The spectral sensitivity of Drosophila photoreceptors

Drosophila melanogaster has long been a popular model insect species, due in large part to the availability of genetic tools and is fast becoming the model for insect colour vision. Key to understanding colour reception in Drosophila is in-depth knowledge of spectral inputs and downstream neural processing. While recent studies have sparked renewed interest in colour processing in Drosophila, photoreceptor spectral sensitivity measurements have yet to be carried out in vivo. We have fully characterised the spectral input to the motion and colour vision pathways, and directly measured the effects of spectral modulating factors, screening pigment density and carotenoid-based ocular pigments. All receptor sensitivities had significant shifts in spectral sensitivity compared to previous measurements. Notably, the spectral range of the Rh6 visual pigment is substantially broadened and its peak sensitivity is shifted by 92 nm from 508 to 600 nm. We show that this deviation can be explained by transmission of long wavelengths through the red screening pigment and by the presence of the blue-absorbing filter in the R7y receptors. Further, we tested direct interactions between inner and outer photoreceptors using selective recovery of activity in photoreceptor pairs.

The spectral sensitivity of Drosophila photoreceptors

Drosophila melanogaster has long been a popular model insect species, due in large part to the availability of genetic tools and is fast becoming the model for insect colour vision. Key to understanding colour reception in Drosophila is in-depth knowledge of spectral inputs and downstream neural processing. While recent studies have sparked renewed interest in colour processing in Drosophila, photoreceptor spectral sensitivity measurements have yet to be carried out in vivo. We have fully characterised the spectral input to the motion and colour vision pathways, and directly measured the effects of spectral modulating factors, screening pigment density and carotenoid-based ocular pigments. All receptor sensitivities had significant shifts in spectral sensitivity compared to previous measurements. Notably, the spectral range of the Rh6 visual pigment is substantially broadened and its peak sensitivity is shifted by 92 nm from 508 to 600 nm. We propose that this deviation can be explained by transmission of long wavelengths through the red screening pigment and by the presence of the blue-absorbing filter in the R7y receptors. Further, we tested direct interactions between photoreceptors and found evidence of interactions between inner and outer receptors, in agreement with previous findings of cross-modulation between receptor outputs in the lamina.

Screening pigment of the camera eyes of stalkeyed mollusks (Pulmonata, Stylommatophora) with different light preferences

Morphological properties of the granules of the screening pigment in the retinae of camera eyes of gastropod mollusks with different light preferences were studied. It was demonstrated that the pigment granules of mollusks can differ by color and size but do not differ by structure, electron density and form. Light conditions of mollusks’ habitats can influence on the amount of the screening pigment, which in its turn does not affect resolving ability of the eyes.

Parietin: an efficient photo-screening pigment in vivo with good photosensitizing and photodynamic antibacterial effects in vitro

In lichens, Parietin forms tiny crystals acting as photo-screening. But in solution it behaves as photosensitizer killing bacteria by photodynamic action.

EFFECT OF DIFFERENT LIGHTING CONDITIONS ON FEEDING ACTIVITY AND EYE ADAPTATION OF POST LARVAE PENAEUS VANNAMEI

This study was conducted to investigate the effect of light and dark conditions on feeding activity and eye adaptations of post larvae (PL5, PL10, PL20 and PL30) Penaeus vannamei fed with frozen Artemia. Shrimp PL were placed individually in beakers and after acclimatization under the light or dark condition, PL were left to ingest known number of Artemia for 30 minutes. Thereafter, each PL was subsequently anesthetized by putting an ice cube into the beakers followed by adding few drops of paraformaldehyde. The results showed that the PL5 ingested significantly more frozen Artemia under light condition compared to dark condition (P<0.05). The eye structures of PL5 comprises of crystalline cone, rhabdom and fasciculated zone. However, it was incomplete due to the lack of clear zone and no migration of the screening pigment granules was observed under light and dark conditions. On the contrary, the number of frozen Artemia ingested by the latter stages PL10, PL20 and PL30 showed no significant differences (P>0.05) under both light conditions and these PL have complete eye structures with define clear zone. The width of clear zone was found to increase proportionally with the growth of the PL. Besides that, the screening pigment granules were able to migrate under light and dark conditions. The ability of the PL10, PL20 and PL30 to ingest almost similar numbers of Artemia under light and dark conditions suggests that different lighting conditions did not affect the feeding activity of the PL and other sensory organs may play roles in detecting food, while PL5 need light to improve their feeding activity. Based on these results, we suggest that in aquaculture practice, during the rearing of early stage of PL (<PL5), a brighter environment or light should be provided to enhance larval feeding activities. Whereas, later stages of PL (>PL10) can be cultured under any light condition.