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Treatments for the Protection of Stored Southern-Grown Corn from Rice Weevil Attack — Exploratory Tests ~
Historic, archived document Do not assume content reflects current scientific l<nowledge, policies, or practices. C~1 ^^ i -»T f-W-t-^-m-—, y>/^ .'3 L i B R •:i;RPEin SERIAL KLUu.^. Marketing Research Report No.272 L- nr.T2 7lS58 '.' S. uEFARTMENT OF AGRICULTURE Treatments for the Protection of Stored Southern-Grown Corn from Rice Weevil Attack — Exploratory Tests ~ Marketing Research Division Agricultural Marketing Service U.S. DEPARTMENT OF AGRICULTURE WARNING No tolerances have been established for the use of lindane, methoxychlor, or ryania as insecticidal applications to the entire bulk of stored grain for the prevention of insect infestation. The tests reported herein were exploratory studies to develop information that could be used in considering the establishment of tolerances. Until such tolerances are announced, lindane, methoxychlor, or ryania protective treatments should not be used. A tolerance of 2 p. p.m. for methoxychlor in grain permits the spraying of bin walls and some surface applications, but is not high enough to cover protective treat- ments in the sense considered here. CONTENTS Page Summary 1 Introduction 2 Techniques 2 Tests with lindane 4 Tests with malathion 6 Tests with methoxychlor 8 Tests with synergized pyrethrum 12 Tests with ryania 16 Findings 19 Washington, D. C. September 1958 sale For by the Superintendent of Documents, U. S. Government Printing Office Washington 25, D. C. - Price 15 cents TREATMENTS FOR THE PROTECTION OF STORED SOUTHERN-GROWN CORN FROM RICE WEEVIL ATTACK—EXPLORATORY TESTS By D. W. La Hue, Herbert Womack, and B. W. Clements, Jr. Stored-Product Insects Laboratory- Georgia Coastal Plain Experiment Station Tifton, Ga.-"- SUMMARY Exploratory studies were made at Tifton, Ga. -
New Brunswick Drug Plans Formulary
New Brunswick Drug Plans Formulary August 2019 Administered by Medavie Blue Cross on Behalf of the Government of New Brunswick TABLE OF CONTENTS Page Introduction.............................................................................................................................................I New Brunswick Drug Plans....................................................................................................................II Exclusions............................................................................................................................................IV Legend..................................................................................................................................................V Anatomical Therapeutic Chemical (ATC) Classification of Drugs A Alimentary Tract and Metabolism 1 B Blood and Blood Forming Organs 23 C Cardiovascular System 31 D Dermatologicals 81 G Genito Urinary System and Sex Hormones 89 H Systemic Hormonal Preparations excluding Sex Hormones 100 J Antiinfectives for Systemic Use 107 L Antineoplastic and Immunomodulating Agents 129 M Musculo-Skeletal System 147 N Nervous System 156 P Antiparasitic Products, Insecticides and Repellants 223 R Respiratory System 225 S Sensory Organs 234 V Various 240 Appendices I-A Abbreviations of Dosage forms.....................................................................A - 1 I-B Abbreviations of Routes................................................................................A - 4 I-C Abbreviations of Units...................................................................................A -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Home Vegetable Garden Insect Pest Control
Oklahoma Cooperative Extension Service EPP-7313 Home Vegetable Garden Insect Pest Control Jonathan Edelson Entomology Specialist Oklahoma Cooperative Extension Fact Sheets are also available on our website at: Brenda Simons http://osufacts.okstate.edu Assistant Extension Specialist -Horticulture David Hillock Assistant Extension Specialist -Horticulture and ‘suck’ liquids from the plants. Examples include squash bugs, aphids, stink bugs, thrips and mites. Many of the insects that feed in this manner defecate a sticky liquid (honeydew) that often builds up on leaves or fruit, leaving a shiny residue What is an Insect Pest? that may support the growth of a black or gray sooty mold. For purposes of this Fact Sheet, we classify insects and Damaged foliage often will turn yellow and eventually brown mites as pests based on their ability to damage vegetable in color or become malformed in shape. plants and reduce your harvest from the home garden. Many insects, and all spiders, found in home vegetable gardens are beneficial and control of these insects is not recommended. Key Pests Those pests that feed directly on the harvested portion of the plant are the most destructive, since they compete directly Monitoring Pest Insects in the Home with you for the food you are trying to grow. You will have little Garden tolerance for the key pests. We recommend controlling key Insects and mites can move into your garden and then pests when found in the garden. Examples include the corn rapidly increase in numbers. You should examine plants in earworm and the tomato fruitworm. and around the garden throughout the season at least twice Many insects and mites feed on leaves or on parts of the weekly. -
