The chromosome complements of thirteen species of the planthopper family Dictyopharidae are described and illustrated. For each species, the structure of testes and, on occasion, ovaries is additionally outlined in terms of the number of seminal follicles and ovarioles. The data presented cover the tribes Nersiini, Scoloptini and Dictyopharini of the subfamily Dictyopharinae and the tribes Ranissini, Almanini, and Orgeriini of the Orgeriinae. The data on the tribes Nersiini and Orgeriini are provided for the first time. Males of Hyalodictyon taurinum and Trimedia cf. viridata (Nersiini) have 2n = 26 + X; Scolops viridis, S. sulcipes, and S. abnormis (Scoloptini) 2n = 36 + X; Callodictya krueperi (Dictyopharini) 2n = 26 + X; Ranissus edirneus and Schizorgerius scytha (Ranissini) 2n = 26 + X. Males of Almana longipes and Bursinia cf. genei (Almanini) have 2n = 26 + X and 2n = 24 + XY, respectively. The latter chromosome complement was not recorded previously for the tribe Almanini. Males of Orgerius ventosus and Deserta cf. bipunctata (Orgeriini) have 2n = 26 + X. The testes of males of A. longipes and B. cf. genei each have 4 seminal follicles, which is characteristic of the tribe Almanini. Males of all other species have 6 follicles per testis. When the ovaries of a species were also studied, the number of ovarioles was coincident with that of seminal follicles. For comparison, Capocles podlipaevi (2n = 24 + X and 6 follicles per testis in males) from the Fulgoridae, the sister family to Dictyopharidae, was also studied. We supplemented all the data obtained with our earlier observations on Dictyopharidae. The chromosomal complement of 2n = 28 + X or that of 2n = 26 + X and 6 follicles per testis are suggested to be the ancestral condition among Dictyopharidae, from which taxa with various chromosome numbers and testes each with 4 follicles have differentiated.
We present the results of the first study on the karyotypes of four European species of Roncus: Roncus alpinus L. Koch, 1873, Roncus lubricus L. Koch, 1873, Roncus transsilvanicus Beier, 1928 and Roncus sp. The diploid number was 2n = 23 in Roncus sp., 2n = 43 in R. alpinus and R. transsilvanicus and 2n = 45 in R. lubricus. Telocentric autosomes predominate in species with a high chromosome number and metacentric autosomes in Roncus sp. We assume that the ancestral situation for this genus is a high number of chromosomes. A low number of chromosomes is very likely a consequence of centric fusions, which have possibly played a very important role in karyotype evolution in the genus Roncus. All the species analyzed have the X0 sex chromosome system. The X chromosome is metacentric and is the smallest element in the karyotypes of all the species analyzed., František Šťáhlavský, Jana Christophoryova, Hans Henderickx., and Obsahuje seznam literatury
The karyotypes of pseudoscorpions of three families, Geogarypidae, Garypinidae and Olpiidae (Arachnida: Pseudoscorpiones), were studied for the first time. Three species of the genus Geogarypus from the family Geogarypidae and 10 species belonging to 8 genera from the family Olpiidae were studied. In the genus Geogarypus the diploid chromosome numbers of males range from 15 to 23. In the family Olpiidae the male chromosome numbers vary greatly, from 7 to 23. The male karyotype of single studied member of the family Garypinidae, Garypinus dimidiatus, is composed of 33 chromosomes. It is proposed that the karyotype evolution of the families Geogarypidae and Olpiidae was characterised by a substantial decrease of chromosome numbers. The diploid numbers of some olpiids are the lowest known 2n within pseudoscorpions and even one of the lowest within the class Arachnida. In spite of a considerable reduction of diploid numbers, all species studied possess a X0 sex chromosome system that is widespread and probably ancestral in pseudoscorpions. Moreover, X chromosomes retain conservative metacentric morphology in the majority of species. During the first meiotic division of males, a high number of chiasmata were observed in some species, up to five per bivalent in Indolpium sp. The transient stage between pachytene and diplotene is typically characterised by extensive decondensation of chromatin in males of geogarypids and in Calocheiridius libanoticus, and we interpret this as a diffuse stage. This is recorded in pseudoscorpions for the first time. The relationships between some species belonging to the family Olpiidae are discussed based on the data obtained.
