Educational Posters on Threatened Plant Communities of North Carolina
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Natural Heritage Program List of Rare Plant Species of North Carolina 2016
Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Revised February 24, 2017 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org C ur Alleghany rit Ashe Northampton Gates C uc Surry am k Stokes P d Rockingham Caswell Person Vance Warren a e P s n Hertford e qu Chowan r Granville q ot ui a Mountains Watauga Halifax m nk an Wilkes Yadkin s Mitchell Avery Forsyth Orange Guilford Franklin Bertie Alamance Durham Nash Yancey Alexander Madison Caldwell Davie Edgecombe Washington Tyrrell Iredell Martin Dare Burke Davidson Wake McDowell Randolph Chatham Wilson Buncombe Catawba Rowan Beaufort Haywood Pitt Swain Hyde Lee Lincoln Greene Rutherford Johnston Graham Henderson Jackson Cabarrus Montgomery Harnett Cleveland Wayne Polk Gaston Stanly Cherokee Macon Transylvania Lenoir Mecklenburg Moore Clay Pamlico Hoke Union d Cumberland Jones Anson on Sampson hm Duplin ic Craven Piedmont R nd tla Onslow Carteret co S Robeson Bladen Pender Sandhills Columbus New Hanover Tidewater Coastal Plain Brunswick THE COUNTIES AND PHYSIOGRAPHIC PROVINCES OF NORTH CAROLINA Natural Heritage Program List of Rare Plant Species of North Carolina 2016 Compiled by Laura Gadd Robinson, Botanist John T. Finnegan, Information Systems Manager North Carolina Natural Heritage Program N.C. Department of Natural and Cultural Resources Raleigh, NC 27699-1651 www.ncnhp.org This list is dynamic and is revised frequently as new data become available. New species are added to the list, and others are dropped from the list as appropriate. -
Sarracenias Aquascapes Seed Grown Hybrids Dutch Treats Collector's
AQUASCAPES UNLIMITED, INC PO Box 364, Pipersville PA 18947 Phone: 215-766-8151, Fax: 215-766-8986 www.aquascapesunlimited.com EMAIL: [email protected] Spring 2014 Our Sarracenias are sold in small, medium and large sizes. The availability is indicated in the chart below with an X=Avail . The pricing reflects age and size: Small - $1.95 (1-2 Years) Multiples of 6, Medium - $3.95 (2-3 Years) Multiples of 5, Large - $8.95 (3-4Years) Multiples of 4. Sarracenias Botanical Name Common Name Small Med. Large Sarracenia alata Pale Pitcher X X X Sarracenia flava Yellow Trumpet X X Sarracenia leucophylla White Trumpet X X Sarracenia leucophylla 'Tarnock' ‘Tarnock’ X X Sarracenia psittacina Parrot Pitcher X Sarracenia purpurea Purple Pitcher X X X Sarracenia rubra Sweet Pitcher X X S. rubra ssp. jonesii (all green) Sweet Pitcher (all green) X Sarracenia x UNC Hybrid ‘Dixie Lace’ X X Sarracenia x UNC Hybrid ‘Doodle Bug’ X Sarracenia x UNC Hybrid ‘Mardi Gras’ X X Sarracenia x UNC Hybrid ‘Red Bug’ X Aquascapes Seed Grown Hybrids Sarracenia Hybrid Botanical Name Small Med. Large S. x areolata S. leucophylla x alata X X X S. x catesbaei S. purp x flava X X X S. readii x moorei S. (leuco x rubra j) (lxf) X X S. x readii All Green S. leuco x rubra jonsii X S. x moorei S. flava x leucophylla X S. x formosa (Limited) S. psitt x minor X Dutch Treats Botanical Name Common Name Size Price S. x 'Farnhamii ' Sarracenia x 'Farnhamii ' PL/72 3.95 S. -
Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae
OPEN ACCESS JCTS Article SERIES B Creation and Carnivory in the Pitcher Plants of Nepenthaceae and Sarraceniaceae R.W. Sanders and T.C. Wood Core Academy of Science, Dayton, TN Abstract The morphological adaptations of carnivorous plants and taxonomic distributions of those adaptations are reviewed, as are the conflicting classifications of the plants based on the adaptations, reproductive morphology, and DNA sequences. To begin developing a creationist understanding of the origin of plant carnivory, we here focus specifically on pitcher plants of Nepenthaceae and Sarraceniaceae because their popularity as cultivated curiosities has generated a literature resource amenable to baraminological analysis. Hybridization records were augmented by total nucleotide differences to assess species similarities. Nonhybridizing species falling within the molecular range of hybridizing species were included in the monobaramin of the hybridizing species. The combined data support each of the three genera of the