290 research outputs found

    Development of lateralization of the magnetic compass in a migratory bird

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    The magnetic compass of a migratory bird, the European robin (Erithacus rubecula), was shown to be lateralized in favour of the right eye/left brain hemisphere. However, this seems to be a property of the avian magnetic compass that is not present from the beginning, but develops only as the birds grow older. During first migration in autumn, juvenile robins can orient by their magnetic compass with their right as well as with their left eye. In the following spring, however, the magnetic compass is already lateralized, but this lateralization is still flexible: it could be removed by covering the right eye for 6 h. During the following autumn migration, the lateralization becomes more strongly fixed, with a 6 h occlusion of the right eye no longer having an effect. This change from a bilateral to a lateralized magnetic compass appears to be a maturation process, the first such case known so far in birds. Because both eyes mediate identical information about the geomagnetic field, brain asymmetry for the magnetic compass could increase efficiency by setting the other hemisphere free for other processes

    AN EXPERIMENT ON THE ENDING OF AUTUMN MIGRATION IN STARLINGS

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    Polyphony in Architecture

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    Based on interviews with a number of architects and managers from a wide range of organizations, we characterize how architecture is perceived in practice. We identify three groups of organizations that differ with respect to their level of architectural thinking and the alignment of business and IT on architectural issues. Analysis of the interviews further indicates that these three groups differ in the architecture aspects and critical success factors they emphasize. Our results provide a starting point for assessing architecture maturity and alignment within organizations, and can be used to help harmonize different architectural tunes played within organizations

    Low migratory connectivity is common in long-distance migrant birds

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    TF benefitted from a Natural Environment Research Council studentship (student number 6109659) and AF from a Natural Environment research grant NE/K006321/1.1. Estimating how much long-distance migrant populations spread out and mix during the non-breeding season (migratory connectivity) is essential for understanding and predicting population dynamics in the face of global change. 2. We quantify variation in population spread and inter-population mixing in long- distance, terrestrial migrant land-bird populations (712 individuals from 98 populations of 45 species, from tagging studies in the Neotropic and Afro-Palearctic flyways). We evaluate the Mantel test as a metric of migratory connectivity, and explore the extent to which variance in population spread can be explained simply by geography. 3. The mean distance between two individuals from the same population during the non- breeding season was 743 km, covering 10–20% of the maximum width of Africa / South America. Individuals from different breeding populations tended to mix during the non-breeding season, though spatial segregation was maintained in species with relatively large non-breeding ranges (and, to a lesser extent, those with low population-level spread). A substantial amount of between-population variation in population spread was predicted simply by geography, with populations using non- breeding zones with limited land availability (e.g. Central America compared to South America) showing lower population spread. 4. The high levels of population spread suggest that deterministic migration strategies are not generally adaptive; this makes sense in the context of the recent evolution of the systems, and the spatial and temporal unpredictability of non-breeding habitat. 5. The conservation implications of generally low connectivity are that the loss (or protection) of any non-breeding site will have a diffuse but widespread effect on many breeding populations. Although low connectivity should engender population resilience to shifts in habitat (e.g. due to climate change), we suggest it may increase susceptibility to habitat loss. We hypothesise that because a migrant species cannot adapt to both simultaneously, migrants generally may be more susceptible to population declines in the face of concurrent anthropogenic habitat and climate change.Publisher PDFPeer reviewe

    Rethinking classic starling displacement experiments : evidence for innate or for learned migratory directions?

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    Funding for the present work came from the Spinoza Premium 2014 awarded to TP by the Netherlands Organization for Scientific Research (NWO), with supplementary funding from an anonymous donor, the Gieskes-Strijbis Fonds and the Ubbo Emmius Fonds of the University of Groningen. TO was supported by Rubicon a grant from NWO (ref. 019.172EN.011)In an attempt to encourage the discourse on sources of individual variation in seasonal migration patterns and the microevolution of bird migration, we here critically examine the published interpretations of a now classic displacement study with starlings Sturnus vulgaris. Based on the ring recoveries after experimental displacement towards the south and southeast of Dutch capture sites of over 18 000 hatch‐year and older starlings, in a series of analyses published in Ardea from 1958 to 1983, A. C. Perdeck established that displaced starlings showed appropriately changed orientations only when they were experienced. During both southward and northward migration, released adults navigated to an apparently previously learned goal (i.e. the wintering or the breeding area) by showing appropriately changed orientations. Juveniles showed appropriate directions when returning to the breeding grounds. In contrast, during their first southward migration displaced juveniles carried on in the direction (and possibly the distance) expected for their release at the Dutch capture site. From the mid‐1970s this work has become cited as evidence for starlings demonstrating ‘innate’ migratory directions. If the definition of innateness is ‘not learned by the individual itself’, then there is a range of non‐innate influences on development that are not ruled out by Perdeck's experimental outcomes. For example, young starlings might have carried on in the direction that they learned to migrate before being caught, e.g. by observing the migratory directions of experienced conspecifics. We argue that, despite over 60 citations to Perdeck as demonstrating innate migratory directions, the jury is out.Publisher PDFPeer reviewe

