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Dive into the research topics where Celia D. Radke is active.

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Featured researches published by Celia D. Radke.


Chemoecology | 1992

Leaf surface chemicals stimulating oviposition byPieris rapae (Lepidoptera: Pieridae) on cabbage

J. Alan A. Renwick; Celia D. Radke; K. Sachdev-Gupta; Erich Städler

SummaryThe chemical stimulation of oviposition byPieris rapae on cabbage was investigated by leaf washing and extraction. Isolation of the stimulant by various chromatographic techniques was monitored by a bioassay using Sieva bean as a surrogate host plant. Cold water, chloroform, or chloroform followed by cold water washes failed to release the stimulant from leaf surfaces. Boiling water or chloroform followed by methanol was required. The most active stimulatory compound was identified as 3-indolylmethyl glucosinolate (glucobrassicin). Other glucosinolates were identified as sinigrin, which was only slightly active, and glucoiberin, which was completely inactive as a stimulant. The significance of the selective response ofP. rapae andP. brassicae to different glucosinolates and the implications of the binding of polar allelochemicals to leaf surfaces is discussed with respect to host utilization and perception mechanisms of pierids.


Physiological Entomology | 1995

Tarsal contact chemoreceptor response to glucosinolates and cardenolides mediating oviposition in Pieris rape

Erich Städler; J. A. A. Renwick; Celia D. Radke; K. Sachdev-Gupta

Abstract. Water‐soluble extracts of a host crucifer (Brassica oleracea L.) and non‐host crucifer (Erysimum cheiranthoides L.) and isolated pure cardenolides and glucosinolates were tested on Pieris rapae L. (Lepidoptera: Pieridae) butterflies in oviposition assays and by electrophysiological recordings from the contact‐chemoreceptor sensilla of the prothoracic tarsi.


Entomologia Experimentalis Et Applicata | 1985

Constituents of host- and non-host plants deterring oviposition by the cabbage butterfly, Pieris rapae

J. A. A. Renwick; Celia D. Radke

Oviposition by Pieris rapae L. on cabbage was deterred by homogenized cabbage tissue sprayed onto intact plants. Ether extracts of cabbage also were deterrent, but water extracts were not. Hexane extracts of other host plants deterred oviposition and water extracts had little or no effect. Polar as well as non‐polar extracts of non‐host plants inhibited oviposition. Polar deterrents in the non‐host crucifers, Erysimum cheiranthoides and Capsella bursa‐pastoris may explain the avoidance of these plants by P. rapae. Chemical deterrents, as well as stimulants, apparently play a major role in the acceptance or rejection of plants as hosts by ovipositing female butterflies.


Journal of Chemical Ecology | 1990

Isolation and identification of oviposition deterrents to cabbage butterfly,Pieris rapae, fromErysimum cheiranthoides.

K. Sachdev-Gupta; J. A. A. Renwick; Celia D. Radke

Avoidance of some crucifer species by the crucifer specialist,Pieris rapae, has been attributed to the presence of oviposition deterrents in these plants. Studies on one such unacceptable plant,Erysimum cheiranthoides, have resulted in the isolation ofn-butanol-soluble deterrents from the alcoholic extract of foliage. The active fraction contained three cardiac glycosides, which were isolated by reversed-phase HPLC and by open column chromatography on silica gel. Chemical and spectral evidence (UV, [1H]NMR, and FAB-MS) led to the characterization of these compounds as erysimoside (1), erychroside (2), and erycordin (3). Erysimoside and erychroside were strongly deterrent toPieris rapae, but erycordin was inactive. Both active compounds have the same aglycone, strophanthidin (5) and the inner sugar in both cases is a 2,6-dideoxy hexose to which the outer sugar is attached at position C-4. These structural features, which are absent in the inactive compound (3), may represent specific requirements for oviposition deterrent activity.


Journal of Chemical Ecology | 1989

Chemical constituents ofErysimum cheiranthoides deterring oviposition by the cabbage butterfly,Pieris rapae

J. A. A. Renwick; Celia D. Radke; K. Sachdev-Gupta

Avoidance ofErysimum cheiranthoides for oviposition byPieris rapae has been attributed to the presence of water-soluble deterrents. The active material was extracted inton-butanol and isolated by a series of HPLC separations. TLC of the active fraction and visualization of individual constituents with Keddes reagent indicated that cardenolides are responsible for deterring oviposition. UV spectra were also characteristic of cardenolides. Bioassays of selected known cardenolides revealed a general lack of activity, except for cymarin, which was as strongly deterrent as the most prominent cardenolide isolated in pure form fromE. cheiranthoides. The results suggest that cardenolides in this plant can explain its escape from cabbage butterflies, but specific structural features of the glycosides are necessary for oviposition-deterring activity.


Journal of Chemical Ecology | 1987

Chemical stimulants and deterrents regulating acceptance or rejection of crucifers by cabbage butterflies.

