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Fern Gazette
ISSN 0308-0838 THE FERN GAZETTE VOLUME ELEVEN PART FIVE 1977 THE JOURNAL OF THE BRITISH PTERIDOLOGICAL SOCIETY THE FERN GAZETTE VOLUME 11 PART 5 1977 CONTENTS Page ECOLOGICAL NOTES Observations on some rare Spanish ferns iri Cadiz Province, Spain - B. Molesworth-AIIen 27 1 Unl:>ranched plants of Equisetum palustre L. - G. Halliday 276 Cyrtomium fa lcatum naturalised on Rhum - P. Corkh i/1 277 MAIN ARTICLES A pteridophyte flora of the Derbyshire Dales National Nature Reserve - A. Wil lmot 279 Ferns in the Cameroons. 11. The pteridophytes of the evergreen forests - G. Ben/ 285 An ecological survey of the ferns of the Canary Islands - C. N. Page 297 A new record of Synchytrium athyrii on Athyrium filix-femina - E. MUller & J.J. Schneller 313 Further cytogenetic studies and a reappraisal of the diploid ancestry in the Dryopteris carthusiana complex - M. Gibby & S. Wa lker 315 Cytology and reproduction of Ch eilanthes fa rinosa from Yemen -S.C. Verma 325 Lunathyrium in the Azores; a postscript- W.A. Sledge 33 1 SHORT NOTES Dryopteris x brathaica Fraser-Jenkins & Reichstein hybr.nov., the putative hybrid of D.carthusiana x D. fil ix-mas - C.R. Fraser-Jenkins & T.· Reichstein 337 No menclatural notes on Dryopteris - C.R. Fraser-Jenkins & A.C. Jermy 378 REVIEWS 278,329,341,342 [THE FERN GAZETTEVolum e 11 Part 4 was published 1st June 1976] Published by THE BRITISH PTERIDOLOGICAL SOCIETY, c/o Department of Botany, British Museum (Natural History), London SW7 5BD. FERN GAZ. 11(5) 1977 271 ECOLOGICAL NOTES OBSERVATIONS ON SOME RARE SPANISH FERNS IN CADIZ PROVINCE, SPAIN PTERIS SERRULATA Forskal. -
A Journal on Taxonomic Botany, Plant Sociology and Ecology Reinwardtia
A JOURNAL ON TAXONOMIC BOTANY, PLANT SOCIOLOGY AND ECOLOGY REINWARDTIA A JOURNAL ON TAXONOMIC BOTANY, PLANT SOCIOLOGY AND ECOLOGY Vol. 13(4): 317 —389, December 20, 2012 Chief Editor Kartini Kramadibrata (Herbarium Bogoriense, Indonesia) Editors Dedy Darnaedi (Herbarium Bogoriense, Indonesia) Tukirin Partomihardjo (Herbarium Bogoriense, Indonesia) Joeni Setijo Rahajoe (Herbarium Bogoriense, Indonesia) Teguh Triono (Herbarium Bogoriense, Indonesia) Marlina Ardiyani (Herbarium Bogoriense, Indonesia) Eizi Suzuki (Kagoshima University, Japan) Jun Wen (Smithsonian Natural History Museum, USA) Managing editor Himmah Rustiami (Herbarium Bogoriense, Indonesia) Secretary Endang Tri Utami Lay out editor Deden Sumirat Hidayat Illustrators Subari Wahyudi Santoso Anne Kusumawaty Reviewers Ed de Vogel (Netherlands), Henk van der Werff (USA), Irawati (Indonesia), Jan F. Veldkamp (Netherlands), Jens G. Rohwer (Denmark), Lauren M. Gardiner (UK), Masahiro Kato (Japan), Marshall D. Sunberg (USA), Martin Callmander (USA), Rugayah (Indonesia), Paul Forster (Australia), Peter Hovenkamp (Netherlands), Ulrich Meve (Germany). Correspondence on editorial matters and subscriptions for Reinwardtia should be addressed to: HERBARIUM BOGORIENSE, BOTANY DIVISION, RESEARCH CENTER FOR BIOLOGY-LIPI, CIBINONG 16911, INDONESIA E-mail: [email protected] REINWARDTIA Vol 13, No 4, pp: 367 - 377 THE NEW PTERIDOPHYTE CLASSIFICATION AND SEQUENCE EM- PLOYED IN THE HERBARIUM BOGORIENSE (BO) FOR MALESIAN FERNS Received July 19, 2012; accepted September 11, 2012 WITA WARDANI, ARIEF HIDAYAT, DEDY DARNAEDI Herbarium Bogoriense, Botany Division, Research Center for Biology-LIPI, Cibinong Science Center, Jl. Raya Jakarta -Bogor Km. 46, Cibinong 16911, Indonesia. E-mail: [email protected] ABSTRACT. WARD AM, W., HIDAYAT, A. & DARNAEDI D. 2012. The new pteridophyte classification and sequence employed in the Herbarium Bogoriense (BO) for Malesian ferns. -
