Guidelines on Biological Nomenclature Brazil Edition
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JVP 26(3) September 2006—ABSTRACTS
Neoceti Symposium, Saturday 8:45 acid-prepared osteolepiforms Medoevia and Gogonasus has offered strong support for BODY SIZE AND CRYPTIC TROPHIC SEPARATION OF GENERALIZED Jarvik’s interpretation, but Eusthenopteron itself has not been reexamined in detail. PIERCE-FEEDING CETACEANS: THE ROLE OF FEEDING DIVERSITY DUR- Uncertainty has persisted about the relationship between the large endoskeletal “fenestra ING THE RISE OF THE NEOCETI endochoanalis” and the apparently much smaller choana, and about the occlusion of upper ADAM, Peter, Univ. of California, Los Angeles, Los Angeles, CA; JETT, Kristin, Univ. of and lower jaw fangs relative to the choana. California, Davis, Davis, CA; OLSON, Joshua, Univ. of California, Los Angeles, Los A CT scan investigation of a large skull of Eusthenopteron, carried out in collaboration Angeles, CA with University of Texas and Parc de Miguasha, offers an opportunity to image and digital- Marine mammals with homodont dentition and relatively little specialization of the feeding ly “dissect” a complete three-dimensional snout region. We find that a choana is indeed apparatus are often categorized as generalist eaters of squid and fish. However, analyses of present, somewhat narrower but otherwise similar to that described by Jarvik. It does not many modern ecosystems reveal the importance of body size in determining trophic parti- receive the anterior coronoid fang, which bites mesial to the edge of the dermopalatine and tioning and diversity among predators. We established relationships between body sizes of is received by a pit in that bone. The fenestra endochoanalis is partly floored by the vomer extant cetaceans and their prey in order to infer prey size and potential trophic separation of and the dermopalatine, restricting the choana to the lateral part of the fenestra. -
Mnemonic Memory Taxonomy
MNEMONIC MEMORY TAXONOMY Overview: In this lesson, students determine proper classification of organisms according to taxonomic levels, explore characteristics that determine classification, and create methods to recall ordered taxonomic terminology. Objectives: The student will: • describe the use and function of a taxonomy, specifically to order and classify living organisms; and • identify and list taxonomic levels of biological classification. Targeted Alaska Grade Level Expectations: Science [7] SC2.2 The student demonstrates an understanding of the structure, function, behavior, development, life cycles, and diversity of living organisms by identifying the seven levels of classification of organisms. [7] SA1.1 The student demonstrates an understanding of the processes of science by asking questions, predicting, observing, describing, measuring, classifying, makign generalizations, inferring, and communicating. Vocabulary: animalia— one of six kingdoms, including most living things that are able to move and digest food internally plantae –one of six kingdoms, including living things that generally manufacture their own food through the use of photosynthesis fungi – one of six kingdoms, mostly living things that are nonmobile and assist in the decomposition process, including yeasts, molds, and mushrooms binomial nomenclature – a scientific naming system that gives a unique name (“scientific name”) to each species, using organisms’ genus and species as its two parts (e.g., “Homo sapiens” for humans) class – a taxonomic rank below -
A NEW SUBGENUS of the GENUS Sabei;Hes (DIPTERA: CULICIDAE) L
