DOCSLIB.ORG

Monocot Families of KY

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Monocot Families of KY MONOCOTYLEDONAE Leucojum L. †L. aestivum L. Snowflake. ♦ ACORACEAE. The Sweet-flag Family. Lycoris Herb. Acorus L. †L. radiata (L’Hér.) Herb. Red spider lily. *A. calamus L. Sweet-flag. Narcissus L. Daffodil, jonquil. ♦ AGAVACEAE. The Agave Family. †N. poeticus L. Poet’s narcissus. †N. pseudonarcissus L. Daffodil. Manfreda Salisb. M. virginica (L.) Rose. False aloe. ♦ ARACEAE. The Arum Family. Yucca L. Spanish-bayonet. Arisaema Mart. *Y. filamentosa L. Adam’s-needle. A. dracontium (L.) Schott. Green-dragon. *Y. flaccida Haw. Beargrass A. triphyllum (L.) Schott. Jack-in-the-pulpit. subsp. quinatum (Nutt.) Huttl. ♦ ALISMATACEAE. The Water-plantain Family. subsp. triphyllum subsp. stewardsonii (Britton) Huttl. Alisma L. Water-plantain. subsp. pusillum (Peck) Huttl. A. subcordatum Raf. Southern w.-p. Orontium L. Echinodorus Rich. Burhead. !O. aquaticum L. Goldenclub. !E. berteroi (Spreng.) Fassett. Tall b. E. cordifolius (L.) Griseb. Creeping b. Peltandra Raf. !E. tenellus (Mart.) Buchenau P. virginica (L.) Raf. ex Schott & Endl. Arrow-arum. var. parvulus (Engelm.) Fassett. Little b. ♦ ASPARAGACEAE. The Asparagus Family. Sagittaria L. Arrowhead. S. australis (J.G.Sm.) Small. Appalachian a. Asparagus L. S. brevirostra Mack. & Bush. Midwestern a. *A. officinalis L. Asparagus. !S. graminea Michx. Grass-leaved sagittaria. S. latifolia Willd. Common a. ♦ COMMELINACEAE. The Spiderwort Family. S. montevidensis Cham. & Schltd. subsp. calycina (Engelm.) Bogin. Mississippi a. Commelina L. Dayflower. !S. platyphylla (Engelm.) J.G. Sm. *C. communis L. Common d. !S. rigida Pursh. Sessile-fruited a. *C. diffusa Burm. f. Creeping d. C. erecta L. Erect d. ♦ ALLIACEAE. The Onion Family. var. angustifolia (Michx.) Fernald C. virginica L. Virginia d. Allium L. Onion. *A. ampeloprasum L. Wild leek. Murdannia Royle. A. burdickii (Hanes) A.G.Jones. Burdick’s wild leek. *M. keisak (Hassk.) Hand.-Mazz. False dayflower. A. canadense L. Wild o. *A. cepa L. Cultivated o. Tradescantia L. Spiderwort. A. cernuum Roth. Nodding onion. T. ohiensis Raf. Smooth s. *A. oleraceum L. Field garlic. T. subaspera Ker Gawl. Wide-leaved s. *A. sativum L. Garlic. T. virginiana L. Virginia s. A. tricoccum Sol. Ramps, wild leek. *A. vineale L. Field garlic. ♦ CONVALLARIACEAE. Lily-of-the-valley Family. Nothoscordum Kunth. Convallaria L. N. bivalve (L.) Britton. False garlic. *C. majalis L. European Lily-of-the-valley. !C. montana Raf. American Lily-of-the-valley. ♦ AMARYLLIDACEAE. The Amaryllis Family. Maianthemum F.H.Wigg. Hymenocallis Salisb. !M. canadense Desf. Canada mayflower. H. occidentalis (Le Conte) Kunth. Spider-lily. M. racemosum (L.) Link. False Solomon’s-seal. !M. stellatum (L.) Link. Starry false Solomon’s-seal. var. debilis var. rudgei L.H.Bailey Polygonatum Mill. Solomon’s-seal. !C. decomposita Muhl. P. biflorum (Walter) Elliott. Smooth S.