BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART III: THE POST-NESTLING DEPENDENCE PERIOD

Brown, C. J. 1990. Breeding biology of the Bearded Vulture in southern Africa, Part III: The post-nestling dependence period. Ostrich 6l: 43–49.

The post-nestling dependence period of the Bearded Vulture Gypaetus barbatus in southern Africa begins with the first flight of the young bird at 126 ± 2 days after latching (November-January) and ends during the pre-laying nod or the parent birds' next breeding attempt (April-June), a nod of about five months. For the first two weeks after first flit young bid remaine6 within about 200m of the nest, moving up to 800 m by the third week. By a month out of the nest young birds spent about 40% of the day in flight, moved up to 3 km from the nest, began bone-dropping and interacting with young birds from neighbouring nests. At six weeks they began to accompany their parents for part of some of their foraging trips, but returned to the nest alone, and by eight weeks they completed foraging forays with parents Pasting up to 3 h. At 2–3 months out of the nest young birds covered an area of about 42 km², excluding the foraging trips with parents, by 3–4 months, 78km² and 4–6 months, 168 km². Parent birds delivered food for at least five months after the young bird's first flight. Young birds left their natal areas of their own accord, usually during the first month of their parents' next breeding attempt.     

THE SOCIABLE WEAVER,PART 2: NEST ARCHITECTURE AND SOCIAL ORGANIZATION

Maclean, G. L. 1973. The Sociable Weaver, Part 2: Nest architecture and social organization. Ostrich 44:191-218.

Sociable Weavers build nest masses in a number of indigenous tree species (especially on Acacia giraffae branches) and on artificial nest sites like telephone poles. They never build in exotic trees. Nest masses are built of grass straws and roofed over with a superstructure of coarser material such as thorn twigs. The grass substructure contains the nest chambers which do not interconnect. The substructure may be divisible into two or more levels, each forming a social unit comprising the birds inhabiting it.

Each social level of birds is confined to its own structural level at all times, but a bird may roost in any chamber within its own level. The superstructure is not divisible into social units and any bird may build or perch on any part of the superstructure. Movements of birds from one colony to another are rare. The colony at one nest mass leaves the nest at about sunrise in summer, a little later in winter, and flies to the feeding grounds; the birds return to the nest mass for a siesta lasting from about 10:00 hours to 14:00 hours in hot weather, less than this in cool weather. They depart again for their feeding grounds until about sunset.

The internal temperature and RH of the nest chambers were not found to be significantly different from ambient temperature and RH when ambient temperatures were > 21,7°C. At ambient temperatures < 26,7°C the RH of the nest chambers was significantly lower than ambient Rh, but temperatures were not significantly different during the day.     

Satellite tracking of a White Stork from Italy to Morocco

Two young White Storks were tracked by satellite during a part of their first migratory journey from the nest colony (settled in Piedmont, NW Italy) to the wintering ground in Western Africa. Both birds left westward, but only one of the two birds provided reliable data which allowed the reconstruction of its migratory route along the coasts of France and Spain up to Morocco. A new aspect of the journey is that the bird did not pass from Europe to Africa at Gibraltar, the storks' known western route. Despite the storks' tendency to avoid flying over large stretches of sea, the tracked bird crossed the Alboran sea from De Gata Cape (Spain) to Tres Forcas Cape (Morocco), thus flying about 120 km over the open sea.     

SOCIAL ORGANIZATION AND NEST-BUILDING IN THE FOREST WEAVER BIRDS OF THE GENUS MALIMBUS (PLOCEINAE)

A comparative study was made of social organization during breeding among the genus Malimbus. In M. nitens, the male chooses the nest site, builds the nest alone, guards the nest during incubation, and feeds the young; the female incubates, broods alone and with the male feeds the young. In M. malimbicus, the male chooses the nest site, builds the nest with the female and guards the nest; the female builds the nest with the male, but incubates alone. In M. racheliae and M. cassini, the nest is built by one female and a multi-male party of two or three. One male drives off the other males when the nest is completed. One male and one female incubate alternately. The female seems to be the leader of the building group, and works like a male. In M. coronatus, the nest is built by a mixed party of males and females (3–6 birds), all working together without any overt leadership. Only one male and one female however, incubate, brood and feed the young. In their morphology and behaviour, Malimbus spp. are close to the weaver birds of the genus Ploceus. M. nitens seems the least evolved species while M. cassini and M. coronatus are behaviourally the most evolved. In the last species, which has a very elaborate nest, the pair of breeding birds is helped by one to four other birds. These helpers are birds in full adult plumage, and are probably capable of breeding and may do so at another period in the long breeding season of at least six months.     

