IUCN Guidelines Using for Assessment of Plants from the Red Book of Russian Federation at Regional Level: a Case Study for the Republic of Mordovia (Russia)
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Vegetation of the Ferdynandovian Interglacial (MIS 13–15) Based on Plant Macrofossils from a New Profile of the Stratotype Site
Acta Palaeobotanica 55(2): 233–251, 2015 DOI: 10.1515/acpa-2015-0011 Vegetation of the Ferdynandovian interglacial (MIS 13–15) based on plant macrofossils from a new profile of the stratotype site RENATA STACHOWICZ-RYBKA W. Szafer Institute of Botany, Polish Academy of Sciences, Lubicz 46, 31-512 Kraków, Poland; e-mail: [email protected] Received 23 September 2015; accepted for publication 19 October 2015 ABSTRACT. Early Middle Pleistocene palaeolacustrine sediments of the Ferdynandów site (E Poland), serving as a stratotype for the Ferdynandovian interglacial, were subjected to a new drilling in 2011. The obtained profile, covering the late Sanian 1 glaciation, two interglacial successions (Ferdynandovian 1 and 2), the cold Ferdynan- dovian 1/2 interval, and the early Sanian 2 glaciation, permitted a high-resolution plant macroremains analysis, correlated with the results of a palynological examination. In detailed studies of plant macroremains from the profile, new taxa were discovered for the Polish Pleistocene flora: specifically, species that are extinct or not found nowadays in Poland. On the basis of the taxonomic diversity and occurrence of bioindicators, the division into warm and cold units of the Ferdynandovian interglacial as well as units associated with the Sanian 1 and 2 glaciations, already applied in pollen studies, were confirmed, and the periods were described in terms of plant macroremains. The Ferdynandovian succession is correlated with the Cromerian Complex (Cromerian III and IV) in the Early Middle Pleistocene of Western Europe, as well as with Marine Isotope Stages (MIS) 13–15. New geological and palaeobotanical data enabled a description of the palaeogeographic context and conditions of functioning, as well as the evolution of the interglacial lake at the stratotype site. -
Á Biologická Klasifikace Rostlin -.. Inovace Studia Molekulární A
Inovace studia molekulární a buněčné biologie Tento projekt je spolufinancován Evropským sociálním fondem a státním rozpočtem České republiky. BIOLOGICKÁ KLASIFIKACE ROSTLIN Radim J. Vašut Gnetoppyhyta Gnetophyta • Dvoudomé i jednodomé dřeviny • Náznak 2-tého oplození • Redukce mikroprotália • Eustélé bez prysky ř. Kanálků, atypické tracheje Ephedridae • 1 rod, 40 druhů, stepní až aridní oblasti • 2vají2 vajíčka / 2 archegonia •Přeličkovitý vzhled Ephedra distachya jediný zástupce ve středoevropské flóře (Slovensko) Gnetidae • Dvoudomé i jednodomé dřeviny • Náznak 2-tého oplození • Redukce mikroprotália • Eustélé bez prysky ř. Kanálků, atypické tracheje Gnetum spp. • Ca. 30 druhů ()(tropy) • Hromada hadrů • EtéExtrémn í suc ho • Až 2000 let Welwitschiidae • Welwitschia mirablis • Náznak 2-tého oplození • RdkRedukce m ikropro tália • Eustélé bez pryskyř. Kanálků, atypické tracheje Welwitschia mirabilis •Namib • Hromada hadrů • EtéExtrémn í suc ho • Až 2000 let Ginkgophyta jinany Ginkgophyta • Nahosemenné druhotně tlopustnoucí dřeviny • Vějiřovitá žilnatina • Listy mikrofilního původu • Vrchol ve druhohorách •Evolučně spojené s Cordaity? • Podstatná složka stravy dinosaurů Ginkgophyta - sex • DdéDvoudomé •Pyl je při vysychání ppyolynační kappyky vtahován do pylové komory. • Uvnitř vyklíčené pylové láčky dva polyciliátní spermatoz oidy • (u cykasů a jinanů se s nimi setkáváme naposledy) • oplození vaječné buňky až po odpadnutí semene na zem Ginkgophyta – generativní orgány Ginkgo biloba •JV Čína • Vyhynulý? • V ku ltivaci po celé m světě -