-s. C. digitalis Willd. P. pubescens (Willd.) Pursh. Hairy S.-s. var. digitalis var. macropoda Fernald ♦ CYPERACEAE. The Sedge Family. C. eburnea Boott. C. emoryi Dewey. Bolboschoenus (Asch.) Palla. C. festucacea Schkuhr. !B. fluviatilis (Torr.) Sojak. River bulrush. C. flaccosperma Dewey. C. frankii Kunth. Bulbostylis Kunth. !C. gigantea Rudge. B. capillaris (L.) C.B.Clarke. Densetuft hairsedge. C. glaucodea Tuck. C. gracilescens Steud. Carex L. Caric sedge. C. gracillima Schwein. C. abscondita Mack. C. granularis Muhl. ex Willd. !C. aestivalis M.A.Curtis. ex A.Gray. C. gravida L.H.Bailey. C. aggregata Mack. C. grayi J.Carey. !C. alata Torr. & A.Gray. C. grisea Wahlenb. C. albicans Willd. ex Spreng. C. gynandra Schwein. var. albicans. C. hirsutella Mack. C. albolutescens Schwein. C. hirtifolia Mack. C. albursina Sheld. C. hitchcockiana Dewey. C. amphibola Steud. C. hyalinolepis Steud. C. annectens (E.P.Bicknell) E.P.Bicknell. !C. hystericina Muhl. var. annectens C. intumescens Rudge. var. xanthocarpa (E.P.Bicknell) Wiegand C. jamesii Schwein. !C. appalachica J.M.Webber & P.W.Ball. !C. joorii L.H.Bailey. !C. atlantica L.H.Bailey. !C. juniperorum Catling, Reznicek, & Crins. subsp. atlantica C. kraliana Naczi & Bryson. subsp. capillacea (L.H. Bailey) Reznicek & P.W.Ball C. lacustris Willd. !C. austrocaroliniana L.H.Bailey. C. laevivaginata (Kük.) Mack. C. baileyi Britton. C. laxiculmis Schwein. C. blanda Dewey. var. laxiculmis C. brevior (Dewey) Mack. ex Lundell. var. copulata (L.H.Bailey) Fernald C. bromoides Schkuhr ex Willd. C. laxiflora Lam. subsp. bromoides. var. laxiflora C. bushii Mack. var. serrulata F.J.Herm. !C. buxbaumii Wahlenb. C. leavenworthii Dewey. C. careyana Torr. ex Dewey. C. leptalea Wahlenb. C. caroliniana Schwein. !C. leptonervia (Fernald) Fernald. C. cephalophora Muhl. ex Willd. C. longii Mack. C. cherokeensis Schwein. C. louisianica L.H.Bailey C. communis L.H.Bailey. C. lucorum Willd. !C. comosa Boott. C. lupuliformis Sartwell. ex Dewey. C. complanata Torr. & Hook. C. lupulina Muhl. ex Willd. C. conjuncta Boott. C. lurida Wahlenb. C. corrugata Fernald C. meadii Dewey. !C. crawei Dewey. C. mesochorea Mack. C. crebriflora Wiegand. C. molesta Mack. C. crinita lam. C. muehlenbergii Schkuhr ex Willd. var. crinita var. muehlenbergii var. brevicrinis Fernald var. enervis Boott. C. cristatella Britton. C. muskingumensis Schwein. C. crus-corvi Shuttlew. ex Kunze. C. nigromarginata Schwein. C. cumberlandensis Naczi, Kral, & Bryson. C. normalis Mack. C. davisii Schwein. & Torr. C. oklahomensis Mack. C. debilis Michx. C. oligocarpa Schkuhr ex Willd. C. ouachitana Kral, Manhart, & Bryson. C. acuminatus Torr. & Hook. Tapertip f. C. oxylepis Torr. & Hook. C. bipartitus Torr. Slender f. var. oxylepis C. compressus