2,4-Dichlorophenoxyacetic Acid Analysis of Risk to Endangered And
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Evolution of Resistance to Auxinic Herbicides: Historical Perspectives, Mechanisms of Resistance, and Implications for Broadleaf Weed Management in Agronomic Crops J
Weed Science 2011 59:445–457 Evolution of Resistance to Auxinic Herbicides: Historical Perspectives, Mechanisms of Resistance, and Implications for Broadleaf Weed Management in Agronomic Crops J. Mithila, J. Christopher Hall, William G. Johnson, Kevin B. Kelley, and Dean E. Riechers* Auxinic herbicides are widely used for control of broadleaf weeds in cereal crops and turfgrass. These herbicides are structurally similar to the natural plant hormone auxin, and induce several of the same physiological and biochemical responses at low concentrations. After several decades of research to understand the auxin signal transduction pathway, the receptors for auxin binding and resultant biochemical and physiological responses have recently been discovered in plants. However, the precise mode of action for the auxinic herbicides is not completely understood despite their extensive use in agriculture for over six decades. Auxinic herbicide-resistant weed biotypes offer excellent model species for uncovering the mode of action as well as resistance to these compounds. Compared with other herbicide families, the incidence of resistance to auxinic herbicides is relatively low, with only 29 auxinic herbicide-resistant weed species discovered to date. The relatively low incidence of resistance to auxinic herbicides has been attributed to the presence of rare alleles imparting resistance in natural weed populations, the potential for fitness penalties due to mutations conferring resistance in weeds, and the complex mode of action of auxinic herbicides in sensitive dicot plants. This review discusses recent advances in the auxin signal transduction pathway and its relation to auxinic herbicide mode of action. Furthermore, comprehensive information about the genetics and inheritance of auxinic herbicide resistance and case studies examining mechanisms of resistance in auxinic herbicide-resistant broadleaf weed biotypes are provided. -
Please Use Caution When Applying Herbicides Near Wine Grapes
Please Use Caution When Applying Herbicides Near Wine Grapes Phenoxy herbicides are very damaging to grapevines Grapevines are extremely sensitive to the application of certain herbicides commonly used by farmers and homeowners, especially phenoxy herbicides. Phenoxy herbicides include 2,4-D, MCPA, Crossbow, Banvel, Garlon, Weed-B-Gone, and Brush Killer, among others. The active ingredient of phenoxy-type herbicides may be listed on the label in “weed and feed” and brush control products for use in home landscaping as 2,4-dichlorophenoxy- acetic acid (2,4-D), 2-methyl-4-chlorophenoxyacetic acid, triclopyr, or dicamba. Sensitivity to phenoxy herbicides exists throughout the grapevine's growing season (mid-March through October). Grapevines are most vulnerable from the early growing season through the bloom and fruit set period (mid-March through June). Phenoxy herbicides do not require a pesticide license for purchase in Oregon and are readily available from home improvement stores, garden centers, retail nurseries, etc. This family of herbicides is very effective and economical for controlling broadleaf weeds. These herbicides are commonly used on a variety of sites such as lawns, golf courses, rights-of-way and agricultural fields and by homeowners. Two forms of spray drift can damage grapevines Drift of spray droplets: Small particles can move with the wind, land on grapes, and be absorbed into the grapevines through the cuticle on the leaf. The smaller the droplet, the further it will travel. Vapor drift: Volatile herbicides may produce vapors that are carried several miles from the target area. Herbicide particles or vapors may be moved from the application site by wind, shifting air currents, climatic inversions or using high pressures when spraying. -
Production of Malonic Acid Through the Fermentation of Glucose
