PLANT LIST for POLLINATORS Part 1 – a Concise List of Suggested Garden Plants That Are Attractive to Pollinating Insects
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Cambridge University Press 978-1-107-11607-8 — a Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P
Cambridge University Press 978-1-107-11607-8 — A Natural History of Ladybird Beetles M. E. N. Majerus , Executive Editor H. E. Roy , P. M. J. Brown Index More Information Index 2-isopropyl-3-methoxy-pyrazine, 238 281, 283, 285, 287–9, 291–5, 297–8, 2-phenylethylamine, 237 301–3, 311, 314, 316, 319, 325, 327, 329, 335 abdomen, 17, 20, 22, 24, 28–9, 32, 38, 42, 110, Adalia 4-spilota,80 114, 125, 128, 172, 186, 189, 209–10, Adalia conglomerata, 255 218 adaline, 108, 237, 241 Acacia, 197, 199 adalinine, 237 acaricides, 316 adelgids, 29, 49, 62, 65, 86, 91, 176, 199, 308, Acaridae, 217 310, 322 Acarina, 205, 217 Adonia, 44, 71 Acer pseudoplatanus, 50, 68, 121 aggregations, 163, 165, 168, 170, 178, 184, Acraea, 228, 297, 302 221, 312, 324 Acraea encedana, 302 Aiolocaria, 78, 93, 133, 276 Acraea encedon, 297, 302 Aiolocaria hexaspilota,78 Acyrthosiphon nipponicum, 101 Aiolocaria mirabilis, 133, 276 Acyrthosiphon pisum, 75, 77, 90, 92, 97–101, albino, 273 116, 239 Alces alces,94 Adalia, 5–6, 10, 22, 34, 44, 64, 70, 78, 80, 86, Aleyrodidae, 91, 310 123, 125, 128, 130, 132, 140, 143, 147, alfalfa, 119, 308, 316, 319, 325 159–60, 166–7, 171, 180–1, 218, 222, alimentary canal, 29, 35, 221 234, 237, 239, 241, 255, 259–60, 262, alkaloids, x, 99–100, 195–7, 202, 236–9, 241–2, 269, 279, 281, 284, 286, 298, 311, 325, 245–6 327, 335 Allantonematidae, 220 Adalia 10-punctata, 22, 70, 80, 86, 98–100, anal cremaster, 38, 40 104, 108, 116, 132, 146–7, 149, Anatis, 4, 17, 23, 41, 44, 66, 76, 89, 102, 131, 154, 156, 160, 174, 181–3, 188, 148, 165, 186, 191, 193, -
Identification of White Campion (Silene Latifolia) Guaiacol O-Methyltransferase Involved in the Biosynthesis of Veratrole, a Key Volatile for Pollinator Attraction
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2012 Identification of white campion (Silene latifolia) guaiacol O-methyltransferase involved in the biosynthesis of veratrole, a key volatile for pollinator attraction Gupta, Alok K ; Akhtar, Tariq A ; Widmer, Alex ; Pichersky, Eran ; Schiestl, Florian P Abstract: BACKGROUND: Silene latifolia and its pollinator, the noctuid moth Hadena bicruris, repre- sent an open nursery pollination system wherein floral volatiles, especially veratrole (1, 2-dimethoxybenzene), lilac aldehydes, and phenylacetaldehyde are of key importance for floral signaling. Despite the important role of floral scent in ensuring reproductive success in S. latifolia, the molecular basis of scent biosyn- thesis in this species has not yet been investigated. RESULTS: We isolated two full-length cDNAs from S. latifolia that show similarity to rose orcinol O-methyltransferase. Biochemical analysis showed that both S. latifolia guaiacol O-methyltransferase1 (SlGOMT1) S. latifolia guaiacol O-methyltransferase2 (SlGOMT2) encode proteins that catalyze the methylation of guaiacol to form veratrole. A large Km value difference between SlGOMT1 ( 10 M) and SlGOMT2 ( 501 M) resulted that SlGOMT1 is31-fold more catalytically efficient than SlGOMT2. qRT-PCR expression analysis showed that theSlGOMT genes are specifically expressed in flowers and male S. latifolia flowers had 3- to 4-folds higher levelof GOMT gene transcripts than female flower tissues. Two related cDNAs, S. dioica O-methyltransferase1 (SdOMT1) and S. dioica O-methyltransferase2 (SdOMT2), were also obtained from the sister species Silene dioica, but the proteins they encode did not methylate guaiacol, consistent with the lack of ver- atrole emission in the flowers of this species. -
Lathyrus Bijugatus
