Ecological Inventory of Fall Mountain State Forest
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ABSTRACT CULATTA, KATHERINE EMILY. Taxonomy, Genetic
ABSTRACT CULATTA, KATHERINE EMILY. Taxonomy, Genetic Diversity, and Status Assessment of Nuphar sagittifolia (Nymphaeaceae). (Under the direction of Dr. Alexander Krings and Dr. Ross Whetten). Nuphar sagittifolia (Walter) Pursh (Nymphaeaceae), Cape Fear spatterdock, is an aquatic macrophyte considered endemic to the Atlantic Coastal Plain and of conservation concern in North Carolina, South Carolina, and Virginia. The existence of populations of unclear taxonomic identity has precluded assessment of the number of populations, distribution, and conservation needs of N. sagittifolia. Thus, the first objective of this thesis was to re-assess the circumscription of the species by evaluating four taxonomic hypotheses: 1) Populations of Nuphar in the N. sagittifolia range, including morphological intermediates, are members of a single polymorphic species; 2) Morphological intermediates in the N. sagittifolia range are hybrids between N. advena subsp. advena and N. sagittifolia; 3) Morphological intermediates are variants of N. advena subsp. advena or N. sagittifolia; 4) Intermediates, distinct from both N. advena subsp. advena and N. sagittifolia, are either disjunct populations of N. advena subsp. ulvacea or members of an undescribed taxon. The second objective was to summarize information on the taxonomy, biology, distribution, and genetic diversity of N. sagittifolia s.s to inform conservation decisions. Approximately 30 individuals from each of 21 populations of Nuphar across the N. sagittifolia range, and the type populations of N. advena subsp. advena, N. advena subsp. ulvacea, and N. sagittifolia were included in genetic and morphological analyses. Individuals were genotyped across 26 SNP loci identified for this study, and 31 leaf, flower and fruit morphological characters were measured. STRUCTURE analysis identified three genetic groups with corresponding morphological differences in the N. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Present-Day Genetic Structure of the Holoparasite Conopholis Americana
Int. J. Plant Sci. 177(2):132–144. 2016. q 2015 by The University of Chicago. All rights reserved. 1058-5893/2016/17702-0003$15.00 DOI: 10.1086/684180 PRESENT-DAY GENETIC STRUCTURE OF THE HOLOPARASITE CONOPHOLIS AMERICANA (OROBANCHACEAE) IN EASTERN NORTH AMERICA AND THE LOCATION OF ITS REFUGIA DURING THE LAST GLACIAL CYCLE Anuar Rodrigues1,* and Saša Stefanović* *Department of Biology, University of Toronto, Mississauga, Ontario L5L 1C6, Canada Editor: Félix Forest Premise of research. Understanding how various organisms respond to previous changes in climate could provide insight into how they may respond or adapt to the current changes. Conopholis americana has a broad distribution across eastern North America, covering both previously glaciated and unglaciated regions. In this study, we investigated the postglacial history and phylogeographic structure of this parasitic plant spe- cies to characterize its genetic variation and structure and to identify the number and locations of refugia. Methodology. Molecular data from 10 microsatellite markers and DNA sequences from the plastid gene/ introns (clpP) were obtained for 281 individuals sampled from 75 populations spanning the current range of the species in eastern North America and analyzed using a variety of phylogeographic methods. Distribution modeling was carried out to determine regions with relatively suitable climate niches for populations at the Last Glacial Maximum (LGM) and present. Pivotal results. We inferred the persistence of a minimum of two glacial refugia for C. americana at the LGM, one in north-central Florida and southern Alabama and another in the Appalachian Mountains near the southern tip of the Blue Ridge Mountains. -
