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Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Flavonoid, Phenylethanoid and Iridoid Glycosides from Globularia Aphyllanthes
Flavonoid, Phenylethanoid and Iridoid Glycosides from Globularia aphyllanthes Hasan Kırmızıbekmeza, Carla Bassarellob, Sonia Piacenteb, Galip Akaydınc, and Ihsan˙ C¸ alıs¸d,e a Yeditepe University, Faculty of Pharmacy, Department of Pharmacognosy, TR-34755, Kayıs¸da˘gı, Istanbul,˙ Turkey b Salerno University, Department of Pharmaceutical Sciences, Via Ponte Don Melillo, 84084 Fisciano, Salerno, Italy c Hacettepe University, Department of Biology Education, TR-06800, Beytepe, Ankara, Turkey d Hacettepe University, Faculty of Pharmacy, Department of Pharmacognosy, TR-06100, Ankara, Turkey e Present address: Near East University, Faculty of Pharmacy, Department of Pharmacognosy and Pharmaceutical Botany, Nicosia, Turkish Republic of Northern Cyprus Reprint requests to Dr. Hasan Kırmızıbekmez. Fax: +90 216 578 00 68. E-mail: [email protected] Z. Naturforsch. 2009, 64b, 252 – 256; received September 4, 2008 A new flavone glycoside, 6-hydroxyluteolin 7-O-[6 -benzoyl-β-D-glucopyranosyl-(1 → 2)]-β- D-glucopyranoside (aphyllanthoside, 1) was isolated from the MeOH extract of the aerial parts of Globularia aphyllanthes. Besides this new compound, two flavonoid glycosides (6-hydroxyluteolin 7-O-[6 -(E)-caffeoyl-β-D-glucopyranosyl-(1 → 2)]-β-D-glucopyranoside and isoquercitrin), three phenylethanoid glycosides (verbascoside, rossicaside A, and trichosanthoside A), and 11 iridoid gly- cosides (aucubin, catalpol, 10-O-benzoylcatalpol, globularin, asperuloside, besperuloside, asperulo- sidic acid, daphylloside, scandoside, alpinoside and baldaccioside) were also obtained and character- ized. Identification of the isolated compounds was carried out by spectroscopic analysis including 1D and 2D NMR experiments as well as HRMS. Key words: Globularia aphyllanthes, Plantaginaceae, Flavonoids, Aphyllanthoside, Phenylethanoid and Iridoid Glycosides Introduction Experimental Section Globularia aphyllanthes Crantz (Plantaginaceae) is General experimental procedures a perennial plant, distributed from northwest Turkey to central and southern Europe [1]. -
Phd Federica Gilardelli A5
Vegetation dynamics and restoration trials in limestone quarries: the Botticino case study (Brescia, Italy) Federica Gilardelli UNIVERSITÀ DEGLI STUDI DI MILANO – BICOCCA Facoltà di Scienze Matematiche, Fisiche e Naturali Vegetation dynamics and restoration trials in limestone quarries: the Botticino case study (Brescia, Italy) Federica Gilardelli PhD thesis in Environmental Science XXV cycle Tutor: Cotutors: Prof. Sandra Citterio Prof. Sergio Sgorbati Dr. Rodolfo Gentili Dr. Stefano Armiraglio Collaborations: Dr. Ing. Sergio Savoldi Dr. Pierangelo Barossi February 2013 To all the quarrymen and their families. A tutti i cavatori e le loro famiglie. Background. All over the world, the naturalistic restoration of abandoned quarry areas represents a real challenge because of the very adverse initial site conditions for plant species colonization. In order to identify the best restoration practices, the present thesis considered, as a case study, the “Botticino extractive basin” (Lombardy, Italy), that is today the second greatest Italian extractive basin and it is famous worldwide for the limestone extraction. In particular, the thesis proposes a multidisciplinary approach based on the study of the local vegetation dynamics, laboratory tests, plant selection for restoration and field experiments to test different restoration techniques. Methods. Spontaneous vegetation dynamics over the whole extractive basin was studied by an ecological approach through 108 plots, that were carried out on surfaces whose “disused time” from quarry abandonment was known; data were analysed by cluster analysis and Canonical Correspondence Analysis (CCA) and compared to the available data on grassland and woodlands related to the study area. We identified successional phases according to the trend of the most common species whose cover significantly increases or decreases with time. -
Vegetation Benchmarks Rainforest and Related Scrub