The Genomic Impact of Mycoheterotrophy in Orchids
fpls-12-632033 June 8, 2021 Time: 12:45 # 1 ORIGINAL RESEARCH published: 09 June 2021 doi: 10.3389/fpls.2021.632033 The Genomic Impact of Mycoheterotrophy in Orchids Marcin J ˛akalski1, Julita Minasiewicz1, José Caius2,3, Michał May1, Marc-André Selosse1,4† and Etienne Delannoy2,3*† 1 Department of Plant Taxonomy and Nature Conservation, Faculty of Biology, University of Gdansk,´ Gdansk,´ Poland, 2 Institute of Plant Sciences Paris-Saclay, Université Paris-Saclay, CNRS, INRAE, Univ Evry, Orsay, France, 3 Université de Paris, CNRS, INRAE, Institute of Plant Sciences Paris-Saclay, Orsay, France, 4 Sorbonne Université, CNRS, EPHE, Muséum National d’Histoire Naturelle, Institut de Systématique, Evolution, Biodiversité, Paris, France Mycoheterotrophic plants have lost the ability to photosynthesize and obtain essential mineral and organic nutrients from associated soil fungi. Despite involving radical changes in life history traits and ecological requirements, the transition from autotrophy Edited by: Susann Wicke, to mycoheterotrophy has occurred independently in many major lineages of land Humboldt University of Berlin, plants, most frequently in Orchidaceae. Yet the molecular mechanisms underlying this Germany shift are still poorly understood. A comparison of the transcriptomes of Epipogium Reviewed by: Maria D. Logacheva, aphyllum and Neottia nidus-avis, two completely mycoheterotrophic orchids, to other Skolkovo Institute of Science autotrophic and mycoheterotrophic orchids showed the unexpected retention of several and Technology, Russia genes associated with photosynthetic activities. In addition to these selected retentions, Sean W. Graham, University of British Columbia, the analysis of their expression profiles showed that many orthologs had inverted Canada underground/aboveground expression ratios compared to autotrophic species. Fatty Craig Barrett, West Virginia University, United States acid and amino acid biosynthesis as well as primary cell wall metabolism were among *Correspondence: the pathways most impacted by this expression reprogramming. -
The Diversity of Wild Orchids in the Southern Slope of Mount Merapi, Yogyakarta, Indonesia Eight Years After the 2010 Eruption
BIODIVERSITAS ISSN: 1412-033X Volume 21, Number 9, September 2020 E-ISSN: 2085-4722 Pages: 4457-4465 DOI: 10.13057/biodiv/d210964 The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption FEBRI YUDA KURNIAWAN1,2,♥, FAUZANA PUTRI2,3, AHMAD SUYOKO2,3, HIMAWAN MASYHURI2,3, MAYA PURQI SULISTIANINGRUM2,3, ENDANG SEMIARTI3,♥♥ 1Postgraduate School, Universitas Gadjah Mada. Jl. Teknika Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax. +62-274-544975, email: [email protected] 2Biology Orchid Study Club (BiOSC), Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia 3Department of Tropical Biology, Faculty of Biology, Universitas Gadjah Mada. Jl. Teknika Selatan, Sekip Utara, Sleman 55281, Yogyakarta, Indonesia. Tel./fax.: +62-274-580839, email: [email protected] Manuscript received: 21 August 2020. Revision accepted: 31 August 2020. Abstract. Kurniawan FY, Putri F, Suyoko A, Masyhuri H, Sulistianingrum MP, Semiarti E. 2020. The diversity of wild orchids in the southern slope of Mount Merapi, Yogyakarta, Indonesia eight years after the 2010 eruption. Biodiversitas 21: 4457-4465. The ecosystem of the slopes of Mount Merapi is mountain tropical forest which is frequently affected by volcanic activities. The dynamics of the volcano affect the diversity and abundance of orchids in the ecosystem. Tritis is an area included in the Turgo Hill of the southern slope of Mount Merapi and is under the management of Mount Merapi National Park. The ecosystem in Tritis area classified as lower mountain forest and it has been affected by Mount Merapi eruption. This study aimed to do an inventory of orchid species in Tritis to know the diversity and abundance of orchids that exist in this area. -
