贵州6种蝙蝠的核型

采用常规骨髓细胞空气干燥法,研究了贵州6种蝙蝠的核型。白腹管鼻蝠(Murina leucogaster)2n=44,染色体臂数(FN)为58;普通长翼蝠(Miniopterus schreibersi)染色体数是2n=46,FN为50,黄大蹄蝠(Hipposideros pratti)2n=32,FN为60;角菊头蝠(Rhinolophus cornutus)2n=62,FN为60;云南菊头蝠(R.yunnanensis)2n=44,FN是60;犬蝠(Cynopterus sphinx)2n=34,FN=58。其中白腹管鼻蝠、云南菊头蝠和犬蝠为国内首次报道。     

四川七种蝙蝠的核型

本报道了四川地区7种蝙蝠的核型。菊头蝠科2种,即角菊头蝠(Rhinolophus comutus)的核型为2n=62,FN=60;栗黄菊头蝠(R．ssinicus)的核型为2n=36,FN=60。蹄蝠科1种,即大蹄蝠(H．armiger)的核型为2n=32,FN=60。蝙蝠科3种,即伏翼(Pipistrellus abramns)的核型为2n=26,FN=44;南蝠(Iaio)的核型为2n=50,FN=48;山蝠(Nyctalus velutinus)的核型为2n=36,FN=50。犬吻蝠科的皱唇蝠(Tadarida teniotis)的核型为2n=48,FN=62。南蝠的核型为首次报道,但栗黄菊头蝠的核型2n=36与安徽张维道报道相同,而与印度和斯里兰卡同种R．rouxii的核型2n=56迥异。分布在中国的栗黄菊头蝠R．sinicus应为独立种而不是R．rouxii的中国亚种。另5种蝙蝠的核型与前人研究结论基本一致。     

广东五种菊头蝠的核型分析

本用蝙蝠的新鲜肺组织和尾椎进行组织培养,然后在光学显微镜下计数30个染色体分散良好的中期分裂相细胞,并进行摄影、剪贴和测量。分析了广东地区5种菊头蝠的核型,即小菊头蝠的核型为2n=62,FN=60;角菊头蝠的核型为2n=62,FN=60;中菊头蝠的核型为2n=62,FN=60;大耳菊头蝠的核型为2n=62,FN=60;中华(栗黄)菊头蝠的核型为2n=36,FN=60。大耳菊头蝠的核型为首次报道。角菊头蝠和中菊头蝠的核型与前人报道的结果基本相同。中华(栗黄)菊头蝠的核型(2n=36)与张维道报道的鲁氏菊头蝠相同,而与印度和斯里兰卡产R．rouxii的核型2n=56迥异。最后对东亚地区菊头蝠多样性进行了探讨。     

Cytogenetic characterization of six species of flatfishes with comments to karyotype differentiation patterns in Pleuronectiformes (Teleostei)

The karyotypes and cytogenetic characteristics of flatfishes species Paralichthys orbignyanus , Paralichthys patagonicus , Citarichthys spilopterus and Etropus crossotus (Paralichthyidae), Bothus ocellatus (Bothidae) and Symphurus tessellatus (Cynoglossidae) were investigated by conventional [Giemsa staining, C-banding, Ag- and chromomycin (CMA₃)-stainings] and molecular [ in situ hybridization (ISH)] cytogenetic techniques. The results showed 2n = 46 and FN = 48 (2msm + 46sta) in P. orbignyanus , 2n = 46 and FN = 46 (46sta) in P. patagonicus , 2n = 26 and FN = 44 (18msm + 8sta) in C. spilopterus , 2n = 38 and FN = 64 (26msm + 12sta) in E. crossotus , 2n = 32 and FN = 50 (18msm + 14sta) in B. ocellatus , and 2n = 46 and FN = 62 (46msm + 62sta) in S. tessellatus . All species exhibited weak C-band positive segments in terminal and centromeric positions of some chromosome pairs. Silver staining of the nucleolus organizer regions (Ag-NOR) technique showed a single Ag-NOR-bearing chromosome pair in all species except E. crossotus . All these sites were CMA₃ positive and showed clear ISH signals after probing with a 18S rRNA probe. Etropus crossotus presented until seven chromosomes with Ag-NORs and CMA₃ positively stained segments in five chromosome pairs. Conversely only one chromosome pair was identified with the ISH experiments in this species. The available results show that the fishes of the order Pleuronectiformes experienced a marked chromosome evolution that included reduction in diploid number, mainly due to Robertsonian rearrangements, and several chromosome inversions.     

