Migration timing and its determinants for nocturnal migratory birds during autumn migration

2015 ◽  
Vol 84 (5) ◽  
pp. 1202-1212 ◽  
Author(s):  
Frank A. La Sorte ◽  
Wesley M. Hochachka ◽  
Andrew Farnsworth ◽  
Daniel Sheldon ◽  
Daniel Fink ◽  
...  
The Auk ◽  
2005 ◽  
Vol 122 (1) ◽  
pp. 71-81 ◽  
Author(s):  
Alexander M. Mills

AbstractProtandry, the earlier arrival of males than of females on breeding areas, occurs in many taxa, including many migratory birds. Numerous hypotheses have been generated to explain protandry. Using bird-banding records, I show that protogyny, the earlier migration of females, frequently occurs in the autumn, though it is less universal and less dramatic than spring protandry. In one species, it occurs in both hatch-year and adult birds. When (1) spring and autumn, (2) departures and arrivals, and (3) breeding and wintering ground conditions are considered, hypotheses generated only to explain spring protandry can be more thoroughly evaluated. Using that approach, the most parsimonious explanation of differential migration between the sexes explains earlier male arrival in spring and later male departure in autumn through either (1) indirect selection operating on intrasexual male competition for territories or (2) direct selection operating on intersexual relations requiring males to be present on breeding territories when females are present. In autumn-protogynous species, males may ”play chicken,” balancing the benefits of remaining longer than females and protecting territories for subsequent years against the costs of remaining in the north under deteriorating conditions and delaying the acquisition of a good winter territory.Protogynie et migration automnale: Est-ce que les mâles ”jouent les dégonflés”?


The Auk ◽  
2019 ◽  
Author(s):  
Émile Brisson-Curadeau ◽  
Kyle H Elliott ◽  
Pascal Côté

Abstract The phenology of migrating birds is shifting with climate change. For instance, short-distance migrants wintering in temperate regions tend to delay their migration in fall during spells of warmer temperature. However, some species do not show strong shifts, and the factors determining which species will react to temperature changes by delaying their migration are poorly known. In addition, it is not known whether a slower migration or a postponed departure creates the observed delays in fall migration because most studies occur far south of the boreal breeding areas making it difficult to separate those 2 mechanisms. We used 22 yr of data at a northern observatory in eastern North America, at the southern edge of the boreal forest, to examine how 21 short-distance migrants responded to changing temperatures. We investigated if those species responding to temperature share life-history features (i.e. diet, size, total migration distance, breeding habitat, timing of migration). The period of migration in each species was, by far, the most important factor predicting the response of a species to temperature. Eight of the 13 species migrating in October changed their migration onset with temperature (usually by delaying migration by 1–2 days/°C), while the migration timing of none of the 8 species migrating in September was dependent on temperature. Furthermore, the absence of a greater migration delay by birds breeding farther from the study site (i.e. Arctic-breeding birds) suggests the mechanism is a postponed departure rather than a slower migration. We conclude that temperature variations in late fall influence the conditions on the breeding grounds, so that birds still present at that time benefit more from postponing their departure in warm weather.


2020 ◽  
Vol 30 (4) ◽  
pp. 634-648
Author(s):  
JULIETA PEDRANA ◽  
KLEMENS PÜTZ ◽  
LUCÍA BERNAD ◽  
SEBASTIÁN MUÑOZ ◽  
ANTONELLA GOROSÁBEL ◽  
...  

SummaryRuddy-headed Goose Chloephaga rubidiceps is the smallest of the five South American sheldgeese and has two separate populations: one sedentary, which resides in the Malvinas/Falkland Islands and one migratory that overwinters mainly in the Pampas region, Argentina and breeds in Southern Patagonia. The Ruddy-headed Goose’s continental population has decreased considerably, and recent estimates indicated that the population size is less than 800 individuals. In Argentina and Chile, this population is categorised as endangered. Understanding migration across vast landscapes is essential for the identification of factors affecting the survival of this endangered population and for the application of effective conservation measures. We aim to provide the first documentation of the complete migration cycle of Ruddy-headed Goose, and to analyse their annual migration in detail, including identification of stop-over, breeding and wintering sites, and to compare migration timing during spring and autumn migration. Adults were captured in the southern Pampas and equipped with solar satellite transmitters in 2015 and 2016. We analysed the influence of season (spring vs autumn migration) on the number and duration of stop-overs, distance travelled and overall migration speed using Generalized Linear Mixed Models. Our results showed that tracked geese used the eastern Patagonian route to reach their breeding grounds and take the same route after breeding. Spring migration was significantly faster than autumn migration, at least based on the number of days spent in their stop-overs. Stop-overs were closer to the final destination, either during spring and autumn migrations, though some of them were not used during subsequent migrations. Our migration cartography for Ruddy-headed Geese, together with the timing and location data, should be used to improve conservation efforts directed at this species and might contribute to the modification of the current status of ‘Least Concern’ under the IUCN criteria.


