Vision and lack of vision in the ocean

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Vision and lack of vision in the ocean Justin Marshall  Current Biology  Volume 27, Issue 11, Pages R494-R502 (June 2017) DOI: 10.1016/j.cub.2017.03.012 Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 1 Light in the ocean. (A) Modern version of the famous Levine and MacNichol representation of light underwater (courtesy of Mike Bok and adapted from original in Further reading - Levine and MacNichol 1982). Upper panel, coloured-in spectrum of light under an irradiance spectrum curve above water, full sunlight. Note ultra-violet wavelengths in black as human vision cannot colour label this range. Middle panel, attenuation of light with depth in clear oceanic water down to 75 m. Bar on right represents how water looks to us. Bottom panel, attenuation of light in green, chlorophyll and dissolved organic matter-laden coastal waters where maximal transmission is around 550 nm. Note also the more rapid reduction in luminance with equivalent depth. (B) The clown triggerfish, Balistoides conspicillum, photographed close up with high resolution (12 megapixel) camera and over distance in near-shore reef water over different distances and with a lower resolution camera (4 megapixel) that approximates to reef fish resolving power. Note the fine patterns and colours disappear rapidly and the contrasting black and white pattern and fish to background has all but vanished at 4.0 m. This water type falls between those in (A) in terms of spectral transmission (maximum at 500 nm) and overall turbidity. Current Biology 2017 27, R494-R502DOI: (10.1016/j.cub.2017.03.012) Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 2 Different spectral sensitivities and colour vision types in the ocean. (A) The spectral sensitivities of the long-nosed butterflyfish, Forcipiger longirostris, including the filtering of ocular media (cornea and lens). The rod sensitivity exactly underlies the central cone. (B) Damselfish spectral sensitivities of the ambon damsel, Pomacentrus ambionensis, and inset photographed through a UV sensitive (350–400 nm) camera. In full spectral photography this fish appears yellow like the butterfly fish above. Cones, solid lines; rod, dotted line. The differences in spectral sensitivity to F. longirostris is one example of many other differences both in cone number and placement among reef fish (Marshall et al. 2003). (C) Stomatopod (mantis shrimp) spectral sensitivities and inset of one of the more flamboyant species, Odontodactylus scyllarus, the peacock mantis shrimp. Current Biology 2017 27, R494-R502DOI: (10.1016/j.cub.2017.03.012) Copyright © 2017 Elsevier Ltd Terms and Conditions

Figure 3 Communication and camouflage colours on the reef. (A) Damselfish, Chromis viridis (green) and Pomacentrus moluccensis (yellow), over a coral head on the reef. Note general match to chosen background. (B) A scorpaenid so well camouflaged a nudibranch has mistaken it for a rock. Both background matching and edge disruptive camouflage principles are used here. Inset shows another scorpaenid species that might appear ‘brightly’ coloured on substrates other than an equally red sponge. (Photographs by Steve Parish.) (C) Healthy branching coral (Acropora sp.) containing a number of different fish species camouflaged through matching or disruption (red arrows mark some fish locations). (D) Bleached Acropora sp. with encroaching algal overgrowth and death from left. Note how both background matching and disruptively camouflaged fish (also present in (C)) are highly conspicuous and indeed not able to use mechanical shelter in overgrown coral. (E) Colours of the moon wrasse, Thalassoma lunare. Top graph, normalised reflectance colours colour matched to areas measured from photograph above. Middle graph, black line shows additive colour from mixing highly contrasting turquoise and pink colours, as would occur at a distance from fish. Bottom graph, overlay of combined colour and background water colour (blue curve). Shaded box indicates spectral region within which reef fish cone sensitivities lie. Current Biology 2017 27, R494-R502DOI: (10.1016/j.cub.2017.03.012) Copyright © 2017 Elsevier Ltd Terms and Conditions