Lesson Title: Aquaadvantage: GMO Salmon
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Early Stages of Fishes in the Western North Atlantic Ocean Volume
ISBN 0-9689167-4-x Early Stages of Fishes in the Western North Atlantic Ocean (Davis Strait, Southern Greenland and Flemish Cap to Cape Hatteras) Volume One Acipenseriformes through Syngnathiformes Michael P. Fahay ii Early Stages of Fishes in the Western North Atlantic Ocean iii Dedication This monograph is dedicated to those highly skilled larval fish illustrators whose talents and efforts have greatly facilitated the study of fish ontogeny. The works of many of those fine illustrators grace these pages. iv Early Stages of Fishes in the Western North Atlantic Ocean v Preface The contents of this monograph are a revision and update of an earlier atlas describing the eggs and larvae of western Atlantic marine fishes occurring between the Scotian Shelf and Cape Hatteras, North Carolina (Fahay, 1983). The three-fold increase in the total num- ber of species covered in the current compilation is the result of both a larger study area and a recent increase in published ontogenetic studies of fishes by many authors and students of the morphology of early stages of marine fishes. It is a tribute to the efforts of those authors that the ontogeny of greater than 70% of species known from the western North Atlantic Ocean is now well described. Michael Fahay 241 Sabino Road West Bath, Maine 04530 U.S.A. vi Acknowledgements I greatly appreciate the help provided by a number of very knowledgeable friends and colleagues dur- ing the preparation of this monograph. Jon Hare undertook a painstakingly critical review of the entire monograph, corrected omissions, inconsistencies, and errors of fact, and made suggestions which markedly improved its organization and presentation. -
UNITED STATES SECURITIES and EXCHANGE COMMISSION Washington, D.C
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-K ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2018 OR TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to . Commission File Number: 001-36042 INTREXON CORPORATION (Exact name of registrant as specified in its charter) Virginia 26-0084895 (State or other jurisdiction of (I.R.S. Employer incorporation or organization) Identification Number) 20374 Seneca Meadows Parkway Germantown, Maryland 20876 (Address of principal executive offices) (Zip Code) Registrant's telephone number, including area code (301) 556-9900 Securities registered pursuant to Section 12(b) of the Act: Title of each class Name of each exchange on which registered Intrexon Corporation Common Stock, No Par Value Nasdaq Global Select Market Securities registered pursuant to Section 12(g) of the Act: None Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes No Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes No Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. -
2019 World Congress Attendee List
2019 World Congress Attendee List Title COMPANY COUNTRY Global Marketing Director AB Enzymes Germany R&D Project Manager Acceligen - A Recombinetics Company United States CEO ACIES BIO Slovenia Head of Business ACIES BIO Slovenia Development Environmental Coordinator Adelante Consulting United States Project Manager Adelante Consulting United States Senior Vice President Advanatage Capital United States Chief Executive Officer Aequor, Inc. United States Chief Investment Officer Aether Earth Fund United States CEO Ag Ventures Alliance United States Chief Innovation Officer AgBiome United States Director, Microbials Agbiome, Inc United States Development Publisher/Editorial Director Agri Marketing Magazine United States Chercheur et chef d'Ãquipe Agrinova Canada Vice President Regulatory Agrisoma Biosciences, Inc United States Affairs Vice President, Business Agrisoma Biosciences, Inc Canada Development General Manager, North Ajinomoto Health & Nutrition North America United States American Research & Innovation Center Director, Forest Alberta Innovates - Bio Solutions Canada Technologies Manager, Clean Technology Alberta Innovates - Bio Solutions Canada Business Development Alderys France Director Head of Business Algenuity United Kingdom Development Senior Business Attraction Alliant Energy United States Manager Senior Economic Alliant Energy United States Development Manager Key Account Manager Alliant Energy United States CEO Altarum Institute France Research Chemical Amalgamated Research LLC United States Engineer Chemical Engineer -
STUDY on RISK ASSESSMENT: APPLICATION of ANNEX I of DECISION CP 9/13 to LIVING MODIFIED FISH Note by the Executive Secretary INTRODUCTION 1
