Karyotypes of tragopogon (Compositae: Lactuceae)

Karyotypes of 24 diploid (2n=12)Tragopogon species are similar with one long pair of chromosomes (A), two medium-length pairs (B and C), and three short pairs (D, E, and F). These species may be divided into three karyotypic groups: 1) seven species with a satellite on A and on D; 2) 14 species with a satellite on A only; and 3) three species with a satellite on D only. Most species within karyotype groups may be separated from each other either by distinctive features of certain chromosomes or by statistical differences in length of chromosome arms or long arm: short arm ratios of chromosome A. Three tetraploid (2n=24) species had two long pairs (A,A′), four medium-length pairs (B,B′;C,C′), and six short pairs (D,D′;E,E′;F,F′). Suggestions are made as to the putative diploid parents of these presumed allotetraploids.     

Ricerche Citotassonomiche in Artemisia Vulgaris L. Ed Artemisia Verlotorum Lamotte

Abstract

Cytotaxonomical studies in Artemisia vulgaris L. and Artemisia verlotorum Lamotte. — Karyotype analysis of A. vulgaris and A. verlotorum has shown in the first species, in agreement with previous data, a chromosome number of 2n=16 and in the second the chromosome number of 2n=48 which does not agree with previous data. This seems to be the first case of polyploidy observed in Artemisia with basic number eight. A few specimens of A. verlotorum had shown 2n=48 + 2B chromosomes. The comparison of karyotypes has shown that, while the two species have, in some respect, the same degree of symmetry (ΣL%=57; ΣC9% = 43), the quality of their chromosomes is different (see karyotype formulas). We see no explanation for such an unlikely phenomenon.     

Exceedingly high chromosome number in Strasburgeriaceae, a monotypic family endemic to New Caledonia

We present the first report on the chromosome number of Strasburgeria robusta, which is confined to montane forests of New Caledonia and is the only known species in Strasburgeriaceae. The species has 2n = 500, which is an exceedingly high chromosome number in angiosperms. Within Crossosomatales, molecular evidence has indicated that S. robusta is sister to Ixerba brexioides, which is endemic to New Zealand and is the sole species in Ixerbaceae. Comparisons to the chromosome number of I. brexioides (2n = 50) support a close affinity between the two species because they share the base number x = 25. It is generally accepted that an increase in ploidy is associated with the origin of novel adaptations. A high level of polyploidy (20x with x = 25) may have allowed S. robusta to survive on a fragment of Gondwana by adapting to its ultrabasic substrate.     

Chromosome evolution in the Brachytheciaceae

Abstract

Twenty-eight moss species have been investigated cytologically. Mitotic karyograms have been presented for most of these species and these show a remarkable similarity in the n = 11 karyotype. Nine of the eleven chromosomes have terminal or sub-terminal centromeres. Lightly staining heterochromatic bands frequently occur along the axis of the chromosomes and very often these are the sites of chromosome bending; it has been suggested that these may be areas of neocentric activity. The karyotypes investigated show a reduction series of chromosome number which is paralleled by an increase in the number of long metacentrics; since the number of major chromosome arms is maintained in most of the species it has been suggested that Robertsonian fusion has been an important mechanism in the evolution of the Bracytheciaceae, and probably in all Diplolepidous mosses. Polyploidy has also played an important role in speciation. Finally it has been proposed that n = 11 is the primary basic number in the Diplolepideae.     

Chromosome rearrangements in Pectinidae (Bivalvia: Pteriomorphia) implied based on chromosomal localization of histone H3 gene in four scallops

Chromosomal structural rearrangement in four scallops, Chlamys farreri (n = 19), Patinopecten yessoensis (n = 19), Chlamys nobilis (n = 16) and Argopecten irradians (n = 16), was studied by fluorescence in situ hybridization using histone H3 gene probes. The results show that histone H3 gene sites differ strikingly with regard to number, location, and intensity among, or even within these species. For example, two histone H3 gene loci were detected on the metaphase chromosomes of P. yessoensis, while one locus was found in the others. In P. yessoensis, differing intensities of hybridization signals were detected between homologues 5 and 11, and within homologue 11. These data suggest that the histone H3 gene is a qualified chromosome marker for the preliminary understanding of the historical chromosomal reconstructing of the Pectinidae family. The variable distribution patterns of the histone H3 gene suggest that gene duplication/diminution as well as chromosome rearrangements by inversion and translocation may have played important roles in the genomic evolution of Pectinidae. We also compiled our present results with former published data regarding the chromosome mapping of rDNAs in species of the Pectinidae family. Such comparative chromosomal mapping should improve our understanding of historical chromosomal reconstructions of modern-day scallops.     

