Insects of the Arboretum
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Diversity of Millipedes Along the Northern Western Ghats
Journal of Entomology and Zoology Studies 2014; 2 (4): 254-257 ISSN 2320-7078 Diversity of millipedes along the Northern JEZS 2014; 2 (4): 254-257 © 2014 JEZS Western Ghats, Rajgurunagar (MS), India Received: 14-07-2014 Accepted: 28-07-2014 (Arthropod: Diplopod) C. R. Choudhari C. R. Choudhari, Y.K. Dumbare and S.V. Theurkar Department of Zoology, Hutatma Rajguru Mahavidyalaya, ABSTRACT Rajgurunagar, University of Pune, The different vegetation type was used to identify the oligarchy among millipede species and establish India P.O. Box 410505 that millipedes in different vegetation types are dominated by limited set of species. In the present Y.K. Dumbare research elucidates the diversity of millipede rich in part of Northern Western Ghats of Rajgurunagar Department of Zoology, Hutatma (MS), India. A total four millipedes, Harpaphe haydeniana, Narceus americanus, Oxidus gracilis, Rajguru Mahavidyalaya, Trigoniulus corallines taxa belonging to order Polydesmida and Spirobolida; 4 families belongs to Rajgurunagar, University of Pune, Xystodesmidae, Spirobolidae, Paradoxosomatidae and Trigoniulidae and also of 4 genera were India P.O. Box 410505 recorded from the tropical or agricultural landscape of Northern Western Ghats. There was Harpaphe haydeniana correlated to the each species of millipede which were found in Northern Western Ghats S.V. Theurkar region of Rajgurunagar. At the time of diversity study, Trigoniulus corallines were observed more than Senior Research Fellowship, other millipede species, which supports the environmental determinism condition. Narceus americanus Department of Zoology, Hutatma was single time occurred in the agricultural vegetation landscape due to the geographical location and Rajguru Mahavidyalaya, habitat differences. Rajgurunagar, University of Pune, India Keywords: Diplopod, Northern Western Ghats, millipede diversity, Narceus americanus, Trigoniulus corallines 1. -
Studies of the Laboulbeniomycetes: Diversity, Evolution, and Patterns of Speciation
Studies of the Laboulbeniomycetes: Diversity, Evolution, and Patterns of Speciation The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:40049989 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA ! STUDIES OF THE LABOULBENIOMYCETES: DIVERSITY, EVOLUTION, AND PATTERNS OF SPECIATION A dissertation presented by DANNY HAELEWATERS to THE DEPARTMENT OF ORGANISMIC AND EVOLUTIONARY BIOLOGY in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the subject of Biology HARVARD UNIVERSITY Cambridge, Massachusetts April 2018 ! ! © 2018 – Danny Haelewaters All rights reserved. ! ! Dissertation Advisor: Professor Donald H. Pfister Danny Haelewaters STUDIES OF THE LABOULBENIOMYCETES: DIVERSITY, EVOLUTION, AND PATTERNS OF SPECIATION ABSTRACT CHAPTER 1: Laboulbeniales is one of the most morphologically and ecologically distinct orders of Ascomycota. These microscopic fungi are characterized by an ectoparasitic lifestyle on arthropods, determinate growth, lack of asexual state, high species richness and intractability to culture. DNA extraction and PCR amplification have proven difficult for multiple reasons. DNA isolation techniques and commercially available kits are tested enabling efficient and rapid genetic analysis of Laboulbeniales fungi. Success rates for the different techniques on different taxa are presented and discussed in the light of difficulties with micromanipulation, preservation techniques and negative results. CHAPTER 2: The class Laboulbeniomycetes comprises biotrophic parasites associated with arthropods and fungi. -
Arthropod Diversity and Conservation in Old-Growth Northwest Forests'