University of Pennsylvania ScholarlyCommons Department of Chemical & Biomolecular Senior Design Reports (CBE) Engineering 4-20-2018 Production of Malonic Acid through the Fermentation of Glucose Emily P. Peters University of Pennsylvania, [email protected] Gabrielle J. Schlakman University of Pennsylvania, [email protected] Elise N. Yang University of Pennsylvania, [email protected] Follow this and additional works at: https://repository.upenn.edu/cbe_sdr Part of the Biochemical and Biomolecular Engineering Commons Peters, Emily P.; Schlakman, Gabrielle J.; and Yang, Elise N., "Production of Malonic Acid through the Fermentation of Glucose" (2018). Senior Design Reports (CBE). 107. https://repository.upenn.edu/cbe_sdr/107 This paper is posted at ScholarlyCommons. https://repository.upenn.edu/cbe_sdr/107 For more information, please contact [email protected]. Production of Malonic Acid through the Fermentation of Glucose Abstract The overall process to produce malonic acid has not drastically changed in the past 50 years. The current process is damaging to the environment and costly, requiring high market prices. Lygos, Inc., a lab in Berkeley, California, has published a patent describing a way to produce malonic acid through the biological fermentation of genetically modified easty cells. This proposed technology is appealing as it is both better for the environment and economically friendly. For the process discussed in this report, genetically modified Pichia Kudriavzevii yeast cells will be purchased from the Lygos lab along with the negotiation of exclusive licensing rights to the technology. The cells will be grown in fermentation vessels, while being constantly fed oxygen, glucose and fermentation media. The cells will excrete malonic acid in the 101 hour fermentation process. -
Preparation of Amine Alanes
Europaisches Patentamt J European Patent Office 00 Publication number: 0 273 229 Office europeen des brevets A2 EUROPEAN PATENT APPLICATION © Application number: 87117901.6 © mt. ci.<: C01B 6/06 , C07C 87/00 © Date of filing: 03.12.87 © Priority: 22.12.86 US 945286 © Applicant: ETHYL CORPORATION Ethyl Tower 451 Florida Boulevard ® Date of publication of application: Baton Rouge Louisiana 70801 (US) 06.07.88 Bulletin 88/27 @ Inventor: Marlett, Everett Michael ® Designated Contracting States: 9355 Greenbriar Drive AT BE CH DE ES FR GB IT LI LU NL SE Baton Rouge Louisiana 7081 5(US) 0 Representative: Sandmair, Kurt, Dr. Patentanwalte Schwabe, Sandmair, Marx Stuntzstrasse 16 D-8000 MUnchen 80(DE) © Preparation of amine alanes. © Process for the preparation of an amine alane, said process comprising reacting: (a) an alkali metal aluminum tetrahydride having the formula MAIH4, wherein M is an alkali metal selected from the class consisting of lithium, sodium and potassium, (b) a hydrogen halide, and (c) a complexing tertiary amine. In this process, NaAlhU, HCI, and (C2H5)3N are preferred reactants. CM CM a. LU Xerox Copy Centre 0 273 229 PREPARATION OF AM1NE ALANES The invention pertains to the formation of amine alanes AIH3«NR3. These materials are useful as chemical intermediates. For example, they can be reacted with a silicon halide such as SiCU or SiF4 to produce silane. Reference is made to U.S. 4,474,743. It pertains to production of silane and aluminum fluoride from silicon tetrafluoride and amine alanes. Reference is also made to U.S. 4,006,095. It teaches, inter alia, that SiCU reacts with a toluene solution of AIH3 containing dimethyl ether or a stabilizing amine. -
WO 2013/089962 Al 20 June 2013 (20.06.2013) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2013/089962 Al 20 June 2013 (20.06.2013) W P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every B01J 31/04 (2006.01) B01J 31/18 (2006.01) kind of national protection available): AE, AG, AL, AM, B01J 31/14 (2006.01) B01J 31/22 (2006.01) AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, (21) Number: International Application DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, PCT/US20 12/065285 HN, HR, HU, ID, IL, IN, IS, JP, KE, KG, KM, KN, KP, (22) International Filing Date: KR, KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, 15 November 2012 (15.1 1.2012) ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, (25) Filing Language: English RW, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, (26) Publication Language: English TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW. (30) Priority Data: 13/323,328 12 December 201 1 (12. 12.201 1) US (84) Designated States (unless otherwise indicated, for every kind of regional protection available): ARIPO (BW, GH, (71) Applicant (for all designated States except US): CHEV¬ GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, SZ, TZ, RON PHILLIPS CHEMICAL COMPANY LP UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, TJ, [US/US]; 10001 Six Pines Drive, The Woodlands, Texas TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, DK, 77380 (US). -
