Compiling the Global Compositae Checklist in the Age of Biodiversity Informatics
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Prospects for Biological Control of Ambrosia Artemisiifolia in Europe: Learning from the Past
DOI: 10.1111/j.1365-3180.2011.00879.x Prospects for biological control of Ambrosia artemisiifolia in Europe: learning from the past EGERBER*,USCHAFFNER*,AGASSMANN*,HLHINZ*,MSEIER & HMU¨ LLER-SCHA¨ RERà *CABI Europe-Switzerland, Dele´mont, Switzerland, CABI Europe-UK, Egham, Surrey, UK, and àDepartment of Biology, Unit of Ecology & Evolution, University of Fribourg, Fribourg, Switzerland Received 18 November 2010 Revised version accepted 16 June 2011 Subject Editor: Paul Hatcher, Reading, UK management approach. Two fungal pathogens have Summary been reported to adversely impact A. artemisiifolia in the The recent invasion by Ambrosia artemisiifolia (common introduced range, but their biology makes them unsuit- ragweed) has, like no other plant, raised the awareness able for mass production and application as a myco- of invasive plants in Europe. The main concerns herbicide. In the native range of A. artemisiifolia, on the regarding this plant are that it produces a large amount other hand, a number of herbivores and pathogens of highly allergenic pollen that causes high rates of associated with this plant have a very narrow host range sensitisation among humans, but also A. artemisiifolia is and reduce pollen and seed production, the stage most increasingly becoming a major weed in agriculture. sensitive for long-term population management of this Recently, chemical and mechanical control methods winter annual. We discuss and propose a prioritisation have been developed and partially implemented in of these biological control candidates for a classical or Europe, but sustainable control strategies to mitigate inundative biological control approach against its spread into areas not yet invaded and to reduce its A. -
Barcoding the Asteraceae of Tennessee, Tribe Coreopsideae
Schilling, E.E., N. Mattson, and A. Floden. 2014. Barcoding the Asteraceae of Tennessee, tribe Coreopsideae. Phytoneuron 2014-101: 1–6. Published 20 October 2014. ISSN 2153 733X BARCODING THE ASTERACEAE OF TENNESSEE, TRIBE COREOPSIDEAE EDWARD E. SCHILLING, NICHOLAS MATTSON, AARON FLODEN Herbarium TENN Department of Ecology & Evolutionary Biology University of Tennessee Knoxville, Tennessee 37996 [email protected]; [email protected] ABSTRACT Results from barcoding studies of tribe Coreopsideae for the Tennessee flora using the nuclear ribosomal ITS marker are presented and include the first complete reports for 2 of the 20 species of the tribe that occur in the state, as well as updated reports for several others. Sequence data from the ITS region separate most of the species of Bidens in Tennessee from one another, but species of Coreopsis, especially those of sect. Coreopsis, have ITS sequences that are identical (or nearly so) to at least one congener. Comparisons of sequence data to GenBank records are complicated by apparent inaccuracies of older sequences as well as potentially misidentified samples. Broad survey of C. lanceolata from across its range showed little variability, but the ITS sequence of a morphologically distinct sample from a Florida limestone glade area was distinct in lacking a length polymorphism that was present in other samples. Tribe Coreopsideae is part of the Heliantheae alliance and earlier was often included in an expanded Heliantheae (Anderberg et al. 2007) in which it was usually treated as a subtribe (Crawford et al. 2009). The tribe shows a small burst of diversity in the southeastern USA involving Bidens and Coreopsis sect. -
Coreopsideae Daniel J
