134 results on '"herbivorous insects"'
Search Results
2. SOIL-INSECT toolbox: A new chamber for analysing the behaviour of herbivorous insects and tri-trophic interactions in soil
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Furmanczyk, Ewa M., Tartanus, Malgorzata, Jóźwiak, Zbigniew B., and Malusà, Eligio
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tri-trophic interactions ,melolontha spp ,Herbivore ,Larva ,biology ,herbivory ,media_common.quotation_subject ,fungi ,Melolontha ,carbon dioxide ,subterranean insects ,Insect ,biology.organism_classification ,biotest arena ,complex mixtures ,behaviour ,QL1-991 ,Insect Science ,Environmental chemistry ,Soil water ,Herbivorous insects ,volatile compounds ,Zoology ,Trophic level ,media_common - Abstract
A chamber, named SOIL-INSECT toolbox, was developed to analyse the effect of various factors on the behaviour of soil-dwelling insects. It is equipped with sensors that continuously monitor the concentration of CO2 in the different compartments of the chamber without disturbing the air balance in the soil. The chamber can be adapted to study different stimuli, including volatile compounds, both in the presence and absence of plants. The chamber was tested using the larvae of Melolontha spp., which confi rmed its suitability for carrying out complex studies on insect-insect and insect-plant-microbiome interactions in a complex environment such as soil. The results of behavioural experiments using L3 larvae of Melolontha spp. in sterilized and natural soils revealed that the soil condition affected the behaviour of the larvae, likely due to its effect on the soil microbiome and physicochemical characteristics.
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- 2021
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3. Nonadaptive host‐use specificity in tropical armored scale insects
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Daniel A. Peterson, Jiufeng Wei, Geoffrey E. Morse, Takao Itioka, Nate B. Hardy, and Benjamin B. Normark
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0106 biological sciences ,host range ,Diaspididae ,Generalist and specialist species ,010603 evolutionary biology ,01 natural sciences ,03 medical and health sciences ,niche breadth ,Specialization (functional) ,polyphagy ,Ecology, Evolution, Behavior and Systematics ,Original Research ,030304 developmental biology ,Nature and Landscape Conservation ,0303 health sciences ,Herbivore ,Ecology ,biology ,herbivory ,Host (biology) ,biology.organism_classification ,ecological specialization ,Spite ,Herbivorous insects ,Armored scale insects - Abstract
Most herbivorous insects are diet specialists in spite of the apparent advantages of being a generalist. This conundrum might be explained by fitness trade‐offs on alternative host plants, yet the evidence of such trade‐offs has been elusive. Another hypothesis is that specialization is nonadaptive, evolving through neutral population‐genetic processes and within the bounds of historical constraints. Here, we report on a striking lack of evidence for the adaptiveness of specificity in tropical canopy communities of armored scale insects. We find evidence of pervasive diet specialization, and find that host use is phylogenetically conservative, but also find that more‐specialized species occur on fewer of their potential hosts than do less‐specialized species, and are no more abundant where they do occur. Of course local communities might not reflect regional diversity patterns. But based on our samples, comprising hundreds of species of hosts and armored scale insects at two widely separated sites, more‐specialized species do not appear to outperform more generalist species., In tropical canopies, we find evidence that diet specialization in armored scale insects might be nonadaptive. Diet generalists occur on more of their potential host plants and are no less abundant than diet specialists.
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- 2020
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4. Bidirectional plant‐mediated interactions between rhizobacteria and shoot‐feeding herbivorous insects: a community ecology perspective
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Marcel Dicke, Joop J. A. van Loon, Ana Pineda, Julia Friman, and Terrestrial Ecology (TE)
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0106 biological sciences ,plant growth promoting rhizobacteria ,media_common.quotation_subject ,Insect ,Biology ,Rhizobacteria ,010603 evolutionary biology ,01 natural sciences ,Laboratory of Entomology ,insect-plant interactions ,Plan_S-Compliant_TA ,Belowground-aboveground interactions ,media_common ,Trophic level ,inducible defence ,Rhizosphere ,Herbivore ,Ecology ,Community ,fungi ,national ,food and beverages ,Laboratorium voor Entomologie ,010602 entomology ,Insect Science ,Shoot ,Herbivorous insects ,EPS ,community ecology - Abstract
1. Plants interact with various organisms, aboveground as well as belowground. Such interactions result in changes in plant traits with consequences for members of the plant-associated community at different trophic levels. Research thus far focussed on interactions of plants with individual species. However, studying such interactions in a community context is needed to gain a better understanding. 2. Members of the aboveground insect community induce defences that systemically influence plant interactions with herbivorous as well as carnivorous insects. Plant roots are associated with a community of plant-growth promoting rhizobacteria (PGPR). This PGPR community modulates insect-induced defences of plants. Thus, PGPR and insects interact indirectly via plant-mediated interactions. 3. Such plant-mediated interactions between belowground PGPR and aboveground insects have usually been addressed unidirectionally from belowground to aboveground. Here, we take a bidirectional approach to these cross-compartment plant-mediated interactions. 4. Recent studies show that upon aboveground attack by insect herbivores, plants may recruit rhizobacteria that enhance plant defence against the attackers. This rearranging of the PGPR community in the rhizosphere has consequences for members of the aboveground insect community. This review focusses on the bidirectional nature of plant-mediated interactions between the PGPR and insect communities associated with plants, including (a) effects of beneficial rhizobacteria via modification of plant defence traits on insects and (b) effects of plant defence against insects on the PGPR community in the rhizosphere. We discuss how such knowledge can be used in the development of sustainable crop-protection strategies.
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- 2020
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5. Herbivore‐induced <scp>DMNT</scp> catalyzed by <scp>CYP82D47</scp> plays an important role in the induction of <scp>JA</scp> ‐dependent herbivore resistance of neighboring tea plants
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Mingyue Zhao, Jieyang Jin, Tingting Jing, Na Zhang, Yi Wu, Wenkai Du, Chuankui Song, Jingming Wang, Ting Gao, Wilfried Schwab, and Xiaochun Wan
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0106 biological sciences ,0301 basic medicine ,Physiology ,Cyclopentanes ,Plant Science ,Alkenes ,Moths ,Biology ,Real-Time Polymerase Chain Reaction ,01 natural sciences ,Camellia sinensis ,03 medical and health sciences ,chemistry.chemical_compound ,Cytochrome P-450 Enzyme System ,Plant Growth Regulators ,Gene Expression Regulation, Plant ,Botany ,Animals ,Oxylipins ,Cloning, Molecular ,Plant Proteins ,Volatile Organic Compounds ,Herbivore ,Resistance (ecology) ,Communication ,Jasmonic acid ,fungi ,food and beverages ,Sequence Analysis, DNA ,030104 developmental biology ,chemistry ,Ectropis obliqua ,Larva ,Plant Defense Against Herbivory ,Herbivorous insects ,010606 plant biology & botany - Abstract
Herbivore-induced plant volatiles play important ecological roles in defense against stresses. However, if and which volatile(s) are involved in the plant-plant communication in response to herbivorous insects in tea plants remains unknown. Here, plant-plant communication experiments confirm that volatiles emitted from insects-attacked tea plants can trigger plant resistance and reduce the risk of herbivore damage by inducing jasmonic acid (JA) accumulation in neighboring plants. The emission of six compounds was significantly induced by geometrid Ectropis obliqua, one of the most common pests of the tea plant in China. Among them, (E)-4,8-dimethyl-1,3,7-nonatriene (DMNT) could induce the accumulation of JA and thus promotes the resistance of neighboring intact plants to herbivorous insects. CsCYP82D47 was identified for the first time as a P450 enzyme, which catalyzes the final step in the biosynthesis of DMNT from (E)-nerolidol. Down-regulation of CsCYP82D47 in tea plants resulted in a reduced accumulation of DMNT and significantly reduced the release of DMNT in response to the feeding of herbivorous insects. The first evidence for plant-plant communication in response to herbivores in tea plants will help to understand how plants respond to volatile cues in response to herbivores and provide new insight into the role(s) of DMNT in tea plants.
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- 2020
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6. Caterpillars’ natural enemies and attack probability in an urbanization intensity gradient across a Neotropical streetscape
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Ian MacGregor-Fors, João Carlos Pena, Felipe Aoki-Gonçalves, Milton Cezar Ribeiro, Wesley Dáttilo, Universidade Estadual Paulista (UNESP), A.C., and Instituto de Ecología A.C.
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0106 biological sciences ,General Decision Sciences ,Context (language use) ,010501 environmental sciences ,010603 evolutionary biology ,01 natural sciences ,Predation ,Pest control ,Urbanization ,Caterpillar ,Ecology, Evolution, Behavior and Systematics ,QH540-549.5 ,0105 earth and related environmental sciences ,Trophic level ,Neotropical city ,Cloud forest ,Herbivore ,biology ,Ecology ,Urban landscapes ,biology.organism_classification ,Herbivorous insects ,Geography ,Habitat ,Predator–prey interactions - Abstract
Made available in DSpace on 2022-05-01T05:29:25Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-09-01 Intensification of urbanization has been shown to be associated with taxonomic and functional modifications of biological communities, leading to changes in trophic interactions. These changes may reduce the delivery of ecosystem services provided by urban ecosystems. For instance, predation on herbivorous insects is an important ecological process operating in urban biological communities. Specifically, on one hand, herbivorous insects serve as food resources for many organisms, and on the other hand predation on herbivorous insects may reduce pest populations on urban vegetation. In this study, we assessed the relationship between urbanization intensity and bird and arthropod predation pressure on herbivorous insects across the streetscape of Xalapa (Mexico), a Neotropical city with half a million people immersed in a cloud forest context. We exposed dummy caterpillar models at 16 sites across the streetscape and two sites in a peri-urban cloud forest patch, comprising a wide range of urbanization intensities. We observed that in streets where the proportion of built cover was higher, dummy caterpillars’ attack probability was substantially lower. Moreover, we observed that caterpillars were most often attacked by arthropods (62.41%), followed by birds (21.53%), independent of built cover. Our study provides evidence that built cover surrounding streets may negatively influence the interactions between herbivorous insects and their natural enemies. Spatial Ecology and Conservation Lab (LEEC) Department of Biodiversity Institute of Biosciences Sao Paulo State University - UNESP Red de Ambiente y Sustentabilidad Instituto de Ecología A.C. Red de Biología Evolutiva Instituto de Ecología A.C. Red de Ecoetología Instituto de Ecología A.C. Spatial Ecology and Conservation Lab (LEEC) Department of Biodiversity Institute of Biosciences Sao Paulo State University - UNESP
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- 2021
7. Jasmonate action in plant defense against insects
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Daoxin Xie, Jiaojiao Wang, Youping Wang, and Dewei Wu
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0106 biological sciences ,0301 basic medicine ,Insecta ,Physiology ,media_common.quotation_subject ,Arabidopsis ,Cyclopentanes ,Plant Science ,Insect ,Biology ,01 natural sciences ,03 medical and health sciences ,Plant Growth Regulators ,Gene Expression Regulation, Plant ,Plant defense against herbivory ,Animals ,Plant Immunity ,Calcium Signaling ,Herbivory ,Oxylipins ,Jasmonate ,Transcription factor ,Plant Diseases ,Plant Proteins ,media_common ,Wound Healing ,Herbivore ,Arabidopsis Proteins ,F-Box Proteins ,fungi ,Ubiquitination ,Cell biology ,030104 developmental biology ,Calcium ,Herbivorous insects ,Signal Transduction ,Transcription Factors ,010606 plant biology & botany ,Cytosolic calcium - Abstract
Herbivorous insects represent one of the major threats to sessile plants. To cope with herbivore challenges, plants have evolved sophisticated defense systems, in which the lipid-derived phytohormone jasmonate plays a crucial role. Perception of insect attack locally and systemically elicits rapid synthesis of jasmonate, which is perceived by the F-box protein COI1 to further recruit JAZ repressors for ubiquitination and degradation, thereby releasing transcription factors that subsequently activate plant defense against insect attack. Here, we review recent progress in understanding the molecular basis of jasmonate action in plant defense against insects.
