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Perennials in Fort Tryon Park

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Fort Tryon Park Plant List Abelia ‘Edward Goucher’ Abelia ‘Little Richard’ Abelia x grandiflora ‘Sherwoodii’ Acanthus hungaricus – Bear’s Breeches Acanthus mollis ‘Latifolius’ Acer negundo Acer saccharum Acer rubrum Achillea filipendula ‘coronation gold’ Achillea filipendula ‘moonshine yellow’ Achillea millefolium ‘Cerise Queen’ Achillea millefolium ‘Terracotta’ Achillea sibirica ‘Love Parade’ Aconitum carmichaelii – Monkshood Aconitum napellus Aescalus x carnea ‘Fort McNair’ Aescalus parviflora Agastache canna ‘Heather Queen’ Agastache canna ‘Apricot Sprite’ Agastache rupestris Agastache foeniculum ‘blue fortune’ Alcea ficifolia – Hollyhock Alcea rosea ‘Chater’s Mixed’ Alcea rosea ‘Nigra’ Alstromeria ‘Sweet Laura’ – Peruvian Lily Alyssum ‘little dorrit’ Alyssum ‘creamy yellow’ Alyssum ‘ purple basket’ Amelanchier laevis Amsonia hubrichtii – Blue Milkweed Anemone hupensis ‘September Charm’ – Japanese Anemone Anemone x hybrida ‘Honorine Jobert’; A.. ‘QueenCharlotte’ Anemone japonica Anemone tomentosa ‘Robustissima’ Anchusa azurea – Italian Alkanet Andropogon virginicus Angelica gigas – Archangel Antirrhinum (snapdragon) ‘rocket rose’ ‘rocket bronze’ Aquilegia caerulea – Columbine Aquilegia flabellata nana ‘alba’ Aquilegia vulgaris’Nora Barlow’ etc. Arabis alpina Arum (skunk cabbage) Arctostaphalos uva-ursi’Massachusetts’(bearberry) Arctotis x ‘wine’ Artemesia ‘Powis Castle’ etc. – Wormwood Aruncus dioicus – Goat’s Beard Asarina ‘violet glow’ Asarum canadensis Asarum europaem Asarum splendens Asclepias incarnata – Butterfly Weed Asclepias tuberosa Asclepias syriaca Aster divaricatus Aster ericoides ‘Erlkonig’ ‘Blue star’ Aster x frikartii ‘monch’ Aster x frikartii ‘Wonder of Stafa’ Aster laevis Aster novae-angliae ‘Helen Lacy’ Aster novae-belgii ‘Blue Gown’ Aster spectabilis Astilbe x arendsii ‘Etna’ – Plume Flower Astilbe x arendsii ‘Europa’ Astilbe x arendsii ‘ostrich plume’ Astilbe x arendsii ‘catteleya’ Astilbe x arendsii ‘prof.van weil Astilbe x arendsii ‘taquetii superba’ Astilbe chinensis ‘Finale’ Astilbe x hybrida ‘Ostrich Plume’ etc. Astrantia major ‘alba’ Athyrium nipponicum ‘Pictum’ – Japanese Painted Fern Aubretia Aurinia saxatilis ‘citrinum’ Aurinia saxatilis ‘Sulphurea’ Azalea calendulaceum Azalea E. ‘Betty Hager’ Azalea ‘flame creeper’ Azalea ‘Kazan’ Azalea ‘Macrantha’ Azalea ‘Pink Pancake’ Azalea ‘Serpiphyllum’ Azalea ‘snowbird’ Azalea visocum Azalea ‘lollipop’ Azalea ‘pink and sweet’ Azalea periclymenoides (Nudiflorum) Azalea prunifolium Azalea viscosum Baptisia australis – False Indigo Baptisia tinctoria Begonia grandis ‘Alba’ Begonia grandis ‘Evansiana’ Berberis x gladwynensis ‘William Penn’ Bergenia cordifolia Betula lenta Betula populifolia Boltonia asteroides – Bolton’s Aster Brunnera