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First published online March 28, 2008
Journal of Experimental Biology 211, 1203-1210 (2008)
Published by The Company of Biologists 2008
doi: 10.1242/jeb.012963
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Visual sensitivity to a conspicuous male cue varies by reproductive state in Physalaemus pustulosus females

Molly E. Cummings1,*, Ximena E. Bernal1, Roberto Reynaga1, A. Stanley Rand2 and Michael J. Ryan1,2

1 Section of Integrative Biology, University of Texas, Austin, TX 78712, USA
2 Smithsonian Tropical Research Institute, Apartado 2072, Balboa, Panama


Figure 1
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Fig. 1. (A) Optomotor device and male túngara with inflated vocal sac. (B) Optomotor stimuli and illumination spectra. Túngara-specific optomotor stripe reflectance: representative male inflated vocal sac spectral reflectance (solid line) and inflated vocal sac imitation stripes (spectral filters: Lee 185 + GamColor 305 + GamColor 1516 above white construction paper; broken line). Moonlight irradiance measurements (filled circles) in air and under clear skies [recreated from figure 4C in McFarland (McFarland, 1991Go)], and spectral irradiance measurements of our optomotor moonlight mimic illumination (open circles; Dolan-Jenner + Lee 138 filter). Both spectra were normalized to the flux at 600 nm. (C) Optomotor illumination intensities for each of the six trial settings.

 

Figure 2
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Fig. 2. Male túngara and background spectral reflectance. (A) Average spectral reflectance of body regions from 15 male túngaras (solid lines) including head (+), dorsal ({blacktriangleup}), ventral ({triangleup}), non-inflated vocal sac (•) and inflated vocal sac ({circ}). Average background material spectral reflectance is also shown (broken lines) including mud (•), stone ({blacksquare}) and dead leaves ({diamondsuit}). (B) Average spectral reflectance of the vocal sac of a representative male túngara frog in non-inflated (•) and inflated ({circ}) states. Mean ± s.e.m. reflectance data include replicates made in left, middle and right areas of the vocal sac.

 

Figure 3
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Fig. 3. Repeat testing of 14 túngara females and the optomotor trial setting of their threshold response. (A) Females initially tested in the reproductive state (N=8), and (B) females initially tested in the non-reproductive state (N=6). Each line connects the threshold responses for a single female with arrowheads indicating the direction of sensitivity change between the first and second testing dates. Asterisks indicate additional females exhibiting the same initial threshold response.

 

Figure 4
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Fig. 4. Box and whisker plots of visual sensitivity thresholds (trial setting of threshold response and corresponding intensity levels) across three testing groups: males (gray, N=22); females in a non-reproductive state (white, N=20) and reproductive state females (cross-hatched; N=12). The center horizontal line marks the median of the sample, and the length of each box shows the range containing 50% of all values with the box edges representing the first and third quartiles. The open circles represent far outside values or outliers (>first or third quartile ± 3xinterquartile range). Each group includes data from individuals obtained on their initial test only. *P<0.05.

 

Figure 5
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Fig. 5. (A) Optomotor threshold response by size (SVL, snout-to-vent length) across all three testing groups: males (gray triangles), non-reproductive females (open circles) and reproductive females (filled circles). (B) Optomotor threshold response by testing month across all three testing groups where 1 is January and 12 is December.

 

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© The Company of Biologists Ltd 2008