The Auk ◽  
2006 ◽  
Vol 123 (2) ◽  
pp. 431-437 ◽  
Author(s):  
Jeffrey F. Kelly

AbstractTracking seasonal movements of songbirds is a key step in understanding the annual cycle of migrants. To better understand autumn migration of wood warblers, I analyzed stable-hydrogen isotope ratios of feathers collected from three species captured during stopover at the Bosque del Apache National Wildlife Refuge, New Mexico. To assess the form and strength of the relationship between timing of migration and breeding origins, I regressed stable-hydrogen isotope ratios of feathers against date of capture. These analyses indicated that Orange-crowned Warblers (Vermivora celata) and Common Yellowthroats (Geothlypis trichas) breeding in the southern portion of these species' ranges precede their northern conspecifics in autumn migration. By contrast, Yellow Warblers (Dendroica petechia) from northern breeding sites arrived before more southerly breeding conspecifics. This pattern is similar to that reported previously in Wilson's Warbler (Wilsonia pusilla). These findings suggest that, among wood warblers, (1) timing of autumn migration is often strongly related to breeding location and (2) interspecific variation in the direction of this relationship is large. The direction and strength of these patterns have implications for our understanding of inter- and intraspecific geographic variation in the life histories of migrants.Evidencia de Isótopos Estables Conecta la Geografía de Nidificación con el Momento de la Migración en Especies de Parulidae


The Auk ◽  
2005 ◽  
Vol 122 (4) ◽  
pp. 1070-1085 ◽  
Author(s):  
Jay D. Carlisle ◽  
Gregory S. Kaltenecker ◽  
David L. Swanson

Abstract Intraspecific patterns of autumn migration timing are not well known, particularly in the western United States. Here, we (1) describe autumn migration timing and age ratios of landbird migrants in southwestern Idaho, (2) examine differences in timing among age and sex classes, and (3) demonstrate how prebasic molt strategies affect migration timing differences between age classes. As a group, Neotropical migrants were most common from late July through early September, whereas temperate migrants were most common from mid-September into early October. Proportion of hatch-year birds was 74.5% for all migrants combined and ranged from 33.3% to 100% for individual species. Timing differences between sex classes were detected in only a few species and no general patterns emerged. In 22 of 31 Neotropical and temperate migrants examined, there were significant differences in timing between adults and hatch-year birds. In species in which adults begin fall migration before replacing flight feathers, adults migrated earlier than hatch-year birds. Conversely, in species in which adults molt flight feathers on or near the breeding grounds before departing on fall migration, hatch-year birds migrated earlier than adults in all but one case. Therefore, it appears that molt strategy is a powerful determinant of intraspecific migration timing differences and, to our knowledge, this is the first study to document this pattern among migrant passerines of North America. Estrategias de Muda y Diferencias en el Momento de Migración Otoñal en Migrantes Terrestres en el Suroeste de Idaho


2020 ◽  
Author(s):  
Ellie Roark ◽  
Willson Gaul

ABSTRACTBecause birds are frequently detected by sound, autonomous audio recorders (called automated recording units or ARUs) are now an established tool in addition to in-person observations for monitoring the status and trends of bird populations. ARUs have been evaluated and applied during breeding seasons, and to monitor the nocturnal flight calls of migrating birds. However, birds behave differently during migration stopover than during the breeding season. Here we present a method for using ARUs to monitor land birds in migration stopover habitat.We conducted in-person point counts next to continuously recording ARUs, and compared estimates of the number of species detected and focal species relative abundance from point counts and ARUs. We used a desk-based audio bird survey method for processing audio recordings, which does not require automated species identification algorithms. We tested two methods of using extended duration ARU recording: surveying consecutive minutes, and surveying randomly selected minutes.Desk-based surveys using randomly selected minutes from extended duration ARU recordings performed similarly to point counts, and better than desk-based surveys using consecutive minutes from ARU recordings. Surveying randomly selected minutes from ARUs provided estimates of relative abundance that were strongly correlated with estimates from point counts, and successfully showed the increase in abundance associated with migration timing. Randomly selected minutes also provided estimates of the number of species present that were comparable to estimates from point counts.ARUs are an effective way to track migration timing and intensity in remote or seasonally inaccessible migration stopover habitats. We recommend that desk-based surveys use randomly sampled minutes from extended duration ARU recordings, rather than using consecutive minutes from recordings. Our methods can be immediately applied by researchers with the skills to conduct point counts, with no additional expertise necessary in automated species identification algorithms.


