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SALT TOLERANT PLANTS Recommended for Pender County Landscapes
North Carolina Cooperative Extension NC STATE UNIVERSITY SALT TOLERANT PLANTS Recommended for Pender County Landscapes Pender County Cooperative Extension Urban Horticulture Leaflet 14 Coastal Challenges Plants growing at the beach are subjected to environmental conditions much different than those planted further inland. Factors such as blowing sand, poor soils, high temperatures, and excessive drainage all influence how well plants perform in coastal landscapes, though the most significant effect on growth is salt spray. Most plants will not tolerate salt accumulating on their foliage, making plant selection for beachfront land- scapes particularly challenging. Salt Spray Salt spray is created when waves break on the beach, throwing tiny droplets of salty water into the air. On-shore breezes blow this salt laden air landward where it comes in contact with plant foliage. The amount of salt spray plants receive varies depending on their proximity to the beachfront, creating different vegetation zones as one gets further away from the beachfront. The most salt-tolerant species surviving in the frontal dune area. As distance away from the ocean increases, the level of salt spray decreases, allowing plants with less salt tolerance to survive. Natural Protection The impact of salt spray on plants can be lessened by physically blocking salt laden winds. This occurs naturally in the maritime forest, where beachfront plants protect landward species by creating a layer of foliage that blocks salt spray. It is easy to see this effect on the ocean side of maritime forest plants, which are “sheared” by salt spray, causing them to grow at a slant away from the oceanfront. -
Western Juniper Woodlands of the Pacific Northwest
Western Juniper Woodlands (of the Pacific Northwest) Science Assessment October 6, 1994 Lee E. Eddleman Professor, Rangeland Resources Oregon State University Corvallis, Oregon Patricia M. Miller Assistant Professor Courtesy Rangeland Resources Oregon State University Corvallis, Oregon Richard F. Miller Professor, Rangeland Resources Eastern Oregon Agricultural Research Center Burns, Oregon Patricia L. Dysart Graduate Research Assistant Rangeland Resources Oregon State University Corvallis, Oregon TABLE OF CONTENTS Page EXECUTIVE SUMMARY ........................................... i WESTERN JUNIPER (Juniperus occidentalis Hook. ssp. occidentalis) WOODLANDS. ................................................. 1 Introduction ................................................ 1 Current Status.............................................. 2 Distribution of Western Juniper............................ 2 Holocene Changes in Western Juniper Woodlands ................. 4 Introduction ........................................... 4 Prehistoric Expansion of Juniper .......................... 4 Historic Expansion of Juniper ............................. 6 Conclusions .......................................... 9 Biology of Western Juniper.................................... 11 Physiological Ecology of Western Juniper and Associated Species ...................................... 17 Introduction ........................................... 17 Western Juniper — Patterns in Biomass Allocation............ 17 Western Juniper — Allocation Patterns of Carbon and -
Bolboschoenus Glaucus (Lam.) S.G. Smith, a New Species in the Flora of the Ancient Near East
