KNOWN COLEOPTERA from FRANKLIN Co

Total Page:16

File Type:pdf, Size:1020Kb

KNOWN COLEOPTERA from FRANKLIN Co KKNOWN COLEOPTERA FROM FRANKLIN Co., MISSOURI Reputedly the largest order of insects, this group includes plant feeders such as leaf beetles, long-horned beetles, and many scarabs; scavengers and coprophages such hide, carrion, and dung beetles; and effective predator among the ground and water beetles. Some beetles are of economic importance as pests of crop and ornamental plants, and stored grain pests. A well-known invasive species is the Japanese beetle Popilia japonica which has spread from the east toward Missouri in recent decades. Most of the species below occur or are likely to at Shaw Nature Reserve. Many on this list are identified to genus level only, a function of both the hugeness of the group, and of much taxonomic work remaining to be done. Records compiled from bugguide.net, especially the exhaustive records of Mr. Jack Foreman, plus those by J. Trager and Jon Rapp. Photos here are all by James C. Trager, taken at SNR. They represent the species whose name is directly above the image. Suborder Archostemata Harpalus pensylvanicus Harpalus spp. Family Cupedidae Lebia analis Tenomerga cinerea Lebia atriventris Lebia solea Suborder Adephaga Lebia viridipennis Lebia viridis Family Carabidae Lebia vittata Acupalpus testaceus Paraclivina bipustulata Agonum sp. Platynus decentis Amara sp. Poecilus chalcites Amphasia sericea Poecilus sp. Anisodactylus caenus Scaphinotus elevatus Anisodactylus harrisii Aspidoglossa subangulata Badister neopulchellus Bembidion sp. Bradycellus festinans Bradycellus tantillus Calosoma scrutator Chlaenius laticollis Chlaenius sp. Chrysochus auratus Cicindela purpurea Stenolophus dissimilis Cicindela repanda Stenolophus lecontei Cicindela sexguttata Stenolophus lineola Cicindelidia rufiventris Stenolophus ochropezus Colliuris pensylvanica Tachys proximus Dicaelus purpuratus Telephanus atricapillus Dicaelus sp. Thalpius dorsalis Galerita sp. Family Dytiscidae Acmaeodora pulchella Acilius sp. Acmaeodora tubulus Family Gyrinidae Dineutus ciliatus Dineutus discolor Family Haliplidae Haliplus triopsis Peltodytes muticus Chrysobothris cf. femorata Suborder Polyphaga Family Callirhipidae Family Aderidae Zenoa picea Aderus sp. Elonus hesperus Family Cantharidae Emelinus melsheimeri Atalantycha bilineata Zonantes hubbardi Atalantycha neglecta Chauliognathus marginatus Family Anthicidae Chauliognathus pensylvanicus Anthicus lutulentus Notoxus murinipennis Omonadus floralis Stricticollis tobias Tomoderus sp. Family Anthribidae Euparius marmoreus Piesocorynus mixtus Polemius repandus Toxonotus cornutus Podabrus flavicollis Podabrus poricollis Family Attelabidae Podabrus rugulosus Eugnamptus angustatus Podabrus tricostatus Merhynchites bicolor Rhagonycha mollis Silis sp. Family Bostrichidae Trypherus sp. Lichenophanes bicornis Tytthonyx erythrocephala Trogoxylon parallelipipedum Xylobiops basilaris Family Cerambycidae Acanthocinus sp. Family Brentidae Anelaphus parallelus Arrhenodes minutus Ataxia crypta Trichapion sayi Batyle suturalis Desmocerus palliates Family Buprestidae Dryobius sexnotatus Agrilaxia flavimana Eburia quadrigeminata Agrilus sp. Ecyrus dasycerus Elytrimitatrix undata Capraita sexmaculata Capraita thyamoides Charidotella sexpunctata Chelymorpha cassidea Chrysomela knabi Enaphalodes atomarius Chrysomela scripta Euderces picipes Colaspis brunnea Eupogonius pauper Colaspis sp. Goes debilis Cryptocephalus leucomelas Graphisurus despectus Cryptocephalus mutabilis Graphisurus fasciatus Cryptocephalus venustus Knullian cincta Cryptocephalus sp. Leptostylus transversus Dectes texanus Necydalis mellita Deloyala guttata Neoclytus acuminatus Derospidea brevicollis Obrium maculatum Diabrotica barberi Odontotaenius disjunctus Diabrotica cristata Oeme rigida Diabrotica undecimpunctata Plinthocoelium