D
Désiré Daloze
Researcher at Université libre de Bruxelles
Publications - 87
Citations - 1742
Désiré Daloze is an academic researcher from Université libre de Bruxelles. The author has contributed to research in topics: Crematogaster & Octocorallia. The author has an hindex of 24, co-authored 87 publications receiving 1691 citations. Previous affiliations of Désiré Daloze include Free University of Brussels & VU University Amsterdam.
Papers
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Journal ArticleDOI
Distribution et activités des alcaloïdes défensifs des Coccinellidae
Jacques M. Pasteels,C. Deroe,Bernard Tursch,Jean Claude Braekman,Désiré Daloze,Claude Hootele +5 more
TL;DR: From a survey of 30 species and varieties of ladybugs the presence of alkaloid appears to be correlated with the existence of aposematic colour and not with being carnivorous or phytophagous, but all the beetles containing alkaloids do not possess the same degree of protection.
Book ChapterDOI
Chemical defense in the Chrysomelidae
TL;DR: Antipredation mechanisms exist in nearly all animals, but are of course better developed in those which appear to be most vulnerable, among them phytophagous insects and above all leaf beetles such as leaf beetles.
Journal ArticleDOI
Absolute configuration of the solenopsins, venom alkaloids of the fire ants
Sabine Leclercq,Isabelle Thirionet,Fabienne Broeders,Désiré Daloze,R. K. Vander Meer,Jean Claude Braekman +5 more
TL;DR: In this article, an effective and practical procedure has been developed that allows the assignment of the absolute configuration of solenopsins from diverse origins to be assigned to a set of different origins.
Journal ArticleDOI
Jaspamide from the Marine Sponge Jaspis johnstoni
Journal ArticleDOI
Chemical ecology of arthropods. X. The structure of myrrhine and the biosynthesis of coccinelline.
TL;DR: The structure elucidation of myrrhine (6), a novel base isolated from Myrrha 18- guttata, is reported in this article, where the biogenesis of the Coccinellidae defensive alkaloids is discussed and coccinelline is shown to be biosynthetized through the polyacetate pathway.