In Which Family Shall We Put the Genus Veronica L.?
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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. -
Veronica Plants—Drifting from Farm to Traditional Healing, Food Application, and Phytopharmacology
molecules Review Veronica Plants—Drifting from Farm to Traditional Healing, Food Application, and Phytopharmacology Bahare Salehi 1 , Mangalpady Shivaprasad Shetty 2, Nanjangud V. Anil Kumar 3 , Jelena Živkovi´c 4, Daniela Calina 5 , Anca Oana Docea 6, Simin Emamzadeh-Yazdi 7, Ceyda Sibel Kılıç 8, Tamar Goloshvili 9, Silvana Nicola 10 , Giuseppe Pignata 10, Farukh Sharopov 11,* , María del Mar Contreras 12,* , William C. Cho 13,* , Natália Martins 14,15,* and Javad Sharifi-Rad 16,* 1 Student Research Committee, School of Medicine, Bam University of Medical Sciences, Bam 44340847, Iran 2 Department of Chemistry, NMAM Institute of Technology, Karkala 574110, India 3 Department of Chemistry, Manipal Institute of Technology, Manipal Academy of Higher Education, Manipal 576104, India 4 Institute for Medicinal Plants Research “Dr. Josif Panˇci´c”,Tadeuša Koš´cuška1, Belgrade 11000, Serbia 5 Department of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, Craiova 200349, Romania 6 Department of Toxicology, University of Medicine and Pharmacy of Craiova, Craiova 200349, Romania 7 Department of Plant and Soil Sciences, University of Pretoria, Gauteng 0002, South Africa 8 Department of Pharmaceutical Botany, Faculty of Pharmacy, Ankara University, Ankara 06100, Turkey 9 Department of Plant Physiology and Genetic Resources, Institute of Botany, Ilia State University, Tbilisi 0162, Georgia 10 Department of Agricultural, Forest and Food Sciences, University of Turin, I-10095 Grugliasco, Italy 11 Department of Pharmaceutical Technology, Avicenna Tajik State Medical University, Rudaki 139, Dushanbe 734003, Tajikistan 12 Department of Chemical, Environmental and Materials Engineering, University of Jaén, 23071 Jaén, Spain 13 Department of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong SAR 999077, China 14 Faculty of Medicine, University of Porto, Alameda Prof. -
Towards Resolving Lamiales Relationships
Schäferhoff et al. BMC Evolutionary Biology 2010, 10:352 http://www.biomedcentral.com/1471-2148/10/352 RESEARCH ARTICLE Open Access Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences Bastian Schäferhoff1*, Andreas Fleischmann2, Eberhard Fischer3, Dirk C Albach4, Thomas Borsch5, Günther Heubl2, Kai F Müller1 Abstract Background: In the large angiosperm order Lamiales, a diverse array of highly specialized life strategies such as carnivory, parasitism, epiphytism, and desiccation tolerance occur, and some lineages possess drastically accelerated DNA substitutional rates or miniaturized genomes. However, understanding the evolution of these phenomena in the order, and clarifying borders of and relationships among lamialean families, has been hindered by largely unresolved trees in the past. Results: Our analysis of the rapidly evolving trnK/matK, trnL-F and rps16 chloroplast regions enabled us to infer more precise phylogenetic hypotheses for the Lamiales. Relationships among the nine first-branching families in the Lamiales tree are now resolved with very strong support. Subsequent to Plocospermataceae, a clade consisting of Carlemanniaceae plus Oleaceae branches, followed by Tetrachondraceae and a newly inferred clade composed of Gesneriaceae plus Calceolariaceae, which is also supported by morphological characters. Plantaginaceae (incl. Gratioleae) and Scrophulariaceae are well separated in the backbone grade; Lamiaceae and Verbenaceae appear in distant clades, while the recently described Linderniaceae are confirmed to be monophyletic and in an isolated position. Conclusions: Confidence about deep nodes of the Lamiales tree is an important step towards understanding the evolutionary diversification of a major clade of flowering plants. The degree of resolution obtained here now provides a first opportunity to discuss the evolution of morphological and biochemical traits in Lamiales. -
