Haustorium #57, July 2010
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"National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary."
Intro 1996 National List of Vascular Plant Species That Occur in Wetlands The Fish and Wildlife Service has prepared a National List of Vascular Plant Species That Occur in Wetlands: 1996 National Summary (1996 National List). The 1996 National List is a draft revision of the National List of Plant Species That Occur in Wetlands: 1988 National Summary (Reed 1988) (1988 National List). The 1996 National List is provided to encourage additional public review and comments on the draft regional wetland indicator assignments. The 1996 National List reflects a significant amount of new information that has become available since 1988 on the wetland affinity of vascular plants. This new information has resulted from the extensive use of the 1988 National List in the field by individuals involved in wetland and other resource inventories, wetland identification and delineation, and wetland research. Interim Regional Interagency Review Panel (Regional Panel) changes in indicator status as well as additions and deletions to the 1988 National List were documented in Regional supplements. The National List was originally developed as an appendix to the Classification of Wetlands and Deepwater Habitats of the United States (Cowardin et al.1979) to aid in the consistent application of this classification system for wetlands in the field.. The 1996 National List also was developed to aid in determining the presence of hydrophytic vegetation in the Clean Water Act Section 404 wetland regulatory program and in the implementation of the swampbuster provisions of the Food Security Act. While not required by law or regulation, the Fish and Wildlife Service is making the 1996 National List available for review and comment. -
Jazani Et Al., Afr J Tradit Complement Altern Med., (2018) 15 (2): 58-67
Jazani et al., Afr J Tradit Complement Altern Med., (2018) 15 (2): 58-67 https://doi.org/10.21010/ajtcam.v15i2.8 INTESTINAL HELMINTHS FROM THE VIEWPOINT OF TRADITIONAL PERSIAN MEDICINE VERSUS MODERN MEDICINE Arezoo Moini Jazani1,4, Ramin Farajpour Maleki1,2,4, Abdol hasan Kazemi3,4, Leila ghasemi 4 4 5 6 matankolaei , Somayyeh Taheri Targhi , Shirafkan kordi , Bahman Rahimi-Esboei and Ramin Nasimi Doost Azgomi1,4* 1Faculty of Traditional Medicine, Tabriz University of Medical Siences, Tabriz, Iran; 2Neuroscience Research center (NSRC) and Student Research Committtee, Tabriz University of Medical Siences, Tabriz, Iran; 3Infectious and tropical diseases research center, Tabriz University of Medical Siences, Tabriz, Iran; 4Medical Philosophy and History Research Center, Tabriz University of Medical Siences, Tabriz, Iran; 5Department of Medical Biotechnology, Faculty of Advanced Medical Science, Tabriz University of Medical Sciences, Tabriz, Iran; 6Department of medical parasitology and mycology, School of public health, Tehran university of Medical Sciences, Tehran, Iran. *Corresponding Author’s E-mail: [email protected] ; [email protected] Article History Received: March. 17, 2017 Revised Received: Dec. 11, 2017 Accepted: Dec.11, 2017 Published Online: Feb. 23, 2018 Abstract Background: Traditional Persian Medicine (TPM) has a history of almost 10,000 years with practice and experience aspects. The existing information and experiences of physicians such as Avicenna clearly show the vast amount of knowledge in the classification and treatment of pathogenic worms. The aim of this paper was the description of the various types of helminths along with their treatment in medieval Persia and comparing them with new medical findings. Materials and Methods: We searched main Traditional Persian Medical and pharmacological texts about etiology, manifestation, diagnosis and treatment of worms in the human digestive system and the out come was compared with the data extracted from modern medical sources. -
Synthesizing Ecosystem Implications of Mistletoe Infection
