Insect Anatomy and Physiology
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Intricate but Tight Coupling of Spiracular Activity and Abdominal Ventilation During Locust Discontinuous Gas Exchange Cycles
© 2018. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2018) 221, jeb174722. doi:10.1242/jeb.174722 RESEARCH ARTICLE Intricate but tight coupling of spiracular activity and abdominal ventilation during locust discontinuous gas exchange cycles Stav Talal1,*, Eran Gefen2 and Amir Ayali1,3 ABSTRACT Based mostly on studies of diapausing lepidopteran pupae, DGE Discontinuous gas exchange (DGE) is the best studied among insect cycles are described as comprising of three phases, defined by the gas exchange patterns. DGE cycles comprise three phases, which state of the spiracles: the closed (C), flutter (F) and open (O) phases are defined by their spiracular state: closed, flutter and open. (Levy and Schneiderman, 1966a). However, spiracle behavior has However, spiracle status has rarely been monitored directly; rather, rarely been monitored, but instead was often assumed based on recorded respiratory gas traces. Unlike lepidopteran pupae (and very it is often assumed based on CO2 emission traces. In this study, we directly recorded electromyogram (EMG) signals from the closer small insects), which rely on gas diffusion (Krogh, 1920) or passive muscle of the second thoracic spiracle and from abdominal ventilation convection resulting from sub-atmospheric tracheal pressures muscles in a fully intact locust during DGE. Muscular activity was during DGE (Levy and Schneiderman, 1966b), diffusion alone may be insufficient for larger and more metabolically active insects. monitored simultaneously with CO2 emission, under normoxia and under various experimental oxic conditions. Our findings indicate that Furthermore, insects that rely on diffusion during DGE may also locust DGE does not correspond well with the commonly described switch to active ventilation (and even to a continuous gas exchange three-phase cycle. -
Hymenoptera (Stinging Wasps)
Return to insect order home Page 1 of 3 Visit us on the Web: www.gardeninghelp.org Insect Order ID: Hymenoptera (Stinging Wasps) Life Cycle–Complete metamorphosis: Queens or solitary adults lay eggs. Larvae eat, grow and molt. This stage is repeated a varying number of times, depending on species, until hormonal changes cause the larvae to pupate. Inside a cell (in nests) or a pupal case (solitary), they change in form and color and develop wings. The adults look completely different from the larvae. Solitary wasps: Social wasps: Adults–Stinging wasps have hard bodies and most have membranous wings (some are wingless). The forewing is larger than the hindwing and the two are hooked together as are all Hymenoptera, hence the name "married wings," but this is difficult to see. Some species fold their wings lengthwise, making their wings look long and narrow. The head is oblong and clearly separated from the thorax, and the eyes are compound eyes, but not multifaceted. All have a cinched-in waist (wasp waist). Eggs are laid from the base of the ovipositor, while the ovipositor itself, in most species, has evolved into a stinger. Thus only females have stingers. (Click images to enlarge or orange text for more information.) Oblong head Compound eyes Folded wings but not multifaceted appear Cinched in waist long & narrow Return to insect order home Page 2 of 3 Eggs–Colonies of social wasps have at least one queen that lays both fertilized and unfertilized eggs. Most are fertilized and all fertilized eggs are female. Most of these become workers; a few become queens. -
(Opiliones: Monoscutidae) – the Genus Pantopsalis
Tuhinga 15: 53–76 Copyright © Te Papa Museum of New Zealand (2004) New Zealand harvestmen of the subfamily Megalopsalidinae (Opiliones: Monoscutidae) – the genus Pantopsalis Christopher K. Taylor Department of Molecular Medicine and Physiology, University of Auckland, Private Bag 92019, Auckland, New Zealand ([email protected]) ABSTRACT: The genus Pantopsalis Simon, 1879 and its constituent species are redescribed. A number of species of Pantopsalis show polymorphism in the males, with one form possessing long, slender chelicerae, and the other shorter, stouter chelicerae. These forms have been mistaken in the past for separate species. A new species, Pantopsalis phocator, is described