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1.
Ian C. T.  Nisbet Lord  Medway 《Ibis》1972,114(4):451-494
A population of 400–600 Acrocephalus orientalis wintering in a Phragmites habitat at 3°N in West Malaysia was studied during four northern hemisphere winters, by means of systematic mist-netting. Data from other study-areas, other habitats and other winters are also used. Intensive mist-netting appears to have made birds move over longer distances than they did in the absence of disturbance, and to have led to the emigration of marked birds from the study-area. Trapping also affected feeding behaviour, resulting in weight-loss; repeated trapping may have increased mortality. Males and females could be separated by means of wing-length in fresh plumage. Females were largely confined to Phragmites; males were more numerous on the edge of reed-beds and in scrub vegetation. Males suffered greater feather-wear than females. As measured by the trapping rate, birds were uniformly distributed throughout the Phragmites habitat, at the same density in different winters. Undisturbed birds used a “home-range” of 1–4 ha, overlapping with 15–50 other individuals. Disturbed birds overlapped with 100–200 others. Individual birds returned to exactly the same “home-range” in successive winters. After correcting for the effects of disturbance and incomplete sampling, the proportion of adults ringed in one winter which returned in the next is estimated as 65% in each of two study-areas. This is a minimum estimate of the annual survival rate for adults. Mean total body-weights were at a minimum in midwinter (November-February). Fat-free weights were also lower in midwinter than in autumn and spring. Body-moult was observed in March and April. Moult of the flight-feathers takes place between July and September, on the breeding grounds or slightly to the south. Females departed on spring migration between 10 and 25 May; males some 11–14 days earlier. Adults arrived in autumn between 8 September and 7 October; males and females often came in in separate “waves”. Females were absent for only about 127 days, about the minimum required for migration, breeding and moult. Dates of migration match those of the more northern breeding populations. Spring departure is later than dates of passage recorded in south China; hence birds of this population appear to make long nights. On average, birds departing in spring carried about 9 g of fat, roughly 40% of total fat-free body-weight. This is about half the energy reserve required for the entire journey. Dates of passage in central China are consistent with a hypothesis that they make the journey (4,500-5,000 km) in two “hops”. A few birds which remained light until very late in the spring showed a significantly lower return rate in the next year. Most birds arriving in autumn appear to have carried 1–2 g of fat, but some were at or below the normal fat-free weight. Many birds appear to have lost weight soon after arrival. Returning ringed adults were amongst the very first birds trapped in September. Individual birds appear to have migrated on very similar dates in different years: many of the dates of trapping differed by 2 days or less in successive years. Trapping rates reached a peak in early October and then declined rapidly, reaching the midwinter level by 21 October. The decline coincided with the differential disappearance of juvenile birds. However, birds collected at this time had adequate fat reserves, and the disappearance appears to have preceded the period of food-shortage. It is suggested that the loss of juvenile birds resulted from behavioural interactions favouring the more dominant individuals, as has been described for several temperate zone residents. The first few weeks in the wintering area may thus be the critical period of mortality during the year. Because birds from different breeding areas are expected to be mixed in the winter-quarters, and vice versa, local mortality factors in winter may affect a number of breeding populations. High adult survival rates have been recorded in several other birds which breed in the temperate zones and winter in the tropics. In general their breeding success appears to be high, so the first-year mortality must be high. The closely related A. arundinaceus, which winters in Africa, differs from A. orientalis in size, wing-shape, timing of spring migration and timing of moult. These differences can be interpreted as adaptations to different environmental (primarily climatic) factors experienced during migration and on the breeding grounds. The segregation of males and females into different habitats probably reduces inter-sexual competition in winter, but this is not necessarily its primary function. Males collected in the evening in Phragmites had smaller fat reserves than females, suggesting that the females are better adapted to this habitat. The large size of the males is probably maintained in part by sexual selection in the breeding season. On the other hand, the size of females and their habitat is probably limited by the specialisation of their nest. These factors would suffice to explain the sexual dimorphism in size and habitat.  相似文献   

2.
We studied the effect of winter rank on survival rate and reproductive success in Willow Tits Parus montanus, a resident passerine living in dominance-structured flocks during the nonbreeding season, in 6 years. Winter survival was dependent on both the birds' age and rank. Adults survived better than first-year birds, and within first-year males, dominants survived better than subordinates. In other sex and age classes, rank did not contribute to survival. Although first-year males were in excess among nonbreeders, no connection existed between breeding status and rank. Female rank did not explain the variation in the start of laying, clutch size, number of fledglings or recruit production. We conclude that social status in Willow Tits affects individual fitness mainly through rank-dependent survival. Acquiring a high rank position seems to be most important for first-year birds, especially first-year males.  相似文献   

3.
Long-distance migrants have evolved complex strategies for the timing of their annual moult, fattening and migration cycles. These strategies are likely to vary at different stages of a bird's life. Ringing data on 6079 Grey Plovers Pluvialis squatarola , caught on the Wash, England, between 1959 and 1996, were analysed to relate migratory strategies to patterns of primary moult and body mass changes. Adults returning from breeding grounds had a shorter and delayed primary moult (duration 90 days, starting date 19 August) in comparison with over-summering birds (duration 109 days, starting date 5 June). Three categories of migrant adults were identified on the basis of primary moult and body mass: (1) birds which did not moult, but increased body mass and migrated further south; (2) birds which moulted 1–3 inner primaries, suspended moult, increased body mass and migrated; and (3) birds which completed or suspended moult and wintered locally. In birds of the second category, timing of primary moult and body mass increase overlapped. Among wintering birds, 38% were in suspended moult. Ninety-six per cent of birds that suspended moult at the beginning of winter were males and almost all completed moult in spring. Grey Plovers which left Britain in autumn had an average body mass of 280 g, enough to reach southern Morocco without refuelling. Both wintering adults and first-year birds showed a prewinter body mass increase, peaking in December. Adults had a synchronized premigratory body mass increase in May, which suggested a negligible presence of African migrants. The average departure mass for spring migration, estimated at 316 g, would allow birds to fly non-stop to the Siberian breeding grounds in western Taymyr.  相似文献   

4.
Brown, C. J. 1989. Plumages and measurements of the Bearded Vulture in southern Africa. Ostrich 60: 165–171.

Four different age classes of the southern African Bearded Vulture Gypaetus barbatus are recognized and their plumages described: juvenile (3–24 months old), immature (24–45 months), subadult (45–60 months) and adult (60+ months). There was no significant difference in size between adult male and female birds. Adults were larger than juvenile birds in bill width, beard length, wingspan and mass, and had a higher aspect ratio and wing loading, while juvenile birds were larger than adults in the length of their outer rectrices, tail area, wing breadth and wing area. These features are considered to be adaptive to young birds inexperienced in flying. Immature and subadult birds were intermediate in size between juveniles and adults. Bearded Vultures differ from other large raptors in two sets of physical characteristics, (a) those adapted to cold, mountainous habitat, e.g. feathered head and face, unusually long wings, a high aspect ratio and a particularly long tail, and (b) those adapted to their diet of mainly bones, e.g. wide gape, beard and relatively long talons for carrying food.  相似文献   

5.
Jiro  Kikkawa 《Ibis》1980,122(4):437-446
Winter survival with respect to dominance classes of 932 individually colour-ringed Silvereyes was examined on Heron Island, Great Barrier Reef, between 1965 and 1969. The dominants (winning two-thirds or more of aggressive encounters) had significantly better chances of survival between May and August (southern winter) than other birds. The 1967/68 year group was studied in detail; the young born early in the breeding season contained proportionately more dominants than those born later in the season and dominant birds tended to survive better in winter. Adults in the same period showed no dominance dependent survival. The weight of birds in winter differed between first-year birds and adults in most cases, but winter mortality within each year-group was not related to the weight of individual birds in May. However, the dominant class had a smaller proportion of birds losing weight through the winter than other classes, and the dominant adults and the intermediate class of first-year birds tended to be heavier than others in August. The lengths of wing, tail, tarsus and exposed culmen examined for the 1967/68 year group showed no significant trends in either survival or dominance classes. Better survival of dominant birds is considered to be a consequence of their feeding advantages over others, but the intensity of selection for an ability for dominance may fluctuate from year to year in relation to the population density and distribution and abundance of food supply.  相似文献   

