安徽沿江地区4种蛇的染色体组型、C带和Ag-NORs研究

本文报道游蛇亚科４种蛇的核型、Ｃ带和ＡｇＮＯＲｓ,结果：黄链蛇２ｎ＝４６．虎斑游蛇２ｎ＝４０,第４号染色体（Ｎｏ．４）有随体．鸟梢蛇和紫灰锦蛇２ｎ＝３６,鸟梢蛇的Ｎｏ．５短臂近着丝粒区有一次缢痕．虎斑游蛇Ｎｏ．５为性染色体,其余３种的性染色体为Ｎｏ．４．这４种蛇均为ＡＦ＝５０;Ｃ带型的种属性特征明显,其中紫灰锦蛇的端粒型Ｃ带特别发育,其余三种以着丝粒Ｃ带较发达．黄链蛇、虎斑游蛇和紫灰锦蛇的Ｗ染色体Ｃ带正染呈现整条异染色质化;银染结果４种蛇均只显示一对ＮＯＲｓ,但其分布不同,其中虎斑游蛇ＮＯＲｓ呈异态现象．文章讨论了核型的演化和次缢痕、ＮＯＲｓ及Ｃ带的关系     

游蛇科4种的核型比较

以骨髓细胞直接制备染色体标本，分析了游蛇属（Ｎａｏｔｒｉｘ）３种和链蛇属（Ｄｉｎｏｄｏｎ）１种蛇的核型．草游蛇（Ｎ．ｓｔｏｌａｔａ）２ｎ＝３６，１８（１５Ｍ＋１ＳＴ＋２Ｔ）·１８ｍ（♀）．渔游蛇（Ｎ．Ｐｉｓｃａｔｏｒ）２ｎ＝４０，１６（１０Ｍ＋１ＳＭ＋３ＳＴ＋２Ｔ）·２４ｍ（♀）．乌游蛇（Ｎ．ｐ．ｐｅｒｃａｒｉｎａｔａ）２ｎ＝４０，１８（８Ｍ十２ＳＭ＋８Ｔ）·２２ｍ（♂）．赤链蛇（Ｄ．ｒｕｆｏｚｏｎａｔｕｍ）２ｎ＝４６，２０（１Ｍ＋３ＳＭ＋１６Ｔ）·２６ｍ（♀）．草游蛇和渔游蛇的Ｎｏｓ，赤链蛇的Ｎｏ３为ＺＺ／ＺＷ型性染色体．草游蛇Ｚ染色体为Ｍ型，Ｗ染色体为ＳＴ型；渔游蛇Ｚ为ＳＭ型，Ｗ也是ＳＴ型；赤链蛇Ｚ为Ｍ型，Ｗ为ＳＭ型．三者Ｚ均略大于Ｗ．草游蛇和渔游蛇Ｎｏ４长臂末端有时可见随体．对游蛇属、链蛇属以及游蛇亚科（Ｃｏｌｕｂｒｉｎａｅ）已知各属种的核型进行了比较和讨论．     

不同寄主植物上烟蚜的染色体组型研究

对采自桃树、油菜和烟草上的烟蚜的核型研究表明：在红、黄绿两种体色的烟蚜中发现５种核型,即２ｎ＝１２,正常;２ｎ＝１２,Ａ１与Ａ３易位;２ｎ＝１１;２ｎ＝１３;３ｎ＝１８,Ａ１与Ａ３易位。同时,在核型为２ｎ＝２３的烟蚜中,体色为红色的个体全为Ａ１与Ａ３易位个体,体色为绿色的个体中既有Ａ１与Ａ３易位个体,又有正常个体。寄主植物不同的烟蚜的各条染色体相对长度在２ｎ＝１２核型中差异不显著（α＝０．０５）。     

Cytogenetic studies in green mussel, Perna viridis (Mytiloida: Pteriomorphia), from West Coast of India

Chromosomes of Perna viridis were characterized by karyotype analysis, C-banding and nucleolus organizer regions (NORs). The diploid chromosome number was confirmed as 30 and the karyotype is composed of ten metacentric and five submetacentric chromosome pairs. Constitutive heterochromatin blocks were found on all chromosomal pairs except chromosomal pair 15, which showed uniform staining throughout the entire chromosomes. Silver staining revealed nucleolus organizer regions on telomeric region of four chromosomal pairs, viz. 1, 3, 7 and 11. This is the first comprehensive study undertaken on chromosomes of Perna viridis.     

