Autosomal polyploidy and male meiotic pattern in the bug family Nabidae (Heteroptera)

Karyotypes of 18 species of Nabidae (Heteroptera), belonging to the genera Nabis (11), Himacerus (3), Hoplistoscelis (1), and Pagasa (1) were studied. The data on Nabis meridionalis Kerzhner 1963, N. tesquorum (Kerzhner 1968), N. ussuriensis (Kerzhner 1962), N. pallidus Fieber 1861, N. sareptanus Dohrn 1862, Hoplistoscelis sordidus (Reuter 1872), and Pagasa fusca (Stein 1857) were obtained for the first time in this study. Karyotypes of Nabis punctatus A. Costa 1847, N. ferus (Linnaeus 1758), N. pseudoferus Remane 1949, N. rugosus (Linnaeus 1758), N. stenoferus Hsiao 1964, N. limbatus Dahlbom 1851, N. reuteri Jakovlev 1876, N. flavomarginatus Scholtz 1847, Himacerus apterus (Fabricius 1798), H. mirmicoides (O. Costa 1834), and H. maracandicus (Reuter 1890) were re-examined. A karyotype of 2n = 18 (16 + XY), which seems to be the most characteristic of Nabidae as a whole, was found in 12 species. Nabis pallidus and N. sareptanus showed a precise numerical doubling of the autosomal complement compared with the modal karyotype, 2n = 34 (32 + XY). Autosomal polyploidy is discussed as a possible evolutionary mechanism for these species. Meiosis in males of the above species was studied in detail. Male meiosis in Nabidae was shown to follow a highly peculiar scenario differing in many aspects from that known in the majority of the Heteroptera taxa.     

长鞭红景天中一个新的葡萄糖甙

从云南怒江产的长鞭红景天(Rhodiola fastigiata (Hook. f. et Thoms.) S. H. Fu)根茎中分离得到13个化合物,它们的结构通过波谱和化学方法得到鉴定.其中,化合物1被鉴定为新的葡萄糖甙(2-O-β-D-吡喃葡糖基-3-甲基-戊酸甲酯),命名为长鞭红景天素甲,化合物2和 5～9首次从该植物中分离得到.     

长鞭红景天中一个新的葡萄糖甙

从云南怒江产的长鞭红景天 (Rhodiolafastigiata (Hook .f.etThoms.)S .H .Fu)根茎中分离得到 13个化合物 ,它们的结构通过波谱和化学方法得到鉴定。其中 ,化合物 1被鉴定为新的葡萄糖甙 (2_O_β_D_吡喃葡糖基_3_甲基_戊酸甲酯 ) ,命名为长鞭红景天素甲 ,化合物 2和 5～ 9首次从该植物中分离得到     

Chromosomes of villadia and altamiranoa (crassulaceae)

Villadia, ranging from Texas to Peru with some 25 species, has a rather distinctive thyrsoid to spicate inflorescence, and we keep it as a genus separate from Sedum. Twenty species show every gametic chromosome number from 9 to 17 and also 20-22 and higher. Chromosome pairing in hybrids shows that the species differ by many translocations and that species with 21 or lower are effectively diploid. More specialized species tend to have fewer and larger chromosomes, suggesting that through time translocations have rearranged the ancestral genome into fewer units. We suspect that relocated genes may be programmed differently, affecting phenotype. Thus Villadia is like Echeveria in having a remarkably long descending series of evidently diploid chromosome numbers. Altamiranoa, often included in Villadia, with about 15 species from Mexico south, more closely resembles Sedum in its broadly cymose inflorescence. It appears polyphyletic, with no clear boundary from Sedum, and we disperse its species in Sedum. The ten species studied have gametic numbers from 20 to 29 that probably are effectively diploid, with a few higher and probably polyploid. Again, chromosome pairing in hybrids shows that the species differ by many translocations. Putative relatives in Sedum section Leptosedum have n = 26 to 31. Thus cytologically as well as morphologically Altamiranoa has remained more similar than Villadia to its Sedum relatives.     

Colchicine-induced polyploidy in phalaenopsis orchids

Colchicine can induce polyploidy in phalaenopsis orchids. When young protocorms are treated in liquid culture with 50 mg/l colchicine, about 50% of the protocorms develop into tetraploids.     