Environmental Research Letters LETTER • OPEN ACCESS Related content - Networks on Networks: Water transport in Mistletoe, friend and foe: synthesizing ecosystem plants A G Hunt and S Manzoni implications of mistletoe infection - Networks on Networks: Edaphic constraints: the role of the soil in vegetation growth To cite this article: Anne Griebel et al 2017 Environ. Res. Lett. 12 115012 A G Hunt and S Manzoni - Impact of mountain pine beetle induced mortality on forest carbon and water fluxes David E Reed, Brent E Ewers and Elise Pendall View the article online for updates and enhancements. This content was downloaded from IP address 137.154.212.215 on 17/12/2017 at 21:57 Environ. Res. Lett. 12 (2017) 115012 https://doi.org/10.1088/1748-9326/aa8fff LETTER Mistletoe, friend and foe: synthesizing ecosystem OPEN ACCESS implications of mistletoe infection RECEIVED 28 June 2017 Anne Griebel1,3 ,DavidWatson2 and Elise Pendall1 REVISED 1 Hawkesbury Institute for the Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW, Australia 12 September 2017 2 Institute for Land, Water and Society, Charles Sturt University, PO box 789, Albury, NSW, Australia ACCEPTED FOR PUBLICATION 3 Author to whom any correspondence should be addressed. 29 September 2017 PUBLISHED E-mail: [email protected] 16 November 2017 Keywords: mistletoe, climate change, biodiversity, parasitic plants, tree mortality, forest disturbance Original content from this work may be used Abstract under the terms of the Creative Commons Biotic disturbances are affecting a wide range of tree species in all climates, and their occurrence is Attribution 3.0 licence. contributing to increasing rates of tree mortality globally. -
A Morphological Cladistic Analysis of Olacaceae
Systematic Botany (2004), 29(3): pp. 569±586 q Copyright 2004 by the American Society of Plant Taxonomists A Morphological Cladistic Analysis of Olacaceae VALE RY MALE COT,1,4 DANIEL L. NICKRENT,2 PIETER BAAS,3 LEEN VAN DEN OEVER,3 and DANIELLE LOBREAU-CALLEN1 1Equipe d'Accueil 3496 Classi®cation Evolution et BiosysteÂmatique, Laboratoire de PaleÂobotanique et PaleÂoeÂcologie, Universite Pierre et Marie Curie, 12 rue Cuvier, 75005 Paris, France; 2Department of Plant Biology, Southern Illinois University, Carbondale, Illinois 62901-6509; 3National Herbarium, Leiden University, P.O. Box 9514, 2300 RA Leiden, Netherlands; 4Author for Correspondence. Present address: UMR A 462 SAGAH, Institut National d'Horticulture, 2 rue Le NoÃtre, 49045 Angers Cedex 01, France ([email protected]) Communicating Editor: Gregory M. Plunkett ABSTRACT. A cladistic study based on morphological characters is presented for all 28 genera of Olacaceae as well as 26 representative genera from ®ve other families of Santalales: Loranthaceae, Misodendraceae, Opiliaceae, Santalaceae, and Viscaceae. The data matrix consists of 80 macro-morphological, palynological, and anatomical characters. The phylogenetic trees obtained show a paraphyletic Olacaceae with four main clades. Some of these clades are congruent with previously recognized tribes, but all of subfamilies are para- or polyphyletic. Examination of character transformations con®rms several assumptions of evolutionary trends within Olacaceae and Santalales, but others appear to be more complex than expected. Optimization of trophic mode on the consensus tree shows that root hemiparasitism had a single origin in Santalales. Whatever the optimization procedure used, the basal-most clade of Olacaceae consists of 12 genera, among which ®ve are known to be autotrophs, whereas the remaining three clades (15 genera) contain four genera known to be root parasites. -
Cassytha Pubescens
Cassytha pubescens: Germination biology and interactions with native and introduced hosts Hong Tai (Steven), Tsang B.Sc. Hons (University of Adelaide) Thesis submitted for the degree of Master of Science School of Earth & Environmental Science University of Adelaide, Australia 03/05/2010 i Table of Contents Table of Contents ........................................................................................................... ii Abstract .......................................................................................................................... v Declaration ................................................................................................................... vii Acknowledgements .................................................................................................... viii Chapter. 1 Introduction .................................................................................................. 1 1.1 General Introduction ............................................................................................ 1 1.2 Literature Review ................................................................................................. 3 1.2.1 Characteristics of parasitic control agents .................................................... 3 1.2.2. Direct impacts on hosts ................................................................................ 7 1.2.3. Indirect impacts on hosts ............................................................................. 8 1.2.4. Summary ................................................................................................... -
