Beneficial Insects
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Meadow Argus Junonia Villida Calybe
Butterfly GardeningFact sheet Nymphalidae family Meadow Argus Junonia villida calybe Abundance in Adelaide area: Common Flight: Throughout the year Wingspan: m 40 mm; f 43 mm Mature larva length: 32 mm The Meadow Argus is a common butterfly that occurs throughout the Adelaide region. Unfortunately, some of its caterpillar food plants are weeds and not desirable in the home garden. Keen gardeners could try some of the native caterpillar food plants listed here. Because its weedy food plants are so widespread and the butterfly is a strong flier that travels widely, even if you don’t succeed in establishing a breeding colony of Argus butterflies, you should still have them as regular visitors to your nectar plants. Caterpillar food plants: Native herbaceous How these eyespots work is a topic of dispute. plants and many invasive weeds. The caterpillars They either scare a predator into thinking the eat the soft parts of the plants. expanded wings of the butterflies are actually the head of a much larger animal, or attract the Adelaide native species: Common Purslane attention of an attacking bird or lizard, causing (Portulaca oleracea), Fairy Fan-flower (Scaevola them to target the edges of the wings, thus aemula). leaving the body and vital organs of the body of the insect alone. Other South Australian species: Spreading Nut-heads (Epaltes australis), Goodenia spp., The butterfly is a brown colour above, with a pair Fan-flowers (Scaevola spp.), Bluerod (Stemodia of blue centered, black eyespots, surrounded in florulenta). orange, near the outer margin of the wings. Foreign species: Snapdragons and weeds— Underneath, the forewing is quite similar to Centaury, Lippia*, Ribwort* (Plantago lanceolata), the upper surface, though much paler. -
THE LITTLE THINGS THAT RUN the CITY 30 AMAZING INSECTS THAT LIVE in MELBOURNE! © City of Melbourne 2017 First Published May, 2017 ISBN 978-1-74250-900-6
THE littleTHINGS that run the city BY KATE CRANNEY, SARAH BEKESSY AND LUIS MATA In partnership with City of Melbourne 30 amazing insects that live in Melbourne! THE LITTLE THINGS THAT RUN THE CITY 30 AMAZING INSECTS THAT LIVE IN MELBOURNE! © City of Melbourne 2017 First published May, 2017 ISBN 978-1-74250-900-6 ABOUT THIS PROJECT This book is an outreach educational resource prepared by Kate Cranney, Sarah Bekessy and Luis Mata for the City of Melbourne. Kate, Sarah and Luis work as part of the Interdisciplinary Conservation Science Research Group at RMIT University in Melbourne, Australia. THE Illustrations: Kate Cranney Ink on paper, www.katecranney.com Photographs: Luis Mata flickr.com/photos/dingilingi/ Graphic Design: Kathy Holowko THANK YOU We wish to acknowledge the support of the Australian Government’s little National Environmental Science Programme - Clean Air and Urban THINGS Landscapes and Threatened Species Hubs, and the Australian Research Council Centre of Excellence for Environmental Decisions. The book was inspired by ‘The Little Things that Run the City – Insect ecology, biodiversity and conservation in the that run the city City of Melbourne’ research project (Mata et al. 2016). We are very grateful to the Australian Museum (http://australianmuseum.net.au/insects), the Museum Victoria BY KATE CRANNEY, SARAH BEKESSY AND LUIS MATA (https://museumvictoria.com.au/bugs/), the CSIRO’s ‘What Bug is That’ program (http://anic.ento.csiro.au/insectfamilies/) In partnership with City of Melbourne and ‘The Insects of Australia - A textbook for students and research workers’ book (Naumann et al. 1991). Thank you to Dr. -
Imidacloprid Movement Into Fungal Conidia Is Lethal to Mycophagous Beetles