suaveolens Disonycha admirabila Prionus imbricornis Disonycha glabrata Psyrassa unicolor Donacia sp. Saperda discoidea Gibbobruchus mimus Saperda tridentata Glyptoscelis sp. Smodicum cucujiforme Kuschelina cf. fimbriata Stenocorus cinnamopterus Labidomera clivicollis Sternidius alpha Luperaltica nigripalpis Sternidius punctatus Neochlamisus sp. Sternidius sp. Odontota scapularis Strangalia sexnotata Pachybrachis sp. Tetraopes tetrophthalmus Parchicola tibialis Typocerus cf. confluens Paria cf. fragariae Xylotrechus colonus Paria sp. Phyllecthris gentilis Family Ceratophytidae Phyllotreta bipustulata Ceratphytum pulsator Rhabdopterus sp. Scolytus sp. Xanthonia sp. Family Chrysomelidae Amblycerus robiniae Aulacothorax copallina Altica chalybea Capraita circumdata Family Cleridae Xyleborus celsus Cymatodera undulata Enoclerus sp. Family Dermestidae Neorthopleura thoracica Anthrenus verbasci Placopterus thoracicus Dermestes lardarius Family Coccinelidae Family Dryopidae Anatis labiculata Helichus lithophilus Coleomegilla maculata Coccinella septempunctata Family Elateridae Cycloneda munda Aeolus mellilus Harmonia axyridis Aeolus sp. Alaus oculatus Family Curculionidae Conoderus bellus Arrhenodes minutus Conderus lividus Chalcodermus sp. Conoderus vespertinus Conotrachelas anaglypticus Glyphonyx sp. Contrachelas buchanani Megapenthes rufilabris Conotrachelas elegans Melanotus sp. Contrachelas fisssunguis Paradonus pectoralis Conotrachelas seniculus Curculio sp. Family Elmidae Stenelmis sp. Family Erotylidae Ischyrus quadripunctatus Languria bicolor Languria trifasciata Cyclorhipidion bodoanum Cyrtepistomus castaneus Eubulus obliquefasciatus Haplorhynchites aeneus Hormops abducens Megalodacne fasciata Lignyodes bischoffi Pseudischyrus extricates Lignyodes fraxini Toramus pulchellus Lignyodes helvolus Listronotus appendiculatus Family Eucnemidae Listronotus humilis Adelothyreus sp. Listronotus sp. Hylochares nigricornis Monarthrum fasciatum Odontocorynus umbellae Family Hydrophilidae Pheloconus cribricollis Enochrus blatchleyi Pheloconus hispidus Enochrus sp. Phyrdenus divergens Hydrochara sp. Rhyssomatus lineaticollis Tropisternus collaris Smicronyx spp. Xanthonia sp. Family Laemophloeidae Laemophloeus biguttatus Family Nitidulidae Cryptarcha ampla Family Lampyridae Epuraea aestiva Lucidota atra Glischrochilus fasciatus Photinus pyralis Lobiopa undulata Photuris sp. Omosita nearctica Pleotomus davisii Pyractomena angulata Family Oedomeridae Oxacis trimaculata Family Latridiidae Corticaria sp. Family Phalacridae Melanopthalma sp. Stilbus sp. Family Leiodidae Family Phengodidae Platypsyllus castoris Phengodes sp. Family Lucanidae Family Ptilodactylidae Lucanus capreolus Ptilodactyla carinata Family Lycidae Family Ptinidae Calopteron reticulatum Ptinus bimaculatus Calopteron terminale Trichodesma gibbosa Plateros sp. Tricorynus sp. Family Melandryidae Family Pyrochroidae Micronotus sericans Dendroides canadensis Neopyrochroa femoralis Family Meloidae Neopyrochroa flabellata Epicauta atrata Pedilus terminalis Epicauta cf. funebris Epicauta pennsylvanica Family Rhipiphoridae Epicauta vittata Macrosiagon limbata Meloe campanicollis Nemognatha nemorensis Nemognatha sp. Family Mordellidae Hoshihananomia octopunctata Mordella insulata Mordella marginata Family Scarabaeidae Necrodes surinamensis Aphodius pseudolividus Nicrophorus orbicollis Aphodius sp. Nicrophorus pustulatus Ataenius imbricatus Ataenius sp. Atinus monilicornis Callistethus marginatus Canthon sp. Cyclocephala lurida Dichotomius carolinus Diplotaxis sp. Dynastes tityus Eucanthus impressus Euphoria sepulcralis Family Staphylinidae Germarotes sp. Arthmius sp. Macrodactylus subspinosus Bledius sp. Odonteus sp. Conotelus sp. Pelidnota punctata Coproporus laevis Phanaeus vindex Gyrophaenina sp. Phyllophaga quercus Homaeotarsus sp. Phyllophaga spp. Lobrathium sp. Mycetoporus sp. Paederus