Cytogenetic Point Of View Research Articles

Parallel anagenetic patterns in endemic Artemisia species from three Macaronesian archipelagos.

Anagenetic speciation is an important mode of evolution in oceanic islands, yet relatively understudied compared to adaptive radiation. In the Macaronesian region, three closely related species of Artemisia (i.e. A. argentea, A. thuscula and A. gorgonum) are each endemic from a single archipelago (i.e. Madeira, Canary Islands and Cape Verde, respectively), representing a perfect opportunity to study three similar but independent anagenetic speciation processes. By analysing plastid and nuclear DNA sequences, as well as nuclear DNA amount data, generated from a comprehensive sampling in all the islands and archipelagos where these species are currently distributed, we intend to find common evolutionary patterns that help us explain the limited taxonomic diversification experienced by endemic Macaronesian Artemisia. Our time-calibrated phylogenetic reconstruction suggested that divergence among the three lineages occurred in a coincidental short period of time during the Pleistocene. Haplotype and genetic differentiation analyses showed similar diversity values among A. argentea, A. thuscula and A. gorgonum. Clear phylogeographic patterns-showing comparable genetic structuring among groups of islands-were also found within the three archipelagos. Even from the cytogenetic point of view, the three species presented similarly lower genome size values compared to the mainland closely related species A. arborescens. We hypothesize that the limited speciation experienced by the endemic Artemisia in Madeira, Canary Islands and Cape Verde archipelagos could be related to their recent parallel evolutionary histories as independent lineages, combined with certain shared characteristics of seed dispersal, pollen transport and type of habitat.

Geographic distribution and climatic niche comparison between diploid and polyploid cytotypes of a South American genus Lessingianthus H.Rob. (Vernonieae, Asteraceae)

The distribution of ploidy levels and their ecological associations were studied using the genus Lessingianthus (Vernonieae, Asteraceae) as a model system. This genus is very complex from a cytogenetic point of view, with high cytotype diversity at the interspecific and intraspecific levels and with a continuous distribution throughout South America. So far, no previous studies have summarized chromosome count data for Lessingianthus or addressed the cytogeography of the genus. In this study, the ploidy levels of Lessingianthus species were determined by chromosome counts during mitosis and ecological niche modelling (ENM) was used to compare the environmental associations of the diploid and polyploid cytotypes. In total, 28 chromosome counts and six ploidy levels (2x, 4x, 6x, 8x, 10x, and 11x) were recorded. Among these counts, the chromosome numbers for three hexaploids with 2 n = 96 (L. parvifolius, L. vepretorum and L. “bolivianensis” sp. ined.) and one decaploid taxon with 2 n = 160 (L. roseus) were reported for the first time. In addition, a new cytotype for L. laniferus (2 n = 6x = 96) was also reported. The cytogeographic analysis resulted in detecting two geographic zones with high diversity of cytotypes and species. The ENMs showed that the areas of climatic suitability of diploids and polyploids are similar in extent, as well as the climatic requirements, showing high values of niche overlap within the environmental space. Our findings suggested that polyploidization in Lessingianthus has not caused expansion to novel environmental conditions and phylogenetic niche conservatism (PNC) may explain the lack of niche differentiation between diploids and polyploids.

Contributions of species Rineloricaria pentamaculata (Loricariidae:Loricariinae) in a karyoevolutionary context