Migration, wintering and breeding of a lesser spotted eagle ( Aquila pomarina) from Slovakia tracked by satellite

In northern Slovakia an adult male Lesser Spotted Eagle (Aquila pomarina) occupied the same nest site for 11 years running (1992–2002), where it was ringed and fitted with two satellite transmitters. In six of these years it successfully reared a young. In 1994 and 2000–2002 its behaviour during migration could be followed in detail by means of satellite telemetry. The eagle took the known route for this species to South Africa. In 2001, it spent 43% of the year at its breeding site, 33% in its winter quarters, the remaining 24% being spent on migration. In three cases the autumn migration took 40, 48 and 61 days respectively. In two cases the spring migration took 49 days. All five recorded autumn and spring migrations averaged a daily flight distance of 178 km. In spring the daily flight distance was in general slightly greater than in autumn. The longest was recorded from 30 March to 2 April 2001, between Uganda and the Red Sea, during which the bird covered a total of 1,650 km, averaging 412 km per day. In 2001, the spring migration from the wintering grounds was 2 weeks later than in 2002. The wintering grounds, where in 2 years the bird spent around 3.5 months, covering at least 1,666 and 2,269 km, respectively, comprised a large part of Zimbabwe together with the Kruger National Park in South Africa and neighbouring parts of Mozambique. The annual journeys flown, including movements around the wintering grounds, amounted in 2000-2001 to at least 20,396 km and in 2001-2002 to 19,041 km. Except during its crossing of the Sahara, the eagle must have taken food on nearly all its days of migration.     

Modelling the energy budget of a colonial bird of prey, the Ruppell's griffon vulture, and consequences for its breeding ecology

Colonial nesting is rare in birds of prey. In this study we develop further Pennycuick's (1979 ) model of energy balance to consider the implications of colonial nesting for the breeding ecology of Ruppell's griffon vultures. To achieve a realistic foraging range, and remain in energy balance, the birds need to do more than fill their crop once on each foraging trip. They must remain in the feeding area and digest some of this food and refill the crop to obtain sufficient energy to pay for the flight costs and have sufficient energy to satisfy their own requirements and that of the chick. Given the known distances that the birds have to travel to forage, it would be impossible for them to rear more than one chick. The low growth rate of griffon vulture chicks may be an adaptation to the low rate at which energy can be delivered by the parents. The optimal time for a bird to be away from the nest changes with the distance they have to travel. Assuming that one parent remains on the nest at all times to guard the chick, it is optimal for both parents to take turns to forage on the same day if the distance to a feeding area is under 150 km, but to switch to each parent being away for a whole day when the distance is greater than this. Soaring flight is essential for such a scavenger, because of the low energy expenditure. If a vulture relied on the more energetically demanding flapping flight its maximum foraging range would be under 40 km. Griffon vultures are known to be able to depress their basal metabolic rate, and this has major implications for their foraging range, which then becomes constrained by the flight speed rather than by the amount of food they need to obtain. Griffon vultures minimize energy expenditure on all activities, because even small increases in their energy demands have a large impact on the foraging range that the bird can use.     

Population dynamics of the bearded vulture Gypaetus barbatus in southern Africa

The essential features of mortality and survivorship of bearded vultures Gypaetus barbatus in southern Africa were deduced from age class plumage characteristics. The population consisted of about 204 adult pairs within a breeding range of about 35,000 sq km. Pairs bred every year and produced, on average, about 0·9 young per pair per year. Young birds made up about 37% of the population, subadults 3·5% and adults 60%. About 182 fledged young were recruited to the population each year. The proportion of young birds in the population in different areas was inversely related to the breeding density of adult birds (range 24–47%). Young bird mortality over the four years to subadult age was 87%, the survival rate of adults was 94% and the mean lifespan of birds surviving to adulthood was 21·4 years. This study demonstrates the need to understand the relationship between adult breeding density and young bird numbers in different parts of their range to accurately deduce population dynamics characteristics.     

