Contribution Fo the Study on the Turkish Penfofomardeo (Heferopfero) Iv
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Maternal Care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)̶Correlated Evolution with Title Morphological Change
Maternal care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)̶correlated evolution with Title morphological change Author(s) Tsai, Jing-Fu; Kudo, Shin-ichi; Yoshizawa, Kazunori BMC Evolutionary Biology, 15, 258 Citation https://doi.org/10.1186/s12862-015-0537-4 Issue Date 2015-11-19 Doc URL http://hdl.handle.net/2115/63251 Rights(URL) http://creativecommons.org/licenses/by/4.0 Type article File Information 10.1186_s12862-015-0537-4.pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP Tsai et al. BMC Evolutionary Biology (2015) 15:258 DOI 10.1186/s12862-015-0537-4 RESEARCH ARTICLE Open Access Maternal care in Acanthosomatinae (Insecta: Heteroptera: Acanthosomatidae)— correlated evolution with morphological change Jing-Fu Tsai1,3*, Shin-ichi Kudo2 and Kazunori Yoshizawa1 Abstract Background: Maternal care (egg-nymph guarding behavior) has been recorded in some genera of Acanthosomatidae. However, the origin of the maternal care in the family has remained unclear due to the lack of phylogenetic hypotheses. Another reproductive mode is found in non-caring species whose females smear their eggs before leaving them. They possess pairs of complex organs on the abdominal venter called Pendergrast’s organ (PO) and spread the secretion of this organ onto each egg with their hind legs, which is supposed to provide a protective function against enemies. Some authors claim that the absence of PO may be associated with the presence of maternal care. No study, however, has tested this hypothesis of a correlated evolution between the two traits. Results: We reconstructed the molecular phylogeny of the subfamily Acanthosomatinae using five genetic markers sequenced from 44 species and one subspecies with and without maternal care. -
Insects of Larose Forest (Excluding Lepidoptera and Odonates)
Insects of Larose Forest (Excluding Lepidoptera and Odonates) • Non-native species indicated by an asterisk* • Species in red are new for the region EPHEMEROPTERA Mayflies Baetidae Small Minnow Mayflies Baetidae sp. Small minnow mayfly Caenidae Small Squaregills Caenidae sp. Small squaregill Ephemerellidae Spiny Crawlers Ephemerellidae sp. Spiny crawler Heptageniiidae Flatheaded Mayflies Heptageniidae sp. Flatheaded mayfly Leptophlebiidae Pronggills Leptophlebiidae sp. Pronggill PLECOPTERA Stoneflies Perlodidae Perlodid Stoneflies Perlodid sp. Perlodid stonefly ORTHOPTERA Grasshoppers, Crickets and Katydids Gryllidae Crickets Gryllus pennsylvanicus Field cricket Oecanthus sp. Tree cricket Tettigoniidae Katydids Amblycorypha oblongifolia Angular-winged katydid Conocephalus nigropleurum Black-sided meadow katydid Microcentrum sp. Leaf katydid Scudderia sp. Bush katydid HEMIPTERA True Bugs Acanthosomatidae Parent Bugs Elasmostethus cruciatus Red-crossed stink bug Elasmucha lateralis Parent bug Alydidae Broad-headed Bugs Alydus sp. Broad-headed bug Protenor sp. Broad-headed bug Aphididae Aphids Aphis nerii Oleander aphid* Paraprociphilus tesselatus Woolly alder aphid Cicadidae Cicadas Tibicen sp. Cicada Cicadellidae Leafhoppers Cicadellidae sp. Leafhopper Coelidia olitoria Leafhopper Cuernia striata Leahopper Draeculacephala zeae Leafhopper Graphocephala coccinea Leafhopper Idiodonus kelmcottii Leafhopper Neokolla hieroglyphica Leafhopper 1 Penthimia americana Leafhopper Tylozygus bifidus Leafhopper Cercopidae Spittlebugs Aphrophora cribrata -
Identification, Biology, Impacts, and Management of Stink Bugs (Hemiptera: Heteroptera: Pentatomidae) of Soybean and Corn in the Midwestern United States
Journal of Integrated Pest Management (2017) 8(1):11; 1–14 doi: 10.1093/jipm/pmx004 Profile Identification, Biology, Impacts, and Management of Stink Bugs (Hemiptera: Heteroptera: Pentatomidae) of Soybean and Corn in the Midwestern United States Robert L. Koch,1,2 Daniela T. Pezzini,1 Andrew P. Michel,3 and Thomas E. Hunt4 1 Department of Entomology, University of Minnesota, 1980 Folwell Ave., Saint Paul, MN 55108 ([email protected]; Downloaded from https://academic.oup.com/jipm/article-abstract/8/1/11/3745633 by guest on 08 January 2019 [email protected]), 2Corresponding author, e-mail: [email protected], 3Department of Entomology, Ohio Agricultural Research