Karyological investigations on several species of genus Rebutia

Abstract These are the first avaiable data about the karyology of the taxa belonging to Rebutia Sect. Digitorebutia, the section of genus Rebutia K. Schum. with more species. Eight species of Sect. Digitorebutia were investigated. Out of the species studied, seven (R. pygmaea, R. raulii, R. steinmannii, R. major, R. diersiana, R. haagei and R. gavazzii) are polyploid, with tetraploid chromosome number 2n=4x = 44, and one (R. leucanthema) is diploid, with chromosome number 2n=2x = 22; x = 11. This is the first karyotype information of all the species investigated

Divergence time estimation and mapping of morphological and cytogenetical data in the southern South American geophyte genus Pterocactus (Cactaceae)

Pterocactus has 10 species endemic to restricted areas of the Argentine Monte and Patagonia regions, also growing in neighbouring Chile. We analysed phylogenetic relationships between its species, based on plastid DNA sequences (psbA-trnH, rpl16, trnH-matK), exomorphological features (spine type and size, stem segment form, flower position, epidermis colour, areole pubescence, stem surface) and cytogenetical traits (genome size, somatic chromosome number). Traits were mapped using character mapping and ancestral state reconstruction to understand the dynamics of evolutionary changes. Pterocactus was monophyletic. Two lineages were recovered: clade A (with P. fischeri diverging early and P. reticulatus, P. valentinii, P. megliolii, P. gonjianii, and both P. tuberosus forms) and clade B (with P. neuquensis diverging first and P. araucanus and P. hickenii). Both samples examined of P. australis were paraphyletic. It was estimated that Pterocactus split from its sister group at 9.38 mya. The crown group age was estimated to be 7.69 myr. Species showed x = 11 with different ploidy levels (2n = 22, 44, 99, ca. 110, and 154); only P. tuberosus f. tuberosus was diploid. The numbers were typical of each taxon studied, and polyploidy was important in its diversification. Two 18S-5.8S-26S sites were detected regardless of the ploidy level, except P. fischeri with four sites and 2n = ca. 110. The number of 5S sites was 2 in P. gonjianii and the diploid P. tuberosus f. tuberosus, 4 in the tetraploid P. tuberosus f. lelongii, 10 in the probably decaploid P. fischeri and 8 in P. araucanus of unknown chromosome number. The genome size ranged from 2C = 4.94 pg in P. megliolii of unknown chromosome number to 2C = 16.68 pg in the tetradecaploid P. hickenii. The ancestor is reconstructed as a dwarf shrub with cylindrical central spines of 16.35–31.2 mm long, non-woolly areoles, cylindrical to globose/obpyriform stem segments, non-tuberculate stem surface, lateral flower position, green/brown to violet epidermis, probably diploid, and with a genome size between 1.10 and 1.23 pg.Fil: Las Peñas, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Bernardello, Gabriel Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentin

Caracterização citogenética em Schlumbergera truncata (Haworth) Moran e Schlumbergera × buckleyi (T. Moore) Tjaden (Cactaceae) Cytogenetic characterization of Schlumbergera truncata (Haworth) Moran and Schlumbergera × buckleyi (T. Moore) Tjaden (Cactaceae)

