Swede Hollow Plant Species List
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Breeding Ecology of Kittlitz's Murrelet at Agattu Island, Alaska, in 2010
AMNWR 2011/01 BREEDING ECOLOGY OF KITTLITZ’S MURRELET AT AGATTU ISLAND, ALASKA, IN 2010: PROGRESS REPORT Photo: R. Kaler/USFWS 1 2 1 1 3 Robb S. A. Kaler , Leah A. Kenney , Jeffrey C. Williams , G. Vernon Byrd , and John F. Piatt Key Words: Alaska, Aleutian Islands, Brachyramphus brevirostris, breeding ecology, growth rates, Kittlitz’s murrelet, Near Islands, nest site selection, parental provisioning, reproductive success. 1Alaska Maritime National Wildlife Refuge 95 Sterling Highway, Suite 1 Homer, Alaska 99603 2Department of Biological Sciences University of Alaska Anchorage Anchorage, Alaska 99501 3Alaska Science Center, US Geological Survey 4210 University Drive Anchorage, Alaska 99508 Cite as: Kaler, R.S.A., L.A. Kenney, J.C. Williams, G.V. Byrd, and J.F. Piatt. 2011. Breeding biology of Kittlitz’s murrelet at Agattu Island, Alaska, in 2010: progress report. U.S. Fish and Wildl. Serv. Rep. AMNWR 2011/01. 2 TABLE OF CONTENTS INTRODUCTION ......................................................................................................................... 3 STUDY AREA .............................................................................................................................. 4 METHODS .................................................................................................................................... 4 RESULTS ...................................................................................................................................... 8 2010 SUMMARY AND RECOMMENDATIONS ................................................................... -
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE
Guide to the Flora of the Carolinas, Virginia, and Georgia, Working Draft of 17 March 2004 -- LILIACEAE LILIACEAE de Jussieu 1789 (Lily Family) (also see AGAVACEAE, ALLIACEAE, ALSTROEMERIACEAE, AMARYLLIDACEAE, ASPARAGACEAE, COLCHICACEAE, HEMEROCALLIDACEAE, HOSTACEAE, HYACINTHACEAE, HYPOXIDACEAE, MELANTHIACEAE, NARTHECIACEAE, RUSCACEAE, SMILACACEAE, THEMIDACEAE, TOFIELDIACEAE) As here interpreted narrowly, the Liliaceae constitutes about 11 genera and 550 species, of the Northern Hemisphere. There has been much recent investigation and re-interpretation of evidence regarding the upper-level taxonomy of the Liliales, with strong suggestions that the broad Liliaceae recognized by Cronquist (1981) is artificial and polyphyletic. Cronquist (1993) himself concurs, at least to a degree: "we still await a comprehensive reorganization of the lilies into several families more comparable to other recognized families of angiosperms." Dahlgren & Clifford (1982) and Dahlgren, Clifford, & Yeo (1985) synthesized an early phase in the modern revolution of monocot taxonomy. Since then, additional research, especially molecular (Duvall et al. 1993, Chase et al. 1993, Bogler & Simpson 1995, and many others), has strongly validated the general lines (and many details) of Dahlgren's arrangement. The most recent synthesis (Kubitzki 1998a) is followed as the basis for familial and generic taxonomy of the lilies and their relatives (see summary below). References: Angiosperm Phylogeny Group (1998, 2003); Tamura in Kubitzki (1998a). Our “liliaceous” genera (members of orders placed in the Lilianae) are therefore divided as shown below, largely following Kubitzki (1998a) and some more recent molecular analyses. ALISMATALES TOFIELDIACEAE: Pleea, Tofieldia. LILIALES ALSTROEMERIACEAE: Alstroemeria COLCHICACEAE: Colchicum, Uvularia. LILIACEAE: Clintonia, Erythronium, Lilium, Medeola, Prosartes, Streptopus, Tricyrtis, Tulipa. MELANTHIACEAE: Amianthium, Anticlea, Chamaelirium, Helonias, Melanthium, Schoenocaulon, Stenanthium, Veratrum, Toxicoscordion, Trillium, Xerophyllum, Zigadenus. -
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. -
Outline of Angiosperm Phylogeny