Acutely / Extremely Hazardous Waste List
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extemely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extemely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extemely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extemely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extemely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extemely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extemely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extemely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extemely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extemely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extemely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extemely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extemely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Bioactivation of N-Alkyl Substituted Phosphor- Amidothioate Insecticides
J. Pesticide Sci. 9, 675-680 (1984) Original Article Bioactivation of N-Alkyl Substituted Phosphor- amidothioate Insecticides Masako UEJI and Chojiro ToMIzAWA National Institute of Agro-Environmental Sciences, Yatabe, Tsukuba-gun, Ibaraki 305, Japan (Received May 15, 1984) The insecticidal activity of O-ethyl O-2-isopropoxycarbonylphenyl N-alkylphoshor- amidothioates was examined with reference to their activation in biologicalsystems. Toxicity to the adzuki bean weevil varied with different N-alkyl groups. N-isopropylphosphoramido- thioate was the most toxic of the compounds tested, and N-unsubstituted, N-methyl- and N-ethylphosphoramidothioates were more toxic than fenitrothion. However, N-propyl and N-butyl homologs were less active than fenitrothion with the exception of the N-isopropyl homolog. LD50 values of the phosphoramidothioates for the insect were not correlated with in vitro anti-AChE activity of the phosphoramidates. 150 of N-isopropylphosphoramidate for acetylcholinesterases from adzuki bean weevil and bovine serum was higher than 10-3 M. When the phosphoramidothioates and phosphoramidate were incubated with rat liver micro- somal system, AChE activity of bovine serum was strongly inhibited in the presence of NADPH. Inhibition of AChE activity was reduced by addition of SKF 525-A to the micro- somal system. The compounds became also potent inhibitors for AChE by treatment with m-chloroperbenzoic acid. From these results, it was concluded that phosphoramidothioates and their oxons were activated oxidatively to inhibit AChE by the microsomal system as well as chemical treatment with peracid. of amide groups of phosphoramidothioate or INTRODUCTION phosphoramidate insecticides except schradan Bioactivity of phosphoramidothioates is vari- (octamethylpyrophosphoramidate). Moreover, able with structural changes. -
Environmental Health Criteria 63 ORGANOPHOSPHORUS
Environmental Health Criteria 63 ORGANOPHOSPHORUS INSECTICIDES: A GENERAL INTRODUCTION Please note that the layout and pagination of this web version are not identical with the printed version. Organophophorus insecticides: a general introduction (EHC 63, 1986) INTERNATIONAL PROGRAMME ON CHEMICAL SAFETY ENVIRONMENTAL HEALTH CRITERIA 63 ORGANOPHOSPHORUS INSECTICIDES: A GENERAL INTRODUCTION This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization World Health Orgnization Geneva, 1986 The International Programme on Chemical Safety (IPCS) is a joint venture of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization. The main objective of the IPCS is to carry out and disseminate evaluations of the effects of chemicals on human health and the quality of the environment. Supporting activities include the development of epidemiological, experimental laboratory, and risk-assessment methods that could produce internationally comparable results, and the development of manpower in the field of toxicology. Other activities carried out by the IPCS include the development of know-how for coping with chemical accidents, coordination -
Thing Natural?
