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We tested 24 microsatellite markers for the red-breasted flycatcher, Ficedula parva, using the primers for the PCR reaction described for other species from genus Ficedula. The amplification efficiency, specificity of the products, and polymorphism of cross-amplified microsatellites were determined based on the genotypes of 65 adult males from a natural population breeding in Białowieża Forest (Eastern Poland). Based on obtained results, we identified 9 highly polymorphic microsatellites, consistently amplifying in majority of individuals. Among those markers between 4 and 26 alleles per locus (mean 15.4) were found and the observed heterozygosity ranged from 0.393 to 0.939. The majority of loci (except for Fhy350 and Fhy458) were in Hardy-Weinberg equilibrium. Accordingly, the values of F IS did not significantly differ from zero 0, except for the locus Fhy350. We suggest that this locus could be loaded with high frequency of null alleles. The polymorphic information content (PIC) for the selected loci set was high and in all cases exceeded 0.82. In addition, we calculated, for each locus, the probability of excluding an improper parent. In majority of loci this parameter distinctly exceeded 0.5. These results demonstrate that tested microsatellite markers can be used to estimate the genetic variability within- and between populations and to establish paternity and parenthood in red-breasted flycatcher populations.
Mammals are common predators on bird nests. However, their species identity frequently remains unknown. Here we present long-term data (1975–2005) from a central European woodland on the predatory effect of three dormice species (Rodentia, Gliridae) on cavity-nesting birds. Dormice are mostly frugivorous during the active late-summer season, but shortly after they terminate hibernation, they frequently depredate cavity-nesting-bird nests. The seven bird species studied, lost on average between 2.9 to 18.4% of their broods. MigratoryFicedula flycatchers suffered the highest brood losses, while the residentParus titmice and the nuthatchSitta europaea had much lower brood losses. The three dormice species differed significantly in their predatory effect during different avian breeding stages. The edible dormouseGlis glis (Linnaeus, 1766) depredated both eggs and nestlings equally, while the common dormouseMuscardinus avellanarius (Linnaeus, 1758) and the forest dormouseDryomys nitedula (Pallas, 1778) destroyed more nests during egg laying and the incubation period. Among adult birds, females were taken more frequently by dormice than males. Among avian species, adultFicedula flycatchers were more often depredated than the titmice and nuthatch. Our study provided further evidence, that among the traditional studies on the costs of reproduction, parental mortality at the nests needs to be considered and that incubating or brooding females might be under higher predation risk than the males.
Our aim was to determine dynamics in a population of tawny owls Strix aluco over 15-year period, in relation to year-to-year variation in environmental conditions. The research was carried out in a habitat mosaic of fields and forest in central Poland, over the 2004–2018 period. Numbers of pairs (territories) were established by the standard playback survey technique supplemented by searches for nest sites. The selected environmental factors studied in parallel were the acorn production, density changes in field and forest rodents, meteorological conditions in winter and density of martens (Martes spp.). At the start of the study period 20 nest boxes designed for tawny owls were placed out in the study area. This number was enlarged by additional 27 nest boxes placed in 2012. The number of owls in the area remained stable – in the range of 26–29 pairs, despite changes in nesting sites availability. However, moderate influence of rodent density and winter conditions on population abundance was detected. Also, peak in the rodent population coincided with greater clutch size and numbers of young owls reared. Densities of martens remained relatively stable throughout the study period, and there were no reported cases of these carnivores killing tawny owls, despite the former taking shelter in the owl-boxes.
Before breeding, hole nesting birds face the problem of the presence of old nest material from previous seasons in their nest sites. This material fills the cavity, making it shallower, resulting in greater brood vulnerability to predators, as well as creating good conditions for ectoparasite development. As a consequence, this may negatively affect many breeding parameters of hole nesters. However, adult birds may compensate the effect of blood sucking ectoparasites by increasing their feeding rates. It is known that the European Starling Sturnus vulgaris L. can deepen its nest site by removing old nest material. Therefore, a study was conducted to find out whether the presence of old nest material influences ectoparasite abundance in newly built nests, reproductive parameters, as well as nestlings’ body parameters and feeding rates in this species. An experiment with nestboxes was carried out in two forested areas. Two groups of nestboxes were prepared – one contained old nests from the previous breeding season, and the other group was cleaned with old nests removed. During the breeding season, data on Starling reproduction were collected, i.e. laying dates, clutch size and number of fledglings. Nestling body parameters were measured on the 6th, 9th, 13th and 17th days of their lives. On the 10th and 15th days of nestling life, the number of feedings was counted over a period of 30 minutes. Nests were collected and analyzed for the presence of ectoparasites. It was found that the average number of ectoparasites, both fleas and mites, was greater in nests built on old nest material, and that this number was highly correlated. In further analysis, two possible effects on reproductive output were investigated separately: the presence of old nest material and the abundance of ectoparasites. Clutch size and number of fledglings were smaller in broods from nestboxes containing old nest material, but there was no such relationship to laying dates and nestlings’ body parameters (weight, tarsus and wing length). The number of feeding trips on the 10th day of nestling life was higher in “cleaned” nestboxes, but a similar level was achieved by the 15th day in both groups of nestboxes. It was found that ectoparasite abundance did not influence any of the studied parameters of Starling reproduction, i.e. breeding, nestlings’ physical condition or number of feedings. This confirmed earlier findings that ectoparasite infestation at a natural level does not affect Starlings’ breeding. It seems that the negative effect of the presence of old nest material in nest sites is connected to the costs of site preparation and old nest material removal, which are borne by the females.
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