The effects of magnetic fields (0-6 kG) on the delayed fluorescence and photoenhanced currents in crystalline pyrene at 300 K can be explained qualitatively using the theories already used for anthracene. It is found that the moving triplet exciton has the same zero-field fine structure as the monomer exciton. In delayed fluorescence, triplet pair formation is diffusion limited with no long range interaction (rate constant 2.7 x 10-10 cm3 s-1) and pair lifetime is of the order of one hopping time, or 10-10 s, with no evidence of pair stabilization. In the study of photocurrents, two magnetic field effects, of opposite sign, are found. If the current is space-charge limited, triplets alter the ratio of free charge to trapped charge ; and the magnetic field acts through modulation of the triplet-trapped charge interaction rate constant. The rate constant for pair formation (1.7 x 10 -9 cm3 s-1) is found to be much larger than diffusion limited for nearest neighbour interaction, and implies a distance for pair formation of several tens of Å. Yet reaction of the pair thus formed to generate a singlet occurs only in about 10 % of cases. If the current is injection limited, triplets enhance the injection ability of the electrode, and the magnetic field acts through modulation of the triplet lifetime (by interaction with trapped charges), hence of the triplet density near the surface and the triplet flux to the electrode