COMPARATIVE KARYOLOGICAL ANALYSIS OF FIVE SPECIES OF VIVIPARUS (GASTROPODA: PROSOBRANCHIA)

Karyological analysis was performed on Viviparus ater (Cristofori& Jan, 1832), V. acerosus Bourguignat, 1862, V. mamillatus (Kuster),V. viviparus (Linnaeus, 1758) and V. contectus (Millet, 1813),collected from different freshwater bodies of Switzerland, Hungary,Albania, Italy and Lithuania. The karyotypes of V. acerosusand V. mamillatus are described for the first time. The diploidnumber of chromosomes in V. contectus equals 14, whereas indiploid sets of other studied species, 18 chromosomes are present.The karyotype formula is in V. contectus (5m + 2sm, NF = 28,in V. ater, 7m + 1sm-m + 1 sm, in V. acerosus and V. viviparus,8m + 1sm, NF = 36, in V. mamillatus, 6m + 1m-sm + 1sm-m + 1sm,NF = 36. In females of V. ater, V. mamillatus and V. acerosus,the heteromorphism of chromosome pair no. 8 was observed, witha sex-determining mechanism — ZW female /ZZ male. Although,Z and W chromosomes are metacentric, significant differences(P > 0.05, or P > 0.001) in their size were determined.The interspecific significant differences (P > 0.05) in karyotypesof V. ater, V. mamillatus, V. acerosus and V. viviparus weredetected by using one-way ANOVA and Bonferronis Multiple Comparisontests. Only chromosomes of the pair no. 5 were of similar shapein all of these species. The smallest interspecific differencewas between V. viviparus and V. acerosus. The intraspecifickaryological differences in relative chromosome length and centromericindex of V. contectus from lakes Garda (Italy), Olauka andAsveja (Lithuania) were observed in the chromosome pair no.5. (Received 29 March 1999; accepted 19 October 1999)     

KARYOTYPES OF FIVE SUBANTARCTIC BIVALVE SPECIES

Chromosomes of five subantarctic species were studied from mitoticmetaphases using cell suspension techniques. Among the Protobranchia,Malletiagigan-lea has a diploid chromosome number of 2n = 38with five metacentric, seven submetacentric, five sub-telocentricand one telocentric pairs, and Yoldia (Aequiyoldia) woodwardialso shows 2n = 38 but with ten metacentric, six submetacentricand three sub-telocentric pairs. Among the Lamellibranchia,the pterioidan Limatula pygmaea has 2n = 38 with six metacentric,eleven submetacentric and two sub-telocentric pairs, the veneroidanCyclocardia astar-toides has 2n = 30 with five metacentric andten telocentric pairs and the anomalodesmatan Laternula ellipticahas 2n = 40 with two metacentric, one submetacentric, two subtelocentricand fifteen telocentric pairs. Our results indicate that in all the Nuculoidea studied so far,a diploid number of 2n = 38 has been found. In addition, thekaryotypes show a close overall appearance in relative lengthswith a majority of meta-centric-submetacentric chromosomes.The species differ in the proportion of the different morphologicaltypes of chromosomes. In the Lamellibranchia, each species correspondsto a particular case within their respective orders (Pterioida,Veneroida, Anomalodesmata). (Received 22 January 1990; accepted 28 March 1990)     

Unusual chromosome complement in the brooding bivalve Lasaea consanguinea

Chromosomes of the brooding species Lasaea consanguinea were studied as part of a general invertigation of evolutionary genetics of antarctic bivalve species. Laseid species are of particular interest because they are widely distributed geographically, they inhabit the high intertidal zone, and they may reproduce apomictically.The diploid number of chromosomes for Lasaea consanguinea ranges from 100 to 120, 110 to 112 being most frequent. Karyological data (2n=108) show 6 groups of chromosomes. Group I includes 8 metacentric (m), 3 submetacentric (sm), 2 subtelocentric (st) and 4 telocentric (t) pairs. Group II has 11 t to st pairs; group III, 9 sm to m pairs; group IV, 8 m to sm pairs; group V, 6 st and group VI, 3 m pairs. Within each of the Groups II to VI chromosome pairs are of about the same size and morphology.The chromosomes of Lasaea consanguinea are unusual because of their abundance, their large size and their numerical variability. We suggest that Lasaea consanguinea has had a hermaphroditic ancestor where abnormal reproduction such as inbreeding, lack of males, and apomixy gave rise to genetic instability, the high number of chromosomes being related to the genetic instability with evolutionary polyploidy or/and supernumerary chromosomes.     

