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Nora M. Bello, Phd
Nora M. Bello, PhD, DVM Curriculum Vitae updated as of 08/14/2020 002 Dickens Hall E-mail: [email protected] Department of Statistics http://www.k-state.edu/stats/people/bello.html Kansas State University https://norabello.weebly.com Manhattan, KS 66506, USA EDUCATION Doctor of Philosophy 2010 Department of Animal Science, Michigan State University, East Lansing, MI Dissertation title: “Hierarchical Bayesian Modeling of Heterogeneity in the Relationship between Milk Production and Reproductive Performance in Dairy Cows”. Emphasis on methodological development and implementation of hierarchical Bayesian multivariate statistical models for heterogeneous covariances. Advisor: Dr. Robert J. Tempelman, Professor Master of Science, Applied Statistics 2008 Department of Statistics and Probability Michigan State University, East Lansing, MI Master of Science, Animal Science 2006 Department of Animal Science Michigan State University, East Lansing, MI Thesis Title: “Optimizing ovulation to first GnRH improved outcomes to each hormonal injection of Ovsynch in lactating dairy cows”. Emphasis in reproductive physiology and management of cattle Advisor: Dr. J. Richard Pursley, Associate Professor Veterinary Medicine Doctor 2003 Catholic University of Cordoba, Cordoba, Argentina Junior Computer Science and Database Management Technician 1997 Cervantes Institution for Computer Sciences, Cordoba, Argentina PROFESSIONAL EMPLOYMENT EXPERIENCE Full Professor 2020 – Present Associate Professor 2015 – 2020 Assistant Professor 2010 – 2015 Department of Statistics, -
Common Greenhouse Insects and Mites Identification and Management the List of Common Greenhouse Insects and Mites in Colorado Is a Fairly Short One
Common Greenhouse Insects and Mites Identification and Management The list of common greenhouse insects and mites in Colorado is a fairly short one: • Aphids (several species) • Whiteflies (one species) • Thrips (two common species) • Twpspotted spider mite • Fungus gnats • Tomato/potato psyllid Aphids Hemiptera: Aphididae Primary aphid species found in greenhouses Green peach aphid Cotton-melon aphid Potato aphid Body plan of a typical, wingless aphid All aphids go through three feeding stages, each punctuated with a molting event “Cast skins”, the discarded remnants of the exoskeleton after molting Diagnostic: “Cast Skins” remain after aphids molt Live birth and asexual reproduction are the norm with aphids Aphid populations can increase rapidly Adults may be winged or wingless Wing pads of late stage aphid nymph Adults may be winged or wingless Piercing-sucking mouthparts of Hemiptera (aphids, whiteflies, mealybugs, leafhoppers, etc.) Probocis (primarily the labium) of an aphid Stylet bundle (mandibles and maxillae) meandering through plant en route to phloem Aphids use their mouthparts to access the fluids of the phloem Little, if any, cell injury is produced by most aphids Important Note: Presence of aphids does not always equate to occurrence of plant injury! Honeydew production Uptake of phloem fluids here Emergence of “honeydew” here Leaf with sparkles of honeydew – and cast skins The leaf above the honeydew – an aphid colony Leaf with sparkles of honeydew – and cast skins Some non-aphid honeydew producing insects Whiteflies Mealybugs -
Further Screening of Entomopathogenic Fungi and Nematodes As Control Agents for Drosophila Suzukii
insects Article Further Screening of Entomopathogenic Fungi and Nematodes as Control Agents for Drosophila suzukii Andrew G. S. Cuthbertson * and Neil Audsley Fera, Sand Hutton, York YO41 1LZ, UK; [email protected] * Correspondence: [email protected]; Tel.: +44-1904-462-201 Academic Editor: Brian T. Forschler Received: 15 March 2016; Accepted: 6 June 2016; Published: 9 June 2016 Abstract: Drosophila suzukii populations remain low in the UK. To date, there have been no reports of widespread damage. Previous research demonstrated that various species of entomopathogenic fungi and nematodes could potentially suppress D. suzukii population development under laboratory trials. However, none of the given species was concluded to be specifically efficient in suppressing D. suzukii. Therefore, there is a need to screen further species to determine their efficacy. The following entomopathogenic agents were evaluated for their potential to act as control agents for D. suzukii: Metarhizium anisopliae; Isaria fumosorosea; a non-commercial coded fungal product (Coded B); Steinernema feltiae, S. carpocapsae, S. kraussei and Heterorhabditis bacteriophora. The fungi were screened for efficacy against the fly on fruit while the nematodes were evaluated for the potential to be applied as soil drenches targeting larvae and pupal life-stages. All three fungi species screened reduced D. suzukii populations developing from infested berries. Isaria fumosorosea significantly (p < 0.001) reduced population development of D. suzukii from infested berries. All nematodes significantly reduced adult emergence from pupal cases compared to the water control. Larvae proved more susceptible to nematode infection. Heterorhabditis bacteriophora proved the best from the four nematodes investigated; readily emerging from punctured larvae and causing 95% mortality. -
VINEYARD BIODIVERSITY and INSECT INTERACTIONS! ! - Establishing and Monitoring Insectariums! !
