DOCSLIB.ORG

Checklist of Kansas Insects

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Checklist of Kansas Insects CHECKLIST OF KANSAS INSECTS REFERENCE: Insects in Kansas, 3rd edition, 2000 By Stephan White and Glenn Salsbury, Kansas Department of Agriculture Order of Springtails (Collembola) Three-banded Grasshopper – Hadrotettix Family Poduridae trifasciatus Water Springtail – Podura aquatica Toothpick Grasshopper – Leptysma Family Sminthuridae marginicollis Alfalfa Springtail – Sminthurus medialis Differential Grasshopper – Melanoplus differentialis Order of Bristletails and Silverfish Pictured Grasshopper – Dactylotum bicolor (Thysanura) pictum Family Machilidae Family Tridactylidae Machilid – Machilis variabilis Large Sand Cricket – Neotridactylus apicalis Family Lepismatidae Family Tettigoniidae Silverfish – Lepisma saccharina Broad-winged Katydid – Microcentrum rhombifolium Order of Mayflies (Ephemeroptera) Swordbearing Katydid – Neoconocephalus spp. Family Ephemeridae Gladiator Katydid – Orchelimum spp. Giant Mayfly – Hexagenia limbata Family Gryllacrididae Cave Cricket – Ceuthophilis spp. Order of Dragonflies and Damselflies Camel Cricket – Udeopsylla robusta (Odonata) Family Gryllidae Family Aeschnidae Field Cricket – Gryllus spp. Common Green Darner – Anax junius House Cricket – Acheta domesticus Family Libellulidae Snowy Tree Cricket – Oecanthus fultoni Green Clearwing – Erythemis simplicicollis Family Gryllotalpidae Widow – Libellula luctuosa Mole Crickets Ten Spot – Libellula pulchella Amberwing – Perithemis tenera Order of Earwigs (Dermaptera) Whitetail – Plathemis lydia Family Carcinophoridae Family Calopterygidae Earwigs Blackwinged Damselfly – Calopteryx maculata American Rubyspot – Hetaerina americana Order of Mantises (Mantodea) Family Lestidae Family Mantidae Spreadwinged Damselfly – Lestes disjunctis Mantids Family Coenagrionidae Civil Bluet – Enallagma civile Order of Cockroaches (Blattodea) Family Blattidae Order of Stoneflies (Plecoptera) Oriental Cockroach – Blatta orientalis Family Perlidae American Cockroach – Periplaneta americana Stoneflies Family Blattellidae German Cockroach – Blattella germanica Order of Walking Sticks (Phasmatodea) Wood Roach – Parcoblatta bolliana Family Heteronemiidae Walking Sticks Order of Termites (Isoptera) Family Rhinotermitidae Order of Crickets, Grasshoppers and Eastern Subterranean Termite – Reticulitermes Katydids (Orthoptera) flavipes Family Acrididae Lubber Grasshopper – Brachystola magna Order of Booklice and Barklice (Psocoptera) Four-spotted Grasshopper – Philbostroma Family Liposcelidae quadrimaculatum Booklice Slant-faced Grasshopper – Mermiria bivittata Family Psocidae Carolina Grasshopper – Dissosteira carolina Barklice Page 1 of 5 Order of Biting Lice (Mallophaga) Family Psyllidae Family Philopteridae Hackberry Nipplegall Maker – Pachypsylla Birdlice celtidismamma Family Trichodectidae Family Aphidae Mammal Chewing Lice Aphids Family Dactylopiidae Order of Sucking Lice (Anoplura) Cochineal Insect – Dactylopius coccus Family Pediculidae Family Diaspididae Head Louse – Pediculus humanus capitus Pine Needle Scale - Chionaspis pinifoliae Order of True Bugs (Hemiptera) Order of Thrips (Thysanoptera) Family Pentatomidae Family Thripidae Green Stink Bug – Acrosternum hilare Grain Thrips – Limothrips cerealium Spined Soldier Bug – Podisus maculiventris Family Coreidae Order of Nerve-winged