Life Cycle of a Dragonfly, and Will Be Broken Down Into Sections Based on the Chronological Life Stages of This Insect
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Ancient Roaches Further Exemplify 'No Land Return' in Aquatic Insects
Gondwana Research 68 (2019) 22–33 Contents lists available at ScienceDirect Gondwana Research journal homepage: www.elsevier.com/locate/gr Ancient roaches further exemplify ‘no land return’ in aquatic insects Peter Vršanský a,b,c,d,1, Hemen Sendi e,⁎,1, Danil Aristov d,f,1, Günter Bechly g,PatrickMüllerh, Sieghard Ellenberger i, Dany Azar j,k, Kyoichiro Ueda l, Peter Barna c,ThierryGarciam a Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia b Slovak Academy of Sciences, Institute of Physics, Research Center for Quantum Information, Dúbravská cesta 9, Bratislava 84511, Slovakia c Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, P.O. BOX 106, 840 05 Bratislava, Slovakia d Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya 123, 117868 Moscow, Russia e Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava 84215, Slovakia f Cherepovets State University, Cherepovets 162600, Russia g Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, D-70191 Stuttgart, Germany h Friedhofstraße 9, 66894 Käshofen, Germany i Bodelschwinghstraße 13, 34119 Kassel, Germany j State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, PR China k Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, PO Box 26110217, Fanar - Matn, Lebanon l Kitakyushu Museum, Japan m River Bigal Conservation Project, Avenida Rafael Andrade y clotario Vargas, 220450 Loreto, Orellana, Ecuador article info abstract Article history: Among insects, 236 families in 18 of 44 orders independently invaded water. We report living amphibiotic cock- Received 13 July 2018 roaches from tropical streams of UNESCO BR Sumaco, Ecuador. -
Lesson: Key Details Lesson Topic: Identify and Explain Key Details Question 1
Lesson: Key Details Lesson Topic: Identify and explain key details Question 1: Read the text below. Sea Stars Written by Lindsey Crowe There are many different kinds of sea stars. For example, some sea stars have five legs and some have ten legs. Some have skinny arms and some have wide arms. Sea stars are found in the ocean. Some sea stars live in warm oceans. Some live in cold oceans. They can be found in deep and shallow waters. Some people call sea stars star fish. Sea stars are not fish. They do not have gills, fins, or bones. Which of the following key details supports the idea that there are many different kinds of sea stars? There are many different kinds of sea stars. Sea stars are found in the ocean. Some sea stars have five legs and some have ten legs. They do not have gills, fins, or bones. Question 2: Read the text below. There are many different kinds of sea stars. For example, some sea stars have five legs and some have ten legs. Some have skinny arms and some have wide arms. Why is the underlined sentence an important key detail? because it explains why the author took pictures and wrote a text about sea stars because it is an important fact that we need to know to understand about different kinds of sea stars because it explains what kind of sea star is in the photograph because it gives the names of different types of sea stars Question 3: Read the text below. -
A New Pupillarial Scale Insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in Coastal New South Wales, Australia
Zootaxa 4117 (1): 085–100 ISSN 1175-5326 (print edition) http://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2016 Magnolia Press ISSN 1175-5334 (online edition) http://doi.org/10.11646/zootaxa.4117.1.4 http://zoobank.org/urn:lsid:zoobank.org:pub:5C240849-6842-44B0-AD9F-DFB25038B675 A new pupillarial scale insect (Hemiptera: Coccoidea: Eriococcidae) from Angophora in coastal New South Wales, Australia PENNY J. GULLAN1,3 & DOUGLAS J. WILLIAMS2 1Division of Evolution, Ecology & Genetics, Research School of Biology, The Australian National University, Acton, Canberra, A.C.T. 2601, Australia 2The Natural History Museum, Department of Life Sciences (Entomology), London SW7 5BD, UK 3Corresponding author. E-mail: [email protected] Abstract A new scale insect, Aolacoccus angophorae gen. nov. and sp. nov. (Eriococcidae), is described from the bark of Ango- phora (Myrtaceae) growing in the Sydney area of New South Wales, Australia. These insects do not produce honeydew, are not ant-tended and probably feed on cortical parenchyma. The adult female is pupillarial