Chapter42 Coreopsideae Daniel J. Crawford, Mes! n Tadesse, Mark E. Mort, "ebecca T. Kimball and Christopher P. "andle HISTORICAL OVERVIEW AND PHYLOGENY In a cladistic analysis of morphological features of Heliantheae by Karis (1993), Coreopsidinae were reported Morphological data to be an ingroup within Heliantheae s.l. The group was A synthesis and analysis of the systematic information on represented in the analysis by Isostigma, Chrysanthellum, tribe Heliantheae was provided by Stuessy (1977a) with Cosmos, and Coreopsis. In a subsequent paper (Karis and indications of “three main evolutionary lines” within "yding 1994), the treatment of Coreopsidinae was the the tribe. He recognized ! fteen subtribes and, of these, same as the one provided above except for the follow- Coreopsidinae along with Fitchiinae, are considered ing: Diodontium, which was placed in synonymy with as constituting the third and smallest natural grouping Glossocardia by "obinson (1981), was reinstated following within the tribe. Coreopsidinae, including 31 genera, the work of Veldkamp and Kre# er (1991), who also rele- were divided into seven informal groups. Turner and gated Glossogyne and Guerreroia as synonyms of Glossocardia, Powell (1977), in the same work, proposed the new tribe but raised Glossogyne sect. Trionicinia to generic rank; Coreopsideae Turner & Powell but did not describe it. Eryngiophyllum was placed as a synonym of Chrysanthellum Their basis for the new tribe appears to be ! nding a suit- following the work of Turner (1988); Fitchia, which was able place for subtribe Jaumeinae. They suggested that the placed in Fitchiinae by "obinson (1981), was returned previously recognized genera of Jaumeinae ( Jaumea and to Coreopsidinae; Guardiola was left as an unassigned Venegasia) could be related to Coreopsidinae or to some Heliantheae; Guizotia and Staurochlamys were placed in members of Senecioneae. -
Sfblake and Tithonia Diversifolia
Prospective agents for the biological control of Tithonia rotundifolia (Mill.) S.F.Blake and Tithonia diversifolia (Hemsl.) A.Gray (Asteraceae) in South Africa D.O. Simelane1*, K.V. Mawela1 & A. Fourie2 1Agricultural Research Council-Plant Protection Research Institute, Private Bag X134, Queenswood, 0121 South Africa 2Agricultural Research Council-Plant Protection Research Institute, Private Bag X5017 Stellenbosch, 7599 South Africa Starting in 2007, two weedy sunflower species, Tithonia rotundifolia (Mill.) S.F.Blake and Tithonia diversifolia (Hemsl.) A.Gray (Asteraceae: Heliantheae), were targeted for biological control in South Africa. Surveys conducted in their native range (Mexico) revealed that there were five potential biological control agents for T.rotundifolia, and three of these are currently undergoing host-specificity and performance evaluations in South Africa. Two leaf-feeding beetles, Zygogramma signatipennis (Stål) and Zygogramma piceicollis (Stål) (Coleoptera: Chrysomelidae), are the most promising biological control agents for T. rotundifolia: prelimi- nary host-specificity trials suggest that they are adequately host-specific. The stem-boring beetle, Lixus fimbriolatus Boheman (Coleoptera: Curculionidae), is also highly damaging to T. rotundifolia, but its host range is yet to be determined. Two other stem-boring beetles, Canidia mexicana Thomson (Coleoptera: Cerambycidae) and Rhodobaenus auctus Chevrolat (Coleoptera: Curculionidae), have also been recorded on T. rotundifolia, and these will be considered for further testing if L. fimbriolatus is found to be unsuitable for release in South Africa. Only two insect species were imported as candidate agents on T. diversifolia, the leaf-feeding butterfly Chlosyne sp. (Lepidoptera: Nymphalidae), and an unidentified stem-boring moth (Lepidoptera: Tortricidae): the latter was tested in quarantine but rejected because it attacked several sunflower cultivars. -
Chromosome Numbers in Compositae, XII: Heliantheae
SMITHSONIAN CONTRIBUTIONS TO BOTANY 0 NCTMBER 52 Chromosome Numbers in Compositae, XII: Heliantheae Harold Robinson, A. Michael Powell, Robert M. King, andJames F. Weedin SMITHSONIAN INSTITUTION PRESS City of Washington 1981 ABSTRACT Robinson, Harold, A. Michael Powell, Robert M. King, and James F. Weedin. Chromosome Numbers in Compositae, XII: Heliantheae. Smithsonian Contri- butions to Botany, number 52, 28 pages, 3 tables, 1981.