Selecting Plants for Pollinators Selecting Plants for Pollinators

Total Page:16

File Type:pdf, Size:1020Kb

Selecting Plants for Pollinators Selecting Plants for Pollinators Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Algonquin- Lake Nipissing Ecoregion SAULT STE. MARIE, ELLIOT LAKE, SUDBURY, NORTH BAY, PARRY SOUND, HUNTSVILLE, AND OTTAWA RIVER VALLEY AREA Table of CONTENTS Why Support Pollinators? 4 Getting Started 5 Algonquin-Lake Nipissing 6 Meet the Pollinators 8 Plant Traits 10 Developing Plantings 12 Farms 13 Public Lands 14 Home Landscapes 15 Plants That Attract Pollinators 16 Habitat hints 20 Habitat and Nesting requirements 21 S.H.A.R.E. 22 Checklist 22 This is one of several guides for different regions of North America. Resources and Feedback 23 We welcome your feedback to assist us in making the future guides useful. Please contact us at [email protected] 2 Selecting Plants for Pollinators Selecting Plants for Pollinators A Guide for Gardeners, Farmers, and Land Managers In the Algonquin-Lake nipissing Ecoregion SAULT STE. MARIE, ELLIOT LAKE, SUDBURY, NORTH BAY, PARRY SOUND, HUNTSVILLE, AND OTTAWA RIVER VALLEY AREA A NAPPC and Pollinator Partnership Canada™ Publication Funding for this ecoregional guide was provided by Growing Forward 2 Algonquin-Lake Nipissing 3 Why support pollinators? IN THEIR 1996 BOOK, THE FORGOttEN POLLINATORS, Buchmann and Nabhan estimated that animal pollinators are needed for the reproduction “Flowering plants of 90% of flowering plants and one third of human food crops. Each of us depends on these industrious pollinators in a practical way to provide us with the wide range of foods we eat. In addition, pollinators are part of the across wild, intricate web that supports the biological diversity in natural ecosystems that helps sustain our quality of life. farmed and even Abundant and healthy populations of pollinators can improve fruit set and quality, and increase fruit size. In farming situations this increases production per hectare. In the wild, biodiversity increases and wildlife urban landscapes food sources increase. Many wild plant species such as lowbush blueberry and red raspberry in addition to field crops such as alfalfa, clover, and actually feed the soybeans are grown in the Algonquin-Lake Nipissing ecoregion that rely on honey bees and native bees for pollination. Honey bees pollinate more than $1 billion worth of crops in Canada each year. terrestrial world, Unfortunately, the numbers of many native pollinators are declining. They are threatened by habitat loss, disease, climate change, and the excessive and pollinators and inappropriate use of pesticides. As a result research and conservation actions supporting native pollinators are increasingly active. Honey bee colony losses have significantly impacted beekeepers. Parasites, disease, are the great pesticide use, insufficient nutrition, and transportation practices all impact honey bee health, and this in turn can impact the commercial pollination services honey bees provide. The efforts to understand the threats to connectors who commercial bees should help us understand other pollinators and their roles in the environment as well. enable this giant It is imperative that we take immediate steps to help pollinator populations thrive. The beauty of the situation is that by supporting pollinators’ need for habitat, we support our own needs for food and support diversity in the food system to natural world. Thank you for taking time to consult this guide. By adding plants to your work for all who landscape that provide food and shelter for pollinators throughout their active seasons and by adopting pollinator friendly landscape practices, you can make a difference to both the pollinators and the people that rely on them. eat... Including us.” – Roger Lang, Chairman, Val Dolcini President & CEO Pollinator Partnership Pollinator Partnership 4 Selecting Plants for Pollinators Getting Started THIS REGIONAL GUIDE IS JUST Framework Report. The National Long before there were homes ONE in a series of plant selection Ecological Framework for Canada and farms in the Algonquin-Lake tools designed to provide you with is a system created as a management Nipissing ecoregion, natural information on how to plant local tool and is used to predict responses vegetation provided essential native plants for pollinators. Each to land management practices opportunities for wildlife, including of us can have a positive impact throughout large areas. This guide pollinators. Farmers, land managers, by providing the essential habitat addresses pollinator-friendly land and gardeners in this region have requirements for pollinators management practices in what is a wide palette of plants to use including