Evolution of reversed sexual size dimorphism and role partitioning among predatory birds, with a size scaling of flight performance

To explain the adaptive significance of sex role partitioning and reversed sexual size dimorphism among raptors, owls and skuas, where females are usually larger than males, we combine several previous hypotheses with some new ideas. Owing to their structural and behavioural adaptations for prey capture, predatory birds have better prospects than other birds of defending their offspring against nest predators. This makes sex role partitioning advantageous; one parent guards the offspring while the other forages for the family. Further, among predators hunting alert prey such as vertebrates, two mates because of interference may not procur much more food than would one mate hunting alone. By contrast, two mates feeding on less alert prey may together obtain almost twice as much food as one mate hunting alone. For these reasons, partitioning of breeding labours might be adaptive only in predatory birds. An initial imbalance favours female nest guarding and male foraging: the developing eggs might be damaged if the female attacks prey; their mass might reduce her flight performance; she must visit the nest to lay; and the male feeds her before she lays (‘courtship feeding’). Increased female body size should enhance egg production, incubation, ability to tear apart prey for the young, and, in particular, offspring protection in predatory birds. Efficient foraging during the breeding period then becomes most important for the male. This imposes great demands on aerial agility in males, particularly among predators of agile prey. Flight performance decreases with increasing size in five of six aspects explored. The male must therefore not be too large in relation to the most important prey. For these reasons, he should be smaller than the female. Among predatory birds, size dimorphism increases with the proportion of birds in the diet, which may be explained as follows. Adult birds have mainly one type of predators: other predatory birds. Because almost only these specialists exploit adult birds, they carry out most of the cropping of this prey. A predator of easier prey competes with many other kinds of predators, which considerably reduce prey abundance in its territory. This is not so for predators of adult birds. Further, because birds are extremely agile, the specialized predator can hunt efficiently only within a limited size range of birds, whose flight skill it can match. Increased size dimorphism among these predators therefore should be particularly important for enlarging the combined food base of the pair. A bird specialist may consume much of the available prey in the suitable size range during the breeding period. When the predator's young are large enough to defend themselves, the female aids better by hunting than by guarding the chicks. It is advantageous among bird specialists if she hunts prey of other sizes than does the male, who has by then reduced prey abundance in his prey size class. But among predatory birds hunting easier prey the female gains little by hunting outside the male's prey spectrum, because other kinds of predators will have reduced the prey abundance outside as well as inside the male's preferred size range. Intra-pair food separation through large sexual size dimorphism therefore should be particularly advantageous among predators of birds. This may be the main reason why the degree of size dimorphism increases with the dietary proportion of birds.     

Nesting success and within-season breeding dispersal in the Orange-breasted Sunbird Anthobaphes violacea

Nest predation is a primary cause of nesting mortality for many bird species, particularly passerines. Nest location can affect predation, and it has also been demonstrated that predation risk can alter nest site selection. Birds can limit predation risk by selecting specific habitat characteristics; by changing nest site characteristics between attempts; and by dispersing between nesting events. Here we report breeding data from a population of Orange-breasted Sunbirds Anthobaphes violacea (L.), for a single breeding season in the Jonkershoek Nature Reserve, South Africa. Neither shrub type nor nest height was found to affect the outcome of a nest. For subsequent breeding attempts, birds were not more likely to change the type of shrub in which they nested after a predation event than when the attempt was successful, nor did they change the height of their nest. However, we found that the distance between a nest and the subsequent one was significantly shorter after a successful nest than after an unsuccessful one. We interpret this as an adaptive strategy to avoid predation.     

NESTING OF THE PURPLE-THROATED CARIB HUMMINGBIRD

We present data on certain parts of the nesting biology of the Purple-throated Carib Humming- bird Eulampis jugularis on the island of Dominica, British West Indies. We watched two nests with eggs and young and a single nest under construction. Incubation was in short periods averaging about six minutes. Females at both nests with eggs continued adding material to the nest until the end of incubation. We suggest that this common practice among hummingbirds may insure that a limited amount of energy at the time of initial nest-building and egg-production is optimally apportioned between the two activities. Brooding ceased in one nest when the young were about 13 days old. Feeding rates stayed relatively constant at one to two per hour throughout the nearly complete nestling period in one nest. Average time per feeding declined, apparently as the female-young interaction became more efficient with maturation of the young. Nesting females foraged on both insects and nectar. We could not be sure what they were feeding the young. Defence of the nest varied with the position of the female and the type of intruder. The aggressive behaviour associated with defence varied according to the size and type of intruder. We concluded that for the one nest of Eulampis for which we had the most complete data, had there been three young, the female would have been unable to provide sufficient food to nourish them. However, the universal clutch size of two and nearly universal promiscuity in humming- birds is strong evidence that factors other than the ability of adults to feed more than two young are important in determining clutch size.     