Chromosomal evolution of the Hawaiian Telmatogeton (Chironomidae,Diptera)

It is only in the Hawaiian Islands that species of the otherwise marine genus Telmatogeton have evolved into freshwater. An analysis of polytene chromosomes and karyotypes of two marine species and five freshwater species revealed that paracentric inversions and centric fusions were important in chromosomal evolution. The sequence of polytene chromosome bands common to most species, established as the Telmatogeton standard sequence, is found in a population of T. torrenticola from West Maui. Most species and other populations of T. torrenticola may be derived from the standard sequence by paracentric inversions. Similarities with the standard band sequence places T. japonicus (n=7) rather than T. pacificus (n=4) in the proposed phylogeny as the species closest to the marine ancestor of the freshwater species. One of three species (T. fluviatilis from Oahu, T. torrenticola from West Maui, or an undescribed species from East Maui), each with seven pairs of chromosomes is considered to be closest to the original freshwater species. T. torrenticola is a complex species in which there is an accumulation of fixed inversions and centric fusions in stepwise fashion in populations from west to east (West Maui n=7; East Maui n=6; Kohala Mountains n=5 and Mauna Kea n=4 both from the island of Hawaii). The population of T. torrenticola from Molokai has a reduced chromosome number (n=4) and fixed inversions. T. abnormis and T. hirtus, the only species which exhibit differentiated sex chromosomes, may be derived from the standard sequency by paracentric inversions. T. abnormis (n=4) has a simple XY system and T. hirtus (n=3/4) has a complex XY₁Y₂ system. Unique sequences of bands, differences in staining intensity of puffs and bands, and an inversion form the basis for the differentiation of the various Y-chromosomes in these species.     

SYSTEMATICS OF POTAMACMAEA FLUVIATILIS (BLANFORD): A BRACKISH WATER PATELLOGASTROPOD (PATELLOIDINAE: LOTTIIDAE)

Potamacmaea fluviatilis (Blanford, 1867), which is known fromestuaries and tributaries that drain into the Bay of Bengal,was studied to assess available material, determine possiblerelationships between P. fluviatilis and other patellogastropodtaxa, and review the current state of our knowledge of thisenigmatic species. Radular and shell structure characters indicatethat P. fluviatilis is referable to the Patelloidinae Chapman& Gabriel, 1923. The radular tooth morphology of P. fluviatilisis similar to that of the wood-eating taxon PectinodontinaePilsbry, 1891; both taxa have multicuspid lateral teeth. Substantialhuman population increase and its accompanying habitat destructionin this region may have had deleterious effects on this uniquepatellogastropod. (Received 22 May 1989; accepted 25 July 1989)     

A note on chromosomes of two species of tree shrews (Tupaiidae)

Karyological studies of five tree shrews showed a diploid number 2n=60 forTupaia glis and 2n=66 forTupaia minor. The Y chromosome ofTupaia glis was found to be a medium-sized submetacentric chromosome in contrast to earlier data in the literature. The karyotype of a femaleTupaia minor showed five pairs of metacentric and submetacentric chromosomes and 28 pairs of acrocentric chromosomes.     

Molecular Cytogenetic Localization and Characterization of 5S and 25S rDNA Loci for Chromosome Identification in Oilseed Rape (Brassica napus L.)