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- 2019
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8. Friend or foe? The role of leaf-inhabiting fungal pathogens and endophytes in tree-insect interactions
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Christin Uhe, Sybille B. Unsicker, and Franziska Eberl
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0106 biological sciences ,Herbivore ,Ecology ,Ecological Modeling ,media_common.quotation_subject ,fungi ,food and beverages ,Plant Science ,Insect ,Biology ,Herbaceous plant ,010603 evolutionary biology ,01 natural sciences ,Plant use of endophytic fungi in defense ,Forest ecology ,Fungal colonization ,Ecosystem ,Herbivorous insects ,Ecology, Evolution, Behavior and Systematics ,010606 plant biology & botany ,media_common - Abstract
Trees are large organisms that structure forest ecosystems by providing an environment for an enormous diversity of animal, microbial and plant species. As these species use trees as their common hosts, many are likely to interact with each other directly or indirectly. From studies on herbaceous plant species we know that microbes can affect the interaction of plants with herbivorous insects, for example via changes in plant metabolite profiles. The consequences of fungal colonization for tree-insect interactions are, however, barely known, despite the importance of these ecological communities. In this review we explore the interaction of leaf-inhabiting pathogenic and endophytic fungi with trees and the consequences for tree-living insect herbivores. We discuss molecular, physiological, chemical, biochemical and ecological aspects of tree-fungus interactions and summarize the current knowledge on the direct and indirect effects of tree-inhabiting fungi on insect herbivores. Our mechanistic understanding of the tripartite interaction of trees with leaf-inhabiting fungi and insect herbivores is still in its infancy. We are currently facing substantial drawbacks in experimental methodology that prevent us from revealing the effect of one single fungal species on a particular insect herbivore species and vice versa. Future studies applying a versatile toolbox of modern molecular, chemical analytical and ecological techniques in combined laboratory and field experiments will unequivocally lead to a better understanding of fungus-tree-insect interactions.
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- 2019
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9. Search for top‐down and bottom‐up drivers of latitudinal trends in insect herbivory in oak trees in Europe
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Ágnes Fürjes-Mikó, Yasmine Kadiri, Thomas Damestoy, Marco Ferrante, Andreas Schuldt, Csaba Béla Eötvös, Arndt Hampe, Marketa Tahadlova, Mihai-Leonard Duduman, Luc Barbaro, Anna Mrazova, Ayco J. M. Tack, Tomas Roslin, Slobodan Milanović, Maria Faticov, Michèle Kaennel-Dobbertin, Andreas Prinzing, György Csóka, Aurélien Sallé, Deborah J. Harvey, Gábor L. Lövei, Katerina Sam, Olivier Bouriaud, Xoaquín Moreira, Michael Scherer-Lorenzen, Lars Opgennoorth, Martin M. Gossner, Juha-Matti Pitkänen, Andrea Galmán, Laurent Augusto, Giada Centenaro, Julia Koricheva, Anne-Maïmiti Dulaurent, Jovan Dobrosavljević, Andrey V. Selikhovkin, Marija Popović, Elena Valdés-Correcher, Manuela Branco, D. Lupaştean, Valentin Queloz, Lassi Suominen, Christophe Bouget, Mikhail V. Kozlov, Rebecca L. Thomas, Anna Yu. Popova, Bastien Castagneyrol, Andy G. Howe, Alexander Kozel, Biodiversité, Gènes & Communautés (BioGeCo), Université de Bordeaux (UB)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Misión Biológica de Galicia, Spanish National Research Council (CSIC), Interactions Sol Plante Atmosphère (UMR ISPA), Ecole Nationale Supérieure des Sciences Agronomiques de Bordeaux-Aquitaine (Bordeaux Sciences Agro)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Dynamiques et écologie des paysages agriforestiers (DYNAFOR), École nationale supérieure agronomique de Toulouse [ENSAT]-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Ecosystèmes forestiers (UR EFNO), Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), University Stefan cel Mare of Suceava (USU), Universidade de Lisboa (ULISBOA), Universita degli Studi di Padova, National Agricultural Research and Innovation Center (NARIC), Agro-écologie, Hydrogéochimie, Milieux et Ressources (AGHYLE), UniLaSalle, Ecosystèmes, biodiversité, évolution [Rennes] (ECOBIO), Centre National de la Recherche Scientifique (CNRS)-Observatoire des Sciences de l'Univers de Rennes (OSUR)-Institut Ecologie et Environnement (INEE), Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES), ANR-10-LABX-0045,COTE,COntinental To coastal Ecosystems: evolution, adaptability and governance(2010), Mision Biologica de Galicia (MBG), Consejo Superior de Investigaciones Científicas [Madrid] (CSIC), École nationale supérieure agronomique de Toulouse (ENSAT), Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Centre d'Ecologie et des Sciences de la COnservation (CESCO), Muséum national d'Histoire naturelle (MNHN)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Universidade de Lisboa = University of Lisbon (ULISBOA), Università degli Studi di Padova = University of Padua (Unipd), University of Belgrade [Belgrade], Universitatea Stefan cel Mare Suceava (USU), Stockholm University, Aarhus University [Aarhus], University of the Azores, Swiss Federal Research Institute, Royal Holloway [University of London] (RHUL), University of Copenhagen = Københavns Universitet (UCPH), Université de Rennes (UR)-Institut Ecologie et Environnement (INEE), Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)-Observatoire des Sciences de l'Univers de Rennes (OSUR), Université de Rennes (UR)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Rennes 2 (UR2)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Centre National de la Recherche Scientifique (CNRS), Georg-August-University = Georg-August-Universität Göttingen, Saint Petersburg State University (SPBU), Biology Centre of the Czech Academy of Sciences (BIOLOGY CENTRE CAS), Czech Academy of Sciences [Prague] (CAS), University of South Bohemia, and This study was carried out with financial support from the French National Research Agency (ANR) in the frame of the Investments for the Future Programme, within the Cluster of Excellence COTE (Continental To coastal Ecosystems: evolution, adaptability and governance) (ANR-10-LABX-45). E.V.C. was funded by the BiodivERsA (BiodivERsA is a network of national and regional funding organisations promoting pan-European research on biodiversity and ecosystem services, and offering innovative opportunities for the conservation and sustainable management of biodiversity) project SPONFOREST (Unraveling the potential of spontaneous forest establishment for improving ecosystem functions and services in dynamic landscapes) (BiodivERsA3-2015-58). The authors warmly thank all the young European citizens and their teachers who made this study possible. They also thank the professional scientists who kindly agreed to participate in this study: Stefan K. Müller (Freie evangelische Schule Lörrach), Olga Mijón Pedreira (teacher IES Rosais 2, Vigo-Spain) and Mickael Pihain (Research Unit 'Ecosystèmes, Biodiversité, Evolution', University of Rennes 1/CNRS, 35042 Rennes, France), and Chloe Mendiondo and Claire Colliaux (Department of Agroecology, Aarhus University, Flakkebjerg Research Centre, DK-4200 Slagelse, Denmark).
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0106 biological sciences ,защита растений ,Range (biology) ,Leaf Chemistry ,media_common.quotation_subject ,Climate ,Plant Defences ,Nutritional quality ,Insect ,Plant defences ,010603 evolutionary biology ,01 natural sciences ,Latitude ,Quercus robur ,biotic interactions ,биотические факторы ,Avian Insectivory ,Artificial Prey ,Avian insectivory ,Natural enemies ,climatic gradients ,pedunculate oak ,Ecology, Evolution, Behavior and Systematics ,media_common ,2. Zero hunger ,[SDV.EE]Life Sciences [q-bio]/Ecology, environment ,Global and Planetary Change ,Herbivore ,насекомые-вредители ,Ecology ,biology ,010604 marine biology & hydrobiology ,Artificial prey ,климатические градиенты ,15. Life on land ,Latitudinal gradients ,biology.organism_classification ,климатические факторы ,climatic factors ,Taxon ,13. Climate action ,широтные градиенты ,Leaf chemistry ,herbivorous insects ,травоядные насекомые ,дуб черешчатый ,010606 plant biology & botany - Abstract
AIM: The strength of species interactions is traditionally expected to increase toward the Equator. However, recent studies have reported opposite or inconsistent latitudinal trends in the bottom-up (plant quality) and top-down (natural enemies) forces driving herbivory. In addition, these forces have rarely been studied together thus limiting previous attempts to understand the effect of large-scale climatic gradients on herbivory. LOCATION: Europe. TIME PERIOD: 2018–2019. MAJOR TAXA STUDIED: Quercus robur. METHODS: We simultaneously tested for latitudinal variation in plant–herbivore–natural enemy interactions. We further investigated the underlying climatic factors associated with variation in herbivory, leaf chemistry and attack rates in Quercus robur across its complete latitudinal range in Europe. We quantified insect leaf damage and the incidence of specialist herbivores as well as leaf chemistry and bird attack rates on dummy caterpillars on 261 oak trees. RESULTS: Climatic factors rather than latitude per se were the best predictors of the large-scale (geographical) variation in the incidence of gall-inducers and leaf-miners as well as in leaf nutritional content. However, leaf damage, plant chemical defences (leaf phenolics) and bird attack rates were not influenced by climatic factors or latitude. The incidence of leaf-miners increased with increasing concentrations of hydrolysable tannins, whereas the incidence of gall-inducers increased with increasing leaf soluble sugar concentration and decreased with increasing leaf C : N ratios and lignins. However, leaf traits and bird attack rates did not vary with leaf damage. MAIN CONCLUSIONS: These findings help to refine our understanding of the bottom-up and top-down mechanisms driving geographical variation in plant–herbivore interactions, and indicate the need for further examination of the drivers of herbivory on trees. This study was carried out with financial support from the French National Research Agency (ANR) in the frame of the Investments for the Future Programme, within the Cluster of Excellence COTE (Continental To coastal Ecosystems: evolution, adaptability and governance) (ANR-10-LABX-45). E.V.C. was funded by the BiodivERsA (BiodivERsA is a network of national and regional funding organisations promoting pan-European research on biodiversity and ecosystem services, and offering innovative opportunities for the conservation and sustainable management of biodiversity) project SPONFOREST (Unraveling the potential of spontaneous forest establishment for improving ecosystem functions and services in dynamic landscapes) (BiodivERsA3-2015-58). info:eu-repo/semantics/publishedVersion
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- 2021
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10. Alternative developmental and transcriptomic responses to host plant water limitation in a butterfly metapopulation
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Guillaume Minard, Vicencio Oostra, Panu Somervuo, Marjo Saastamoinen, Aapo Kahilainen, Organismal and Evolutionary Biology Research Programme, Life-history Evolution Research Group, Helsinki Institute of Life Science HiLIFE, Organismal and Evolutionary Biological Research Programme (OEB), Faculty of Biological and Environmental Sciences [Helsinki], University of Helsinki-University of Helsinki, University of Liverpool, Laboratoire d'Ecologie Microbienne - UMR 5557 (LEM), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Ecole Nationale Vétérinaire de Lyon (ENVL)-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Helsinki Institute of Life Science (HiLIFE), and University of Helsinki
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0106 biological sciences ,LIFE-HISTORY ,RNA-Seq ,phenotypic plasticity ,01 natural sciences ,IRIDOID GLYCOSIDE CONTENT ,Transcriptome ,transcriptomics ,insects ,METABOLOMIC ANALYSIS ,GENE-EXPRESSION ,2. Zero hunger ,species interactions ,0303 health sciences ,education.field_of_study ,CLIMATE-CHANGE ,biology ,RICE STEM BORER ,Plants ,ECOLOGICAL CONSEQUENCES ,Larva ,[SDE]Environmental Sciences ,1181 Ecology, evolutionary biology ,Butterflies ,Population ,Glanville fritillary ,Climate change ,Metapopulation ,010603 evolutionary biology ,03 medical and health sciences ,Genetic variation ,Genetics ,Metabolome ,Humans ,Animals ,[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology ,life-history evolution ,Herbivory ,education ,Ecology, Evolution, Behavior and Systematics ,030304 developmental biology ,Phenotypic plasticity ,Herbivore ,fungi ,Water ,15. Life on land ,biology.organism_classification ,13. Climate action ,Evolutionary biology ,DIFFERENTIAL EXPRESSION ANALYSIS ,1182 Biochemistry, cell and molecular biology ,sense organs ,lepidoptera ,HERBIVOROUS INSECTS - Abstract
Predicting how climate change affects biotic interactions and their evolution poses a challenge. Plant-insect herbivore interactions are particularly sensitive to climate change, as climate-induced changes in plant quality cascade into the performance of insect herbivores. Whereas the immediate survival of herbivore individuals depends on plastic responses to climate change induced nutritional stress, long-term population persistence via evolutionary adaptation requires genetic variation for these responses. In order to assess the prospects for population persistence under climate change, it is therefore crucial to characterise response mechanisms to climate change induced stressors, and quantify their variability in natural populations. Here, we test developmental and transcriptomic responses to water limitation induced host plant quality change in a Glanville fritillary butterfly (Melitaea cinxia) metapopulation. We combine nuclear magnetic resonance spectroscopy on the plant metabolome, larval developmental assays and an RNA seq analysis of the larval transcriptome. We observed that responses to feeding on water limited plants, in which amino acids and aromatic compounds are enriched, showed marked intrapopulation variation, with individuals of some families performing better on control and others on water limited plants. The transcriptomic responses were concordant with the developmental responses: Families exhibiting opposite developmental responses also produced opposite transcriptomic responses, e.g. in growth associated intracellular signalling. The opposite developmental and transcriptomic responses are associated with between families differences in organic compound catabolism and storage protein production. The results reveal heritable intrapopulation variability in plasticity, suggesting potential for evolutionary responses to drought-induced changes in host plant quality in the Finnish M. cinxia metapopulation.
