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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. -
Ajo Peak to Tinajas Altas: a Flora of Southwestern Arizona
Felger, R.S., S. Rutman, and J. Malusa. 2014. Ajo Peak to Tinajas Altas: A flora of southwestern Arizona. Part 6. Poaceae – grass family. Phytoneuron 2014-35: 1–139. Published 17 March 2014. ISSN 2153 733X AJO PEAK TO TINAJAS ALTAS: A FLORA OF SOUTHWESTERN ARIZONA Part 6. POACEAE – GRASS FAMILY RICHARD STEPHEN FELGER Herbarium, University of Arizona Tucson, Arizona 85721 & Sky Island Alliance P.O. Box 41165, Tucson, Arizona 85717 *Author for correspondence: [email protected] SUSAN RUTMAN 90 West 10th Street Ajo, Arizona 85321 JIM MALUSA School of Natural Resources and the Environment University of Arizona Tucson, Arizona 85721 [email protected] ABSTRACT A floristic account is provided for the grass family as part of the vascular plant flora of the contiguous protected areas of Organ Pipe Cactus National Monument, Cabeza Prieta National Wildlife Refuge, and the Tinajas Altas Region in southwestern Arizona. This is the second largest family in the flora area after Asteraceae. A total of 97 taxa in 46 genera of grasses are included in this publication, which includes ones established and reproducing in the modern flora (86 taxa in 43 genera), some occurring at the margins of the flora area or no long known from the area, and ice age fossils. At least 28 taxa are known by fossils recovered from packrat middens, five of which have not been found in the modern flora: little barley ( Hordeum pusillum ), cliff muhly ( Muhlenbergia polycaulis ), Paspalum sp., mutton bluegrass ( Poa fendleriana ), and bulb panic grass ( Zuloagaea bulbosa ). Non-native grasses are represented by 27 species, or 28% of the modern grass flora. -
Introductory Grass Identification Workshop University of Houston Coastal Center 23 September 2017
Broadleaf Woodoats (Chasmanthium latifolia) Introductory Grass Identification Workshop University of Houston Coastal Center 23 September 2017 1 Introduction This 5 hour workshop is an introduction to the identification of grasses using hands- on dissection of diverse species found within the Texas middle Gulf Coast region (although most have a distribution well into the state and beyond). By the allotted time period the student should have acquired enough knowledge to identify most grass species in Texas to at least the genus level. For the sake of brevity grass physiology and reproduction will not be discussed. Materials provided: Dried specimens of grass species for each student to dissect Jewelry loupe 30x pocket glass magnifier Battery-powered, flexible USB light Dissecting tweezer and needle Rigid white paper background Handout: - Grass Plant Morphology - Types of Grass Inflorescences - Taxonomic description and habitat of each dissected species. - Key to all grass species of Texas - References - Glossary Itinerary (subject to change) 0900: Introduction and house keeping 0905: Structure of the course 0910: Identification and use of grass dissection tools 0915- 1145: Basic structure of the grass Identification terms Dissection of grass samples 1145 – 1230: Lunch 1230 - 1345: Field trip of area and collection by each student of one fresh grass species to identify back in the classroom. 1345 - 1400: Conclusion and discussion 2 Grass Structure spikelet pedicel inflorescence rachis culm collar internode ------ leaf blade leaf sheath node crown fibrous roots 3 Grass shoot. The above ground structure of the grass. Root. The below ground portion of the main axis of the grass, without leaves, nodes or internodes, and absorbing water and nutrients from the soil. -
Enneapogon Cenchroides (Roem
This report was generated from the SEPASAL database ( www.kew.org/ceb/sepasal ) in August 2007. This database is freely available to members of the public. SEPASAL is a database and enquiry service about useful "wild" and semi-domesticated plants of tropical and subtropical drylands, developed and maintained at the Royal Botanic Gardens, Kew. "Useful" includes plants which humans eat, use as medicine, feed to animals, make things from, use as fuel, and many other uses. Since 2004, there has been a Namibian SEPASAL team, based at the National Botanical Research Institute of the Ministry of Agriculture which has been updating the information on Namibian species from