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Autumn Migration (autumn + migration)
Selected AbstractsIs there a connection between weather at departure sites, onset of migration and timing of soaring-bird autumn migration in Israel?GLOBAL ECOLOGY, Issue 6 2006Judy Shamoun-Baranes ABSTRACT Aims, Different aspects of soaring-bird migration are influenced by weather. However, the relationship between weather and the onset of soaring-bird migration, particularly in autumn, is not clear. Although long-term migration counts are often unavailable near the breeding areas of many soaring birds in the western Palaearctic, soaring-bird migration has been systematically monitored in Israel, a region where populations from large geographical areas converge. This study tests several fundamental hypotheses regarding the onset of migration and explores the connection between weather, migration onset and arrival at a distant site. Location, Globally gridded meteorological data from the breeding areas in north-eastern Europe were used as predictive variables in relation to the arrival of soaring migrants in Israel. Methods, Inverse modelling was used to study the temporal and spatial influence of weather on initiation of migration based on autumn soaring-bird migration counts in Israel. Numerous combinations of migration duration and temporal influence of meteorological variables (temperature, sea-level pressure and precipitable water) were tested with different models for meteorological sensitivity. Results, The day of arrival in Israel of white storks, honey buzzards, Levant sparrowhawks and lesser spotted eagles was significantly and strongly related to meteorological conditions in the breeding area days or even weeks before arrival in Israel. The cumulative number of days or cumulative value above or below a meteorological threshold performed significantly better than other models tested. Models provided reliable estimates of migration duration for each species. Main conclusions, The meteorological triggers of migration at the breeding grounds differed between species and were related to deteriorating living conditions and deteriorating migratory flight conditions. Soaring birds are sensitive to meteorological triggers at the same period every year and their temporal response to weather appears to be constrained by their annual routine. [source] Changes in the timing of spring and autumn migration in North American migrant passerines during a period of global warmingIBIS, Issue 2 2005ALEXANDER M. MILLS Butler (2003) used first arrival dates (FADs) of 103 migrant birds in northeastern USA and found that both long-distance migrants (LDMs; wintering south of the USA) and short-distance migrants (SDMs; wintering in the southern USA) arrived earlier in the second half of the 20th century than they had in the first, consistent with scenarios of global warming; the trend was stronger in SDMs. Using FADs to characterize migration systems can be problematic because they are data from one tail of a distribution, they comprise a mostly male population and they may not correlate well with the balance of the migration period. FADs also provide no information about autumn migration. This paper uses a banding dataset from Long Point Bird Observatory, Ontario, for 14 passerines for a period of global warming (1975,2000), taking these issues into account. The data were filtered to minimize effects of unequal netting effort (147 491 resulting records), and the passage dates then calculated in each season of each year for the 1st, 2nd and 3rd quartiles for regression analysis. Only two of 13 species analysed in the spring showed significantly earlier passage times, although the overall trend was towards earlier spring migration, especially among SDMs. Autumn responses were more prevalent, however, and in some cases more dramatic with six of 13 species showing delayed migration (four SDMs, two LDMs). Two LDMs exhibited earlier autumn migration. Where earlier spring migration occurred, both sexes appeared to contribute to the change. Where delayed migration occurred in autumn, both sexes and both adults and hatch-year birds appeared to contribute in at least some cases. The spring FAD results are consistent with those of Butler, but when the whole migration is considered, change is far from universal in spring and is in fact more substantial and complex in autumn. [source] Fuel reserves affect migratory orientation of thrushes and sparrows both before and after crossing an ecological barrier near their breeding groundsJOURNAL OF AVIAN BIOLOGY, Issue 1 2009Mark E. Deutschlander Fat reserves influence the orientation of migrating songbirds at ecological barriers, such as expansive water crossings. Upon encountering a body of water, fat migrants usually cross the barrier exhibiting ,forward' migration in a seasonally appropriate direction. In contrast, lean birds often exhibit temporary ,reverse' orientation away from the water, possibly to lead them to suitable habitats for refueling. Most examples of reverse orientation are restricted to autumn migration and, in North America, are largely limited to transcontinental migrants prior to crossing the Gulf of Mexico. Little is known about the orientation of lean birds after crossing an ecological barrier or on the way to their breeding grounds. We examined the effect of fat stores on migratory orientation of both long- and short-distance migrants before and after a water crossing near their breeding grounds; Catharus thrushes (Swainson's and gray-cheeked thrushes, C. ustulatus and C. minimus) and white-throated sparrows Zonotrichiaalbicollis were tested for orientation at the south shore of Lake Ontario during spring and autumn. During both spring and autumn, fat birds oriented in a seasonally appropriate, forward direction. Lean thrushes showed a tendency for reverse orientation upon encountering water in the spring and axial, shoreline orientation after crossing water in the autumn. Lean sparrows were not consistently oriented in any direction during either season. The responses of lean birds may be attributable to their stopover ecology and seasonally-dependent habitat quality. [source] Hunting strategies and foraging performance of the short-toed eagle in the Dadia-Lefkimi-Soufli National Park, north-east GreeceJOURNAL OF ZOOLOGY, Issue 3 2010D. E. Bakaloudis Abstract The foraging performance and the hunting strategies of foraging short-toed eagles Circaetus gallicus were studied in Dadia-Lefkimi-Soufli National Park during 1996,1998. A general linear model analysis showed that the eagle's hunting mode was related to wind velocity. At low wind speeds, the eagles more frequently soared and/or hovered, whereas on windy days, they hung more frequently than soared or hovered. Individuals appear to compensate for the high-cost foraging method (hovering) with a high capture rate or a low capture rate with low-cost foraging methods (soaring and hanging). In addition, their foraging activities exhibited two patterns. In the early (April) and late (September) breeding season, eagles foraged mainly during midday, while from May to August eagles foraged largely during the morning and a little during the afternoon, reflecting to some extent the diurnal activity of prey (reptiles) throughout the breeding season. Short-toed eagles tended to forage for longer as the breeding season progressed, peaking during August due to additional food requirements before autumn migration. Following a mixed foraging strategy throughout the breeding season, short-toed eagles increased their hunting efficiency, which may benefit increased breeding success and energy reserves for migration. [source] Detecting genetic structure in migrating bowhead whales off the coast of Barrow, AlaskaMOLECULAR ECOLOGY, Issue 10 2007P. E. JORDE Abstract We develop a general framework for analysing and testing genetic structure within a migratory assemblage that is based on measures of genetic differences between individuals. We demonstrate this method using microsatellite DNA data from the Bering-Chukchi-Beaufort stock of bowhead whales (Balaena mysticetus), sampled via Inuit hunting during the spring and autumn migration off Barrow, Alaska. This study includes a number of covariates such as whale ages and the time separation between captures. Applying the method to a sample of 117 bowhead whales, we use permutation methods to test for temporal trends in genetic differences that can be ascribed to age-related effects or to timing of catches during the seasons. The results reveal a pattern with elevated genetic differences among whales caught about a week apart, and are statistically significant for the autumn migration. In contrast, we find no effects of time of birth or age-difference on genetic differences. We discuss possible explanations for the results, including population substructuring, demographic consequences of historical overexploitation, and social structuring during migration. [source] | ||||||||||