Poxvirus infections have been found in 230 species of wild and domestic birds worldwide in both terrestrial and marine environments. This ubiquity raises the question of how infection has been transmitted and globally dispersed. We present a comprehensive global phylogeny of 111 novel poxvirus isolates in addition to all available sequences from GenBank. Phylogenetic analysis of the Avipoxvirus genus has traditionally relied on one gene region (4b core protein). In this study we expanded the analyses to include a second locus (DNA polymerase gene), allowing for a more robust phylogenetic framework, finer genetic resolution within specific groups, and the detection of potential recombination. Our phylogenetic results reveal several major features of avipoxvirus evolution and ecology and propose an updated avipoxvirus taxonomy, including three novel subclades. The characterization of poxviruses from 57 species of birds in this study extends the current knowledge of their host range and provides the first evidence of the phylogenetic effect of genetic recombination of avipoxviruses. The repeated occurrence of avian family or order-specific grouping within certain clades (e.g., starling poxvirus, falcon poxvirus, raptor poxvirus, etc.) indicates a marked role of host adaptation, while the sharing of poxvirus species within prey-predator systems emphasizes the capacity for crossspecies infection and limited host adaptation. Our study provides a broad and comprehensive phylogenetic analysis of the Avipoxvirus genus, an ecologically and environmentally important viral group, to formulate a genome sequencing strategy that will clarify avipoxvirus taxonomy.

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Shortage of breeding sites is an important limiting factor of bird populations. Artificial breeding platforms, nest-boxes or man-made twig nests often present solutions with remarkable results, however long-term sustainability of these populations remains to be resolved. Furthermore, the question whether the inference of results of studies conducted on birds breeding in artificial breeding sites can be generalized to other populations, still remains open. Here we present the history, and the results of a 20 year old (1995-2015) nest-box programme initiated to increase potential breeding possibilities of Red-footed Falcons in an area, where nest-site shortage was a severe limiting factor. We show how various other species (Jackdaws, Kestrels and Long-eared Owls) have utilized these resources, and present descriptive statistics on their reproductive performance. Analysing the data of a total of 1432 breeding attempts, we show that Red-footed Falcons have similar clutch sizes, and nesting success (i.e. ratio of nests with at least on fledgling), however fledging success (ratio of the number of eggs/fledged nestlings) was different in artificial nest-boxes. When we excluded closed box types from artificial nests, this difference was not apparent. In case of Kestrels (n=1626 breeding attempts) clutch size was significantly higher in artificial nests, while we found no difference in fledging or nesting success. When only comparing open boxes to natural nests, the difference in clutch size was no longer significant. We also analysed the effect of nest box design on reproductive parameters of the two species using regression trees. Inter annual effects were the most important in shaping clutch size and fledging rate of both falcon species, however we also found nest-box design effects, but only in Red-footed Falcons. In years when mean clutch size was high, these birds had lower clutch size in an older, darker nest-box type compared to an alternative design, and to open boxes. However, fledging rate in the same years was lower for both open boxes and older nest-boxes. We conclude that artificial colonies are an important and successful tool in Red-footed Falcon conservation, and that the breeding parameters measured in artificial colonies depend on nest-box design. We present correlative evidence that closed boxes have a significant positive species specific effect on reproduction, probably due to their protection against weather. We also show that birds may have a preference for a certain nest-box design, and that the breeding success in the less favoured box type may be similar to that in open nests. We recommend that future studies incorporate nest-type and nest-box design effects in all comparisons made on reproductive performance in case of Red-footed Falcons and Kestrels.

The Red-footed Falcon is a facultatively colonial species that exploits rookeries, artificial nest-box colonies and solitary corvid nests for breeding. Moreover, the remain gregarious in the post breeding period using communal roost sites prior to migration. We developed and implemented a survey protocol to allow to precisely estimate the number of breeding pairs in all three breeding types and to assess large scale spatio-temporal changes in roost site usage. Our results show that the lowest number of breeding pairs (558) was in 2006. However, in 2014 the number of pairs showed a two fold increase, mainly due to a large scale nest-box programme implemented in the past decade. We identified a total of 105 roost sites throughout the country. The number of birds peaked in the second week of September in the past 10 years. We formulate a recommendation to maintain population monitoring efficiency by reducing the frequency of full surveys to 5 years and using designated study areas to control for temporal trends in between.

Fehérvári et al.: Modeling habitat selection of the red-footed falcon (Falco vespertinus)-59 - Abstract. Due to a severe population decline and shrinkage of distribution range in the past decades, the red-footed falcon has gained top priority in both worldwide and Hungarian nature conservation. As a facultative colonial breeder, in Hungary, this species predominantly nests in rookeries. The number of rooks (Corvus frugilegus) has also dramatically fallen recently, but population decline did not affect the large scale breeding distribution of this species. In our study we analyzed the presence of red-footed falcons at a colony in the case of current and historical breeding ranges based on landscape scaled habitat variables. We used a potential colony home-range size, estimated from observed home-range sizes in order to determine the scale of influential habitat variables. According to our results, the primary cause of the observed range shift is the urbanization of rooks in definable regions of Hungary. The ratio of forests and open water surfaces within the potential home-range had negative, while the ratio of grasslands had a positive effect on the probability of red-footed falcon presence. None of our models predicted red-footed falcon presence at colonies outside the current breeding range, suggesting that a probable increase in redfooted falcon population numbers will not be accompanied by the expansion of the current breeding range.