Pyrethrum – Pyrethrins, Pyrethroid – Permethrin: Let’s Call the Whole Thing Natural? By Mike Catangui, Ph.D., Entomologist Manager, MWI Animal Health Technical Services Terminology This might be the reason why, despite being used for Pyrethrum: Liquid extract or dry preparation from hundreds of years, natural pyrethrins are still very effective the flowers of the pyrethrum plant (Chrysanthemum against many insect pests. Insects have not yet developed cinerariifolium). widespread resistance to natural pyrethrins despite being used for centuries. In comparison, many insect species, Pyrethrins: Collective name of the six naturally-occurring such as the house fly, can develop resistance against much insecticidal active ingredients (esters) found in pyrethrum. simpler man-made or laboratory-synthesized insecticides Pyrethroid: A manmade or laboratory-synthesized like permethrin (a synthetic pyrethroid) if used continuously insecticide patterned after one of the pyrethrins. for three to four years without employing resistance Permethrin: A pyrethroid. management strategies. Through the course of civilization, perhaps through keen observation and happenstance, humans have figured out that extracts from certain chrysanthemum flowers (Scientific Name: Chrysanthemum cinerariifolium; Common Names: pyrethrum plant, Dalmatian chrysanthemum, insect flowers) [Fig. 1] have insecticidal properties. Legend has it that a person picked certain chrysanthemum flowers as beautiful adornment—and then noticed dead insects around the flowers once they had dried and withered several days later. It is possible that pyrethrum extracts have been used for hundreds of years as insecticides in the Middle East. Persian Fig 1. Flowers of the pyrethrum plant (Chrysanthemum cinerariifolium). (Photo: Botanical Resources Australia http://botanicalra.com.au) pellitory, Persian powder and Zacherlin were names used by early Europeans to refer to preparations from pyrethrum extracts originating from the Middle East and the Balkans. -
Appendix Common, Trade, and Chemical Names of Pesticides Mentioned in the Present Volume
Appendix Common, trade, and chemical names of pesticides mentioned in the present volume Commonname Tradename Chemical name aldrin Octalene 1,2,3,4,10,1 O-hexachloro-1 ,4,4a,S,8,8a hexahydro-1,4-endo-exo-S,8-dimethano naphthalene amidithion Thiocron O,O-dimethyl S-(2-methoxyethyl carbamoylmethyl) phosphorodithioate azinphos methyl Guthion, Gusathion O,O-dimcthyl S-( 4-oxo-l ,2,3-benzotri azin-3-( 4H)-ylmethyl) phosphorodithioate captan Orthocid N -(trichloromethylthio) cyclohex-4-ene- 1,2-dicarboximide carbaryl Sevin 1-naphthyl-mcthylcarbamate carbophenothion Trithion O,O-diethyl S-[(p-chlorophenylthio) methyl] phosphorodithioate chlorfenvinphos Birlane (Shell), 2-chloro-1-(2,4-dichlorophenyl) vinyl Sapecron (e/BA) diethyl phosphate chlorphenamidine Galecron N'-( 4-chloro-o-tolyl)-N,N-dimethyl formamidine chlorthion Chlorthion O,O-dimethyIO-(3-chloro-4-nitro phenyl)-phosphorothioate coumaphos Asuntol, Co-Ral O,O-diethyl O-(3-chloro-4-methyl- 2-oxo-2H-1-benzopyran-7-yl) phosphorothioate DDT Gesarol 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane demeton Systox O,O-diethyl O-(and S)-2-(ethylthio)ethyl phosphorothioates DEF S,S,S-tributyltrithiophosphate demeton methyl Metasystox O,O-dimethyl O-(and S)-2-(ethylthio) ethyl phosphorothioates diazinon Diazinon, Basudin O,O-diethyIO-(2-isopropyl-4-methyl- 6-pyrimidyl) phosphorothioate dichlorvos Vapona (Shell), O,O-dimethyl-2,2-dichlorovinyl Nuvan (e/BA) phosphate dicrotophos Bidrin (Shell), O,O-dimethyl O-(2-dimethyl-carbamyl-1- Carbicron (e/BA) methyl) vinyl phosphate dieldrin Octalox -
Nobel Lecture, December 11, 1948
P AUL H. MÜLLE R Dichloro-diphenyl-trichloroethane and newer insecticides Nobel Lecture, December 11, 1948 Ladies and Gentlemen. Since Perkin synthesized the first dyestuff in 1856, about 90 years have elapsed. During this period the synthesis of artificial dyestuffs has gone through enormous development. The discovery of fuchsines by Emanuel Verguin in 1859, unlocked the tri- phenylmethane dyestuffs for the dyestuffs chemist. The very important discovery of the diazo compounds by Peter Griess, in 1858, certainly brought about the most significant reaction in the chemistry of dyestuffs, a quite unique impetus to the development of this field of organic chemistry. The most important milestones in this development are: the preparation of Bismarck brown by C. Martius in 1863, of Chrysoidine by O. N. Witt in 1876, and Congo Red, the first dyestuff