insects Communication Imidacloprid Movement into Fungal Conidia Is Lethal to Mycophagous Beetles 1, 2, , 3 4 Robin A. Choudhury y , Andrew M. Sutherland * y, Matt J. Hengel , Michael P. Parrella and W. Douglas Gubler 5 1 School of Earth, Environmental, and Marine Sciences, University of Texas Rio Grande Valley, Edinburg, TX 78539, USA; [email protected] 2 University of California Cooperative Extension, Alameda County, Hayward, CA 94544, USA 3 Department of Environmental Toxicology, University of California, Davis, Davis, CA 95616, USA; [email protected] 4 Department of Entomology, Plant Pathology and Nematology, University of Idaho, Moscow, ID 83844, USA; [email protected] 5 Department of Plant Pathology, University of California, Davis, Davis, CA 95616, USA; [email protected] * Correspondence: [email protected] These authors contributed equally to the writing, design and completion of this work. y Received: 1 July 2020; Accepted: 30 July 2020; Published: 3 August 2020 Simple Summary: Some insects are beneficial to plants because they eat pest insects and disease-causing fungi; integrating the use of these insects into pest management can help to reduce the need for costly pesticide applications. Twenty-spotted ladybeetles eat plant pathogenic fungi, which helps to reduce disease severity for many economically important crops. In this study, we applied a systemic insecticide to the roots of pumpkin plants and monitored to see if it would be detectable in the spores of a plant pathogenic fungus and whether the insecticide-tainted fungal spores would hurt the ladybeetle larvae. We were able to chemically detect the systemic insecticide in the fungal spores up to 21 days after the plants had been treated with the fungus. -
Supporting Information
Supporting Information Campbell et al. 10.1073/pnas.1421386112 SI Materials and Methods transformed into Escherichia coli JM109 High Efficiency Com- Genome Sequencing. The following amount of data were generated petent Cells. Transformed cells were grown in 3 mL of LB broth at for each sequencing technology: 136,081,956 pairs of 100 × 2 37 °C overnight, and plasmids were purified with E.Z.N.A. plas- short insert Illumina HiSeq reads for about 27 Gb total; 50,884,070 mid DNA mini kit I. The purified plasmids were used as PCR pairs of 100 × 2 large insert HiSeq reads for about 10 Gb total; templates to for further amplification of the probe region. The and 259,593 reads averaging 1600 nt for about 421 Mb total of amplified probes were subject to nick translation (>175 ng/μL PacBio data. DNA, 1× nick-translation buffer, 0.25 mM unlabeled dNTPs, 50 μM labeled dNTPs, 2.3 U/μL DNA polymerase I, 9 mU/μL Genome Annotation. Annotation of Hodgkinia DNA was done Dnase), using either Cy3 (MAGTRE006 and MAGTRE005), or using the phmmer module of HMMER v3.1b1 (1). All ORFs Cy5 (MAGTRE001 and MAGTRE012), and size selected for beginning with a start codon that overlapped a phmmer hit sizes in the range of 100–500 bp using Ampure XP beads. Probes were searched against a database of all Hodgkinia genes using with at least seven incorporated labeled dNTPs per 1,000 nucle- BLASTX 2.2.28+. MAGTRE Hodgkinia genes were considered otides as determined by spectroscopy were used for hybridization. -
Developing Biodiverse Green Roofs for Japan: Arthropod and Colonizer Plant Diversity on Harappa and Biotope Roofs
20182018 Green RoofsUrban and Naturalist Urban Biodiversity SpecialSpecial Issue No. Issue 1:16–38 No. 1 A. Nagase, Y. Yamada, T. Aoki, and M. Nomura URBAN NATURALIST Developing Biodiverse Green Roofs for Japan: Arthropod and Colonizer Plant Diversity on Harappa and Biotope Roofs Ayako Nagase1,*, Yoriyuki Yamada2, Tadataka Aoki2, and Masashi Nomura3 Abstract - Urban biodiversity is an important ecological goal that drives green-roof in- stallation. We studied 2 kinds of green roofs designed to optimize biodiversity benefits: the Harappa (extensive) roof and the Biotope (intensive) roof. The Harappa roof mimics vacant-lot vegetation. It is relatively inexpensive, is made from recycled materials, and features community participation in the processes of design, construction, and mainte- nance. The Biotope roof includes mainly native and host plant species for arthropods, as well as water features and stones to create a wide range of habitats. This study is the first to showcase the Harappa roof and to compare biodiversity on Harappa and Biotope roofs. Arthropod species richness was significantly greater on the Biotope roof. The Harappa roof had dynamic seasonal changes in vegetation and mainly provided habitats for grassland fauna. In contrast, the Biotope roof provided stable habitats for various arthropods. Herein, we outline a set of testable hypotheses for future comparison of these different types of green roofs aimed at supporting urban biodiversity. Introduction Rapid urban growth and associated anthropogenic environmental change have been identified as major threats to biodiversity at a global scale (Grimm et al. 2008, Güneralp and Seto 2013). Green roofs can partially compensate for the loss of green areas by replacing impervious rooftop surfaces and thus, contribute to urban biodiversity (Brenneisen 2006). -
