Three-dimensional visualization of insect morphology using confocal laser scanning microscopy

被引:92
作者
Klaus, AV [1 ]
Kulasekera, VL
Schawaroch, V
机构
[1] Amer Museum Nat Hist, Microscopy & Imaging Facil, New York, NY 10024 USA
[2] Amer Museum Nat Hist, Div Invertebrate Zool, New York, NY 10024 USA
[3] New York City Dept Hlth & Mental Hyg, New York, NY 10013 USA
关键词
autofluorescence; axial distortion; Culex; Diptera; Drosophila; exoskeleton; male genitalia; signal loss; spherical aberration; systematics;
D O I
10.1046/j.1365-2818.2003.01235.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
Cuticular structures of insects are often microscopic and intricately complex; among the most complex structures are male genitalia. Genitalic structures are essential in taxonomic and phylogenetic studies of insects. Using well-described species from two disparate dipteran genera, we demonstrate the utility of confocal laser scanning microscopy for studying the morphological characters of fly genitalia by taking advantage of the autofluorescent properties of cuticle material. Reconstructions of confocal data sets obtained from genitalic structures embedded in two commonly used entomological mounting media (euparal and glycerin jelly) are presented. Aberration artefacts often observed in confocal data obtained from thick specimens were analysed and strategies for their minimization are discussed. Our results indicate that confocal laser scanning microscopy and 3D reconstruction are excellent techniques for visualizing small, complex, autofluorescent structures in flies. These techniques could have a profound impact on the quality of information provided by 3D representations of insect structures over more traditional methods of visualization.
引用
收藏
页码:107 / 121
页数:15
相关论文
共 49 条
[41]  
SKALIORA I, 2002, CONFOCAL 2 PHOTON MI, P365
[42]  
SNODGRASS, 1935, PRINCIPLES INSECT MO
[43]  
Tsien Roger Y., 1995, P267
[44]  
TUXEN SL, 1978, TAXONOMISTS GLOSSARY
[45]  
VANDERVOORT HTM, 1995, J MICROSC-OXFORD, V178, P165, DOI 10.1111/j.1365-2818.1995.tb03593.x
[46]   AN EVALUATION OF CONFOCAL VERSUS CONVENTIONAL IMAGING OF BIOLOGICAL STRUCTURES BY FLUORESCENCE LIGHT-MICROSCOPY [J].
WHITE, JG ;
AMOS, WB ;
FORDHAM, M .
JOURNAL OF CELL BIOLOGY, 1987, 105 (01) :41-48
[47]   Aberration control in quantitative imaging of botanical specimens by multidimensional fluorescence microscopy [J].
White, NS ;
Errington, RJ ;
Fricker, MD ;
Wood, JL .
JOURNAL OF MICROSCOPY-OXFORD, 1996, 181 :99-116
[48]  
Zill S, 2000, MICROSC RES TECHNIQ, V48, P367, DOI 10.1002/(SICI)1097-0029(20000315)48:6<367::AID-JEMT7>3.3.CO
[49]  
2-P