Variation in Plant Defense Traits and Population Genetics Within A
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Polyploidy and the Evolutionary History of Cotton
POLYPLOIDY AND THE EVOLUTIONARY HISTORY OF COTTON Jonathan F. Wendel1 and Richard C. Cronn2 1Department of Botany, Iowa State University, Ames, Iowa 50011, USA 2Pacific Northwest Research Station, USDA Forest Service, 3200 SW Jefferson Way, Corvallis, Oregon 97331, USA I. Introduction II. Taxonomic, Cytogenetic, and Phylogenetic Framework A. Origin and Diversification of the Gossypieae, the Cotton Tribe B. Emergence and Diversification of the Genus Gossypium C. Chromosomal Evolution and the Origin of the Polyploids D. Phylogenetic Relationships and the Temporal Scale of Divergence III. Speciation Mechanisms A. A Fondness for Trans-oceanic Voyages B. A Propensity for Interspecific Gene Exchange IV. Origin of the Allopolyploids A. Time of Formation B. Parentage of the Allopolyploids V. Polyploid Evolution A. Repeated Cycles of Genome Duplication B. Chromosomal Stabilization C. Increased Recombination in Polyploid Gossypium D. A Diverse Array of Genic and Genomic Interactions E. Differential Evolution of Cohabiting Genomes VI. Ecological Consequences of Polyploidization VII. Polyploidy and Fiber VIII. Concluding Remarks References The cotton genus (Gossypium ) includes approximately 50 species distributed in arid to semi-arid regions of the tropic and subtropics. Included are four species that have independently been domesticated for their fiber, two each in Africa–Asia and the Americas. Gossypium species exhibit extraordinary morphological variation, ranging from herbaceous perennials to small trees with a diverse array of reproductive and vegetative -
Designations for Individual Genomes and Chromosomes in Gossypium WANG Kunbo1*, WENDEL Jonathan F.2 and HUA Jinping3
WANG et al. Journal of Cotton Research (2018) 1:3 Journal of Cotton Research https://doi.org/10.1186/s42397-018-0002-1 REVIEW Open Access Designations for individual genomes and chromosomes in Gossypium WANG Kunbo1*, WENDEL Jonathan F.2 and HUA Jinping3 Abstract Gossypium, as the one of the biggest genera, the most diversity, and the highest economic value in field crops, is assuming an increasingly important role in studies on plant taxonomy, polyploidization, phylogeny, cytogenetics, and genomics. Here we update and provide a brief summary of the emerging picture of species relationships and diversification, and a set of the designations for individual genomes and chromosomes in Gossypium. This cytogenetic and genomic nomenclature will facilitate comparative studies worldwide, which range from basic taxonomic exploration to breeding and germplasm introgression. Keywords: Nomenclature, Individual genome, Individual chromosome, Gossypium Because of its diversity and economic significance, the cotton diversity, from consisting of only a single species (F gen- genus (Gossypium) has been subjected to decades of taxo- ome) to larger genome groups containing more than a nomic, cytogenetic, and phylogenetic analyses. Accordingly, dozen species each (D, K). The important allopolyploid a reasonably well-documented phylogenetic and taxonomic clade, which includes G. hirsutum and G. barbadense,con- understanding has developed, as recently summarized tains 7 species, including two described only in the last (Wendel and Grover 2015). Work published since that time 10 years (G.ekmanianum,G.stephensii) (Krapovickas and also supports the emerging picture of species relationships Seijo 2008; Gallagher et al. 2017). and diversification (Grover et al. 2015a, 2015b;Chenetal. Many Gossypium species are taxonomically well- 2016; Gallagher et al. -
Largest Species, Citheronia Splendens Sinaloensis (Hoffmann) and Ea Cles Oslari Rothschild, Is Poorly Known
