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TAXON:Costus Malortieanus H. Wendl. SCORE:7.0 RATING:High Risk
TAXON: Costus malortieanus H. SCORE: 7.0 RATING: High Risk Wendl. Taxon: Costus malortieanus H. Wendl. Family: Costaceae Common Name(s): spiral flag Synonym(s): Costus elegans Petersen spiral ginger stepladder ginger Assessor: Chuck Chimera Status: Assessor Approved End Date: 2 Aug 2017 WRA Score: 7.0 Designation: H(HPWRA) Rating: High Risk Keywords: Perennial Herb, Ornamental, Shade-Tolerant, Rhizomatous, Bird-Dispersed Qsn # Question Answer Option Answer 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? 103 Does the species have weedy races? Species suited to tropical or subtropical climate(s) - If 201 island is primarily wet habitat, then substitute "wet (0-low; 1-intermediate; 2-high) (See Appendix 2) High tropical" for "tropical or subtropical" 202 Quality of climate match data (0-low; 1-intermediate; 2-high) (See Appendix 2) High 203 Broad climate suitability (environmental versatility) y=1, n=0 n Native or naturalized in regions with tropical or 204 y=1, n=0 y subtropical climates Does the species have a history of repeated introductions 205 y=-2, ?=-1, n=0 y outside its natural range? 301 Naturalized beyond native range y = 1*multiplier (see Appendix 2), n= question 205 y 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) n 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see Appendix 2) n 304 Environmental weed n=0, y = 2*multiplier (see Appendix 2) n 305 Congeneric weed 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic 403 Parasitic y=1, n=0 n 404 Unpalatable to grazing animals 405 Toxic to animals y=1, n=0 n 406 Host for recognized pests and pathogens 407 Causes allergies or is otherwise toxic to humans y=1, n=0 n 408 Creates a fire hazard in natural ecosystems y=1, n=0 n 409 Is a shade tolerant plant at some stage of its life cycle y=1, n=0 y Creation Date: 2 Aug 2017 (Costus malortieanus H. -
[The Pond\. Odonatoptera (Odonata)]
Odonatological Abstracts 1987 1993 (15761) SAIKI, M.K. &T.P. LOWE, 1987. Selenium (15763) ARNOLD, A., 1993. Die Libellen (Odonata) in aquatic organisms from subsurface agricultur- der “Papitzer Lehmlachen” im NSG Luppeaue bei al drainagewater, San JoaquinValley, California. Leipzig. Verbff. NaturkMus. Leipzig 11; 27-34. - Archs emir. Contam. Toxicol. 16: 657-670. — (US (Zur schonen Aussicht 25, D-04435 Schkeuditz). Fish & Wildl. Serv., Natn. Fisheries Contaminant The locality is situated 10km NW of the city centre Res. Cent., Field Res, Stn, 6924 Tremont Rd, Dixon, of Leipzig, E Germany (alt, 97 m). An annotated CA 95620, USA). list is presented of 30 spp., evidenced during 1985- Concentrations of total selenium were investigated -1993. in plant and animal samplesfrom Kesterson Reser- voir, receiving agricultural drainage water (Merced (15764) BEKUZIN, A.A., 1993. Otryad Strekozy - — Co.) and, as a reference, from the Volta Wildlife Odonatoptera(Odonata). [OrderDragonflies — km of which Area, ca 10 S Kesterson, has high qual- Odonatoptera(Odonata)].Insectsof Uzbekistan , pp. ity irrigationwater. Overall,selenium concentrations 19-22,Fan, Tashkent, (Russ.). - (Author’s address in samples from Kesterson averaged about 100-fold unknown). than those from Volta. in and A rather 20 of higher Thus, May general text, mentioning (out 76) spp. Aug. 1983, the concentrations (pg/g dry weight) at No locality data, but some notes on their habitats Kesterson in larval had of 160- and vertical in Central Asia. Zygoptera a range occurrence 220 and in Anisoptera 50-160. In Volta,these values were 1.2-2.I and 1.1-2.5, respectively. In compari- (15765) GAO, Zhaoning, 1993. -
Aristolochic Acids Affect the Feeding Behaviour and Development of Battus Polydamas Archidamas Larvae (Lepidoptera: Papilionidae: Troidini)