L. Poorland f. var. pubescens J.K.Underwood C. croceus Vahl. Baldwin’s f. C. pedunculata Willd. C. difformis L. Variable f. !C. pellita Muhl. ex Willd. C. echinatus (L.) Alph.Wood. Globe f. C. pensylvanica Lam. C. engelmannii Steud. Engelmann’s f. C. picta Steud. C. erythrorhizos Muhl. Redroot f. C. planispicata Naczi. C. esculentus L. Chufa f. C. plantaginea Lam. C. flavescens L. Yellow f. C. platyphylla J.Carey. C. flavicomus Michx. White-edge f. C. prasina Wahlenb. *C. iria L. Ricefield f. C. purpurifera Mack. C. lancastriensis Porter. Many-flower f. C. radiata (Wahlenb.) Small. C. lupulinus (Spreng.) Marcks. Great Plain f. !C. reniformis (L.H.Bailey) Small. subsp. lupulinus C. retroflexa Muhl. subsp. macilentus (Fernald) Marcks. !C. roanensis F.J.Herm. C. microiria Steud. Asian f. C. rosea Schkuhr ex Willd. C. odoratus L. Frangant f. !C. rugosperma Mack. !C. plukenetii Fern. Plukenet’s f. C. scabrata Schwein. C. polystachyos Rottb. var. texensis (Torr.) Fernald. Texan f. C. scoparia Schkuhr. C. pseudovegetus Steud. Marsh f. !C. seorsa Howe. C. refractus Engelm. ex Steud. Relaxed f. C. shortiana Dewey. C. retroflexus Buckley. One-flower f. C. socialis Mohlenbr. & Schwegman. C. retrofractus (L.) Torr. Rough f. C. sparganoides Muhl. ex Willd. C. retrorsus Chapm. Pine barren f. C. squarrosa L. *C. rotundus L. Nut-grass f. !C. stipata Muhl. ex Willd. C. schweinitzii Torr. Schweinitz’s f. var. stipita C. squarrosus L. Bearded f. var. maxima Chapm. C. strigosus L. Straw-colored f. !C. straminea Willd. C.striatula Michx. Dulichium Pers. C. stricta Lam. D. arundinaceum (L.) Britton. Three-way sedge. C. styloflexa Buckley. C. superata Naczi, Reznicek, & B.A.Ford. Eleocharis R. Br. Spikerush. C. swanii (Fernald) Mack. E. acicularis (L.) Roem. & Schult. Needle s. !C. tetanica Schkuhr. E. bifida S.G. Smith C. texensis (Torr.) L.H.Bailey. E. compressa Sull. Flatstem s. C. timida Naczi & B.A.Ford. E. erythropoda Steud. Bald s. C. torta Boott. E. flavescens (Poir.) Urb. Yellow s. C. triangularis Boeck. E. ovata (Roth) Roem. & Schult. Ovate s. C. tribuloides Wahlenb. E. palustris (L.) Roem. & Schult. Common s. var. tribuloides E. quadrangulata (Michx.) Roem. & Schult. Squarestem s. var. sangamonensis Clokey E. tenuis (Willd.) Schult. Slender s. C. typhina Michx. var. pseudoptera (Weath.) Svenson. C. umbellata Schkuhr ex Willd. var. tenuis C. virescens Muhl. ex Willd. var. verrucosa (Svenson) Svenson C. vulpinoidea Michx. E. tuberculosa (Michx.) Roem. & Schult. Cone-cup s. C. willdenowii Schkuhr ex Willd. C. woodii Dewey Eriophorum L. Cotton-grass. !E. virginicum L. Tawny cotton-grass. Cladium C. mariscoides (Muhl.) Torr. Smooth sawgrass Fimbristylis Vahl. Fimbry F. annua (All.) Roem. & Schult. Annual f. Cymophyllus Mack. ex Britton F. autumnalis (L.) Roem. & Schult. Slender f. !C. fraserianus (Ker Gawl.) Kartesz & Gandhi. Fraser’s sedge. *F. miliacea (L.) Vahl. Grasslike f. !F. puberula (Michx.) Vahl. Hairy f. Cyperus L. Flat sledges. F. vahlii (Lam.) Link. Vahl’s f. *D. polystachya Turcz. Cinnamon-vine. Fuirena Rottb. Umbrella-Grass D. villosa L. Colicroot. F. simplex Vahl. Western u.