AUGUST1991 1 A NEW SUBGENUS OF THE GENUS sABEI;HEs (DIPTERA: CULICIDAE) l RALPH E. HARBACH~ Walter Reed Biosystematics Unit, Department of Entomology, Walter Reed Army Institute of Research, Washington, DC 20307-5100. ABSTRACT. A new subgenus, Peytonulus, of the genus Sabethes Robineau-Desvoidy is estab- lished for seven species previously included in the subgenus Sabethinus Lutz. The subgenus is contrasted with the other subgenera of Sabethes and the type species is illustrated. INTRODUCTION The new subgenus is uniquely characterized by several autapomorphic features, the highly Because mosquitoes of the genus Sabethes modified larval seta l-VII and its missing pupal Robineau-Desvoidy are known to harbor and homolog being the most notable and conspicu- transmit arboviruses (Galindo et al. 1959, Mat- ous. Based on these distinctive features, the tingly et al. 1973), information on their identifi- subgenus PeytonuZus is erected for the seven cation andphylogenetic relationships isof great species listed above, and the following informa- importance. This is the third in a series of tion isprovided for its separation from the other papers that deals with taxonomic problems in- subgenera within the genus Sabethes. volving nominal taxa within this genus. The first The descriptive terminology and abbrevia- paper dealt with the transfer of a species from tions follow Harbach and Knight (1980, 1982) Sabethesto a new subgenusin WyeomyiaTheobald and Harbach and Peyton (1990a, 1990b). The (Harbach and Peyton 1990a). The second dealt illustrations are based on specimens deposited with the transfer of the subgenus Davismyia in the National Museum of Natural History, Lane and Cerqueira and its type species from Smithsonian Institution. -
Seed Ecology Iii
SEED ECOLOGY III The Third International Society for Seed Science Meeting on Seeds and the Environment “Seeds and Change” Conference Proceedings June 20 to June 24, 2010 Salt Lake City, Utah, USA Editors: R. Pendleton, S. Meyer, B. Schultz Proceedings of the Seed Ecology III Conference Preface Extended abstracts included in this proceedings will be made available online. Enquiries and requests for hardcopies of this volume should be sent to: Dr. Rosemary Pendleton USFS Rocky Mountain Research Station Albuquerque Forestry Sciences Laboratory 333 Broadway SE Suite 115 Albuquerque, New Mexico, USA 87102-3497 The extended abstracts in this proceedings were edited for clarity. Seed Ecology III logo designed by Bitsy Schultz. i June 2010, Salt Lake City, Utah Proceedings of the Seed Ecology III Conference Table of Contents Germination Ecology of Dry Sandy Grassland Species along a pH-Gradient Simulated by Different Aluminium Concentrations.....................................................................................................................1 M Abedi, M Bartelheimer, Ralph Krall and Peter Poschlod Induction and Release of Secondary Dormancy under Field Conditions in Bromus tectorum.......................2 PS Allen, SE Meyer, and K Foote Seedling Production for Purposes of Biodiversity Restoration in the Brazilian Cerrado Region Can Be Greatly Enhanced by Seed Pretreatments Derived from Seed Technology......................................................4 S Anese, GCM Soares, ACB Matos, DAB Pinto, EAA da Silva, and HWM Hilhorst -
BAST1986050004005.Pdf
BASTERIA, 50: 93-150, 1986 Alphabetical revision of the (sub)species in recent Conidae. 9. ebraeus to extraordinarius with the description of Conus elegans ramalhoi, nov. subspecies H.E. Coomans R.G. Moolenbeek& E. Wils Institute of Taxonomic Zoology (Zoological Museum) University of Amsterdam INTRODUCTION In this ninth part of the revision all names of recent Conus taxa beginning with the letter e are discussed. Amongst these are several nominal species of tent-cones with a C.of close-set lines, the shell a darker pattern consisting very giving appearance (e.g. C. C. The elisae, euetrios, eumitus). phenomenon was also mentioned for C. castaneo- fasciatus, C. cholmondeleyi and C. dactylosus in former issues. This occurs in populations where with normal also that consider them specimens a tent-pattern are found, so we as colour formae. The effect is known shells in which of white opposite too, areas are present, leaving 'islands' with the tent-pattern (e.g. C. bitleri, C. castrensis, C. concatenatus and C. episco- These colour formae. patus). are also art. Because of a change in the rules of the ICZN (3rd edition, 1985: 73-74), there has risen a disagreement about the concept of the "type series". In cases where a museum type-lot consists of more than one specimen, although the original author(s) did not indicate that more than one shell was used for the description, we will designate the single originally mentioned and/or figured specimen as the "lectotype". Never- theless a number of taxonomists will consider that "lectotype" as the holotype, and disregard the remaining shells in the lot as type material. -
