Genetic assessment of the subspecies status of Eurasian Magpies (Pica pica) in Norway

Based on phenotypes, two subspecies of Eurasian Magpies (Pica pica) are recognized in Norway, with nominate P. p. pica in southern Norway, and P. p. fennorum in northern Norway. In this study, we investigated whether there are genetically distinct groups of Magpies in Norway, which can be considered in the discussion of the subspecies status. We collected DNA from 61 Magpies from seven locations in Norway, and measured genetic diversity using two types of markers: mitochondrial DNA sequences and microsatellites. Genetic differentiation among the Magpies was extremely low. Most of the variance was within populations, and th e population identity and the putative subspecies border did not explain the genetic variance among the samples. Although microsatellite markers indicated genetic differentiation, the pattern was not consistent with the geographic locations of the sampling sites. Mismatch analysis suggested that the Magpie populations in Norway were formed by rapid expansion. Our results suggest that all the Magpies in Norway have originated from the same refugia after the last glaciation, their colonization in Norway happened quickly, and that the subspecies status of Magpies in Norway needs to be reconsidere

Microbial abundance on the eggs of a passerine bird and related fitness consequences between urban and rural habitats

<div><p>Urban environments present novel and challenging habitats to wildlife. In addition to well-known difference in abiotic factors between rural and urban environments, the biotic environment, including microbial fauna, may also differ significantly. In this study, we aimed to compare the change in microbial abundance on eggshells during incubation between urban and rural populations of a passerine bird, the Eurasian Magpie (<i>Pica pica</i>), and examine the consequences of any differences in microbial abundances in terms of hatching success and nestling survival. Using real-time PCR, we quantified the abundances of total bacteria, <i>Escherichia coli/Shigella</i> spp., surfactin-producing <i>Bacillus</i> spp. and <i>Candida albicans</i> on the eggshells of magpies. We found that urban magpie eggs harboured greater abundances of <i>E</i>. <i>coli/Shigella</i> spp. and <i>C</i>. <i>albicans</i> before incubation than rural magpie eggs. During incubation, there was an increase in the total bacterial load, but a decrease in <i>C</i>. <i>albicans</i> on urban eggs relative to rural eggs. Rural eggs showed a greater increase in <i>E</i>. <i>coli/Shigella</i> spp. relative to their urban counterpart. Hatching success of the brood was generally lower in urban than rural population. Nestling survival was differentially related with the eggshell microbial abundance between urban and rural populations, which was speculated to be the result of the difference in the strength of the interaction among the microbes. This is the first demonstration that avian clutches in urban and rural populations differ in eggshell microbial abundance, which can be further related to the difference in hatching success and nestling survival in these two types of environments. We suggest that future studies on the eggshell microbes should investigate the interaction among the microbes, because the incubation and/or environmental factors such as urbanization or climate condition can influence the dynamic interactions among the microbes on the eggshells which can further determine the breeding success of the parents.</p></div

Changes in microbial abundance.

<p>Comparisons of changes in the microbial abundance on the naturally incubated magpie eggs between rural (n = 14 nests) and urban (n = 17 nests) populations; (a) total bacteria, (b) <i>Escherichia coli/Shigella</i> spp., (c) surfactin-producing <i>Bacillus</i> spp., and (d) <i>Candida albicans</i>. Paired responses of each nest (connected circles) are given along with the average aligned ranks (circles with error bars). Open circles (connected with solid lines) and closed circles (connected with dashed lines) denote the responses of the rural and urban populations respectively. Units of Y axis values for the microbial abundance are log₁₀ (copy numbers of microbes) per cm² of the eggshells for (a), (b) and (c), and log₁₀ (copy numbers+1) per cm² of the eggshells for (d). Error bars for the aligned ranks denote standard errors. Significance level of the comparison of aligned ranks is given as “*” for 0.01</p

Microbial abundance, hatching success and nestling survival.

<p>The relationships between population and microbial abundance on the hatching success and the nestling survival.</p

Microbes and primer sequences.

<p>Target microbes and the primer sequences used in this study.</p

Changes in microbial abundance.

<p>Results of Wilcoxon signed-rank tests on the changes in microbial loads. The change in microbial loads was calculated by subtracting microbial load at day 3 from that at day 18; thus positive signed-rank value mean increases in microbial loads during incubation and vice versa.</p