Plants That Missed the Marketing Push About Odyssey Bulbs
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Plant List 2016
Established 1990 PLANT LIST 2016 European mail order website www.crug-farm.co.uk CRÛG FARM PLANTS • 2016 Welcome to our 2016 list hope we can tempt you with plenty of our old favourites as well as some exciting new plants that we have searched out on our travels. There has been little chance of us standing still with what has been going on here in 2015. The year started well with the birth of our sixth grandchild. January into February had Sue and I in Colombia for our first winter/early spring expedition. It was exhilarating, we were able to travel much further afield than we had previously, as the mountainous areas become safer to travel. We are looking forward to working ever closer with the Colombian institutes, such as the Medellin Botanic Gardens whom we met up with. Consequently we were absent from the RHS February Show at Vincent Square. We are finding it increasingly expensive participating in the London shows, while re-branding the RHS February Show as a potato event hardly encourages our type of customer base to visit. A long standing speaking engagement and a last minute change of date, meant that we missed going to Fota near Cork last spring, no such problem this coming year. We were pleasantly surprised at the level of interest at the Trgrehan Garden Rare Plant Fair, in Cornwall. Hopefully this will become an annual event for us, as well as the Cornwall Garden Society show in April. Poor Sue went through the wars having to have a rush hysterectomy in June, after some timely results revealed future risks. -
Size Variations of Flowering Characters in Arum Italicum (Araceae)
M. GIBERNAU,]. ALBRE, 2008 101 Size Variations of Flowering Characters in Arum italicum (Araceae) Marc Gibernau· and Jerome Albre Universite Paul Sabatier Laboratoire d'Evolution & Diversite Biologique (UMR 5174) Bat.4R3-B2 31062 Toulouse cedex 9 France *e-mail: [email protected] ABSTRACT INTRODUCTION In Arum, bigger individuals should An extreme form of flowering character proportionally invest more in the female variations according to the size is gender function (number or weight of female modification, which occurs in several flowers) than the male. The aim of this species of Arisaema (Clay, 1993). Individ paper is to quantify variations in repro ual plant gender changes from pure male, ductive characters (size of the spadix when small, to monoecious (A. dracon parts, number of inflorescences) in rela tium) or pure female (A. ringens) when tion to plant and inflorescence sizes. The large (Gusman & Gusman, 2003). This appendix represents 44% of the spadix gender change is reversible, damaged length. The female zone length represents female individuals will flower as male the 16.5% of the spadix length and is much following year (Lovett Doust & Cavers, longer than the male zone (6%). Moreover 1982). These changes are related to change these three spadix zones increase with in plant size and are explained by the plant vigour indicating an increasing size-advantage model. The size-advantage investment into reproduction and pollina model postulates a sex change when an tor attraction. It appears that the length of increase in body size is related to differen appendix increased proportionally more tial abilities to produce or sire offspring than the lengths of the fertile zones. -
Appendix 2: Plant Lists
Appendix 2: Plant Lists Master List and Section Lists Mahlon Dickerson Reservation Botanical Survey and Stewardship Assessment Wild Ridge Plants, LLC 2015 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Acalypha rhomboidea Native 1 Forb 9 Acer palmatum Invasive 0 Tree 1 Acer pensylvanicum Native 7 Tree 2 Acer platanoides Invasive 0 Tree 4 Acer rubrum Native 3 Tree 27 Acer saccharum Native 5 Tree 24 Achillea millefolium Native 0 Forb 18 Acorus calamus Alien 0 Forb 1 Actaea pachypoda Native 5 Forb 10 Adiantum pedatum Native 7 Fern 7 Ageratina altissima v. altissima Native 3 Forb 23 Agrimonia gryposepala Native 4 Forb 4 Agrostis canina Alien 0 Graminoid 2 Agrostis gigantea Alien 0 Graminoid 8 Agrostis hyemalis Native 2 Graminoid 3 Agrostis