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Stored Grain Insects and Pea Weevil (Live) Insects Large – Dead Or Alive
To whom it may concern, Proposal for GTA Standards change regarding Cereal grains for categories: Stored Grain Insects and Pea Weevil (live) Insects Large – dead or alive Currently there is a lack of reference with insects of NIL tolerance applied by DA for export and that listed within GTA standards. This has the potential to cause contract disputes especially in the grower direct to port transactions. At present if a supplier delivers grain with live insects for example Small-eyed flour beetles and Black fungus beetles, there is no reference in the standards that declare such insects as NIL tolerance. If the buyer was loading a container direct for export this would pose a problem due to the NIL tolerance being applied by DA for export phytosanitary requirements. These insects are in the same category as Psocids which are listed in GTA receival standards. I would like to see the GTA "Stored Grain Insects and Pea Weevil (live)" & "Insects Large – dead or alive" reflect the Department of Agriculture PEOM 6a: Pests, Diseases and Contaminants of Grain and Plant Products (excluding horticulture) http://www.agriculture.gov.au/SiteCollectionDocuments/aqis/exporting/plants-exports-operation-manual/vol6A.pdf I put forward the motion to have all major and minor injurious pests listed within PEOM 6a that apply to cereal grains to be of NIL tolerance within the GTA standards. 1) This would involve moving the Hairy Fungus Beetle Typhaea stercorea from “Insects Large – dead or alive” to the list of “Stored Grain Insects and Pea Weevil (live)”. Thus taking it from a tolerance level of 3 per half litre to NIL. -
Darkling Beetles and Mealworms Theresa A
Darkling Beetles and Mealworms Theresa A. Dellinger and Eric R. Day, Department of Entomology, Virginia Tech Description Darkling beetles belong in the beetle family Tenebrionidae, which consists of more than 20,000 species of beetles. Adult darkling beetles widely range in shape and size, with most measuring from 2 – 19 mm (0.13” – 0.75”). Adults are usually a reddish-brown to brownish-black in color and can be shiny or dull. The elytra (the wing covers) can be smooth, grooved, or otherwise sculptured. Most do not have colorful patterns on their wing covers. Adults are most active at night and tend to avoid bright lights. Darkling beetle larvae are often referred to as mealworms or false wireworms. They are long, hard-bodied grubs with a cylindrical shape and are shiny yellow-brown to darKer brown in color. They are active crawlers. Yellow mealworm larva, top. Dark mealworm larva, bottom. Clemson University-USDA Cooperative Adult yellow mealworm, Tenebrio molitor. Extension Slide Series, Bugwood.org. Clemson University-USDA Cooperative Extension Slide Series, Bugwood.org. Life Cycle Darkling beetles have a complete life cycle with egg, larval, pupal, and adult stages. Most species of darkling beetles have a slow rate of development and may live for a year as an adult. Species living on grains or other stored products may develop faster. Habitat/Distribution Darkling beetles are found throughout the world except for places with very cold climates. They are scavengers and omnivores, feeding on decomposing plant material, dead insects, fungi, and stored products. Only a handful of darkling beetles are considered pests; the vast majority of them live in the wild and pose no harm. -
State-Of-The-Art on Use of Insects As Animal Feed
State-of-the-art on use of insects as animal feed Harinder P.S. Makkar1, Gilles Tran2, Valérie Heuzé2 and Philippe Ankers1 1 Animal Production and Health Division, FAO, Rome 2 Association Française de Zootechnie, Paris, France Full reference of the paper: Animal Feed Science and Technology, Volume 197, November 2014, pages 1-33 Link: http://www.animalfeedscience.com/article/S0377-8401(14)00232-6/abstract http://dx.doi.org/10.1016/j.anifeedsci.2014.07.008 Abstract A 60-70% increase in consumption of animal products is expected by 2050. This increase in the consumption will demand enormous resources, the feed being the most challenging because of the limited availability of natural resources, ongoing climatic changes and food-feed-fuel competition. The costs of conventional feed resources such as soymeal and fishmeal are very high and moreover their availability in the future will be limited. Insect rearing