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Craseonycteris thonglongyai (Chiroptera: Craseonycteridae), an enigmatic taxon which shares morphological traits with both Rhinopomatidae and Emballonuridae was for the first time investigated with the aid of molecular phylogenetic techniques. Three methods of phylogenetic inference, parsimony, maximum-likelihood, and Bayesian phylogenetics were used. Based on 402 bp of DNA sequence from the mitochondrial cytochrome b gene, placement of Craseonycteridae within the superfamily Rhinolophoidea was demonstrated. Our results also suggest close proximity of Craseonycteridae to Hipposideridae rather than to Rhinopomatidae, close relationships between Megadermatidae and Rhinolophidae, sister group position of Pteropodidae to Rhinolophoidea, and closer affiliation of Nycteridae with the infraorder Yangochiroptera. Spectral analysis was in agreement with all these outcomes except for closer relationships of Craseonyeteris with Rhinopomatidae.
The distribution of pipistrelles of the Pipistrellus pipistrellus complex (= P. pipistrellus s.l.) reaches only marginally the African continent. These bats are known only from a narrow belt of the Mediterranean zone in Maghreb and from NE Libya. We analysed museum specimens of African populations of P. pipistrellus s.l. using both morphologic and genetic techniques and compared them with Eurasian specimens of the complex. The African representatives of P. pipistrellus complex include two morphologically, genetically and geographically distinct populations. One of them inhabits the Mediterranean part of Cyrenaica, Libya. Belonging to the P. pygmaeus genetic lineage, these bats are represented by larger and more rusty coloured individuals with large massive rostrum and canines. In morphologic traits, this population differs significantly from all Western Palaearctic populations of the P. pipistrellus complex. These bats differ by about 6–7% in genetic distance from P. pygmaeus s. str. Within the P. pygmaeus lineage Libyan bats seem to be unique in their echolocation calls: the maximum energy of terminal frequencies was recorded at about 45 kHz. We consider the Libyan pipistrelles to represent a separate species, Pipistrellus hanaki sp. nov. Another distinct African pipistrelle population inhabits the Mediterranean parts of NW African countries, Morocco, Algeria and Tunisia. Individuals from the latter population are small and somewhat darker members of the P. pipistrellus genetic lineage, with relatively short and narrow mesial part of rostrum. Although both morphological and genetic differences between this population and Eurasian P. pipistrellus s. str. were found (genetic distance about 3–5%), they are probably not sufficient for the separation of this form at the specific level. However, the differences from European samples show rather not a cline character and therefore potential subspecific level of NW African P. pipistrellus has to be taken into consideration.
With the recent and continuing discovery of further cryptic bat species, it is essential to find morphological species discriminating characters. Pipistrellus pipistrellus (common pipistrelle) and Pipistrellus pygmaeus (soprano pipistrelle) have been recognized as separate species since 1997, but no reliable morphological species discriminating trait has yet been found. The most commonly used morphological species discrimination traits are ‘wing vein’ pattern and shape and color of the penis, but these have not been validated on sets of genetically identified specimens. The baculum (os penis) has long been used successfully in species discrimination in bats and other mammals. In this study, we tested the reliability of the established traits and demonstrated how to reliably separate the common pipistrelle and the soprano pipistrelle by simple baculum measurements. The bacula of museum specimens of these two species and of Pipistrellus hanaki were imaged with high-resolution microCT. Several measurements were taken on the size-calibrated volume images, and their value for species discrimination was tested by discriminant analysis with leave-one-out cross validation. We showed that P. pipistrellus and P. pygmaeus specimens can be discriminated by measuring the projected length, height, and width of the baculum (n = 48; all but one classified correctly). Geometric morphometrics was used to analyze and locate variations in baculum shape. Principal component analysis of baculum variation was not sufficient to separate these species. Most of the interspecific variation in baculum shape can be found in the proximal third (the base) of the baculum, and most individual variation can be observed in lateral view, especially in the dorsoventral curve. Quantitative details of morphology are becoming more important to distinguish cryptic species and understand their phylogeographic distributions. The simple baculum measurements can be used to classify single specimens and could be taken without microCT, on a resected baculum.
Miniopterus schreibersii is a complex, polytypic species group with a wide distribution ranging from Northern Africa, Southern Europe to Asia, the Solomon Islands and Northern Australia. Two subspecies previously recognized in Turkey, M. s. schreibersii and M. s. pallidus, differ significantly in nuclear and mitochondrial DNA, and in morphology. Until now, the distribution records of M. s. schreibersii and M. s. pallidus showed that they were allopatric and hence even though there was clear morphological and genetic differentiation between the two taxa, whether they represented separate species or subspecies was still not determined with certainty. Here we present the first data on syntopic occurrence of both forms in three caves in south-eastern Turkey. We show that the three caves host individuals of both taxa by using mitochondrial DNA, nuclear DNA and morphometric analyses. These findings provide the final line of evidence to date, for designation of M. s. schreibersii and M. s. pallidus as two separate species, M. schreibersii and M. pallidus. This will raise the number of species in the Eurobats agreement area from 45 to 46.
Between 2001 and 2008, we recorded Myotis alcathoe at nine sites within three distant areas in the Czech Republic. The species identification was confirmed with cyt b sequences and four distinct haplotypes were identified. All the localities exhibit surprisingly uniform habitat characteristics: (1) old full-grown oak-hornbeam forests, with (2) numerous large trees in advanced stages of decay are present, and (3) a very small to large water bodies and/or patches of riparian vegetation surrounded by the forest. Using radiotracking techniques, we discovered 27 day roosts of M. alcathoe, located mostly in big oak, birch and lime trees inside extensive forest stands. All roosts were fissures or small cavities in a tree trunk and in branches in the canopies, some 16 m above the ground. Bats preferred trees that were higher, had higher canopy and canopy basement and had larger diameter at breast height than other available trees. Roost trees were surrounded by lower trees with lower canopy basements than available trees. Roost trees were in a poorer condition than other available trees. Roosts were occupied by up to 83 individuals in July but usually single individuals were found in the roosts in September. In contrast to syntopic M. mystacinus and M. brandtii, M. alcathoe has never been found in an anthropogenic roost (except for a fissure in concrete electricity pole). Preliminary analysis of the diet showed that nematoceran flies were the most important prey item along with spiders, caddis flies, small moths and neuropterans. In the observed ecological characteristics, M. alcathoe markedly differs from other European species of the genus Myotis. Its restricted habitat requirements are perhaps responsible for an islet-like pattern of its distribution and suggest an essential conservation value of the habitats of its occurrence.
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