perennans Native 5 Graminoid 18 Agrostis stolonifera Invasive 0 Graminoid 3 Ailanthus altissima Invasive 0 Tree 8 Ajuga reptans Invasive 0 Forb 3 Alisma subcordatum Native 3 Forb 3 Alliaria petiolata Invasive 0 Forb 17 Allium tricoccum Native 8 Forb 3 Allium vineale Alien 0 Forb 2 Alnus incana ssp rugosa Native 6 Shrub 5 Alnus serrulata Native 4 Shrub 3 Ambrosia artemisiifolia Native 0 Forb 14 Amelanchier arborea Native 7 Tree 26 Amphicarpaea bracteata Native 4 Vine, herbaceous 18 2015 MASTER PLANT LIST MAHLON DICKERSON RESERVATION SCIENTIFIC NAME NATIVENESS S-RANK CC PLANT HABIT # OF SECTIONS Anagallis arvensis Alien 0 Forb 4 Anaphalis margaritacea Native 2 Forb 3 Andropogon gerardii Native 4 Graminoid 1 Andropogon virginicus Native 2 Graminoid 1 Anemone americana Native 9 Forb 6 Anemone quinquefolia Native 7 Forb 13 Anemone virginiana Native 4 Forb 5 Antennaria neglecta Native 2 Forb 2 Antennaria neodioica ssp. -
Araliaceae.Pdf
ARALIACEAE 五加科 wu jia ke Xiang Qibai (向其柏 Shang Chih-bei)1; Porter P. Lowry II2 Trees or shrubs, sometimes woody vines with aerial roots, rarely perennial herbs, hermaphroditic, andromonoecious or dioecious, often with stellate indumentum or more rarely simple trichomes or bristles, with or without prickles, secretory canals pres- ent in most parts. Leaves alternate, rarely opposite (never in Chinese taxa), simple and often palmately lobed, palmately compound, or 1–3-pinnately compound, usually crowded toward apices of branches, base of petiole often broad and sheathing stem, stipules absent or forming a ligule or membranous border of petiole. Inflorescence terminal or pseudo-lateral (by delayed development), um- bellate, compound-umbellate, racemose, racemose-umbellate, or racemose-paniculate, ultimate units usually umbels or heads, occa- sionally racemes or spikes, flowers rarely solitary; bracts usually present, often caducous, rarely foliaceous. Flowers bisexual or unisexual, actinomorphic. Pedicels often jointed below ovary and forming an articulation. Calyx absent or forming a low rim, some- times undulate or with short teeth. Corolla of (3–)5(–20) petals, free or rarely united, mostly valvate, sometimes imbricate. Stamens usually as many as and alternate with petals, sometimes numerous, distinct, inserted at edge of disk; anthers versatile, introrse, 2- celled (or 4-celled in some non-Chinese taxa), longitudinally dehiscent. Disk epigynous, often fleshy, slightly depressed to rounded or conic, sometimes confluent with styles. Ovary inferior (rarely secondarily superior in some non-Chinese taxa), (1 or)2–10(to many)-carpellate; carpels united, with as many locules; ovules pendulous, 2 per locule, 1 abortive; styles as many as carpels, free or partially united, erect or recurved, or fully united to form a column; stigmas terminal or decurrent on inner face of styles, or sessile on disk, circular to elliptic and radiating. -
Atoll Research Bulletin No. 503 the Vascular Plants Of
ATOLL RESEARCH BULLETIN NO. 503 THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS BY NANCY VANDER VELDE ISSUED BY NATIONAL MUSEUM OF NATURAL HISTORY SMITHSONIAN INSTITUTION WASHINGTON, D.C., U.S.A. AUGUST 2003 Uliga Figure 1. Majuro Atoll THE VASCULAR PLANTS OF MAJURO ATOLL, REPUBLIC OF THE MARSHALL ISLANDS ABSTRACT Majuro Atoll has been a center of activity for the Marshall Islands since 1944 and is now the major population center and port of entry for the country. Previous to the accompanying study, no thorough documentation has been made of the vascular plants of Majuro Atoll. There were only reports that were either part of much larger discussions on the entire Micronesian region or the Marshall Islands as a whole, and were of a very limited scope. Previous reports by Fosberg, Sachet & Oliver (1979, 1982, 1987) presented only 115 vascular plants on Majuro Atoll. In this study, 563 vascular plants have been recorded on Majuro. INTRODUCTION The accompanying report presents a complete flora of Majuro Atoll, which has never been done before. It includes a listing of all species, notation as to origin (i.e. indigenous, aboriginal introduction, recent introduction), as well as the original range of each. The major synonyms are also listed. For almost all, English common names are presented. Marshallese names are given, where these were found, and spelled according to the current spelling system, aside from limitations in diacritic markings. A brief notation of location is given for many of the species. The entire list of 563 plants is provided to give the people a means of gaining a better understanding of the nature of the plants of Majuro Atoll. -