Eur. J. Entomol. 106: 357–361, 2009 http://www.eje.cz/scripts/viewabstract.php?abstract=1462 ISSN 1210-5759 (print), 1802-8829 (online) Aristolochic acids affect the feeding behaviour and development of Battus polydamas archidamas larvae (Lepidoptera: Papilionidae: Troidini) CARLOS F. PINTO1, ALEJANDRA J. TRONCOSO1, ALEJANDRO URZÚA2 and HERMANN M. NIEMEYER1* 1 Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Casilla 653, Santiago, Chile 2 Facultad de Química y Biología, Universidad de Santiago de Chile, Casilla 40, Santiago-33, Chile Key words. Lepidoptera, Papilionidae, Battus polydamas archidamas, Aristolochia chilensis, aristolochic acid content, foraging substrate, larval development Abstract. The feeding behaviour of specialist butterflies may be affected by the mechanical and chemical characteristics of the tis- sues of their host-plants. Larvae of the butterfly, Battus polydamas archidamas feed only on Aristolochia chilensis, which contains aristolochic acids. We studied the oviposition pattern of adults and the foraging of larvae of B. polydamas archidamas over time in relation to variations in hardness of the substrate and concentration of aristolochic acids in different plant tissues. We further tested the effect of two artificial diets containing different concentrations of aristolochic acids on larval performance. B. polydamas archi- damas oviposited mostly on young leaves and the larvae fed on this tissue until the second instar. Third instar larvae fed also on mature leaves and fourth and higher instars fed also on stems. Young leaves are softer and contain higher concentrations of aris- tolochic acids than mature leaves, and stems are both harder and contain a high concentration of aristolochic acids. Larvae reared on artificial diets containing a high concentration of aristolochic acids suffered less mortality and were heavier than those reared on a diet with a lower concentration of aristolochic acids, which suggests they are phagostimulatory. -
Butterfly Migrations in Florida: Seasonal Patterns and Long-Term
POPULATION ECOLOGY Butterfly Migrations in Florida: Seasonal Patterns and Long-Term Changes THOMAS J. WALKER1 Department of Entomology and Nematology, University of Florida, Gainesville, FL 32611Ð0620 Environ. Entomol. 30(6): 1052Ð1060 (2001) ABSTRACT Flight traps at Gainesville, in north-central Florida, operating from 1984 to spring 2000, separated butterßies migrating into the Florida peninsula (SSE Ϯ 90Њ) from those migrating out of the Florida peninsula (NNW Ϯ 90Њ). Five species ßew southward in the fall and northward in the spring: Phoebis sennae (L.), Agraulis vanillae (L.), Junonia coenia (Hu¨ bner), Urbanus proteus (L.), and Eurema lisa (Boisduval & LeConte). Five species had signiÞcant northward ßights in spring but no signiÞcant migration in fall: Pieris rapae (L.), Vanessa virginiensis (Drury), Vanessa atalanta (L.), Eurytides marcellus (Cramer), and Libytheana bachmanii (Kirtland). Danaus plexippus (L.) had a southward ßight in fall but no signiÞcant migration in spring. Eurema daira (Godart) switched from a net movement northward in early fall to a net movement southward in late fall, whereas Eurema nicippe (Cramer) maintained a net movement northward throughout the fall. The major migrants differed signiÞcantly in the seasonal timing and duration of peak migration. When the numbers trapped were greatest, the proportion of those ßying in the migratory direction was greatest. The numbers of spring migrants of A. vanillae increased during the course of the study, whereas both the spring and fall migrations of J. coenia declined. The fall migrations of P. sennae and U. proteus declined sharply. In 1990Ð1999, the fall migrations of P. sennae and U. proteus averaged only 37 and 15% of what they had averaged in 1984Ð1989. -
Monarch Butterflies and Their Habitat Across North America
Monitoring Monarch Butterflies and Their Habitat across North America Inventory and Monitoring Protocols and Data Standards for Monarch Conservation Please cite as: CEC. 2017. Monitoring Monarch Butteries and eir Habitat across North America: Inventory and Monitoring Protocols and Data Standards for Monarch Conservation. Montreal, Canada: Commission for Environmental Cooperation. 48 pp. is publication was prepared by Holly Holt of Monarch Joint Venture (University of Minnesota) for the Secretariat of the Commission for Environmental Cooperation. e information contained herein is the responsibility of the author and does not necessarily reect the views of [the CEC, or] the governments of Canada, Mexico or the United States of America. Reproduction of this document in whole or in part and in any form for educational or non-prot purposes may be made without special permission from the CEC Secretariat, provided acknowledgment of the source is made. e CEC would appreciate receiving a copy of any publication or material that uses this document as a source. Except where otherwise noted, this work is protected under a Creative Commons Attribution Noncommercial–NoDerivative Works License. © Commission for Environmental Cooperation, 2017 ISBN: 978-2-89700-221-3 (e-version) Disponible en français – ISBN: 978-2-89700-223-7 (e-version) Disponible en español – ISBN: 978-2-89700-222-0 (e-version) Legal deposit – Bibliothèque et Archives nationales du Québec, 2017 Legal deposit – Library and Archives Canada, 2017 Publication Details Document category: -
