Marcel Dicke

Professor of Entomology
Wageningen University · Department of Entomology

Topics (17) View all

Skills (4)

Research experience

  • Jan 1983–
    present
    Research: Wageningen University
    Wageningen UR · Entomology
    Netherlands · Wageningen
    www.ent.wur.nl

Awards & achievements

  • Jun 2011
    Award: eleced member of the Royal Netherlands Academy of Arts and Sciences
  • Nov 2007
    Award: Spinoza Award (aka 'Dutch Nobel Prize'

Other

  • Languages
    Dutch
    English
    German
  • Scientific Memberships
    Elected member of the Royal Netherlands Academy of Arts and Sciences (Koninklijke Nederlandse Akademie van Wetenschappen, abbreviated: KNAW)
    Elected Member of The Royal Holland Society of Sciences and Humanities (Koninklijke Hollandse Maatschappij der Wetenschappen).
    International Organisation for Biological Control
    International Society for Chemical Ecology
    Netherlands Institute for Biologists
    Netherlands Ecological Society
    Netherlands Entomological Society
  • Other Interests
    Insects in art

Questions and Answers (2) View all

  • Answer added in Ecology
    8 How relevant do you think genomics will be in understanding community ecology?
    By Joshua Thia · University of Canterbury
    Marcel Dicke · Wageningen University
    Genomics is getting more and more importan in population ecology and community ecology-seee.g. https://www.researchgate.net/publication/225634640_The_... [more]
  • Answer added in Biological Pest Control
    7 Antibiotics use on predatory mites
    By Eitan (Amiel) Recht · Ben-Gurion University of the Negev
    Marcel Dicke · Wageningen University
    Hi Eitan See our publication on bacterial diseases in predatory mites: 244. Schütte, C., Poitevin, O. & Dicke, M. 2008. A novel disease affecting the... [more]