Aquatic Vascular Plant Species Distribution Maps
Appendix 11.5.1: Aquatic Vascular Plant Species Distribution Maps These distribution maps are for 116 aquatic vascular macrophyte species (Table 1). Aquatic designation follows habitat descriptions in Haines and Vining (1998), and includes submergent, floating and some emergent species. See Appendix 11.4 for list of species. Also included in Appendix 11.4 is the number of HUC-10 watersheds from which each taxon has been recorded, and the county-level distributions. Data are from nine sources, as compiled in the MABP database (plus a few additional records derived from ancilliary information contained in reports from two fisheries surveys in the Upper St. John basin organized by The Nature Conservancy). With the exception of the University of Maine herbarium records, most locations represent point samples (coordinates were provided in data sources or derived by MABP from site descriptions in data sources). The herbarium data are identified only to township. In the species distribution maps, town-level records are indicated by center-points (centroids). Figure 1 on this page shows as polygons the towns where taxon records are identified only at the town level. Data Sources: MABP ID MABP DataSet Name Provider 7 Rare taxa from MNAP lake plant surveys D. Cameron, MNAP 8 Lake plant surveys D. Cameron, MNAP 35 Acadia National Park plant survey C. Greene et al. 63 Lake plant surveys A. Dieffenbacher-Krall 71 Natural Heritage Database (rare plants) MNAP 91 University of Maine herbarium database C. Campbell 183 Natural Heritage Database (delisted species) MNAP 194 Rapid bioassessment surveys D. Cameron, MNAP 207 Invasive aquatic plant records MDEP Maps are in alphabetical order by species name. -
Ficha Catalográfica Online
UNIVERSIDADE ESTADUAL DE CAMPINAS INSTITUTO DE BIOLOGIA – IB SUZANA MARIA DOS SANTOS COSTA SYSTEMATIC STUDIES IN CRYPTANGIEAE (CYPERACEAE) ESTUDOS FILOGENÉTICOS E SISTEMÁTICOS EM CRYPTANGIEAE CAMPINAS, SÃO PAULO 2018 SUZANA MARIA DOS SANTOS COSTA SYSTEMATIC STUDIES IN CRYPTANGIEAE (CYPERACEAE) ESTUDOS FILOGENÉTICOS E SISTEMÁTICOS EM CRYPTANGIEAE Thesis presented to the Institute of Biology of the University of Campinas in partial fulfillment of the requirements for the degree of PhD in Plant Biology Tese apresentada ao Instituto de Biologia da Universidade Estadual de Campinas como parte dos requisitos exigidos para a obtenção do Título de Doutora em Biologia Vegetal ESTE ARQUIVO DIGITAL CORRESPONDE À VERSÃO FINAL DA TESE DEFENDIDA PELA ALUNA Suzana Maria dos Santos Costa E ORIENTADA PELA Profa. Maria do Carmo Estanislau do Amaral (UNICAMP) E CO- ORIENTADA pelo Prof. William Wayt Thomas (NYBG). Orientadora: Maria do Carmo Estanislau do Amaral Co-Orientador: William Wayt Thomas CAMPINAS, SÃO PAULO 2018 Agência(s) de fomento e nº(s) de processo(s): CNPq, 142322/2015-6; CAPES Ficha catalográfica Universidade Estadual de Campinas Biblioteca do Instituto de Biologia Mara Janaina de Oliveira - CRB 8/6972 Costa, Suzana Maria dos Santos, 1987- C823s CosSystematic studies in Cryptangieae (Cyperaceae) / Suzana Maria dos Santos Costa. – Campinas, SP : [s.n.], 2018. CosOrientador: Maria do Carmo Estanislau do Amaral. CosCoorientador: William Wayt Thomas. CosTese (doutorado) – Universidade Estadual de Campinas, Instituto de Biologia. Cos1. Savanas. 2. Campinarana. 3. Campos rupestres. 4. Filogenia - Aspectos moleculares. 5. Cyperaceae. I. Amaral, Maria do Carmo Estanislau do, 1958-. II. Thomas, William Wayt, 1951-. III. Universidade Estadual de Campinas. Instituto de Biologia. IV. Título. -