Fire Effects Information System (FEIS) FEIS Home Page Lathyrus bijugatus Table of Contents SUMMARY INTRODUCTION DISTRIBUTION AND OCCURRENCE BOTANICAL AND ECOLOGICAL CHARACTERISTICS FIRE ECOLOGY AND MANAGEMENT OTHER MANAGEMENT CONSIDERATIONS APPENDIX REFERENCES Figure 1—Drypark pea in flower. Photo by Tara Luna, used with permission. SUMMARY This Species Review summarizes the scientific information that was available on drypark pea as of February 2021. Drypark pea is a rare, leguminous forb that occurs in eastern Washington and Oregon, northern Idaho, and northwestern Montana. Within that distribution, it grows in a broad range of biogeoclimatic zones and elevations. As its common name "drypark pea" suggests, it prefers dry soils and open sites. Drypark pea grows in sagebrush-conifer and sagebrush-grassland transition zones; in ponderosa pine, Douglas-fir, and subalpine fir-Engelmann spruce woodlands and forests; and subalpine fir parklands. In conifer communities, it is most common in open stands. Drypark pea has rhizomes that grow out from its taproot. Its roots host nitrogen-fixing Rhizobium bacteria. Drypark pea regenerates from seed and has a soil-stored seed bank; however, information on seed dispersal, viability, and seedling establishment of drypark pea was not available in the literature. Fire probably top-kills drypark pea, and it likely sprouts from its rhizomes and/or caudex after top-kill; however, these responses are undocumented. Only one study provided information on the response of drypark pea to fire. In ponderosa pine forest in northern Idaho, cover and frequency of drypark pea were similar on unburned plots and plots burned under low or high intensity, when 1 averaged across 3 postfire years. -
Leptidea Reali (Real’S Wood White) in Northern Ireland
The ecology and conservation of Leptidea reali (Real’s Wood White) in Northern Ireland © Neal Warnock Neal Warnock September 2008 11753072 MSc Ecological Management and Conservation Biology, Queen’s University Belfast TABLE OF CONTENTS CONTENTS PAGE NUMBER Acknowledgements…………………………………………………………………….…....i Abstract……………………………………………………………………………………...ii List of tables………………………………………………………………………………...iii List of figures……………………………………………………………………………..... iv 1 Introduction……………………………………………………………….1 1.1 Background……………………………………………………………………...1 1.2 ‘Wood White’ butterflies……………………… ……………………………...2 1.2.1 The ‘sinapis-reali’ complex………………………………………....2 1.2.2 Leptidea reali in Northern Ireland- what we know and what we Don’t know………………………………………………………………….9 1.3 Summary and Aims of study…………………………………………………...12 2 Sites and Methods……………………………………………………….15 2.1 Site locations…………………………………………………………………..15 2.2 Relationships with previous research……………………………………….…16 2.3 Site descriptions............................................................................................…..18 2.3.1 Craigavon Lakes…………………………………………………………18 2.3.2 Oxford Island National Nature Reserve……………………………….....20 2.4 Numbers………………………………………………………………………..23 2.5 Oviposition choice- flight cage experiment……………………………...…….24 2.6 Oviposition preference- field observations…………………………………….24 2.7 Larvae and pupae………………………………………………………………25 2.8 Nectaring preference…………………………………………………..……….25 2.9 Courtship……………………………………………………………………….25 2.10 Species identification…………………………………………………………26 2.11 -
Effect of Broad Bean Varieties and Faba Bean Upon Populations Dynamic of Bruchus Rufimanus (Coleoptera: Chrysomelidae: Bruchinae) in Kabylia Region (Algeria)
International Journal of Agricultural Science and Research (IJASR) ISSN(P): 2250-0057; ISSN(E): 2321-0087 Vol. 5, Issue 6, Dec 2015, 79-88 © TJPRC Pvt. Ltd. EFFECT OF BROAD BEAN VARIETIES AND FABA BEAN UPON POPULATIONS DYNAMIC OF BRUCHUS RUFIMANUS (COLEOPTERA: CHRYSOMELIDAE: BRUCHINAE) IN KABYLIA REGION (ALGERIA) MEZANI SAMIR, KHELFANE-GOUCEM KARIMA & MEDJDOUB-BENSAAD FERROUDJA Biology Department, Mouloud Mammeri University, Tizi-Ouzou, Algeria ABSTRACT The present study aimed to examine the process and conditions of broad bean Bruchid B. rufimanus infestation in the field in Kabylia region (Algeria). B. rufimanus adults colonized progressively the cultures of Aguadulce variety and faba bean at the beginning of the flowering period, while it colonized Seville variety culture during the flowering period. This colonization seemed to depend upon climatic factors and host plant phenology. The presence of adults in plots spanned about 5 weeks for Aguadulce variety, 6 for faba bean and 4 weeks for Seville variety. At the end of the flowering period, the number of adults decreased whereas the number of mature pods increased for all plots. The egg-laying was spread over a period of approximately 8 and 7 weeks for