-g. F. squarrosa Michx. Hairy u.-g. ♦ HEMEROCALLIDACEAE. The Day-lily Family. Isolepis R.Br. Hemerocallis L. Day-lily. I. carinata Hook. & Torr. Keeled bulrush. †H. fulva (L.)L. Day-lily. Kyllinga Rottb. ♦ HYACINTHACEAE. The Grape-hyacinth Family. *K. gracillima Miq. Pasture s. K. pumila Michx. Low s. Camassia Lindl. C. scilloides (Raf.) Cory. Wild hyacinth, camas-lily. Lipocarpha R.Br. L. micrantha (Vahl.) G.C.Tucker. Halfchaff sedge. Hyacinthoides Heist. †H. non-scripta (L.) Chouard. English bluebell. Rhynchospora Beak-rush. R. capitellata (Michx.) Vahl. Slender b.-r. Muscari Grape-hyacinth. R. corniculata (Lam.) A.Gray. Shortbristle horned b.-r. †M. botryoides (L.) Mill. Common g.-h. !R. globularis (Chapm.) Small. Globe b.-r. †M. comosum (L.) Mill. Tassel g.-h. var. globularis. †M. neglectum Guss. ex Ten. Starch g.-h. R. glomerata
Load more

Recommended publications
  • Illustrated Flora of East Texas --- Taxa in Volume 1 (May 2004)
    Illustrated Flora of East Texas --- Taxa in Volume 1 (May 2004) Family Genus Species Var. or Subsp. Native or Intro Ferns & Fern Allies Psilotaceae Psilotum nudum N Isoetaceae Isoetes butleri N Isoetaceae Isoetes melanopoda N Lycopodiaceae Lycopodiella alopecuroides N Lycopodiacae Lycopodiella appressa N Lycopodiaceae Lycopodiella prostrata N Lycopodiaceae Palhinhaea cernua N Lycopodiaceae Pseudolycopodiella caroliniana N Selaginellaceae Selaginella apoda var. apoda N Selaginellaceae Selaginella arenicola subsp. riddellii N Equisetaceae Equisetum hyemale subsp. affine N Equisetaceae Equisetum laevigatum N Anemiaceae Anemia mexicana N Aspleniaceae Asplenium platyneuron N Aspleniaceae Asplenium resiliens N Azollaceae Azolla caroliniana N Azollaceae Azolla mexicana N Blechnaceae Woodwardia areolata N Blechnaceae Woodwardia virginica N Dennstaedtiaceae Pteridium aquilinum var. pseudocaudatum N Dryopteridaceae Athyrium filix-femina subsp. asplenioides N Dryopteridaceae Cyrtomium falcatum I Dryopteridaceae Cystopteris protrusa N Dryopteridaceae Dryopteris celsa N Dryopteridaceae Dryopteris ludoviciana N Dryopteridaceae Nephrolepis exaltata I Dryopteridaceae Onoclea sensibilis N Dryopteridaceae Polystichum acrostichoides N Dryopteridaceae Tectaria heracleifolia N Dryopteridaceae Woodsia obtusa subsp. obtusa N Dryopteridaceae Woodsia obtusa subsp. occidentalis N Lygodiaceae Lygodium japonicum I Marsileaceae Marsilea macropoda N Marsileaceae Marsilea vestita N Marsileaceae Pilularia americana N Ophioglossaceae Botrychium biternatum N Ophioglossaceae
    [Show full text]
  • 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.
