Allelopathy and Chemical Defense - Franz Hadacek
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Fishing for Toxins
000 - Applied Bio Systems Article 19/7/06 11:37 am Page 2 Fishing for Toxins ENVIRONMENTAL Professor Allan Cembella, Professor in the Faculty of Biology and Chemistry at the University of Bremen ANALYSIS and Head of Biological Sciences at the Alfred Wegener Institute. Email: [email protected] Abstract Researchers at the Alfred Wegener Institute (AWI) for Polar and Marine Research in Bremerhaven, Germany are applying advanced chemical and molecular biological technologies to answer ecological questions. They are analysing trace levels of natural bioactive substances in seawater and marine biotoxins produced by various phytoplankton (microalgae), bacteria and cyanobacteria (“blue- green algae”), trying to understand how these bioactive metabolites are produced and sequestered and what effects they have on the ecosystem. Allan Cembella, Professor in the Faculty of Biology and Chemistry at the University of Bremen and Head of Biological Sciences at AWI, describes how the division is using sophisticated chemical analytical technology, including liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS), and limited genomics approaches to define the genetic regulation of marine biotoxin production and eventually determine the distribution and functional ecology of these toxins in marine food webs. Introduction The Alfred Wegener Institute in Bremerhaven, named after the famous polar explorer and geomorphologist responsible for the continental drift theory, was established in 1980 as a research institute focusing primarily on the polar regions. Since then its mandate has enlarged to embrace other disciplines in marine and coastal research in temperate waters and global climate change studies. The Division of Biological Sciences at the Institute is involved in research on projects covering organismal biology, physiology and genetics, functional ecology, molecular biology, marine and natural products chemistry and, now, ecological chemistry - chemical aspects of biological and ecological processes and mechanisms. -
National Resource Material Green and Black Poison Frog (Dendrobates Auratus)
Indicative 10 Project National Resource Material Green and Black Poison frog (Dendrobates auratus) Michelle T. Christy and Win Kirkpatrick 2017 Department of Primary Industries and Regional Development 3 Baron-Hay Court, South Perth, WA 6151 An Invasive Animals CRC Project Contents Summary ............................................................................. 2 Key Messages ................................................................... 2 Classification ................................................................... 2 Common names ................................................................ 3 Biology and Ecology ................................................................ 3 Identification ................................................................... 3 Behaviours and Traits ......................................................... 4 Food and Foraging ............................................................. 4 Reproduction and Lifecycle ................................................. 5 Habitat ......................................................................... 5 Global Range ........................................................................ 5 Potential for Introduction ........................................................ 6 Potential for Eradication.......................................................... 7 Impacts ............................................................................... 7 Economic ........................................................................ 7 Environmental -
Role of Secondary Metabolites in Defense Mechanisms of Plants
