3. Archaeology of the Urban Environment
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
Smithsonian Institution Archives (SIA)
SMITHSONIAN OPPORTUNITIES FOR RESEARCH AND STUDY 2020 Office of Fellowships and Internships Smithsonian Institution Washington, DC The Smithsonian Opportunities for Research and Study Guide Can be Found Online at http://www.smithsonianofi.com/sors-introduction/ Version 2.0 (Updated January 2020) Copyright © 2020 by Smithsonian Institution Table of Contents Table of Contents .................................................................................................................................................................................................. 1 How to Use This Book .......................................................................................................................................................................................... 1 Anacostia Community Museum (ACM) ........................................................................................................................................................ 2 Archives of American Art (AAA) ....................................................................................................................................................................... 4 Asian Pacific American Center (APAC) .......................................................................................................................................................... 6 Center for Folklife and Cultural Heritage (CFCH) ...................................................................................................................................... 7 Cooper-Hewitt, -
Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America North of Mexico with a Key to Species
Zootaxa 2835: 30–40 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America north of Mexico with a key to species J. E. McPHERSON1, RICHARD J. PACKAUSKAS2, ROBERT W. SITES3, STEVEN J. TAYLOR4, C. SCOTT BUNDY5, JEFFREY D. BRADSHAW6 & PAULA LEVIN MITCHELL7 1Department of Zoology, Southern Illinois University, Carbondale, Illinois 62901, USA. E-mail: [email protected] 2Department of Biological Sciences, Fort Hays State University, Hays, Kansas 67601, USA. E-mail: [email protected] 3Enns Entomology Museum, Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211, USA. E-mail: [email protected] 4Illinois Natural History Survey, University of Illinois at Urbana-Champaign, Illinois 61820, USA. E-mail: [email protected] 5Department of Entomology, Plant Pathology, & Weed Science, New Mexico State University, Las Cruces, New Mexico 88003, USA. E-mail: [email protected] 6Department of Entomology, University of Nebraska-Lincoln, Panhandle Research & Extension Center, Scottsbluff, Nebraska 69361, USA. E-mail: [email protected] 7Department of Biology, Winthrop University, Rock Hill, South Carolina 29733, USA. E-mail: [email protected] Abstract A review of Acanthocephala of America north of Mexico is presented with an updated key to species. A. confraterna is considered a junior synonym of A. terminalis, thus reducing the number of known species in this region from five to four. New state and country records are presented. Key words: Coreidae, Coreinae, Acanthocephalini, Acanthocephala, North America, review, synonymy, key, distribution Introduction The genus Acanthocephala Laporte currently is represented in America north of Mexico by five species: Acan- thocephala (Acanthocephala) declivis (Say), A. -
A Phylogeny of the Hubbardochloinae Including Tetrachaete (Poaceae: Chloridoideae: Cynodonteae)