Nest boxes for Cape Parrots Poicephalus robustus in the Hogsback area,Eastern Cape,South Africa

Breeding propensity of tree-cavity nesting bird species are often limited by a shortage of natural nesting sites. Artificial nests can be used to provide alternative nest sites. Cape Parrots Poicephalus robustus are nationally endangered and nest in existing tree-cavities in high-altitude fragmented Afromontane forests in South Africa, assumed to be in short supply due to historic and current logging practices. To increase nest site availability, 179 wooden bird boxes and 28 bee boxes (to ‘pull’ bees) were erected during 2011–2012 in Hogsback, Eastern Cape. In 2016, no bird boxes were occupied by Cape Parrots. A total of 43% were used by other species, 51% were unused and 6% could not be inspected due to tree instability and inaccessibility. Two bird boxes were inspected by two pairs of Cape Parrots, but were never occupied. Occupancy of boxes by birds was not associated with nest, tree or habitat characteristics. However, occupancy of boxes by bees was associated with habitat type and tree species. Future conservation efforts will include locating natural Cape Parrot nesting sites and reforestation efforts to ensure the long-term availability of natural nesting sites.     

Foraging behaviour and time allocation of chick-rearing Razorbills Alca torda at Græsholmen, central Baltic Sea

A new type of bird-borne data logger, which stores data from flight and depth sensors at pre-set intervals, was used to investigate the foraging pattern and diving behaviour of chick-rearing Razorbills Alca torda breeding on the islet of Græsholmen (central Baltic Sea, Denmark). The instruments recorded all relevant events in the 35 foraging trips accomplished by six different individual birds; a seventh bird, equipped with a direction recorder, provided information on directional preferences exhibited on seven different trips. A foraging trip usually consisted of a number of flights interrupted by a small number of dives probably performed to explore the site for prey availability. True foraging occurred during the last stops in the outbound trip, after which the bird returned to the nest with a single flight or a sequence of a few flights. The duration of nocturnal trips was significantly longer than diurnal trips, possibly due to a preference for the familiar marine environment shown by birds when they are not 'on duty' in the nest. The majority of dives consisted of V-shaped dives in which birds descend to a maximum depth and then start ascending. A clear diurnal variation of the dive depth, which never exceeded 43 m, was recorded. Our results show that the new types of recording devices can be used to answer basic questions about the foraging strategies of marine birds.     

The white-backed woodpecker: umbrella species for forest conservation planning?

In northern Europe, a long history of land use has led to profound changes within forest ecosystems. The white-backed woodpecker (Dendrocopos leucotos) is one of several specialised forest species whose populations have declined. Conservation management directed at this species’ habitat has made it a de facto umbrella species for conservation of the biodiversity associated with forests rich in deciduous trees and dead wood. We assessed empirically the value of the white-backed woodpecker as an indicator and umbrella species in central Sweden. Occurrence of the woodpecker in breeding bird atlas squares (5 × 5 km²) indicated high species richness of forest birds, particularly species of special conservation concern, which included on average 13% more species in squares with than without the woodpecker. The number of red-listed cryptogam species expected to benefit from conservation actions directed at white-backed woodpecker habitats was higher in squares where the woodpecker bred compared to where is was absent. However, no such pattern was found for red-listed beetles, a group with very few records in the studied squares. White-backed woodpecker occurrence was positively associated with the current area of deciduous and mixed forest of high conservation value. Considering its indicator value, its specialised habitat requirements and its potential as a communication tool, using the white-backed woodpecker as an umbrella species may provide a coarse filter for the conservation of several other deciduous forest species. However, focusing solely on white-backed woodpecker habitat may not provide for the conservation of all such species, which stresses the need for a suite of complementary planning approaches.     