Journal of the Lepidopterists' Society 40(4), 1986, 264- 270 BIOLOGY AND IMMATURE STAGES OF CITHERONIA SPLENDENS SINALOENSIS AND EACLES OSLARI IN ARIZONA (SATURNIIDAE) PAUL M. TUSKES 7900 Cambridge IllD, Houston, Texas 77054 ABSTRACT. Citheronia splendens sinaloensis and Eacles oslari occur in Cochise, Pima, and Santa Cruz counties in southern Arizona. Both species have one generation per year. The flight season of E. oslari extends from early June to mid-August, and the larval host plants include Quercus species. The flight season of C. splendens extends from July to mid-August, and the larval host plants include wild cotton, manzanita, and New Mexico evergreen sumac. The immature stages are described for the first time. The citheroniine fauna of Arizona is unique in that all seven species are primarily of Mexican origin (Tuskes 1985). The biology of the two largest species, Citheronia splendens sinaloensis (Hoffmann) and Ea cles oslari Rothschild, is poorly known. Ferguson (1971) illustrated the adults, summarized existing information, and indicated that their im mature stages were undescribed. The purpose of this paper is to de scribe the immature stages of both species and to present additional biological and distributional information. Citheronia splendens sinaloensis (Figs. 1-4) Citheronia splendens sinaloensis is the only member of the genus presently known to occur in Arizona. Citheronia mexicana G. & R. occurs just south of Arizona, in Sonora, Mexico. Although reported from Arizona before the turn of the century, there are no recent United States records. Citheronia regalis (F.) and C. sepulcralis (Druce) are common in the eastern or central United States but do not occur farther west than central Texas. -
Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America Adam P
Entomology Publications Entomology 2012 Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America Adam P. Kuester Iowa State University, [email protected] Robert W. Jones Centro Universitario Queretaro Thomas W. Sappington Iowa State University, [email protected] Kyung Seok Kim Seoul National University NFoorllomwa nthi Bs. Bandarr additional works at: https://lib.dr.iastate.edu/ent_pubs UnitPeda Srta oftes theDepaArtmgricenulturt of Agalric Sulctuierence Commons, Agriculture Commons, Agronomy and Crop Sciences Commons, Biology Commons, Entomology Commons, Genetics Commons, and the See next page for additional authors Systems Biology Commons The ompc lete bibliographic information for this item can be found at https://lib.dr.iastate.edu/ ent_pubs/198. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Entomology at Iowa State University Digital Repository. It has been accepted for inclusion in Entomology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Population Structure and Genetic Diversity of the Boll Weevil (Coleoptera: Curculionidae) on Gossypium in North America Abstract Although the boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a devastating pest in the United States and Mexico, its population structure and genetic diversity -
Evolutionary Consequences of Dioecy in Angiosperms: the Effects of Breeding System on Speciation and Extinction Rates
EVOLUTIONARY CONSEQUENCES OF DIOECY IN ANGIOSPERMS: THE EFFECTS OF BREEDING SYSTEM ON SPECIATION AND EXTINCTION RATES by JANA C. HEILBUTH B.Sc, Simon Fraser University, 1996 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY in THE FACULTY OF GRADUATE STUDIES (Department of Zoology) We accept this thesis as conforming to the required standard THE UNIVERSITY OF BRITISH COLUMBIA July 2001 © Jana Heilbuth, 2001 Wednesday, April 25, 2001 UBC Special Collections - Thesis Authorisation Form Page: 1 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. The University of British Columbia Vancouver, Canada http://www.library.ubc.ca/spcoll/thesauth.html ABSTRACT Dioecy, the breeding system with male and female function on separate individuals, may affect the ability of a lineage to avoid extinction or speciate. Dioecy is a rare breeding system among the angiosperms (approximately 6% of all flowering plants) while hermaphroditism (having male and female function present within each flower) is predominant. Dioecious angiosperms may be rare because the transitions to dioecy have been recent or because dioecious angiosperms experience decreased diversification rates (speciation minus extinction) compared to plants with other breeding systems. -
Review and Advances in Style Curvature for the Malvaceae Cheng-Jiang Ruan*
