Morella Cerifera Wax Myrtle Myricaceae
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Caterpillars Moths Butterflies Woodies
NATIVE Caterpillars Moths and utter flies Band host NATIVE Hackberry Emperor oodies PHOTO : Megan McCarty W Double-toothed Prominent Honey locust Moth caterpillar Hackberry Emperor larva PHOTO : Douglas Tallamy Big Poplar Sphinx Number of species of Caterpillars n a study published in 2009, Dr. Oaks (Quercus) 557 Beeches (Fagus) 127 Honey-locusts (Gleditsia) 46 Magnolias (Magnolia) 21 Double-toothed Prominent ( Nerice IDouglas W. Tallamy, Ph.D, chair of the Cherries (Prunus) 456 Serviceberry (Amelanchier) 124 New Jersey Tea (Ceanothus) 45 Buttonbush (Cephalanthus) 19 bidentata ) larvae feed exclusively on elms Department of Entomology and Wildlife Willows (Salix) 455 Larches or Tamaracks (Larix) 121 Sycamores (Platanus) 45 Redbuds (Cercis) 19 (Ulmus), and can be found June through Ecology at the University of Delaware Birches (Betula) 411 Dogwoods (Cornus) 118 Huckleberry (Gaylussacia) 44 Green-briar (Smilax) 19 October. Their body shape mimics the specifically addressed the usefulness of Poplars (Populus) 367 Firs (Abies) 117 Hackberry (Celtis) 43 Wisterias (Wisteria) 19 toothed shape of American elm, making native woodies as host plants for our Crabapples (Malus) 308 Bayberries (Myrica) 108 Junipers (Juniperus) 42 Redbay (native) (Persea) 18 them hard to spot. The adult moth is native caterpillars (and obviously Maples (Acer) 297 Viburnums (Viburnum) 104 Elders (Sambucus) 42 Bearberry (Arctostaphylos) 17 small with a wingspan of 3-4 cm. therefore moths and butterflies). Blueberries (Vaccinium) 294 Currants (Ribes) 99 Ninebark (Physocarpus) 41 Bald cypresses (Taxodium) 16 We present here a partial list, and the Alders (Alnus) 255 Hop Hornbeam (Ostrya) 94 Lilacs (Syringa) 40 Leatherleaf (Chamaedaphne) 15 Honey locust caterpillar feeds on honey number of Lepidopteran species that rely Hickories (Carya) 235 Hemlocks (Tsuga) 92 Hollies (Ilex) 39 Poison Ivy (Toxicodendron) 15 locust, and Kentucky coffee trees. -
Alphabetical Lists of the Vascular Plant Families with Their Phylogenetic
Colligo 2 (1) : 3-10 BOTANIQUE Alphabetical lists of the vascular plant families with their phylogenetic classification numbers Listes alphabétiques des familles de plantes vasculaires avec leurs numéros de classement phylogénétique FRÉDÉRIC DANET* *Mairie de Lyon, Espaces verts, Jardin botanique, Herbier, 69205 Lyon cedex 01, France - [email protected] Citation : Danet F., 2019. Alphabetical lists of the vascular plant families with their phylogenetic classification numbers. Colligo, 2(1) : 3- 10. https://perma.cc/2WFD-A2A7 KEY-WORDS Angiosperms family arrangement Summary: This paper provides, for herbarium cura- Gymnosperms Classification tors, the alphabetical lists of the recognized families Pteridophytes APG system in pteridophytes, gymnosperms and angiosperms Ferns PPG system with their phylogenetic classification numbers. Lycophytes phylogeny Herbarium MOTS-CLÉS Angiospermes rangement des familles Résumé : Cet article produit, pour les conservateurs Gymnospermes Classification d’herbier, les listes alphabétiques des familles recon- Ptéridophytes système APG nues pour les ptéridophytes, les gymnospermes et Fougères système PPG les angiospermes avec leurs numéros de classement Lycophytes phylogénie phylogénétique. Herbier Introduction These alphabetical lists have been established for the systems of A.-L de Jussieu, A.-P. de Can- The organization of herbarium collections con- dolle, Bentham & Hooker, etc. that are still used sists in arranging the specimens logically to in the management of historical herbaria find and reclassify them easily in the appro- whose original classification is voluntarily pre- priate storage units. In the vascular plant col- served. lections, commonly used methods are systema- Recent classification systems based on molecu- tic classification, alphabetical classification, or lar phylogenies have developed, and herbaria combinations of both. -
Invasive Trees of Georgia Pub10-14