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. -
Pollen Morphology of Fridericia Mart. (Bignoniaceae) from Brazilian Forest Fragments
Braz. J. Bot (2014) 37(1):83–94 DOI 10.1007/s40415-013-0042-1 Pollen morphology of Fridericia Mart. (Bignoniaceae) from Brazilian forest fragments Cintia Neves de Souza • Eduardo Custo´dio Gasparino Received: 18 October 2013 / Accepted: 3 December 2013 / Published online: 17 December 2013 Ó Botanical Society of Sao Paulo 2013 Abstract A pollen morphology study of 10 Brazilian Introduction native species of Fridericia (Bignoniaceae) from forest fragments was performed using light microscopy and The fragmentation process of forest habitats has increased scanning electron microscopy, in search of new characters in most ecosystems particularly in the tropics, so this has that might increase knowledge of pollen morphology of the caused, in general, the loss of the biodiversity (Turner species, and also to help the taxonomic characterization of 1996; Myers et al. 2000). The northwestern of Sa˜o Paulo the genus. The pollen grains were acetolysed, measured, State, Brazil, is a region consisting of vegetation that photographed, and described qualitatively. The quantitative includes small fragments of semideciduous forest and large data were analyzed by descriptive statistics and multivar- areas of Cerrado (Kronka et al. 1993). This structure is a iate statistics. Non-acetolysed pollen grains were observed result of fragmentation in natural forest (Atlantic Forest of under scanning electron microscopy for further details of Brazil), which currently only take up 5 % of the original exine and pollen surface. The pollen grains are isopolar, forest -
Pollen and Stamen Mimicry: the Alpine Flora As a Case Study
Arthropod-Plant Interactions DOI 10.1007/s11829-017-9525-5 ORIGINAL PAPER Pollen and stamen mimicry: the alpine flora as a case study 1 1 1 1 Klaus Lunau • Sabine Konzmann • Lena Winter • Vanessa Kamphausen • Zong-Xin Ren2 Received: 1 June 2016 / Accepted: 6 April 2017 Ó The Author(s) 2017. This article is an open access publication Abstract Many melittophilous flowers display yellow and Dichogamous and diclinous species display pollen- and UV-absorbing floral guides that resemble the most com- stamen-imitating structures more often than non-dichoga- mon colour of pollen and anthers. The yellow coloured mous and non-diclinous species, respectively. The visual anthers and pollen and the similarly coloured flower guides similarity between the androecium and other floral organs are described as key features of a pollen and stamen is attributed to mimicry, i.e. deception caused by the flower mimicry system. In this study, we investigated the entire visitor’s inability to discriminate between model and angiosperm flora of the Alps with regard to visually dis- mimic, sensory exploitation, and signal standardisation played pollen and floral guides. All species were checked among floral morphs, flowering phases, and co-flowering for the presence of pollen- and stamen-imitating structures species. We critically discuss deviant pollen and stamen using colour photographs. Most flowering plants of the mimicry concepts and evaluate the frequent evolution of Alps display yellow pollen and at least 28% of the species pollen-imitating structures in view of the conflicting use of display pollen- or stamen-imitating structures. The most pollen for pollination in flowering plants and provision of frequent types of pollen and stamen imitations were pollen for offspring in bees. -
