The “Early-Diverging” Flowering Plants
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Native Herbaceous Perennials and Ferns for Shade Gardens
Green Spring Gardens 4603 Green Spring Rd ● Alexandria ● VA 22312 Phone: 703-642-5173 ● TTY: 703-803-3354 www.fairfaxcounty.gov/parks/greenspring NATIVE HERBACEOUS PERENNIALS AND FERNS FOR � SHADE GARDENS IN THE WASHINGTON, D.C. AREA � Native plants are species that existed in Virginia before Jamestown, Virginia was founded in 1607. They are uniquely adapted to local conditions. Native plants provide food and shelter for a myriad of birds, butterflies, and other wildlife. Best of all, gardeners can feel the satisfaction of preserving a part of our natural heritage while enjoying the beauty of native plants in the garden. Hardy herbaceous perennials form little or no woody tissue and live for several years. Some of these plants are short-lived and may live only three years, such as wild columbine, while others can live for decades. They are a group of plants that gardeners are very passionate about because of their lovely foliage and flowers, as well as their wide variety of textures, forms, and heights. Most of these plants are deciduous and die back to the ground in the winter. Ferns, in contrast, have no flowers but grace our gardens with their beautiful foliage. Herbaceous perennials and ferns are a joy to garden with because they are easily moved to create new design combinations and provide an ever-changing scene in the garden. They are appropriate for a wide range of shade gardens, from more formal gardens to naturalistic woodland gardens. The following are useful definitions: Cultivar (cv.) – a cultivated variety designated by single quotes, such as ‘Autumn Bride’. -
Floral MADS Box Genes and Homeotic Gender Dimorphism in Thalictrum Dioicum (Ranunculaceae) – a New Model for the Study of Dioecy
The Plant Journal (2005) 41, 755–766 doi: 10.1111/j.1365-313X.2005.02336.x Floral MADS box genes and homeotic gender dimorphism in Thalictrum dioicum (Ranunculaceae) – a new model for the study of dioecy Vero´ nica S. Di Stilio1,*,†, Elena M. Kramer1 and David A. Baum1,2 1Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA, and 2Department of Botany, University of Wisconsin, Madison, WI 53706, USA Received 23 September 2004; revised 8 December 2004; accepted 14 December 2004. *For correspondence (fax þ206 616 2011; e-mail [email protected]). †Present address: Department of Biology, University of Washington, Seattle, WA 98195, USA. Summary In most dioecious angiosperm species, flowers are initially perfect but abort either stamens or carpels during their development, indicating that sex determination occurs after floral organ identity has been established. Dioecious members of the genus Thalictrum (meadow-rue), however, produce flowers that lack aborted organs. Examination of early flower development of T. dioicum confirms that flowers are male or female from inception, raising the possibility that genetic mechanisms working at or above the level of organ identity promote sex determination through a homeotic-like mechanism. In order to investigate this possibility, we identified homologs of the organ identity genes PISTILLATA (PI), APETALA3 (AP3) and AGAMOUS (AG) from T. dioicum and the hermaphroditic species T. thalictroides. A combination of early and late duplication events was uncovered in these gene lineages and expression analyses indicate that these events are generally associated with divergence in gene regulation. In light of these findings, we discuss the potential of T. -
Variation in Susceptibility of Giant Buttercup (Ranunculus Acris L. Subsp. Acris) Populations to Herbicides
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. i Variation in susceptibility of giant buttercup (Ranunculus acris L. subsp. acris) populations to herbicides A thesis presented in partial fulfillment of the requirements for the degree of Master of AgriScience In Agriculture at Massey University, Palmerston North, New Zealand. Carolyn Sarah Lusk 2012 ii ABSTRACT Giant buttercup (Ranunculus acris L.) is a serious weed of dairy pastures throughout New Zealand causing substantial economic losses from lost pasture productivity. It has developed resistance to the phenoxy herbicides (MCPA and MCPB) at many sites around New Zealand, particularly in Golden Bay. Since the discovery of resistance in the 1980s, two newer herbicides from a different mode-of-action group (acetolactate synthase inhibitor, ALS), flumetsulam and thifensulfuron-methyl, have been used widely, which appeared to overcome the resistance problem. A survey of farmers in Golden Bay indicated that most have herbicide control programmes for giant buttercup based around flumetsulam but some have reported poor control with this herbicide, particularly after several years of use. The research in this thesis was undertaken to determine whether this may be due to evolved resistance. Seedling progeny from 15 populations of giant buttercup, with known spraying history, were sprayed with a range of doses of flumetsulam, thifensulfuron-methyl and MCPA (Experiment 1) to test for differences in susceptibility. The experiment revealed a large difference in susceptibility between the populations (83-100% and 58-100% mortality at the recommended rate and 2.2 times that rate of flumetsulam applied, respectively). -
