The karyotype, C-banding and Ag-NORs of Spermophilus xanthoprymnus (Anatolian souslik) from the Konya in Central Anatolia were examined. The diploid number of chromosomes (2n) is 42, the fundamental number (FN ) is 81, the number of autosomal arms (NFa) is 78. C-banding positive regions appeared to be restricted to the pericentromeric regions in all autosome chromosome pairs and the X chromosome. The relative amount of C-positive heterochromatin is 28.9 % of the total length of the set. Nucleolar organizer regions (NORs), identified by the silver-staining technique, were found on the terminal region of the short arm of three pairs of subtelocentric chromosomes.
A cytogenetic study of bisexual species belonging to the genera Cirrorhynchus, Dodecastichus and Otiorhynchus is presented in order to confirm their taxonomic position. The karyotype characterization was accomplished by an analysis of mitotic and meiotic chromosomes after differential staining, namely by C-banding, silver impregnation, DAPI and CMA3. A review of the cytogenetic data for the tribe Otiorhynchini contributed to knowledge of chromosomal evolution in this group. An investigation of five of the species studied showed some similarities such as a sex chromosome system of "parachute type" (Xyp), the presence of 10 autosomal bivalents (2n = 22) and heterochromatin localized around centromeres. These observations are similar to those already described for Otiorhynchini species, and confirm the karyological conservatism of this weevil group. In contrast, another species Cirrorhynchus kelecsenyi has an additional four autosomal bivalents (n% = 14 + Xyp, 2n = 30), which differs considerably from the chromosomal homogeneity of the other genera. Karyotypic evolution in this species was achieved most probably by increasing the number of chromosomes by centric fissions, resulting in variation in the number of acrocentric chromosomes. DAPI-positive and CMA3-negative reactions of heterochromatic DNA in all the species studied suggest that it has an AT-rich composition. Impregnating chromosomes with silver nitrate reveals NORs on one pair of autosomes, and probably argentophilic material in the interspace between the X and y sex chromosomes. The karyological findings support the taxonomical revision of Otiorhynchini based on morphological characters.
Extensive karyotype variation was found in both somatic and meiotic cells of the progeny in a laboratory-reared family of the loach Misgurnus anguillicaudatus. Only one of seven individuals examined showed the standard karyotype, 2n = 50 comprising 10 metacentrics, 4 submetacentrics and 36 telocentrics. However, the other six individuals exhibited hyperdiploid karyotypes due to the presence of additional telocentrics and micro-chromosomes, resulting in chromosome numbers 2n = 51 to 53, or 58 plus 0 to 5 micro-chromosomes within or between individuals. Such inter- and/or intra-individual variation in chromosome number was also observed in primary spermatocytes of three males with an increase of bivalents and univalents involving additional telocentrics, although micro-chromosomes were seldom paired. Accumulation of additional chromosomes was apparent in spermatogonia and spermatocytes with greater incidence than in somatic cells. Euploid and aneuploid loaches were not discriminated by the external morphology, suggesting the observed additional chromosomes to be genetically neutral.
Karyotyped specimens from three populations of spined loaches, genus Cobitis, that occurred in the Veleka (Bulgaria), Chernaya (Crimean Peninsula) and Southern Bug (Ukraine) Rivers in north-western Pontic region were subjected to enzyme electrophoresis (for 5 loci), comparative morphological studies, and phylogenetic analysis (based on PCR of a 1230 bp fragment of mtDNA and the cytochrome b gene). These studies resulted in the description of loaches from the Crimean Peninsula as a new species Cobitis taurica, while the taxonomic status of populations from the Veleka and S. Bug rivers appeared to be controversial and in need of further investigation.
The aim of this study was to characterize karyotypes of central European spiders of the genera Arctosa, Tricca, and Xerolycosa (Lycosidae) with respect to the diploid chromosome number, chromosome morphology, and sex chromosomes. Karyotype data are reported for eleven species, six of them for the first time. For selected species the pattern in the distributions of the constitutive heterochromatin and the nucleolar organizer regions (NORs) was determined. The silver staining technique for detecting NORs of lycosid spiders was standardized. The male karyotype consisted of 2n = 28 (Arctosa and Tricca) or 2n = 22 (Xerolycosa) acrocentric chromosomes. The sex chromosome system was X1X20 in all species. The sex chromosomes of T. lutetiana and X. nemoralis showed unusual behaviour during late diplotene, namely temporary extension due to decondensation. C-banding technique revealed a small amount of constitutive heterochromatin at the centromeric region of the chromosomes. Two pairs of autosomes bore terminal NORs. Differences in karyotypes among Arctosa species indicate that the evolution of the karyotype in this genus involved autosome translocations and size changes in the sex chromosomes. Based on published results and those recorded in this study it is suggested that the ancestral male karyotype of the superfamily Lycosoidea consisted of 28 acrocentric chromosomes. and Petr DOLEJŠ, Tereza KOŘÍNKOVÁ, Jana MUSILOVÁ, Věra OPATOVÁ, Lenka KUBCOVÁ, Jan BUCHAR, Jiří KRÁL.