In vitro induction of polyploidy in japanese quince (Chaenomeles japonica)

In vitro conditions for Japanese quince polyploidisation were investigated. Microshoots and isolated cotyledons were treated with colchicine and oryzalin. Morphogenesis was more dependent on the concentration of colchicine or oryzalin than on the duration of exposure, genotype differences were observed. Low oryzalin concentrations had no impact on morphogenesis. Plants with changed chromosome numbers were obtained at 0.25–38 mM colchicine and 10–50 μM oryzalin concentrations. It was determined that stomata length is a suitable parameter for identifying putative Japanese quince tetraploids. Stomata of tetraploid shoots of the same clone were approximately 1/3 longer than in the diploids. It was shown that through polyploidisation gigas effect was not obtained in fruit size but tetraploids have reduced seed set and an increased proportion of fruit flesh.     

Occurrence of polyploidy in the fishes

Polyploidy, the multiplication of entire setsof chromosomes beyond the normal set of two,has occurred extensively, independently, and isoften repeated in many groups of fish, from thesharks to the higher teleosts. While there areseveral ways that a polyploid fish can develop,environmental change and hybrid stabilizationmay play a large role in the initiation of anew polyploid species. Despite its prevalence,the importance of polyploidy in the evolutionof the fishes is unclear. Polyploidy is morecommon in the lower teleosts than the higherteleosts, possibly due to an advantage gainedthrough decreased specialization in the lowerteleosts, a decreased viability of polyploidyin the higher fish, or both. Polyploid fishcould gain an advantage over diploid fishthrough increased heterozygosity, divergence ofduplicate genes, and/or increased expression ofkey physiological proteins. While polyploidfish do not differ considerably from diploidsphenotypically, they may be at a disadvantage,or certain advantages may be lessened due to anoverall decrease in cell number. This papersummarizes all polyploid species of fish knownto-date, and discusses the possible roles andpathways for establishment of polyploidy in theevolution of the fishes.     

Evolution of clonality and polyploidy in a weevil system

The increased interest in asexual organisms calls for in-depth studies of asexual complexes that actively give rise to new clones. We present an extensive molecular study of the Otiorhynchus scaber (Coleoptera, Curculionidae) weevil system. Three forms have traditionally been recognized: diploid sexuals, triploid, and tetraploid parthenogens. All forms coexist in a small central area, but only the polyploid parthenogens have colonized marginal areas. Analyzing the phylogenetic relationship, based on three partial mitochondrial genes, of 95 individuals from 19 populations, we find that parthenogenesis and polyploidy have originated at least three times from different diploid lineages. We observe two major mitochondrial lineages, with over 2.5% sequence divergence between the most basal groups within them, and find that current distribution and phylogenetic relationships are weakly correlated. Quite unexpectedly, we also discover diploid clones that coexist with, and are morphologically indistinguishable from, the diploid sexual females. Our results support that these diploid clones are derived directly from the diploid sexuals. We also find that it is mainly an increase in ploidy level and not the benefits of asexual reproduction that confers to polyploid parthenogens the advantage over their diploid sexual relatives.     

Origins of domestication and polyploidy in oca (Oxalis tuberosa : Oxalidaceae): nrDNA ITS data

As part of a study aimed at elucidating the origins of the octoploid tuber crop "oca," Oxalis tuberosa, DNA sequences of the internal trancribed spacer of nuclear ribosomal DNA (nrDNA ITS) were determined for oca and several wild Oxalis species, mostly from Bolivia. Phylogenetic analysis of these data supports a group of these species as being close relatives of oca, in agreement with morphology and cytology, but at odds with traditional infrageneric taxonomy. Variation in ITS sequences within this group is quite low (0-7 substitutions in the entire ITS region), contrasting with the highly divergent (unalignable in some cases) sequences within the genus overall. Some groups of morphologically differentiated species were found to have identical sequences, notably a group that includes oca, wild populations of Oxalis that bear small tubers, and several other clearly distinct species. The presence of a second, minor sequence type in at least some oca accessions suggests a possible contribution from a second genome donor, also from within this same species group. ITS data lack sufficient variation to elucidate the origins of oca precisely, but have identified a pool of candidate species and so can be used as a tool to screen yet unsampled species for possible progenitors.     

Unequal X Chromosomes in Bradysia Hygida (Diptera:Sciaridae) Females: Karyotype Assembly and Morphometric Analysis

The mitotic chromosomes of Bradysia hygida(Diptera:Sciaridae) neuroblast cells are described together with their morphometric data. Giemsa-stained neuroblast chromosomes from female and male larvae confirm the chromosome number of this species, 2n=8 (XX) and 2n=7 (XO), respectively. The karyotype assembly reveals two metacentric autosomic pairs, the A and B chromosome; a subtelocentric, the C chromosome, the smallest one; and a sexual unequal metacentric pair, X chromosome, in female karyotype and a one sexual metacentric X chromosome in male. The implications of the unequal X chromosome pair are discussed.     

