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06-Secondary Productivity.Pptx
BIO 3072 !Ecology !Eric L. Peters! Ecological (Biomass) Production! Earth Area Available to Support Humans! Primary Production:! Productive sea and land area Production of autotroph (producer)" biomass! available to support each Autotrophs capture and store their own" energy and synthesize their own" person in Africa: ! structural materials! 1.36 ha! Limited by photosynthetic rates! …on Earth: 1.90 ha! Secondary Production:! Production of heterotroph" Used by each W. European/U.S. (consumer) biomass! citizen:" Heterotrophs’ structural" 5.06/5.26 ha! materials (and energy) must be" World obtained from their food! Productive sea and land area needed to produce Wildlife Limited by primary productivity, number and efficiency of energy the products consumed by each U.S. citizen:" Fund," transfers, and other factors. Many chemical elements (e.g., Ca and P) 9.71 ha (the CSU campus is 64.75 ha: enough to Living Planet must be provided in specific chemical forms or combinations! sustain 12.3 U.S. citizens) ! Report 2002. ! Nutrient Requirements of Consumers! Energy-bearing Nutrients and Respiration! !Edible, adj. good to eat and wholesome to digest, as a worm Cells use many organic molecules as fuel for respiration:! to a toad, a toad to a snake, a snake to a pig, a pig to a man, and a man to a worm.! –Ambrose Bierce, The Devil’s Dictionary !" ! There is tremendous variability in organismal nutritional requirements, as well as in the adaptations to meet those needs, e.g.,! Insects require a dietary source of cholesterol, mammals manufacture -
4 Reproductive Biology of Cerambycids
4 Reproductive Biology of Cerambycids Lawrence M. Hanks University of Illinois at Urbana-Champaign Urbana, Illinois Qiao Wang Massey University Palmerston North, New Zealand CONTENTS 4.1 Introduction .................................................................................................................................. 133 4.2 Phenology of Adults ..................................................................................................................... 134 4.3 Diet of Adults ............................................................................................................................... 138 4.4 Location of Host Plants and Mates .............................................................................................. 138 4.5 Recognition of Mates ................................................................................................................... 140 4.6 Copulation .................................................................................................................................... 141 4.7 Larval Host Plants, Oviposition Behavior, and Larval Development .......................................... 142 4.8 Mating Strategy ............................................................................................................................ 144 4.9 Conclusion .................................................................................................................................... 148 Acknowledgments ................................................................................................................................. -
Fungal Transformation of Tree Stumps Into a Suitable Resource for Xylophagous Beetles Via Changes in Elemental Ratios
insects Brief Report Fungal Transformation of Tree Stumps into a Suitable Resource for Xylophagous Beetles via Changes in Elemental Ratios Michał Filipiak *, Łukasz Sobczyk and January Weiner Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387 Kraków, Poland; [email protected] (L.S.); [email protected] (J.W.) * Correspondence: michal.fi[email protected]; Tel.: +48-12-664-5134 Academic Editors: Tsuyoshi Yoshimura, Wakako Ohmura, Vernard Lewis and Ryutaro Iwata Received: 10 February 2016; Accepted: 5 April 2016; Published: 9 April 2016 Abstract: The elements present in dead pine stumps inhabited by larvae of wood-boring beetles (Stictoleptura rubra, Arhopalus rusticus and Chalcophora mariana) were analyzed over the initial (first 5 years; a chronosequence) stages of wood decay. The quantities of N, P, K, Ca, Mg, Fe, Zn, Mn, Cu and Na (but not S) increased with increases in the content of ergosterol (used as a proxy for the amount of fungal tissue). In fact, the amounts of P, N, K, Fe and Cu presented marked increases. These findings show that fungi stoichiometrically rearrange dead wood by importing externally occurring nutrients to decaying stumps. During the first years of wood decay, the ratios of C to other elements decrease substantially, but differently, for various elements, whereas the N:Fe, N:Cu, N:P and N:K ratios remain relatively stable. Therefore, the stoichiometric mismatch between xylophages and their food is greatly reduced. By changing the nutritional stoichiometry of dead wood, fungi create a nutritional niche for wood-eaters, and these changes enable the development of xylophages. -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