CBD Distr. GENERAL CBD/CP/RA/AHTEG/2020/1/3 19 February 2020 ENGLISH ONLY AD HOC TECHNICAL EXPERT GROUP ON RISK ASSESSMENT AND RISK MANAGEMENT Montreal, Canada, 31 March to 3 April 2020 Item 3 of the provisional agenda* STUDY ON RISK ASSESSMENT: APPLICATION OF ANNEX I OF DECISION CP 9/13 TO LIVING MODIFIED FISH Note by the Executive Secretary INTRODUCTION 1. In decision CP-9/13, the Conference of the Parties serving as the meeting of the Parties to the Cartagena Protocol on Biosafety decided to establish the Ad Hoc Technical Expert Group (AHTEG) on Risk Assessment and Risk Management, which would work in accordance with the terms of reference contained in annex II to that decision. In the same decision, the Conference of the Parties serving as the meeting of the Parties to the Protocol requested the Executive Secretary to commission a study informing the application of annex I of the decision to (a) living modified organisms containing engineered gene drives and (b) living modified fish and present it to the online forum and the AHTEG. 2. Pursuant to the above, and with the financial support of the Government of the Netherlands, the Secretariat commissioned a study informing the application of annex I to living modified fish to facilitate the process referred to in paragraph 6 of decision CP-9/13. The study was presented to the Open-Ended Online Forum on Risk Assessment and Risk Management, which was held from 20 January to 1 February 2020, during which registered participants provided feedback and comments.1 3. -
Genetically Engineered Fish: an Unnecessary Risk to the Environment, Public Health and Fishing Communities
Issue brief Genetically engineered fish: An unnecessary risk to the environment, public health and fishing communities On November 19, 2015, the U.S. Food & Drug Administration announced its approval of the “AquAdvantage Salmon,” an Atlantic salmon that has been genetically engineered to supposedly be faster-growing than other farmed salmon. This is the first-ever genetically engineered animal allowed to enter the food supply by any regulatory agency in the world. At least 35 other species of genetically engineered fish are currently under development, including trout, tilapia, striped bass, flounder and other salmon species — all modified with genes from a variety of organisms, including other fish, coral, mice, bacteria and even humans.1 The FDA’s decision on the AquAdvantage genetically engineered salmon sets a precedent and could open the floodgates for other genetically engineered fish and animals (including cows, pigs and chickens) to enter the U.S. market. Genetically engineered salmon approved by FDA Despite insufficient food safety or environmental studies, the FDA announced its approval of the AquAdvantage Salmon, a genetically engineered Atlantic salmon produced by AquaBounty Technologies. The company originally submitted its application to the FDA in 2001 and the FDA announced in the summer of 2010 it was considering approval of this genetically engineered fish — the first genetically engineered animal intended for human consumption. In December 2012, the FDA released its draft Environmental Assessment of this genetically engineered salmon, and approved it in November 2015. This approval was made despite the 1.8 million people who sent letters to FDA opposing approval of the so-called “frankenfish,” and the 75 percent of respondents to a New York Times poll who said they would not eat genetically engineered salmon.2 The FDA said it would probably not require labeling of the fish; however Alaska, a top wild salmon producer, requires labeling of genetically engineered salmon and momentum is growing for GMO labeling in a number of states across the U.S. -
Problems in Gene Therapy and Transgenesis
Problems in Gene Therapy and Transgenesis Prof. Dr. Oliver Kayser Technische Biochemie TU Dortmund 16.03.2015 Chapter 5 - Transgenesis and Gene 1 Therapy Producing transgenic animals Purpose: Production of heterolog proteins in transgenic animals Principle: Integration of heterolog DNA with selected genetic information in fertilised eggs Methods: Mikroinjektion (-) Retrovirus vectors (-) Genetically modified embryonic stem cells (++) 16.03.2015 Chapter 5 - Transgenesis and Gene Therapy 2 16.03.2015 Chapter 5 - Transgenesis and Gene Therapy 3 Dolly 16.03.2015 Chapter 5 - Transgenesis and Gene 4 Therapy Telomers 16.03.2015 Chapter 5 - Transgenesis and Gene 5 Therapy klausurrelevant 16.03.2015 Chapter 5 - Transgenesis and Gene Therapy 6 16.03.2015 Chapter 5 - Transgenesis and Gene Therapy 7 Advantage of sheeps and goats as transgenic animals • high milk production capacity (2-3 l/ day) • short gestation period and quick maturation • low capital investment • easy handling and breeding • high expression level of proteins (35g protein/ l milk) • easy downstream processing • ongoing supply of product is guaranteed by breeding 16.03.2015 Chapter 5 - Transgenesis and Gene 8 Therapy Drug safety • Genetic stability from animal to anmial • Variation in produktion und purity during lactation • Microbial, varial, and mykoplasm contamination • TSE, Scrapie • Age and general conditions of animals 16.03.2015 Chapter 5 - Transgenesis and Gene 9 Therapy Atryn • First recombinant therapeutic protein approved in 2009 • Anticoagulant for treatment of antithrombin -
Putting the Cartel Before the Horse ...And Farm, Seeds, Soil, Peasants, Etc