Insects (Neuroptera) Leaf-footed Bug – Leptoglossus phyllopus Family Sialidae Boxelder Bug – Boisea trivittata Alderflies Family Lygaeidae Family Corydalidae Large Milkweed Bug – Oncopeltus fasciatus Dobsonfly – Corydalus cornutus Chinch Bug – Blissus leucopterus Family Mantispidae Longnecked Seed Bug – Myodocha serripes Mantispid – Climaciella brunnea Family Tingidae Family Chrysopidae Lace bugs Lacewings Family Phymatidae Family Myrmeleontidae Ambush Bugs. Antlions Famly Reduviidae Family Ascalaphidae Wheel Bug – Arilus cristatus Owlflies Family Gerridae Water Strider – Gerris remigis Order of Beetles (Coleoptera) Family Notonectidae Family Cicindelidae Backswimmer – Notonecta undulata Tiger Beetles Family Corixidae Family Carabidae Water Boatman – Sigara alternata Caterpillar Hunter – Calosoma scrutator Family Nepidae Bluemargined Ground Beetle – Pasimachus Water Scorpion – Ranatra fusca elongatus Family Belostomatidae Ground Beetle – Galerita janus Electric Light Bug – Lethocerus griseus Family Dytiscidae Toe Biter – Belostoma flumineum Predacious Diving Beetle – Cybister fimbriolatus Family Gelastocoridae Family Gyrinidae Toad Bug – Gelastocoris oculatus Whirligig Beetle – Dineutus assimilis Family Silphidae Order of Aphids, Leafhoppers and Cicadas Carrion Beetle – Nicrophorus marginatus (Homoptera) Family Staphylinidae Family Flatidae Rove Beetles Citrus Planthopper – Metcalfa pruinosa Family Lucanidae Family Cercopidae Stag Beetle – Pseudolucanus placidus Twolined Spittlebug – Prosapia bicincta Family Scarabaeidae Family Cicadidae Dung Beetle – Dichotomius carolinus Bush Cicada – Tibicen dorsata May Beetle – Phyllophaga spp. Dog Day Cicada – Tibicen pruinosa Tenlined June Beetle – Polyphylla decemlineata Periodical Cicada – Magicicada septendecim Green June Beetle – Cotinus nitida Prairie Cicada – Melampsalta calliope Family Elmidae Family Cicadellidae Scott’s Riffle Beetle – Optioservus phaeus Saddled Leafhopper – Coladonus clitellarius Family Buprestidae Family Membracidae Wood Borers Buffalo Treehopper – Stictocephala bisonia Page 2 of 5 Family Elateridae Family Formicidae Eyed Click Beetle – Alaus oculatus Western Harvester Ant – Pogonomyrmex Click Beetle – Neotrichophorus carolinensis occidentalis Family Lampyridae Acrobat Ant – Crematogaster lineolata Eastern Firefly – Photinus pyralis Black Carpenter Ant – Camponotus Family Cantharidae pennsylvanicus Goldenrod Soldier Beetle – Chauliognathus Family Vespidae pennsylvanicus Potter Wasp – Eumenes spp. Family Lycidae Eastern Yellowjacket – Vespula maculifrons Netwinged Beetle – Calopteron terminale Common Paper Nest Wasp – Polistes Family Coccinelidae exclamans Sevenspotted Lady Beetle – Coccinella Family Pompilidae septempunctata Tarantula Hawk – Pepsis formosa Pinkspotted Lady Beetle – Coleomegilla Family Sphecidae maculata Steelblue Cricket Hunter – Chlorion aerarium Family Tenebrionidae Black & Yellow Mud Dauber – Sceliphron Darkling Beetles caementarium Family Meloidae Great Golden Digger Wasp – Sphex Blister Beetles ichneumoneus Family Cerambycidae Great Black Wasp – Sphex pennsylvanicus Locust Borer – Megacyllene robiniae Pipe Organ Wasp – Trypoxylon politum Flowerloving Longhorn – Typocerus sinuatus Cicada Killer – Sphecius speciosus Cottonwood Borer – Plectrodera scalator Family Halictidae Red Milkweed Beetle – Tetraopes Sweat Bees tetrophthalmus Family Megachilidae Family Chrysomelidae