Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cajas

In processed products of the tropical fruit caja and in some cultivars of persimmons, all-tran P-cryptoxanthin was found to be the major carotenoid, contributing to 31 to 38% of the total carotenoid contents in both fruits (Table... [Pg.218]

Hamano, PS. and Mercadante, A.Z., Composition of carotenoids from commercial products of caja (Spondias lutea), J. Food Compos. Anal, 14, 335, 2001. [Pg.236]

Gomez-Prieto MS, Caja MM and Santa-Maria G. 2002. Solubility in supercritical carbon dioxide of the predominant carotenes in tomato skin. J Am Oil Chem Soc 79(9) 897—902. [Pg.266]

Gomez-Prieto MS, Caja MM, Herraiz M and Santa-Maria G. 2003. Supercritical fluid extraction of all trans-lycopene from tomato. J Agric Food Chem 51(1 ) 3—7. [Pg.266]

However, in the case of dietary alkaloids, it would seem that more than only traces of alkaloids, which do not exhibit selective toxicity to antagonist organisms, would be needed for defensive purposes. These trace alkaloids probably have a role in the organism s metabolism, development and behaviour. The traces of alkaloids in the eggs of Arctia caja also suggest a potential participation of these compounds in reproduction. Moreover, attention should be given to the fact that alkaloids are dietary sequestrations acquired from feeding on plants. [Pg.210]

Arctia caja Danaus piexippus Danaus chrysippus Idea ieuconoe Tyria jacobaeae Utethesia omatix Utethesia pulchelloides... [Pg.211]

LEPIDOPTERA Arctia caja Danaus piexippus Danaus chrysippus... [Pg.211]

Figure 98. A diagram of the accumuiation of pyrroiizidine aikaloids in some insect species during various developmentai stages. It shouid be noted that it is not often that these aikaloids are present in the eggs, as in the case of the Arctia caja. Natural sources are pyrroiizidine alkaloid-rich plant species Senecio spp., Homoptera Senecio and Adenostyles spp., Coleoptera and Senecio, Adenostyles, Petasites, Crotalaria and Heliotropium spp., Lep-idoptera). Figure 98. A diagram of the accumuiation of pyrroiizidine aikaloids in some insect species during various developmentai stages. It shouid be noted that it is not often that these aikaloids are present in the eggs, as in the case of the Arctia caja. Natural sources are pyrroiizidine alkaloid-rich plant species Senecio spp., Homoptera Senecio and Adenostyles spp., Coleoptera and Senecio, Adenostyles, Petasites, Crotalaria and Heliotropium spp., Lep-idoptera).
Moure, G., ed. Duchamp Exposicion organizada par la Fundacion Caja de Pensiones y la Fundacion Joan Mird. Madrid Fundacion Caja de Pensiones, 1984. [Pg.446]

Dalman Arctia caja L. Polyphagous Larva Hair brushes Rothschild, 1972b,c Rothschild et al 1979 Bisset et al., 1959, 1960 Rothschild... [Pg.257]

Aplin, R. T. and Rothschild, M. (1972). Poisonous alkaloids in the body tissues of the garden tiger moth (Arctia caja L.) and the cinnabar moth (Tyria (= Callimorpha) jacobaeae L.) (Lepidoptera). In Toxins of Animal and Plant Origin, eds. A. de Vries and K. Kochva. pp. 579-595. London Gordon and Breach. [Pg.274]

Bisset, G. W., Grazer, J. F. D., Rothschild, M. and Schachter, M. (1959). A choline ester and other substances in the garden tiger moth, Arctia caja (L.). Journal of Physiology 146 38-39. [Pg.275]

Pheromones. 84. The sex pheromone complex of the arctiid moth Arctia caja (Lepidoptera Arctiidae). Z. Naturforsch. C, 47,132-135. [Pg.434]

W.W. Au, C.H. Sierra-Torres, N. Cajas-Salazar, B.K. Shipp, M.S. Legator, Cytogenetic effects from exposure to mixed pesticides and the influence from genetic susceptibility. Environ. Health Perspect. 107(6) 501, 1999. [Pg.117]

Blanch, G.P., Caja, M.M., Leon, M. and Herraiz, M. (2000) Determination of (E)-5-methylhept-2-en-4-one in deodorised hazelnut oil. Application to the detection of adulterated olive oils. J. Sci. Food Agric., 80, 140-144. [Pg.20]

Hydroxytryptamine Ananas comosus (Bromeliaceae), Hippophae Tiger moth (Arctia caja)... [Pg.438]

Figure 14.5 Charge-discharge curves for the cell U/EMPBF4 0.8 molar LiAsFe/LIMnsO at room temperature. (Adapted from Caja, Dunstan, and Katovic [22]). Figure 14.5 Charge-discharge curves for the cell U/EMPBF4 0.8 molar LiAsFe/LIMnsO at room temperature. (Adapted from Caja, Dunstan, and Katovic [22]).
The best-studied group of acquired alkaloids are the pyrrolizidines, which are produced by plants, especially in the families Asteraceae and Boraginaceae (502). Some arctiid larvae of Tyria Jacobaea, Cycnia men-dica, Amphicallia bellafrix, Arginia cribaria, and Arctia caja were shown... [Pg.98]


See other pages where Cajas is mentioned: [Pg.68]    [Pg.124]    [Pg.350]    [Pg.44]    [Pg.219]    [Pg.457]    [Pg.68]    [Pg.275]    [Pg.435]    [Pg.435]    [Pg.68]    [Pg.124]    [Pg.350]    [Pg.270]    [Pg.191]    [Pg.197]    [Pg.393]    [Pg.263]    [Pg.20]    [Pg.153]    [Pg.200]    [Pg.438]    [Pg.54]    [Pg.54]    [Pg.186]    [Pg.186]    [Pg.223]   
See also in sourсe #XX -- [ Pg.347 ]




SEARCH



Arctia caja

© 2024 chempedia.info