from Codfish Island. Megalopsalis luna Forster, 1944 is transferred to Pantopsalis. Pantopsalis distincta Forster, 1964, P. wattsi Hogg, 1920, and P. grayi Hogg, 1920 are transferred to Megalopsalis Roewer, 1923. Pantopsalis nigripalpis nigripalpis Pocock, 1902, P. nigripalpis spiculosa Pocock, 1902, and P. jenningsi Pocock, 1903 are synonymised with P. albipalpis Pocock, 1902. Pantopsalis trippi Pocock, 1903 is synonymised with P. coronata Pocock, 1903, and P. mila Forster, 1964 is synonymised with P. johnsi Forster, 1964. A list of species described to date from New Zealand and Australia in the Megalopsalidinae is given as an appendix. KEYWORDS: taxonomy, Arachnida, Opiliones, male polymorphism, sexual dimorphism. examines the former genus, which is endemic to New Introduction Zealand. The more diverse Megalopsalis will be dealt with Harvestmen (Opiliones) are abundant throughout New in another publication. All Pantopsalis species described to Zealand, being represented by members of three different date are reviewed, and a new species is described. suborders: Cyphophthalmi (mite-like harvestmen); Species of Monoscutidae are found in native forest the Laniatores (short-legged harvestmen); and Eupnoi (long- length of the country, from the Three Kings Islands in the legged harvestmen; Forster & Forster 1999). -
Ovipositor of the Braconid Wasp
JHR 83: 73–99 (2021) doi: 10.3897/jhr.83.64018 RESEARCH ARTICLE https://jhr.pensoft.net Ovipositor of the braconid wasp Habrobracon hebetor: structural and functional aspects Michael Csader1, Karin Mayer1, Oliver Betz1, Stefan Fischer1,2, Benjamin Eggs1 1 Evolutionary Biology of Invertebrates, Institute of Evolution and Ecology, University of Tübingen, Auf der Morgenstelle 28, 72076, Tübingen, Germany 2 Tübingen Structural Microscopy Core Facility (TSM), Center for Applied Geosciences, University of Tübingen, Schnarrenbergstrasse 94–96, 72076, Tübingen, Germany Corresponding author: Michael Csader ([email protected]) Academic editor: J. Fernandez-Triana | Received 5 February 2021 | Accepted 22 April 2021 | Published 28 June 2021 http://zoobank.org/FEA676AD-6473-4EA3-8F74-E7F83A572234 Citation: Csader M, Mayer K, Betz O, Fischer S, Eggs B (2021) Ovipositor of the braconid wasp Habrobracon hebetor: structural and functional aspects. Journal of Hymenoptera Research 83: 73–99. https://doi.org/10.3897/jhr.83.64018 Abstract The Braconidae are a megadiverse and ecologically highly important group of insects. The vast majority of braconid wasps are parasitoids of other insects, usually attacking the egg or larval stages of their hosts. The ovipositor plays a crucial role in the assessment of the potential host and precise egg laying. We used light- and electron-microscopic techniques to investigate all inherent cuticular elements of the ovipositor (the female 9th abdominal tergum, two pairs of valvifers, and three pairs of valvulae) of the braconid Habrobra- con hebetor (Say, 1836) in detail with respect to their morphological structure and microsculpture. Based on serial sections, we reconstructed the terebra in 3D with all its inherent structures and the ligaments connecting it to the 2nd valvifers. -
Phylum Onychophora
Lab exercise 6: Arthropoda General Zoology Laborarory . Matt Nelson phylum onychophora Velvet worms Once considered to represent a transitional form between annelids and arthropods, the Onychophora (velvet worms) are now generally considered to be sister to the Arthropoda, and are included in chordata the clade Panarthropoda. They are no hemichordata longer considered to be closely related to echinodermata the Annelida. Molecular evidence strongly deuterostomia supports the clade Panarthropoda, platyhelminthes indicating that those characteristics which the velvet worms share with segmented rotifera worms (e.g. unjointed limbs and acanthocephala metanephridia) must be plesiomorphies. lophotrochozoa nemertea mollusca Onychophorans share many annelida synapomorphies with arthropods. Like arthropods, velvet worms possess a chitinous bilateria protostomia exoskeleton that necessitates molting. The nemata ecdysozoa also possess a tracheal system similar to that nematomorpha of insects and myriapods. Onychophorans panarthropoda have an open circulatory system with tardigrada hemocoels and a ventral heart. As in arthropoda arthropods, the fluid-filled hemocoel is the onychophora main body cavity. However, unlike the arthropods, the hemocoel of onychophorans is used as a hydrostatic acoela skeleton. Onychophorans feed mostly on small invertebrates such as insects. These prey items are captured using a special “slime” which is secreted from large slime glands inside the body and expelled through two oral papillae on either side of the mouth. This slime is protein based, sticking to the cuticle of insects, but not to the cuticle of the velvet worm itself. Secreted as a liquid, the slime quickly becomes solid when exposed to air. Once a prey item is captured, an onychophoran feeds much like a spider. -
