16.20 TRIPOGON Roem. & Schult.^ 16.22 DINEBRA Jacq.^ 16.21
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A Phylogeny of the Hubbardochloinae Including Tetrachaete (Poaceae: Chloridoideae: Cynodonteae)
Peterson, P.M., K. Romaschenko, and Y. Herrera Arrieta. 2020. A phylogeny of the Hubbardochloinae including Tetrachaete (Poaceae: Chloridoideae: Cynodonteae). Phytoneuron 2020-81: 1–13. Published 18 November 2020. ISSN 2153 733 A PHYLOGENY OF THE HUBBARDOCHLOINAE INCLUDING TETRACHAETE (CYNODONTEAE: CHLORIDOIDEAE: POACEAE) PAUL M. PETERSON AND KONSTANTIN ROMASCHENKO Department of Botany National Museum of Natural History Smithsonian Institution Washington, D.C. 20013-7012 [email protected]; [email protected] YOLANDA HERRERA ARRIETA Instituto Politécnico Nacional CIIDIR Unidad Durango-COFAA Durango, C.P. 34220, México [email protected] ABSTRACT The phylogeny of subtribe Hubbardochloinae is revisited, here with the inclusion of the monotypic genus Tetrachaete, based on a molecular DNA analysis using ndhA intron, rpl32-trnL, rps16 intron, rps16- trnK, and ITS markers. Tetrachaete elionuroides is aligned within the Hubbardochloinae and is sister to Dignathia. The biogeography of the Hubbardochloinae is discussed, its origin likely in Africa or temperate Asia. In a previous molecular DNA phylogeny (Peterson et al. 2016), the subtribe Hubbardochloinae Auquier [Bewsia Gooss., Dignathia Stapf, Gymnopogon P. Beauv., Hubbardochloa Auquier, Leptocarydion Hochst. ex Stapf, Leptothrium Kunth, and Lophacme Stapf] was found in a clade with moderate support (BS = 75, PP = 1.00) sister to the Farragininae P.M. Peterson et al. In the present study, Tetrachaete elionuroides Chiov. is included in a phylogenetic analysis (using ndhA intron, rpl32- trnL, rps16 intron, rps16-trnK, and ITS DNA markers) in order to test its relationships within the Cynodonteae with heavy sampling of species in the supersubtribe Gouiniodinae P.M. Peterson & Romasch. Chiovenda (1903) described Tetrachaete Chiov. with a with single species, T. -
Mohammad Karbaschi Thesis
STRUCTURAL, PHYSIOLOGICAL AND MOLECULAR CHARACTERISATION OF THE AUSTRALIAN NATIVE RESURRECTION GRASS TRIPOGON LOLIIFORMIS (F.MUELL.) C.E.HUBB. DURING DEHYDRATION AND REHYDRATION Mohammad Reza Karbaschi Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Centre for Tropical Crops and Biocommodities Science and Engineering Faculty Queensland University of Technology November 2015 Keywords Arabidopsis thaliana; Agrobacterium-mediated transformation; Anatomy; Anti-apoptotic proteins; BAG4; Escherichia coli; Bulliform cells; C4 photosynthesis; Cell wall folding; Cell membrane integrity; Chaperone-mediated autophagy; Chlorophyll fluorescence; Hsc70/Hsp70; Desiccation tolerance, Dehydration; Drought; Electrolyte leakage; Freehand sectioning; Homoiochlorophyllous; Leaf structure; Leaf folding; Reactive oxygen species (ROS); Resurrection plant; Morphology; Monocotyledon; Nicotiana benthamiana; Photosynthesis; Physiology; Plant tissue; Programed cell death (PCD); Propidium iodide staining; Protein microarray chip; Sclerenchymatous tissue; Stress; Structure; Tripogon loliiformis; Ubiquitin; Vacuole fragmentation; Kranz anatomy; XyMS+; Structural, physiological and molecular characterisation of the Australian native resurrection grass Tripogon loliiformis (F.Muell.) C.E.Hubb. during dehydration and rehydration i Abstract Plants, as sessile organisms must continually adapt to environmental changes. Water deficit is one of the major environmental stresses that affects plants. While most plants can tolerate moderate dehydration -
Long-Term Growth Patterns of Welwitschia Mirabilis, a Long-Lived Plant of the Namib Desert (Including a Bibliography)