sp. Philonthus rufulus Pinophilus sp. Platydracus sp. Popilia japonica Tomarus gibbosus Rugilus angularis Trichiopeltastes delta Tachyporus sp. Trichiotinus piger Trichiotinus viridans Family Tenebrionidae Family Scirtidae Alobates sp. Contacyphon sp. Bolitotherus cornutus Scirtes tibialis Cynaeus angustus Scirtes sp. Diaperis maculata Lobopoda punctulata Neatus tenebrioides Family Silvanidae Platydema erythrocerum Ahasverus advena Platydema ruficorne Statira sp. Tenebrio molitor Family Scraptiidae Allopoda lutea Family Silphidae Family Tetratomidae Penthe pimelia Family Trogidae Omorgus sp. Family Trogossitidae Temebroides sp. Family Zopheridae Colydium lineola .
Recommended publications
  • Checklist of the Coleoptera of New Brunswick, Canada
    A peer-reviewed open-access journal ZooKeys 573: 387–512 (2016)Checklist of the Coleoptera of New Brunswick, Canada 387 doi: 10.3897/zookeys.573.8022 CHECKLIST http://zookeys.pensoft.net Launched to accelerate biodiversity research Checklist of the Coleoptera of New Brunswick, Canada Reginald P. Webster1 1 24 Mill Stream Drive, Charters Settlement, NB, Canada E3C 1X1 Corresponding author: Reginald P. Webster ([email protected]) Academic editor: P. Bouchard | Received 3 February 2016 | Accepted 29 February 2016 | Published 24 March 2016 http://zoobank.org/34473062-17C2-4122-8109-3F4D47BB5699 Citation: Webster RP (2016) Checklist of the Coleoptera of New Brunswick, Canada. In: Webster RP, Bouchard P, Klimaszewski J (Eds) The Coleoptera of New Brunswick and Canada: providing baseline biodiversity and natural history data. ZooKeys 573: 387–512. doi: 10.3897/zookeys.573.8022 Abstract All 3,062 species of Coleoptera from 92 families known to occur in New Brunswick, Canada, are re- corded, along with their author(s) and year of publication using the most recent classification framework. Adventive and Holarctic species are indicated. There are 366 adventive species in the province, 12.0% of the total fauna. Keywords Checklist, Coleoptera, New Brunswick, Canada Introduction The first checklist of the beetles of Canada by Bousquet (1991) listed 1,365 species from the province of New Brunswick, Canada. Since that publication, many species have been added to the faunal list of the province, primarily from increased collection efforts and
    [Show full text]
  • Swede's Forest SNA Bioblitz Results
    Swede Forest SNA Bioblitz Findings Species found at the June 17, 2017 bioblitz. Bacteria: Birds: • Apical chlorosis of Canada thistle aka PST – • Ring-necked Pheasant (Phasianus colchicus) (Pseudomonas syringae pv. tagetis) • Pied-billed Grebe (Podilymbus podiceps) Fungi and Lichens: • American White Pelican (Pelecanus erythrorhynchos) • Crown Rust (Puccinia coronata) • Green Heron (Butorides virescens) Amphibians: • Killdeer (Charadrius vociferus) • Mourning Dove (Zenaida macroura) • Northern Leopard Frog (Rana pipiens) • Turkey Vulture (Cathartes aura) • Eastern Gray Treefrog (Hyla versicolor) • Bald Eagle (Haliaeetus leucocephalus) • Belted Kingfisher (Megaceryle alcyon) Reptiles: • Eastern Kingbird (Tyrannus tyrannus) • Red-sided Garter Snake (Thamnophis sirtalis • Great Crested Flycatcher (Myiarchus crinitus) parietalis) • Eastern Wood-Pewee (Contopus virens) • Plains Garter Snake (Thamnophis radix) • Brown-headed Cowbird (Molothrus ater) • Redbelly Snake (Storeria occipitomaculata) • Red-winged Blackbird (Agelaius phoeniceus) • Five-lined Skink (Plestiodon fasciatus) • Orchard Oriole (Icterus spurius) • Western Painted Turtle (Chrysemys picta belli) • Baltimore Oriole (Icterus galbula) • Common Grackle (Quiscalus quiscula) Mammals: • American Goldfinch (Spinus tristis) • Eastern Cottontail (Sylvilagus floridanus) • Lark Sparrow (Chondestes grammacus)— • Whitetail Deer (Odocoileus virginianus) confirmed nesting • White-footed Mouse (Peromyscus leucopus) • Chipping Sparrow (Spizella passerina) • Coyote (Canis latrans) scat • Clay-colored