Namibian and southern African literature and unpublished sources. By August 2007, over 700 Namibian species had been updated. Work on updating species information, and adding new species to the database, is ongoing. It may be worth visiting the web site and querying the database to obtain the latest information for this species. Internet SEPASAL New query Edit query View query results Display help In names list include: synonyms vernacular names and display: All names per page Your query found 1 taxon Enneapogon cenchroides (Roem. & Schult.) C.E.Hubb. [ 5104 ] Family: POACEAE Synonyms Enneapogon mollis Lehm. Pappophorum cenchroides (Roem. & Schult.) Vernacular names Afrikaans (Namibia) eenjarige negenaaldgras [ 5083 ] [ 5115 ] [ 6711 ], suurgras [ 2259 ] Afrikaans (South Africa) gewone negenaaldgras [ 2259 ], negenaaldgras [ 5117 ], suurgras [ 2259 ], tuingras [ 2259 ] Afrikaans -
Landscaping with Native Grasses
Landscaping with native Grasses Keith Pawelek Assistant Director of South Texas Natives • STN formalized in 2001 by founding grant from the Robert J. Kleberg, Jr. and Helen C. Kleberg Foundation • 2001: commercial seeds of native plants for south Texas were not available-the looming IH-69 corridor brought persistent concerns about a lack of native seed to the forefront • Pasture, rangeland, restoration, and reclamation plantings used exotic grass seed • Landowners and agencies desired native seeds for these uses, but could not obtain them History Texas Native Seeds • Allow multiple use of the landscape • Best meet habitat requirements of wildlife • Support today’s economic opportunities (hunting, wildlife, ecotourism, and other forms of outdoor recreation) • Facilitate ecosystem services (water, pollination, biodiversity, carbon sequestration, clean air, etc.) Why native plants? • Few (if any) demonstrated benefits to wildlife • Limit biodiversity and multiple use • Tendency to spread from areas they are planted to • Gradual, yet profound alteration of ecosystem processes • Shift in landowner goals and objectives • Change in economic factors benefitting ranches Why not exotic plants? Mimic nature Layer Still needs some care Set up Plants native to your area Preferably from seed or plant stock from your area Proven releases or cultivars for your area Grasses that meet your criteria (annual, perennial, warm season, cool season) What plants should I use? Desired look Size Desired maintenance Water requirements Desired timeline -
GRAPHIE by Cornelia D. Niles with INTRODUCTION and BOTANICAL
A BIBLIOGRAPHIC STUDY OF BEAUVOIS' AGROSTO- • GRAPHIE By Cornelia D. Niles WITH INTRODUCTION AND BOTANICAL NOTES By Aones Chase nrntODTJCTiON The Essai d?une Nouvelle Agrostographie ; ou Nouveaux Genres des Graminees; avec figures representant les Oaracteres de tous les Genres, by A. M. F. J. Palisot de Beauvois, published in 1812, is, from the standpoint of the nomenclature of grasses, a very important work, its importance being due principally to its innumerable errors, less so because of its scientific value. In this small volume 69 new genera are proposed and some 640 new species, new binomials, and new names are published. Of the 69 genera proposed 31 are to-day recognized as valid, and of the 640 names about 61 are commonly accepted. There is probably not a grass flora of any considerable region anywhere in the world that does not contain some of Beauvois' names. Many of the new names are made in such haphazard fashion that they are incorrectly listed in the Index Kewensis. There are, besides, a number of misspelled names that have found their way into botanical literature. The inaccuracies are so numerous and the cita- tions so incomplete that only a trained bibliographer* could solve the many puzzles presented. Cornelia D. Niles in connection with her work on the bibliography of grasses, maintained in the form of a card catalogue in the Grass Herbarium, worked out the basis in literature of each of these new names. The botanical problems involved, the interpretation of descriptions and figures, were worked out by Agnes Chase, who is also respon- sible for the translation and summaries from the Advertisement, Introduction, and Principles. -
SELECCIÓN ENTRE Panicum Urvilleanum, Pappophorum Caespitosum, Y CUATRO GENOTIPOS DE Leptochloa Crinita, BAJO SALINIDAD Y SEQUÍA, CON PERSPECTIVA DE REVEGETACIÓN