Plant Ecology 150: 7–26, 2000. 7 © 2000 Kluwer Academic Publishers. Printed in the Netherlands. Long-term growth patterns of Welwitschia mirabilis, a long-lived plant of the Namib Desert (including a bibliography) Joh R. Henschel & Mary K. Seely Desert Ecological Research Unit, Desert Research Foundation of Namibia, Gobabeb Training and Research Centre, P.O. Box 953, Walvis Bay, Namibia (E-mail: [email protected]) Key words: Episodic events, Long-term ecological research, Namibia, Population dynamics, Seasonality, Sex ratio Abstract Over the past 14 years, long-term ecological research (LTER) was conducted on the desert perennial, Welwitschia mirabilis (Gnetales: Welwitschiaceae), located in the Welwitschia Wash near Gobabeb in the Central Namib Desert. We measured leaf growth of 21 plants on a monthly basis and compared this with climatic data. The population structure as well as its spatial distribution was determined for 110 individuals. Growth rate was 0.37 mm day−1, but varied 22-fold within individuals, fluctuating seasonally and varying between years. Seasonal patterns were correlated with air humidity, while annual differences were affected by rainfall. During three years, growth rate quadrupled following episodic rainfall events >11 mm during mid-summer. One natural recruitment event followed a 13-mm rainfall at the end of summer. Fog did not appear to influence growth patterns and germination. Plant loca- tion affected growth rate; plants growing on the low banks, or ledges, of the main drainage channel grew at a higher rate, responded better and longer to rainfall and had relatively larger leaves than plants in the main channel or its tributaries. -
22. Tribe ERAGROSTIDEAE Ihl/L^Ä Huameicaozu Chen Shouliang (W-"^ G,), Wu Zhenlan (ß^E^^)
POACEAE 457 at base, 5-35 cm tall, pubescent. Basal leaf sheaths tough, whit- Enneapogon schimperianus (A. Richard) Renvoize; Pap- ish, enclosing cleistogamous spikelets, finally becoming fi- pophorum aucheri Jaubert & Spach; P. persicum (Boissier) brous; leaf blades usually involute, filiform, 2-12 cm, 1-3 mm Steudel; P. schimperianum Hochstetter ex A. Richard; P. tur- wide, densely pubescent or the abaxial surface with longer comanicum Trautvetter. white soft hairs, finely acuminate. Panicle gray, dense, spike- Perennial. Culms compactly tufted, wiry, erect or genicu- hke, linear to ovate, 1.5-5 x 0.6-1 cm. Spikelets with 3 fiorets, late, 15^5 cm tall, pubescent especially below nodes. Basal 5.5-7 mm; glumes pubescent, 3-9-veined, lower glume 3-3.5 mm, upper glume 4-5 mm; lowest lemma 1.5-2 mm, densely leaf sheaths tough, lacking cleistogamous spikelets, not becom- villous; awns 2-A mm, subequal, ciliate in lower 2/3 of their ing fibrous; leaf blades usually involute, rarely fiat, often di- length; third lemma 0.5-3 mm, reduced to a small tuft of awns. verging at a wide angle from the culm, 3-17 cm, "i-^ mm wide, Anthers 0.3-0.6 mm. PL and &. Aug-Nov. 2« = 36. pubescent, acuminate. Panicle olive-gray or tinged purplish, contracted to spikelike, narrowly oblong, 4•18 x 1-2 cm. Dry hill slopes; 1000-1900 m. Anhui, Hebei, Liaoning, Nei Mon- Spikelets with 3 or 4 florets, 8-14 mm; glumes puberulous, (5-) gol, Ningxia, Qinghai, Shanxi, Xinjiang, Yunnan [India, Kazakhstan, 7-9-veined, lower glume 5-10 mm, upper glume 7-11 mm; Kyrgyzstan, Mongolia, Pakistan, E Russia; Africa, America, SW Asia]. -
The Resurrection Plant Tripogon Spicatus (Poaceae) Harbors a Diversity of Plant Growth Promoting Bacteria in Northeastern Brazilian Caatinga
THE RESURRECTION PLANT Tripogon spicatus (POACEAE) HARBORS A DIVERSITY OF PLANT GROWTH PROMOTING BACTERIA IN NORTHEASTERN BRAZILIAN CAATINGA Paulo Ivan Fernandes-Júnior(1)*, Saulo de Tarso Aidar(1), Carolina Vianna Morgante(1), Carlos Alberto Tuão Gava(1), Jerri Édson Zilli(2), Layane Silva Barbosa de Souza(3), Rita de Cássia Nunes Marinho(4), Rafaela Simão Abrahão Nóbrega(5), Marivaine da Silva Brasil(6), Sirando Lima Seido(7) and Lindete Míria Vieira Martins(8) (1) Empresa Brasileira de Pesquisa Agropecuária, Centro de Pesquisa Agropecuária do Trópico Semiárido, Petrolina, Pernambuco, Brasil. (2) Empresa Brasileira de Pesquisa Agropecuária, Centro Nacional de Pesquisa em Agrobiologia, Seropédica, Rio de Janeiro, Brasil. (3) Universidade do Estado da Bahia, Departamento de Tecnologia e Ciências Sociais, Programa de Pós-graduação em Horticultura Irrigada, Juazeiro, Bahia, Brasil. (4) Universidade Federal do Piauí, Campus Universitário Professora Cinobelina Elvas, Programa de Pós-graduação em Produção Vegetal, Bom Jesus, Piauí, Brasil. (5) Universidade Federal