INSECT, WEED, Anddisease CONTROL in TURFGRASS
SC-039 5/17 WEED,INSECT, and DISEASE CONTROL in TURFGRASS 2017–18 WEED, INSECT, and DISEASE CONTROL in TURFGRASS Editor Casey Reynolds, Assistant Professor and Extension Turfgrass Specialist Authors Casey Reynolds, Assistant Professor and Extension Turfgrass Specialist Matt Elmore, Assistant Professor and Extension Turfgrass Specialist Young-Ki Jo, Associate Professor and Extension Turfgrass Specialist Diane Silcox Reynolds, Post-doctoral Research Associate, Entomology AggieTurf: http://aggieturf.tamu.edu Contents Introduction . 1 Herbicide Mode of Action (MOA) classification . 3 Herbicides for general control of grassy and broadleaf weeds . 4 Preemergence herbicides for grassy and broadleaf weeds . 4 Selective postemergence herbicides . 9 Synthetic auxin postemergence herbicides for broadleaf weeds . 19 Product formulations containing synthetic auxin herbicides . 21 Nonsynthetic auxin postemergence herbicides for broadleaf weeds . 23 Nonselective herbicides for general weed control . 24 Herbicides for commonly occurring weeds . 25 Crabgrass (Digitaria spp ). 25 Goosegrass (Eleusine indica) . 27 Sandbur (Cenchrus spp ). 30 Annual bluegrass (Poa annua L ). 33 Dallisgrass (Paspalum dilatatum Poir ). 39 WEEDS Bermudagrass (Cynodon spp ). 41 Nutsedge (Cyperus spp ). and kyllinga (Kyllinga spp ). 43 Khakiweed and mat chafflower (Alternanthera spp ). 46 Herbicides containing sulfentrazone . 47 Herbicides containing quinclorac . 48 Turfgrass tolerance to postemergence herbicides . 49 Plant growth regulators . 51 Insect pests in turfgrasses . 53 Insecticide Mode of Action (MOA) classification . 55 Insecticides registered for use in turfgrasses . 56 Ants . 56 Armyworms . 58 Billbugs . 61 Black turfgrass ataenius . 63 Chinch bugs . 66 Cutworms . 69 Green June beetles . 72 Mealybugs . 74 Mites . 75 INSECTS Mole crickets . 76 Red imported fire ants . 79 Sod webworms . 81 White grubs . 84 Diseases in Texas turfgrasses . 86 Fungicide Mode of Action (MOA) classification . -
PESTICIDES Criteria for a Recommended Standard
CRITERIA FOR A RECOMMENDED STANDARD OCCUPATIONAL EXPOSURE DURING THE MANUFACTURE AND FORMULATION OF PESTICIDES criteria for a recommended standard... OCCUPATIONAL EXPOSURE DURING THE MANUFACTURE AND FORMULATION OF PESTICIDES * U.S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Public Health Service Center for Disease Control National Institute for Occupational Safety and Health July 1978 For sale by the Superintendent of Documents, U.S. Government Printing Office, Washington, D.C. 20402 DISCLAIMER Mention of company names or products does not constitute endorsement by the National Institute for Occupational Safety and Health. DHEW (NIOSH) Publication No. 78-174 PREFACE The Occupational Safety and Health Act of 1970 emphasizes the need for standards to protect the health and provide for the safety of workers occupationally exposed to an ever-increasing number of potential hazards. The National Institute for Occupational Safety and Health (NIOSH) has implemented a formal system of research, with priorities determined on the basis of specified indices, to provide relevant data from which valid criteria for effective standards can be derived. Recommended standards for occupational exposure, which are the result of this work, are based on the effects of exposure on health. The Secretary of Labor will weigh these recommendations along with other considerations, such as feasibility and means of implementation, in developing regulatory standards. Successive reports will be presented as research and epideiriologic studies are completed and as sampling and analytical methods are developed. Criteria and standards will be reviewed periodically to ensure continuing protection of workers. The contributions to this document on pesticide manufacturing and formulating industries by NIOSH staff members, the review consultants, the reviewer selected by the American Conference of Governmental Industrial Hygienists (ACGIH), other Federal agencies, and by Robert B. -
Phenoxy Reference Guide 3