Contributions to the cytotaxonomy of the Commelinaceae*

Further material of Gibasis geniculata (Jacq.) Rohw. (syn. Tradescantia geniculata Jacq.) and other Gibasis species collected in the field has been studied. The existence of several species in our earlier experimental material is confirmed. These include G. geniculata itself (2n= 32 or 48 small chromosomes), G. oaxacana D. R. Hunt (2n= 16 small chromosomes) and G. schiedeana (Kunth) D. R. Hunt, which has two chromosome forms, 2n= 10 and 2n= 16, both with large chromosomes. These forms are diploid and tetraploid based on x= 5 and x= 4 respectively and show a Robertsonian relationship with each other. The cytology of tetraploid (2n= 20) G. karwinskyana is confirmed and that of a diploid form (2n=10) described. The recently described G. consobrina D. R. Hunt (2n= 20) is shown to be cytologically comparable with G. karwinskyana, but to differ in significant details. Next, the cytology of G. pulchella (Kunth) Rafin., the type species of Gibasis, is described and also that of the allied G. matudae D. R. Hunt. Both G. pulchella (2n= 10, 15) and G. matudae (2n= 10) show interchange heterozygosity, with complete rings of ten chromosomes at meiosis in some plants of G. pulchella. Preliminary comments are made on the cytology of G. aguensis (Standl. & Steyerm.) Rohw. (2n= 10), another ally of G. pulchella, and on the G. linearis group, where the basic number appears to be x= 6 but two karyotype patterns have been found. A discussion of chromosome architecture in Gibasis in relation to the taxonomy of the genus concludes the paper.     

Karyomorphology of Taiwanese Begonia (Begoniaceae): taxonomic implications

 The karyomorphology of all 14 species of Taiwanese Begonia was investigated to elucidate their chromosome features and chromosomal evolution. Among all species investigated, differences in chromosome features are found in: (1) chromosome number 2n = 22, 26, 36, 38, 52, 60, 64, 82, and (2) frequencies of chromosomes with secondary, tertiary, and/or small constrictions of polyploids, ranging from 23% to 63%, which is higher than the expected value of about 9%. It is suggested that after polyploidization from the diploid species (i.e., 2n = 22 and frequencies of chromosomes with secondary, tertiary, and/or small constrictions of polyploids of about 9%), chromosome translocations occurred, followed by a decrease in chromosome number, and subsequently stabilized genomes were formed in various species in Taiwan. The karyomorphological evidence also suggested that the chromosome morphology has evolved in parallel in the begonias belonging to different sections in Taiwan. The variation in chromosomal features is more complex than the variation in floral and fruit morphologies. Karyomorphological data also supports the recognition of five new species in Taiwan: Begonia bouffordii, B. chuyunshanensis, B. pinglinensis, B. tengchiana, and B. wutaiana. Based on detailed karyomorphological analyses, the taxonomic implications, speciation, and chromosomal evolution in Taiwanese Begonia are discussed. Received: January 22, 2002 / Accepted: March 4, 2002     