Publications (693) View all

  • Source
    Article: Phenotypic plasticity of plant response to herbivore eggs: effects on resistance to caterpillars and plant development.
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    ABSTRACT: Herbivory induces direct resistance responses in plants that negatively affect subsequently colonizing herbivores. Moreover, eggs of herbivorous insects can also activate plant resistance, which in some cases prevents hatching larvae from feeding. Until now, plantmediated effects of eggs on subsequent herbivory, and the specificity of such responses, have remained poorly understood. We studied the specificity and effects of plant resistance induced by herbivore egg deposition against lepidopteran larvae of species with different dietary breadths, feeding on a wild annual plant, the crucifer Brassica nigra. We examined whether this plant-mediated response affects the growth of caterpillars of a specialist (Pieris brassicae) that feeds on B. nigra leaves and flowers, and a generalist (Mamestra brassicae) that rarely attacks this wild crucifer. We measured growth rates of neonate larvae to the end of their second instar after the larvae had hatched on plants exposed to eggs vs. plants without eggs, under laboratory and semi-field conditions. Moreover, we studied the effects of egg deposition by the two herbivore species on plant height and flowering rate before and after larval hatching. Larvae of both herbivore species that developed on plants previously infested with eggs of the specialist butterfly P. brassicae gained less mass compared with larvae that developed on egg-free plants. Plants exposed to butterfly eggs showed accelerated plant growth and flowering compared to egg-free plants. Egg deposition by the generalist moth M. brassicae, in contrast, had no effect on subsequent performance by either herbivore species, or on plant development. Our results demonstrate that B. nigra plants respond differently to eggs of two herbivore species in terms of plant development and induced resistance to caterpillar attack. For this annual crucifer, the retardation of caterpillar growth in response to deposition of eggs by P. brassicae in combination with enhanced growth and flowering likely result in reproductive assurance, after being exposed to eggs from an herbivore whose larvae rapidly reduce the plant’s reproductive potential through florivory.
    Ecology 04/2013; 94:702-713. · 4.85 Impact Factor
  • Source
    Article: Rhizobacteria modify plant-aphid interactions: a case of induced systemic susceptibility.
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    ABSTRACT: Beneficial microbes, such as plant growth-promoting rhizobacteria and mycorrhizal fungi, may have a plant-mediated effect on insects aboveground. The plant growth-promoting rhizobacterium Pseudomonas fluorescens can induce systemic resistance in Arabidopsis thaliana against several microbial pathogens and chewing insects. However, the plant-mediated effect of these beneficial microbes on phloem-feeding insects is not well understood. Using Arabidopsis as a model, we here report that P. fluorescens has a positive effect on the performance (weight gain and intrinsic rate of increase) of the generalist aphid Myzus persicae, while no effect was recorded on the crucifer specialist aphid Brevicoryne brassicae. Additionally, transcriptional analyses of selected marker genes revealed that in the plant-microbe interaction with M. persicae, rhizobacteria (i) prime the plant for enhanced expression of LOX2, a gene involved in the jasmonic acid (JA)-regulated defence pathway, and (ii) suppress the expression of ABA1, a gene involved in the abscisic acid (ABA) signalling pathway, at several time points. In contrast, almost no effect of the plant-microbe interaction with B. brassicae was found at the transcriptional level. This study presents the first data on rhizobacteria-induced systemic susceptibility to an herbivorous insect, supporting the pattern proposed for other belowground beneficial microbes and aboveground phloem feeders. Moreover, we provide further evidence that at the transcript level, soil-borne microbes modify plant-aphid interactions.
    Plant Biology 03/2012; 14 Suppl 1:83-90. · 2.39 Impact Factor
  • Article: Herbivore‐induced volatiles of cabbage (Brassica oleracea) prime defence responses in neighbouring intact plants
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    ABSTRACT: When attacked by herbivores, plants release herbivore-induced plant volatiles (HIPV) that may function in direct defence by repelling herbivores or reducing their growth. Emission of HIPV may also contribute to indirect defence by attracting natural enemies of the herbivore. Here, cabbage (Brassica oleracea L.) plants (receiver plants) previously exposed to HIPV and subsequently induced through feeding by five Pieris brassicae L. caterpillars attracted more Cotesia glomerata L. parasitoids than control plants. HIPVs to which receiver plants had been exposed were emitted by B. oleracea infested with 50 P. brassicae caterpillars. Control plants had been exposed to volatiles from undamaged plants. In contrast, there were no differences in the attraction of wasps to receiver plants induced through feeding of one or ten larvae of P. brassicae compared to control plants. In addition, RT-PCR demonstrated higher levels of LIPOXYGENASE (BoLOX) transcripts in HIPV-exposed receiver plants. Exposure to HIPV from emitter plants significantly inhibited the growth rate of both P. brassicae and Mamestra brassicae caterpillars compared to growth rates of caterpillars feeding on control receiver plants. Our results demonstrate plant–plant signalling leading to priming of both indirect and direct defence in HIPV-exposed B. oleracea plants.
    Plant Biology 02/2011; 13(2):276 - 284. · 2.39 Impact Factor
  • Article: CREB expression in the brains of two closely related parasitic wasp species that differ in long‐term memory formation
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    ABSTRACT: The cAMP/PKA signalling pathway and transcription factor cAMP response element-binding protein (CREB) play key roles in long-term memory (LTM) formation. We used two closely related parasitic wasp species, Cotesia glomerata and Cotesia rubecula, which were previously shown to be different in LTM formation, and sequenced at least nine different CREB transcripts in both wasp species. The splicing patterns, functional domains and amino acid sequences were similar to those found in the CREB genes of other organisms. The predicted amino acid sequences of the CREB isoforms were identical in both wasp species. Using real-time quantitative PCR we found that two low abundant CREB transcripts are differentially expressed in the two wasps, whereas the expression levels of high abundant transcripts are similar.
    Insect Molecular Biology 05/2010; 19(3):367 - 379. · 2.53 Impact Factor
  • Article: The role of volatiles in aggregation and host-seeking of the haematophagous poultry red mite Dermanyssus gallinae (Acari: Dermanyssidae).
    C J M Koenraadt, M Dicke
    [show abstract] [hide abstract]
    ABSTRACT: Infestations with ectoparasitic poultry red mites (Dermanyssus gallinae) pose an increasing threat to poultry health and welfare. Because of resistance to acaricides and higher scrutiny of poultry products, alternative and environmentally safe management strategies are warranted. Therefore, we investigated how volatile cues shape the behavior of D. gallinae and how this knowledge may be exploited in the development of an attract-and-kill method to control mite populations. A Y-tube olfactometer bio-assay was used to evaluate choices of mites in response to cues related to conspecific mites as well as related to their chicken host. Both recently fed and starved mites showed a strong preference (84 and 85%, respectively) for volatiles from conspecific, fed mites as compared to a control stream of clean air. Mites were also significantly attracted to 'aged feathers' (that had remained in the litter for 3-4 days), but not to 'fresh feathers'. Interestingly, an air stream containing 2.5% CO(2), which mimics the natural concentration in air exhaled by chickens, did attract fed mites, but inhibited the attraction of unfed mites towards volatiles from aged feathers. We conclude that both mite-related cues (aggregation pheromones) and host-related cues (kairomones) mediate the behavior of the poultry mite. We discuss the options to exploit this knowledge as the 'attract' component of attract-and-kill strategies for the control of D. gallinae.
    Experimental and Applied Acarology 09/2009; 50(3):191-9. · 1.39 Impact Factor

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