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First published online January 5, 2005
Journal of Experimental Biology 208, 327-344 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01356
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Body-induced vortical flows: a common mechanism for self-corrective trimming control in boxfishes

Ian K. Bartol1,*, Morteza Gharib2, Paul W. Webb3, Daniel Weihs4 and Malcolm S. Gordon5

1 Department of Biological Sciences, Old Dominion University, Nor folk, VA 23529-0266, USA
2 Options of Bioengineering and Aeronautics, California Institute of Technology, Pasadena, CA 91125, USA
3 School of Natural Resources and Department of Biology, University of Michigan, Ann Arbor, MI 48109, USA
4 Department of Aerospace Engineering, Technion, Haifa, 3200, Israel
5 Department of Ecology and Evolutionary Biology, University of California, Los Angeles, CA 90095-1606, USA



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Fig. 1. Anterior, posterior, and lateral views of a spotted boxfish, scrawled cowfish, buffalo trunkfish, and smooth trunkfish. The smooth trunkfish was examined in Bartol et al. (2003Go). Some distinguishing features of each boxfish are highlighted in the figure. Scale bars, 1 cm.

 


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Fig. 2. Vorticity contour fields around and in the wake of the spotted boxfish (upper row), scrawled cowfish (middle row), and buffalo trunkfish (bottom row) models positioned at a pitch angle of +10°. The data are viewed in transverse planes at various locations along the body and in the wake. Each plot is the mean result of 30 paired images (1 representative trial). From left to right, the locations, which are highlighted in the upper corner of the figures, are: eye ridge, maximum girth, midpoint between maximum girth and posterior edge of the carapace, posterior edge of the carapace, caudal peduncle, and wake. The shadows beneath the models represent areas that were shielded from laser light. White dots in scrawled cowfish and buffalo trunkfish figures are the tips of the ventral keel extensions. Mean circulation magnitude and mean peak vorticity magnitude for a dorsal vortex ({Gamma}D and P{omega}D, respectively) and ventral vortex ({Gamma}V and P{omega}V, respectively) are included beneath the plots. In the wake of the spotted boxfish, ventral and dorsal vortices merge and thus dorsal and ventral distinctions are not necessary.

 


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Fig. 3. Vorticity contour fields around and in the wake of the spotted boxfish (upper row), scrawled cowfish (middle row) and buffalo trunkfish (bottom row) models positioned at a pitch angle of -10°. The data are viewed in transverse planes at various locations along the body and in the wake. Each plot is the mean result of 30 image pairs (1 representative trial). From left to right, the locations, which are highlighted in the upper corner of figures, are: eye ridge, maximum girth, midpoint between maximum girth and posterior edge of the carapace, posterior edge of the carapace, caudal peduncle, and wake. The shadows on the sides of or beneath models represent areas that were shielded from laser light. White dots in scrawled cowfish and buffalo trunkfish figures are the tips of the ventral keels extensions. Mean circulation magnitude and mean peak vorticity magnitude for a dorsal vortex ({Gamma}D and P{omega}D, respectively) and a ventral vortex ({Gamma}V and P{omega}V, respectively) are included beneath the vorticity contour plots. In the scrawled cowfish, mean circulation magnitude and mean peak vorticity magnitude for a lateral vortex ({Gamma}L and P{omega}L, respectively) also are included. In the wake, dorsal and ventral distinctions are not necessary for the spotted boxfish and buffalo trunkfish since ventral and dorsal vortices merge.

 


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Fig. 4. Vorticity contour fields around the posterior edge of the carapace of the spotted boxfish (upper row), scrawled cowfish (middle row), and buffalo trunkfish (bottom row) models positioned (from left to right) at pitch angles of +20°, +10°, 0°, -10°, and -20°, and a yaw angle of 10°. The data are viewed in transverse planes, and sampling locations are highlighted in the upper corner of figures. Each plot is the mean result of 30 image pairs (1 representative trial). The shadows underneath or to the side of models represent areas that were shielded from laser light. White dots in scrawled cowfish and buffalo trunkfish figures are the tips of the ventral keels extensions. Mean circulation magnitude and mean peak vorticity magnitude for a dorsal vortex ({Gamma}D, and P{omega}D, respectively) and a ventral vortex ({Gamma}V and P{omega}V, respectively are included beneath the vorticity contour plots. For the yaw angles, circulation and peak vorticity values for each side of the carapace are included (right side, in normal text = far-field; left side, in italicized text = near-field).

 


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Fig. 5. Pressure coefficients (Cp) plotted as a function of location along various dorso-ventral transects (A-F) on the spotted boxfish model positioned at positive (left) and negative (right) pitch angles. The locations of the pressure ports included in each graph are highlighted in images to the left of the graphs. The location of each dorso-ventral transect is expressed as a percentage of ventral keel length (measured from the anterior leading edge) in the lower left-hand corner of each image. Ports in blue, red and black are located on the dorsum, sides, and ventrum of the model, respectively. {dagger}Denotes ports that were slightly out of alignment with other ports along the dorso-ventral transect; * represent transects that were considered in DPIV studies. Blue and red rectangles highlight ports where local pressure minima were consistently detected at dorsal and ventral locations, respectively. An ambient pressure line (Cp=0) was included in the most posteriorly located transect (F).

 


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Fig. 6. Pressure coefficients (Cp) plotted as a function of location along various dorso-ventral transects (A-F) on the scrawled cowfish model positioned at positive (left) and negative (right) pitch angles. The locations of the pressure ports included in each graph are highlighted in images to the left of the graphs. The location of each dorso-ventral transect is expressed as a percentage of ventral keel length (measured from the anterior leading edge) in the lower left-hand corner of each image. Ports in red and white are located on the sides and ventrum of the model, respectively. {dagger}Denotes ports that were slightly out of alignment with other ports along the dorso-ventral transect; * represent transects that were considered in DPIV studies. Blue and red rectangles highlight ports where local pressure minima were consistently detected at dorsal and ventral locations, respectively. An ambient pressure line (Cp=0) was included in the most posteriorly located transect (F).

 


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Fig. 7. Pressure coefficients (Cp) plotted as a function of location along various dorso-ventral transects (A-F) on the buffalo trunkfish model positioned at positive (left) and negative (right) pitch angles. The locations of the pressure ports included in each graph are highlighted in images to the left of the graphs. The location of each dorso-ventral transect is expressed as a percentage of ventral keel length (measured from the anterior leading edge) in the lower left-hand corner of each image. Ports in red and black are located on the sides and ventrum of the model, respectively. {dagger}Denotes ports that were slightly out of alignment with other ports along the dorso-ventral transect; * represent transects that were considered in DPIV studies. Blue and red rectangles highlight ports where local pressure minima were consistently detected at dorsal and ventral locations, respectively. An ambient pressure line (Cp=0) was included in the most posteriorly located transect (F).

 


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Fig. 8. Lift coefficients CL (A), drag coefficients CD (B), and pitching moment coefficients about the center of mass CM (C) for four boxfishes (smooth trunkfish, buffalo trunkfish, scrawled cowfish and spotted boxfish) positioned at various pitch angles. In A, CL values for a delta wing of similar aspect ratio (0.83) to that of the boxfishes are also depicted. Delta wing data are from Schlichting and Truckenbrodt (1969Go), and smooth trunkfish data are from Bartol et al. (2003Go). Positive CM values indicate a nose-down pitching moment about the center of mass, whereas negative CM values indicate a nose-up pitching moment about the center of mass.

 





© The Company of Biologists Ltd 2005