Vegetation Benchmarks Rainforest and related scrub Eucryphia lucida Vegetation Condition Benchmarks version 1 Rainforest and Related Scrub RPW Athrotaxis cupressoides open woodland: Sphagnum peatland facies Community Description: Athrotaxis cupressoides (5–8 m) forms small woodland patches or appears as copses and scattered small trees. On the Central Plateau (and other dolerite areas such as Mount Field), broad poorly– drained valleys and small glacial depressions may contain scattered A. cupressoides trees and copses over Sphagnum cristatum bogs. In the treeless gaps, Sphagnum cristatum is usually overgrown by a combination of any of Richea scoparia, R. gunnii, Baloskion australe, Epacris gunnii and Gleichenia alpina. This is one of three benchmarks available for assessing the condition of RPW. This is the appropriate benchmark to use in assessing the condition of the Sphagnum facies of the listed Athrotaxis cupressoides open woodland community (Schedule 3A, Nature Conservation Act 2002). Benchmarks: Length Component Cover % Height (m) DBH (cm) #/ha (m)/0.1 ha Canopy 10% - - - Large Trees - 6 20 5 Organic Litter 10% - Logs ≥ 10 - 2 Large Logs ≥ 10 Recruitment Continuous Understorey Life Forms LF code # Spp Cover % Immature tree IT 1 1 Medium shrub/small shrub S 3 30 Medium sedge/rush/sagg/lily MSR 2 10 Ground fern GF 1 1 Mosses and Lichens ML 1 70 Total 5 8 Last reviewed – 2 November 2016 Tasmanian Vegetation Monitoring and Mapping Program Department of Primary Industries, Parks, Water and Environment http://www.dpipwe.tas.gov.au/tasveg RPW Athrotaxis cupressoides open woodland: Sphagnum facies Species lists: Canopy Tree Species Common Name Notes Athrotaxis cupressoides pencil pine Present as a sparse canopy Typical Understorey Species * Common Name LF Code Epacris gunnii coral heath S Richea scoparia scoparia S Richea gunnii bog candleheath S Astelia alpina pineapple grass MSR Baloskion australe southern cordrush MSR Gleichenia alpina dwarf coralfern GF Sphagnum cristatum sphagnum ML *This list is provided as a guide only. -
Edition 2 from Forest to Fjaeldmark the Vegetation Communities Highland Treeless Vegetation
Edition 2 From Forest to Fjaeldmark The Vegetation Communities Highland treeless vegetation Richea scoparia Edition 2 From Forest to Fjaeldmark 1 Highland treeless vegetation Community (Code) Page Alpine coniferous heathland (HCH) 4 Cushion moorland (HCM) 6 Eastern alpine heathland (HHE) 8 Eastern alpine sedgeland (HSE) 10 Eastern alpine vegetation (undifferentiated) (HUE) 12 Western alpine heathland (HHW) 13 Western alpine sedgeland/herbland (HSW) 15 General description Rainforest and related scrub, Dry eucalypt forest and woodland, Scrub, heathland and coastal complexes. Highland treeless vegetation communities occur Likewise, some non-forest communities with wide within the alpine zone where the growth of trees is environmental amplitudes, such as wetlands, may be impeded by climatic factors. The altitude above found in alpine areas. which trees cannot survive varies between approximately 700 m in the south-west to over The boundaries between alpine vegetation communities are usually well defined, but 1 400 m in the north-east highlands; its exact location depends on a number of factors. In many communities may occur in a tight mosaic. In these parts of Tasmania the boundary is not well defined. situations, mapping community boundaries at Sometimes tree lines are inverted due to exposure 1:25 000 may not be feasible. This is particularly the or frost hollows. problem in the eastern highlands; the class Eastern alpine vegetation (undifferentiated) (HUE) is used in There are seven specific highland heathland, those areas where remote sensing does not provide sedgeland and moorland mapping communities, sufficient resolution. including one undifferentiated class. Other highland treeless vegetation such as grasslands, herbfields, A minor revision in 2017 added information on the grassy sedgelands and wetlands are described in occurrence of peatland pool complexes, and other sections. -
1 Contrasting Habitat and Landscape Effects on the Fitness of a Long-Lived Grassland Plant Under 1 Forest Encroachment