Arctic and Boreal Plant Species Decline at Their Southern Range Limits in the Rocky Mountains
Ecology Letters, (2017) 20: 166–174 doi: 10.1111/ele.12718 LETTER Arctic and boreal plant species decline at their southern range limits in the Rocky Mountains Abstract Peter Lesica1,2* and Climate change is predicted to cause a decline in warm-margin plant populations, but this hypoth- Elizabeth E. Crone3 esis has rarely been tested. Understanding which species and habitats are most likely to be affected is critical for adaptive management and conservation. We monitored the density of 46 populations representing 28 species of arctic-alpine or boreal plants at the southern margin of their ranges in the Rocky Mountains of Montana, USA, between 1988 and 2014 and analysed population trends and relationships to phylogeny and habitat. Marginal populations declined overall during the past two decades; however, the mean trend for 18 dicot populations was À5.8% per year, but only À0.4% per year for the 28 populations of monocots and pteridophytes. Declines in the size of peripheral populations did not differ significantly among tundra, fen and forest habitats. Results of our study support predicted effects of climate change and suggest that vulnerability may depend on phylogeny or associated anatomical/physiological attributes. Keywords arctic-alpine plants, boreal plants, climate change, fens, marginal populations, peripheral popula- tions, range margins, Rocky Mountains. Ecology Letters (2017) 20: 166–174 2009; Sexton et al. 2009; Brusca et al. 2013), which suggests INTRODUCTION that in some cases climate does not determine a species’ range. Climate of the earth is changing at an unprecedented rate Nonetheless, most plant ecologists believe that climate is an (Jackson & Overpeck 2000; IPCC 2013) and is predicted to important factor determining geographic range limits. -
Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date
Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date EQUISETACEAE HORSETAIL FAMILY Equisetum arvense L. Field Horsetail FF Equisetum fluviatile L. Water Horsetail LRB Equisetum hyemale L. ssp. affine (Engelm.) Stone Common Scouring-rush BS Equisetum laevigatum A. Braun Smooth Scouring-rush WM Equisetum variegatum Scheich. ex Fried. ssp. Small Horsetail LRB Variegatum DENNSTAEDIACEAE BRACKEN FAMILY Pteridium aquilinum (L.) Kuhn Bracken-Fern COF DRYOPTERIDACEAE TRUE FERN FAMILILY Athyrium filix-femina (L.) Roth ssp. angustum (Willd.) Northeastern Lady Fern FF Clausen Cystopteris bulbifera (L.) Bernh. Bulblet Fern FF Dryopteris carthusiana (Villars) H.P. Fuchs Spinulose Woodfern FF Matteuccia struthiopteris (L.) Tod. Ostrich Fern FF Onoclea sensibilis L. Sensitive Fern FF Polystichum acrostichoides (Michaux) Schott Christmas Fern FF ADDER’S-TONGUE- OPHIOGLOSSACEAE FERN FAMILY Botrychium virginianum (L.) Sw. Rattlesnake Fern FF FLOWERING FERN OSMUNDACEAE FAMILY Osmunda regalis L. Royal Fern WM POLYPODIACEAE POLYPODY FAMILY Polypodium virginianum L. Rock Polypody FF MAIDENHAIR FERN PTERIDACEAE FAMILY Adiantum pedatum L. ssp. pedatum Northern Maidenhair Fern FF THELYPTERIDACEAE MARSH FERN FAMILY Thelypteris palustris (Salisb.) Schott Marsh Fern WM LYCOPODIACEAE CLUB MOSS FAMILY Lycopodium lucidulum Michaux Shining Clubmoss OF Lycopodium tristachyum Pursh Ground-cedar COF SELAGINELLACEAE SPIKEMOSS FAMILY Selaginella apoda (L.) Fern. Spikemoss LRB CUPRESSACEAE CYPRESS FAMILY Juniperus communis L. Common Juniper Jun-E DS Juniperus virginiana L. Red Cedar Jun-E SD Thuja occidentalis L. White Cedar LRB PINACEAE PINE FAMILY Larix laricina (Duroi) K. Koch Tamarack Jun LRB Pinus banksiana Lambert Jack Pine COF Pinus resinosa Sol. ex Aiton Red Pine Jun-M CF Pinery Provincial Park Vascular Plant List 1 Pinery Provincial Park Vascular Plant List Flowering Latin Name Common Name Community Date Pinus strobus L. -
