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Despite the importance of polyploidy for the evolution of Opuntia, few researches have been focused to identify the ploidy of cultivars used in plant breeding programmes. We aimed to provide chromosome numbers, ploidy and heterochromatin band patterns of seven species and 24 cultivars from Opuntia, and investigate the relationship between phenotypic characteristics and ploidy in these species. All cultivars analyzed of Opuntia atropes, O. cochenillifera, and one cultivar of O. undulata are diploids, O. larreyi, one cultivar of O. stricta and two cultivars of O. undulata are tetraploids and all cultivars of O. ficus-indica, one cultivar of O. stricta and four cultivars of Opuntia sp. are octoploids. CMA/DAPI banding revealed the occurrence of terminal bands in all cultivars and pericentromeric bands in six cultivars. Polyploid species of Opuntia had superior mean values than diploid ones in relation to the cladode width, cladode length, cladode area, cladode thickness and plant height. Diploids had superior mean values than polyploids in relation to the number of cladodes. Polyploidy may be a useful tool for obtaining Opuntia cultivars with quantitative characteristics of interest. [ABSTRACT FROM AUTHOR]

Nine new species in Australian Nicotiana section Suaveolentes are described, including N. clarksonii M.W.Chase & Christenh., N. erytheia M.W.Chase & Christenh., N. latifolia M.W.Chase & Christenh., N. latzii M.W.Chase, R.W.Jobson & Christenh., N. gibbosa M.W.Chase, D.D.Andrew & J.J.Bruhl, N. olens M.W.Chase & Christenh., N. praecipitis M.W.Chase & K.Durham, N. karara M.W.Chase & Christenh. and N. bungonia M.W.Chase & Taseski. Some have been known from herbarium specimens for a long time, but their distinction from other species concepts was unsuspected until DNA studies showed their divergent nature. Others are known from one or only a few new localities. All are morphologically and genetically distinct from their close relatives. Increased sampling of populations in our molecular studies has led us to the conclusion that the widespread, recently described species N. insecticida is a species complex, comprising as many as six genetically distinct taxa, one of which includes material from the type locality of N. hesperis. Here, we describe a new name, N. erytheia, for all material we previously assigned to N. hesperis that is phylogenetically distinct from that of the type locality. To make the relationships of the new species clearer, we provide a tree produced by analysis of nuclear (RADseq) DNA data. [ABSTRACT FROM AUTHOR]

Background and Aims The extent to which genome size and chromosome numbers evolve in concert is little understood, particularly after polyploidy (whole-genome duplication), when a genome returns to a diploid-like condition (diploidization). We study this phenomenon in 46 species of allotetraploid Nicotiana section Suaveolentes (Solanaceae), which formed <6 million years ago and radiated in the arid centre of Australia. Methods We analysed newly assessed genome sizes and chromosome numbers within the context of a restriction site-associated nuclear DNA (RADseq) phylogenetic framework. Key Results RADseq generated a well-supported phylogenetic tree, in which multiple accessions from each species formed unique genetic clusters. Chromosome numbers and genome sizes vary from n = 2x = 15 to 24 and 2.7 to 5.8 pg/1C nucleus, respectively. Decreases in both genome size and chromosome number occur, although neither consistently nor in parallel. Species with the lowest chromosome numbers (n = 15–18) do not possess the smallest genome sizes and, although N. heterantha has retained the ancestral chromosome complement, n = 2x = 24, it nonetheless has the smallest genome size, even smaller than that of the modern representatives of ancestral diploids. Conclusions The results indicate that decreases in genome size and chromosome number occur in parallel down to a chromosome number threshold, n = 20, below which genome size increases, a phenomenon potentially explained by decreasing rates of recombination over fewer chromosomes. We hypothesize that, more generally in plants, major decreases in genome size post-polyploidization take place while chromosome numbers are still high because in these stages elimination of retrotransposons and other repetitive elements is more efficient. Once such major genome size change has been accomplished, then dysploid chromosome reductions take place to reorganize these smaller genomes, producing species with small genomes and low chromosome numbers such as those observed in many annual angiosperms, including Arabidopsis. [ABSTRACT FROM AUTHOR]