SELECCIÓN ENTRE Panicum urvilleanum, Pappophorum caespitosum, Y CUATRO GENOTIPOS DE Leptochloa crinita, BAJO SALINIDAD Y SEQUÍA, CON PERSPECTIVA DE REVEGETACIÓN. TESIS DE GRADO INGENIERÍA EN RECURSOS NATURALES RENOVABLES 2020 Tesista: Yanina Cristina, Buccolini Lucas Directora: Sartor, Carmen Elena Codirectora: Kozub, Perla Carolina Facultad de Ciencias Agrarias Universidad Nacional de Cuyo Almirante Brown 500, Chacras de Coria, Mendoza M5528AHB- (54 261) 4135000. SELECCIÓN ENTRE Panicum urvilleanum, Pappophorum caespitosum, Y CUATRO GENOTIPOS DE Leptochloa crinita, BAJO SALINIDAD Y SEQUÍA, CON PERSPECTIVA DE REVEGETACIÓN. Tesista: Yanina Cristina, Buccolini Lucas [email protected] Directora: Dra. Sartor, Carmen Elena [email protected] Codirectora: Dra. Kozub, Perla Carolina [email protected] Jurado: Mg. Ing. Greco, Silvina Alicia [email protected] Dra. Fernández, María Emilia [email protected] Ing. Domínguez, Deolindo Luis Esteban [email protected] ii RESUMEN: La desertificación es una de las preocupaciones ambientales más relevantes en la Argentina, con el 75% del territorio bajo condiciones áridas y semiáridas. Es por ello que las prácticas productivas en estas zonas áridas y semiáridas, se desarrollan en oasis bajo riego, en los cuales el 40% de su superficie presenta problemas de degradación, provocados en gran medida por la salinización. En este contexto, los oasis mendocinos utilizan íntegramente los caudales de los ríos, mientras que las áreas deprimidas del desierto no reciben aportes hídricos superficiales. La vegetación evidencia estos impactos, y es ella quien brinda recursos fundamentales para la recuperación de estos ambientes. Siendo la revegetación con especies nativas, una de las herramientas más promisorias para la restauración de estos ambientes sensibles y de baja recuperación natural. -
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. -
A Molecular Phylogeny and Classification of the Cynodonteae
TAXON 65 (6) • December 2016: 1263–1287 Peterson & al. • Phylogeny and classification of the Cynodonteae A molecular phylogeny and classification of the Cynodonteae (Poaceae: Chloridoideae) with four new genera: Orthacanthus, Triplasiella, Tripogonella, and Zaqiqah; three new subtribes: Dactylocteniinae, Orininae, and Zaqiqahinae; and a subgeneric classification of Distichlis Paul M. Peterson,1 Konstantin Romaschenko,1,2 & Yolanda Herrera Arrieta3 1 Smithsonian Institution, Department of Botany, National Museum of Natural History, Washington, D.C. 20013-7012, U.S.A. 2 M.G. Kholodny Institute of Botany, National Academy of Sciences, Kiev 01601, Ukraine 3 Instituto Politécnico Nacional, CIIDIR Unidad Durango-COFAA, Durango, C.P. 34220, Mexico Author for correspondence: Paul M. Peterson, [email protected] ORCID PMP, http://orcid.org/0000-0001-9405-5528; KR, http://orcid.org/0000-0002-7248-4193 DOI https://doi.org/10.12705/656.4 Abstract Morphologically, the tribe Cynodonteae is a diverse group of grasses containing about 839 species in 96 genera and 18 subtribes, found primarily in Africa, Asia, Australia, and the Americas. Because the classification of these genera and spe cies has been poorly understood, we conducted a phylogenetic analysis on 213 species (389 samples) in the Cynodonteae using sequence data from seven plastid regions (rps16-trnK spacer, rps16 intron, rpoC2, rpl32-trnL spacer, ndhF, ndhA intron, ccsA) and the nuclear ribosomal internal transcribed spacer regions (ITS 1 & 2) to infer evolutionary relationships and refine the -
Flora of Southwestern Arizona
Felger, R.S., S. Rutman, and J. Malusa. 2014. Ajo Peak to Tinajas Altas: A flora of southwestern Arizona. Part 6. Poaceae – grass family. Phytoneuron 2014-35: 1–139. Published 17 March 2014. ISSN 2153 733X AJO PEAK TO TINAJAS ALTAS: A FLORA OF SOUTHWESTERN ARIZONA Part 6. POACEAE – GRASS FAMILY RICHARD STEPHEN FELGER Herbarium, University of Arizona Tucson, Arizona 85721 & Sky Island Alliance P.O. Box 41165, Tucson, Arizona 85717 *Author for correspondence: [email protected] SUSAN RUTMAN 90 West 10th Street Ajo, Arizona 85321 JIM MALUSA School of Natural Resources and the Environment University of Arizona Tucson, Arizona 85721 [email protected] ABSTRACT A floristic account is provided for the grass family as part of the vascular plant flora of the contiguous protected areas of Organ Pipe Cactus National Monument, Cabeza Prieta National Wildlife Refuge, and