Aguadulce and Seville varieties respectively and 6 for faba bean. Females seemed Article Original to deposit their eggs randomly on the available young pods and old pods of each host. Our results showed also that the varieties act significantly on the rate of infestation by B. rufimanus females on V. faba plots studied. KEYWORDS: Vicia Faba, Bruchus Rufimanus, Egg-Laying, Varieties, Host Plant Colonization, Kabylia Region Received: Oct 06, 2015; Accepted: Oct 19, 2015; Published: Oct 27, 2015; Paper Id.: IJASRDEC201511 INTRODUCTION Bean or faba bean ( Vicia faba Linné) is a most cultivated Leguminosae seeds for human consumption in the Maghreb (Kharrat and al., 2002). -
Section Elisanthe)
POPULATION GENETICS AND SPECIATION IN THE PLANT GENUS SILENE (SECTION ELISANTHE) by ANDREA LOUISE HARPER A thesis submitted to The University of Birmingham for the degree of DOCTOR OF PHILOSOPHY School of Biosciences The University of Birmingham 2009 University of Birmingham Research Archive e-theses repository This unpublished thesis/dissertation is copyright of the author and/or third parties. The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation. Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the permission of the copyright holder. ABSTRACT This thesis is concerned with speciation and population genetics in the plant genus Silene (section Elisanthe). The introductory chapter is a literature review covering characteristics of the species studied, and the current literature on their evolutionary dynamics and population genetics. The second and third chapters cover techniques used in all experiments, such as DNA extraction, sequencing and genotyping protocols, and explain the rationale behind the initial experimental design. The fourth chapter focuses on the multi-locus analysis of autosomal gene sequences from S. latifolia and S. dioica. The relationship between the two species was investigated using various analyses such as isolation modeling and admixture analysis providing estimates of evolutionary distance and extent of historical gene flow. The maintenance of the species despite frequent hybridization at present-day hybrid zones is discussed. -
Review of Coverage of the National Vegetation Classification
JNCC Report No. 302 Review of coverage of the National Vegetation Classification JS Rodwell, JC Dring, ABG Averis, MCF Proctor, AJC Malloch, JHJ Schaminée, & TCD Dargie July 2000 This report should be cited as: Rodwell, JS, Dring, JC, Averis, ABG, Proctor, MCF, Malloch, AJC, Schaminée, JNJ, & Dargie TCD, 2000 Review of coverage of the National Vegetation Classification JNCC Report, No. 302 © JNCC, Peterborough 2000 For further information please contact: Habitats Advice Joint Nature Conservation Committee Monkstone House, City Road, Peterborough PE1 1JY UK ISSN 0963-8091 1 2 Contents Preface .............................................................................................................................................................. 4 Acknowledgements .......................................................................................................................................... 4 1 Introduction.............................................................................................................................................. 5 1.1 Coverage of the original NVC project......................................................................................................... 5 1.2 Generation of NVC-related data by the community of users ...................................................................... 5 2 Methodology............................................................................................................................................. 7 2.1 Reviewing the wider European scene......................................................................................................... -
2020 Plant List 1
