CHROMOSOME NUMBERS IN THE GENUS ANTHURIUM

Chromosome numbers were determined for 63 Anthurium species. Thirty-eight of these were newly determined. Generally the present work confirmed existing chromosome counts when these were available for comparison. The most common somatic chromosome number found was 30, but counts ranged from 2n = 20 to 90. In a few instances conflicting counts were obtained. B chromosomes were found frequently in Sect. Cardiolonchium and varied in number from one to three. Four polyploid series were evident from all available counts: 20-40, 24-30-48-84, 28-56 and 30-60-90-ca 124. Most species were part of the polyploid complex based on 30. Although species were not observed with n = 5, 6 or 7, movement among the basic numbers was considered to have occurred at this level. The relationship among these basic numbers and n = 15 (x₂) is still obscure.     

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.     

Extensive chromosome number variation in Aster ageratoides var. pendulus (Asteraceae)

Aster ageratoides var. pendulus, a recently described taxon, is endemic to Mt Hupingshan of north‐western Hunan, China. Field observations and collections were made from the only known population. Root‐tip squashes were used to determine the chromosome numbers of 96 plants and 61 seedlings from the achenes of eight sample plants. The results show that var. pedulus is a swarm of 30 cytotypes with nearly continuous chromosome numbers from 2n = 60 to 2n = 92. Chromosome numbers of 61 seedlings vary from 2n = 61 to 2n = 91, belonging to 18 cytotypes. The chromosome number variation of var. pendulus is highly unusual not only in the A. ageratoides polyploid complex but also in angiosperms. Such an enormous continuous variation of chromosome numbers could have arisen by the combined effect of hybridization, recent origin and high levels of polyploidy. © 2011 The Linnean Society of London, Botanical Journal of the Linnean Society, 2011, 165 , 378–387.     

MODELS OF RETICULATE EVOLUTION IN THE CORAL GENUS ACROPORA BASED ON CHROMOSOME NUMBERS: PARALLELS WITH PLANTS

Somatic chromosome number was determined for 22 species of the scleractinian coral genus Acropora, three species of Montipora, and one species of Fungia, using colchicine-treated cells of externally developing embryos. Most had 28 chromosomes, except for six species of Acropora, which had somatic numbers of 24, 30, 30, 42, 48, and 54. Two models that invoke a combination of polyploidy and aneuploidy are presented to account for the observed intrageneric variation in somatic chromosome number. The ability to propagate clones through vegetative fragmentation plus the opportunities for hybridization during multispecies spawning events may have contributed to the development of polyploidy and rapid, sympatric speciation in the uniquely speciose coral genus Acropora.     

Culture studies on the life history of Haplospora globosa and Tilopteris mertensii (tilopteridales,phaeophyceae)

The complete life histories of Tilopteris mertensii and haplospora globosa were followed in culture. Tilopteris shows a succession of identical plants through uninucleate “eggs” which develop parthenogenetically. In Haplospora, sporophytes alternate with gametophytes without sexuality and nuclear alternation. However, evidence for meiotic stages is found in sporangium initials. Gametophytes produce oogonia and antheridia, and eggs develop parthenogenetically. The chromosome number of Tilopteris is n = 62 (60–65). In both phases of Haplospora numbers are n = 50 (43–54). Haplospora from Heligoland perpetuates the sporophyte only at chromosome numbers of n = 25 (22–28).     

ISOZYME NUMBER IN SUBTRIBE ONCIDIINAE (ORCHIDACEAE): AN EVALUATION OF POLYPLOIDY

The Oncidiinae has attracted attention because of the variation it exhibits in chromosome number, n = 5–30, which is greater than the range in the rest of the Orchidaceae. The genus Psygmorchis, with n = 5 and 7, has been a particular focus of controversy, and many authors have suggested that 5 and 7 are the base numbers for the subtribe. The other taxa in the subtribe presumably evolved through hybridization and polyploidy. Other workers have found that the lowest counts correlate with derived morphological conditions and have hypothesized that these low numbers result from aneuploid reductions, while higher numbers are associated with ancestral morphologies and are not the result of polyploidy. These two hypotheses were evaluated by determining isozyme numbers for 13 enzymes in species that span the chromosomal range known for the Oncidiinae (n = 5–30). Isozyme number has been shown to be a reliable indicator of polyploidy in angiosperms because polyploids display isozyme multiplicity relative to diploids. This analysis revealed no differences among species in isozyme number for the enzymes examined. Therefore, our data reject the hypothesis that species with higher chromosome numbers are polyploid.     