could be a part of the solutions. Although some studies have been conducted on evaluation of insects, insect larvae or insect meals as an ingredient in the diets of some animal species, this field is in infancy. Here we collate, synthesize and discuss the available information on five major insect species studied with respect to evaluation of their products as animal feed. The nutritional quality of black soldier fly larvae, the house fly maggots, mealworm, locusts- grasshoppers-crickets, and silkworm meal and their use as a replacement of soymeal and fishmeal in the diets of poultry, pigs, fish species and ruminants are discussed. The crude protein contents of these alternate resources are high: 42 to 63% and so are the lipid contents (up to 36% oil), which could possibly be extracted and used for various applications including biodiesel production. -
Handbook 2007-2008
FLORIDA STATE UNIVERSITY DEPARTMENT OF BIOLOGICAL SCIENCE UNDERGRADUATE HANDBOOK 2007 – 2008 0 THE DEPARTMENT OF BIOLOGICAL SCIENCE ADMINISTRATION The Department of Biological Science administration and faculty are housed in multiple buildings on the Florida State campus including Conradi Building, Biology Unit I, and the Biomedical Research Facility. Biological science faculty is also housed in the Institute of Molecular Biophysics and the Nuclear Research Building. The department consists of 50 faculty members; over 60 administrative, technical, and support staff; 100 graduate students; and 1,800 undergraduate majors. UNDERGRADUATE ADVISING FACULTY & STAFF Dr. Robert Reeves Dr. Joanna Carter Mr. Delmar Little Dr. D. Craig Filar Assoc.Chair, Undergrad Studies Academic Advisor Academic Advisor Academic Advisor 330 Conradi 205 Conradi 204 Conradi 204 Conradi [email protected] [email protected] [email protected] [email protected] (850) 644-2248 (850) 644-3099 (850) 644-9351 (850) 644-4781 ADMINISTRATIVE CONTACTS IN BIOLOGICAL SCIENCE Dr. Timothy S. Moerland Dr. Lloyd Epstein Chairman, Department of Biological Science Associate Chairman for Curriculum and Development 214 Conradi 239 BIO Unit I [email protected] [email protected] (850) 644-4424 (850) 644-4560 Dr. George Bates Dr. Walter Tschinkel Associate Chairman for Graduate Studies Director, Honors In The Major 202 Conradi 203 BIO Unit I [email protected] [email protected] (850) 644-3023 (850) 644-4489 Judy Bowers Dr. Ann Lumsden Graduate Academic Affairs Coordinator Director, Non-Major Biology Curriculum 202 Conradi 428 Carothers [email protected] [email protected] (850) 644-3023 (850) 644-6826 ADMINISTRATIVE CONTACTS IN RELATED PROGRAMS Ms. -
Use Them for What They Are Good At: Mealworms in Circular Food Systems
insects Article Use Them for What They Are Good at: Mealworms in Circular Food Systems Hartmut Derler 1,2,*, Andrea Lienhard 1, Simon Berner 1, Monika Grasser 1, Alfred Posch 2 and René Rehorska 1 1 Institute of Applied Production Sciences, Sustainable Food Management, University of Applied Sciences FH JOANNEUM, Eggenberger Allee 11, 8020 Graz, Austria; [email protected] (A.L.); [email protected] (S.B.); [email protected] (M.G.); [email protected] (R.R.) 2 Institute of Systems Sciences, Innovation and Sustainability Research, University of Graz, Merangasse 18/1, 8010 Graz, Austria; [email protected] * Correspondence: [email protected] Simple Summary: Different challenges exist, such as climate change and a growing number of people living on the planet, that put pressure on current and future food systems. In the future, more food must be produced on less land. At the same time, food-related greenhouse gas emissions must be reduced to be in line with the 2 ◦C climate goal, to limit potential risks of climate change. In this context, mealworms have been discussed as a sustainable and resource-efficient protein production option in circular food systems. They are an efficient biomass converter of low-quality by-products, such as wheat bran and brewer’s spent grain. In this article, we provide an overview of by-products that have been used in mealworm feeding trials. We quantify commonly available by-product types in Austria, and discuss potentials and limitations associated with mealworm farming. We found that further research is needed to better understand the strengths of mealworms in circular food systems, and several hurdles need to be addressed so that mealworm farming becomes more attractive in Western countries. -
4 Biology, Behavior, and Ecology of Insects in Processed Commodities