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- 2021
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11. Genetic and Ecological Basis of Resistance to Herbivorous Insects in Mediterranean Pines
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Carla Vázquez-González, Luis Sampedro, Xosé López-Goldar, and Rafael Zas
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Abiotic component ,Mediterranean climate ,Herbivore ,Resistance (ecology) ,Range (biology) ,Ecology ,media_common.quotation_subject ,fungi ,food and beverages ,Insect ,Biology ,Genetic variation ,Herbivorous insects ,media_common - Abstract
As massive, sessile and long-lived organisms, Mediterranean pines are exposed to a wide array of insect herbivores that feed on their tissues causing damage and ultimately, tree death. To protect themselves against biotic risks, pines have a complex battery of chemical and physical defenses, that act directly to kill or repel the antagonist organisms. Defense production, however, is not constant throughout time, but can be fine-tuned to the particular biotic risk to which the individuals and populations are exposed, producing the so called induced defenses. Moreover, the defensive state of a tree might also be determined by mutualistic interactions between the tree and other organisms that act as indirect defenses by means of top-down effects on the herbivore populations. Knowledge about these intriguing interactions in Mediterranean pines is still very limited but most of the theoretical progress made in model plant species could be hopefully translated to these long-lived plants. The defensive arsenal that a tree produces requires large amounts of resources that are no longer available for other life functions (i.e. growth, reproduction). Pine resistance to biotic threats must thus be understood as a general function integrated with other life-history traits, where defensive allocation, ultimately leading to biotic resistance, is shaped by the optimal resource allocation across life functions according to the particular biotic and abiotic environment. Thus, environmental variation across the distribution range of Mediterranean pines generates patterns of phenotypic diversity in defensive investment, by means of both adaptive (genetic) and plastic responses. Genetic variation and plasticity in the expression of defenses in Meditteranean pines have inmidiate implications in the resistance capacity of these long-lived species. Understanding the sources of phenotypic variation driving allocation to defenses in Mediterranean pines is therefore specially relevant to forecast species responses to ongoing environmental changes, particularly those casued by increased biotic stresses associated with global change.
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- 2021
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12. Role of Phytohormones in Plant Defence Against Insects: Signalling and Crosstalk
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C. Selvi, R. Poorniammal, and A. R. Sakthi
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Herbivore ,Mechanism (biology) ,media_common.quotation_subject ,fungi ,Defence mechanisms ,food and beverages ,Insect ,Biology ,Cell biology ,Crosstalk (biology) ,Signalling ,Herbivorous insects ,Function (biology) ,media_common - Abstract
Plants possess their own defence mechanisms to combat infestations of herbivorous insects and pathogens. It has few preexisting defence mechanisms, whereas most of the defence response is activated only after insect or pathogen invasion. Crosstalk between defence signalling pathways induced in response to herbivore/pathogen attack offer plants to regulate defence mechanism in an effective manner. Crosstalk and interaction of signalling pathways can function synergistically, or either one is suppressed under stress condition. Crosstalk enables the plant to utilize less energy for defence response and allocate energy for its growth and development. Host plant resistance against herbivores can be manipulated using chemical elicitors, which induces defence signalling mechanism in plants. Unravelling of defence mechanisms and phytohormonal signalling pathway under stress condition, the induced responses of the herbivores can be predicted, that can be further utilized for pest management and reduction in crop losses.
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- 2021
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13. Microbiota, pathogens, and parasites as mediators of tritrophic interactions between insect herbivores, plants, and pollinators
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Ikkei Shikano and Christina L. Mogren
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0106 biological sciences ,0301 basic medicine ,Insecta ,media_common.quotation_subject ,Foraging ,Insect ,Biology ,01 natural sciences ,Host-Parasite Interactions ,03 medical and health sciences ,Pollinator ,medicine ,Host plants ,Animals ,Microbiome ,Herbivory ,Pollination ,Ecology, Evolution, Behavior and Systematics ,Epizootic ,Plant Physiological Phenomena ,media_common ,Herbivore ,Ecology ,Microbiota ,fungi ,food and beverages ,medicine.disease ,010602 entomology ,030104 developmental biology ,Host-Pathogen Interactions ,Herbivorous insects - Abstract
Insect-associated microbes, including pathogens, parasites, and symbionts, influence the interactions of herbivorous insects and pollinators with their host plants. Moreover, herbivory-induced changes in plant resource allocation and defensive chemistry can influence pollinator behavior. This suggests that the outcomes of interactions between herbivores, their microbes and host plants could have implications for pollinators. As epizootic diseases occur at high population densities, pathogen and parasite-mediated effects on plants could have landscape-level impacts on foraging pollinators. The goal of this minireview is to highlight the potential for an herbivore's multitrophic interactions to trigger plant-mediated effects on the immunity and health of pollinators. We highlight the importance of plant quality and gut microbiomes in bee health, and how caterpillars as model herbivores interact with pathogens, parasites, and symbionts to affect plant quality, which forms the centerpiece of multitrophic interactions between herbivores and pollinators. We also discuss the impacts of other herbivore-associated factors, such as agricultural inputs aimed at decreasing herbivorous pests, on pollinator microbiomes.
- Published
- 2020
14. Predation and parasitism on herbivorous insects change in opposite directions in a latitudinal gradient crossing a boreal forest zone
- Author
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Vitali Zverev, Mikhail V. Kozlov, and Elena L. Zvereva
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0106 biological sciences ,Insecta ,media_common.quotation_subject ,Parasitism ,Insect ,Biology ,010603 evolutionary biology ,01 natural sciences ,Predation ,Latitude ,law.invention ,law ,Taiga ,Animals ,Herbivory ,Ecology, Evolution, Behavior and Systematics ,media_common ,Herbivore ,Ecology ,010604 marine biology & hydrobiology ,15. Life on land ,Europe ,Predatory Behavior ,Animal Science and Zoology ,Plasticine ,Herbivorous insects - Abstract
The latitudinal biotic interaction hypothesis (LBIH) predicts that the strength of various biotic interactions decreases from low to high latitudes. Inconsistency between studies testing this hypothesis may result from variations among different types of interactions and among study systems. Therefore, exploration of multiple interactions within one system would help to disentangle latitudinal patterns across individual interactions and to evaluate latitudinal changes in the overall impact of enemies on prey. We tested the prediction based on the LBIH that the pressure of natural enemies on herbivorous insects decreases with increase in latitude across the boreal forest zone. We also asked whether the impacts of major groups of these enemies exhibit similar latitudinal patterns and whether these patterns are consistent across study years. In 10 forest sites located from 60°N to 69°N in Northern Europe, each summer, from 2016 to 2019, we measured (a) mortality of three groups of leafmining insects caused by birds, ants, parasitoids and unknown factors, (b) bird attacks on caterpillar-shaped plasticine models and (c) birch foliar damage caused by defoliators and leafminers. Latitudinal patterns in both insect herbivory on birch and top-down pressure on herbivorous insects varied considerably and inconsistently among the four study years, so that only some of the year-specific correlations with latitude were statistically significant. Nevertheless, meta-analysis combining correlations across years, preys and enemies revealed general decreases in predation by birds (on both natural and model prey) and ants, but an increase in parasitism rates, from low to high latitudes. We found that the direction of latitudinal changes in the strength of biotic interactions was interaction-specific: predation and herbivory supported LBIH, whereas parasitism exhibited an opposite trend. Consequently, the overall impact of natural enemies on herbivorous insects did not change with latitude and was therefore an unlikely reason for the poleward decrease in herbivory observed in our gradient. Considerable among-year variation in the strength of the latitudinal patterns in all the studied interactions suggests that this variation is a widespread phenomenon.
- Published
- 2020
15. Contradictory effects of leaf rolls in a leaf-mining weevil
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Chisato Kobayashi, Kazunori Matsuo, and Masakado Kawata
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0106 biological sciences ,Evolution ,Oviposition ,Wasps ,Zoology ,Parasitism ,lcsh:Medicine ,010603 evolutionary biology ,01 natural sciences ,Environmental stress ,Article ,Predation ,Betulaceae ,Animals ,Natural enemies ,Herbivory ,lcsh:Science ,Ovum ,Herbivore ,Multidisciplinary ,biology ,Behavior, Animal ,Ecology ,Weevil ,lcsh:R ,fungi ,food and beverages ,biology.organism_classification ,010601 ecology ,Plant Leaves ,Larva ,Predatory Behavior ,Weevils ,Herbivorous insects ,lcsh:Q ,Female - Abstract
Leaf rolls by herbivorous insects evolved in various lepidopteran groups, aphids, and some attelabid weevil species. Leaf rolls are known to have a positive effect on the survival of immature insects, protecting them from natural enemies such as birds, ants, predatory wasps, and parasitoids as well as environmental stress. On the other hand, leaf rolls are considered to have a negative effect on immature survival, attracting natural enemies because of their noticeability and subsequent learning or specialization. In this study, we directly tested the effects of leaf rolls using an attelabid species by comparing the fate of immature insects between artificial leaf rolls and unrolled leaves. The results showed the following positive effects of leaf rolls: avoidance of parasitism by eulophid wasps and avoidance of egg predation by unknown predators. On the other hand, a negative effect of leaf rolls was also detected, specifically and increase in mortality via leaf roll herbivory. This study indicated that leaf shelters are not only protective refuges but are also sometimes risky hiding places, although total survival rates increased in leaf shelters.
- Published
- 2020
16. Learning in herbivorous insects: dispersing aphids spend less time evaluating familiar than novel non-host plant species
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Lauren M. Mathews
- Subjects
0106 biological sciences ,0301 basic medicine ,Zoology ,Solidago altissima ,010603 evolutionary biology ,01 natural sciences ,Host Specificity ,03 medical and health sciences ,Animals ,Herbivory ,Ecosystem ,Ecology, Evolution, Behavior and Systematics ,Herbivore ,biology ,Host (biology) ,food and beverages ,biochemical phenomena, metabolism, and nutrition ,biology.organism_classification ,Solidago ,Aphis ,030104 developmental biology ,Habitat ,Aphids ,Host finding ,Biological dispersal ,Herbivorous insects - Abstract
For many organisms, dispersal may be a high-risk activity, and dispersers are likely to have behavioral, physiological, or other adaptations that increase the probability they will successfully settle in new habitat. Dispersing aphids, for example, are small-bodied, relatively weak flyers that must navigate through a complex landscape where non-host species may be much more common than suitable hosts are. While previous research has focused on how dispersing aphids locate and evaluate host species, little is known about how they interact with the non-host species they encounter while host searching. Here, I report on an experiment to test the hypothesis that dispersers of Aphis fabae spend less time evaluating non-host species with which they have had prior experience than novel non-host species. Aphids consistently spent less time in contact with familiar non-host species than novel non-host species, but the magnitude of this effect varied for different non-host species. Aphids that had previously encountered rose spent less time interacting with rose than with raspberry or goldenrod, and aphids that had previously encountered raspberry spent less time interacting with raspberry than with goldenrod. Aphids that had previously encountered goldenrod showed a less pronounced and statistically non-significant reduction in time spent interacting with goldenrod relative to either raspberry or rose. The ability to recognize previously encountered non-hosts may allow aphids to navigate more efficiently through an environment in which they face many more non-hosts than hosts, and therefore increase the probability that a disperser will ultimately locate and settle on an appropriate host plant.