AMER. ZOOL., 33:578-587 (1993) Arthropod Diversity and Conservation in Old-Growth mon et al., 1990; Hz Northwest Forests complex litter layer 1973; Lattin, 1990; JOHN D. LATTIN and other features Systematic Entomology Laboratory, Department of Entomology, Oregon State University, tural diversity of th Corvallis, Oregon 97331-2907 is reflected by the 14 found there (Lawtt SYNOPSIS. Old-growth forests of the Pacific Northwest extend along the 1990; Parsons et a. e coastal region from southern Alaska to northern California and are com- While these old posed largely of conifer rather than hardwood tree species. Many of these ity over time and trees achieve great age (500-1,000 yr). Natural succession that follows product of sever: forest stand destruction normally takes over 100 years to reach the young through successioi mature forest stage. This succession may continue on into old-growth for (Lattin, 1990). Fire centuries. The changing structural complexity of the forest over time, and diseases, are combined with the many different plant species that characterize succes- bances. The prolot sion, results in an array of arthropod habitats. It is estimated that 6,000 a continually char arthropod species may be found in such forests—over 3,400 different ments and habitat species are known from a single 6,400 ha site in Oregon. Our knowledge (Southwood, 1977 of these species is still rudimentary and much additional work is needed Lawton, 1983). throughout this vast region. Many of these species play critical roles in arthropods have lx the dynamics of forest ecosystems. They are important in nutrient cycling, old-growth site, tt as herbivores, as natural predators and parasites of other arthropod spe- mental Forest (HJ cies. -
TERRESTRIAL ARTHROPODS 2012-2016 BIOBLITZ VASHON ISLAND List Compiled By: Harsi Parker
COMPLETE LIST OF TERRESTRIAL ARTHROPODS 2012-2016 BIOBLITZ VASHON ISLAND List compiled by: Harsi Parker Number Species name Common name Notes Year Location Taxonomic Order 1 Gammaridae sp. scud 2016 J Amphipoda – Gammaridae 2 Hyalella sp. amphipod 2014, 2016 CH, J Amphipoda – Hyalellidae 3 Acari sp. #1 mite 2012, 2013, 2015, 2016 NP, SH, M, J Arachnida 4 Acari sp. #2 mite 2014 CH Arachnida 5 Opiliones sp. harvestman 2013, 2015 SH, M Arachnida 6 Callobius sp. hacklemesh weaver 2012 NP Arachnida – Amaurobiidae 7 Araneidae sp. orb weaver 2016 J Arachnida – Araneidae 8 Araneus diadematus Cross Orbweaver 2012, 2014 NP, CH Arachnida – Araneidae 9 Clubiona sp. leafcurling sac spider 2012 NP Arachnida – Clubionidae 10 Linyphiinae sp. sheetweb spider tentative ID 2012 NP Arachnida – Linyphiidae 11 Neriene sp. sheetweb spider tentative ID 2014 CH Arachnida – Linyphiidae 12 Pardosa sp. thinlegged wolf spider 2012 NP Arachnida – Lycosidae 13 Philodromus dispar running crab spider 2012 NP Arachnida – Philodromidae 14 Tibellus sp. slender crab spider tentative ID 2014 CH Arachnida – Philodromidae 15 Eris militaris Bronze Jumper tentative ID 2014 CH Arachnida – Salticidae 16 Metaphidippus manni jumping spider tentative ID 2014, 2016 CH, J Arachnida – Salticidae 17 Salticidae sp. #1 jumping spider 2014 CH Arachnida – Salticidae 18 Salticidae sp. #2 jumping spider 2015 M Arachnida – Salticidae 19 Salticus scenicus Zebra Jumper 2013, 2014, 2015 SH, CH, M Arachnida – Salticidae 20 Metellina sp. long-jawed orb weaver 2012 NP Arachnida – Tetragnathidae 21 Tetragnatha sp. long-jawed orb weaver 2013 SH Arachnida – Tetragnathidae 22 Theridiidae sp. cobweb spider 2012 NP Arachnida – Theridiidae 23 Misumena vatia Goldenrod Crab Spider 2013, 2016 SH, J Arachnida – Thomisidae 24 Thomisidae sp. -
The Ecology of British Upland Peatlands: Climate Change, Drainage, Keystone Insects and Breeding Birds
The ecology of British upland peatlands: climate change, drainage, keystone insects and breeding birds Matthew John Carroll PhD University of York Department of Biology September 2012 Abstract Northern peatlands provide important ecosystem services and support species adapted to cold, wet conditions. However, drainage and climate change could cause peatlands to become drier, threatening ecosystem functions and biodiversity. British blanket bogs occur towards the southern extent of northern peatlands and have been extensively drained, so present an excellent opportunity to examine climate change and drainage impacts. Craneflies (Diptera: Tipulidae) are a major component of upland peatland invertebrate