O APPENDIX F. Natural Communities Information
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Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
Despite Introgressive Hybridization, North American Birches (Betula Spp.) Maintain Strong Differentiation at Nuclear Microsatellite Loci
Tree Genetics & Genomes (2015) 11:101 DOI 10.1007/s11295-015-0922-6 ORIGINAL ARTICLE Despite introgressive hybridization, North American birches (Betula spp.) maintain strong differentiation at nuclear microsatellite loci Ashley M. Thomson1,2,3 & Christopher W. Dick3 & Ana L. Pascoini4 & Selvadurai Dayanandan1,2 Received: 20 March 2015 /Revised: 27 June 2015 /Accepted: 28 August 2015 # Springer-Verlag Berlin Heidelberg 2015 Abstract Extensive chloroplast introgression has been docu- between B. alleghaniensis and B. papyrifera increased signif- mented in polyploid Betula species of eastern North America. icantly moving northward into the sympatric zone, suggesting However, the extent to which the nuclear genomes of these the occurrence of hybridization in previously glaciated habi- species are differentiated is unknown. Therefore, we evaluated tats. In contrast, admixture proportions of B. papyrifera and genetic differentiation among largely sympatric Betula B. alleghaniensis did not show a significant geographic trend, papyrifera, B. alleghaniensis,andB. lenta using nuclear mi- which points to recent ancestry as the likely cause of allele crosatellite markers. Principal components analysis (PCA) sharing between these two species. We suggest that allele and analysis of molecular variation (AMOVA) were used to sharing of B. papyrifera and B. alleghaniensis results from a evaluate genetic differentiation. Bayesian model-based clus- combination of ongoing gene flow and historic introgression tering was used to identify putatively admixed individuals. via pollen swamping during northward colonization into post- Despite a high incidence of allele sharing, all of the species glacial environments. were significantly differentiated even within zones of sympat- ry. A number of individuals were identified as possibly Keywords Allele sharing . -
1Alan S. Weakley, 2Bruce A. Sorrie, 3Richard J. Leblond, 4Derick B
NEW COMBINATIONS, RANK CHANGES, AND NOMENCLATURAL AND TAXONOMIC COMMENTS IN THE VASCULAR FLORA OF THE SOUTHEASTERN UNITED STATES. IV 1Alan S. Weakley, 2Bruce A. Sorrie, 3Richard J. LeBlond, 4Derick B. Poindexter UNC Herbarium (NCU), North Carolina Botanical Garden, Campus Box 3280, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3280, U.S.A. [email protected], [email protected], [email protected], [email protected] 5Aaron J. Floden 6Edward E. Schilling Missouri Botanical Garden (MO) Dept. of Ecology & Evolutionary Biology (TENN) 4344 Shaw Blvd. University of Tennessee Saint Louis, Missouri 63110, U.S.A. Knoxville, Tennessee 37996 U.S.A. [email protected] [email protected] 7Alan R. Franck 8John C. Kees Dept. of Biological Sciences, OE 167 St. Andrew’s Episcopal School Florida International University, 11200 SW 8th St. 370 Old Agency Road Miami, Florida 33199, U.S.A. Ridgeland, Mississippi 39157, U.S.A. [email protected] [email protected] ABSTRACT As part of ongoing efforts to understand and document the flora of the southeastern United States, we propose a number of taxonomic changes and report a distributional record. In Rhynchospora (Cyperaceae), we elevate the well-marked R. glomerata var. angusta to species rank. In Dryopteris (Dryopteridaceae), we report a state distributional record for Mississippi for D. celsa, filling a range gap. In Oenothera (Onagraceae), we continue the reassessment of the Oenothera fruticosa complex and elevate O. fruticosa var. unguiculata to species rank. In Eragrostis (Poaceae), we address typification issues. In the Trilliaceae, Trillium undulatum is transferred to Trillidium, providing a better correlation of taxonomy with our current phylogenetic understanding of the family. -
Betula Alleghaniensis Britton Yellow Birch Betu Laceae Birch Family G
Betula alleghaniensis Britton Yellow Birch Betu laceae Birch family G. G. Erdmann Yellow birch (Bet&a alleghaniensis) is the most precipitation may be snow. Snowfall ranges from 152 valuable of the native birches. It is easily recognized to 356 cm (60 to 140 in) and averages 229 cm (90 in) by the yellowish-bronze exfoliating bark for which it in the north. The growing season ranges from 60 to is named. The inner bark is aromatic and has a 150 days and averages about 120 days. flavor of winter-green. Other names are gray birch, silver birch, and swamp birch. This slow-growing Soils and Topography long-lived tree is found with other hardwoods and conifers on moist well-drained soils of the uplands Yellow birch grows over a large area