Leafcutter Bee – Megachile parallela Threelined Potato Beetle – Lema trilineata Family Anthophoridae Dogbane Beetle – Chrysochus auratus Carpenter Bee – Xylocopa virginica Sunflower Beetle – Zygogramma exclamationis Subfamily Apinae Elm Leaf Beetle – Pyrrhalta luteola Bumble Bee – Bombus pennsylvanicus Spotted Cucumber Beetle – Diabrotica Honey Bee – Apis mellifera undecimpunctata howardi Tortoise Beetle – Deloyala guttata Order of Caddisflies (Trichoptera) Family Rhynchitidae Family Hydropsychidae Rose Curculio – Merhynchites bicolor Seinemaking Caddisflies Family Curculionidae Family Phryganeidae Acorn weevils – Curculio spp. Giant Casemaker Caddisfly – Phryganea Milkweed Curculio – Rhyssomatus lineaticollis cinerea Ironweed Curculio – Rhodobaenus Family Leptoceridae tredecimpunctatus Longhorned Casemaker – Nectopsyche candida Order of Ants, Bees and Wasps Order of Butterflies and Moths (Lepidoptera) (Hymenoptera) Family Incurvariidae Family Siricidae Yucca Moth – Tegeticula yuccasella Pigeon Tremex – Tremex columba Family Psychidae Family Ichneumonidae Bagworm – Thyridopteryx ephemeraeformis Longtailed Megarhyssa – Megarhyssa atrata Family Gelechiidae Megarhyssa Wasp – Megarhyssa macrurus Redbud Leaffolder – Fascista cercerisella Family Pelecinidae Family Yponomeutidae Pelecinid Wasp – Pelecinus polyturator Ailanthus Webworm – Atteva punctella Family Chrysididae Family Sesiidae Cuckoo Wasp – Chrysis smaragdula Glorious Squashvine Borer – Melittia gloriosa Family Mutillidae Family Cossidae Velvet Ants Carpenterworm Moth – Prionoxystus robiniae Family Scoliidae Family Tortricidae Scoliid Wasp – Scolia bicincta Codling Moth – Cydia pomonella Page 3 of 5 Family Limacodidae Family Pieridae Spiny Oakslug Caterpillar – Euclea delphinii Imported Cabbageworm – Pieris rapae Family Crambidae Alfalfa Caterpillar – Colias eurytheme Grape Leaffolder – Desmia funeralis Dogface Butterfly – Zerene cesonia Family Pterophoridae Cloudless Sulphur – Phoebis sennae eubule Geranium Plume Moth – Amblyptilia pica Little Sulphur – Pyrisitia lisa lisa Family Geometridae Dwarf Yellow – Nathalis iole Buttercup Moth – Xanthotype urticaria Family Lycaenidae Chickweed Geometer – Haematopsis grataria Redbanded Hairstreak – Calycopis cecrops Family Lasiocampidae Olive Hairstreak – Mitoura gryneus Eastern Tent Caterpillar – Malacosoma Spring Azure – Celastrina argiolus ladon americanum Family Libytheidae Family Saturniidae Snout Butterfly – Libytheana bachmanii Imperial Moth – Eacles imperialis bachmanii Io Moth – Automeris io Family Heliconidae Polyphemus Moth – Antheraea polyphemus Gulf Fritillary – Agraulis vanillae Luna Moth – Actias luna Family Nymphalidae Cecropia Moth – Hyalophora cecropia Common Variegated Fritillary – Euptoieta Family Sphingidae claudia Tomato Hornworm – Manduca quinquemaculata Great Spangled Fritillary – Speyeria cybele Elm Sphinx – Ceratomia
Load more

Recommended publications
  • Bulletin No. 206-Treehopper Injury in Utah Orchards