Ecography ECOG-02578 Pinkert, S., Brandl, R
Ecography ECOG-02578 Pinkert, S., Brandl, R. and Zeuss, D. 2016. Colour lightness of dragonfly assemblages across North America and Europe. – Ecography doi: 10.1111/ecog.02578 Supplementary material Appendix 1 Figures A1–A12, Table A1 and A2 1 Figure A1. Scatterplots between female and male colour lightness of 44 North American (Needham et al. 2000) and 19 European (Askew 1988) dragonfly species. Note that colour lightness of females and males is highly correlated. 2 Figure A2. Correlation of the average colour lightness of European dragonfly species illustrated in both Askew (1988) and Dijkstra and Lewington (2006). Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Note that the extracted colour values of dorsal dragonfly drawings from both sources are highly correlated. 3 Figure A3. Frequency distribution of the average colour lightness of 152 North American and 74 European dragonfly species. Average colour lightness ranges from 0 (absolute black) to 255 (pure white). Rugs at the abscissa indicate the value of each species. Note that colour values are from different sources (North America: Needham et al. 2000, Europe: Askew 1988), and hence absolute values are not directly comparable. 4 Figure A4. Scatterplots of single ordinary least-squares regressions between average colour lightness of 8,127 North American dragonfly assemblages and mean temperature of the warmest quarter. Red dots represent assemblages that were excluded from the analysis because they contained less than five species. Note that those assemblages that were excluded scatter more than those with more than five species (c.f. the coefficients of determination) due to the inherent effect of very low sampling sizes. -
GENOME EVOLUTION in MONOCOTS a Dissertation
GENOME EVOLUTION IN MONOCOTS A Dissertation Presented to The Faculty of the Graduate School At the University of Missouri In Partial Fulfillment Of the Requirements for the Degree Doctor of Philosophy By Kate L. Hertweck Dr. J. Chris Pires, Dissertation Advisor JULY 2011 The undersigned, appointed by the dean of the Graduate School, have examined the dissertation entitled GENOME EVOLUTION IN MONOCOTS Presented by Kate L. Hertweck A candidate for the degree of Doctor of Philosophy And hereby certify that, in their opinion, it is worthy of acceptance. Dr. J. Chris Pires Dr. Lori Eggert Dr. Candace Galen Dr. Rose‐Marie Muzika ACKNOWLEDGEMENTS I am indebted to many people for their assistance during the course of my graduate education. I would not have derived such a keen understanding of the learning process without the tutelage of Dr. Sandi Abell. Members of the Pires lab provided prolific support in improving lab techniques, computational analysis, greenhouse maintenance, and writing support. Team Monocot, including Dr. Mike Kinney, Dr. Roxi Steele, and Erica Wheeler were particularly helpful, but other lab members working on Brassicaceae (Dr. Zhiyong Xiong, Dr. Maqsood Rehman, Pat Edger, Tatiana Arias, Dustin Mayfield) all provided vital support as well. I am also grateful for the support of a high school student, Cady Anderson, and an undergraduate, Tori Docktor, for their assistance in laboratory procedures. Many people, scientist and otherwise, helped with field collections: Dr. Travis Columbus, Hester Bell, Doug and Judy McGoon, Julie Ketner, Katy Klymus, and William Alexander. Many thanks to Barb Sonderman for taking care of my greenhouse collection of many odd plants brought back from the field. -
Sequestration of Aristolochic Acids from Meridic Diets by Larvae of Battus Polydamas Archidamas (Papilionidae: Troidini)
