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Journal of Experimental Biology, Vol 204, Issue 8 1421-1431, Copyright © 2001 by Company of Biologists
JOURNAL ARTICLES |
S Gorb, E Gorb and V Kastner
Biological Microtribology Group, Biochemistry Department, Max-Planck-Institute of Developmental Biology, Spemannstrasse 35, D-72076 Tubingen, Germany. Stas.Gorb@tuebingen.mpg.de
To test the role of constructional and dimensional factors in the generation of friction force by systems of setose attachment pads, six species of syrphid fly (Platycheirus angustatus, Sphaerophoria scripta, Episyrphus balteatus, Eristalis tenax, Myathropa florea and Volucella pellucens) were studied using light and scanning electron microscopy. Flies were selected according to their various body mass and attachment pad dimensions. Such variables as pad area, setal density, the area of a single setal tip and body mass were individually measured. A centrifugal force tester, equipped with a fibre-optic sensor, was used to measure the friction forces of the pads on a smooth horizontal surface made of polyvinylchloride. Friction force, which is the resistance force of the insect mass against the sum of centrifugal and tangential forces, was greater in heavier insects such as Er. tenax, M. florea and V. pellucens. Although lighter species generated lower frictional forces, the acceleration required to detach an insect was greater in smaller species. The area of attachment pads, setal tip area and setal density differed significantly in the species studied, and the dependence of these variables on body mass was significant. The frictional properties of the material of the setal tips were not dependent on the dimensions of the fly species. Similar results were obtained for the frictional properties of the pulvillus as a whole. Thus, the properties of the secretion and the mechanical properties of the material of the setal tips are approximately constant among the species studied. It is concluded that differences in friction force must be related mainly to variations in the real contact area generated by the pad on the smooth surface. The real contact area can be estimated as the summed area of the broadened setal tips of the pad in contact with the surface. The real contact area depends on such morphological variables as setal density and the area of a single setal tip. Although individual variables vary among flies with different dimensions, they usually compensate such that smaller setal tip area is partially compensated for by higher setal density.
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