Notes on chromosome numbers and C-banding patterns in karyotypes of some weevils from central Europe (Coleoptera, Curculionoidea: Apionidae, Nanophyidae, Curculionidae)

Chromosome numbers and C-banding patterns of sixteen weevil species are presented. The obtained results confirm the existence of two groups of species with either a small or large amount of heterochromatin in the karyotype. The first group comprises twelve species (Apionidae: Oxystoma cerdo, Eutrichapion melancholicum, Ceratapion penetrans, Ceratapion austriacum, Squamapion flavimanum, Rhopalapion longirostre; Nanophyidae: Nanophyes marmoratus; Curculionidae: Centricnemus (=Peritelus) leucogrammus, Sitona humeralis, Sitona lineatus, Sitona macularis, Sitona suturalis). In weevils with a small amount of heterochromatin, tiny grains on the nucleus during interphase are visible, afterwards appearing as dark dots during mitotic and meiotic prophase. The second group comprises four species from the curculionid subfamily Cryptorhynchinae (Acalles camelus, Acalles commutatus, Acalles echinatus, Ruteria hypocrita) which possess much larger heteropycnotic chromosome parts visible during all nuclear divisions. The species examined have pericentromeric C-bands on autosomes and on the X chromosome.     

C-bands on chromosomes of 32 beetle species (Coleoptera: Elateridae, Cantharidae, Oedemeridae, Cerambycidae, Anthicidae, Chrysomelidae, Attelabidae and Curculionidae)

C-banding patterns of 32 beetle species from the families Elateridae, Cantharidae, Oedemeridae, Cerambycidae, Anthicidae, Chrysomelidae, Attelabidae and Curculionidae were studied using the C-banding technique. Mitotic and meiotic chromosomes were previously described for 14 species. From among 18 species that had never been cytogenetically studied, we determined the diploid and haploid chromosome numbers and the sex determination system for 12 beetles. The karyotype for 6 species is not described because of a lack of mitotic and meiotic metaphases. Results confirm that most of the beetle species possess a small amount of heterochromatin and C-positive segments are weakly visible in pachytene stages and weakly or imperceptible in mitotic and meiotic metaphases. In some species with a large amount of heterochromatin, C-bands were observed in the centromeric region in all autosomes and the X chromosome. The Y chromosome does not show C-bands with the exception of Oedemera viridis in which it possesses a small band of heterochromatin.     

C-heterochromatin and extra (B) chromosome distribution in six species of the Nabis (Heteroptera, Nabidae) with the modal male karyotype 2n = 16 + XY

The basic male karyotype of the six Nabis species (Heteroptera, Nabidae) is confirmed as being 2n=16+XY. The chromosomes are holokinetic while male meiosis is achiasmatic. The sex chromosomes undergo postreduction and in second metaphase show distance pairing, registered in all nabid species examined so far. Using C-banding technique for the first time in the family Nabidae, the heterochromatin was revealed on chromosomes of six species. The species showed different amount and distribution of C-heterochromatin. Only in Nabis (Dolichonabis) limbatus did the C-bands distribution make possible the identification of every chromosome pair in the karyotype. In other species, C-bands were found in some of the autosomes and the X, localized either interstitially or at telomeres. Only the Y usually showed relative stability ofthe C-banding pattern. In four of six species, extra (B) chromosomes were observed and their behaviour in meiosis described.     

C-bands on chromosomes of four beetle species (Coleoptera: Carabidae, Silphidae, Elateridae, Scarabaeidae)

The C-banding pattern of Bembidion geniculatum, Silpha atrata, Prosternon tesselatum, and Epicometis hirta are presented. All analysed species have pracentromeric C-bands on autosomes and chromosome X but the widest ones are visible in the karyotype of B. geniculatum. In S. atrata, P. tesselatum, and E. hirta sex chromosome y is heterochromatic, only B. geniculatum having the Y chromosome wholly euchromatin. The results indicate that on the chromosomes of the investigated species do not have a terminal and an intercalar segments of heterochromatin.     