macrophylla ; B. ‘Langtrees’ – Siberian Bugloss Buddleia ‘Honeycomb’ Buxus x ‘Green velvet’ Calluna vulgaris ‘Silver Queen’ Calluna vulgaris ‘Silver Knight’ Calluna vulgaris ‘Beoly Gold’ Calluna vulgaris ‘Blaze away’ Calluna vulgaris ‘Wickwar Flame’ Calluna vulgaris ‘Barnett Anley’ Calluna vulgaris ‘County Wicklow’ Calluna vulgaris ‘Kerstin’ Calluna vulgaris ‘Allison Yates’ Calluna vulgaris ‘Gold Haze’ Calluna vulgaris ‘Firefly’ Calluna vulgaris ‘Finale’ Calluna vulgaris ‘Cuprea’ Calluna vulgaris ‘Tib’ Calluna vulgaris ‘Alba Plena’ Calluna vulgaris ‘Kuphaldtii’ Calluna vulgaris ‘Mrs. Ronald Gray’ Calluna vulgaris ‘Mair’s variety’ Calluna vulgaris ‘Pyramidalis’ Calluna vulgaris ‘Hibernica’ Calluna vulgaris ‘E.F.Brown’ Annemarie Calluna vulgaris ‘Bray Head’ Calluna vulgaris ‘Dart’s Flamboyant’ Calluna vulgaris ‘Fritz Kircher’ Calluna vulgaris ‘Goldsworth crimson’ Calluna vulgaris ‘Long White’ Calluna vulgaris ‘My Dream’ Calluna vulgaris ‘Roland Haagen’ Calluna vulgaris ‘Sally Ann Proudley’ Calluna vulgaris ‘Spitfire’ Calluna vulgaris ‘Green Cardinal’ Calluna vulgaris ‘Perestrojka’ Caltha palustris – Marsh Marigold Campanula glomerata superba Carpinus caroliniana Carya cordiformis Carya ovata (Shagbark hickory) Catananche caerulea Ceanothus americana Celtis occidentalis Cerastium alpinum Cerastium tomentosum Ceratostigma plumbaginoides Cercis canadensis Chaenomeles x superba ‘Cameo’ Chelone lyonii (turtlehead) Chionanthus virginicus (American Fringe tree) Cimicifuga racemosa Clematis cirrhosa ‘ Comtesse de Bouchaud’ – Virgin’s Bower Clematis grandiflora ‘Niobe’ Clematis jouiniana ‘Praecox’ Clematis montana Clematis virginiana Clematis viticella ‘Polish Spirit’ Clethra alnifolia ‘September Beauty’ Clethra alnifolia ‘Sixteen Candles’ Clethra alnifolia ‘Ruby Spice’ Clethra alnifolia ‘Hummingbird’ Convallaria majalis – Lily of the Valley Coreopsis grandiflora – Tickseed Coreopsis verticillata ‘golden showers’ Coreopsis verticillata ‘moonbeam’ Cornus florida Cornus rosea ‘Sweet Dreams’ Cornus verticilata – Threadleaf Coreopsis Corydalis ochroleuca – Yellow Bleeding Heart Corydalis ‘Blackberry Wine’ Corylopsis pauciflora (boskoop) Corylopsis spicata Corylus americana Cotoneaster dammeri ‘Coral Beauty’ Crocosmia ‘Lucifer’ – Montbrietia (corm) Cryptomeria japonica ‘Black Dragon’ Cynaria cardunculus – Cardoon Cytisus ‘Allgold’ Cytisus ‘Bi-color red’ Cytisus ‘Carla’ Cytisus decumbens Cytisus ‘Hollandia’ Cytisus ‘Kencasis’ Cytisus ‘Lilac Time’ Cytisus ‘Lucky’ Cytisus ‘Warmeister’ Calluna vulgaris ‘Bray Head’ Calluna vulgaris ‘Dart’s Flamboyant’ Calluna vulgaris ‘Fritz Kircher’ Calluna vulgaris ‘Goldsworth crimson’ Calluna vulgaris ‘Long White’ Calluna vulgaris ‘My Dream’ Calluna vulgaris ‘Roland Haagen’ Calluna vulgaris ‘Sally Ann Proudley’ Calluna vulgaris ‘Spitfire’ Calluna vulgaris ‘Green Cardinal’ Calluna vulgaris ‘Perestrojka’ Daboecia –lavender