CHROMOSOMES AND SYSTEMATICS OF ASPLENIUM SECT. HYMENASPLENIUM (ASPLENIACEAE)

Gametic and somatic chromosome numbers of eight Asian species belonging to Asplenium sect. Hymenasplenium were determined. Seven species were observed to have chromosome numbers based on x = 39, and one on x = 38. These chromosome numbers are exceptional in Asplenium which is well known to have chromosomes of n = 36 or multiples thereof. Decisions on the taxonomic status of the species of section Hymenasplenium were facilitated by cytological observations. Systematic recognition of this section is also supported by the peculiarity in the chromosome numbers, and evidence for the addition to the section of several other species is presented.     

CHROMOSOME NUMBERS IN UMBELLIFERAE. II

Bell , C. Ritchie (U. of North Carolina, Chapel Hill.), and Lincoln Constance . Chromosome Numbers in Umbelliferae. II. Amer. Jour. Bot. 47(1) : 24-32. Illus. 1960.–Chromosome numbers are reported for plants representing an additional 100 taxa of Umbelliferae. Chromosome numbers for 77 of these taxa are published here for the first time, previously published chromosome numbers of 19 taxa are verified, and numbers differing from those previously published are reported in 4 instances. Ten of the genera included here have been previously unknown cytologically. Polyploidy has been discovered in Bowlesia and confirmed in Pimpinella. Aneuploid series appear to occur in Eremocharis, Eryngium, Oenanthe, Perideridia, and Ptilimnium. Every chromosome count is referable to a cited herbarium specimen.     

ANEUPLOIDY IN CLAYTONIA VIRGINICA

Rothwell , Norman V. (Long Island U., Brooklyn, N. Y.) Aneuploidy in Claytonia virginica. Amer. Jour. Bot. 46(5): 353–360. Illus. 1959.—Within the taxon, Claytonia virginica L., an extensive aneuploid series has been found including the following chromosome numbers: 2n = 12, 14, 16, 17, 18, 19, 20, 22, 24, 26, 28, 30, 32, 34, 36, 48, and 72. Studies revealed that a population could be composed of individuals differing in chromosome number. Pollen fertility appears to be high in natural populations and in plants showing meiotic irregularities. Different karyotypes were found within the taxon; plants having the same chromosome number may have different karyotypes. Hybrids have been obtained as the result of crossing plants differing both in number and karyotype. From all the evidence, C. virginica appears to be able to tolerate transitions from one cytological type to another. The hypothesis is proposed that most of the various numbers have been derived from a haploid complement of 8 chromosomes possessing median centromeres. The following factors are suggested to account for the origin of the different numbers: nondisjunction, univalent lagging, misdivision of univalents, polyploidy, and fertile triploids.     

Somatic hybridization between potato and Nicotiana plumbaginifolia

Summary Electrofusion was carried out between mesophyll protoplasts from the transformed diploid S. tuberosum clone 413 (2n=2x=24) which contains various genetic markers (hormone autotrophy, opine synthesis, kanamycin resistance, -glucuronidase activity) and mesophyll protoplasts of a diploid wild-type clone of N. plumbaginifolia (2n=2x=20). Hybrid calli were obtained after continuous culture on selection medium containing kanamycin. Parental chromosome numbers, determined at 2 months after fusion, revealed hybrid-specific differences between the individual calli. On the basis of these differences three categories of hybrids were distinguished. Category I hybrids contained between 8 and 24 potato chromosomes and more than 20 N. plumbaginifolia chromosomes; category II hybrids had between 1 and 20 N. plumbaginifolia chromosomes and more than 24 potato chromosomes; category III hybrids contained diploid or subdiploid numbers of chromosomes from both parents. The hybrids were evenly distributed over the three categories. After a 1-year culture of 24 representative hybrid callus lines on selection medium the karyotype of 10 hybrids remained stable, whereas 8 hybrids showed polyploidization of the genome of one parent, together with no or minor changes of the chromosome numbers of the other parent. Six hybrids showed slight changes in the hybrid karyotype. The elimination of chromosomes of a particular parent was not correlated to their metaphase location. The processes of spontaneous biparental chromosome elimination leading to the production of asymmetric hybrids of different categories are discussed.     

Cytogeography of Gentianaceae–Exaceae in Africa,with a special focus on Sebaea: the possible role of dysploidy and polyploidy in the evolution of the tribe

Unlike other tribes of Gentianaceae, Exaceae have so far received little attention regarding their karyological evolution. Indeed, only 35 chromosome number counts (19 species) have been referenced to date, representing only a negligible fraction of the tribal diversity. In this paper, we performed an intensive chromosome count on material collected in the field (South and central Africa, plus Madagascar), encompassing 155 populations and c. 60 species from four genera of Exaceae, including Exacum, Ornichia, Sebaea and Tachiadenus. Fifty nine species (14 Exacum, one Ornichia, 42 Sebaea and two Tachiadenus) were examined for the first time, revealing a broad set of chromosome numbers (2n = 18, 28, 32, 36, 42, 56) and the occurrence of polyploid systems within Exacum and Sebaea. These results allow us to postulate x = 7, 8 or 9 as possible base chromosome numbers for Exaceae and emphasize the importance of both dysploidy and polyploidy processes in the evolution of the tribe. Finally, chromosome numbers appear to be associated to some morphological or geographical traits, suggesting new systematic combinations and likely active speciation patterns in the group. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 556–566.     