    Utah State University DigitalCommons@USU UAES Bulletins Agricultural Experiment Station 6-1928 Bulletin No. 206 - Treehopper Injury in Utah Orchards Charles J. Sorenson Follow this and additional works at: https://digitalcommons.usu.edu/uaes_bulletins Part of the Agricultural Science Commons Recommended Citation Sorenson, Charles J., "Bulletin No. 206 - Treehopper Injury in Utah Orchards" (1928). UAES Bulletins. Paper 178. https://digitalcommons.usu.edu/uaes_bulletins/178 This Full Issue is brought to you for free and open access by the Agricultural Experiment Station at DigitalCommons@USU. It has been accepted for inclusion in UAES Bulletins by an authorized administrator of DigitalCommons@USU. For more information, please contact [email protected]. Bulletin 2 06 June, 1928 Treehopper Injury in Utah Orchards By CHARLES J. SORENSON 3 Dorsal and side views of the following species of treehoppers: 1. Ceresa bubalus (Fabr.) ( Buffalo treehopper) 2. Stictocephala inermis (Fabr.) 3. Stictocephala gillettei Godg. (x 10 ) UTAH AGRICULTURAL EXPERIMENT STATION LOGAN. UTAH UTAH AGRICULTURAL EXPERIMENT STATION , BOARD OF TRUSTEES . ANTHONY W. IVINS, President __ _____ ____________________ __ ___________________ Salt Lake City C. G. ADNEY, Vice-President ____ ___ ________________________________ ________________________ Corinne ROY B ULLEN ________ __________________________ _______ _____ _____ ________ ___ ____ ______ ____ Salt Lake City LORENZO N . STOHL ______ ___ ____ ___ ______________________ __ ___ ______ _____ __________ Salt Lake City MRS. LEE CHARLES MILLER ___ ______ ___ _________ ___ _____ ______ ___ ____ ________ Salt Lake City WE S TON V ERN ON, Sr. ________________________ ___ ____ ____ _____ ___ ____ ______ __ __ _______ ________ Loga n FRANK B. STEPHENS _____ ___ __ ____ ____________ ____ ______________ __ ___________ __.___ Salt Lake City MRS.
    [Show full text]
  • Morphology and Adaptation of Immature Stages of Hemipteran Insects
    © 2019 JETIR January 2019, Volume 6, Issue 1 www.jetir.org (ISSN-2349-5162) Morphology and Adaptation of Immature Stages of Hemipteran Insects Devina Seram and Yendrembam K Devi Assistant Professor, School of Agriculture, Lovely Professional University, Phagwara, Punjab Introduction Insect Adaptations An adaptation is an environmental change so an insect can better fit in and have a better chance of living. Insects are modified in many ways according to their environment. Insects can have adapted legs, mouthparts, body shapes, etc. which makes them easier to survive in the environment that they live in and these adaptations also help them get away from predators and other natural enemies. Here are some adaptations in the immature stages of important families of Hemiptera. Hemiptera are hemimetabolous exopterygotes with only egg and nymphal immature stages and are divided into two sub-orders, homoptera and heteroptera. The immature stages of homopteran families include Delphacidae, Fulgoridae, Cercopidae, Cicadidae, Membracidae, Cicadellidae, Psyllidae, Aleyrodidae, Aphididae, Phylloxeridae, Coccidae, Pseudococcidae, Diaspididae and heteropteran families Notonectidae, Corixidae, Belastomatidae, Nepidae, Hydrometridae, Gerridae, Veliidae, Cimicidae, Reduviidae, Pentatomidae, Lygaeidae, Coreidae, Tingitidae, Miridae will be discussed. Homopteran families 1. Delphacidae – Eg. plant hoppers They comprise the largest family of plant hoppers and are characterized by the presence of large, flattened spurs at the apex of their hind tibiae. Eggs are deposited inside plant tissues, elliptical in shape, colourless to whitish. Nymphs are similar in appearance to adults except for size, colour, under- developed wing pads and genitalia. 2. Fulgoridae – Eg. lantern bugs They can be recognized with their antennae inserted on the sides & beneath the eyes.