and Development Center, The Ohio State University, 210 Thorne, 1680 Madison Ave. Wooster, OH 44691 ([email protected]), and 4Department of Entomology, University of Nebraska, Haskell Agricultural Laboratory, 57905 866 Rd., Concord, NE 68728 ([email protected]) Subject Editor: Jeffrey Davis Received 12 December 2016; Editorial decision 22 March 2017 Abstract Stink bugs (Hemiptera: Heteroptera: Pentatomidae) are an emerging threat to soybean and corn production in the midwestern United States. An invasive species, the brown marmorated stink bug, Halyomorpha halys (Sta˚ l), is spreading through the region. However, little is known about the complex of stink bug species associ- ated with corn and soybean in the midwestern United States. In this region, particularly in the more northern states, stink bugs have historically caused only infrequent impacts to these crops. To prepare growers and agri- cultural professionals to contend with this new threat, we provide a review of stink bugs associated with soybean and corn in the midwestern United States. -
Maternal Care in Pygoplatys Bugs (Heteroptera: Tessaratomidae)
NOTE Eut. J. Entomol. 95: 311-315, 1998 ISSN 1210-5759 Maternal care inPygoplatys bugs (Heteroptera: Tessaratomidae) M atija GOGALA', Hoi-Sen YONG2 andC arsten BRÜHL3 1 1 Prirodoslovni muzej Slovenije, Presemova 20, P.O. Box 290, SI-1001 Ljubljana, Slovenia; e-mail: [email protected] departm ent of Zoology, University of Malaya, 50603 Kuala Lumpur, Malaysia 3Zoologie III, Theodor-Boveri-Biozentrum der Universität, Am Hubland, D-97074 Würzburg, Germany Tessaratomidae,Pygoplatys, maternal care, egg guarding Abstract.Cases of maternal care and egg guarding were observed and photographed in bugs of the family Tessaratomidae. Females of one still undescribed speciesPygoplatys of from Doi Inthanon, Thailand, and ofPygoplatys acutus from Borneo are carrying their young larvae on the venter. The egg guarding was also observed inPygoplatys acutus from Kepong, Peninsular Malaysia. It seems, that maternal care is a characteristic behavior in bugs of the genusPygoplatys. Introduction Parental care at various levels is present in many insect groups. The guarding of eggs and attendance of the early instars probably reduces the levels of mortality during these stages, even in subsocial species which lack any nesting behavior. The parental (and usually maternal) care is known in the orthopteroid orders and in many other groups, e.g. Embioptera, Psocoptera, Thysanoptera, Heteroptera, Homoptera, Coleóptera and Hymenoptera (Tallamy & Wood, 1986). In Heteroptera, cases of maternal egg guarding and early instar attendance have been reported for many terrestrial and some aquatic species (Melber & Schmidt, 1977; Schuh & Slater, 1995). In families Reduviidae and Belostomatidae, cases of paternal care of the young are known (Tallamy & Wood, 1986). Until now, however, the only report of parental care in family Tessaratomidae has been published by Tachikawa (1991, egg guarding in the Japanese species of Pygoplatys and Erga; after Tallamy & Schaefer, 1997). -
Actinobacteria and the Vitamin Metabolism of Firebugs
Actinobacteria and the Vitamin Metabolism of Firebugs - Characterizing a mutualism's specificity and functional importance - Seit 1558 Dissertation To Fulfill the Requirements for the Degree of „Doctor of Philosophy“ (PhD) Submitted to the Council of the Faculty of Biology and Pharmacy of the Friedrich Schiller University Jena by M.S. Hassan Salem Born on 16.01.1986 in Cairo, Egypt i Das Promotionsgesuch wurde eingereicht und bewilligt am: Gutachter: 1) 2) 3) Das Promotionskolloquium wurde abgelegt am: ii To Nagla and Samy, for ensuring that life’s possibilities remain endless To Aly, for sharing everything* And to Aileen, my beloved HERC2 mutant * Everything except our first Gameboy (circa 1993). For all else, I am profoundly grateful. i ii CONTENTS LIST OF PUBLICATIONS ................................................................................................... 1 CHAPTER 1: SYMBIOSIS AND THE EVOLUTION OF BIOLOGICAL NOVELTY IN INSECTS ............................................................................................................................ 3 1.1 The organism in the age of the holobiont: It, itself, they .................................................. 3 1.2 Adaptive significance of symbiosis .................................................................................. 4 1.3 Symbiont-mediated diversification ................................................................................... 5 1.4 Revisiting Darwin’s mystery of mysteries: The role of symbiosis in species formation 6 1.5 Homeostasis of symbioses -