as it is retained within the cuticle of the penultimate (second) instar. The crawlers (mobile first-instar nymphs) emerge via a flap or operculum at the posterior end of the abdomen of the second-instar exuviae. The adult and second-instar females, second-instar male and first-instar nymph, as well as salient features of the apterous adult male, are described and illustrated. The adult female of this new taxon has some morphological similarities to females of the non-pupillarial palm scale Phoenicococcus marlatti Cockerell (Phoenicococcidae), the pupillarial palm scales (Halimococcidae) and some pupillarial genera of armoured scales (Diaspididae), but is related to other Australian Myrtaceae-feeding eriococcids. -
Dragonflies and Damselflies in Your Garden
Natural England works for people, places and nature to conserve and enhance biodiversity, landscapes and wildlife in rural, urban, coastal and marine areas. Dragonflies and www.naturalengland.org.uk © Natural England 2007 damselflies in your garden ISBN 978-1-84754-015-7 Catalogue code NE21 Written by Caroline Daguet Designed by RR Donnelley Front cover photograph: A male southern hawker dragonfly. This species is the one most commonly seen in gardens. Steve Cham. www.naturalengland.org.uk Dragonflies and damselflies in your garden Dragonflies and damselflies are Modern dragonflies are tiny by amazing insects. They have a long comparison, but are still large and history and modern species are almost spectacular enough to capture the identical to ancestors that flew over attention of anyone walking along a prehistoric forests some 300 million river bank or enjoying a sunny years ago. Some of these ancient afternoon by the garden pond. dragonflies were giants, with This booklet will tell you about the wingspans of up to 70 cm. biology and life-cycles of dragonflies and damselflies, help you to identify some common species, and tell you how you can encourage these insects to visit your garden. Male common blue damselfly. Most damselflies hold their wings against their bodies when at rest. BDS Dragonflies and damselflies belong to Dragonflies the insect order known as Odonata, Dragonflies are usually larger than meaning ‘toothed jaws’. They are often damselflies. They are stronger fliers and referred to collectively as ‘dragonflies’, can often be found well away from but dragonflies and damselflies are two water. When at rest, they hold their distinct groups. -
Damselflies & Dragonflies of the Tees and Humber Industrial Sites
Damselflies & Dragonflies of the Tees and Humber Industrial Sites Introduction Damselflies and dragonflies belong to the same ‘order’ of insects called the Odonata. Although the adults are flying insects, the other stages of their life cycle are spent in water. Adults lay their eggs on aquatic plants or in the mud of still or slow moving freshwater. The larval or ‘nymph’ form is the immature stage which is wingless. Nymphs eat other aquatic insects and small animals such as tadpoles and small fish. They shed their skin as they grow and larger species can take several years to reach the point Damsel or Dragon? where they become full-grown. At this point The following key points will give an they climb out of the water onto surrounding indication of the main differences vegetation and after a short period the adult between dragonflies and damselflies: insect emerges from the old larval skin. The adults are also fearsome predators, catching • Both have two large ‘compound’ eyes at other flying insects on the wing. Damselflies the front of their head. A dragonfly’s eyes eat smaller species, such as greenfly or are so large that they meet in the middle midges, but a dragonfly’s diet includes larger or at the top of the head, but those of a flying insects such as butterflies, moths and damselfly are smaller and always separate. even smaller dragonflies and damselflies! • Both have four wings, but when resting, damselflies fold their wings back This leaflet is a useful field guide, that covers along their bodies or at 45 degrees, the Odonata species which can be seen in whereas dragonflies rest with their the Tees and Humber industrial areas. -
Monitoring Dragonfly Migration in North America Protocols for Citizen Scientists