Fern Classification
16 Fern classification ALAN R. SMITH, KATHLEEN M. PRYER, ERIC SCHUETTPELZ, PETRA KORALL, HARALD SCHNEIDER, AND PAUL G. WOLF 16.1 Introduction and historical summary / Over the past 70 years, many fern classifications, nearly all based on morphology, most explicitly or implicitly phylogenetic, have been proposed. The most complete and commonly used classifications, some intended primar• ily as herbarium (filing) schemes, are summarized in Table 16.1, and include: Christensen (1938), Copeland (1947), Holttum (1947, 1949), Nayar (1970), Bierhorst (1971), Crabbe et al. (1975), Pichi Sermolli (1977), Ching (1978), Tryon and Tryon (1982), Kramer (in Kubitzki, 1990), Hennipman (1996), and Stevenson and Loconte (1996). Other classifications or trees implying relationships, some with a regional focus, include Bower (1926), Ching (1940), Dickason (1946), Wagner (1969), Tagawa and Iwatsuki (1972), Holttum (1973), and Mickel (1974). Tryon (1952) and Pichi Sermolli (1973) reviewed and reproduced many of these and still earlier classifica• tions, and Pichi Sermolli (1970, 1981, 1982, 1986) also summarized information on family names of ferns. Smith (1996) provided a summary and discussion of recent classifications. With the advent of cladistic methods and molecular sequencing techniques, there has been an increased interest in classifications reflecting evolutionary relationships. Phylogenetic studies robustly support a basal dichotomy within vascular plants, separating the lycophytes (less than 1 % of extant vascular plants) from the euphyllophytes (Figure 16.l; Raubeson and Jansen, 1992, Kenrick and Crane, 1997; Pryer et al., 2001a, 2004a, 2004b; Qiu et al., 2006). Living euphyl• lophytes, in turn, comprise two major clades: spermatophytes (seed plants), which are in excess of 260 000 species (Thorne, 2002; Scotland and Wortley, Biology and Evolution of Ferns and Lycopliytes, ed. -
Tree Ferns: Monophyletic Groups and Their Relationships As Revealed by Four Protein-Coding Plastid Loci
Molecular Phylogenetics and Evolution 39 (2006) 830–845 www.elsevier.com/locate/ympev Tree ferns: Monophyletic groups and their relationships as revealed by four protein-coding plastid loci Petra Korall a,b,¤, Kathleen M. Pryer a, Jordan S. Metzgar a, Harald Schneider c, David S. Conant d a Department of Biology, Duke University, Durham, NC 27708, USA b Department of Phanerogamic Botany, Swedish Museum of Natural History, Stockholm, Sweden c Albrecht-von-Haller Institute für PXanzenwissenschaften, Georg-August-Universität, Göttingen, Germany d Natural Science Department, Lyndon State College, Lyndonville, VT 05851, USA Received 3 October 2005; revised 22 December 2005; accepted 2 January 2006 Available online 14 February 2006 