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II. Vision in Deep-Sea Crustaceans Tamara M Nova Southeastern University NSUWorks Marine & Environmental Sciences Faculty Articles Department of Marine and Environmental Sciences 10-1-2012 Light and Vision in the Deep-Sea Benthos: II. Vision in Deep-Sea Crustaceans Tamara M. Frank Nova Southeastern University, [email protected] Sönke Johnsen Duke University Thomas W. Cronin University of Maryland Find out more information about Nova Southeastern University and the Halmos College of Natural Sciences and Oceanography. Follow this and additional works at: https://nsuworks.nova.edu/occ_facarticles Part of the Marine Biology Commons, and the Oceanography and Atmospheric Sciences and Meteorology Commons NSUWorks Citation Tamara M. Frank, Sönke Johnsen, and Thomas W. Cronin. 2012. Light and Vision in the Deep-Sea Benthos: II. Vision in Deep-Sea Crustaceans .Journal of Experimental Biology , (19) : 3344 -3353. https://nsuworks.nova.edu/occ_facarticles/396. This Article is brought to you for free and open access by the Department of Marine and Environmental Sciences at NSUWorks. It has been accepted for inclusion in Marine & Environmental Sciences Faculty Articles by an authorized administrator of NSUWorks. For more information, please contact [email protected]. 3344 The Journal of Experimental Biology 215, 3344-3353 © 2012. Published by The Company of Biologists Ltd doi:10.1242/jeb.072033 RESEARCH ARTICLE Light and vision in the deep-sea benthos: II. Vision in deep-sea crustaceans Tamara M. Frank1,*, Sönke Johnsen2 and Thomas W. Cronin3 1Oceanographic Center, Nova Southeastern University, Dania Beach, FL 33004, USA, 2Biology Department, Duke University, Durham, NC 27708, USA and 3Department of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD 21250, USA *Author for correspondence ([email protected]) SUMMARY Using new collecting techniques with the Johnson-Sea-Link submersible, eight species of deep-sea benthic crustaceans were collected with intact visual systems. Their spectral sensitivities and temporal resolutions were determined shipboard using electroretinography. Useable spectral sensitivity data were obtained from seven species, and in the dark-adapted eyes, the spectral sensitivity peaks were in the blue region of the visible spectrum, ranging from 470 to 497nm. Under blue chromatic adaptation, a secondary sensitivity peak in the UV portion of the spectrum appeared for two species of anomuran crabs: Eumunida picta (max363nm) and Gastroptychus spinifer (max383nm). Wavelength-specific differences in response waveforms under blue chromatic adaptation in these two species suggest that two populations of photoreceptor cells are present. Temporal resolution was determined in all eight species using the maximum critical flicker frequency (CFFmax). The CFFmax for the isopod Booralana tricarinata of 4Hz proved to be the lowest ever measured using this technique, and suggests that this species is not able to track even slow-moving prey. Both the putative dual visual pigment system in the crabs and the extremely slow eye of the isopod may be adaptations for seeing bioluminescence in the benthic environment. Key words: vision, deep-sea, benthic, bioluminescence. Received 1 March 2012; Accepted 18 June 2012 INTRODUCTION 1988), whereas in benthic species, there is a depth-related increase The large eyes of deep-sea animals have been remarked upon since in both parameters, resulting in the eyes of many benthic crustaceans the first specimens were pulled up in trawl nets. In addition to large being larger, relative to body length, than those of pelagic eyes, early structural studies on mesopelagic species (i.e. those living crustaceans (Hiller-Adams and Case, 1985). Similar trends are found in the water column) demonstrated further adaptations for increasing among deep-sea fish: eyes decrease in size with increasing habitat sensitivity to the dim environmental light field, including larger depth among a variety of pelagic species, but many deep-sea benthic apertures, longer photoreceptor cells, reductions in screening or near-benthic species retain large, well-developed eyes (Murray pigments and the presence of reflecting tapeta (reviewed in Warrant and Hjort, 1912; Locket, 1977). Many of these benthic species have and Locket, 2004). Studies on visual pigment absorption maxima depth ranges well below the depths at which there is sufficient from mesopelagic species have shown a shift in peak sensitivity to daylight remaining to have any significance for vision (Denton, shorter, ‘bluer’ wavelengths compared with those of shallow-water 1990), suggesting that these species may be adapted for seeing species [e.g. fish (reviewed in Douglas et al., 2003; Turner et al., bioluminescence. 