    [Show full text]
  • Forest Disturbance and Arthropods: Small‐Scale Canopy Gaps Drive
    Forest disturbance and arthropods: Small-scale canopy gaps drive invertebrate community structure and composition 1, 2,3 4 1,5 KAYLA I. PERRY , KIMBERLY F. WALLIN, JOHN W. WENZEL, AND DANIEL A. HERMS 1Department of Entomology, Ohio Agricultural Research and Development Center, The Ohio State University, 1680 Madison Avenue, Wooster, Ohio 44691 USA 2Rubenstein School of Environment and Natural Resources, University of Vermont, 312H Aiken Center, Burlington, Vermont 05405 USA 3USDA Forest Service, Northern Research Station, 312A, Aiken, Burlington, Vermont 05405 USA 4Powdermill Nature Reserve, Carnegie Museum of Natural History, 1847 PA-381, Rector, Pennsylvania 15677 USA 5The Davey Tree Expert Company, 1500 Mantua Street, Kent, Ohio 44240 USA Citation: Perry, K. I., K. F. Wallin, J. W. Wenzel, and D. A. Herms. 2018. Forest disturbance and arthropods: Small-scale canopy gaps drive invertebrate community structure and composition. Ecosphere 9(10):e02463. 10.1002/ecs2.2463 Abstract. In forest ecosystems, disturbances that cause tree mortality create canopy gaps, increase growth of understory vegetation, and alter the abiotic environment. These impacts may have interacting effects on populations of ground-dwelling invertebrates that regulate ecological processes such as decom- position and nutrient cycling. A manipulative experiment was designed to decouple effects of simultane- ous disturbances to the forest canopy and ground-level vegetation to understand their individual and combined impacts on ground-dwelling invertebrate communities. We quantified invertebrate abundance, richness, diversity, and community composition via pitfall traps in response to a factorial combination of two disturbance treatments: canopy gap formation via girdling and understory vegetation removal. For- mation of gaps was the primary driver of changes in invertebrate community structure, increasing activity- abundance and taxonomic richness, while understory removal had smaller effects.
    [Show full text]
  • Evaluation of Wood and Cellulosic Materials As Fillers in Artificial Diets for Lyctus Africanus Lesne (Coleoptera: Bostrichidae)
    Insects 2015, 6, 696-703; doi:10.3390/insects6030696 OPEN ACCESS insects ISSN 2075-4450 www.mdpi.com/journal/insects/ Article Evaluation of Wood and Cellulosic Materials as Fillers in Artificial Diets for Lyctus africanus Lesne (Coleoptera: Bostrichidae) Titik Kartika 1,2,†,*, and Tsuyoshi Yoshimura 1,† 1 Research Institute for Sustainable Humanosphere, Kyoto University, Uji Campus, Kyoto 6110011, Japan; E-Mail: [email protected] 2 Research Centre for Biomaterials, Indonesian Institute of Sciences, Jl. Raya Bogor Km. 46, Cibinong 16911, Indonesia † These authors contributed equally to this work. * Author to whom correspondence should be addressed; E-Mail: [email protected] or [email protected]; Tel.: +81-744-38-3664; Fax: +81-744-38-3666. Academic Editor: Brian T. Forschler Received: 29 January 2015 / Accepted: 11 June 2015 / Published: 23 July 2015 Abstract: We studied the usefulness of wood- and cellulose-based diets for L. africanus Lesne. Three diets were prepared which differed on the base ingredients; wood particles (Diet 1), cellulose powder (Diet 2), and alpha-cellulose (Diet 3). The diets were provided to adult L. africanus and the number of larvae, as well as the number of adults that emerged sex ratio, and body weight of the progeny was determined. Findings indicated similar results for the number of larvae, sex ratio and body weight of the emerged L. africanus fed on each diet. However, the number of adult produced by L. africanus on Diet 3 was significantly lower. The results indicate that the amount of vital nutrients is not the only important factor in selecting a suitable diet for L.
