In the fish retina, retinomotor movement, spinule formation, and alteration of connexon density within gap junctions occur in response to changes in ambient light conditions. All of these morphological parameters can also be influenced by the application of dopamine. This study examines whether the morphological alterations of these structures are correlated with the activity of endogenous dopamine during an entrained 12-h light/12-h dark cycle and after 1-h sort-term adaptation periods.

The two measured parameters of retinomotor movement, cone inner segment length and pigment dispersion, were well-correlated with endogenous cyclic dopamine activity. However, retinomotor movement was initiated already at the end of the entrained dark period, before the onset of light and before the onset of dopamine turnover. Furthermore, a 1-h dark-adaptation period in the middle of the light phase reduced dopamine activity but did not affect retinomotor movement. At the switch from light to dark and after a 1-h light period at midnight retinomotor movement correlated exactly with dopamine turnover and illumination conditions. The formation of spinules was correlated with dopaminergic activity during all phases of the light/dark cycle and during short-term adaptation periods. Spinules were expressed in the light when dopamine activity was high and they were retracted when dopamine activity was reduced during darkness. Connexon density of horizontal cell gap junctions showed a weaker correlation with the endogenous dopamine turnover. In this case, a high activity of endogenous dopamine was paralleled by a high density of connexons.

Our results suggest that endogenous dopamine is involved in the cyclic regulation of the observed morphological alterations and that dopamine is part of the light signal for these mechanisms.

In this study, we investigated the potency of dopamine for being an intrinsic signal for cyclic events in the fish retina. Dopaminergic activity was measured during different light/dark cycles, during continuous darkness, and during short-term light and dark adaptation within 1 h. During a 12-h light/12-h dark cycle, the total content of endogenous dopamine was high during the dark phase and low during the light phase. The potassium-induced release of endogenous dopamine followed a parallel time course. The concentration of the dopamine breakdown product 3,4-dihydroxyphenylacetic acid (DOPAC), which reflects the endogenous dopaminergic activity, was high during the light phase and low during the dark phase. Similar alterations occurred in accelerated 6-h light/6-h dark cycles, again indicating a strong coupling of dopaminergic activity with light. The cyclic alterations in the total endogenous dopamine content persisted during continuous darkness after an entrainment of the fish to a 12-h light/12-h dark cycle. Although the magnitude of the change was weaker, changes in dopamine content, potassium-induced dopamine release, and DOPAC were also measured during 1 h of light or dark adaptation. During a 1-h period of dark adaptation, the total content of dopamine and the potassium-induced release of endogenous dopamine increased, while DOPAC values decreased. These values changed in the opposite direction during 1 h of light adaptation.

Our findings strongly suggest that dopamine is the intrinsic signal for light during both the light and dark phases and during short-term adaptation. Light seems to be the major trigger for dopaminergic activity within the fish retina. An endogenous clock might participate in the control of the dopaminergic activity. This has to be, however, confirmed by further investigations.

Growth rates in terms of area expansion per 30 min were measured in the red alga Porphyra leucosticta under different light/dark (LD) cycles, irradiance levels and light qualities. Twelve hours per day under white light (35 μmol m−2 s−1) promoted a dramatic and rapid increase in thallus expansion during the first part of the light period followed by low values during the remaining light and dark phase. Light/dark regimes of 8[ratio ]8 h, 6[ratio ]6 h, 3[ratio ]3 h and 1·5[ratio ]1·5 h resulted in a discontinuous growth pattern where thallus expansion was restricted to the light phase while no growth occurred in the dark phase, and there was even a significant thallus contraction just after light-off. Growth rates in terms of percentage area increased with irradiance at LD 12[ratio ]12. This was due to: (1) the phase of high growth rate following the initial ‘morning peak’ extending from the first 6 h of the light phase to cover almost the entire light phase, and (2) an increase in growth rate during the second half of the night phase. Saturation was reached at an irradiance of 125 μmol m−2 s−1. An irradiance of 500 μmol m−2 s−1 decreased thallus expansion rate during the light and dark culture phases relative to the other irradiances used. Light quality also caused changes in growth rate: the maximum value was reached under yellow light followed by red; both of these were higher than the growth rate under white light. Blue light (35 μmol m−2 s−1) caused a decrease of more than 50% in thallus expansion compared with white or red light due to a very dramatic decrease in the ‘morning peak’ of thallus expansion and very low values in the rest of the light and dark phases. Increasing the percentage of blue light in different white light sources also decreased thallus expansion. It is suggested that light influences the growth of Porphyra in three ways: as an external signal matching thallus expansion with light and dark cycles; as an energy source promoting thallus expansion with increasing irradiance; and, at a morphogenetic level, inhibiting growth in blue light.