Review Article Biology and Medicine, 3 (2) Special Issue: 232-249, 2011 eISSN: 09748369, www.biolmedonline.com Role of secondary metabolites in defense mechanisms of plants *Mazid M1, Khan TA2, Mohammad F1 1 Plant Physiology Division, Department of Botany, Faculty of Life Sciences, AMU, Aligarh, India. 2 Department of Biochemistry, Faculty of Life Sciences, AMU, Aligarh, India. *Corresponding Author: [email protected] Abstract In all natural habitats, plants are surrounded by an enormous number of potential enemies (biotic) and various kinds of abiotic environmental stress. Nearly all ecosystems contain a wide variety of bacteria, viruses, fungi, nematodes, mites, insects, mammals and other herbivorous animals, greatly responsible for heavy reduction in crop productivity. By their nature, plants protect themselves by producing some compounds called as secondary metabolites. Secondary metabolites, including terpenes, phenolics and nitrogen (N) and sulphur (S) containing compounds, defend plants against a variety of herbivores and pathogenic microorganisms as well as various kinds of abiotic stresses. This review presents an overview about some of the mechanisms by which plants protect themselves against herbivory, pathogenic microbes and various abiotic stresses as well as specific plant responses to pathogen attack, the genetic control of host-pathogen interactions. Keywords: Secondary metabolites; defense mechanism; phytoalexins; terpenes; alkaloids; phenolics; cynogenic glucosides. Abbreviations: GST, glucosinolate synthase transferase; SIR, systematic induced resistance; GSL, glucosinolates; GSH, glutathione; HCN, hydrogen cyanide. Introduction (Schaller et al., 1996). Once infected, some In natural systems, plants face a plethora of plants also develop immunity to subsequent antagonists and thus posses a myriad of microbial attacks (Putnam and Heisey, 1983; defense and have evolved multiple defense Putnam and Tang, 1986; Bernays, 1989; mechanisms by which they are able to cope Elakovich, 1987). -
Tropical Insect Chemical Ecology - Edi A
TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol.VII - Tropical Insect Chemical Ecology - Edi A. Malo TROPICAL INSECT CHEMICAL ECOLOGY Edi A. Malo Departamento de Entomología Tropical, El Colegio de la Frontera Sur, Carretera Antiguo Aeropuerto Km. 2.5, Tapachula, Chiapas, C.P. 30700. México. Keywords: Insects, Semiochemicals, Pheromones, Kairomones, Monitoring, Mass Trapping, Mating Disrupting. Contents 1. Introduction 2. Semiochemicals 2.1. Use of Semiochemicals 3. Pheromones 3.1. Lepidoptera Pheromones 3.2. Coleoptera Pheromones 3.3. Diptera Pheromones 3.4. Pheromones of Insects of Medical Importance 4. Kairomones 4.1. Coleoptera Kairomones 4.2. Diptera Kairomones 5. Synthesis 6. Concluding Remarks Acknowledgments Glossary Bibliography Biographical Sketch Summary In this chapter we describe the current state of tropical insect chemical ecology in Latin America with the aim of stimulating the use of this important tool for future generations of technicians and professionals workers in insect pest management. Sex pheromones of tropical insectsUNESCO that have been identified to– date EOLSS are mainly used for detection and population monitoring. Another strategy termed mating disruption, has been used in the control of the tomato pinworm, Keiferia lycopersicella, and the Guatemalan potato moth, Tecia solanivora. Research into other semiochemicals such as kairomones in tropical insects SAMPLErevealed evidence of their presence CHAPTERS in coleopterans. However, additional studies are necessary in order to confirm these laboratory results. In fruit flies, the isolation of potential attractants (kairomone) from Spondias mombin for Anastrepha obliqua was reported recently. The use of semiochemicals to control insect pests is advantageous in that it is safe for humans and the environment. The extensive use of these kinds of technologies could be very important in reducing the use of pesticides with the consequent reduction in the level of contamination caused by these products around the world. -
Stingless Bee Nesting Biology David W
Stingless bee nesting biology David W. Roubik To cite this version: David W. Roubik. Stingless bee nesting biology. Apidologie, Springer Verlag, 2006, 37 (2), pp.124-143. hal-00892207 HAL Id: hal-00892207 https://hal.archives-ouvertes.fr/hal-00892207 Submitted on 1 Jan 2006 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Apidologie 37 (2006) 124–143 124 c INRA/DIB-AGIB/ EDP Sciences, 2006 DOI: 10.1051/apido:2006026 Review article Stingless bee nesting biology* David W. Ra,b a Smithsonian Tropical Research Institute, Apartado 0843-03092, Balboa, Ancón, Panamá, República de Panamá b Unit 0948, APO AA 34002-0948, USA Received 2 October 2005 – Revised 29 November 2005 – Accepted 23 December 2005 Abstract – Stingless bees diverged since the Cretaceous, have 50 times more species than Apis,andare both distinctive and diverse. Nesting is capitulated by 30 variables but most do not define clades. Both architectural features and behavior decrease vulnerability, and large genera vary in nest habit, architecture and defense. Natural stingless bee colony density is 15 to 1500 km−2. Symbionts include mycophagic mites, collembolans, leiodid beetles, mutualist coccids, molds, and ricinuleid arachnids. -