food, water, shelter, and known as the Algonquin-Lake in the landscape. In choosing enough space to raise their young. Nipissing ecoregion. plants, aim to create habitat for pollinators that allow adequate food, Pollinators travel through the The seasonal cycle of sun and shade shelter, and water sources. Most landscape without regard to within the forests has created a pollinators have very small home property ownership or provincial changing pattern of bloom time for ranges. You will make a difference boundaries. We’ve chosen to use food plants and shelter needs for by understanding the vegetation the ecoregional classification system foraging, nesting, and migrating patterns on the farm, forest, or and to underscore the connections pollinators. Farms and residential neighbour’s yard adjacent to your between climate and vegetation areas provide a diverse range of soil property. With this information in types that affect the diversity of types in both sunny and shady areas. hand, your planting choices will pollinators in the environment. With this diversity of locations many better support the pollinators’ need different species of plants may be for food and shelter as they move The Canadian ecoregions are used to improve pollinator habitats through the landscape. based on the National Ecological where they are lacking. Algonquin-Lake Nipissing 5 Understanding the Algonquin-Lake Nipissing n The Algonquin-Lake Nipissing ecoregion is part of the Boreal Shield ecozone which includes the following ecoregions; Lac Seul Upland, Big Trout Lake, Lake of the Woods, Thunder Bay- Quetico, Lake Nipigon, Abitibi Plains, and Lake Temiskaming Lowland. This ecoregion is situated at the southern extant of the boreal shield ecozone between Sault Ste. Marie and the Ottawa River valley in southern Ontario. The characteristic mixed forests of this ecoregion are distinct from the predominately deciduous forests to the south and the coniferous forests to the north. Significant land uses include forestry, mining, and tourism. Low-intensity farming, primarily grazing operations are also scattered throughout much of the ecoregion. n Not sure about which region you live or work in? Go to www. pollinator.org and click on Ecoregion Locator for help. n 74,479 square kilometres in Ontario. n The topography is mostly forested and exposed bedrock is common particularly north and west of Lake Nipissing. n Elevations ranging from 81 to 579 metres. n The mean summer temperature is 15.5°C and the mean winter temperature is -8.5°C. Photo courtesy of Balalaika n Annual year round precipitation is between 900-1000 mm. Characteristics n Dominated by mixed, deciduous and coniferous forest types (77% of the total landcover for the ecoregion). n Fewer flowering species due to less nutrient rich soil types and dense forest canopies, and colder mean annual and minimum winter temperatures.. n Dissected by forestry activities, settlements, and summer homes. 6 Selecting Plants for Pollinators Algonquin-Lake Nipissing includes: Sault Ste. Marie, Elliot Lake, Sudbury, North Bay, Mattawa,Parry Sound, Bracebridge, Gravenhurst Huntsville, Deep River, Minden, Bancroft, and Barry’s Bay. Algonquin-Lake Nipissing 7 Meet the Pollinators Who are the Sweat bees (family Halictidae) are medium to small-sized, slender bees pollinators? that commonly nest underground. Bees Various species are solitary while others form loose colonies, nesting Bees are the best documented side-by-side. Other common solitary pollinators in the natural and bees include mining bees (Andrena agricultural landscapes of the spp.), which nest underground and Algonquin-Lake Nipissingt. A wide are common in the spring; leaf- range of plants in the Aster and Rose cutter bees (Megachile spp.), which families, blueberry, raspberry and prefer dead trees or branches for strawberry crops are just a few plants their nest sites; and mason bees that benefit from bee pollinators. (Osmia spp.), which utilize cavities Most of us are familiar with the they find in stems and dead wood colonies of honey bees that have that they fill with mud. been the workhorses of agricultural pollination for years in Canada. Butterfl ies They were imported from Europe Butterflies prefer open and sunny almost 400 years ago and continue areas such as meadows and along to be managed for honey production woodland edges that provide bright and pollination services. There are flowers, water sources, and specific over 800 species of native ground host plants for their caterpillars. and twig nesting bees in Canada. Gardeners have been attracting Photo courtesy of Tim Dunne Photo courtesy of Tim Most of these bee species live a butterflies to their gardens for some Ruby-throated Hummingbird, a solitary life; a minority are social and time. To