4 Biology, Behavior, and Ecology of Insects in Processed Commodities Rizana M. Mahroof David W. Hagstrum Most insects found in storage facilities consume Red flour beetle, Tribolium commodities, but some feed on mold growing castaneum (Herbst) on stored products. Others may be predators and parasitoids. Insects that attack relatively dry pro- Red flour beetle adults (Figure 1) are reddish brown. cessed commodities (those with about 10% or more Eggs are oblong and white. Adults show little moisture content at 15 to 42oC) can cause signifi- preference for cracks or crevices as oviposition sites. cant weight losses during storage. Insects occur in Eggshells are coated with a sticky substance that aids flour mills, rice mills, feed mills, food processing in attaching the eggs to surfaces and causes small facilities, breakfast and cereal processing facilities, particles to adhere to them (Arbogast 1991). Larvae farm storages, grain bins, grain elevators, bakeries, are yellowish white with three pair of thoracic legs. warehouses, grocery stores, pet-food stores, herbari- ums, museums, and tobacco curing barns. Economic Typically, there are six to seven larval instars, losses attributed to insects include not only weight depending on temperature and nutrition. Larvae loss of the commodity, but also monitoring and pest move away from light, living concealed in the food. management costs and effects of contamination on Full-grown larvae move to the food surface or seek product trade name reputation. shelter for pupation. Pupae are white and exarate, which means that appendages are not fused to the body. External genitalic characters on pupae can be Life Histories used to differentiate males and females (Good 1936). -
Alternative Reproductive Tactics and Male-Dimorphism in the Horned Beetle Onthophagus Acuminatus (Coleoptera: Scarabaeidae)
Behav Ecol Sociobiol (1997) 41: 335±341 Ó Springer-Verlag 1997 Douglas J. Emlen Alternative reproductive tactics and male-dimorphism in the horned beetle Onthophagus acuminatus (Coleoptera: Scarabaeidae) Received: 12 October 1996 / Accepted after revision: 8 August 1997 Abstract Adult dung beetles (Onthophagus acuminatus) Key words Alternative reproductive behavior á exhibit continuous variation in body size resulting from Male dimorphism á Male competition á dierential nutritional conditions experienced during Horned beetles á Onthophagus larval development. Males of this species have a pair of horns that protrude from the base of the head, and the lengths of these horns are bimodally distributed in nat- Introduction ural populations. Males growing larger than a threshold body size develop long horns, and males that do not Males in many animal species show variation in mor- achieve this size grow only rudimentary horns or no phology which is associated with dierences in behavior horns at all. Previous studies of other horned beetle (e.g., Austad 1984; Dominey 1984; Travis 1994). For species have shown that horned and hornless males often example, large and small males frequently utilize strik- have dierent types of reproductive behavior. Here I ingly dierent behaviors to encounter and mate with describe the mating behaviors of the two male morphs of females (Dominey 1980; Rubenstein 1980, 1987; How- O. acuminatus during encounters with females. Females ard 1984; Gross 1985; Kodric-Brown 1986; Arak 1988; excavate tunnels beneath dung, where they feed, mate Reynolds et al. 1993). Occasionally, variation in male and provision eggs. Large, horned males were found to morphology is dimorphic, and two or more distinct male guard entrances to tunnels containing females. -
Natural Selection and Genetic Differentiation of Behaviour Between Parasitoids from Wild and Cultivated Habitats