Chromosome identification in oilseed rape (Brassica napus L.)is extremely difficult using conventional cytogenetic techniquesbecause amphidiploid Brassica species possess numerous verysmall chromosomes with few cytogenetic landmarks. In combinationwith methods for improved chromosome preparations, we used asimplified fluorescencein situ hybridization (FISH) techniqueto localize simultaneously the gene families coding for 5S and25S rDNA in B. napus. The resulting hybridization patterns enabledten of the 19 oilseed rape chromosome pairs to be unequivocallyidentified. Copyright 2000 Annals of Botany Company Brassica napus, oilseed rape, rDNA, molecular cytogenetics, FISH, chromosome identification     

The polymorphism and distribution of B chromosomes in germline and somatic cells of Tscherskia triton de Winton (Rodentia, Cricetinae)

The karyotypes of 13 greater long-tailed hamsters (Tscherskia triton de Winton, 1899) (eight males and five females) from Primorskii krai (Russia), including six males and one female from the vicinity of the city of Ussuriisk and two males and four females from the vicinity of the village of Pogranichnyi, have been studied. The karyotypes of five males (four from the vicinity of Ussuriisk and one from the vicinity of Pogranichnyi) have been found to contain one or two small acrocentric B chromosomes each. In males with B chromosomes, each germline cell contains one or two B chromosomes. The proportion of somatic cells carrying B chromosomes varies from 34.9 to 55.9% in these males. Karyological study of a total of 45 Tscherskia triton (30 males and 15 females) from Primorskii krai has been performed, B chromosomes being found in only five males (11.1%). In T. triton populations of Korea and China, also only a few animals have been found to carry one or two B chromosomes. The greater long-tailed hamster belongs to the monotypic genus Tscherskia; the animals described earlier under the names T. (Cricettilus) triton albipes Ognev, 1914 and T. (Cricettilus) triton nestor Thomas, 1907 belong to the only species in the genus, T. triton de Winton, 1899.     

Comparative cytogenetics of opisthorchid species (Trematoda, Opisthorchiidae)

In the present study karyotypes and chromosomes of five species of the family Opisthorchiidae (Opisthorchis felineus (Rivolta, 1884), O. viverrini (Poirier, 1886), Metorchis xanthosomus (Creplin, 1846), M. bilis (Braun, 1893), and Clonorchis sinensis (Cobbold, 1875)) were compared. Karyotypes of O. felineus, M. xanthosomus, M. bilis and C. sinensis consist of two pairs of large meta- and submetacentrics and five pairs of small chromosomes (2n = 14). The karyotype of O. viverrini is 2n = 12, which indicates a fusion of two chromosomes of opisthorchid ancestral karyotype. Analysis of mitotic and meiotic chromosomes was performed by heterologous in situ hybridization of microdissected DNA probes obtained from chromosomes 1 and 2 of O. felineus and chromosomes 1 and 2 of M. xanthosomus. Results of chromosome staining (C- and AgNOR-banding) and FISH of telomeric probes and ribosomal DNA probe on opisthorchid chromosomes were used for chromosome comparison. Data on chromosome number in opisthorchid species were also discussed.     

Identifizierung der genetischen Geschlechtschromosomen bei der monogenen Schmeißfliege Chrysomya rufifacies (Calliphoridae,Diptera)

Previous investigations have shown the sex determination in the monogenic blowfly Chrysomya rufifacies to be controlled by a cytologically not discernible homogamety-heterogamety mechanism in the female. Female-producing (thelygenic) females are assumed to be heterozygous for a dominant female sex realizer (F′) with sex-predetermining properties, while male-producing (arrhenogenic) females as well as males are supposed to be homozygous for the recessive allele (f). In order to identify the genetic sex chromosomes of C. rufifacies among its five pairs of long euchromatic chromosomes (nos.1–5) plus one pair of small heterochromatic ones (no. 6), all chromosomes were marked by reciprocal translocations induced by X-ray treatment of adult males. The inheritance of thirteen different heterozygous translocations has been analyzed. All of the translocations (eleven) between two of the four longer chromosomes did not show sex-linked inheritance, thus demonstrating the autosomal character of the chromosomes nos 1, 2, 3 and 4. The same is true for the translocation T6 (2/6). Therefore the small heterochromatic chromosome no. 6, corresponding to the morphologically differentiated sex chromosomes within the amphogenic calliphorid species, remains without sex determining function in the monogenic fly. This could be confirmed by the analysis of monosomic (monosomy-6) and trisomic (trisomy-6) individuals, which resulted from meiotic non-disjunction in T6/+ translocation heterozygotes. Contrary to these translocations, the heterozygous 5/2 translocation (T14) exhibited sex-linked inheritance: There was but a very low frequency (0,76 per cent) of recombinants resulting from crossing-over between F′/f and the translocation breakage point in thelygenic F₁ T14/+ females. The sex-linked inheritance of T14 was confirmed by the progeny of a thelygenic F₁ T14/+ female crossed to a homozygous T14/T14 translocation male. Among the offspring of that F₁ T14/+ female, which had received the translocation from its father, all of the F₂ T14/+ females were thelygenic compared to their arrhenogenic T14/T14 sisters. These results prove that the chromosomes of pair no. 5 genetically act as X′X-XX sex chromosomes in C. rufifacies.     