communities and provide a key food resource to breeding birds. However, larvae are highly susceptible to desiccation, so environmental changes that dry peat surfaces could harm cranefly populations and, in turn, bird populations. This thesis aims to examine effects of soil moisture, drainage and climate change on craneflies, and the relationship between craneflies and birds. A large-scale field experiment showed that adult cranefly abundance increased with soil moisture. Areas with blocked drainage ditches showed significantly higher soil moisture and cranefly abundance than areas with active drainage. A model of monthly peatland water tables driven by simple climate data was developed. The model accurately predicted water table position, and predicted up to two thirds of water table variation over time. Performance declined when modelling drained sites. The water table model was combined with empirical relationships to model cranefly abundance under climate change. Falling summer water tables were projected to drive cranefly population declines. Drain blocking would increase abundance and slow declines, thus aiding population persistence. -
Apheloria Polychroma, a New Species of Millipede from the Cumberland Mountains (Polydesmida: Xystodesmidae) PAUL E. MAREK1*
Apheloria polychroma, a new species of millipede from the Cumberland Mountains (Polydesmida: Xystodesmidae) PAUL E. MAREK1*, JACKSON C. MEANS1, DEREK A. HENNEN1 1Virginia Polytechnic Institute and State University, Department of Entomology, Blacksburg, Virginia 24061, U.S.A. *Corresponding author, email: [email protected] Abstract Millipedes of the genus Apheloria occur in temperate broadleaf forests throughout eastern North America and west of the Mississippi River in the Ozark and Ouachita Mountains. Chemically defended with toxins made up of cyanide and benzaldehyde, the genus is part of a community of xystodesmid millipedes that compose several Müllerian mimicry rings in the Appalachian Mountains. We describe a model species of these mimicry rings, Apheloria polychroma n. sp., one of the most variable in coloration of all species of Diplopoda with more than six color morphs, each associated with a separate mimicry ring. Keywords: aposematic, Appalachian, Myriapoda, taxonomy, systematics Introduction Millipedes in the family Xystodesmidae are most diverse in the Appalachian Mountains where about half of the family’s species occur. In the New World, the family is distributed throughout eastern and western North America and south to El Salvador (Marek et al. 2014, Marek et al. 2017). Xystodesmidae occur in the Old World in the Mediterranean, the Russian Far East, Japan, western and eastern China, Taiwan and Vietnam. Taxa include species that are bioluminescent (genus Motyxia) and highly gregarious (genera Parafontaria and Pleuroloma); some form Müllerian mimicry rings. Despite their fascinating biology and critical ecological function as native decomposers in broadleaf deciduous forests in the U.S., their alpha-taxonomy is antiquated, and scores of new species remain undescribed. -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Biological Solutions for Chafer Grub and Leatherjacket Control in Turf Chafer Grubs and Leatherjackets Cause Extensive Damage by Feeding on Plant Roots in Turf
Biological solutions for Chafer Grub and Leatherjacket control in turf Chafer Grubs and Leatherjackets cause extensive damage by feeding on plant roots in turf. The secondary damage is just as desctructive when birds, badgers, foxes, moles and other small mammals rip up the already weakened turf in search of their protein rich larvae. Tell-tale signs of infestation include birds pecking at the grass, poor grass growth, the appearance of yellow patches and the ability to pull the turf up because there is little or no root growth. Beneficial nematodes are effective biological control agents that are safe to users and the environment. Key points Most turf specialists use chemical methods to control pest problems, however insects are known for their ability to develop resistance to synthetic chemicals