with diverse and mountain ravines. It is an important source of hardwood lumber and a good browse plant for deer geology, topography, and soil and moisture condi- and moose. Other wildlife feed on the buds and tions. In Michigan and Wisconsin it is found on gla- cial tills, outwash sands, lacustrine deposits, shallow seeds. loess deposits, and residual soils derived from sandstone, limestone, and igneous and metamorphic Habitat rock (95). Soils are also derived from granites, schists, and shales in other parts of its range. Native Range Growth of yellow birch is affected by soil texture, drainage, rooting depth, stone content in the rooting Yellow birch (fig. 1) ranges from Newfoundland, zone, elevation, aspect, and fertility. Yellow birch Nova Scotia, New Brunswick, and Anticosti Island grows best on well-drained, fertile loams and west through southern Ontario to extreme moderately well-drained sandy loams within the soil southeastern Manitoba; south to Minnesota and orders Spodosols and Inceptisols and on flats and northeastern Iowa; east to northern Illinois, Ohio, lower slopes (45). -
Ground Vegetation Patterns of the Spruce-Fir Area of the Great Smoky Mountains National Park
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Doctoral Dissertations Graduate School 12-1957 Ground Vegetation Patterns of the Spruce-Fir Area of the Great Smoky Mountains National Park Dorothy Louise Crandall University of Tennessee - Knoxville Follow this and additional works at: https://trace.tennessee.edu/utk_graddiss Part of the Botany Commons Recommended Citation Crandall, Dorothy Louise, "Ground Vegetation Patterns of the Spruce-Fir Area of the Great Smoky Mountains National Park. " PhD diss., University of Tennessee, 1957. https://trace.tennessee.edu/utk_graddiss/1624 This Dissertation is brought to you for free and open access by the Graduate School at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. To the Graduate Council: I am submitting herewith a dissertation written by Dorothy Louise Crandall entitled "Ground Vegetation Patterns of the Spruce-Fir Area of the Great Smoky Mountains National Park." I have examined the final electronic copy of this dissertation for form and content and recommend that it be accepted in partial fulfillment of the equirr ements for the degree of Doctor of Philosophy, with a major in Botany. Royal E. Shanks, Major Professor We have read this dissertation and recommend its acceptance: James T. Tanner, Fred H. Norris, A. J. Sharp, Lloyd F. Seatz Accepted for the Council: Carolyn R. Hodges Vice Provost and Dean of the Graduate School (Original signatures are on file with official studentecor r ds.) December 11, 19)7 To the Graduate Council: I am submitting herewith a thesis written by DorothY Louise Crandall entitled "Ground Vegetation Patterns of the Spruce-Fir Area of the Great Smoky Hountains National Park." I recommend that it be accepted in partial fulfillment of the requirements for the degree of Doctor of Philosophy, with a major in Botany. -
Trillium Reliquum)
REPRODUCTIVE BIOLOGY OF RELICT TRILLIUM (Trillium reliquum) Except where reference is made to the work of others, the work described in this thesis is my own or was done in collaboration with my advisory committee. This thesis does not include proprietary or classified information. _________________________________________ Melissa Gwynne Brooks Waddell Certificate of Approval: ________________________ _________________________ Robert Boyd Debbie R. Folkerts, Chair Professor Assistant Professor Biological Sciences Biological Sciences _____________________ _________________________ Robert Lishak Stephen L. McFarland Associate Professor Acting Dean Biological Sciences Graduate School REPRODUCTIVE BIOLOGY OF RELICT TRILLIUM (Trillium reliquum) Melissa Gwynne Brooks Waddell A Thesis Submitted to the Graduate Faculty of Auburn University in Partial Fulfillment of the Requirements for the Degree of Master of Science Auburn, Alabama August 7, 2006 REPRODUCTIVE BIOLOGY OF RELICT TRILLIUM (Trillium reliquum) Melissa Gwynne Brooks Waddell Permission is granted to Auburn University to make copies of this thesis at its discretion, upon request of individuals or institutions and at their expense. The author reserves all publication rights. ______________________________ Signature of Author ______________________________ Date of Graduation iii VITA Melissa Gwynne (Brooks) Waddell, daughter of Robert and Elaine Brooks, graduated from the University of North Alabama in 1996 with a bachelor’s degree in Geography and a minor in Biology. She graduated from Auburn University in 1998, in Horticulture and Landscape Design, and returned to Auburn University to pursue a master’s of science in 1999. Married in May 2004 to Erik Waddell, she accepted a position teaching seventh grade science and environmental science in December 2005. In July 2006, she begins a master’s degree in Education at the University of North Alabama. -
