Learn Which Ornamental Plants Can Be Invasive in Our Area
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Mimulus Is an Emerging Model System for the Integration of Ecological and Genomic Studies
Heredity (2008) 100, 220–230 & 2008 Nature Publishing Group All rights reserved 0018-067X/08 $30.00 www.nature.com/hdy SHORT REVIEW Mimulus is an emerging model system for the integration of ecological and genomic studies CA Wu, DB Lowry, AM Cooley, KM Wright, YW Lee and JH Willis Department of Biology, Duke University, Durham, NC, USA The plant genus Mimulus is rapidly emerging as a model direct genetic studies with Mimulus can address a wide system for studies of evolutionary and ecological functional spectrum of ecological and evolutionary questions. In genomics. Mimulus contains a wide array of phenotypic, addition, we present the genomic resources currently ecological and genomic diversity. Numerous studies have available for Mimulus and discuss future directions for proven the experimental tractability of Mimulus in laboratory research. The integration of ecology and genetics with and field studies. Genomic resources currently under bioinformatics and genome technology offers great promise development are making Mimulus an excellent system for for exploring the mechanistic basis of adaptive evolution and determining the genetic and genomic basis of adaptation and the genetics of speciation. speciation. Here, we introduce some of the phenotypic and Heredity (2008) 100, 220–230; doi:10.1038/sj.hdy.6801018; genetic diversity in the genus Mimulus and highlight how published online 6 June 2007 Keywords: adaptation; ecological genetics; floral evolution; Mimulus guttatus; Mimulus lewisii; speciation The broad goal of ecological and evolutionary functional Because the expression of such fitness traits can vary genomics (EEFG) is to understand both the evolutionary depending on the environment (for example, Campbell processes that create and maintain genomic and pheno- and Waser, 2001), a comprehensive assessment of the typic diversity within and among natural populations and adaptive significance of these traits also requires the species, and the functional significance of such variation. -
An Updated Checklist of Aquatic Plants of Myanmar and Thailand
Biodiversity Data Journal 2: e1019 doi: 10.3897/BDJ.2.e1019 Taxonomic paper An updated checklist of aquatic plants of Myanmar and Thailand Yu Ito†, Anders S. Barfod‡ † University of Canterbury, Christchurch, New Zealand ‡ Aarhus University, Aarhus, Denmark Corresponding author: Yu Ito ([email protected]) Academic editor: Quentin Groom Received: 04 Nov 2013 | Accepted: 29 Dec 2013 | Published: 06 Jan 2014 Citation: Ito Y, Barfod A (2014) An updated checklist of aquatic plants of Myanmar and Thailand. Biodiversity Data Journal 2: e1019. doi: 10.3897/BDJ.2.e1019 Abstract The flora of Tropical Asia is among the richest in the world, yet the actual diversity is estimated to be much higher than previously reported. Myanmar and Thailand are adjacent countries that together occupy more than the half the area of continental Tropical Asia. This geographic area is diverse ecologically, ranging from cool-temperate to tropical climates, and includes from coast, rainforests and high mountain elevations. An updated checklist of aquatic plants, which includes 78 species in 44 genera from 24 families, are presented based on floristic works. This number includes seven species, that have never been listed in the previous floras and checklists. The species (excluding non-indigenous taxa) were categorized by five geographic groups with the exception of to reflect the rich diversity of the countries' floras. Keywords Aquatic plants, flora, Myanmar, Thailand © Ito Y, Barfod A. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. -
Oxeye Daisy(Chrysanthemum Leucanthemum Syn.Leucanthemum
