Post‐breeding movements of Wood Storks in Brazil and Argentina

Seasonal migration and the dispersal of juvenile and adult Wood Storks (Mycteria americana) after breeding have been documented in the United States, but little is known about the post‐breeding movements of Wood Storks in South America. Our objective was to identify the locations of post‐breeding areas used by Wood Storks banded as nestlings in breeding colonies in Brazil by analyzing banding data. During the period from 1984 to 2007, 2543 nestlings were banded at breeding colonies in three regions of Brazil, with most (94%) banded in the Pantanal wetland in west‐central Brazil. Seventeen bands were subsequently recovered, with most (14) recovered in southern Brazil and northern Argentina. The mean distance between banding and recovery sites was 1265 km. Our results suggest that Wood Stork movements from breeding areas in Brazil are, as also reported in the United States, in response to changing water levels. The rainy season begins at the end of the breeding season and, in apparent response to rising water levels, Wood Storks in our study moved to drier areas further south with shallower water where they can forage more efficiently. Because only a small percentage of the area where Wood Stork bands were recovered in our study is currently protected, measures are needed to prevent habitat destruction and preserve wetland habitats used by Wood Storks during the post‐breeding period in southern Brazil and Argentina.     

Seasonal variation in energy expenditure and body composition in captive White Storks (Ciconia ciconia)

North Western European populations of White Storks (Ciconia ciconia) appear to have been saved from extinction by settling, i.e. stopping migration. Settled storks exposed to winter conditions must cope with periods of potentially high energy demands that would otherwise be avoided by the migration process. Doubly labeled water (DLW) was therefore used to examine the seasonal variation (summer vs winter) in daily energy expenditure (DEE) and the body composition of adult and immature storks of both sexes. Male White Storks showed a higher DEE over the winter period than in summer compared with females; in particular, immature males exhibited greater energy expenditure in winter than adult males. Thus, the DEE did not significantly differ between summer and winter (except for immature males), reflecting an absence of thermoregulation cost in winter. For both age classes, total body mass increased in winter, which was mainly due to an increase in fat mass. Adult storks were 5% heavier than immature storks. The sexes differed in body mass, with males weighing significantly more than females by 11%. Mean LBM (lean body mass) was 8.5% higher in adults than in immatures, and was 11.5% higher in males compared with females. Between their first and second summers, immatures accumulated a lean body mass to finally reach the same values as adults, indicating a phase of muscle development. The mean fat mass of the storks did not differ between age classes or between sexes. Based on physiological parameters, this study shows that settled White Storks are able to cope with mild winter periods when they are artificially provided with food. In a view to preserve favourable habitats for this species, it is therefore necessary to decide on a plan of action for breeding areas.     

THE AUTUMN MIGRATION OF SOARING BIRDS AT THE BOSPHORUS

The migration of soaring birds was observed at Küçük Çamlica at the southern end of the Bosphorus between 14 July and 8 November 1966. Simultaneous watches were also carried out at other points on the Bosphorus on a number of dates. The largest movements of birds of prey occurred on days of light northeasterly winds, the largest movements of storks on days of light winds with a southerly component. On most days the stream of migrants appeared to be concentrated over the southern end of the Bosphorus. Migration frequently occurred right throughout the day, though the peak period was usually not spread over more than three hours. Figures are given for the daily times of migration of the commonest soaring birds. Daily counts of soaring birds (storks, raptors and Cranes) migrating over the Bosphorus at Küçük Çamlica are given. The main species found migrating were (with total number recorded in brackets) White Stork Ciconia ciconia (207,145), Black Stork C. nigra (6,194), Honey Buzzard Pernis upivorus (8,997), Buzzard Buteo buteo (12,949), "Spotted" Eagle Aquila clanga/pomarina (4,309) and sparrowhawk Accipiter nisus / brevipes (5,224). The autumn migration of 1966 is discussed in detail in a systematic list. Buzzards B. buteo were recorded in large numbers for the first time at the Bosphorus, and were the commonest bird of prey. Cranes Grus grus were also recorded for the first time. Comparison is made between our results and those of previous workers, though differences of coverage rule out any firm conclusions.     

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.     