Communiqué www.etcgroup.org September 2013 No. 111 Putting the Cartel before the Horse ...and Farm, Seeds, Soil, Peasants, etc. Who Will Control Agricultural Inputs, 2013? In this Communiqué, ETC Group identifies the major corporate players that control industrial farm inputs. Together with our companion poster, Who will feed us? The industrial food chain or the peasant food web?, ETC Group aims to de-construct the myths surrounding the effectiveness of the industrial food system. Table of contents Introduction: 3 Messages 3 Seeds 6 Commercial Seeds 7 Pesticides and Fertilizers 10 Animal pharma 15 Livestock Genetics 17 Aquaculture Genetics Industry 26 Conclusions and Policy Recommendations 31 Introduction: 3 Messages ETC Group has been monitoring the power and global reach of agro-industrial corporations for several decades – including the increasingly consolidated control of agricultural inputs for the industrial food chain: proprietary seeds and livestock genetics, chemical pesticides and fertilizers and animal pharmaceu- ticals. Collectively, these inputs are the chemical and biological engines that drive industrial agriculture. This update documents the continuing concentration (surprise, surprise), but it also brings us to three conclusions important to both peasant producers and policymakers… 1. Cartels are commonplace. Regulators have lost sight of the well-accepted economic principle that the market is neither free nor healthy whenever 4 companies control more than 50% of sales in any commercial sector. In this report, we show that the 4 firms / 50% line in the sand has been substan- tially surpassed by all but the complex fertilizer sector. Four firms control 58.2% of seeds; 61.9% of agrochemicals; 24.3% of fertilizers; 53.4% of animal pharmaceuticals; and, in livestock genetics, 97% of poultry and two-thirds of swine and cattle research. -
Should Genetically Modified Salmon Be Part of the Human Food Chain? Todd Biddle Cumberland Valley High School July 2011
Should Genetically Modified salmon be part of the Human Food Chain? Todd Biddle Cumberland Valley High School July 2011 Authors note: This case study is based on a real and current political upheaval amongst the United States House of Representatives, the Senate, the FDA, the consumer, and AquaBountyTechnologies®. Photo courtesy of Living in a Modern World. Modernest. Photo courtesy of AquaBounty Technologies. Aqu Advantage Fish. AquaBounty September 2010. Technologies 2011. http://www.aquabounty.com/PressRoom/ http://blog.modernest.com/2010/09/21/an-upstream- swim-to-stop-ge-salmon/ Introduction: What is for dinner? The choices for our dinner plate continue to evolve due to modern technologies and new information about human health. One way the “undesirable” genetics of edible plants and animals can be changed over time is through the process of artificial selection, a form of selective breeding. Artificial selection involves agriculturists selecting plants and animals that have the most desirable traits for producing our food. These plants and animals become the parent stock of future generations. In recent years, creating genetically modified crops and now animals has become an alternative to artificial selection. Even though genetically modified crops have been part of the human diet since the 1990s, genetically modified foods are often met with criticism from global consumers (Note: the European Commission has received responses from some European countries who wish to ban genetically modified organisms). There is a lack of public trust in their safety and they flag a number of environmental concerns. Genetically modified salmon, AquAdvantage® Salmon, engineered by the company AquaBounty Technologies may become the first genetically modified animal protein approved by the Food and Drug Administration, FDA. -
The Ocean Genome: Conservation and the Fair, Equitable and Sustainable Use of Marine Genetic Resources
Commissioned by BLUE PAPER The Ocean Genome: Conservation and the Fair, Equitable and Sustainable Use of Marine Genetic Resources LEAD AUTHORS Robert Blasiak, Rachel Wynberg, Kirsten Grorud-Colvert and Siva Thambisetty CONTRIBUTING AUTHORS Narcisa M. Bandarra, Adelino V.M. Canário, Jessica da Silva, Carlos M. Duarte, Marcel Jaspars, Alex D. Rogers, Kerry Sink and Colette C.C. Wabnitz oceanpanel.org About this Paper Established in September 2018, the High Level Panel for a Sustainable Ocean Economy (HLP) is a unique initiative of 14 serving heads of government committed to catalysing bold, pragmatic solutions for ocean health and wealth that support the Sustainable Development Goals and build a better future for people and the planet. By working with governments, experts and stakeholders from around the world, the HLP aims to develop a road map for rapidly transitioning to a sustainable ocean economy, and to trigger, amplify and accelerate responsive action worldwide. The HLP consists of the presidents or prime ministers of Australia, Canada, Chile, Fiji, Ghana, Indonesia, Jamaica, Japan, Kenya, Mexico, Namibia, Norway, Palau and Portugal, and is supported by an Expert Group, Advisory Network and Secretariat that assist with analytical work, communications and stakeholder engagement. The Secretariat is based at World Resources Institute. The HLP has commissioned a series of ‘Blue Papers’ to explore pressing challenges at the nexus of the ocean and the economy. These Blue Papers summarise the latest science and state-of-the-art thinking about innovative ocean solutions in the technology, policy, governance and finance realms that can help accelerate a move into a more sustainable and prosperous relationship with the ocean. -