THE PROBLEM OF PLOIDY IN ECHEVERIA (CRASSULACEAE) II. TETRAPLOIDY IN E. SECUNDA

Every chromosome number from n = 12 to n =34 and also many higher numbers are known in one or more of the 130+ species of Echeveria, and the numerical boundary between diploids and tetraploids is not immediately apparent. Echeveria also is extraordinary for the number and diversity of hybrids that it can produce in cultivation, both within the genus and with species of several related genera. In 42 collections studied, the morphologically and cytologically variable E. secunda of central Mexico has n = 30-32, often with one or more B-chromosomes, and some quadrivalents are formed at meiosis in nearly every cell. Twenty-four hybrids of E. secunda, with 22 species or cytotypes considered diploids, resemble the former much more closely in appearance, and at meiosis 15-16 paired elements (bivalents and multivalents) are formed, never more, regardless of the number of chromosomes, 12 to 34, that were received from the other parent. It is concluded that the 15-16 paired elements in these hybrids are formed by the 30-32 chromosomes received from E. secunda, and that most chromosomes from the other parents occur as univalents, although usually a few associate with pairs from E. secunda to produce multivalents. Hybrids of E. secunda with 11 definitely tetraploid species having n = 34 to n = 68 are nicely intermediate in morphology between their parents, form mostly or entirely bivalents at meiosis, and most, probably all, including five intergeneric hybrids, are fertile. These observations are all consistent with the conclusion that E. secunda is an autotetraploid, even though no plants of the species having n = 15 or 16 have been found, and even though some other species of Echeveria having as many as 34 gametic chromosomes appear to be effectively diploid. Observations on pollen stainability and on second-generation hybrids are all compatible with this conclusion. The high chromosome numbers in many Mexican Crassulaceae that are now effectively diploid may have originated as polyploids that have become diploidized by mutation, loss, or suppression of duplicated chromosomes, segments, and genes. Hybrids of E. secunda, with three other species that appear to be tetraploids, have less regular meiosis, apparently because all of the chromosomes from the other parents do not regularly form pairs in the hybrids. These three species may represent intermediate stages in the processes of diploidization.     

THE CHROMOSOME NUMBER AND POSSIBLE ANCESTRY OF PELLAEA WRIGHTIANA

Knobloch , Irving W. (Michigan State U., E. Lansing), and D. M. Britton . The chromosome number and possible ancestry of Pellaea wrightiana . Amer. Jour. Bot. 50(1): 52–55. Illus. 1963.—Meiotic and somatic chromosome number determinations show that Pellaea wrightiana Hook, is a triploid (2n = 87) of hybrid origin. P. ternifolia (Cav.) Link (4x) and P. longimucronata Hook. (2x) (2n = 58) are considered to be the probable parents.     

Karyological notes on another eight species of Achillea (Asteraceae) from Turkey

The chromosome number and morphology in eight species of the sections Ptarmica (Mill.) W. D. J. Koch, Anthemoideae (DC.) Heimerl, Arthrolepis Boiss., Santolinoideae (DC.) Heimerl and Achillea of the genus Achillea L. (Asteraceae) were investigated using karyological techniques. Sample plants and seeds of A. biserrata M. Bieb., A. fraasii var. troiana Aschers. & Heimerl, A. multifida (DC.) Boiss., A. brachyphylla Boiss. & Hausskn., A. pseudaleppica Hub.-Mor., A. cretica L., A. latiloba Ledeb. ex Nordm., and A. kotschyi Boiss. subsp. kotschyi) were collected from natural habitats in 2003 and 2004. The chromosome number found in seven species was 2n = 18, while only A. kotschyi had 2n = 36. All chromosomes had median point (M), median region (m), and submedian (sm) centromers. In addition, only A. biserrata species had one subterminal (st) chromosome. An increase in asymmetry was not observed in the karyotypes of the species studied. None of the studied species had any B chromosomes.     

Karyological and taxonomical notes on three species of the genus<Emphasis Type="Italic">Epipactis (Neottioideae,Orchidaceae)</Emphasis> in the central-western Iberian Peninsula

Studies on the karyotypes and chromosome numbers of species ofEpipactis from the central-western Iberian Peninsula show that the species harbour enormous chromosome variability, have very asymmetric karyotypes and possess extraordinary diversity of aneuploidy. This paper provides the first report of a chromosome number forE. fageticola (2n=36, 40 + 0–2 B), as well as the first counts for Portuguese populations ofE. helleborine (2n=18, 32, 38) and first counts for Iberian populations ofE. tremolsii (n=20, 30, 2n=16, 24, 32, 34, 36, 38 + 1B, 40 + 1B, 52, 60). Among populations ofE. tremolsii there is a significant differentiation in ecology and somatic chromosome number, suggesting that there may be two different taxa in the region studied. Chromosomes are large to small, ranging in length from 10.8 μm to 1.8 μm. Karyotype asymmetry is of type 3C inE. fageticola andE. tremolsii and 2C inE. helleborine andE. tremolsii.     