First Report of Ancylostoma Ceylanicum in Wild Canids Q ⇑ Felicity A
International Journal for Parasitology: Parasites and Wildlife 2 (2013) 173–177 Contents lists available at SciVerse ScienceDirect International Journal for Parasitology: Parasites and Wildlife journal homepage: www.elsevier.com/locate/ijppaw Brief Report First report of Ancylostoma ceylanicum in wild canids q ⇑ Felicity A. Smout a, R.C. Andrew Thompson b, Lee F. Skerratt a, a School of Public Health, Tropical Medicine and Rehabilitation Sciences, James Cook University, Townsville, Queensland 4811, Australia b School of Veterinary and Biomedical Sciences, Murdoch University, Murdoch, Western Australia 6150, Australia article info abstract Article history: The parasitic nematode Ancylostoma ceylanicum is common in dogs, cats and humans throughout Asia, Received 19 February 2013 inhabiting the small intestine and possibly leading to iron-deficient anaemia in those infected. It has pre- Revised 23 April 2013 viously been discovered in domestic dogs in Australia and this is the first report of A. ceylanicum in wild Accepted 26 April 2013 canids. Wild dogs (dingoes and dingo hybrids) killed in council control operations (n = 26) and wild dog scats (n = 89) were collected from the Wet Tropics region around Cairns, Far North Queensland. All of the carcasses (100%) were infected with Ancylostoma caninum and three (11.5%) had dual infections with A. Keywords: ceylanicum. Scats, positively sequenced for hookworm, contained A. ceylanicum, A. caninum and Ancylos- Ancylostoma ceylanicum toma braziliense, with A. ceylanicum the dominant species in Mount Windsor National Park, with a prev- Dingo Canine alence of 100%, but decreasing to 68% and 30.8% in scats collected from northern and southern rural Hookworm suburbs of Cairns, respectively. -
INTRODUCTION to ALGEBRAIC GEOMETRY, CLASS 25 Contents 1
INTRODUCTION TO ALGEBRAIC GEOMETRY, CLASS 25 RAVI VAKIL Contents 1. The genus of a nonsingular projective curve 1 2. The Riemann-Roch Theorem with Applications but No Proof 2 2.1. A criterion for closed immersions 3 3. Recap of course 6 PS10 back today; PS11 due today. PS12 due Monday December 13. 1. The genus of a nonsingular projective curve The definition I’m going to give you isn’t the one people would typically start with. I prefer to introduce this one here, because it is more easily computable. Definition. The tentative genus of a nonsingular projective curve C is given by 1 − deg ΩC =2g 2. Fact (from Riemann-Roch, later). g is always a nonnegative integer, i.e. deg K = −2, 0, 2,.... Complex picture: Riemann-surface with g “holes”. Examples. Hence P1 has genus 0, smooth plane cubics have genus 1, etc. Exercise: Hyperelliptic curves. Suppose f(x0,x1) is a polynomial of homo- geneous degree n where n is even. Let C0 be the affine plane curve given by 2 y = f(1,x1), with the generically 2-to-1 cover C0 → U0.LetC1be the affine 2 plane curve given by z = f(x0, 1), with the generically 2-to-1 cover C1 → U1. Check that C0 and C1 are nonsingular. Show that you can glue together C0 and C1 (and the double covers) so as to give a double cover C → P1. (For computational convenience, you may assume that neither [0; 1] nor [1; 0] are zeros of f.) What goes wrong if n is odd? Show that the tentative genus of C is n/2 − 1.(Thisisa special case of the Riemann-Hurwitz formula.) This provides examples of curves of any genus. -
Botanical Nomenclature: Concept, History of Botanical Nomenclature