Species of Rineloricaria demonstrate an interesting evolutionary history from a cytogenetic point of view, due to the occurrence of extensive variation in diploid number (2n=36 -70 chromosomes), with Robertsonian rearrangements mostly responsible for this karyotypic diversity. In this study we present the karyotypic data for a population of Rineloricaria pentamaculata, collected in the Itiz stream, a tributary of the Paraná River Basin (Paraná, Brazil), which exhibited 2n=56 chromosomes distributed in 8m/sm+48st/a (number fundamental equal to 64) and simple NOR system revealed by fluorescent in situ hybridization (FISH) with 18S rDNA probe, silver nitrate and positive C band, located on the first submetacentric chromosome pair (pair 5). In addition, the NOR pair showed a size heteromorphism for this region, rich in GC composition (positive CMA3). Clusters of 5S rDNA were located in 14 chromosomes and the FISH with a telomeric probe was used to map possible evidence of chromosomal fusions, however, it showed only telomeric sites. These results corroborate the data for the species R. pentamaculata and the genus Rineloricaria, showing that they are similar to most of the populations analyzed. About the cytogenetic data of R. pentamaculata, we reaffirm that most populations were conserved, but in those with derived characteristics, Robertsonian chromosomal rearrangements probably contributed to the karyotypic evolution of the group.

Tracing the Evolution of the Angiosperm Genome from the Cytogenetic Point of View

Cytogenetics constitutes a branch of genetics that is focused on the cellular components, especially chromosomes, in relation to heredity and genome structure, function and evolution. The use of modern cytogenetic approaches and the latest microscopes with image acquisition and processing systems enables the simultaneous two- or three-dimensional, multicolour visualisation of both single-copy and highly-repetitive sequences in the plant genome. The data that is gathered using the cytogenetic methods in the phylogenetic background enable tracing the evolution of the plant genome that involve changes in: (i) genome sizes; (ii) chromosome numbers and morphology; (iii) the content of repetitive sequences and (iv) ploidy level. Modern cytogenetic approaches such as FISH using chromosome- and genome-specific probes have been widely used in studies of the evolution of diploids and the consequences of polyploidy. Nowadays, modern cytogenetics complements analyses in other fields of cell biology and constitutes the linkage between genetics, molecular biology and genomics.

Revisiting the Karyotypes of Alligators and Caimans (Crocodylia, Alligatoridae) after a Half-Century Delay: Bridging the Gap in the Chromosomal Evolution of Reptiles.

Although crocodilians have attracted enormous attention in other research fields, from the cytogenetic point of view, this group remains understudied. Here, we analyzed the karyotypes of eight species formally described from the Alligatoridae family using differential staining, fluorescence in situ hybridization with rDNA and repetitive motifs as a probe, whole chromosome painting (WCP), and comparative genome hybridization. All Caimaninae species have a diploid chromosome number (2n) 42 and karyotypes dominated by acrocentric chromosomes, in contrast to both species of Alligatorinae, which have 2n = 32 and karyotypes that are predominantly metacentric, suggesting fusion/fission rearrangements. Our WCP results supported this scenario by revealing the homeology of the largest metacentric pair present in both Alligator spp. with two smaller pairs of acrocentrics in Caimaninae species. The clusters of 18S rDNA were found on one chromosome pair in all species, except for Paleosuchus spp., which possessed three chromosome pairs bearing these sites. Similarly, comparative genomic hybridization demonstrated an advanced stage of sequence divergence among the caiman genomes, with Paleosuchus standing out as the most divergent. Thus, although Alligatoridae exhibited rather low species diversity and some level of karyotype stasis, their genomic content indicates that they are not as conserved as previously thought. These new data deepen the discussion of cytotaxonomy in this family.

Study of frequency and types of chromosomal abnormalities in phenotypically female patients with amenorrhea in Eastern Indian population.

This comprehensive review article aims to comprehend the frequency and prevalence of chromosomal abnormalities in both primary amenorrhea (PA) and secondary amenorrhea (SA) cases and correlating it with their phenotypes, clinical features and hormonal profiles. Research publications on prevalence of chromosomal abnormalities in both PA and SA cases worldwide and its etiology, clinical features, hormonal profiles; their correlation with chromosomal profiles were searched for on the internet, including general search engines and respective scientific sites. Only published, relevant and authentic data conducted on phenotypically female patients were considered. Another aspect of amenorrhea occurs due to several clinical conditions apart from cytogenetic viewpoint were not considered or discussed in detail. As literature study suggests; considering various etiology of amenorrhea counting anatomic defect of the hypothalamus or genetic defect, and various acquired causes of chromosomal anomalies contribute to be one of the major etiologies of both PA and SA; ranging from 15.9% to 63.3% in case of PA and from 3.9% to 44.4% in case of SA. In spite of the presence of any other factors responsible condition, the genetic factors need to be emphasized, which might include single gene disorders or chromosomal disorders. Individuals with chromosomal anomalies reported a wide range of abnormalities in phenotypes, as well as in other clinical features and hormonal profiles. This comprehensive review is the first structured review article that encompasses the cytogenetic profile of the amenorrhea cases and correlating it with their phenotypes, clinical features and hormonal profiles from Eastern India.