Heredity 83 (1999) 127±137 Received 20 November 1998, accepted 18 March 1999 Natural selection and genetic differentiation of behaviour between parasitoids from wild and cultivated habitats SASKYA VAN NOUHUYS* & SARA VIA Department of Entomology, Cornell University, Ithaca, New York 14853, U.S.A. Dierences in behaviour between individuals in populations living in dierent environments may result from evolution proceeding dierently in each population. The parasitoid wasp Cotesia glomerata (L.) (Hymenoptera: Braconidae) parasitizes early instar larvae of butter¯ies in the family Pieridae. In the study area the only host of C. glomerata is the Small Cabbage White Butter¯y [Pieris rapae (L.) (Lepidoptera: Pieridae)], which feeds on cruciferous host plants in a variety of habitats. The behaviour of this parasitoid wasp collected from two habitat types (wild and agricultural) was observed in a reciprocal transplant-style experiment in a greenhouse. Dierences in behaviour between wasp sources and test habitat type were analysed using canonical analysis in multivariate analysis of variance. Directional selection on parasitoid behaviour in each test habitat type was estimated by regressing the relative rate of parasitism (a measure of relative ®tness) on the behavioural character state. We found that there is genetic dierentiation of behaviour between wasps from wild and cultivated habitats and that a dierent set of behaviours is associated with short-term ®tness within models of each source habitat. There was no evidence of local adaptation of wasps to either habitat. Keywords: Cotesia glomerata, evolution, foraging behaviour, Pieris rapae, tritrophic interaction. Introduction have been shown to orientate upwind towards odour sources (see van Alphen & Vet, 1986; Turlings et al., Natural selection in dierent habitat types can lead to 1991; Benrey et al., 1997), and to orientate towards genetic divergence and local adaptation of populations. -
Arthropods and the Current Great Mass Extinction: Effective Themes to Decrease Arthropod Fear and Disgust and Increase Positive Environmental Beliefs in Children?
International Journal Journal of Environmental of Environmental & Science & Educat Scienceion Education (2014), 9, 197-214 Vol. 3, No. 3, July 2008, xx-xx Arthropods and the Current Great Mass Extinction: Effective Themes to Decrease Arthropod Fear and Disgust and Increase Positive Environmental Beliefs in Children? Amy Wagler The University of Texas at El Paso Ron Wagler The University of Texas at El Paso Received 16 October 2013; Accepted 14 February 2014 Doi: 10.12973/ijese.2014.211a Earth is experiencing a great mass extinction (GME) that has been caused by the environmentally destructive activities of humans. This GME is having and will have profound effects on Earth’s biodiversity if environmental sustainability is not reached. Activities and curriculum tools have been developed to assist teachers in integrating the current GME theme into their existing curriculum. There has also been a recent appeal to incorporate the current GME theme into science and environmental education research but this research has yet to be conducted. This study presents the first time the current GME theme has been assessed in a research setting. This study analyzed the effect living Poecilotheria spider activities had on United States children. The variables measured included 1) human fear toward the Poecilotheria spiders; 2) human disgust toward the Poecilotheria spiders; and 3) human environmental beliefs associated with the current GMEs impact on the Poecilotheria spiders. New to this study is the finding that the use of living spiders in a positive educational setting that addresses the current GME are effective tools in decreasing fear and disgust and increasing positive environmental beliefs toward Poecilotheria spiders in children. -
Sterile Insect Technique. Principles and Practice in Area-Wide Integrated Pest Management, 3–36
Sterile Insect Technique Principles and Practice in Area-Wide Integrated Pest Management Edited by V. A. DYCK J. HENDRICHS and A.S. ROBINSON Joint FAO/IAEA Programme Vienna, Austria A C.I.P. Catalogue record for this book is available from the Library of Congress. ISBN-10 1-4020-4050-4 (HB) ISBN-13 978-1-4020-4050-4 (HB) ISBN-10 1-4020-4051-2 ( e-book) ISBN-13 978-1-4020-4051-1 (e-book) Published by Springer, P.O. Box 17, 3300 AA Dordrecht, The Netherlands. www.springeronline.com Printed on acid-free paper Photo Credits: A.S. Robinson and M.J.B. Vreysen provided some of the photos used on the front and back covers. All Rights Reserved © 2005 IAEA All IAEA scientific and technical publications are protected by the terms of the Universal Copyright Convention on Intellectual Property as adopted in 1952 (Berne) and as revised in 1972 (Paris). The copyright has since been extended by the World Intellectual Property Organization (Geneva) to include electronic and virtual intellectual property. Permission to use whole or parts of texts contained in IAEA publications in printed or electronic form must be obtained and is usually subject to royalty agreements. Proposals for non- commercial reproductions and translations are welcomed and considered on a case-by-case basis. Inquiries should be addressed to the Publishing Section, IAEA, Wagramer Strasse 5, A-1400 Vienna, Austria. Printed in the Netherlands. PREFACE It is a challenge to bring together all relevant information about the sterile insect technique (SIT) and its application in area-wide integrated pest management (AW- IPM) programmes; this book is the first attempt to do this in a thematic way. -
