| scholarly article | Q13442814 |
| P50 | author | Jarmo K Holopainen | Q42305879 |
| James Blande | Q42862991 | ||
| P2860 | cites work | Effects of feeding Spodoptera littoralis on lima bean leaves. II. Continuous mechanical wounding resembling insect feeding is sufficient to elicit herbivory-related volatile emission | Q24520346 |
| Caterpillar-induced nocturnal plant volatiles repel conspecific females | Q28209236 | ||
| Effects of air pollution on biogenic volatiles and ecological interactions | Q30448152 | ||
| Within-plant signaling by volatiles leads to induction and priming of an indirect plant defense in nature | Q30479175 | ||
| Restoring a maize root signal that attracts insect-killing nematodes to control a major pest | Q30489500 | ||
| Smelling global climate change: mitigation of function for plant volatile organic compounds | Q33422704 | ||
| Biogenic volatile organic compounds in the Earth system | Q33440814 | ||
| Two terpene synthases are responsible for the major sesquiterpenes emitted from the flowers of kiwifruit (Actinidia deliciosa). | Q33465449 | ||
| New particle formation in forests inhibited by isoprene emissions | Q33504015 | ||
| BVOCs and global change | Q33526133 | ||
| Deceptive chemical signals induced by a plant virus attract insect vectors to inferior hosts | Q33734401 | ||
| Ecological role of volatiles produced by plants in response to damage by herbivorous insects. | Q33763784 | ||
| Gaia: the living Earth | Q34285043 | ||
| Physiological and physicochemical controls on foliar volatile organic compound emissions | Q34311038 | ||
| Plant volatiles induced by herbivore egg deposition affect insects of different trophic levels | Q34389700 | ||
| Recruitment of entomopathogenic nematodes by insect-damaged maize roots | Q34409563 | ||
| Ecosystem engineering in space and time. | Q34606759 | ||
| Exploitation of herbivore-induced plant odors by host-seeking parasitic wasps | Q34683516 | ||
| Airborne signals prime plants against insect herbivore attack | Q36162493 | ||
| Defense-inducing volatiles: in search of the active motif | Q36638940 | ||
| Male-derived butterfly anti-aphrodisiac mediates induced indirect plant defense. | Q36786790 | ||
| Behavioural and community ecology of plants that cry for help | Q37330575 | ||
| Deposition Fluxes of Terpenes over Grassland | Q37417956 | ||
| The underestimated role of roots in defense against leaf attackers | Q37593281 | ||
| The evolutionary context for herbivore-induced plant volatiles: beyond the 'cry for help'. | Q37667232 | ||
| Induced BVOCs: how to bug our models? | Q37673473 | ||
| Plant volatile organic compounds (VOCs) in ozone (O3) polluted atmospheres: the ecological effects. | Q37677608 | ||
| Abiotic stresses and induced BVOCs | Q37687625 | ||
| Multiple stress factors and the emission of plant VOCs | Q37689942 | ||
| Perception of plant volatile blends by herbivorous insects--finding the right mix. | Q37877355 | ||
| Detection of diseased plants by analysis of volatile organic compound emission. | Q37887781 | ||
| Can forest trees compensate for stress-generated growth losses by induced production of volatile compounds? | Q37960262 | ||
| The specificity of herbivore-induced plant volatiles in attracting herbivore enemies | Q38002641 | ||
| Evolutionary models of extended phenotypes | Q38029453 | ||
| Defoliation of alders (Alnus glutinosa) affects herbivory by leaf beetles on undamaged neighbours | Q38762460 | ||
| Damage-induced resistance in sagebrush: volatiles are key to intra- and interplant communication | Q39121094 | ||
| Short signalling distances make plant communication a soliloquy | Q41140744 | ||
| Impact of changes in diffuse radiation on the global land carbon sink | Q41996830 | ||
| Plasma membrane potential depolarization and cytosolic calcium flux are early events involved in tomato (Solanum lycopersicon) plant-to-plant communication. | Q42011429 | ||
| Function of defensive volatiles in pedunculate oak (Quercus robur) is tricked by the moth Tortrix viridana | Q42013003 | ||
| Volatile emissions from Alnus glutionosa induced by herbivory are quantitatively related to the extent of damage | Q42018660 | ||
| Real-time monitoring of herbivore induced volatile emissions in the field | Q42022810 | ||
| Herbivore-induced volatiles in the perennial shrub, Vaccinium corymbosum, and their role in inter-branch signaling | Q42026599 | ||
| Priming defense genes and metabolites in hybrid poplar by the green leaf volatile cis-3-hexenyl acetate. | Q42028191 | ||
| Within-plant signalling via volatiles overcomes vascular constraints on systemic signalling and primes responses against herbivores | Q42033367 | ||
| Oviposition by pierid butterflies triggers defense responses in Arabidopsis | Q42035267 | ||
| Role of the lipoxygenase/lyase pathway of host-food plants in the host searching behavior of two parasitoid species, Cotesia glomerata and Cotesia plutellae | Q42037195 | ||