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Diposit Digital de Documents de la UAB 1 Contrasting habitat and landscape effects on the fitness of a long-lived grassland plant under 2 forest encroachment: do they provide evidence for extinction debt? 3 4 Guillem Bagaria1,2*, Ferran Rodà1,2, Maria Clotet1, Silvia Míguez1 and Joan Pino1,2 5 6 1CREAF, Cerdanyola del Vallès 08193, Spain; 2Univ Autònoma Barcelona, Cerdanyola del Vallès 7 08193, Spain. 8 9 *Correspondence author. CREAF, Cerdanyola del Vallès 08193, Spain. 10 E-mail: [email protected] 11 Phone: +34 935814851 12 FAX: +34 93 5814151 13 14 Running title: Plant fitness and extinction debt 15 This is the accepted version of the following article: Bagaria, G. , et al.“Contrasting habitat and landscape effects on the fitness of a long-lived grassland plant under forest encroachment: do they provide evidence for extinction debt?” in Journal of ecology (Ed. Wiley), vol. 106, issue 1 (Jan. 2018), p. 278-288, which has been published in final form at DOI 10.1111/1365-2745.12860. 1 16 Summary 17 1. Habitat loss, fragmentation and transformation threaten the persistence of many species 18 worldwide. Population and individual fitness are often compromised in small, degraded and isolated 19 habitats, but extinction can be a slow process and extinction debts are common. 20 2. Long-lived species are prone to persist as remnant populations in low quality habitats for a long 21 time, but the population and individual-level mechanisms of extinction debt remain poorly explored 22 so far. -
Gilia Sedifolia Brandeg. (Stonecrop Gilia): a Technical Conservation Assessment
Gilia sedifolia Brandeg. (stonecrop gilia): A Technical Conservation Assessment Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project August 9, 2004 David G. Anderson Colorado Natural Heritage Program 8002 Campus Delivery — Colorado State University Fort Collins, CO 80523 Peer Review Administered by Society for Conservation Biology Anderson, D.G. (2004, August 9). Gilia sedifolia Brandeg. (stonecrop gilia): a technical conservation assessment. [Online]. USDA Forest Service, Rocky Mountain Region. Available: http://www.fs.fed.us/r2/projects/scp/ assessments/giliasedifolia.pdf [date of access]. ACKNOWLEDGEMENTS This research was facilitated by the helpfulness and generosity of many experts, particularly Bill Jennings, Susan Komarek, Peggy Lyon, J. Mark Porter, and James Reveal. Their interest in the project and time spent answering questions were extremely valuable, and their insights into the distribution, habitat, classification, and ecology ofGilia sedifolia were crucial to this project. The rediscovery of this species and its subsequent documentation are solely the work of Susan Komarek; without her efforts very little could be said about this species. J. Mark Porter’s thoughts and insights into this species have contributed greatly to our understanding of G. sedifolia. Greg Hayward, Gary Patton, Jim Maxwell, Andy Kratz, Beth Burkhart, and Joy Bartlett assisted with questions and project management. Jane Nusbaum, Carmen Morales, Betty Eckert, Candyce Jeffery, and Barbara Brayfield provided crucial financial oversight. Amy Lavender assisted with the production of the potential habitat distribution map. Annette Miller provided information for the report on seed storage status. Nan Lederer and Tim Hogan provided valuable assistance and insights at the CU Herbarium, as did Janet Wingate and Loraine Yeatts at the Kalmbach Herbarium. -
Kosipe Revisited
Peat in the mountains of New Guinea G.S. Hope Department of Archaeology and Natural History, Australian National University, Canberra, Australia _______________________________________________________________________________________ SUMMARY Peatlands are common in montane areas above 1,000 m in New Guinea and become extensive above 3,000 m in the subalpine zone. In the montane mires, swamp forests and grass or sedge fens predominate on swampy valley bottoms. These mires may be 4–8 m in depth and up to 30,000 years in age. In Papua New Guinea (PNG) there is about 2,250 km2 of montane peatland, and Papua Province (the Indonesian western half of the