Karyotype, nucleolus organiser regions and constitutive heterochromatin in Ostrea angasi (Molluscae: Bivalvia): evidence of taxonomic relationships within the Ostreidae

Chromosome preparations from gill tissue of the Australian flat oyster Ostrea angasi Sowerby were studied with conventional Giemsa staining, C-banding and silver staining techniques. A diploid complement of 2n = 20 was observed, consisting of five metacentric, three submetacentric and two subtelocentric pairs. Constitutive heterochromatin was distributed as large centromeric blocks in Chromosome Pairs 3, 6, 8, 9 and 10. The nucleolus organizer regions (NORs) were located terminally on long arms of Chromosome Pairs 9 and 10. This allowed the identification of homologous chromosomes in submetacentric and subtelocentric pairs. Intraspecific variability in NOR pattern as revealed by differences in the number of silver-stained NORs (Ag-NORs) per cell was found to be very common. Comparison of the patterns of karyotype, C-band and Ag-NORs between species of the larviparous oysters for which data have been published demonstrate that the chromosomal structure of the endemic Australian and New Zealand species O. angasi shows little similarity to the Southern Hemisphere oysters O. (Eostrea)puelchana Orbigny and Tiostrea chilensis (Philippi) and the Indo-West Pacific oyster O. denselamellosa, but very high resemblance to the European species O. edulis. Received: 12 August 1996 / Accepted: 16 September 1996     

Cytogenetic analysis of Epinephelus marginatus (Pisces: Serranidae), with the chromosome localization of the 18S and 5S rRNA genes and of the (TTAGGG)n telomeric sequence

 A cytogenetic analysis was carried out on specimens of Epinephelus marginatus (Lowe, 1834) from three localities in the Mediterranean Sea, to deepen knowledge of the chromosome complement of the species and identify any possible population-specific cytogenetic markers. All specimens had a 2n = 48 acrocentric karyotype with two Ag-, chromomycin A₃- and C-positive NORs (nucleolar organizer regions) in the subcentromeric region of the smallest chromosome pair. The constitutive heterochromatin was distributed centromerically. Except for NORs, neither eu- nor heterochromatin show fluorescence after fluorochrome staining, i.e. there is no localized increase of AT- or GC-rich DNA. In all populations, the (TTAGGG) _n telomeric sequences are restricted to the telomeres, and the 18S and the 5S rDNA clusters are located on different chromosome pairs. In specimens from Sardinia, additional signals after C-banding, Ag-staining and FISH (fluorescence in situ hybridization) with 18S rDNA can be observed in the telomeric region of one or two large-sized chromosomes, classified as No. 2. This suggests that additional and variable NORs could be detected in the species in addition to those on the genus-specific, NOR-bearing Chromosome Pair 24. Received: 20 October 1999 / Accepted: 14 April 2000     

Cytogenetic analysis of Oedalechilus labeo (Pisces: Mugilidae), with a report of NOR variability

 A cytogenetic analysis by several staining techniques was carried out on Oedalechilus labeo specimens from the west coast of Italy, in order to extend the karyological knowledge on Mediterranean mullets. The karyotype of the species is composed of 46 acrocentric and 2 subtelocentric chromosomes. Constitutive heterochromatin was found to be restricted to the centromeres. Fluorochrome staining revealed a uniform base composition along the chromosome arms. Nucleolus organizer regions (NORs) are located on the short arms of chromosome pair 9 and can be either homomorphic or quite heteromorphic in size. In some specimens chromomycin A₃-staining and fluorescence in situ hybridization with 18S rDNA revealed a third additional and inactive NOR on the short arms of a medium-sized chromosome. This is the first report of NOR variability in Mugilidae, a family generally characterized by a quite conservative karyotype. Heterochromatin composition and NOR location differentiate O. labeo from a cytotaxonomical point of view from the Liza species studied, Liza being considered the genus from which the genus Oedalechilus derived. Received: 10 April 1999 / Accepted: 21 October 1999     

Karyology of the toadfish Porichthys plectrodon (Jordan and Gilbert, 1882) (Batrachoididae) from Margarita Island,Venezuela