Pub. No. 39 October 2016 Invasive Trees of Georgia by Dr. Kim D. Coder, Professor of Tree Biology & Health Care Warnell School of Forestry & Natural Resources, University of Georgia Georgia has many species of trees. Some are native trees and some have been introduced from outside the state, nation, or continent. Most of Georgia’s trees are well- behaved and easily develop into sustainable shade and street trees. A few tree species have an extrodinary ability to upsurp resources and take over sites from other plants. These trees are called invasive because they effectively invade sites, many times eliminat- ing other species of plants. There are a few tree species native to Georgia which are considered invasive in other parts of the country. These native invasives, may be well-behaved in Georgia, but reproduce and take over sites elsewhere, and so have gained an invasive status from at least one other invasive species list. Table 1. There are hundreds of trees which have been introduced to Georgia landscapes. Some of these exotic / naturalized trees are considered invasive. The selected list of Georgia invasive trees listed here are notorious for growing rampantly and being difficult to eradicate. Table 2. Table 1: Native trees considered invasive in other parts of the country. scientific name common name scientific name common name Acacia farnesiana sweet acacia Myrica cerifera Southern bayberry Acer negundo boxelder Pinus taeda loblolly pine Acer rubrum red maple Populus deltoides Eastern cottonwood Fraxinus americana white ash Prunus serotina black cherry Fraxinus pennsylvanica green ash Robinia pseudoacacia black locust Gleditsia triacanthos honeylocust Toxicodendron vernix poison sumac Juniperus virginiana eastern redcedar The University of Georgia is committed to principles of equal opportunity and affirmative action. -
In China: Phylogeny, Host Range, and Pathogenicity
Persoonia 45, 2020: 101–131 ISSN (Online) 1878-9080 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE https://doi.org/10.3767/persoonia.2020.45.04 Cryphonectriaceae on Myrtales in China: phylogeny, host range, and pathogenicity W. Wang1,2, G.Q. Li1, Q.L. Liu1, S.F. Chen1,2 Key words Abstract Plantation-grown Eucalyptus (Myrtaceae) and other trees residing in the Myrtales have been widely planted in southern China. These fungal pathogens include species of Cryphonectriaceae that are well-known to cause stem Eucalyptus and branch canker disease on Myrtales trees. During recent disease surveys in southern China, sporocarps with fungal pathogen typical characteristics of Cryphonectriaceae were observed on the surfaces of cankers on the stems and branches host jump of Myrtales trees. In this study, a total of 164 Cryphonectriaceae isolates were identified based on comparisons of Myrtaceae DNA sequences of the partial conserved nuclear large subunit (LSU) ribosomal DNA, internal transcribed spacer new taxa (ITS) regions including the 5.8S gene of the ribosomal DNA operon, two regions of the β-tubulin (tub2/tub1) gene, plantation forestry and the translation elongation factor 1-alpha (tef1) gene region, as well as their morphological characteristics. The results showed that eight species reside in four genera of Cryphonectriaceae occurring on the genera Eucalyptus, Melastoma (Melastomataceae), Psidium (Myrtaceae), Syzygium (Myrtaceae), and Terminalia (Combretaceae) in Myrtales. These fungal species include Chrysoporthe deuterocubensis, Celoporthe syzygii, Cel. eucalypti, Cel. guang dongensis, Cel. cerciana, a new genus and two new species, as well as one new species of Aurifilum. These new taxa are hereby described as Parvosmorbus gen. -
Waxmyrtle-- a Shrub for a Natural Riparian Buffer