Characterization of constitutive heterochromatin of Callithrix geoffroyi (Callitrichidae, Primates) by restriction enzymes and fluorochrome bands

The neotropical primate genus Callithrix comprises two groups of species, jacchus and argentata, which inhabit distinct geographical regions and manifest different fur coloration and constitutive heterochromatin (CH) markers in their karyotypes. In this investigation the CH of a representative of the jacchus group, Callithrix geoffroyi, was analysed using fluorochromes and restriction enzymes in situ. To clarify the source of the constitutive heterochromatin of both groups, the data obtained in the jacchus group were compared with those published in the argentata group obtained by the same techniques. The C-bands of C. geoffroyi (four specimens, 2n = 46) were centromeric in all chromosomes, and distally located in pairs 6 and 22. The Alu I, Hae III, Hin fI, Rsa I, Dde I, Mbo I, and Msp I restriction endonucleases and CMA3 and DAPI fluorochromes produced different bands, which allowed the characterization of four distinct types of constitutive heterochromatin in the C. geoffroyi genome. Several of these types of heterochromatin were present in the ancestor of the two groups of species, jacchus and argentata, while others originated after their cladogenesis.     

Heterochromatin and interstitial telomeric DNA homology

The purpose of this investigation was twofold. The first objective was to demonstrate that, in most of ten mammalian species commonly used in biomedical research, not all constitutive heterochromatin (C-bands) represents telomeric DNA. For example, the C-bands in human chromosomes, the long arm of the X and the entire Y chromosome of Chinese hamster, and most of the short arms of Peromyscus and Syrian hamster chromosomes are not telomeric DNA. In addition to the usual terminal telomeric DNA in the chromosomes of these mammalian species, the pericentromeric regions of seven or eight Syrian hamster chromosomes and all Chinese hamster chromosomes except pair one have pericentromeric regions that hybridize with telomeric DNA, some in C-bands and some not. The second objective was to describe a simple fluorescence in situ hybridization (FISH) reverse-printing procedure to produce black-and-white microphotographs of metaphase and interphase cells showing locations of telomeric DNA with no loss of resolution. Thus, at least three different types of heterochromatin (telomeric heterochromatin, nontelomeric heterochromatin and a combination of both) are present in these mammalian species, and this simple black-and-white reverse printing of telomeric FISH preparations can depict them economically without sacrificing clarity.     

Restrictive localization of centromeric heterochromatin (C-bands) in Presbytis e. entellus (Dufresne) as compared to Macaca mulatta (Zimmerman)

C-bands are observed in the centromeric regions of only three pairs of autosomes and the distal portion of the small acrocentric Y in a total complement of 44 chromosomes of a male Presbytis e. entellus. Simultaneously treated slides of a Rhesus monkey, however, have C-bands in all the 42 chromosomes. The lack of C-bands may be due to (1) absence of highly repetitive DNA in the centromeric region of certain chromosomes or (2) presence of minute quantity of such DNA which is imperceptible or (3) different types of centromeric heterochromatin with a varying degree of repetition of DNA sequences all of which do not react in similar manner to various techniques employed at present. It is hypothesized that the centromeric heterochromatin rich in satellite DNA helps in withstanding the force of excessive coiling of chromosomes at the centromere to facilitate the functioning of the genes for microtubular protein during cell division when other genes are rendered inactive due to compactness of chromosomes.     

Karyological investigations on seven weevil species (Coleoptera, Curculionidae)

Karyological studies were carried out on seven Palaearctic weevils. The following chromosome numbers were found in individual species, i.e. Otiorhynchus niger (F.), Phyllobius viridearis (Laich.), Phyllobius scutellaris Redt., Phyllobius calcaratus (F.), Polydrusus cervinus (L.), and Brachyderes incanus (L.) 2n = 22, n Male = 10 + Xyp, in Lixus elegantulus (Boh.) 2n = 22, n Male = 21 + Xyp. The heterochromosomes of all the examined species form, in the first meiotic metaphase, a typical parachute bivalent.     