Influence of Host Phylogeny, Geographical Location and Seed Harvesting Diet on the Bacterial Community of Globally Distributed Pheidole Ants
Influence of host phylogeny, geographical location and seed harvesting diet on the bacterial community of globally distributed Pheidole ants Cíntia Martins1,2 and Corrie S. Moreau2,3 1 Department of Biological Science, Campus Ministro Reis Velloso, Universidade Federal do Piauí, Parnaíba, Piauí, Brazil 2 Department of Science and Education, Field Museum of Natural History, Chicago, IL, United States of America 3 Departments of Entomology and Ecology & Evolutionary Biology, Cornell University, Ithaca, NY, United States of America ABSTRACT The presence of symbiotic relationships between organisms is a common phenomenon found across the tree of life. In particular, the association of bacterial symbionts with ants is an active area of study. This close relationship between ants and microbes can significantly impact host biology and is also considered one of the driving forces in ant evolution and diversification. Diet flexibility of ants may explain the evolutionary success of the group, which may be achieved by the presence of endosymbionts that aid in nutrition acquisition from a variety of food sources. With more than 1,140 species, ants from the genus Pheidole have a worldwide distribution and an important role in harvesting seeds; this behavior is believed to be a possible key innovation leading to the diversification of this group. This is the first study to investigate the bacterial community associated with Pheidole using next generation sequencing (NGS) to explore the influences of host phylogeny, geographic location and food preference in shaping the microbial community. In addition, we explore if there are any microbiota signatures related to granivory. We identified Proteobacteria and Firmicutes as the major phyla associated with these ants. -
An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna
© Copyright Australian Museum, 2005 Records of the Australian Museum (2005) Vol. 57: 375–446. ISSN 0067-1975 An Appraisal of the Higher Classification of Cicadas (Hemiptera: Cicadoidea) with Special Reference to the Australian Fauna M.S. MOULDS Australian Museum, 6 College Street, Sydney NSW 2010, Australia [email protected] ABSTRACT. The history of cicada family classification is reviewed and the current status of all previously proposed families and subfamilies summarized. All tribal rankings associated with the Australian fauna are similarly documented. A cladistic analysis of generic relationships has been used to test the validity of currently held views on family and subfamily groupings. The analysis has been based upon an exhaustive study of nymphal and adult morphology, including both external and internal adult structures, and the first comparative study of male and female internal reproductive systems is included. Only two families are justified, the Tettigarctidae and Cicadidae. The latter are here considered to comprise three subfamilies, the Cicadinae, Cicadettinae n.stat. (= Tibicininae auct.) and the Tettigadinae (encompassing the Tibicinini, Platypediidae and Tettigadidae). Of particular note is the transfer of Tibicina Amyot, the type genus of the subfamily Tibicininae, to the subfamily Tettigadinae. The subfamily Plautillinae (containing only the genus Plautilla) is now placed at tribal rank within the Cicadinae. The subtribe Ydiellaria is raised to tribal rank. The American genus Magicicada Davis, previously of the tribe Tibicinini, now falls within the Taphurini. Three new tribes are recognized within the Australian fauna, the Tamasini n.tribe to accommodate Tamasa Distant and Parnkalla Distant, Jassopsaltriini n.tribe to accommodate Jassopsaltria Ashton and Burbungini n.tribe to accommodate Burbunga Distant. -
The Signal Environment Is More Important Than Diet Or Chemical Specialization in the Evolution of Warning Coloration