    [Show full text]
  • Richard Chinn Environmental Training, Inc. Info
    Scientific Name Common Name Region 6 Habit Scientific Name Common Name Region 6 Habit Abies balsamea FIR,BALSAM FACW NT Amaranthus californicus AMARANTH,CALIFORNIA NI ANF Abutilon theophrasti VELVET-LEAF NI AIF Amaranthus crassipes AMARANTH,TROPICAL FAC+ AIF Acacia greggii ACACIA,CATCLAW UPL NST Amaranthus greggii AMARANTH,GREGGIS FAC ANF Acacia smallii HUISACHE FACU NTS Amaranthus obcordatus AMARANTH,TRANS PECOS NI ANF Acalypha rhomboidea COPPER-LEAF,COMMON UPL* ANF Amaranthus palmeri AMARANTH,PALMER'S FACU- ANF Acalypha virginica MERCURY,THREE-SEEDED UPL* ANF Amaranthus retroflexus AMARANTH,RED-ROOT FACU- ANF Acer negundo BOX-ELDER FACW- NT Amaranthus rudis AMARANTH,TALL FAC ANF Acer rubrum MAPLE,DRUMMOND RED FACW NT Amaranthus spinosus AMARANTH,SPINY FACU- ANF Acer rubrum MAPLE,TRIDENT RED NI NT Amaranthus tuberculatus AMARANTH,ROUGH-FRUIT NI ANF Acer rubrum MAPLE,RED FAC NT Ambrosia artemisiifolia RAGWEED,ANNUAL FACU- ANF Acer saccharinum MAPLE,SILVER FAC NT Ambrosia grayi BURSAGE,WOOLLY-LEAF FACW PNF Acer saccharum MAPLE,SUGAR UPL NT Ambrosia psilostachya RAGWEED,NAKED-SPIKE FAC- PNF Achillea millefolium YARROW,COMMON FACU PNF Ambrosia trifida RAGWEED,GREAT FAC ANF Acorus calamus SWEETFLAG OBL PIEF Amelanchier alnifolia SERVICE-BERRY,SASKATOON FAC- NS Adiantum capillus-veneris FERN,SOUTHERN MAIDEN-HAIR FACW+ PNF3 Amelanchier arborea SERVICE-BERRY,DOWNY FACU NT Adiantum pedatum FERN,NORTHERN MAIDEN-HAIR FAC PNF3 Amianthium muscaetoxicum FLYPOISON FAC PNF Adiantum tricholepis FERN,HAIRY MAIDEN-HAIR FAC PNF3 Ammannia auriculata AMMANNIA,RED-STEM
    [Show full text]
  • ATLAS of FLORIDA PLANTS - 7/29/19 Lake County Native Species
    ATLAS OF FLORIDA PLANTS - 7/29/19 Lake County Native Species Scientific_Name Common_Name Endemic State US 1 Abutilon hulseanum MAUVE N 2 Acalypha gracilens SLENDER THREESEED MERCURY N 3 Acalypha ostryifolia PINELAND THREESEED MERCURY N 4 Acer negundo BOXELDER N 5 Acer rubrum RED MAPLE N 6 Acrolejeunea heterophylla 7 Acrostichum danaeifolium GIANT LEATHER FERN N 8 Aeschynomene americana SHYLEAF N 9 Aeschynomene viscidula STICKY JOINTVETCH N 10 Aesculus pavia RED BUCKEYE N 11 Agalinis fasciculata BEACH FALSE FOXGLOVE N 12 Agalinis filifolia SEMINOLE FALSE FOXGLOVE N 13 Agalinis linifolia FLAXLEAF FALSE FOXGLOVE N 14 Agalinis plukenetii PLUKENET'S FALSE FOXGLOVE N 15 Agarista populifolia FLORIDA HOBBLEBUSH; PIPESTEM N 16 Ageratina jucunda HAMMOCK SNAKEROOT N 17 Aletris lutea YELLOW COLICROOT N 18 Allium canadense var. canadense MEADOW GARLIC N 19 Amaranthus australis SOUTHERN AMARANTH N 20 Amblystegium serpens 21 Ambrosia artemisiifolia COMMON RAGWEED N 22 Amorpha fruticosa BASTARD FALSE INDIGO N 23 Amorpha herbacea var. herbacea CLUSTERSPIKE FALSE INDIGO N 24 Amphicarpum muehlenbergianum BLUE MAIDENCANE N 25 Amsonia ciliata FRINGED BLUESTAR N 26 Andropogon brachystachyus SHORTSPIKE BLUESTEM N 27 Andropogon floridanus FLORIDA BLUESTEM N 28 Andropogon glomeratus var. glaucopsis PURPLE BLUESTEM N 29 Andropogon glomeratus var. hirsutior BUSHY BLUESTEM N 30 Andropogon glomeratus var. pumilus BUSHY BLUESTEM N 31 Andropogon gyrans ELLIOTT'S BLUESTEM N 32 Andropogon longiberbis HAIRY BLUESTEM N 33 Andropogon ternarius SPLITBEARD BLUESTEM N 34 Andropogon
    [Show full text]
  • 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.