Heterochromatin organization in the nucleus of Indian muntjac (Muntiacus muntjak)

The heterochromatin in Indian muntjac (Muntiacus muntjak) is located at the periphery of primary constrictions of all the chromosomes. The X chromosome contains significantly larger amounts of heterochromatin than the rest of the complement by C-banding technique. However, the small portion of C-band region was found to be resistant by restriction endonuclease HaeIII (5'...GG decreases CC...3') and was clearly visible on the nucleus. Therefore, the position of this large heterochromatic segment is examined at somatic metaphases. The distribution of the heterochromatin of the X chromosome observed in Indian muntjac is contrary to the general pattern observed in other species, i.e., the chromosomes consisting greater amount of heterochromatin are located more peripherally than those with lesser amount. However, the smaller Y chromosome (Y1) is frequently found at the periphery. The present findings suggest that the role of heterochromatin organization in the nucleus vary between different heterochromatic segments of the same species and vary from species to species.     

Quantitative analysis of C-segments of chromosomes 1, 9, 16 and Y in couples with reproductive disorders

A comparative analysis of structural variability of C-bands on chromosomes 1, 9, 16 and Y was conducted in 50 phenotypically normal adults and 25 couples with repeated spontaneous abortions. Reduction of both the total amount of heterochromatin in the cell and the lengths of these regions on chromosomes 1, 9, and 16 is revealed in the group of pathology. No differences were found in the lengths of C-bands on Y chromosome.     

Karyotypic characterization of three weevil species (Coleoptera: Curculionidae, Brachyderini)

Karyotypes of three species, Brachyderes incanus, Brachysomus setiger and Paophilus afflatus, belonging to the tribe Brachyderini, were studied using C-banding technique. The species share the same chromosome number 2n = 22 and meioformula n = 10+Xy(p) at all metaphase 1 plates of spermatid division. Some differences between karyotypes were observed in terms of centromere positions and C-band sizes. Most chromosomes are meta- or submetacentric and form a graded series in respect to length. The chromosomes resemble one another in having a rather small amount of heterochromatin restricted to the pericentromeric region and visible as dark stained blocks mainly during early stages of nuclear division. Only in Brachyderes incanus do larger bands occur at mitotic metaphase and diakinesis. These cytogenetic data are in agreement with karyological findings obtained in other species of Brachyderini so far examined.     

Equilocality of heterochromatin distribution and heterochromatin heterogeneity in acridid grasshoppers

Comparative fluorescence studies on the chromosome of ten species of acridid grasshoppers, with varying amounts and locations of C-band positive heterochromatin, indicate that the only regions to fluoresce differentially are those that C-band. Within a given species there is a marked tendency for groups of chromosomes to accumulate heterochromatin with similar fluorescence behaviour at similar sites. This applies to all three major categories of heterochromatin — centric, interstitial and telomeric. Different sites within the same complement, however, tend to have different fluorescence properties. In particular, centric C-bands within a given species are regularly distinguishable in their behaviour from telomeric C-bands. Different species, on the other hand, may show distinct forms of differential fluorescence at equilocal sites. These varying patterns of heterochromatin heterogeneity, both within and between species, indicate that whatever determines the differential response to fluorochromes has tended to operate both on an equilocal basis and in a concerted fashion. This is reinforced by the fact that structural rearrangements that lead to the relocation of centric C-bands, either within or between species, may also be accompanied by a change in fluorescence behaviour.We dedicate this paper, with affection, to Professor Hans Bauer on the occasion of his 80th birthday, and in appreciation of his singular contribution to the study of chromosomes     

The reaction to c-banding of c-banded constituents during mitotic cycle ofCrepis capillaris