2020 issima Introductions Sesleria nitida Artemisia lactiflora ‘Smoke Show’ Succisella inflexa 'Frosted Pearls' Impatiens omeiana ‘Black Ice’ Thalictrum contortum Kniphofia ‘Corn Dog’ Thalictrum rochebrunianum var. grandisepalum Kniphofia ‘Dries’ Tiarella polyphylla (BO) Kniphofia ‘Takis Fingers’ Verbascum roripifolium hybrids Persicaria amplexicaulis ‘Ruby Woo’ Veronica austriaca 'Ionian Skies' Sanguisorba ‘Unicorn Tails’ Sanguisorba obtusa ‘Tickled Pink’ Stock Woody and Herbaceous Perennials, New & Returning for 2020 indexed alphabetically: Alchemilla alpina Acanthus ‘Summer Beauty’ Aletris farinosa Acanthus Hollard’s Gold’ Anemone nemorosa ‘Vestal’ Acanthus syriacus Anemone nemorosa Virescens Actaea pachypoda Anemone ranunculoides Actaea rubra leucocarpa Anemone seemannii Adenophora triphylla Berkheya purpurea Pink Flower Agastache ‘Linda’ Berkheya species (Silver Hill) Agastache ‘Serpentine’ Boehmeria spicata 'Chantilly' Ajuga incisa ‘Blue Enigma’ Callirhoe digitata Amorphophallus konjac Carex plantaginea Anemonella thalictroides ‘Cameo’ Carex scaposa Anemonella thalictroides ‘Oscar Schoaff’ Deinanthe caerulea x bifida Anemonopsis macrophylla – dark stems Dianthus superbus var. speciosus Anemonopsis macrophylla – White Flower Digitalis ferruginea Angelica gigas Disporum sessile ‘Variegatum’ Anthemis ‘Cally Cream’ Echium amoenum Anthericum ramosum Echium russicum Arisaema fargesii Echium vulgare Arisaema ringens Erigeron speciosus (KDN) Arisaema sikokianum Eriogonum annuum (KDN) Artemisia lactiflora ‘Elfenbein’ Geranium psilostemon -
Floerkea Proserpinacoides Willdenow False Mermaid-Weed
New England Plant Conservation Program Floerkea proserpinacoides Willdenow False Mermaid-weed Conservation and Research Plan for New England Prepared by: William H. Moorhead III Consulting Botanist Litchfield, Connecticut and Elizabeth J. Farnsworth Senior Research Ecologist New England Wild Flower Society Framingham, Massachusetts 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, December 2003 1 SUMMARY Floerkea proserpinacoides Willdenow, false mermaid-weed, is an herbaceous annual and the only member of the Limnanthaceae in New England. The species has a disjunct but widespread range throughout North America, with eastern and western segregates separated by the Great Plains. In the east, it ranges from Nova Scotia south to Louisiana and west to Minnesota and Missouri. In the west, it ranges from British Columbia to California, east to Utah and Colorado. Although regarded as Globally Secure (G5), national ranks of N? in Canada and the United States indicate some uncertainly about its true conservation status in North America. It is listed as rare (S1 or S2) in 20% of the states and provinces in which it occurs. Floerkea is known from only 11 sites total in New England: three historic sites in Vermont (where it is ranked SH), one historic population in Massachusetts (where it is ranked SX), and four extant and three historic localities in Connecticut (where it is ranked S1, Endangered). The Flora Conservanda: New England ranks it as a Division 2 (Regionally Rare) taxon. Floerkea inhabits open or forested floodplains, riverside seeps, and limestone cliffs in New England, and more generally moist alluvial soils, mesic forests, springy woods, and streamside meadows throughout its range. -
The Electronic Publication
The electronic publication Phänologische und symphänologische Artengruppen von Blütenpflanzen Mitteleuropas (Dierschke 1995) has been archived at http://publikationen.ub.uni-frankfurt.de/ (repository of University Library Frankfurt, Germany). Please include its persistent identifier urn:nbn:de:hebis:30:3-425536 whenever you cite this electronic publication. Tuexenia 15: 523-560. Göttingen 1995. Phänologische und symphänologische Artengruppen von Blütenpflanzen Mitteleuropas - Hartmut Dierschke- Zusammenfassung Mit Hilfe blühphänologischer Merkmale von Waldpflanzen wird die Vegetationsperiode in Phäno- phasen nach phänologischen Artengruppen eingeteilt. Diesen Phasen werden 1577 Blütenpflanzen Mittel- europas, vorwiegend solche mit Hauptverbreitung im planaren bis montanen Bereich, zugeordnet, aufge teilt auf 12 grobe G esellschaftsgruppen (А-M). Hieraus ergeben sich zwei Artenlisten mit phänologischen bzw. symphänologischen Angaben in gesellschaftsspezifischer Gliederung und alphabetischer Reihenfol ge (Anhang 1-2). Für die Gesellschaftsgruppen werden symphänologische Gruppenspektren erstellt und kommentiert. Abstract: Phenological and symphenological species groups of flowering plants of central Europe By means of phenological characteristics (time from