Outline of angiosperm phylogeny: orders, families, and representative genera with emphasis on Oregon native plants Priscilla Spears December 2013 The following listing gives an introduction to the phylogenetic classification of the flowering plants that has emerged in recent decades, and which is based on nucleic acid sequences as well as morphological and developmental data. This listing emphasizes temperate families of the Northern Hemisphere and is meant as an overview with examples of Oregon native plants. It includes many exotic genera that are grown in Oregon as ornamentals plus other plants of interest worldwide. The genera that are Oregon natives are printed in a blue font. Genera that are exotics are shown in black, however genera in blue may also contain non-native species. Names separated by a slash are alternatives or else the nomenclature is in flux. When several genera have the same common name, the names are separated by commas. The order of the family names is from the linear listing of families in the APG III report. For further information, see the references on the last page. Basal Angiosperms (ANITA grade) Amborellales Amborellaceae, sole family, the earliest branch of flowering plants, a shrub native to New Caledonia – Amborella Nymphaeales Hydatellaceae – aquatics from Australasia, previously classified as a grass Cabombaceae (water shield – Brasenia, fanwort – Cabomba) Nymphaeaceae (water lilies – Nymphaea; pond lilies – Nuphar) Austrobaileyales Schisandraceae (wild sarsaparilla, star vine – Schisandra; Japanese -
Round-Lobed Hepatica (Anemone Americana) – Wooly Harbinger of Spring
Round-lobed Hepatica (Anemone americana) – Wooly Harbinger of Spring Did you Know? Hepaticas are one of the first flowers to bloom in Spring. Native Americans used a tea derived from the leaves to cure a number of ailments. Hepaticas are poisonous in large doses. They can also be irritating to the skin if handled. Photo : 2013 Brian Popelier Habitat – Upland woods and forests, deciduous forests Size – 70-170 cm in height Range – Manitoba, Ontario and Quebec south into the eastern United States Flowering Date – March - May Status – S5/ Common in Ontario Other Common Names – Liverleaf, Snow Trillium, Blue Anemone, Kidneywort The Bruce Trail Conservancy | PO Box 857 Hamilton, ON L8N 3N9 | 1.800.665.4453 | [email protected] Identification: Purple, pink or white six - ten petaled flowers sit atop a single, leafless stem covered in wooly hairs. Flowers often found in clumps. The leaves are distinct with three lobes ending in a rounded tip. The flower stocks are upright standing over the flattened basal leaves. The leaves are light green at first but turn a purplish, wine colour as the season wears on and can often be seen standing out from the snow in the winter. Photo : 2013 Brian Popelier Interesting Facts The plant gets its name from the leathery purple-brown basal leaves, which resemble the shape of the liver. Many early herbalists believed that the shape of the plant determined its usefulness in the treatment of liver ailments. Bees and flies are the primary pollinators. The plant uses ants to distribute their seeds. As the seeds drop ants pick them up and disperse the seeds to other areas. -
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. -
Etude Sur L'origine Et L'évolution Des Variations Florales Chez Delphinium L. (Ranunculaceae) À Travers La Morphologie, L'anatomie Et La Tératologie
Etude sur l'origine et l'évolution des variations florales chez Delphinium L. (Ranunculaceae) à travers la morphologie, l'anatomie et la tératologie : 2019SACLS126 : NNT Thèse de doctorat de l'Université Paris-Saclay préparée à l'Université Paris-Sud ED n°567 : Sciences du végétal : du gène à l'écosystème (SDV) Spécialité de doctorat : Biologie Thèse présentée et soutenue à Paris, le 29/05/2019, par Felipe Espinosa Moreno Composition du Jury : Bernard Riera Chargé de Recherche, CNRS (MECADEV) Rapporteur Julien Bachelier Professeur, Freie Universität Berlin (DCPS) Rapporteur Catherine Damerval Directrice de Recherche, CNRS (Génétique Quantitative et Evolution Le Moulon) Présidente Dario De Franceschi Maître de Conférences, Muséum national d'Histoire naturelle (CR2P) Examinateur Sophie Nadot Professeure, Université Paris-Sud (ESE) Directrice de thèse Florian Jabbour Maître de conférences, Muséum national d'Histoire naturelle (ISYEB) Invité Etude sur l'origine et l'évolution des variations florales chez Delphinium L. (Ranunculaceae) à travers la morphologie, l'anatomie et la tératologie Remerciements Ce manuscrit présente le travail de doctorat que j'ai réalisé entre les années 2016 et 2019 au sein de l'Ecole doctorale Sciences du végétale: du gène à l'écosystème, à l'Université Paris-Saclay Paris-Sud et au Muséum national d'Histoire naturelle de Paris. Même si sa réalisation a impliqué un investissement personnel énorme, celui-ci a eu tout son sens uniquement et grâce à l'encadrement, le soutien et l'accompagnement de nombreuses personnes que je remercie de la façon la plus sincère. Je remercie très spécialement Florian Jabbour et Sophie Nadot, mes directeurs de thèse. -