    [Show full text]
  • (Pueraria Montana Var. Lobata Willd) in North Carolina
    ABSTRACT THORNTON, MELISSA ROSE. Arthopod Fauna Associated With Kudzu (Pueraria montana var. lobata Willd) In North Carolina. (Under the direction of David Orr.) The purpose of this research was to obtain background information to aid the implementation of a biological control program against the weed, kudzu (Pueraria montana var. lobata Willd). This research had several specific objectives that examined: 1) potential insect pollinators and seed production of kudzu in NC; 2) phytophagous insects and insect herbivory of kudzu foliage, seeds, vines and roots in NC; 3) abundance and diversity of foliar, vine, and root feeding insect communities on kudzu in comparison with those found on soybeans, the closest North American relative of kudzu in the United States. Kudzu is pollinated by native and naturalized insects in NC, in a pattern that varies by flower apparency rather than density. Arthropod herbivory by native generalists almost eliminated kudzu seed viability, while a naturalized Asian specialist consumed a nominal proportion of seeds. These data indicate that seed feeding arthropods would be poor candidates for importation biological control. Kudzu and soybeans shared the same foliar feeding insect communities and levels of defoliation, suggesting that foliage feeders are also poor choices for importation. No kudzu vine or root feeding insects or damage were found during the two years of this study, suggesting that future importation biological control research should focus on such feeders from Asia. ARTHROPOD FAUNA ASSOCIATED WITH KUDZU (PUERARIA MONTANA VAR. LOBATA WILLD) IN NORTH CAROLINA by MELISSA ROSE THORNTON A thesis submitted to the Graduate Faculty of North Carolina State University in partial fulfillment of the requirements for the Degree of Master of Science DEPARTMENT OF ENTOMOLOGY Raleigh 2004 APPROVED BY: ______________________________ ______________________________ Dr.
    [Show full text]
  • The Evolution and Genomic Basis of Beetle Diversity
    The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State
    [Show full text]
  • Express PRA Lyctus Africanus
    Express PRA for Lyctus africanus – Interception – Prepared by: Julius Kühn-Institute, Institute for national and international Plant Health; by: Dr. Thomas Schröder, Dr. Gritta Schrader, Dr. Anne Wilstermann; on: 18-12-2019 (replaces version of: 12-03-2015). Revision in red and italics. (translated by Elke Vogt- Arndt) Initiation: Interception of wooden packaging material by the plant protection service of the Federal State Brandenburg Initiation for the revision: Application on the update of the risk analysis by the plant protection service of the Federal State Brandenburg Express Pest Risk analysis Lyctus africanus Lesne 1907 Phytosanitary risk for Germany high medium low Phytosanitary risk for high medium low EU-Member States Certainty of the assessment high medium low Conclusion The beetle Lyctus africanus is endemic in Africa and so far, it does not occur in Germany and very likely not in the EU. So far, it is not listed – neither in the Annexes of Regulation (EU) 2019/2072 nor by the EPPO. Lyctus africanus infests various tropical and subtropical trees and wood. Due to inappropriate climatic conditions and very likely the lack of host plants in Germany and Central Europe, it is assumed that L. africanus is not capable to establish outdoors. The establishment in south European Member States cannot be totally ruled out but the risk is assessed as low. Eventually, the establishment in protected cultivation (tropical greenhouses) would be possible. The transfer from infested wooden packaging to plants under glass seems very unlikely. Thus, Lyctus africanus is not classified as a potential quarantine pest and Article 29 of the Regulation (EU) 2016/2031 does not apply.