Eur. J. Entomol. 108: 41–45, 2011 http://www.eje.cz/scripts/viewabstract.php?abstract=1585 ISSN 1210-5759 (print), 1802-8829 (online) Sequestration of aristolochic acids from meridic diets by larvae of Battus polydamas archidamas (Papilionidae: Troidini) CARLOS F. PINTO1, ALEJANDRO URZÚA2 and HERMANN M. NIEMEYER1* 1Laboratorio de Química Ecológica, Universidad de Chile, Casilla 653, Santiago, Chile 2Laboratorio de Química Ecológica, Universidad de Santiago de Chile, Casilla 40, C-33 Santiago, Chile Key words. Lepidoptera, Papilionidae, Battus polydamas archidamas, Aristolochia chilensis, aristolochic acids, sequestration of toxins, uptake of toxins Abstract. Larvae of the butterfly, Battus polydamas archidamas (Papilionidae: Troidini) feed exclusively on aristolochic acid (AAs)-containing Aristolochia species (Aristolochiaceae). The distribution of sequestrated AAs in the tissues (body, integument and osmeterial secretions) of B. polydamas archidamas larvae during their development, when fed on a meridic diet containing either a higher or lower concentration of AAs (AAI and AAII) than occurs naturally in the aerial tissues of their host plant, was determined. Accumulation of AAs in the body and integument was proportional to the weight of larvae and greater in the larvae that fed on the diet containing the higher concentration of AAs. Phenolic AAs (AAIa and AAIVa) not present in the diets were found in all larval tissues examined. Integument and body extracts had a higher AAI/AAII ratio than in the original diet and also a relatively high AAIa/AAIVa ratio, suggesting a preferred AAII to AAIa transformation in those larval tissues. In the osmeterial secretion, the value of the AAI/AAII ratio was similar to that in the diets and the AAIa/AAIVa ratio close to 1, which suggests that hydroxylation of AAI to AAIVa and of AAII to AAIa occur to similar extents. -
Butterflies of Citrus County and Host Plants
Butterflies of Citrus County ~---4- --•;... ____ - Family I Species Host plant Hesperiidae SkipQers Phocides Qigmalion Mangrove Skipper ~mangrove herbs, vines, shrubs, and trees in the pea family (Fabaceae) including false indigobush (Amorpha fruticosa L.), American hogpeanut (Amphicarpaea bracteata [L.) Fernald), Atlantic pidgeonwings or butterfly pea (Clitoria mariana L.), groundnut (Apios ~vreus clarus Silver-spotted Skip~ americana Medik.), American wisteria (Wisteria frutescens [L.) Poir.) and the introduced Dixie ticktrefoil (Desmodium tortuosum [Sw.] DC.), kudzu (Pueraria montana [Lour.] Merr.), black locust (Robinia pseudoacacia L.), Chinese wisteria (Wisteria sinensis [Sims) DC.) and a variety of other legumes Urbanus prqJg_µs Long-t~.Ued SkiQpec vine legumes including various beans (Phaseolus), hog peanuts (Amphicarpa bracteata), beggar's ticks (Desmodium), blue peas (Clitoria), and wisteria (Wisteria) Various legumes inclu ding wild and cu ltivated beans (Phaseolus), begga r's ticks Urbanus dorantes Dorantes Longtail (Desmodium), and bl ue peas (Clit oria ) -· Beggar\'s ticks (Desmodium); occasionally false indigo (Baptisia) and bush clover Achalarus ly-ciades Hoar.y_r;_ggg {Lespedeza); all in the pea family {Fabaceae) - pea family (Fabaceae) including beggar's ticks (Desmodium), bush clover (Lespedeza), Thor'lbes P'llades Northern Cloud'lwing clover (Trifolium), lotus (Hosackia), and others. -----· Thory-bes bathy-llus Southern Cloudywing Potato bean, Apios americana. Ozark milkvetch, Astragalus distortus var. engelmanni ~ ---- Lespedezas (Lespedeza spp .) are reported as well as Florida Hoarypea (Tephrosia l ibQr:_y_bes confusis Confused Cloudy-wing florid a) . -· -- -------- Staphy:lus hayhurst_ii Ha yh u r?J?-5.IAJ.\QQ Wi ri_g Lambsquart ers {Che nopodium) in the goosefoot family (Chenopodiaceae ), and occasiona lly chaff flower (Alternanthera) in the pigweed family (Amaranthaceae). -
Butterflies (Lepidoptera: Papilionoidea) of Grassland Areas in the Pampa Biome, Southern Brazil
11 5 1772 the journal of biodiversity data 19 October 2015 Check List LISTS OF SPECIES Check List 11(5): 1772, 19 October 2015 doi: http://dx.doi.org/10.15560/11.5.1772 ISSN 1809-127X © 2015 Check List and Authors Butterflies (Lepidoptera: Papilionoidea) of grassland areas in the Pampa biome, southern Brazil Ana Paula dos Santos de Carvalho*, Geisa Piovesan and Ana Beatriz Barros de Morais Universidade Federal de Santa Maria, Centro de Ciências Naturais e Exatas, Pós-Graduação em Biodiversidade Animal, Faixa de Camobi, km 09, CEP 97105-900, Santa Maria, RS, Brazil * Corresponding author. E-mail: [email protected] Abstract: The temperate and subtropical grassland Agricultural activities and the introduction of exotic ecosystems are among the most threatened ecosystems species are the main threats to the local biodiversity in the world due to habitat loss. This study aimed to make (Martino 2004; Behling et al. 2009; Roesch