Importance of the connectivity of Spanish stopovers for Black Storks

Capsule?Sixteen Black Storks (Ciconia nigra) were tracked by satellite during their autumnal and spring migrations in order to identify their major stopover sites and connections between stopovers in Europe and Africa. Among journeys with stopovers, the longest distance that a stork travelled without stopover was 2433?km (defined here as ‘accessible distance’) meaning that those storks which have stopovers use only a single stopover on average, and this is usually in Spain. We identified nine crucial stopovers (seven in Spain and two in Africa) with high connectivity highlighting the importance of Spanish stopover locations on the flyway of Black Storks.     

Satelliten-Telemetrie beim Wei?storchCiconia ciconia: Wanderung eines Ost-Storchs westlich bis Nigeria

A male White Stork, for the first time equipped with a mini-transmitter operated by a solar battery, was tracked on the eastern migration route from E Germany to central African winter quarters and during part of the return migration, for a total distance of about 10 000 km. The individual moved westward into Nigeria, i.e. into the wintering area of western Storks. Since a number of other eastern Storks were tracked as far as Chad, the possibility is discussed that individuals migrating to central Africa along the eastern or western route may eventually return on the opposite route when attracted to flocks of the population from the other side of the migration divide. Some ringing recoveries are consistent with a U-shaped abmigration.     

Movements and diving of grey seal females (Halichoerus grypus) in the Gulf of St. Lawrence, Canada

Five female grey seals were tracked with satellite-linked time-depth recorders during September to April 1993-1994. Seals remained in the northern Gulf of St. Lawrence (Gulf) for 1-2.5 months after capture. Four females dove primarily to depths <10 m and 20-70 m, while all dives of the fifth female, a blind animal, were <10 m. During October/November, all animals moved into the southern Gulf or onto the Scotian Shelf. This migration lasted 6-10 days, during which time animals covered 350-800 km. During that migration, all females, including the blind animal, dove up to 100 m, but the majority of dives were to depths of 40-70 m. Two seals stayed in the southern Gulf through the winter while the others left the Gulf in January. When in the southern Gulf and on the Scotian Shelf, dive depths and bathymetry information indicated that dives were to the bottom.     

Long-term satellite tracking sheds light upon variable migration strategies of White Storks (Ciconia ciconia)

Summary During investigations on the migration of 120 individual White Storks by means of satellite tracking, four birds were tracked into their winter quarters several times, one bird on nine successive journeys. These storks did not exhibit strong winter-site fidelity, but instead occupied somewhat different winter quarters from one year to the next, probably depending on the food supply.

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Langzeit Satelliten-Telemetrie beim Wei?storch gibt Hinweise auf variable Zug- und überwinterungsstrategien

Zusammenfassung Bisher konnten wir 120 Wei?st?rche auf ihrem Zug mit Hilfe der Satelliten-Telemetrie verfolgen, 4 V?gel mehrfach und einen auf neun aufeinander folgenden Wanderungen. Dabei zeichnet sich ab, dass Wei?st?rche im Gegensatz zu vielen anderen Afrikaziehern nur geringe Winterquartiertreue zeigen und im Laufe von Jahren in verschiedenen Gebieten überwintern, wahrscheinlich in Abh ?ngigkeit vom Nahrungsangebot.

     

Is population structure in the European white stork determined by flyway permeability rather than translocation history?

European white stork are long considered to diverge to eastern and western migration pools as a result of independent overwintering flyways. In relatively recent times, the western and northern distribution has been subject to dramatic population declines and country‐specific extirpations. A number of independent reintroduction programs were started in the mid 1950s to bring storks back to historical ranges. Founder individuals were sourced opportunistically from the Eastern and Western European distributions and Algeria, leading to significant artificial mixing between eastern and western flyways. Here we use mitochondrial and microsatellite DNA to test the contention that prior to translocation, eastern and western flyways were genetically distinct. The data show a surprising lack of structure at any spatial or temporal scale suggesting that even though birds were moved between flyways, there is evidence of natural mixing prior to the onset of translocation activities. Overall a high retention of genetic diversity, high N_ef, and an apparent absence of recent genetic bottleneck associated with early 20th century declines suggest that the species is well equipped to respond to future environmental pressures.     