Conserving Europe's Threatened Plants
Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation Conserving Europe’s threatened plants Progress towards Target 8 of the Global Strategy for Plant Conservation By Suzanne Sharrock and Meirion Jones May 2009 Recommended citation: Sharrock, S. and Jones, M., 2009. Conserving Europe’s threatened plants: Progress towards Target 8 of the Global Strategy for Plant Conservation Botanic Gardens Conservation International, Richmond, UK ISBN 978-1-905164-30-1 Published by Botanic Gardens Conservation International Descanso House, 199 Kew Road, Richmond, Surrey, TW9 3BW, UK Design: John Morgan, [email protected] Acknowledgements The work of establishing a consolidated list of threatened Photo credits European plants was first initiated by Hugh Synge who developed the original database on which this report is based. All images are credited to BGCI with the exceptions of: We are most grateful to Hugh for providing this database to page 5, Nikos Krigas; page 8. Christophe Libert; page 10, BGCI and advising on further development of the list. The Pawel Kos; page 12 (upper), Nikos Krigas; page 14: James exacting task of inputting data from national Red Lists was Hitchmough; page 16 (lower), Jože Bavcon; page 17 (upper), carried out by Chris Cockel and without his dedicated work, the Nkos Krigas; page 20 (upper), Anca Sarbu; page 21, Nikos list would not have been completed. Thank you for your efforts Krigas; page 22 (upper) Simon Williams; page 22 (lower), RBG Chris. We are grateful to all the members of the European Kew; page 23 (upper), Jo Packet; page 23 (lower), Sandrine Botanic Gardens Consortium and other colleagues from Europe Godefroid; page 24 (upper) Jože Bavcon; page 24 (lower), Frank who provided essential advice, guidance and supplementary Scumacher; page 25 (upper) Michael Burkart; page 25, (lower) information on the species included in the database. -
151-170 Peruzzi
INFORMATORE BOTANICO ITALIANO, 42 (1) 151-170, 2010 151 Checklist dei generi e delle famiglie della flora vascolare italiana L. PERUZZI ABSTRACT - Checklist of genera and families of Italian vascular flora -A checklist of the genera and families of vascular plants occurring in Italy is presented. The families were grouped according to the main six taxonomic groups (e.g. sub- classes: Lycopodiidae, Ophioglossidae, Equisetidae, Polypodiidae, Pinidae, Magnoliidae) and put in systematic order accord- ing to the most recent criteria (e.g. APG system etc.). The genera within each family are arranged in alphabetic order and delimited through recent literature survey. 55 orders (51 native and 4 exotic) and 173 families were recorded (158 + 24), for a total of 1297 genera (1060 + 237). Families with the highest number of genera were Poaceae (126 + 23) and Asteraceae (125 + 23), followed by Apiaceae (85 + 5), Brassicaceae (64 + 5), Fabaceae (45 + 19) etc. A single genus resulted narrow endemic of Italy (Sicily): the monotypic Petagnaea (Apiaceae). Three more genera are instead endemic to Sardinia and Corse: Morisia (Brassicaceae), Castroviejoa and Nananthea (Asteraceae). Key words: classification, families, flora, genera, Italy Ricevuto il 16 Novembre 2009 Accettato il 5 Marzo 2010 INTRODUZIONE Successivamente alla “Flora d’Italia” di PIGNATTI Flora Europaea (BAGELLA, URBANI, 2006; (1982), i progressi negli studi biosistematici e filoge- BOCCHIERI, IIRITI, 2006; LASTRUCCI, RAFFAELLI, netici hanno prodotto una enorme mole di cono- 2006; ROMANO et al., 2006; MAIORCA et al., 2007; scenze circa le piante vascolari. Nella recente CORAZZI, 2008) a tentantivi di aggiormanento Checklist della flora vascolare italiana e sua integra- “misti”, basati sul totale o parziale accoglimento di zione (CONTI et al., 2005, 2007a) non vengono prese classificazioni successive, spesso non ulteriormente in considerazione le famiglie di appartenenza delle specificate (es. -