the Tinajas Altas Region in southwestern Arizona. This is the second largest family in the flora area after Asteraceae. A total of 97 taxa in 46 genera of grasses are included in this publication, which includes ones established and reproducing in the modern flora (86 taxa in 43 genera), some occurring at the margins of the flora area or no long known from the area, and ice age fossils. At least 28 taxa are known by fossils recovered from packrat middens, five of which have not been found in the modern flora: little barley ( Hordeum pusillum ), cliff muhly ( Muhlenbergia polycaulis ), Paspalum sp., mutton bluegrass ( Poa fendleriana ), and bulb panic grass ( Zuloagaea bulbosa ). Non-native grasses are represented by 27 species, or 28% of the modern grass flora. -
Classification and Biogeography of Panicoideae (Poaceae) in the New World Fernando O
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Scholarship@Claremont Aliso: A Journal of Systematic and Evolutionary Botany Volume 23 | Issue 1 Article 39 2007 Classification and Biogeography of Panicoideae (Poaceae) in the New World Fernando O. Zuloaga Instituto de Botánica Darwinion, San Isidro, Argentina Osvaldo Morrone Instituto de Botánica Darwinion, San Isidro, Argentina Gerrit Davidse Missouri Botanical Garden, St. Louis Susan J. Pennington National Museum of Natural History, Smithsonian Institution, Washington, D.C. Follow this and additional works at: http://scholarship.claremont.edu/aliso Part of the Botany Commons, and the Ecology and Evolutionary Biology Commons Recommended Citation Zuloaga, Fernando O.; Morrone, Osvaldo; Davidse, Gerrit; and Pennington, Susan J. (2007) "Classification and Biogeography of Panicoideae (Poaceae) in the New World," Aliso: A Journal of Systematic and Evolutionary Botany: Vol. 23: Iss. 1, Article 39. Available at: http://scholarship.claremont.edu/aliso/vol23/iss1/39 Aliso 23, pp. 503–529 ᭧ 2007, Rancho Santa Ana Botanic Garden CLASSIFICATION AND BIOGEOGRAPHY OF PANICOIDEAE (POACEAE) IN THE NEW WORLD FERNANDO O. ZULOAGA,1,5 OSVALDO MORRONE,1,2 GERRIT DAVIDSE,3 AND SUSAN J. PENNINGTON4 1Instituto de Bota´nica Darwinion, Casilla de Correo 22, Labarde´n 200, San Isidro, B1642HYD, Argentina; 2([email protected]); 3Missouri Botanical Garden, PO Box 299, St. Louis, Missouri 63166, USA ([email protected]); 4Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20013-7012, USA ([email protected]) 5Corresponding author ([email protected]) ABSTRACT Panicoideae (Poaceae) in the New World comprise 107 genera (86 native) and 1357 species (1248 native). -
21. Tribe PAPPOPHOREAE 123. ENNEAPOGON Desvaux Ex P. Beauvois, Ess. Agrostogr. 81. 1812
456 POACEAE 1. Stipagrostis pennata (Trinius) De Winter, Kirkia 3: 135. This species provides good fodder when young and is also good 1963. for binding sand. 羽毛针禾 yu mao zhen he 2. Stipagrostis grandiglumis (Roshevitz) Tzvelev, Zlaki SSSR, 618. 1976. Aristida pennata Trinius, Mém. Acad. Imp. Sci. St. Péters- bourg Hist. Acad. 6: 488. 1815; Aristida pungens var. pennata 大颖针禾 da ying zhen he (Trinius) Trautvetter; Arthratherum pennatum (Trinius) Tzve- Aristida grandiglumis Roshevitz, Bot. Mater. Gerb. Bot. lev. Inst. Komarova Akad. Nauk SSSR 11: 18. 1949. Perennial with slender rhizomes, roots tomentose. Culms tussocky, 20–60 cm tall, much branched at base. Leaf sheaths Perennial, roots tomentose. Culms densely tufted, 30–65 smooth or scabrid, longer than internodes; leaf blades involute, cm tall, branched at base. Leaf sheaths smooth or scabrid, 10–30 cm, glaucous, abaxial surface scabrid, adaxial surface longer than internodes; leaf blades involute, 10–35 cm, abaxial puberulent; ligule short, margin with 0.5–1 mm hairs. Panicle surface smooth, adaxial surface pubescent; ligule short, ciliate. lax, open, base usually included in uppermost leaf sheath, 5–20 Panicle lax with few spikelets, 15–30 cm; branches capillary, cm; branches paired, rarely solitary. Spikelets 1.3–1.7 cm, stra- solitary, 3–10 cm. Spikelets 2.5–3 cm, stramineous or yellowish mineous; glumes narrowly lanceolate, smooth or scabrid, pu- white; glumes narrowly lanceolate, smooth or scabrid, densely bescent within, subequal, lower slightly longer than upper, low- pubescent within upward, unequal, lower glume 2.5–3 cm, 5–7- er glume 3–5-veined, upper glume 3-veined, apex acuminate; veined, marginal veins obscure, upper glume 2–2.3 cm, 3- callus ca.