6.
We studied the nonbreeding ecology of Bristle-thighed Curlews Numenius tahitiensis from 1988 to 1991 on Laysan Island in the Northwestern Hawaiian Islands. Using capture-recapture analysis, we estimated that 300–350 curlews wintered on the island. Annual survival was >85% for adults and 92% for first-year birds. Young birds remained on the island until at least their third calendar year, when some individuals made "exploratory" visits to other islands in the Northwestern chain. Most of the birds marked in their first year migrated north to the breeding grounds when they were 3 years old; several birds remained on the island until they were at least 4 years old. Adults returned to the same discrete home ranges year after year, whereas subadults (which do not migrate) tended to use a greater portion of the island. At least 60% of the subadults marked from 1988 to 1990 returned to the island to winter as adults. Because young curlews arrived after adults and experienced high survivorship while on the island, there did not appear to be intense competition for space at Laysan even though the island is at the northern end of the species' winter range.  相似文献   

7.
D. J. Pearson 《Ibis》1984,126(1):1-15
Moult data were collected during 1967–80 from some 6900 Little Stints in the southern Kenyan rift valley.
Adults typically moulted from summer to winter body and head plumage during September and early October, soon after arrival. The complete pre-winter wing and tail moult began in most adults between mid-September and early October. Some birds finished by December, but others continued until February and March. Individual duration was usually between 100 and 150 days. Adults which completed this moult early often remoulted outer primaries between January and early April.
Young birds acquired first-winter body plumage during October and early November. Some 90% had a complete pre-winter wing and tail moult. This usually began between December and early February, and finished during March or early April, taking about 70–100 days. In about 10% of young birds, flight feather moult was restricted to the outer primaries and inner secondaries. Birds adopting this strategy typically began moult late, during January or February. Short periods of suspension were common during pre-winter wing moult, particularly in adults. The difference in moult speed between adult arid first-winter birds was attributable in the primary, secondary and tail tracts to differences in numbers of growing feathers.
Practically all birds completed a pre-summer moult involving the entire body and head plumage, most of the tertials, some or all of the tail feathers and many wing coverts. Most birds began this moult between early February and late March, and finished between mid-April and early May. It was typically later and more rapid in first-year birds than adults. In late birds, the onset of pre-summer moult was linked to the final stages of pre-winter moult.
The wing moult of the Little Stint in different wintering areas is discussed. First-winter moult strategy is compared with that in other small Calidris species.  相似文献   

8.
The moult of Barred Warblers Sylvia nisoria was studied during three winter seasons in southeastern Kenya at a southward passage site (Ngulia) and a wintering site (Mtito Andei). Most Barred Warblers migrating through Ngulia in November had yet to commence winter moult. These birds probably moulted subsequently in winter in northern Tanzania. In December, birds were found in heavy moult at Mtito Andei, and some of these birds were known to stay throughout the winter. By contrast, most birds reaching southeastern Kenya from late December onwards had already completed part or all of their winter moult, presumably at stopover sites in northern and eastern Kenya or in Ethiopia. Thus, winter moult in Barred Warblers takes place mainly in late November and December, either just before or soon after the final leg of autumn migration. In general, first-year birds renewed all tertials and tail feathers, about three to five secondaries per wing and commonly also the outer one to four large primaries per wing. Adults renewed all tertials and tail feathers, almost all secondaries and only occasionally an outer primary. The replacement of relatively fresh juvenile secondaries during the birds' first winter implies that the split moult pattern of this species (secondaries, tertials and tail moulted in winter; primaries and tertials in summer) is endogenously controlled.  相似文献   