Phylogeny and higher classification of the cerambycid subfamily Lepturinae remain controversial. Here we report the results of a cytogenetic study of 18 species currently classified in Lepturini and 12 species in other tribes of Lepturinae (1 in Oxymirini, 1 in Rhamnusiini and 10 in Rhagiini) from Western Europe. The male sex chromosome formula is XY in all Rhagiini, Oxymirini and in Grammoptera ruficornis in the Lepturini (whose tribal placement may be doubtful), and X0 in all the remaining Lepturini. The rarity of the X0 formula in other Cerambycidae indicates that the Y chromosome was lost in a common ancestor of the Lepturini or a subgroup thereof, indicating its monophyletic origin. The number of chromosomes is stable in the Lepturini that lack a Y chromosome (19,X/20,XX in males and females, respectively), but varies from 20 to 24 in the remaining genera, probably the consequence of evolution by chromosome fission. Whereas all the males with 19 or 20 chromosomes have an early gametogenesis, which is achieved before the imago stage, the species with more than 20 chromosomes seem to have a delayed male gametogenesis, which is still active in the young imagoes. The species of Rhagiini with 22 chromosomes may constitute a monophyletic group.
We compared cranial, dental, bacular and chromosomal variables between a population of Graphiurus murinus collected in riverine forest in the Andries Vosloo Kudu Reserve (AVKR) near Grahamstown (N= 32), and another from Afromontane forest at Hobbiton on Hogsback (HH), in the Amathole Mountains (N=21), Eastern Cape, South Africa. AVKR dormice were significantly larger in 13 out of a total of 23 cranial dimensions and they had a relatively longer rostrum. The 4th upper premolar was clearly longer and the tip of the baculum broader in the sample from HH. Discriminant function analyses of cranial and dental parameters perfectly separated the two samples. The karyotypes were the same at both localities (2n= 46; NFa = 92) but differed from previously reported karyotypes of Graphiurus species from Africa.
Almost after a century, the occurrence of Zingel streber (Siebold, 1863) was recorded again in the area of confluence of the rivers Morava and Dyje. The population consisted of fish 0+ to 5+, with 0+ group predominating in the sample, indicating that the species had successfully reproduced in 2003. Analysis was made of their karyotype (n=5) and meristic characters (n=10). The following was the result of a study of growth of standard lengths (n=16): SL1 – 81 mm, SL2 – 114 mm, SL3 – 130 mm, SL4 – 146 mm, SL5 – 166 mm. The biggest individual was a female 5+ of age, TL 200 mm, SL 180 mm. The habitat types preferred by individuals 0+ were the rapidly flowing sections with gravel bottom, in which the stream velocity was 0.2–0.6 m.s-1. Re-occurrence of this species was facilitated by the marked improvement of water quality after 1990 as well as by the barrier-free connection of sections of the rivers Morava and Dyje with the Danube via the Slovakian-Austrian part of the River Morava. Further dispersal of this species is limited by the weir in r.km 26.7 on the Dyje, and six weirs between r.km 74.1 and r.km 101.8 on the Morava. Z. streber is protected by national law and the area mentioned above has been proposed as a pSCI for the NATURA 2000 system.
The Lama forest is the largest natural forest in southern Benin, and one of the last remnant forests within the Dahomey Gap. It harbours several species of major importance in terms of conservation. Small mammals are known to represent more than 80% of the African mammalian species diversity but they have received little attention in Benin. In this article we present the results of the first terrestrial small mammal species inventory (murid rodents and shrews) in the Lama forest. In September and October 2007, we captured 280 small mammals belonging to 12 species, identified by morphological and genetic analysis. We also provide detailed cytogenetic data for six of the 12 captured species. For five of them, we compare our data with previously published karyotypes, and for the sixth one (Hylomyscus pamfi), the karyotype is published here for the first time. Two of the captured species are closed-forest specialists (Praomys misonnei, H. pamfi), and H. pamfi is endemic to the Dahomey Gap region. Our results are congruent with those obtained on other animal groups, and highlight the importance of the Lama forest for the conservation of the country's forest biodiversity.
The history and value of cytogenetic features for addressing questions of the evolution and systematics of tapeworms (Cestoda) are briefly reviewed along with instructions for collecting karyological data. As a supplement to worm morphology, chromosome number and morphology have been helpful in determining the systematic status of some genera in the Diphyllobothriidae and species in the Bothriocephallidea. In addition, many new techniques for chromosome analysis have been recently applied in morphological and molecular studies of invertebrates, including tapeworms. Methods of molecular karyology, fluorescence in situ hybridisation, and chromosomal location of satellite DNA, microsatellites or histone genes may also provide useful data to inference of taxonomic relationships and for revealing trends or general lines of chromosome evolution. However, as karyological data are available only for few tapeworms, they are seldom an integral part of evolutionary and taxonomic studies of cestodes. A primary reason for this lack of karyological data may lie in general difficulties in working with tapeworm chromosomes. To address these problems, herein we present a well-tested, step-by-step illustrated guide on the fixation of tapeworm material and preparation of their chromosomes for cytogenetic studies. The technique requires standard glassware, few reagents and simple equipment such as needles; it can also be used on other neodermatan flatworms., Martina Orosová, Marta Špakulová., and Obsahuje bibliografii