Benefical Insects
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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, -
Spiders of the Hawaiian Islands: Catalog and Bibliography1
Pacific Insects 6 (4) : 665-687 December 30, 1964 SPIDERS OF THE HAWAIIAN ISLANDS: CATALOG AND BIBLIOGRAPHY1 By Theodore W. Suman BISHOP MUSEUM, HONOLULU, HAWAII Abstract: This paper contains a systematic list of species, and the literature references, of the spiders occurring in the Hawaiian Islands. The species total 149 of which 17 are record ed here for the first time. This paper lists the records and literature of the spiders in the Hawaiian Islands. The islands included are Kure, Midway, Laysan, French Frigate Shoal, Kauai, Oahu, Molokai, Lanai, Maui and Hawaii. The only major work dealing with the spiders in the Hawaiian Is. was published 60 years ago in " Fauna Hawaiiensis " by Simon (1900 & 1904). All of the endemic spiders known today, except Pseudanapis aloha Forster, are described in that work which also in cludes a listing of several introduced species. The spider collection available to Simon re presented only a small part of the entire Hawaiian fauna. In all probability, the endemic species are only partly known. Since the appearance of Simon's work, there have been many new records and lists of introduced spiders. The known Hawaiian spider fauna now totals 149 species and 4 subspecies belonging to 21 families and 66 genera. Of this total, 82 species (5596) are believed to be endemic and belong to 10 families and 27 genera including 7 endemic genera. The introduced spe cies total 65 (44^). Two unidentified species placed in indigenous genera comprise the remaining \%. Seventeen species are recorded here for the first time. In the catalog section of this paper, families, genera and species are listed alphabetical ly for convenience. -
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. -
Checklist of Non-Insect Invertebrates of Steele Creek Park
Checklist of Non-Insect Invertebrates of Steele Creek Park Harvestmen (Order Opiliones) __ Leiobunum aldrichi __ Leiobunum vittatum (Eastern Harvestman) __ Odiellus nubivagus __ Odiellus pictus __ Vonones sayi (Ornate Harvestman) Centipedes (Class Chilopoda) __ Geophilus vittatus (Diamondback Soil Centipede) __ Hemiscolopendra marginata (Florida Blue Centipede, Eastern Bark Centipede) __ Scolopocryptops nigridius __ Scolopocryptops sexspinosus (Eastern Fire Centipede) __ Strigamia bothriopus __ Theatops posticus (Smooth-tailed Forceps Centipede) __ Cryptops leucopodus Millipedes (Class Diplopoda) __ Apheloria montana (Cherry Millipede) __ Brachycybe lecontii (Feather Millipede) __ Cambala annulata __ Oxidus gracilis (Greenhouse Millipede)* __ Pseudopolydesmus canadensis __ Abacion magnum __ Abacion tesselatum __ Euryurus leachii __ Andrognathus corticarius (Cope’s Noodle Millipede) __ Narceus americanus-annularis (American Giant Millipede) Spiders (Order Araneae) __ Agelenopsis sp. (Grass Spider) __ Araneus marmoreus (Marbled Orbweaver) __ Araniella displicata (Six-spotted Orbweaver) __ Dolomedes albineus (White-striped Fishing Spider) __ Dolomedes tenebrosus (Dark Fishing Spider) __ Dolomedes triton (Six-spotted Fishing Spider) __ Dolomedes vittatus (Banded Fishing Spider) __ Larinioides cornutus (Furrow Orbweaver) __ Leucage venusta (Orchard Orbweaver) __ Micrathena gracilis (Spiny Micrathena) __ Micrathena mitrata (White Micrathena) __ Micrathena sagitatta (Arrow-shaped Micrathena) __ Misumenoides formosipes (White-banded Crab Spider) __ Neoscona crucifera (Spotted Orbweaver) __ Phidippus audax (Bold Jumping Spider) __ Phidippus otiosus (Canopy Jumping Spider) __ Phidippus putnami (Putnam’s Jumping Spider) __ Platycryptus undatus (Tan Jumping Spider) __ Pardosa sp. (Thin-legged Wolf Spider) __ Pirata sp. (Pirate Wolf Spider) __ Rabidosa rabida (Rabid Wolf Spider) __ Schizocosa crassipes (Brush-footed Wolf Spider) __ Synema parvulum (Black-banded Crab Spider) __ Tetragnatha sp. -
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<! -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
Visual Reactions to Auditory Stimulus by the Jumping Spider Phidippus Princeps (Araneae, Salticidae)