encourage butterflies place summer species in the Algonquin- form colonies or nest in aggregations. flowering plants where they have Lake Nipissing ecoregion. Native bees visit and pollinate full sun and are protected from the many crops; in many cases they wind. They usually look for flowers are better at transferring pollen that provide a good landing platform. than honey bees. Our native bees Butterflies need open areas (e.g., can be encouraged to do more to bare earth, large stones) where support agricultural endeavours if they can bask, and moist soil from their needs for nesting habitat are which they wick needed minerals. met and if suitable sources of nectar, Butterflies eat rotten fruit and even dung, so don’t clean up all the messes Eastern Tiger Swallowtail. pollen, and water are provided.
Recommended publications
  • State of New York City's Plants 2018
    STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species.
    [Show full text]
  • Literature Cited
    Literature Cited Robert W. Kiger, Editor This is a consolidated list of all works cited in volume 9, whether as selected references, in text, or in nomenclatural contexts. In citations of articles, both here and in the taxonomic treatments, and also in nomenclatural citations, the titles of serials are rendered in the forms recommended in G. D. R. Bridson and E. R. Smith (1991), Bridson (2004), and Bridson and D. W. Brown (http://fmhibd.library.cmu.edu/fmi/iwp/cgi?-db=BPH_Online&-loadframes). When those forms are abbreviated, as most are, cross references to the corresponding full serial titles are interpolated here alphabetically by abbreviated form. In nomenclatural citations (only), book titles are rendered in the abbreviated forms recommended in F. A. Stafleu and R. S. Cowan (1976–1988) and Stafleu et al. (1992–2009). Here, those abbreviated forms are indicated parenthetically following the full citations of the corresponding works, and cross references to the full citations are interpolated in the list alphabetically by abbreviated form. Two or more works published in the same year by the same author or group of coauthors will be distinguished uniquely and consistently throughout all volumes of Flora of North America by lower-case letters (b, c, d, ...) suffixed to the date for the second and subsequent works in the set. The suffixes are assigned in order of editorial encounter and do not reflect chronological sequence of publication. The first work by any particular author or group from any given year carries the implicit date suffix “a”; thus, the sequence of explicit suffixes begins with “b”.
    [Show full text]
  • 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.
    [Show full text]
  • Pollen Morphology and Variability of Invasive Spiraea Tomentosa L. (Rosaceae) from Populations in Poland
    RESEARCH ARTICLE Pollen morphology and variability of invasive Spiraea tomentosa L. (Rosaceae) from populations in Poland 1 1 2 Dorota Wrońska-PilarekID *, Blanka Wiatrowska , Jan BocianowskiID 1 Department of Forest Botany, Poznan University of Life Sciences, Poznań, Poland, 2 Department of Mathematical and Statistical Methods, Poznan University of Life Sciences, Poznań, Poland * [email protected] Abstract a1111111111 The aim of this study was to investigate the pollen morphology and the ranges of intraspe- a1111111111 a1111111111 cific and interindividual variability of the North American steeplebushÐSpiraea tomentosa a1111111111 L., an invasive species in Poland. Steeplebush inflorescences were collected randomly from a1111111111 30 localities of S. tomentosa in Poland. In total, 900 pollen grains were analysed with both a light and a scanning electron microscope. Nine quantitative and three qualitative pollen fea- tures were studied. The diagnostic features were: exine ornamentation (size and direction of the muri), operculum and perforation size. For the first time, the intraspecific and interindivid- OPEN ACCESS ual variability of the pollen grains of the highly invasive S. tomentosa were investigated. Pol- Citation: Wrońska-Pilarek D, Wiatrowska B, len grain features were so similar, that they did not allow to differentiate individual samples Bocianowski J (2019) Pollen morphology and of S. tomentosa and only groups of samples were recognized. variability of invasive Spiraea tomentosa L. (Rosaceae) from populations in Poland. PLoS ONE 14(8): e0218276. https://doi.org/10.1371/journal. pone.0218276 Editor: Ramasamy Perumal, Kansas State Introduction University, UNITED STATES The genus L. belongs to the Juss. family, to the Amygdaloideae subfamily and Received: February 4, 2019 Spiraea Rosaceae to the Spiraeeae tribe, which is the subject of considerable speculation regarding its internal Accepted: May 29, 2019 divisions.