| Priming of plant defense responses in nature by airborne signaling between Artemisia tridentata and Nicotiana attenuata | Q42038458 | ||
| Emission of Plutella xylostella-induced compounds from cabbages grown at elevated CO2 and orientation behavior of the natural enemies. | Q42043956 | ||
| Individual variability in herbivore-specific elicitors from the plant's perspective | Q42044299 | ||
| On the direct effect of clouds and atmospheric particles on the productivity and structure of vegetation. | Q42044406 | ||
| Defensive function of herbivore-induced plant volatile emissions in nature. | Q42054565 | ||
| Leaf rust induced volatile organic compounds signalling in willow during the infection | Q43085772 | ||
| Birch (Betula spp.) leaves adsorb and re-release volatiles specific to neighbouring plants--a mechanism for associational herbivore resistance? | Q43125151 | ||
| Attacks by a piercing-sucking insect (Myzus persicae Sultzer) or a chewing insect (Leptinotarsa decemlineata Say) on potato plants (Solanum tuberosum L.) induce differential changes in volatile compound release and oxylipin synthesis | Q43160584 | ||
| Foliar methyl salicylate emissions indicate prolonged aphid infestation on silver birch and black alder | Q43185292 | ||
| Airborne induction and priming of plant defenses against a bacterial pathogen. | Q43265417 | ||
| The effects of abiotic factors on induced volatile emissions in corn plants | Q44062049 | ||
| Needle removal by pine sawfly larvae increases branch-level VOC emissions and reduces below-ground emissions of Scots pine | Q44391873 | ||
| Change in acceptability of barley plants to aphids after exposure to allelochemicals from couch-grass (Elytrigia repens). | Q44434063 | ||
| Cross-kingdom effects of plant-plant signaling via volatile organic compounds emitted by tomato (Solanum lycopersicum) plants infested by the greenhouse whitefly (Trialeurodes vaporariorum). | Q44669054 | ||
| Qualitative and quantitative variation among volatile profiles induced by Tetranychus urticae feeding on plants from various families | Q44837488 | ||
| The major volatile organic compound emitted from Arabidopsis thaliana flowers, the sesquiterpene (E)-β-caryophyllene, is a defense against a bacterial pathogen | Q44971700 | ||
| Exposure of lima bean leaves to volatiles from herbivore-induced conspecific plants results in emission of carnivore attractants: active or passive process? | Q45123092 | ||
| Self-recognition affects plant communication and defense. | Q46014218 | ||
| The role of ozone-reactive compounds, terpenes, and green leaf volatiles (glvs), in the orientation of Cotesia plutellae. | Q50659626 | ||
| Ozone degrades common herbivore-induced plant volatiles: does this affect herbivore prey location by predators and parasitoids? | Q50695041 | ||
| Explaining evolution of plant communication by airborne signals. | Q51647259 | ||
| Plant VOC emissions: making use of the unavoidable. | Q51727313 | ||
| Dynamic pathway allocation in early terpenoid biosynthesis of stress-induced lima bean leaves. | Q51729737 | ||
| Developmental stage of herbivorePseudaletia separata affects production of herbivore-induced synomone by corn plants. | Q52209543 | ||
| Priming of indirect defences. | Q52669351 | ||
| Effect of bark beetle infestation on secondary organic aerosol precursor emissions. | Q52736968 | ||
| Specific herbivore-induced volatiles defend plants and determine insect community composition in the field. | Q52740567 | ||
| Kin recognition affects plant communication and defence. | Q52751169 | ||
| Growth parameters and resistance against Drechslera teres of spring barley (Hordeum vulgare L. cv. Scarlett) grown at elevated ozone and carbon dioxide concentrations. | Q53738564 | ||
| Gaia and natural selection. | Q55067737 | ||
| An amorphous solid state of biogenic secondary organic aerosol particles | Q57113715 | ||
| Air pollution impedes plant-to-plant communication by volatiles | Q57555615 | ||
| Direct Observations of Atmospheric Aerosol Nucleation | Q57689182 | ||
| Clean the Air, Heat the Planet? | Q58065040 | ||
| ATMOSPHERIC SCIENCE: How Particles Nucleate and Grow | Q58065371 | ||
| Soil Nitrite as a Source of Atmospheric HONO and OH Radicals | Q58684312 | ||
| Transgenic, non-isoprene emitting poplars don’t like it hot | Q59603130 | ||
| Foliar limonene uptake scales positively with leaf lipid content: “non-emitting” species absorb and release monoterpenes | Q60448907 | ||
| Induced plant volatiles: from genes to climate change | Q61761923 | ||
| Attraction of Phytoseiulus persimilis (Acari: Phytoseiidae) towards volatiles from various Tetranychus urticae-infested plant species | Q61762053 | ||
| A Significant Role for Nitrate and Peroxide Groups on Indoor Secondary Organic Aerosol | Q63487806 | ||
| Volatile dose and exposure time impact perception in neighboring plants | Q83427989 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | herbivore | Q59099 |
| herbivory | Q45874067 | ||
| plant volatile | Q124159016 | ||
| P304 | page(s) | 185 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | Frontiers in Plant Science | Q27723840 |
| P1476 | title | Where do herbivore-induced plant volatiles go? | |
| P478 | volume | 4 |
| Q35518522 | Associational susceptibility in broccoli: mediated by plant volatiles, impeded by ozone |
| Q41139799 | Atmospheric transformation of plant volatiles disrupts host plant finding |
| Q39065656 | Biological Activities of Essential Oils: From Plant Chemoecology to Traditional Healing Systems. |
| Q41109834 | Bottom-up effects on herbivore-induced plant defences: a case study based on compositional patterns of rhizosphere microbial communities |
| Q90713650 | Copitarsia decolora Guenée (Lepidoptera: Noctuidae) females avoid larvae competition by detecting larvae damaged plants |
| Q92007906 | Defense of pyrethrum flowers: repelling herbivores and recruiting carnivores by producing aphid alarm pheromone |
| Q49290672 | Disproportionate photosynthetic decline and inverse relationship between constitutive and induced volatile emissions upon feeding of Quercus robur leaves by large larvae of gypsy moth (Lymantria dispar). |
| Q57555587 | Do Insectivorous Birds use Volatile Organic Compounds from Plants as Olfactory Foraging Cues? Three Experimental Tests |
| Q90186625 | Eavesdropping on gall-plant interactions: the importance of the signaling function of induced volatiles |
| Q41991951 | Elevated Ozone Modulates Herbivore-Induced Volatile Emissions of Brassica nigra and Alters a Tritrophic Interaction |
| Q38971944 | Elm leaves 'warned' by insect egg deposition reduce survival of hatching larvae by a shift in their quantitative leaf metabolite pattern |
| Q41766972 | Environmental conditions regulate the impact of plants on cloud formation |
| Q89876984 | Environmental decomposition of olefinic cuticular hydrocarbons of Periplaneta americana generates a volatile pheromone that guides social behaviour |
| Q38801690 | Herbivory by an Outbreaking Moth Increases Emissions of Biogenic Volatiles and Leads to Enhanced Secondary Organic Aerosol Formation Capacity |
| Q41504218 | Identification of an insect-produced olfactory cue that primes plant defenses. |
| Q41902344 | Induced plant responses to microbes and insects |
| Q37502283 | Innate and Learned Olfactory Responses in a Wild Population of the Egg Parasitoid Trichogramma (Hymenoptera: Trichogrammatidae). |
| Q49578682 | Methyl jasmonate-induced emission of biogenic volatiles is biphasic in cucumber: a high-resolution analysis of dose dependence |
| Q92267133 | Non-invasive plant disease diagnostics enabled by smartphone-based fingerprinting of leaf volatiles |
| Q91936766 | Olfactory response of Mahanarva spectabilis (Hemiptera: Cercopidae) to volatile organic compounds from forage grasses |
| Q98772275 | Ozone affects plant, insect, and soil microbial communities: A threat to terrestrial ecosystems and biodiversity |
| Q51335530 | Ozone degrades floral scent and reduces pollinator attraction to flowers. |
| Q38205015 | Plant volatiles in polluted atmospheres: stress responses and signal degradation |
| Q100752718 | Policy, toxicology and physicochemical considerations on the inhalation of high concentrations of food flavour |
| Q35750802 | Priming and memory of stress responses in organisms lacking a nervous system |
| Q38254533 | Recent Advances in the Application of Metabolomics to Studies of Biogenic Volatile Organic Compounds (BVOC) Produced by Plant |
| Q97548212 | Seasonal and environmental variation in volatile emissions of the New Zealand native plant Leptospermum scoparium in weed-invaded and non-invaded sites |
| Q90218902 | Sequestration of Exogenous Volatiles by Plant Cuticular Waxes as a Mechanism of Passive Associational Resistance: A Proof of Concept |
| Q28068326 | Stress-Mediated cis-Element Transcription Factor Interactions Interconnecting Primary and Specialized Metabolism in planta |
| Q40623626 | Temperature dependencies of Henry's law constants for different plant sesquiterpenes |
| Q38936262 | Three odorant binding proteins may regulate the behavioural response of Chrysopa pallens to plant volatiles and the aphid alarm pheromone (E)-β-farnesene |
| Q58763327 | Understorey Rhododendron tomentosum and Leaf Trichome Density Affect Mountain Birch VOC Emissions in the Subarctic |
| Q38476928 | Volatile organic compounds as non-invasive markers for plant phenotyping. |
| Q55259159 | Volatile β-Ocimene Can Regulate Developmental Performance of Peach Aphid Myzus persicae Through Activation of Defense Responses in Chinese Cabbage Brassica pekinensis. |
| Q41987360 | Volatile-Mediated Interactions between Cabbage Plants in the Field and the Impact of Ozone Pollution. |
| Q92079899 | What makes a volatile organic compound a reliable indicator of insect herbivory? |
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