No abstract

During late summer and early autumn in temperate zones of the Northern Hemisphere, thousands of bats gather at caves, mainly for the purpose of mating. We demonstrated that this swarming behavior most probably leads not only to breeding among bats of the same species but also interbreeding between different species. Using 14 nuclear microsatellites and three different methods (the Bayesian assignment approaches of STRUCTURE and NEWHYBRIDS and a principal coordinate analysis of pairwise genetic distances), we analyzed 375 individuals belonging to three species of whiskered bats (genus Myotis) at swarming sites across their sympatric range in southern Poland. The overall hybridization rate varied from 3.2 to 7.2%. At the species level, depending on the method used, these values ranged from 2.1–4.6% in M. mystacinus and 3.0–3.7% in M. brandtii to 6.5–30.4% in M. alcathoe. Hybrids occurred in about half of the caves we studied. In all three species, the sex ratio of hybrids was biased towards males but the observed differences did not differ statistically from those noted at the population level. In our opinion, factors leading to the formation of these admixed individuals and their relatively high frequency are: i) swarming behaviour at swarming sites, where high numbers of bats belonging to several species meet; ii) male-biased sex ratio during the swarming period; iii) the fact that all these bats are generally polygynous. The highly different population sizes of different species at swarming sites may also play some role. Swarming sites may represent unique hybrid hotspots, which, as there are at least 2,000 caves in the Polish Carpathians alone, may occur on a massive scale not previously observed for any group of mammal species in the wild. Evidently, these sites should be treated as focal points for the conservation of biodiversity and evolutionary processes.

No abstract

We examined selected external characteristics and measurements of Pipistrellus k. kuhlii and P. k. lepidus representatives from the Balkans and Central Europe, whose ranges have rapidly expanded over the past few decades. We also sequenced and analysed two mitochondrial (16S and COI genes) and one nuclear (RAG2) markers of these two bat morphotypes to determine haplotype diversity and distribution patterns with a wider geographic perspective. We found that bats of the two taxa differed markedly with regard to the overall body coloration, size (P. k. lepidus is larger than P. k. kuhlii), extent and shape of the pale wing margin, and penis coloration, a finding which seems to be of diagnostic value, similarly to other Pipistrellus species. No polymorphism in RAG2 marker was found, but in both mtDNA markers we detected different haplotypes characteristic for both taxa, corresponding to morphological and morphometric patterns established in this study. Our genetic analysis results confirmed a clear division into two phylogenetic lineages and may indicate their allopatric speciation and a very recent simultaneous expansion to the Balkans and Central Europe from the Mediterranean region (P. kuhlii/deserti) and south-west Asia across eastern Europe (P. k. lepidus). We also show that P. k. lepidus distribution is wider than previously reported, and that the ranges of P. k. lepidus and P. k. kuhlii have already contacted in Central Europe.

No abstract

We investigated the occurrence and pathogenicity of Beauveria spp. (Hypocreales: Cordycipitaceae) in forest soils in Poland, in outbreak areas of cockchafers (Coleoptera: Scarabaeidae): Melolontha melolontha L. and M. hippocastani F. We also examined the occurrence of Beauveria in relation to soil pH. Beauveria spp. isolates were characterised at species and genotype levels using ITS and microsatellite markers. Beauveria spp., which were detected at over 80% of sites, were sensitive to pH, preferring neutral or alkaline soils. This suggests that the acidity of forest soils in Poland can affect their efficacy as biological control agents (BCAs). B. brongniartii (Sacc.) Petch as a pathogen of cockchafers occurred at 41% of sites, but often at densities below the threshold values for infection, and it infected only 1.3% of cockchafer grubs. Our results suggest that B. brongniartii genotype isolated from cockchafers in forest soils can potentially expand the pool of BCAs in this environment.

No abstract

Summary Real‐time PCR assays based on the TaqMan system and using ITS sequences were developed for the identification of Phytophthora species, including P. cactorum, P. megasperma, P. plurivora, P. pseudosyringae and P. quercina, all of which are currently causing significant damage to roots of forest trees in both managed stands and natural ecosystems. Total genomic DNA was extracted from mycelia of aforementioned Phytophthora isolates. Species‐specific primers for P. cactorum, P. megasperma, P. plurivora, P. pseudosyringae and P. quercina were designed based on ITS sequences of rDNA. The amplification efficiency of target DNA varied from 93.1% (P. pseudosyringae) to 106.8% (P. quercina). The limit of the detection was calculated as 100 – 1,000 fg DNA, depending on the Phytophthora species. In mixed soil samples, all Phytophthora species were detected for Ct values shifted by 0.7 – 2.1 cycles. Based on these real‐time PCR assays we were able to identify the five Phytophthora species. These techniques will be of value in the identification of these pathogens, which may cause up to 80 – 90% fine root loss in oak stands.