    [Show full text]
  • Native Plants for Wildlife Habitat and Conservation Landscaping Chesapeake Bay Watershed Acknowledgments
    U.S. Fish & Wildlife Service Native Plants for Wildlife Habitat and Conservation Landscaping Chesapeake Bay Watershed Acknowledgments Contributors: Printing was made possible through the generous funding from Adkins Arboretum; Baltimore County Department of Environmental Protection and Resource Management; Chesapeake Bay Trust; Irvine Natural Science Center; Maryland Native Plant Society; National Fish and Wildlife Foundation; The Nature Conservancy, Maryland-DC Chapter; U.S. Department of Agriculture, Natural Resource Conservation Service, Cape May Plant Materials Center; and U.S. Fish and Wildlife Service, Chesapeake Bay Field Office. Reviewers: species included in this guide were reviewed by the following authorities regarding native range, appropriateness for use in individual states, and availability in the nursery trade: Rodney Bartgis, The Nature Conservancy, West Virginia. Ashton Berdine, The Nature Conservancy, West Virginia. Chris Firestone, Bureau of Forestry, Pennsylvania Department of Conservation and Natural Resources. Chris Frye, State Botanist, Wildlife and Heritage Service, Maryland Department of Natural Resources. Mike Hollins, Sylva Native Nursery & Seed Co. William A. McAvoy, Delaware Natural Heritage Program, Delaware Department of Natural Resources and Environmental Control. Mary Pat Rowan, Landscape Architect, Maryland Native Plant Society. Rod Simmons, Maryland Native Plant Society. Alison Sterling, Wildlife Resources Section, West Virginia Department of Natural Resources. Troy Weldy, Associate Botanist, New York Natural Heritage Program, New York State Department of Environmental Conservation. Graphic Design and Layout: Laurie Hewitt, U.S. Fish and Wildlife Service, Chesapeake Bay Field Office. Special thanks to: Volunteer Carole Jelich; Christopher F. Miller, Regional Plant Materials Specialist, Natural Resource Conservation Service; and R. Harrison Weigand, Maryland Department of Natural Resources, Maryland Wildlife and Heritage Division for assistance throughout this project.