Castilleja Coccinea and C. Indivisa (Orobanchaceae)
Nesom, G.L. and J.M. Egger. 2014. Castilleja coccinea and C. indivisa (Orobanchaceae). Phytoneuron 2014-14: 1–7. Published 6 January 2014. ISSN 2153 733X CASTILLEJA COCCINEA AND C. INDIVISA (OROBANCHACEAE) GUY L. NESOM 2925 Hartwood Drive Fort Worth, Texas 76109 www.guynesom.com J. M ARK EGGER Herbarium, Burke Museum of Natural History and Culture University of Washington Seattle, Washington 98195-5325 [email protected] ABSTRACT Castilleja coccinea and C. indivisa are contrasted in morphology and their ranges mapped in detail in the southern USA, where they are natively sympatric in small areas of Oklahoma, Arkansas, and Louisiana. Castilleja indivisa has recently been introduced and naturalized in the floras of Alabama and Florida. Castilleja ludoviciana , known only by the type collection from southwestern Louisiana, differs from C. coccinea in subentire leaves and relatively small flowers and is perhaps a population introgressed by C. indivisa . Castilleja coccinea and C. indivisa are allopatric except in small areas of Oklahoma, Arkansas, and Lousiana, but assessments of their native distributions are not consistent among various accounts (e.g. Thomas & Allen 1997; Turner et al. 2003; OVPD 2012; USDA, NRCS 2013). Morphological contrasts between the two species, via keys in floristic treatments (e.g., Smith 1994; Wunderlin & Hansen 2003; Nelson 2009; Weakley 2012), have essentially repeated the differences outlined by Pennell (1935). The current study presents an evaluation and summary of the taxonomy of these two species. We have examined specimens at CAS, TEX-LL, SMU-BRIT-VDB, MO, NLU, NO, USF, WS, and WTU and viewed digital images available through Florida herbaria and databases. -
José Guadalupe García-Franco
CURRICULUM VITAE JOSÉ GUADALUPE GARCÍA-FRANCO 20/08/2015 Curriculun Vitae García-Franco Contenido 1. DATOS PERSONALES ..................................................................................................................... 5 2. DATOS LABORALES ....................................................................................................................... 5 3. FORMACIÓN PROFESIONAL ............................................................................................................ 5 3.1. Licenciatura: .......................................................................................................................... 5 3.2. Maestría: ................................................................................................................................ 5 3.3. Doctorado: ............................................................................................................................. 5 4. PERTENENCIA AL SISTEMA NACIONAL DE INVESTIGADORES ......................................................... 5 5. DOMINIO DE IDIOMAS EXTRANJEROS ............................................................................................ 5 6. BECAS OBTENIDAS PARA SU FORMACIÓN PROFESIONAL ............................................................... 5 7. EXPERIENCIA LABORAL ................................................................................................................ 6 8. ASISTENCIA A CURSOS Y TALLERES DE CAPACITACIÓN .............................................................. 6 9. -
Cassytha) and Insights Into the Plastid Phylogenomics of Lauraceae