! VINEYARD BIODIVERSITY AND INSECT INTERACTIONS! ! - Establishing and monitoring insectariums! ! Prepared for : GWRDC Regional - SA Central (Adelaide Hills, Currency Creek, Kangaroo Island, Langhorne Creek, McLaren Vale and Southern Fleurieu Wine Regions) By : Mary Retallack Date : August 2011 ! ! ! !"#$%&'(&)'*!%*!+& ,- .*!/'01)!.'*&----------------------------------------------------------------------------------------------------------------&2 3-! "&(')1+&'*&4.*%5"/0&#.'0.4%/+.!5&-----------------------------------------------------------------------------&6! ! &ABA <%5%+3!C0-72D0E2!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!F! &A&A! ;D,!*2!G*0.*1%-2*3,!*HE0-3#+3I!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!J! &AKA! ;#,2!0L!%+D#+5*+$!G*0.*1%-2*3,!*+!3D%!1*+%,#-.!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!B&! 7- .*+%)!"/.18+&--------------------------------------------------------------------------------------------------------------&,2! ! ! KABA ;D#3!#-%!*+2%53#-*MH2I!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!BN! KA&A! O3D%-!C#,2!0L!L0-H*+$!#!2M*3#G8%!D#G*3#3!L0-!G%+%L*5*#82!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!&P! KAKA! ?%8%53*+$!3D%!-*$D3!2E%5*%2!30!E8#+3!AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA!&B! 9- :$"*!.*;&5'1/&.*+%)!"/.18&-------------------------------------------------------------------------------------&3<! -
Ecology and Role of the Rove Beetle, Dalotia Coriaria, and Insidious Flower Bug, Orius Insidiosus, in Greenhouse Biological Control Programs
Advances in Entomology, 2017, 5, 115-126 http://www.scirp.org/journal/ae ISSN Online: 2331-2017 ISSN Print: 2331-1991 Ecology and Role of the Rove Beetle, Dalotia coriaria, and Insidious Flower Bug, Orius insidiosus, in Greenhouse Biological Control Programs Raymond A. Cloyd*, Nathan J. Herrick Department of Entomology, Kansas State University, Manhattan, KS, USA How to cite this paper: Cloyd, R.A. and Abstract Herrick, N.J. (2017) Ecology and Role of the Rove Beetle, Dalotia coriaria, and Insidious Greenhouse production systems typically involve growing multiple crop types Flower Bug, Orius insidiosus, in Greenhouse simultaneously, including ornamentals and vegetables. Therefore, greenhouse Biological Control Programs. Advances in producers commonly deal with multiple pest complexes. Two important insect Entomology, 5, 115-126. https://doi.org/10.4236/ae.2017.54012 pests of greenhouse-grown horticultural crops are fungus gnats (Bradysia spp.) and western flower thrips (Frankliniella occidentalis). A plant protection Received: July 6, 2017 strategy that can be used to manage both pests is biological control. The rove Accepted: August 7, 2017 Published: August 10, 2017 beetle (Dalotia coriaria) and insidious flower bug (Orius insidiosus) are generalist predators commercially available for use in greenhouse production Copyright © 2017 by authors and systems targeting fungus gnats and the western flower thrips. This article Scientific Research Publishing Inc. describes the biology, behavior, ecology, and role of both natural enemies in This work is licensed under the Creative Commons Attribution International greenhouse production systems, and discusses the direct and indirect effects License (CC BY 4.0). of pesticides (insecticides, miticides, and fungicides) on D. -
Carpophilus Mutilatus) (Coleoptera: Nitidulidae) in Relation to Different Concentrations of Carbon Dioxide (CO2) - 6443
Nor-Atikah et al.: Evaluation on colour changes, survival rate and life span of the confused sap beetle (Carpophilus mutilatus) (Coleoptera: Nitidulidae) in relation to different concentrations of carbon dioxide (CO2) - 6443 - EVALUATION OF COLOUR CHANGES, SURVIVAL RATE AND LIFE SPAN OF THE CONFUSED SAP BEETLE (Carpophilus mutilatus) (COLEOPTERA: NITIDULIDAE) IN DIFFERENT CONCENTRATIONS OF CARBON DIOXIDE (CO2) NOR-ATIKAH, A. R. – HALIM, M. – NUR-HASYIMAH, H. – YAAKOP, S.* Centre for Insect Systematics, Department of Biological Sciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor, Malaysia *Corresponding author e-mail: [email protected]; phone: +60-389-215-698 (Received 8th Apr 2020; accepted 13th Aug 2020) Abstract. This study conducted in a rearing room (RR) (300-410 ppm) and in an open roof ventilation greenhouse system (ORVS) (800-950 ppm). No changes observed on Carpophilus mutilatus colouration after treatment in the ORVS. The survival rate increased from 61.59% in the F1 to 73.05% in the F2 generation reared in the RR. However, a sharp decline was observed from 27.05% in F1 to 1.5% in F2 in the ORVS. There was significant difference in number of individuals between RR and ORVS in F1 and F2 (F 12.76 p= 0.001< 0.05). The life span of F1 and F2 in the RR took about 46 days to complete; 7-21 days from adult to larvae stage, 5-15 days from the larval to pupal stage and 3-10 days from adult to pupal stage. Whereas in ORVS, F1 and F2 took about 30 and 22 days, respectively to complete their life cycles; that is 7-14, 7-14 days (adult to larval stage), 5-10, 0-5 days (larval to pupal stage) and 3-6, 0-3 days (pupal to adult stage), respectively. -