J. A. A. Renwick; Celia D. Radke

GravidPieris rapae butterflies oviposit on many, but not all, crucifers. Rejection ofErysimum cheiranthoides andCapsella bursa-pastoris was initially explained by the presence of chemical deterrents in the plants. Analyses and bioassays of plant extracts indicated the absence of oviposition stimulants inC. bursa-pastoris, but similar chemical separation ofE. cheiranthoides extracts revealed the presence of stimulants as well as deterrents. Choice tests illustrate how acceptance or rejection of a plant by an insect may depend on the balance of positive and negative chemical stimuli within the plant.


Journal of Chemical Ecology | 1993

Cardenolides fromErysimum cheiranthoides: Feeding deterrents toPieris rapae larvae

K. Sachdev-Gupta; Celia D. Radke; J. A. A. Renwick; M. B. Dimock

Larvae of the cabbage butterfly,Pieris rapae, refuse to feed on the wild mustard,Erysimum cheiranthoides, due to the presence of alcoholextractable deterrents. The active components were extracted inton-BuOH, and this extract was separated into four fractions (I–IV) by reverse-phase HPLC. Fractions III and IV retained the feeding deterrent activity. The activity of fraction III was found to be due to the cardenolide diglycosides 1 and 2, which were previously reported as oviposition deterrents for gravidP. rapae butterflies. Three active compounds were isolated from fraction IV by column chromatography on silica gel followed by reverse-phase HPLC. These compounds were identified as a monoglycoside, digitoxigenin 3-O-β-D-glucoside (4), and two diglycosides, glucodigigulomethyloside (5) and glucodigifucoside (6). An additional cardenolide isolated from fraction II was identified as cheirotoxin (7). All compounds were identified by UV, NMR (1H and13C), and mass spectrometry, as well as hydrolysis experiments. The feeding deterrent activity of these compounds was compared with that of related commercially available chemicals and other compounds isolated fromE. cheiranthoides.


Phytochemistry | 1993

Antifeedant activity of cucurbitacins from Iberis amara against larvae of Pieris rapae

K. Sachdev-Gupta; Celia D. Radke; J. Alan A. Renwick

Abstract Two cucurbitacins isolated from Iberis amara foliage were identified by UV and NMR spectroscopy and acid catalysed hydrolysis as 2- O -β- d -glucopyranosyl cucurbitacin E and 2- O -β- d -glucopyranosyl cucurbitacin I. The first compound was found to be a potent antifeedant to the larvae of Pieris rapae in a choice test.


Entomologia Experimentalis Et Applicata | 1981

Host plant constituents as oviposition deterrents for the Cabbage Looper, Trichoplusia ni

J. A. A. Renwick; Celia D. Radke

Boch, R., & Shearer, D. A. (t962). Identification of geraniol as an active component in the Nassanoff pheromone of the honey bee. Nature (Lond.) 194 : 704--706. Boch, R., & Shearer, D. A. (1964). Identification of nerolic and geranic acids in the Nassanoff pheromone of the honey bee. Nature (Lond.) 202 : 320----321. Butler, C. G. & Calam, D. H. (1969). Pheromones of the honeybee the secretion of the Nassanoff gland of the worker. J. Insect Physiol. 15 : 237-244. Pickett, J. A., Williams, Ingrid H., Martin, A. P. & Smith, M. C. (1980). Nasonov pheromone of the honey bee, Apis mellifera L. (Hymenoptera: Apidae) Part I. Chemical characterization. J. Chem. Ecol. 6 : 425~434. Waller, G. D. (1970). Attracting honeybees to alfalfa with citral, geraniol and anise. J. apic. Res. 9 : 9--12. Weaver, N., Weaver, E. C., & Law, J. H. (1964). The attractiveness of citral to foraging honey bees. Prog. Rep. Texas Agric. Exp. Sta. No. 2324, 7 pp. Williams, Ingrid, H., Pickett, J. A. & Martin, A. P. (1981) Nasonov pheromone of the honey bee, Apis mellifera L. (Hymenoptera: Apidae) Part II. Bioassay of the components using foragers. J. Chem. Ecol. 7 : 225---237.


Journal of Chemical Ecology | 1991

Chemical constituents of an unacceptable crucifer,Erysimum cheiranthoides, deter feeding byPieris rapae

M. B. Dimock; J. A. A. Renwick; Celia D. Radke; K. Sachdev-Gupta

The wild cruciferErysimum cheiranthoides was found to contain extractable constituents that deterred feeding by larvae of the crucifer specialistPieris rapae when applied to cabbage leaf disks in both choice and nochoice bioassays. High-performance liquid chromatography was used to separate the extract into several fractions, two of which retained the feeding deterrent activity of the extract. UV-absorption spectra of the fractions suggested that one contained cardenolides similar or identical to those reported to deter oviposition byP. rapae onE. cheiranthoides. The other active fraction evidently contains a compound that deters larval feeding but not adult oviposition. The results suggest that the chemical defense ofE. cheiranthoides depends on two types of compounds acting on separate developmental stages of the insect.

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J. A. A. Renwick

Boyce Thompson Institute for Plant Research

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K. Sachdev-Gupta

Boyce Thompson Institute for Plant Research

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J. Alan A. Renwick

Boyce Thompson Institute for Plant Research

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M. B. Dimock

Boyce Thompson Institute for Plant Research

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Erich Städler

University of New Brunswick

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