Oxeye Daisy (Chrysanthemum leucanthemum syn. Leucanthemum vulgare) Provincial Designation: Noxious Overview: Identification: Introduced from Europe in the early 1800’s Stems: Multiple, un-branched stems grow up primarily as a grass seed contaminant, and to 1 m tall and are smooth, frequently grooved subsequently spread as an ornamental, and generally hairless. Oxeye daisy has become a serious invader Leaves: Basal and lower leaves are lance- of pastures and natural areas throughout shaped with “toothed” margins and petioles North America. It is a perennial herb that that may be as long as the leaves. The upper reproduces both by seed and shallow leaves are alternately arranged, narrow, and rhizomes. Single plants quickly become stalkless with wavy margins. Leaves progres- patches that continually increase in size. sively decrease in size upward on the stem. Control: Plants flower June-August and its seed Flowers: Flowers are borne singly at the end germinates throughout the growing season. of stems and can be up to 5 cm in diameter, Grazing: Not grazed. Livestock may physically Oxeye Daisy and the very similarly flowered with yellow centers, and 20 to 30 white petals damage oxeye plants by trampling under high Scentless Chamomile can be considered radiating from the center. The petals are slightly stocking rates, but the subsequent overgrazing conspicuous, as there are no native white notched at the tip. of desirable vegetation and soil disturbance will flowered daisies in Alberta. worsen the infestation. Plants consumed by Seed: Individual plants can produce over 500 dairy cattle can give the milk an off-flavour. flat, black seeds that are viable in the soil for Habitat: 2-3 years or more. -
Oregon City Nuisance Plant List
Nuisance Plant List City of Oregon City 320 Warner Milne Road , P.O. Box 3040, Oregon City, OR 97045 Phone: (503) 657-0891, Fax: (503) 657-7892 Scientific Name Common Name Acer platanoides Norway Maple Acroptilon repens Russian knapweed Aegopodium podagraria and variegated varieties Goutweed Agropyron repens Quack grass Ailanthus altissima Tree-of-heaven Alliaria officinalis Garlic Mustard Alopecuris pratensis Meadow foxtail Anthoxanthum odoratum Sweet vernalgrass Arctium minus Common burdock Arrhenatherum elatius Tall oatgrass Bambusa sp. Bamboo Betula pendula lacinata Cutleaf birch Brachypodium sylvaticum False brome Bromus diandrus Ripgut Bromus hordeaceus Soft brome Bromus inermis Smooth brome-grasses Bromus japonicus Japanese brome-grass Bromus sterilis Poverty grass Bromus tectorum Cheatgrass Buddleia davidii (except cultivars and varieties) Butterfly bush Callitriche stagnalis Pond water starwort Cardaria draba Hoary cress Carduus acanthoides Plumeless thistle Carduus nutans Musk thistle Carduus pycnocephalus Italian thistle Carduus tenufolius Slender flowered thistle Centaurea biebersteinii Spotted knapweed Centaurea diffusa Diffuse knapweed Centaurea jacea Brown knapweed Centaurea pratensis Meadow knapweed Chelidonium majou Lesser Celandine Chicorum intybus Chicory Chondrilla juncea Rush skeletonweed Cirsium arvense Canada Thistle Cirsium vulgare Common Thistle Clematis ligusticifolia Western Clematis Clematis vitalba Traveler’s Joy Conium maculatum Poison-hemlock Convolvulus arvensis Field Morning-glory 1 Nuisance Plant List -
DICOTS Aceraceae Maple Family Anacardiaceae Sumac Family
FLOWERINGPLANTS Lamiaceae Mint family (ANGIOSPERMS) Brassicaceae Mustard family Prunella vulgaris - Self Heal Cardamine nutallii - Spring Beauty Satureja douglasii – Yerba Buena Rubiaceae Madder family DICOTS Galium aparine- Cleavers Boraginaceae Borage family Malvaceae Mallow family Galium trifidum – Small Bedstraw Aceraceae Maple family Cynoglossum grande – Houndstongue Sidalcea virgata – Rose Checker Mallow Acer macrophyllum – Big leaf Maple Oleaceae Olive family MONOCOTS Anacardiaceae Sumac family Fraxinus latifolia - Oregon Ash Toxicodendron diversilobum – Poison Oak Cyperaceae Sedge family Plantaginaceae Plantain family Carex densa Apiaceae Carrot family Plantago lanceolata – Plantain Anthriscus caucalis- Bur Chervil Iridaceae Iris family Daucus carota – Wild Carrot Portulacaceae Purslane family Iris tenax – Oregon Iris Ligusticum apiifolium – Parsley-leaved Claytonia siberica – Candy Flower Lovage Claytonia perforliata – Miner’s Lettuce Juncaceae Rush family Osmorhiza berteroi–Sweet Cicely Juncus tenuis – Slender Rush Sanicula graveolens – Sierra Sanicle Cynoglossum Photo by C.Gautier Ranunculaceae Buttercup family Delphinium menziesii – Larkspur Liliaceae Lily family Asteraceae Sunflower family Caryophyllaceae Pink family Ranunculus occidentalis – Western Buttercup Allium acuminatum – Hooker’s Onion Achillea millefolium – Yarrow Stellaria media- Chickweed Ranunculus uncinatus – Small-flowered Calochortus tolmiei – Tolmie’s Mariposa Lily Adendocaulon bicolor – Pathfinder Buttercup Camassia quamash - Camas Bellis perennis – English -