Peterson, P.M., K. Romaschenko, and Y. Herrera Arrieta. 2020. A phylogeny of the Hubbardochloinae including Tetrachaete (Poaceae: Chloridoideae: Cynodonteae). Phytoneuron 2020-81: 1–13. Published 18 November 2020. ISSN 2153 733 A PHYLOGENY OF THE HUBBARDOCHLOINAE INCLUDING TETRACHAETE (CYNODONTEAE: CHLORIDOIDEAE: POACEAE) PAUL M. PETERSON AND KONSTANTIN ROMASCHENKO Department of Botany National Museum of Natural History Smithsonian Institution Washington, D.C. 20013-7012 [email protected]; [email protected] YOLANDA HERRERA ARRIETA Instituto Politécnico Nacional CIIDIR Unidad Durango-COFAA Durango, C.P. 34220, México [email protected] ABSTRACT The phylogeny of subtribe Hubbardochloinae is revisited, here with the inclusion of the monotypic genus Tetrachaete, based on a molecular DNA analysis using ndhA intron, rpl32-trnL, rps16 intron, rps16- trnK, and ITS markers. Tetrachaete elionuroides is aligned within the Hubbardochloinae and is sister to Dignathia. The biogeography of the Hubbardochloinae is discussed, its origin likely in Africa or temperate Asia. In a previous molecular DNA phylogeny (Peterson et al. 2016), the subtribe Hubbardochloinae Auquier [Bewsia Gooss., Dignathia Stapf, Gymnopogon P. Beauv., Hubbardochloa Auquier, Leptocarydion Hochst. ex Stapf, Leptothrium Kunth, and Lophacme Stapf] was found in a clade with moderate support (BS = 75, PP = 1.00) sister to the Farragininae P.M. Peterson et al. In the present study, Tetrachaete elionuroides Chiov. is included in a phylogenetic analysis (using ndhA intron, rpl32- trnL, rps16 intron, rps16-trnK, and ITS DNA markers) in order to test its relationships within the Cynodonteae with heavy sampling of species in the supersubtribe Gouiniodinae P.M. Peterson & Romasch. Chiovenda (1903) described Tetrachaete Chiov. with a with single species, T. -
Improving Our Understanding of Environmental Controls on the Distribution of C3 and C4 Grasses STEPHANIE PAU*, ERIKA J
Global Change Biology (2013) 19, 184–196, doi: 10.1111/gcb.12037 Improving our understanding of environmental controls on the distribution of C3 and C4 grasses STEPHANIE PAU*, ERIKA J. EDWARDS† andCHRISTOPHER J. STILL‡§ *National Center for Ecological Analysis and Synthesis (NCEAS), 735 State Street, Suite 300, Santa Barbara, CA 93101, USA, †Department of Ecology and Evolutionary Biology, Brown University, Providence, RI 02912, USA, ‡Department of Geography, University of California, Santa Barbara, CA 93106-4060, USA, §Forest Ecosystems and Society, Oregon State University, 321 Richardson Hall, Corvallis, OR 97331-5752, USA Abstract A number of studies have demonstrated the ecological sorting of C3 and C4 grasses along temperature and moisture gradients. However, previous studies of C3 and C4 grass biogeography have often inadvertently compared species in different and relatively unrelated lineages, which are associated with different environmental settings and distinct adaptive traits. Such confounded comparisons of C3 and C4 grasses may bias our understanding of ecological sorting imposed strictly by photosynthetic pathway. Here, we used MaxEnt species distribution modeling in combination with satellite data to understand the functional diversity of C3 and C4 grasses by comparing both large clades and closely related sister taxa. Similar to previous work, we found that C4 grasses showed a preference for regions with higher temperatures and lower precipitation compared with grasses using the C3 pathway. However, air temperature differences were smaller (2 °C vs. 4 °C) and precipitation and % tree cover differences were larger (1783 mm vs. 755 mm, 21.3% vs. 7.7%, respectively) when comparing C3 and C4 grasses within the same clade vs. -
State of New York City's Plants 2018
STATE OF NEW YORK CITY’S PLANTS 2018 Daniel Atha & Brian Boom © 2018 The New York Botanical Garden All rights reserved ISBN 978-0-89327-955-4 Center for Conservation Strategy The New York Botanical Garden 2900 Southern Boulevard Bronx, NY 10458 All photos NYBG staff Citation: Atha, D. and B. Boom. 2018. State of New York City’s Plants 2018. Center for Conservation Strategy. The New York Botanical Garden, Bronx, NY. 132 pp. STATE OF NEW YORK CITY’S PLANTS 2018 4 EXECUTIVE SUMMARY 6 INTRODUCTION 10 DOCUMENTING THE CITY’S PLANTS 10 The Flora of New York City 11 Rare Species 14 Focus on Specific Area 16 Botanical Spectacle: Summer Snow 18 CITIZEN SCIENCE 20 THREATS TO THE CITY’S PLANTS 24 NEW YORK STATE PROHIBITED AND REGULATED INVASIVE SPECIES FOUND IN NEW YORK CITY 26 LOOKING AHEAD 27 CONTRIBUTORS AND ACKNOWLEGMENTS 30 LITERATURE CITED 31 APPENDIX Checklist of the Spontaneous Vascular Plants of New York City 32 Ferns and Fern Allies 35 Gymnosperms 36 Nymphaeales and Magnoliids 37 Monocots 67 Dicots 3 EXECUTIVE SUMMARY This report, State of New York City’s Plants 2018, is the first rankings of