    [Show full text]
  • Introduction to Botany. Lecture 37
    Monday test Rosidae, or rosids (Part II) Introduction to Botany. Lecture 37 Alexey Shipunov Minot State University December 6th, 2010 Shipunov BIOL 154.37 Monday test Rosidae, or rosids (Part II) Outline 1 Monday test 2 Rosidae, or rosids (Part II) Rosaceae—rose family Leguminosae, or Fabaceae—legume family Cruciferae, or Brassicaceae—cabbage family Shipunov BIOL 154.37 Monday test Rosidae, or rosids (Part II) Outline 1 Monday test 2 Rosidae, or rosids (Part II) Rosaceae—rose family Leguminosae, or Fabaceae—legume family Cruciferae, or Brassicaceae—cabbage family Shipunov BIOL 154.37 5 Name one economically important representative of Cucurbitaceae. Monday test Rosidae, or rosids (Part II) Monday test (5 points) 1 Name one difference between Cyperaceae (sedge family) and Gramineae (grass family) Shipunov BIOL 154.37 1 Name one difference between Cyperaceae (sedge family) and Gramineae (grass family) 5 Name one economically important representative of Cucurbitaceae. Monday test Rosidae, or rosids (Part II) Monday test (5 points) 2 Which family this diagram belongs to? Shipunov BIOL 154.37 1 Name one difference between Cyperaceae (sedge family) and Gramineae (grass family) 5 Name one economically important representative of Cucurbitaceae. Monday test Rosidae, or rosids (Part II) Monday test (5 points) 3 What is wrong with this picture? Shipunov BIOL 154.37 1 Name one difference between Cyperaceae (sedge family) and Gramineae (grass family) 5 Name one economically important representative of Cucurbitaceae. Monday test Rosidae, or rosids (Part II) Monday test (5 points) 4 What is united Rosidae (rosids)? (≥ 1 character) Shipunov BIOL 154.37 1 Name one difference between Cyperaceae (sedge family) and Gramineae (grass family) Monday test Rosidae, or rosids (Part II) Monday test (5 points) 5 Name one economically important representative of Cucurbitaceae.
    [Show full text]
  • INTRODUCTION This Check List of the Plants of New Jersey Has Been
    INTRODUCTION This Check List of the Plants of New Jersey has been compiled by updating and integrating the catalogs prepared by such authors as Nathaniel Lord Britton (1881 and 1889), Witmer Stone (1911), and Norman Taylor (1915) with such other sources as recently-published local lists, field trip reports of the Torrey Botanical Society and the Philadelphia Botanical Club, the New Jersey Natural Heritage Program’s list of threatened and endangered plants, personal observations in the field and the herbarium, and observations by other competent field botanists. The Check List includes 2,758 species, a botanical diversity that is rather unexpected in a small state like New Jersey. Of these, 1,944 are plants that are (or were) native to the state - still a large number, and one that reflects New Jersey's habitat diversity. The balance are plants that have been introduced from other countries or from other parts of North America. The list could be lengthened by hundreds of species by including non-persistent garden escapes and obscure waifs and ballast plants, many of which have not been seen in New Jersey since the nineteenth century, but it would be misleading to do so. The Check List should include all the plants that are truly native to New Jersey, plus all the introduced species that are naturalized here or for which there are relatively recent records, as well as many introduced plants of very limited occurrence. But no claims are made for the absolute perfection of the list. Plant nomenclature is constantly being revised. Single old species may be split into several new species, or multiple old species may be combined into one.
    [Show full text]
  • Appendices I Through VIII
    APPENDIX I: Standards for Ecological Classification A given terrestrial ecological system is defined as a group of plant community types that tend to co-occur within landscapes with similar ecological processes, substrates, and/or environmental gradients. A given terrestrial ecological system will typically manifest itself in a landscape at intermediate geographic scales of 10s to 1,000s of hectares and persist for 50 or more years. Ecological processes include natural disturbances such as fire and flooding. Substrates may include a variety of soil surface and bedrock features, such as shallow soils, alkaline parent materials, sandy/gravelling soils, or peatlands. Finally, environmental gradients include hydrologically defined patterns in coastal zones, arid grassland or desert areas, or montane, alpine or subalpine zones defined by climate. By plant community type, we mean a vegetation classification unit at the association or alliance level of the US National Vegetation Classification (US-NVC) (Grossman et al. 1998, Jennings et al. 2003, NatureServe 2004), or, if these are not available, other comparable vegetation units. US-NVC associations are used wherever possible to describe the component biotic communities of each terrestrial system. Ecological systems are defined using both spatial and temporal criteria that influence the grouping of associations. Associations that consistently co-occur on the landscape therefore define biotic components of each ecological system type. Our approach to ecological systems definition using US-NVC associations is similar to the biotope or habitat approach used, for example, by the EUNIS habitat classification, which explicitly links meso-scale habitat units to European Vegetation Survey alliance units (Rodwell et al. 2002).