Routes of migrating soaring birds

Soaring migrants travelling through Israel use three principal routes which are used in the opposite directions during the spring and autumn: (1) the Western Route lies mainly along the western edge of the central mountain range, (2) the Eastern Route lies mainly along the Jordan Valley, crossing the mountain range during part of the day, continuing southward along the Dead Sea towards the Sinai, and joining the Western Route in autumn and (3) the Southern-Elat Mountains Route. The geomorphological structure of Israel, with a central mountain range dividing the country roughly into three landscape units, plays a central role in route selection. In the autumn, the Western Route migration axis is deflected at the beginning of the day from east to west for 10–25 km, depending on weather conditions and the flock's roosting locations. Between 10.00 h and 11.00 h, the daily breeze blowing from the Mediterranean Sea influences the migration axis, which is slowly deflected back to the east. A parallel deflection of the migration axis occurs in the Eastern Route in the autumn. The route moves southwest over the eastern slopes of the central mountain range during the morning hours and over the slope, which absorbs direct radiation from the sun, creating good soaring conditions. Towards late afternoon, when the breeze from the sea starts, the axis is deflected to the east, to the Jordan Valley. In the Elat Mountains, the wind flow plays a similar role, but because the topography of the southern Arava Valley causes a change in wind direction, the axis moves during the day in a north-south direction. In addition to the axis movement on a daily scale, a seasonal deflection of the migration axis from east to west also exists. During autumn migration, early migrants (e.g. White Storks Ciconia ciconia) tend to travel on an eastern route, while late migrants (e.g. White Pelican Pelecanus onocrotalus) travel along the Mediterranean coast. This fluctuation was probably because of sub-optimal soaring conditions along the coastal plain during August. In September, temperature differences between the sea and land decrease and the influence of the marine inversion gradually declines, until its influence disappears completely in October. A comparison of the numbers of soaring birds seen over Israel in the autumn and spring shows significant seasonal differences in the use of the various routes. For example, only one species, the Steppe Eagle Aquila nipalensis, flies over the Elat Mountains in the autumn, compared to more than 30 species in the spring. In the autumn, White Storks pass over only along the Jordan Valley axis, whereas in the spring, about half the migrating storks also pass over the western edge of the central mountain range. Honey Buzzards Pernis apivorus fly along the Western Route in large numbers in the autumn, while concentrating almost totally over the Elat Mountains in the spring. These differences are related to the global migration routes between the breeding and the wintering grounds in relation to the Red Sea, which birds avoid crossing, thus causing them to follow different routes in autumn, and spring.     

African Odyssey project – satellite tracking of black storks Ciconia nigra breeding at a migratory divide

The African Odyssey project focuses on studying the migration of the black stork Ciconia nigra breeding at a migratory divide. In 1995–2001, a total of 18 black storks breeding in the Czech Republic were equipped with satellite (PTT) and VHF transmitters. Of them, 11 birds were tracked during at least one migration season and three birds were tracked repeatedly. The birds migrated either across western or eastern Europe to spend the winter in tropical west or east Africa, respectively. One of the juveniles made an intermediate route through Italy where it was shot during the first autumn migration. The mean distance of autumn migration was 6,227 km. The eastern route was significantly longer than the western one (7,000 km and 5,667 km respectively). Important stopover sites were discovered in Africa and Israel. Wintering areas were found from Mauritania and Sierra Leone in the west to Ethiopia and Central African Republic in the east and south. One of the storks migrating by the eastern migration route surprisingly reached western Africa. Birds that arrived early in the wintering areas stayed longer than those arriving later. On the average, birds migrating via the western route spent 37 d on migration compared to 80 d for birds migrating via the eastern route. The mean migration speed in the autumn was 126 km/d and the fastest stork flew 488 km/d when crossing the Sahara. The repeatedly tracked storks showed high winter site fidelity.     

The effect of wind, season and latitude on the migration speed of white storks Ciconia ciconia, along the eastern migration route

The relation between wind, latitude and daily migration speed along the entire migration route of white storks was analysed. Mean daily migration speed was calculated using satellite telemetry data for autumn and spring migration of white storks from their breeding grounds in Germany and Poland to wintering grounds in Africa and back. The National Center for Environmental Prediction (NCEP) reanalysis data were used to systematically fit 850 mb wind vectors to daily migration speed along the migration route. White storks migrated significantly faster and had a shorter migration season in autumn (10 km/h) compared to spring (6.4 km/h). In autumn mean daily migration speed was significantly slower in Europe (8.0 km/h) than in the Middle East (11.1 km/h) and Africa (11.0 km/h). In spring mean daily migration speed was significantly faster in Africa (10.5 km/h) as birds left their wintering grounds than in the Middle East (4.3 km/h). Migration speed then increased in Europe (6.5 km/h) as birds approached their breeding grounds. In both spring and autumn tailwind (at 850mb) and latitude were found to be significant variables related to daily migration speed.     