Karyology of the genus Epidendrum (Orchidaceae: Laeliinae) with emphasis on subgenus Amphiglottium and chromosome number variability in Epidendrum secundum

Epidendrum is one of the largest Neotropical genera of Orchidaceae and comprises approximately 1500 species. Only 2.8% of these species have been studied cytologically, demonstrating chromosome numbers ranging from n = 12 in E. fulgens to n = 120 in E. cinnabarinum. The present work evaluated the evolution of the karyotypes of Epidendrum spp. based on data gathered from the literature and from analyses of the karyotypes of 16 Brazilian species (nine previously unpublished). The appearance of one karyotype with n = 12 with one larger chromosome pair in subgenus Amphiglottium appears to have occurred at the beginning of the divergence of this lineage, and x = 12 probably represents the basic number of this subgenus. Epidendrum secundum exhibits wide variation in chromosome numbers, with ten different cytotypes found in 22 Brazilian populations, seven of which were new counts: 2n = 30, 42, 50, 54, 56, 58 and 84. Most lineages of Epidendrum seem to have been secondarily derived from one ancestral stock with x = 20, as is seen in the majority of the present‐day representatives of the genus. © 2013 The Linnean Society of London, Botanical Journal of the Linnean Society, 2013, 172 , 329–344.     

CYTOTAXONOMIC STUDIES IN ELEOCHARIS SUBSER. PALUSTRES: CENTRAL UNITED STATES TAXA

Comparative chromosomal and morphological studies indicate that four species are present in the area surveyed. Eleocharis smallii Britt. is primarily diploid with 2n = 16, although sporadic polyploids with 2n = 36 also occur. E. macrostachya Britt. is morphologically similar with unstable polyploid numbers ranging around 2n = 38 and multivalents and univalents present in meiosis. E. xyridiformis Fern. & Brack., a species generally synonymized with E. macrostachya, is shown to be a morphologically distinct species with 2n = 18, 19, and 20. The 19-chromosome types are trisomic for one of the long chromosomes, the three homologs pairing in meiosis as a large chain trivalent. The trivalent separates equationally in the first division and preferentially in the second so that only 9- or 10-chromosome pollen grains containing an extra chromosome are formed. Trisomic cytotypes may potentially produce normal (18), reconstituted trisomies (19), or tetrasomic (20) plants, although tetrasomics have not been found. The 20-chromosome cytotype is not the expected tetrasomic, as it is karyotypically distinct from either the 18 or 19 cytotypes. In all species somatic mutations including translocations, translocation-retranslocations, and chromosome fragmentation (agmatoploidy) have been observed of which the significance, if any, has not been determined.     

SUPERNUMERARY CHROMOSOMES IN SAXIFRAGA VIRGINIENSIS (SAXIFRAGACEAE)

Acetocarmine squashes of root tips have demonstrated that 2n = 20 and 38 in Saxifraga virginiensis. These contrast with the earlier reported count of 2n = 28 for this species. In several populations supernumerary chromosomes were detected. Both intrapopulational and interpopulational variation in supernumerary chromosome number were detected, with the largest number of supernumerary chromosomes observed being six. Because these supernumerary chromosomes are equal in size to many of the smaller A chromosomes during mitotic metaphase, the presence of supernumerary chromosomes in this species could not be ascertained by analysis of mitotic metaphase preparations alone. During mitotic prophase, however, the supernumerary chromosomes of S. virginiensis are highly heterochromatic, appearing more densely coiled and darkly stained than the A chromosomes. This characteristic facilitated the recognition of supernumerary chromosomes in this species. The similarity in size of A and supernumerary chromosomes during mitotic metaphase and the observation of six supernumerary chromosomes in one population suggest that the count of 2n = 28 reported earlier for S. virginiensis may actually be a misinterpretation of 2n = 20 plus 8 supernumerary chromosomes. Furthermore, these findings and the observation of this same supernumerary chromosome phenomenon in other species of Saxifraga raise the possibility that some of the many disparate chromosome counts attributed to aneuploidy in the large genus Saxifraga may also be the result of misinterpretations of supernumerary chromosomes as A chromosomes.     