    [Show full text]
  • Species Convergence Into Life-Forms in a Hyperseasonal Cerrado in Central Brazil Silva, IA.* and Batalha, MA
    Species convergence into life-forms in a hyperseasonal cerrado in central Brazil Silva, IA.* and Batalha, MA. Laboratório de Ecologia Vegetal, Departamento de Botânica, Universidade Federal de São Carlos – UFSCar, CP 676, CEP 13565-905, São Carlos, SP, Brazil *e-mail: [email protected] Received September 21, 2006 – Accepted November 30, 2006 – Distributed May 31, 2008 (With 3 figures) Abstract Whether the functional structure of ecological communities is deterministic or historically contingent is still quite con- troversial. However, recent experimental tests did not find effects of species composition variation on trait convergence and therefore the environmental constraints should play the major role on community convergence into functional groups. Seasonal cerrados are characterized by a sharp seasonality, in which the water shortage defines the community functioning. Hyperseasonal cerrados experience additionally waterlogging in the rainy season. Here, we asked whether waterlogging modifies species convergences into life-forms in a hyperseasonal cerrado. We studied a hyperseasonal cerrado, comparing it with a nearby seasonal cerrado, never waterlogged, in Emas National Park, central Brazil. In each area, we sampled all vascular plants by placing 40 plots of 1 m2 plots in four surveys. We analyzed the species convergences into life-forms in both cerrados using the Raunkiaer’s life-form spectrum and the index of divergence from species to life-form diversity (IDD). The overall life-form spectra and IDDs were not different, indicating that waterlogging did not affect the composition of functional groups in the hyperseasonal cerrado. However, there was a seasonal variation in IDD values only in the hyperseasonal cerrado. As long as we did not find a seasonal variation in life-form diversity, the seasonal variation of convergence into life-forms in the hyperseasonal cerrado was a conse- quence of the seasonal variation of species diversity.
    [Show full text]
  • Fire in the Southeastern Grasslands, By
    Fire in the Southeastern Grasslands RICHARD J. VOGL Department of Biology California State University Los Angeles, CA 90032 INTRODUCTION ~ERE has been more research on the effects of fire in the southeastern United States than in any region of North America. Most studies have been concerned with the effects of fire on the trees, including the role of fire in controlling hardwood suc­ cession, fire damage to trees, the effects of fire on soils and litter, the influence of fire on conifer growth and reproduction, and the relationships of fire to tree diseases (Garren 1943; Ahlgren and Ahlgren 1960; Cushwa 1968). A lesser, but stilI substantial number of studies have been focused on the effects of fire on forage yields and livestock production (Wahlenberg et al. 1939), and the use of fire in wildlife management in the Southeast. But academic or phy­ tosociological studies of the vegetational composition and of the effects of fire on the understory vegetation are generally lacking. Except for some range and wildlife research and several general studies (Wells and Shunk 1931; Leukel and St<Jkes 1939; Biswell and Lemon 1943; Burton 1944; Lemon 1949, 1967; Campbell 1955; Biswell1958; Hodgkins 1958; Arata 1959; Cushwa et al. 1966, 1970; Wolters 1972) , most investigators have ignored the herbaceous cover or grassland vegetation under southeastern trees. Even early botanists often became more interested in the unusual botanical features such as the southern extent of Appalachian tree species (Harper 1943, 1952), the description of the silaceous dunes of the 175 RICHARD J. VOGL Gulf Coast (Kurz 1942), the habits of eastern red cedar (Harper 1912), the vegetation of the Okefenokee Swamp (Wright and Wright 1932), or why the Black Belt Prairie of Alabama was treeless (Ranking and Davis 1971), thereby neglecting the widespread and common grassland vegetation and its relationship to fire.