Flora Mediterranea 26
FLORA MEDITERRANEA 26 Published under the auspices of OPTIMA by the Herbarium Mediterraneum Panormitanum Palermo – 2016 FLORA MEDITERRANEA Edited on behalf of the International Foundation pro Herbario Mediterraneo by Francesco M. Raimondo, Werner Greuter & Gianniantonio Domina Editorial board G. Domina (Palermo), F. Garbari (Pisa), W. Greuter (Berlin), S. L. Jury (Reading), G. Kamari (Patras), P. Mazzola (Palermo), S. Pignatti (Roma), F. M. Raimondo (Palermo), C. Salmeri (Palermo), B. Valdés (Sevilla), G. Venturella (Palermo). Advisory Committee P. V. Arrigoni (Firenze) P. Küpfer (Neuchatel) H. M. Burdet (Genève) J. Mathez (Montpellier) A. Carapezza (Palermo) G. Moggi (Firenze) C. D. K. Cook (Zurich) E. Nardi (Firenze) R. Courtecuisse (Lille) P. L. Nimis (Trieste) V. Demoulin (Liège) D. Phitos (Patras) F. Ehrendorfer (Wien) L. Poldini (Trieste) M. Erben (Munchen) R. M. Ros Espín (Murcia) G. Giaccone (Catania) A. Strid (Copenhagen) V. H. Heywood (Reading) B. Zimmer (Berlin) Editorial Office Editorial assistance: A. M. Mannino Editorial secretariat: V. Spadaro & P. Campisi Layout & Tecnical editing: E. Di Gristina & F. La Sorte Design: V. Magro & L. C. Raimondo Redazione di "Flora Mediterranea" Herbarium Mediterraneum Panormitanum, Università di Palermo Via Lincoln, 2 I-90133 Palermo, Italy [email protected] Printed by Luxograph s.r.l., Piazza Bartolomeo da Messina, 2/E - Palermo Registration at Tribunale di Palermo, no. 27 of 12 July 1991 ISSN: 1120-4052 printed, 2240-4538 online DOI: 10.7320/FlMedit26.001 Copyright © by International Foundation pro Herbario Mediterraneo, Palermo Contents V. Hugonnot & L. Chavoutier: A modern record of one of the rarest European mosses, Ptychomitrium incurvum (Ptychomitriaceae), in Eastern Pyrenees, France . 5 P. Chène, M. -
Systematic Treatment of Veronica L
eISSN: 2357-044X Taeckholmia 38 (2018): 168-183 Systematic treatment of Veronica L. Section Beccabunga (Hill) Dumort (Plantaginaceae) Faten Y. Ellmouni1, Mohamed A. Karam1, Refaat M. Ali1, Dirk C. Albach2 1Department of Botany, Faculty of Science, Fayoum University, 63514 Fayoum, Egypt. 2Institute of biology and environmental sciences, Carl von Ossietzky-University, 26111 Oldenburg, Germany. *Corresponding author: [email protected] Abstract Veronica species mostly occur in damp fresh water places and in the Mediterranean precipitation regime. Members of this genus grow at different altitudes from sea level to high alpine elevations. They show a high level of polymorphism and phenotypic plasticity in their responses to variations of the enviromental factors, a quality that allows them to occur over a wide range of conditions. A group with particular high levels of polymorphism is the group of aquatic Veronica L. species in V. sect. Beccabunga (Hill) Dumort. Here, we attempt to unravel some confusion in the taxonomic complexity in V. section Beccabunga. We recognize 20 taxa in V. sect. Beccabunga and explore the occurrence of V. section Beccabunga, mainly in the Mediterranean basin; especially in Egypt (Nile delta and Sinai), Turkey and Iran with each country containing 10 taxa, from a total of 20 taxa, and characterized by endemics, or near-endemic as Veronica anagalloides ssp. taeckholmiorum.The results confirmed that V. section Beccabunga is divided into three subsections Beccabunga, Anagallides and Peregrinae, which essentially can be differentiated by the absence or presence of apetiole. Keywords: Morphological key, systematic treatment, Veronica, V. section Beccabunga Introduction The tribe Veroniceae, formerly part of the genus include: life-form (subshrubby/perennial vs. -