广东7 种蝙蝠的核型研究

对采集于广东的4 科7 种蝙蝠进行了核型分析,它们的核型分别是:犬蝠(Cynopterus sphinx)2n =34,FN= 58;印度假吸血蝠(Megaderma lyra)2n = 54,FN = 104;大耳双色蹄蝠(Hipposideros pomona)2n = 32,FN =60;中蹄蝠(H. larvatus)2n = 32,FN = 60;大卫鼠耳蝠(Myotis davidii)2n = 46,FN = 52;大黄蝠(Scotophilus heathi)2n = 36,FN = 54;南长翼蝠(Miniopterus australis)2n =46,FN = 50。其中大耳双色蹄蝠和大卫鼠耳蝠的核型为首次报道,犬蝠、印度假吸血蝠、中蹄蝠、大黄蝠和南长翼蝠的核型为中国第一次报道。     

New Ctenomys karyotypes (Rodentia,Octodontidae) from north-eastern Argentina and from Paraguay confirm the extreme chromosomal multiformity of the genus

Bone-marrow karyotypes of 68 specimens of the subterranean octodontid rodent genus Ctenomys from 16 different populations of north east Argentina and one from Paraguay have been studied. A surprising variety of chromosome numbers was found, ranging from 2n=42 to 2n=70. Some of the karyomorphs are clearly assigned to named species by topotypy: C. conoveris 2n=50, FN=56; C. argentinus, 2n=44, FN=54; C. perrensi, 2n=50, FN=84; C. dorbignyi, 2n=70, FN=84; C. roigi, 2n=48, FN=80; C. yolandae, 2n=50, FN=78. Four populations of Corrientes Province similar in morphology to C. perrensi were found to be polymorphic and polytypic; they maintain the same FN=84, but diploid numbers increase from 2n=54 to 2n=58 from SW to the NE, thus suggesting Robertsonian rearrangements. In the middle of this cline, a stable karyomorph of 2n=62, FN=84 was found in two different populations, suggesting to belong to an undescribed species. Another karyomorph of 2n=42, FN=76 found in Curuzú Laurel, Corrientes, may also prove to represent another undescribed species. One karyomorph of 2n=52, FN=74, and another of 2n=56, FN=78 from Paraná and Ubajaý (Entre Ríos Province, Argentina) respectively are close to C. rionegrensis. The relationships among these karyomorphs is considered in light of data on sperm morphology. The hypothesis is advanced that karyotypic rearrangements among the FN=84 group may be the result of Robertsonian repatterning from a 2n=70 original widespread form. Fixation of chromosomal variants is correlated with patchy distribution and small size of unstable demes, and may or may not have resulted in reproductive isolation.     

贵州五种菊头蝠的核型分析 *

采用常规骨髓细胞空气干燥法,研究了贵州5种菊头蝠的核型。贵州菊头蝠和中菊头蝠2n=62,两者染色体臂数(NF)均为60;托氏菊头蝠、小菊头蝠和栗黄菊头蝠的染色体数是2n=36,其中托氏菊头蝠和小菊头蝠染色体臂数(NF)是58,栗黄菊头蝠是60。5种菊头蝠的性别决定机制均是xY。     

Chromosome evolution in Australian rodents

A total of 219 wild caught specimens representing 12 of the currently recognised 13 species and subspecies of Australian Rattus have been karyotyped. No two species possessed karyotypes in common, most species and several subspecies differing markedly in chromosome number. While the diploid number varied from 2n=32 to 2n=50, the fundamental number (FN) varied only from 60 to 62, suggesting that Robertsonian rearrangements have played a major role in karyotypic evolution in the group. — Karyotypically the Australian species of Rattus fall into two groups. — the R. lutreolus group and the R. sordidus group. Of the karyotypic forms encountered in the former group, that of R. lutreolus is probably most ancestral because it is identical to that of many Asian species of Rattus. Other karyotypic forms in the R. lutreolus group can be derived as follows: That of (1) R. tunneyi tunneyi and R. t. culmorum by a single fixed pericentric inversion; (2) R. fuscipes fuscipes, R. f. greyi, R. f. assimilis and R. f. coracius by two fixed fusions; (3) R. leucopus cooktownensis by three fixed fusions; and (4) R. leucopus leucopus by four fixed fusions. Of the R. sordidus group, R. s. villosissimus may possess the most ancestral karyotype with 2n=50 (FN=60), from which R. s. colletti (2n=42; FN=60) is derived by four fusions and R. s. sordidus (2n=32; FN=60) by nine fusions, four of which appear to be homologous with those R. s. colletti. — The karyotypic data are in accord with Taylor and Horner's (1973) suggestions that (1) R. t. tunneyi and R. t. culmorum belong to one species; (2) R. lut. lutreolus and R. lut. velutinus belong to one species; (3) R. leu. leucopus and R. leu. cooktownensis belong to one species and (4) R. f. fuscipes, R. f. greyi, R. f. assimilis and R. f. coracius belong to one species. However, the large karyotypic difference between R. s. sordidus and R. s. colletti and R. s. villosissimus may indicate that these groups belong to different biological species. — Supernumerary or B-chromosomes were found in R. f. assimilis and R. t. tunneyi. A single R. t. culmorum was heterozygous for a centric fusion.     