Veget Hist Archaeobot DOI 10.1007/s00334-011-0305-3 ORIGINAL ARTICLE Bolboschoenus glaucus (Lam.) S.G. Smith, a new species in the flora of the ancient Near East Miche`le M. Wollstonecroft • Zdenka Hroudova´ • Gordon C. Hillman • Dorian Q. Fuller Received: 5 October 2010 / Accepted: 23 May 2011 Ó Springer-Verlag 2011 Abstract Taxonomic advancement in the genus Bolbo- Bolboschoenus in present-day Turkey, indicating that it has schoenus (Cyperaceae, formerly included in the genus a long history of occurrence in this region. The environ- Scirpus) have resulted in the re-classification of the plant mental, ecological and economic implications of this new previously known as Bolboschoenus maritimus (synonym information suggest that it is entirely feasible that this plant Scirpus maritimus) into several closely-related but distinct provided late Pleistocene and Holocene Near Eastern Bolboschoenus species This improved taxonomy is of people with a dependable and possibly a staple food source. importance for archaeobotanical investigations of ancient sites within the temperate zones, where this genus fre- Keywords Bolboschoenus glaucus Á Epipalaeolithic Á quently occurs, because it allows more precise definitions Near East Á Neolithic Á Taxonomy Á Nutlet characteristics of the ecological requirements and growing habits of each species. Moreover, it details the distinct morphological and anatomical characteristics of the fruit (nutlets) of each Introduction species. Using these new nutlet classification criteria, we re-examined charred archaeological specimens which had Bolboschoenus maritimus (sea club-rush) is a semi-aquatic previously been identified as B. maritimus (or S. mariti- species of the Cyperaceae that produces edible nutlets, mus), from five Near Eastern late Pleistocene and early tubers and shoots (Fig. -
Flowering Plants Eudicots Apiales, Gentianales (Except Rubiaceae)
Edited by K. Kubitzki Volume XV Flowering Plants Eudicots Apiales, Gentianales (except Rubiaceae) Joachim W. Kadereit · Volker Bittrich (Eds.) THE FAMILIES AND GENERA OF VASCULAR PLANTS Edited by K. Kubitzki For further volumes see list at the end of the book and: http://www.springer.com/series/1306 The Families and Genera of Vascular Plants Edited by K. Kubitzki Flowering Plants Á Eudicots XV Apiales, Gentianales (except Rubiaceae) Volume Editors: Joachim W. Kadereit • Volker Bittrich With 85 Figures Editors Joachim W. Kadereit Volker Bittrich Johannes Gutenberg Campinas Universita¨t Mainz Brazil Mainz Germany Series Editor Prof. Dr. Klaus Kubitzki Universita¨t Hamburg Biozentrum Klein-Flottbek und Botanischer Garten 22609 Hamburg Germany The Families and Genera of Vascular Plants ISBN 978-3-319-93604-8 ISBN 978-3-319-93605-5 (eBook) https://doi.org/10.1007/978-3-319-93605-5 Library of Congress Control Number: 2018961008 # Springer International Publishing AG, part of Springer Nature 2018 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. -
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 -
Medicinal Practices of Sacred Natural Sites: a Socio-Religious Approach for Successful Implementation of Primary
Medicinal practices of sacred natural sites: a socio-religious approach for successful implementation of primary healthcare services Rajasri Ray and Avik Ray Review Correspondence Abstract Rajasri Ray*, Avik Ray Centre for studies in Ethnobiology, Biodiversity and Background: Sacred groves are model systems that Sustainability (CEiBa), Malda - 732103, West have the potential to contribute to rural healthcare Bengal, India owing to their medicinal floral diversity and strong social acceptance. *Corresponding Author: Rajasri Ray; [email protected] Methods: We examined this idea employing ethnomedicinal plants and their application Ethnobotany Research & Applications documented from sacred groves across India. A total 20:34 (2020) of 65 published documents were shortlisted for the Key words: AYUSH; Ethnomedicine; Medicinal plant; preparation of database and statistical analysis. Sacred grove; Spatial fidelity; Tropical diseases Standard ethnobotanical indices and mapping were used to capture the current trend. Background Results: A total of 1247 species from 152 families Human-nature interaction has been long entwined in has been documented for use against eighteen the history of humanity. Apart from deriving natural categories of diseases common in tropical and sub- resources, humans have a deep rooted tradition of tropical landscapes. Though the reported species venerating