-Chromosome reports are provided for 145 populations, including first reports for 33 species and three genera, Garcilassa, Riencourtia, and Helianthopsis. Chromosome numbers are arranged according to Robinson’s recently broadened concept of the Heliantheae, with citations for 212 of the ca. 265 genera and 32 of the 35 subtribes. Diverse elements, including the Ambrosieae, typical Heliantheae, most Helenieae, the Tegeteae, and genera such as Arnica from the Senecioneae, are seen to share a specialized cytological history involving polyploid ancestry. The authors disagree with one another regarding the point at which such polyploidy occurred and on whether subtribes lacking higher numbers, such as the Galinsoginae, share the polyploid ancestry. Numerous examples of aneuploid decrease, secondary polyploidy, and some secondary aneuploid decreases are cited. The Marshalliinae are considered remote from other subtribes and close to the Inuleae. Evidence from related tribes favors an ultimate base of X = 10 for the Heliantheae and at least the subfamily As teroideae. OFFICIALPUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution’s annual report, Smithsonian Year. SERIESCOVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllumjaponicum Siebold and Zuccarini. Library of Congress Cataloging in Publication Data Main entry under title: Chromosome numbers in Compositae, XII. -
2003 Vol. 6, Issue 3
Department of Systematic Biology - Botany & the U.S. National Herbarium The Plant Press New Series - Vol. 6 - No. 3 July-September 2003 Botany Profile A Colossus of the Compositae By Robert DeFilipps e has named or described 2,800 employment in Washington, D.C., as labored. For example, just a glance at the new species and subtribes, a Associate Curator of lower plants (1962- South American journal Ernstia will figure equal to one-quarter the 1964) at the Smithsonian Institution, and reveal that in the Tribe Eupatorieae as Hnumber of flowering plants named by Carl successively as Associate Curator (1964- represented in Venezuela with 35 genera, Linnaeus, the originator of binomial 1971) and Curator of Botany from 1971 to Robinson (with co-worker King) has nomenclature, and the equivalent of the present. named at least one species in 27 of the approximately one-tenth the total number An incisive, perennially questing mind genera (V. Badillo, vol. 11. 2001). Similarly, of species in his chosen family of has allowed him to delve, often with new country records of species named expertise, the immense Compositae collaborators, into the taxonomy of groups by Robinson seem to appear everywhere, (Asteraceae). His singular contribution of as diverse as the bryophytes of many such as in Peru, from which three species more than 650 publications advancing the regions; green algae (a new genus Struve- of Eupatorieae previously regarded as taxonomy of the composites, as well as of opsis from Diego Garcia, Indian Ocean, endemic to Ecuador have recently been the bryophytes (mosses and liverworts), with Charlie Rhyne); the Brazilian members reported (Cronquistianthus leucophyl- the insect family Dolichopodidae, and of the dicot family Hippocrateaceae, with lus, Crossothamnus gentryi, Ophryos- many other groups, reflect both the Lyman Smith; scanning electron micros- porus integrifolia; H. -
Heliantheae of Iowa. I
Proceedings of the Iowa Academy of Science Volume 36 Annual Issue Article 27 1929 Heliantheae of Iowa. I M. Rae Johns Let us know how access to this document benefits ouy Copyright ©1929 Iowa Academy of Science, Inc. Follow this and additional works at: https://scholarworks.uni.edu/pias Recommended Citation Johns, M. Rae (1929) "Heliantheae of Iowa. I," Proceedings of the Iowa Academy of Science, 36(1), 147-184. Available at: https://scholarworks.uni.edu/pias/vol36/iss1/27 This Research is brought to you for free and open access by the Iowa Academy of Science at UNI ScholarWorks. It has been accepted for inclusion in Proceedings of the Iowa Academy of Science by an authorized editor of UNI ScholarWorks. For more information, please contact [email protected]. Johns: Heliantheae of Iowa. I HELIANTHEAE OF row A. I lVI. RAE JOIINS Heliantheae is one of the nine tribes of the Family Compositae. It is believed to have originated in South America soon after the appearance of the Family and may be regarded as the oldest and most primitive of the tribes. The near approach to the earliest composite form is said to be retained in the more foliaceous outer invol ucral bracts, the more normally developed and more firmly attached paleae subtending the disk flowers, the 0 less transformed calyx-limb of persistent teeth or aristae directly continuous with the ribs of the ovary, and in some genera, the less firmly united or nearly free anthers. (Bentham, 1873.) The characters which today distinguish it from the other tribes are: Receptacle: chaffy, depressed, horizontal, convex, or columnar. -