Karyotypes of three rat species (Mammalia: Rodentia: Muridae) from Hainan Island, China, and the valid specific status of Niviventer lotipes

The karyotypes of three rat species from Hainan Island, China, were examined. Niviventer fulvescens (Gray, 1847) had 2n=46 and FN=64, similar to the karyotypes reported for N. fulvescens from Southeast Asia, while Niviventer lotipes () had 2n=52 and FN=66, which is distinct from the known karyotypes of other Niviventer species. Niviventer lotipes was recently considered conspecific with N. tenaster (), but the two were found to have extremely different karyotypes (2n=52 and FN=66 in N. lotipes; 2n=46 and FN=54 in N. tenaster). Therefore, in this paper N. lotipes is considered a valid species for the first time; it is distinct from N. tenaster and endemic to Hainan Island, where N. lotipes is differentiated from N. fulvescens by larger body and skull sizes, a shorter tail, and darker coloration. Rattus nitidus (Hodgson, 1845) from Hainan Island had 2n=42 and FN=62, which is similar to the reported karyotypes of conspecific populations in Southeast Asia.     

Chromosome counts of some MongolianPotentilla species

Chromosome numbers are reported for 26 collections representing 12 MongolianPotentilla taxa. The first chromosome records are reported forP.[x]agrimonioides Bieb. (2n = 42, 49–50),P. [x]chionea Soják (2n = 64, 74+1B, 84–86, 86),P. [x]stepposa Soják (2n = 62) andP. supina, L. subsp.costata Soják (2n = 42). Tetraploid and pentaploid populations ofP. sericea L. (2n = 28, 34, 35) and hexaploid populations ofP. omithopoda Tausch (2n = 42) were found in Mongolia. Chromosome numbers of the following species were confirmed:P. longifolia Willd. exSchlecht. (2n = 14),P. multifida L. (2n = 28),P. sanguisorba Willd. exSchlecht. (2n = 28),P. sericea L. (2n = 42),P. supina L. subsp.paradoxa (Nutt.) Soják (2n = 28 China) andP. tanacetifolia Willd. exSchlecht. (2n = 28). Taxonomic observations are briefly discussed.     

Comparative Chromosome Painting in Six Species of Oligoryzomys (Rodentia,Sigmodontinae) and the Karyotype Evolution of the Genus

Oligoryzomys belongs to the tribe Oryzomyini, and contains about 22 species. Diploid numbers range from 2n = 44 in Oligoryzomys sp. 2 to 2n = 72 in O. utiaritensis and phylogenetic relationships are not well defined. The high morphological convergence leads to misidentification of taxonomic entities and the species are often identified by chromosomal characters. Until now, the genus has been studied only by classical cytogenetic approaches. To understand the chromosomal evolution of Oligoryzomys, we developed chromosome probes from a female of Oligoryzomys moojeni (OMO) with 2n = 70 and hybridized to other five Oligoryzomys species. The probes painted 31 segments on O. fornesi (OFO) with 2n = 62; 32 segments on O. microtis (OMI), 2n = 64; 33 segments on O. nigripes (ONI), 2n = 62 and on O. rupestris (ORU), 2n = 46; and 34 on Oligoryzomys sp. 2 (OSP), 2n = 44. OMO probes 4 and 5 showed a syntenic association in O. fornesi, O. microtis and O. nigripes and were also presented in the same pair, although disrupted, in O. rupestris and Oligoryzomys sp. 2. Concerning O. rupestris and Oligoryzomys sp. 2, species with the lowest diploid numbers of the genus, a total of 8 probes hybridized to 11 segments on the largest pair of ORU 1 and 9 probes hybridized to 12 segments on OSP 1. Also, OMO 6 painted three segments in ORU, corresponding to the proximal segment of ORU 2q, and the whole of ORU 19 and 20. In OSP, the segment corresponding to ORU 20 was homologous to OSP 1p. OMO X showed signals of hybridization in both X and Y chromosomes. Extensive chromosomal rearrangements, that could not be detected by classical cytogenetic techniques, such as pericentric inversions or repositioning of centromeres, Robertsonian rearrangements and tandem fusions/fissions, as well as gain/activation or loss/inactivation of centromeres and telomeric sequences have driven the huge genome reshuffling in these closely related species.     