ANEUSOMATY IN ANEUPLOID POPULATIONS OF CLAYTONIA VIRGINICA

Lewis Walter H. (Stephen F. Austin State Coll., Nacogdoches, Texas.) Aneusomaty in aneuploid populations of Claytonia virginica. Amer. Jour. Bot. 49(9): 918–928. Illus. 1962.—From 2 central east Texas populations of Claytonia virginica, 15 chromosome numbers, 2n = 14, 15, 16, 18, 25, 26, 27, 28, 29 30, 31, 32, 33, 36, and 58, were found among a sample of 181 plants. The most frequently encountered numbers were 2n = 14, 28, and 29. Among an additional 14 plants the pollen mother cells in the same bud differed from one another in chromosome number, as well as the pollen and premeiotic cells from the same plant. The chromosomes of the most unstable plant varied from 2n = 14–36. Numerous meiotic abnormalities, including inversions, dicentrics, bridges, fragments, non-disjunctions, univalents, and multivalents, were observed for the aneusomatic and trisomic plants. It is suggested that the origin of the aneusomatics is related to the numerical disparity of the gametic chromosomes composing them. Since the species is perennial in habit, thereby allowing the unstable plants to produce gametes with varying chromosome numbers year after year, it is further proposed that the wide range of aneuploid known for C. virginica resulted, at least in part from the presence of aneusomatic individuals.     

BIOSYSTEMATIC STUDIES IN THE BOUTELOUA CURTIPENDULA COMPLEX. III. POLLEN SIZE AS RELATED TO CHROMOSOME NUMBERS

Pollen size statistics are presented for 10 closely related species of Bouteloua and relationships between pollen size and chromosome numbers are presented for 13 populations of 5 species and 3 varieties. With 1 exception, all populations of all taxa conformed to a general pattern of pollen size dependent upon chromosome number. Chromosome numbers varied from 2n = 20 to 2n = ca. 103, with several independent aneuploid series. Statistical analyses were made of pollen size as related to chromosome number in the 3 varieties of B. curtipendula. These data showed that tetraploids (2n = 40) of var. tenuis had significantly greater pollen size and coefficient of variation than diploids (2n = 20) of the same variety. Similarly, aneuploids of var. curtipendula with 2n = 45 to 2n = 64 chromosomes had significantly larger and more variable pollen than tetraploids (2n = 40) of the same variety. Highly significant positive regression coefficients were obtained from analyses of chromosome numbers and mean pollen size, and chromosome numbers and coefficient of variation, for var. curtipendula. Regression coefficients for var. caespitosa populations with chromosome numbers over the hexaploid (2n = 60) level were not significant.     

Karyotypes of parasitic Hymenoptera: Diversity, evolution and taxonomic significance

Haploid chromosome numbers (n) of parasitic Hymenoptera (= traditional Parasitica + Chrysidoidea) vary from 2 to 23. However, this range can be subdivided into three intervals with n= 14–23 (less derived parasitic wasps, e.g., some Ichneumonidae and Braconidae as well as Gasteruptiidae), 8–13 (many other parasitic Hymenoptera) and 2–7 (Dryinidae, the majority of Chalcidoidea and some advanced Braconidae, e.g. Aphidiinae). The symmetric karyotype with a relatively high chromosome number (n= 14–17) and the prevalence of biarmed chromosomes must be considered as a groundplan feature of parasitic Hymenoptera. Independent reductions of chromosome numbers (n≤ 10–11) occurred in some groups of the superfamily Ichneumonoidea as well as in the common ancestor of the Proctotrupoidea sensu lato, Ceraphronoidea, Cynipoidea and Chalcidoidea. Further multiple decreases in chromosome numbers (n≤ 4–6) took place in some Braconidae, various lineages of the superfamily Chalcidoidea as well as in the family Dryinidae. Two main trends prevailed in the karyotype evolution of parasitic wasps: the reduction of chromosome numbers (mainly due to tandem fusions and less frequently due to centric ones) and karyotypic dissymmetrization (through an increase in size differentiation of chromosomes and/or in the share of acrocentrics in a chromosome set). Although karyotypic features of parasitic Hymenoptera can be used for solving taxonomic problems at various levels, this method is the most effective at the species level.     