Oogenesis and the Chromosomes of Twelve Bisexual Species of Heterodera (Nematoda: Heteroderidae)

Twelve bisexual species of Heterodera reproduced by amphimixis and had the same number of n=9 (2n=18) chromosomes in maturing oocytes. H. schachtii had slightly larger chromosomes than all other species. Only sperm nuclei with n=9 chromosomes were observed inside maturing oocytes and no specialized sex chromosomes were detected in any case. A "supernumerary" chromosome was observed occasionally in oocytes of H. schachtii and H. weissi and was transmitted regularly to one-half of the progeny of the nematodes that possessed it. Cytological characteristics were not very instructive in differentiating amphimictic tleterodera species. Such karyotypic uniformity indicates cytogenetic stability of the genus and close interrelationship among its members.     

Chromosomes of caryophyllidean cestodes: Diploidy, triploidy, and parthenogenesis in Glaridacris catostomi

Mitotic and meiotic chromosomes were studied in Giemsa post-stained Feulgen squashes of testicular, ovarian, and vitelline cells. G. catostomi is 2n = 20 with eight pairs of metacentrics and two pairs of submetacentrics in its karyotype. The fundamental number of chromosome arms is FN = 40. At mitotic metaphase the mean total chromosome length (TCL) of the complement was 111·4 μm; the largest chromosomes were 8 μm (7% TCL) and the smallest 3 μm (3% TCL). Karyotype variation was not found among five diploid populations from New York State and Canada. Meiotic activity was abundant in spermatogenesis which proceeds as usual with sperm developing after two meiotic divisions. Chiasma frequency at diakinesis was 37/cell; as many as five chiasmata were observed in a single bivalent. A triploid ‘race’ (3n = 30) of G. catostomi was discovered in Bozenkill Creek near Albany, New York. Karyotype analysis confirms the triploid nature of these variants. Spermatogenesis in triploids is abnormal to the point of complete failure. The presence of an extra set of chromosomes has resulted in a breakdown of meiosis with subsequent sterility of the male system. Eggs remain unfertilized and parthenogenetic reproduction is presumed to occur. The possible origins of this unusual condition and its evolutionary implications are discussed. Seventeen figures, two tables of measurements, and a system of chromosome nomenclature supplement the paper.     

The Leptynia hispanica species complex (Insecta Phasmida): polyploidy, parthenogenesis, hybridization and more

The Leptynia hispanica stick insect species complex includes bisexuals, triploid and tetraploid parthenogenetic populations, suggesting that polyploidy has played a central role in the evolution of this complex. An analysis of karyotype, mitochondrial DNA (cox2) and nuclear DNA (ef1-alpha) markers was carried out to clarify phylogenetic relationships and microevolutionary/phylogeographical patterns of the L. hispanica complex. Our analyses suggested a subdivision of bisexual populations into four groups, tentatively proposed as incipient species. Moreover, triploids and tetraploids showed two independent origins, the latter being more ancient than the former. From ef1-alpha analysis, triploids showed hybrid constitution, while the hybrid constitution of tetraploids is likely, but more data are needed. We suggest that L. hispanica is a case of 'geographical parthenogenesis' with parthenogenetic strains colonizing large peripheral ranges, and bisexuals confined to glacial refuge areas. Moreover, the age, wide distribution and competitive advantage of polyploids over diploids, demonstrate their significance in the evolution of the L. hispanica species complex.     

The effect of B chromosomes and T-DNA on chromosomal variation in callus cells and regenerated roots of Crepis capillaris

The chromosome behaviour has been compared in three Crepis capillaris callus culture lines and the roots regenerated from these calli. The calli were obtained from explants derived from plants without and with two B chromosomes and the hairy roots were obtained from plants transformed with Agrobacterium rhizogenes. Cytological studies demonstrated that the presence of additional DNA as B chromosomes or as T-DNA had an influence on the numerical and structural variability of the standard chromosome in long-term callus cultures and in regenerated organs. The callus with two B chromosomes displayed higher levels of polyploidyzation than callus without B chromosomes. The roots regenerated from both these calli were only diploid, while roots regenerated from transformed callus were also polyploid. This revised version was published online in June 2006 with corrections to the Cover Date.     

Chromosomes of lemuriformes. I. A chromosome complement of Lepilemur mustelinus (I. Geoffroy 1851)

The diploid chromosome number of two specimens of Lepilemur mustelinus (I. Geoffroy 1851) is 2N = 20. All of the chromosomes, except the Y chromosome, are metacentric or submetacentric; the Y chromosome is acrocentric and is the shortest chromosome in the complement. Satellites on autosomal pair 5 provide marked chromosomes for the animals studied and may be a marked pair for the species.