Morphological and karyotypic differences within and among populations of Radopholus similis

Twenty populations of Radopholus similis from three countries and different hosts (19 populations from ornamental plants and one population from ginger) were compared using morphological characters, morphometrics and karyotype between progeny from both single females and 30 females of each population. Morphological diversity existed in and among the populations, even within the progeny nematodes from single nematodes compared to that of 30 females. The labial disc shape, the number of head annuli, the terminated position of lateral lips, the number of genital papillae before cloacal apertures and female and male tail terminal shape showed variation. In addition, genital papillae arranged in a double row before cloacal apertures was first found in two ornamental populations. The karyotype of all the 20 populations was n = 5. Combining our results and previous studies, we support that Radopholus citrophilus is a synonym of Radopholus similis, and that it is not possible to distinguish physiological races or pathotypes of Radopholus similis according to morphological characters or karyotype.     

Evolutionary significance of hybridization in Onosma (Boraginaceae): analyses of stabilized hemisexual odd polyploids and recent sterile hybrids

Interspecific hybridization is an important evolutionary force promoting plant speciation. In the genus Onosma, one of three main evolutionary lineages presumably evolved by hybrid speciation. The assumed hybrid lineage (Heterotricha) consists of two species complexes with bimodal karyotypes containing different numbers of large (L) and small (S) chromosomes, the tetraploid Onosma pseudoarenaria (2n = 12 L + 14S) and the triploid Onosma arenaria (2n = 12 L + 8S). The latter represents a rare case of hemisexual, asymmetrically compensating allopolyploids. Representatives of the other two lineages of the genus, Haplotricha (2n = 12 L) and Asterotricha (2n = 14S), have been considered to be the ancestral taxa of O. pseudoarenaria and O. arenaria, although this has yet to be investigated critically. In the present study, we examined genetic [amplified fragment length polymorphism (AFLP), internal transcribed spacer (ITS) , and chloroplast (cp)DNA)], reproductive (pollen viability and seed production) and cytogenetic (chromosome counts, genome size assessment) patterns to resolve the hypothesized allopolyploid formations in the Heterotricha group, single or polytopic allopolyploid origins, as well as ongoing interspecific gene flow as one piece of evidence for understanding past hybrid speciation events in the genus. Discordant patterns in maternally inherited cpDNA (Heterotricha accessions bearing the haplotypes related to asterotrichous species) and the nuclear ITS and AFLP markers (Heterotricha clustering with haplotrichous Onosma fastigiata), as well as karyological features, support the hybrid origin of the stabilized Heterotricha lineage. Genetic variation that is both large and geographically correlated indicates multiple origins of Heterotricha allopolyploids or, less likely, a single origin with recurring introgression from the progenitor species. The nuclear markers and cytogenetic features also provide evidence for the ongoing hybridization between O. arenaria and Onosma echioides (2n = 14S), which gives rise to sterile triploids of 2n = 6 L + 15S. We contrast the two cases of triploids with LLS (hemisexual O. arenaria from the stabilized Heterotricha lineage) and LSS (recent sterile hybrids) karyotypes, which could help to understand the mechanisms ensuring the establishment and reproductive fitness of the odd allopolyploids in Onosma. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 112 , 89–107.     

Recent changes in the distribution of carboxylesterase genes and associated chromosomal rearrangements in Greek populations of the tobacco aphid Myzus persicae nicotianae

We present data on the frequency of amplified E4 and FE4 carboxylesterase genes in Myzus persicae s.l. clones collected during the years 2002–2007 and 2012 in Greece. Most clones were of the tobacco aphid, Myzus persicae nicotianae. Samples from 2012 were genotyped with microsatellite DNA markers and a number of them were karyotyped. Aphid clones with amplified FE4 genes predominated in all years, whereas E4 was present in only 3.5% of all samples and always occurred in clones with FE4. Most of the clones examined showed high carboxylesterase activity levels (R2 resistant category). The results showed marked changes in the frequencies of the two carboxylesterase genes in the tobacco aphid populations compared to published data that were collected in Greece in the mid 1990s, when E4 was recorded on its own in 20% of all samples and in 32% of samples from tobacco. A parallel change in karyotype was also observed because the A1,3 translocation, which had a worldwide association with amplified E4 genes in the 1990s, was not detected in the clones analyzed in 2012. Possible causes for these changes are discussed, although selection as a result of pest management practices appears to be the major one. Novel chromosomal rearrangements were also found in M. persicae nicotianae clones. These rearrangements could be a result of clastogenic effects of nicotine, which could persist because of the holocentric nature of aphid chromosomes. The results are discussed in relation to rapid evolution events that have taken place in the tobacco aphid in Greece during the last two decades. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 113 , 455–470.     