Phenoxy Reference Guide www.nufarm.com.au 3 Contents Introduction 4 Mode of Action 4 Cereal Crop Growth Stages (including Zadok’s guide) 5 A Numerical Cereal Growth Scale – Zadok’s 6 What Phenoxy Where? 6 Common Weeds Controlled 7 Using the Growth Stage of Cereal Crops to Time Herbicide Applications 8 Damage to Cereal Crops from Incorrect Phenoxy Herbicide Applications 9 Salvage Spraying of Winter Crops 10 Cereal Tolerance Guide 11-13 Plant Back Periods for Fallow Seed Bed Preparation 14-15 Spray Grazing 16 Withholding Periods 16 Reducing Off-Target Herbicide Drift 16-19 Herbicide Resistance Management 20 4 Introduction At Nufarm, we are committed to supporting Australian growers Phenoxys were first developed in the USA in the early 1940’s with the highest quality crop protection and weed control and used commercially in 1946. Today they remain amongst products so maximum outputs can be achieved. the world’s most widely used herbicides, providing farmers and other users with broadleaf weed control in a multitude of Our commitment starts with the utilisation of world-leading agricultural and non-agricultural uses. Phenoxys work by manufacturing and environmental control technology. This is disrupting plant cell growth and form a part of the Group I reflected in research and development, container management, herbicides. and the establishment of regional service centres across Australia. Nufarm guarantees its Phenoxy products, which include Nufarm Amicide® 625, Nufarm Estercide® 800, Nufarm LV Nufarm, an Australian company, is a global leader in the Estercide® 600, Nufarm Surpass® 300, Nufarm Buttress®, manufacture, supply and marketing of 'phenoxys', with Baton®, Nufarm LVE MCPA and Nufarm MCPA 500. -
Item N Number °3632 D N0t Scanned
3632 item n Number ° D n0t scanned Author House, W.B. Corporate Author Midwest Research Institute, Kansas City, Missouri Report/Article TltlB Assessment of Ecological Effects of Extensive or Repeated Use of Herbicides Journal/Book Title Year Month/Day Color D Number of Images 386 DescrlOtOU NOtBS Project monitored by the Department of the Army under contract no. DAHC15-68-C-0119; ARPA Order No. 1086 Monday, December 31, 2001 Page 3632 of 3802 UNCLASSIFIED AD 824 314 ASSESSMENT OF ECOLOGICAL EFFECTS OF EXTENSIVE OR REPEATED USE bF H2RBICIDES: FINAL REPORT Midwest Research Institute Kansas City, Missouri Processed for. .. DEFENSE DOCUMENTATION CENTER DEFENSE SUPPLY AGENCY FOR FEDERAL SCIENTIFIC AND TECHNICAL INFORMATION U. S. DEPARTMENT OF COMMERCE / NATIONAL BUREAU OF STANDARDS / INSTITUTE FOR APPLIED TECHNOLOGY UNCLASSIFIED ASSESSMENT OF ECOLOGICAL EFFECTS OF EXTENSIVE OR REPEATED USE OF HERBICIDES FINAL REPORT 15 August - 1 December 1967 Contract No. DAHC15-68-C-0119 MRI Project No. 3103-B Sponsored by Advanced Research Projects Agency ARPA Order No. 1086 MIDV i: '':«'; RIL.GF-1- '< ;H iNi.-iTITUTH 42S VOLKER BOULEVARD/KANSAS CITY, MISSOURI 6411O/AC 816 LO 1-O2O2 This research was supported by the Advanced Research Projects Agency of the Department of Defense and was monitored by Department of Army under Contract No. DAHCl5-68-C-Oll9._ Reproduced by the CLEARINGHOUSE | for Federal Scientific & Technical > Information Springfield Va. 221S1 Disclaimer: The findings in this report are not to be construed as an of- ficial position of the Department of Army, unless so designated "by other authorized documents. WST., ) AVAIL ASSESSMENT OF ECOLOGICAL EFFECTS OF EXTENSIVE OR REPEATED USE OF HERBICIDES by W. -
Long Island Pesticide Pollution Prevention Strategy
LONG ISLAND PESTICIDE POLLUTION PREVENTION STRATEGY New York State Department of Environmental Conservation July 11, 2014 THIS PAGE INTENTIONALLY LEFT BLANK LONG ISLAND PESTICIDE POLLUTION PREVENTION STRATEGY NYS DEPARTMENT OF ENVIRONMENTAL CONSERVATION 7/11/2014 TABLE OF CONTENTS EXECUTIVE SUMMARY The Challenge of Pesticide Use and Groundwater on Long Island………………….. ES-1 Pesticide Pollution Prevention Goal…………………………………………………. ES-3 Pesticide P2 Blueprint………….…………………………………………………….. ES-4 Summary of Long Island P2 Strategy Contents……………………………………… ES-8 CHAPTER 1: GOAL, PHILOSOPHY AND PURPOSE .......................................................... 1 CHAPTER 2: OVERVIEW: GROUNDWATER AND PESTICIDE USE ON LONG ISLAND Introduction……………………….…………………………………………….…………2 Groundwater and the Importance of Protecting It…………………………………….......2 Overview of Pesticide Use on Long Island……………………….