CHROMOSOME NUMBERS IN CUPHEA (LYTHRACEAE): NEW COUNTS AND A SUMMARY

The American genus Cuphea with ca. 260 species is extremely diverse with respect to chromosome number. Counts are now available for 78 species and/or varieties, or 29% of the genus. Included in this study are first reports for 15 taxa from Brazil, Cuba, Dominican Republic, Mexico, and Venezuela. Twenty-two different numbers are known for the genus, ranging from n = 6 to n = 54. The most common number in the primary center of species diversity in Brazil is n = 8, which is regarded as the base number of the genus. Two numbers are most common in the secondary center in Mexico, n = 10 and n = 12. Species with n = 14 or higher are considered to be of polyploid origin. Polyploids comprise 46% of the total species counted and appear in 9 of the 11 sections for which chromosome numbers have been reported. Aneuploid species comprise ca. 25% of the genus and are known from 7 of the 11 sections. The two subgenera are not characterized by different chromosome numbers or sequences of numbers. None of the 14 sections are circumscribed by a single chromosome number. Morphological and ecological variability in widespread, weedy species is correlated with differing chromosome numbers in some species whereas in others the chromosome number is stable. Summary of chromosome numbers by taxonomic section is presented. Section Euandra, centered in eastern Brazil, and the largest section of the genus, appears to be chromosomally most diverse. In section Trispermum, characterized by difficult, variable species with intermediate forms, two of the four species studied have polyploid races. Section Heterodon, endemic to Mexico and Central America and comprising most of the annual species of the genus, is best known chromosomally. Chromosome numbers have been counted for 25 of 28 species, and 12 different numbers are reported. The most advanced sections, Melvilla and Diploptychia, with numerous species occurring at higher altitudes, are characterized by high polyploids. Apomictic species occur in sect. Diploptycia. The cytoevolution of Cuphea is complex with frequent polyploid and aneuploid events apparently playing a significant role in speciation in both centers of diversity.     

DIFFERENTIAL STAINING WITH ORCEIN,GIEMSA, CMA,AND DAPI FOR COMPARATIVE CHROMOSOME STUDY OF 12 SPECIES OF AUSTRALIAN DROSERA (DROSERACEAE)

Differential stainings with orcein, Giemsa, CMA, and DAPI were compared in 12 species of Western Australian Drosera. Chromosome numbers of D. roseana, D. barbigera, D. leioblasta, D. oreopodion, D. mannii, D. walyunga, D. sewelliae, D. helodes, and D. echinoblasta are reported here for the first time. A marked difference regarding chromosome number was observed in Drosera dichrosepala (2n = 12) from that of the previous report (2n = 18). The karyotypes of the species showed commonly that degree of asymmetry in chromosome length was directly proportional to the mean chromosomal length whereas the number of chromosomes was inversely proportional. Bimodal karyotypes were observed in D. oreopodion, D. walyunga, D. barbigera, and D. echinoblasta, which perhaps resulted from interspecific hybridization of the former two and fragmentation in the latter two. Sat-chromosomes found in D. falconeri, D. sewelliae, D. helodes, and D. echinoblasta responded differently in differential staining. The C and fluorescent bands at the mostly terminal region revealed that maximum C-positive heterochromatin-rich segments, GC-rich segments, and AT-rich segments were accumulated at the ends of Drosera chromosomes. Some chromosomes could be identified by their specific staining property. On the basis of chromosome number and C- and fluorescent-banding pattern, we suggest that D. helodes and D. sewelliae are closely related.     

The cytology of Brachycome lineariloba

A comparison of the karyotypes of races D (2n=8), E (2n=10), B (2n=12) and C (2n=16) of B. lineariloba suggests that these races have in common a basic set of four chromosome pairs, and that the higher chromosome number races are related to race D by successive chromosome addition. — A study of meiosis in B × C and A₁ × B hybrids supports this contention and elucidates the homologies of the additional chromosomes. — Meiotic pairing in hybrids between A and C is very complex. At present it can only be stated that there are extensive interchromosomal homologies between the two races. — Two phyletic schemes of the relationships of the races are considered. The second, which is favoured, involves successive chromosome addition, with the quasidiploid race E (2n = 10) giving rise to race B by diploidisation of the univalent chromosomes. This scheme is supported by features of univalent behaviour in the various races and their hybrids. — The ecogeographic distribution pattern of the races shows replacement of D by E by B by C as the species extends into more arid and more harsh environments. This replacement is also associated with increasing vigour. — It seems most likely that the addition chromosomes are derived from a race A (2n=4) source since they are added always by twos, and each addition increases both vigour and drought tolerance. Race A is the most vigorous and one of the most drought tolerant of the five races.It is suggested that the evolution of the races can be related to the increasing aridity of the Late Pleistocene and Recent geological epochs.     