Maine Coefficient of Conservatism
Coefficient of Coefficient of Scientific Name Common Name Nativity Conservatism Wetness Abies balsamea balsam fir native 3 0 Abies concolor white fir non‐native 0 Abutilon theophrasti velvetleaf non‐native 0 3 Acalypha rhomboidea common threeseed mercury native 2 3 Acer ginnala Amur maple non‐native 0 Acer negundo boxelder non‐native 0 0 Acer pensylvanicum striped maple native 5 3 Acer platanoides Norway maple non‐native 0 5 Acer pseudoplatanus sycamore maple non‐native 0 Acer rubrum red maple native 2 0 Acer saccharinum silver maple native 6 ‐3 Acer saccharum sugar maple native 5 3 Acer spicatum mountain maple native 6 3 Acer x freemanii red maple x silver maple native 2 0 Achillea millefolium common yarrow non‐native 0 3 Achillea millefolium var. borealis common yarrow non‐native 0 3 Achillea millefolium var. millefolium common yarrow non‐native 0 3 Achillea millefolium var. occidentalis common yarrow non‐native 0 3 Achillea ptarmica sneezeweed non‐native 0 3 Acinos arvensis basil thyme non‐native 0 Aconitum napellus Venus' chariot non‐native 0 Acorus americanus sweetflag native 6 ‐5 Acorus calamus calamus native 6 ‐5 Actaea pachypoda white baneberry native 7 5 Actaea racemosa black baneberry non‐native 0 Actaea rubra red baneberry native 7 3 Actinidia arguta tara vine non‐native 0 Adiantum aleuticum Aleutian maidenhair native 9 3 Adiantum pedatum northern maidenhair native 8 3 Adlumia fungosa allegheny vine native 7 Aegopodium podagraria bishop's goutweed non‐native 0 0 Coefficient of Coefficient of Scientific Name Common Name Nativity -
Invisible Connections: Introduction to Parasitic Plants Dr
Invisible Connections: Introduction to Parasitic Plants Dr. Vanessa Beauchamp Towson University What is a parasite? • An organism that lives in or on an organism of another species (its host) and benefits by deriving nutrients at the other's expense. Symbiosis https://www.superpharmacy.com.au/blog/parasites-protozoa-worms-ectoparasites Food acquisition in plants: Autotrophy Heterotrophs (“different feeding”) • True parasites: obtain carbon compounds from host plants through haustoria. • Myco-heterotrophs: obtain carbon compounds from host plants via Image Credit: Flickr User wackybadger, via CC mycorrhizal fungal connection. • Carnivorous plants (not parasitic): obtain nutrients (phosphorus, https://commons.wikimedia.org/wiki/File:Pin nitrogen) from trapped insects. k_indian_pipes.jpg http://www.welivealot.com/venus-flytrap- facts-for-kids/ Parasite vs. Epiphyte https://chatham.ces.ncsu.edu/2014/12/does-mistletoe-harm-trees-2/ By © Hans Hillewaert /, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=6289695 True Parasitic Plants • Gains all or part of its nutrition from another plant (the host). • Does not contribute to the benefit of the host and, in some cases, causing extreme damage to the host. • Specialized peg-like root (haustorium) to penetrate host plants. https://www.britannica.com/plant/parasitic-plant https://chatham.ces.ncsu.edu/2014/12/does-mistletoe-harm-trees-2/ Diversity of parasitic plants Eudicots • Parasitism has evolved independently at least 12 times within the plant kingdom. • Approximately 4,500 parasitic species in Monocots 28 families. • Found in eudicots and basal angiosperms • 1% of the dicot angiosperm species • No monocot angiosperm species Basal angiosperms Annu. Rev. Plant Biol. 2016.67:643-667 True Parasitic Plants https://www.alamy.com/parasitic-dodder-plant-cuscuta-showing-penetration-parasitic-haustor The defining structural feature of a parasitic plant is the haustorium. -