® International Journal of Plant Developmental Biology ©2010 Global Science Books Review and Advances in Style Curvature for the Malvaceae Cheng-Jiang Ruan* Key Laboratory of Biotechnology & Bio-Resources Utilization, Dalian Nationalities University, Dalian City, Liaoning 116600, China Correspondence : * [email protected] ABSTRACT The flowers of the Malvaceae with varying levels of herkogamy via style curvature have long intrigued evolutionary botanists. This review covers the flower opening process, approach herkogamy, style curvature and character evolution based on molecular phylogenetic trees, adaptive significances of style curvature and the mating system in some portions of the genera in this family. Hermaphroditic flowers of some species have showy petals and pollen and nectar rewards to pollinators. Approach herkogamy, in which stigmas are located on the top of a monadelphous stamen, has evolved as a mechanism to reduce the frequency of intra-floral self-pollination or the interference between male-female organs. Protandrous or monochogamous flowers in the fields open at about 5-7 days and 1-2 days respectively, and pollination is conducted by insects and birds. Interestingly, un-pollinated styles in some species curve when pollination fails. According to our observations and published or internet data, this curvature occurs in 23 species distributed in eight genera of four tribes (Malvavisceae, Ureneae, Hibisceae, Malveae) and appears to have evolved at least eight times. A shift to use style curvature is associated with a shift to annual or perennial herbs, and an unpredictable pollinator environment is likely an important trigger for this evolution. The adaptive significances of style curvature in the Malvaceae include delayed selfing, promotion of outcrossing or reduction in intrafloral male-female interference, sometimes two or three of which simultaneously occur in style curvature of one species (e.g., Kosteletzkya virginica). -
Explorations in Ethnobiology: the Legacy of Amadeo Rea
Explorations in Ethnobiology: The Legacy of Amadeo Rea Edited by Marsha Quinlan and Dana Lepofsky Explorations in Ethnobiology: The Legacy of Amadeo Rea Edited by Marsha Quinlan and Dana Lepofsky Copyright 2013 ISBN-10: 0988733013 ISBN-13: 978-0-9887330-1-5 Library of Congress Control Number: 2012956081 Society of Ethnobiology Department of Geography University of North Texas 1155 Union Circle #305279 Denton, TX 76203-5017 Cover photo: Amadeo Rea discussing bird taxonomy with Mountain Pima Griselda Coronado Galaviz of El Encinal, Sonora, Mexico, July 2001. Photograph by Dr. Robert L. Nagell, used with permission. Contents Preface to Explorations in Ethnobiology: The Legacy of Amadeo Rea . i Dana Lepofsky and Marsha Quinlan 1 . Diversity and its Destruction: Comments on the Chapters . .1 Amadeo M. Rea 2 . Amadeo M . Rea and Ethnobiology in Arizona: Biography of Influences and Early Contributions of a Pioneering Ethnobiologist . .11 R. Roy Johnson and Kenneth J. Kingsley 3 . Ten Principles of Ethnobiology: An Interview with Amadeo Rea . .44 Dana Lepofsky and Kevin Feeney 4 . What Shapes Cognition? Traditional Sciences and Modern International Science . .60 E.N. Anderson 5 . Pre-Columbian Agaves: Living Plants Linking an Ancient Past in Arizona . .101 Wendy C. Hodgson 6 . The Paleobiolinguistics of Domesticated Squash (Cucurbita spp .) . .132 Cecil H. Brown, Eike Luedeling, Søren Wichmann, and Patience Epps 7 . The Wild, the Domesticated, and the Coyote-Tainted: The Trickster and the Tricked in Hunter-Gatherer versus Farmer Folklore . .162 Gary Paul Nabhan 8 . “Dog” as Life-Form . .178 Eugene S. Hunn 9 . The Kasaga’yu: An Ethno-Ornithology of the Cattail-Eater Northern Paiute People of Western Nevada . -
Conservation Status of the Genus Hampea (Malvaceae: Gossypieae) in Mexico