Cytogenetics of entelegyne spiders (Arachnida, Araneae) from southern Africa.

Spiders represent one of the most studied arachnid orders. They are particularly intriguing from a cytogenetic point of view, due to their complex and dynamic sex chromosome determination systems. Despite intensive research on this group, cytogenetic data from African spiders are still mostly lacking. In this study, we describe the karyotypes of 38 species of spiders belonging to 16 entelegyne families from South Africa and Namibia. In the majority of analysed families, the observed chromosome numbers and morphology (mainly acrocentric) did not deviate from the family-level cytogenetic characteristics based on material from other continents: Tetragnathidae (2n♂ = 24), Ctenidae and Oxyopidae (2n♂ = 28), Sparassidae (2n♂ = 42), Gnaphosidae, Trachelidae and Trochanteriidae (2n♂ = 22), and Salticidae (2n♂ = 28). On the other hand, we identified interspecific variability within Hersiliidae (2n♂ = 33 and 35), Oecobiidae (2n♂ = 19 and 25), Selenopidae (2n♂ = 26 and 29) and Theridiidae (2n♂ = 21 and 22). We examined the karyotypes of Ammoxenidae and Gallieniellidae for the first time. Their diploid counts (2n♂ = 22) correspond to the superfamily Gnaphosoidea and support their placement in this lineage. On the other hand, the karyotypes of Prodidominae (2n♂ = 28 and 29) contrast with all other Gnaphosoidea. Similarly, the unusually high diploid number in Borboropactus sp. (2n♂ = 28) within the otherwise cytogenetically uniform family Thomisidae (mainly 2n♂ = 21–24) supports molecular data suggesting a basal position of the genus in the family. The implementation of FISH methods for visualisation of rDNA clusters facilitated the detection of complex dynamics of numbers of these loci. We identified up to five loci of the 18S rDNA clusters in our samples. Three different sex chromosome systems (X0, X1X20 and X1X2X30) were also detected among the studied taxa.

Cytogenetic Investigations in Emballonuroidea. II. Chromosome Painting in Nycteridae Reveals Cytogenetic Signatures Pointing to Common Ancestry of Nycteris and Emballonura

Two species of the monogeneric family Nycteridae were studied for the first time with chromosome banding techniques and chromosome painting. The diploid chromosome number of Nycteris macrotis and N. tragata is 40 and 38, respectively. Both karyotypes differ by a translocation, a telomeric fusion and a pericentric inversion. The genus Nycteris shows a highly derived karyotype where the 25 chiropteran evolutionarily conserved units (ECUs) are represented in 37 segments. Chromosome painting with Myotis probes revealed three common features of Nycteris and Emballonura, which are not present in Taphozous. From a cytogenetic point of view, Nycteris is therefore closer related to Emballonura than to Taphozous. Further, an additional synapomorphy for Vespertilioniformes is described, i.e. the synteny of a segment homologous to human chromosome 13 and ECU12a-22a in elements homologous to Myotis chromosome MMY6.

Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation?