Spring Ephemerals)
1 Sex Lives of Woodland Herbs Spring in the forest begins with a smorgasbord of flowering herbs. Hillsides become carpeted in white, pink, and maroon as trillium flowers open. The yellow bell-shaped flowers and mottled leaves of trout lily blaze in the April sunlight. Yellow, white, and blue violets flower in profusion along trails and creeks. Squirrel corn (Dicentra canadensis) flowers flavor the air with a sweet aroma (Figure Spring Ephemerals). The early woodland herbs, or spring ephemerals, spring forth quickly with leaves, flowers, and fruits and then wither just as summer heats up. Their strategy is to perform energy demanding activities quickly while sunlight abounds under the bare forest trees. In a few short weeks, many of these perennials will shift from a cryptic underground phase to a robust plant with conspicuous flowers only to return to hiding by July. The above ground growth phase is never prolonged. April trillium flowers progress to fruits and seeds in late July. Trout lily (Erythronium americanum), on the other hand, has one of the shortest above ground periods. They send both leaves and flowers to the surface in early April, then six weeks later the plant senesces as the fruit capsule lies quietly on forest soil. Special contractile roots, common among lily members, pull the expanding trout lily corm further beneath the soil. The large, colorful spring ephemeral flowers advertise their pollen and nectar rewards to early flies and bees in the forest. Insects are efficient and abundant pollinators on warm sunny days in the spring forest. Insect pollinators feed intensively with deliberate flights between flowers. -
Northern Hardwoods – Hemlock – White Pine Forest
Classification of the Natural Communities of Massachusetts Terrestrial Communities Descriptions Northern Hardwoods – Hemlock – White Pine Forest Community Code: CT1C000000 State Rank: S5 Concept: A matrix forest of northern areas, with a closed canopy dominated by a mix of deciduous and evergreen trees, with sparse shrub and herbaceous layers. Environmental Setting: The Northern Hardwoods - Hemlock - White Pine Forest is the prevailing, or matrix, forest in higher elevations of western and north-central Massachusetts, with smaller occurrences throughout on north-facing slopes and in ravines. It is an uneven-aged forest with a closed canopy dominated by a mix of long-lived deciduous and evergreen trees, with sparse shrub and herbaceous layers. The forest structure is dominated by single tree falls and replacements, with occasional small to medium blowdown events; stand replacement events are uncommon. The community occurs on neutral to moderately acidic soils with moderate levels of nutrients that retain some moisture except during extreme droughts. Sugar maple leaf litter is relatively high in nitrogen and decomposes rapidly which leads to a shallow layer of leaf litter and rapid turnover of nutrients. Vegetation Description: Dominant and characteristic species of Northern Hardwoods - Hemlock - White Pine Forests occur in different combinations between and within occurrences: occurrences are generally predominantly deciduous with scattered hemlocks and white pines, but may have internal patches of nearly pure conifers. Canopies include variable combinations of sugar maple (Acer saccharum), white ash (Fraxinus americana), yellow birch (Betula alleghaniensis), American beech (Fagus grandifolia), black cherry (Prunus serotina), red oak (Quercus rubra), bitternut hickory (Carya cordiformis), eastern hemlock (Tsuga canadensis), and, usually, emergent white pine (Pinus strobus). -
Identifying Organisms Answer the Following Questions Using Information from the Textbook
NAME DATE CLASS Chapter 15 Use with Section 3 REINFORCEMENT Identifying Organisms Answer the following questions using information from the textbook. 1. Why don’t scientists use common names to identify organisms?____________________________ 2. Why are scientific names important? Give four functions for scientific names. a. b. c. d. 3. The system of ______________________________ gives each organism a unique scientific name. Use the key to species of birch trees below to answer the questions that follow. 1a. bark dark, reddish-brown, yellowish-brown to black . go to 2 1b. bark creamy white, pinkish, or gray . go to 6 2a. bark and twigs with wintergreen fragrance when cut . go to 3 2b. bark and twigs without a fragrance when cut . go to 5 3a. leaves with 8–12 pairs of veins . go to 4 3b. leaves with 4–6 pairs of veins . Betula uber 4a. bark dark red to almost black; scales smooth, 6–12 mm long . Betula lenta 4b. bark reddish-brown, peeling in loose, ragged sheets, scales hairy, 5–7 mm . Betula alleghaniensis 5a. branchlets covered near tip with many small glands, Rocky Mountains or Western Canada . Betula occidentalis 5b. branchlets smooth, shiny, no glands present, eastern U.S. Betula nigra 6a. leaves hairy on lower surface . go to 7 6b. leaves smooth, hairless underside . go to 8 7a. leaves 5–13 cm long, pointed tip . Betula papyrifer 7b. leaves 3–7 cm long, pointed tip, winter buds shiny . Betula pendula 8a. bark dull gray to grayish-white, smooth and not peeling . Betula populifolia 8b. bark white to pinkish-white, peeling . -