nature which is extensively observed are clustered around a few widely distributed across continents (Verschuuren 2010). The tradition families, 71% of them are uniquely represented from has attracted attention of researchers and policy- any single biogeographic region. The use of multiple makers for its impact on local ecological and socio- species in treating an ailment, high use value of the economic dynamics. Ethnomedicine that emanated popular plants, and cross-community similarity in from this tradition, deals health issues with nature- disease treatment reflects rich community wisdom to derived resources. -
Page 1 植物研究雜誌 J. Jpn. Bot. 76: 339-343 (2001) Delineation Of
植物研究雑誌 J. J. Jpn. Bo t. 76: 76: 339-343 (200 1) Delineation Delineation of Schoenoplectus sect. Malacogeton (Cyperaceae) , New Combination ,and Distinctions of Species a b S. S. Galen SMITH and Eisuke HA YASAKA aDepartment aDepartment of Biology ,University of Wisconsin-Whitewater , Whitewater ,Wisconsin , 53190 U.S. A.; bBotanical bBotanical Garden ,Graduate School of Science ,Tohoku University ,Sendai , 980-0862 JAPAN (Received (Received on 乱1ay 14 , 2001) The new combination ,Schoenoplectus sec t. Malacogeton (Ohwi) S. G. Smith & Hayasaka , is made and a description of the section is provided. Schoenoplectus nipponicus ,Sc h. etuberculatus ,Sch. torreyi and Sch. subterminalis 訂 e included in sec t. Malacogeton , and a key to these is given. We recognize the sections Schoenoplectus , Actaeogeton , Malacogeton and Supini in the genus Schoenoplectus , and a key to the sec- tions tions and a list of North American and East Asian species included in each section are provided. provided. Key words: Cyperaceae , new combination , Schoenoplectus sec t. Malacogeton , taxonomy taxonomy The polymorphic and polyphyletic Scirpus 2000 , Koyama et al. 2000 , Smith and L. L. s. la t. in recent ye 紅 s has been subdivided Yatskievych 1996 ,Wilson 1981). Of these into into about 17 genera (Bruhl 1995 , segregate genera Schoenoplectus is comp 紅 a- Goetghebeur 1998 , Wilson 1981 , 1989). tively large , with species distributed world- Scirpus Scirpus as stric t1 y defined includes about 30 wide , the number of which is v紅 iously species species occurring mainly in the temperate re- estimated at 50 spp. (Goetghebeur 1998) ,60 gions gions of the Northem Hemisphere , with S. -
Environmental and Vegetational Gradients on an Arizona
ENVIRONMENTAL AND VEGETATIONAL GRADIENTS ON AN ARIZONA PONDEROSA PINE LANDSCAPE: IMPLICATIONS FOR ECOLOGICAL RESTORATION by Scott R. Abella A Dissertation Submitted in Partial Fulfillment of the Requirements for the degree of Doctor of Philosophy in Forest Science Northern Arizona University May 2005 Approved: __________________________________ W. Wallace Covington, Ph.D., Chair __________________________________ Peter Z. Fulé, Ph.D. __________________________________ Margaret M. Moore, Ph.D. __________________________________ Carolyn H. Sieg, Ph.D. ABSTRACT ENVIRONMENTAL AND VEGETATIONAL GRADIENTS ON AN ARIZONA PONDEROSA PINE LANDSCAPE: IMPLICATIONS FOR ECOLOGICAL RESTORATION SCOTT R. ABELLA This research was performed in northern Arizona ponderosa pine (Pinus ponderosa) forests to enhance the ecological basis for restoration projects currently ongoing in these forests. My objectives were to: (i) develop a forest ecosystem classification on a 110,000-ha ponderosa pine landscape, (ii) determine geomorphic and soil gradients associated with the distribution of plant communities on this landscape, (iii) assess potential contributions of the soil seed bank for reestablishing understory communities, and (iv) determine understory responses to forest-floor manipulations in an existing ecological restoration experiment. I identified 10 landscape ecosystem types on this landscape, ranging from black cinders/Phacelia ecosystems low in available moisture and total N, to mesic basalt/Festuca and aspen/Lathyrus ecosystems. Distribution of plant communities was chiefly correlated with soil texture and resource levels reflecting influences of parent materials. Soil seed bank composition was partly ecosystem- specific, and was dominated by graminoids and short-lived forbs such as aspen fleabane (Erigeron divergens). I did not detect any short-term (2 year) treatment effects on understory vegetation in the forest-floor manipulation experiment. -