The signal environment is more important than diet or chemical specialization in the evolution of warning coloration Kathleen L. Prudic†‡, Jeffrey C. Oliver§, and Felix A. H. Sperling¶ †Department of Ecology and Evolutionary Biology and §Interdisciplinary Program in Insect Science, University of Arizona, Tucson, AZ 85721; and ¶Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada T6G 2E9 Edited by May R. Berenbaum, University of Illinois at Urbana–Champaign, Urbana, IL, and approved October 11, 2007 (received for review June 13, 2007) Aposematic coloration, or warning coloration, is a visual signal that in ref. 13). Prey can become noxious by consuming other organisms acts to minimize contact between predator and unprofitable prey. with defensive compounds (e.g., refs. 15 and 16). By specializing on The conditions favoring the evolution of aposematic coloration re- a particular toxic diet, the consumer becomes noxious and more main largely unidentified. Recent work suggests that diet specializa- likely to evolve aposematic coloration as a defensive strategy tion and resultant toxicity may play a role in facilitating the evolution (reviewed in ref. 13). Diet specialization, in which a consumer feeds and persistence of warning coloration. Using a phylogenetic ap- on a limited set of related organisms, allows the consumer to tailor proach, we investigated the evolution of larval warning coloration in its metabolism to efficiently capitalize on the specific toxins shared the genus Papilio (Lepidoptera: Papilionidae). Our results indicate that by a suite of related hosts. Recent investigations suggest that diet there are at least four independent origins of aposematic larval specialization on toxic organisms promotes the evolution of apose- coloration within Papilio. -
Australian Cicadidae. the Mating of <I>Cyclochila Australasiae</I>, Don
AUSTRALIAN MUSEUM SCIENTIFIC PUBLICATIONS Rainbow, W. J., 1904. Australian Cicadidae. The mating of Cyclochila australasiae, Don. and Thopha saccata, Amyot. Records of the Australian Museum 5(2): 116–117, plate xi. [28 January 1904]. doi:10.3853/j.0067-1975.5.1904.1044 ISSN 0067-1975 Published by the Australian Museum, Sydney nature culture discover Australian Museum science is freely accessible online at http://publications.australianmuseum.net.au 6 College Street, Sydney NSW 2010, Australia AUSTRALIAN CICADIDJE. THE MATING OF CYCLOCHILA AUSTRALASlJE, Don. AND THOPHA SACCATA, Amyot. By W. J. RAINBOW, F.L.S., F.E.S., Entomologist. (Plate xi.) A short time ago, Mr. T. M. McGregor, of Rockdale, presented to the Trustees, a green male of Cyclochile atLstmlasiOJ, Don, (" Green Monday"), and a female of the "Double-drummer," Thopha saccata, Amyot, which he had taken in cop. last summer, when collecting around Sydney. Numerous instances of insects of distinct species and genera taken in the act of coition, have, from time to time been recorded in the Old World, but this appears to be the first instance of the kind reported from Australia. Mr. McGregor informs me that w ben bis attention was attracted to these insects, he at first thought he had discovered an unusually large Cicada, and it was not until he had captured them, that he discovered he had secured two Cicadas of distinct genera in the act of coition. These when taken were placed in the cyanide bottle. When captured the female was suspended to a branch, which she had firmly grasped with her legs, whilst the male was hanging head downwards, but grasping his partner round her abdomen. -
Traces and Burrowing Behaviors of the Cicada Nymph Cicadetta Calliope: Neoichnology and Paleoecological Significance of Extant Soil-Dwelling Insects
PALAIOS, 2008, v. 23, p. 503–513 Research Article DOI: 10.2110/palo.2007.p07-063r TRACES AND BURROWING BEHAVIORS OF THE CICADA NYMPH CICADETTA CALLIOPE: NEOICHNOLOGY AND PALEOECOLOGICAL SIGNIFICANCE OF EXTANT SOIL-DWELLING INSECTS JON J. SMITH1* and STEPHEN T. HASIOTIS1,2 1Kansas Geological Survey, 1930 Constant Ave., Lawrence, Kansas 66047-3726, USA; 2Natural History Museum and Biodiversity Research Center, Lawrence, Kansas 66045-7613, USA e-mail: [email protected] ABSTRACT documented the burrowing traces of extant temporary and permanent soil- dwelling arthropods (e.g., Clark and Ratcliffe, 1989; Hasiotis and Mitch- This study documents the traces and burrowing behaviors of nymphs ell, 1993; Tschinkel, 2003), despite their role as primary agents of pe- of the prairie cicada Cicadetta