    [Show full text]
  • 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.
    [Show full text]
  • Bastrop County Grasses Only As of February 21, 2014 Common Name Scientific Name Grass Family Poaceae
    Bastrop County Grasses Only As of February 21, 2014 This checklist of the vascular plants of Bastrop County is primarily based on the collections in the herbarium at Plant Resource Center (PRC), University of Texas, Austin. Additional records were added from the USDA files, historic plant lists from Bastrop and Buescher State Parks (including the Stengl Research Station), recent McKinney Roughs Natural Area bio-surveys, and from the Bill Carr post-fire survey in 2012. Special codes used: asterisk (*) USDA, percent (%) Bill Carr, pound sign (#) added to the PRC from surveys. Rare plants listed from Rare Plants of Texas by Poole, et.al. are indicated with an exclamation point (!). New Biota of North Ameaica (BONAP) modern family names have an ampersand (&). Species marked in bold are listed on the Texas Department of Agriculture Noxious Weeds list, on the USDA list, or introduced. Scientific Name Common Name Poaceae Grass Family Agostris hyemalis winter bentgrass # Agostris scabra rough bentgrass # Aira caryophyllea hairgrass Alopecurus caroliniana Carolina foxtail Andropogon gerardii big bluestem Andropogon glomeratus bushy bluestem # Andropogon ternarius split-beard bluestem Andropogon virginicus broomsedge Anthaenantus rufa purple silky scale Aristida affinis three-awn grass Aristida desmantha church mouse three-awn Aristida dichotoma poverty grass Aristida glauca smooth three-awn Aristida lanosa woolly three-awn Aristida longespica slim-spike three-awn Aristida oligantha old-field three-awn Aristida purpurascens arrow feather three-awn
    [Show full text]
  • Floristic Composition of the South-Central Florida Dry Prairie Landscape Steve L
    Floristic Composition of the South-Central Florida Dry Prairie Landscape Steve L. Orzell Avon Park Air Force Range, 29 South Blvd., Avon Park Air Force Range, FL 33825-5700 [email protected] Edwin L. Bridges Botanical and Ecological Consultant, 7752 Holly Tree Place NW, Bremerton, WA 98312-1063 [email protected] ABSTRACT Floristic composition of the Florida dry prairie landscape was compiled from 291 sites in nine south-central peninsular counties. Floristic lists were based upon field inventory and compilation from reliable sources to- taling 11,250 site and community type-specific observations and were analyzed by region (Kissimmee River, Desoto/Glades “Big Prairie,” and Myakka). The known vascular flora consists of 658 vascular plant taxa, rep- resenting 317 genera and 115 families. Families with the highest number of species are Poaceae (103), Asteraceae (78), Cyperaceae (76), Fabaceae (23), Scrophulariaceae (20), and Orchidaceae (18). The most diverse genera are Rhynchospora (29), Dichanthelium (17), Ludwigia (13), Xyris (12), and Andropogon (11). Of this flora 24 taxa are endemic to central or southern peninsular Florida, primarily within the pine savanna- flatwood/dry prairie landscape, and 41 taxa are of Floridian biotic affinity. Although most species are not re- gionally specific, a few (Carphephorus carnosus, Ctenium aromaticum, and Liatris spicata) appear to be ab- sent from the Myakka prairie region, while Marshallia tenuifolia appears to be absent from both the Desoto/ Glades and Myakka prairie regions. Within the dry prairie landscape Hypericum edisonianum is restricted to the Desoto/Glades region. A few other species somewhat differentiate between prairie regions; however, most occur in other habitats in the counties where they are absent or nearly absent from dry prairie.