BackgroundSynbranchidae or swamp eels are fishes belonging to the order Synbranchiformes that occur in both freshwater and occasionally in brackish. They are worldwide distributed in tropical and subtropical rivers of four different continents. A large degree of chromosomal variation has been found in this family, mainly through the use of conventional cytogenetic investigations. Inside this group, a still almost unexplored species under the cytogenetic point of view is the Asian swamp eel Monopterus albus, a widely distributed species throughout Asia. Here, we tested the hypothesis of chromosomal speciation, where a case of sympatric speciation may occur as the primary consequence of chromosomal rearrangements. We performed a comparative chromosomal analysis of M. albus from 22 different localities in Thailand, using distinct staining methods (C-banding, Ag-NO3, and Chromomycin A3), and FISH with repetitive DNA probes (5S rDNA, 18S rDNA, Rex1 element and microsatellite repeats).ResultsThis approach evidenced two contrasting karyotypes (named karyomorphs A and B) that varied concerning their 2n and repetitive DNAs distribution, where chromosomal fusions and pericentric inversions were involved in such differentiation. While the karyomorph A has 2n = 24 chromosomes, the karyomorph B has only 2n = 18, both with NF = 24. In addition, karyomorph A contains only acrocentric chromosomes, while karyomorph B contains three unique metacentric pairs. These features highlight that M. albus has already gone through a significant genomic divergence, and may include at least two cryptic species.ConclusionsThis marked chromosomal differentiation, likely linked to the lifestyle of these fishes, point to the occurrence of a chromosomal speciation scenario, in which fusions and inversions had a prominent role. This highlights the biodiversity of M. albus and justifies its taxonomic revision, since this nominal species may constitute a species complex.

Toxicity and removal of Direct Red 28 diazo dye in living polymeric systems

Aquatic environments are often contaminated with various compounds, with potential toxicity towards aquatic organisms, which may enter the food chain. Azo dyes are used in various industries and contamination of waters has been reported. The present paper assesses the toxicity of the synthetic, water soluble Congo Red dye towards Lemna minor from a physiological and cytogenetical point of view. The dye was tested in 5-5000 ppm concentrations. Total frond surface, root growth and fresh mass reductions were registered from 5 ppm dye concentration, with a concentration-dependent response and calculated EC50 of 1530 ppm. Plant growth was completely inhibited above 2500 ppm. Dye accumulation was observed in tissues, along with necrosis formation. Chlorophyll a contents decreased, while carotenoid contents increased above 2500 ppm. Significant inhibition of PSII efficiency was recorded above 1000 ppm. Mitotic indices were decreased at 5 and 1000 ppm dye and were 0 at 5000 ppm. The number of chromosomal aberrations significantly increased at 5 and 1000 ppm dye. The growth medium was decontaminated up to 56% at 250 ppm dye concentration by Lemna plants. Congo Red azo dye presented toxicity towards Lemna minor, from a physiological and cyotgenetical point of view, especially at higher concentrations. In the same time, a phytoremediation potential of duckweed with respect to the tested dye was demonstrated.

Presentations of Clinical, Ultrasonographic and Pathological Features of Nodular Fasciitis from an Established Cytogenetic Viewpoint: Review of the Case Series

Even though nodular fasciitis (NF) is benign and self-limited, the clinical, ultrasonographyic and pathological presentations have been described as mimicking sarcoma. We have reported that proliferative findings on both US and histology may be caused by the cytogenetic nature of NF. When the lesion showed the proliferative findings of the margin on both US and pathology, accompanied with clinical rapid growth and self-limited course, NF should be strongly suggested as one of the skin tumors as previously described. NF has been cytogenetically considered as a novel model of transient neoplasia induced by MYH9-USP6 gene fusion. It has been suggested that strong overexpression of USP6 under MYH9 promoter appears to drive tumorigenesis. A clear association between NF and a recurrent genetic abnormality had been established in fluorescence in-situ hybridization (FISH) analysis. In this article, we reviewed the clinical, ultrasonographic and pathological features of NF in the case series from an established cytogenetic viewpoint. Our study indicated that proliferative findings of the margin on US and pathology may be caused by the driving force of USP6 transcriptional upregulation behind the high proliferative activity and growth of NF. All nodules clinically represented rapid growing, self-limited and/or regress course, suggesting the high proliferative growth and involutional nature of NF. We emphasize that the presentations of clinical, ultrasonographic and pathological features of NF are contributed to the cytogenetic nature, having the high proliferative growth and involutional nature.