Crop Reports
CROP REPORTS Classification, origin, and environmental requirements Stokes aster initially was described and classified as Carthamus laevis by J. Hill in 1769. The genus Stokesia was Crop described by L’Héritier de Brutelle (1788), who proposed that the type specimen used by J. Hill to describe C. laevis should be selected as the type Reports specimen for the new genus Stokesia. L’Héritier de Brutelle (1788) also re- ferred to S. cyanea but failed to describe the species; therefore, the name S. cyanea is illegitimate. The final authority re- Stokes Aster (12,13-epoxy-cis-9-octadecenoic) garding the nomenclature of stokes as- acid, a fatty acid that is converted to ter is Greene (1893), who stated that epoxy oil products for use in the manu- the proper binomial for the specimen 1 facture of plastics and adhesives called C. laevis by J. Hill and S. cyanea by Lyn A. Gettys and (Campbell, 1981; Kleiman, 1990). Oil L’Héritier de Brutelle should be Stokesia Dennis J. Werner2 content in seeds can be as high as 40%, laevis. The genus is named for the En- with about 70% of this oil being vernolic glish botanist Jonathan Stokes (1755- acid (Gunn and White, 1974). In the 1831). 1980s, the annual global market for Stokesia is one of about 950 genera ADDITIONAL INDEX WORDS. Stokesia seed-derived epoxy oils was between laevis, Asteraceae, Vernonieae, oilseed in the aster family (Asteraceae Dumont) crop, native plant, propagation 45 and 90 billion tons (40.8 and 81.6 and is monotypic, with S. laevis the only × 109 t) per year (Campbell, 1981; species (Bailey, 1949; Els, 1994; Greene, Princen, 1983). -
Compositae: Cichorioideae
Systematic Botany (2011), 36(1): pp. 191–208 © Copyright 2011 by the American Society of Plant Taxonomists DOI 10.1600/036364411X553270 A Monograph of the Small Tribe Platycarpheae (Compositae: Cichorioideae) V. A. Funk , 1 , 3 and Marinda Koekemoer 2 1 U.S. National Herbarium, National Museum of Natural History, Smithsonian Institution, Washington, DC 20013-7012, U.S.A. 2 South African National Biodiversity Institute, Private Bag X101, Pretoria 0001, South Africa 3 Author for correspondence ( [email protected] ) Communicating Editor: Victoria Sosa Abstract— The tribe Platycarpheae has three species; they are found from South Africa, to Namibia and Botswana. The three species have traditionally been placed in a single genus but were recently divided into two ( Platycarpha and Platycarphella ). All have ‘secondary heads’ formed by tightly clustered heads on the crown of the rhizome. The three species are easily separated from one another based on characters such as leaf type, head size, style and corolla length, and pollen type. Morphological and molecular data support Platycarpheae as a monophyl- etic group within the subfamily Cichorioideae but no firm sister-group relationship has been determined. The three species form a monophyl- etic group on a long branch: Platycarphella carlinoides and Platycarphella parvifolia share more characters and are sister-taxa; Platycarpha glomerata has the largest number of unique features and is the sister taxon to the other two species. The distributions and flowering times of the three spe- cies are different. Platycarphella carlinoides is the most widespread of the species and grows in northwestern South Africa, the central highlands of Namibia, and southwestern Botswana; its peak flowering time is March-July. -
Asteraceae: Astereae), a New Genus and Species from Northern Chile
Phytotaxa 177 (5): 280–290 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.177.5.4 Kieslingia chilensis (Asteraceae: Astereae), a new genus and species from northern Chile PATRICIO SALDIVIA1, LUIS FAÚNDEZ1,2, ALICIA MARTICORENA3 & JOSÉ L. PANERO4 1Biota, Gestión y Consultorías Ambientales Ltda. Av. Miguel Claro 1224, Providencia, Santiago, Chile; email: [email protected], [email protected] 2Laboratorio de Morfología y Taxonomía Vegetal, Facultad de Ciencias Agronómicas, Universidad de Chile. Av. Santa Rosa 11315, Casilla 1004, La Pintana, Santiago, Chile 3Departamento de Botánica, Universidad de Concepción, Casilla 160-C, Concepción, Chile; email: [email protected] 4Department of Integrative Biology, 1 University Station C 0930, The University of Texas, Austin, TX 78712, USA; email: panero@ utexas.edu Abstract Kieslingia chilensis, a new genus and species of tribe Astereae (Asteraceae) from northern Chile restricted to the Huasco river basin of the Andes pre-mountain Range in the Atacama region is described and illustrated. The combination of its diagnostic characters including discoid homogamous capitula, alveolate epaleate receptacles, and deeply trifid leaves, is not found in any other species of South American Astereae. An ITS phylogenic analysis placed Kieslingia chilensis within subtribe Hinterhuberinae, and sister to the genus Guynesomia, also endemic to Chile. The morphological characteristics of Kieslingia chilensis are compared and contrasted to sister taxa as identified by the molecular phylogenetic studies and the environmental features of the area where the species is found are discussed. A key to distinguish Kieslingia from other Astereae genera of northern Chile is given. -
A Phylogenetic Analysis of the Inflated Fruiting Calyx in the Ph
bioRxiv preprint doi: https://doi.org/10.1101/425991; this version posted September 25, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Original article 2 3 Repeated evolution of a morphological novelty: a phylogenetic analysis of the inflated 4 fruiting calyx in the Physalideae tribe (Solanaceae) 5 6 Rocío Deanna1,2,3,4, Maximilien D. Larter2, Gloria E. Barboza1,2,3, Stacey D. Smith2 7 1Instituto Multidisciplinario de Biología Vegetal, IMBIV (CONICET-UNC). CC 495, 8 Córdoba 5000, Argentina. 9 2Department of Ecology and Evolutionary Biology, University of Colorado, Boulder, 10 Colorado 80305, United States of America. 11 3Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Químicas (FCQ, UNC). 12 Medina Allende s.n., Córdoba 5000, Argentina. 13 4Corresponding author. E-mail: [email protected] 14 15 Manuscript received __ _____; revision accepted ____ ___. 16 17 Running title: Fruiting calyx evolution in Physalideae 18 1 bioRxiv preprint doi: https://doi.org/10.1101/425991; this version posted September 25, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 19 PREMISE OF THE STUDY: The evolution of novel fruit morphologies has been integral 20 to the success of angiosperms. The inflated fruiting calyx, in which the balloon-like calyx 21 swells to completely surround the fruit, has evolved repeatedly across angiosperms and is 22 postulated to aid in protection and dispersal. -
Towards a Phylogenetic Classification of Lychnophorinae (Asteraceae: Vernonieae)
Benoît Francis Patrice Loeuille Towards a phylogenetic classification of Lychnophorinae (Asteraceae: Vernonieae) São Paulo, 2011 Benoît Francis Patrice Loeuille Towards a phylogenetic classification of Lychnophorinae (Asteraceae: Vernonieae) Tese apresentada ao Instituto de Biociências da Universidade de São Paulo, para a obtenção de Título de Doutor em Ciências, na Área de Botânica. Orientador: José Rubens Pirani São Paulo, 2011 Loeuille, Benoît Towards a phylogenetic classification of Lychnophorinae (Asteraceae: Vernonieae) Número de paginas: 432 Tese (Doutorado) - Instituto de Biociências da Universidade de São Paulo. Departamento de Botânica. 1. Compositae 2. Sistemática 3. Filogenia I. Universidade de São Paulo. Instituto de Biociências. Departamento de Botânica. Comissão Julgadora: Prof(a). Dr(a). Prof(a). Dr(a). Prof(a). Dr(a). Prof(a). Dr(a). Prof. Dr. José Rubens Pirani Orientador To my grandfather, who made me discover the joy of the vegetal world. Chacun sa chimère Sous un grand ciel gris, dans une grande plaine poudreuse, sans chemins, sans gazon, sans un chardon, sans une ortie, je rencontrai plusieurs hommes qui marchaient courbés. Chacun d’eux portait sur son dos une énorme Chimère, aussi lourde qu’un sac de farine ou de charbon, ou le fourniment d’un fantassin romain. Mais la monstrueuse bête n’était pas un poids inerte; au contraire, elle enveloppait et opprimait l’homme de ses muscles élastiques et puissants; elle s’agrafait avec ses deux vastes griffes à la poitrine de sa monture et sa tête fabuleuse surmontait le front de l’homme, comme un de ces casques horribles par lesquels les anciens guerriers espéraient ajouter à la terreur de l’ennemi.