THE JEPSON GLOBE a Newsletter from the Friends of the Jepson Herbarium
THE JEPSON GLOBE A Newsletter from the Friends of The Jepson Herbarium VOLUME 29 NUMBER 1, Spring 2019 Curator’s column: Don Kyhos’s Upcoming changes in the Con- legacy in California botany sortium of California Herbaria By Bruce G. Baldwin By Jason Alexander In early April, my Ph.D. advisor, In January, the Northern California Donald W. Kyhos (UC Davis) turns 90, Botanists Association hosted their 9th fittingly during one of the California Botanical Symposium in Chico, Cali- desert’s most spectacular blooms in fornia. The Consortium of California recent years. Don’s many contributions Herbaria (CCH) was invited to present to desert botany and plant evolution on upcoming changes. The CCH be- in general are well worth celebrating gan as a data aggregator for California here for their critical importance to our vascular plant specimen data and that understanding of the California flora. remains its primary purpose to date. Those old enough to have used Munz’s From 2003 until 2017, the CCH grew A California Flora may recall seeing in size to over 2.2 million specimen re- the abundant references to Raven and cords from 36 institutions. Responding Kyhos’s chromosome numbers, which to requests from participants to display reflect a partnership between Don and specimen data from all groups of plants Peter Raven that yielded a tremendous Rudi Schmid at Antelope Valley Califor- and fungi, from all locations (including body of cytogenetic information about nia Poppy Reserve on 7 April 2003. Photo those outside California), we have de- our native plants. Don’s talents as a by Ray Cranfill. -
Alien Flora of Europe: Species Diversity, Temporal Trends, Geographical Patterns and Research Needs
Preslia 80: 101–149, 2008 101 Alien flora of Europe: species diversity, temporal trends, geographical patterns and research needs Zavlečená flóra Evropy: druhová diverzita, časové trendy, zákonitosti geografického rozšíření a oblasti budoucího výzkumu Philip W. L a m b d o n1,2#, Petr P y š e k3,4*, Corina B a s n o u5, Martin H e j d a3,4, Margari- taArianoutsou6, Franz E s s l7, Vojtěch J a r o š í k4,3, Jan P e r g l3, Marten W i n t e r8, Paulina A n a s t a s i u9, Pavlos A n d r i opoulos6, Ioannis B a z o s6, Giuseppe Brundu10, Laura C e l e s t i - G r a p o w11, Philippe C h a s s o t12, Pinelopi D e l i p e t - rou13, Melanie J o s e f s s o n14, Salit K a r k15, Stefan K l o t z8, Yannis K o k k o r i s6, Ingolf K ü h n8, Hélia M a r c h a n t e16, Irena P e r g l o v á3, Joan P i n o5, Montserrat Vilà17, Andreas Z i k o s6, David R o y1 & Philip E. H u l m e18 1Centre for Ecology and Hydrology, Hill of Brathens, Banchory, Aberdeenshire AB31 4BW, Scotland, e-mail; [email protected], [email protected]; 2Kew Herbarium, Royal Botanic Gardens Kew, Richmond, Surrey, TW9 3AB, United Kingdom; 3Institute of Bot- any, Academy of Sciences of the Czech Republic, CZ-252 43 Průhonice, Czech Republic, e-mail: [email protected], [email protected], [email protected], [email protected]; 4Department of Ecology, Faculty of Science, Charles University, Viničná 7, CZ-128 01 Praha 2, Czech Republic; e-mail: [email protected]; 5Center for Ecological Research and Forestry Applications, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain, e-mail: [email protected], [email protected]; 6University of Athens, Faculty of Biology, Department of Ecology & Systematics, 15784 Athens, Greece, e-mail: [email protected], [email protected], [email protected], [email protected], [email protected]; 7Federal Environment Agency, Department of Nature Conservation, Spittelauer Lände 5, 1090 Vienna, Austria, e-mail: [email protected]; 8Helmholtz Centre for Environmental Research – UFZ, Department of Community Ecology, Theodor-Lieser- Str. -
Host Range and Impact of Dichrorampha Aeratana, the First Potential Biological Control Agent for Leucanthemum Vulgare in North America and Australia