Helpful Tool or Oversimplification? Concept of the Monosomal Karyotype from the Clinical and Cytogenetic Point of View.

Helpful Tool or Oversimplification? Concept of the Monosomal Karyotype from the Clinical and Cytogenetic Point of View.

General trends of chromosomal evolution in Aphidococca (Insecta, Homoptera, Aphidinea + Coccinea).

Parallel trends of chromosomal evolution in Aphidococca are discussed, based on the catalogue of chromosomal numbers and genetic systems of scale insects by Gavrilov (2007) and the new catalogue for aphids provided in the present paper. To date chromosome numbers have been reported for 482 species of scale insects and for 1039 species of aphids, thus respectively comprising about 6% and 24% of the total number of species. Such characters as low modal numbers of chromosomes, heterochromatinization of part of chromosomes, production of only two sperm instead of four from each primary spermatocyte, physiological sex determination, "larval" meiosis, wide distribution of parthenogenesis and chromosomal races are considered as a result of homologous parallel changes of the initial genotype of Aphidococca ancestors. From a cytogenetic point of view, these characters separate Aphidococca from all other groups of Paraneoptera insects and in this sense can be considered as additional taxonomic characters. In contrast to available paleontological data the authors doubt that Coccinea with their very diverse (and partly primitive) genetic systems may have originated later then Aphidinea with their very specialised and unified genetic system.

Phylogenetic reconstruction by cross-species chromosome painting and G-banding in four species of Phyllostomini tribe (Chiroptera, Phyllostomidae) in the Brazilian Amazon: an independent evidence for monophyly.

The subfamily Phyllostominae comprises taxa with a variety of feeding strategies. From the cytogenetic point of view, Phyllostominae shows different rates of chromosomal evolution between genera, with Phyllostomus hastatus probably retaining the ancestral karyotype for the subfamily. Since chromosomal rearrangements occur rarely in the genome and have great value as phylogenetic markers and in taxonomic characterization, we analyzed three species: Lophostoma silvicola (LSI), Phyllostomus discolor (PDI) and Tonatia saurophila (TSA), representing the tribe Phyllostomini, collected in the Amazon region, by classic and molecular cytogenetic techniques in order to reconstruct the phylogenetic relationships within this tribe. LSA has a karyotype of 2n=34 and FN=60, PDI has 2n=32 and FN=60 and TSA has 2n=16 and FN=20. Comparative analysis using G-banding and chromosome painting show that the karyotypic complement of TSA is highly rearranged relative to LSI and PHA, while LSI, PHA and PDI have similar karyotypes, differing by only three chromosome pairs. Nearly all chromosomes of PDI and PHA were conserved in toto, except for chromosome 15 that was changed by a pericentric inversion. A strongly supported phylogeny (bootstrap=100 and Bremer=10 steps), confirms the monophyly of Phyllostomini. In agreement with molecular topologies, TSA was in the basal position, while PHA and LSI formed sister taxa. A few ancestral syntenies are conserved without rearrangements and most associations are autapomorphic traits for Tonatia or plesiomorphic for the three genera analyzed here. The karyotype of TSA is highly derived in relation to that of other phyllostomid bats, differing from the supposed ancestral karyotype of Phyllostomidae by multiple rearrangements. Phylogenies based on chromosomal data are independent evidence for the monophyly of tribe Phyllostomini as determined by molecular topologies and provide additional support for the paraphyly of the genus Tonatia by the exclusion of the genus Lophostoma.

Cytogenetic evidences of genome rearrangement and differential epigenetic chromatin modification in the sea lamprey (Petromyzon marinus).