    [Show full text]
  • The Acridiidae of Minnesota
    Wqt 1lluitttr11ity nf :!alliuur11nta AGRICULTURAL EXPERIMENT STATION BULLETIN 141 TECHNICAL THE ACRIDIIDAE OF MINNESOTA BY M. P. SOMES DIVISION OF ENTOMOLOGY UNIVERSITY FARM, ST. PAUL. JULY 1914 THE UNIVERSlTY OF l\ll.'\1\ESOTA THE 130ARD OF REGENTS The Hon. B. F. :.JELsox, '\finneapolis, President of the Board - 1916 GEORGE EDGAR VINCENT, Minneapolis Ex Officio The President of the l.:niversity The Hon. ADOLPH 0. EBERHART, Mankato Ex Officio The Governor of the State The Hon. C. G. ScnuLZ, St. Paul l'.x Oflicio The Superintendent of Education The Hon. A. E. RICE, \Villmar 191.3 The Hon. CH.\RLES L. Sol\DfERS, St. Paul - 1915 The Hon. PIERCE Bun.ER, St. Paul 1916 The Hon. FRED B. SNYDER, Minneapolis 1916 The Hon. W. J. J\Lwo, Rochester 1919 The Hon. MILTON M. \NILLIAMS, Little Falls 1919 The Hon. }OIIN G. vVILLIAMS, Duluth 1920 The Hon. GEORGE H. PARTRIDGE, Minneapolis 1920 Tl-IE AGRICULTURAL C0:\1MITTEE The Hon. A. E. RrCE, Chairman The Hon. MILTON M. vVILLIAMS The Hon. C. G. SCHULZ President GEORGE E. VINCENT The Hon. JoHN G. \VrLLIAMS STATION STAFF A. F. VlooDs, M.A., D.Agr., Director J. 0. RANKIN, M.A.. Editor HARRIET 'vV. SEWALL, B.A., Librarian T. J. HORTON, Photographer T. L.' HAECKER, Dairy and Animal Husbandman M. H. REYNOLDS, B.S.A., M.D., D.V.:'d., Veterinarian ANDREW Boss, Agriculturist F. L. WASHBURN, M.A., Entomologist E. M. FREEMAN, Ph.D., Plant Pathologist and Botanist JonN T. STEWART, C.E., Agricultural Engineer R. W. THATCHER, M.A., Agricultural Chemist F. J.
    [Show full text]
  • Spatial Vision in Band-Winged Grasshoppers (Orthoptera: Acrididae: Oedipodinae)
    Spatial vision in band-winged grasshoppers (Orthoptera: Acrididae: Oedipodinae) A Senior Thesis Presented to the Faculty of the Department of Organismal Biology and Ecology, Colorado College By Alexander B. Duncan Bachelor of Arts Degree in Organismal Biology and Ecology May, 2017 Approved by: _________________________________________ Dr. Nicholas Brandley Primary Thesis Advisor ________________________________________ Dr. Emilie Gray Secondary Thesis Advisor ABSTRACT Visual acuity, the ability to resolve fine spatial details, can vary dramatically between and within insect species. Body-size, sex, behavior, and ecological niche are all factors that may influence an insect’s acuity. Band-winged grasshoppers (Oedipodinae) are a subfamily of grasshoppers characterized by their colorfully patterned hindwings. Although researchers have anecdotally suggested that this color pattern may attract mates, few studies have examined the visual acuity of these animals, and none have examined its implications on intraspecific signaling. Here, we compare the visual acuity of three bandwing species: Dissosteira carolina, Arphia pseudonietana, and Spharagemon equale. To measure acuity in these species we used a modified radius of curvature estimation (RCE) technique. Visual acuity was significantly coarser 1) in males compared to females, 2) parallel to the horizon compared to the perpendicular, and 3) in S. equale compared to other bandwings. Unlike many insect families, body size within a species did not correlate with visual acuity. To examine the functional implications of these results, we modeled the appearance of different bandwing patterns to conspecifics. These results suggest that hind- wing patterning could only be used as a signal to conspecifics at short distances (<50cm). This study furthers the exploration of behavior and the evolution of visual systems in bandwings.
    [Show full text]
  • Insetos Do Brasil
    COSTA LIMA INSETOS DO BRASIL 2.º TOMO HEMÍPTEROS ESCOLA NACIONAL DE AGRONOMIA SÉRIE DIDÁTICA N.º 3 - 1940 INSETOS DO BRASIL 2.º TOMO HEMÍPTEROS A. DA COSTA LIMA Professor Catedrático de Entomologia Agrícola da Escola Nacional de Agronomia Ex-Chefe de Laboratório do Instituto Oswaldo Cruz INSETOS DO BRASIL 2.º TOMO CAPÍTULO XXII HEMÍPTEROS ESCOLA NACIONAL DE AGRONOMIA SÉRIE DIDÁTICA N.º 3 - 1940 CONTEUDO CAPÍTULO XXII PÁGINA Ordem HEMÍPTERA ................................................................................................................................................ 3 Superfamília SCUTELLEROIDEA ............................................................................................................ 42 Superfamília COREOIDEA ............................................................................................................................... 79 Super família LYGAEOIDEA ................................................................................................................................. 97 Superfamília THAUMASTOTHERIOIDEA ............................................................................................... 124 Superfamília ARADOIDEA ................................................................................................................................... 125 Superfamília TINGITOIDEA .................................................................................................................................... 132 Superfamília REDUVIOIDEA ...........................................................................................................................