    [Show full text]
  • Rhexia Mariana L
    New England Plant Conservation Program Rhexia mariana L. Maryland Meadowbeauty Conservation and Research Plan For New England Prepared by: Stephen I. Craine Department of Biology Tufts University For: New England Wild Flower Society 180 Hemenway Road Framingham, MA 01701 508/877-7630 e-mail: [email protected] • website: www.newfs.org Approved, Regional Advisory Council, 2002 1 SUMMARY Rhexia mariana L., Maryland meadowbeauty, (Melastomataceae) is a regionally rare, but globally secure, species that is listed S1 (Endangered) in Massachusetts and has never been documented in any other New England state. There are nine extant and four historical occurrences in Massachusetts, all of which are on Cape Cod. Only three of these sites were found to include over 500 stems in the 2001 season; several others had less than 50. The small number of sites for this species, their small populations, and the instability of population numbers from year to year all make R. mariana very vulnerable in the region. This perennial herb of pond shores and wet meadows is common in the southern Atlantic coastal plain from central New Jersey to Florida and on the Gulf coast to Texas. Although R. mariana is secure in the heart of its range, preserving the species in New England is important because such peripheral populations often serve as reservoirs of genetic diversity for a species as a whole. The Massachusetts occurrences represent a disjunct population at the northern extreme of the species’ range. Here, it is found along with other characteristic coastal plain species on the acidic and nutrient-poor, sandy beaches of freshwater ponds, in full sun.
    [Show full text]
  • Acta Pr Ů Honiciana
    ACTA PRŮ HONICIANA 72 2002 VÝZKUMNÝ ÚSTAV SILVA TAROUCY PRO KRAJINU A OKRASNÉ ZAHRADNICTVÍ PRŮHONICE THE GENUS SPIRAEA IN CULTIVATION IN BOHEMIA, MORAVIA AND SLOVAKIA Rod Spiraea v kultuře v Čechách, na Moravě a na Slovensku Roman Businský, Ludmila Businská Průhonice 2002 Cover photograph: Spiraea ×blanda Zab. in the Dendrological garden at Průhonice, May 22, 2001. ISSN: 0374-5651 ISBN: 80-85116-27-8 ii CONTENTS Abstract & Keywords . 1 Introduction . 2 History of the classification of the genus Spiraea . 2 History of the genus Spiraea cultivation in the world . 6 Spireas in cultivation in Bohemia, Moravia and Slovakia . 7 Evaluation of spireas in the Dendrological garden at Průhonice . 10 Material and methods used . 11 Evaluation of taxa from horticultural points of view . 12 Systematic Treatment . 13 Natural species inclusive of infraspecific taxa and derived cultivars . 14 Spiraea L. Sect. Glomerati Nakai . 14 Sect. Chamaedryon Ser. 21 Sect. Calospira K. Koch . 45 Sect. Spiraea . 90 Interspecific hybrids and hybrid cultivars . 101 Hybrids within the sect. Chamaedryon Ser. 101 Hybrids within the sect. Calospira K. Koch . 106 Hybrids within the sect. Spiraea . 110 Hybrids between species from different sections of the genus . 117 New cultivars . 130 Conclusions . 138 Acknowledgement . 138 References . 139 Czech Summary . 141 Appendix – Survey of accepted taxa cultivated in Bohemia, Moravia and Slovakia in historic context . 153 Index of scientific names and cultivars . 160 iii iv ACTA PRŮHONICIANA 72, Průhonice 2002 ____________________________________________________________________________________ The genus Spiraea in cultivation in Bohemia, Moravia and Slovakia ROMAN BUSINSKÝ 1, LUDMILA BUSINSKÁ 2 1 Silva Tarouca Research Institute for Landscape and Ornamental Gardening, CZ-252 43 Průhonice; [email protected] –– 1, 2 Kodaňská 51, CZ-101 00 Praha 10 ABSTRACT History of the classification of the genus Spiraea (spirea, Rosaceae) with a view to the infrageneric division is given.