Developments in avian cytotaxonomy: implications for Afro-avian Species

Ejere. VC. 2000. Developments in avian cytotaxonomy: implications for Afro-avian Species. Ostrich 71 (1 & 2): 40.

Karyological studies of the extant species of birds have progressed slower than those of other animal groups. To date, a paltry proportion of less than 20% of about an estimated 9 000 avian species have been karyotyped, such that for most orders, karyological information remains largely scanty. Data accumulated so far, has revealed a lot of interesting features of the typical avian karyotype. Essentially, the karyotype is dichotomous, containing several pairs of fairly big chromosomes (= macrochomosomes) and very small to minute chromosome elements (= microchromosmes). The diploid chromosome number is also variable, ranging from 2n = 40 to 2n = 92 with a mode of 2n = 80 chromosomes observed in a majority of species. Studies have further revealed that chromosomal evolution in birds is highly conservative especially with reference to the first 3 pairs of macrochromosomes. (Group A), while considerable variability in number and morphology occurs in the remaining groups of chromosome elements. These variabilities, as well as the homologies revealed by chromosome banding techniques, have aided the cytotaxonomy of various individual avian groups. In this review, the karyological as well as the phylogenetic relationships of the various avian species so far karyotyped, vis-a-vis the cytotaxonomic implications for the abundant Afro-avian fauna are highlighted. Similarly, the significance of the observed peculiarities in the avian karyotype is briefly discussed. Suggestions are proffered in respect of the application of karyotype analysis technique to bird conservation in Africa. This will focus mainly on the identification of the gender of birds for the singular purpose of breeding rare and endangered species for zoological gardens and related institutions.     

COMPARATIVE SPERM MORPHOLOGY OF THE PULMONATE LIMPETS TRIMUSCULUS COSTATUS, T. RETICULATUS (TRIMUSCULIDAE) AND BURNUPIA STENOCHORIAS AND ANCYLUS FLUVIATILIS (ANCYLIDAE)

Sperm ultrastructure is described for the first time in representativesof the pulmonate ‘limpet’ families Trimusculidae(Trimusculus costatus, T. reticulatus: marine) and Ancylidae(Burnupia stenochorias, Ancylus fluviatilis: freshwater). Allshow characteristic heterobranch sperm features (a spheroidalacrosomal vesicle supported by an acrosomal pedestal; a helicallykeeled nucleus and a complex, very elongate midpiece featuringparacrystalline and matrix layers sheathing the axoneme, coarsefibers and one or more glycogen helices). Posterior to the midpiece,a glycogen piece (axoneme sheathed by glycogen granules) andannulus are also present in all species. Taxonomically usefuldifferences in the shape and dimensions of the acrosome, nucleusand midpiece occur between the species. Results support thedecision of recent workers to transfer the Trimusculidae fromthe Siphonarioidea to a separate superfamily Trimusculoidea(characteristic sperm features including: narrow acrosomal pedestaloverlapping with nuclear apex; heavily keeled nucleus; midpiecewith strongly projecting secondary and glycogen helices). Therelationship of the Trimusculoidea to other pulmonates, as indicatedby sperm ultrastructure, remains uncertain largely because comparativedata for several important groups are unavailable. Spermatozoaof the two ancylids most closely resemble those of other investigatedplanor-boideans and to a lesser extent, those of the Lym-naeoidea.However, differences between Burnupia stenochorias (unique(?)accessory structure on the acrosomal pedestal; glycogen wedgeswithin the nuclear fossa; other features similar to planorbids)and Ancylus fluviatilis (all sperm features very similar toplanorbids) suggests that these patelliform ancylids are notclosely related. (Received 20 November 1997; accepted 23 January 1998)     