9.
Despite its relevance for the dynamics of populations, the ecological mechanisms underlying juvenile and adult survival are poorly known in most bird species. This study focuses on the effect of habitat fragmentation on early post-fledging, first-year and adult survival of the middle spotted woodpecker Dendrocopus medius by combining data of radio-tagged and ringed birds. Among juveniles, most deaths occurred during the first three weeks after fledging (survival rate: 0.359±0.077) and were mainly caused by predation. After independence, birds faced another critical period during their first autumn-winter that lowered first-year survival further (0.255±0.044), whereas adult mortality was considerably lower (annual survival rate: 0.786±0.074). We did not find any significant effect of habitat fragmentation (measured as patch size and connectivity) on juvenile or adult survival. Sex ratio at fledging did not differ significantly from parity (proportion of females: 0.513) and was not correlated to patch size. Regardless of age, survival did not differ between the sexes, suggesting that a female-biased mortality was not the mechanism behind the presence of unpaired territorial males in this population. Lighter nestlings underwent significantly higher post-fledging mortality, indicating that conditions in the nest may substantially affect survival later in life.  相似文献   

10.
The feeding behaviour of the Caspian Gull Larus cachinnans was analysed in southern Poland in 2001. During the pre-breeding period, most birds foraged on a refuse dump and some foraged in a river valley. During incubation, similar numbers of birds foraged on fishponds, gravel pits and the refuse dump. During the chick-rearing period, fishponds were the most important foraging grounds. The foraging success of three main foraging tactics was analysed: digging on refuse, fishing and kleptoparasitism. We found that digging success was higher in juveniles than in immature or adult birds. However, older birds moved and ate more items per unit of time than juveniles, which indicates that older birds improved their energy gain simply by a higher speed of searching. The opposite was found for fishing success. As juvenile birds made fewer attempts than immature or adult birds, fishing success was higher in adults. Adults and immature birds interrupted more attacks than juveniles, which indicates that older birds were better able to assess the probability of fish catching than juveniles. Kleptoparasitism was observed almost exclusively on the refuse dump during the pre-breeding period. Young birds kleptoparasitised more frequently than adults, but they had a lower rate of success. However, the lower success in young birds was due to victim choice, rather than differences in flight skills. Young birds kleptoparasitised Black-headed Gulls Larus ridibundus and Jackdaws Corvus monedula more frequently than adults, but none of the attacks towards these species was successful. Generally, Caspian Gulls kleptoparasitised conspecifics more often than expected from species frequency. Only attacks towards conspecifics yielded any success.  相似文献   

11.
Most small birds wintering in the tropics should show little subcutaneous fat deposition (SFD), except in habitats where food availability may decline in late winter or, for some resident species, to prepare for incubation or brooding fasts. However, these predictions need re‐examination in light of a new, precise, cross‐validated method to compare SFD among habitats and species. We sampled 170 Nearctic‐Neotropical migrant and 279 resident birds during early and late winter in 1993 and 1994 in Jamaica, West Indies. Habitats, from greatest to least expected availability of insect prey, were (1) mangrove forest, (2) montane/foothills forest and cultivation, (3) dry limestone forest, and (4) acacia scrub. Percent lipid, estimated from multiple‐regression models using visual fat scoring (0–8 scale), total‐body electrical conductivity, and a variety of morphometrics, was categorized by percentile ranks to determine if SFD varied by habitat, season, or age for all species, resident species, migrant species, and several individual species. SFD averaged ~ 13% total mass for all birds, ranging from 8–24% for well‐sampled species. The few bird species in acacia scrub, primarily two facultative long‐distance migrants, averaged ~ 26% lipid content, significantly more than birds in other habitats. Most birds did not vary in SFD in the other three habitats, although Common Yellowthroats (Geothlypis trichas) had greater SFD in dry limestone habitat than in montane habitat. Bananaquits (Coereba flaveola) and Jamaican Euphonias (Euphonia jamaica) in montane habitat, especially in early winter, had higher SFD than other resident species. Contrary to our prediction, adults and juveniles had similar SFD, with the exception of juveniles having more SFD than adults in acacia scrub habitat. Winter fat deposition (or, in some cases, muscle‐protein catabolism) in the tropics may be an overlooked strategy, potentially important as a hedge against fasting for floaters, facultative migrants, some territorial migrants in habitats with seasonal declines in food resources, and some resident species prior to breeding.  相似文献   