    [Show full text]
  • NRCS West Virginia Pollinator Handbook
    West Virginia Pollinator Handbook NRCS West Virginia Pollinator Handbook WV NRCS Ecological Sciences In conjunction with the WV Division of Natural Resources and The Xerces Society for Invertebrate Conservation A Field Office Technical Guide Reference to management of pollinators and their habitats 1 West Virginia Pollinator Handbook Cover Photo: Eastern tiger swallowtail on milkweed in Randolph County, WV. Photo: C. Shrader NRCS, WV 2 West Virginia Pollinator Handbook ACKNOWLEDGEMENTS PARTNERING AGENCIES: U.S. DEPARTMENT OF AGRICULTURE, NATURAL RESOURCES CONSERVATION SERVICE WEST VIRGINIA DIVISION OF NATURAL RESOURCES THE XERCES SOCIETY FOR INVERTEBRATE CONSERVATION CONTRIBUTORS: Elizabeth Byers, Wildlife Diversity Biologist, WVDNR, Elkins, WV Harry W. Godwin, Research Scientist, Agricultural Research Service, Beaver, WV Walt Kordek, Assistant Chief, Wildlife Div. & Tech. Support Units, WVDNR, Elkins, WV Barbara McWhorter, Forester, USDA NRCS, Morgantown, WV Eric Mader, Assistant Pollinator Program Director, The Xerces Society, Portland Oregon Susan Olcott, Wildlife Diversity Biologist, WVDNR, Elkins, WV Casey Shrader, WV State Biologist, USDA Natural Resources Conservation Service, Morgantown, WV 3 West Virginia Pollinator Handbook 4 West Virginia Pollinator Handbook Table of Contents PAGE INTRODUCTION 7 POLLINATION SERVICES IN WEST VIRGINIA 8 WEST VIRGINIA NATIVE BEE AND BUTTERFLY DIVERSITY 10 POLLINATOR BIOLOGY AND HABITAT 13 POLLINATOR CONSERVATION AND FARM PLANNING 15 I RECOGNIZING EXISTING POLLINATOR HABITAT 17 A Existing Plant
    [Show full text]
  • Diversity and Evolution of Rosids
    Diversity and Evolution of Rosids . roses, currants, peonies . Eudicots • continue survey through the eudicots or tricolpates • vast majority of eudicots are Rosids (polypetalous) and Asterids core (sympetalous) eudicots rosid asterid Eudicots • unlike Asterids, Rosids (in orange) now represent a diverse set of families *Saxifragales • before examining the large Rosid group, look at a small but important order of flowering plants - Saxifragales Paeonia Sedum *Saxifragales • small group of 16 families and about 2500 species sister to Rosids • ancient lineage from 120 mya and underwent rapid radiation Paeonia Sedum *Saxifragales • part of this ancient radiation may involve this small family of holo-parasites - Cynomoriaceae *Saxifragales • they generally can be identified by their two or more separate or semi-fused carpels, but otherwise quite variable Paeonia Sedum Paeoniaceae 1 genus / 33 species • like many of these families, Paeonia exhibits an Arcto-Tertiary distribution Paeoniaceae 1 genus / 33 species • small shrubs with primitive features of perianth and stamens • hypogynous with 5-8 separate carpels developing into follicles Cercidiphyllaceae 1 genus / 2 species • small trees (kadsura-tree) restricted to eastern China and Japan . • . but fossils in North America and Europe from Tertiary Cercidiphyllaceae 1 genus / 2 species • unisexual, wind-pollinated but do produce follicles Hamamelidaceae 27 genera and 80 species - witch hazels • family of trees and shrubs in subtropical and temperate areas but only 1 species in Wisconsin - witch
    [Show full text]