SR-112 Science of Hemp: Production and Pest Management
University of Kentucky College of Agriculture, Food and Environment Agricultural Experiment Station SR-112 Science of Hemp: Production and Pest Management Science of Hemp: Production and Pest Management October 10 –11, 2019 Agricultural Kentucky Tobacco Research and Development Center | Veterinary Diagnostic Laboratory | Division of Regulatory Services | Research and Education Center Experiment Station Robinson Forest | Robinson Center for Appalachian Resource Sustainability | University of Kentucky Superfund Research Center | Equine Programs emp (Cannabis sativa with <0.3% THC content) is grown for fiber, grain, and cannabinoid extraction in Asia, Europe, and the Americas. Until recently, HCannabis sativa has been classified as a Schedule 1 controlled substance in the US. The Agricultural Act of 2014 (Farm Bill) allowed for reintroduction of industrial hemp under a pilot research program. Acreage increases and addition of state legislation resulted in over 78,000 acres of hemp grown in 23 states by the end of 2018. Hemp became a legal commodity under the 2018 Farm Bill, and by the end of 2019, over 500,000 licensed acres were documented across 45 states. Canada re-introduced the crop in 1998, and in 2018, almost 78,000 acres of hemp were licensed and planted. With this increase in acreage and the lack of modern scientific data, university and government agricultural specialists began to work on various components of production and a range of realized challenges. This new information, however, had either not been shared or was not readily accessible to the scientific community, especially early results and nonpublished data. The first annual meeting of the Science of Hemp: Production and Pest Management was held on October 10-11, 2019 at the University of Kentucky in Lexington, KY. -
List of Biological Control Agents Widely Used in the Eppo Region
EPPO Standards SAFE USE OF BIOLOGICAL CONTROL LIST OF BIOLOGICAL CONTROL AGENTS WIDELY USED IN THE EPPO REGION PM 6/3 English 2021 VERSION oepp eppo European and Mediterranean Plant Protection Organization 21 Boulevard Richard Lenoir, 75011 Paris, France APPROVAL EPPO Standards are approved by EPPO Council. The date of approval appears in each individual standard. In the terms of Article II of the IPPC, EPPO Standards are Regional Standards for the members of EPPO. REVIEW EPPO Standards are subject to periodic review and amendment. The next review date for this set of EPPO Standards is decided by the EPPO Working Party on Phytosanitary Regulations. AMENDMENT RECORD Amendments will be issued as necessary, numbered and dated. The dates of amendment appear in each individual standard (as appropriate). DISTRIBUTION EPPO Standards are distributed by the EPPO Secretariat to all EPPO member governments. Copies are available to any interested person under particular conditions upon request to the EPPO Secretariat. SCOPE The EPPO Standards on the safe use of biological control are intended to be used by NPPOs or equivalent authorities, in their capacity as bodies responsible for overseeing and, if appropriate, regulating the introduction and use of biological control agents. OUTLINE OF REQUIREMENTS NPPOs of the EPPO region generally promote the use of biological control in plant protection because, like other aspects of integrated pest management, it reduces risks to human health and the environment. Use of biological control agents may, nevertheless, present some risks, in particular for the environment if exotic agents are introduced from other continents, and for the user if agents are formulated as plant protection products. -
Hox-Logic of Body Plan Innovations for Social Symbiosis in Rove Beetles
bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 Hox-logic of body plan innovations for social symbiosis in rove beetles 2 3 Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman4 and Steven R. Davis5 4 5 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, 6 CA 91125, USA 7 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity 8 Institute, University of Kansas, Lawrence, KS, USA 9 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New 10 York, NY 10032, USA 11 4Laboratory of Neurophysiology and Behavior, The Rockefeller University, New York, NY 10065, 12 USA 13 5Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, 14 USA 15 *correspondence: [email protected] 16 17 18 19 20 21 22 23 24 25 26 27 1 bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 How symbiotic lifestyles evolve from free-living ecologies is poorly understood. In 2 Metazoa’s largest family, Staphylinidae (rove beetles), numerous lineages have evolved 3 obligate behavioral symbioses with ants or termites. -
Hox-Logic of Preadaptations for Social Insect Symbiosis in Rove Beetles
bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. All rights reserved. No reuse allowed without permission. Hox-logic of preadaptations for social insect symbiosis in rove beetles Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman3 and Steven R. Davis3,4 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity Institute, University of Kansas, Lawrence, KS, USA 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New York, NY 10032, USA 4Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, USA *correspondence: [email protected] bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder. All rights reserved. No reuse allowed without permission. How symbiotic lifestyles evolve from free-living ecologies is poorly understood. Novel traits mediating symbioses may stem from preadaptations: features of free- living ancestors that predispose taxa to engage in nascent interspecies relationships. In Metazoa’s largest family, Staphylinidae (rove beetles), the body plan within the subfamily Aleocharinae is preadaptive for symbioses with social insects. Short elytra expose a pliable abdomen that bears targetable glands for host manipulation or chemical defense. The exposed abdomen has also been convergently refashioned into ant- and termite-mimicking shapes in multiple symbiotic lineages. Here we show how this preadaptive anatomy evolved via novel Hox gene functions that remodeled the ancestral coleopteran groundplan. -
Hox-Logic of Preadaptations for Social Insect Symbiosis in Rove Beetles
bioRxiv preprint doi: https://doi.org/10.1101/198945; this version posted October 5, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Hox-logic of preadaptations for social insect symbiosis in rove beetles Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman3 and Steven R. Davis3,4 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity Institute, University of Kansas, Lawrence, KS, USA 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New York, NY 10032, USA 4Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, USA *correspondence: [email protected] bioRxiv preprint doi: https://doi.org/10.1101/198945; this version posted October 5, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. How symbiotic lifestyles evolve from free-living ecologies is poorly understood. Novel traits mediating symbioses may stem from preadaptations: features of free- living ancestors that predispose taxa to engage in nascent interspecies relationships. In Metazoa’s largest family, Staphylinidae (rove beetles), the body plan within the subfamily Aleocharinae is preadaptive for symbioses with social insects. Short elytra expose a pliable abdomen that bears targetable glands for host manipulation or chemical defense. The exposed abdomen has also been convergently refashioned into ant- and termite-mimicking shapes in multiple symbiotic lineages. -
Effects of the Rove Beetle, Dalotia Coriaria, on Western Flower Thrips, Frankliniella Occidentalis, Under Laboratory Conditions
Effects of the rove beetle, Dalotia coriaria, on western flower thrips, Frankliniella occidentalis, under laboratory conditions; and integrating the entomopathogenic fungus, Beauveria bassiana, with D. coriaria to suppress western flower thrips populations under greenhouse conditions by Yinping Li B.S., Agricultural University of Hebei, 2009 M.S., Chinese Academy of Agricultural Sciences, 2012 AN ABSTRACT OF A DISSERTATION submitted in partial fulfillment of the requirements for the degree DOCTOR OF PHILOSOPHY Department of Entomology College of Agriculture KANSAS STATE UNIVERSITY Manhattan, Kansas 2019 Abstract Western flower thrips, Frankliniella occidentalis, is one of the most destructive insect pests in greenhouse production systems due to direct and indirect plant damage resulting in substantial economic losses. In addition, western flower thrips has developed resistance to many insecticides. Therefore, alternative plant protection strategies are warranted, such as augmentative biological control. This research was designed to evaluate 1) the effect of different absolute numbers of predator (rove beetle, Dalotia coriaria) and prey (western flower thrips) on predation efficacy of rove beetle under laboratory conditions; 2) the effect of western flower thrips pupal stage, predator-prey ratio, predator-prey number, and searchable area on predation efficacy of rove beetle in the laboratory; and 3) the effectiveness and cost of integrating the entomopathogenic fungus, Beauveria bassiana, and the rove beetle, D. coriaria, in suppressing western flower thrips populations under greenhouse conditions. Three laboratory experiments were conducted to assess predation efficacy of rove beetle adults on three western flower thrips pupal stages [prepupa, pupa, and prepupa-pupa combination (50%:50%)]. In each experiment, there were six numbers (0, 1, 2, 3, 4, and 5) of rove beetle adults and four initial numbers (15, 20, 25, and 30) of one western flower thrips pupal stage.