In order to understand the effect of nitrogen sources on the growth and toxicity of harmful dinoflagellate Alexandrium tamarense, four nitrogen sources (nitrate, ammonium, urea and glycine) were added into artificial seawater enriched with F/20 and cells were batchcultured at 20 oC and 200 μmol photons·m-2·s-1. Cells of A. tamarense at exponential phase were collected to test the acute toxic effect on zebrafish embryo in 48 hours. The results showed that four nitrogen sources were all utilized by A. tamarense, but the growth rate was different, being ammonium (0.25 d-1) > nitrate (0.20 d-1) > urea = glycine (0.12 d-1). However, the pigment contents were not influenced. Compared with the control group (embryo medium), the rude extract of A. tamarense at 2
×104 cells·mL-1 had significantly teratogenic effects on the zebrafish embryos, resulting in embryo coagulation, developmental retardation, vitelline membrane rupture, yolk sac edema and tail bending. When the cell density increased to 8×104 cells·mL-1, the toxicity increased accordingly, moreover, a significant difference was found among the four nitrogen sources, showing nitrate > urea = glycine > ammonium. In summary, A. tamarense can maintain relatively high growth rate and make algal blooms outbreak continuously regardless of environmental changes, which threatens the ecological environment in coastal areas.