Zum Vorkommen Von Hajas Ihihoi' All. Im Mitteleibegebiet
Hercynia N. F., Leipzig 10 (1973) 3, S. 264-275 Aus der Sektion Biowissenschaften der Martin-Luther-Universität Halle-Wittenberg, Fachbereich Botanik (Fachbereichsleiter : Prof. Dr. H. Meusel) Zum Vorkommen von Hajas IHiHOI' All. im Mitteleibegebiet Von W erner Hilbig und Horst Jage Mit 2 Karten und 1 Tabelle (Eingegangen am 5. April 1973) Das seit dem Jahre 1787 aus dem Mitteleibegebiet bekannte und im 19. Jahr hundert mehrfach belegte Kleine Nixkraut (Najas minor All.) war seit der 2. Hälfte des 19. Jahrhunderts verschollen. Seit dem ersten Wiederfund der Art im Mittelelbe gebiet im Jahre 1970 (vgl. Reichhoff u. Voigt 1972) sind weitere Vorkommen im Gebiet festgestellt worden. Auch im südlichen Brandenburg wurde die Art in neuerer Zeit mehrfach beobachtet. Wir halten es deshalb für angebracht, auf die bisherigen Funde von Najas minor im Mitteleibegebiet zusammenfassend aufmerksam zu machen und gleichzeitig auf die anderen in Europa auftretenden Najas-Arten und ihre Verbreitung hinzuweisen. Ein Bestimmungsschlüssel für die europäischen Najas-Arten wird am Schlu6 des Beitrages gegeben. Für verschiedenartige Mitteilungen und Hinweise möchten wir folgenden Kollegen danken: Dr. K. Faber - Magdeburg, Dr. W. Fischer - Potsdam, D. Heidecke - Steckby, Dr. W. Hempel - Dresden, H. Illig - Luckau, Dr. E. Jäger - Halle/S., P. Konczak - Wriezen, Dr. habil. H.-D. Krausch - Potsdam, M. Nicht - Magdeburg, L. Reichhoff - Halle/S., 0 . Voigt - Dessau. Herr P. Konczak stellte uns freundlicher weise die Originalaufnahmen der Bestände mit Najas minor zur Verfügung, die seiner Tabelle 2 (Konczak 1968) zugrunde liegen; eine weitere Einzelaufnahme verdanken wir Herrn L. Reichhoff. Vorkommen im Mitteleibegebiet und seiner Umgebung Während Najas marina gegenwärtig im gesamten Mitteleibegebiet verschollen ist, konnte Najas minor seit 1970 an vier verschiedenen Fundorten, teilweise an mehreren Stellen der Gewässer und in reichen Beständen sowie in aufeinanderfolgenden Jahren beobachtet werden. -
Cypripediaceae Lindl
Acta Botanica Neerlandica 14 (1965) 230-241 The Place of Epipogium in the System of Orchidales P. Vermeulen [Hugo de Vries-Laboratorium, Amsterdam) (;received April 13lh, 1965) Abstract stamen The (Ai) of Epipogium has a discrete filament and there is no broad in sertion of the large anther. In the anther the pollinia and the caudicles develop from of Orchioideae in of differently those the a way characteristic the genus. The rostellum consists of a simple gland crowning the top of the median stigma- tic lobe. This gland lies on top (is acrotonic) of the pollinia (and not basitonic). make should be refer- The common characteristics it clear that the genus Epipogium red to the contribe of the Neottianthae (subfamilia Epidendroideae). 