    [Show full text]
  • <I>Tibraca Limbativentris</I> (Hemiptera: Pentatomidae)
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 2018 Resistance in Rice to Tibraca limbativentris (Hemiptera: Pentatomidae) Influenced yb Plant Silicon Content Lincoln Luis França University of Goias State, Unidade Universitária de Ipameri, [email protected] Cássio Antonio Dierings Federal Goiano Institute, Campus Urutaí, Rodovia, [email protected] André Cirilo de Sousa Almeida Federal Goiano Institute, Campus Urutaí, Rodovia, [email protected] Marcio da Silva Araújo University of Goias State, Unidade Universitária de Ipameri Elvis Arden Heinrichs University of Nebraska-Lincoln, [email protected] See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/entomologyfacpub Part of the Agriculture Commons, and the Entomology Commons França, Lincoln Luis; Dierings, Cássio Antonio; de Sousa Almeida, André Cirilo; Araújo, Marcio da Silva; Heinrichs, Elvis Arden; da Silva, Anderson Rodrigo; Freitas Barrigossi, José Alexandre; and de Jesus, Flávio Gonçalves, "Resistance in Rice to Tibraca limbativentris (Hemiptera: Pentatomidae) Influenced yb Plant Silicon Content" (2018). Faculty Publications: Department of Entomology. 900. https://digitalcommons.unl.edu/entomologyfacpub/900 This Article is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Faculty Publications:
    [Show full text]
  • Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2
    Insects of Western North America 4. Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Survey of Selected Insect Taxa of Fort Sill, Comanche County, Oklahoma 2. Dragonflies (Odonata), Stoneflies (Plecoptera) and selected Moths (Lepidoptera) by Boris C. Kondratieff, Paul A. Opler, Matthew C. Garhart, and Jason P. Schmidt C.P. Gillette Museum of Arthropod Diversity Department of Bioagricultural Sciences and Pest Management Colorado State University, Fort Collins, Colorado 80523 March 15, 2004 Contributions of the C.P. Gillette Museum of Arthropod Diversity Colorado State University Cover illustration (top to bottom): Widow Skimmer (Libellula luctuosa) [photo ©Robert Behrstock], Stonefly (Perlesta species) [photo © David H. Funk, White- lined Sphinx (Hyles lineata) [photo © Matthew C. Garhart] ISBN 1084-8819 This publication and others in the series may be ordered from the C.P. Gillette Museum of Arthropod Diversity, Department of Bioagricultural Sciences, Colorado State University, Fort Collins, Colorado 80523 Copyrighted 2004 Table of Contents EXECUTIVE SUMMARY……………………………………………………………………………….…1 INTRODUCTION…………………………………………..…………………………………………….…3 OBJECTIVE………………………………………………………………………………………….………5 Site Descriptions………………………………………….. METHODS AND MATERIALS…………………………………………………………………………….5 RESULTS AND DISCUSSION………………………………………………………………………..…...11 Dragonflies………………………………………………………………………………….……..11
    [Show full text]
  • Nesting Behavior of Osmia Tingitana Benoist
    Journal of Entomology and Zoology Studies 2017; 5(2): 1181-1186 E-ISSN: 2320-7078 P-ISSN: 2349-6800 Nesting behavior of Osmia tingitana Benoist JEZS 2017; 5(2): 1181-1186 © 2017 JEZS (1969) (Hymenoptera: Megachilidae), endemic Received: 04-01-2017 Accepted: 05-02-2017 species of North Africa with first observation of Aguib Sihem its parasite Chrysura barbata Lucas (1849) Laboratory of Biosystematics and Ecology of Arthropods, (Hymenoptera: Chrysididae) University of Mentouri Constantine, Road Ain-El-Bey, 25000 Constantine, Algeria Aguib Sihem, Benachour Karima, Maghni Noudjoud and Louadi Kamel Benachour Karima Laboratory of Biosystematics Abstract and Ecology of Arthropods, The analysis of six Osmia tingitana nests found in snail shells showed that the female selects shells University of Mentouri belonging to the Hygromiidae family and whose diameter was between 1.8 and 3.5 cm. The nest building Constantine, Road Ain-El-Bey, materials consist essentially of sand, small pebbles, plant fragments (stems or flower petals) mixed with 25000 Constantine, Algeria the pollen grains. The nest was closed with a cap formed of a greenish paste consisting of pine needles chewed and mixed with the bee saliva and pieces of the shell. The number of cells per nest was variable, Maghni Noudjoud and range between 4 and 7 cells for multicellular nests.The different development stages were found in Laboratory of Biosystematics and Ecology of Arthropods, the nests analyzed with observation for the first time in one nest of the parasitic species of osmia, namely University of Mentouri a cuckoo wasp, Chrysura barbata of the Chrysididae family. Constantine, Road Ain-El-Bey, 25000 Constantine, Algeria Keywords: Osmia tingitana, nesting behavior, parasite, Chrysura barbata Louadi Kamel 1.