capable of direct application to cotton, by P. Böttiger in 1884. This large-scale development and the vast mass of experimental material available have called for a variety of attempted explanations. The relation- ships between composition and colour on the one hand, and fastness on the other, were the subjects of several attempts at theoretical explanation. Particularly fruitful in this respect was the theory of O. N. Witt on chro- mophores and auxochromes, and the theory - valid only in special cases - of E. Schirm, J. Prakt. Chem., 144 (1936) 69, concerning the connexion between composition and affinity to cellulose fibre. Thanks to these results the dyestuffs chemist today, after about 90 years of untiring detailed study, is in the fortunate position to possess certain points of reference enabling him to set up his programme of work in bold outlines. -
US EPA, Pesticide Product Label, EVERGREEN PYRETHRUM
UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, DC 20460 OFFICE OF CHEMICAL SAFETY AND POLLUTION PREVENTION April 19, 2017 Steven K. Ditto McLaughlin Gormley King Company D/B/A MGK 8810 10th Ave. N Minneapolis, MN 55427 Subject: Notification per PRN 98-10 – Revised Dilution Directions Product Name: EVERGREEN PYRETHRUM CONCENTRATE EPA Registration Number: 1021-2560 Application Date: 3/24/2017 Decision Number: 527604 Dear Mr. Ditto: The Agency is in receipt of your Application for Pesticide Notification under Pesticide Registration Notice (PRN) 98-10 for the above referenced product. The Registration Division (RD) has conducted a review of this request for its applicability under PRN 98-10 and finds that the action requested falls within the scope of PRN 98-10. The label submitted with the application has been stamped “Notification” and will be placed in our records. Should you wish to add/retain a reference to the company’s website on your label, then please be aware that the website becomes labeling under the Federal Insecticide Fungicide and Rodenticide Act and is subject to review by the Agency. If the website is false or misleading, the product would be misbranded and unlawful to sell or distribute under FIFRA section 12(a)(1)(E). 40 CFR 156.10(a)(5) list examples of statements EPA may consider false or misleading. In addition, regardless of whether a website is referenced on your product’s label, claims made on the website may not substantially differ from those claims approved through the registration process. Therefore, should the Agency find or if it is brought to our attention that a website contains false or misleading statements or claims substantially differing from the EPA approved registration, the website will be referred to the EPA’s Office of Enforcement and Compliance. -
Managing Pesticide Poisoning Risk and Understanding the Signs and Symptoms Clyde L
EC2505 Revised June 2018 Managing Pesticide Poisoning Risk and Understanding the Signs and Symptoms Clyde L. Ogg, Extension Educator Jan R. Hygnstrom, Project Manager Cheryl A. Alberts, Project Coordinator Erin C. Bauer, Entomology Lecturer The potential for accidents with pesticides is real. Ac- cidental exposure or overexposure to pesticides can have seri- ous consequences. While most pesticides can be used with relatively little risk when label directions are followed, some are extremely toxic and require special precautions. The Poison Control Centers receive about 90,000 calls each year related to pesticide exposures. Pesticides are re- sponsible for about 3 percent of all accidental exposures to children 5 years and younger and about 4 percent for adults. In addition, pesticides are the cause of about 3 percent of children’s deaths reported to the Poison Control Centers. Routes of Exposure Pesticides can enter the human body three ways: 1) der- mal exposure, by absorption through the skin or eyes; 2) oral exposure, through the mouth; and 3) through inhalation or respiratory exposure, by inhaling into the lungs. Some classify exposure through the eyes as ocular exposure. Dermal exposure results in absorption immediately after Figure 1. Absorption rates of different a pesticide contacts the skin or eyes. Absorption will contin- parts of the body based on the absorption ue as long as the pesticide remains in contact with the skin or of parathion into the forearm over 24 eyes. The rate at which dermal absorption occurs is different hours. for each part of the body (Figure 1). Maiback and Feldman (1974) measured the amount of the pesticide parathion absorbed by different parts of the human body over 24 hours.