    [Show full text]
  • Utilizing Novel Grasslands for the Conservation and Restoration Of
    Iowa State University Capstones, Theses and Graduate Theses and Dissertations Dissertations 2014 Utilizing novel grasslands for the conservation and restoration of butterflies nda other pollinators in agricultural ecosystems John Thomas Delaney Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/etd Part of the Biodiversity Commons, Ecology and Evolutionary Biology Commons, Natural Resources and Conservation Commons, and the Natural Resources Management and Policy Commons Recommended Citation Delaney, John Thomas, "Utilizing novel grasslands for the conservation and restoration of butterflies and other pollinators in agricultural ecosystems" (2014). Graduate Theses and Dissertations. 14097. https://lib.dr.iastate.edu/etd/14097 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Utilizing novel grasslands for the conservation and restoration of butterflies and other pollinators in agricultural ecosystems by John Thomas Delaney A dissertation submitted to the graduate faculty in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Major: Ecology and Evolutionary Biology Program of Study Committee: Diane M. Debinski, Major Professor David M. Engle Mary A. Harris Amy L. Toth Brian J. Wilsey Iowa State University Ames, Iowa 2014 Copyright © John Thomas Delaney, 2014. All rights reserved. ii Dedication I dedicate this dissertation to all of my family, friends, and mentors who have helped me along in this journey.
    [Show full text]
  • Of Peru: a Survey of the Families
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 2015 Beetles (Coleoptera) of Peru: A Survey of the Families. Scarabaeoidea Brett .C Ratcliffe University of Nebraska-Lincoln, [email protected] M. L. Jameson Wichita State University, [email protected] L. Figueroa Museo de Historia Natural de la UNMSM, [email protected] R. D. Cave University of Florida, [email protected] M. J. Paulsen University of Nebraska State Museum, [email protected] See next page for additional authors Follow this and additional works at: http://digitalcommons.unl.edu/entomologyfacpub Part of the Entomology Commons Ratcliffe, Brett .;C Jameson, M. L.; Figueroa, L.; Cave, R. D.; Paulsen, M. J.; Cano, Enio B.; Beza-Beza, C.; Jimenez-Ferbans, L.; and Reyes-Castillo, P., "Beetles (Coleoptera) of Peru: A Survey of the Families. Scarabaeoidea" (2015). Faculty Publications: Department of Entomology. 483. http://digitalcommons.unl.edu/entomologyfacpub/483 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: Department of Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Authors Brett .C Ratcliffe, M. L. Jameson, L. Figueroa, R. D. Cave, M. J. Paulsen, Enio B. Cano, C. Beza-Beza, L. Jimenez-Ferbans, and P. Reyes-Castillo This article is available at DigitalCommons@University of Nebraska - Lincoln: http://digitalcommons.unl.edu/entomologyfacpub/ 483 JOURNAL OF THE KANSAS ENTOMOLOGICAL SOCIETY 88(2), 2015, pp. 186–207 Beetles (Coleoptera) of Peru: A Survey of the Families.
    [Show full text]
  • And Lepidoptera Associated with Fraxinus Pennsylvanica Marshall (Oleaceae) in the Red River Valley of Eastern North Dakota
    A FAUNAL SURVEY OF COLEOPTERA, HEMIPTERA (HETEROPTERA), AND LEPIDOPTERA ASSOCIATED WITH FRAXINUS PENNSYLVANICA MARSHALL (OLEACEAE) IN THE RED RIVER VALLEY OF EASTERN NORTH DAKOTA A Thesis Submitted to the Graduate Faculty of the North Dakota State University of Agriculture and Applied Science By James Samuel Walker In Partial Fulfillment of the Requirements for the Degree of MASTER OF SCIENCE Major Department: Entomology March 2014 Fargo, North Dakota North Dakota State University Graduate School North DakotaTitle State University North DaGkroadtaua Stet Sacteho Uolniversity A FAUNAL SURVEYG rOFad COLEOPTERA,uate School HEMIPTERA (HETEROPTERA), AND LEPIDOPTERA ASSOCIATED WITH Title A FFRAXINUSAUNAL S UPENNSYLVANICARVEY OF COLEO MARSHALLPTERTAitl,e HEM (OLEACEAE)IPTERA (HET INER THEOPTE REDRA), AND LAE FPAIDUONPATLE RSUAR AVSESYO COIFA CTOEDLE WOIPTTHE RFRAA, XHIENMUISP PTENRNAS (YHLEVTAENRICOAP TMEARRAS),H AANLDL RIVER VALLEY OF EASTERN NORTH DAKOTA L(EOPLIDEAOCPTEEAREA) I ANS TSHOEC RIAETDE RDI VWEITRH V FARLALXEIYN UOSF P EEANSNTSEYRLNV ANNOICRAT HM DAARKSHOATALL (OLEACEAE) IN THE RED RIVER VAL LEY OF EASTERN NORTH DAKOTA ByB y By JAMESJAME SSAMUEL SAMUE LWALKER WALKER JAMES SAMUEL WALKER TheThe Su pSupervisoryervisory C oCommitteemmittee c ecertifiesrtifies t hthatat t hthisis ddisquisition isquisition complies complie swith wit hNorth Nor tDakotah Dako ta State State University’s regulations and meets the accepted standards for the degree of The Supervisory Committee certifies that this disquisition complies with North Dakota State University’s regulations and meets the accepted standards for the degree of University’s regulations and meetMASTERs the acce pOFted SCIENCE standards for the degree of MASTER OF SCIENCE MASTER OF SCIENCE SUPERVISORY COMMITTEE: SUPERVISORY COMMITTEE: SUPERVISORY COMMITTEE: David A. Rider DCoa-­CCo-Chairvhiadi rA.