Module – 15; Content writer: AvishekBhattacharjee Module 15: Botanical Nomenclature: Concept, history of botanical nomenclature (local and scientific) and its advantages, formation of code. Content writer: Dr.AvishekBhattacharjee, Central National Herbarium, Botanical Survey of India, P.O. – B. Garden, Howrah – 711 103. Module – 15; Content writer: AvishekBhattacharjee Botanical Nomenclature:Concept – A name is a handle by which a mental image is passed. Names are just labels we use to ensure we are understood when we communicate. Nomenclature is a mechanism for unambiguous communication about the elements of taxonomy. Botanical Nomenclature, i.e. naming of plants is that part of plant systematics dealing with application of scientific names to plants according to some set rules. It is related to, but distinct from taxonomy. A botanical name is a unique identifier to which information of a taxon can be attached, thus enabling the movement of data across languages, scientific disciplines, and electronic retrieval systems. A plant’s name permits ready summarization of information content of the taxon in a nested framework. A systemofnamingplantsforscientificcommunicationmustbe international inscope,andmustprovideconsistencyintheapplicationof names.Itmustalsobeacceptedbymost,ifnotall,membersofthe scientific community. These criteria led, almost inevitably, to International Botanical Congresses (IBCs) being the venue at which agreement on a system of scientific nomenclature for plants was sought. The IBCs led to publication of different ‘Codes’ which embodied the rules and regulations of botanical nomenclature and the decisions taken during these Congresses. Advantages ofBotanical Nomenclature: Though a common name may be much easier to remember, there are several good reasons to use botanical names for plant identification. Common names are not unique to a specific plant. -
Their Botany, Essential Oils and Uses 6.86 MB
MELALEUCAS THEIR BOTANY, ESSENTIAL OILS AND USES Joseph J. Brophy, Lyndley A. Craven and John C. Doran MELALEUCAS THEIR BOTANY, ESSENTIAL OILS AND USES Joseph J. Brophy School of Chemistry, University of New South Wales Lyndley A. Craven Australian National Herbarium, CSIRO Plant Industry John C. Doran Australian Tree Seed Centre, CSIRO Plant Industry 2013 The Australian Centre for International Agricultural Research (ACIAR) was established in June 1982 by an Act of the Australian Parliament. ACIAR operates as part of Australia's international development cooperation program, with a mission to achieve more productive and sustainable agricultural systems, for the benefit of developing countries and Australia. It commissions collaborative research between Australian and developing-country researchers in areas where Australia has special research competence. It also administers Australia's contribution to the International Agricultural Research Centres. Where trade names are used this constitutes neither endorsement of nor discrimination against any product by ACIAR. ACIAR MONOGRAPH SERIES This series contains the results of original research supported by ACIAR, or material deemed relevant to ACIAR’s research and development objectives. The series is distributed internationally, with an emphasis on developing countries. © Australian Centre for International Agricultural Research (ACIAR) 2013 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from ACIAR, GPO Box 1571, Canberra ACT 2601, Australia, [email protected] Brophy J.J., Craven L.A. and Doran J.C. 2013. Melaleucas: their botany, essential oils and uses. ACIAR Monograph No. 156. Australian Centre for International Agricultural Research: Canberra. -
1 an Annotated Checklist of the Chondrichthyans of South Africa 1 2 3
1 An annotated checklist of the chondrichthyans of South Africa 2 3 4 DAVID A. EBERT1, 2, 3, 6, SABINE P. WINTNER4 & PETER M. KYNE5 5 6 1 Pacific Shark Research Center, Moss Landing Marine Laboratories, Moss Landing, 7 USA 8 2 South African Institute for Aquatic Biodiversity, Grahamstown, South Africa 9 3 Department of Ichthyology, California Academy of Sciences, San Francisco, USA 10 4 University of KwaZulu-Natal, School of Life Sciences, Durban, South Africa 11 5 Research Institute for the Environment and Livelihoods, Charles Darwin University, 12 Darwin, Australia 13 14 6 Corresponding author: E-mail: [email protected] 15 16 David A. Ebert ORCID ID 0000-0003-4604-8192 17 Sabine P. Wintner ORCID ID 0000-0001-7350-5999 18 Peter M. Kyne ORCID ID 