Sarraceniaceae as a monobaramin, but the three could not be combined into a larger monobaramin. With the Nepenthaceae, the data unequivocally place 73% of the species in a single monobaramin, strongly suggesting the whole genus (and, thus, family) is a monobaramin. The lack of variation in the carnivorous habit provides no evidence for the intrabaraminic origin of carnivory from non-carnivorous plants. An array of fascinating symbiotic relationships of pitchers in some species with unusual bacteria, insects, and vertebrates are known and suggest the origin of carnivory from benign functions of the adaptive structures. However, these symbioses still do not account for the apparent complex design for carnivory characteristic of all species in the two families. Editor: J.W. -
Carnivorous Plant Newsletter V42 N3 September 2013
Technical Refereed Contribution Phylogeny and biogeography of the Sarraceniaceae JOHN BRITTNACHER • Ashland, Oregon • USA • [email protected] Keywords: History: Sarraceniaceae evolution The carnivorous plant family Sarraceniaceae in the order Ericales consists of three genera: Dar- lingtonia, Heliamphora, and Sarracenia. Darlingtonia is represented by one species that is found in northern California and western Oregon. The genus Heliamphora currently has 23 recognized species all of which are native to the Guiana Highlands primarily in Venezuela with some spillover across the borders into Brazil and Guyana. Sarracenia has 15 species and subspecies, all but one of which are located in the southeastern USA. The range of Sarracenia purpurea extends into the northern USA and Canada. Closely related families in the plant order Ericales include the Roridu- laceae consisting of two sticky-leaved carnivorous plant species, Actinidiaceae, the Chinese goose- berry family, Cyrillaceae, which includes the common wetland plant Cyrilla racemiflora, and the family Clethraceae, which also has wetland plants including Clethra alnifolia. The rather charismatic plants of the Sarraceniaceae have drawn attention since the mid 19th century from botanists trying to understand how they came into being, how the genera are related to each other, and how they came to have such disjunct distributions. Before the advent of DNA sequencing it was very difficult to determine their relationships. Macfarlane (1889, 1893) proposed a phylogeny of the Sarraceniaceae based on his judgment of the overlap in features of the adult pitchers and his assumption that Nepenthes is a member of the family (Fig. 1a). He based his phy- logeny on the idea that the pitchers are produced from the fusion of two to five leaflets. -
2019 Domain Management Plan
Domain Management Plan 2019-2029 FINAL DRAFT 12/20/2019 Owner Contact: Amy Turner, Ph.D., CWB Director of Environmental Stewardship and Sustainability The University of the South Sewanee, Tennessee Office: 931-598-1447 Office: Cleveland Annex 110C Email: [email protected] Reviewed by: The Nature Conservancy Forest Stewards Guild ____________________________________________________________________________ Tract Location: Franklin and Marion Counties, Tennessee Centroid Latitude 35.982963 Longitude -85.344382 Tract Size: 13,036 acres | 5,275 hectares Land Manager: Office of Environmental Stewardship and Sustainability, The University of the South, Sewanee, Tennessee 2 Executive Summary The primary objective of this management plan is to provide a framework to outline future management and outline operations for the Office of Environmental Stewardship and Sustainability (OESS) over the next ten years. In this plan, we will briefly introduce the physical and biological setting, past land use, and current uses of the Domain. The remainder of the plan consists of an assessment of the forest, which has been divided into six conservation areas. These conservation areas contain multiple management compartments, and the six areas have similarities in topographical position and past land use. Finally, the desired future condition and project summary of each conservation area and compartment has been outlined. Background The University of the South consists of an academic campus (382 acres) with adjacent commercial and residential areas (783 acres) that are embedded within and surrounded by diverse natural lands (11,838 acres). The term “Domain” is used interchangeably to describe both the entire ~13,000 acres and the 11,800-acre natural land matrix (also referred to as the “Greater Domain”). -