- Published
- 2018
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17. Patterns of herbivory and leaf morphology in two Mexican hybrid oak complexes: Importance of fluctuating asymmetry as indicator of environmental stress in hybrid plants
- Author
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Armando Canché-Delgado, Yurixhi Maldonado-López, G. Wilson Fernandes, Antonio González-Rodríguez, Ken Oyama, and Pablo Cuevas-Reyes
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0106 biological sciences ,Herbivore ,Ecology ,General Decision Sciences ,Morphology (biology) ,Biology ,010603 evolutionary biology ,01 natural sciences ,Environmental stress ,Fluctuating asymmetry ,Interspecific hybridization ,Evolutionary biology ,Plant species ,Herbivorous insects ,Ecology, Evolution, Behavior and Systematics ,010606 plant biology & botany ,Hybrid - Abstract
Interspecific hybridization is a prevalent process in plant species that may have different ecological and evolutionary consequences. Interactions with herbivorous insects may be altered because of hybridization among host plants. These changes result from the morphological, physiological and chemical traits expressed in hybrid individuals. Therefore, it is of interest to document the changes in traits such as leaf morphology and their consequences on patterns of herbivory by insects in hybrid complexes of plants. Another useful indicator that may serve to evaluate developmental instability resulting from genetic or environmental stress in hybrid plants is fluctuating asymmetry. In this study, we used two previously genetically characterized complexes of hybridizing Mexican oaks as models to compare and understand the relationships between leaf morphology, fluctuating asymmetry and herbivory levels in parental and hybrid individuals. Results indicated that in the Quercus affinis × Q. laurina complex, hybrid individuals show a distinct morphology in relation to the parental species, while in the Q. magnoliifolia × Q. resinosa complex, hybrids were similar to Q. resinosa. In both hybrid complexes, our results show that hybrid individuals have higher levels of fluctuating asymmetry and herbivory levels, which may reflect higher levels of genetic or environmental stress in comparison to the parental species. These results might help explain why oak species usually remain distinct despite the high frequency of hybridization characteristic of the genus.
- Published
- 2018
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18. The ecological role of microsymbionts in the interaction of plants and herbivorous insects
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Igor V. Maksimov, G. V. Benkovskaya, A. V. Sorokan, and S. D. Rumyantsev
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0301 basic medicine ,Abiotic component ,Herbivore ,Resistance (ecology) ,Ecology ,Ecology (disciplines) ,fungi ,food and beverages ,General Medicine ,Biology ,03 medical and health sciences ,030104 developmental biology ,Symbiosis ,Plant defense against herbivory ,Herbivorous insects ,Adaptation - Abstract
A lot of evidence on the involvement of microsymbionts in the adaptation of hosts to adverse environmental impacts of both abiotic and biotic natures has recently been collected. In particular, microorganisms living in plants are involved in the development of induced systemic resistance to pathogens and pests, which allows them to be regarded as a reserve for the design of ecologically safe plant defense tools. However, the endosymbionts of herbivores are also putatively involved in both the adaptation of a macrosymbiont to the environment and the effect on host plant immune system in order to reduce the efficiency of defense responses. The obtained data show that the understanding of the mechanisms underlying the interaction of plants and pathogens or pests is incomplete without knowledge about the role of “hidden players,” microsymbionts that are present in both parties.
- Published
- 2017
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19. Grazing limits natural biological controls of woody encroachment in Inner Mongolia Steppe
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Yinhua Wang, Hongyu Guo, Chengcang Ma, Chelse M. Prather, Chunguang Liu, Lina Xie, and Linjing Guan
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0106 biological sciences ,010504 meteorology & atmospheric sciences ,QH301-705.5 ,Parasitic plant ,Science ,ved/biology.organism_classification_rank.species ,Caragana ,010603 evolutionary biology ,01 natural sciences ,Shrub ,General Biochemistry, Genetics and Molecular Biology ,Caragana microphylla ,Grazing ,Inner Mongolia Steppe ,Biology (General) ,Overgrazing ,Parasitic plants ,Woody encroachment ,0105 earth and related environmental sciences ,Herbivore ,biology ,ved/biology ,Ecology ,Herbaceous plant ,biology.organism_classification ,Herbivorous insects ,General Agricultural and Biological Sciences ,Woody plant ,Research Article - Abstract
Woody encroachment in grasslands has become increasingly problematic globally. Grazing by domestic animals can facilitate woody encroachment by reducing competition from herbaceous plants and fire frequency. Herbivorous insects and parasitic plants can each exert forces that result in the natural biological control of encroaching woody plants through reducing seeding of their host woody plants. However, the interplay of grazing and dynamics of herbivorous insects or parasitic plants, and its effects on the potential biological control of woody encroachment in grasslands remains unclear. We investigated the flower and pod damage by herbivorous insects, and the infection rates of a parasitic plant on the shrub Caragana microphylla, which is currently encroaching in Inner Mongolia Steppe, under different grazing management treatments (33-year non-grazed, 7-year non-grazed, currently grazed). Our results showed that Caragana biomass was highest at the currently grazed site, and lowest at the 33-year non-grazed site. Herbaceous plant biomass followed the opposite pattern, suggesting that grazing is indeed facilitating the encroachment of Caragana plants in Inner Mongolia Steppe. Grazing also reduced the abundance of herbivorous insects per Caragana flower, numbers of flowers and pods damaged by insect herbivores, and the infection rates of the parasitic plant on Caragana plants. Our results suggest that grazing may facilitate woody encroachment in grasslands not only through canonical mechanisms (e.g. competitive release via feeding on grasses, reductions in fires, etc.), but also by limiting natural biological controls of woody plants (herbivorous insects and parasitic plants). Thus, management efforts must focus on preventing overgrazing to better protect grassland ecosystems from woody encroachment., Summary: Grazing can negatively affect herbivorous insects and parasitic plants on woody plants, and thus limit the effectiveness of their natural biological control effects on woody encroachment.
- Published
- 2017
20. Diversity and impact of herbivorous insects on Brazilian peppertree in Florida prior to release of exotic biological control agents
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Ganesh P. Bhattarai, Bernardette Stange, Rodrigo Diaz, Lyle J. Buss, William A. Overholt, Veronica Manrique, and William W. Turechek
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0106 biological sciences ,Herbivore ,Schinus ,biology ,Ecology ,media_common.quotation_subject ,fungi ,Biological pest control ,Insect ,biology.organism_classification ,Generalist and specialist species ,010603 evolutionary biology ,01 natural sciences ,010602 entomology ,Insect Science ,South american ,Herbivorous insects ,Anacardiaceae ,Agronomy and Crop Science ,media_common - Abstract
Brazilian peppertree, Schinus terebinthifolia Raddi (Anacardiaceae), is a South American plant that is highly invasive in Florida. The impact of insect herbivores on the performance of Brazilian peppertree was evaluated at two locations in Florida using an insecticide exclusion method. Although 38 species of insect herbivores were collected on the invasive tree, there were no differences in growth or reproductive output of insecticide protected and unprotected trees, providing evidence that insect feeding had no measurable impact on tree performance. The majority of insects collected on Brazilian peppertree were generalists, and several were serious agricultural pests.
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- 2017
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21. Symbiotic solutions to nitrogen limitation and amino acid imbalance in insect diets
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Allison K. Hansen, Daniel Pers, and Jacob A. Russell
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Ecological niche ,Herbivore ,Symbiosis ,Ecology ,media_common.quotation_subject ,Herbivorous insects ,Genomics ,Limiting ,Insect ,Biology ,Limited resources ,media_common - Abstract
Although comprising ~ 80% of the Earth's air, nitrogen (N), in a usable form, is a limited resource for herbivorous insects. Additionally, much of the consumed dietary N is lost through-excretion, further challenging such insects, while limiting their growth and reproduction. To meet this challenge, many insect groups have evolved symbiotic relationships with microbes, enabling success within otherwise inhospitable niches. These mutualistic microbes contribute to their hosts' N-economies through nitrogen recycling, fixation and/or upgrading, using divergent metabolic strategies with varying precursors and physiological requirements. In this chapter we highlight each strategy, organizing our discussion by insect taxonomy, while enumerating the various microbes and innovations that have converged upon N-centric, nutritive functions. Our overview places a large emphasis on N-recycling, due in part to a lack of recent reviews on this topic. In reviewing N-fixation, we take a termite-centred approach, capitalizing upon an extensive bank of research performed across several decades. We also emphasize essential amino acid (EAA) and precursor biosynthesis, discussing non-fixing, non-recycling mutualisms in which symbionts make up for dietary shortcomings and missing pathways for nutrient biosynthesis in their hosts. In these explorations, we discuss the specificity and evolutionary histories between herbivorous insect hosts and their often ancient N-metabolizing symbionts. We focus, further, on correlations between dietary evolution and altered symbioses, which cast light on the causes and consequences of these nutritional relationships. We, finally, describe the evidence supporting prior arguments for N-centric mutualisms, emphasizing how a pairing of genomics and experimentation can uncover mechanism, while pinpointing just how symbiont metabolism shapes the fitness and N-budgets of diverse, herbivorous hexapods.
- Published
- 2020
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22. Release from Above- and Belowground Insect Herbivory Mediates Invasion Dynamics and Impact of an Exotic Plant
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Harald Auge, Lotte Korell, Susanne Schreiter, Martin Schädler, and Roland Brandl
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0106 biological sciences ,enemy release ,productivity ,Population ,biological invasions ,Introduced species ,Plant Science ,Solidago canadensis ,010603 evolutionary biology ,01 natural sciences ,Article ,diversity ,education ,Ecology, Evolution, Behavior and Systematics ,trophic interactions ,Herbivore ,education.field_of_study ,Ecology ,biology ,Species diversity ,Plant community ,Native plant ,biology.organism_classification ,plant communities ,Plant ecology ,ecosystem functions ,herbivorous insects ,long-term experiment ,010606 plant biology & botany - Abstract
The enemy-release hypothesis is one of the most popular but also most discussed hypotheses to explain invasion success. However, there is a lack of explicit, experimental tests of predictions of the enemy-release hypothesis (ERH), particularly regarding the effects of above- and belowground herbivory. Long-term studies investigating the relative effect of herbivores on invasive vs. native plant species within a community are still lacking. Here, we report on a long-term field experiment in an old-field community, invaded by Solidago canadensis s. l., with exclusion of above- and belowground insect herbivores. We monitored population dynamics of the invader and changes in the diversity and functioning of the plant community across eight years. Above- and belowground insects favoured the establishment of the invasive plant species and thereby increased biomass and decreased diversity of the plant community. Effects of invertebrate herbivores on population dynamics of S. canadensis appeared after six years and increased over time, suggesting that long-term studies are needed to understand invasion dynamics and consequences for plant community structure. We suggest that the release from co-evolved trophic linkages is of importance not only for the effect of invasive species on ecosystems, but also for the functioning of novel species assemblages arising from climate change.