2009) and crustaceans (reviewed in Marshall et al., 2003)]. This However, there is virtually no information on the visual pigments shift to blue sensitivity is an adaptation to both downwelling light, of benthic species because of the difficulty in collecting them without which becomes more monochromatic and blue with increasing depth exposing their eyes to damaging light levels. Even minimal exposure (Jerlov, 1976), and bioluminescence, the vast majority of which lies to light (1min of daylight) can cause irreparable damage to between 450 and 510nm (Herring, 1983; Widder et al., 1983; photoreceptors adapted for dim-light environments (Loew, 1976; Haddock and Case, 1999). Lindström et al., 1988). Photoreceptors of hydrothermal vent shrimp The only vision studies that have been conducted on benthic caught under the lights of a submersible also show significant light- (bottom-dwelling) species are structural, and these show that there induced damage, with disordered microvilli and disruption to are similar structural adaptations for increasing light sensitivity, photoreceptor membranes (O’Neill et al., 1995; Lakin et al., 1997), including reflecting tapeta [e.g. crustaceans (Hiller-Adams and Case, whereas those of their pelagic larvae, caught with a net that 1985; Eguchi et al., 1997) and fish (Denton and Shaw, 1963; Somiya, prevented exposure to light, show orthogonal layers of microvilli 1980)], enlarged photoreceptive membranes (Hiller-Adams and with intact membranes typical of crustacean rhabdoms (Gaten et Case, 1985; Eguchi et al., 1997) and aphakic spaces [allowing light al., 1998). The structural organization of the compound eye of the to hit the retina without going through the lens (Denton, 1990)]. giant deep-sea isopod Bathynomus giganteus, collected with a dredge However, in mesopelagic crustaceans, eye growth rates relative to and brought up in bright sunlight, showed similar severe disruption body growth rates decline with depth, as does the eye size relative of the microvilli, even after 2months maintenance in constant to body length (Hiller-Adams and Case, 1984; Adams and Case, darkness (Chamberlain et al., 1986). Therefore, it is imperative that THE JOURNAL OF EXPERIMENTAL BIOLOGY Vision in deep-sea crustaceans 3345 these benthic species be collected without exposure to light. Deep- living pelagic species have successfully been collected alive and with intact eyes with the aid of insulated and light-tight containers attached to the end of trawl nets (Childress et al., 1978; Frank and Widder, 1994), but trawling in the benthic environment (other than sparsely populated muddy bottom) with such a device would seriously damage the environment and destroy the net. Using new technologies developed for the Johnson-Sea-Link (JSL) submersible, the photoreceptor function of eight species of deep-sea benthic crustaceans were examined on a series of research expeditions funded by the NOAA Ocean Exploration program. These studies demonstrated unusual spectral sensitivity in two species of deep-sea crabs, in addition to extraordinarily low temporal resolution in a species of deep-sea isopod, indicative of an integration time so long that this species may not be able to track even slow- moving prey. Preliminary data from this study have been published in abstract form (Frank, 2006; Frank, 2008; Frank et al., 2010). MATERIALS AND METHODS Animal collections One species of isopod, two species of caridean shrimp, four species of anomuran crabs and one species of brachyuran crab were collected on a series of research cruises in the Gulf of Mexico and in the Bahamas (Fig.1, Table1). Crustaceans were collected with the JSL submersible using several techniques. Baited traps were deployed in several locations, collected 6 to 24h later under red light and placed into light-tight Bio-Boxes. These containers were constructed out of 1.5cm thick black Plexiglas with lids fitted with O-ring seals, making the boxes light-tight, water-tight and thermally insulated. Pressure relief valves on the Bio-Boxes released excess pressure as the submersible ascended from the collection depths to the surface. In addition, animals attracted to a bait bag placed near the traps were collected under red light with the suction sampler on the JSL, and deposited directly into the Bio-Box. The red lights used in collections were two submersible lights, one filtered with a Schott OG 590nm cutoff filter (transmission below 560nm Fig.1. Seven of the eight species of deep-sea crustaceans examined in <0.001%; Dalton, GA, USA) and the other with a HOYA O-58 cut- this study. These are the seven species for which spectral sensitivity data off filter (transmission below 560nm <0.1%; THK Photo Products are shown in Fig.2. Scale bars are 1cm, to show the relative sizes of the Inc., Huntington Beach, CA, USA). Once back at the
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