rare, threatened, endangered, and extinct species of what is envisioned by the Center for Conservation Strategy known from New York City, and based on this compilation of The New York Botanical Garden as annual updates thirteen percent of the City’s flora is imperiled or extinct in New summarizing the status of the spontaneous plant species of the York City. five boroughs of New York City. This year’s report deals with the City’s vascular plants (ferns and fern allies, gymnosperms, We have begun the process of assessing conservation status and flowering plants), but in the future it is planned to phase in at the local level for all species. -
The Genera of Bambusoideae (Gramineae) in the Southeastern United States Gordon C
Eastern Illinois University The Keep Faculty Research & Creative Activity Biological Sciences January 1988 The genera of Bambusoideae (Gramineae) in the southeastern United States Gordon C. Tucker Eastern Illinois University, [email protected] Follow this and additional works at: http://thekeep.eiu.edu/bio_fac Part of the Biology Commons Recommended Citation Tucker, Gordon C., "The eg nera of Bambusoideae (Gramineae) in the southeastern United States" (1988). Faculty Research & Creative Activity. 181. http://thekeep.eiu.edu/bio_fac/181 This Article is brought to you for free and open access by the Biological Sciences at The Keep. It has been accepted for inclusion in Faculty Research & Creative Activity by an authorized administrator of The Keep. For more information, please contact [email protected]. TUCKER, BAMBUSOIDEAE 239 THE GENERA OF BAMBUSOIDEAE (GRAMINEAE) IN THE SOUTHEASTERN UNITED STATESu GoRDON C. T ucKER3 Subfamily BAMBUSOIDEAE Ascherson & Graebner, Synop. Mitteleurop. Fl. 2: 769. 1902. Perennial or annual herbs or woody plants of tropical or temperate forests and wetlands. Rhizomes present or lacking. Stems erect or decumbent (some times rooting at the lower nodes); nodes glabrous, pubescent, or puberulent. Leaves several to many, glabrous to sparsely pubescent (microhairs bicellular); leaf sheaths about as long as the blades, open for over tf2 their length, glabrous; ligules wider than long, entire or fimbriate; blades petiolate or sessile, elliptic to linear, acute to acuminate, the primary veins parallel to-or forming an angle of 5-10• wi th-the midvein, transverse veinlets numerous, usually con spicuous, giving leaf surface a tessellate appearance; chlorenchyma not radiate (i.e., non-kranz; photosynthetic pathway C.,). -
Micromorphology and Anatomy of the Leaf Blade: a Contribution to the Taxonomy of Luziola (Poaceae, Oryzoideae) from the Pantanal, Brazil
Plant Syst Evol (2016) 302:265–273 DOI 10.1007/s00606-015-1260-8 ORIGINAL ARTICLE Micromorphology and anatomy of the leaf blade: a contribution to the taxonomy of Luziola (Poaceae, Oryzoideae) from the Pantanal, Brazil 1 2 2 Thales D. Leandro • Edna Scremin-Dias • Rosani do Carmo de Oliveira Arruda Received: 5 January 2015 / Accepted: 19 October 2015 / Published online: 12 November 2015 Ó Springer-Verlag Wien 2015 Abstract Luziola comprises nine monoecious, aquatic A key for the identification of the studied species is pre- species and has its center of diversity in South America. sented based on the leaf blade features. Due to the morphological similarities among Luziola spe- cies in the vegetative stage, the micromorphology and Keywords Aquatic grasses Á Leaf anatomy Á Luziolinae Á anatomy of the leaf blade of five Luziola species were Oryzeae Á Poales Á Zizaniinae studied to survey potentially useful features for taxon identification. Oryzoid silica bodies; silicified unicellular trichomes with a rounded apex; stomata in furrows on the Introduction adaxial surface; a complex midrib consisting of at least two vascular bundles; superposed vascular bundles in the The subfamily Oryzoideae (syn. Ehrhartoideae) is mono- mesophyll; and fusoid cells are features shared by some of phyletic and a member of the BOP clade [Bambu- these species. Conversely, features unique to a single soideae ? Oryzoideae ? Pooideae] of grasses (Grass species include: vertically elongated epidermal cells sur- Phylogeny Working Group (GPWG) II 2012; Soreng et al. rounding pointed unicellular trichomes, flat midrib and leaf 2015). Oryzoideae (excluding Streptogyneae) share a margin dimorphism (L. fragilis), and an obtuse leaf blade combination of characters including spikelets with two margin (L. -