Waxmyrtle-- A Shrub for a Natural Riparian Buffer By Susan Camp When you live on a tidal creek or river, as do many of us on the Middle Peninsula, you bear a special responsibility to maintain a healthy interface between land and water. The plants that grow along a shoreline help to protect the adjacent waterway from erosion and pollutants, and they provide valuable habitat for the wildlife that live and feed along the banks. Jim and I are fortunate to live on property that was left in a natural state by the previous owners, and we have maintained the banks for 25 years with a minimum amount of labor and no expense. The native trees, shrubs, and grasses along the water’s edge maintain themselves with minor pruning of dead wood, trimming of greenbriers, and eradication of poison ivy. One of my favorite native shrubs is waxmyrtle (Myrica cerifera or Morella cerifera), also called southern waxmyrtle or southern bayberry. Waxmyrtle is a small tree or large, multi-trunked, fast- growing shrub, depending on how it is pruned. Waxmyrtle produces numerous suckers that lend the shrub an irregular, leggy appearance, but it can be maintained with a single trunk. Waxmyrtle is found from New Jersey south to Mexico, Central America and the Caribbean, and west to Texas and Oklahoma, surviving in a wide range of environments from wet swamps to elevated forestland, although it is most often found in marshes and along tidal creeks and stream banks. The shrub grows well in USDA Hardiness Zones 6b to 11. It is evergreen where winters are mild, but is classified as semi-evergreen in colder environments, which means it will lose its leaves when the temperature drops below 0 F. -
Field Instructions for The
FIELD INSTRUCTIONS FOR THE INVENTORY OF THE PACIFIC ISLANDS 2013 Hawaii Edition Forest Inventory and Analysis Program Pacific Northwest Research Station USDA Forest Service THIS MANUAL IS BASED ON: FOREST INVENTORY AND ANALYSIS NATIONAL CORE FIELD GUIDE FIELD DATA COLLECTION PROCEDURES FOR PHASE 2 PLOTS VERSION 5.1 TABLE OF CONTENTS 1 INTRODUCTION ........................................................................................................................................................................ 1 1.1 PURPOSES OF THIS MANUAL ................................................................................................................................................... 1 1.2 ORGANIZATION OF THIS MANUAL .......................................................................................................................................... 1 1.2.1 UNITS OF MEASURE ................................................................................................................................................................. 2 1.2.2 GENERAL DESCRIPTION ............................................................................................................................................................ 2 1.2.3 PLOT SETUP .............................................................................................................................................................................. 3 1.2.4 PLOT INTEGRITY ...................................................................................................................................................................... -
100 of the World's Worst Invasive Alien Species
100 OF THE WORLD’S WORST INVASIVE ALIEN SPECIES A SELECTION FROM THE GLOBAL INVASIVE SPECIES DATABASE Published by Contribution to the Global Invasive Species Programme (GISP) In Association with SPECIES SURVIVAL COMMISSION Citation Lowe S., Browne M., Boudjelas S., De Poorter M. (2000) 100 of the World’s Worst Invasive Alien Species A selection from the Global Invasive Species Database. Published by The Invasive Species Specialist Group (ISSG) a specialist group of the Species Survival Commission (SSC) of the World Conservation Union (IUCN), 12pp. First published as special lift-out in Aliens 12, December 2000. Updated and reprinted version: November 2004. Electronic version available at: www.issg.org/booklet.pdf For information, or copies of the booklet in English, French or Spanish, please contact: ISSG Office: School of Geogra- phy and Environmental Sciences (SGES) University of Auckland (Tamaki Campus) Private Bag 92019 Auckland, New Zealand Phone: #64 9 3737 599 x85210 Fax: #64 9 3737 042 E-mail: [email