species Dahlia ssp. Daphne ‘eximia’ Daphne ‘ruby glow’ Daphne ‘pygmea’ Daphne ‘jim’s pride’ Delphinium ‘Gentian Blue’ ‘Magic Fountain’ Delphinium P.G. ‘blue bird’ Dennstaedtia puntiloba – Hay Scented Fern Delphinium belladonna ‘bellamosum’ Delphinium belladonna ‘clived beauty’ Dennstaedtia punctiloba Deutzia elegance ‘Rosalind’ Deutzia gracilis ‘Nikko’ Dianthus barbatus ‘Sooty’ – Sweet William Dianthusbarbatus x D. chinensis ‘Ideal Pearl’ – Pinks Dianthus ‘Bath’s Pink’; D. ‘Crimsona’; D. ‘Spangled Star’ Dicentra eximia – Fringed Bleeding Heart Dicentra spectabilis ‘Alba’ – Bleeding Heart Digitalis ferruginea Digitalis grandiflora – Yellow Foxglove Digitalis mertonensis Digitalis purpurea; D. ‘Apricot’ – Foxglove Dimorphotheca ‘glistening white’ Doronicum magnificum Echinacea pallida - Pink Coneflower Echinacea purpurea ‘Magnus’; ‘White Swan’ Echinacea ‘Green Wizard’ Echinops bannaticus ‘Veitch’s Blue’ – Globe Thistle Echinops exaltus Echinops ritro Enkianthus campanulatus Epimedium perralchicum(Barrenwort) ‘Frohnleiten ‘ Epimedium x versicolor ‘Sulphureum’ Erica arborea ‘Alpina’ Erica carnea ‘James Backhouse’ Erica carnea ‘Springwood Pink’ Erica carnea ‘Springwood white’ Erica carnea ‘Myretown Ruby’ Erica carnea ‘Winter Beauty’ Erica carnea ‘Pink Spangles’ Erica cinerea ‘Iberion Beauty’ Erica x darleyensis ‘Kramer’s Rote’ Erica x darleyensis ‘Darley Dale’ Erica x darleyensis ‘May Helen’ Erica x darleyensis ‘Silberschmeize’ Erica x darleyensis ‘Furzey’ Erica x darleyensis ‘Adrian Duncan’ Erica x darleyensis ‘Rosalie’ Erica vagens ‘Mrs. D.F. Maxwell’ Erica vagens ‘lyoness’ Eryngium gigantium. – Sea Holly Euonymus f. ‘coloratus’ Eupatorium coelestinum – Hardy Ageratum Eupatorium rugosum (White Snakeroot) Euphorbia palustris ; etc. - Spurge Fagus grandiflora Fothergilla gardenii ‘Blue Mist’ Fothergilla major ‘Mt. Airy’ Galium odoratum – Sweet Woodruff Gaura lindheimerii ‘Crimson Butterflies’ Gaura lindheimerii . ‘Siskiyou Pink’ Genista pilosa Genista sagittalis Gentiana Geranium cinereum ‘Ballerina’ – Cranesbill Geranium endressii Geranuim maculatum Geranium Maxfrei Gymnocladus dioicus Gypsophila paniculata ‘Pink Fairy’; G. ssp. – Baby’s Breath Hakonechloa macra ‘Aureola’ – Golden Hakonechloa Grass Halesia carolina ‘rosea’ Halesia diptera ‘Magnolifolia’ Hamamelis virginiana Hamamelis ‘goldcrest’ Hedera helix – English Ivy Helenium autumnale ‘Moerheim Beauty’ Helenium autumnale ‘Red-Gold Hybrids’ Helianthemum ssp. – Sun Rose Helianthus divaricatus Helleborus foetidus – Stinking Hellebore Helleborus x orientalis ‘Lady Series’ (Lenten Rose) Hemerocallis ssp. – Daylily Heuchera ‘Chatterbox’; H. ‘Chocolate Ruffles’; H. ‘Pewter Moon’ ‘Sioux Falls’ Heuchera americana ’Dale’s Strain’ Heuchera sanguinea –Coral Bells Heliotrope ‘marine’ Heucherella ‘Silver Streak’ Hibiscus moscheutos ‘Disco Belle Series’ Hibiscus ‘Bird’ Hosta ‘Frances Williams’ Hosta