GBE Plastome Evolution in the Sole Hemiparasitic Genus Laurel Dodder (Cassytha) and Insights into the Plastid Phylogenomics of Lauraceae Chung-Shien Wu1,†, Ting-Jen Wang1,†,Chia-WenWu1, Ya-Nan Wang2, and Shu-Miaw Chaw1,* 1Biodiversity Research Center, Academia Sinica, Taipei 11529, Taiwan 2School of Forestry and Resource Conservation, Nation Taiwan University, Taipei 10617, Taiwan *Corresponding author: E-mail: [email protected]. †These authors contributed equally to this work. Accepted: September 6, 2017 Data deposition: This project has been deposited at DDBJ under the accession numbers LC210517, LC212965, LC213014, and LC228240. Abstract To date, little is known about the evolution of plastid genomes (plastomes) in Lauraceae. As one of the top five largest families in tropical forests, the Lauraceae contain many species that are important ecologically and economically. Lauraceous species also provide wonderful materials to study the evolutionary trajectory in response to parasitism because they contain both nonparasitic and parasitic species. This study compared the plastomes of nine Lauraceous species, including the sole hemiparasitic and herbaceous genus Cassytha (laurel dodder; here represented by Cassytha filiformis). We found differential contractions of the canonical inverted repeat (IR), resulting in two IR types present in Lauraceae. These two IR types reinforce Cryptocaryeae and Neocinnamomum— Perseeae–Laureae as two separate clades. Our data reveal several traits unique to Cas. filiformis, including loss of IRs, loss or pseudogenization of 11 ndh and rpl23 genes, richness of repeats, and accelerated rates of nucleotide substitutions in protein- coding genes. Although Cas. filiformis is low in chlorophyll content, our analysis based on dN/dS ratios suggests that both its plastid house-keeping and photosynthetic genes are under strong selective constraints. -
Minnesota and Federal Prohibited and Noxious Plants List 6-22-2011
Minnesota and Federal Prohibited and Noxious Plants List 6-22-2011 Minnesota and Federal Prohibited and Noxious Plants by Scientific Name (compiled by the Minnesota DNR’s Invasive Species Program 6-22-2011) Key: FN – Federal noxious weed (USDA–Animal Plant Health Inspection Service) SN – State noxious weed (Minnesota Department of Agriculture) RN – Restricted noxious weed (Minnesota Department of Agriculture) PI – Prohibited invasive species (Minnesota Department of Natural Resources) PS – State prohibited weed seed (Minnesota Department of Agriculture) RS – State restricted weed seed (Minnesota Department of Agriculture) (See explanations of these classifications below the lists of species) Regulatory Scientific Name Common Name Classification Aquatic Plants: Azolla pinnata R. Brown mosquito fern, water velvet FN Butomus umbellatus Linnaeus flowering rush PI Caulerpa taxifolia (Vahl) C. Agardh Mediterranean strain (killer algae) FN Crassula helmsii (Kirk) Cockayne Australian stonecrop PI Eichomia azurea (Swartz) Kunth anchored water hyacinth, rooted water FN hyacinth Hydrilla verticillata (L. f.) Royle hydrilla FN, PI Hydrocharis morsus-ranae L. European frog-bit PI Hygrophila polysperma (Roxburgh) T. Anders Indian swampweed, Miramar weed FN, PI Ipomoea aquatica Forsskal water-spinach, swamp morning-glory FN Lagarosiphon major (Ridley) Moss ex Wagner African oxygen weed FN, PI Limnophila sessiliflora (Vahl) Blume ambulia FN Lythrum salicaria L., Lythrum virgatum L., (or any purple loosestrife PI, SN variety, hybrid or cultivar thereof) Melaleuca quenquinervia (Cav.) Blake broadleaf paper bank tree FN Monochoria hastata (Linnaeus) Solms-Laubach arrowleaf false pickerelweed FN Monochoria vaginalis (Burman f.) C. Presl heart-shaped false pickerelweed FN Myriophyllum spicatum Linnaeus Eurasian water mifoil PI Najas minor All. brittle naiad PI Ottelia alismoides (L.) Pers. -
Lodgepole Pine Dwarf Mistletoe in Taylor Park, Colorado Report for the Taylor Park Environmental Assessment
Lodgepole Pine Dwarf Mistletoe in Taylor Park, Colorado Report for the Taylor Park Environmental Assessment Jim Worrall, Ph.D. Gunnison Service Center Forest Health Protection Rocky Mountain Region USDA Forest Service 1. INTRODUCTION ............................................................................................................................... 2 2. DESCRIPTION, DISTRIBUTION, HOSTS ..................................................................................... 2 3. LIFE CYCLE....................................................................................................................................... 3 4. SCOPE OF TREATMENTS RELATIVE TO INFESTED AREA ................................................. 4 5. IMPACTS ON TREES AND FORESTS ........................................................................................... 4 5.1 TREE GROWTH AND LONGEVITY .................................................................................................... 4 5.2 EFFECTS OF DWARF MISTLETOE ON FOREST DYNAMICS ............................................................... 6 5.3 RATE OF SPREAD AND INTENSIFICATION ........................................................................................ 6 6. IMPACTS OF DWARF MISTLETOES ON ANIMALS ................................................................ 6 6.1 DIVERSITY AND ABUNDANCE OF VERTEBRATES ............................................................................ 7 6.2 EFFECT OF MISTLETOE-CAUSED SNAGS ON VERTEBRATES ............................................................12 -