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY
Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- BIBLIOGRAPHY BIBLIOGRAPHY Ackerfield, J., and J. Wen. 2002. A morphometric analysis of Hedera L. (the ivy genus, Araliaceae) and its taxonomic implications. Adansonia 24: 197-212. Adams, P. 1961. Observations on the Sagittaria subulata complex. Rhodora 63: 247-265. Adams, R.M. II, and W.J. Dress. 1982. Nodding Lilium species of eastern North America (Liliaceae). Baileya 21: 165-188. Adams, R.P. 1986. Geographic variation in Juniperus silicicola and J. virginiana of the Southeastern United States: multivariant analyses of morphology and terpenoids. Taxon 35: 31-75. ------. 1995. Revisionary study of Caribbean species of Juniperus (Cupressaceae). Phytologia 78: 134-150. ------, and T. Demeke. 1993. Systematic relationships in Juniperus based on random amplified polymorphic DNAs (RAPDs). Taxon 42: 553-571. Adams, W.P. 1957. A revision of the genus Ascyrum (Hypericaceae). Rhodora 59: 73-95. ------. 1962. Studies in the Guttiferae. I. A synopsis of Hypericum section Myriandra. Contr. Gray Herbarium Harv. 182: 1-51. ------, and N.K.B. Robson. 1961. A re-evaluation of the generic status of Ascyrum and Crookea (Guttiferae). Rhodora 63: 10-16. Adams, W.P. 1973. Clusiaceae of the southeastern United States. J. Elisha Mitchell Sci. Soc. 89: 62-71. Adler, L. 1999. Polygonum perfoliatum (mile-a-minute weed). Chinquapin 7: 4. Aedo, C., J.J. Aldasoro, and C. Navarro. 1998. Taxonomic revision of Geranium sections Batrachioidea and Divaricata (Geraniaceae). Ann. Missouri Bot. Gard. 85: 594-630. Affolter, J.M. 1985. A monograph of the genus Lilaeopsis (Umbelliferae). Systematic Bot. Monographs 6. Ahles, H.E., and A.E. -
Arisaema Triphyllum) by a Specialist Thrips (Heterothrips Arisaemae)
162 THRIPS AND TOSPOVIRUSES: PROCEEDINGS OF THE 7TH INTERNATIONAL SYMPOSIUM ON THYSANOPTERA 163 Sex-biased herbivory in Jack-in-the-pulpit (Arisaema triphyllum) by a specialist thrips (Heterothrips arisaemae) Ilka C. Feller2, Hiroshi Kudoh2,3, Christopher E. Tanner5 and Dennis F. Whigham2 2Smithsonian Environmental Research Center, Edgewater, MD 21037, USA; 3Current address: Department of Biological Sciences, Tokyo Metropolitan University, Minamiohsawa 1-1, Hachiohji-shi, Tokyo 192-03, JAPAN 5St. Mary’s College of Maryland, St. Mary’s City, MD 20686, USA E-mail: [email protected] Abstract: We document through observational, correlative, and experimental studies evidence of sex-biased herbivory in the gender-labile, functionally dioecious plant, Jack-in-the-pulpit (Arisaema triphyllum). Jack-in-the-pulpit is the host for a specialist thrips, Heterothrips arisaemae. Second instar larvae of this thrips feed on the abaxial surface of Jack-in-the-pulpit leaves. We found that the level of herbivory by H. arisaemae was dependent on the gender expressed by plants. Significantly more damage was found on leaves of male plants than on leaves of female and asexual plants. Concentration of total phenols and nitrogen concentrations of leaf tissue did not explain different herbivory levels between genders. Spathe removal significantly reduced thrips damage, particularly in male plants. Our results suggests that adult feeding behavior and developmental phenologies of H. arisaemae are major factors in determining the observed patterns of male-biased herbivory in Jack-in-the-pulpit, rather than differences in levels in defensive chemicals or nutritional quality of leaf tissue. Heterothrips arisaemae was the most common insect in Jack-in-the-pulpit spathes, and male plants consistently contained significantly more adult thrips and thrips eggs than female flowers. -
Streptopus Lanceolatus (Rosy Twisted-Stalk)