Interstitial telomere‐like repeats in the monocot family Araceae

Combining molecular cytogenetics and phylogenetic modelling of chromosome number change can shed light on the types of evolutionary changes that may explain the haploid numbers observed today. Applied to the monocot family Araceae, with chromosome numbers of 2n = 8 to 2n = 160, this type of approach has suggested that descending dysploidy has played a larger role than polyploidy in the evolution of the current chromosome numbers. To test this, we carried out molecular cytogenetic analyses in 14 species from 11 genera, using probes for telomere repeats, 5S rDNA and 45S rDNA and a plastid phylogenetic tree covering the 118 genera of the family, many with multiple species. We obtained new chromosome counts for six species, modelled chromosome number evolution using all available counts for the family and carried out fluorescence in situ hybridization with three probes (5S rDNA, 45S rDNA and Arabidopsis‐like telomeres) on 14 species with 2n = 14 to 2n = 60. The ancestral state reconstruction provides support for a large role of descending dysploidy in Araceae, and interstitial telomere repeats (ITRs) were detected in Anthurium leuconerum, A. wendlingeri and Spathyphyllum tenerum, all with 2n = 30. The number of ITR signals in Anthurium (up to 12) is the highest so far reported in angiosperms, and the large repeats located in the pericentromeric regions of A. wendlingeri are of a type previously reported only from the gymnosperms Cycas and Pinus. © 2014 The Linnean Society of London, Botanical Journal of the Linnean Society, 2015, 177 , 15–26.     

A SYSTEMATIC REVISION OF PHYLLANTHUS SUBSECTION URINARIA (EUPHORBIACEAE)

The examination of several taxa from various tropical regions of the world, previously classified as Phyllanthus urinaria L., indicates that they do not belong to a single species. On the basis of morphology, cytology, genetics, and biometry, a new classification is presented in which the collective species P. urinaria, or “urinaria complex,” is elevated to the subsection level: Phyllanthus subsection Urinaria. Within the subsection, two subgroups may be recognized on the basis of seed coat ornamentation. Each of these lines is represented by two species which differ from each other in chromosome number: P. embergeri nov. spec. (2n = 100) and P. nozeranii nov. spec. (2n = 50) in the “spiraled” line, P. hookeri Muell. Arg. (2n = 100) and P. urinaria L. (2n = 50) in the “radiated” line. In the latter species, which has undergone diversification, two subspecies may be distinguished: P. urinaria urinaria and P. urinaria nudicarpus subspec. nova.     

Chromosomes tell half of the story: the correlation between karyotype rearrangements and genetic diversity in sedges,a group with holocentric chromosomes

Chromosome rearrangements may affect the rate and patterns of gene flow within species, through reduced fitness of structural heterozygotes or by reducing recombination rates in rearranged areas of the genome. While the effects of chromosome rearrangements on gene flow have been studied in a wide range of organisms with monocentric chromosomes, the effects of rearrangements in holocentric chromosomes—chromosomes in which centromeric activity is distributed along the length of the chromosome—have not. We collected chromosome number and molecular genetic data in Carex scoparia, an eastern North American plant species with holocentric chromosomes and highly variable karyotype (2n = 56–70). There are no deep genetic breaks within C. scoparia that would suggest cryptic species differentiation. However, genetic distance between individuals is positively correlated with chromosome number difference and geographic distance. A positive correlation is also found between chromosome number and genetic distance in the western North American C. pachystachya (2n = 74–81). These findings suggest that geographic distance and the number of karyotype rearrangements separating populations affect the rate of gene flow between those populations. This is the first study to quantify the effects of holocentric chromosome rearrangements on the partitioning of intraspecific genetic variance.