A chromosomal study on Greek populations of the genusApodemus (Rodentia, Murinae) reveals new data on B chromosome distribution

During this study, 94 specimens (51 males, 43 females) of the wood mouseApodemus sylvaticus (Linnaeus, 1758), the yellow-necked mouseA. flavicollis (Melchior, 1834) and the western broad-toothed mouseA. epimelas (Nehring, 1902) from 20 localities of Greece were karyologically examined. The first two species were found to be widely distributed and their otherwise very similar karyotype (2n=48, FN=48) could be clearly distinguished, based on C-banding pattern. The third species appeared to have a more limited geographical distribution and its karyotype was distinguished from that of the previous two species, since it contained two pairs of small metacentric autosomes (2n=48, FN=52). The chromosomal study further revealed that nine individuals ofA. flavicollis possessed supernumerary B chromosomes (2n=49–50, FN=49–50). Meiotic chromosome preparations revealed that in contrast to sex chromosomes and autosomes, B chromosomes do not participate in bivalent formation. On the other hand, no supernumerary chromosomes were found in the studiedA. sylvaticus andA. epimelas material.     

Karyotypic changes associated to the dispersive potential on Pomacentridae (Pisces, Perciformes)

When comparing karyotypic diversification between freshwater and marine fish, a notable increase in modifications associated to the former environment can be noticed in relation to the latter one. This fact is related to the great number of physical partitions (barriers) that exist in continental waters. Furthermore, in the marine environment, the barriers to the gene flow are complex and not always identifiable, especially when considering the participation of dynamic factors such as currents and winds associated to the dispersive potentialities of a living group. Within Perciformes fish, the Pomacentridae family stands out from the others for its intimate relation with the coral reefs, as well as for its diversity of forms and biological characteristics, providing an adequate model for studying the influence of the pelagic period of the larval stage upon the karyotypic evolution. In the present work, cytogenetic analyses were carried out on three Pomacentridae species, typical representatives of the coral reefs, Abudefduf saxatilis (2n=48, FN=52, 2 m+2sm+44a), Microspathodon chrysurus (2n=48, FN=64, 6 m+10st+32a) and Amphiprion frenatus (2n=48, FN=92, 14 m+22sm+8st+4a) that have different pelagic larval periods. The analyses between subfamilies showed a trend that the lower the dispersive potential, the greater the quantity of fixed pericentric inversions based on the basal karyotype of the Perciformes.     

First cytogenetic information for Drymoreomys albimaculatus (Rodentia,Cricetidae), a recently described genus from Brazilian Atlantic Forest

The recently described taxon Drymoreomys albimaculatus is endemic to the Brazilian Atlantic Forest and its biology and genetics are still poorly known. Herein, we present, for the first time, the karyotype of the species using classical and molecular cytogenetics, which showed 2n=62, FN=62, and interstitial telomeric signals at the sex chromosomes. Nuclear and mitochondrial DNA sequences from the two karyotyped individuals verify the taxonomic identity as the recently described Drymoreomys albimaculatus and confirm the relationship of the species with other Oryzomyini. Additionally, external morphological information is provided.     

Chromosome numbers of thirty-one species of Indian Lepidoptera

Chromosome numbers are reported for 31 Indian species. Results forPsara stultalis (2n=60, n=30),Malacosoma indica (50, 25) andPygaera fulgurita (62, 31) differ from data reported by earlier workers. Eighteen species are new to cytology.     

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.     