    [Show full text]
  • COMMON Plants Longleaf PINE
    COMMON PlANTS OF lONGlEAF PINE - BlUE STEM RANGE Harold E. Grelen Vinson L. Duvall In preparing this handbook, the authors have received substantial assistance from predecessors and colleagues. Much of the information is from the Forest Service's "Field Book of Forage Plants on Longleaf Pine-Biuestem Ranges," by 0. Gordon Langdon, the late Miriam L. Bomhard, and John T. Cassady ( 1952). Charles Feddema, Lowell K. Halls, J. B. Hilmon, and Alfred W. Johnson, U. S. Forest Service, and Thomas N. Shiflet, U. S. Soil Conservation Service, reviewed the manu­ script and made important suggestions regarding content and organiza­ tion. Phil D. Goodrum, Bureau of Sport Fisheries and Wildlife, U. S. Fish and Wildlife Service, supplied much information on values of range plants to wildlife. Jane Roller, Forest Service, prepared illustrated keys as well as many technical descriptions and drawings. Most other drawings were by the late Leta Hughey, Forest Service, and the senior author; several are from other U.S. Department of Agriculture publica­ tions. U. S. FOREST SERVICE RESEARCH PAPER S0-23 COMMON PLANTS OF LONGLEAF PINE·BLUESTEM RANGE Harold E. Grelen V-inson L. Duvall SOUTHERN FO!;<.EST EXPERIMENT STAT ION Thomas, c·. Nelson, Director FOREST SERVICE U.S. DEPARTMENT OF AGRICULTURE 1966 Contents The type 1 Grasses 3 Bluestems 3 Panicums 13 Paspalums 21 Miscellaneous grasses 25 Grasslike plants 37 Forbs . 47 Legumes 47 Composites 59 Miscellaneous forbs 74 Shrubs and woody vines 78 Bibliography 90 Glossary . 91 Index of plant names 94 COMMON PLANTS OF LONGLEAF PINE· BLUEST EM RANGE This publication describes many grasses, salient taxonomic features of species mention­ grasslike plants, forbs, and shrubs that inhabit ed briefly as well as of those described fully.
    [Show full text]
  • A Comparison of Native Versus Old-Field Vegetation in Upland Pinelands Managed with Frequent Fire, South Georgia, Usa
    A COMPARISON OF NATIVE VERSUS OLD-FIELD VEGETATION IN UPLAND PINELANDS MANAGED WITH FREQUENT FIRE, SOUTH GEORGIA, USA Thomas E. Ostertag1 and Kevin M. Robertson2 Tall Timbers Research Station, 13093 Henry Beadel Drive, Tallahassee, FL 32312, USA ABSTRACT Fire-maintained, herb-dominated upland pinelands of the southeastern U.S. Coastal Plain may be broadly divided into those that have arisen through secondary succession following abandonment of agriculture (old-field pinelands) and those that have never been plowed (native pinelands). The ability to distinguish these habitat types is important for setting conservation priorities by identifying natural areas for conservation and appropriate management and for assessing the ecological value and restoration potential for old-field pine forests managed with frequent fire. However, differences in species composition have rarely been quantified. The goals of this study were to characterize the species composition of native and old-field pineland ground cover, test the ability to distinguish communities of previously unknown disturbance history, and suggest indicator species for native versus old-field pinelands. Plant composition was surveyed in areas known to be native ground cover, those known to be old fields, and those with an uncertain disturbance history. Twelve permanent plots were established in each cover type and sampled in spring (April–May) and fall (October–November) in 2004 and 2005. Of the 232 species identified in the plots, 56 species were present only in native ground-cover plots, of which 17 species occurred in a sufficient number of plots to have a statistically significant binomial probability of occurring in native ground cover and might be considered indicator species.
    [Show full text]