…………….…………4 Pesticides Impacting Groundwater on Long Island…………………………………….....8 Water Quality Criteria…………………………...………………………………..……...11 CHAPTER 3: ACTION PLAN TO IMPLEMENT THE LONG ISLAND PESTICIDE POLLUTION PREVENTION STRATEGY Pesticide Pollution Prevention……………………………………………………….......14 A Pesticide P2 Blueprint …………………………………………………………...........14 Conduct Initial Assessment of Specific Active Ingredients and Pesticide P2 Needs …..18 Maximize Use of Water Quality Monitoring for Pesticides………..………………...….19 Establish, Convene and Chair Pesticide P2 Workgroups………...……………….…......20 P2 Workgroups Consider Specified Active Ingredients and Related P2……….……......24 DEC -
Synthesis of Insecticidal Mono- and Diacylhydrazines for Disruption of K+ Voltage-Gated Channels, Elucidation of Regiochemistry, And
Synthesis of Insecticidal Mono- and Diacylhydrazines for Disruption of K+ Voltage-Gated Channels, Elucidation of Regiochemistry, and Description of Conformational Isomerism by NMR Spectroscopy and Computation Joseph Shelby Clements II Dissertation submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy In Chemistry Paul R. Carlier, Chair David G. I. Kingston James M. Tanko Gordon T. Yee May 2, 2017 Blacksburg, VA Keywords: Hydrazine, acylation, α-effect, regioselectivity, hydrazide, voltage- gated, (E)-/(Z)-, 19F NMR, single electron transfer (SET), rotational barrier, N-N bond rotation, rotational isomerism, helicity, transition state, dihedral angle Copyright 2017, Joseph S. Clements II Synthesis of Insecticidal Mono- and Diacylhydrazines for Disruption of K+ Voltage-Gated Channels, Elucidation of Regiochemistry, and Description of Conformational Isomerism by NMR Spectroscopy and Computation Joseph Shelby Clements II ABSTRACT Based on the success of diacyl-tert-butylhydrazines RH-5849 and RH-1266 in controlling agricultural crop pests, we endeavored to synthesize our own diacylbenzyl- and arylhydrazine derivatives for use against the malaria vector Anopheles gambiae. In the process of producing a library of compounds for assay against An. gambiae, it became clear that employing regioselective acylation techniques (in molecules that feature two nucleophilic, acyclic nitrogen atoms α to one another) would be imperative. Synthesis of the library derivatives proceeded rapidly and after topical assay, we found three compounds that were more toxic than the RH- series leads. One of the three displayed an LD50 value of half that of RH-1266, though patch clamp assay concluded that toxicity was not necessarily linked to inhibition of mosquito K+ channel Kv2.1. -
5. Key Post-Emergent Modes of Action
5. KEY POST-EMERGENT MODES OF ACTION When new mode of action herbicides are first introduced, of this enzyme is reduction in the production of fatty acids manufacturers typically provide robust formulations and use required for construction of cell membranes needed for rates. There is often a high level of “forgiveness” in the label. new cell production. As resistant populations are selected over time, there is The ACCase enzyme in most broadleaf plants is insensitive sometimes a period where the herbicide may still be useful, to herbicides from this herbicide mode of action, and hence albeit with reduced performance. In these situations of low- there is acceptable crop tolerance in most broadleaf crops level or emerging resistance, it is critical that users seek to and no efficacy on most broadleaf weeds. Some exceptions maximise application conditions to ensure everything possible exist. For example, haloxyfop is able to control the broadleaf is done to enhance the herbicide performance. weed storksbill or geranium (Erodium spp.) while high rates of clethodim can damage canola, particularly when flowering. Understanding how each of the key modes of action available for post-emergent weed control work, how they The three sub-groups of Group A herbicides bind to the target enter and translocate in the plant, and what is required to enzyme at slightly different, and overlapping, amino acids. This differential binding can lead to differences in target site maximise efficacy is critical knowledge for maximising field herbicide resistance patterns both between and within the performance. sub groups (refer to the Acetyl CoA Carboxylase inhibitors This chapter coves the key modes of actions used for post- section under section 6.3.1.1.