1. The System of Orchidales Before assigning Epipogium a place in the system of orchidaceous plants, one has to choose the system one prefers to follow. My personal opinion being at variance with that of other modern taxonomists (Mansfeld, Dressler & Dodson, Garay and Melchior), it seems best to outline here the system I prefer. Ordo: ORCHIDALES, flowers zygomorphic, usually resupinate, epi- with the abaxial gynous, a gynostemium only stamens present (Ai + ai + aa) and these fertile or partly staminodial. Seeds dust- fine (usually) and after germination mycotrophic. (Fig. 1) Familia 1. Apostasiaceae Lindl.: perianth nearly regular, gynostemium short with Ai fertile or a staminodial, ai + a fertile, style and stamens partly free, anthers oblong; pollen powdery. No rostel- lum. Stigma terminal. Familia 2. Cypripediaceae Lindl.: median petal (lip) forming the label- lum slipper-like; gynostemium longer andbent with Ai represented orbicular by a staminod, ai + aa fertile, anther to oblong; pollen sticky, no pollinia. -
Circumscribing Genera in the European Orchid Flora: a Subjective
Ber. Arbeitskrs. Heim. Orchid. Beiheft 8; 2012: 94 - 126 Circumscribing genera in the European orchid lora: a subjective critique of recent contributions Richard M. BATEMAN Keywords: Anacamptis, Androrchis, classiication, evolutionary tree, genus circumscription, monophyly, orchid, Orchidinae, Orchis, phylogeny, taxonomy. Zusammenfassung/Summary: BATEMAN , R. M. (2012): Circumscribing genera in the European orchid lora: a subjective critique of recent contributions. – Ber. Arbeitskrs. Heim. Orch. Beiheft 8; 2012: 94 - 126. Die Abgrenzung von Gattungen oder anderen höheren Taxa erfolgt nach modernen Ansätzen weitestgehend auf der Rekonstruktion der Stammesgeschichte (Stamm- baum-Theorie), mit Hilfe von großen Daten-Matrizen. Wenngleich aufgrund des Fortschritts in der DNS-Sequenzierungstechnik immer mehr Merkmale in der DNS identiiziert werden, ist es mindestens genauso wichtig, die Anzahl der analysierten Planzen zu erhöhen, um genaue Zuordnungen zu erschließen. Die größere Vielfalt mathematischer Methoden zur Erstellung von Stammbäumen führt nicht gleichzeitig zu verbesserten Methoden zur Beurteilung der Stabilität der Zweige innerhalb der Stammbäume. Ein weiterer kontraproduktiver Trend ist die wachsende Tendenz, diverse Datengruppen mit einzelnen Matrizen zu verquicken, die besser einzeln analysiert würden, um festzustellen, ob sie ähnliche Schlussfolgerungen bezüglich der Verwandtschaftsverhältnisse liefern. Ein Stammbaum zur Abgrenzung höherer Taxa muss nicht so robust sein, wie ein Stammbaum, aus dem man Details des Evo- lutionsmusters -
Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences
d i v e r s i t y , p h y l o g e n y , a n d e v o l u t i o n i n t h e monocotyledons e d i t e d b y s e b e r g , p e t e r s e n , b a r f o d & d a v i s a a r h u s u n i v e r s i t y p r e s s , d e n m a r k , 2 0 1 0 Phylogenetics of Stipeae (Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences Konstantin Romaschenko,1 Paul M. Peterson,2 Robert J. Soreng,2 Núria Garcia-Jacas,3 and Alfonso Susanna3 1M. G. Kholodny Institute of Botany, Tereshchenkovska 2, 01601 Kiev, Ukraine 2Smithsonian Institution, Department of Botany MRC-166, National Museum of Natural History, P.O. Box 37012, Washington, District of Columbia 20013-7012 USA. 3Laboratory of Molecular Systematics, Botanic Institute of Barcelona (CSIC-ICUB), Pg. del Migdia, s.n., E08038 Barcelona, Spain Author for correspondence ([email protected]) Abstract—The Stipeae tribe is a group of 400−600 grass species of worldwide distribution that are currently placed in 21 genera. The ‘needlegrasses’ are char- acterized by having single-flowered spikelets and stout, terminally-awned lem- mas. We conducted a molecular phylogenetic study of the Stipeae (including all genera except Anemanthele) using a total of 94 species (nine species were used as outgroups) based on five plastid DNA regions (trnK-5’matK, matK, trnHGUG-psbA, trnL5’-trnF, and ndhF) and a single nuclear DNA region (ITS). -