Chapter 5 Phylogeny of Poaceae Based on Matk Gene Sequences
Chapter 5 Phylogeny of Poaceae Based on matK Gene Sequences 5.1 Introduction Phylogenetic reconstruction in the Poaceae began early in this century with proposed evolutionary hypotheses based on assessment of existing knowledge of grasses (e.g., Bew, 1929; Hubbard 1948; Prat, 1960; Stebbins, 1956, 1982; Clayton, 1981; Tsvelev, 1983). Imperical approaches to phylogenetic reconstruction of the Poaceae followed those initial hypotheses, starting with cladistic analyses of morphological and anatomical characters (Kellogg and Campbell, 1987; Baum, 1987; Kellogg and Watson, 1993). More recently, molecular information has provided the basis for phylogenetic hypotheses in grasses at the subfamily and tribe levels (Table 5.1). These molecular studies were based on information from chloroplast DNA (cpDNA) restriction sites and DNA sequencing of the rbcL, ndhF, rps4, 18S and 26S ribosomal DNA (rDNA), phytochrome genes, and the ITS region (Hamby and Zimmer, 1988; Doebley et al., 1990; Davis and Soreng, 1993; Cummings, King, and Kellogg, 1994; Hsiao et al., 1994; Nadot, Bajon, and Lejeune, 1994; Barker, Linder, and Harley, 1995; Clark, Zhang, and Wendel, 1995; Duvall and Morton, 1996; Liang and Hilu, 1996; Mathews and Sharrock, 1996). Although these studies have refined our concept of grass evolution at the subfamily level and, to a certain degree, at the tribal level, major disagreements and questions remain to be addressed. Outstanding discrepancies at the subfamily level include: 1) Are the pooids, bambusoids senso lato, or herbaceous bamboos the -
Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences
d i v e r s i t y , p h y l o g e n y , a n d e v o l u t i o n i n t h e monocotyledons e d i t e d b y s e b e r g , p e t e r s e n , b a r f o d & d a v i s a a r h u s u n i v e r s i t y p r e s s , d e n m a r k , 2 0 1 0 Phylogenetics of Stipeae (Poaceae: Pooideae) Based on Plastid and Nuclear DNA Sequences Konstantin Romaschenko,1 Paul M. Peterson,2 Robert J. Soreng,2 Núria Garcia-Jacas,3 and Alfonso Susanna3 1M. G. Kholodny Institute of Botany, Tereshchenkovska 2, 01601 Kiev, Ukraine 2Smithsonian Institution, Department of Botany MRC-166, National Museum of Natural History, P.O. Box 37012, Washington, District of Columbia 20013-7012 USA. 3Laboratory of Molecular Systematics, Botanic Institute of Barcelona (CSIC-ICUB), Pg. del Migdia, s.n., E08038 Barcelona, Spain Author for correspondence ([email protected]) Abstract—The Stipeae tribe is a group of 400−600 grass species of worldwide distribution that are currently placed in 21 genera. The ‘needlegrasses’ are char- acterized by having single-flowered spikelets and stout, terminally-awned lem- mas. We conducted a molecular phylogenetic study of the Stipeae (including all genera except Anemanthele) using a total of 94 species (nine species were used as outgroups) based on five plastid DNA regions (trnK-5’matK, matK, trnHGUG-psbA, trnL5’-trnF, and ndhF) and a single nuclear DNA region (ITS). -
Ornamental Grasses for the Midsouth Landscape
Ornamental Grasses for the Midsouth Landscape Ornamental grasses with their variety of form, may seem similar, grasses vary greatly, ranging from cool color, texture, and size add diversity and dimension to season to warm season grasses, from woody to herbaceous, a landscape. Not many other groups of plants can boast and from annuals to long-lived perennials. attractiveness during practically all seasons. The only time This variation has resulted in five recognized they could be considered not to contribute to the beauty of subfamilies within Poaceae. They are Arundinoideae, the landscape is the few weeks in the early spring between a unique mix of woody and herbaceous grass species; cutting back the old growth of the warm-season grasses Bambusoideae, the bamboos; Chloridoideae, warm- until the sprouting of new growth. From their emergence season herbaceous grasses; Panicoideae, also warm-season in the spring through winter, warm-season ornamental