Ecological restauration Conservation status of the genus Hampea (Malvaceae: Gossypieae) in Mexico ROBERT W. JONES*, M. FERNANDA CRUZ-TORRES, CARLOS LÓPEZ-GONZÁLEZ, AND MAGDALENA A. DUARTE-FERNÁNDEZ Botanical Sciences 96 (3): 426-442, 2018 DOI: 10.17129/botsci.1857 Abstract Received: Background. The genus Hampea (Malvaceae: Gossypieae) has 21 reported species and occurs in Mexico, August 28th, 2017 Central America and Colombia. Mexico has eleven species, of which seven are endemic. Hampea is of Accepted: special conservation interest because its members are wild relatives of cultivated cotton and several spe- April 26th, 2018 cies are apparently threatened by anthropogenic activities. Associated editor: Questions. What is the conservation status of species of Hampea in Mexico? Salvador Arias Study site and years of study. Observations were made in the field during 1991-1995, 2012 and 2016 in southern Mexico. Specimen data was obtained from the CONABIO data base and from national and international herbaria from 2014-2016. Methods. The conservation status of species of Hampea in Mexico was evaluated using criteria given in the Methods of the Evaluation of Risk of Extinction of Plants (MER-Plantas) (NOM-059-SEMARNAT- 2010). The potential distribution was calculated using Maximum Entropy Algorithm and biological data for species were obtained from literature and field observations. Results. Seven species of the genus Hampea were considered to be in a category of risk under the MER- Plantas criteria. Hampea montebellensis, H. breedlovei, and H. longipes were categorized as “at Risk of Extinction,” (En Peligro de Extinción ); H. latifolia was categorized as “Threatened” (Amenazada) and H. stipitata, H. mexicana, and H. -
Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site
Powell, Schmidt, Halvorson In Cooperation with the University of Arizona, School of Natural Resources Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site Plant and Vertebrate Vascular U.S. Geological Survey Southwest Biological Science Center 2255 N. Gemini Drive Flagstaff, AZ 86001 Open-File Report 20 Southwest Biological Science Center Open-File Report 2005-1167 February 2007 05-1 U.S. Department of the Interior 167 U.S. Geological Survey National Park Service In cooperation with the University of Arizona, School of Natural Resources Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site By Brian F. Powell, Cecilia A. Schmidt , and William L. Halvorson Open-File Report 2005-1167 December 2006 USGS Southwest Biological Science Center Sonoran Desert Research Station University of Arizona U.S. Department of the Interior School of Natural Resources U.S. Geological Survey 125 Biological Sciences East National Park Service Tucson, Arizona 85721 U.S. Department of the Interior DIRK KEMPTHORNE, Secretary U.S. Geological Survey Mark Myers, Director U.S. Geological Survey, Reston, Virginia: 2006 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod Telephone: 1-888-ASK-USGS For more information on the USGS-the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web:http://www.usgs.gov Telephone: 1-888-ASK-USGS Suggested Citation Powell, B. F, C. A. Schmidt, and W. L. Halvorson. 2006. Vascular Plant and Vertebrate Inventory of Fort Bowie National Historic Site. -
U5b5c4e4 OA.Pdf
Downloaded from genome.cshlp.org on September 9, 2019 - Published by Cold Spring Harbor Laboratory Press Letter Differential lineage-specific amplification of transposable elements is responsible for genome size variation in Gossypium Jennifer S. Hawkins,1 HyeRan Kim,2 John D. Nason,1 Rod A. Wing,2 and Jonathan F. Wendel1,3 1Iowa State University, Department of Ecology, Evolution and Organismal Biology, Ames, Iowa 50011, USA; 2University of Arizona, Department of Plant Sciences, Arizona Genomics Institute, Tucson, Arizona 85721, USA The DNA content of eukaryotic nuclei (C-value) varies ∼200,000-fold, but there is only a ∼20-fold variation in the number of protein-coding genes. Hence, most C-value variation is ascribed to the repetitive fraction, although little is known about the evolutionary dynamics of the specific components that lead to genome size variation. To understand the modes and mechanisms that underlie variation in genome composition, we generated sequence data from whole genome shotgun (WGS) libraries for three representative diploid (n = 13) members of Gossypium that vary in genome size from 880 to 2460 Mb (1C) and from a phylogenetic outgroup, Gossypioides kirkii, with an estimated genome size of 588 Mb. Copy number estimates including all dispersed repetitive sequences indicate that 40%–65% of each genome is composed of transposable elements. Inspection of individual sequence types revealed differential, lineage-specific expansion of various families of transposable elements among the different plant lineages. Copia-like retrotransposable element sequences have differentially accumulated in the Gossypium species with the smallest genome, G. raimondii, while gypsy-like sequences have proliferated in the lineages with larger genomes. -