The reaction to C-banding was investigated throughout the mitotic cycle ofCrepis capillaris (2n=6): (1) 18–22 C-bodies or C-bands were found during mid telophase and interphase to prophase and metaphase, and also 12–14 at late anaphase to early telophase in the mitotic cycle. Fewer C-bands in late anaphase to early telophase were due to the absence of minute bands; (2) large and medium sized C-bands were strongly stained by Giemsa, while small and minute bands stained palely. It is suggested that inCrepis capillaris the difference of color in C-banded segments following Giemsa staining is referable to the amount of constitutive heterochromatin rather than to the difference in the condensation and decondensation; (3) the size of C-bodies changed during telophase to interphase and prophase. It is inferred that the extent of C-bodies is regulated by both the length of DNA sequences of constitutive heterochromatin and the amount of proteins combined with C-banded DNA. It was shown that the reaction to C-banding is neither due to the differential condensation of chromatin nor to a higher concentration of DNA in the C-banded regions, in the C-banding mechanism as has been suggested so far at least.     

New data on the cytology of parthenogenetic weevils (Coleoptera,Curculionidae)

Parthenogenesis and, in particular, polyploidy are rare in animals. A number of cases, known among weevils, represent apomictic parthenogenesis-a reproductive mode in which eggs undergo one maturation division, the chromosomes divide equationally, and no reduction takes place. Among parthenogenetic weevils there are two diploids, 48 triploids, 18 tetraploids, six pentaploids, three hexaploids and one decaploid. Eight examined parthenogenetic species are triploids with 33 chromosomes of different morphology, confirming that triploidy is the most common level of ploidy in weevils. The karyotypes are heterogeneous with the presence of meta-, submeta-, subtelo- and acrocentric chromosomes. The C-banding method showed that only two species possess a large amount of heterochromatin visible as a band around the centromere during mitotic metaphase. This agrees with observations that weevils are characterized by a small amount of heterochromatin, undetectable in metaphase plates after C-banding. In three species an atypical course of apomictic oogenesis occurs with stages similar to meiosis, in which chromosomes form bivalents and multivalent clusters. This association of chromosomes probably represents the remnants of meiosis, although these events have nothing to do with recombination. The results support the hypothesis that the evolution of apomictic parthenogenesis in weevils has proceeded through a stage of automixis.     

C-banding in the polytene chromosomes of species of the plumosus group (Diptera,Chironomidae) and their experimental hybrids

The localization and amount of heterochromatin in the plumosus group were studied, including the species Chironomus plumosus L., C. vancouveri and C. balatonicus. The appearance of C bands of Chironomus plumosus in several European populations is traced. The role of the C heterochromatin in the differentiation of this species is discussed. From the evolutionary point of view the Swiss populations, in which large centromere heterochromatin blocks have been discovered, are more varied as to the amount of heterochromatin. The importance of duplications for this process is pointed out. The chromosomes of the individuals from C. vancouveri and C. balatonicus have centromeric, telomeric and interstitial heterochromatin. The centromeric heterochromatin is represented by thin C-bands. The particularities in the appearance of C heterochromatin in C. vancouveri and C. balatonicus reflect the structural peculiarities of their chromosomes. The change in the euchromatin regions in these forms is discussed in the light of transformation of euchromatin to heterochromatin in the process of evolution.The appearance of heterochromatin in hybrids (between populations and between species) created experimentally is traced. A change has been discovered in the appearance of heterochromatin in the hybrids compared to the initial parent forms. This difference is expressed more strongly in inter-species hybrids than in interpopulation hybrids of C. plumosus.     

Chromosome banding in amphibia

In the chromosomes of 12 frog species of the suborder Diplasiocoela (Amphibia, Anura), the constitutive heterochromatin and the nucleolus organizer regions (NORs) have been specifically stained. On most of the chromosomes, aside from the centric heterochromatin, telomeric and interstitial C-bands were also found. The various C-bands display a very variable reaction to alkaline pretreatment; this indicates heterogeneity in the constitutive heterochromatin. Sex chromosomes could not be identified in any of the species studied. The number and chromosomal positions of the NORs vary quite strongly between species and between families. In 4 species of the genus Rana, there were, aside from the standard-NORs in chromosome pair 10, between 4 and 14 extra, small NORs detectable in the smaller chromosome pairs. As possible causal mechanism of these additional small NORs the reintegration of amplified rDNA during amphibian oogenesis is suggested. Q- or G-bands could only be recognized in mitotic prophase chromosomes. The strong spiralization of metaphase chromosomes prevents the differential demonstration of Q- or G-bands in the euchromatic regions.     

