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.     

CRYSTALLOGRAPHY AND DIAGENESIS IN FOSSIL CRANIID BRACHIOPODS

Abstract:  One of the fundamental questions in biomineralization is how organisms control crystallographic orientation during biomineral production. The understanding of how diagenetic changes influence the preservation of original crystallographic patterns in fossilized biomineral structures provides a priori fundamental information for such an assessment. Fossil craniid brachiopods Petrocrania scabiosa (Late Ordovician) and Crania craniolaris (Late Cretaceous) are analysed using electron backscattered diffraction (EBSD) to provide crystallographic data at high spatial resolution in the structural context. EBSD analyses show that P. scabiosa maintains most of the original crystallographic signature, including data from individual calcite tablets and laminae, while C. craniolaris only retains fragmentary crystallographic data reflecting the crystallographic continuity of tablets across laminae. Data show that the preservation of the original crystallographic signature is independent of that of shell ultrastructure and geological time. In addition, results allow us to propose a series of steps in the evolution of 'crystallographic loss' due to diagenesis.     

Gametophyte morphology and gametangial ontogeny of Asplenium foreziense and related taxa (Aspleniaceae: Pteridophyta)

Gametophytes of Asplenium foreziense and related taxa have been studied by culture of spores on mineral agar and soil. Those of A. obovatum ssp. obovatum var. protobillotii and var. deltoideum , ssp. numidicum , and of A. macedonicum are described for the first time. Gametophyte development follows the Adiantum type in the A. obovatum group, and the Aspidium type in A. fontanum . Both types of development have been found in A. foreziense , depending on the sporophytic sample. The taxa with hairy gametophytes show significant differences in hair density. As in most of the homosporous ferns, antheridia are formed first and in a high proportion of gametophytes in the A. obovatum group and in A. fontanum , except for one sample; most of these male gametophytes become bisexual. In A. foreziense and A. macedonicum archegonia are formed first or at the same time as antheridia, but the proportion of female gametophytes is higher than in the other taxa; some of the gametophytes become bisexual, most of them differentiated from the female ones. © 2002 The Linnean Society of London, Botanical Journal of the Linnean Society , 2002, 139 , 87–98.     

Electrophoretic Analysis of Endonuclease-Generated Fragments of k-DNA,of Esterase Isoenzymes,and of Surface Proteins as Aids for Species Identification of Insect Trypanosomatids1

In order to verify the applicability of biochemical methods for species identification of Trypanosomatidae, 13 species of monoxenic trypanosomatids plus the heteroxenous Trypanosoma cruzi were comparatively analyzed by three different biochemical methods. Insect trypanosomatids examined were: Crithidia acanthocephali, C. fasciculata (three varieties), C. luciliae luciliae, C. luciliae thermophila, C. deanei, C. oncopelti, Herpetomonas muscarum muscarum, H. megaseliae, H. samuelpessoai, H. mariadeanei, Leptomonas seymouri, L. collosoma, L. samueli, and Blastocrithidia culicis. Also included in the survey were aposymbiotic strains of C. deanei and C. oncopelti. Methods used were: electrophoretic profiling of endonuclease-generated fragments of k-DNA, esterase isoenzymes profiling, and polyacrylamide-gel electrophoresis (SDS-PAGE) of radioiodinated cell surface proteins. Interspecific but not intraspecific differences were detected by all three methods among the 13 monoxenic species examined. Thus, it is concluded that these methods can be successfully used, in addition to classical criteria, for species identification of insect trypanosomatids.