November 2018 Serving the Mountain Empire Communities of Canelo, Elgin, Patagonia and Sonoita Vol
NOVEMBER 2018 SERVING THE MOUNTAIN EMPIRE COMMUNITIES OF CANELO, ELGIN, PATAGONIA AND SONOITA VOL. 8, ISSUE 9 By Aisha Sander The 30th Patagonia Fall Festival faced some unforeseen A Rainy Fall Festival challenges due to unfavorable weather conditions as well as discontent expressed by some of the participants with changes in the structure of the event. This year the event was outsourced to a professional event management company, South- ern Arizona Arts & Cultural Alliance (SAACA). For the past 29 years the Fall festival has been man- aged and put on by locals, volunteers and most recently by Sky Island Tourist Association (SITA). A SAACA representative said they were very excited to work at the Fall Festival, and that it was a perfect fit, as they specialize in creating art experiences. Their goals were to keep the artists happy and to give them opportunities for business and marketing. They also hoped to provide overall support to the town and the business community. As an organization that has primarily worked in the urban areas of Arizona, SAACA was excited to branch out to a rural area and merge the best of both worlds for the Fall Festival. SAACA intends to reinvest the funds generated from the festival by giving a portion to the town and retaining a portion for their own arts programming around Arizona. There were some significant changes with the new management. The first change was to remove Photo by Aisha Sander Friday as a full day for vendors, limiting it to a com- Two young boys enjoy the chance to play in the mud puddles in the Patagonia Park at the Fall Festival munity kick-off celebration. -
Downloaded from Genbank on That Full Plastid Genomes Are Not Sufficient to Reject Al- February 28, 2012
Ruhfel et al. BMC Evolutionary Biology 2014, 14:23 http://www.biomedcentral.com/1471-2148/14/23 RESEARCH ARTICLE Open Access From algae to angiosperms–inferring the phylogeny of green plants (Viridiplantae) from 360 plastid genomes Brad R Ruhfel1*, Matthew A Gitzendanner2,3,4, Pamela S Soltis3,4, Douglas E Soltis2,3,4 and J Gordon Burleigh2,4 Abstract Background: Next-generation sequencing has provided a wealth of plastid genome sequence data from an increasingly diverse set of green plants (Viridiplantae). Although these data have helped resolve the phylogeny of numerous clades (e.g., green algae, angiosperms, and gymnosperms), their utility for inferring relationships across all green plants is uncertain. Viridiplantae originated 700-1500 million years ago and may comprise as many as 500,000 species. This clade represents a major source of photosynthetic carbon and contains an immense diversity of life forms, including some of the smallest and largest eukaryotes. Here we explore the limits and challenges of inferring a comprehensive green plant phylogeny from available complete or nearly complete plastid genome sequence data. Results: We assembled protein-coding sequence data for 78 genes from 360 diverse green plant taxa with complete or nearly complete plastid genome sequences available from GenBank. Phylogenetic analyses of the plastid data recovered well-supported backbone relationships and strong support for relationships that were not observed in previous analyses of major subclades within Viridiplantae. However, there also is evidence of systematic error in some analyses. In several instances we obtained strongly supported but conflicting topologies from analyses of nucleotides versus amino acid characters, and the considerable variation in GC content among lineages and within single genomes affected the phylogenetic placement of several taxa.