and Nemasys G contains the insect parasitic some pesticides may be non-specific and kill beneficial nematode Heterohabditis bacteriophora for insects. That, added to the increasing legislation the control of Chafer Grubs and withdrawing of existing chemical controls, has increased the use of natural biological control agents Nemasys J contains Steinernema feltiae for as part of an integrated pest management programme the control of Leatherjackets for controlling pest populations. Kills larvae within 10–14 days Nemasys G (controls Chafer Grubs) and Nemasys J (controls Leatherjackets) contain nematodes that provide Safe for turf and wildlife the perfect biological control by entering the larvae, One tray contains 250 million nematodes which stops them feeding within three days of infection. and treats 500m2 The larvae then die within 10-14 days. The nematodes complete their life cycle within the larvae, then enter Follow application instructions and timings the soil seeking more hosts, so the pest control for optimum results continues naturally. -
Insects and Related Arthropods Associated with of Agriculture
USDA United States Department Insects and Related Arthropods Associated with of Agriculture Forest Service Greenleaf Manzanita in Montane Chaparral Pacific Southwest Communities of Northeastern California Research Station General Technical Report Michael A. Valenti George T. Ferrell Alan A. Berryman PSW-GTR- 167 Publisher: Pacific Southwest Research Station Albany, California Forest Service Mailing address: U.S. Department of Agriculture PO Box 245, Berkeley CA 9470 1 -0245 Abstract Valenti, Michael A.; Ferrell, George T.; Berryman, Alan A. 1997. Insects and related arthropods associated with greenleaf manzanita in montane chaparral communities of northeastern California. Gen. Tech. Rep. PSW-GTR-167. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Dept. Agriculture; 26 p. September 1997 Specimens representing 19 orders and 169 arthropod families (mostly insects) were collected from greenleaf manzanita brushfields in northeastern California and identified to species whenever possible. More than500 taxa below the family level wereinventoried, and each listing includes relative frequency of encounter, life stages collected, and dominant role in the greenleaf manzanita community. Specific host relationships are included for some predators and parasitoids. Herbivores, predators, and parasitoids comprised the majority (80 percent) of identified insects and related taxa. Retrieval Terms: Arctostaphylos patula, arthropods, California, insects, manzanita The Authors Michael A. Valenti is Forest Health Specialist, Delaware Department of Agriculture, 2320 S. DuPont Hwy, Dover, DE 19901-5515. George T. Ferrell is a retired Research Entomologist, Pacific Southwest Research Station, 2400 Washington Ave., Redding, CA 96001. Alan A. Berryman is Professor of Entomology, Washington State University, Pullman, WA 99164-6382. All photographs were taken by Michael A. Valenti, except for Figure 2, which was taken by Amy H. -
Insects Carolina Mantis Mayfly
I l l i n o i s Insects Carolina mantis mayfly elephant stag beetle widow skimmer ichneumon wasp click beetle black locust borer birdwing grasshopper large milkweed bug (adults and nymphs) mantisfly walking stick lady beetle stink bug crane fly stonefly (nymph) horse fly wheel bug bot fly prairie cicada leafhopper robber fly katydid alderfly syrphid fly Order Ephemeroptera mayfly Species List Order Coleoptera black locust borer click beetle This poster was made possible by: nsects and their relatives (arthropods) make up nearly 80 percent of the known animal species. Scientists elephant stag beetle lady beetle Illinois Department of Natural Resources Order Plecoptera stonefly currently estimate that 5 to 15 million species of insects exist. In contrast, 5,000 species of mammals are Order Orthoptera birdwing grasshopper Carolina mantis Division of Education found on our planet. In Illinois, we have more than 20,000 species of insects, and many more likely katydid Illinois Natural History Survey I Order