations of Yellow Warblers in North America, but these techniques have low spatial resolution. During the 2015 breeding season, we tagged male Yellow Warblers breeding in Maine (N = 10) and Wisconsin (N = 10) with light‐level geolocators to elucidate fine‐scale migratory connectivity within the eastern haplotype of this species and determine fall migration timing, routes, and wintering locations. We recovered seven of 20 geolocators (35%), including four in Maine and three in Wisconsin. The mean duration of fall migration was 49 d with departure from breeding areas in late August and early September and arrival in wintering areas in mid‐October. Most individuals crossed the Gulf of Mexico to Central America before completing the final eastward leg of their migration to northern South America. Yellow Warblers breeding in Maine wintered in north‐central Colombia, west of those breeding in Wisconsin that wintered in Venezuela and the border region between Brazil, Colombia, and Venezuela. Our results provide an example of crosswise migration, where the more easterly breeding population wintered farther west than the more westerly breeding population (and vice versa), a seldom‐documented phenomenon in birds. Our results confirm earlier work demonstrating that the eastern haplotype of northern Yellow Warblers winters in northern South America, and provide novel information about migratory strategies, timing, and wintering locations of birds from two different populations.     

Timing of events on the breeding grounds for five species of sympatric warblers

ABSTRACT On the breeding grounds, migratory birds have limited time to breed and molt before autumn migration. However, few studies of long‐distance migrants have examined the phenology of these events to determine what life‐history trade‐offs might result if these activities overlap. From 2000 to 2007, I used banding data to determine the timing of migration, breeding, and primary molt for Yellow Warblers (Dendroica petechia), Yellow‐rumped Warblers (D. coronata coronata), American Redstarts (Setophaga ruticilla), Ovenbirds (Seiurus aurocapilla), and Canada Warblers (Wilsonia canadensis) at a study site in Alberta, Canada. Hatching date did not differ among species (P= 0.63), with means ranging from 27 June to 3 July. All species began primary molt between 12 July and 18 July, near the expected fledging date of offspring, and therefore all species exhibited overlap between postfledging parental care and molt. The duration of primary molt ranged from 28 d for Canada Warblers to 69 d for Yellow‐rumped Warblers. Yellow Warblers, Yellow‐rumped Warblers, and American Redstarts began autumn migration having completed about 50% of their primary molt. However, Ovenbirds departed when 21% of molt was complete, and Canada Warblers departed 2 d after completing molt. For all five species of warblers, molt did not overlap with nest‐bound breeding activities. However, molt did overlap with both postfledging care and migration. This suggests that initiating migration as soon as possible is important, possibly because earlier arrival on the wintering grounds may improve access to high quality winter habitat. Overall, warblers may maximize individual fitness by combining life‐history events that result in overlapping portions of the breeding cycle, molt, and migration.     

Isotopic (δ2Hf) evidence of “loop migration” and use of the Gulf of Maine Flyway by both western and eastern breeding populations of Blackpoll Warblers

Declining numbers of Blackpoll Warblers (Setophaga striata) have been documented at long‐term migration monitoring sites as well as in breeding areas. However, the “loop migration” of Blackpoll Warblers makes it difficult to ascribe population change at migration monitoring sites to specific breeding populations. Individuals from all populations across the breeding range of Blackpoll Warblers concentrate in fall along the Atlantic coastline of eastern North America prior to initiating a transoceanic flight to wintering areas. In spring, Blackpoll Warblers return along a different route, moving north into the southeastern United States where birds from eastern and western breeding populations then diverge during migration to reach their respective breeding areas. To monitor breeding populations outside of breeding areas and identify factors potentially affecting those populations, we must be able to identify where birds captured during migration breed and map seasonal variation in population‐specific flyways. To “map” population‐specific migration movements of Blackpoll Warblers, we used feather deuterium (δ²H_f) values and a spatially explicit model to assign molt origins of 289 Blackpoll Warblers moving through sites in the Gulf of Maine (GOM) region and at three locations further west and south (northern Great Lakes area, Pennsylvania, and Florida). The assignment method was validated with feather samples from 35 birds captured during the breeding season at Churchill, Manitoba, Canada. As predicted, the spatial pattern of movement within and between seasons reflected “loop migration.” Blackpoll Warblers captured during fall migration in the GOM region included birds from across their breeding range, whereas birds captured during the spring were exclusively from northeastern populations. During fall migration, Blackpoll Warblers captured at two sites west of the GOM were from breeding areas further northwest than those from western Canada that were captured in the GOM. Blackpoll Warblers captured in eastern Florida during spring migration were assigned exclusively to breeding areas in the northeast, suggesting that eastern and western populations diverge soon after entering the United States. Finally, most Blackpoll Warblers sampled at Manomet Bird Observatory originated from breeding populations in Alaska and western Canada that have shown a similar (70–90%) decline over the same period. Our results, therefore, not only document the “loop migration” pattern of Blackpoll Warblers, but, by mapping patterns of connectivity between breeding and non‐breeding areas, may help target conservation efforts for breeding populations of Blackpoll Warblers where most needed.     