O número cromossômico diplóide de Schlumbergera truncata e Schlumbergera x buckleyi, de indivíduos com diferentes tipos de coloração de pétalas, foi determinado usando-se pontas de raízes. A utilização de 8-hidroxiquinoleína 0,003 M à 36 &deg;C por 3 horas possibilitou melhor separação cromossômica. Técnica de bandeamento C e de coloração Giemsa permitiram o estudo cariológico dessas espécies. O híbrido Schlumbergera &times; buckleyi (rósea) apresenta 2n = 22 cromossomos com fórmula cariotípica 16 M + 6 SM. Schlumbergera truncata, apresentando pétalas nas cores vermelha, branca e pink, possui 2n = 22 cromossomos, formulação cariotípica idêntica à de Schlumbergera &times; buckleyi, enquanto a planta com flores de coloração amarelada mostrou 2n = 34 cromossomos. A classificação cromossômica foi baseada no índice centromérico. Nas plantas que apresentam coloração vermelha, branca, pink e rósea nas pétalas, o melhor período de obtenção de metáfases corresponde ao período de florescimento. Schlumbergera truncata com flores amareladas apresenta dois picos anuais de divisão mitótica. Esses resultados dão suporte à um melhor entendimento da biologia no gênero Schlumbergera e auxiliam na classificação taxonômica nos casos onde apenas as características fenotípicas não são suficientemente confiáveis para a classificação das plantas no mesmo táxon.<br>The diploid chromosome number of Schlumbergera truncata and Schlumbergera &times; buckleyi, in individuals with different types of petal color, was determined using root tips. The use of 8-hydroxyquinolein 0.003 M at 36 ºC provided better chromosome separation. C-banding technique and Giemsa coloration allowed the karyological study of these species. Schlumbergera &times; buckleyi hybrid (light pink) species has 2n = 22 chromosomes with karyotype formula 16M + 6SM. Schlumbergera truncata with red, white, and pink petals and 2n = 22 chromosomes has karyotype formula identical to Schlumbergera &times; buckleyi, while the plant with yellowish flowers has 2n = 34 chromosomes. Chromosome classification was based on the centromeric index. In plants with white, red, pink and light pink petal color, the best time to obtain metaphases is during flowering. Schlumbergera truncata with yellowish flowers has two annual peaks of mitotic division. These results give us a better understanding of the biology of the genus Schlumbergera and aid in taxonomic classification where phenotypic characteristics alone are not reliable enough to classify plants of the same taxon

Phylogenetic reconstruction of the genus Tephrocactus (Cactaceae) based on molecular, morphological, and cytogenetical data

Tephrocactus comprises species mainly endemic to Argentina. Molecular phylogenetic analyses of all proposed species of the genus as well as classical (chromosome number, karyotype) and molecular cytogenetical techniques (DNA content, heterochromatin amount, rDNA genes) were conducted. Sequence data of two plastid DNA markers of Tephrocactus taxa were analyzed. Evolution of character states of cytogenetical and morphological (growth form, presence of leaves, glochids and tepal spiny mucrons, flower color) traits were reconstructed. Species show x = 11 with different ploidy levels (2n = 22, 44, 66, 77, 242, 319), small chromosomes, and symmetrical karyotypes. Tephrocactus was recovered as monophyletic with three main clades including 12 species, using molecular and morphological data. Tephrocactus geometricus, T. halophilus, and T. paediophilus are recognized as distinct species. Banding patterns showed CMA+/DAPI− constitutive heterochromatin associated with nuclear organized regions. Heterochromatin amount ranged from 2.99% to 6.50%. The 18S-5.8S-26S ribosomal DNA (rDNA) sites coincided with the CMA+/DAPI− signals. The 5S sites varied with ploidy levels of the taxa. DNA content (2C = 1.99–24.50 pg) had a significant and positive correlation with ploidy level and the number of rDNA genes. The ancestor is reconstructed to have been a dwarf shrub with strong articulation, glochids, and deciduous leaves, white, pink or pearly tepals without spiny mucrons, 2n = 22, low DNA content, and one pair of each rDNA gene followed by three polyploidization events. Tephrocactus diversification has been associated with polyploidy and few cumulative small cryptic chromosomal changes.Fil: Las Peñas, Maria Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba; ArgentinaFil: Kiesling, Roberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mendoza. Instituto Argentino de Investigaciones de las Zonas Áridas. Provincia de Mendoza. Instituto Argentino de Investigaciones de las Zonas Áridas. Universidad Nacional de Cuyo. Instituto Argentino de Investigaciones de las Zonas Áridas; ArgentinaFil: Bernardello, Gabriel Luis Mario. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; Argentina. Universidad Nacional de Córdoba; Argentin