Of Coiylus(Betulaceae)
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Asteraceae; Heliantheae
The JapaneseSocietyJapanese Society forforPlantSystematics Plant Systematics ISSNOOOI-6799 Acta Phytotax. Geobot. 43 (2): 135-137 (1992) Chromosomesof Tuxtla pittieri (Asteraceae; Heliantheae) KAZUO OGINUMA*, GUILLERMO IBARRA-MANRfQUEZ**, AND HIROSHI TOBE*** 'Codege 'tEstacitin of Child Deveiqpment Kbchi PVbmenir Uhiversity, Ohara-cho, Kbchi 78dr de Biotogia 7}'opicalLos Tzaxtts instituto de Bilogit(, UlriiversidbdIVIxcionalAut6noma de Man'co, Apartado Postal 94 San Andres TtLxtleq Vleratcru4 MtExico; '"'IFticulty ofintqgrated Htzman Studias, Kyoto Uhiversity, Kyoto 60cFOI Abstract 7letxtlapittieri (Asteraceae; Heliantheae), which was reeently described as the only species of a new genus from Costa Rica and Mexico, is found to have 2n=34 (x= 17) and interphase nucleus of difftJse-complex chromocenter type. Of 34 metaphase chromosomes, 30 have centromeres at median position, two at submedian position, and two at terminal-subterrninal position. Shared basic chromosome number x=17 suggests close relationships of Tttxtla to P2irbesina. (Rcceived August 28, 1992; Accepted October 8, 1992) Key words:Asteraceae, Chromosome, Compositae,7leixtla. Tttxtla pittieri is a woody liana of Asteraceae (Compositae) and was recently described by Villasenor and Strother (1989) as the only species of a new genus from Costa Rica and southern Veracruz of Mexico. Villasenor and Strother (1989) made intensive and extensive observations on its vegetative and reproductive morphology, and, on the basis of phenetic analyses using 129 characters, suggest a distant relationship of 7le{xtla to any of other possibly related genera Otopmppus, SaLmea, Vkrbayina, and Zexmenia. The present paper reports on chromosome number and morphology of 7letxtla pittieri that is not known yet, and discusses similarities and dissimilarities in chfornosome features between 7}txtla and the other genera. -
Guillermo Ibarra-Manríquez * Y Santiago Sinaca Colín
Rev. Bio!. Trop., 43(1-3): 75-115,1995 Lista florÍstica comentada de la Estación de Biología Tropical "Los Thxtlas", Veracruz, México GuillermoIbarra-Manríquez * y Santiago Sinaca Colín Departamento de BoL Inst. de Biología. Universidad Nac. Autónoma de México. Apartado Postal 70-233. México 04510. D. F. (Revisado I-XI-1994. Aceptado 23-XI-1994) Abstract: The Estación de Biología Tropical "Los Tuxtlas", (México) an ecological reserve of about 640 ha with tro pical rain forest, has a vascular flora of about 940 species, 543 genera, and 137 families. For each species, a short des cription, growth form, height, kind and position of leaves, flowercolor, fruitcolor and type, phenology, uses, common name, and revisedspecimens are provided. The most diverse families in the preserve are Orchidaceae (108 species), Polypodiaceae s. l. (62), Asteraceae (60), Fabaceae s. l. (58) and Rubiaceae (39). The numerically more important ge nera are Epidendrum (16), Ficus (15), Piper (13), Eupatorium (11), and Psychotria (11). Trees and herbs are the most frequentgrowth forms: 31.7% and 30.4% respectively. This paper ¡neludes part 1 of the listo Key words: Phenology, vascular plants, floristics, Tropical rain forest, uses, Mexico, Veracruz. En los últimos años se ha incrementado de cies, facilitando el desarrollo de métodos para manera notable el interés por aumentar los co un aprovechamiento sostenible de los Rec. na nocimientos que se tienen sobre la diversidad y turales. funcionamiento de las selvas cálido-húmedas Esta contribución ha sido elaborada con este del mundo. No obstante, es aún muy largo el enfoque y brinda información para la determina camino que se tendrá que recorrer para imple ción de las plantas nativas de la Estación de Bio mentar métodos que permitanconjugar el apro logía Tropical "Los Tuxtlas" (México), por me vechamiento y conservación de los múltiples dio de breves descripciones de todaslas especies, Recursos que estos ambientes proporcionan al enfatizando cuando es factible sus caracteres ser humano. -
HOTSPOTS for CONSERVATION Acta Botánica Mexicana, Núm
