Cultures of Ceratium fusus were grown at seven light intensities (5 to 400 μmol photons m−2 s−1 as photosynthetically active radiation (PAR)) in the laboratory. Measurements of bioluminescence capacity (BCAP), division rate, and cell size were made at each intensity and compared to similar data from natural populations. In cultures, BCAP increased by a factor of 5–10 with increasing light. Division rates ranged from 0 d−1 (5 μmol photons m−2 s−1) to about 0.16 d−1 (100 μmol photons m−2 s−1). In these cultures, BCAP was highly correlated with both the log of light (r2 = 0.89) and division rate (r2 = 0.69), suggesting that BCAP may be of use as an in‐situ indicator of division rate. In both cultures and natural populations, BCAP was poorly correlated with cell size (r2 ≈ 0.3 and r2 ≈ 0.1 respectively). For populations from the Gulf of Maine ( ∼42°N, 69° W) and the Marine light‐Mixed Layers (MLML) site (∼59°N, 21° W), division rates in the mixed‐layer could only be determined with statistical certainty at the Gulf of Maine station (0.04 to 0.17 d−1). At the MLML site, BCAP in C. fusus was greater in the mixed‐layer in May and below the mixed‐layer in August. The August result is opposite to what culture photoenhancement studies would predict if light was the factor controlling BCAP.