Wool-Grass – Mannagrass Mixed Shrub Marsh
Wool-grass – Mannagrass Mixed Shrub Marsh System: Palustrine Subsystem: Herbaceous PA Ecological Group(s): Vernal Pool Global Rank: GNR State Rank: S4 General Description The Wool-grass – mannagrass mixed shrub marsh pool occurs in seasonally to somewhat permanently inundated depressions throughout Pennsylvania. The type can be described as a seasonally flooded, herbaceous swamp with well defined boundaries; some pools of this type exhibit somewhat poorly defined boundaries. The surrounding plant community varies with region, soils, and geology. The pools are generally deeper than those of the Rice cutgrass – bulrush marsh pool and may not dry completely over the summer months. This community is characterized as an open, seasonally to permanently flooded depression, dominated by herbaceous and shrubby species; wool-grass (Scirpus cyperinus) is usually dominant. Common co- dominant and associate species include floating mannagrass (Glyceria septentrionalis), rattlesnake mannagrass (Glyceria canadensis), rice cutgrass (Leersia oryzoides), pale meadowgrass (Torreyochloa pallida), sedges (e.g. Carex crinita, C. lurida, C. lupulina, C. vesicaria, C. folliculata), three-way sedge (Dulichium arundinaceum), mild water-pepper (Persicaria hydropiperoides), marsh-purslane (Ludwigia palustris), marsh St. Johns-wort (Triadenum fraseri). The federally endangered species, northeastern bulrush (Scirpus ancistrochaetus), is also found in this type. Shrubs include hardhack (Spiraea tomentosa), meadow-sweet (S. alba), northern arrow-wood (Viburnum recognitum), highbush blueberry (Vaccinium corymbosum), and buttonbush (Cephalanthus occidentalis). Canopy trees, which are limited to the pool margins, most often include white oak (Quercus alba), sourgum (Nyssa sylvatica), and red maple (Acer rubrum). Rank Justification Uncommon but not rare; some cause for long-term concern due to declines or other factors. Identification Open, seasonally flooded depression, dominated by herbaceous plants, usually graminoids. -
Carex Barrattii Schwein
New England Plant Conservation Program Conservation and Research Plan Carex barrattii Schwein. & Torr. Barratt's Sedge Prepared by: Penelope C. Sharp Environmental Consultant Northford, Connecticut For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, May 2001 SUMMARY Barratt’s sedge (Carex barrattii) is a regionally rare plant species that ranges from Alabama northward along the Atlantic coastal states to Connecticut. Primarily a species of the Atlantic Coastal Plain, it has also been documented at a number of disjunct sites in Virginia, Tennessee, North Carolina, South Carolina, Georgia, and Alabama. Its presence in New England is limited to Connecticut where there are seven occurrences, five of which are historic. The two extant sites for C. barrattii are in relatively close proximity, and the occurrences may be considered to be sub-populations of a single population. Population size is estimated to exceed 10,000 ramets. The state rank for the species is S1, and it is listed under Connecticut’s Endangered Species Act as State Endangered. The occurrence locations are on private property; therefore, C. barrattii is vulnerable to a number of potential threats including alteration of wetland hydrology and development activities. Natural succession and canopy closure also threaten the species, which appears to produce few fruiting culms under dense shade. Carex barrattii is an obligate wetland species and, in Connecticut, grows in seasonally saturated, acidic, sandy wetlands. In other parts of its range, it is found in wetland depressions in pine barrens, along the shores of rivers and ponds or in peaty bogs.