The functional significance of multiple nest-building in the Australian Reed Warbler Acrocephalus australis

The vast majority of bird species build a nest in which to breed. Some species build more than one nest, but the function of most multiple nest-building remains unclear. Here we describe the unusual nest-building behaviour of the Australian Reed Warbler Acrocephalus australis , and test experimentally the hypotheses that multiple nest-building is related to individual condition or territory quality, and plays a role in mate assessment. Australian Reed Warblers built two types of nest structures: 'type I' nests, which were used for eggs and nestlings, and 'type II' nests, which were structurally distinct from type I nests, did not support eggs, nestlings or adults and were not essential for successful breeding. The number of type II nests built in each territory varied. Type II nests were only built before breeding had commenced in a territory and females were not observed participating in their construction, supporting a role in female mate choice. Birds provided with supplementary food built significantly more type II nests than control birds. However, supplementary-fed birds did not have greater pairing success, and the addition of further type II nests to territories did not increase the pairing rate or type II nest construction in those territories. There was no relationship between the presence of type II nests and either reproductive success or likelihood of nest predation. We discuss the implications of these results in light of previous suggestions regarding the function of multiple nest-building in birds.     

Behavioural plasticity under a changing climate; how an experimental local climate affects the nest construction of the zebra finch Taeniopygia guttata

Successful reproduction in most avian species is dependent on the construction of a nest that provides protection and a suitable microclimate for the eggs and developing nestlings. Observational studies suggest that climatic variation may affect the structure of the nest, but to date there have been no attempts to experimentally determine the role that local climate plays in the construction of a suitable nest. Using a within‐individual counter balanced design we investigated how nest composition and construction differ in zebra finches breeding in ambient conditions of 18°C and 30°C. We found that at 18°C birds built nests that were over 20% heavier, and with significantly more thread and less grass than those built at 30°C. Our results highlight the degree of plasticity in nest building behaviour in relation to local ambient conditions. These results suggest that nest building behaviour is one route through which birds can respond to a changing climate and modify the microclimate of their nest in line with projected changes in ambient conditions.     

How avian nest site selection responds to predation risk: testing an 'adaptive peak hypothesis'

1. Nest predation limits avian fitness, so birds should favour nest sites that minimize predation risk. Nevertheless, preferred nest microhabitat features are often uncorrelated with apparent variation in predation rates. 2. This lack of congruence between theory-based expectation and empirical data may arise when birds already occupy 'adaptive peaks'. If birds nest exclusively in low-predation microhabitats, microhabitat and nest predation may no longer be correlated even though predation ultimately shaped microhabitat selection. 3. This 'adaptive peak hypothesis' was tested for a population of Yellow Warblers (Dendroica petechia) focusing on two nest microhabitat features: concealment and height. Experimental nests measured relative predation risk both within and outside the microhabitat range typically occupied by natural nests to examine whether nest site choices made by birds restricted our ability to detect microhabitat effects on predation. 4. Within the natural range (30-80% concealment, >75 cm height), microhabitat-predation relationships were weak and inconsistent, and similar for experimental and natural nests. Over an extended range, however, experimental predation rates were elevated in exposed sites (<30% concealed), indicating a concealment-related 'adaptive plateau'. 5. Clay egg bite data revealed a concealment effect on avian predators, and the abundance of one avian predator group correlated with nest concealment among years, suggesting these predators may cue birds to modulate nest concealment choices. 6. This study demonstrates how avian responses to predation pressure can obscure the adaptive significance of nest site selection, so predation influences may be more important than apparent from published data.     

Predators at bird nests in a northern hardwood forest in New Hampshire

ABSTRACT.   Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure.     