12.
This paper describes the strategies of resource utilization in the course of the breeding season by five radio-tagged Grey Herons Ardea cinerea. The seasonal changes in exploitation of the environment by two breeding adults, one non-breeding adult and two non-breeding first-year birds were studied from March to August 1982, near Zonhoven in Belgium. Two adult breeding birds could be followed continuously from the end of March until the middle of June. During the first month they explored an extended area all around the colony, but each concentrated its search in a specific direction. From the end of April until the beginning of June, most probably from egg-hatching until the end of breeding activities, each bird spent a very large proportion of its time at a particular feeding site, from which other herons were actively excluded. In the first part of June they again visited different sites, each maintaining its preferred direction. From the middle of June onwards they seemed to have left the fish-pond area. The pattern of movements of the first-year birds differed markedly from that of the breeding adults. In April, although both non-breeding and breeding birds explored large areas, only the areas used by non-breeders were centred on the colony. From the end of April onwards, probably after general egg-hatching in the colony, the non-breeders very rarely revisited the colony, and from May till August their ranges became more and more restricted to very small areas at an increasing distance from the colony. They were never observed defending particular sites. The results are discussed with regard to recent speculations about the evolution of colonies as an adaptation for the exploitation of food resources. Breeding herons seem to explore a large part of the environment during incubation and defend a particular site while feeding their young. Choice of feeding site by non-breeding birds may be influenced by the site defence of the breeding birds. Non-breeding birds exploit a large area when breeding birds occupy feeding territories. Perhaps they are forced to forage in less suitable places at this time. Colonies might have evolved as a strategy to minimize effort in resource esploitation as, especially at the beginning of the breeding season, the colony could act as an assembly point in the exploration of the environment. However, its importance as an assembly point diminishes in the course of the season, as non-breeding birds no longer visit the colony and adults defend territories.  相似文献   

13.
Whether to disperse, and where to, are two of the most prominent decisions in an individual's life, with major consequences for reproductive success. We studied natal and breeding dispersal in the monogamous black‐tailed godwit Limosa limosa limosa in the Netherlands, where they breed in agricultural grasslands. The majority of these grasslands recently changed from wet herb‐rich meadows into well‐drained grassland monocultures, on which godwits have a lower reproductive success. Here we examine habitat selection with a multistate mark–recapture analysis. Habitat transition probabilities between meadows and monocultures were estimated on the basis of 1810 marked chicks and 531 adults during seven years in a 8500 ha study area. Young and adult godwits may differ in habitat selection because: 1) adults may have gained experience from previous nest success where to settle, 2) younger individuals may find it harder to compete for the best territories. Both young and adults moved at a higher rate from the predominant monocultures to meadows than the other way around, thus actively selecting the habitat with better quality. However, dispersal distance of adults was not affected by previous nest success. The average dispersal distance from place of birth of godwits breeding for the first time was ten times larger than that of adult godwits. That godwits breeding in their second calendar year arrived and laid at similar dates and were equally able to select territories in areas with high breeding densities, suggests that young birds were not competitively inferior to adults. Although on monocultures reproduction is insufficient to maintain constant populations, birds sometimes moved from meadows to monocultures. This explains why even after 30 years of land‐use intensification, godwits still breed in low‐quality habitat. The adjustment to changing habitat conditions at the population level appears to be a slow process.  相似文献   