Satelliten-Telemetrie beim Wei?storch (Ciconia ciconia) auf dem Wegzug — eine Pilotstudie

Zusammenfassung (1) 1991 konnten erstmals 4 mit Kleinsendern ausgerüstete Weißstörche mit Hilfe der Satelliten-Telemetrie auf Teilstrecken ihres Wegzugs bis zu 46 Tage lang verfolgt werden. Die japanischen Sender betrugen nur etwa 2 % des Körpergewichts der Vögel; die Ortung erfolgte durch das ARGOS-System. Die Versuchsvögel zeigten völlig normales Zugverhalten. — (2) Drei der in Brandenburg und Sachsen-Anhalt markierten Vögel waren Ostzieher und konnten über Strecken von etwa 640–4700 km verfolgt werden, 1 Storch bis zur ägyptisch-sudanesischen Grenze. Ein Westzieher konnte rund 1400 km bis zu den Pyrenäen geortet werden. — (3) Die Vögel wanderten individuell recht verschieden. 2 zogen weitgehend kontinuierlich bis in den Sudan bzw. zu den Pyrenäen, die anderen legten längere Pausen ein. Die ermittelten Zugstrecken verliefen recht geradlinig; Richtungsänderungen erfolgten vor allem an der Donau, den Karpaten, am Mittelmeer und auf der Sinai-Halbinsel. Tagesetappen betrugen mindestens bis zu 370 km, in einem Fall in 21 Tagen durchschnittlich 224 km/Tag. Die Zuggeschwindigkeit lag in der Größenordnung von 30–90 km/h. — (4) Verbesserte Sender mit längerer Lebensdauer und mehreren Ortungen pro Tag dürften es bald ermöglichen, individuelle Wanderrouten von Weißstörchen und anderen Großvögeln praktisch lückenlos zu ermitteln. Begleitmannschaften werden zudem die Zug- und Rastökologie mit Sendern ausgerüsteter Vögel mit erfassen können. Damit dürfte der Vogelschutz auf dem Zug eine neue Dimension gewinnen.

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Satellite tracking of White Storks during the autumn migratory period — a pilot study

Summary (1) In 1991 parts of the routes of White Storks migrating in autumn could be recorded for the first time by satellite tracking. Four individuals could be followed for up to 46 days. Transmitter weight accounted for only about 2 % of body mass. Locations were obtained by the ARGOS system. Migratory behaviour of the experimental birds appeared to be absolutely normal. — (2) The birds were equipped with transmitters in eastern Germany. Three of them followed the eastern migration route and could be tracked from 640 up to 4700 km, the latter reaching the borders of Egypt and Sudan. A western migrant could be followed over a distance of about 1400 km towards the Pyrenees. — (3) Migration showed considerable individual variation. Whereas in two birds migration was largely continuous towards the Sudan and the Pyrenees, respectively, the other birds rested for longer periods. The tracked migration routes were fairly straight. Marked directional shifts occurred towards the Danube valley, at the Carpathian mountains, the Mediterranean and on the Sinai. Capacity per day was at least 370 km. One bird covered 224 km/day on average during a period of 21 days. Migration speed ranged in the magnitude of 30–90 km/h. — (4) Improved transmitters with increased lifetime giving several locations per day will presumably allow to record migration routes of White Storks and other large birds more completely in the near future. Escorts should then be able to closely analyse the ecology of migration and staging of their test birds. These possibilities may give a new dimension to bird conservation measures during migration.

