The symbiotic association between the acoel flatworm Symsagittifera roscoffensis and the prasinophyte microalgae Tetraselmis convolutae was studied regarding its photophysiology and photobehaviour. The photoacclimation status and the photophysiological responses to high light of the algal endosymbiont were studied non-destructively on individual S. roscoffensis using pulse amplitude modulated fluorometry. Specimens collected in an intertidal sandy shore were characterized regarding the maximum quantum yield of photosystem II (PSII), Fv/Fm, and the light response of photosynthetic activity, by constructing rapid light-response curves of the relative electron transport rate of PSII, rETR. The studied population could be considered as high light-acclimated when compared with other intertidal photosynthetic organisms (e.g. macroalgae), with the light-saturation parameter Ek averaging 250 μmol m−2 s−1. Light stress experiments showed S. roscoffensis to be able to withstand the exposure to high light without displaying signs of photoinhibition, suggesting the operation of efficient physiological photoprotective processes. The photobehaviour of S. roscoffensis was studied by characterizing the distribution of the flatworms under a light gradient, using a custom-made photoaccumulation chamber. The results showed a photoaccumulation pattern evidencing a clear avoidance of extreme low or high light levels, and with maximum photoaccumulation values being found for a range of irradiances (150–400 μmol m−2 s−1) that generally coincided with the optima for photosynthetic activity. This matching between the optimum light levels for photosynthetic activity and photoaccumulation suggested that S. roscoffensis may use vertical migration as a form of behavioural photoprotection. This behavioural response may be used to rapidly and flexibly control light exposure, avoiding photodamage to the endosymbiont photosynthetic apparatus by direct exposure to sunlight.

Many pelagic animal species in the marine environment and in lakes migrate to deeper water layers before sunrise and return around sunset. The amplitude of these diel vertical migrations (DVM) varies from several hundreds of metres in the oceans to approx. 5–20 m in lakes. DVM can be studied from a proximate and an ultimate point of view. A proximate analysis is intended to reveal the underlying behavioural mechanism and the factors that cause the daily displacements. The ultimate analysis deals with the adaptive significance of DVM and the driving forces that were responsible for the selection of the traits essential to the behavioural mechanism. The freshwater cladoceran Daphnia is the best studied species and results can be used to model migration behaviour in general. Phototaxis in Daphnia spp., which is defined as a light-oriented swimming towards (positive phototaxis) or away (negative phototaxis) from a light source, is considered the most important mechanism basic to DVM. A distinction has been made between primary phototaxis which occurs when light intensity is constant, and secondary phototaxis which is caused by changes in light intensity. Both types of reaction are superimposed on normal swimming. This swimming of Daphnia spp. consists of alternating upwards and downwards displacements over small distances. An internal oscillator seems to be at the base of these alternations. Primary phototaxis is the result of a dominance of either the upwards or the downwards oscillator phase, and the direction depends on internal and external factors: for example, fish-mediated chemicals or kairomones induce a downwards drift. Adverse environmental factors may produce a persistent primary phototaxis. Rare clones of D. magna have been found that show also persistent positive or negative primary phototaxis and interbreeding of the two types produces intermediate progeny: thus a genetic component seems to be involved. Also secondary phototaxis is superimposed on normal swimming: a continuous increase in light intensity amplifies the downwards oscillator phase and decreases the upwards phase. A threshold must be succeeded which depends on the rate and the duration of the relative change in light intensity. The relation between both is given by the stimulus strength versus stimulus duration curve. An absolute threshold or rheobase exists, defined as the minimum rate of change causing a response if continued for an infinitely long time. DVM in a lake takes place during a period of 1·5–2 h when light changes are higher than the rheobase threshold. Accelerations in the rate of relative increase in light intensity strongly enhance downwards swimming in Daphnia spp. and this enhancement increases with increasing fish kairomone and food concentration. This phenomenon may represent a ‘decision-making mechanism’ to realize the adaptive goal of DVM: at high fish predator densities, thus high kairomone concentrations, and sufficiently high food concentrations, DVM is profitable but not so at low concentrations. Body axis orientation in Daphnia spp. is controlled with regard to light–dark boundaries or contrasts. Under water, contrasts are present at the boundaries of the illuminated circular window which results from the maximum angle of refraction at 48·9° with the normal (Snell's window). Contrasts are fixed by the compound eye and appropriate turning of the body axis orients the daphnid in an upwards or an obliquely downwards direction. A predisposition for a positively or negatively phototactic orientation seems to be the result of a disturbed balance of the two oscillators governing normal swimming.

Some investigators have tried to study DVM at a laboratory scale during a 24 h cycle. To imitate nature, properties of a natural water column, such as a large temperature gradient, were compressed into a few cm. With appropriate light intensity changes, vertical distributions looking like DVM were obtained. The results can be explained by phototactic reactions and the artificial nature of the compressed environmental factors but do not compare with DVM in the field.

A mechanistic model of DVM based on phototaxis is presented. Both, primary and secondary phototaxis is considered an extension of normal swimming. Using the light intensity changes of dawn and the differential enhancement of kairomones and food concentrations, amplitudes of DVM could be simulated comparable to those in a lake.

The most important adaptive significance of DVM is avoidance of visual predators such as juvenile fish. However, in the absence of fish kairomones, small-scale DVMs are often present, which were probably evolved for UV-protection, and are realized by not enhanced phototaxis. In addition, the ‘decision-making mechanism’ was probably evolved as based on the enhanced phototactic reaction to accelerations in the rate of relative changes in light intensity and the presence of fish kairomones.