Joint Phylogenetic Estimation of Geographic Movements and Biome Shifts During the Global Diversification of Viburnum
Copyedited by: YS MANUSCRIPT CATEGORY: Systematic Biology Syst. Biol. 70(1):67–85, 2021 © The Author(s) 2020. Published by Oxford University Press, on behalf of the Society of Systematic Biologists. All rights reserved. For permissions, please email: [email protected] DOI:10.1093/sysbio/syaa027 Advance Access publication April 8, 2020 Joint Phylogenetic Estimation of Geographic Movements and Biome Shifts during the Global Diversification of Viburnum , ,∗ MICHAEL J. LANDIS1 2 ,DEREN A. R. EATON3,WENDY L. CLEMENT4,BRIAN PARK5,ELIZABETH L. SPRIGGS6, , , PATRICK W. SWEENEY7,ERIKA J. EDWARDS2 7, AND MICHAEL J. DONOGHUE2 7 1Department of Biology, Washington University in St. Louis, One Brookings Drive, St. Louis, MO 63130, USA; 2Department of Ecology & Evolutionary Biology, Yale University, PO Box 208106, New Haven, CT 06520, USA; 3Department of Ecology, Evolution & Environmental Biology, Columbia University, New York, NY 10027, USA; 4Department of Biology, The College of New Jersey, 2000 Pennington Road, Ewing, NJ 08628 USA; 5Department of Plant Biology, University of Georgia, Miller Plant Sciences Building, Athens, GA 30602, USA; 6The Arnold Arboretum of Harvard University, 1300 Centre Street, Boston, MA 02131, USA; and 7Division of Botany, Yale Peabody Museum of Natural History, P.O. Box 208118, New Haven, CT 06520, USA; ∗ Correspondence to be sent to: Department of Biology, Washington University in St. Louis, One Brookings Drive, St. Louis, MO 63130, USA; ∗ Email: [email protected] Downloaded from https://academic.oup.com/sysbio/article/70/1/67/5817834 by Yale University user on 17 December 2020 Received 21 October 2019; reviews returned 13 March 2020; accepted 30 March 2020 Associate Editor: Alexandre Antonelli Abstract.—Phylogeny, molecular sequences, fossils, biogeography, and biome occupancy are all lines of evidence that reflect the singular evolutionary history of a clade, but they are most often studied separately, by first inferring a fossil-dated molecular phylogeny, then mapping on ancestral ranges and biomes inferred from extant species. -
Ordre Dipsacales
Ordre Dipsacales Avant-Propos § Le Vol 18 de FNA n’a pas encore été publié... Les clés présentées ici devraient être modifiées lorsque la parution sera effective. (in prep.) La nouvelle classification phylogénétique APG IV (2016) a confirmé que les genres Sambucus (sureau) et Viburnum (viorne), anciennement de la famille des Caprifoliacées (97), doivent être séparées des Caprifoliacées. Ils doivent plutôt être reliés au genre Adoxa, représenté par l'espèce Adoxa moschatellina, native du nord-ouest de l'Ontario jusque dans l'Ouest du Canada, mais non présente au Québec. Ils font maintenant partie de la famille des Viburnacées (anc. Les Adoxacées). N.B. Le nom à attribuer à la familles est un sujet de controverse et a dû être soumis au vote… (2016) https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4859216/ L'ordre des Dipsacales est donc constitué de 2 familles : les Viburnacées et les Caprifoliacées. Les principales différences entre les deux familles sont que les fleurs des Caprifoliacées sont à symétrie bilatérale (zygomorphes), corolles tubulaires à 2 pétales dorsaux, 2 pétales latéraux et un ventral et leurs fruits secs sont à multiples akènes (sauf Linnaea), alors que chez les Viburnacées, les corolles sont à symétrie radiale (actinomorphes) et leurs fruits sont des drupes, donc à un seul noyau ... Les Viburnacées comprennent maintenant 5 genres : Sambucus, Viburnum et trois autres genres, dont Adoxa, que nous n'avons pas au Québec et Sinadoxa et Tetradoxa que nous n’avons pas non plus… Des 7 genres des Caprifoliacées de la Flore laurentienne, on doit donc en soustraire deux, soit les Sambucus et les Viburnum, mais on doit leur en rajouter 6, pour un total de 10 genres sur notre territoire seulement, soient les Diervilla, Dipsacus, Knautia, Linnaea, Lonicera, Succisella, Symphoricarpos, Triosteum, Valeriana et Wiegela.