Bovine Fascioliasis with Emphasis on Fasciola Hepatica
PEER REVIEWED Bovine fascioliasis with emphasis on Fasciola hepatica Gary L. Zimmerman, MS, PhD, DVM 1106 West Park 424, Livingston, MT 59047 Corresponding author: Gary L. Zimmerman, [email protected], 406-223-3704 Abstract over 135 million years, with the divergent evolution of Fasciola hepatica and F. gigantica occurring ap Fasciola hepatica, the common liver fluke, is an proximately 19 million years ago. 14 In the continental economically important parasite of ruminants. Although United States, Fasciola hepatica is the most common and infections in cattle are generally chronic and sub-clinical, economically important fluke infecting domestic large the overall impacts on health and productivity can be and small ruminants. The related species F. gigantica, significant, including decreased feed efficiency, weight which is common worldwide, has also been reported in 24 32 gain, reproductive rates, immunity, immunodiagnostic the southeastern United States. • Fascioloides magna, tests, and responses to vaccinations. Acute infections normally a parasite of deer, elk, and moose, also occurs can occur in cattle, but are more common in sheep. There in cattle as an incidental finding at necropsy or slaugh 9 38 are no pathognomonic signs of fascioliasis. Fecal ex ter, whereas in sheep it is often fatal. • Previously aminations using sedimentation or filtration techniques reported to infect Bison bison, recent research efforts remain the most commonly used diagnostic tools. In the to experimentally infect bison with Fascioloides magna United States, albendazole and a combined clorsulon/ have not been successful.10,38 Dicrocoelium dendriticum ivermectin formulation are the only currently approved is a smaller and less pathogenic liver fluke ofruminants products for treatment of liver flukes. -
Anemone Acutiloba – Hepatica
Friends of the Arboretum Native Plant Sale Anemone acutiloba – Hepatica COMMON NAME: Hepatica, Sharp-lobed hepatica SCIENTIFIC NAME: Anemone acutiloba – the Greek word anemos is wind and acutiloba refers to the pointed leaves. The common name of hepatica comes from the fancied resemblance of the 3-lobed leaves to the liver. FLOWER: white, pink, lavender with six (usually) petal-like sepals. The color tends to fade with age. BLOOMING PERIOD: April, but maybe March with global warming! This is one of the earliest spring flowers. SIZE: 4 to 6 inches BEHAVIOR: This is a perennial herb with its distinctive 3-lobed leaves and fibrous roots. It will spread from seed and should be divided in fall. SITE REQUIREMENTS: Does best in rich, moist soil and dense shade of maple forests, but tolerates less shady habitats and drier, rocky soils. Look for it on steep, rocky hillsides and steep banks of creeks. NATURAL RANGE; Nova Scotia to northern Florida, west to Manitoba, Iowa, Missouri and even in Alaska. In Wisconsin it is more common in the southern 2/3 of the state. SPECIAL FEATURES: Old leaves may still be present in early spring, but will be looking kind of coppery. Then furry stems unfurl and hold the fragrant pastel flowers. The new leaves appear after flowering and will remain sort of green until the following spring. SUGGESTED CARE: Provide ample water in spring and fall, especially the first few years. Cover in winter with light mulch of maple leaves, but remove the mulch in mid to late March. COMPANION PLANTS: trillium, Solomon’s plume, toothwort, Dutchman’s breeches, spring beauty, wild geranium, bloodroot, troutlily, bedstraw, rue anemone SPECIAL NOTE: There is a similar specials, Anemone Americana, with round-lobed leaves. -
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.