Ants: Major Functional Elements in Fruit Agro-Ecosystems and Biological Control Agents
sustainability Review Ants: Major Functional Elements in Fruit Agro-Ecosystems and Biological Control Agents Lamine Diamé 1,2,*, Jean-Yves Rey 1,3,6, Jean-François Vayssières 3,6, Isabelle Grechi 4,6, Anaïs Chailleux 3,5,6 ID and Karamoko Diarra 2 1 Institut Sénégalais de Recherches Agricoles, Centre pour le Développement de l’Horticulture, BP 3120 Dakar, Senegal; [email protected] 2 Université Cheikh Anta Diop de Dakar, BP 7925 Dakar, Senegal; [email protected] 3 Centre de Coopération Internationale de Recherche Agronomique pour le Développement, UPR HortSys, F-34398 Montpellier, France; jean-franç[email protected] (J.F.V.); [email protected] (A.C.) 4 Centre de Coopération Internationale de Recherche Agronomique pour le Développement, UPR HortSys, F-97455 Saint-Pierre, La Réunion, France; [email protected] 5 Biopass, Institut Sénégalais de Recherches Agricoles—University Cheikh Anta Diop de Dakar—Institut de Recherche pour le Développement, BP 2274 Dakar, Senegal 6 University de Montpellier, Centre de Coopération Internationale de Recherche Agronomique pour le Développement, HortSys, F-34398 Montpellier, France * Correspondence: [email protected] Received: 15 October 2017; Accepted: 12 December 2017; Published: 22 December 2017 Abstract: Ants are a very diverse taxonomic group. They display remarkable social organization that has enabled them to be ubiquitous throughout the world. They make up approximately 10% of the world’s animal biomass. Ants provide ecosystem services in agrosystems by playing a major role in plant pollination, soil bioturbation, bioindication, and the regulation of crop-damaging insects. Over recent decades, there have been numerous studies in ant ecology and the focus on tree cropping systems has given added importance to ant ecology knowledge. -
Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico
insects Article Vertical and Horizontal Trophic Networks in the Aroid-Infesting Insect Community of Los Tuxtlas Biosphere Reserve, Mexico Guadalupe Amancio 1 , Armando Aguirre-Jaimes 1, Vicente Hernández-Ortiz 1,* , Roger Guevara 2 and Mauricio Quesada 3,4 1 Red de Interacciones Multitróficas, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 2 Red de Biologia Evolutiva, Instituto de Ecología A.C., Xalapa, Veracruz 91073, Mexico 3 Laboratorio Nacional de Análisis y Síntesis Ecológica, Escuela Nacional de Estudios Superiores Unidad Morelia, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico 4 Instituto de Investigaciones en Ecosistemas y Sustentabilidad, Universidad Nacional Autónoma de México, Morelia 58190 Michoacán, Mexico * Correspondence: [email protected] Received: 20 June 2019; Accepted: 9 August 2019; Published: 15 August 2019 Abstract: Insect-aroid interaction studies have focused largely on pollination systems; however, few report trophic interactions with other herbivores. This study features the endophagous insect community in reproductive aroid structures of a tropical rainforest of Mexico, and the shifting that occurs along an altitudinal gradient and among different hosts. In three sites of the Los Tuxtlas Biosphere Reserve in Mexico, we surveyed eight aroid species over a yearly cycle. The insects found were reared in the laboratory, quantified and identified. Data were analyzed through species interaction networks. We recorded 34 endophagous species from 21 families belonging to four insect orders. The community was highly specialized at both network and species levels. Along the altitudinal gradient, there was a reduction in richness and a high turnover of species, while the assemblage among hosts was also highly specific, with different dominant species. -
Nutrional Ecology in Social Insects