island) probably contains much more. Above 3,000 m, peat soils form under blanket bog on slopes as well as on valley floors. Vegetation types include cushion bog, grass bog and sedge fen. Typical peat depths are 0.5‒1 m on slopes, but valley floors and hollows contain up to 10 m of peat. The estimated total extent of mountain peatland is 14,800 km2 with 5,965 km2 in PNG and about 8,800 km2 in Papua Province. The stratigraphy, age structure and vegetation histories of 45 peatland or organic limnic sites above 750 m have been investigated since 1965. These record major vegetation shifts at 28,000, 17,000‒14,000 and 9,000 years ago and a variable history of human disturbance from 14,000 years ago with extensive clearance by the mid- Holocene at some sites. While montane peatlands were important agricultural centres in the Holocene, the introduction of new dryland crops has resulted in the abandonment of some peatlands in the last few centuries. -
Doctorat De L'université De Toulouse
En vue de l’obt ention du DOCTORAT DE L’UNIVERSITÉ DE TOULOUSE Délivré par : Université Toulouse 3 Paul Sabatier (UT3 Paul Sabatier) Discipline ou spécialité : Ecologie, Biodiversité et Evolution Présentée et soutenue par : Joeri STRIJK le : 12 / 02 / 2010 Titre : Species diversification and differentiation in the Madagascar and Indian Ocean Islands Biodiversity Hotspot JURY Jérôme CHAVE, Directeur de Recherches CNRS Toulouse Emmanuel DOUZERY, Professeur à l'Université de Montpellier II Porter LOWRY II, Curator Missouri Botanical Garden Frédéric MEDAIL, Professeur à l'Université Paul Cezanne Aix-Marseille Christophe THEBAUD, Professeur à l'Université Paul Sabatier Ecole doctorale : Sciences Ecologiques, Vétérinaires, Agronomiques et Bioingénieries (SEVAB) Unité de recherche : UMR 5174 CNRS-UPS Evolution & Diversité Biologique Directeur(s) de Thèse : Christophe THEBAUD Rapporteurs : Emmanuel DOUZERY, Professeur à l'Université de Montpellier II Porter LOWRY II, Curator Missouri Botanical Garden Contents. CONTENTS CHAPTER 1. General Introduction 2 PART I: ASTERACEAE CHAPTER 2. Multiple evolutionary radiations and phenotypic convergence in polyphyletic Indian Ocean Daisy Trees (Psiadia, Asteraceae) (in preparation for BMC Evolutionary Biology) 14 CHAPTER 3. Taxonomic rearrangements within Indian Ocean Daisy Trees (Psiadia, Asteraceae) and the resurrection of Frappieria (in preparation for Taxon) 34 PART II: MYRSINACEAE CHAPTER 4. Phylogenetics of the Mascarene endemic genus Badula relative to its Madagascan ally Oncostemum (Myrsinaceae) (accepted in Botanical Journal of the Linnean Society) 43 CHAPTER 5. Timing and tempo of evolutionary diversification in Myrsinaceae: Badula and Oncostemum in the Indian Ocean Island Biodiversity Hotspot (in preparation for BMC Evolutionary Biology) 54 PART III: MONIMIACEAE CHAPTER 6. Biogeography of the Monimiaceae (Laurales): a role for East Gondwana and long distance dispersal, but not West Gondwana (accepted in Journal of Biogeography) 72 CHAPTER 7 General Discussion 86 REFERENCES 91 i Contents. -
Annotated Checklist of Vascular Flora, Bryce
National Park Service U.S. Department of the Interior Natural Resource Program Center Annotated Checklist of Vascular Flora Bryce Canyon National Park Natural Resource Technical Report NPS/NCPN/NRTR–2009/153 ON THE COVER Matted prickly-phlox (Leptodactylon caespitosum), Bryce Canyon National Park, Utah. Photograph by Walter Fertig. Annotated Checklist of Vascular Flora Bryce Canyon National Park Natural Resource Technical Report NPS/NCPN/NRTR–2009/153 Author Walter Fertig Moenave Botanical Consulting 1117 W. Grand Canyon Dr. Kanab, UT 84741 Sarah Topp Northern Colorado Plateau Network P.O. Box 848 Moab, UT 84532 Editing and Design Alice Wondrak Biel Northern Colorado Plateau Network P.O. Box 848 Moab, UT 84532 January 2009 U.S. Department of the Interior National Park Service Natural Resource Program Center Fort Collins, Colorado The Natural Resource Publication series addresses natural resource topics that are of interest and applicability to a broad readership in the National Park Service and to others in the management of natural resources, including the scientifi c community, the