    No experimental evidence for local competition in the nestling phase as a driving force for density-dependent avian clutch size

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    1. In birds, local competition for food between pairs during the nestling phase may affect nestling growth and survival. A decrease in clutch size with an increase in breeding density could be an adaptive response to this competition. To investigate whether breeding density causally affected the clutch size of great tits (Parus major), we manipulated breeding density in three out of eight study plots by increasing nest-box densities. We expected clutch size in these plots to be reduced compared to that in control plots. 2. We analysed both the effects of variation in annual mean density (between-year comparisons) and experimental density (within-year comparison between plots) on clutch size variation, the occurrence of second broods and nestling growth. We examined within-female variation in clutch size to determine whether individual responses explain the variation over years. 3. Over the 11 years, population breeding density increased (from 0·33 to 0·50 pairs ha–1) while clutch size and the occurrence of second broods decreased (respectively from 10·0 to 8·5 eggs and from 0·39 to 0·05), consistent with a negative density-dependent effect for the whole population. Nestling growth showed a declining but nonsignificant trend over years. 4. The decline in population clutch size over years was primarily explained by changes occurring within individuals rather than selective disappearance of individuals laying large clutches. 5. Within years, breeding density differed significantly between manipulated plots (0·16 pairs ha–1 vs. 0·77 pairs ha–1) but clutch size, occurrence of second broods and nestling growth were not affected by the experimental treatment, resulting in a discrepancy between the effects of experimental and annual variation in density on reproduction. 6. We discuss two hypotheses that could explain this discrepancy: (i) the decline in breeding performance over time was not due to density, but resulted from other, unknown factors. (ii) Density did cause the decline in breeding performance, but this was not due to local competition in the nestling phase. Instead, we suggest that competition acting in a different phase (e.g. before egg laying or after fledgling) was responsible for the density effect on clutch size among years.

    Geographical origin of dabbling ducks wintering in Iberia: Sex differences and implications for pair formation

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    Los humedales ibéricos naturales y antropógenos del sur de Europa son bien conocidos por sustentar a un gran número de aves migratorias acuáticas del Palaearctico en cada invierno. Sin embargo, la información sobre el origen geográfico de los patos de humedal que pasan el invierno en estos espacios es escasa y se limita principalmente a datos de sonar. Aquí, hemos utilizado marcadores isotópicos para determinar el origen geográfico de machos y hembras de Pintails septentrional, Anas acuta y Anas crecca euroasiática en Extremadura, en el interior de la península Ibérica, sitio clave para invernar los patos de humedal. Además, hemos instalado seis etiquetas GPSGSM en Pintails septentrional para complementar los datos derivados del análisis de isótopos estables. La mayoría (> 70%) de los Pintails septentrional, dentro del primer año calendario, fueron asignados a regiones situadas por encima de los 55° N, volando 2600-5600 km desde sus regiones de procedencia a Extremadura. Los valores promedio de δ2Hf variaron significativamente entre macho y hembra de Pintails septentrional, sugiriendo que los sexos tienen diferentes orígenes geográficos. Los datos de los adultos etiquetados Pintails septentrional apoyan los datos isotópicos, un macho volando más de 5000 km de la costa de la mar Pechora (Rusia). La mayoría (> 70%) de los Teal euroasiáticos, dentro del primer año calendario, fueron asignados a la región situada entre 48° y 60° N y viajaron 1500-4500 km para llegar en Extremadura. Los machos y hembras de Cerceta euroasiáticos mostraron diferencias marginales en valores promedio de δ2Hf. En patos de humedal migratorios, el emparejamiento se produce normalmente en las zonas de invernada, y los patos en su primer invierno pueden reproducirse en la primavera siguiente. Para Pintails septentrional, la formación de parejas en Extremadura podría suceder entre individuos con diferentes orígenes geográficos, lo que podría contribuir a la variabilidad genética de su descendencia.Natural and anthropogenic Iberian wetlands in southern Europe are well known for supporting large numbers of migratory Palaearctic waterbirds each winter. However, information on the geographical origin of dabbling ducks overwintering in these wetlands is scarce and mostly limited to data from ringing recoveries. Here, we used intrinsic isotopic markers to determine the geographical origin of male and female Northern Pintails Anas acuta and Eurasian Teal Anas crecca in Extremadura, inland Iberia, a key site for overwintering dabbling ducks. Additionally, we fitted six Northern Pintails with GPSGSM tags to complement the data derived from stable isotope analysis. Most (> 70%) first calendar-year Northern Pintails were assigned to regions above 55°N, flying 2600–5600 km from their main natal regions to Extremadura. Mean values of δ2Hf varied significantly between male and female Northern Pintails, suggesting that the sexes had different geographical origins. Data from tagged adult Northern Pintails supported the isotopic data, one male flying more than 5000 km to the coast of the Pechora Sea (Russia). Most (> 70%) first calendar-year Eurasian Teal were assigned to the region between 48° and 60°N, travelling 1500–4500 km to arrive in Extremadura. Male and female Eurasian Teal showed marginal differences in mean values of δ2Hf. In migratory dabbling ducks, pairing typically occurs on the wintering grounds, and ducks in their first winter can breed the following spring. For Northern Pintails, pair formation in Extremadura could occur between individuals with different geographical origins, which could contribute to the genetic variability of their offspring.Trabajo patrocinado por: Junta de Extremadura. Proyecto PRI 09C128 Gobierno de Extremadura y Fondos FEDER. Ayuda GR10174 Confederación Hidrográfica del Guadiana (Ministerio de Medio Ambiente). Ayuda financierapeerReviewe

