| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1890/14-1474.1 |
| P8608 | Fatcat ID | release_bxv63fyucrdzzjunb73ps5vsxm |
| P698 | PubMed publication ID | 26236859 |
| P5875 | ResearchGate publication ID | 270591138 |
| P50 | author | Anurag A. Agrawal | Q16769581 |
| André Kessler | Q57548782 | ||
| Robert A. Raguso | Q61948939 | ||
| Angela E. Douglas | Q64358875 | ||
| Georg Jander | Q64810691 | ||
| Jennifer S. Thaler | Q109208569 | ||
| Katja Poveda | Q31043012 | ||
| P2860 | cites work | Hyperparasitoids use herbivore-induced plant volatiles to locate their parasitoid host | Q21092708 |
| The evolution of cooperation | Q22065515 | ||
| Glucosinolate metabolites required for an Arabidopsis innate immune response | Q24645375 | ||
| Achieving food security for one million sub-Saharan African poor through push-pull innovation by 2020 | Q26829253 | ||
| Hawaiian ant–flower networks: nectar-thieving ants prefer undefended native over introduced plants with floral defenses | Q56761720 | ||
| Herbivore-induced plant responses inBrassica oleraceaprevail over effects of constitutive resistance and result in enhanced herbivore attack | Q56998913 | ||
| Marine chemical ecology: what's known and what's next? | Q57067967 | ||
| Floral volatiles controlling ant behaviour | Q57230006 | ||
| Rhizobacterial volatile emissions regulate auxin homeostasis and cell expansion in Arabidopsis | Q58324758 | ||
| Ecological Complexity and Pest Control in Organic Coffee Production: Uncovering an Autonomous Ecosystem Service | Q58709918 | ||
| Acute olfactory response of Culex mosquitoes to a human- and bird-derived attractant | Q27490228 | ||
| The raison d'ĕtre of secondary plant substances; these odd chemicals arose as a means of protecting plants from insects and now guide insects to food | Q28185035 | ||
| Control of witchweed Striga hermonthica by intercropping with Desmodium spp., and the mechanism defined as allelopathic | Q28216023 | ||
| Postsecretory hydrolysis of nectar sucrose and specialization in ant/plant mutualism | Q28246427 | ||
| The use of push-pull strategies in integrated pest management | Q28263171 | ||
| Widespread adoption of Bt cotton and insecticide decrease promotes biocontrol services | Q28269361 | ||
| Mirid bug outbreaks in multiple crops correlated with wide-scale adoption of Bt cotton in China | Q28282425 | ||
| Whiteflies interfere with indirect plant defense against spider mites in Lima bean | Q28472362 | ||
| Exposure of unwounded plants to chemical cues associated with herbivores leads to exposure-dependent changes in subsequent herbivore attack | Q28535311 | ||
| Floral scents repel facultative flower visitors, but attract obligate ones | Q28752439 | ||
| Evolutionary ecology of pungency in wild chilies | Q28756712 | ||
| The evolution of chemical defences and mating systems in tiger moths (Lepidoptera: Arctiidae) | Q29028485 | ||
| The exploitation of mutualisms | Q29396946 | ||
| Alarm pheromone habituation in Myzus persicae has fitness consequences and causes extensive gene expression changes | Q30476970 | ||
| Neuroecology, chemical defense, and the keystone species concept | Q33310584 | ||
| Sex pheromones and their impact on pest management | Q33527025 | ||
| Pseudomonas syringae manipulates systemic plant defenses against pathogens and herbivores | Q33818683 | ||
| Keys to symbiotic harmony | Q33994648 | ||
| Malaria-induced changes in host odors enhance mosquito attraction | Q34002514 | ||
| A plant flavone, luteolin, induces expression of Rhizobium meliloti nodulation genes | Q34189021 | ||
| Community ecology and the evolution of molecules of keystone significance | Q34308991 | ||
| How caterpillar-damaged plants protect themselves by attracting parasitic wasps | Q34309694 | ||
| 'Real time' genetic manipulation: a new tool for ecological field studies | Q34309707 | ||
| Evolutionary change from induced to constitutive expression of an indirect plant resistance | Q34331974 | ||
| Insect resistance to Bt crops: lessons from the first billion acres | Q34349837 | ||
| A bacterial symbiont is converted from an inedible producer of beneficial molecules into food by a single mutation in the gacA gene | Q34360678 | ||
| Phenotypic plasticity in the interactions and evolution of species | Q34399753 | ||
| Biochemistry and genetics of insect resistance to Bacillus thuringiensis. | Q34453767 | ||
| Linking aboveground and belowground interactions via induced plant defenses | Q34526239 | ||
| Integrated pest management: the push-pull approach for controlling insect pests and weeds of cereals, and its potential for other agricultural systems including animal husbandry | Q34655737 | ||
| Fragments of ATP synthase mediate plant perception of insect attack. | Q34695548 | ||
| Field experiments with transformed plants reveal the sense of floral scents | Q34816501 | ||
| Suppression of cotton bollworm in multiple crops in China in areas with Bt toxin-containing cotton. | Q34831042 | ||
| Distinguishing mechanisms for the evolution of co-operation | Q45002918 | ||
| Dosage-dependent impacts of a floral volatile compound on pollinators, larcenists, and the potential for floral evolution in the alpine skypilot Polemonium viscosum | Q45242844 | ||
| Damaged-self recognition in plant herbivore defence. | Q45961966 | ||
| Herbivory-mediated pollinator limitation: negative impacts of induced volatiles on plant-pollinator interactions | Q46330361 | ||
| Response of economically important aphids to components of Hemizygia petiolata essential oil. | Q46628802 | ||
| Prey perception of predation risk: volatile chemical cues mediate non-consumptive effects of a predator on a herbivorous insect | Q46836917 | ||
| The sensory ecology of nonconsumptive predator effects | Q46861938 | ||
| Exploring plant defense theory in tall goldenrod, Solidago altissima. | Q46921853 | ||
| Petunia flowers solve the defence/apparency dilemma of pollinator attraction by deploying complex floral blends. | Q50547975 | ||
| Chemical ecology in the post genomics era. | Q51162745 | ||
| Forest succession suppressed by an introduced plant-fungal symbiosis. | Q51709155 | ||
| Benzoxazinoid metabolites regulate innate immunity against aphids and fungi in maize. | Q51861985 | ||
| Above- and below-ground impacts of introduced predators in seabird-dominated island ecosystems. | Q52575122 | ||
| AFTER PESTICIDES--WHAT? | Q52632254 | ||
| Host plant influences on sex pheromone behavior of phytophagous insects. | Q52646423 | ||
| Oceanic phytoplankton, atmospheric sulphur, cloud albedo and climate | Q55868942 | ||
| Plant-Animal Mutualistic Networks: The Architecture of Biodiversity | Q56136814 | ||
| Evolutionary stability of mutualism between yuccas and yucca moths | Q56623286 | ||
| The genetic architecture of maize flowering time. | Q34996049 | ||
| Explaining intraspecific diversity in plant secondary metabolites in an ecological context | Q35015487 | ||
| Symbiotic bacteria appear to mediate hyena social odors | Q35039174 | ||
| The contribution of trait-mediated indirect effects to the net effects of a predator | Q35045483 | ||
| Novel chemistry of invasive exotic plants | Q35104138 | ||
| New synthesis: parallels between biodiversity and chemodiversity | Q35109781 | ||
| Synthesis of caeliferins, elicitors of plant immune responses: accessing lipophilic natural products via cross metathesis | Q35551187 | ||
| Parasitoid-specific induction of plant responses to parasitized herbivores affects colonization by subsequent herbivores. | Q35621376 | ||
| PROGRAMMED CELL DEATH IN PLANT-PATHOGEN INTERACTIONS. | Q35687230 | ||
| Marine chemical ecology: chemical signals and cues structure marine populations, communities, and ecosystems. | Q36049139 | ||
| Botanical insecticides, deterrents, and repellents in modern agriculture and an increasingly regulated world | Q36332731 | ||
| Sexually transmitted chemical defense in a moth (Utetheisa ornatrix). | Q36358955 | ||
| The role of root exudates in rhizosphere interactions with plants and other organisms | Q36466505 | ||
| Exposure of Solidago altissima plants to volatile emissions of an insect antagonist (Eurosta solidaginis) deters subsequent herbivory | Q36512380 | ||
| Potential of mass trapping for long-term pest management and eradication of invasive species | Q36635296 | ||
| Chemical cues, defence metabolites and the shaping of pelagic interspecific interactions | Q36727257 | ||
| Salmon lice--impact on wild salmonids and salmon aquaculture. | Q36910247 | ||
| Codling moth management and chemical ecology | Q36945042 | ||
| Phytohormone-based activity mapping of insect herbivore-produced elicitors. | Q37062129 | ||
| Overexpression of the Bacillus thuringiensis (Bt) Cry2Aa2 protein in chloroplasts confers resistance to plants against susceptible and Bt-resistant insects | Q37160225 | ||
| A gain-of-function polymorphism controlling complex traits and fitness in nature. | Q37413418 | ||
| Evidence that dimethyl sulfide facilitates a tritrophic mutualism between marine primary producers and top predators | Q37659968 | ||