insects Article Host Range and Impact of Dichrorampha aeratana, the First Potential Biological Control Agent for Leucanthemum vulgare in North America and Australia Sonja Stutz 1,* , Rosemarie De Clerck-Floate 2 , Hariet L. Hinz 1, Alec McClay 3 , Andrew J. McConnachie 4 and Urs Schaffner 1 1 CABI, Rue des Grillons 1, CH-2800 Delémont, Switzerland; [email protected] (H.L.H.); [email protected] (U.S.) 2 Agriculture and Agri-Food Canada, Lethbridge Research and Development Centre, 5403—1 Ave. S., Lethbridge, AB T1J 4B1, Canada; rosemarie.declerck-fl[email protected] 3 12 Roseglen Private, Ottawa, ON K1H 1B6, Canada; [email protected] 4 Weed Research Unit, New South Wales Department of Primary Industries, Biosecurity and Food Safety, Orange, NSW 2800, Australia; [email protected] * Correspondence: [email protected] Simple Summary: Oxeye daisy, a Eurasian member of the daisy family, has become invasive in several parts of the world, including North America and Australia. We investigated whether a root-feeding moth found closely associated with oxeye daisy in Europe could be used as a biological control agent for the plant when weedy. We found that the moth could develop on 11 out of 74 plant species that we tested in laboratory conditions when it was given no choice of plants. When the Citation: Stutz, S.; De Clerck-Floate, moths were given a choice of food plants outdoors, we found its larvae only on the ornamentals R.; Hinz, H.L.; McClay, A.; Shasta daisy and creeping daisy. Larval feeding had no impact on the weight and number of flowers McConnachie, A.J.; Schaffner, U. -
(Linaria Vulgaris) and Dalmatian Toadflax (Linaria
DISSERTATION VIABILITY AND INVASIVE POTENTIAL OF HYBRIDS BETWEEN YELLOW TOADFLAX (LINARIA VULGARIS) AND DALMATIAN TOADFLAX (LINARIA DALMATICA) Submitted by Marie F.S. Turner Department of Soil and Crop Sciences In partial fulfillment of the requirements For the Degree of Doctor of Philosophy Colorado State University Fort Collins, Colorado Fall 2012 Doctoral Committee: Advisor: Sarah Ward Christopher Richards David Steingraeber George Beck Sharlene Sing Copyright by Marie Frances Sundem Turner 2012 All Rights Reserved ABSTRACT VIABILITY AND INVASIVE POTENTIAL OF HYBRIDS BETWEEN YELLOW TOADFLAX (LINARIA VULGARIS) AND DALMATIAN TOADFLAX (LINARIA DALMATICA) Although outcomes of hybridization are highly variable, it is now considered to play an important role in evolution, speciation, and invasion. Hybridization has recently been confirmed between populations of yellow (or common) toadflax (Linaria vulgaris) and Dalmatian toadflax (Linaria dalmatica) in the Rocky Mountain region of the United States. The presence of hybrid toadflax populations on public lands is of concern, as both parents are aggressive invaders already listed as noxious weeds in multiple western states. A common garden experiment was designed to measure differences in quantitative (shoot length, biomass, flowering stems, seed capsule production) phenological (time of emergence, first flowering and seed maturity) and ecophysiological (photosynthesis, transpiration and water use efficiency (WUE)) traits for yellow and Dalmatian toadflax, F1 and BC1 hybrids, as well as natural field-collected hybrids from two sites. Genotypes were cloned to produce true replicates and the entire common garden was also replicated at two locations (Colorado and Montana); physiological data were collected only in Colorado. All genotypes grew larger and were more reproductively active in Colorado than in Montana, and hybrids outperformed parent taxa across vegetative and reproductive traits indicating heterosis. -
Wildflowers of Scotland
Seed Origin and Quality Wildflowers of Scotland At Scotia Seeds we use our years of experience to ensure that the wildflower seed We are the leading producers of wildflower we supply is of the highest quality possible and seeds in Scotland and are committed to can be traced back to original collections in the providing the range and quality of seeds you wild. require. We have a wide range of species that we can Seed Origin provide. As well as the ones here in the All of the wildflower seeds we produce can be catalogue; please contact us if you are looking traced back to the sites where the original wild for a species not in our catalogue. plants grow. From these sites we collect a small amount of seed which is then sown on page Contents our farm to give us crops from which we can harvest a larger amount of seed. Seed Quality and Origin 2 We are signatories to the Flora Locale Code of Practice for Collectors, Growers and Suppliers Seed Packets 3 of Native Flora that ensures responsible collection and sale of native British plants. Establishing a Wildflower Meadow 11 Quality Yellow Rattle 13 We test samples of all our seed crops for germination and purity, to ensure that they have reached our stringent standards. Sowing Rates 14 Our quality laboratory specialises in testing the seeds of wildflowers and trees. For most of the Meadow Mixtures 15 species we test we have developed our own procedures in a research programme funded by How to Order 26 a Scottish Executive SMART Award. -