Streptopus lanceolatus Rosy Twisted-Stalk Liliaceae Streptopus lanceolatus by Rob Routledge (CC BY 3.0) Streptopus lanceolatus Rare Plant Profile New Jersey Department of Environmental Protection Division of Parks and Forestry New Jersey Forest Service Office of Natural Lands Management New Jersey Natural Heritage Program 501 East State Street P.O. Box 420 Trenton, NJ 08625-0420 Prepared by: Rebekah Buczynski [email protected] August 21, 2019 This report should be cited as follows: Buczynski, Rebekah. 2019. Streptopus lanceolatus Rare Plant Profile. New Jersey Department of Environmental Protection, Division of Parks and Forestry, New Jersey Forest Service, Office of Natural Lands Management, New Jersey Natural Heritage Program, Trenton, NJ. 15 pp. Streptopus lanceolatus Rare Plant Profile, Page 2 of 15 Introduction Rosy Twisted-stalk is a NJ state endangered plant whose name can arguably be attributed to either its zigzag stem (Peterson and McKenny 1968 and Lady Bird Johnson Wildflower Center 2019 [hereafter, "LBJWC"]) or perhaps more accurately the arching angle of the flowering stalks (LBJWC 2019; Minnesota Wildflowers 2019 [hereafter, "MNWF"]). The translation of the Latin genus Streptopus is literally "Twisted foot" (USDA U.S. Forest Service 2019). One of the common names, "Scootberry" possibly refers to the purgative effect of consuming too much of the fruit (Flowering Plants in Voyageur Country 2007). Another point of taxonomic contention with this species is that Streptopus lanceolatus may be divided into several subordinate taxa depending upon where it exists in its range (MNWF 2019) but for the purposes of this profile we will simply refer to all variations as Streptopus lanceolatus. -
Title Insect-Flower Relationship in the Temperate Deciduous Forest Of
Insect-flower Relationship in the Temperate Deciduous Forest Title of Kibune, Kyoto : An Overview of the Flowering Phenology and the Seasonal Pattern of Insect Visits INOUE, Tamiji; KATO, Makoto; KAKUTANI, Takehiko; Author(s) SUKA, Takeshi; ITINO, Takao Contributions from the Biological Laboratory, Kyoto Citation University (1990), 27(4): 377-464 Issue Date 1990-08-20 URL http://hdl.handle.net/2433/156100 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University Contr. biol, Lab. Kyoto Univ,, Vol. 27, pp. 377-463 Issued 20 August 1990 Insect-flower Relationship in the Temperate Deciduous 'Forest of Kibune, Kyoto: An Overview of the Flowering Phenology and the Seasonal Pattern of Insect Visits' Tamiji INouE, Makoto KATo, Takehiko KAKuTANi, Takeshi SuKA and Takao IT[No ABSTRACT In 1984 -1987, insect visitors to fiowers werebimonthly or weekly surveyed on a total of 115 plant species or 49 families in the temperate deciduous forest of Kibune, Kyoto, Japan. Flowering was observed from early April to early November, The number of plant species that concurrently bloomed was nine to 17 from May to September. Themonthly total number of flowering plant species peaked twice in May (34 spp.) and September (33 spp,). From April to August, floweringperiods werestaggered arnong congeneric woody species, e.g., Lindera, Rubus, Hydrangea and Deutzia. A total of 4603 individuals of 889 species in 12 orders of Insecta and 2 orders of Arachnoidea were collected. The most abundant order was Hymeno- ptera (46 O/o of the total number of individuals), and it was followed by Diptera (30 O/o) and Coleoptera (140/o). -
New Plant Records for the Hawaiian Islands 2010–20111
Records of the Hawaii Biological Survey for 2011. Edited by 27 Neal L. Evenhuis & Lucius G. Eldredge. Bishop Museum Occasional Papers 113: 27 –54 (2012) New plant records for the Hawaiian Islands 2010 –2011 1 DANielle FRoHliCH 2 & A lex lAU 2 O‘ahu Early Detection, Bishop Museum, 1525 Bernice Street, Honolulu, Hawai‘i 96817-2704; emails: [email protected]; [email protected] o‘ahu early Detection here documents 26 new naturalized records, 8 new state records, 31 new island records, 1 range extension, and 2 corrections found by us and other indi - viduals and agencies. in addition, several species showing signs of naturalization are men - tioned. A total of 42 plant families are discussed. information regarding the formerly known distribution of flowering plants is based on the Manual of the flowering plants of Hawai‘i (Wagner et al . 