do Recôncavo da Bahia, Centro de Ciências Agrárias, Ambientais e Biológicas, Cruz das Almas, Bahia, Brasil. (6) Universidade Federal do Mato Grosso do Sul, Centro de Ciências Ambientais, Corumbá, Mato Grosso do Sul, Brasil. (7) Universidade Federal Rural de Pernambuco, Departamento de Agronomia, Programa de Pós-graduação em Genética e Melhoramento de Plantas, Recife, Pernambuco, Brasil. (8) Universidade do Estado da Bahia, Departamento de Tecnologia e Ciências Sociais, Juazeiro, Bahia, Brasil. * Corresponding author. E-mail: [email protected] ABSTRACT Plant species that naturally occur in the Brazilian Caatinga (xeric shrubland) adapt in several ways to these harsh conditions, and that can be exploited to increase crop production. -
Inselbergs) As Centers of Diversity for Desiccation-Tolerant Vascular Plants
Plant Ecology 151: 19–28, 2000. 19 © 2000 Kluwer Academic Publishers. Printed in the Netherlands. Dedicated to Prof. Dr Karl Eduard Linsenmair (Universität Würzburg) on the occasion of his 60th birthday. Granitic and gneissic outcrops (inselbergs) as centers of diversity for desiccation-tolerant vascular plants Stefan Porembski1 & Wilhelm Barthlott2 1Universität Rostock, Institut für Biodiversitätsforschung, Allgemeine und Spezielle Botanik, Rostock, Germany (E-mail: [email protected]); 2Botanisches Institut der Universität, Bonn, Germany (E-mail: [email protected]) Key words: Afrotrilepis, Borya, Desiccation tolerance, Granitic outcrops, Myrothamnus, Poikilohydry, Resurrection plants, Velloziaceae, Water stress Abstract Although desiccation tolerance is common in non-vascular plants, this adaptive trait is very rare in vascular plants. Desiccation-tolerant vascular plants occur particularly on rock outcrops in the tropics and to a lesser extent in temperate zones. They are found from sea level up to 2800 m. The diversity of desiccation-tolerant species as mea- sured by number of species is highest in East Africa, Madagascar and Brazil, where granitic and gneissic outcrops, or inselbergs, are their main habitat. Inselbergs frequently occur as isolated monoliths characterized by extreme environmental conditions (i.e., edaphic dryness, high degrees of insolation). On tropical inselbergs, desiccation- tolerant monocotyledons (i.e., Cyperaceae and Velloziaceae) dominate in mat-like communities which cover even steep slopes. Mat-forming desiccation-tolerant species may attain considerable age (hundreds of years) and size (several m in height, for pseudostemmed species). Both homoiochlorophyllous and poikilochlorophyllous species occur. In their natural habitats, both groups survive dry periods of several months and regain their photosynthetic activity within a few days after rainfall. -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
Grasses of Namibia Contact
Checklist of grasses in Namibia Esmerialda S. Klaassen & Patricia Craven For any enquiries about the grasses of Namibia contact: National Botanical Research Institute Private Bag 13184 Windhoek Namibia Tel. (264) 61 202 2023 Fax: (264) 61 258153 E-mail: [email protected] Guidelines for using the checklist Cymbopogon excavatus (Hochst.) Stapf ex Burtt Davy N 9900720 Synonyms: Andropogon excavatus Hochst. 47 Common names: Breëblaarterpentyngras A; Broad-leaved turpentine grass E; Breitblättriges Pfeffergras G; dukwa, heng’ge, kamakama (-si) J Life form: perennial Abundance: uncommon to locally common Habitat: various Distribution: southern Africa Notes: said to smell of turpentine hence common name E2 Uses: used as a thatching grass E3 Cited specimen: Giess 3152 Reference: 37; 47 Botanical Name: The grasses are arranged in alphabetical or- Rukwangali R der according to the currently accepted botanical names. This Shishambyu Sh publication updates the list in Craven (1999). Silozi L Thimbukushu T Status: The following icons indicate the present known status of the grass in Namibia: Life form: This indicates if the plant is generally an annual or G Endemic—occurs only within the political boundaries of perennial and in certain cases whether the plant occurs in water Namibia. as a hydrophyte. = Near endemic—occurs in Namibia and immediate sur- rounding areas in neighbouring countries. Abundance: The frequency of occurrence according to her- N Endemic to southern Africa—occurs more widely within barium holdings of specimens at WIND and PRE is indicated political boundaries of southern Africa. here. 7 Naturalised—not indigenous, but growing naturally. < Cultivated. Habitat: The general environment in which the grasses are % Escapee—a grass that is not indigenous to Namibia and found, is indicated here according to Namibian records. -