    [Show full text]
  • Coleoptera: Nitidulidae, Kateretidae)
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida March 2006 An annotated checklist of Wisconsin sap and short-winged flower beetles (Coleoptera: Nitidulidae, Kateretidae) Michele B. Price University of Wisconsin-Madison Daniel K. Young University of Wisconsin-Madison Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Price, Michele B. and Young, Daniel K., "An annotated checklist of Wisconsin sap and short-winged flower beetles (Coleoptera: Nitidulidae, Kateretidae)" (2006). Insecta Mundi. 109. https://digitalcommons.unl.edu/insectamundi/109 This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. INSECTA MUNDI, Vol. 20, No. 1-2, March-June, 2006 69 An annotated checklist of Wisconsin sap and short-winged flower beetles (Coleoptera: Nitidulidae, Kateretidae) Michele B. Price and Daniel K. Young Department of Entomology 445 Russell Labs University of Wisconsin-Madison Madison, WI 53706 Abstract: A survey of Wisconsin Nitidulidae and Kateretidae yielded 78 species through analysis of literature records, museum and private collections, and three years of field research (2000-2002). Twenty-seven species (35% of the Wisconsin fauna) represent new state records, having never been previously recorded from the state. Wisconsin distribution, along with relevant collecting techniques and natural history information, are summarized. The Wisconsin nitidulid and kateretid faunae are compared to reconstructed and updated faunal lists for Illinois, Indiana, Michigan, Minnesota, Ohio, and south-central Canada.
    [Show full text]
  • Conspicuousness, Phylogenetic Structure, and Origins of Müllerian
    www.nature.com/scientificreports OPEN Conspicuousness, phylogenetic structure, and origins of Müllerian mimicry in 4000 lycid beetles from all zoogeographic regions Michal Motyka1, Dominik Kusy1, Michal Masek1, Matej Bocek1, Yun Li1, R. Bilkova1, Josef Kapitán2, Takashi Yagi3 & Ladislav Bocak1* Biologists have reported on the chemical defences and the phenetic similarity of net-winged beetles (Coleoptera: Lycidae) and their co-mimics. Nevertheless, our knowledge has remained fragmental, and the evolution of mimetic patterns has not been studied in the phylogenetic context. We illustrate the general appearance of ~ 600 lycid species and ~ 200 co-mimics and their distribution. Further, we assemble the phylogeny using the transcriptomic backbone and ~ 570 species. Using phylogenetic information, we closely scrutinise the relationships among aposematically coloured species, the worldwide diversity, and the distribution of aposematic patterns. The emitted visual signals difer in conspicuousness. The uniform coloured dorsum is ancestral and was followed by the evolution of bicoloured forms. The mottled patterns, i.e. fasciate, striate, punctate, and reticulate, originated later in the course of evolution. The highest number of sympatrically occurring patterns was recovered in New Guinea and the Andean mountain ecosystems (the areas of the highest abundance), and in continental South East Asia (an area of moderate abundance but high in phylogenetic diversity). Consequently, a large number of co-existing aposematic patterns in a single region and/or locality is the rule, in contrast with the theoretical prediction, and predators do not face a simple model-like choice but cope with complex mimetic communities. Lycids display an ancestral aposematic signal even though they sympatrically occur with diferently coloured unproftable relatives.
    [Show full text]