1999) and information subse - quently published in the Records of the Hawai ‘i Biological Survey . Voucher specimens are deposited at Bishop Museum’s Herbarium Pacificum (BiSH), Honolulu, Hawai‘i. Acanthaceae Megaskepasma erythroclamys lindau New island record This species, which was previously found naturalizing on o‘ahu, can be distinguished by its 1 –2" long showy burgundy bracts and white, tubular, 2-lipped corollas with 2 fertile stamens (Staples & Herbst 2005). Parker & Parsons (this volume) report this species as naturalized on Hawai‘i island. Material examined . KAUA ‘I: Hā‘ena, in neighborhood makai of highway, near Tunnels Beach, UTM 442390, 2457621. Coastal residential setting; sparingly-branched shrub to 6 ft tall, growing out of a hedge. inflorescence bracts magenta. Species is planted as an ornamental and sparingly natural - ized in the area, 9 Mar 2010, OED 2010030904. -
Fall 2012 Mail Order Catalog Cistus Nursery
Fall 2012 Mail Order Catalog Cistus Nursery 22711 NW Gillihan Road Sauvie Island, OR 97231 503.621.2233 phone order by phone 9 - 5 pst, visit 10am - 5pm, mail, or email: [email protected] 24-7-365 www.cistus.com Fall 2012 Mail Order Catalog 2 Abelia x grandiflora 'Margarita' margarita abelia New and interesting abelia with variegated leaves, green with bright yellow margins, on red stems, dressing up a smallish shrub, expected to be 4 ft tall and wide. A cheerful addition to the garden. Flowers are typical of the species, beginning in May and continuing sporadically throughout the season. Best in sun -- they tend to be leggy in shade -- with average summer water. Frost hardy to -20F, USDA zone 6. $14 Caprifoliaceae Abutilon 'Savitzii' flowering maple One of the few abutilons we sell that is quite tender. Grown since the 1800s for its wild variegation -- the leaves large and pale, almost white with occasional green blotches -- and long, salmon-orange, peduncled flowers. A medium grower, to 4-6 ft tall, needing consistent water and nutrients in sun to part shade. Winter mulch increases frost hardiness as does some overstory. Frost hardy to 25 F, mid USDA zone 9. Where temperatures drop lower, best in a container or as cuttings to overwinter. Well worth the trouble! $9 Malvaceae Acanthus sennii A most unusual and striking species from the highlands of Ethiopia, a shrub to 3 ft or more with silvery green leaves to about 3" wide, ruffle edged and spined, and spikes of nearly red flowers in summer and autumn. -
15. SCHEFFLERA J. R. Forster & G. Forster, Char. Gen. Pl. 23. 1775
Flora of China 13: 454–463. 2007. 15. SCHEFFLERA J. R. Forster & G. Forster, Char. Gen. Pl. 23. 1775, nom. cons. 鹅掌柴属 e zhang chai shu Agalma Miquel; Heptapleurum Gaertner; Sciodaphyllum P. Browne. Shrubs or trees, sometimes climbers or epiphytes, evergreen, hermaphroditic or andromonoecious, unarmed. Leaves palmately compound, rarely unifoliolate (not in China), margins entire to serrate; stipules united within petiole. Inflorescence a terminal or pseudo-lateral panicle or compound raceme; flowers arranged in umbels, heads, or racemes; bracts pubescent, deciduous or persistent. Pedicels not articulate below ovary. Calyx rim entire or 5-toothed. Petals 5–11, valvate. Stamens 5–11. Ovary (4 or)5–11- carpellate; styles partly or completely united into a column or stigmas sessile. Fruit a drupe, globose or ovoid. Seeds (4 or)5–11, laterally compressed; endosperm uniform or slightly ruminate. Nearly 1100 species: widely distributed in tropics and subtropics of both hemispheres; 35 species (14 endemic) in SW and SE China. Several recent phylogenetic studies have shown that Schefflera is clearly polyphyletic (Lowry et al., S. Afr. J. Bot. 70: 382–392. 2004; Plunkett et al., Pl. Syst. Evol. 245: 1–39. 2004; Plunkett et al., Ann. Missouri Bot. Gard. 92: 202–224. 2005) and that the Asian species belong to a single, well- supported, morphologically coherent clade. The name Schefflera will ultimately have to be restricted to a small group of species from the SW Pacific while the Asian species will have to be transferred to one or more other genera. We were unable to treat Schefflera cavaleriei (H. Léveillé) Frodin (World Checklist Bibliogr.