herbaceous grasses; and Pooideae, a cool-season subfamily. grasses add drama, grace, and motion to the landscape Their habitats also vary. Grasses are found across the unlike any other plants. globe, including in Antarctica. They have a strong presence One of the unique and desirable contributions in prairies, like those in the Great Plains, and savannas, like ornamental grasses make to the landscape is their sound. those in southern Africa. It is important to recognize these Anyone who has ever been in a pine forest on a windy day natural characteristics when using grasses for ornament, is aware of the ethereal music of wind against pine foliage. since they determine adaptability and management within The effect varies with the strength of the wind and the a landscape or region, as well as invasive potential. -
Baccharis Neglecta (Roosevelt Weed)
BELL COUNTY MASTER GARDENER Tip of the Week By Beverly Wickersham The “Neglected” Shrub A casual glance into the fields or pastures around the Bell County area will reveal numerous sightings of Baccharis neglecta , a multi-stemmed, 5 to 9 foot tall spreading shrub belonging to the Asteraceae (Sunflower) family. The genus name Baccharis is a Greek name given to a plant with a fragrant root. The species name, neglecta, is a Latin word meaning “overlooked”, “disregarded”, “slighted”. This “overlooked” plant is actually being used as a specimen planting in several yards in the Killeen/Harker Heights area. When the rains return, the entire shrub will be covered in white flowers. The male and female flowers are borne on separate plants with the female plants producing a profusion of dense, fuzzy, white flowers heads. Several common names for this plant refer to the Oklahoma/Texas Panhandle Dust Bowl and Depression period of the 1930s and to Roosevelt’s presidency. Baccharis neglecta was eventually planted in the fields as a fast and easy way to rejuvenate the severely damaged soil. Therefore, common names for the shrub are Roosevelt Weed , New Deal Weed , and Poverty Weed . Additional common names are False-willow (the leaves resemble willow leaves), Groundsel , and Jara Dulce , a reference to the shrub’s sweet root. Baccharis neglecta has several positive qualities: 1. Adapts well to numerous soil types, 2. Rehabilitates damaged, worn-out soil, 3.Tolerates high salt levels in the soil making it an ideal plant for sea shore plantings to reduce beach erosion, 4. Performs well in specimen plantings, as a screen or background plant, and in neglected sites such as along roadsides, median strips, and in parking lots. -
Subclass 2. Monochlamydeae Order: Centrospermae (Caryophyllales) (Curvembryeae)
Subclass 2. Monochlamydeae Perianth undifferentiated into Ca. and Co. or absent. Order: Centrospermae (Caryophyllales) (Curvembryeae) The order is of interest as indicating a passage from Monochlamydeae to the Dialypetalous type. The simplest flower forms of Chenopodiaceae show a similar plan of floral structure to Urticales, while more advanced families are typically dichlamydous reaching in Caryophyllaceae. Key to families of order Centrospermae (Caryophyllales) 1a. Stem nodded, dichasially branched, leaves opposite…………............................…..…….Caryophyllaceae 1b.Not So.........................................................................................2 2a. Carpels 2 or more.....................................................................3 2b. Carpel one.................................................................................6 3a. Fruit achene, inflated...............................................................4 3b. Fruit capsule..............................................................................5 4a. Perianth memberanous…………...…..………Amarantaceae 4b. Perianth herbaceous…….....….......………..Chenopodiaceae 5a. Perianth differentiated into K2 and C 4-6........Portulaccaceae 5b. Perianth single of 5 tepals……………........………Aizoaceae 6a Perianth petaloid………………..…………….Nyctaginaceae 6b. Perianth sepaloid…………..……...………….Phytolaccaceae Family: Amarantaceae Vegetative characters: Leaves: With reticulate venation. Floral characters: Inflorescence: Dense small showy cymose. Flower: Small dry pentamerous. Bract: