COLOR-VISION IN LYCAENA BUTTERFLIES - SPECTRAL TUNING OF RECEPTOR ARRAYS IN RELATION TO BEHAVIORAL ECOLOGY

被引:118
作者
BERNARD, GD [1 ]
REMINGTON, CL [1 ]
机构
[1] YALE UNIV,DEPT BIOL,OSBORN MEM LAB,NEW HAVEN,CT 06511
关键词
ANTIHYBRIDIZATION; EYESHINE; OVIPOSITION; TERRITORIALITY; VISUAL PIGMENTS;
D O I
10.1073/pnas.88.7.2783
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Males of two closely related, co-occurring species of Lycaena butterflies have dorsally blue (Lycaena heteronea) or red-orange plus ultraviolet (Lycaena rubidus) wings. Males are selectively territorial against conspecific males. Virgin females accept only conspecific males, probably chosen by wing color. Females are nonterritorial and spend most of their adult activity ovipositing on the correct larval food plants. Eyes of both species contain four spectral types of visual pigments (P360, P437, P500, and P568) but the distribution of these pigments within the receptor mosaic is quite different between both species and sexes. The ventral eye region of L. heteronea is tetrachromatic but that of L. rubidus is trichromatic, lacking the blue-sensitive visual pigment P437. The dorsal eye region of males of both species is dichromatic (P360 and P437). Visual-pigment spectra and wing-reflectance spectra are well matched for effective discrimination of wings of conspecific males from those of other species. The dorsal region of female eyes is trichromatic, containing P360, P437, and P568. The third visual pigment, P568, is important for long-range detection by ovipositing females of red coloration on Eriogonum and Rumex food plants. P568 has the same absorbance spectrum as the human red-cone and is considerably red-shifted compared to the P530 possessed by most insects. That the sexes and closely related species can have such major differences in distribution of visual pigments indicates that the visual system is as readily altered as wing coloration in the course of adaptive evolution.
引用
收藏
页码:2783 / 2787
页数:5
相关论文
共 12 条
[1]  
BERNARD G D, 1988, Investigative Ophthalmology and Visual Science, V29, P350
[2]   RED-ABSORBING VISUAL PIGMENT OF BUTTERFLIES [J].
BERNARD, GD .
SCIENCE, 1979, 203 (4385) :1125-1127
[3]  
BERNARD GD, 1982, METHOD ENZYMOL, V81, P752
[4]   DARK-PROCESSES FOLLOWING PHOTOCONVERSION OF BUTTERFLY RHODOPSINS [J].
BERNARD, GD .
BIOPHYSICS OF STRUCTURE AND MECHANISM, 1983, 9 (04) :277-286
[5]  
BERNARD GD, 1988, J OPT SOC AM A, V4, P123
[6]  
Cornsweet T., 1970, VISUAL PERCEPTION
[7]   OPTIMIZATION, CONSTRAINT, AND HISTORY IN THE EVOLUTION OF EYES [J].
GOLDSMITH, TH .
QUARTERLY REVIEW OF BIOLOGY, 1990, 65 (03) :281-322
[8]   A UNIFYING PRESENTATION OF PHOTOPIGMENT SPECTRA [J].
MACNICHOL, EF .
VISION RESEARCH, 1986, 26 (09) :1543-1556
[9]   GENETIC-DIFFERENCES IN SOLUTIONS TO THE CRISES OF HYBRIDIZATION AND COMPETITION IN EARLY SYMPATRY [J].
REMINGTON, CL .
BOLLETTINO DI ZOOLOGIA, 1985, 52 (1-2) :21-43
[10]   BEHAVIORAL-EXPERIMENTS ON THE VISUAL PROCESSING OF COLOR STIMULI IN PIERIS-BRASSICAE L (LEPIDOPTERA) [J].
SCHERER, C ;
KOLB, G .
JOURNAL OF COMPARATIVE PHYSIOLOGY A-NEUROETHOLOGY SENSORY NEURAL AND BEHAVIORAL PHYSIOLOGY, 1987, 160 (05) :645-656