- Published
- 2019
23. Leaf shape deters plant processing by an herbivorous weevil
- Author
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Atsushi Kawakita and Yumiko Higuchi
- Subjects
0106 biological sciences ,0301 basic medicine ,Herbivore ,Larva ,Lamiaceae ,biology ,Host (biology) ,Weevil ,Oviposition ,Isodon ,Plant Science ,biology.organism_classification ,01 natural sciences ,Plant Leaves ,03 medical and health sciences ,030104 developmental biology ,Botany ,Animals ,Weevils ,Herbivorous insects ,Female ,Herbivory ,010606 plant biology & botany - Abstract
The shapes of plant leaves are remarkably diverse, but their ecological functions are largely unknown. Reports on the effects of leaf shape on biotic interactions such as herbivory are especially scarce, partly because herbivorous insects rarely rely on leaf shape for host selection. Here, we show that leaf shape acts as a physical deterrent against a leaf-processing herbivore. Plants in the genus Isodon (Lamiaceae) host a specialized leaf-rolling weevil (Apoderus praecellens) whose ovipositing females process an entire leaf into a leaf roll to serve as larval food and shelter. Among the species of Isodon, I. umbrosus var. hakusanensis is exceptional in that it has deeply lobed leaves. Because leaf processing follows a consistent sequence of complex behaviours, the unusual shape of I. umbrosus leaves may disrupt this process. Under both natural and laboratory conditions, female weevils preferred I. trichocarpus, a close relative with non-lobed leaves, over I. umbrosus. Nutritional properties of the leaves do not explain this preference because weevil larvae developed equally well on both hosts. Modifying the non-lobed I. trichocarpus leaves to mimic the shape of I. umbrosus leaves also discouraged leaf processing. Leaf processing often terminated because weevils failed to complete the inspection routine on I. umbrosus leaves. Leaf shape may be an important but overlooked factor that affects the interactions between plants and leaf-processing herbivores.
- Published
- 2019
24. Before the ‘Big Chill’: Patterns of plant-insect associations from the Neogene of Iceland
- Author
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Friðgeir Grímsson and Torsten Wappler
- Subjects
0106 biological sciences ,Herb layer ,Global and Planetary Change ,Herbivore ,010504 meteorology & atmospheric sciences ,Community assembly ,Ecology ,Biogeography ,fungi ,Late Miocene ,Biology ,Oceanography ,Neogene ,Herbivorous insects ,Island ecology ,010603 evolutionary biology ,01 natural sciences ,Subarctic climate ,Structural complexity ,Palaeobiogeography ,Climate driven changes ,Sedimentary rock ,0105 earth and related environmental sciences - Abstract
Iceland is the only known terrestrial place in the subarctic North Atlantic providing a fairly continuous sedimentary and plant fossil record over the past 15 million years. While the basic palaeobotanical framework of this pattern has been well established during the last decade, less attention has been paid to the abundant insect traces on fossil leaves/leaflets. Here, we assess the diversity and frequency of insect herbivory on 4349 fossil angiosperm leaves/leaflets from six plant-bearing sedimentary formations exposed at 18 localities. By combining analyses of environmental factors, species interactions, ecology, biogeography, and the geological history, our results demonstrate how patterns of herbivory have changed over time in relation to temperature fluctuations that profoundly influenced levels of insect-mediated damage diversity and frequency. In addition, higher structural complexity, particularly the establishment of species-rich herb layer communities seems to have positively influenced the structure of insect communities in early late Miocene palaeoforests of Iceland.
- Published
- 2016
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25. Periodic solutions in a herbivore-plant system with time delay and spatial diffusion
- Author
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Li Li, Jing Li, and Zhen Jin
- Subjects
Hopf bifurcation ,Herbivore ,Differential equation ,Applied Mathematics ,01 natural sciences ,010305 fluids & plasmas ,symbols.namesake ,Control theory ,Modeling and Simulation ,0103 physical sciences ,symbols ,Quantitative Biology::Populations and Evolution ,Herbivorous insects ,Plant system ,Biological system ,Spatial diffusion ,010301 acoustics ,Center manifold ,Mathematics - Abstract
Empirical studies indicate that many populations of herbivorous insects exhibit periodic outbreaks, but the intrinsic causes of this behavior are not well understood. Thus, in this study, we investigated a herbivore-plant system with time delay based on reaction-diffusion equations. Using normal formal theory and the center manifold theorem for partial functional differential equations, we show that this model exhibits the property of Hopf bifurcation. Therefore, interactions between the time delay and spatial diffusion will induce periodic outbreaks in herbivore populations. These results may suggest a new mechanism for herbivore outbreaks.
- Published
- 2016
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26. The relative importance of plant-soil feedbacks for plant-species performance increases with decreasing intensity of herbivory
- Author
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Nadja K. Simons, Guntram Weithoff, Daniel Prati, T. Martijn Bezemer, Martin M. Gossner, Johannes Heinze, Jasmin Joshi, Alexander Wacker, Sebastian Seibold, and Terrestrial Ecology (TE)
- Subjects
0106 biological sciences ,Plant soil ,Nutritional quality ,Biology ,580 Plants (Botany) ,010603 evolutionary biology ,01 natural sciences ,Grassland ,Soil ,ddc:570 ,Animals ,Ecosystem ,Herbivory ,Institut für Biochemie und Biologie ,Ecology, Evolution, Behavior and Systematics ,Invertebrate ,geography ,Herbivore ,geography.geographical_feature_category ,Ecology ,010604 marine biology & hydrobiology ,Selective herbivory ,Plants ,Herbivorous insects ,Invertebrates ,international ,Plant-soil feedback ,Plant species ,Field conditions ,Intensity (heat transfer) - Abstract
Under natural conditions, aboveground herbivory and plant-soil feedbacks (PSFs) are omnipresent interactions strongly affecting individual plant performance. While recent research revealed that aboveground insect herbivory generally impacts the outcome of PSFs, no study tested to what extent the intensity of herbivory affects the outcome. This, however, is essential to estimate the contribution of PSFs to plant performance under natural conditions in the field. Here, we tested PSF effects both with and without exposure to aboveground herbivory for four common grass species in nine grasslands that formed a gradient of aboveground invertebrate herbivory. Without aboveground herbivores, PSFs for each of the four grass species were similar in each of the nine grasslands—both in direction and in magnitude. In the presence of herbivores, however, the PSFs differed from those measured under herbivory exclusion, and depended on the intensity of herbivory. At low levels of herbivory, PSFs were similar in the presence and absence of herbivores, but differed at high herbivory levels. While PSFs without herbivores remained similar along the gradient of herbivory intensity, increasing herbivory intensity mostly resulted in neutral PSFs in the presence of herbivores. This suggests that the relative importance of PSFs for plant-species performance in grassland communities decreases with increasing intensity of herbivory. Hence, PSFs might be more important for plant performance in ecosystems with low herbivore pressure than in ecosystems with large impacts of insect herbivores.
- Published
- 2019
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27. Settling on leaves or flowers: herbivore feeding site determines the outcome of indirect interactions between herbivores and pollinators
- Author
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Quint Rusman, Dani Lucas-Barbosa, Erik H. Poelman, and Peter N. Karssemeijer
- Subjects
0106 biological sciences ,Insecta ,media_common.quotation_subject ,Flowers ,Insect ,Biology ,010603 evolutionary biology ,01 natural sciences ,Folivory ,Plant-Microbe-Animal Interactions–Original Research ,Pollinator ,Florivory ,Plant defense ,Plant defense against herbivory ,Preference–performance ,Animals ,Herbivory ,Laboratory of Entomology ,Pollination ,Antagonist-mutualist interactions ,Plant-mediated interactions ,Preference-performance ,Ecology, Evolution, Behavior and Systematics ,media_common ,Herbivore ,Ecology ,15. Life on land ,Laboratorium voor Entomologie ,Plant tissue ,Plant Leaves ,Herbivorous insects ,EPS ,010606 plant biology & botany - Abstract
Herbivore attack can alter plant interactions with pollinators, ranging from reduced to enhanced pollinator visitation. The direction and strength of effects of herbivory on pollinator visitation could be contingent on the type of plant tissue or organ attacked by herbivores, but this has seldom been tested experimentally. We investigated the effect of variation in feeding site of herbivorous insects on the visitation by insect pollinators on flowering Brassica nigra plants. We placed herbivores on either leaves or flowers, and recorded the responses of two pollinator species when visiting flowers. Our results show that variation in herbivore feeding site has profound impact on the outcome of herbivore–pollinator interactions. Herbivores feeding on flowers had consistent positive effects on pollinator visitation, whereas herbivores feeding on leaves did not. Herbivores themselves preferred to feed on flowers, and mostly performed best on flowers. We conclude that herbivore feeding site choice can profoundly affect herbivore–pollinator interactions and feeding site thereby makes for an important herbivore trait that can determine the linkage between antagonistic and mutualistic networks. Electronic supplementary material The online version of this article (10.1007/s00442-019-04539-1) contains supplementary material, which is available to authorized users.
- Published
- 2019
28. Ecological interactions shape the adaptive value of plant defence: Herbivore attack versus competition for light
- Author
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Erik H. Poelman, Jorad de Vries, Marcel Dicke, and Jochem B. Evers
- Subjects
0106 biological sciences ,Plant growth ,Adaptive value ,ecological costs ,plant defence ,media_common.quotation_subject ,Context (language use) ,plant ,Biology ,010603 evolutionary biology ,01 natural sciences ,functional‐structural plant modelling ,Competition (biology) ,Laboratory of Entomology ,Ecology, Evolution, Behavior and Systematics ,Plant–Animal Interactions ,media_common ,Herbivore ,Ecology ,herbivory ,Brassica nigra ,fungi ,food and beverages ,15. Life on land ,Investment (macroeconomics) ,PE&RC ,Laboratorium voor Entomologie ,growth-defence trade-off ,functional-structural plant modelling ,herbivore interactions ,Herbivorous insects ,growth‐defence trade‐off ,EPS ,Crop and Weed Ecology ,Limited resources ,competition ,010606 plant biology & botany ,Research Article - Abstract
Plants defend themselves against diverse communities of herbivorous insects. This requires an investment of limited resources, for which plants also compete with neighbours. The consequences of an investment in defence are determined by the metabolic costs of defence as well as indirect or ecological costs through interactions with other organisms. These ecological costs have a potentially strong impact on the evolution of defensive traits, but have proven to be difficult to quantify.We aimed to quantify the relative impact of the direct and indirect or ecological costs and benefits of an investment in plant defence in relation to herbivory and intergenotypic competition for light. Additionally, we evaluated how the benefits of plant defence balance its costs in the context of herbivory and intergenotypic competition.To this end, we utilised a functional‐structural plant (FSP) model of Brassica nigra that simulates plant growth and development, morphogenesis, herbivory and plant defence. In the model, a simulated investment in defences affected plant growth by competing with other plant organs for resources and affected the level and distribution of herbivore damage.Our results show that the ecological costs of intergenotypic competition for light are highly detrimental to the fitness of defended plants, as it amplifies the size difference between defended and undefended plants. This leads to herbivore damage counteracting the effects of intergenotypic competition under the assumption that herbivore damage scales with plant size. Additionally, we show that plant defence relies on reducing herbivore damage rather than the dispersion of herbivore damage, which is only beneficial under high levels of herbivore damage.We conclude that the adaptive value of plant defence is highly dependent on ecological interactions and is predominantly determined by the outcome of competition for light. plain language summary is available for this article.
- Published
- 2019
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29. Jasmonates mediate plant defense responses toSpodoptera exiguaherbivory in tomato and maize foliage
- Author
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Wafaa Al-Zahrani, Manal El-Zohri, and Sameera O. Bafeel
- Subjects
0106 biological sciences ,0301 basic medicine ,Herbivore ,biology ,Jasmonic acid ,fungi ,food and beverages ,Plant Science ,Spodoptera ,medicine.disease_cause ,biology.organism_classification ,01 natural sciences ,03 medical and health sciences ,chemistry.chemical_compound ,Horticulture ,030104 developmental biology ,chemistry ,Beet armyworm ,Infestation ,Exigua ,medicine ,Plant defense against herbivory ,Herbivorous insects ,010606 plant biology & botany - Abstract
Plants evolve diverse strategies to cope with herbivorous insects, in which the lipid-derived phytohormone jasmonic acid (JA) plays a crucial role. This study was conducted to investigate the differential responses of tomato and maize plants to Spodoptera exiguaherbivory and to clarify the role played by JA, methyl-jasmonate (MeJA) and jasmonoyl-L-isoleucine (JA-L-Ile) in their defense responses. JA, MeJA and JA-L-Ile were quantified using HPLC-MS/MS. The results showed that maize plant was more tolerant toS. exiguaherbivory than tomato. Spodopteraexigua attack induced JA, MeJA, and JA-L-Ile to high levels after 2 h of infestation in both test plants. Then, all studied JAsconcentration decreased gradually by increasing infestation time up to 1 week. JA concentration in infested maize was much higher than that in infested tomato leaves. However, MeJA concentration in infested tomato leaves was higher than that in maize. In control plants, JA was not recorded, while MeJA was recorded in comparable values both in tomato and maize. Our results showed that JA plays the main role in increasing defense responses to S. exigua infestation in the studied plants as a direct signaling molecule; however, MeJA could play an indirect role by inducing JA accumulation. JA-L-Ile indicated a less efficient role in defense responses to S. exigua attack in both test plants where its level is much lower than JA and MeJA.
