about
Hyperparasitoids use herbivore-induced plant volatiles to locate their parasitoid hostAttractiveness of volatiles from different body parts to the malaria mosquito Anopheles coluzzii is affected by deodorant compoundsSynergism in the effect of prior jasmonic acid application on herbivore-induced volatile emission by Lima bean plants: transcription of a monoterpene synthase gene and volatile emissionPlant volatiles induced by herbivore egg deposition affect insects of different trophic levels.Understanding the long-lasting attraction of malaria mosquitoes to odor baitsHerbivore-mediated effects of glucosinolates on different natural enemies of a specialist aphid.Rhizobacterial colonization of roots modulates plant volatile emission and enhances the attraction of a parasitoid wasp to host-infested plantsCovariation and phenotypic integration in chemical communication displays: biosynthetic constraints and eco-evolutionary implications.Integrating Insect Life History and Food Plant Phenology: Flexible Maternal Choice Is Adaptive.Qualitative and Quantitative Differences in Herbivore-Induced Plant Volatile Blends from Tomato Plants Infested by Either Tuta absoluta or Bemisia tabaci.Drought stress affects plant metabolites and herbivore preference but not host location by its parasitoids.Virulence factors of geminivirus interact with MYC2 to subvert plant resistance and promote vector performance.Attraction of egg-killing parasitoids toward induced plant volatiles in a multi-herbivore context.Parasitism overrides herbivore identity allowing hyperparasitoids to locate their parasitoid host using herbivore-induced plant volatiles.To be in time: egg deposition enhances plant-mediated detection of young caterpillars by parasitoids.Effect of sequential induction by Mamestra brassicae L. and Tetranychus urticae Koch on lima bean plant indirect defense.Body odors of parasitized caterpillars give away the presence of parasitoid larvae to their primary hyperparasitoid enemies.Caterpillar-induced plant volatiles remain a reliable signal for foraging wasps during dual attack with a plant pathogen or non-host insect herbivore.Canopy light cues affect emission of constitutive and methyl jasmonate-induced volatile organic compounds in Arabidopsis thaliana.Solid phase extraction in combination with comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry for the detailed investigation of volatiles in South African red wines.Analysis of volatiles in Pinotage wines by stir bar sorptive extraction and chemometric profiling.Genetic engineering of plant volatile terpenoids: effects on a herbivore, a predator and a parasitoid.Altered volatile profile associated with precopulatory mate guarding attracts spider mite males.Trading direct for indirect defense? Phytochrome B inactivation in tomato attenuates direct anti-herbivore defenses whilst enhancing volatile-mediated attraction of predators.Application of a headspace sorptive extraction method for the analysis of volatile components in South African wines.Non-pathogenic rhizobacteria interfere with the attraction of parasitoids to aphid-induced plant volatiles via jasmonic acid signalling.Compatible and incompatible pathogen-plant interactions differentially affect plant volatile emissions and the attraction of parasitoid waspsVolatile-mediated foraging behaviour of three parasitoid species under conditions of dual insect herbivore attackDo apes smell like humans? The role of skin bacteria and volatiles of primates in mosquito host selectionNeonates know better than their mothers when selecting a host plantCharacterisation of volatile components of Pinotage wines using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC–TOFMS)Chemometric investigation of the volatile content of young South African wines
P50
Q21092708-685D0C91-0416-45FD-9FFC-B6B022E175CDQ26315414-BC4EDB1C-1538-4B42-9EC4-D6840300896DQ28542551-CC180250-6661-44A4-A118-B229BBDBBE76Q34389700-41BF048B-11CB-4EE2-9736-B33C261CE04AQ35208605-608007AF-A432-4212-B6F7-9C4E83B0DF7AQ35714311-3180815A-393B-4DD4-A232-5973D11A707EQ35863330-965D3DCD-E11E-4154-88FA-6F1EBE3959C3Q36296355-3F359022-2ED5-4AF1-8C35-061466CE866BQ37210007-99DB39D7-A850-4144-9C99-FBDF991BA8FBQ37672485-1A17ED7F-FE6A-4717-B950-735807821DA4Q39585975-C2113D55-EBEE-4BCE-9535-043889A6C4CAQ41608521-AD494887-C8F3-4386-9EA4-7187F2D22B4BQ41998244-F9EB30BC-8F9A-47E4-900D-2A5B42371F3CQ41998979-C8690D4F-A1C2-4784-BF85-5A36B7DB3D0EQ42001355-71BF18D1-EEA2-4E09-8F3B-742E82CC404DQ42001510-C142CFA9-67A1-4EE3-90B3-198166BEA54EQ42001563-ABB8AF1B-E4FF-4F0C-B1E0-9E79C56A7D8AQ42004108-2CA716A9-6590-4A42-BC69-5180C5AD7889Q42007701-8D85ADCD-BC97-4EDF-9632-2A4BE4CCFB78Q45967487-7CC9B85F-B341-4EBB-BCA4-65E578048C74Q46211491-5F0A076F-8ED3-48F6-9B4F-10209CC4151DQ46215264-D7A458FE-E1E4-48DC-ADE6-CD25FA3FA081Q46783554-4E3DE214-1055-4943-B1FD-877DF3FAD109Q50227953-8FBB6E87-E484-4023-AAE2-C76021463878Q50674059-FB445D29-EEF1-4018-B9EA-000CA5159291Q51556026-8939C9AC-D2D9-437B-9F88-629461A453D7Q60546317-1ABDD8E3-B70E-4D17-9A90-AEA93568DD5FQ60546322-15F3DBC2-B3BF-4E78-B552-EFEFD77F8EBDQ61761769-7E8487B3-A707-40F9-B338-2623E7EA607EQ61761867-280DA3AE-084F-45F3-895B-2AB485E8B435Q61948943-B61827F6-902C-4C1B-817D-A10BA14C7501Q61948944-1D53B6E8-28E3-4AF8-9F4C-557D1476F634
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Berhane T Weldegergis
@nl
Berhane T Weldegergis
@sl
Berhane T. Weldegergis
@en
Berhane T. Weldegergis
@es
type
label
Berhane T Weldegergis
@nl
Berhane T Weldegergis
@sl
Berhane T. Weldegergis
@en
Berhane T. Weldegergis
@es
prefLabel
Berhane T Weldegergis
@nl
Berhane T Weldegergis
@sl
Berhane T. Weldegergis
@en
Berhane T. Weldegergis
@es
P106
P1153
22942807900
P21
P31
P496
0000-0001-8838-7876
P569
2000-01-01T00:00:00Z