Visual reactions to auditory stimulus by the jumping spider Phidippus princeps (Araneae, Salticidae) Philip Denbaum Degree project in biology, Master of science (2 years), 2019 Examensarbete i biologi 45 hp till masterexamen, 2019 Biology Education Centre, Uppsala University, and Elizabeth Jakob lab, University of Massachusetts Supervisors: Elizabeth Jakob and Anders Berglund External opponent: Emilie Laurent & Julian Baur Table of contents Abstract 2 Introduction 3 Methods and Materials 5 Spider collection and care 5 General experimental setup 5 Overview of the eyetracker 5 Securing the spider 6 Aligning spider and finding retinas 6 Experiment 7 Data analysis 8 Statistical analyses 9 Results 10 Analysis 1 10 Analysis 2 13 Discussion 14 Future studies 15 Conclusions 16 Acknowledgements 16 References 17 Appendix 19 !1 Abstract Jumping spiders (Family Salticidae) are known for their exceptional vision, including color vision and spatial acuity. Salticids use their vision in many behaviors, including predation and courtship. Recently evidence of their ability to sense airborne vibrations, i.e. sound, was published. I used a specialized jumping-spider-specific eyetracker to study the visual reaction of the retinas of the jumping spider Phidippus princeps when exposed to the sound of a predator. I used a generic wasp sound, previously shown to induce a startle response, as stimulus and played it from different directions. The spiders showed strong reactions to the sound stimulus by large increases in retinal movement when exposed to the stimulus, and they showed no habituation to the stimulus over three rounds of exposure. However, I found no indication that the direction of retinal movement corresponded to the location of the sound source. -
Natural Prey of the Jumping Spider Menemerus Semilimbatus (Hahn, 1827) (Araneae: Salticidae), with Notes on Its Unusual Predatory Behaviour
EUROPEAN ARACHNOLOGY 2003 (LOGUNOV D.V. & PENNEY D. eds.), pp. 93100. © ARTHROPODA SELECTA (Special Issue No.1, 2004). ISSN 0136-006X (Proceedings of the 21st European Colloquium of Arachnology, St.-Petersburg, 49 August 2003) Natural prey of the jumping spider Menemerus semilimbatus (Hahn, 1827) (Araneae: Salticidae), with notes on its unusual predatory behaviour Åñòåñòâåííàÿ äîáû÷à ïàóêà ñêàêóí÷èêà Menemerus semilimbatus (Hahn, 1827) (Araneae: Salticidae) ñ çàìåòêàìè î åãî íåîáû÷íîì õèùíè÷åñêîì ïîâåäåíèè E.F. GUSEINOV Ý.Ô. ÃÓÑÅÉÍΠInstitute of Zoology, Azerbaijan Academy of Sciences, block 504, passage 1128, Baku 370073, Azerbaijan. email: [email protected] Èíñòèòóò çîîëîãèè ÍÀÍ Àçåðáàéäæàíà, êâàðòàë 504, ïðîåçä 1128, Áàêó 370073, Àçåðáàéäæàí. email: [email protected] ABSTRACT. Prey composition and the hunting behaviour of the jumping spider, Menemerus semilimbatus, which inhabits stone walls was studied. Less than 10% of the specimens in the population studied were observed feeding. Adult males fed significantly less frequently than adult females and juveniles. Diptera, the dominant prey group, accounted for more than 70% of all prey consumed. No other single prey type was present in significant numbers. M. semilimbatus adopts a specialized predatory behaviour towards flies that is unusual for salticids. This behaviour depends on how the fly is orientated towards the spider. If the fly is facing away from the spider, M. semilimbatus approaches it directly. When the fly is facing the spider, M. semilimbatus keeps its distance and encircles it until the prey is facing away from the spider. Only then, will the spider start to approach the fly directly. The specific habitat of M. -
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. -
Life History of Phidippus Johnsoni (Araneae, Salticidae )
Jackson, R . R . 1978 . The life history of Phidippus johnsoni (Araneae : Saltiicidae) . J. Arachnol. 6 :1-29 . LIFE HISTORY OF PHIDIPPUS JOHNSONI (ARANEAE, SALTICIDAE ) Robert R. Jackson ' Department of Zoology University of California, Berkeley Berkeley, California 9472 0 ABSTRACT In the laboratory, P. johnsoni oviposit successive batches of eggs with a trend toward a decrease i n both number of eggs and proportion of eggs that hatch in later batches . Approximately one month elapses between copulation and the first oviposition, and another month elapses between each succes- sive oviposition . Eggs hatch three weeks after oviposition, and spiderlings disperse from the materna l nest after another three weeks. Males mature earlier, pass through fewer molts, reach smaller adult siz e and have lesser adult longevity than females . There is considerable intrasexual variability in adult size , maturation time, and number of instars before reaching maturity . Males mature in 5 to 7 molts; females, 6 to 8 . Instar duration and variability in instar duration is greater in later than in earlier instars. Morphometric data from the laboratory were employed for estimating the number of molt s that spiders undergo in the Coastal Range of California . Spiders in nature matured later in the year an d probably passed through more molts before reaching maturity (6 to 8 for males ; 7 to 9 for females) than was the case for laboratory-reared spiders . Phenology and density were investigated in six popula- tions : two from the Coastal Range of California, two from Beach habitats (sea level, next to th e ocean) in California, and two from Alpine habitats (Sierra Nevada, California ; Rocky Mountains, Wyoming) .