Heterochromatin study and geographical distribution of Microtus species (Rodentia,Arvicolinae) from Greece

In a sample of 108 underground voles from 23 Greek localities, the species Microtus felteni, M. guentheri, M. rossiaemeridionalis and M. subterraneus were identified, based on external body morphology and karyotype. Moreover, the implemented C-banding staining technique revealed the heterochromatin distribution in the chromosomes of the above species. All M. guentheri (2n=54, FN=54) and M. rossiaemeridionalis (2n=54, FN=56) specimens displayed the typical karyotypes of these species, respectively. The M. subterraneus specimens belonged to the chromosomal race with 2n=52, FN=60 of this species, apart from a single individual that demonstrated a medium-sized, subtelocentric autosome in heterozygous condition (2n=52, FN=61). Furthermore, M. felteni individuals, trapped again after many years, were karyologically studied (2n=54, FN=56) and the C-banding pattern for this species is hereby presented for the first time. Finally, the study of meiotic preparations in M. guentheri and M. rossiaemeridionalis males verified the asynaptic behaviour of their sex chromosomes. The karyotype of the four studied Microtus species does not seem to have diversified much from the putative ancestral arvicoline karyotype (2n=56, FN=56). On the other hand, the heterochromatin accumulation in the sex chromosomes, particularly prominent in M. felteni and M. rossiaemeridionalis, represents this common tendency in several Microtus species.     

Chromosomal polymorphism and small karyotypic differentiation in a group of Ctenomys species from Central Argentina (Rodentia: Octodontidae)

Cytogenetic analysis was performed in six nominal taxa of the genus Ctenomys with a diploid number of 2n=47/48. The studied species were: C. australis (2n=48, FN=76); C. mendocinus (2n=47/48, FN=68/75/76); C. porteousi (2n=47/48, FN=71/72/73); C. azarae (2n=47, FN=71); C. sp. (chasiquensis) (2n=47/48); and C. talarum (2n=48, FN=80). The first three species shared the whole complement, C. talarum shares with them 19 arms from a total of 43 (44%). In all species analyzed constitutive heterochromatin was detected in most short arms, and in several centromeres. Polymorphisms for several pairs involving the heterochromatic short arms together with a complex polymorphism of pair A1 were found in C. azarae, C. sp., C. mendocinus and C. porteousi. Intraindividual variation found in one specimen of C. porteousi involving heterochromatic arms is discussed.These results lead us to propose the inclusion of all species except C. talarum, within a complex called the mendocinus-group. A new case of conservatism for chromosomal number in the genus Ctenomys is found in this group.     

Conventional karyotype, nucleolar organizer regions and genome size in five Mediterranean species of Syngnathidae (Pisces, Syngnathiformes)

Conventional karyotypes, NOR-bearing chromosomes by means of silver impregnation and genome size were investigated in five Mediterranean species in three genera of the Syngnathidae. A karyotype of 48 subtelocentric-acrocentric chromosomes was found in the seahorse Hippocampus hippocampus (FN=48) while a diploid value of 44 occurred in H. guttulatus (2 sm-m+42 a; FN=46) and the pipefish Syngnathus abaster (44 a; FN=44) and S. typhle (44 a; FN=44). The pipefish Nerophis ophidion , possessing a diploid chromosomal set of 58 made up of 50 meta-submetacentric and eight subteloacrocentric elements (FN=108) and a genome size three to four times larger than those known to date, differs cytogenetically from all other Syngnathids studied so far. A single pair of active NOR-bearing chromosomes was found in both species of the genus Hippocampus while in Syngnathus and Nerophis species more than two silver positive chromosomes were found to be involved in nucleolus organization giving rise to NOR-bearing chromosome polymorphism. The possible evolutionary routes of quantitative and qualitative changes in chromosome and DNA are discussed. The resulting phylogenetic scheme is shown to coincide with that constructed from morphological characters.     

Chromosome Banding and 18S rDNA in situ Hybridization Analysis of Seven Species of the Family Achiridae (Teleostei: Pleuronectiformes)

Achiridae is an important family of the order Pleuronectiformes widely distributed in North, Central, and South America with freshwater and marine species. In the present study cytogenetic analyses comprising conventional and molecular techniques were carried out in seven species of this family. The following diploid numbers (2n) and fundamental numbers (FN) were obtained: Achirus declivis 2n = 34, FN = 52; Achirus lineatus 2n = 40, FN = 66; Catathyridium jenynsi 2n = 40 and FN = 50; Gymnachirus nudus 2n = 36 and FN = 50; Hypoclinemus mentalis 2n = 38 and FN = 54; Trinectes paulistanus 2n = 42 and FN = 52; and Trinectes sp. 2n = 38 and FN = 54. All species presented a single nucleolar organizer region (NOR) bearing chromosome pair and C-band positive segments mainly distributed at the pericentromeric position. The wide variation observed in chromosome number and FN suggests the occurrence of larger chromosome rearrangements in the family Achiridae if compared with other families of the same order.