     

Network analysis of potential migration routes for Oriental White Storks (<Emphasis Type="Italic">Ciconia boyciana</Emphasis>)

From 1998 through to 2000, we satellite-tracked the movements of 13 Oriental White Storks (Ciconia boyciana) on their autumnal migration in order to identify their important stopover sites for preserving links from the Russian Far East breeding sites to the wintering sites in south-eastern China. New analytical methods of satellite tracking data were employed to derive robust information on the locations of stay sites, the number of stopovers made during migration, and the distance traveled without making stopovers. Based on the derived information, we modeled a stay site network as an abstraction of the storks potential migration routes from their breeding sites to wintering sites. Using network analysis techniques, we explored how the loss of stopover sites could affect the connectivity of potential migration routes. The results suggested that if the seashore stopover sites facing Bohai Bay in eastern China were lost, the storks wintering sites along the Yangtze River in south-eastern China would be isolated. Among the seashore stopover sites, Jiantuozhi Gley Mire (39.185°N, 118.627°E), located on the northern seashore of Bohai Bay, was considered particularly important for migrating storks, because it was used every year by the storks we tracked. If conservation needs of this critically located site fail to be addressed, the stay site network of storks can create weak links in the chain of migration and, if broken, storks will have great difficulties in completing their autumnal migration.     

Coastal forests of eastern Africa: status, endemism patterns and their potential causes

Eastern African coastal forests are located within the Swahili regional centre of endemism and Swahili-Maputaland regional transition zone in eastern Africa, between 1d? North and 25d? South, and 34—41d? East. Approximately 3167 km² coastal forest remains: 2 km² in Somalia, 660 km² in Kenya, 697 km² in Tanzania, 16 km² in Malawi, 3 km² in Zimbabwe and perhaps 1790 km² in Mozambique. Most forests are small (≤ 20 km²), and all but 19 are under 30 km² in area. Over 80% of coastal forest is located on government land, principally Forest Reserves; only 8.3 km² is found in National Parks (6.2 km² in Kenya (Arabuko-Sokoke), 2 km² in Tanzania (Mafia Island) and tiny patches in Zimbabwe). Coastal forests are an important and highly threatened centre of endemism for plants (c 550 endemic species), mammals (6 species), birds (9 species), reptiles (26 species), frogs (2 species), butterflies (79 species), snails (>86 species) and millipedes (>20 species). Endemic species are concentrated in the forests of the Tana River, between Malindi in Kenya to Tanga in northern Tanzania, and in southern Tanzania. Forests with highest numbers of endemics are: lower Tana River, Arabuko-Sokoke, Shimba Hills (Kenya); lowland East Usambara, Pugu Hills, Matumbi Hills, Rondo and Litipo and other plateaux near Lindi (Tanzania); the Tanzanian offshore island of Pemba; Bazaruto archipelago (Mozambique), and tiny forest remnants of southern Malawi, eastern Zimbabwe and Mozambique. Most coastal forest endemics have a narrow distributional range, often exhibiting single-site endemism or with scattered or disjunct distributional patterns. They are best interpreted as relicts and not the result of recent evolution. Relictualization probably started with the separation of the ancient Pan African rainforest into two parts during the Miocene. The coastal forests are interpreted as a ‘vanishing refuge’ with the endemic species gradually becoming more and more relict (and presumably extinct) due historically to climatic desiccation and more recently to human destruction.     

THE MIGRATION OF RAPTORS AND STORKS THROUGH THE NEAR EAST IN AUTUMN

Between 1963 and 1965 three expeditions have investigated the autumn migration of raptors and storks, on two occasions in southeast Turkey, and once in Lebanon.
Nearly all the soaring birds leaving Europe by the Bosphorus cross Asia Minor and turn south at the Gulf of Iskenderun. The commonest of these migrants are White Stork Ciconia ciconia , Honey Buzzard Pernis apivorus , and Eagles Aquila spp.
Other species such as Common Buzzard Buteo buteo are not usually seen crossing the Bosphorus, but occur in large numbers in the flocks seen south of the Gulf of Iskenderun. It is suggested that these are birds from Russia and north Turkey. Common Buzzards also occur on Cyprus in autumn, but their point of origin is not clear. Short-toed Eagles Circuetus gullicus and vultures join the migration from their breeding grounds in Turkey and the Levant.
Different species tend to migrate at different times of year. White Storks, Egyptian Vultures Neophron percnopterus and Black Kites Milvus migruns move chiefly between late August and mid-September, while eagles Aquilu spp. start in late September and continue until November. Other species are intermediate, or spread their migration out over a longer period.
The volume of migration at different times of day is discussed. No general conclusions are possible but in 1964 a correlation was obtained between cloud cover and the start of the migration.     