fortunei ‘Aurea’ Hosta plantiginea Hosta sieboldiana Hypericum androsaemum ‘Aloury Purple’ Hypericum calycinum – St. John’s Wort Hydrangea anomola sub. Petiolaris Hydrangea Lilacina Hydrangea macrophylla ‘Blaumeise’ Hydrangea macrophylla ‘glowing embers’ Hydrangea petiolaris Hydrangea quercifolia ‘Alison’ Hydrangea quercifolia ‘Pee Wee’ Hydrangea quercifolia ‘snow queen’ Hydrangea tardiva Hydrangea ‘Blue Bird’ Hydrangea ‘Taube’ Hydrangea ‘the swan’ Hydrangea ‘Blue Billow’ Hydrangea ‘Beni Gaku’ Hydrangea ‘Coerulea’ Hydrangea ‘Enziandan’ Hydrangea ‘All Summer Beauty’ Hypericum calycinum Iberis sempervirens – Candytuft Ilex glabra Ilex opaca Inula helenium – Elecampane Iris cristata Iris ensata ssp. – Japanese Iris Iris germanica ssp. – German Iris Iris kaempferi Iris siberica ssp. – Siberian Iris Juglans nigra Juniperus confecta ‘Emerald Sea’ Juniperus horizontalis ‘Wiltonii’ Kalmia angustifolia Kalmia latifolia Knautia macedonica Kniphofia ‘Citrina’ etc. – Red Hot Poker Larkspur ‘miss california’ Latifolium Laurentia Lavandula angustifolia ‘Munstead’ – Lavender
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    Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, Robin Duponnois, Mohamed Hafidi To cite this version: Ahlam Hamim, Lucie Miche, Ahmed Douaik, Rachid Mrabet, Ahmed Ouhammou, et al.. Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems. Comptes Rendus Biologies, Elsevier Masson, 2017, 340 (4), pp.226-237. 10.1016/j.crvi.2017.02.003. hal- 01681523 HAL Id: hal-01681523 https://hal.archives-ouvertes.fr/hal-01681523 Submitted on 23 Apr 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/315062117 Diversity of fungal assemblages in roots of Ericaceae in two Mediterranean contrasting ecosystems Article in Comptes rendus biologies · March 2017 DOI: 10.1016/j.crvi.2017.02.003 CITATIONS READS 0 37 7 authors, including: Ahmed Douaik Rachid Mrabet Institut National de Recherche Agronomique
  • Ranunculaceae) for Asian and North American Taxa

    Ranunculaceae) for Asian and North American Taxa

    Mosyakin, S.L. 2018. Further new combinations in Anemonastrum (Ranunculaceae) for Asian and North American taxa. Phytoneuron 2018-55: 1–11. Published 13 August 2018. ISSN 2153 733X FURTHER NEW COMBINATIONS IN ANEMONASTRUM (RANUNCULACEAE) FOR ASIAN AND NORTH AMERICAN TAXA SERGEI L. MOSYAKIN M.G. Kholodny Institute of Botany National Academy of Sciences of Ukraine 2 Tereshchenkivska Street Kiev (Kyiv), 01004 Ukraine [email protected] ABSTRACT Following the proposed re-circumscription of genera in the group of Anemone L. and related taxa of Ranunculaceae (Mosyakin 2016, Christenhusz et al. 2018) and based on recent molecular phylogenetic and partly morphological evidence, the genus Anemonastrum Holub is recognized here in an expanded circumscription (including Anemonidium (Spach) Holub, Arsenjevia Starod., Tamuria Starod., and Jurtsevia