First published online June 7, 2004
Journal of Experimental Biology 207, 2471-2485 (2004)
Published by The Company of Biologists 2004
doi: 10.1242/jeb.01047
Interspecific and intraspecific views of color signals in the strawberry poison frog Dendrobates pumilio
Afsheen Siddiqi1,
Thomas W. Cronin1,*,
Ellis R. Loew2,
Misha Vorobyev3 and
Kyle Summers4
1 Department of Biological Sciences, University of Maryland Baltimore
County, Baltimore, MD 21250, USA
2 Department of Biomedical Sciences, Cornell University, Ithaca, NY 14853,
USA
3 Vision Touch and Hearing Research Centre, University of Queensland,
Brisbane, Queensland 4072, Australia
4 Department of Biology, East Carolina University, Greenville, NC 27858,
USA

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Fig. 1. Images of 14 of the 15 color morphs of Dendrobates pumilio
included in the current study, all from the Bocas del Toro region of Panama.
The name designating each type indicates the location at which the particular
color morph is collected. The one color morph not illustrated is from Pelican
Key, and it is very similar in appearance to the `Shepherd Island' type.
Photographs by K. Summers, except for Bocas Island and Solarte Island images,
which were taken by Marcos Guerra.
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Fig. 2. Representative reflectance spectra from leaves used as backgrounds for
spectral comparisons. (A) Purple leaf from Zebrina pendula. (B) Red
leaf from Neoreglia carolinae. (C) Yellow dry leaf. (D) Green leaf of
Aglaonema commutatum.
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Fig. 3. Spectra used in data analyses of spectral discriminability. See text for a
description of the model used for this analysis. (A) Irradiance spectra. D65
(standard daylight), D55 (direct sunlight) and D75 (`north' skylight), from
Wyszecki and Stiles (1982 ).
Green (light under the natural forest canopy in D. pumilio habitat,
Pelican Key), from Summers et al.
(2003 ). (B) Templates
representing cone visual pigments of D. pumilio. (C) Spectral
sensitivities of avian cones, taken from Parus caeruleus (generously
provided by N. Hart). Thin lines indicate visual pigments, while thick lines
represent spectral sensitivities computed taking cone oil droplet absorption
into account, used for actual analyses. (D) Normalized absorptance of an avian
double cone, including the contribution of the associated oil droplet, used in
achromatic analyses (provided by N. Hart). UVS, ultraviolet sensitive; SWS,
short-wavelength sensitive; MWS, medium-wavelength sensitive; LWS,
long-wavelength sensitive.
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Fig. 5. Results of analyses comparing frog spectral reflectances as discriminated
by frog or bird visual systems. Each panel is a histogram plot of the number
of comparisons (each a pair of spectra) vs. jnds
(`just-noticeable-differences'); see text for details. Data plotted here
represent results for the `Green' illuminant, but overall results were similar
for all illuminants; see also Table
1. (A) Frog spectral pairs, as seen by frog vision. (B) Frog
spectra compared to background spectra, as seen by frog vision. (C) Frog
spectral pairs, as seen by bird vision. (D) Frog spectra compared to
background spectra, as seen by bird vision.
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Fig. 6. Results of analyses comparing frog spectral reflectances within single
color morphs, as viewed by frog or bird visual systems. Each panel plots the
discriminability (in jnds; just-noticeable-differences) of spectral pairs,
each indicated by a dot, for color morphs indicated along the abscissa. Al,
Almirante; Ag, Aguacate; Ba, Bastimentos; Bo, Bocas; Ca, Cayo Agua; Cg,
Chiriqui Grande; Gu, Guabo; Po, Pope; Ra, Rambala; Rb, Robalo; Rd, Roldan
(Pelican Key); Sc, San Cristobal; Sh, Shepherd; So, Solarte; Uy, Uyama.
Results plotted here are for the `Green' illuminant, but similar results were
found for all illuminants. See also Table
2. (A) Frog spectral pairs, as seen by frog vision. (B) Frog
spectra compared to background spectra, as seen by frog vision. (C) Frog
spectral pairs, as seen by bird vision. (D) Frog spectra compared to
background spectra, as seen by bird vision. Note that there are many more
points in the panels for frogs vs. backgrounds, because each frog
color was compared to all background colors, not only to the few colors
present in any given frog color morph as in A and C.
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Fig. 7. Results of analyses comparing frog spectral reflectances as discriminated
by frog or bird visual systems, using only `bright' frog colors in the
analysis. Each panel is a histogram plot of the number of comparisons (each a
pair of spectra) vs. jnds (`just-noticeable-differences'); see text
for details. Data plotted here represent results for the `Green' illuminant,
but overall results were similar for all illuminants; see also
Table 3. (A) Frog spectral
pairs, as seen by frog vision. (B) Frog spectra compared to background
spectra, as seen by frog vision. (C) Frog spectral pairs, as seen by bird
vision. (D) Frog spectra compared to background spectra, as seen by bird
vision.
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Fig. 8. Results of analyses comparing spectral reflectances from dorsal or ventral
frog body regions, as discriminated from backgrounds by frog or bird visual
systems. All discriminations plotted here are for the `Green' illuminant, but
results were similar for all illuminants. Open bars, dorsal frog colors; solid
bars, ventral frog colors. (A) Frog visual systems, (B) bird visual
systems.
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Fig. 9. Results of analyses comparing frog spectral reflectances as discriminated
by only the achromatic channel of frog or bird visual systems. Data plotted
here represent results for the `Green' illuminant, but overall results were
similar for all illuminants; see also Table
4. (A) Frog spectral pairs, as seen by frog vision. (B) Frog
spectra compared to background spectra, as seen by frog vision. (C) Frog
spectral pairs, as seen by bird vision. (D) Frog spectra compared to
background spectra, as seen by bird vision.
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© The Company of Biologists Ltd 2004