Structuration Écologique Et Évolutive Des Symbioses Mycorhiziennes Des
Universit´ede La R´eunion { Ecole´ doctorale Sciences Technologie Sant´e{ Facult´edes Sciences et des Technologies Structuration ´ecologique et ´evolutive des symbioses mycorhiziennes des orchid´ees tropicales Th`ese de doctorat pr´esent´eeet soutenue publiquement le 19 novembre 2010 pour l'obtention du grade de Docteur de l'Universit´ede la R´eunion (sp´ecialit´eBiologie des Populations et Ecologie)´ par Florent Martos Composition du jury Pr´esidente: Mme Pascale Besse, Professeur `al'Universit´ede La R´eunion Rapporteurs : Mme Marie-Louise Cariou, Directrice de recherche au CNRS de Gif-sur-Yvette M. Raymond Tremblay, Professeur `al'Universit´ede Porto Rico Examinatrice : Mme Pascale Besse, Professeur `al'Universit´ede La R´eunion Directeurs : M. Thierry Pailler, Ma^ıtre de conf´erences HDR `al'Universit´ede La R´eunion M. Marc-Andr´e Selosse, Professeur `al'Universit´ede Montpellier Laboratoire d'Ecologie´ Marine Institut de Recherche pour le D´eveloppement 2 R´esum´e Les plantes n'exploitent pas seules les nutriments du sol, mais d´ependent de champignons avec lesquels elles forment des symbioses mycorhiziennes dans leurs racines. C'est en particulier vrai pour les 25 000 esp`ecesd'orchid´eesactuelles qui d´ependent toutes de champignons mycorhiziens pour accomplir leur cycle de vie. Elles produisent des graines microscopiques qui n'ont pas les ressources nutritives pour germer, mais qui d´ependent de la pr´esencede partenaires ad´equatspour nourrir l'embryon (h´et´erotrophie)jusqu’`al'apparition des feuilles (autotrophie). Les myco- rhiziens restent pr´esents dans les racines des adultes o`uils contribuent `ala nutrition, ce qui permet d'´etudierplus facilement la diversit´edes symbiotes `al'aide des ou- tils g´en´etiques.Conscients des biais des ´etudesen faveur des r´egionstemp´er´ees, nous avons ´etudi´ela diversit´edes mycorhiziens d'orchid´eestropicales `aLa R´eunion. -
The Threads That Bind: Symbiotic Fungi in the Garden
veryone knows that a plant they formed a symbiosis with fungi, has leaves and flowers, and whose growing network of threads (the below ground its roots mycelium) allowed them to explore branch and explore the soil. the soil and forage for phosphate. In Yet that picture misses an return the plant provided the fungus essential component as with organic compounds. EEvirtually all plants live with a fungus in Three lines of evidence support this a symbiosis called a mycorrhiza (from story: first, molecular evidence shows the Greek, meaning ‘fungus root’) that that this group of fungi originated at or is essential to both partners. The plants before that distant time; second, we get phosphate and some other nutrients find plants that form this type of mycor- from the fungus, and the fungus gets all rhiza in all branches of the evolutionary its sugars from the plant. Plants gain tree of land plants, showing that they The threads other benefits too from the symbiosis must all have shared a common mycor- and sustainable farming, forestry and rhizal ancestor; and most convincingly, gardening will all increasingly rely on there are fossils from Devonian rocks understanding how it behaves. nearly 400 million years old that contain the fungal structures (Fig. 1a) that bind: Meet the ancestors and older Ordovician spores that are To explain why they are mycorrhizal, unequivocally from the group. This we need to go back to when plants first ancestral type is known as an arbus- colonized the land more than 400 cular mycorrhiza, after the tiny struct- million years ago, in the Ordovician ures called arbuscules that develop symbiotic fungi and Devonian periods.