2021 ◽  
Author(s):  
Peter Pyle

Two broad nomenclatures have emerged to describe moult strategies in birds, the "life-cycle" system which describes moults relative to present-day breeding and other life-history events and the Humphrey-Parkes (H-P) system which reflects the evolution of moults along ancestral lineages. Using either system, challenges have arisen defining strategies in migratory species with more than one moult per year. When all or part of two moults occur in non-breeding areas they may fail to be recognized as two moults or have been discriminated temporally, whether feathers are replaced in fall, winter, or spring. But in some cases feather replacement can span the non-breeding period, and this has resulted in an inability to identify inserted moults and to compare moult strategies between species. Furthermore, recent analyses on factors influencing the extent of the postjuvenile or preformative moults have either confined this moult to the summer grounds or presumed that it can be suspended and resumed on winter grounds, which has lead to quite divergent results. Evolutionarily, the timing, extent, and location of moults are very plastic whereas the sequence in which feathers are replaced is comparatively fixed. As, such, I propose taking an evolutionary approach to define moults on the basis of feather-replacement sequences as opposed to timing or location of replacement, including strategies in which moults can overlap temporally. I provide examples illustrating the functionality of a sequence-based definition in three migratory North American passerines that can undergo feather replacement twice in non breeding areas, and I demonstrate how this system can effectively apply to moults in many other passerine and non-passerine species. I recommend that authors studying the evolutionary drivers of moult strategies in migratory birds adopt a sequence-based approach or carefully consider replacement strategies both prior to and following autumn migration.


2012 ◽  
Vol 3 (2) ◽  
pp. 238-251 ◽  
Author(s):  
David G. Krementz ◽  
Kwasi Asante ◽  
Luke W. Naylor

Abstract We used satellite telemetry to study autumn migration timing, routes, stopover duration, and final destinations of mallards Anas platyrhynchos captured the previous spring in Arkansas from 2004 to 2007. Of those mallards that still had functioning transmitters on September 15 (n  =  55), the average date when autumn migration began was October 23 (SE  =  2.62 d; range  =  September 17–December 7). For those mallards that stopped for >1 d during migration, the average stopover length was 15.4 d (SE  =  1.47 d). Ten mallards migrated nonstop to wintering sites. The eastern Dakotas were a heavily utilized stopover area. The total distance migrated per mallard averaged 1,407 km (SE  =  89.55 km; range  =  142–2,947 km). The average time spent on migration per individual between September 15 and December 15 was 27 d (SE  =  2.88 d; range  =  2–84 d). The state where most mallards were located on December 15 was Missouri (11) followed by Arkansas (8), while 5 mallards were still in Canada, and only 8 of 43 females and 0 of 10 males were present in Arkansas. The eastern Dakotas are a heavily utilized migration stopover for midcontinent mallards that may require more attention for migration habitat management. The reasons for so few mallards, especially male mallards, returning to Arkansas the following year deserves further research.


2019 ◽  
Vol 286 (1897) ◽  
pp. 20182821 ◽  
Author(s):  
Martins Briedis ◽  
Silke Bauer ◽  
Peter Adamík ◽  
José A. Alves ◽  
Joana S. Costa ◽  
...  

In many taxa, the most common form of sex-biased migration timing is protandry—the earlier arrival of males at breeding areas. Here we test this concept across the annual cycle of long-distance migratory birds. Using more than 350 migration tracks of small-bodied trans-Saharan migrants, we quantify differences in male and female migration schedules and test for proximate determinants of sex-specific timing. In autumn, males started migration about 2 days earlier, but this difference did not carry over to arrival at the non-breeding sites. In spring, males on average departed from the African non-breeding sites about 3 days earlier and reached breeding sitesca4 days ahead of females. A cross-species comparison revealed large variation in the level of protandry and protogyny across the annual cycle. While we found tight links between individual timing of departure and arrival within each migration season, only for males the timing of spring migration was linked to the timing of previous autumn migration. In conclusion, our results demonstrate that protandry is not exclusively a reproductive strategy but rather occurs year-round and the two main proximate determinants for the magnitude of sex-biased arrival times in autumn and spring are sex-specific differences in departure timing and migration duration.


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