Evidence of selection for egg crypsis in conspicuous nests

ABSTRACT The value of egg coloration as crypsis, once accepted as a general principle, has recently been questioned because most experiments have failed to show that egg coloration deters predation. The nest‐crypsis hypothesis postulates that, among species that build conspicuous nests, selection for egg crypsis is relaxed or absent because visually searching predators detect nests prior to eggs. I tested the nest‐crypsis hypothesis using the large, relatively conspicuous nests of American Robins (Turdus migratorius), and eggs that differed markedly in color that were collected from the nests of Red‐winged Blackbirds (Agelaius phoeniceus), Brewer's Blackbirds (Euphagus cyanocephalus), and Yellow‐headed Blackbirds (Xanthocephalus xanthocephalus). Each nest (N= 22) received a clutch of each species during three sequential predation trials that were 16 d in duration. The order of clutch presentation was randomized for each nest. Survival trends for Brewer's and Yellow‐headed Blackbirds were similar, and higher than those for clutches of Red‐winged Blackbirds. By the end of trials, overall survival of the three clutch types was roughly equivalent. However, clutches of Red‐winged Blackbird eggs, the most conspicuous egg type to the human eye, were discovered sooner by predators. Because the experimental design controlled for effects of nest crypsis, nest location, and nest size, this difference in egg survival can be attributed to differences in egg pigmentation. Thus, my results support a role for egg coloration as camouflage in conspicuous nests.     

Evidence of Territoriality and Species Interactions from Spatial Point-Pattern Analyses of Subarctic-Nesting Geese

Quantifying spatial patterns of bird nests and nest fate provides insights into processes influencing a species’ distribution. At Cape Churchill, Manitoba, Canada, recent declines in breeding Eastern Prairie Population Canada geese (Branta canadensis interior) has coincided with increasing populations of nesting lesser snow geese (Chen caerulescens caerulescens) and Ross’s geese (Chen rossii). We conducted a spatial analysis of point patterns using Canada goose nest locations and nest fate, and lesser snow goose nest locations at two study areas in northern Manitoba with different densities and temporal durations of sympatric nesting Canada and lesser snow geese. Specifically, we assessed (1) whether Canada geese exhibited territoriality and at what scale and nest density; and (2) whether spatial patterns of Canada goose nest fate were associated with the density of nesting lesser snow geese as predicted by the protective-association hypothesis. Between 2001 and 2007, our data suggest that Canada geese were territorial at the scale of nearest neighbors, but were aggregated when considering overall density of conspecifics at slightly broader spatial scales. The spatial distribution of nest fates indicated that lesser snow goose nest proximity and density likely influence Canada goose nest fate. Our analyses of spatial point patterns suggested that continued changes in the distribution and abundance of breeding lesser snow geese on the Hudson Bay Lowlands may have impacts on the reproductive performance of Canada geese, and subsequently the spatial distribution of Canada goose nests.     

Issue Information

The population of Yellow‐naped Amazons (Amazona auropalliata) declined by an estimated 50% between 1980 and 2000, and the current population is estimated to be between 10,000 and 50,000. Poaching of young has been a persistent problem, but the species is also threatened by habitat loss and degradation. Because most aspects of their life history, behavior, and ecology have not been examined in wild populations, we studied Yellow‐naped Amazons with the following objectives: (1) identify the species of trees used for nesting, (2) determine the size and potential function of breeding territories, (3) determine nesting success, and (4) examine their duetting behavior. We located nests at 16 sites on the Pacific Slope of Costa Rica from 1999 to 2008. We searched for nests from January to May. Every nest was visited at least once and some nests were visited every 2–3 weeks throughout the breeding season. We also collected territory and duetting data at one site (Ahogados). The breeding season of Yellow‐naped Amazons was during the dry season (January–May). Yellow‐naped Amazons nested in 21 species of trees, but 68% of nests were located in only five species, and cavities in dead coyols (Acrocomia aculeata) were used most often. We found no association between breeding success and the species of tree in which birds nested. Mean territory size was 25,578 m², and these small areas generally consisted of several trees surrounding a nest tree. Pairs continued to duet throughout the breeding season, suggesting that duetting is important for territory defense. The nest failure rate in our study was 89%, and most nest failures (64%) were due to poaching for the pet trade. We recommend immediate population management and conservation actions, including increased law enforcement to reduce nest poaching, protection of key nesting areas, educational programs, and habitat conservation.     

The effect of investigators on the breeding success of royal,Eudyptes schlegeli,and rockhopper penguins,E. chrysocome,at Macquarie Island

The impact on reproductive success of investigators studying the breeding biology of royal and rockhopper penguins was assessed. Control and experimental transects were established in a colony of each species and the number of active nests, from egg laying to creche stage, were compared. Experimental nests were those used in breeding biology work, where birds were measured and banded, and nest checks were carried out at least once per week. Control nests were in equivalent locations but birds were not handled, and no contact was made with the nests once breeding had begun. There were no significant differences in the number of active nests between the control and experimental transects (and, therefore, breeding success) in either species. It is concluded that, provided care is taken when working with these species, no impacts on the short-term (up to creche stage, in one breeding season) breeding success of these populations will occur.     

Vegetation structure influences predation rates of early nests in subarctic breeding waders

Ground-nesting species are vulnerable to a wide range of predators and often experience very high levels of nest predation. Strategies to reduce nest vulnerability can include concealing nests in vegetation and/or nesting in locations in which nests and eggs are camouflaged and less easy for predators to locate. These strategies could have important implications for the distribution of ground-nesting species and the success rates of nests in areas with differing vegetation structure. However, the factors influencing the success of nest concealment and camouflage strategies in ground-nesting species are complex. Here we explore the effects of local vegetation structure and extent of nest concealment on nest predation rates in a range of ground-nesting, sympatric wader species with differing nest concealment strategies (open-nest species: Oystercatcher Haematopus ostralegus, Golden Plover Pluvialis apricaria and Whimbrel Numenius phaeopus; concealed-nest species: Black-tailed Godwit Limosa limosa, Redshank Tringa totanus and Snipe Gallinago gallinago) in south Iceland, in landscapes that comprise substantial variability in vegetation structure at a range of scales. We monitored 469 nests of these six wader species in 2015 and 2016 and ~40% of these nests were predated. Nest predation rates were similar for open-nest and concealed-nest species and did not vary with vegetation structure in the surrounding landscape, but nest-concealing species were ~10% more likely to have nests predated when they were poorly concealed, and the frequency of poorly concealed nests was higher in colder conditions at the start of the breeding season. For concealed-nest species, the reduced capacity to hide nests in colder conditions is likely to reflect low rates of vegetation growth in such conditions. The ongoing trend for warmer springs at subarctic latitudes could result in more rapid vegetation growth, with consequent increases in the success rates of early nests of concealed-nest species. Temperature-related effects on nest concealment from predators could thus be an important mechanism through which climate change affecting vegetation could have population-level impacts on breeding birds at higher latitudes.     

Nesting Success in Crimson Finches: Chance or Choice?

In avian systems, nest predation is one of the most significant influences on reproductive success. Selection for mechanisms and behaviours to minimise predation rates should be favoured. To avoid predation, breeding birds can often deter predators through active nest defence or by modifying behaviours around the nest (e.g. reducing feeding rates and vocalisations). Birds might also benefit from concealing nests or placing them in inaccessible locations. The relative importance of these strategies (behaviour vs. site selection) can be difficult to disentangle and may differ according to life history. Tropical birds are thought to experience higher rates of predation than temperate birds and invest less energy in nest defence. We monitored a population of crimson finches (Neochmia phaeton), in the Australian tropics, over two breeding seasons. We found no relationship between adult nest defence behaviour (towards a model reptile predator) and the likelihood of nest success. However, nest success was strongly related to the visibility of the nest and the structure of the vegetation. We found no evidence that adult nest building decisions were influenced by predation risk; individuals that re‐nested after a predation event did not build their nest in a more concealed location. Therefore, predator avoidance, and hence nest success, appears to be largely due to chance rather than due to the behaviour of the birds or their choice of nesting sites. To escape high predation pressures, multiple nesting attempts both within and between seasons may be necessary to increase reproductive success. Alternatively, birds may be limited in their nest‐site options; that is, high‐quality individuals dominate quality nest sites.     

Nesting biology of Eastern Yellow Wagtails at Cape Romanzof, Alaska

ABSTRACT.   The nesting biology of the Eastern Yellow Wagtail ( Motacilla tschutschensis ) was studied at Cape Romanzof, Alaska, an arctic tundra site on the Bering Sea coast near the northeastern limit of the breeding distribution of the Yellow Wagtail ( Motacilla flava/citreola/tschutschensis ) species complex. Ninety-four nests were located and monitored from 1996 to 1999. Females built nests in 5–7 d, and nests were located on the ground. The mean clutch size was 5.6 eggs, and the mean incubation period was 11 d. Both adults incubated, and some males had a partial brood patch. The mean duration of the nestling period was 11.6 d, and both parents brooded and fed the young. Some adults began the complete prebasic molt (including primaries) while their young were still in the nest. Nestling development was similar to that reported for other Yellow Wagtails ( sensu lato ), but the breeding cycle and breeding season of Eastern Yellow Wagtails was compressed relative to Western Yellow Wagtails in Europe and to other passerine species breeding in western Alaska. Some breeding events overlapped, including initiation of egg laying before completion of nest building and initiation of adult molt while young were still in the nest. Clutch sizes were larger than reported for most European relatives. Clutch size generally fit with models predicting an increase of about one egg per 19 degrees of increased latitude. Rapid nest initiation, overlap of breeding cycle events, nest attendance (including incubation) by males, and slightly larger clutches appear to be adaptations to high-latitude breeding in this long-distance migrant.     

Host range and dynamics of mycoplasmal conjunctivitis among birds in North America

An epidemic of conjunctivitis among house finches (Carpodacus mexicanus) caused by Mycoplasma gallisepticum (MG) bacterial infections was first described in 1994. The disease exhibits high primary host specificity, but has been isolated from a limited number of secondary avian hosts at various times and locations. We used records from the House Finch Disease Survey, a continent-wide, volunteer monitoring project, to document the host range of conjunctivitis in birds at feeding stations and to investigate how disease in house finches might influence the spread of conjunctivitis to other hosts. Between 1994 and 1998, participants recorded 675 cases of conjunctivitis in 31 species other than house finches in eastern North America. Seventy five % of these cases were observed among three species: American goldfinches (Carduelis tristis), purple finches (Carpodacus purpureus) and house sparrows (Passer domesticus). The proportion of sites with diseased wintering populations of the three species increased over the 4 yr study and coincided with range expansion of conjunctivitis in house finches. Sites with diseased house finches present were significantly more likely to report conjunctivitis in each of the three species during the same month. These observations are most consistent with transmission of an infectious agent (presumably MG) from house finches to these secondary hosts via spillover of localized epidemics, rather than sustained interspecific transmission.     

Macrogeographic variations in food choice of mainland citril finches Carduelis [citrinella] citrinella versus insular Corsican (citril) finches Carduelis [citrinella] corsicanus

We studied variations in diet composition in sub-populations of mainland citril finches Carduelis [citrinella] citrinella in European mountain chains, compared to closely related insular Corsican (citril) finches Carduelis [citrinella] corsicanus on several Mediterranean Islands with a special emphasis on key food plants used during the breeding period. We found that citril finch sub-populations of the Pre-Pyrenees and the Black Forest rely mostly on mountain pine and dandelion seeds as main food resources during the breeding season. In contrast, insular Corsican finches on the Mediterranean islands of Capraia and Corsica fed mainly on various herb species. Finches in Corsica fed predominantly on shepherd’s purse, while birds from Capraia were choosing rosemary as their main food plant during the breeding period. These observations confirmed the previously expected difference in food choice between the two forms due to the observed increased niche breadth on Corsica. However, Corsican finches on Sardinia showed a food choice more similar to that of the citril finch populations, in that they fed predominantly on black pine seeds during breeding season. Thus we were not able to find clear behavioural differences in diet composition between all studied sub-populations of citril and Corsican finches. To conclude, food choice of both forms is highly adaptive and, in the different breeding areas, distinct key plants may be of special importance during the breeding season. The preference for these plants is likely to be linked to their abundance and their energetic and nutritional content.     

Urban living influences the nesting success of Darwin’s finches in the Galápagos Islands

Urbanization is expanding worldwide with major consequences for organisms. Anthropogenic factors can reduce the fitness of animals but may have benefits, such as consistent human food availability. Understanding anthropogenic trade‐offs is critical in environments with variable levels of natural food availability, such as the Galápagos Islands, an area of rapid urbanization. For example, during dry years, the reproductive success of bird species, such as Darwin''s finches, is low because reduced precipitation impacts food availability. Urban areas provide supplemental human food to finches, which could improve their reproductive success during years with low natural food availability. However, urban finches might face trade‐offs, such as the incorporation of anthropogenic debris (e.g., string, plastic) into their nests, which may increase mortality. In our study, we determined the effect of urbanization on the nesting success of small ground finches (Geospiza fuliginosa; a species of Darwin''s finch) during a dry year on San Cristóbal Island. We quantified nest building, egg laying and hatching, and fledging in an urban and nonurban area and characterized the anthropogenic debris in nests. We also documented mortalities including nest trash‐related deaths and whether anthropogenic materials directly led to entanglement‐ or ingestion‐related nest mortalities. Overall, urban finches built more nests, laid more eggs, and produced more fledglings than nonurban finches. However, every nest in the urban area contained anthropogenic material, which resulted in 18% nestling mortality while nonurban nests had no anthropogenic debris. Our study showed that urban living has trade‐offs: urban birds have overall higher nesting success during a dry year than nonurban birds, but urban birds can suffer mortality from anthropogenic‐related nest‐materials. These results suggest that despite potential costs, finches benefit overall from urban living and urbanization may buffer the effects of limited resource availability in the Galápagos Islands.     

Factors affecting nesting success of a bird assembly in the central Monte Desert, Argentina

We estimated nesting success of a breeding bird assemblage in the central Monte Desert in four breeding seasons (1995–1999). We analyzed the effect of year, period within the breeding season, nest type, and nest location on daily survival rates (DSR). Averaged nesting success of passeriforms in natural habitats was very low (<20% on average, n=12 species). DSR tended to be lower during the egg-laying stage in Furnariidae, Rhinocryptidae, Mimidae, and Emberizidae. Tyrannidae had the highest DSR for all nesting stages and Emberizidae the lowest. Predation was the main cause of nest failure (>90% on average, n=12 species). DSR differed among years, being higher in the driest year (1995) and lower in the most humid year (1997). Nests initiated in the first half of the breeding season had higher DSR than those initiated in the second half. Closed nests had similar survival rates to open nests. DSR differed according to species of plant that supported the nest. Nest predation in the central Monte Desert may be an important selective pressure in birds' life history, which is in accordance with other results for South American temperate birds.     

Lifespan Analyses of Forest Raptor Nests: Patterns of Creation,Persistence and Reuse

Structural elements for breeding such as nests are key resources for the conservation of bird populations. This is especially true when structural elements require a specific and restricted habitat, or if the construction of nests is costly in time and energy. The availability of nesting-platforms is influenced by nest creation and persistence. In a Mediterranean forest in southeastern Spain, nesting-platforms are the only structural element for three forest-dwelling raptor species: booted eagle Aquila pennata, common buzzard Buteo buteo and northern goshawk Accipiter gentilis. From 1998 to 2013, we tracked the fate of 157 nesting-platforms built and reused by these species with the aim of determining the rates of creation and destruction of nesting-platforms, estimating nest persistence by applying two survival analyses, describing the pattern of nest reuse and testing the effects of nest use on breeding success. Nest creation and destruction rates were low (0.14 and 0.05, respectively). Using Kaplan Meier survival estimates and Cox proportional-hazards regression models we found that median nest longevity was 12 years and that this was not significantly affected by nest characteristics, nest-tree dimensions, nest-builder species, or frequency of use of the platform. We also estimated a transition matrix, considering the different stages of nest occupation (vacant or occupied by one of the focal species), to obtain the fundamental matrix and the average life expectancies of nests, which varied from 17.9 to 19.7 years. Eighty six percent of nests were used in at least one breeding attempt, 67.5% were reused and 17.8% were successively occupied by at least two of the study species. The frequency of nest use had no significant effects on the breeding success of any species. We conclude that nesting-platforms constitute an important resource for forest raptors and that their longevity is sufficiently high to allow their reuse in multiple breeding attempts.     

Testing hypotheses about the function of repeated nest abandonment as a life history strategy in a passerine bird

Nest structures are essential for successful reproduction in most bird species. Nest construction costs time and energy, and most bird species typically build one nest per breeding attempt. Some species, however, build more than one nest, and the reason for this behaviour is often unclear. In the Grey Fantail Rhipidura albiscapa, nest abandonment before egg‐laying is very common. Fantails will build up to seven nests within a breeding season, and pairs abandon up to 71% of their nests before egg‐laying. We describe multiple nest‐building behaviour in the Grey Fantail and test four hypotheses explaining nest abandonment in this species: cryptic depredation, destruction of nests during storm events, and two anti‐predatory responses (construction of decoy nests to confuse predators, and increasing concealment to ‘hide’ nests more effectively). We found support for only one hypothesis – that abandonment is related to nest concealment. Abandoned nests were significantly less concealed than nests that received eggs. Most abandoned nests were not completely built and none received eggs, thus ruling out cryptic predation. Nests were not more likely to be abandoned following storm events. The decoy nest hypothesis was refuted as abandoned nests were constructed at any point during the breeding season and some nests were dismantled and the material used to build the subsequent nest. Thus, Grey Fantails are flexible about nest‐site locations during the nest‐building phase and readily abandon nest locations if they are found to have deficient security.