protected] Development of the 100 of the World’s Worst Invasive Alien Spe- cies list has been made possible by Cover image: Brown tree snake the support of the Fondation (Boiga irregularis). d’Entreprise TOTAL (1998 - 2000). Photo: Gordon Rodda Printed in New Zealand by: Hollands Printing Ltd Contact: Otto van Gulik Email: [email protected] 2 Biological Invasion What happens when a species is in- The list of “100 of the World’s precedented rate. A number of the troduced into an ecosystem where Worst Invasive Alien Species” in invasive alien species featured in it doesn’t occur naturally? Are eco- this booklet illustrates the incred- this booklet are contributing to systems flexible and able to cope ible variety of species that have the these losses. -
Texas Big Tree Registry a List of the Largest Trees in Texas Sponsored by Texas a & M Forest Service
Texas Big Tree Registry A list of the largest trees in Texas Sponsored by Texas A & M Forest Service Native and Naturalized Species of Texas: 320 ( D indicates species naturalized to Texas) Common Name (also known as) Latin Name Remarks Cir. Threshold acacia, Berlandier (guajillo) Senegalia berlandieri Considered a shrub by B. Simpson 18'' or 1.5 ' acacia, blackbrush Vachellia rigidula Considered a shrub by Simpson 12'' or 1.0 ' acacia, Gregg (catclaw acacia, Gregg catclaw) Senegalia greggii var. greggii Was named A. greggii 55'' or 4.6 ' acacia, Roemer (roundflower catclaw) Senegalia roemeriana 18'' or 1.5 ' acacia, sweet (huisache) Vachellia farnesiana 100'' or 8.3 ' acacia, twisted (huisachillo) Vachellia bravoensis Was named 'A. tortuosa' 9'' or 0.8 ' acacia, Wright (Wright catclaw) Senegalia greggii var. wrightii Was named 'A. wrightii' 70'' or 5.8 ' D ailanthus (tree-of-heaven) Ailanthus altissima 120'' or 10.0 ' alder, hazel Alnus serrulata 18'' or 1.5 ' allthorn (crown-of-thorns) Koeberlinia spinosa Considered a shrub by Simpson 18'' or 1.5 ' anacahuita (anacahuite, Mexican olive) Cordia boissieri 60'' or 5.0 ' anacua (anaqua, knockaway) Ehretia anacua 120'' or 10.0 ' ash, Carolina Fraxinus caroliniana 90'' or 7.5 ' ash, Chihuahuan Fraxinus papillosa 12'' or 1.0 ' ash, fragrant Fraxinus cuspidata 18'' or 1.5 ' ash, green Fraxinus pennsylvanica 120'' or 10.0 ' ash, Gregg (littleleaf ash) Fraxinus greggii 12'' or 1.0 ' ash, Mexican (Berlandier ash) Fraxinus berlandieriana Was named 'F. berlandierana' 120'' or 10.0 ' ash, Texas Fraxinus texensis 60'' or 5.0 ' ash, velvet (Arizona ash) Fraxinus velutina 120'' or 10.0 ' ash, white Fraxinus americana 100'' or 8.3 ' aspen, quaking Populus tremuloides 25'' or 2.1 ' baccharis, eastern (groundseltree) Baccharis halimifolia Considered a shrub by Simpson 12'' or 1.0 ' baldcypress (bald cypress) Taxodium distichum Was named 'T. -
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. -
Diversity of Wisconsin Rosids
Diversity of Wisconsin Rosids . oaks, birches, evening primroses . a major group of the woody plants (trees/shrubs) present at your sites The Wind Pollinated Trees • Alternate leaved tree families • Wind pollinated with ament/catkin inflorescences • Nut fruits = 1 seeded, unilocular, indehiscent (example - acorn) *Juglandaceae - walnut family Well known family containing walnuts, hickories, and pecans Only 7 genera and ca. 50 species worldwide, with only 2 genera and 4 species in Wisconsin Carya ovata Juglans cinera shagbark hickory Butternut, white walnut *Juglandaceae - walnut family Leaves pinnately compound, alternate (walnuts have smallest leaflets at tip) Leaves often aromatic from resinous peltate glands; allelopathic to other plants Carya ovata Juglans cinera shagbark hickory Butternut, white walnut *Juglandaceae - walnut family The chambered pith in center of young stems in Juglans (walnuts) separates it from un- chambered pith in Carya (hickories) Juglans regia English walnut *Juglandaceae - walnut family Trees are monoecious Wind pollinated Female flower Male inflorescence Juglans nigra Black walnut *Juglandaceae - walnut family Male flowers apetalous and arranged in pendulous (drooping) catkins or aments on last year’s woody growth Calyx small; each flower with a bract CA 3-6 CO 0 A 3-∞ G 0 Juglans cinera Butternut, white walnut *Juglandaceae - walnut family Female flowers apetalous and terminal Calyx cup-shaped and persistant; 2 stigma feathery; bracted CA (4) CO 0 A 0 G (2-3) Juglans cinera Juglans nigra Butternut, white -