    [Show full text]
  • Lepidoptera of Albany Hill, Alameda Co., California
    LEPIDOPTERA OF ALBANY HILL, ALAMEDA CO., CALIFORNIA Jerry A. Powell Essig Museum of Entomology University of California, Berkeley and Robert L. Langston Kensington, CA November 1999; edited 2009 The following list summarizes observations of Lepidoptera (moths and butterflies) at Albany Hill, Alameda Co., California, during 1995-1999. Data originate from about 75 daytime and crepuscular visits of 0.5 to 3.5 hrs, in all months of the year. All of the butterfly species and some of the moths were recorded by RLL, most of the moth species and their larval host plants by JAP. A total of 145 species is recorded (30 butterflies, 115 moths), a modest number considering the extent and diversity of the flora. However, many of the potential larval host plants may be present in too small patches to support populations of larger moths or butterflies. Nonetheless, we were surprised that colonies of some of the species survive in a small area that has been surrounded by urban development for many decades, including some rare ones in the East Bay region, as annotated below. Moreover, the inventory is incomplete. A more comprehensive census would be accomplished by trapping moths attracted to ultraviolet lights. In a habitat of this size, however, such survey would attract an unknown proportion of species from surrounding areas. Larval collections are indicated by date-based JAP lot numbers (e.g. 95C37 = 1995, March, 37th collection). Larval foods of most of the other species are documented in other populations. Host plants are recorded at Albany Hill for 75 species (65% of the moths, 52% of the total); the rest were observed as adults only.
    [Show full text]
  • Moth Checklist Pagemaker
    thePembrokeAreaFieldNaturalists presents a MothChecklist of central Renfrew County, Ontario compiled by Jason J. Dombroskie ©chris michener February 2003 Checklist of Moths of the Pembroke Area Field Naturalists Compiled by Jason J. Dombroskie. Status: VR = very rare, R = rare, U = uncommon, C = common Scientific Name Common Name status Family Hepialidae Ghost Moths Sthenopis argenteomaculatus (Harris) Silver-spotted Ghost Moth U Sthenopis quadriguttatus (Grote) Four-spotted Ghost Moth U Family Nepticulidae Minute Eye-cap Moths Ectoedemia populella Busck Poplar Petiolegall Moth C Ectoedemia ulmella (Braun) C Glaucolepis saccharella (Braun) Stigmella corylifoliella (Clemens) U Stigmella saginella (Clemens) R Family Heliozelidae Shield Bearer Moths Antispila freemani Lafontaine R Family Adelidae Fairy Moths Adela purpurea Walker Willow Fairy Moth U Family Incurvariidae Leafcutter Moths Paraclemensia acerifoliella (Fitch) Maple Leafcutter C Family Tineidae Fungus Moths Eccritothrix trimaculella (Chambers) R Nemapogon granella (Linnaeus) R Family Gracillariidae Leaf Miner Moths Caloptilia fraxinella (Ely) Privet Leaf Miner C Caloptilia invariabilis (Braun) Cherry Leafcone Caterpillar C Caloptilia near stigmatella (Fabricus) C Caloptilia umbratella (Braun) R Parornix crataegifoliella (Clemens) R Parornix inusitatumella (Chambers) R Phyllonorycter aeriferella (Clemens) R Phyllonorycter argentifimbriella (Clemens) R Phyllonorycter basistrigella (Clemens) R Phyllonorycter lucetiella (Clemens) Basswood Squareblotch Miner U Phyllonorycter ostryaefoliella
    [Show full text]
  • Arriving at the Whole Story President Chris Hepburn, Vice President Michael Clarke, Secretary Katherine Howard, Treasurer