Cytogenetic aspects of phylogeny in the Bovidae. II. C-banding

Constitutive heterochromatin in the Bovidae, as revealed by C-banding, was mostly located in the centromeric regions. Considerable variation was, however, evident in the size of the C-bands both within and between subfamilies. Some evidence was found for a reduction in the amount of centromeric heterochromatin in bi-armed relative to acrocentric autosomes, and these findings are discussed in relation to karyotype evolution in the group.     

Regularities and restrictions governing C-band variation in acridoid grasshoppers

C-band patterns have been analysed in embryonic neuroblast chromosomes of 23 Australian species of acridoids. All of them showed paracentromeric C-bands but these varied considerably in size both within and between species. Many of them also showed interstitial C-bands in from 1–5 members of the haploid complement and in two cases (Atractomorpha similis and Genus nov. 95 ochracea) larger numbers of interstitial bands were present. Terminal C-bands were the least common though again when present they could be found in 1–6 members of the complement except in the cases of A. similis and Genus nov. 95 ochracea where still larger numbers occur. In 5 of the 23 species the megameric chromosome pair was distinctively C-banded. The B-chromosomes found in 3 of the species were also strikingly different in C-band characteristics compared to the standard A-chromosomes. Differences in the number of very small chromosomes present in different species clearly cannot be explained in terms of differences in their C-band content. Neither are differences in genome size simply related to differences in the total amount of C-band material indicating that changes in the size of the genome in this group have involved alterations in both eu and heterochromatin content. Finally similar amounts of C-band material may be distributed throughout the complement in very different ways in different species.To Hans Bauer with respect and affection on the occasion of his 75th birthday.     

Identification of the pattern of heterochromatin distribution in Passiflora species with C-banding

We tested four C-banding protocols to obtain heterochromatic bands in the passion fruit species Passiflora edulis and P. cacaoensis (Passifloraceae). Three of these protocols had been previously described. The three published protocols were not adequate to obtain C-bands in these species. An adapted protocol demonstrated heterochromatin distribution in metaphasic chromosomes of species of Passiflora for the first time. The differentiated coloration for C-bands was obtained with immersion of the slides in 99% ethanol, 45% acetic acid (additional step), 0.2 N hydrochloric acid, hydroxide of barium, 45% acetic acid, and 2X standard saline citrate at four different temperatures. The C-bands were observed in the satellites and in the telomere and centromere regions of all chromosomes, both in P. edulis and in P. cacaoensis.     

A new karyotype in Callicebus torquatus (Cebidae, Primates)

We describe a new karyotype of Callicebus torquatus using conventional staining, G-banding with Wright Stain, CBG, Ag-NOR staining and fluorescence in situ hybridization (FISH) with human telomere probes and comparative analysis with the previously reported karyotype of C. torquatus torquatus (2n = 20). We studied a female specimen maintained in captivity at the Centro Nacional de Primatas (Para, Brazil). This titi monkey presented 2n = 22, with four large biarmed and six acrocentric autosome pairs; the X chromosome is a medium submetacentric. C-bands were revealed at the centromeric region of all acrocentrics and X chromosome; punctual C-bands also are visualized at the centromeric region in the large biarmed pairs. The NOR site was located at the long arm of pair 4, at the position of a conspicuous secondary constriction. Hybridization signals were detected exclusively at the terminal region of all chromosomes. The karyotype described here has one acrocentric pair more than that found in the literature and also differs by amount and distribution of constitutive heterochromatin. Our data support the notion that the torquatus group may be composed of distinct species, each with its own karyotype.