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  • 1
    ISSN: 1570-7458
    Keywords: antixenosis ; host-plant resistance ; host preference ; oviposition behaviour ; contact chemoreception ; glucosinolates ; Delia radicum ; Delia floralis ; Anthomyiidae ; Diptera ; Brassica ; Cruciferae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In Brassica crops differences in susceptibility to root fly attack can be largely attributed to antixenotic resistance. Plants of four genotypes (two swedes and two kales) with widely differing resistance in field trials, were compared in laboratory choice assays for their susceptibility to oviposition by the root flies Delia radicum (L.) and D. floralis (Fallen) (Diptera, Anthomyiidae). For both species the preference among the genotypes corresponded to the susceptibility of the genotypes in the field. The preference ranking in response to surrogate leaves treated with methanolic surface extracts of the four genotypes was identical to the preference among potted plants, demonstrating that chemical factors on the leaf surface mediate host preference for oviposition in these species. For both species of fly, glucosinolates are major oviposition stimulants and for D. radicum an additional, nonglucosinolate oviposition stimulant, presently called CIF, is known. We describe a procedure for chromatographic separation of glucosinolates from CIF in leaf surface extracts. In oviposition-choice assays with D. radicum, the CIF-fractions of the two swede genotypes applied to surrogate leaves received a 1.8 and 4.6 times higher proportion of eggs than the respective glucosinolate-fractions, confirming the major importance of CIF as an oviposition stimulant. The genotype of swede that was preferred by both fly species in tests with plants and methanolic leaf surface extracts, also stimulated oviposition more in tests with the glucosinolate-fractions or the CIF-fractions derived from the surface extracts, respectively. Thus, glucosinolates and CIF together account for the observed preference among the genotypes and may also be responsible for their susceptibility under field conditions. In the two kale genotypes the preference for plants or surface extracts differed from the preference among the corresponding glucosinolate- and CIF-fractions, indicating that additional, as yet unknown chemical factors may also be involved. For both groups of stimulants tarsal chemoreceptors allow electrophysiological monitoring of glucosinolate- and CIF-activity in fractionated surface extracts. For D. radicum the chemosensory activity of both glucosinolate- and CIF-fractions corresponded to the respective behavioural activity in the oviposition preference tests, suggesting that preference for oviposition among genotypes can be predicted from the electrophysiological activity of their fractions. The chemosensory response of D. floralis, in particular to the CIF-fractions, was less pronounced than the response of D. radicum, indicating interspecific differences in the perception of the major oviposition stimulants. We discuss the potential application of electrophysiological techniques in support of other screening methods used in breeding for root fly resistance in Brassica crops.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1561
    Keywords: Delia floralis ; turnip root fly ; oviposition stimuli ; chemoreception ; leaf surface chemistry ; Brassica ; host plant resistance ; glucosinolates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The role of leaf surface compounds influencing the oviposition of the turnip root fly, Delia floralis, was investigated using bioassays and fractionation of leaf surface extracts from four Brassica genotypes. Polar leaf surface extracts contained between 65 and 175 nM/g leaf equivalent of glucosinolates. However, following fractionation it was found that nonglucosinolates were the major stimuli for D. floralis oviposition. Electrophysiological studies of leaf surface extracts and their fractions were performed by using D. radicum, the cabbage root fly, as an analytical tool. The most behaviorally active fractions contained stimulatory compound(s) that had an activity profile identical to that previously described for recently discovered nonglucosinolate compounds. The role of leaf surface chemicals in influencing antixenotic resistance to D. floralis is discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 39 (1956), S. 722-728 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex formation of cis- and trans-1,2-Diaminocyclohexan with the ions H+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+ has been studied. The metal complexes of the trans-diamine are slightly more stable than the corresponding complexes of ethylenediamine, which is probably due to a somewhat more positive entropy term of the formation reaction. The complexes of the cis-compound are somewhat less stable than those of the trans-diamine. The distance between the two basic nitrogen atoms are almost certainly the same in both diamine molecules. The cis-compound, however, has a less favourable geometry for complex formation, because the chelate ring and the 6-membered carbon ring do not lie in the same plane as will be the case with the complexes of the trans-diamine.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 842-847 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the solutions of some double cyanides MNi(CN)4 (M = Cu2+, Cd2+, Zn2+) in ammonia clathrates can be obtained with benzene which are of the type of HOFMANN's compound {Ni(CN)2NH3C6H6}. The conditions of formation of these new clathrates have been studied and their structure is discussed. The dry salt [Cd(NH3)6] [Ni(CN)4] has been degraded to CdNi(CN)4, the reaction having been followed by means of tensiometric measurements; thereby the triammonate has been found to be the only intermediate.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 45 (1962), S. 775-783 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From a solution containing a mercury(II)salt and thiocyanate (ratio of about 1:4), a solution of a cobalt(II) salt precipitates, in presence of benzene, a bright pink mikrocrystalline compound of the exact composition: {CoHg2(SCN)6, C6H6}, which can be also obtained in well developed cristals. Reflexion and IR. Spectra show that CoII is octahedrally coordinated and that all six thiocyanate groups serve to bridge the two metal atoms: Hg…SCN…Co. It is suggested that the molecule of benzene formes π-bonds simultaneously with two mercury atoms, being the fourth ligand of each Hg2+. Benzene can be replaced by toluene, the three xylenes, naphthalene, anthracene, but not by aliphatic cyclic hydrocarbons. CoII can be replaced by octahedral NiII and CdII, but not by ZnII and CuII. The compounds are thermodynamically unstable. At about 100°C the cobalt-benzene compound loses the hydrocarbon rapidly and the colour of the solid residue turns from pink to a brilliant blue, due to the formation of a 1:1 mixture of {CoHg(SCN)4} and {Hg(SCN)2}. The compound {CoHg2(SCN)6} is non-existent, and it is unlikely therefore that it can serve as a host-lattice for benzene in a clathrate.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 29 (1884), S. 489-493 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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