Coptis Trifolia Conservation Assessment
CONSERVATION ASSESSMENT for Coptis trifolia (L.) Salisb. Originally issued as Management Recommendations December 1998 Marty Stein Reconfigured-January 2005 Tracy L. Fuentes USDA Forest Service Region 6 and USDI Bureau of Land Management, Oregon and Washington CONSERVATION ASSESSMENT FOR COPTIS TRIFOLIA Table of Contents Page List of Tables ................................................................................................................................. 2 List of Figures ................................................................................................................................ 2 Summary........................................................................................................................................ 4 I. NATURAL HISTORY............................................................................................................. 6 A. Taxonomy and Nomenclature.......................................................................................... 6 B. Species Description ........................................................................................................... 6 1. Morphology ................................................................................................................... 6 2. Reproductive Biology.................................................................................................... 7 3. Ecological Roles ............................................................................................................. 7 C. Range and Sites -
Repeated Climate-Linked Host Shifts Have Promoted Diversification in a Temperate Clade of Leaf-Mining Flies
Repeated climate-linked host shifts have promoted SPECIAL FEATURE diversification in a temperate clade of leaf-mining flies Isaac S. Winklera,b,1, Charles Mitterb, and Sonja J. Schefferc aDepartment of Entomology, North Carolina State University, Campus Box 7613, Raleigh, NC 27695-7613; bDepartment of Entomology, University of Maryland, 4112 Plant Sciences Building, College Park, MD 20742; and cSystematic Entomology Laboratory, Plant Science Institute, Agricultural Research Service, United States Department of Agriculture, 10300 Baltimore Avenue, Building 003, Room 231, BARC-West, Beltsville, MD 20705 Edited by Anurag A. Agrawal, Cornell University, Ithaca, NY, and accepted by the Editorial Board July 30, 2009 (received for review May 1, 2009) A central but little-tested prediction of ‘‘escape and radiation’’ ever, there is still little evidence on the degree to which changes coevolution is that colonization of novel, chemically defended host in either plant defense or insect ‘‘offense’’ promote diversifica- plant clades accelerates insect herbivore diversification. That the- tion (7). Progress on the insect side has come from several recent ory, in turn, exemplifies one side of a broader debate about the reports plausibly attributing an instance of significantly elevated relative influence on clade dynamics of intrinsic (biotic) vs. extrinsic insect diversity to a co-occurring shift to a new host taxon (5, 10, (physical-environmental) forces. Here, we use a fossil-calibrated 11). Any single instance of elevated diversification, however, molecular chronogram to compare the effects of a major biotic could reflect other influences that happen to be confounded factor (repeated shift to a chemically divergent host plant clade) with the host shift. -
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 -
Introduction to Common Native & Invasive Freshwater Plants in Alaska
Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska Cover photographs by (top to bottom, left to right): Tara Chestnut/Hannah E. Anderson, Jamie Fenneman, Vanessa Morgan, Dana Visalli, Jamie Fenneman, Lynda K. Moore and Denny Lassuy. Introduction to Common Native & Potential Invasive Freshwater Plants in Alaska This document is based on An Aquatic Plant Identification Manual for Washington’s Freshwater Plants, which was modified with permission from the Washington State Department of Ecology, by the Center for Lakes and Reservoirs at Portland State University for Alaska Department of Fish and Game US Fish & Wildlife Service - Coastal Program US Fish & Wildlife Service - Aquatic Invasive Species Program December 2009 TABLE OF CONTENTS TABLE OF CONTENTS Acknowledgments ............................................................................ x Introduction Overview ............................................................................. xvi How to Use This Manual .................................................... xvi Categories of Special Interest Imperiled, Rare and Uncommon Aquatic Species ..................... xx Indigenous Peoples Use of Aquatic Plants .............................. xxi Invasive Aquatic Plants Impacts ................................................................................. xxi Vectors ................................................................................. xxii Prevention Tips .................................................... xxii Early Detection and Reporting -
Next-Generation Sequencing Identification and Characterization
Next-generation sequencing identification and characterization of microsatellite markers in Aconitum austrokoreense Koidz., an endemic and endangered medicinal plant of Korea Y.-E. Yun, J.-N. Yu, G.H. Nam, S.-A. Ryu, S. Kim, K. Oh and C.E. Lim National Institute of Biological Resources, Environmental Research Complex, Incheon, Korea Corresponding author: C.E. Lim E-mail: [email protected] Genet. Mol. Res. 14 (2): 4812-4817 (2015) Received June 11, 2014 Accepted October 29, 2014 Published May 11, 2015 DOI http://dx.doi.org/10.4238/2015.May.11.13 ABSTRACT. We used next-generation sequencing to develop 9 novel microsatellite markers in Aconitum austrokoreense, an endemic and endangered medicinal plant in Korea. Owing to its very limited distribution, over-harvesting for traditional medicinal purposes, and habitat loss, the natural populations are dramatically declining in Korea. All novel microsatellite markers were successfully genotyped using 64 samples from two populations (Mt. Choejeong, Gyeongsangbuk- do and Ungseokbong, Gyeongsangnam-do) of Gyeongsang Province. The number of alleles ranged from 2 to 7 per locus in each population. Observed and expected heterozygosities ranged from 0.031 to 0.938 and from 0.031 to 0.697, respectively. The novel markers will be valuable tools for assessing the genetic diversity of A. austrokoreense and for germplasm conservation of this endangered species. Key words: Aconitum austrokoreense; Microsatellite marker; Endemic and endangered medicinal plant, Next-generation sequencing; Genetic diversity Genetics and Molecular Research 14 (2): 4812-4817 (2015) ©FUNPEC-RP www.funpecrp.com.br Novel microsatellite markers in A. austrokoreense 4813 INTRODUCTION Aconitum austrokoreense Koidz. -
Aquatic Vascular Plant Species Distribution Maps
Appendix 11.5.1: Aquatic Vascular Plant Species Distribution Maps These distribution maps are for 116 aquatic vascular macrophyte species (Table 1). Aquatic designation follows habitat descriptions in Haines and Vining (1998), and includes submergent, floating and some emergent species. See Appendix 11.4 for list of species. Also included in Appendix 11.4 is the number of HUC-10 watersheds from which each taxon has been recorded, and the county-level distributions. Data are from nine sources, as compiled in the MABP database (plus a few additional records derived from ancilliary information contained in reports from two fisheries surveys in the Upper St. John basin organized by The Nature Conservancy). With the exception of the University of Maine herbarium records, most locations represent point samples (coordinates were provided in data sources or derived by MABP from site descriptions in data sources). The herbarium data are identified only to township. In the species distribution maps, town-level records are indicated by center-points (centroids). Figure 1 on this page shows as polygons the towns where taxon records are identified only at the town level. Data Sources: MABP ID MABP DataSet Name Provider 7 Rare taxa from MNAP lake plant surveys D. Cameron, MNAP 8 Lake plant surveys D. Cameron, MNAP 35 Acadia National Park plant survey C. Greene et al. 63 Lake plant surveys A. Dieffenbacher-Krall 71 Natural Heritage Database (rare plants) MNAP 91 University of Maine herbarium database C. Campbell 183 Natural Heritage Database (delisted species) MNAP 194 Rapid bioassessment surveys D. Cameron, MNAP 207 Invasive aquatic plant records MDEP Maps are in alphabetical order by species name. -
Southwestern Showy Sedge in the Black Hills National Forest, South Dakota and Wyoming