NUTRIONAL ECOLOGY IN SOCIAL INSECTS Laure-Anne Poissonnier Thesis submitted the 16th of July 2018 for the degree of Doctor of Philosophy Department of Agricultural Science School of Agriculture, Food and Wine Faculty of Sciences, The University of Adelaide Supervisors: Jerome Buhl and Audrey Dussutour “If all mankind were to disappear, the world would regenerate back to the rich state of equilibrium that existed ten thousand years ago. If insects were to vanish, the environment would collapse into chaos.” E.O.Wilson Table of Contents Tables of contents i Abstract v Declaration vii Acknowledgements ix Statements of authorship x Chapter 1 – General introduction 1 1. Nutrition is a complex process that influences and links all living organisms 3 2. Towards an integrative approach to study nutrition, the Nutritional Geometric Framework 4 2.a. Nutrient regulation 5 2.b. Nutrient effects on life history traits and feeding rules 8 3. Nutrition and sociality 10 3.a. Nutrition and immunity in social insects 12 3.a. Humoral and cellular defence against pathogens in insects 13 3.b Behavioural strategies used by social insects to fight parasites 14 3.c Physiological strategies used by social insects to fight parasites 16 3.d Role of nutrition in insects’ immunity 16 4. Nutrition in insect colonies 18 4.a. Self-organisation and foraging in social insects 19 4.b. Ending mass recruitment 21 4.c. Modulating recruitment according to food quality 22 4.d. Information exchange and food sharing between castes 23 4.e. Distribution of nutrients in the colony 25 4.f. The insight brought by NGF studies in social insect nutrition 29 5. -
A Comparison of Predation Rates Measured by Various Types of Sentinel Prey
Author Manuscript This is the author manuscript accepted for publication and has undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/jen.12745 This article is protected by copyright. All rights reserved Fresh, frozen or fake: a comparison of predation rates measured by various types of sentinel prey Rebecca K. Nagya,b, Nancy A. Schellhornb† and Myron P. Zaluckia aSchool of Biological Sciences, The University of Queensland, St Lucia, Qld 4072, Australia bCSIRO, Brisbane, Qld 4001, Australia †RapidAim, Brisbane, Qld 4000, Australia Acknowledgements Thanks goes to UQAuthor Manuscript Gatton for allowing access to their property to conduct this research. Thanks also to Anna Marcora for her help procuring insects from Narrabri and Dr Lynda Perkins for her help with statistics. R.K.N.’s research is funded by the Australian This article is protected by copyright. All rights reserved Government Research Training Program (RTP), AW Howard Memorial Trust and Advance Queensland. Author Manuscript This article is protected by copyright. All rights reserved 1 2 MRS. REBECCA NAGY (Orcid ID : 0000-0002-5562-7957) 3 4 5 Article type : Advances in Methodology 6 7 Formatted: Left, Line spacing: Multiple 1.08 li 8 Corresponding author mail id: [email protected] Formatted: Font: 12 pt 9 Fresh, frozen or fake: a comparison 10 of predation rates measured by 11 various types of sentinel prey 12 13 Rebecca K. Nagya,b, Nancy A. -
Sexual Dimorphism in the Multielemental Stoichiometric Phenotypes and Stoichiometric Niches of Spiders
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 29 July 2020 doi:10.20944/preprints202007.0073.v2 Peer-reviewed version available at Insects 2020, 11, 484; doi:10.3390/insects11080484 Communication Sexual Dimorphism in the Multielemental Stoichiometric Phenotypes and Stoichiometric Niches of Spiders Łukasz Sobczyk, Michał Filipiak * and Marcin Czarnoleski Institute of Environmental Sciences, Jagiellonian University, ul. Gronostajowa 7, 30-387 Kraków, Poland; [email protected] (Ł.S.); [email protected] (M.C.) * Correspondence: [email protected]; Tel.: +48-12-664-5134 Abstract: Nutritional limitations may shape populations and communities of organisms. This phenomenon is often studied by treating populations and communities as pools of homogenous individuals with average nutritional optima and experiencing average constraints and trade-offs that influence their fitness in a standardized way. However, populations and communities consist of individuals belonging to different sexes, each with specific nutritional demands and limitations. Taking this into account, we used the ecological stoichiometry framework to study sexual differences in the stoichiometric phenotypes, reflecting stoichiometric niches, of four spider taxa differing in hunting mode. The species and sexes differed fundamentally in their elemental phenotypes, including elements beyond those most commonly studied (C, N and P). Both species and sexes were distinguished by the C:N ratio and concentrations of Cu, K and Zn. Species additionally differed in concentrations of Na, Mg and Mn. Phosphorous was not involved in this differentiation. Sexual dimorphism in spiders’ elemental phenotypes, related to differences in their stoichiometric niches, suggests different nutritional optima and differences in nutritional limitation experienced by different sexes and species. -
Using Species Traits to Understand the Mechanisms Driving Pollination and Pest Control Ecosystem Services