Biological Differences Reflect Host Preference in Two Parasitoids Attacking the Bark Beetle Ips Typographus (Coleoptera : Scolytidae) in Belgium
UC Berkeley UC Berkeley Previously Published Works Title Biological differences reflect host preference in two parasitoids attacking the bark beetle Ips typographus (Coleoptera : Scolytidae) in Belgium Permalink https://escholarship.org/uc/item/64h0k3qr Journal Bulletin of Entomological Research, 94(4) ISSN 0007-4853 Authors Hougardy, Evelyne Gregoire, J C Publication Date 2004-08-01 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Bulletin of Entomological Research (2004) 94, 341–347 DOI: 10.1079/BER2004305 Biological differences reflect host preference in two parasitoids attacking the bark beetle Ips typographus (Coleoptera: Scolytidae) in Belgium E. Hougardy* and J.-C. Grégoire Lutte biologique et Ecologie spatiale CP 160/12, Université Libre de Bruxelles, 50 av. F.D. Roosevelt, 1050 Bruxelles, Belgium Abstract The basic reproductive biology of two ectoparasitoids developing on the late larval instars of the scolytid Ips typographus Linnaeus, a pest of spruce forests in Eurasia, was studied with the purpose of explaining which biological features allow the two species to share the same host. The anautogenous braconid Coeloides bostrichorum Giraud had a longer pre-oviposition period (5.1 vs. 3.3 days), a greater egg load (8.1 vs. 6.1 eggs), survived longer and emerged later than the pteromalid Rhopalicus tutela (Walker). In contrast, R. tutela was autogenous and tended to be more fecund under constrained conditions (9.7 vs. 5.1 total offspring per female). The longer pre-oviposition period of the specialist C. bostrichorum, coupled with its greater longevity, afforded the opportunity of better synchronization of ovipositing females with late instar larvae of I. -
STRUCTURE and FUNCTIONS of RESPIRATORY SYSTEM Similar To
STRUCTURE AND FUNCTIONS OF RESPIRATORY SYSTEM Similar to aerobic animals, insects must obtain oxygen from their environment and eliminate carbon dioxide respired by their cells. This is gas exchange through series of gas filled tubes providing surface area for gaseous exchange (Respiration strictly refers to oxygen- consuming, cellular metabolic processes). Air is supplied directly to the tissue and no haemolymph (blood) is involved in the respiratory role. Gas exchange occurs by means of internal air-filled tracheae. These tubes branch and ramify through the body. The finest branches called tracheloe contact all internal organs and tissues and are numerous in tissues with high oxygen requirements. Air usually enters the tracheae via spiracular openings positioned laterally on the body. No insect has more than ten pairs (two thoracic and eight abdominal). Based on the number and location of functional spiracles respiratory system is classified as follows 1. Holopneustic 10 pairs, 2 in thorax and 8 in abdomen. e.g. grasshopper 2. Hemipneustic Out of 10 pairs, one or two non functional 3. Peripneustic 9 pairs - 1 in thorax 8 in abdomen. e.g. Caterpillar 4. Amphipneustic 2 pairs - One anterior, one posterior, e.g. maggot 5. Propneustic 1 pair -anterior pair e.g. Puparium 6. Metapneustic 1 pair - posterior pair e.g.Wriggler 7. Hypopneustic 10 pairs - 7 functional (1 thorax + 6 abdominal), 3 non functional. e.g. head louse 8. Apneustic All spiracles closed, closed tracheal system e.g. naiad of may fly. ORGANS OF RESPIRATION SPIRACLES Spiracles have a chamber or atrium with a opening and closing mechanism called valve. -
Evolution of the Insects