Transgenic Animals
IQP-43-DSA-4208 IQP-43-DSA-6270 TRANSGENIC ANIMALS An Interactive Qualifying Project Report Submitted to the Faculty of WORCESTER POLYTECHNIC INSTITUTE In partial fulfillment of the requirements for the Degree of Bachelor of Science By: _________________________ _________________________ William Caproni Erik Dahlinghaus August 24, 2012 APPROVED: _________________________ Prof. David S. Adams, PhD WPI Project Advisor ABSTRACT A transgenic animal contains genes not native to its species. The use of these animals in research and medicine has dramatically increased our understanding of genetics and disease modeling. This IQP aims to provide an overview of the technical development and applications of transgenic animals, as well as the ethical, legal, and societal ramifications of creating these animals. Finally, this IQP will draw conclusions from the research performed and the information gathered. 2 TABLE OF CONTENTS Signature Page …………………………………………..…………………………….. 1 Abstract …………………………………………………..……………………………. 2 Table of Contents ………………………………………..…………………………….. 3 Project Objective ……………………………………….....…………………………… 4 Chapter-1: Transgenic Animal Technology …….……….…………………………… 5 Chapter-2: Applications of Transgenics in Animals …………..…………………….. 19 Chapter-3: Transgenic Ethics ………………………………………………………... 32 Chapter-4: Transgenic Legalities ……………………..………………………………. 43 Project Conclusions...…………………………………..….…………………………… 53 3 PROJECT OBJECTIVES The objective of this project was to research and present a multifaceted view of transgenics, including the technology itself and its effects on mankind. Chapter one offers an overview of the different methods for creating and testing transgenic animals. Chapter two provides information on how the different types of transgenic animals are used, and how they affect our daily lives. Chapter three presents the many ethical issues surrounding this controversial technology, and its impact on society. Chapter four describes the legal issues regarding this emerging technology and the patenting of life. -
Aquabounty Technologies, Inc. (Exact Name of the Registrant As Specified in Its Charter)
Table of Contents UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 _____________________________ Form 10-K ☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2020 ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from ________________ to ________________ Commission file number: 001-36426 _____________________________ AquaBounty Technologies, Inc. (Exact name of the registrant as specified in its charter) Delaware 04-3156167 (State or other jurisdiction of (I.R.S. employer incorporation or organization) identification no.) 2 Mill & Main Place, Suite 395 Maynard, Massachusetts 01754 (978) 648-6000 (Address and telephone number of the registrant’s principal executive offices) Securities registered pursuant to Section 12(b) of the Securities Exchange Act of 1934 (the “Exchange Act”): Title of each class Trading Symbol(s) Name of exchange on which registered Common Stock, par value $0.001 per share AQB The NASDAQ Stock Market LLC Securities registered pursuant to Section 12(g) of the Act: None Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act of 1933. Yes ☐ No ☒ Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Exchange Act. Yes ☐ No ☒ Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. -
TRANSGENIC SALMON IS FRAUGHT with UNCERTAINTIES and IRREVERSIBLE HARMFUL CONSEQUENCES 2.Pdf
www.theguardian.com TRANSGENIC SALMON IS FRAUGHT WITH UNCERTAINTIES AND IRREVERSIBLE HARMFUL CONSEQUENCES. In May 2016, the Canadian Food Inspection Agency approved the sale of the GM fish. In July 2017, AquaBounty Technologies said they had sold 4.5 tons of AquaAdvantage salmon fillets to customers in Canada. AquaBounty first asked the FDA to approve the fish for human consumption in 1996. But the FDA said because this was the first genetically modified animal that would be eaten by humans, the agency wanted to take it slow and weigh the pros and cons.Nov 19, 2015 Aquadvantage salmon FDA Approval The Food and Drug Administration (FDA) approved AquaBounty Technologies' application to sell the AquAdvantage salmon to U.S. consumers on November 19, 2015. ... The decision marks the first time a genetically modified animal has been approved to enter the United States food supply. The AquaBounty transgenic Salmon are only allowed to be raise in two land-bases tanks Submission to the FDA TRANSGENIC SALMON IS FRAUGHT WITH UNCERTAINTIES AND IRREVERSIBLE HARMFUL CONSEQUENCES. Sunday, 20 October 2013 21:54 By Joan Russow PhD Global Compliance Research Project It is reported that the FDA is poised to approve Genetically engineered Aquabounty Salmon for human consumption; If approved, it would be the first-ever GE animal permitted for human consumption in the U.S. On April 26 2013 the 120-day comment period ended with 1.8 million submissions opposing the approval of Aquabounty salmon. Once approved, will it be exported everywhere? Unless there is a global ban on genetically engineered food and crops, global citizens will have to be constantly vigilant and have to oppose over and over again each new product introduced by this rogue technology.