Five Trichoptera species, representing four different families of three suborders, have been examined for sex chromatin status in relation to their sex chromosome system. These were Hydropsyche sp., Polycentropus flavomaculatus (Pictet), Rhyacophila sp., Anabolia furcata Brauer and Limnephilus decipiens (Kolenatý). None of the species displayed sex-specific heterochromatin in highly polyploid nuclei of the Malpighian tubule cells. Such sex chromatin is a characteristic trait of the heterogametic female sex in the sister order Lepidoptera; it is derived from the heterologous sex chromosome W. Hence, the absence of sex chromatin in somatic nuclei of Trichoptera females indicated the lack of a W chromosome in their karyotype. Correspondingly, diploid chromosome sets of the females consisted of an odd chromosome number, two sets of autosomes and one sex chromosome Z. Thus, the Z/ZZ chromosome mechanism of sex determination has been confirmed. In pachytene and postpachytene oocytes, the Z chromosome having no pairing partner formed a univalent. In Hydropsyche sp., the Z-univalent was distinct as a compact, positively heteropycnotic element. Whereas, in two other caddis-flies, P. flavomaculatus and L. decipiens, it formed a negatively heteropycnotic thread. In postpachytene nuclei of nurse cells of A. furcata, two sister chromatids of the Z chromosome separated as a result of chromosome degeneration and formed a negatively heteropycnotic pseudobivalent. The species-specific differences in pycnosis may reflect a transcriptional activity/inactivity of the Z chromosome during meiotic prophase. The absence of sex chromatin and the sex chromosome system in Trichoptera are characters in common with the "primitive" Lepidoptera. This supports a hypothesis that the commcommon with the "primitive" Lepidoptera. This supports a hypothesis that the common ancestor of both orders had a ZJZZ sex chromosome
mechanism.
Genetic variation among populations of commensal house mice was studied across the territories of the Czech and Slovak Republics and in some adjacent areas of Germany. We used six diagnostic allozyme loci (Es-2, Gpd-1, Idh-1, Mpi, Np, Sod-1) and the following molecular markers: B1 insertion in the Btk gene (X chromosome), Zfy2 18-bp deletion (Y chromosome), BamH I restriction site in the mt-Nd1 gene (mtDNA) and Hba-4ps 16-bp insertion (diagnosing the presence of t haplotypes). In total, 544 individuals taken from 49 localities were examined. Almost the entire territories of the Czech Republic and Slovakia were found to be occupied by Mus musculus, the only exception being the westernmost parts of the Czech Republic, where M. musculus meets the range of M. domesticus and forms a narrow belt of hybrid populations. Despite this, domesticus-type alleles of some allozyme markers (notably Es-2) were also found at sites well within the range of M. musculus, either tens or hundreds of kilometres behind the hybrid zone. This provides evidence of either: (1) introgression of some markers into the species’ genome due to free gene flow through the zone, or (2) human-mediated long-distance migrations, or (3) incomplete lineage sorting. Conversely, variants of molecular markers typical for M. domesticus in Btk, Zfy2 and mt-Nd1were only found in the westernmost populations studied. t haplotypes were quite frequent in some populations, irrespective of whether M. domesticus, M. musculus or their hybrids, yet no t/t homozygotes were found. The mean frequency of t/+ heterozygotes found within the study populations was 13%.
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.
In Mormidea paupercula (n = 6 + XY in males), the presence of a CMA3-bright band in the telomeric regions on both sex chromosomes allowed the analysis of the kinetic activity of the sex univalents and XY pseudobivalent at the first and second meiotic divisions, respectively. The separation of the sister chromatids of the sex chromosomes occurs from a pair of telomeric regions (with or without a band), with opposite telomeric regions remaining associated with each other at meiosis I; the behaviour of both sex chromosomes differs, on the X chromosome both telomeric regions are similarly active, while on the Y chromosome the telomeric region without a band is more frequently active. At the second division, the most frequent associations in the pseudobivalent occur between the telomeric regions of both sex chromosomes with bands or without bands. Therefore, in both meiotic divisions, the same telomeric region on the sex chromosomes could lead the migration, in contrast to that observed usually in autosomal bivalents. These results provide evidence that the sex chromosomes of Heteroptera show more than one pattern of attachment to the spindle.
Although a monophyletic group, male (XX/XY) and female heterogametic (WZ/ZZ) sex chromosome systems with a couple of variants like XX/X, Z/ZZ and multiple sex chromosome systems occur in insects. Molecular and morphological differences between X and Y or W and Z range from imperceptible to conspicuous. This article illustrates sex chromosome differentiation mainly in two fly species, Drosophila melanogaster and Megaselia scalaris, and in Lepidoptera. The earliest phases of XY evolution are present in the fly M. scalaris. Occasionally in this species, the male determining gene jumps to another chromosome, transforming the new host chromosome to a functional Y chromosome. Thus, in M. scalaris there are strains with virtually no XY differentiation (except for the sex determining function) and others with a moderate degree of differentiation. Base substitutions and alterations like sequence deletions, duplications, and insertions of mobile sequences mark the onset of molecular differentiation. Accumulation of molecular changes and coarser alterations are thought to lead to the morphological differences seen in WZ chromosome pairs of Lepidoptera. The W chromosome probably evolved in the most numerous clade of Lepidoptera, the Ditrysia, after it diverged from the common lepidopteran stem. Extant species display various degrees of molecular and morphological differentiation of the W chromosome, translocation or fusion with autosomes, and loss of the W.