An empirical relationship between the cellular cross-section absorption coefficient (a) and the Chl a fluorescence of individual plankton cells was established. Chl a fluorescence of single cells was measured in a flow cytometer with 488-nm argon-ion laser excitation. Absorption by dilute suspensions of cells was measured spectrophotometrically and normalized to cell number for computation of (r(488) (m2 cell-l). At the high excitation irradiances characteristic of lasers, a constant proportion of photons absorbed by photosynthetic pigments was re-emitted as Chl a fluorescence; a strong correlation was observed between absorption at 488 nm and Chl a fluorescence (r2 = 0.93; P << 0.00 1). The regression predicted the total phytoplankton absorption coefficient [a,,,,(488) (m-l)] at 488 nm for mixtures of five monospecific cultures with <9% error. For field samples, discrepancies between the flow cytometric method and the filter pad spectrophotometric method for estimating a,,,,(488) were greater. Relatively large, rare phytoplankton cells accounted for a disproportionate percentage of total a,,,,(488). The coherence between absorption at 488 nm and at other wavelengths was high and provides a basis for extrapolating from (r(488) to single-cell absorption coefficients at all visible wavelengths. The single-cell spectral absorption coefficients can be used to compute total in situ photon absorption for modeling light-limited photosynthetic rates of individual phytoplankton cells in the ocean.