Evolutionary History of Floral Key Innovations in Angiosperms Elisabeth Reyes
Evolutionary history of floral key innovations in angiosperms Elisabeth Reyes To cite this version: Elisabeth Reyes. Evolutionary history of floral key innovations in angiosperms. Botanics. Université Paris Saclay (COmUE), 2016. English. NNT : 2016SACLS489. tel-01443353 HAL Id: tel-01443353 https://tel.archives-ouvertes.fr/tel-01443353 Submitted on 23 Jan 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. NNT : 2016SACLS489 THESE DE DOCTORAT DE L’UNIVERSITE PARIS-SACLAY, préparée à l’Université Paris-Sud ÉCOLE DOCTORALE N° 567 Sciences du Végétal : du Gène à l’Ecosystème Spécialité de Doctorat : Biologie Par Mme Elisabeth Reyes Evolutionary history of floral key innovations in angiosperms Thèse présentée et soutenue à Orsay, le 13 décembre 2016 : Composition du Jury : M. Ronse de Craene, Louis Directeur de recherche aux Jardins Rapporteur Botaniques Royaux d’Édimbourg M. Forest, Félix Directeur de recherche aux Jardins Rapporteur Botaniques Royaux de Kew Mme. Damerval, Catherine Directrice de recherche au Moulon Président du jury M. Lowry, Porter Curateur en chef aux Jardins Examinateur Botaniques du Missouri M. Haevermans, Thomas Maître de conférences au MNHN Examinateur Mme. Nadot, Sophie Professeur à l’Université Paris-Sud Directeur de thèse M. -
Reproductive Ecology of Granite Outcrop Plants from the South-Eastern United States
JournalJournal of theof the Royal Royal Society Society of Westernof Western Australia, Australia, 80(3), 80:123-129, September 1997 1997 Reproductive ecology of granite outcrop plants from the south-eastern United States R Wyatt Institute of Ecology, University of Georgia, Athens, Georgia 30602 USA email: [email protected] Abstract Most of the Piedmont Physiographic Province of the southeastern United States is covered with mixed mesophytic forest of oaks, hickories, and pines. Within this “sea”, however, are “islands” of exposed granite and gneiss. A characteristic, and largely endemic, assemblage of plants has adapted to the environmental extremes that bare rock provides by strongly altering their morphology, physiology, and life history. With respect to their reproductive ecology, however, these plants appear very similar to their congeners and to the Piedmont flora as a whole. Except for ant-pollinated Diamorpha smallii, most species show the expected range of pollen vectors, including wind, bees, flies, butterflies, moths and one species of hummingbird. Fruit and/or seed dispersal appears to be highly localised and effected primarily by wind and water. If anything, most species appear to possess adaptations against long-distance dispersal, which would carry propagules into the inhospitable matrix of oak-hickory-pine forest. Mating systems are variable, including examples of both self-compatible and self-incompatible taxa. Consistent with the expectation of low gene flow between populations on isolated outcrops, genetic data show strong differentiation and suggest the potential for genetic drift and/or natural selection to result in divergence. Some of the endemic species on granite outcrops have originated by allopolyploidy, whereas others appear to represent products of more gradual divergence in geographical isolation. -
Rare Plants of Louisiana
Rare Plants of Louisiana Agalinis filicaulis - purple false-foxglove Figwort Family (Scrophulariaceae) Rarity Rank: S2/G3G4 Range: AL, FL, LA, MS Recognition: Photo by John Hays • Short annual, 10 to 50 cm tall, with stems finely wiry, spindly • Stems simple to few-branched • Leaves opposite, scale-like, about 1mm long, barely perceptible to the unaided eye • Flowers few in number, mostly born singly or in pairs from the highest node of a branchlet • Pedicels filiform, 5 to 10 mm long, subtending bracts minute • Calyx 2 mm long, lobes short-deltoid, with broad shallow sinuses between lobes • Corolla lavender-pink, without lines or spots within, 10 to 13 mm long, exterior glabrous • Capsule globe-like, nearly half exerted from calyx Flowering Time: September to November Light Requirement: Full sun to partial shade Wetland Indicator Status: FAC – similar likelihood of occurring in both wetlands and non-wetlands Habitat: Wet longleaf pine flatwoods savannahs and hillside seepage bogs. Threats: • Conversion of habitat to pine plantations (bedding, dense tree spacing, etc.) • Residential and commercial development • Fire exclusion, allowing invasion of habitat by woody species • Hydrologic alteration directly (e.g. ditching) and indirectly (fire suppression allowing higher tree density and more large-diameter trees) Beneficial Management Practices: • Thinning (during very dry periods), targeting off-site species such as loblolly and slash pines for removal • Prescribed burning, establishing a regime consisting of mostly growing season (May-June) burns Rare Plants of Louisiana LA River Basins: Pearl, Pontchartrain, Mermentau, Calcasieu, Sabine Side view of flower. Photo by John Hays References: Godfrey, R. K. and J. W. Wooten. -
(Sarracenia) Provide a 21St-Century Perspective on Infraspecific Ranks and Interspecific Hybrids: a Modest Proposal* for Appropriate Recognition and Usage
Systematic Botany (2014), 39(3) © Copyright 2014 by the American Society of Plant Taxonomists DOI 10.1600/036364414X681473 Date of publication 05/27/2014 Pitcher Plants (Sarracenia) Provide a 21st-Century Perspective on Infraspecific Ranks and Interspecific Hybrids: A Modest Proposal* for Appropriate Recognition and Usage Aaron M. Ellison,1,5 Charles C. Davis,2 Patrick J. Calie,3 and Robert F. C. Naczi4 1Harvard University, Harvard Forest, 324 North Main Street, Petersham, Massachusetts 01366, U. S. A. 2Harvard University Herbaria, Department of Organismic and Evolutionary Biology, 22 Divinity Avenue, Cambridge, Massachusetts 02138, U. S. A. 3Eastern Kentucky University, Department of Biological Sciences, 521 Lancaster Avenue, Richmond, Kentucky 40475, U. S. A. 4The New York Botanical Garden, 2900 Southern Boulevard, Bronx, New York 10458, U. S. A. 5Author for correspondence ([email protected]) Communicating Editor: Chuck Bell Abstract—The taxonomic use of infraspecific ranks (subspecies, variety, subvariety, form, and subform), and the formal recognition of interspecific hybrid taxa, is permitted by the International Code of Nomenclature for algae, fungi, and plants. However, considerable confusion regarding the biological and systematic merits is caused by current practice in the use of infraspecific ranks, which obscures the meaningful variability on which natural selection operates, and by the formal recognition of those interspecific hybrids that lack the potential for inter-lineage gene flow. These issues also may have pragmatic and legal consequences, especially regarding the legal delimitation and management of threatened and endangered species. A detailed comparison of three contemporary floras highlights the degree to which infraspecific and interspecific variation are treated inconsistently. -
Delete Darlingtonia Californica from Appendix II
Prop. 11.11 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II Proposals resulting from reviews by the Plants Committees A. Proposal Delete Darlingtonia californica from Appendix II. B. Proponent Swiss Confederation. C. Supporting Statement 1. Taxonomy 1.1 Class: Dicotyledonae 1.2 Order: Nepenthales 1.3 Family: Sarraceniaceae 1.4 Genus: Darlingtonia 1.4.1: Species: Darlingtonia californica Torrey 1.5 Scientific synonyms: 1.6 Common names: English: California pitcherplant, cobra lily French: Spanish: 1.7 Code numbers: 2. Biological Parameters 2.1 Distribution USA, West Coast, from Oregon to North California on a 160 km long strip between Roseburg (Oregon) and Santa Rosa (California). Along the coast, it appears in northern Curry County and extends north sporadically to Sandlake in Tillamook County. 2.2 Habitat availability From sea level to 2800 m. 2.3 Population status In the center of its range from Del Norte-Trinity-Shasta-Siskiyou County (California) to Curry & Josephine County (Oregon) this species is rather abundant. It is not uncommon throughout this area to find several colonies numbering between 1000-3000 specimens with abundant habitat for expansion and few threats to their survival because many locations are very difficult to access (Rondeau, pers.comm. to von Arx, 1999). At the southern limit of its range in Nevada County it is quite abundant and grows on remote sites; while in 3 nearby Counties (Butte, Plumas and Sierra) it has never been abundant, and it is now scattered and diminishing due to the combined effects of logging and succession into other vegetation types. Prop. 11.11 – p. -