CY501-C11[407-467].qxd 3/2/05 12:56 PM Page 407 quark11 Quark11:Desktop Folder:CY501-Grimaldi:Quark_files: But, for the point of wisdom, I would choose to Know the mind that stirs Between the wings of Bees and building wasps. –George Eliot, The Spanish Gypsy 11HHymenoptera:ymenoptera: Ants, Bees, and Ants,Other Wasps Bees, and The order Hymenoptera comprises one of the four “hyperdi- various times between the Late Permian and Early Triassic. verse” insectO lineages;ther the others – Diptera, Lepidoptera, Wasps and, Thus, unlike some of the basal holometabolan orders, the of course, Coleoptera – are also holometabolous. Among Hymenoptera have a relatively recent origin, first appearing holometabolans, Hymenoptera is perhaps the most difficult in the Late Triassic. Since the Triassic, the Hymenoptera have to place in a phylogenetic framework, excepting the enig- truly come into their own, having radiated extensively in the matic twisted-wings, order Strepsiptera. Hymenoptera are Jurassic, again in the Cretaceous, and again (within certain morphologically isolated among orders of Holometabola, family-level lineages) during the Tertiary. The hymenopteran consisting of a complex mixture of primitive traits and bauplan, in both structure and function, has been tremen- numerous autapomorphies, leaving little evidence to which dously successful. group they are most closely related. Present evidence indi- While the beetles today boast the largest number of cates that the Holometabola can be organized into two major species among all orders, Hymenoptera may eventually rival lineages: the Coleoptera ϩ Neuropterida and the Panorpida. or even surpass the diversity of coleopterans (Kristensen, It is to the Panorpida that the Hymenoptera appear to be 1999a; Grissell, 1999). -
Life History, Habits, and Control of the Mormon Cricket'
TECHNICAL BULLETIN NO. 161 DECEMBER, 1929 UNITED STATES DEPARTMENT OF AGRICULTURE WASHINGTON, D. C. LIFE HISTORY, HABITS, AND CONTROL OF THE MORMON CRICKET' Hy FRANK T. COWAN '' Junior lintuiiiolui/iët, Division of Cereal and Foraye Insovt Bureau of Entomologii CONTENTS rage I'age Introduction 1 Description of stages—Continued. Historioiil 2 Adult 12 iioouraphlcal distribution 3 Molting _- 12 Habitat 4 Reactions 14 Economic importance 4 Food plants 16 I*]xtent of infestations T» Cannibalism 16 Nature of injury 5 Migrations 17 Seasonal liistory (i Reproduction 18 Experiments in rearing 7 Natural control 21 Description of stages 8 Predatory enemies J^l Egg 8 Insect parasites -2 First instar - 0 Artiflcial control 23 Second instar 10 Byan masli 2;^ Third instar 10 Raxriers 24 Eourtll initar 10 .\rseiiites 25 I'"ifth instar 11 Summary 26 Sixtli instar 11 Literature cited 28 Seventh instar 11 INTRODUCTION The work reported in this bulletin was begun in Hot Springs County, Wyo., in 1923 by F. W. Boyd.-' Experimental work dealing with the life history, habits, and control of the Mormon cricket was carried on by Mr. Boyd in that section until 1924. Little or no work was done in 1925, but in 1926 and 1927 the writer did similar work in Lake and Sanders Counties in western Montana. As a sequel to this experimental work a control campaign was instituted by the State of Montana in 1927, in cooperation with these counties. So highly successful was it that another campaign, based on its results, was carried on by the writer in the spring of 1928 in Iloutt and Moffat Counties, in northwestern Coloraclo. -
BITING, STINGING and VENOMOUS PESTS: INSECTS (For Non-Insects Such As Scorpions and Spiders, See Page 23)
BITING, STINGING AND VENOMOUS PESTS: INSECTS (For non-insects such as scorpions and spiders, see page 23). Bees include a large number of insects that are included in different families under the order Hymenoptera. They are closely related to ants and wasps, and are common and important components of outdoor community environments. Bees have lapping-type mouthparts, which enable them to feed on nectar and pollen from flowers. Most bees are pollinators and are regarded as beneficial, but some are regarded as pests because of their Pollination by honey bees stings, or damage that they cause due to Photo: Padmanand Madhavan Nambiar nesting activities. NOTABLE SPECIES Common name(s): Bee, honey bee Scientific name, classification: Apis spp., Order: Hymenoptera, Family: Apidae. Distribution: Worldwide. The western honey bee A. mellifera is the most common species in North America. Description and ID characters: Adults are medium to large sized insects, less than ¼ to Western honey bee, Apis mellifera slightly over 1 inch in length. Sizes and Photo: Charles J. Sharp appearances vary with the species and the caste. Best identifying features: Robust black or dark brown bodies, covered with dense hair, mouthparts (proboscis) can be seen extending below the head, hind pair of wings are smaller than the front pair, hind legs are stout and equipped to gather pollen, and often have yellow pollen-balls attached to them. Pest status: Non-pest, although some are aggressive and can sting in defense. Damage/injury: Usually none, and are regarded as the most beneficial insects. Swarming colonies near homes and buildings may cause concern, but they often move on. -