Shield Bugs and \Toodland Composition in Epping Forest
Field Studies6 (1985),253-268 SHIELD BUGS AND \TOODLAND COMPOSITION IN EPPING FOREST PAUL H. DULSTICH* EppingForest Conseraation Centre ABsrRAcr The distribution of five speciesof shield bug was studied with different host plant species,structure, condition and age in Epping Forest, Essex. Stands of beech, birch and oak-hornbeam, as well as scrubland gorse and hawthorn, were sampled, each tree being characterisedb1 a variet.vofparameters including bole circumference, pollard- ing and defoliation class. Correlations between shield bug species and host plant character were expressedthtough chi-squared analysesof presencelabsencedata for the samples.Resuits suggesta high degreeofhost specificity amongst the phytophage species studied and probably a preference for earlv successionalplant stages.Prei- erential utilisation of mature and non-defoliated hosts is aiso apparenr. The resuits are discussedin terms ofthe requirements ofthe bugs and the nutritional vaiue ofthe host. Ir is conciuded that nitrogen availability within and between host plant species is likeiy to be highly influential in deterrnining the diet and distribution of shielcj bugs, and indeed other selecrive-feedingheteroptera. INrRonucrroN Epprxc Fonssr comprisesof 2430hectares of woodland and grasslandwith small pockets of scrub and heathland, extending from the Wanstead Flats in the London Borough of Redbridge, north for approximarely l9 krn, just beyond Epping in Essex.The principal trce speciesare treech(Fagus sylz;atica),birch (Betula pendula and B. pubescens))common oak (Qtte r ctrs r obur) and hornbeam (C arp inus be tulu s). Pollen data indicate the late survival of the lir-:.e(Tilia) until about AD600 as the dominant tree species)then giving way to the familiar woodland associationsseen today. -
Shieldbugs of Norfolk Copyright
Shieldbugs of Norfolk Copyright Norfolk & Norwich Naturalists’ Society (registered charity 291604) Presentation compiled by David Richmond and Rob Coleman (county recorder). All photographs copyright of the credited authors. Bibliography Bernard Nau, Guide to Shieldbugs of the British Isles, Field Studies Council (2004) (laminated identification sheet) Paul D. Brock, A comprehensive guide to Insects of Britain & Ireland Pisces Publications (2014) pp 66-81 Cover illustration: Gorse Shieldbug (Hans Watson) Revision date 13.11.20 Shieldbugs are members of the heteroptera, in its laminated Guide to the Shieldbugs of the or true-bugs, a sub-order of insects with over 500 British Isles. We have used the same names in this different species in Gt Britain. presentation, except for a few species where different names have been adopted by the national The shieldbugs take their name from their recording scheme. For formal use the two-part distinctive outline which resembles a heraldic scientific names should always be used. shield. The forewing is leathery with a membranous tip (see front cover illustration). The Six families are considered in this presentation: hindwing is transparent and is folded out of sight when the insect is at rest. • The Acanthosomatidae (keeled shieldbugs) with four Norfolk species. The larval forms are like miniature versions of the adult but may have a different colour pattern and • The Pentatomidae (typical shieldbugs) with are without wings. They pass through five fourteen species in Norfolk. nymphal instars before moulting into fully winged • The Scutelleridae (tortoise shieldbugs) with adults. Many species hibernate so that adults two species in Norfolk. can be seen in both autumn and spring. -
Great Lakes Entomologist the Grea T Lakes E N Omo L O G Is T Published by the Michigan Entomological Society Vol