Dwarf Mistletoes: Biology, Pathology, and Systematics
This file was created by scanning the printed publication. Errors identified by the software have been corrected; however, some errors may remain. CHAPTER 10 Anatomy of the Dwarf Mistletoe Shoot System Carol A. Wilson and Clyde L. Calvin * In this chapter, we present an overview of the Morphology of Shoots structure of the Arceuthobium shoot system. Anatomical examination reveals that dwarf mistletoes Arceuthobium does not produce shoots immedi are indeed well adapted to a parasitic habit. An exten ately after germination. The endophytic system first sive endophytic system (see chapter 11) interacts develops within the host branch. Oftentimes, the only physiologically with the host to obtain needed evidence of infection is swelling of the tissues near the resources (water, minerals, and photosynthates); and infection site (Scharpf 1967). After 1 to 3 years, the first the shoots provide regulatory and reproductive func shoots are produced (table 2.1). All shoots arise from tions. Beyond specialization of their morphology (Le., the endophytic system and thus are root-borne shoots their leaves are reduced to scales), the dwarf mistle (Groff and Kaplan 1988). In emerging shoots, the toes also show peculiarities of their structure that leaves of adjacent nodes overlap and conceal the stem. reflect their phylogenetic relationships with other As the internodes elongate, stem segments become mistletoes and illustrate a high degree of specialization visible; but the shoot apex remains tightly enclosed by for the parasitic habit. From Arceuthobium globosum, newly developing leaf primordia (fig. 10.lA). Two the largest described species with shoots 70 cm tall oppositely arranged leaves, joined at their bases, occur and 5 cm in diameter, toA. -
Arceuthobium Tsugense Subsp. Amabilae, a New Subspecies of Hemlock Dwarf Mistletoe (Viscaceae) from Oregon
Arceuthobium tsugense subsp. amabilae, a New Subspecies of Hemlock Dwarf Mistletoe (Viscaceae) from Oregon Robert L. Mathiasen School of Forestry, Northern Arizona University, Flagstaff, Arizona 86011, U.S.A. [email protected] Carolyn M. Daugherty Department of Geography, Planning, and Recreation, Northern Arizona University, Flagstaff, Arizona 86011, U.S.A. ABSTRACT . The dwarf mistletoe severely parasitizing Hawksworth and Wiens (1972) only included white fir Pacific silver fir in Oregon is described as a new (Abies concolor Lindley & Gordon), grand fir (Abies subspecies of hemlock dwarf mistletoe. This classifi grandis (Douglas ex D. Don) Lindley), California red cation is based on morphological and host range fir (Abies magnifica A. Murray), and noble fir (Abies differences between hemlock dwarf mistletoe, Ar procera Rehder) as hosts of Arceuthobium abietinum in ceuthobium tsugense (Rosendahl) G. N. Jones subsp. Oregon; they included only grand fir in Washington. tsugense, and the new subspecies, Pacific silver fir Hawksworth (1987) summarized the taxonomy of dwarf mistletoe, Arceuthobium tsugense subsp. am Arceuthobium tsugense and separated this species into abilae Mathiasen & C. Daugherty. three different races: a western hemlock race, a shore Key words: Arceuthobium, Hemlock dwarf mis pine race, and a mountain hemlock race. Hawksworth tletoe, IUCN Red List, mountain hemlock, noble fir, indicated that only the western hemlock race Oregon, Pacific silver fir, Viscaceae, western hem parasitized species of Abies. Hawksworth et al. lock. (1992) presented another interpretation for the classification of A. tsugense. They described the The taxonomic classification of the dwarf mistletoes western hemlock and mountain hemlock races pro severely parasitizing Pacific silver fir (Abies amabilis posed by Hawksworth (1987) as subspecies of A.