Acta Botánica Mexicana ISSN: 0187-7151 [email protected] Instituto de Ecología, A.C. México Sosa, Victoria; De-Nova, J. Arturo ENDEMIC ANGIOSPERM LINEAGES IN MEXICO: HOTSPOTS FOR CONSERVATION Acta Botánica Mexicana, núm. 100, 2012, pp. 293-315 Instituto de Ecología, A.C. Pátzcuaro, México Available in: http://www.redalyc.org/articulo.oa?id=57424406010 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Acta Botanica Mexicana 100: 293-315 (2012) ENDEMIC ANGIOSPERM LINEAGES IN MEXICO: HOTSPOTS FOR CONSERVATION Victoria SoSa1,4 and J. arturo de-noVa2,3 1Instituto de Ecología A.C., Biología Evolutiva, Apdo. postal 63, 91070 Xalapa, Veracruz, Mexico. 2Universidad Autónoma de San Luis Potosí, Instituto de Investigación en Zonas Desérticas, Altair 200, 78377 San Luis Potosí, Mexico. 3Universidad Autónoma de San Luis Potosí, Facultad de Agronomía, km 14.5 carretera San Luis Potosí-Matehuala, 78321 San Luis Potosí, Mexico. 4Autor para la correspondencia: [email protected] ABSTRACT As a megadiverse country, Mexico harbors 4 to 8% of the flora of the world and of this, 51% is endemic. There is concern because several factors are impeding its conservation. In this paper, areas of endemism for the flowering plants of Mexico are identified to prioritize regions for conservation. To categorize zones for preservation, the approach followed takes biodiversity, weighted endemism and evolutionary history into account. Lineages of angiosperms, families, genera, and formal or informal groups within genera previously retrieved as monophyletic are selected to represent evolutionary history in equivalent spatial units. -
Karyomorphology of Corylopsis Glabrescens and C. Gotoana Endemic to Japan (Hamamelidaceae; Hamamelidoideae)
Chromosome Botany (2008) 3: 27-29 © Copyright 2008 by the International Society of Chromosome Botany Karyomorphology of Corylopsis glabrescens and C. gotoana endemic to Japan (Hamamelidaceae; Hamamelidoideae) Yoshiko Kono1,2, Masahisa Okada3, Hiroaki Setoguchi4 and Kazuo Oginuma5,6 1Graduate School of Human Health Science, Kochi Women’s University, Eikokuji-cho 5-15, Kochi 780-8515, Japan; 2Research Center for Biodiversity, Academia Sinica, Taipei 115, Taiwan; 3Kochi Agricultural Research Center, Amaeda 1100, Nankoku 783-0023, Japan; 4Deparment of Biology, Graduate School of Human and Environmental Studies, Kyoto University, Yoshida Nihonmatsu-cho, Sakyo-ku, Kyoto 606-8501, Japan; 5Department of Environmental Science, Faculty of Human Life and Environmental Science, Kochi Women’s University, Eikokuji-cho 5-15, Kochi 780-8515, Japan 6Author for correspondence: ([email protected]) Received May 10, 2008; accepted July 21, 2008 ABSTRACT. Chromosome numbers and karyotypes of Corylopsis glabrescens and C. gotoana in the Hamamelidaceae were investigated. Corylopsis glabrescens was diploid with 2n=24=14m+8sm+2st, while C. gotoana was tetraploid with 2n=48=36m+8sm+4st. The karyotype of the diploid C. glabrescens was different from that of the diploid C. pauciflora previously reported in Japan, suggesting a heterogeneous origin of the two species. The karyotype of the tetraploid C. gotoana seemed to share a homogeneous karyotype composition with the hexaploid C. spicata previously reported in Japan. KEYWORDS: Chromosome number, Corylopsis, Hamamelidaceae, karyotype Plants of Corylopsis, the Hamamelidaceae are small JP2702) and that of C. gotoana was collected in Nantan deciduous trees that tend to grow at forest edges on rocky City, Kyoto Prefecture, Japan (Voucher: H. -
Of Coiylus(Betulaceae): Walt. (Voucher
The JapaneseSocietyJapanese Society forforPlant Plant Systematics ISSN OOOI-6799 Acta Phytotax. Geobot. 49 (2): 99-104 (1998) Chromosome Base Number of Coiylus (Betulaceae): Correction, and Evolution KAZUO OGINUMAi HIDETOSHI KAT02 and HIROSHI TOBE3 ' ithculty of Human Lijle and Enyironmental Seiences, Kochi Women's [Jhiversity, Kochi 780-8515, 2Makino Japan; Herbarium, thculty ofScience, 7bkyo Metropolitan Uhiversity, Hl chioji, Tokyo, "Flaculty 192-0364, Japan; of integrated Human Studies, K),oto Vhiversity, 1<Yoto 606-8501, Japan Abstract. The chromosome base number of Corytus (15 species) has long been considered to be x=14 on the basis of the early report of Woodworth, but in later publieations different chromosome nurnbers have been reported in most species of the genus. This paper, on the basis of review of the earlier publications and additional observations in three species of Ceryltts (C. americana, C, heterqphylla var, thunbergii, C. sieboldiana), demonstrates that the generic chromosome base number is not x=14 but x=11. Molecular phylogeny of Betulaceae (published elsewhere in this issue) suggests that x=11 is an autapomorphy of Corylus derived from x=8 common to three other genera of Coryloideae. Key words: Betulaceae, chremosome number, CoTyloideae, Corylus, evolution Received September 11, 1998; accepted January 4, 1999 The family Betulaceae is well known cytologically, and all the six genera have been studied with respect to their gametic andlor somatic chromosome numbers. The generic chromosome base number is determined as x=14 for Alnus and Betula and x=8 for Carpinus, Ostrlya, and Ostryopsis (see Johnson and Wilson, 1993). Concerning the remaining genus Corylus, 14 of the 15 species are known cytologically, and its chromosome base number has usually been considered to be x=14 (e.g., Bousquet et at., 1992; Johnson and Wilson, 1993; Takhtajan, 1997). -