United States Department of Agriculture Conservation Assessment Forest Service Rocky of the Southwestern Mountain Region Black Hills Showy Sedge in the Black National Forest Custer, Hills National Forest, South South Dakota May 2003 Dakota and Wyoming Bruce T. Glisson Conservation Assessment of Southwestern Showy Sedge in the Black Hills National Forest, South Dakota and Wyoming Bruce T. Glisson, Ph.D. 315 Matterhorn Drive Park City, UT 84098 email: [email protected] Bruce Glisson is a botanist and ecologist with over 10 years of consulting experience, located in Park City, Utah. He has earned a B.S. in Biology from Towson State University, an M.S. in Public Health from the University of Utah, and a Ph.D. in Botany from Brigham Young University EXECUTIVE SUMMARY Southwestern showy sedge, Carex bella Bailey, is a cespitose graminoid that occurs in the central and southern Rocky Mountain region of the western United States and Mexico, with a disjunct population in the Black Hills that may be a relict from the last Pleistocene glaciation (Cronquist et al., 1994; USDA NRCS, 2001; NatureServe, 2001). Southwestern showy sedge is quite restricted in range and habitat in the Black Hills. There is much that we don’t know about the species, as there has been no thorough surveys, no monitoring, and very few and limited studies on the species in the area. Long term persistence of southwestern showy sedge is enhanced due to the presence of at least several populations within the Black Elk Wilderness and Custer State Park. Populations in Custer State Park may be at greater risk due to recreational use and lack of protective regulations (Marriott 2001c). -
The Ranunculus Acris L. Complex in Europe S
Watsonia, 8, 237-261 (1971). 237 The Ranunculus acris L. complex in Europe s. M. COLES Department ofBotany, Birmingham University ABSTRACT The geographical variation of the Ranunculus acris L. complex within Europe has been exam ined. The following taxa are recognised in this present work: Ranunculus granatensis Boiss. R. strigulosus Schur R. acris L. sensu stricto subsp. acris var. acris var. ,,;llosus (Drabble) S. M. Coles, comb. et stat. novo var. pumilus Wahlenb. subsp. borealis (Trautv.) Nyman subsp.friesanus (Jord.) Rouy & Fouc. var.friesanus var.pyrenaeus S. M. Coles, var. novo R. granatensis and R. strigulosus have a restricted distribution and are relatively uniform in appearance. R. acris sensu stricto occurs over most of Europe and is a very variable plant. The main clinal variation in R. acris is in an east-west direction. R. acris subsp. friesanus forms no part of this variational pattern although its distribution is completely overlapped by that of subsp. acris. INTRODUCTION The plants investigated in this study are those included in Ranunculus acris L. as defined by Tutin (1964). R. acris L. sensu stricto in the present study excludes R. acris subsp. granatensis (Boiss.) Nyman and subsp. strigulosus (Schur) Hyl., which are given specific status. The R. acris complex belongs to the section Ranunculus of the subgenus Ranunculus. It can be separated from most other European species of this section by having a terete pedicel, patent sepals and a glabrous receptacle. The diploid chromosome number of R. acris L. sensu stricto is 14; within the genus a basic chromosome number of 8 is more common than one of 7. -
Phylogenetic Reconstruction Prompts Taxonomic Changes in Sauropus, Synostemon and Breynia (Phyllanthaceae Tribe Phyllantheae)
Blumea 59, 2014: 77–94 www.ingentaconnect.com/content/nhn/blumea RESEARCH ARTICLE http://dx.doi.org/10.3767/000651914X684484 Phylogenetic reconstruction prompts taxonomic changes in Sauropus, Synostemon and Breynia (Phyllanthaceae tribe Phyllantheae) P.C. van Welzen1,2, K. Pruesapan3, I.R.H. Telford4, H.-J. Esser 5, J.J. Bruhl4 Key words Abstract Previous molecular phylogenetic studies indicated expansion of Breynia with inclusion of Sauropus s.str. (excluding Synostemon). The present study adds qualitative and quantitative morphological characters to molecular Breynia data to find more resolution and/or higher support for the subgroups within Breynia s.lat. However, the results show molecular phylogeny that combined molecular and morphological characters provide limited synergy. Morphology confirms and makes the morphology infrageneric groups recognisable within Breynia s.lat. The status of the Sauropus androgynus complex is discussed. Phyllanthaceae Nomenclatural changes of Sauropus species to Breynia are formalised. The genus Synostemon is reinstated. Sauropus Synostemon Published on 1 September 2014 INTRODUCTION Sauropus in the strict sense (excluding Synostemon; Pruesapan et al. 2008, 2012) and Breynia are two closely related tropical A phylogenetic analysis of tribe Phyllantheae (Phyllanthaceae) Asian-Australian genera with up to 52 and 35 species, respec- using DNA sequence data by Kathriarachchi et al. (2006) pro- tively (Webster 1994, Govaerts et al. 2000a, b, Radcliffe-Smith vided a backbone phylogeny for Phyllanthus L. and related 2001). Sauropus comprises mainly herbs and shrubs, whereas genera. Their study recommended subsuming Breynia L. (in- species of Breynia are always shrubs. Both genera share bifid cluding Sauropus Blume), Glochidion J.R.Forst. & G.Forst., or emarginate styles, non-apiculate anthers, smooth seeds and and Synostemon F.Muell.