0000-0003-4494-2625 19 20 21 1 1 Abstract 2 3 An annotated checklist of chondrichthyan fishes (sharks, batoids, and chimaeras) 4 occurring in South African waters is presented. The checklist is the result of decades of 5 research and on-going systematic revisions of the regional fauna. The chondrichthyan 6 fauna of South Africa is one of the richest in the world with 191 species, comprising 50 7 families and 103 genera. It consists of 30 families, 64 genera, and 111 species of sharks; 8 17 families, 36 genera, and 72 species of batoids; and, 3 families, 5 genera, and 8 species 9 of chimaeras. The most species-rich shark families are the whaler sharks Carcharhinidae 10 with 20 species followed by the deepwater catsharks Pentanchidae with 13 species. -
Indigenous Plants of Bendigo
Produced by Indigenous Plants of Bendigo Indigenous Plants of Bendigo PMS 1807 RED PMS 432 GREY PMS 142 GOLD A Gardener’s Guide to Growing and Protecting Local Plants 3rd Edition 9 © Copyright City of Greater Bendigo and Bendigo Native Plant Group Inc. This work is Copyright. Apart from any use permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the City of Greater Bendigo. First Published 2004 Second Edition 2007 Third Edition 2013 Printed by Bendigo Modern Press: www.bmp.com.au This book is also available on the City of Greater Bendigo website: www.bendigo.vic.gov.au Printed on 100% recycled paper. Disclaimer “The information contained in this publication is of a general nature only. This publication is not intended to provide a definitive analysis, or discussion, on each issue canvassed. While the Committee/Council believes the information contained herein is correct, it does not accept any liability whatsoever/howsoever arising from reliance on this publication. Therefore, readers should make their own enquiries, and conduct their own investigations, concerning every issue canvassed herein.” Front cover - Clockwise from centre top: Bendigo Wax-flower (Pam Sheean), Hoary Sunray (Marilyn Sprague), Red Ironbark (Pam Sheean), Green Mallee (Anthony Sheean), Whirrakee Wattle (Anthony Sheean). Table of contents Acknowledgements ...............................................2 Foreword..........................................................3 Introduction.......................................................4 -
A Review of the International Code of Botanical Nomenclature with Respect to Its Compatibility with Phylogenetic Classification
TAXON 53 (1) • February 2004: 159-161 Barkley & al. • A review of the ICBN A review of the International Code of Botanical Nomenclature with respect to its compatibility with phylogenetic classification Theodore M. Barkley1, Paula DePriest2, Vicki Funk2, Robert W. Kiger3, W. John Kress3, John McNeill4, Gerry Moore5, Dan H. Nicolson2, Dennis W. Stevenson6 & Quentin D. Wheeler7 [note: order of authors determined alphabetically] 1 Botanical Research Institute of Texas, 509 Pecan Street, Fort Worth, Texas 76102, U.S.A. barkley® brit.org 2 Botany, MRC-166, United States National Herbarium, National Museum of Natural History, Smithsonian Institution, P.O. Box 37012, Washington D.C. 20013, U.S.A. [email protected]; funk.vicki@ nmnh.si.edu; [email protected]; [email protected] 3 Hunt Institute for Botanical Documentation, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, U.S.A. [email protected] 4Royal Botanic Garden, Edinburgh, EH3 SLR, Scotland, U.K. [email protected] 5Brooklyn Botanic Garden, 1000 Washington Avenue, Brooklyn, New York 11225, U.S.A. gerrymoore@bbg. org (author for correspondence) 6 The New York Botanical Garden, Bronx, New York 10458 U.S.A. [email protected] 7Division of Environmental Biology, National Science Foundation, 4201 Wilson Boulevard, Arlington, Virginia 22230, U.S.A. [email protected] This article presents a summary of a discussion on believe that this assertion is the case, but many others do the current Code of botanical nomenclature (Greuter & not. al., 2000) that took place at the Linnaean Nomenclature Discussion: From a nomenclatural perspective, the Workshop held on 26-28 June 2002 at the Hunt Institute rank of species is indeed basic.