Abstract Volume
th German Zoological Society 105 Annual Meeting Abstract Volume September 21 – 24, 2012 University of Konstanz, Germany Sponsored by: Dear Friends of the Zoological Sciences! Welcome to Konstanz, to the 105 th annual meeting of the German Zoological Society (Deutsche ZoologischeGesellschaft, DZG) – it is a great pleasure and an honor to have you here as our guests! We are delighted to have presentations of the best and most recent research in Zoology from Germany. The emphasis this year is on evolutionary biology and neurobiology, reflecting the research foci the host laboratories from the University of Konstanz, but, as every year, all Fachgruppen of our society are represented – and this promisesto be a lively, diverse and interesting conference. You will recognize the standard schedule of our yearly DZG meetings: invited talks by the Fachgruppen, oral presentations organized by the Fachgruppen, keynote speakers for all to be inspired by, and plenty of time and space to meet and discuss in front of posters. This year we were able to attract a particularly large number of keynote speakers from all over the world. Furthermore, we have added something new to the DZG meeting: timely symposia about genomics, olfaction, and about Daphnia as a model in ecology and evolution. In addition, a symposium entirely organized by the PhD-Students of our International Max Planck Research School “Organismal Biology” complements the program. We hope that you will have a chance to take advantage of the touristic offerings of beautiful Konstanz and the Bodensee. The lake is clean and in most places it is easily accessed for a swim, so don’t forget to bring your swim suits.A record turnout of almost 600 participants who have registered for this year’s DZG meeting is a testament to the attractiveness of Konstanz for both scientific and touristic reasons. -
Surprisingly Little Population Genetic Structure in a Fungus-Associated Beetle Despite Its Exploitation of Multiple Hosts"
Swarthmore College Works Biology Faculty Works Biology 6-1-2013 Surprisingly Little Population Genetic Structure In A Fungus- Associated Beetle Despite Its Exploitation Of Multiple Hosts Corlett W. Wood , '08 H. M. Donald Vincent A. Formica Swarthmore College, [email protected] E. D. Brodie III Follow this and additional works at: https://works.swarthmore.edu/fac-biology Part of the Biology Commons, and the Evolution Commons Let us know how access to these works benefits ouy Recommended Citation Corlett W. Wood , '08; H. M. Donald; Vincent A. Formica; and E. D. Brodie III. (2013). "Surprisingly Little Population Genetic Structure In A Fungus-Associated Beetle Despite Its Exploitation Of Multiple Hosts". Ecology And Evolution. Volume 3, Issue 6. 1484-1494. DOI: 10.1002/ece3.560 https://works.swarthmore.edu/fac-biology/110 This work is brought to you for free by Swarthmore College Libraries' Works. It has been accepted for inclusion in Biology Faculty Works by an authorized administrator of Works. For more information, please contact [email protected]. Surprisingly little population genetic structure in a fungus- associated beetle despite its exploitation of multiple hosts Corlett W. Wood1, Hannah M. Donald1, Vincent A. Formica2 & Edmund D. Brodie III1 1Mountain Lake Biological Station, Department of Biology, University of Virginia, Charlottesville, Virginia, 22904 2Department of Biology, Swarthmore College, Swarthmore, Pennsylvania, 19801 Keywords Abstract Bolitotherus cornutus, community diversity, environmental heterogeneity, resource- In heterogeneous environments, landscape features directly affect the structure associated population structure. of genetic variation among populations by functioning as barriers to gene flow. Resource-associated population genetic structure, in which populations that use Correspondence different resources (e.g., host plants) are genetically distinct, is a well-studied Corlett W.