Estimating Soil Seed Bank Characteristics in Ponderosa Pine Forests Using Vegetation and Forest-Floor Data
Estimating Soil Seed Bank Characteristics in Ponderosa Pine Forests Using United States Department of Agriculture Vegetation and Forest-Floor Data Forest Service Rocky Mountain Research Station Research Note Scott R. Abella and Judith D. Springer RMRS-RN-35 September 2008 Abstract—Soil seed banks are important for vegetation management because they contain propagules of species that may be considered desirable or undesirable for site colonization after management and disturbance events. Knowledge of seed bank size and composition before planning management activities facilitates proactive management by providing early alerts of exotic species presence and of abilities of seed banks to promote colonization by desirable species. We developed models in ponderosa pine (Pinus ponderosa) forests in northern Arizona to estimate the size and richness of mineral soil seed banks using readily observable vegetation and forest- floor characteristics. Regression models using three or fewer predictors explained 41 to 59 percent of the variance in 0- to 2-inch (0- to 5-cm) seed densities of total and native perennial seed banks. Key predictors included aboveground plant species richness/10.8 ft2 (1 m2), litter weight and thickness, and tree canopy type (open or closed). Both total and native perennial seed banks were larger and richer in plots containing: (1) species-rich understories, (2) sparse litter, and (3) tree canopy openings. A regression tree model estimated that seed bank density of native perennials is 14-fold greater if aboveground plant richness exceeds eight species/10.8 ft2, forest-floor leaf litter is < 1 inch (2.5 cm) thick, and tree canopies are open. Introduction Soil seed banks are important for vegetation man- agement in ponderosa pine forests in at least four ways. -
Circumscription of Apiaceae Tribe Oenantheae
South African Journal of Botany 2004, 70(3): 393–406 Copyright © NISC Pty Ltd Printed in South Africa — All rights reserved SOUTH AFRICAN JOURNAL OF BOTANY ISSN 0254–6299 Circumscription of Apiaceae tribe Oenantheae TM Hardway1, K Spalik2, MF Watson3, DS Katz-Downie1 and SR Downie1* 1 Department of Plant Biology, University of Illinois, Urbana 61801, United States of America 2 Department of Plant Systematics and Geography, Warsaw University, Aleje Ujazdowskie 4, 00-478 Warsaw, Poland 3 Royal Botanic Garden Edinburgh, 20A Inverleith Row, Edinburgh EH3 5LR, Scotland, United Kingdom * Corresponding author, email: [email protected] Received 18 August 2003, accepted in revised form 17 November 2003 Previous molecular systematic investigations into the Sium and Trepocarpus. Relationships inferred from higher-level relationships of Apiaceae subfamily phylogenetic analyses of nuclear rDNA ITS sequences Apioideae have revealed a strongly supported clade from 64 accessions representing all 17 genera reveal recognised as tribe Oenantheae Dumort. These plants that four genera are not monophyletic. Bifora and may have clusters of fibrous or tuberous-thickened Cryptotaenia have members that fall outside of the tribe; roots, corky-thickened fruits, and other adaptations for Berula and Sium each comprise two or more lineages existence in wet or aquatic habitats. In some species, within Oenantheae. The St Helena endemics, Sium the leaves may be finely dissected or linear-septate and bracteatum and S. burchellii, ally with African Berula much reduced. We have initiated collaborative studies erecta; this clade is sister to the African endemic to produce a comprehensive estimate of phylogeny of species Sium repandum and Afrocarum imbricatum, the tribe, but such investigations are thwarted because and this entire group is allied closely with north tem- information on the composition of the tribe is lacking. -