Flowering Plants of South Norwood Country Park
Flowering Plants Of South Norwood Country Park Robert Spencer Introduction South Norwood Country Park relative to its size contains a wide range habitats and as a result a diverse range of plants can be found growing on site. Some of these plants are very conspicuous, growing in great abundance and filling the park with splashes of bright colour with a white period in early May largely as a result of the Cow Parsley, this is followed later in the year by a pink period consisting of mainly Willow herbs. Other plants to be observed are common easily recognisable flowers. However there are a great number of plants growing at South Norwood Country Park that are less well-known or harder to spot, and the casual observer would likely be surprised to learn that 363 species of flowering plants have so far been recorded growing in the park though this number includes invasive species and garden escapes. This report is an update of a report made in 2006, and though the site has changed in the intervening years the management and fundamental nature of the park remains the same. Some plants have diminished and some have flourished and the high level of diversity is still present. Many of these plants are important to other wildlife particularly in their relationship to invertebrate pollinators, and some of these important interactions are referenced in this report. With so many species on the plant list there is a restriction on how much information is given for each species, with some particularly rare or previously observed but now absent plants not included though they appear in the index at the back of the report including when they were last observed. -
Evolution of Flower Shape in Plantago Lanceolata
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by MURAL - Maynooth University Research Archive Library Plant Mol Biol (2009) 71:241–250 DOI 10.1007/s11103-009-9520-z Evolution of flower shape in Plantago lanceolata Wesley Reardon Æ David A. Fitzpatrick Æ Mario A. Fares Æ Jacqueline M. Nugent Received: 16 December 2008 / Accepted: 25 June 2009 / Published online: 11 July 2009 Ó Springer Science+Business Media B.V. 2009 Abstract Plantago lanceolata produces small actino- Introduction morphic (radially symmetric), wind-pollinated flowers that have evolved from a zygomorphic, biotically pollinated Flowering plants have evolved huge diversity in their floral ancestral state. To understand the developmental mecha- form and in their pollination strategies. One of the most nisms that might underlie this change in flower shape, and variable morphological characters is flower shape. Flowers associated change in pollination syndrome, we analyzed can be classified as zygomorphic (having only one plane of the role of CYC-like genes in P. lanceolata. Related reflectional symmetry or bilaterally symmetric), actino- zygomorphic species have two CYC-like genes that are morphic (having multiple planes of symmetry or radially expressed asymmetrically in the dorsal region of young symmetric) or asymmetric (having no plane of symmetry) floral meristems and in developing flowers, where they (Endress 2001). The gene regulatory network that deter- affect the rate of development of dorsal petals and stamens. mines zygomorphy is best understood in the model plant Plantago has a single CYC-like gene (PlCYC) that is not Antirrhinum majus (Corley et al. -