Hemiptera large milkweed bug Illinois State Museum occur, as yet undetected in our state! The scientific study of insects is known as entomology. Entomologists stink bug wheel bug Order Diptera bot fly study insects for many reasons, including their incredible number of species and their wide variety of sizes, crane fly horse fly colors, shapes, and lifestyles. The 24 species depicted on this poster were selected by Michael R. Jeffords of robber fly syrphid fly Order Homoptera leafhopper the Illinois Department of Natural Resources, Illinois Natural History Survey, to represent the variety of prairie cicada Order Phasmida walking stick insects occurring in our state. -
A Seasonal Guide to New York City's Invertebrates
CENTER FOR BIODIVERSITY AND CONSERVATION A Seasonal Guide to New York City’s Invertebrates Elizabeth A. Johnson with illustrations by Patricia J. Wynne CENTER FOR BIODIVERSITY AND CONSERVATION A Seasonal Guide to New York City’s Invertebrates Elizabeth A. Johnson with illustrations by Patricia J. Wynne Ellen V. Futter, President Lewis W. Bernard, Chairman, Board of Trustees Michael J. Novacek, Senior Vice-President and Provost of Science TABLE OF CONTENTS Introduction.................................................................................2-3 Rules for Exploring When to Look Where to Look Spring.........................................................................................4-11 Summer ...................................................................................12-19 Fall ............................................................................................20-27 Winter ......................................................................................28-35 What You Can Do to Protect Invertebrates.............................36 Learn More About Invertebrates..............................................37 Map of Places Mentioned in the Text ......................................38 Thanks to all those naturalists who contributed information and to our many helpful reviewers: John Ascher, Allen Barlow, James Carpenter, Kefyn Catley, Rick Cech, Mickey Maxwell Cohen, Robert Daniels, Mike Feller, Steven Glenn, David Grimaldi, Jay Holmes, Michael May, E.J. McAdams, Timothy McCabe, Bonnie McGuire, Ellen Pehek, Don -
Biomechanical Basis of Wing and Haltere Coordination in Flies
Biomechanical basis of wing and haltere coordination in flies Tanvi Deora, Amit Kumar Singh, and Sanjay P. Sane1 National Centre for Biological Sciences, Tata Institute of Fundamental Research, Bangalore 560065, India Edited by M. A. R. Koehl, University of California, Berkeley, CA, and approved December 16, 2014 (received for review June 30, 2014) The spectacular success and diversification of insects rests critically unclear, especially in its ability to mediate rapid wing movement. on two major evolutionary adaptations. First, the evolution of flight, Moreover, faster wing movements require rapid sensory motor which enhanced the ability of insects to colonize novel ecological integration by the insect nervous system. The hind wings of habitats, evade predators, or hunt prey; and second, the miniatur- Diptera have evolved into a pair of mechanosensory halteres that ization of their body size, which profoundly influenced all aspects of detect gyroscopic forces during flight (10–13). The rapid feed- their biology from development to behavior. However, miniaturi- back from halteres is essential for flies to sense and control self- zation imposes steep demands on the flight system because smaller rotations during complex aerobatic maneuvers (13–15). In the insects must flap their wings at higher frequencies to generate majority of flies, the bilateral wings move in-phase, whereas sufficient aerodynamic forces to stay aloft; it also poses challenges halteres move antiphase relative to the wings. This relative co- to the sensorimotor system because precise control of wing ordination between wings and halteres is extremely precise even kinematics and body trajectories requires fast sensory feedback. at frequencies far exceeding 100 Hz.