Á. Löve & D. Löve) covering members of the “Anemone ” clade with x=7, but excluding Hepatica Mill., a genus well outlined morphologically and forming a separate subclade (accepted by Hoot et al. (2012) as Anemone subg. Anemonidium (Spach) Juz. sect. Hepatica (Mill.) Spreng.) within the clade earlier recognized taxonomically as Anemone subg. Anemonidium (sensu Hoot et al. 2012). The following new combinations at the section and subsection ranks are validated: Anemonastrum Holub sect. Keiskea (Tamura) Mosyakin, comb. nov . ( Anemone sect. Keiskea Tamura); Anemonastrum [sect. Keiskea ] subsect. Keiskea (Tamura) Mosyakin, comb. nov .; Anemonastrum [sect. Keiskea ] subsect. Arsenjevia (Starod.) Mosyakin, comb. nov . ( Arsenjevia Starod.); and Anemonastrum [sect. Anemonastrum ] subsect. Himalayicae (Ulbr.) Mosyakin, comb. nov. ( Anemone ser. Himalayicae Ulbr.). The new nomenclatural combination Anemonastrum deltoideum (Hook.) Mosyakin, comb. nov . ( Anemone deltoidea Hook.) is validated for a North American species related to East Asian Anemonastrum keiskeanum (T.
  • Development and Characterization of EST-SSR Markers for Tricyrtissect

    Development and Characterization of EST-SSR Markers for Tricyrtissect

    ISSN 1346-7565 Acta Phytotax. Geobot. 71 (1): 73–76 (2020) doi: 10.18942/apg.201907 Primer Note Development and Characterization of EST-SSR Markers for Tricyrtis sect. Tricyrtis (Liliaceae) * riku Nakamasu, shota sakaguchi aNd hiroaki setoguchi Graduate School of Human and Environmental Studies, Kyoto University, Yoshida-Nihonmatsu-cho, Sakyo-ku, Kyoto 606-8501, Japan. *[email protected] (author for correspondence) A set of 8 polymorphic EST-SSR markers has been developed to evaluate the genetic diversity and ge- netic structure of the populations of Tricyrtis sect. Tricyrtis (Liliaceae) in Kyushu, which reproduces sexually and asexually by bulbils. The total number of alleles for each locus ranged from 2 to 11 with an average of 5.5, while the values of observed and expected heterozygosity ranged from 0.043 to 0.875 and 0.043 to 0.849, respectively. The combined probabilities of identity (PI = 6.0E-07 and PI-Sib = 2.7E-03) of these markers suggest that they are useful for not only evaluating genetic diversity but also for estimat- ing clonal diversity within populations. Cross-species amplification was evaluated for three phylogenet- ically related species, T. macropoda, T. setouchiensis, and T. affinis, to show that all the EST-SSR mark- ers are transferrable among these species. Key words: EST-SSR, genetic diversity, microsatellite loci, next generation sequencing, population genetics, Tricyrtis Tricyrtis Wall. (Liliaceae) comprises approxi- cable to sect. Tricyrtis. To determine the genetic mately 20 species of perennial herbs in temperate structure and the spatial extent of genets within to subtropical mesic forests of eastern Asia.