public, and the NPS conservation and environmental constituencies. Manuscripts are peer-reviewed to ensure that the information is scientifi cally credible, technically accurate, appropriately written for the intended audience, and is designed and published in a professional manner. The Natural Resource Technical Report series is used to disseminate the peer-reviewed results of scientifi c studies in the physical, biological, and social sciences for both the advancement of science and the achievement of the National Park Service’s mission. The reports provide contributors with a forum for displaying comprehensive data that are often deleted from journals because of page limitations. -
ABSTRACTS 117 Systematics Section, BSA / ASPT / IOPB
Systematics Section, BSA / ASPT / IOPB 466 HARDY, CHRISTOPHER R.1,2*, JERROLD I DAVIS1, breeding system. This effectively reproductively isolates the species. ROBERT B. FADEN3, AND DENNIS W. STEVENSON1,2 Previous studies have provided extensive genetic, phylogenetic and 1Bailey Hortorium, Cornell University, Ithaca, NY 14853; 2New York natural selection data which allow for a rare opportunity to now Botanical Garden, Bronx, NY 10458; 3Dept. of Botany, National study and interpret ontogenetic changes as sources of evolutionary Museum of Natural History, Smithsonian Institution, Washington, novelties in floral form. Three populations of M. cardinalis and four DC 20560 populations of M. lewisii (representing both described races) were studied from initiation of floral apex to anthesis using SEM and light Phylogenetics of Cochliostema, Geogenanthus, and microscopy. Allometric analyses were conducted on data derived an undescribed genus (Commelinaceae) using from floral organs. Sympatric populations of the species from morphology and DNA sequence data from 26S, 5S- Yosemite National Park were compared. Calyces of M. lewisii initi- NTS, rbcL, and trnL-F loci ate later than those of M. cardinalis relative to the inner whorls, and sepals are taller and more acute. Relative times of initiation of phylogenetic study was conducted on a group of three small petals, sepals and pistil are similar in both species. Petal shapes dif- genera of neotropical Commelinaceae that exhibit a variety fer between species throughout development. Corolla aperture of unusual floral morphologies and habits. Morphological A shape becomes dorso-ventrally narrow during development of M. characters and DNA sequence data from plastid (rbcL, trnL-F) and lewisii, and laterally narrow in M. -
High-Elevation Limits and the Ecology of High-Elevation Vascular Plants: Legacies from Alexander Von Humboldt1
a Frontiers of Biogeography 2021, 13.3, e53226 Frontiers of Biogeography REVIEW the scientific journal of the International Biogeography Society High-elevation limits and the ecology of high-elevation vascular plants: legacies from Alexander von Humboldt1 H. John B. Birks1,2* 1 Department of Biological Sciences and Bjerknes Centre for Climate Research, University of Bergen, PO Box 7803, Bergen, Norway; 2 Ecological Change Research Centre, University College London, Gower Street, London, WC1 6BT, UK. *Correspondence: H.J.B. Birks, [email protected] 1 This paper is part of an Elevational Gradients and Mountain Biodiversity Special Issue Abstract Highlights Alexander von Humboldt and Aimé Bonpland in their • The known uppermost elevation limits of vascular ‘Essay on the Geography of Plants’ discuss what was plants in 22 regions from northernmost Greenland known in 1807 about the elevational limits of vascular to Antarctica through the European Alps, North plants in the Andes, North America, and the European American Rockies, Andes, East and southern Africa, Alps and suggest what factors might influence these upper and South Island, New Zealand are collated to provide elevational limits. Here, in light of current knowledge a global view of high-elevation limits. and techniques, I consider which species are thought to be the highest vascular plants in twenty mountain • The relationships between potential climatic treeline, areas and two polar regions on Earth. I review how one upper limit of closed vegetation in tropical (Andes, can try to