Monitoring Dragonfly Migration in North America Protocols for Citizen Scientists Migratory Dragonfly Partnership Blank on purpose Monitoring Dragonfly Migration in North America Protocols for Citizen Scientists Migratory Dragonfly Partnership Canada • United States • Mexico www.migratorydragonflypartnership.org © 2014 by The Migratory Dragonfly Partnership The Migratory Dragonfly Partnership uses research, citizen science, education, and outreach to under- stand North American dragonfly migration and promote conservation. MDP steering committee members represent a range of organizations, including: Ontario Ministry of Natural Resources; Peggy Notebaert Nature Museum; Pronatura Veracruz; Rutgers University; Slater Museum of Natural History, University of Puget Sound; Smithsonian Conservation Biology Institute; St. Edward's University; U. S. Forest Service International Programs; U. S. Geological Survey; Vermont Center for Ecostudies; and the Xerces Society for Invertebrate Conservation. Migratory Dragonfly Partnership Project Coordinator, Celeste Mazzacano [email protected] 628 NE Broadway, Suite 200, Portland, OR 97232 Tel (855) 232-6639 Fax (503) 233-6794 www.migratorydragonflypartnership.org Acknowledgements Funding for the Migratory Dragonfly Partnership's work is provided by the U.S. Forest Service Inter- national Programs. We thank the photographers who generously allowed use of their images. Copyright of all photographs remains with the photographers. Front and Back Cover Photographs Common Green Darner (Anax junius) male. Photograph © John C. Abbott/Abbott Nature Photography. CONTENTS Summary Page 1 1. Introduction Page 3 1.1 Objectives and Goals Page 3 Box 1: Citizen Science Projects, page 4. 2. Citizen Science Projects Page 5 2.1 Migration Monitoring Page 5 2.1.1 Fall Migration Observations Page 5 - Objectives, page 5. Box 2: MDP Monitoring Projects, page 6. -
Wetlands Invertebrates Banded Woollybear(Isabella Tiger Moth Larva)
Wetlands Invertebrates Banded Woollybear (Isabella Tiger Moth larva) basics The banded woollybear gets its name for two reasons: its furry appearance and the fact that, like a bear, it hibernates during the winter. Woollybears are the caterpillar stage of medium sized moths known as tiger moths. This family of moths rivals butterflies in beauty and grace. There are approximately 260 species of tiger moths in North America. Though the best-known woollybear is the banded woollybear, there are at least 8 woollybear species in the U.S. with similar dense, bristly hair covering their bodies. Woollybears are most commonly seen in the autumn, when they are just about finished with feeding for the year. It is at this time that they seek out a place to spend the winter in hibernation. They have been eating various green plants since June or early July to gather enough energy for their eventual transformation into butterflies. A full-grown banded woollybear caterpillar is nearly two inches long and covered with tubercles from which arise stiff hairs of about equal length. Its body has 13 segments. Middle segments are covered with red-orange hairs and the anterior and posterior ends with black hairs. The orange-colored oblongs visible between the tufts of setae (bristly hairs) are spiracles—entrances to the respiratory system. Hair color and band width are highly variable; often as the caterpillar matures, black hairs (especially at the posterior end) are replaced with orange hairs. In general, older caterpillars have more black than young ones. However, caterpillars that fed and grew in an area where the fall weather was wetter tend to have more black hair than caterpillars from dry areas. -
Body-Enlarging Effect of Royal Jelly in a Non-Holometabolous Insect Species, Gryllus Bimaculatus
© 2016. Published by The Company of Biologists Ltd | Biology Open (2016) 5, 770-776 doi:10.1242/bio.019190 RESEARCH ARTICLE Body-enlarging effect of royal jelly in a non-holometabolous insect species, Gryllus bimaculatus Atsushi Miyashita, Hayato Kizaki, Kazuhisa Sekimizu and Chikara Kaito* ABSTRACT (Conlon and Raff, 1999; Otto, 2007). These studies have provided Honeybee royal jelly is reported to have body-enlarging effects in significant insight into the principles of size regulation of living holometabolous insects such as the honeybee, fly and silkmoth, but organisms, although recent concerns over genetically modified its effect in non-holometabolous insect species has not yet been organisms have led researchers to evaluate other types of strategies examined. The present study confirmed the body-enlarging effect in to enlarge animals for industrial purposes. silkmoths fed an artificial diet instead of mulberry leaves used in the As a non-genetic size manipulation, oral ingestion of royal jelly previous