- Published
- 2020
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30. Evolutionary dynamics of specialisation in herbivorous stick insects
- Author
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Sergio Rasmann, Tanja Schwander, and Chloé Larose
- Subjects
0106 biological sciences ,Ecological niche ,Herbivore ,Insecta ,Ecology ,010604 marine biology & hydrobiology ,media_common.quotation_subject ,fungi ,Niche ,food and beverages ,Insect ,Plants ,Generalist and specialist species ,010603 evolutionary biology ,01 natural sciences ,Biological Evolution ,Animals ,Ecosystem ,Herbivorous insects ,Herbivory ,Evolutionary dynamics ,Ecology, Evolution, Behavior and Systematics ,media_common - Abstract
Understanding the evolutionary dynamics underlying herbivorous insect mega-diversity requires investigating the ability of insects to shift and adapt to different host plants. Feeding experiments with nine related stick insect species revealed that insects retain the ability to use ancestral host plants after shifting to novel hosts, with host plant shifts generating fundamental feeding niche expansions. These expansions were, however, not accompanied by expansions of the realised feeding niches, as species on novel hosts are generally ecologically specialised. For shifts from angiosperm to chemically challenging conifer hosts, generalist fundamental feeding niches even evolved jointly with strong host plant specialisation, indicating that host plant specialisation is not driven by constraints imposed by plant chemistry. By coupling analyses of plant chemical compounds, fundamental and ecological feeding niches in multiple insect species, we provide novel insights into the evolutionary dynamics of host range expansion and contraction in herbivorous insects.
- Published
- 2018
31. Evolutionary dynamics of specialization in herbivorous stick insects
- Author
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Chloé Larose, Sergio Rasmann, and Tanja Schwander
- Subjects
Ecological niche ,Herbivore ,Ecology ,media_common.quotation_subject ,Niche ,fungi ,Host plants ,food and beverages ,Herbivorous insects ,Insect ,Evolutionary dynamics ,Generalist and specialist species ,media_common - Abstract
Understanding the evolutionary dynamics underlying herbivorous insect mega-diversity requires investigating the ability of insects to shift and adapt to different host plants. Feeding experiments with nine related stick insect species revealed that insects retain the ability to use ancestral host plants after shifting to novel hosts, with host plant shifts generating fundamental feeding niche expansions. These expansions were not accompanied by expansions of the realized feeding niches however, as species on novel hosts are generally ecologically specialized. For shifts from angiosperm to chemically challenging conifer hosts, generalist fundamental feeding niches even evolved jointly with strong host plant specialization, indicating that host plant specialization is more likely driven by species interactions than by constraints imposed by plant chemistry. By coupling analyses of plant chemical compounds, fundamental and ecological feeding niches in multiple insect species, we provide novel insights into the evolutionary dynamics of host range expansion and contraction in herbivorous insects.
- Published
- 2018
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32. Livestock grazing disrupts plant-insect interactions on salt marshes
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Roel van Klink, Andreas Fichtner, and Corinna Rickert
- Subjects
0106 biological sciences ,Biology ,010603 evolutionary biology ,01 natural sciences ,Grassland ,Grazing ,moths ,grazing management ,Conservation grazing ,Ecology, Evolution, Behavior and Systematics ,Herbivore ,geography ,geography.geographical_feature_category ,Ecology ,Host (biology) ,010604 marine biology & hydrobiology ,fungi ,livestock ,Habitat ,Ecosystems Research ,Insect Science ,Salt marsh ,Rarefaction (ecology) ,herbivorous insects ,grassland - Abstract
1. Studies of grassland communities have demonstrated that increasingvertebrate grazing decreases the diversity of specialised herbivorous insects,while plant diversity is maintained or increased. However, we still have a limitedunderstanding of the causal mechanisms underlying these contrasting observations of two tightly linked groups of organisms.2. We used spatially linked plant and moth observations from salt marshes,sampled for 3 years along an experimental sheep-grazing gradient (0, 1–2, 3–4and 10 sheep ha1), to test whether the disruption of plant–insect interactionsby large herbivores accounts for these contrasting grazing effects. Moths werecaught using emergence traps, which were moved and repositioned every3 weeks.3. Firstly, we quantified species turnover between the grazing regimes forboth taxa (measured as Sørensen dissimilarity) using a null-model approach.Secondly, we analysed the number of observed insect ̶ host associations underthe different regimes.4. Species turnover between grazing regimes was significant (after correctingfor rarefaction effects) for moth species, but not for plants, indicating very fewand random effects of grazing on plant species composition. The percentage ofrealised plant–moth associations decreased from 37% in the absence of grazingto 6.5% under high stocking densities.5. We thus conclude that vertebrate grazing caused a disruption of plant–moth associations, probably by rendering the host-plants unsuitable for most ofthe moth species. Our findings provide further mechanistic understanding onhow large herbivores shape arthropod communities and illustrate the importance of host-plant associations in explaining effects of natural or anthropogenic habitat modification. 1. Studies of grassland communities have demonstrated that increasingvertebrate grazing decreases the diversity of specialised herbivorous insects,while plant diversity is maintained or increased. However, we still have a limited understanding of the causal mechanisms underlying these contrasting observations of two tightly linked groups of organisms.2. We used spatially linked plant and moth observations from salt marshes,sampled for 3 years along an experimental sheep-grazing gradient (0, 1–2, 3–4 and 10 sheep ha1), to test whether the disruption of plant–insect interactions by large herbivores accounts for these contrasting grazing effects. Moths were caught using emergence traps, which were moved and epositioned every 3 weeks.3. Firstly, we quantified species turnover between the grazing regimes forboth taxa (measured as Sørensen dissimilarity) using a null-model approach.Secondly, we analysed the number of observed insect ̶ host associations underthe different regimes.4. Species turnover between grazing regimes was significant (after correctingfor rarefaction effects) for moth species, but not for plants, indicating very fewand random effects of grazing on plant species composition. The percentage of realised plant–moth associations decreased from 37% in the absence of grazing to 6.5% under high stocking densities.5. We thus conclude that vertebrate grazing caused a disruption of plant–moth associations, probably by rendering the host-plants unsuitable for most of the moth species. Our findings provide further mechanistic understanding on how large herbivores shape arthropod communities and illustrate the importance of host-plant associations in explaining effects of natural or anthropogenic habitat modification.
- Published
- 2018
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33. Forest Fragmentation Drives the Loss of Insectivorous Birds and an Associated Increase in Herbivory
- Author
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Graham R.H. Grieve, Franziska Peter, Dana G. Berens, and Nina Farwig
- Subjects
Herbivore ,Ecology ,fungi ,Tropics ,Insectivore ,Herbivorous insects ,Forest fragmentation ,Biology ,Regeneration (ecology) ,Tropical and subtropical moist broadleaf forests ,Ecology, Evolution, Behavior and Systematics ,Trophic level - Abstract
Insectivorous birds are known to play a decisive role for the natural control of herbivorous insects. Thus, they enhance the growth, reproduction, and survival of plant individuals and in the long-term benefit plant regeneration. However, particularly in the tropics, forest fragmentation has been suggested to cause a loss of insectivorous birds. Yet, it is unclear whether this hampers the trophic control of herbivorous insects with potential consequences for plants. Therefore, we investigated the effect of increasing forest fragmentation on tritrophic interactions between insectivorous birds, herbivorous insects, and plants in a subtropical forest landscape, South Africa. We monitored the community composition of birds and estimated insectivorous bird abundances along a gradient of forest fragmentation. In the same sites, we installed bird exclosures on a common plant species (Englerophytum natalense) to assess effects of the trophic control of insectivorous birds on herbivorous insects and leaf area loss (LAL). Forest fragmentation strongly shaped the functional composition of bird communities, particularly through a loss of forest-dependent insectivorous birds. Moreover, LAL was higher within bird exclosures than on control branches and increased with increasing forest fragmentation on the control branches. Altogether, forest fragmentation seems to hamper the trophic control of herbivorous insects by insectivorous birds through changes in the community composition. This, in turn, may interfere with tritrophic interactions and ecological processes. Thus, conservation efforts aiming at enhancing the natural control of herbivorous insects should focus on the maintenance of continuous indigenous forests that are well-connected to smaller forest fragments on the landscape scale.
- Published
- 2015
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34. Host specialization by reproductive interference between closely related herbivorous insects
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Koh-Ichi Takakura, Keisuke Iwao, and Takayoshi Nishida
- Subjects
Herbivore ,Ecology ,Host (biology) ,Host plants ,Herbivorous insects ,Interspecific competition ,Biology ,Generalist and specialist species ,Ecology, Evolution, Behavior and Systematics - Abstract
Host specialization among closely related herbivores is common and is therefore a major theme in ecology. Despite its ecological importance, no general explanatory framework for host specialization is currently available. We introduce a new model of the evolution of host specialization in herbivorous insects. We use a two-dimensional lattice comprising 32 × 32 cells. Moreover, the model incorporates reproductive interference, defined as any negative outcomes resulting from interspecific mating, between two species of herbivores feeding on two different host plants as well as ordinary resource competition and differences in host suitability. Our simulation showed that reproductive interference, together with other factors such as host-related performance and resource competition, can actually drive the evolution of host specialization and thereby host partitioning between herbivorous insects during secondary contact. Host specialization arises particularly when levels of both reproductive interference and resource competition are intermediate. In contrast, host specialization seldom occurs if reproductive interference is absent. Thus, reproductive interference is as key to specialization as is spatial partitioning, which was not regarded as a realistic outcome when only resource competition was considered.
- Published
- 2015
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35. Application and Theory of Plant–Soil Feedbacks on Aboveground Herbivores
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Kaplan, Ian, Pineda, Ana, Bezemer, T.M., Ohgushi, Takayuki, Wurst, Susanne, Johnson, Scott N., and Terrestrial Ecology (TE)
- Subjects
0106 biological sciences ,Herbivore ,Restoration ecology ,Ecology ,Soil biology ,Context (language use) ,Plant soil ,010603 evolutionary biology ,01 natural sciences ,Crop protection ,international ,Plant species ,Environmental science ,Herbivorous insects ,Cover crop ,010606 plant biology & botany - Abstract
Plant–soil feedbacks are legacy effects created by an initial plant on the growth of subsequent plants using the same soil. These indirect soil-mediated interactions are primarily studied in the context of changes in the belowground biotic community. Here, we review current evidence surrounding plant–soil feedbacks, focusing on how these interactions are studied from an experimental standpoint and expand this discussion into new directions surrounding the influence of feedbacks on interactions with aboveground herbivorous insects. The taxon-specific impact of individual soil groups on foliar-feeding insects is well-described, but expanding this framework to plant–soil feedbacks is challenging because different plant species cause simultaneous and dramatic shifts in the composition of all soil life, sometimes in contradictory directions (i.e., certain fungi may increase, while nematodes decrease). Thus, expanding simple pair-wise root herbivore–plant–insect relationships to more holistic approaches that account for the full spectrum of changes in soil biota represents both a mechanistic and analytical challenge. These community-wide shifts, however, are representative of true legacy effects encountered by plants and insects in nature. We end our chapter on a discussion of how plant–soil feedbacks can be functionally used to steer the microbiome for enhanced crop protection in applied agricultural systems.