    NEWSLETTER Newton’s land trust working to preserve open space since 1961 WINTER ISSUE NEWTONCONSERVATORS.ORG • WINTER 2020-2021 2020 Officers and Directors Ted Kuklinski, Arriving at the Whole Story President Chris Hepburn, Vice President Michael Clarke, Secretary Katherine Howard, Treasurer AnnaMaria Abernathy David Backer Peter Barrer Barbara Bates Dan Brody Bonnie Carter Margaret Doris ALL PHOTOS THIS ARTICLE: SAM JAFFE Henry Finch Left to right: Cecropia Giant Silk Moth, Hyalophora cecropia: found on buttonbush,Boston MA. Maurice Gilmore Elm Sphinx, Ceratomia amyntor: Mimic of dried elm leaves, found at Oxbow National Wildlife Refuge, Harvard MA. Daniel Green Abbott’s Sphinx, Sphecodina abbottii: False-eye and grape-patterns, found in Newton, MA on fox grape. William Hagar Ken Mallory George Mansfield y name is Sam Jaffe, and I founded bright warning colors, or strange inflatable Nyssa Patten The Caterpillar Lab — an tails and false eye-spots drew people in, Larry Smith Meducational outreach, art, and sparked interest and imagination. But today, Beth Wilkinson science non-profit organization that uses caterpillars represent so much more to native caterpillars and their stories to engage me. From working so closely with these Advisors and inspire the public with their own, local, insects for so long, from rearing over five Margaret Albright and ecologically important creatures. The hundred species and countless thousands of Lisle Baker Caterpillar Lab is a fluid thing, constantly individuals, and from bringing them to meet John Bliss changing as we learn from our audiences audiences every spring, summer, and fall, the Lee Breckenridge Lalor Burdick and our creatures alike. I would like to share world of caterpillars has exploded in size.
    [Show full text]
  • Occurrence and Biology of Pseudogonalos Hahnii (Spinola, 1840) (Hymenoptera: Trigonalidae) in Fennoscandia and the Baltic States
    © Entomologica Fennica. 1 June 2018 Occurrence and biology of Pseudogonalos hahnii (Spinola, 1840) (Hymenoptera: Trigonalidae) in Fennoscandia and the Baltic states Simo Väänänen, Juho Paukkunen, Villu Soon & Eduardas Budrys Väänänen, S., Paukkunen, J., Soon, V. & Budrys, E. 2018: Occurrence and bio- logy of Pseudogonalos hahnii (Spinola, 1840) (Hymenoptera: Trigonalidae) in Fennoscandia and the Baltic states. Entomol. Fennica 29: 8696. Pseudogonalos hahnii is the only known species of Trigonalidae in Europe. It is a hyperparasitoid of lepidopteran larvae via ichneumonid primary parasitoids. Possibly, it has also been reared from a symphytan larva. We report the species for the first time from Estonia, Lithuania and Russian Fennoscandia, and list all known observations from Finland and Latvia. An overview of the biology of the species is presented with a list of all known host records. S. Väänänen, Vantaa, Finland; E-mail: [email protected] J. Paukkunen, Finnish Museum of Natural History, Zoology Unit, P.O. Box 17, FI-00014 University of Helsinki, Finland; E-mail: [email protected] V. Soon, Natural History Museum, University of Tartu, Vanemuise 46, 51014 Tartu, Estonia; E-mail: [email protected] E. Budrys, Nature Research Centre, Akademijos 2, LT-08412 Vilnius, Lithuania; E-mail: [email protected] Received 27 June 2017, accepted 22 September 2017 1. Introduction ovipositor with Aculeata (Weinstein & Austin 1991). The trigonalid ovipositor is reduced and Trigonalidae is a moderately small family of par- hidden within the abdomen and it is not known if asitic wasps of little over 100 species and about it is used in egg placement (Quicke et al. 1999).
    [Show full text]