The Raison D'tre of Chemical Ecology
ESA CENTENNIAL PAPER Ecology, 96(3), 2015, pp. 617–630 Ó 2015 by the Ecological Society of America The raison d’eˆtre of chemical ecology 1,5 2,3 3 4 2 ROBERT A. RAGUSO, ANURAG A. AGRAWAL, ANGELA E. DOUGLAS, GEORG JANDER, ANDRE´KESSLER, 3 2,3 KATJA POVEDA, AND JENNIFER S. THALER 1Department of Neurobiology and Behavior, Cornell University, Ithaca, New York 14853 USA 2Department of Ecology and Evolutionary Biology, Cornell University, Ithaca, New York 14853 USA 3Department of Entomology, Cornell University, Ithaca, New York 14853 USA 4Boyce Thompson Institute for Plant Research, Cornell University, Ithaca, New York 14853 USA Abstract. Chemical ecology is a mechanistic approach to understanding the causes and consequences of species interactions, distribution, abundance, and diversity. The promise of chemical ecology stems from its potential to provide causal mechanisms that further our understanding of ecological interactions and allow us to more effectively manipulate managed systems. Founded on the notion that all organisms use endogenous hormones and chemical compounds that mediate interactions, chemical ecology has flourished over the past 50 years since its origin. In this essay we highlight the breadth of chemical ecology, from its historical focus on pheromonal communication, plant–insect interactions, and coevolution to frontier themes including community and ecosystem effects of chemically mediated species interactions. Emerging approaches including the -omics, phylogenetic ecology, the form and function of microbiomes, and network analysis, as well as emerging challenges (e.g., sustainable agriculture and public health) are guiding current growth of this field. Nonetheless, the directions and approaches we advocate for the future are grounded in classic ecological theories and hypotheses that continue to motivate our broader discipline. -
Disruption of Coniferophagous Bark Beetle (Coleoptera: Curculionidae: Scolytinae) Mass Attack Using Angiosperm Nonhost Volatiles: from Concept to Operational Use
The Canadian Entomologist (2021), 153,19–35 Published on behalf of the doi:10.4039/tce.2020.63 Entomological Society of Canada ARTICLE Disruption of coniferophagous bark beetle (Coleoptera: Curculionidae: Scolytinae) mass attack using angiosperm nonhost volatiles: from concept to operational use Dezene P.W. Huber1* , Christopher J. Fettig2 , and John H. Borden3 1Faculty of Environment, University of Northern British Columbia, 3333 University Way, Prince George, British Columbia, V2N 4Z9, Canada, 2Pacific Southwest Research Station, United States Department of Agriculture Forest Service, 1731 Research Park Drive, Davis, California, 95618, United States of America, and 3JHB Consulting, 6552 Carnegie Street, Burnaby, British Columbia, V5B 1Y3, Canada *Corresponding author. Email: [email protected] (Received 24 June 2020; accepted 22 September 2020; first published online 13 November 2020) Abstract Although the use of nonhost plants intercropped among host crops has been a standard agricultural prac- tice for reducing insect herbivory for millennia, the use of nonhost signals to deter forest pests is much more recent, having been developed over the past several decades. Early exploratory studies with synthetic nonhost volatile semiochemicals led to targeted electrophysiological and trapping experiments on a variety of bark and ambrosia beetles (Coleoptera: Curculionidae: Scolytinae) across three continents. This work disclosed a suite of antennally and behaviourally active nonhost volatiles, which are detected in common across a range of coniferophagous bark beetles. It also established the fact that dispersing bark and ambro- sia beetles detect nonhost signals while in flight and avoid nonhost trees without necessarily landing on them. Later work showed that groups of synthetic nonhost volatiles, sometimes combined with insect- derived antiaggregants, are effective in protecting individual trees and forest stands. -