- Published
- 2018
36. Plant Responses to Insect Egg Deposition
- Author
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Monika Hilker and Nina E. Fatouros
- Subjects
Insecta ,pieris-brassicae ,Oviposition ,media_common.quotation_subject ,Insect egg ,parasitoid anagrus-nilaparvatae ,Insect ,ovicidal substance ,Pheromones ,sogatella-furcifera horvath ,Plant defense against herbivory ,Animals ,Herbivory ,Laboratory of Entomology ,medfly ceratitis-capitata ,Plant Physiological Phenomena ,Ecology, Evolution, Behavior and Systematics ,media_common ,Pieris brassicae ,Herbivore ,Larva ,oryza-sativa l ,biology ,host location ,Ecology ,elm leaf beetle ,fungi ,food and beverages ,PE&RC ,Laboratorium voor Entomologie ,biology.organism_classification ,phytophagous insects ,Insect Science ,embryonic structures ,defense responses ,Herbivorous insects - Abstract
Plants can respond to insect egg deposition and thus resist attack by herbivorous insects from the beginning of the attack, egg deposition. We review ecological effects of plant responses to insect eggs and differentiate between egg-induced plant defenses that directly harm the eggs and indirect defenses that involve egg parasitoids. Furthermore, we discuss the ability of plants to take insect eggs as warning signals; the eggs indicate future larval feeding damage and trigger plant changes that either directly impair larval performance or attract enemies of the larvae. We address the questions of how egg-associated cues elicit plant defenses, how the information that eggs have been laid is transmitted within a plant, and which molecular and chemical plant responses are induced by egg deposition. Finally, we highlight evolutionary aspects of the interactions between plants and insect eggs and ask how the herbivorous insect copes with egg-induced plant defenses and may avoid them by counteradaptations.
- Published
- 2015
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37. Plant Volatiles as Mate-Finding Cues for Insects
- Author
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Hao Xu and Ted C. J. Turlings
- Subjects
0106 biological sciences ,Male ,Insecta ,Combined use ,Zoology ,Plant Science ,Biology ,010603 evolutionary biology ,01 natural sciences ,Predation ,Sexual Behavior, Animal ,Host plants ,Animals ,Herbivory ,Mating ,Sex Attractants ,Herbivore ,Volatile Organic Compounds ,fungi ,food and beverages ,Plants ,010602 entomology ,Sex pheromone ,Herbivorous insects ,Female ,Plant Structures ,Signal Transduction - Abstract
Plant volatiles are used not only by herbivorous insects to find their host plants, but also by the natural enemies of the herbivores to find their prey. There is also increasing evidence that plant volatiles, in addition to species-specific pheromones, help these insects to find mating partners. Plant structures such as flowers, fruit, and leaves are frequently rendezvous sites for mate-seeking insects. Here we propose that the combined use of plant volatiles and pheromones can efficiently guide insects to these sites, where they will have access to both mates and food. This notion is supported by the fact that plant volatiles can stimulate the release of sex pheromones and can render various insects more receptive to potential mates.
- Published
- 2017
38. Altering Plant Defenses: Herbivore-Associated Molecular Patterns and Effector Arsenal of Chewing Herbivores
- Author
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Suresh Varsani, Saumik Basu, and Joe Louis
- Subjects
0106 biological sciences ,0301 basic medicine ,Insecta ,Physiology ,media_common.quotation_subject ,Insect ,Biology ,01 natural sciences ,03 medical and health sciences ,Symbiosis ,Plant defense against herbivory ,Animals ,Herbivory ,media_common ,Herbivore ,Ecology ,Effector ,Host (biology) ,Frass ,fungi ,Pathogen-Associated Molecular Pattern Molecules ,General Medicine ,Plants ,030104 developmental biology ,Mastication ,Herbivorous insects ,Agronomy and Crop Science ,010606 plant biology & botany - Abstract
Chewing herbivores, such as caterpillars and beetles, while feeding on the host plant, cause extensive tissue damage and release a wide array of cues to alter plant defenses. Consequently, the cues can have both beneficial and detrimental impacts on the chewing herbivores. Herbivore-associated molecular patterns (HAMPs) are molecules produced by herbivorous insects that aid them to elicit plant defenses leading to impairment of insect growth, while effectors suppress plant defenses and contribute to increased susceptibility to subsequent feeding by chewing herbivores. Besides secretions that originate from glands (e.g., saliva) and fore- and midgut regions (e.g., oral secretions) of chewing herbivores, recent studies have shown that insect frass and herbivore-associated endosymbionts also play a critical role in modulating plant defenses. In this review, we provide an update on a growing body of literature that discusses the chewing insect HAMPs and effectors and the mechanisms by which they modulate host defenses. Novel “omic” approaches and availability of new tools will help researchers to move forward this discipline by identifying and characterizing novel insect HAMPs and effectors and how these herbivore-associated cues are perceived by host plant receptors.
- Published
- 2017
39. Does Ozone Alter the Attractiveness of Japanese White Birch Leaves to the Leaf Beetle Agelastica coerulea via Changes in Biogenic Volatile Organic Compounds (BVOCs): An Examination with the Y-Tube Test
- Author
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Noboru Masui, Takayoshi Koike, Toshihiro Watanabe, Akira Tani, Tomoki Mochizuki, Evgenios Agathokleous, and Hideyuki Matsuura
- Subjects
atmospheric lifetime ,010504 meteorology & atmospheric sciences ,media_common.quotation_subject ,biogenic volatile organic compounds (BVOCs) ,Insect ,010501 environmental sciences ,01 natural sciences ,Alder ,Japonica ,biogenic volatile organic compounds (BVOCs), herbivorous insects ,leaf beetle ,Botany ,Grazing ,olfactory response ,0105 earth and related environmental sciences ,media_common ,Herbivore ,biology ,Chemistry ,fungi ,Forestry ,lcsh:QK900-989 ,biology.organism_classification ,ozone ,lcsh:Plant ecology ,herbivorous insects ,Composition (visual arts) ,Leaf beetle ,Betula platyphylla - Abstract
Elevated ground-level ozone (O3) reduced C-based defense chemicals, however, severe grazing damages were found in leaves grown in the low O3 condition of a free air O3-concentration enrichment (O3-FACE) system. To explain this phenomenon, this study investigates the role of BVOCs (biogenic volatile organic compounds) as signaling compounds for insect herbivores. BVOCs act as scents for herbivore insects to locate host plants, while some BVOCs show high reactivity to O3, inducing changes in the composition of BVOCs in atmospheres with elevated O3. To assess the aforementioned phenomenon, profiles of BVOCs emitted from birch (Betula platyphylla var. japonica Hara) leaves were analyzed ex situ, and Y-tube insect preference tests were conducted in vitro to study the insect olfactory response. The assays were conducted in June and August or September, according to the life cycle of the adult alder leaf beetle Agelastica coerulea Baly (Coleoptera: Chrysomelidae). The Y-tube tests revealed that the leaf beetles were attracted to BVOCs, and O3 per se had neither an attractant nor a repellent effect. BVOCs became less attractant when mixed with highly concentrated O3 (>, 80 ppb). About 20% of the total BVOCs emitted were highly O3-reactive compounds, such as &beta, ocimene. The results suggest that BVOCs emitted from the birch leaves can be altered by elevated O3, thus potentially reducing the attractiveness of leaves to herbivorous insects searching for food.
- Published
- 2020
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40. Biodiversity Has Been Maintained with Intermediate Disturbance in Traditional Agricultural Lands
- Author
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Kei Uchida and Atushi Ushimaru
- Subjects
Herbivore ,Ecology ,business.industry ,Agroforestry ,Biodiversity ,General Medicine ,Geography ,Intermediate Disturbance Hypothesis ,Agriculture ,Abandonment (emotional) ,Agricultural biodiversity ,Herbivorous insects ,Species richness ,business - Abstract
Richness and diversity of plant and herbivorous insect species were significantly lower in abandoned and intensified grasslands than in traditional grasslands. This trend was consistent throughout the seasons in 2011 and 2012. Changes in mowing frequency and surrounding landscape due to land abandonment and intensification explained plant richness declines around paddy terraces. Declines in herbivorous insects were well explained by plant richness declines and changes in mowing frequency. Plant and herbivore richness were maximized at an intermediate mowing frequency (about twice per year), which is a typical practice on traditional terraces.
- Published
- 2014
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41. Plant Immune Responses: Aphids Strike Back
- Author
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Thierry Calandra, Isabelle De Kaenel, and Philippe Reymond
- Subjects
0106 biological sciences ,Insect Proteins/genetics ,Plant Immunity ,Zoology ,Biology ,01 natural sciences ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Immune system ,Aphids/genetics ,Animals ,Herbivory ,Macrophage Migration-Inhibitory Factors ,030304 developmental biology ,0303 health sciences ,Herbivore ,Agricultural and Biological Sciences(all) ,Ecology ,Biochemistry, Genetics and Molecular Biology(all) ,fungi ,food and beverages ,Macrophage Migration-Inhibitory Factors/genetics ,Vicia faba/immunology ,biochemical phenomena, metabolism, and nutrition ,Vicia faba ,Aphids ,Insect Proteins ,Herbivorous insects ,General Agricultural and Biological Sciences ,010606 plant biology & botany - Abstract
SummaryTo survive and complete their life cycle, herbivorous insects face the difficult challenge of coping with the arsenal of plant defences. A new study reports that aphids secrete evolutionarily conserved cytokines in their saliva to suppress host immune responses.
- Published
- 2015
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42. Alien plants versus alien herbivores: does it matter who is non-native in a novel trophic interaction?
- Author
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Gaylord A. Desurmont and Ian S. Pearse
- Subjects
0106 biological sciences ,0303 health sciences ,Herbivore ,Ecology ,media_common.quotation_subject ,Context (language use) ,Alien ,Insect ,15. Life on land ,Biology ,010603 evolutionary biology ,01 natural sciences ,Predation ,03 medical and health sciences ,Insect Science ,Herbivorous insects ,Ecosystem ,Ecology, Evolution, Behavior and Systematics ,030304 developmental biology ,media_common ,Trophic level - Abstract
Introductions of both plants and herbivorous insects have had tremendous impacts on the world's ecosystems. Novel herbivorous insect-plant interactions are important consequences of introductions of either plants or herbivorous insects. We contrast novel herbivorous insect-plant interactions that arise due to plant versus insect introductions with the aim of understanding whether the causes and consequences of the interaction depend on which party is non-native. The biotic context of the herbivore-plant interaction, in terms of mutualists, predators, and competitors can limit the prevalence of that interaction and varies between native and introduced ranges. Introduced plants can have a large, direct impact on their environment, whereas the impact of introduced herbivorous insects is often mediated through the plants that they consume.
- Published
- 2014
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43. Aphids decelerate litter nitrogen mineralisation through changes in litter quality
- Author
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Takayuki Ohgushi, Noboru Katayama, Osamu Kishida, and Alessandro Oliveria Silva
- Subjects
Aphid ,Herbivore ,Ecology ,biology ,fungi ,food and beverages ,chemistry.chemical_element ,Aphis glycines ,biochemical phenomena, metabolism, and nutrition ,Plant litter ,biology.organism_classification ,Decomposition ,Nitrogen ,Agronomy ,chemistry ,Insect Science ,Litter ,Herbivorous insects ,reproductive and urinary physiology - Abstract
Herbivorous insects may have significant impacts on litter decomposi- tion through modification of plant litter quality and quantity. The effects of herbivorous insects on decomposition processes are of growing interest. 2. Here, experiments were conducted to examine how sap-feeding aphids modify plant litter and whether the aphid-induced modification influences litter decomposition processes, using a plant-herbivore system consisting of soybean (Glycine max (L.)) and soybean aphids (Aphis glycines Matsumura). 3. First, litter traits produced by aphid-free and aphid-infected plants were compared, and it was found that aphids did not affect litter mass and carbon concentration, but significantly decreased the nitrogen concentration. Such aphid-mediated modification of litter quality may cause deceleration of litter decomposition as the higher C/N ratio inhibits litter decomposition. 4. A decomposition experiment was then carried out to compare the decomposition of litter between the aphid-free and aphid-infected plants. No impacts of aphid herbivory were found on litter carbon mineralisation but negative impacts were found on nitrogen mineralisation. Litter nitrogen mineralisation of aphid-infected plants decreased by 40% and 28% compared with that of aphid-free plants 1 and 3 months after commencement of the experiment, respectively. 5. The experimental results clearly showed that aphids decelerated litter nitrogen mineralisation by modifying litter quality.