This work explores both the chromatin loss and the differential genome methylation in the sea lamprey (Petromyzon marinus) from a molecular cytogenetic point of view. Fluorescent in situ hybridization experiments on meiotic bivalents and mitotic chromosomes corroborate the chromatin loss previously observed during the development of the sea lamprey and demonstrate that the elimination affects not only to Germ1 sequences but also to the rpt200 satellite DNA and most part of the major ribosomal DNA present on the germinal line. 5-Methylcytosine immunolocation revealed that the GC-rich heterochromatin is highly methylated in the germ line but significantly less in somatic chromosomes. These findings not only support previous observations about genome rearrangements but also give new information about epigenetic changes in P. marinus. The key position of lampreys in the vertebrate phylogenetic tree makes them an interesting taxon to provide relevant information about genome evolution in vertebrates.

The chromosome banding pattern in two cytotypes (2n = 36 and 38) of blind mole rats from Turkey (Mammalia: Spalaxidae)

Two cytotypes (2n = 36 and 38) of blind mole rats, Nannospalax xanthodon (Nordmann, 1840), from the Aydın and Manisa provinces in Turkey were investigated. Conventional chromosome staining, Ag-NOR staining and C-banding analysis were carried out. From the cytogenetic point of view, the particular phylogenetic position of these populations is supported by their low diploid numbers only, and the Cbanding pattern and the NORs distribution seem generally similar to populations with higher chromosome numbers. Several autosomal pairs with centromeric dark Cbands were observed in the 2n=36 cytotype. One autosomal pair possessed an interstitial dark C-band on the short arm; another pair possessed an interstitial dark Cband on the long arm. Whole C-heterochromatic short arms were observed in three subtelocentric autosomal pairs in the 2n=38 cytotype. Most of the other autosomal pairs possessed centromeric dark C-bands. Distinct dark C-bands were observed also in the presumed X chromosomes of both the cytotypes. The Ag-NOR regions were found on three autosomal pairs of both the cytotypes. These sites were located in telomeric areas of the short arms of two subtelocentric and one submetacentric pair.

Comparative cytogenetics of two species of genus Scobinancistrus (Siluriformes, Loricariidae, Ancistrini) from the Xingu River, Brazil

The family Loricariidae encompasses approximately 800 species distributed in six subfamilies. The subfamily Hypostominae consists of five tribes; of them, the tribe Ancistrini is relatively diverse, but it is not well known from the cytogenetic point of view. Genus Scobinancistrus Isbrücker et Nijssen, 1989, which is part of the tribe Ancistrini, has two species that occur in sympatry in the Xingu River, Brazil. In this work, we performed the first karyotypic characterizations of these two species and sought to identify the processes involved in their karyotypic evolution. Chromosomal preparations were subjected to Giemsa staining, silver nitrate impregnation, C-banding, CMA3 staining, DAPI staining, and FISH (fluorescence in situ hybridization) with 18S rDNA and telomeric probes. We found that Scobinancistrus aureatus Burgess, 1994 and Scobinancistrus pariolispos Isbrücker et Nijssen, 1989 shared the diploid number, 2n=52, but differed in their karyotypic formulae (KFs), distribution of constitutive heterochromatin (CH), and the localizations of their nucleolus organizer regions (NORs), which were found on the interstitial and distal regions of the long arm of chromosome pair 3 in Scobinancistrus aureatus and Scobinancistrus pariolispos respectively. We suggest that these interspecific variations may have arisen via paracentric inversion or transposition of the NOR. The karyotypic differences found between these two Scobinancistrus species can be used to identify them taxonomically, and may have functioned as a mechanism of post-zygotic reproductive isolation during the speciation process.