Abstract Tree ferns are a well-established clade within leptosporangiate ferns. Most of the 600 species (in seven families and 13 genera) are arbo- rescent, but considerable morphological variability exists, spanning the giant scaly tree ferns (Cyatheaceae), the low, erect plants (Plagiogy- riaceae), and the diminutive endemics of the Guayana Highlands (Hymenophyllopsidaceae). In this study, we investigate phylogenetic relationships within tree ferns based on analyses of four protein-coding, plastid loci (atpA, atpB, rbcL, and rps4). Our results reveal four well-supported clades, with genera of Dicksoniaceae (sensu Kubitzki, 1990) interspersed among them: (A) (Loxomataceae, (Culcita, Pla- giogyriaceae)), (B) (Calochlaena, (Dicksonia, Lophosoriaceae)), (C) Cibotium, and (D) Cyatheaceae, with Hymenophyllopsidaceae nested within. How these four groups are related to one other, to Thyrsopteris, or to Metaxyaceae is weakly supported. Our results show that Dicksoniaceae and Cyatheaceae, as currently recognised, are not monophyletic and new circumscriptions for these families are needed. © 2006 Elsevier Inc. -
Phytochrome Diversity in Green Plants and the Origin of Canonical Plant Phytochromes
ARTICLE Received 25 Feb 2015 | Accepted 19 Jun 2015 | Published 28 Jul 2015 DOI: 10.1038/ncomms8852 OPEN Phytochrome diversity in green plants and the origin of canonical plant phytochromes Fay-Wei Li1, Michael Melkonian2, Carl J. Rothfels3, Juan Carlos Villarreal4, Dennis W. Stevenson5, Sean W. Graham6, Gane Ka-Shu Wong7,8,9, Kathleen M. Pryer1 & Sarah Mathews10,w Phytochromes are red/far-red photoreceptors that play essential roles in diverse plant morphogenetic and physiological responses to light. Despite their functional significance, phytochrome diversity and evolution across photosynthetic eukaryotes remain poorly understood. Using newly available transcriptomic and genomic data we show that canonical plant phytochromes originated in a common ancestor of streptophytes (charophyte algae and land plants). Phytochromes in charophyte algae are structurally diverse, including canonical and non-canonical forms, whereas in land plants, phytochrome structure is highly conserved. Liverworts, hornworts and Selaginella apparently possess a single phytochrome, whereas independent gene duplications occurred within mosses, lycopods, ferns and seed plants, leading to diverse phytochrome families in these clades. Surprisingly, the phytochrome portions of algal and land plant neochromes, a chimera of phytochrome and phototropin, appear to share a common origin. Our results reveal novel phytochrome clades and establish the basis for understanding phytochrome functional evolution in land plants and their algal relatives. 1 Department of Biology, Duke University, Durham, North Carolina 27708, USA. 2 Botany Department, Cologne Biocenter, University of Cologne, 50674 Cologne, Germany. 3 University Herbarium and Department of Integrative Biology, University of California, Berkeley, California 94720, USA. 4 Royal Botanic Gardens Edinburgh, Edinburgh EH3 5LR, UK. 5 New York Botanical Garden, Bronx, New York 10458, USA. -
On the Phylogenetic Position of Cystodium: It's Not a Tree Fern – It's a Polypod!
