New data on the evolution of the Cretan spiny mouse,Acomys minous (Rodentia: Murinae), shed light on the phylogenetic relationships in the cahirinus group

The karyotype of the Cretan spiny mouse Acomys minous was examined with chromosome banding techniques in 53 individuals from 12 localities of Crete, aiming to gain a more detailed knowledge on the chromosomal constitution and variability of its natural populations. We found that it consists of three Robertsonian (Rb) populations with 2n = 38, 2n = 40 and 2n = 42, respectively, the last one being reported for the first time, and with stable fundamental number (FNa = 66, FN = 68). The G‐banding pattern proves that the Rb populations are closely linked phylogenetically by the many common Rb fusions and the lack of monobrachial homologies. In addition, they appear to freely mate at their contact areas, producing viable and fertile hybrids. No other type of chromosomal rearrangement appears to have played part in the chromosomal evolution of this species, at least in the recent past, as indicated also by the study of the telomeric sequences. Heterochromatin appears to be restricted to the pericentromeric position of all acrocentric and most biarmed autosomes, as well as of the X chromosome, whereas the Y chromosome is uniformly, yet faintly heterochromatic. Chromosome banding comparison of the karyotypes in A. minous with those of the other species in the cahirinus group (i.e. Acomys cahirinus, Acomys cilicicus, and Acomys nesiotes) proves their very close phylogenetic relationship, further reinforced by the study of the cytochrome b sequences, and that A. minous possesses the ancestral karyotype of the group. It is suggested that at least two of the karyotypes that characterize A. minous today, pre‐existed in North Africa before it colonized Crete and that the specific status of the four members in the cahirinus group may need to be revisited. © 2011 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102 , 498–509.     

Isolation and amplification of shrew DNA from barn owl pellets

The last decade has seen a number of studies reporting the extraction of DNA from ancient sources, such as fossil bones. Owl pellets, which contain an excellent skeletal record of small mammals consumed, can be used in a non-invasive sampling method for genetic studies of free-ranging animals without the need for direct capture or even observation. Such a non-invasive sampling method will allow us to address questions that cannot be answered using conventional methods and will lead to a more integrated study of micromammals. In the present study, various protocols used for ancient DNA extraction were investigated, in order to determine the applicability of owl pellets as a source of DNA for phylogenetic and phylogeographical studies of micromammals. Of the 12 bone samples used in this study, 11 gave sequences of expected species ( Crocidura , Rattus and Mus ) and size (around 300 bp), using the pair of primers L14841/H15149, which target a highly conserved region of the cytochrome b gene. The results obtained demonstrate that mitochondrial DNA can be isolated and amplified using bones of micromammals found in barn owl ( Tyto alba ) pellets. The recovery of genetic data from owl pellets will enable the identification of prey species for several phylogenetic and phylogeographical studies of small mammals (Muridae and Insectivora) appearing in the owl's diet. The main advantages of this new approach are that (a) the pellets are very easy to find and collect, (b) the pellets can potentially provide a large number of individuals of small mammals, and (c) the method can cover a wide geographical area complementary to the range of owls of this type.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 85 , 331–340.     

Taxonomy, evolutionary history and biogeography of the broad-toothed field mouse (Apodemus mystacinus) in the eastern Mediterranean area based on mitochondrial and nuclear genes

The broad-toothed field mouse ( Apodemus mystacinus ) is distributed throughout the Balkan Peninsula, Asia Minor and the Middle East. It is generally split into two different specific entities: Apodemus epimelas occurs on the Balkan Peninsula and A. mystacinus inhabits Asia Minor and the Middle East. This analysis, based on two mitochondrial regions (cytochrome b and the D-loop) and the interstitial retinol binding protein (IRBP) nuclear gene, confirms an important level of genetic divergence between the animals from these regions and their separation from each other at least 4.2–5.1 Mya, which is in favour of a distinct specific status. Finally, the broad-toothed field mice from south-western Turkey appear to be closely related to the animals from Crete but highly distinct from the populations of the other Oriental regions. This supports a distinct subspecific level ( A. m. rhodius ) for the insular animals and also for those from south-western Turkey. From a biogeographical point of view, it can be assumed that either late Pliocene or early Pleistocene cooling led to the isolation of two main groups of A. mystacinus , one in the Balkan region and the other one in Turkey and the Near East (Syria and Israel). In this region, it is suggested that a more recent event appeared during the Quaternary period, isolating broad-toothed field mice in Crete and leading to the appearance of two well-differentiated genetic groups: one in Crete and south-western Turkey, and the other widespread in northern and eastern Turkey as well as in the Near East.  © 2005 The Linnean Society of London, Biological Journal of the Linnean Society , 2005, 85 , 53–63.