A new method for sexing Oriental White Storks

ABSTRACT.   For species where males and females are monomorphic, or nearly so, determining the sex of individual birds generally requires either capturing birds or collecting samples, such as feathers, for DNA analysis. We developed a new method, involving the use of photographs, to determine the sex of endangered Oriental White Storks ( Ciconia boyciana ). Using photographs, we analyzed the lateral features of the heads of 25 captive storks of known sex (12 males and 13 females) and found differences between males and females in the distance from the bill tip to the nape and the distance from the bill tip to the commissural point. These differences were used to generate a discriminant function that was then tested on 22 captive storks at Hyogo Homeland Park (Toyooka, Japan), and we correctly determined the sex of 18 individuals (82%). In addition, the sex of two wild storks was correctly assigned. Our results suggest that good-quality photographs can be useful for determining the sex of both captive and wild Oriental White Storks and, further, that similar methods may prove useful for determining sex in other species of birds.     

Movements by juvenile and immature Steller's Sea Eagles Haliaeetus pelagicus tracked by satellite

Twenty‐four juvenile Steller's Sea Eagles Haliaeetus pelagicus were tracked via satellite from natal areas in Magadan, Kabarovsk, Amur, Sakhalin and Kamchatka. Nestling dispersal occurred between 9 September and 6 December (n = 24), mostly 14 September–21 October, and did not differ among regions or years. Most eagles made stopovers of 4–28 days during migration. Migration occurred 9 September–18 January, mostly along previously described routes, taking 4–116 days to complete (n = 18). Eagles averaged 47.8 km/day excluding stopovers; 22.9 km/day including stopovers. The mean degrees of latitude spanned during migration was: Kamchatka, 2.1; Magadan, 11.6; Amur, 7.3; and Sakhalin, 1.1. Eagle winter range sizes varied. Eagles concentrated in 1–3 subareas within overall winter ranges. The mean size of the first wintering subareas was 274 km², the second 529 km², and the third 1181 km². Second wintering areas were south of first wintering areas. Spring migration started between 2 February and 31 March. Two eagles from Magadan were tracked onto summering grounds, well south of their natal areas. Both had early and late summering areas. One bird was followed for 25 months. It initiated its second autumn migration in the first half of October and arrived on its wintering grounds on 26 December. The second autumn migration covered 1839 km (20.9–22.4 km/day). Unlike its first winter when it used two subareas, this bird used only one subarea in 1998–99, but this was located near wintering areas used in 1997–98. It left its wintering ground between 13 April and 13 May, and arrived on its summering grounds between 7 June and 8 July. Unlike most satellite radiotracking studies, data are presented from a relatively large number of birds from across their breeding range, including new information on eagle movements on the wintering grounds and during the second year.     

Poleward shifts in breeding bird distributions in New York State

Like other regions of the northern hemisphere, the northeastern United States has experienced a general increase in regional temperatures over the past 20 years. Quantifying the ecological implications of these changing temperatures has been severely constrained by a lack of multispecies distributional data by which to compare long-term changes. We used the New York State Breeding Bird Atlas, a statewide survey of 5332 25 km² blocks surveyed in 1980–1985 and 2000–2005, to test several predictions that the birds of New York State are responding to climate change. Our objective was to use an information-theoretic approach to analyze changes in three geographic range characteristics, the center of occurrence, range boundaries, and states of occurrence to address several predictions that the birds of New York State are moving polewards and up in elevation. As expected, we found all bird species ( n =129) included in this analysis showed an average northward range shift in their mean latitude of 3.58 km [ Prob ( H _a|data)=0.87)]. Past studies have found that northern range boundaries are more likely to be influenced by climatic factors than southern range boundaries. Consequently, we predicted that northward shifts would be more evident in northern as opposed to southern range boundaries. We found, however, that the southern range boundaries of northerly birds moved northward by 11.4 km [ n =43, Prob ( H _a|data)=0.92], but this pattern was less evident in northern range boundaries of southerly birds. In addition, we found that bird species demonstrated a general shift downhill in their mean elevation, but demonstrated little change in their elevational boundaries. The repeated pattern of a predicted northward shift in bird ranges in various geographic regions of the world provides compelling evidence that climate change is driving range shifts.