American Fern Journal 96(2):45–53 (2006) On the Phylogenetic Position of Cystodium: It’s Not a Tree Fern – It’s a Polypod! 1 PETRA KORALL Department of Biology, Duke University, Durham, NC 27708, USA, and Swedish Museum of Natural History, Stockholm, Sweden DAVID S. CONANT Natural Science Department, Lyndon State College, Lyndonville, VT 05851, USA HARALD SCHNEIDER Albrecht-von-Haller Institute of Plant Sciences, Georg-August University, Go¨ttingen, Germany KUNIHIKO UEDA Division of Life Science, Graduate School of Natural Science and Technology, Kanazawa University, Kanazawa, Japan HARUFUMI NISHIDA Faculty of Science and Engineering, Chuo University, 1-13-27 Kasuga, Bunkyo, Tokyo 112-8551, Japan KATHLEEN M. PRYER Department of Biology, Duke University, Durham, NC 27708, USA ABSTRACT.—The phylogenetic position of Cystodium J. Sm. is studied here for the first time using DNA sequence data. Based on a broad sampling of leptosporangiate ferns and two plastid genes (rbcL and atpB), we show that Cystodium does not belong to the tree fern family Dicksoniaceae, as previously thought. Our results strongly support including Cystodium within the large polypod clade, and suggest its close relationship to the species-poor grade taxa at the base of the polypod topology (Sphenomeris and Lonchitis,orSaccoloma in this study). Further studies, with an expanded taxon sampling within polypods, are needed to fully understand the more precise phylogenetic relationships of Cystodium. Cystodium J. Sm., with its single species C. sorbifolium (Sm.) J. Sm., has traditionally been included in Dicksoniaceae (Christensen, 1938; Pichi Sermolli, 1977; Tryon and Tryon, 1982; Kramer, 1990; Stevenson and Loconte, 1996) and, more specifically, has been considered to be closely related to Dicksonia L’He´r. -
Historical Reconstruction of Climatic and Elevation Preferences and the Evolution of Cloud Forest-Adapted Tree Ferns in Mesoamerica
Historical reconstruction of climatic and elevation preferences and the evolution of cloud forest-adapted tree ferns in Mesoamerica Victoria Sosa1, Juan Francisco Ornelas1,*, Santiago Ramírez-Barahona1,* and Etelvina Gándara1,2,* 1 Departamento de Biología Evolutiva, Instituto de Ecología AC, Carretera antigua a Coatepec, El Haya, Xalapa, Veracruz, Mexico 2 Instituto de Ciencias/Herbario y Jardín Botánico, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico * These authors contributed equally to this work. ABSTRACT Background. Cloud forests, characterized by a persistent, frequent or seasonal low- level cloud cover and fragmented distribution, are one of the most threatened habitats, especially in the Neotropics. Tree ferns are among the most conspicuous elements in these forests, and ferns are restricted to regions in which minimum temperatures rarely drop below freezing and rainfall is high and evenly distributed around the year. Current phylogeographic data suggest that some of the cloud forest-adapted species remained in situ or expanded to the lowlands during glacial cycles and contracted allopatrically during the interglacials. Although the observed genetic signals of population size changes of cloud forest-adapted species including tree ferns correspond to predicted changes by Pleistocene climate change dynamics, the observed patterns of intraspecific lineage divergence showed temporal incongruence. Methods. Here we combined phylogenetic analyses, ancestral area reconstruction, and divergence time estimates with climatic and altitudinal data (environmental space) for phenotypic traits of tree fern species to make inferences about evolutionary processes Submitted 29 May 2016 in deep time. We used phylogenetic Bayesian inference and geographic and altitudinal Accepted 18 October 2016 distribution of tree ferns to investigate ancestral area and elevation and environmental Published 16 November 2016 preferences of Mesoamerican tree ferns. -
Evolution of Vascular Plants Through Redeployment of Ancient Developmental Regulators