Georgia Native Trees Considered Invasive in Other Parts of the Country. Scientific Name Common Name Scientific Name Common Name
Invasive Trees of Georgia Dr. Kim D. Coder, Professor of Tree Biology & Health Care, Warnell School, UGA Georgia has many species of trees. Some are native trees and some have been introduced from outside the state, nation, or continent. Most of Georgia’s trees are well-behaved and easily develop into sustainable shade and street trees. A few tree species have an extrodinary ability to upsurp resources and take over sites from other plants. These trees are called invasive because they effectively invade sites, many times eliminating other species of plants. There are a few tree species native to Georgia which are considered invasive in other parts of the country. These native invasives, may be well-behaved in Georgia, but reproduce and take over sites elsewhere, and so have gained an invasive status from at least one other invasive species list. Table 1. There are hundreds of trees which have been introduced to Georgia landscapes. Some of these exotic / naturalized trees are considered invasive. The selected list of Georgia invasive trees listed here are notorious for growing rampantly and being diffi- cult to eradicate. Table 2. They should not be planted. Table 1: Georgia native trees considered invasive in other parts of the country. scientific name common name scientific name common name Acacia farnesiana sweet acacia Myrica cerifera Southern bayberry Acer negundo boxelder Pinus taeda loblolly pine Acer rubrum red maple Populus deltoides Eastern Fraxinus americana white ash cottonwood Fraxinus pennsylvanica green ash Prunus serotina black cherry Gleditsia triacanthos honeylocust Robinia pseudoacacia black locust Juniperus virginiana eastern Toxicodendron vernix poison sumac redcedar Table 2: Introduced (exotic) tree / shrub species found in Georgia listed at a regional / national level as being ecologically invasive. -
Antimicrobial Properties of Traditional Brewing Herbs
ANTIMICROBIAL PROPERTIES OF TRADITIONAL BREWING HERBS - Ledum palustre, Myrica gale & Humulus lupulus Gordon Virgo Project work in Ethnobiology 15 hp, 2010 Evolutionary Biology Centre (EBC) Supervisor: Hugo J. de Boer ACKNOWLEDGEMENTS I would like to thank my supervisor Hugo de Boer for encouragement and his excellent input to this project. Thanks to Stallhagen Brewery and Marcus Lindborg for providing material and literature. Also, I would like to thank Stefan Roos at SLU and Marianne Svarvare for guidance and technique. ABSTRACT In this study, three different brewing herbs that have been used through the history are evaluated as inhibitors of common beer spoilage organisms. The three species are Ledum palustre (Marsh Tea), Myrica gale (Bog Myrtle) and Humulus lupulus (Hops). Experimental batches of 10 L were made with all the three herbs and one without any additives. For each herb, two batches were made with different concentration, one batch with 3g/L and the other with 6g/L. All batches were treated the same and fermentation pattern for all of them were similar. Inoculations of four common beer spoilage organisms were practiced in order to examine microbial resistance of the different beers. Antibacterial activity was analyzed by membrane filtration and by measure the optical density during the incubation time. Both Humulus lupulus and Myrica gale showed clear resistance to the three gram-positive bacteria. 1 INTRODUCTION Throughout history, several different plant species have been used as beer additives for flavour and above all as preservatives. Particularly two species, Myrica gale and Humulus lupulus were widely used as beer additives in Europe (Behre 1999).