The distribution and biology of nomadic birds in the Karoo, South Africa

Dryland nomadic bird species, as a proportion of all bird species in a biome in southern Africa, are highest in the arid grassland and arid and semi-arid Karoo in South Africa. Nomadic birds, of which the most widespread species is the greybacked finchlark Eremopterix verticalis (Smith), are most frequently observed in the north-central and north western Nama Karoo. The species richness of nomadic species is inversely correlated with species richness of all bird species in the Karoo. Since the distribution of nomadic birds is in areas where rainfall is patchy, low (<250 mm per year) and aseasonal, this supports the idea that fewer species are able to cope with resources that are patchy in time and space, and that there has been selection for nomadism in the species that are able to use patchy environments. Species richness and abundance of nomadic birds is negatively correlated with rainfall amount but positively correlated with the coefficient of variation of the rainfall and with rainfall in autumn. The frequency of nomadic birds is inversely correlated with altitude range; nomadic species are most often recorded in structurally simple habitats (shrubland and grassland) on open plains. Most nomadic bird species in the Karoo are granivorous. Perennial desert grasses are important components of the habitat and diet of small nomadic granivores, and also provide nest sites and nest material. Nomadic birds can breed throughout the year, without a clearly defined ‘season’ in both the Succulent and Nama Karoo. Average clutch sizes do not differ significantly between resident and all nomadic species in the arid and semi-arid Karoo. Nomadism is an evolutionary stable strategy for individual species only when extremes in environmental conditions are frequent enough, and unpredictable enough, to maintain movements to high resource patches or to maintain dispersal away from low resource patches. If high rainfall years are too regular or infrequent, or peaks in fluctuations of resources in the environment too low, or rainfall patches are randomly distributed, nomadism would not be maintained as part of the individual behaviour pattern.     

Nest-mediated seed dispersal

Many plant seeds travel on the wind and through animal ingestion or adhesion; however, an overlooked dispersal mode may lurk within those dispersal modes. Viable seeds may remain attached or embedded within materials birds gather for nest building. Our objective was to determine if birds inadvertently transport seeds when they forage for plant materials to build, insulate, and line nests. We also hypothesized that nest-mediated dispersal might be particularly useful for plants that use mating systems with self-fertilized seeds embedded in their stems. We gathered bird nests in temperate forests and fields in eastern North America and germinated the plant material. We also employed experimental nest boxes and performed nest dissections to rule out airborne and fecal contamination. We found that birds collect plant stem material and mud for nest construction and inadvertently transport the seeds contained within. Experimental nest boxes indicated that bird nests were not passive recipients of seeds (e.g., carried on wind), but arrived in the materials used to construct nests. We germinated 144 plant species from the nests of 23 bird species. A large proportion of the nest germinants were graminoids containing self-fertilized seeds inside stems—suggesting that nest dispersal may be an adaptive benefit of closed mating systems. Avian nest building appears as a dispersal pathway for hundreds of plant species, including many non-native species, at distances of at least 100–200 m. We propose a new plant dispersal guild to describe this phenomenon, caliochory (calio = Greek for nest).     

Incubation rhythm in the great snipe Gallinago media

The incubation rhythm of four female great snipe was monitored with telemetric equipment. The mean daily incubation constancy was 90.3 ± 2.0 (SD) per cent, and the mean daily time off the nest amounted to 139.8 ± 28.8 min. The number of recesses per day averaged 8.7 ± 1.9, with a mean duration of 15.7 ± 6.1 min. Generally, the birds incubated for long bouts during the night, and left the nest frequently during the daylight hours.
Recesses were concentrated in the warmest part of the day in cool periods, but were more evenly distributed throughout the day in warmer periods. Recess duration decreased with decreasing temperature. These adjustments minimize egg cooling when the bird is off the nest, and thus allow the incubating bird more time to feed without lowering the mean egg temperature.
Calculations of the cooling rates of eggs indicate that the bird minimizes incubation energy expenditure as far as possible, but without letting the eggs cool beyond the temperature of no embryonic development.     

Nest site competition between cavity nesting passerines and golden paper wasps Polistes fuscatus

Nest boxes provide sheltered nesting sites for both passerines and paper wasps. Although neither wasps nor birds appear to evict the other once one is fully established, it is unclear which is the dominant competitor at the onset of the breeding season. Using wire mesh, we excluded birds but not golden paper wasps Polistesfuscatus from alternating boxes along a transect through edge habitat in North Carolina from 2006 – 2008. If wasps dominate Carolina chickadees Poecile carolinensis and eastern bluebirds Sialia sialis during the early spring (all have similar nest initiation dates), we would expect wasps to settle in both box types at equal frequencies. However, if birds dominate wasps, we would expect wasp nests to be concentrated in “bird‐proof” boxes. We found wasps in bird‐proof boxes significantly more often than in bird‐accessible boxes, indicating that secondary‐cavity nesting birds are able to exclude wasps from available nest sites. Additionally, we found that during the period of nest initiation, birds usurp wasps more often than vice versa.     