    (Micro)evolutionary changes and the evolutionary potential of bird migration

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    Seasonal migration is the yearly long-distance movement of individuals between their breeding and wintering grounds. Individuals from nearly every animal group exhibit this behavior, but probably the most iconic migration is carried out by birds, from the classic V-shape formation of geese on migration to the amazing nonstop long-distance flights undertaken by Arctic Terns Sterna paradisaea. In this chapter, we discuss how seasonal migration has shaped the field of evolution. First, this behavior is known to turn on and off quite rapidly, but controversy remains concerning where this behavior first evolved geographically and whether the ancestral state was sedentary or migratory (Fig. 7.1d, e). We review recent work using new analytical techniques to provide insight into this topic. Second, it is widely accepted that there is a large genetic basis to this trait, especially in groups like songbirds that migrate alone and at night precluding any opportunity for learning. Key hypotheses on this topic include shared genetic variation used by different populations to migrate and only few genes being involved in its control. We summarize recent work using new techniques for both phenotype and genotype characterization to evaluate and challenge these hypotheses. Finally, one topic that has received less attention is the role these differences in migratory phenotype could play in the process of speciation. Specifically, many populations breed next to one another but take drastically different routes on migration (Fig. 7.2). This difference could play an important role in reducing gene flow between populations, but our inability to track most birds on migration has so far precluded evaluations of this hypothesis. The advent of new tracking techniques means we can track many more birds with increasing accuracy on migration, and this work has provided important insight into migration's role in speciation that we will review here

    Collective animal navigation and migratory culture: From theoretical models to empirical evidence

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    Animals often travel in groups, and their navigational decisions can be influenced by social interactions. Both theory and empirical observations suggest that such collective navigation can result in individuals improving their ability to find their way and could be one of the key benefits of sociality for these species. Here, we provide an overview of the potential mechanisms underlying collective navigation, review the known, and supposed, empirical evidence for such behaviour and highlight interesting directions for future research. We further explore how both social and collective learning during group navigation could lead to the accumulation of knowledge at the population level, resulting in the emergence of migratory culture

    Sea buckthorn berries <i>Hippophae rhamnoides</i> L. predict size and composition of a great tit population <i>Parus major</i> L.

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    In seasonal environments variation in food abundance in the non-breeding season is thought to affect songbird population dynamics. In a unique tit-sea buckthorn berry system we can estimate the berry abundance and both the tit consumption and population dynamics. Six hundred nest boxes were available to great and blue tits Cyanistes caeruleus for breeding in spring and roosting in winter. We followed the dynamics including the recapture histories of individually marked great tits from 2008 to 2014. In each year we estimated 1) the winter sea buckthorn berry availability, 2) an index of berry consumption in December based on the colour of the faeces of roosting birds, 3) the number of breeding great and blue tits, 4) both recapture probability and the return rate of the great tits and 5) immigration rates. December berry abundance positively predicted the number of breeding pairs of both species in the subsequent season and great tit return rates in the second half of the winter. There was support for a sex specific berry effect on the adult return rate in the great tit: female return rate was associated less strongly to berry abundance than male return rate. This skewed the sex ratio of the local breeders in the following breeding season. Intriguingly, annual berry consumption in December was not related to berry abundance, and individuals consuming more berries tended to have slightly lower return rates. Reproductive rate was not related to berry abundance. There was hardly support for a relation between immigration rates of first year breeders and berry abundance. Taken together these results imply that berry stock not only affected population size but also the population composition through sex specific exchange with the surroundings. Since population density covaried with berry abundance, density dependent effects provide an alternative explanation for the patterns observed
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