New particle formation during the oxidation of <font face="Symbol" >a</font>- and <font face="Symbol" >b</font>-pinene (C<sub>10</sub>H<sub>16</sub>) by ozone, OH and NO<sub>3</sub> was studied by measuring the particle size distributions with a scanning mobility particle sizer (TSI 3936). The results indicate a drastically higher nucleation potential of the ozonolysis than in the reaction with either OH or NO<sub>3</sub>. On the contrary, the contribution of the individual oxidation reactions to form new aerosol volume was found to depend on the location of the carbon double bond to be oxidized: for the <i>endocyclic</i> <font face="Symbol" >a</font>-pinene reactions the ozonolysis contributed mostly to the aerosol volume yield, whereas for the <i>exocyclic</i> <font face="Symbol" >b</font>-pinene reactions the oxidation by O<sub>3</sub>, OH and NO<sub>3</sub> yielded a similar aerosol volume.<br> <br> In a second part of this study the influence of water vapour on the nucleation in all three possible oxidation routes was examined. The observations revealed only an effect of water vapour during the ozonolysis reactions.