Using species traits to understand the mechanisms driving pollination and pest control ecosystem services Arran Greenop (B.Sc., MRes) March 2020 Thesis submitted for the degree of Doctor of Philosophy Contents Summary ...................................................................................................................... iv List of figures ................................................................................................................. v List of tables .................................................................................................................. vi Acknowledgements ...................................................................................................... viii Declarations ................................................................................................................. viii Statement of authorship ................................................................................................ ix 1. Chapter 1. Thesis introduction ....................................................................................... 1 1.1. Background ............................................................................................................... 1 1.2. Thesis outline ............................................................................................................ 8 2. Chapter 2. Functional diversity positively affects prey suppression by invertebrate predators: a meta-analysis ................................................................................................. -
Handbook of Zoology
Handbook of Zoology Founded by Willy Kükenthal Editor-in-chief Andreas Schmidt-Rhaesa Arthropoda: Insecta Editors Niels P. Kristensen & Rolf G. Beutel Authenticated | [email protected] Download Date | 5/8/14 6:22 PM Richard A. B. Leschen Rolf G. Beutel (Volume Editors) Coleoptera, Beetles Volume 3: Morphology and Systematics (Phytophaga) Authenticated | [email protected] Download Date | 5/8/14 6:22 PM Scientific Editors Richard A. B. Leschen Landcare Research, New Zealand Arthropod Collection Private Bag 92170 1142 Auckland, New Zealand Rolf G. Beutel Friedrich-Schiller-University Jena Institute of Zoological Systematics and Evolutionary Biology 07743 Jena, Germany ISBN 978-3-11-027370-0 e-ISBN 978-3-11-027446-2 ISSN 2193-4231 Library of Congress Cataloging-in-Publication Data A CIP catalogue record for this book is available from the Library of Congress. Bibliografic information published by the Deutsche Nationalbibliothek The Deutsche Nationalbibliothek lists this publication in the Deutsche Nationalbibliografie; detailed bibliographic data are available in the Internet at http://dnb.dnb.de Copyright 2014 by Walter de Gruyter GmbH, Berlin/Boston Typesetting: Compuscript Ltd., Shannon, Ireland Printing and Binding: Hubert & Co. GmbH & Co. KG, Göttingen Printed in Germany www.degruyter.com Authenticated | [email protected] Download Date | 5/8/14 6:22 PM Cerambycidae Latreille, 1802 77 2.4 Cerambycidae Latreille, Batesian mimic (Elytroleptus Dugés, Cerambyc inae) feeding upon its lycid model (Eisner et al. 1962), 1802 the wounds inflicted by the cerambycids are often non-lethal, and Elytroleptus apparently is not unpal- Petr Svacha and John F. Lawrence atable or distasteful even if much of the lycid prey is consumed (Eisner et al. -
Appendix 2. Additional Information Supporting an Application to Introduce Exotic Pastoral Dung Beetles Into New Zealand
Appendix 2. Additional information supporting an application to introduce exotic pastoral dung beetles into New Zealand 1. Scope of the literature used in this appendix 2. Introduction: Native dung beetle diversity 2.1 Reproduction 3. The effect of exotic species on native species: habitat and soil preference 3.1 Habitat Specificity 3.2 Habitat preferences of native dung beetles 3.3 Habitat preferences of pastoral dung beetles in New Zealand 3.4 Soil preference 4. Benefits to the pastoral habitat above and below ground 4.1 Soil Compaction 4.2 Nutrient Cycling 5. Benefits to availability of pasture and calculating dung production 6. Benefits to the health of livestock 6.1 Destruction of nematode eggs 6.2 Dung Beetles and the suppression of nematodes 6.3 Dung beetles aiding in parasitic survival and dispersal 6.4 Dung beetle burial activity reduces pest fly numbers 6.5 Benefits to pest fly control in Australia 6.6 Dung removal and human disease transmission by flies 7. Dung beetle activity increases earthworm populations and depth at which earthworms are found 8. Effect of dung beetles on the rate at which water infiltrates soil 9. Agricultural emissions 9.1 Methane 10. Economic benefits 10.1 Calculating future benefits of dung beetles in New Zealand 10.2 Estimating production increases from dung burial by Bubas bison, a winter active species considered for release in New Zealand 11. References 1. Scope of the literature used in this appendix A literature search of online journals and data bases yielded over 1,720 published articles and reports covering all aspects of dung beetle ecological research.