Integrative taxonomy and evolutionary history of a newly revealed spider Dysdera ninnii complex (Araneae: Dysderidae)

The spider genus Dysdera is a species‐rich clade of specialized woodlice predators, composed typically of complexes of sibling species. Here, we analyse the Dysdera ninnii complex, distinguishing three species that exhibit slight but constant differences in the morphology of their copulatory organs, and in their genetic background. We designate a neotype for D. ninnii and redescribe it. We consider Dysdera pavesii Thorell, 1873 to be a junior synonym of Dysdera ninnii Canestrini, 1868. In addition, we describe two new species ( D ysdera moravica sp. nov. and D ysdera microdonta sp. nov. ). All three species occur in the region of north‐eastern Italy, Slovenia, and north‐western Croatia. D ysdera moravica sp. nov. expanded to central Europe. The species occur allopatrically or parapatrically. All three species possess the same diploid number and X0 sex chromosome determination. In some individuals we found chromosome fusions, and such polymorphism is common in spiders with holokinetic chromosomes. The analysis of mitochondrial (cytochrome c oxidase subunit I, COI) and nuclear ribosomal (internal transcribed spacer 2, ITS2) DNA markers revealed two clades, one formed by D. ninnii and D . microdonta sp. nov. , and a second by D . moravica sp. nov. Species of the first clade are not well defined by DNA markers. We noticed only weak separation of maternally inherited COI, and even overlap of autosomally inherited ITS2 sequences. We suggest that either short speciation time, unfinished lineage sorting, or rare hybridization events caused this pattern. In one sample of D . microdonta sp. nov. we detected the coxA gene of a Rickettsia species, which is the first record of this parasitic bacteria from the spider family Dysderidae. D ysdera microdonta sp. nov. occurs at higher altitudes than D. ninnii, and their distribution ranges form a long contact zone. Remarkably, we did not record any overlap of the two distribution ranges, suggesting that the lack of a precopulatory interspecific barrier causes a loss of reproduction potential. We hypothesize that because of the unsolved interspecific barrier together with only tiny differences in morphology and COI sequences, and no differences in karyotypes and ITS2 sequences, the D. ninnii species complex is evolutionarily young. © 2014 The Linnean Society of London     

中国两种波腿蝗（蝗总科：癞蝗科）染色体C带核型研究

报道中国两种波腿蝗的染色体C带核型,结果表明：红胫波腿蝗Asiotmethis zacharjini (Bei-Bienko, 1926) 2n ♂ =18, neo-X为亚中着丝粒染色体,其他均为近端着丝粒染色体,染色体除强染的着丝粒C带,S8染色体具强染端部C带带纹,neo-Y染色体还具有一条宽的弱染的近着丝粒端居间C带,性别决定机制是neo-XY ♂型,该种染色体组成和性别决定机制在我国癞蝗中为首次报道,蓝胫波腿蝗Asiotmethis jubatus (Uvarov, 1926) 2n＝19♂,均为近端着丝粒染色体,仅具有明显强染的着丝粒C带,性别决定机制是XO ♂型;两种波腿蝗的异染色质含量存在显著性差异（α=0.05）。     

Microsatellites confirm the authenticity of inter-varietal chromosome substitution lines of wheat (Triticum aestivum L.)

Ninety-five wheat microsatellite markers (WMS) were used to verify the authenticity of the set of Saratovskaya 29/Yanetzkis Probat inter-varietal wheat chromosome substitution lines developed using Saratovskaya 29 as the recipient variety. Polymorphic markers were available for all chromosome arms except 4DS, 6DS and 7DS. Each chromosome substitution line was tested by 2–8 microsatellite markers. The results demonstrate that most of the lines are correct. Out of 21 lines tested 17 showed the expected microsatellite pattern of the donor variety. Two entire chromosomes, 1B and 7A, and two chromosome arms, 3AL and 6DS, were not substituted with Yanetzkis Probat in their respective lines. Three microsatellite markers located in the distal regions of chromosome arms 4AL, 3BS and 5BL in the corresponding substitution lines did not reveal the expected microsatellite pattern of the recipient variety. The possible causes of the incorrect substitution line development and the appearance of incorrect distal microsatellite markers are discussed. The data confirm the idea that microsatellite markers provide ideal tools for testing the authenticity of genetic stocks of wheat. Received: 27 August 1999 / Accepted: 8 October 1999     

应用显微操作和PCR技术进行基因的染色体定位

介绍了一种将染色体显微操作和ＰＣＲ技术结合起来进行基因染色体定位的方法,具有简便易行,特异性和敏感性很高等特点。分析了这种定位方法的技术特点,以及ＳＳＣＰ和ＤＮＡ序列分析等方法在排除错误结果中的运用。     

New chromosome counts inStreptocarpus (Gesneriaceae) from Madagascar and the Comoro Islands and their taxonomic significance

This study records the chromosome numbers of 10 species ofStreptocarpus; nine of the counts are new. With the exception ofS. buchananii of mainland Africa, all the results are for plants endemic to Madagascar and the Comoro Islands. While there is a strong correlation between basic number and growth form in the two subgenera of the genus on the African mainland (x = 15 among caulescent species in subgenusStreptocarpella; x = 16 among acaulescent species in subgenusStreptocarpus), the situation appears more complex among Madagascan and Comoro Island species. One notable example of deviation from this correlation is shown byS. papangae, a shrubby caulescent species, with 2n = 32 (x = 16). Polyploidy in the genus appears to be absent on mainland Africa, but is present in Madagascar and the Comoro Islands, ranging from tetraploidy to octoploidy. Evolutionary implications of the cytological observations are considered.     

鹌鹑的核型及G带分析

分别采用外周血淋巴细胞培养法和胰酶处理法,对鹌鹑染色体的核型和G带进行了研究。结果表明,鹌鹑染色体数目为2n=78,有10对大染色体（包括Z、W）,29对小染色体。染色体形态分别为：NO.1染色体为sm型,NO.2、Z染色体为m型,其余染色体均为t型,这与前人研究结果存在一定差异。G带分析结果显示,鹌鹑的前9对大染色体及Z、W染色体G带可分为27个区,134带。