Endemic Angiosperm Lineages in Mexico: Hotspots for Conservation
Acta Botanica Mexicana 100: 293-315 (2012) ENDEMIC ANGIOSPERM LINEAGES IN MEXICO: HOTSPOTS FOR CONSERVATION Victoria SoSa1,4 and J. arturo de-noVa2,3 1Instituto de Ecología A.C., Biología Evolutiva, Apdo. postal 63, 91070 Xalapa, Veracruz, Mexico. 2Universidad Autónoma de San Luis Potosí, Instituto de Investigación en Zonas Desérticas, Altair 200, 78377 San Luis Potosí, Mexico. 3Universidad Autónoma de San Luis Potosí, Facultad de Agronomía, km 14.5 carretera San Luis Potosí-Matehuala, 78321 San Luis Potosí, Mexico. 4Autor para la correspondencia: [email protected] ABSTRACT As a megadiverse country, Mexico harbors 4 to 8% of the flora of the world and of this, 51% is endemic. There is concern because several factors are impeding its conservation. In this paper, areas of endemism for the flowering plants of Mexico are identified to prioritize regions for conservation. To categorize zones for preservation, the approach followed takes biodiversity, weighted endemism and evolutionary history into account. Lineages of angiosperms, families, genera, and formal or informal groups within genera previously retrieved as monophyletic are selected to represent evolutionary history in equivalent spatial units. A database with 9416 entries based on specimens of species belonging to 259 monophyletic groups of angiosperms from Mexico was compiled, and their presence-absence recorded for every unit area. Species richness and weighted endemism index was calculated for each of these units. The results indicate that the majority of the regions with -
I ABSTRACT a BIOINFORMATIC STUDY on the EVOLUTION OF
i ABSTRACT A BIOINFORMATIC STUDY ON THE EVOLUTION OF BAMBOOS AND OTHER GRAMINOID POALES William P. Wysocki, Ph.D. Department of Biological Sciences Northern Illinois University, 2016 Melvin R. Duvall, Director For the past decade, next-generation sequencing (NGS) has been used to undertake genomics-scale projects in molecular biology. This method of sequencing involves randomly fragmenting a sample of nucleic acid and randomly generating millions of short reads. The large number of reads moves the assembly and other analyses to be performed by computer algorithms. As well as sequencing full chromosomes, full RNA extracts can be sequenced to determine levels of gene expression and exon boundaries. In this study, NGS is used to examine the evolution of bamboos (Bambusoideae), which are a subfamily of grasses (Poaceae). Bamboos are divided into two main phenotypes: woody and herbaceous. Woody bamboos are characterized by lignified culms, bisexual florets and undergo gregarious monocarpy, while herbaceous bamboos have less lignified shoots, unisexual florets and flower annually. The evolution of this subfamily was examined in a phylogenomic framework using full chloroplast genome (plastome) sequences. First, a set of methods for plastome assembly was developed using automatable scripts and accuracy-testing steps. These methods were then used to generate full plastomes from bamboos. Full plastomes were then analyzed phylogenomically under a maximum-likelihood and Bayesian framework. This analysis ii revealed paraphyly between the temperate woody and tropical woody clades. Previously established tribal and subtribal relationships were also confirmed. Nuclear transcripts were assembled from four bamboo species by sequencing RNA from floral tissue using NGS. Two assembly methods were performed: a de novo assembly used only overlapping reads to produce transcripts and a reference-based assembly used a previously sequenced nuclear genome from a bamboo to place reads and assemble them into transcripts. -
Lianas of Mexico
!"#$%&'$()*'&+%'+,$%!$&!'($!"#)*+,-$./+# !"#$"% 012($+/3+,+.%456789:3+.! LIANAS OF MEXICO GUILLERMO IBARRA-MANRÍQUEZ1,3, FRANCISCO JAVIER RENDÓN-SANDOVAL1, GUADALUPE CORNEJO-TENORIO1 AND PABLO CARRILLO-REYES2 1Instituto de Investigaciones en Ecosistemas y Sustentabilidad, Universidad Nacional Autónoma de México. Morelia, Michoacán, México. 2Instituto de Botánica, Departamento de Botánica y Zoología, Centro Universitario de Ciencias Biológicas y Agropecuarias, Universidad de Guadalajara. Zapopan, Jalisco, México. 3Corresponding author: [email protected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