This paper reports the results of cytogenetic analyses carried out on Porichthys plectrodon using conventional Giemsa staining, C-banding and silver staining techniques. A diploid chromosome count of 2n=44 was observed, consisting of 8 metacentric, 10 submetacentric, 6 subtelocentric and 20 acrocentric chromosomes. Differences in length made it possible to identify homologous chromosomes within the metacentric group. Constitutive heterochromatin was distributed as large pericentromeric blocks in pairs 1 and 2, while the rest of the chromosomes were marked in centromeric regions, some more conspicuously than others. One pair of small-sized acrocentric NOR-bearing chromosomes (21) was identified by the nucleolar regions located terminally on their short arms.Communicated by P.W. Sammarco, Chauvin     

Cytogenetic characterization of the greater amberjack, Seriola dumerili (Pisces: Carangidae), by different staining techniques and fluorescence in situ hybridization

A cytogenetic analysis by several staining techniques was carried out on specimens of Seriola dumerili from the Tyrrhenian coast of Sicily. The karyotype was found to be composed of 48 chromosomes in all the specimens examined. All chromosomes are subtelo- and acrocentrics, except for one pair of small-sized submetacentric chromosomes. After Ag-staining, nucleolus organizer regions (NORs) can be observed on the short arms of a medium-sized subtelocentric chromosome pair, and after chromomycin A₃-staining a bright fluorescent signal is evident at the same sites. The 18S rDNA mapping by fluorescence in situ hybridization confirms this unique NOR location. The constitutive heterochromatin is mainly restricted to centromeres and the fluorochrome-staining by chromomycin A₃ and 4′,6-diamidino-2-phenylindole revealed a uniform base composition along the chromosomal arms; therefore stock/population-specific marker chromosomes cannot be identified. Such cytogenetic features, however, rule out the presence of morphologically differentiated sex-chromosomes in the greater amberjack. Received: 16 January 1997 / Accepted: 31 January 1997     

Divergence between populations of a monogamous polychaete with male parental care: Premating isolation and chromosome variation

Low dispersal and sexual selection are characteristic of the coastal polychaeteNereis acuminata Ehlers 1868 [also known asNereis arenaceodentata Moore 1903 andNereis (Neanthes) caudata Delle Chiaje 1841]. We assessed levels of premating isolation between populations of this polychaete. Four North American populations were used, two from the Atlantic and two from the Pacific. Worms from all sites (1) were collected in 1987 and 1988 from the same habitat type, (2) were morphologically similar and keyed out asN. acuminata, and (3) reproduced monogamously and exhibited male parental care, an extremely rare reproductive mode in marine invertebrates. There was no evidence from 10-min or 36-h trials of premating isolation between the two Pacific populations. Incomplete premating isolation was found between the two Atlantic populations. High aggression and non-pairing occurred in some 10-min trials between males and females. However, in 36-h trials males and females from the two Atlantic populations always paired to mate. Complete premating isolation was found between Atlantic and Pacific populations. During 10-min trials, males and females from different oceans often attacked and then avoided each other, and they never paired to mate. Nor did they pair to mate in longer, 36-h trials. One Pacific and one Atlantic population were compared for tolerance to cold temperature. Pacific individuals were less able to tolerate cold water than Atlantic individuals. Two Atlantic populations studied had karyotypes with 11 pairs of small acrocentric chromosomes (2n=22), while the two Pacific populations had nine pairs of large metacentric or submetacentric chromosomes (2n=18). Such extreme dissimilarity in karyotype was not expected considering the similarity in morphology, habitat, and reproductive mode. Results suggest strongly that the Atlantic and Pacific populations have been allopatric for a long time, and are different species.     

Karotypic characterization of turbot (Scophthalmus maximus) with conventional,fluorochrome and restriction endonuclease-banding techniques

A karyotypic analysis was carried out in turbot (Scophthalmus maximus) using conventional banding techniques, fluorochromes and restriction endonucleasebanding. The standard karyotype of turbot is 2n=44 chromosomes, with 48 chromosome arms. Nucleolar organizer regions, which were localized in the short arm of Chromosome Pair No. 3, showed C-and chromomycin A₃-positive staining. C-bands were mainly located at the centromeres, but were also present in some interstitial and telomeric locations. No differences were revealed among constitutive heterochromatin bands after treatment of fixed chromosomes with fluorochrome staining and restriction endonucleases. Digestion with DdeI restriction enzyme produced a pattern of interstitial banding which suggested some degree of differentiation along the chromosome arms in turbot. Neither variation in chromosome number of arm number nor polymorphism in nucleolar organizer regions was revealed in the turbot analyzed.