The Great Lakes Entomologist THE GREA Published by the Michigan Entomological Society Vol. 45, Nos. 3 & 4 Fall/Winter 2012 Volume 45 Nos. 3 & 4 ISSN 0090-0222 T LAKES Table of Contents THE Scholar, Teacher, and Mentor: A Tribute to Dr. J. E. McPherson ..............................................i E N GREAT LAKES Dr. J. E. McPherson, Educator and Researcher Extraordinaire: Biographical Sketch and T List of Publications OMO Thomas J. Henry ..................................................................................................111 J.E. McPherson – A Career of Exemplary Service and Contributions to the Entomological ENTOMOLOGIST Society of America L O George G. Kennedy .............................................................................................124 G Mcphersonarcys, a New Genus for Pentatoma aequalis Say (Heteroptera: Pentatomidae) IS Donald B. Thomas ................................................................................................127 T The Stink Bugs (Hemiptera: Heteroptera: Pentatomidae) of Missouri Robert W. Sites, Kristin B. Simpson, and Diane L. Wood ............................................134 Tymbal Morphology and Co-occurrence of Spartina Sap-feeding Insects (Hemiptera: Auchenorrhyncha) Stephen W. Wilson ...............................................................................................164 Pentatomoidea (Hemiptera: Pentatomidae, Scutelleridae) Associated with the Dioecious Shrub Florida Rosemary, Ceratiola ericoides (Ericaceae) A. G. Wheeler, Jr. .................................................................................................183 -
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises
Building-Up of a DNA Barcode Library for True Bugs (Insecta: Hemiptera: Heteroptera) of Germany Reveals Taxonomic Uncertainties and Surprises Michael J. Raupach1*, Lars Hendrich2*, Stefan M. Ku¨ chler3, Fabian Deister1,Je´rome Morinie`re4, Martin M. Gossner5 1 Molecular Taxonomy of Marine Organisms, German Center of Marine Biodiversity (DZMB), Senckenberg am Meer, Wilhelmshaven, Germany, 2 Sektion Insecta varia, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 3 Department of Animal Ecology II, University of Bayreuth, Bayreuth, Germany, 4 Taxonomic coordinator – Barcoding Fauna Bavarica, Bavarian State Collection of Zoology (SNSB – ZSM), Mu¨nchen, Germany, 5 Terrestrial Ecology Research Group, Department of Ecology and Ecosystem Management, Technische Universita¨tMu¨nchen, Freising-Weihenstephan, Germany Abstract During the last few years, DNA barcoding has become an efficient method for the identification of species. In the case of insects, most published DNA barcoding studies focus on species of the Ephemeroptera, Trichoptera, Hymenoptera and especially Lepidoptera. In this study we test the efficiency of DNA barcoding for true bugs (Hemiptera: Heteroptera), an ecological and economical highly important as well as morphologically diverse insect taxon. As part of our study we analyzed DNA barcodes for 1742 specimens of 457 species, comprising 39 families of the Heteroptera. We found low nucleotide distances with a minimum pairwise K2P distance ,2.2% within 21 species pairs (39 species). For ten of these species pairs (18 species), minimum pairwise distances were zero. In contrast to this, deep intraspecific sequence divergences with maximum pairwise distances .2.2% were detected for 16 traditionally recognized and valid species. With a successful identification rate of 91.5% (418 species) our study emphasizes the use of DNA barcodes for the identification of true bugs and represents an important step in building-up a comprehensive barcode library for true bugs in Germany and Central Europe as well. -
Notes on the Bionomics of Elasmucha Grisea (LINNAEUS 1758
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Denisia Jahr/Year: 2006 Band/Volume: 0019 Autor(en)/Author(s): Roth Steffen, Adaschkiewitz Wolfgang, Fischer Christian Artikel/Article: Notes on the bionomics of Elasmucha grisea (LINNAEUS 1758) (Heteroptera, Acanthosomatidae) with special regard to joint brood guarding 1153-1167 © Biologiezentrum Linz/Austria; download unter www.biologiezentrum.at Notes on the bionomics of Elasmucha grisea (LINNAEUS 1758) (Heteroptera, Acanthosomatidae) with special regard to joint brood guarding1 S. ROTH, W. ADASCHKIEWITZ & C. FISCHER Abstract: Females of Elasmucha grisea are known to guard their eggs and nymphs. We investigated this behaviour in several populations in Germany. While in Scandinavia a high proportion of females have been observed to guard their eggs jointly, in German populations less than 5 % (n=114) of females do so. For the first time, interactions between joint guarding females and nymphs are reported. Observa- tions and data from experiments in the field and in the laboratory reported here contribute to aspects of the distribution