et al. 2009; a list of butterfly species present in native grassland Medan et al. 2011). fields in the city of Santa Maria, southern Brazil. The In Rio Grande do Sul state, where the largest sampling field effort was 225 h using entomological nets, remains of preserved grasslands are still found, the from 2009 to 2011. In total, 117 species of butterflies were floristic composition of these fields is fairly well recorded, distributed in six families and 18 subfamilies. known, and they are estimated to contain a richness Nymphalidae was the richest family, with 56 species, of 2,200 species (Boldrini et al. 2010; Iganci et al. 2011). while Lycaenidae was the least rich family, with six Apiaceae, Asteraceae, Cyperaceae, Fabaceae, Iridaceae, species. -
II. a Cladistic Analysis of Rbcl Sequences and Morphology
Systematic Botany (2003), 28(2): pp. 270±292 q Copyright 2003 by the American Society of Plant Taxonomists Phylogenetic Relationships in the Commelinaceae: II. A Cladistic Analysis of rbcL Sequences and Morphology TIMOTHY M. EVANS,1,3 KENNETH J. SYTSMA,1 ROBERT B. FADEN,2 and THOMAS J. GIVNISH1 1Department of Botany, University of Wisconsin, 430 Lincoln Drive, Madison, Wisconsin 53706; 2Department of Systematic Biology-Botany, MRC 166, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington, DC 20013-7012; 3Present address, author for correspondence: Department of Biology, Hope College, 35 East 12th Street, Holland, Michigan 49423-9000 ([email protected]) Communicating Editor: John V. Freudenstein ABSTRACT. The chloroplast-encoded gene rbcL was sequenced in 30 genera of Commelinaceae to evaluate intergeneric relationships within the family. The Australian Cartonema was consistently placed as sister to the rest of the family. The Commelineae is monophyletic, while the monophyly of Tradescantieae is in question, due to the position of Palisota as sister to all other Tradescantieae plus Commelineae. The phylogeny supports the most recent classi®cation of the family with monophyletic tribes Tradescantieae (minus Palisota) and Commelineae, but is highly incongruent with a morphology-based phylogeny. This incongruence is attributed to convergent evolution of morphological characters associated with pollination strategies, especially those of the androecium and in¯orescence. Analysis of the combined data sets produced a phylogeny similar to the rbcL phylogeny. The combined analysis differed from the molecular one, however, in supporting the monophyly of Dichorisandrinae. The family appears to have arisen in the Old World, with one or possibly two movements to the New World in the Tradescantieae, and two (or possibly one) subsequent movements back to the Old World; the latter are required to account for the Old World distribution of Coleotrypinae and Cyanotinae, which are nested within a New World clade. -
BUTTERFLIES in Thewest Indies of the Caribbean
PO Box 9021, Wilmington, DE 19809, USA E-mail: [email protected]@focusonnature.com Phone: Toll-free in USA 1-888-721-3555 oror 302/529-1876302/529-1876 BUTTERFLIES and MOTHS in the West Indies of the Caribbean in Antigua and Barbuda the Bahamas Barbados the Cayman Islands Cuba Dominica the Dominican Republic Guadeloupe Jamaica Montserrat Puerto Rico Saint Lucia Saint Vincent the Virgin Islands and the ABC islands of Aruba, Bonaire, and Curacao Butterflies in the Caribbean exclusively in Trinidad & Tobago are not in this list. Focus On Nature Tours in the Caribbean have been in: January, February, March, April, May, July, and December. Upper right photo: a HISPANIOLAN KING, Anetia jaegeri, photographed during the FONT tour in the Dominican Republic in February 2012. The genus is nearly entirely in West Indian islands, the species is nearly restricted to Hispaniola. This list of Butterflies of the West Indies compiled by Armas Hill Among the butterfly groupings in this list, links to: Swallowtails: family PAPILIONIDAE with the genera: Battus, Papilio, Parides Whites, Yellows, Sulphurs: family PIERIDAE Mimic-whites: subfamily DISMORPHIINAE with the genus: Dismorphia Subfamily PIERINAE withwith thethe genera:genera: Ascia,Ascia, Ganyra,Ganyra, Glutophrissa,Glutophrissa, MeleteMelete Subfamily COLIADINAE with the genera: Abaeis, Anteos, Aphrissa, Eurema, Kricogonia, Nathalis, Phoebis, Pyrisitia, Zerene Gossamer Wings: family LYCAENIDAE Hairstreaks: subfamily THECLINAE with the genera: Allosmaitia, Calycopis, Chlorostrymon, Cyanophrys,