BREEDING PERFORMANCE OF PUFFINS FRATERCULA ARCTICA IN RELATION TO NEST DENSITY, LAYING DATE AND YEAR

The paper presents data on the breeding and predation of Puffins in two areas of different nest density within a single colony on Dun, St Kilda group, Outer Hebrides in 1973-78.
Within a season birds laying early had a slightly higher nesting success than birds laying late, but laying date had little influence on the peak and fledging weights of young. The main disadvantage in late laying was a reduced chance of relaying if the first egg was lost.
Breeding success and chick weights varied from year to year. The 1974 season was the least successful with the lowest nesting success, lowest frequency of feeds, lowest calorific value of feeds, lightest chicks and slowest growth. Overall breeding performance was not related to the annual mean laying dates.
In all years pairs nesting in the area of high nest density did better than pairs nesting at low density. The effect is attributed to differential predation and disturbance by predatory gulls. At least 4.2% of adult Puffins breeding in the area of low burrow density were killed by gulls each breeding season; this is higher than the total annual mortality found in three other studies. Only 0.9% of adults from the high density area were found killed. The subpopulation in the low density area cannot survive without much immigration, yet there is no evidence that this happens.     

The influence of weather on the flight altitude of nocturnal migrants in mid‐latitudes

By altering its flight altitude, a bird can change the atmospheric conditions it experiences during migration. Although many factors may influence a bird's choice of altitude, wind is generally accepted as being the most influential. However, the influence of wind is not clearly understood, particularly outside the trade‐wind zone, and other factors may play a role. We used operational weather radar to measure the flight altitudes of nocturnally migrating birds during spring and autumn in the Netherlands. We first assessed whether the nocturnal altitudinal distribution of proportional bird density could be explained by the vertical distribution of wind support using three different methods. We then used generalized additive models to assess which atmospheric variables, in addition to altitude, best explained variability in proportional bird density per altitudinal layer each night. Migrants generally remained at low altitudes, and flight altitude explained 52 and 73% of the observed variability in proportional bird density in spring and autumn, respectively. Overall, there were weak correlations between altitudinal distributions of wind support and proportional bird density. Improving tailwind support with height increased the probability of birds climbing to higher altitude, but when birds did fly higher than normal, they generally concentrated around the lowest altitude with acceptable wind conditions. The generalized additive model analysis also indicated an influence of temperature on flight altitudes, suggesting that birds avoided colder layers. These findings suggested that birds increased flight altitudes to seek out more supportive winds when wind conditions near the surface were prohibitive. Thus, birds did not select flight altitudes only to optimize wind support. Rather, they preferred to fly at low altitudes unless wind conditions there were unsupportive of migration. Overall, flight altitudes of birds in relation to environmental conditions appear to reflect a balance between different adaptive pressures.     

Changes in timing, duration, and symmetry of molt of Hawaiian forest birds

Food limitation greatly affects bird breeding performance, but the effect of nutritive stress on molt has barely been investigated outside of laboratory settings. Here we show changes in molting patterns for an entire native Hawaiian bird community at 1650-1900 m elevation on the Island of Hawaii between 1989-1999 and 2000-2006, associated with severe food limitation throughout the year beginning in 2000. Young birds and adults of all species took longer to complete their molt, including months never or rarely used during the 1989-1999 decade. These included the cold winter months and even the early months of the following breeding season. In addition, more adults of most species initiated their molt one to two months earlier, during the breeding season. Suspended molt, indicated by birds temporarily not molting primary flight feathers during the months of peak primary molt, increased in prevalence. Food limitation reached the point where individuals of all species had asymmetric molt, with different primary flight feathers molted on each wing. These multiple changes in molt, unprecedented in birds, had survival consequences. Adult birds captured during January to March, 2000-2004, had lower survival in four of five species with little effect of extended molt. Extended molt may be adaptive for a nutrient stressed bird to survive warm temperatures but not cool winter temperatures that may obliterate the energy savings. The changing molt of Hawaiian birds has many implications for conservation and for understanding life history aspects of molt of tropical birds.