Table S2.
Experiment | Experiment description | Consistent with model? |
1950: Kühn (21) | (A) Test of camouflage response on textured colored backgrounds vs. greyscale; (B) training experiment on Octopus vulgaris using stationary targets | Yes for both. Kühn (21) concludes a wavelength sensing capability; both of his experimental designs (A and B) allow for the determination of chromatically induced defocus |
1973: Messenger et al. (9) | (C) Training experiments on octopus under fluorescent lighting using colored rods vibrated at 3 Hz; (D) nystagmus response in octopus to alternating colored stripes | Yes, rapidly vibrating color cues would make color assessment by chromatic defocus impossible. Yes, under our model, they are unable to judge coloration absent fine-scale structure; adjacent colors are not resolvable |
1975: Roffe (10) | (E) Training experiment on octopus with unfocused monochromatic light projected onto a white screen without focusing cues | Yes, light projected onto uniform disk would not allow for determination of chromatic defocus |
1977: Messenger (8) | (F) Training experiments on octopus with rectangles of colored cues vibrated at 3 Hz | Yes, rapid vibration makes color assessment by chromatic defocus impossible |
1996: Marshall and Messenger (11) | (G) Camouflage assay using two adjacent colors of artificial fine gravel | Yes, under our model, adjacent colors are not resolvable |
2006: Mäthger et al. (7) | (H) Nystagmus tracking response in Sepia using alternating adjacent colored bars rotated around the head of the animal; (i) camouflage assay using two adjacent colors in a uniform checkerboard | Yes for both. Both lines of evidence (H and I) use adjacent colors without fine-scale structure; this degeneracy defeats a spectral discrimination model using chromatically dependent defocus as seen in Fig. 3 |
This table provides a summary of how prior laboratory cephalopod behavior and vision experiments compare with the chromatic aberration model proposed here.