A Review of Chemical Defense in Poison Frogs (Dendrobatidae): Ecology, Pharmacokinetics, and Autoresistance
Chapter 21 A Review of Chemical Defense in Poison Frogs (Dendrobatidae): Ecology, Pharmacokinetics, and Autoresistance Juan C. Santos , Rebecca D. Tarvin , and Lauren A. O’Connell 21.1 Introduction Chemical defense has evolved multiple times in nearly every major group of life, from snakes and insects to bacteria and plants (Mebs 2002 ). However, among land vertebrates, chemical defenses are restricted to a few monophyletic groups (i.e., clades). Most of these are amphibians and snakes, but a few rare origins (e.g., Pitohui birds) have stimulated research on acquired chemical defenses (Dumbacher et al. 1992 ). Selective pressures that lead to defense are usually associated with an organ- ism’s limited ability to escape predation or conspicuous behaviors and phenotypes that increase detectability by predators (e.g., diurnality or mating calls) (Speed and Ruxton 2005 ). Defended organisms frequently evolve warning signals to advertise their defense, a phenomenon known as aposematism (Mappes et al. 2005 ). Warning signals such as conspicuous coloration unambiguously inform predators that there will be a substantial cost if they proceed with attack or consumption of the defended prey (Mappes et al. 2005 ). However, aposematism is likely more complex than the simple pairing of signal and defense, encompassing a series of traits (i.e., the apose- matic syndrome) that alter morphology, physiology, and behavior (Mappes and J. C. Santos (*) Department of Zoology, Biodiversity Research Centre , University of British Columbia , #4200-6270 University Blvd , Vancouver , BC , Canada , V6T 1Z4 e-mail: [email protected] R. D. Tarvin University of Texas at Austin , 2415 Speedway Stop C0990 , Austin , TX 78712 , USA e-mail: [email protected] L. -
"Curing" of Nicotiana Attenuata Leaves by Small Mammals Does Not Decrease Nicotine Contents
Western North American Naturalist Volume 63 Number 1 Article 15 1-31-2003 "Curing" of Nicotiana attenuata leaves by small mammals does not decrease nicotine contents Ian T. Baldwin Max-Planck Institute for Chemical Ecology, Jena, Germany Follow this and additional works at: https://scholarsarchive.byu.edu/wnan Recommended Citation Baldwin, Ian T. (2003) ""Curing" of Nicotiana attenuata leaves by small mammals does not decrease nicotine contents," Western North American Naturalist: Vol. 63 : No. 1 , Article 15. Available at: https://scholarsarchive.byu.edu/wnan/vol63/iss1/15 This Article is brought to you for free and open access by the Western North American Naturalist Publications at BYU ScholarsArchive. It has been accepted for inclusion in Western North American Naturalist by an authorized editor of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Western North American Naturalist 63(1), ©2003, pp. 114–117 “CURING” OF NICOTIANA ATTENUATA LEAVES BY SMALL MAMMALS DOES NOT DECREASE NICOTINE CONTENTS Ian T. Baldwin1 ABSTRACT.—Basal leaves of Nicotiana attenuata are frequently found neatly excised at the petiole and piled on rocks or soil in the sun until dry, after which they disappear, sometimes to be found again in the nests of Neotoma lepida. In response to herbivore attack, N. attenuata increases the concentration of nicotine in its leaves, where it functions as an induced defense. Since excision of leaves at the petiole allows for leaf removal without substantially activating this induced defense, and air-drying at high temperatures can volatilize nicotine, we examined the hypothesis that the observed leaf “curing” behavior decreased nicotine contents. -
Chemical Ecology Example 1. Pyrrolizidine Alkaloids (Pas)
Alkaloids Part 2 Chemical Ecology p. 1 Alkaloids Part 2: Chemical Ecology Example 1. Pyrrolizidine Alkaloids (PAs) - Senecionine-N-oxides Background - basic structural type, but many variations - occurrence in plants in Compositae, Boragincaceae, Orchidaceae - extremely toxic to both mammals and insects but complex interactions - documented co-evolution with specialist insects, and sophisticated use of plant defenses by insects Biosynthesis Senecionine-N-oxide synthesized from two separate pathways/moieties - necine moiety, from arginine via putrescine (decarboxylate, condense, cyclize) - dicarboxylic acid moiety, from isoleucine => both form the macrocyclic diester = senecionine - key enzyme: homospermine