FATE OF IRIDOID GLYCOSIDES IN DIFFERENT LIFE STAGES OF THE BUCKEYE, JUNONIA-COENIA (LEPIDOPTERA, NYMPHALIDAE)

被引:86
作者
BOWERS, MD
COLLINGE, SK
机构
[1] UNIV COLORADO, DEPT EPO BIOL, BOULDER, CO 80309 USA
[2] HARVARD UNIV, MUSEUM COMPARAT ZOOL, CAMBRIDGE, MA 02138 USA
关键词
JUNONIA-COENIA; LEPIDOPTERA; NYMPHALIDAE; PLANTAGO-LANCEOLATA; CHEMICAL DEFENSE; EVOLUTION OF UNPALATABILITY; IRIDOID GLYCOSIDES; AUCUBIN; CATALPOL; ECOLOGICAL CHEMISTRY; SEQUESTRATION;
D O I
10.1007/BF00988322
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The buckeye butterfly, Junonia coenia (Lepidoptera:Nymphalidae), specializes on plants that contain iridoid glycosides. To determine the fate of these compounds in larvae, pupae, and adults of this species, we reared larvae on artificial diets with and without iridoid glycosides, and on leaves of a host plant, Plantago lanceolata (Plantaginaceae). Quantification by gas chromatography showed that newly molted third-, fourth-, and fifth-instar larvae reared on leaves of P. lanceolata contained means of 5.13, 2.88, and 6.83% dry weight iridoid glycoside. In contrast, the mean iridoid glycoside concentration of actively feeding fifth-instar larvae was 0.28% dry weight, that of pupae was 0.19% dry weight iridoids, and adults contained no detectable iridoids. Feeding experiments suggested that this reduction in actively feeding larvae was due to the metabolism of iridoid glycosides. P. lanceolata leaves in these experiments contained a mean of 1.00% dry weight iridoid glycoside, with a 2:1 ratio of aucubin to catalpol. Calculation of iridoid consumption and utilization indices showed that larvae fed artificial diets consumed, digested, and sequestered aucubin and catalpol in similar ways. When these indices were calculated for larvae fed leaves of P. lanceolata, catalpol was sequestered twice as efficiently as aucubin.
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页码:817 / 831
页数:15
相关论文
共 47 条
[1]   IRIDOID GLYCOSIDES OF AUREOLARIA-FLAVA AND THEIR SEQUESTRATION BY EUPHYDRYAS-PHAETON BUTTERFLIES [J].
BELOFSKY, G ;
BOWERS, MD ;
JANZEN, S ;
STERMITZ, F .
PHYTOCHEMISTRY, 1989, 28 (06) :1601-1604
[2]  
Blum M., 1981, CHEM DEFENSES ARTHRO
[3]  
BLUM MS, 1983, ACS SYM SER, V208, P265
[4]  
Bobbitt JM, 1969, CYCLOPENTANOID TERPE, P1
[5]   PROCESSING OF IRIDOID GLYCOSIDE ANTIRRINOSIDE FROM MAURANDYA-ANTIRRHINIFLORA (SCROPHULARIACEAE) BY MERIS-PARADOXA (GEOMETRIDAE) AND LEPIPOLYS SPECIES (NOCTUIDAE) [J].
BOROS, CA ;
STERMITZ, FR ;
MCFARLAND, N .
JOURNAL OF CHEMICAL ECOLOGY, 1991, 17 (06) :1123-1133
[6]  
Bowers M.D., 1988, P133
[7]  
Bowers M.D., 1988, P273
[8]  
BOWERS MD, 1981, EVOLUTION, V35, P367, DOI 10.1111/j.1558-5646.1981.tb04895.x
[9]  
BOWERS MD, 1990, ANIM BEHAV, V39, P699
[10]  
BOWERS MD, 1980, EVOLUTION, V34, P586, DOI 10.1111/j.1558-5646.1980.tb04846.x