beginning to full development of flowering) of forest plant species, 9 phenological groups have been established which characterize phenophases 1-9 of the vegetation period. Afterwards, 1577 plant species of central Europe were classified into these phenolo gical groups, especially those growing in lower to montane areas (i.e. excluding alpine plants). These species belong to 12 groups of plant communities (А-M ; some with subgroups a-b). On this basis two species lists are prepared, one with symphenological groups related to the community groups A- M (appendix 1) and one in alphabetic sequence (appendix 2). Symphenological group spectra were estab lished and are discussed for the community groups. -
Assessment Report on Plantago Lanceolata L., Folium Based on Article 16D(1), Article 16F and Article 16H of Directive 2001/83/EC As Amended (Traditional Use)
22 November 2011 EMA/HMPC/437859/2010 Committee on Herbal Medicinal Products (HMPC) Assessment report on Plantago lanceolata L., folium Based on Article 16d(1), Article 16f and Article 16h of Directive 2001/83/EC as amended (traditional use) Final Herbal substance(s) (binomial scientific whole or fragmented, dried leaf and scape of Plantago name of the plant, including plant part) lanceolata L. Herbal preparation(s) Traditional use: a) Herbal substance, comminuted b) Herbal substance, powdered c) Dry extract (DER 3-6:1); extraction solvent: water d) Liquid extract (DER 1:0.8-1.2); extraction solvent: ethanol 20%-40% (V/V) e) Soft extract (DER 1.5-1.7:1); extraction solvent ethanol 20% (m/m) f) Expressed juice (DER 1:0.5-0.9) from the fresh herb g) Syrup according to ÖAB 2009 (formally, the native herbal preparation is a liquid extract (DER 1:11); extraction solvent: water) h) Dry extract (DER 3-5:1); extraction solvent: ethanol 20% (m/m) i) Liquid extract (DER 1:5.8-5.9); extraction solvent: water Pharmaceutical form(s) Traditional use: Comminuted herbal substance as herbal tea for oral use. Powdered herbal substance in a solid dosage form and other herbal preparations in liquid or solid dosage forms for oral and/or oromucosal use. The pharmaceutical form should be described by the European Pharmacopoeia full standard term. Rapporteur(s) Werner Knöss Jacqueline Wiesner Assessor(s) 7 Westferry Circus ● Canary Wharf ● London E14 4HB ● United Kingdom Telephone +44 (0)20 7418 8400 Facsimile +44 (0)20 7523 7051 E-mail [email protected] Website www.ema.europa.eu An agency of the European Union © European Medicines Agency, 2012. -
Diversity of Sexual Systems Within Different Lineages of the Genus Silene
Research Article Diversity of sexual systems within different lineages of the genus Silene Ine´s Casimiro-Soriguer1,2*, Maria L. Buide1 and Eduardo Narbona1 1 A´ rea de Bota´nica, Departamento de Biologı´a Molecular e Ingenierı´a Bioquı´mica, Universidad Pablo de Olavide, Ctra. de Utrera, km 1, 41013 Sevilla, Spain 2 A´ rea de Bota´nica, Departamento de Biologı´a Vegetal y Ecologı´a, Universidad de Sevilla, Avenida Reina Mercedes s/n, 41012 Sevilla, Spain Received: 16 December 2014; Accepted: 26 March 2015; Published: 10 April 2015 Associate Editor: Diana Wolf Citation: Casimiro-Soriguer I, Buide ML, Narbona E. 2015. Diversity of sexual systems within different lineages of the genus Silene. AoB PLANTS 7: plv037; doi:10.1093/aobpla/plv037 Abstract. Species and populations can be categorized by their sexual systems, depending on the spatial distribu- tion of female and male reproductive structures within and among plants. Although a high diversity of sexual systems exists in Silene, their relative frequency at the genus and infrageneric level is unknown. Here, we carried out an exten- sive literature search for direct or indirect descriptions of sexual systems in Silene species. We found descriptions of sexual systems for 98 Silene species, where 63 and 35 correspond to the phylogenetically supported subgenera Silene and Behenantha, respectively. Hermaphroditism was the commonest sexual system (58.2 %), followed by dioecy (14.3 %), gynodioecy (13.3 %) and gynodioecy–gynomonoecy (i.e. hermaphroditic, female and gynomonoecious plants coexisting in the same population; 12.2 %). The presence of these sexual systems in both subgenera suggests their multiple origins.