New cytogenetic data on Coreoidea (Hemiptera: Heteroptera) with special reference to Coreidae

Some cytogenetic aspects of six Chinese species of Coreoidea were studied. The material included five species from the familyCoreidae: Hydarella orientalis (Distant), Homoeocerus bannaensis Hsiao, Cletus graminis Hsiao & Cheng, Paradasynus lon-girostris Hsiao, Acanthocoris scaber (Linnaeus), and one species from the family Stenocephalidae: Stenocephalus femoralisReuter. All species show holokinetic chromosomes, post-reductional meiotic division of XO sex chromosomes, a pre-reduc-tional type of meiosis for autosomes and m-chromosomes, intersticial chiasmata in most autosomes, and one chiasma per biva-lent in male meiosis. In the species studied, the diploid chromosome number ranged from 13 to 21. It was 13 in S. femoralis (10+ 2m + XO), 15 in Hy. orientalis (12 + 2m + XO), 17 in Ho. bannaensis (14 + 2m + XO) and C. graminis (14 + 2m + XO), 19in P. longirostris (16 + 2m + XO), and 21 in A. scaber (18 + 2m + XO). Hy. orientalis represents the first cytogenetically stud-ied species in subfamily Hydarinae. The phylogenetic relationships among Coreoidea are briefly discussed from a cytogenetic point of view.

Cytogenetical characterization of six orb-weaver species and review of cytogenetical data for Araneidae

The family Araneidae is the third largest among spiders and the third most studied from a cytogenetical point of view. In spite of this, only 2% of all araneids have been karyotyped. The majority of araneids analyzed possess 2n 5 24 chromosomes in males; however, the study of additional species could reveal unusual karyotype characteristics. Thus, the aim of this work is to analyze chromosomally, for the first time, six species belonging to three araneid genera from Brazil. The specimens of Alpaida leucogramma (White 1841), Alpaida truncata (Keyserling 1865), Alpaida veniliae (Keyserling 1865), Parawixia kochi (Taczanowski 1873), Parawixia velutina (Taczanowski 1878) and Wagneriana sp. were collected in Parque Nacional de Ilha Grande and in the municipality of Rio Claro. The gonads were treated with colchicine and hypotonic solution before fixation with Carnoy I solution. The results were 2nL 5 24 (11II+X1X2 )i nA. leucogramma and P. velutina, and 2nL 5 22 (10II+X1X2 )i nA. truncata, A. veniliae, P. kochi and Wagneriana sp. When the chromosomal morphologies were established, we observed telocentric chromosomes in all specimens save one female specimen of P. velutina. The univalent sex chromosomes were easily recognized on diplotenes. The unpaired metacentric element found in one female specimen of P. velutina with 2n 5 25 probably arises by centric fusion/fission. Araneidae is a megadiverse family composed of ,3000 species distributed mainly in the tropics; thus the analysis of more species may provide new insights about orb-weaver chromosome evolution.

Karyotype plasticity in crickets: numerical, morphological, and nucleolar organizer region distribution pattern of Anurogryllus sp.

Within the Orthopteran species, those of the suborder Ensifera have been rarely studied from the cytogenetic point of view, mainly due to the difficulties for taxonomic identification of its species. The Gryllidae is the second largest family of this suborder and possesses some genera, such as Anurogryllus, that occur only on the American continents. The aim of this work was to determine the karyotype characteristics, the meiotic chromosome behaviour, and the nucleolar organizer region (NOR) pattern of Anurogryllus sp (Orthoptera: Gryllidae). In the analyzed sample, high levels of numerical, morphological, and NORs polymorphisms were detected. Within five distinct karyotypes that were found, the basic karyotype of Anurogryllus sp. showed 2n(♂) = 22 + X0 with acrocentric autosomes and a metacentric X sex chromosome; furthermore, a conspicuous secondary constriction related to the NOR was present along the entire short arm on pair 5. The other four types of karyotypes arose from centric fusions between elements of pairs 1/3, 2/6, 4/7 and a NOR partial translocation from pair 5 onto the long arm terminal region of one element of the fused pair 2/6. Such intraspecific variability and the consequences of high levels of polymorphism are discussed, leading to conjectures about the mechanisms that led to these chromosome rearrangements.