pattern of guarding females, selection of oviposition site, host plant shift, mating be- haviour, and survival patterns of males and females. We found evidence that in early nymphal instar stages the synchronity of development can become lost. While some nymphs are still in the first instar stage, others already hatched to second instar nymphs and leave the brood leaf. The female then no longer is able to provide an effective shelter for all her nymphs. Consequently, nymphs of different fe- males contact and form mixed groups. In such cases, both single and joint guarding females perform guarding behaviour regardless of whether the nymphs are hers or another female’s offspring. -
Shieldbugs of Norfolk Copyright
Shieldbugs of Norfolk Copyright Norfolk & Norwich Naturalists’ Society (registered charity 291604) Presentation compiled by David Richmond and Rob Coleman (county recorder). All photographs copyright of the credited authors. Bibliography Bernard Nau, Guide to Shieldbugs of the British Isles, Field Studies Council (2004) (laminated identification sheet) K C Durrant, Norfolk Terrestrial Heteroptera, Transactions of Norfolk & Norwich Naturalists’ Society (2002) vol 35 (part 1) pp 54-66 Paul D. Brock, A comprehensive guide to Insects of Britain & Ireland Pisces Publications (2014) pp 66-81 Cover illustration: Gorse Shieldbug (Hans Watson) Revision date 11.3.16 Shieldbugs are members of the heteroptera, in its laminated Guide to the Shieldbugs of the or true-bugs, a sub-order of insects with over 500 British Isles. We have used the same names in this different species in Gt Britain. presentation, except for a few species where different names have been adopted by the national The shieldbugs take their name from their recording scheme. For formal use the two-part distinctive outline which resembles a heraldic scientific names should always be used. shield. The forewing is leathery with a membranous tip (see front cover illustration). The Five families are considered in this presentation: hindwing is transparent and is folded out of sight when the insect is at rest. • The Acanthosomatidae (keeled shieldbugs) with four Norfolk species. The larval forms are like miniature versions of the adult but may have a different colour pattern and • The Pentatomidae (typical shieldbugs) with are without wings. They pass through five thirteen species in Norfolk. nymphal instars before moulting into fully winged adults. -
Preempting the Arrival of the Brown Marmorated Stink Bug, Halyomorpha Halys: Biological Control Options for Australia
insects Article Preempting the Arrival of the Brown Marmorated Stink Bug, Halyomorpha halys: Biological Control Options for Australia Valerie Caron 1,* , Tania Yonow 1, Cate Paull 2, Elijah J. Talamas 3, Gonzalo A. Avila 4 and Kim A. Hoelmer 5 1 CSIRO, Health and Biosecurity, Black Mountain, Acton, ACT 2601, Australia; [email protected] 2 CSIRO, Agriculture and Food, Dutton Park, QLD 4102, Australia; [email protected] 3 Florida Department of Agriculture and Consumer Services, Division of Plant Industry, Bureau of Entomology, Nematology and Plant Pathology, Gainesville, FL 32608, USA; [email protected] 4 The New Zealand Institute for Plant and Food Research Limited, Auckland 1025, New Zealand; [email protected] 5 USDA, Agriculture Research Service, Beneficial Insects Introduction Research Unit, Newark, DE 19713, USA; [email protected] * Correspondence: [email protected]; Tel.: +61-02-6218-3475 Simple Summary: The brown marmorated stink bug Halyomorpha halys (Stål) (Hemiptera: Pentato- midae) is native to Northeast Asia, but has become a serious invasive species in North America and Europe, causing major economic damage to crops. Halyomorpha halys has not established itself in Australia, but it has been intercepted several times at the border, therefore future incursions and establishment are likely. There are few control options for this species and biological control may be a useful management method in Australia. This study summarizes the literature on natural enemies of H. halys in its native and invaded ranges and prioritizes potential biological control agents that could be suitable for use in Australia. The results show two egg parasitoid species as the Citation: Caron, V.; Yonow, T.; Paull, best candidates: Trissolcus japonicus (Ashmead) and Trissolcus mitsukurii (Ashmead) (Hymenoptera: C.; Talamas, E.J.; Avila, G.A.; Hoelmer, Scelionidae).