calliope (Hemiptera: Cicadidae), as doturbation and great abundances in modern soils (Wallwork, 1970; Hole, observed in neoichnological experiments. Cicada nymphs were col- 1981; Hasiotis, 2002). lected from the C horizons of sandy Fluvents along the Kansas River It has been hypothesized (Hasiotis and Bown, 1992; Hasiotis and Du- east of Lawrence, Kansas. The nymphs appeared to be fifth instars, biel, 1994; Hasiotis and Demko, 1996; Hasiotis, 2004) that soil-dwelling 13–17 mm long and 6–7 mm wide. Nymphs were placed in plastic hemipterans should produce meniscate, backfilled burrows similar to enclosures containing layers of colored, moist, very fine-grained sand. some fossil burrows in Mesozoic paleosols. This suggestion is based on They burrowed immediately, excavating air-filled, sediment-enclosed research by Willis and Roth (1962), who examined the behavioral re- cells between 20 mm and 40 mm long and averaging 9 mm wide. -
Papua New Guinea I
This cracking Wallace´s Fairywren was voted bird of thet trip. (DLV) PAPUA NEW GUINEA I 30 MAY– 16 / 20 JUNE 2018 LEADER: DANI LOPEZ VELASCO and JOSH BERGMARK Our first tour to Papua New Guinea –including New Britain- in 2018 was a great success and delivered a high number of quality birds. A total of 21 species of Birds-of-paradise (BoPs) - undoubtedly one of the most extraordinary, and “out of this world” bird families in the world-, were recorded, perhaps most memorable being a superb male Blue BoP, seen at close range near Kumul for as long as we wished. Just as impressive though were spectacular performances by displaying Raggiana and Greater BoPs in excellent light, stunning males King and Twelve-wired BoPs in the Kiunga area, a cracking adult male Growling Riflebird at Varirata, several amazing King-of-Saxony BoPs, waving their incredible head plumes like some strange insect antennae in the mossy forest of Tari Valley, great sightings of both Princess Stephanie´s and Ribbon-tailed Astrapias with their ridiculously long tail feathers, superb scope studies of Black –doing full display!- and Brown Sicklebills, uttering their machine-gun like calls, and so on. While Birds-of-paradise are certainly the signature family in PNG, there is of course plenty more besides, and this year the cracking and little-known Wallace´s Fairywren was awarded bird of the trip, ahead of BoPs, crowned pigeons and owlet- nightjars! We recorded a grand total of 33 species of pigeons and doves, -they reach their greatest diversity here in New Guinea, as do kingfishers-, including 11 Fruit Doves, and, during the extension, the rare Eastern Bronze Ground Dove. -
Imidacloprid Movement Into Fungal Conidia Is Lethal to Mycophagous Beetles
bioRxiv preprint doi: https://doi.org/10.1101/2020.01.11.901751; this version posted January 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Imidacloprid Movement into Fungal Conidia is Lethal to Mycophagous Beetles ROBIN A. CHOUDHURY*, ANDREW M. SUTHERLAND*, MATHEW J. HENGEL, MICHAEL P. PARRELLA, and W. DOUGLAS GUBLER *these authors contributed equally to the writing, design and completion of this work First author: University of Texas Rio Grande Valley, School of Earth, Environmental, & Marine Sciences; second author: University of California Cooperative Extension, Alameda County; third author: University of California, Davis Department of Environmental Toxicology; fourth author: University of Idaho, College of Agriculture and Life Sciences; fifth author: University of California, Davis Department of Plant Pathology. Abstract. 1. Applications of systemic pesticides can have unexpected direct and indirect effects on nontarget organisms, producing ecosystem-level impacts. 2. We investigated whether a systemic insecticide (imidacloprid) could be absorbed by a plant pathogenic fungus infecting treated plants and whether the absorbed levels were high enough to have detrimental effects on the survival of a mycophagous beetle. Beetle larvae fed on these fungi were used to assess the survival effects of powdery mildew and imidacloprid in a factorial design. Fungal conidia were collected from treated and untreated plants and were tested for the presence and concentration of imidacloprid. 3. Survival of beetles fed powdery mildew from imidacloprid-treated leaves was significantly lower than that of beetles from all other treatments.