| Chemical interaction between undamaged plants--effects on herbivores and natural enemies | Q37851195 | ||
| Plants and insect eggs: how do they affect each other? | Q37858024 | ||
| Evolution of jasmonate and salicylate signal crosstalk | Q38002244 | ||
| The physiological importance of glucosinolates on plant response to abiotic stress in Brassica | Q38110726 | ||
| Allelochemics: Chemical Interactions between Species | Q38586220 | ||
| Genetic architecture of maize kernel composition in the nested association mapping and inbred association panels | Q39680279 | ||
| Some general comments on the evolution and design of animal communication systems. | Q40711293 | ||
| Recent advances in systemic acquired resistance research--a review | Q41256945 | ||
| Marine tubeworm metamorphosis induced by arrays of bacterial phage tail-like structures | Q41814136 | ||
| Synergistic Effects of Amides from Two Piper Species on Generalist and Specialist Herbivores | Q42019866 | ||
| Insect eggs suppress plant defence against chewing herbivores | Q42021666 | ||
| Tree fruit IPM programs in the western United States: the challenge of enhancing biological control through intensive management | Q42024093 | ||
| Early season herbivore differentially affects plant defence responses to subsequently colonizing herbivores and their abundance in the field. | Q42028862 | ||
| Silencing the jasmonate cascade: induced plant defenses and insect populations | Q42044346 | ||
| Herbivory: caterpillar saliva beats plant defences. | Q42051801 | ||
| Identification of olfactory cues used in host-plant finding by diamondback moth,Plutella xylostella (Lepidoptera: Plutellidae). | Q42068217 | ||
| Responses of Glossina morsitans morsitans to blends of electroantennographically active compounds in the odors of its preferred (buffalo and ox) and nonpreferred (waterbuck) hosts | Q44697989 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P6104 | maintained by WikiProject | WikiProject Ecology | Q10818384 |
| P1104 | number of pages | 14 | |
| P304 | page(s) | 617-630 | |
| P577 | publication date | 2015-03-01 | |
| P1433 | published in | Ecology | Q1013420 |
| P1476 | title | The raison d'être of chemical ecology | |
| P478 | volume | 96 |
| Q36196344 | A multifunctional chemical cue drives opposing demographic processes and structures ecological communities |
| Q48741063 | Beyond the beaten path: improving natural products bioprospecting using an eco-evolutionary framework - the case of the octocorals |
| Q98946167 | Chemical novelty facilitates herbivore resistance and biological invasions in some introduced plant species |
| Q92051900 | Context-Dependence and the Development of Push-Pull Approaches for Integrated Management of Drosophila suzukii |
| Q55284839 | Current Challenges in Plant Eco-Metabolomics. |
| Q36381192 | Defence syndromes in lodgepole - whitebark pine ecosystems relate to degree of historical exposure to mountain pine beetles. |
| Q30316300 | Diacetin, a reliable cue and private communication channel in a specialized pollination system |
| Q55249134 | Discovering variation of secondary metabolite diversity and its relationship with disease resistance in Cornus florida L. |
| Q41990687 | Feeding guild of non-host community members affects host-foraging efficiency of a parasitic wasp. |
| Q57066695 | Herbivore-specific induction of defence metabolites in a grass-endophyte association |
| Q57147868 | Horizontal gene cluster transfer increased hallucinogenic mushroom diversity |
| Q51309093 | Introduction to a Virtual Special Issue on plant volatiles. |
| Q33834080 | Marine Mollusk-Derived Agents with Antiproliferative Activity as Promising Anticancer Agents to Overcome Chemotherapy Resistance. |
| Q57470826 | Modelling habituation of introduced predators to unrewarding bird odors for conservation of ground-nesting shorebirds |
| Q107038814 | Plant Secondary Metabolite Diversity and Species Interactions |
| Q38605749 | Plant Volatilome in Greece: a Review on the Properties, Prospects, and Chemogeography |
| Q28551637 | Possible Synergistic Effects of Thymol and Nicotine Against Crithidia bombi Parasitism in Bumble Bees |
| Q39129970 | The geographic mosaic of plant chemistry and its effects on community and population genetic diversity. |
| Q114866709 | Tree species richness differentially affects the chemical composition of leaves, roots and root exudates in four subtropical tree species |
| Q38948837 | Why do plants produce so many terpenoid compounds? |
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