Grass Genera of Southern Africa: Interactive Identification and Information Retrieval from an Automated Data Bank
452 S.-Afr.Tydskr. Plantk. , 1989, 55(4): 452-463 Grass genera of southern Africa: Interactive identification and information retrieval from an automated data bank L. Watson*, G.E. Gibbs Russell 1 and M.J. Dallwitz Taxonomy Laboratory, Research School of Biological Sciences, Australian National University, GPO Box 475, A.C.T. 2601, Australia; Botanical Research Institute, Private Bag X1 01, Pretoria, 0001 Republic of South Africa and Division of Entomology, Commonwealth Scientific and Industrial Research Organization, GPO Box 1700, Canberra City, A.C.T. 2601, Australia 1 Present address: Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri, USA 63166-0299 A new interactive system for computerized taxonomic identification and information retrieval, operable on MS DOS microcomputers, is now available. In this application to southern African grass genera the data include synonyms, morphology, anatomy, physiology, cytology, classification, pathogens, world and local distribu tions and references. The program is part of the DELTA system, which also provides natural language descriptions and printed keys. The data for the southern African genera can be provided separately, or inclu ded in the complete data for the grass genera of the world. 'n Nuwe interaktiewe stelsel vir gerekenariseerde taksonomiese identifisering en inligtingsherwinning, bedryf baar op MS-DOS-mikrorekenaars, is nou beskikbaar. Hierdie toepassing op Suider-Afrikaanse grasgenusse bevat data oor sinonieme, morfologie, anatomie, fisiologie, sitologie, klassifikasie, patogene, wereldwye en plaaslike verspreidings en verwysings. Die program is deel van die DELTA-stelsel, wat ook voorsiening maak vir beskrywings in gewone taal en gedrukte sleutels. Die data vir die Suider-Afrikaanse genusse kan afsonderlik verskaf word, of by die volledige data vir die grasgenusse van die wereld ingesluit word. -
A Classification of the Chloridoideae (Poaceae)
Molecular Phylogenetics and Evolution 55 (2010) 580–598 Contents lists available at ScienceDirect Molecular Phylogenetics and Evolution journal homepage: www.elsevier.com/locate/ympev A classification of the Chloridoideae (Poaceae) based on multi-gene phylogenetic trees Paul M. Peterson a,*, Konstantin Romaschenko a,b, Gabriel Johnson c a Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013, USA b Botanic Institute of Barcelona (CSICÀICUB), Pg. del Migdia, s.n., 08038 Barcelona, Spain c Department of Botany and Laboratories of Analytical Biology, Smithsonian Institution, Suitland, MD 20746, USA article info abstract Article history: We conducted a molecular phylogenetic study of the subfamily Chloridoideae using six plastid DNA Received 29 July 2009 sequences (ndhA intron, ndhF, rps16-trnK, rps16 intron, rps3, and rpl32-trnL) and a single nuclear ITS Revised 31 December 2009 DNA sequence. Our large original data set includes 246 species (17.3%) representing 95 genera (66%) Accepted 19 January 2010 of the grasses currently placed in the Chloridoideae. The maximum likelihood and Bayesian analysis of Available online 22 January 2010 DNA sequences provides strong support for the monophyly of the Chloridoideae; followed by, in order of divergence: a Triraphideae clade with Neyraudia sister to Triraphis; an Eragrostideae clade with the Keywords: Cotteinae (includes Cottea and Enneapogon) sister to the Uniolinae (includes Entoplocamia, Tetrachne, Biogeography and Uniola), and a terminal Eragrostidinae clade of Ectrosia, Harpachne, and Psammagrostis embedded Classification Chloridoideae in a polyphyletic Eragrostis; a Zoysieae clade with Urochondra sister to a Zoysiinae (Zoysia) clade, and a Grasses terminal Sporobolinae clade that includes Spartina, Calamovilfa, Pogoneura, and Crypsis embedded in a Molecular systematics polyphyletic Sporobolus; and a very large terminal Cynodonteae clade that includes 13 monophyletic sub- Phylogenetic trees tribes. -