Arbuscular Mycorrhizal Fungi and Dark Septate Fungi in Plants Associated with Aquatic Environments Doi: 10.1590/0102-33062016Abb0296
Arbuscular mycorrhizal fungi and dark septate fungi in plants associated with aquatic environments doi: 10.1590/0102-33062016abb0296 Table S1. Presence of arbuscular mycorrhizal fungi (AMF) and/or dark septate fungi (DSF) in non-flowering plants and angiosperms, according to data from 62 papers. A: arbuscule; V: vesicle; H: intraradical hyphae; % COL: percentage of colonization. MYCORRHIZAL SPECIES AMF STRUCTURES % AMF COL AMF REFERENCES DSF DSF REFERENCES LYCOPODIOPHYTA1 Isoetales Isoetaceae Isoetes coromandelina L. A, V, H 43 38; 39 Isoetes echinospora Durieu A, V, H 1.9-14.5 50 + 50 Isoetes kirkii A. Braun not informed not informed 13 Isoetes lacustris L.* A, V, H 25-50 50; 61 + 50 Lycopodiales Lycopodiaceae Lycopodiella inundata (L.) Holub A, V 0-18 22 + 22 MONILOPHYTA2 Equisetales Equisetaceae Equisetum arvense L. A, V 2-28 15; 19; 52; 60 + 60 Osmundales Osmundaceae Osmunda cinnamomea L. A, V 10 14 Salviniales Marsileaceae Marsilea quadrifolia L.* V, H not informed 19;38 Salviniaceae Azolla pinnata R. Br.* not informed not informed 19 Salvinia cucullata Roxb* not informed 21 4; 19 Salvinia natans Pursh V, H not informed 38 Polipodiales Dryopteridaceae Polystichum lepidocaulon (Hook.) J. Sm. A, V not informed 30 Davalliaceae Davallia mariesii T. Moore ex Baker A not informed 30 Onocleaceae Matteuccia struthiopteris (L.) Tod. A not informed 30 Onoclea sensibilis L. A, V 10-70 14; 60 + 60 Pteridaceae Acrostichum aureum L. A, V, H 27-69 42; 55 Adiantum pedatum L. A not informed 30 Aleuritopteris argentea (S. G. Gmel) Fée A, V not informed 30 Pteris cretica L. A not informed 30 Pteris multifida Poir. -
Communications
COMMUNICATION S FACULTY OF SCIENCES DE LA FACULTE DES SCIENCES UNIVERSITY OF ANKARA DE L’UNIVERSITE D’ANKARA Series C: Biology VOLUME: 29 Number: 1 YEAR: 2020 Faculy of Sciences, Ankara University 06100 Beşevler, Ankara-Turkey ISSN: 1303-6025 E-ISSN: 2651-3749 COMMUNICATION S FACULTY OF SCIENCES DE LA FACULTE DES SCIENCES UNIVERSITY OF ANKARA DE L’UNIVERSITE D’ANKARA Series C: Biolog y Volume 29 Number : 1 Year: 2020 Owner (Sahibi) Selim Osman SELAM, Dean of Faculty of Sciences Editor-in-Chief (Yazı İşleri Müdürü) Nuri OZALP Managing Editor Nur Münevver PINAR Area Editors Ilgaz AKATA (Botany) Nursel AŞAN BAYDEMİR (Zoology) İlker BUYUK (Biotechnology) Talip ÇETER (Plant Anatomy and Embryology) Ilknur DAĞ (Microbiology, Histology) Türker DUMAN (Moleculer Biology) Borga ERGONUL (Hydrobiology) Sevgi ERTUĞRUL KARATAY (Biotechnology) Esra KOÇ (Plant Physiology) G. Nilhan TUĞ (Ecology) A. Emre YAPRAK ( Botany) Mehmet Kürşat Şahin (Zoology) Şeyda Fikirdeşici Ergen (Hydrobiology) Alexey YANCHUKOV (Populations Genetics, Molecular Ecology and Evolution Biology) Language Editor: Sümer ARAS Technical Editor: Aydan ACAR ŞAHIN Editors Nuray AKBULUT (Hacettepe University, Turkey) Hasan AKGUL (Akdeniz University, Turkey) Şenol ALAN (Bülent Ecevit University, Turkey) Dirk Carl ALBACH (Carl Von Ossietzky University, Germany) Ahmet ALTINDAG (Ankara University, Turkey) Rami ARAFEH (Palestine Polytechnic University, Palestine) Belma BINLI ASLIM (Gazi University, Turkey) Tahir ATICI (Gazi University,Turkey) Dinçer AYAZ (Ege University, Turkey) Zeki AYTAÇ (Gazi University,Turkey) Jan BREINE (Research Institute for Nature and Forest, Belgium) Kemal BUYUKGUZEL (Bulent Ecevit University, Turkey) Suna CEBESOY (Ankara University, Turkey) A. Kadri ÇETIN (Fırat University, Turkey) Nuran ÇIÇEK (Hacettepe University, Turkey) Elif SARIKAYA DEMIRKAN (Uludag University, Turkey) Mohammed H.