The Trichocentrum cepula complex comprises three species, T. caatingaense, T. cepula and T. sprucei, endemic to tropical forests east of the Andes in South America. The delimitation of these species has been diversely interpreted due to the extensive morphological variation in the complex. We applied an integrative approach to achieve a better understanding of these biological units, using geometric morphometrics, cytogenetic analysis (chromosome counts and CMA/DAPI banding) and molecular phylogenetics (ITS and rpl32-trnL). An initial morphometric analysis using the pre-identified specimens into three taxa suggested that T. sprucei is distinct from the other two, which show some overlap. A subsequent analysis of the labellum, including only T. caatingaense and T. cepula organized in six pseudo-populations, suggested the existence of four morphological groups. All analysed specimens presented 2n = 36 chromosomes, CMA+/DAPI− terminal bands and CMA−/DAPI+ pericentromeric bands, which varied in number across species, localities or even individuals from the same locality. The notable variation in DAPI+ pericentromeric bands may be related to transposable elements that could also be a factor influencing the wide morphological variation in the flowers. In the phylogenetic analysis, the specimens belonging to T. caatingaense formed a strongly supported clade sister to the rest, whereas the specimens belonging to T. cepula and T. sprucei emerged together, with their relationships tending to be determined by geographic proximity. The evidence we generated suggests that treating the Brazilian populations of this species complex under a single name, T. cepula, provides more taxonomic stability and utility, thus the necessary taxonomic changes are implemented. [ABSTRACT FROM AUTHOR]

Some groups in Epidendrum have stable chromosome numbers, whereas the species of Epidendrum subgenus Amphiglottium exhibit high levels of chromosome number variability and other genomic alterations. Polyploidy and dysploidy have both been invoked to explain chromosome number variation in the subgenus, but little is known about what is driving the high frequency of chromosome modification within some species in this group. To test whether hybridization and introgression are involved, we use fluorochrome staining to evaluate the chromosome numbers and heterochromatin bands in E. subgenus Amphiglottium , including individual parental genotypes from introgressed and non-introgressed populations. Two main types of heterochromatin were observed forming CMA and DAPI bands in Epidendrum spp. B chromosomes were identified in some individuals. In non-introgressed populations, E. secundum has three cytotypes, 2 n = 28, 56 and 84, found in different parts of its geographical range and a small number of DAPI bands. In introgressed populations of E. secundum , there was dysploid variation among individuals that were morphologically typical parental plants, and in one introgressed population a high number of DAPI bands was observed in what appeared on morphological grounds to be pure parental individuals. Our data corroborate the hypothesis that hybridization and introgression play a role in generating chromosome variation (number and form) and heterochromatin diversification in E. subgenus Amphiglottium. [ABSTRACT FROM AUTHOR]

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Here we study a challenging group of karyotypically highly variable Epidendrum spp. using phylogenetic methods to help understand how hybridization/introgression contributes to karyotype evolution. We hypothesize that species with great chromosome number variation are a result of past hybridization/introgression. Conflicting topologies in trees constructed using separate plastid and nuclear datasets suggest past hybridization events that occurred most probably at least 3.7 Mya. A basic number x = 14 and substantial karyotype change followed by species divergence are suggested. Descending dysploidy and polyploidy were the most frequent changes estimated across the phylogenetic tree of the group. Two species, Epidendrum secundum and E. xanthinum , have probably experienced unidirectional gene flow involving their ancestors (the pollen recipients) and ancestors of E. puniceoluteum and E. denticulatum/E. flammeum , respectively, the pollen donors. However, it is not possible to say whether hybridization participated in the origin of E. secundum and E. xanthinum or merely contributed to their genomic divergence and karyotype change through introgression as has been observed in modern hybrid zones in Epidendrum. This pattern of introgression causing karyotype disruption and divergence could help explain the enigma of some highly diverse genera, such as Epidendrum. Further studies using a wider sampling of the genus could test if gene flow and karyotype variability are associated with the increase of speciation rates. [ABSTRACT FROM AUTHOR]

Summary: In this volume of Curtis's Botanical Magazine, we increase the number of species recognised in Nicotiana sect. Suaveolentes to 38, up from the 21 recorded in the Flora of Australia published 39 years ago, but we estimate the final number is likely to exceed 60. We examine the reasons why so many unrecognised species exist. Several Australian and American botanists have previously specialised in Nicotiana but did not detect such diversity. We have carried out many fieldtrips, seen most known species in the wild and have grown these accessions from diverse areas side‐by‐side in cultivation to avoid basing decisions about species characteristics on features heavily influenced by environmental plasticity. In the end, we conclude that it is a mixture of focused and extensive fieldwork and more recent genomic, genetic and karyological studies combined in the process of reciprocal illumination, that has enabled us to describe so many new species. We also briefly focus on the topic of why Nicotiana is so species‐rich in Australia. [ABSTRACT FROM AUTHOR]

Summary: Plants collected in Towarri National Park in New South Wales were cultivated at the Royal Botanic Gardens, Kew. It is illustrated here and described as the new species, Nicotiana notha. Its origin, cytology, taxonomic history, ecology and cultivation are discussed. [ABSTRACT FROM AUTHOR]