A small (2.4 Mb) Bacillus cereus chromosome corresponds to a conserved region of a larger (5.3 Mb) Bacillus cereus chromosome

We have determined the sizes of the chromosomes of six Bacillus cereus strains (range 2.4–4.3 Mb) and constructed a physical map of the smallest B. cereus chromosome (2.4 Mb). This map was compared to those of the chromosomes of four B. cereus strains and one B. thuringiensis strain previously determined to be 5.4-6.3 Mb. Of more than 50 probes, 30 were localized to the same half of the larger B. cereus and B. thuringiensis chromosomes. All 30 were also present on the small chromosome. Twenty of the probes present on the other half of the larger chromosomes were either present on extrachromosomal DNA, or absent from the B. cereus strain carrying the small chromosome. We propose that the genome of B. cereus and B. thuringiensis has one constant part and another less stable part which is more easily mobilized into other genetic elements. This part of the genome is localized to one region of the chromosome and may be subject to deletions or more frequent relocations between the chromosome and episomal elements of varying sizes up to the order of megabases.     

半蒴苣苔属植物染色体制片优化及染色体数目和倍性研究

染色体数目和倍性是系统与进化生物学和遗传学研究中十分重要的基础信息。为探索半蒴苣苔属染色体制片的适宜条件以及染色体数目的进化模式及其与物种的进化关系，该研究基于半蒴苣苔属染色体数目的进化历史，并根据该属植物具有叶片扦插繁殖的特性，采用叶片水培生根法获取半蒴苣苔(Hemiboea subcapitata)、弄岗半蒴苣苔(H.longgangensis)、龙州半蒴苣苔(H.longzhouensis)、江西半蒴苣苔(H.subacaulis var.jiangxiensis)、华南半蒴苣苔(H.follicularis)和永福半蒴苣苔(H.yongfuensis)6种植物的根尖材料，分析不同实验条件对染色体制片效果的影响，对染色体制片实验的条件进行优化及染色体计数，结果表明：(1)9:30—10:00取材，解离10 min以及染色15 min为半蒴苣苔属染色体制片的适宜条件。(2)上述6种半蒴苣苔属植物均为二倍体，染色体数目均为32(2n=2x=32)。(3)除个别物种染色体数目有变化以外，该属大部分物种染色体数目可能为2n=2x=32且染色体数目变化可能是非整倍化的作用，与物种进化没有明...     

CHROMOSOMES OF GRAPTOPETALUM AND THOMPSONELLA (CRASSULACEAE)

Chromosome numbers are reported for probably all 11 species of Graptopetalum (x = 30–35) and for both species of Thompsonella (x = 26). Plants of two species of Graptopetalum have gametic numbers from about 240–275, more than have been reported in any other seed plants. In hybrids the 30–35 chromosomes in the basic genome of Graptopetalum and likewise the 26 in Thompsonella apparently do not pair among themselves, and the genomes seem to be no more potent genetically than those of other species in their subfamily having as few as 12 chromosomes. Species with these gametic numbers are therefore considered to be diploid. On the other hand, in hybrids between a diploid and a plant with a very high chromosome number the phenotype of the latter predominates, and most of its chromosomes pair with each other. Many such hybrids are fertile. These facts suggest that the high polyploids arose by autoploidy rather than by alloploidy. Nevertheless, they may store heterozygosity at some gene loci and release it in various dosages and proportions each generation.     

Chromosome numbers of Turkish Crocus (Liliiflorae,Iridaceae) and their geographical distribution

The genus Crocus is known for its widely varying chromosome numbers (from 2n = 6 to 2n = 70) with varying numbers occurring even within species, as it is the case for Crocus biflorus Miller (2n = 8, 10, 12, 14, 16, 18, 20, 22, 24). After we found morphological diverse C. biflorus populations in Turkey doubts arose about their rank of being subspecies of the Italian C. biflorus (2n = 8). Here we publish the chromosome numbers for 76 populations of C. biflorus sensu lato distributed all over Turkey. The chromosome numbers ranged from 2n = 8 to 2n = 36, with the higher numbers occurring in the mountain ranges of the Anatolian Diagonal and east of it, while lower numbers were found only southwest of these mountains. Closely related taxa with similar distribution mostly differ in their chromosome numbers. This led us to assume that chromosomal changes influence speciation processes in the genus. Therefore, chromosome numbers may represent an important character for the establishment of a new taxonomic treatment of the Crocus species, especially within section Nudiscapus. (© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Chromosome numbers of miscellaneous Malagasy Acanthaceae

Meiotic chromosome numbers are reported for 12 species in eight genera of Acanthaceae from Madagascar. Chromosome numbers of 11 species are reported for the first time. Counts inMendoncia (n=19) andNeuracanthus (n=20) are the first for these genera. A new chromosome number (n=30) is reported inJusticia. Systematic implications of the chromosome counts are addressed and basic chromosome numbers for these eight genera of Malagasy Acanthaceae are discussed.