Telomeric DNA in chromosomes of five opisthorchid species

The analysis of telomere repeat distribution in chromosomes of five opisthorchid species (Opisthorchis felineus (Rivolta, 1884), Opisthorchis viverrini (Poirier, 1886), Metorchis xanthosomus (Creplin, 1846), Metorchis bilis (Braun, 1890), Clonorchis sinensis (Cobbold, 1875)) was performed with fluorescent in situ hybridization (FISH) of labeled (TTAGGG)n DNA-probe and PNA telomere probe on mitotic and meiotic chromosomes of these species. It was shown that chromosome telomeres of all studied species contain large clusters of (TTAGGG)n telomeric repeats. Interstitial clusters of the (TTAGGG)n repeats have not been revealed in the chromosomes of any studied species even when FISH of PNA telomere probe on pachytene chromosomes was performed. Furthermore interstitial clusters of the (TTAGGG)n repeats have not been detected in the chromosomes of O. viverrini, one of chromosomes of this species is the result of a fusion of two ancestral opisthorchid chromosomes.     

Studio Cariologico Di Helictotrichon Versicolor (Villar) Pilger Ssp. Praetutianum (Arc.) Nov. Comb

Abstract

Karyological study of «Helictotrichon versicolor» (Villar) Pilger ssp. «praetutianum» (Arc.) nov. comb. — Karyological investigations on Helictotrichon versicolor (Vill.) Pilger ssp. praetutianum (Arc.) nov. comb. (Graminaceae), from Alpi Apuane, have been made. The species, endemic of Alpi Apuane and Central-Southern Appennino, is diploid (2n=14), as Avena versicolor Vill. already studied by SKALINSKA (1956). The author reports on the karyotype, characterized by seven pairs of chromosomes, as follows: z = 2n = 14 = 2M^s ₁ + 2M₂ + 2M₃ + 2M₄ + 2M₅ + 2M₆ + 2M₇.     

The Close Relationship Between the A and B Genomes in Avena L. (Poaceae) Determined by Molecular Cytogenetic Analysis of Total Genomic, Tandemly and Dispersed Repetitive DNA Sequences

The genusAvena L. (Poaceae) consists of diploid, tetraploid,and hexaploid species, with the B genome known only in tetraploidspecies and the D genome in the hexaploid species. DNA:DNAinsitu hybridization, using total genomic DNA from diploidAvenastrigosa Schreb. (A_sgenome) as a probe, labelled all 28 chromosomesof the AB tetraploidAvena vaviloviana (Malz.) Mordv. stronglyand uniformly, revealing the close relationship between thesetwo genomes. Comparison of patterns of size-separated DNA restrictionfragments between the diploidA. strigosa and the tetraploidA.vaviloviana , using 32 different restriction enzymes, revealedno differences. Southern hybridization using total AB genomicDNA as a probe also gave no differences in banding patternsbetween the two genomes, even when a large excess of A genomicDNA was used as a block. From anA. vaviloviana genomic library,1800 colonies were blotted and probed sequentially with A andAB genomic DNA, but no colony was identified to be B genomespecific. DNA digests of AB genome tetraploids with restrictionenzymeHae III gave a strong band at 4.2 kb. Clone pAbKB3, derivedfrom the 4.2 kb band, was found to be part of aTy1-copia -likeretrotransposon present in A and B genome chromosomes. ClonedrRNA genes were used forin situ hybridization and showed thatdiploidA. strigosa has four major sites for 18S-25S rDNA andtwo pairs of sites for 5S rDNA (pairs on the same satellitedchromosome, on different chromosome arms), while 4xA. vavilovianahas eight major sites for 18S-25S rDNA and four pairs of sitesfor 5S rDNA (pairs on the same satellited chromosome, on differentchromosome arms). A repetitive sequence from rye pSc119.2, showeddispersed hybridization, while the telomeric sequence in clonepLT11 hybridized to telomeres. Again no discrimination was possiblebetween A and B genome chromosomes. The molecular similaritiesbetween the diploidA. strigosa and thebarbata group tetraploidsclearly indicate that thebarbata group of tetraploids arosefrom A_sdiploids through autotetraploidization. Avena ; evolution; repetitive sequences; in situ hybridization; retrotransposons; genome organization     