14.
The study objectives were to identify the horizontal and vertical distributions of adult Chinese sturgeon (Acipenser sinensis) in relation to the Habitat Suitability Index (HSI) in order to assess the utility of the only remaining spawning grounds by adults and to understand the effects of river alterations on habitat use. Twenty‐five adults were surgically implanted with ultrasonic transmitters and located by mobile tracking and fixed monitoring stations during the 2006–2009 spawning seasons. Fish locations and depths along with water depth and bottom characteristics (topography, velocity, and embeddedness) were measured during tracking and used to determine HSI curves for non‐spawning and spawning adults. Most fish locations (91%) were on the spawning grounds (GZD to Miaozui reaches). Horizontal distribution differed before and after spawning, among years, and between the sexes. Adults used deeper depths during the day than at night (P < 0.001), while also preferring shallower depths on the day of spawning rather than the days before and after. Mature females used deeper water than other females (P < 0.001). Comparison of horizontal and vertical distributions before and after river alterations found fewer adults using the grounds impacted by a diversion dike which was built on the spawning grounds. Adults also used shallower depths after the Three Gorges Dam regulated river flow over the spawning grounds. The HSI model and the use of Weighed Usable Areas (WUA) for mature and immature adults indicated suitable habitat was available, but was reduced by the river alterations resulting in reduced spawning success and placing the population into a situation close to extirpation.  相似文献   

15.
Using a broad-scale automated telemetry array, we explored post-fledging movements of blackpoll warblers breeding in Atlantic Canada. We sought to determine the full spatial scale of post-fledging dispersal, to assess support for three hypotheses for regional-scale post-fledging movement, and to determine whether learning influenced movement during this period. We demonstrated that both young and adults moved over distances more than 200 km prior to initiating migration. Adults moved southwest, crossing the Gulf of Maine (GOM), consistent with the commencement of migration hypothesis. Hatch-year birds exhibited less directional movements constrained geographically by the GOM. Their movements were most consistent with exploration hypotheses—that young birds develop a regional-scale map to aid in habitat selection, natal dispersal and subsequent migrations.  相似文献   

16.
The post‐fledging period is a critical life stage for young grassland birds. Habitat selection by recently fledged birds may differ from that of adults and may change as juveniles transition from the care and protection of parents to independence. To describe patterns of habitat selection during these important life stages, we studied habitat use by juvenile Grasshopper Sparrows (Ammodramus savannarum) in a Conservation Reserve Program grassland in Maryland. We used radio‐telemetry to track daily movement patterns of two age classes of Grasshopper Sparrows during the post‐fledging period. Sparrows were classified as either dependent (<32‐d‐old) or independent (≥32‐d‐old). We characterized the vegetation at 780 vegetation plots (390 plots where birds were located and 390 paired random plots). Microhabitats where dependent birds were found had significantly more bare ground, litter, and plant species richness than paired random plots. In addition, dependent birds were found in plots with less bare ground, more warm‐season grass cover, more total vegetation cover, and more forb cover than plots used by independent birds. Plots where independent birds were located also had significantly more bare ground than random plots. Dependent birds are less able to escape from predators because their flight feathers are not fully grown so they may benefit from remaining in areas of greater vegetation cover. However, juveniles transitioning from dependence to independence must forage on their own, possibly explaining their increased use of more open areas where foraging may be easier. To properly manage habitat for grassland birds, management strategies must consider the changing needs of birds during different stages of development. Our results highlight the importance of diverse grassland ecosystems for juvenile grassland birds during the transition to independence.  相似文献   

17.
刘超  丁志锋  丁平 《生态学报》2015,35(20):6759-6768
为探究千岛湖陆桥岛屿不同鸟类集团对栖息地片段化敏感性的差异和季节变化,于2009年4月—2012年1月鸟类繁殖季(4、5、6月)和冬季(11、12、1月)对千岛湖41个陆桥岛屿鸟类集团进行了研究。结果表明,冬季杂食鸟对片段化敏感性高于食虫鸟,繁殖季时二者无显著差异,繁殖季和冬季时下层鸟对片段化敏感性均高于林冠鸟,冬季留鸟对片段化敏感性高于候鸟,繁殖季则无显著差异。杂食鸟和留鸟对片段化敏感性存在季节差异,而食虫鸟、林冠鸟、下层鸟和候鸟对片段化敏感性均无季节差异。不同鸟类集团对栖息地片段化敏感性的差异和季节变化规律,有助于人们在栖息地管理和保护区设计时采取更有针对性的鸟类保护措施。  相似文献   