synthase. Evolved independently at least four time - different plant families - from deoxyhypusine synthase, and enzyme of primary metabolism (activates eukaryotic translation initiation factor eIF5A) - five distinct structural types, that vary in macrocyclic diester bridge component Pyrrolizidine alkaloid localization and transport - root synthesis of senecionine, then transported to shoot - final accumulation of alkaloids is in flowers and shoot apex - further biochemical elaboration and structural diversification (decoration of macrocycle) occurs in shoot - population differentiation (diverse mixtures of pyrrolizidine alkaloids in different plant populations) - > variable target for pests. Pyrrolizidine Alkaloid Toxicity and its Avoidance - PA-containing plants are generally avoided by herbivores ( bitter taste, toxicity) - N-oxide -
Appendix A: Monarch Biology and Ecology
Appendix A: Monarch Biology and Ecology Materials for this appendix were adapted from MonarchNet.org, MonarchJointVenture.org, MonarchLab.org, and MonarchParasites.org. Monarch Life Cycle Biology: Overview: All insects change in form as they grow; this process is called metamorphosis. Butterflies and moths undergo complete metamorphosis, in which there are four distinct stages: egg, larva (caterpillar) pupae (chrysalis) and adult. It takes monarchs about a month to go through the stages from egg to adult, and it is hormones circulating within the body that trigger the changes that occur during metamorphosis. Once adults, monarchs will live another 3-6 weeks in the summer. Monarchs that migrate live all winter, or about 6-9 months. Monarch larvae are specialist herbivores, consuming only host plants in the milkweed family (Asclepiadacea). They utilize most of the over 100 North American species (Woodson 1954) in this family, breeding over a broad geographical and temporal range that covers much of the United States and southern Canada. Adults feed on nectar from blooming plants. Monarchs have specific habitat needs: Milkweed provides monarchs with an effective chemical defense against many predators. Monarchs sequester cardenolides (also called cardiac glycosides) present in milkweed (Brower and Moffit 1974), rendering them poisonous to most vertebrates. However, many invertebrate predators, as well as some bacteria and viruses, may be unharmed by the toxins or able to overcome them. The extent to which milkweed protects monarchs from non-vertebrate predators is not completely understood, but a recent finding that wasps are less likely to prey on monarchs consuming milkweed with high levels of cardenolides suggests that this defense is at least somewhat effective against invertebrate predators (Rayor 2004). -
Sequestered Alkaloid Defenses in the Dendrobatid Poison Frog Oophaga Pumilio Provide Variable Protection from Microbial Pathogens
John Carroll University Carroll Collected Masters Theses Theses, Essays, and Senior Honors Projects Summer 2016 SEQUESTERED ALKALOID DEFENSES IN THE DENDROBATID POISON FROG OOPHAGA PUMILIO PROVIDE VARIABLE PROTECTION FROM MICROBIAL PATHOGENS Kyle Hovey John Carroll University, [email protected] Follow this and additional works at: http://collected.jcu.edu/masterstheses Part of the Biology Commons Recommended Citation Hovey, Kyle, "SEQUESTERED ALKALOID DEFENSES IN THE DENDROBATID POISON FROG OOPHAGA PUMILIO PROVIDE VARIABLE PROTECTION FROM MICROBIAL PATHOGENS" (2016). Masters Theses. 19. http://collected.jcu.edu/masterstheses/19 This Thesis is brought to you for free and open access by the Theses, Essays, and Senior Honors Projects at Carroll Collected. It has been accepted for inclusion in Masters Theses by an authorized administrator of Carroll Collected. For more information, please contact [email protected]. SEQUESTERED ALKALOID DEFENSES IN THE DENDROBATID POISON FROG OOPHAGA PUMILIO PROVIDE VARIABLE PROTECTION FROM MICROBIAL PATHOGENS A Thesis Submitted to the Office of Graduate Studies College of Arts & Sciences of John Carroll University in Partial Fulfillment of the Requirements for the Degree of Master of Science By Kyle J. Hovey 2016 Table of Contents Abstract ................................................................................................................................1 Introduction ..........................................................................................................................3 Methods