Understanding the Coexistence of Sperm-Dependent Asexual Species
Understanding the coexistence of sperm-dependent asexual species and their sexual hosts: the role of biogeography, mate choice, and relative fitness in the Phoxinus eos-neogaeus (Pisces: Cyprinidae) system by Jonathan Alan Mee B.Sc.F., The University of British Columbia, 2002 M.Sc., The University of Toronto, 2005 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in The Faculty of Graduate Studies (Zoology) THE UNIVERSITY OF BRITISH COLUMBIA (Vancouver) December 2011 © Jonathan Alan Mee, 2011 !"#$%&'$( In sperm-dependent asexual reproduction, sperm is not required for its genetic contribution, but it is required for stimulating zygote development. In my dissertation, I address several questions related to the coexistence of sperm-dependent asexuals and the sexually-reproducing species on which they depend. I have focused my research on a sperm-dependent asexual fish, Phoxinus eos-neogaeus, that originated via hybridization between P. eos and P. neogaeus. Using a mathematical model of mate choice among sexuals and sperm-dependent asexuals, I showed that stable coexistence can occur when there is variation among males in the strength of preference for mating with sexual females and when males with stronger preference pay a higher cost of preference. My model also predicts that coexistence is facilitated when the asexuals suffer a fitness disadvantage relative to the sexuals. Subsequent empirical work, in which I compared the repeat swimming performance, fecundity, and growth rate of asexual and sexual Phoxinus, provided results that are consistent with this prediction: the asexuals are, at best, as fit as the sexuals. I sampled Phoxinus populations from across the species’ North American distribution and the pattern of mitochondrial DNA variation across these populations suggests that all P. -
Oklahoma Natural Heritage Inventory Plant Tracking List
OKLAHOMA NATURAL HERITAGE INVENTORY PLANT TRACKING LIST FAMILY UPDATED NAME COMMON NAME SRANK GRANK Acanthaceae Dyschoriste linearis (Torr. & A. Gray) Kuntze var. linearis polkadots S1T1 G4G5TNR Aizoaceae Sesuvium verrucosum Raf. winged sea purslane S1 G5 Alismataceae Alisma triviale Pursh northern water plantain S2 G5 Echinodorus tenellus (Mart.) Buchenau dwarf burhead SH G5? Sagittaria ambigua J.G. Sm. Kansas arrowhead S2 G2? Sagittaria cuneata E. Sheld. Wapatum arrowhead S2 G5 Amaranthaceae Amaranthus scleropoides Uline & W.L. Bray bone-bract pigweed SH G5 Chenopodium pallescens Standl. narrow-leaved goosefoot S1 G5 Guilleminea densa (Humb. & Bonpl. ex Schult.) Moq. cottonflower SNRTNR G5TNR var. aggregata Uline & W.L. Bray Guilleminea densa (Humb. & Bonpl. ex Schult.) Moq. cottonflower SNRTNR G5TNR var. densa Krascheninnikovia lanata (Pursh) A. Meeuse & A. Smit winterfat S1 G5 Suckleya suckleyana (Torr.) Rydb. poison suckleya S1 G5 Amaryllidaceae Hymenocallis liriosme (Raf.) Shinners Texas spiderlily S2 G4? Hymenocallis occidentalis (J. Le Conte) Kunth var. northern spiderlily S1T1 GNRTNR eulae (Shinners) G. Lom. Sm. & Flory Hymenocallis occidentalis (J. Le Conte) Kunth var. S1T1 GNRTNR occidentalis northern spiderlily Anacardiaceae Cotinus obovatus Raf. American smoketree S2 G4 Rhus copallinum L. var. lanceolata A. Gray prairie sumac SNAT1 G5T4T5 Rhus microphylla Engelm. ex A. Gray little-leaved sumac S1 G4G5 Apiaceae Berula erecta (Huds.) Coville wild parsnip S2 G4G5 Bowlesia incana Ruiz & Pav. hoary bowlesia SH G5 Erigenia bulbosa (Michx.) Nutt. harbinger-of-spring S1 G5 Eryngium diffusum Torr. spreading eryngo SH G4? Eryngium hookeri Walp. Hooker's eryngo S1 G3G5 Eryngium integrifolium Walter blue-flower coyotethistle S1 G5 Perideridia americana (Nutt. ex DC.) Rchb. eastern eulophus S1 G4 Ptilimnium costatum Raf.