18.
ABSTRACT Dispersal events can affect the distribution, abundance, population structure, and gene flow of animal populations, but little is known about long‐distance movements due to the difficulty of tracking individuals across space. We documented the natal and breeding dispersal of shrubland birds among 13 study sites in a 1000 km2 area in southeastern Ohio. In addition, we radio‐marked and tracked 37 adult males of one shrubland specialist, the Yellow‐breasted Chat (Icteria virens). We banded 1925 juveniles and 2112 adults of nine shrubland species from 2002 to 2005. Of these, 33 (1.7%) juveniles were encountered in subsequent years (2003–2006) as adults (natal dispersal) and 442 (20.9%) birds initially banded as breeding adults were re‐encountered in subsequent years (breeding dispersal). Apparent survival of juvenile shrubland birds on their natal patches was 0.024 (95% CI 0.016–0.036). After accounting for the probability of detection, we found that 21% of birds banded as juveniles and recaptured as adults returned to their natal patches, whereas 78% of adult birds showed fidelity to the patch where they were originally captured. Moreover, natal dispersers tended to move farther than breeding dispersers (corrected natal median = 1.7 km ± 0.37; corrected breeding median = 0.23 km ± 0.10). We used our estimates of natal dispersal and annual apparent survival to estimate true survival at 0.11 (95% CI 0.07–0.18) for juveniles in their first year. However, this estimate was only applicable for birds dispersing within 7 km of their natal patches. Interpatch movements of radio‐marked Yellow‐breasted Chats were not uncommon, with 13 of 37 males located in more than one habitat patch. Overall, we observed low natal philopatry, but high adult site fidelity for shrubland birds in our study area. Considering the frequency of short‐distance movements observed (median = 531 m, range = 88–1045 m), clustering of patches within 1 km might facilitate use of shrubland habitat.  相似文献   

19.
J. Cooper 《Ostrich》2013,84(2):154-156
Cooper, J. 1975. Primary moult, weight and breeding cycles of the Rock Pigeon on Dassen Island. Ostrich 46:154-156.

The primary moult season of the adult Rock Pigeon Columba guinea on Dassen Island is spread over at least nine months. Individual duration is estimated at eight months. Adult birds were heaviest in the winter months outside the breeding season. Overlap between the breeding and moulting seasons occurred and evidence was obtained of incubating birds with active primary moult. Juveniles were lighter than adults. Adults fed on the mainland and probably made daily flights there.  相似文献   

20.
Abstract: Common reed (Phragmites australis) forms dense stands with deep layers of residual organic matter that negatively affects plant diversity and possibly habitat use by wetland birds. We sought to determine whether seasonal relative abundance and species richness of birds varied among 3 habitat types in Great Lakes coastal wetland complexes recently invaded by common reed. We used fixed-distance point counts to determine species relative abundances and species richness in edge and interior locales within common reed, cattail (Typha spp.), and meadow marsh habitats of various sizes during 2 summers (2001 and 2002) and 1 autumn (2001) at Long Point, Lake Erie, Ontario, Canada. We found that total relative abundance and species richness of birds were greater in common reed habitat compared to cattail or meadow marsh habitats. However, we also found that relative abundance of marsh-nesting birds was greater in meadow marsh habitat than in cattail and common reed during summer. Lastly, we found that, irrespective of habitat type, habitat edges had higher total relative abundance and species richness of birds than did habitat interiors. Our results show that common reed provides suitable habitat for a diversity of landbirds during summer and autumn but only limited habitat for many marsh-nesting birds during summer. Based on these results, we recommend restoration of meadow marsh habitat through reduction of common reed in Great Lakes wetlands where providing habitat for breeding marsh-nesting birds is an objective. Managers also might consider reducing the size of nonnative common reed stands to increase edge effect and use by birds, possibly including wetland birds.  相似文献   

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