Micromorphological and Histochemical Attributes of Flowers and Floral Reward in Linaria Vulgaris (Plantaginaceae)
Protoplasma https://doi.org/10.1007/s00709-018-1269-2 ORIGINAL ARTICLE Micromorphological and histochemical attributes of flowers and floral reward in Linaria vulgaris (Plantaginaceae) Jacek Jachuła1 & Agata Konarska1 & Bożena Denisow1 Received: 21 February 2018 /Accepted: 23 May 2018 # The Author(s) 2018 Abstract The self-incompatible flowers of Linaria vulgaris have developed a range of mechanisms for attraction of insect visitors/ pollinators and deterrence of ineffective pollinators and herbivores. These adaptive traits include the flower size and symmetry, the presence of a spur as a Bsecondary nectar presenter,^ olfactory (secondary metabolites) and sensual (scent, flower color, nectar guide—contrasting palate) signals, and floral rewards, i.e. pollen and nectar. Histochemical tests revealed that the floral glandular trichomes produced essential oils and flavonoids, and pollen grains contained flavonoids, terpenoids, and steroids, which play a role of olfactory attractants/repellents. The nectary gland is disc-shaped and located at the base of the ovary. Nectar is secreted through numerous modified stomata. Nectar secretion began in the bud stage and lasted to the end of anthesis. The amount of produced nectar depended on the flower age and ranged from 0.21 to 3.95 mg/flower (mean = 1.51 mg). The concentration of sugars in the nectar reached up to 57.0%. Both the nectar amount and sugar concentration demonstrated a significant year and population effect. Pollen production was variable between the years of the study. On average, a single flower of L. vulgaris produced 0.31 mg of pollen. The spectrum of insect visitors in the flowers of L. vulgaris differed significantly between populations. -
RHS Perfect for Pollinators Wildflowers Rhs.Org.Uk/Perfectforpollinators
RHS Perfect for Pollinators Wildflowers rhs.org.uk/perfectforpollinators RHS Registered Charity No: 222879 / SC038262 Get your garden buzzing ► Plant flowers that are on the RHS Perfect for Pollinators plant lists ► Grow a range of plants for year- round flowering ► Avoid plants with double or multi- petalled flowers ► Never use pesticides on plants in flower ► Provide nest sites for solitary bees Short grass (up to 15cm) Ajuga reptans bugle H Bellis perennis daisy H Campanula rotundifolia common harebell H Hippocrepis comosa horseshoe vetch H Lotus corniculatus bird’s foot trefoil H Potentilla anserina silverweed H Potentilla erecta tormentil H Potentilla reptans creeping cinquefoil H Primula veris common cowslip H Prunella vulgaris selfheal H Ranunculus repens creeping buttercup H Sanguisorba minor salad burnet H Taraxacum officinale dandelion H Thymus polytrichus wild thyme H Thymus pulegioides large thyme H Trifolium pratense red clover H Photo: RHS / Carol Sheppard (hoverfly on Leucanthemum vulgare, ox-eye daisy). Clinopodium vulgare wild basil H Cornus sanguinea common dogwood S Crataegus monogyna common hawthorn S or T Cytisus scoparius common broom S Digitalis purpurea common foxglove Bi Euonymus europaeus spindle S Fragaria vesca wild strawberry H Frangula alnus alder buckthorn S Galium mollugo hedge bedstraw H Galium odoratum sweet woodruff H Galium verum lady’s bedstraw H Geranium robertianum herb robert A/Bi Geum urbanum wood avens H Hedera helix common ivy C Helleborus foetidus stinking hellebore H Hyacinthoides non-scripta bluebell B Ilex aquifolium common holly T Lamium album white deadnettle H Lamium galeobdolon yellow archangel H Ligustrum vulgare wild privet S Lonicera periclymenum common honeysuckle C Malus sylvestris crab apple T Malva sylvestris common mallow H Myosotis sylvatica wood forget-me-not H Primula vulgaris primrose H Prunus avium wild cherry, gean T Photo: RHS / Carol Sheppard (brimstone butterfly on purple loosestrife, Lythrum Prunus padus bird cherry T salicaria).