The eye of the opossum shrimp Mysis relicta (Crustacea, Mysidae) contains two visual pigments located in different photoreceptor cells

2013 ◽  
Vol 449 (1) ◽  
pp. 68-72 ◽  
Author(s):  
P. P. Zak ◽  
M. Lindström ◽  
Ju. V. Demchuk ◽  
K. Donner ◽  
M. A. Ostrovsky
2008 ◽  
Vol 34 (3) ◽  
pp. 461-471 ◽  
Author(s):  
Christian Schlechtriem ◽  
Ora E. Johannsson ◽  
Kelly L. Bowen ◽  
Richard W. Smith ◽  
Michael T. Arts

2020 ◽  
Vol 206 (6) ◽  
pp. 871-889
Author(s):  
Tatiana Feldman ◽  
Marina Yakovleva ◽  
Martta Viljanen ◽  
Magnus Lindström ◽  
Kristian Donner ◽  
...  

Abstract We have studied dark-adaptation at three levels in the eyes of the crustacean Mysis relicta over 2–3 weeks after exposing initially dark-adapted animals to strong white light: regeneration of 11-cis retinal through the retinoid cycle (by HPLC), restoration of native rhodopsin in photoreceptor membranes (by MSP), and recovery of eye photosensitivity (by ERG). We compare two model populations (“Sea”, Sp, and “Lake”, Lp) inhabiting, respectively, a low light and an extremely dark environment. 11-cis retinal reached 60–70% of the pre-exposure levels after 2 weeks in darkness in both populations. The only significant Lp/Sp difference in the retinoid cycle was that Lp had much higher levels of retinol, both basal and light-released. In Sp, rhodopsin restoration and eye photoresponse recovery parallelled 11-cis retinal regeneration. In Lp, however, even after 3 weeks only ca. 25% of the rhabdoms studied had incorporated new rhodopsin, and eye photosensitivity showed only incipient recovery from severe depression. The absorbance spectra of the majority of the Lp rhabdoms stayed constant around 490–500 nm, consistent with metarhodopsin II dominance. We conclude that sensitivity recovery of Sp eyes was rate-limited by the regeneration of 11-cis retinal, whilst that of Lp eyes was limited by inertia in photoreceptor membrane turnover.


2002 ◽  
Vol 42 (supplement2) ◽  
pp. S26
Author(s):  
S. Tachibanaki ◽  
S. Tsushima ◽  
Y. Shimauchi-Matsukawa ◽  
S. Kawamura

2003 ◽  
Vol 20 (4) ◽  
pp. 411-419 ◽  
Author(s):  
PETRI ALA-LAURILA ◽  
RAULI-JAN ALBERT ◽  
PIA SAARINEN ◽  
ARI KOSKELAINEN ◽  
KRISTIAN DONNER

Effects of temperature on the spectral properties of visual pigments were measured in the physiological range (5–28°C) in photoreceptor cells of bullfrog (Rana catesbeiana) and crucian carp (Carassius carassius). Absorbance spectra recorded by microspectrophotometry (MSP) in single cells and sensitivity spectra recorded by electroretinography (ERG) across the isolated retina were combined to yield accurate composite spectra fromca. 400 nm to 800 nm. The four photoreceptor types selected for study allowed three comparisons illuminating the properties of pigments using the dehydroretinal (A2) chromophore: (1) the two members of an A1/A2 pigment pair with the same opsin (porphyropsinvs.rhodopsin in bullfrog “red” rods); (2) two A2 pigments with similar spectra (porphyropsin rods of bullfrog and crucian carp); and (3) two A2 pigments with different spectra (rodsvs.long-wavelength-sensitive (L-) cones of crucian carp). Qualitatively, the temperature effects on A2 pigments were similar to those described previously for the A1 pigment of toad “red” rods. Warming caused an increase in relative sensitivities at very long wavelengths but additionally a small shift of λmaxtoward shorter wavelengths. The former effect was used for estimating the minimum energy required for photoactivation (Ea) of the pigment. Bullfrog rod opsin with A2 chromophore hadEa= 44.2 ± 0.9 kcal/mol, significantly lower (one-tailedP< 0.05) than the valueEa= 46.5 ± 0.8 kcal/mol for the same opsin coupled to A1. The A2 rod pigment of crucian carp hadEa= 42.3 ± 0.6 kcal/mol, which is significantly higher (one-tailedP< 0.01) than that of the L-cones in the same retina (Ea= 38.3 ± 0.4 kcal/mol), whereas the difference compared with the bullfrog A2 rod pigment is not statistically significant (two-tailedP= 0.13). No strict connection between λmaxandEaappears to exist among A2 pigments any more than among A1 pigments. Still, the A1 → A2 chromophore substitution in bullfrog opsin causes three changes correlated as originally hypothesized by Barlow (1957): a red-shift of λmax, a decrease inEa, and an increase in thermal noise.


2005 ◽  
Vol 280 (50) ◽  
pp. 41184-41191 ◽  
Author(s):  
Guang W. Shi ◽  
Jiayan Chen ◽  
Francis Concepcion ◽  
Khatereh Motamedchaboki ◽  
Paul Marjoram ◽  
...  

1996 ◽  
Vol 108 (1) ◽  
pp. 27-34 ◽  
Author(s):  
C L Makino ◽  
R L Dodd

Although a given retina typically contains several visual pigments, each formed from a retinal chromophore bound to a specific opsin protein, single photoreceptor cells have been thought to express only one type of opsin. This design maximizes a cell's sensitivity to a particular wavelength band and facilitates wavelength discrimination in retinas that process color. We report electrophysiological evidence that the ultraviolet-sensitive cone of salamander violates this rule. This cell contains three different functional opsins. The three opsins could combine with the two different chromophores present in salamander retina to form six visual pigments. Whereas rods and other cones of salamander use both chromophores, they appear to express only one type of opsin per cell. In visual pigment absorption spectra, the bandwidth at half-maximal sensitivity increases as the pigment's wavelength maximum decreases. However, the bandwidth of the UV-absorbing pigment deviates from this trend; it is narrow like that of a red-absorbing pigment. In addition, the UV-absorbing pigment has a high apparent photosensitivity when compared with that of red- and blue-absorbing pigments and rhodopsin. These properties suggest that the mechanisms responsible for spectrally tuning visual pigments separate two absorption bands as the wavelength of maximal sensitivity shifts from UV to long wavelengths.


1982 ◽  
Vol 39 (1) ◽  
pp. 203-208 ◽  
Author(s):  
Scott D. Cooper ◽  
Charles R. Goldman

Mysis relicta was fed Epischura nevadensis late instars or Diaptomus tyrrelli males in a series of feeding experiments. Mysis clearance rates were not affected by the time of day mysids were collected, the time of day experiments were conducted, or conditioning of experimental water by predators and prey. Mysis fed as efficiently in the dark as in bright light, and exhibited increasing clearance rates with increasing container size. When Diaptomus males were used as prey Mysis clearance rates were significantly higher at 5 °C than 10 and 15 °C; temperature did not affect clearance rates with Epischura as prey. Mean clearance rates tended to decline with increasing prey density, but the only significant differences were recorded when Epischura was used as prey. Prior acclimation to experimental light and temperature conditions had no effect on the results. When presented with an abundant food supply, freshly collected Mysis fed at initially low rates. Subsequent feeding rate peaks were followed by feeding rate declines to low levels over a 24-h period. Individual Mysis consumption rates remained relatively constant from day to day.Key words: Mysis relicta, predation, copepods, clearance rates, opossum shrimp


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