- Published
- 2013
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44. Patterns of insect herbivory on four Australian understory plant species
- Author
-
Sabine S. Nooten and Lesley Hughes
- Subjects
Herbivore ,Ecology ,Sclerophyll ,Fauna ,media_common.quotation_subject ,fungi ,Leaf damage ,food and beverages ,Insect ,Understory ,Biology ,stomatognathic system ,Insect Science ,Plant species ,Herbivorous insects ,Agronomy and Crop Science ,Ecology, Evolution, Behavior and Systematics ,media_common - Abstract
Australia harbours a very diverse phytophagous insect fauna, but little is known about the patterns of insect herbivory in dominant forest systems, especially in dry sclerophyll forests. Here, we assess variation in leaf herbivory in four species of narrow-ranged sclerophyllous shrubs across their geographical distribution. We assessed leaf herbivory as the percentage of missing leaf area, and estimated the proportion of damage types, such as chewing, sucking and mining. We found that the levels of leaf herbivory and the proportions of damage types were consistent among plant species but showed considerable variability within single plant species among sites and individual plants. This variability is most likely due to the patchy distribution of herbivorous insects in space and time. Leaf damage was dominated by chewing, but mining and sucking occurred on all plant four species. Sap sucking, although much less conspicuous, was found to be a major damage type, demonstrating that neglect of sap sucking damage in leaf herbivory assessments could lead to a considerable underestimation of the total herbivore damage inflicted on host plants.
- Published
- 2013
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45. Effects of clipping and N fertilization on insect herbivory and infestation by pathogenic fungi on bilberry
- Author
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José Ramón Obeso and Joaquina Pato
- Subjects
Herbivore ,Bilberry ,biology ,ved/biology ,media_common.quotation_subject ,ved/biology.organism_classification_rank.species ,Insect ,Vaccinium myrtillus ,biology.organism_classification ,medicine.disease_cause ,Shrub ,Human fertilization ,Agronomy ,Botany ,Infestation ,medicine ,Herbivorous insects ,Ecology, Evolution, Behavior and Systematics ,media_common - Abstract
Interactions among herbivores or between herbivores and other plant natural enemies, such as fungal pathogens, range from competition to facilitation. Moreover, the outcome of these interactions depends on the ecological context where they occur. In this study we examined the effects of clipping, as a surrogate of herbivory by ungulates, on the damage caused by two types of natural enemies (herbivorous insects and foliar fungal pathogens) on bilberry, Vaccinium myrtillus, in combination with nitrogen (N) fertilization representing current N atmospheric deposition. To examine whether the responses of both these natural enemies were mediated by changes in the plant, we estimated the effects of the treatments on bilberry growth and branching and on chlorophyll content as proxy of N content in leaves. Clipping increased the proportion of leaves damaged by herbivorous insects regardless of whether it was combined with N fertilization or not in 2008. In 2007 and 2009 repeated damage to the shrub also facilitated insect herbivory but only under N applications. Regarding fungal infestation incidence, clipping decreased the proportion of infected leaves in all the years considered but only in fertilized plots. Our results suggest that vertebrate herbivores facilitate insect herbivory and reduce fungal infestation but that these effects are dependent on nutritional conditions. Moreover, we found a negative residual correlation between insect herbivory and fungal infestation on bilberry leaves. Therefore, interactions between insect herbivores and fungal pathogens could be implicated in the final outcome of interactions between browsing ungulates and both bilberry natural enemies.
- Published
- 2013
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46. Plant Communication With Herbivores
- Author
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J.D. Blande
- Subjects
0106 biological sciences ,Herbivore ,Pollination ,Ecology ,media_common.quotation_subject ,fungi ,food and beverages ,Eavesdropping ,Biology ,010603 evolutionary biology ,01 natural sciences ,Competition (biology) ,Sex pheromone ,Evolutionary ecology ,Herbivorous insects ,010606 plant biology & botany ,media_common ,Trophic level - Abstract
Plants and herbivores both release volatile organic compounds that have important roles in mediating important biological functions related to defence and reproduction. Plants emit complex blends of chemicals that are involved in multitrophic interactions, coordination of systemic defence responses and pollination, whereas herbivorous insects release pheromones that play important roles in attracting mates, instigating defence responses and initiating aggregation. Interactions between plants and herbivores have been subject to a wealth of studies and knowledge on their biology, biochemistry, ecology and evolution is constantly expanding. In this chapter the idea of communication between plants and herbivores will be explored. Communication between organisms of consecutive trophic levels is somewhat controversial due to unidirectional reliance and competition precluding some of the requirements of a conventional communication process, but there are growing examples of where chemically mediated interactions between plants and herbivores can be viewed as eavesdropping by a signal recipient, or even as true communication where both chemical emitter and receiver gain a benefit from communication. Examples of herbivores responding to plant-emitted cues and plants responding to herbivore-emitted cues are both explored, and suggestions for future directions in this field are provided.
- Published
- 2017
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47. Higher plasticity in feeding preference of a generalist than a specialist : Experiments with two closely related Helicoverpa species
- Author
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Chen-Zhu Wang, Su Xia Gao, Joop J. A. van Loon, Xin Cheng Zhao, Ying Ma, Qing Bo Tang, Yan Wang, and Dongsheng Zhou
- Subjects
0106 biological sciences ,Oviposition ,lcsh:Medicine ,Zoology ,Helicoverpa armigera ,Generalist and specialist species ,010603 evolutionary biology ,01 natural sciences ,Article ,Life Science ,Animals ,Herbivory ,Laboratory of Entomology ,lcsh:Science ,Helicoverpa ,Herbivore ,Larva ,Multidisciplinary ,biology ,lcsh:R ,fungi ,food and beverages ,Feeding Behavior ,Plants ,biology.organism_classification ,Laboratorium voor Entomologie ,Preference ,Diet ,Lepidoptera ,010602 entomology ,Instar ,lcsh:Q ,Herbivorous insects ,EPS ,Specialization - Abstract
Herbivorous insects have been categorized as generalists or specialists depending on the taxonomic relatedness of the plants they use as food or oviposition substrates. The plasticity in host plant selection behavior of species belonging to the two categories received little attention. In the present work, fifth instar caterpillars of the generalist herbivore Helicoverpa armigera and its closely related species, the specialist Helicoverpa assulta, were fed on common host plants or artificial diet, after which their feeding preference was assessed individually by using dual - and triple- plant choice assays. Results show both the two Helicoverpa species have a preference hierarchy for host plants. Compared to the fixed preference hierarchy of the specialist H. assulta, the generalist H. armigera exhibited extensive plasticity in feeding preference depending on the host plant experienced during larval development. Whereas the specialist H. assulta exhibited a rigid preference in both dual and triple-plant choice assays, our findings demonstrate that the generalist H. armigera expressed stronger preferences in the dual-plant choice assay than in the triple-plant choice assay. Our results provide additional evidence supporting the neural constraints hypothesis which predicts that generalist herbivores make less accurate decisions than specialists when selecting plants.
- Published
- 2017
- Full Text
- View/download PDF
48. Hylobius Abietis L. Feeding On The Novel Host Pinus Brutia Ten. Increases Emission Of Volatile Organic Compounds
- Author
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Jarmo K. Holopainen, Gürkan Semiz, and N. Erbilgin
- Subjects
0106 biological sciences ,volatile organic compound ,seedling ,010603 evolutionary biology ,01 natural sciences ,Terpene ,host plant ,Pinus brutia ,volatile organic compounds ,Botany ,Hylobius abietis ,terpene ,2. Zero hunger ,Herbivore ,biology ,Host (biology) ,Organic chemicals ,herbivory ,Weevil ,beetle ,emission inventory ,fungi ,Hexapoda ,15. Life on land ,biology.organism_classification ,Insect Science ,coniferous tree ,Herbivorous insects ,host expansion ,Agronomy and Crop Science ,terpenes ,feeding ,010606 plant biology & botany ,plant-herbivore interaction - Abstract
Plants respond to feeding by herbivorous insects by producing volatile organic chemicals, which mediate interactions between herbivores and plants. Yet, few studies investigated whether such plant responses to herbivory differ between historical host and novel plants. Here, we investigated whether herbivory by the pine weevil Hylobius abietis causes a release of volatile organic chemicals from a novel tree Pinus brutia and compared the relative amounts of volatiles released from herbivore's historical hosts and P. brutia. We collected volatiles emitted from P. brutia seedlings that were either subjected to feeding by H. abietis or no feeding. Our results indicated that feeding increased emission of volatile compounds, composed of monoterpenes and sesquiterpenes, and that the emission was several fold higher in the damaged seedlings than in undamaged seedlings. In particular, emission of monoterpenes and sesquiterpenes increased by 4.4-and 10-fold in the damaged plants, respectively. Strikingly, individual monoterpenes and sesquiterpenes showed much greater dissimilarity between damaged and undamaged seedlings. Furthermore, several minor monoterpenes showed negative relationships with the weevil gnawed area. We discussed these results with the results of previous studies focused on historical host plants of H. abietis and hypothesized the ecological relevance and importance of our results pertaining relevance to the plant–herbivory interactions. © 2016 Blackwell Verlag GmbH
- Published
- 2017
49. Nonadaptive Radiation: Pervasive diet specialization by drift in scale insects?
- Author
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Daniel A. Peterson, Benjamin B. Normark, and Nate B. Hardy
- Subjects
0106 biological sciences ,0301 basic medicine ,Scale (anatomy) ,Insecta ,Diversification (marketing strategy) ,Biology ,010603 evolutionary biology ,01 natural sciences ,Evolution, Molecular ,03 medical and health sciences ,Magnoliopsida ,Genetic drift ,Phylogenetics ,Specialization (functional) ,Genetics ,Animals ,Biomass ,Herbivory ,Ecology, Evolution, Behavior and Systematics ,Phylogeny ,030304 developmental biology ,0303 health sciences ,Herbivore ,Extinction ,Phylogenetic tree ,Models, Genetic ,Ecology ,Host (biology) ,Genetic Drift ,Genetic Variation ,Adaptation, Physiological ,030104 developmental biology ,Negative relationship ,Evolutionary biology ,Plant species ,Herbivorous insects ,General Agricultural and Biological Sciences - Abstract
At least half of metazoan species are herbivorous insects. Why are they so diverse? Most herbivorous insects feed on few plant species, and adaptive host specialization is often invoked to explain their diversification. Nevertheless, it is possible that the narrow host ranges of many herbivorous insects are non-adaptive. Here, we test predictions of this hypothesis with comparative phylogenetic analyses of scale insects, a group for which there appears to be few host-use tradeoffs that would select against polyphagy, and for which passive wind-dispersal should make host specificity costly. We infer a strong positive relationship between host range and diversification rate, and a marked asymmetry in cladogenetic changes in diet breadth. These results are consonant with a system of pervasive non-adaptive host specialization in which small, drift-and extinction-prone populations are frequently isolated from persistent and polyphagous source populations. They also contrast with the negative relationship between diet breadth and taxonomic diversification that has been estimated in butterflies, a disparity which likely stems from differences in the average costs and benefits of host specificity and generalism in scale insects vs. butterflies. Our results indicate the potential for non-adaptive processes to be important to diet-breadth evolution and taxonomic diversification across herbivorous insects.
- Published
- 2016
- Full Text
- View/download PDF
50. Resisting the onset of herbivore attack: plants perceive and respond to insect eggs
- Author
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Monika Hilker and Nina E. Fatouros
- Subjects
0106 biological sciences ,0301 basic medicine ,Insecta ,media_common.quotation_subject ,Plant Science ,Insect ,Biology ,01 natural sciences ,03 medical and health sciences ,Botany ,Plant defense against herbivory ,Life Science ,Animals ,Herbivory ,media_common ,Larva ,Herbivore ,Hatching ,fungi ,food and beverages ,Plants ,Biosystematiek ,Plant Leaves ,030104 developmental biology ,embryonic structures ,Biosystematics ,Herbivorous insects ,EPS ,Desiccation ,010606 plant biology & botany - Abstract
Plants can respond to attack by herbivorous insects very soon after herbivores start producing a new generation by depositing eggs onto their leaves. Egg-induced plant responses may result in killing the attacker in its egg stage. However, if the eggs do survive, they can also prime feeding-induced plant defenses against the larvae hatching from eggs. In this paper we focus first on egg-induced plant responses that resemble hypersensitive responses (HR) to phytopathogens and lead to egg desiccation or detachment from plants. We then summarize the current knowledge about egg-mediated effects on feeding-induced plant defenses against larvae. Finally, we discuss the insect species specificity of plant responses to eggs and the variability of insect susceptibility to these responses.
- Published
- 2016
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