literature. Administration of honeybee royal jelly to silkmoth by larvae of the honeybee, Apis mellifera, a holometabolous from early larval stage increased the size of female pupae and hymenopteran insect, induces queen differentiation, leading to adult moths, but not larvae (at the late larval stage) or male pupae. enlarged bodies. Royal jelly contains 12-15% protein, 10-16% We further examined the body-enlarging effect of royal jelly in a sugar, 3-6% lipids (percentages are wet-weight basis), vitamins, non-holometabolous species, the two-spotted cricket Gryllus salts, and free amino acids (Buttstedt et al., 2014). Royal jelly bimaculatus, which belongs to the evolutionarily primitive group contains proteins, named major royal jelly proteins (MRJPs), which Polyneoptera. -
Periodical Cicadas SP 341 3/21 21-0190 Programs in Agriculture and Natural Resources, 4-H Youth Development, Family and Consumer Sciences, and Resource Development
SP 341 Periodical Cicadas Frank A. Hale, Professor Originally developed by Harry Williams, former Professor Emeritus and Jaime Yanes Jr., former Assistant Professor Department of Entomology and Plant Pathology The periodical cicada, Magicicada species, has the broods have been described by scientists and are longest developmental period of any insect in North designated by Roman numerals. There are three 13-year America. There is probably no insect that attracts as cicada broods (XIX, XXII and XXIII) and 12 17-year much attention in eastern North America as does the cicada broods (I-X, XIII, and XIV). Also, there are three periodical cicada. Their sudden springtime emergence, distinct species of 17-year cicadas (M. septendecim, filling the air with their high-pitched, shrill-sounding M. cassini, and M. septendecula) and three species of songs, excites much curiosity. 13-year cicadas (M. tredecim, M. tredecassini, and M. tredecula). Two races of the periodical cicada exist. One race has a life cycle of 13 years and is common in the southeastern In Tennessee, Brood XIX of the 13-year cicada had a United States. The other race has a life cycle of 17 years spectacular emergence in 2011 (Map 1). In 2004 and and is generally more northern in distribution. Due 2021, Brood X of the 17-year cicada primarily emerged to Tennessee’s location, both the 13-year and 17-year in East Tennessee (Map 2). Brood X has the largest cicadas occur in the state. emergence of individuals for the 17-year cicada in the United States. Brood XXIII of the 13-year cicada last Although periodical cicadas have a 13- or 17-year cycle, emerged in West Tennessee in 2015 (Map 3). -
Wax, Wings, and Swarms: Insects and Their Products As Art Media
Wax, Wings, and Swarms: Insects and their Products as Art Media Barrett Anthony Klein Pupating Lab Biology Department, University of Wisconsin—La Crosse, La Crosse, WI 54601 email: [email protected] When citing this paper, please use the following: Klein BA. Submitted. Wax, Wings, and Swarms: Insects and their Products as Art Media. Annu. Rev. Entom. DOI: 10.1146/annurev-ento-020821-060803 Keywords art, cochineal, cultural entomology, ethnoentomology, insect media art, silk 1 Abstract Every facet of human culture is in some way affected by our abundant, diverse insect neighbors. Our relationship with insects has been on display throughout the history of art, sometimes explicitly, but frequently in inconspicuous ways. This is because artists can depict insects overtly, but they can also allude to insects conceptually, or use insect products in a purely utilitarian manner. Insects themselves can serve as art media, and artists have explored or exploited insects for their products (silk, wax, honey, propolis, carmine, shellac, nest paper), body parts (e.g., wings), and whole bodies (dead, alive, individually, or as collectives). This review surveys insects and their products used as media in the visual arts, and considers the untapped potential for artistic exploration of media derived from insects. The history, value, and ethics of “insect media art” are topics relevant at a time when the natural world is at unprecedented risk. INTRODUCTION The value of studying cultural entomology and insect art No review of human culture would be complete without art, and no review of art would be complete without the inclusion of insects. Cultural entomology, a field of study formalized in 1980 (43), and ambitiously reviewed 35 years ago by Charles Hogue (44), clearly illustrates that artists have an inordinate fondness for insects. -