Tripogonella Final.Pmd
396 Tripogonella minima, a new record for Asia Vol. 30(3):30(2): 396–399270–277 (2020) RHEEDEA ISSN: 0971-2313 (Print edition) ISSN: 2582-2438 (Online edition) Journal of the Indian Association for Angiosperm Taxonomy https://dx.doi.org/10.22244/rheedea.2020.30.03.06https://dx.doi.org/10.22244/rheedea.2020.30.02.02 Tripogonella minima (Poaceae: Chloridoideae: Cynodonteae: Tripogoninae), a new record for Asia from Peninsular India J. Swamy Botanical Survey of India, Deccan Regional Centre, Kendriya Sadan, GPOA, Sultan Bazar, Koti, Hyderabad, Telangana – 500 095, India. E-mail: [email protected] southwards to Natal, Cape Verde Islands and Abstract: Tripogonella minima (A.Rich.) P.M.Peterson & Romasch. (Poaceae: Chloridoideae: Cynodonteae: Madagascar (Phillips & Launert, 1971), while Tripogoninae), a species indigenous to tropical Africa Tripogonella spicata is distributed in North is reported here as an addition to the angiosperm flora America, Central America, South America, and of Asia from Telangana state, India. Detailed description, the Caribbean Islands. photographs and notes are provided for easy identification. While exploring the grasses of Telangana state, a small population of a Tripogonella species was Key words: India, New record, Poaceae, Telangana. observed in Medak district and a few specimens were collected from the existing population by Introduction the author. The voucher specimens were studied critically and identified as Tripogonella minima. Tripogonella P.M.Peterson & Romasch. is a newly The species is similar to Tripogon purpurascens established genus based on molecular studies of Duthie by its habit and 2-lobed lemma with a Tripogon Roem. & Schult. and is distributed in midvein that extends into a small mucro and tropical and subtropical America, Africa, awnless lateral lobes but differs by its smaller Madagascar, New Guinea and Australia (Peterson habit, glabrous leaf-blades, number of florets, et al., 2016). -
Illustration Sources
APPENDIX ONE ILLUSTRATION SOURCES REF. CODE ABR Abrams, L. 1923–1960. Illustrated flora of the Pacific states. Stanford University Press, Stanford, CA. ADD Addisonia. 1916–1964. New York Botanical Garden, New York. Reprinted with permission from Addisonia, vol. 18, plate 579, Copyright © 1933, The New York Botanical Garden. ANDAnderson, E. and Woodson, R.E. 1935. The species of Tradescantia indigenous to the United States. Arnold Arboretum of Harvard University, Cambridge, MA. Reprinted with permission of the Arnold Arboretum of Harvard University. ANN Hollingworth A. 2005. Original illustrations. Published herein by the Botanical Research Institute of Texas, Fort Worth. Artist: Anne Hollingworth. ANO Anonymous. 1821. Medical botany. E. Cox and Sons, London. ARM Annual Rep. Missouri Bot. Gard. 1889–1912. Missouri Botanical Garden, St. Louis. BA1 Bailey, L.H. 1914–1917. The standard cyclopedia of horticulture. The Macmillan Company, New York. BA2 Bailey, L.H. and Bailey, E.Z. 1976. Hortus third: A concise dictionary of plants cultivated in the United States and Canada. Revised and expanded by the staff of the Liberty Hyde Bailey Hortorium. Cornell University. Macmillan Publishing Company, New York. Reprinted with permission from William Crepet and the L.H. Bailey Hortorium. Cornell University. BA3 Bailey, L.H. 1900–1902. Cyclopedia of American horticulture. Macmillan Publishing Company, New York. BB2 Britton, N.L. and Brown, A. 1913. An illustrated flora of the northern United States, Canada and the British posses- sions. Charles Scribner’s Sons, New York. BEA Beal, E.O. and Thieret, J.W. 1986. Aquatic and wetland plants of Kentucky. Kentucky Nature Preserves Commission, Frankfort. Reprinted with permission of Kentucky State Nature Preserves Commission.