Evolution of vascular plants through redeployment of ancient developmental regulators Kuan-Ju Lua,1, Nicole van ’t Wout Hoflanda,1, Eliana Morb,c, Sumanth Muttea, Paul Abrahamsa, Hirotaka Katoa, Klaas Vandepoeleb,c, Dolf Weijersa,2, and Bert De Rybela,b,c,2 aLaboratory of Biochemistry, Wageningen University, 6708 WE Wageningen, The Netherlands; bDepartment of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium; and cVIB-UGent Center for Plant Systems Biology, 9052 Ghent, Belgium Edited by Dominique C. Bergmann, Stanford University, Stanford, CA, and approved December 2, 2019 (received for review July 29, 2019) Vascular plants provide most of the biomass, food, and feed on Results earth, yet the molecular innovations that led to the evolution of TMO5/LHW Acts as an Obligate Heterodimer in Arabidopsis Vascular their conductive tissues are unknown. Here, we reveal the Development. In Arabidopsis, both TMO5 and LHW have several evolutionary trajectory for the heterodimeric TMO5/LHW tran- paralogues, and higher-order mutants in either subclade strongly scription factor complex, which is rate-limiting for vascular cell reduce the number of vascular cell files, leading to nearly indis- Arabidopsis thaliana proliferation in . Both regulators have origins tinguishable phenotypes. Simultaneous misexpression of TMO5 predating vascular tissue emergence, and even terrestrialization. We and LHW triggers periclinal and radial cell divisions (PRD) in all further show that TMO5 evolved its modern function, including root meristem -
A Classification for Extant Ferns
55 (3) • August 2006: 705–731 Smith & al. • Fern classification TAXONOMY A classification for extant ferns Alan R. Smith1, Kathleen M. Pryer2, Eric Schuettpelz2, Petra Korall2,3, Harald Schneider4 & Paul G. Wolf5 1 University Herbarium, 1001 Valley Life Sciences Building #2465, University of California, Berkeley, California 94720-2465, U.S.A. [email protected] (author for correspondence). 2 Department of Biology, Duke University, Durham, North Carolina 27708-0338, U.S.A. 3 Department of Phanerogamic Botany, Swedish Museum of Natural History, Box 50007, SE-104 05 Stock- holm, Sweden. 4 Albrecht-von-Haller-Institut für Pflanzenwissenschaften, Abteilung Systematische Botanik, Georg-August- Universität, Untere Karspüle 2, 37073 Göttingen, Germany. 5 Department of Biology, Utah State University, Logan, Utah 84322-5305, U.S.A. We present a revised classification for extant ferns, with emphasis on ordinal and familial ranks, and a synop- sis of included genera. Our classification reflects recently published phylogenetic hypotheses based on both morphological and molecular data. Within our new classification, we recognize four monophyletic classes, 11 monophyletic orders, and 37 families, 32 of which are strongly supported as monophyletic. One new family, Cibotiaceae Korall, is described. The phylogenetic affinities of a few genera in the order Polypodiales are unclear and their familial placements are therefore tentative. Alphabetical lists of accepted genera (including common synonyms), families, orders, and taxa of higher rank are provided. KEYWORDS: classification, Cibotiaceae, ferns, monilophytes, monophyletic. INTRODUCTION Euphyllophytes Recent phylogenetic studies have revealed a basal dichotomy within vascular plants, separating the lyco- Lycophytes Spermatophytes Monilophytes phytes (less than 1% of extant vascular plants) from the euphyllophytes (Fig. -
European Red List of Vascular Plants Melanie Bilz, Shelagh P
European Red List of Vascular Plants Melanie Bilz, Shelagh P. Kell, Nigel Maxted and Richard V. Lansdown European Red List of Vascular Plants Melanie Bilz, Shelagh P. Kell, Nigel Maxted and Richard V. Lansdown IUCN Global Species Programme IUCN Regional Office for Europe IUCN Species Survival Commission Published by the European Commission This publication has been prepared by IUCN (International Union for Conservation of Nature). The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of the European Commission or IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of the European Commission or IUCN. Citation: Bilz, M., Kell, S.P., Maxted, N. and Lansdown, R.V. 2011. European Red List of Vascular Plants. Luxembourg: Publications Office of the European Union. Design and layout by: Tasamim Design - www.tasamim.net Printed by: The Colchester Print Group, United Kingdom Picture credits on cover page: Narcissus nevadensis is endemic to Spain where it has a very restricted distribution. The species is listed as Endangered and is threatened by modifications to watercourses and overgrazing. © Juan Enrique Gómez. All photographs used in this publication remain the property of the original copyright holder (see individual captions for details). Photographs should not be reproduced or used in other contexts without written permission from the copyright holder. Available from: Luxembourg: Publications Office of the European Union, http://bookshop.europa.eu IUCN Publications Services, www.iucn.org/publications A catalogue of IUCN publications is also available. -