Anatomy and Affinities of Penthorum Melanie Lynn Haskins
University of Richmond UR Scholarship Repository Biology Faculty Publications Biology 2-1987 Anatomy and Affinities of Penthorum Melanie Lynn Haskins W. John Hayden University of Richmond, [email protected] Follow this and additional works at: http://scholarship.richmond.edu/biology-faculty-publications Part of the Botany Commons, Other Plant Sciences Commons, and the Plant Biology Commons Recommended Citation Haskins, Melanie Lynn, and W. John Hayden. "Anatomy and Affinities of Penthorum." American Journal of Botany 74, no. 2 (February 1987): 164-77. This Article is brought to you for free and open access by the Biology at UR Scholarship Repository. It has been accepted for inclusion in Biology Faculty Publications by an authorized administrator of UR Scholarship Repository. For more information, please contact [email protected]. Amer. J. Bot. 74(2): 164-177. 1987. ANATOMY AND AFFINITIES OF PENTHORUM' MELANIE L. HASKINS AND W. JOHN HAYDEN Department of Biology, University of Richmond, Richmond, Virginia 23173 ABSTRACT The genus Penthorum L. consists of two species of perennial herbs, P. sedoides of eastern North America and P. chinense ofeastern Asia. Pentho rum has long been considered intermediate between Crassulaceae and Saxifragaceae. An anatomical study of both species was undertaken to contribute to a better understanding of the relationships ofthese plants. Prominent anatomical features of Penthorum include: an aerenchymatous cortex and closely-spaced collateral vascular bundles of stems; one-trace unilacunar nodes; brochidodromous venation, rosoid teeth bearing hydathodes, and anomocytic stomata of leaves; angular vessel elements with many-barred scalariform perforation plates and alternate to scattered intervascular pits; thin-walled non septate fiber-tracheids; abundant homocellular erect uniseriate and biseriate rays; and absence of axial xylem parenchyma. -
Conservation Genetic Inferences in the Carnivorous Pitcher Plant Sarracenia Alata (Sarraceniaceae)
Conserv Genet DOI 10.1007/s10592-010-0095-7 RESEARCH ARTICLE Conservation genetic inferences in the carnivorous pitcher plant Sarracenia alata (Sarraceniaceae) Margaret M. Koopman • Bryan C. Carstens Received: 16 September 2009 / Accepted: 2 May 2010 Ó Springer Science+Business Media B.V. 2010 Abstract Conservation geneticists make inferences about nerable to increased competition following fire suppression their focal species from genetic data, and then use these (Schnell 1976; Weiss 1980; Folkerts 1982; Barker and inferences to inform conservation decisions. Since different Williamson 1988; Brewer 2005), habitat fragmentation and biological processes can produce similar patterns of genetic degradation as well as overcollecting (CITES May 2009, diversity, we advocate an approach to data analysis that IUCN Red List). Among the most important habitats for considers the full range of evolutionary forces and attempts Sarracenia in this region are the Longleaf pine savannahs, to evaluate their relative contributions in an objective herb-dominated wetlands that were once extensive manner. Here we collect data from microsatellites and throughout the Gulf Coast of North America, but have been chloroplast loci and use these data to explore models of severely reduced in the last several hundred years. In historical demography in the carnivorous Pitcher Plant, Louisiana only 1–3% of the original Longleaf pine sa- Sarracenia alata. Findings indicate that populations of vannahs remain (Conservation Habitat Species Assessment S. alata exhibit high degrees of population genetic struc- 16, 36). Sarracenia alata is locally abundant (CITES: LR ture, likely caused by dispersal limitation, and that popu- (nt)) throughout these habitats in Louisiana but remains lation sizes have decreased in western populations and vulnerable to all the pressures that jeopardize more rare increased in eastern populations.