Differential Accumulation of Heterochromatin as a Cause for Karyotype Variation in Phalaenopsis Orchids

Karyotypes of nine Phalaenopsis species and the closely relatedDoritis pulcherrima were compared based on Feulgen- and DAPI-stainedsomatic metaphase chromosomes prepared from root tips. All specieshad the same chromosome number (2n = 2x = 38), but their karyotypesdiffered markedly in absolute chromosome size, relative chromosomesize, and the position of the centromere. Both genome size andthe amount of constitutive heterochromatin (CH) varied widelyamong the species studied, and there was a positive correlationbetween these two parameters. The distribution of CH in thegenomes was non-random: one or both arms of long chromosomesusually possessed large blocks of CH, while the small chromosomescontained little or no CH. DAPI-staining revealed that mostCH regions are rich in AT base pairs. We suggest that differentialaccumulation of CH is a major cause for karyotype variationin Phalaenopsis orchids. Copyright 2001 Annals of Botany Company Phalaenopsis, Doritis pulcherrima, karyotype differentiation, constitutive heterochromatin, total chromosome volume, nuclear DNA content     

贵州两种黄脊蝗核型和C-带的比较研究

本文研究了贵州日本黄脊蝗 Patanga japonica Bolivar和印度黄脊蝗 P.Succincta Johansson的核型和c-带。结果表明：两种黄脊蝗的染色体数目均为2n(♂)=22+x.=23,全部为端着丝粒染色体;核型公式2n(♂)=2X=231,NF=23. 但日本黄脊蝗的染色体绝对长度总和(79.75±2.22μm)比印度黄脊蝗的(71.4 7±0.63μm)长;异染色质总量(35.65±0.14μm)比印度黄脊蝗的(10.76±0.11μm多;日本黄脊蝗的核型属“1B”核型,印度黄脊蜱的核型属“lc”核型。     

Occurrence of macro B chromosomes in Astyanax scabripinnis paranae (Pisces,Characiformes, Characidae)

B chromosomes occur in several Neotropical fish species. Cytogenetic analysis of 27 specimens (15 females and 12 males) of Astyanax scabripinnis paranae from the Araquá river (a small headwater tributary of the Tietê river) shows that this population has 2n=50 chromosomes (4M+30 SM+4ST+12A), two chromosome pairs with NORs and conspicuous C-band positive blocks in the terminal position of the long arm of four chromosome pairs. In this population, eight females presented 2n=51 chromosomes and the extra chromosome was a large metacentric similar in size and morphology to the first chromosome pair in the karotype. This accessory chromosome is entirely heterochromatic in C-banded metaphases and shows a late replication pattern evidenced by BrdU incorporation. There was no significant correlation between the presence of B chromosomes and increased NOR activity at the P>0.05 level. Some aspects related to these B chromosomes are discussed.     

Cytogenetic and molecular analysis of the pufferfish Tetraodon fluviatilis (Osteichthyes)

In view of their compact genome, pufferfish (Tetraodontiformes) have been proposed as model animal for the study of the vertebrate genome. Despite such interest, cytogenetic information about puffers is still scanty. To fill this gap, a cytogenetic analysis of T. fluviatilis has been performed using both classical and molecular techniques. C-banding, followed by DAPI staining, evidenced that in T. fluviatilis, like all other puffer species so far examined, heterochromatin is essentially AT-rich and it is located at centromeres, whereas staining with CMA₃, silver staining and FISH with a 28S ribosomal RNA gene DNA probe showed 2–4 nucleolar organizing regions (NORs) located in heterochromatic regions in the considered puffer species. FISH with the 5S probe put in evidence both in T. fluviatilis and in T. nigroviridis only a 5S cluster per haploid genome that is physically unlinked with the major ribosomal RNA genes including the 28S rRNA genes. Hybridization with the (TTAGGG)_n probe showed in all the puffers brightly fluorescent signals uniform both in size and intensity at the end of all the chromosomes. Finally, mariner-like elements (MLEs) have been identified in T. fluviatilis and they have located into the NOR-associated heterochromatin.