Free Download Available
In: Ferns ISBN: 978-1-53613-018-8 Editors: Lucjan Nowicki et al. © 2018 Nova Science Publishers, Inc. No part of this digital document may be reproduced, stored in a retrieval system or transmitted commercially in any form or by any means. The publisher has taken reasonable care in the preparation of this digital document, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. No liability is assumed for incidental or consequential damages in connection with or arising out of information contained herein. This digital document is sold with the clear understanding that the publisher is not engaged in rendering legal, medical or any other professional services. Chapter 1 ECOPHYSIOLOGY AND ADAPTABILITY OF TERRESTRIAL FERNS: PERSPECTIVES IN A CHANGING GLOBAL CLIMATE O. Roger Anderson* Biology and Paleo Environment, Lamont-Doherty Earth Observatory of Columbia University, Palisades, NY, US ABSTRACT During millions of years of biological evolution, fern species have exhibited remarkable adaptive radiation, inhabiting environmental niches in all of the major biomes of the world, exclusive of the most formidable polar regions; although some occur in less hostile portions of the Arctic. Fern species occur widely in a variety of ecosystems including moist temperate and tropical forests, dry forests, wetlands, arid lands or deserts, and mountain domains, and have become highly specialized to exploit * Corresponding Author Email: [email protected]. 2 O. Roger Anderson niches that complement their particular life profile. Some have become entirely aquatic. However, this chapter focuses on epiphytic and terrestrial ferns to highlight peculiar challenges that global climate change may bring for their adaptation or survival. -
Change the Current Listings of Cyatheaceae Spp. to Cyathea Spp
Prop. 11.8 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II Proposals resulting from reviews by the Plants Committees A. Proposal a) Change the current listings of Cyatheaceae spp. to Cyathea spp. (including Alsophila, Nephelea, Sphaeropteris, Trichipteris). b) Change the current listing of Dicksoniaceae spp. to Dicksonia spp. (originating in the Americas only) and Cibotium barometz. B. Proponent Swiss Confederation. C. Supporting Statement 1. Taxonomy 1.1 Class: a) Filicidae b) Filicidae 1.2 Order: a) Cyatheales b) Dicksoniales 1.3 Family: a) Cyatheaceae b) Dicksoniaceae 1.4 Genus: a) Cyathea spp. (including Alsophila, Nephelea, Sphaeropteris, Trichipteris) b) i) Dicksonia spp. (originating in the Americas) ii) Cibotium: Cibotium barometz 1.5 Scientific synonyms: 1.6 Common names: a) English: tree ferns French: fougères arborescentes Spanish: helechos arborescentes b) i) English: tree ferns French: fougères arborescentes Spanish: helechos arborescentes ii) English: Golden haired dog fern French: Spanish: 1.7 Code numbers: 2. Biological Parameters 2.1 Distribution Prop. 11.8 - p. 1 Representatives of the Cyatheaceae and Dicksoniaceae can be found in all tropical regions of the world. Some smaller genera have a more restricted, continental distribution. Family Genus Comments Com- mercial Trade Cyatheaceae Alsophila Included in Cyathea as subgenus --- Cyatheaceae Cnemidaria Tropical America; ca. 23 species No Cyatheaceae Cyathea Pantropical, 600 species Yes Cyatheaceae Nephelea Included in Cyathea as subgenus --- Cyatheaceae Sphaeropteris Included in Cyathea as subgenus --- Cyatheaceae Trichipteris Included in Cyathea as subgenus --- Dicksoniaceae* Calochlaena Tropical Asia, Oceania, segregated from Yes Culcita senso stricto Dicksoniaceae Cibotium Pantropical 12 species, only C. barometz Yes reported to be in trade Dicksoniaceae* Culcita Tropical America, 1 species No Dicksoniaceae Cystodium Tropical Asia, Oceania, 1 species No Dicksoniaceae Dicksonia Tropical America, Oceania, South East Asia (high elevations); D.