Fine Morphology of Antennal and Ovipositor Sensory Structures of the Gall Chestnut Wasp, Dryocosmus Kuriphilus
insects Article Fine Morphology of Antennal and Ovipositor Sensory Structures of the Gall Chestnut Wasp, Dryocosmus kuriphilus Milos Sevarika 1 , Marco Valerio Rossi Stacconi 2 and Roberto Romani 1,* 1 Department of Agricultural, Food and Environmental Sciences, University of Perugia, 06121 Perugia, Italy; [email protected] 2 Research and Innovation Center, Fondazione Edmund Mach, S. Michele all’Adige, 38098 Trento, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-075-585-6032 Simple Summary: Hymenoptera encompass a large group of insects with different habits, ranging from phytophagy to parasitic/predatory lifestyles. This is also true in the superfamily Cynipoidea, where phytophagy becomes highly specialized towards the exploitation of specific plant tissues (i.e., buds), leading to the induction of galls. In this paper, we investigated the organization of antennal and ovipositor sensory structures in the chestnut gall wasp, Dryocosmus kuriphilus. This insect became a major threat to chestnut production in Italy in the last 15 years. We investigated only females (this is a parthenogenetic species with thelytoky), and on the antennae we found several sensilla with the clear functional specialization to different groups of stimuli, with almost no overlapping among each sensilla. Similarly, specialization was also found on the ovipositor where groups of gustatory and mechanoreceptive sensilla were observed. This information represents an advancement in the Citation: Sevarika, M.; Rossi knowledge of this pest, which may be useful to understand the biological role of plant derived Stacconi, M.V.; Romani, R. Fine chemical cues or to implement new control methods. Morphology of Antennal and Ovipositor Sensory Structures of the Abstract: Dryocosmus kuriphilus is a gall-inducing insect, which can cause significant damage on Gall Chestnut Wasp, Dryocosmus plants of the genus Castanea Mill., 1754. -
The Spiracular Morphology of the Hawaiian Damselfly Megalagrion Blackburni (Odonata)1
Vol. XX, No, I, June, 1968 213 The Spiracular Morphology of the Hawaiian Damselfly Megalagrion blackburni (Odonata)1 Ruth L. Willey DEPARTMENT OF BIOLOGICAL SCIENCES UNIVERSITY OF ILLINOIS AT CHICAGO CIRCLE CHICAGO, ILLINOIS INTRODUCTION In the Odonata, growth and differentation is gradual throughout the nymphal stages although much of the final differentiation of adult structures takes place during the final (ultimate) instar. The environment shifts radically from water to air at the emergence of the adult and most differences in the respiratory system can be correlated with this change. Three stages can be observed: (1) the aquatic nymph, (2) the semi- aquatic nymph of the ultimate instar and (3) the terrestrial, air-breathing adult. The major nymphal respiratory mechanism of the odonate nymph is the diffusion of oxygen through the surface of the body and the surface area may be increased by caudal lamellae (damselflies) or by a rectal branchial basket (dragonflies). The odonate adult has a generalized tracheal system open to the air through 10 pairs of spiracles. The semi-aquatic stage of the final instar retains the nymphal structures and has a single, functional pair of spiracles on the mesothorax. The major structural changes which take place between the nymph and the adult at final metamorphosis are (1) the loss of the caudal lamellae or rectal gills, (2) the shift from the single pair of functional spiracles of the ultimate instar nymph to the 10 pairs of functional spiracles of the adult and (3) the replacement of most of the cylindrical diffusion tracheae of the nymph by compressible, thin-walled air sacs in the adult.