<p>Nitrous acid (HONO) can produce hydroxyl radicals (OH) by photolysis and plays an important role in atmospheric photochemistry. Over the years, high concentrations of HONO have been found in the Pearl River Delta region (PRD), which may be one of the reasons for the high atmospheric oxidation capacity. A comprehensive atmospheric observation was conducted at an urban site in Guangzhou from 27 September to 9 November 2018. During the period, HONO ranged from 0.02 to 4.43 ppbv with an average of 0.74&#177;0.70 ppbv. The combustion emission ratio (HONO/NOx) of 0.9&#177;0.4% was derived from 11 fresh plumes. The primary emission rate of HONO during night was calculated with the emission source inventory data to be between 0.04&#177;0.02 and 0.30&#177;0.15 ppbv/h. And the HONO produced by the homogeneous reaction of OH+NO at night was 0.26&#177;0.08 ppbv/h, which can be seemed as secondary results from primary emission. They were both much higher than the increase rate of HONO (0.02 ppbv/h) during night. Soil emission rate of HONO at night was calculated to be 0.019&#177;0.0003 ppbv/h. Deposition was the dominant removal process of HONO during night, and a deposition rate of at least 2.5 cm/s is required to balance the direct emissions and OH+NO reaction. Correlation analysis shows that NH<sub>3</sub> and relative humidity (RH) may participate in the heterogeneous transformation from NO<sub>2</sub> to HONO during night. In the daytime, the average primary emission P<sub>emis</sub> was 0.12&#177;0.01 ppbv/h, and the homogeneous reaction P<sub>OH+NO</sub> was 0.79&#177;0.61 ppbv/h, which was even larger than the unknown sources P<sub>Unknown</sub> (0.65&#177;0.46 ppbv/h). The results showed that the direct and indirect contributions of primary emission to HONO are great at the site, both during daytime and nighttime. Similar to previous studies, P<sub>Unknown</sub> was suggested to be related to the photo-enhanced reaction of NO<sub>2</sub>. The mean OH production rates by photolysis of HONO and O<sub>3</sub> were 3.7&#215;10<sup>6</sup> cm<sup>-3</sup>&#183;s<sup>-1</sup> and 4.9&#215;10<sup>6</sup> cm<sup>-3</sup>&#183;s<sup>-1</sup>, respectively. We further studied the impact of HONO on the atmospheric oxidation by a Master Chemical Mechanism (MCM) box model. When constraining observed HONO in the model, OH and O<sub>3 </sub>increased 59% and 68.8% respectively, showing a remarkable contribution of HONO to the atmospheric oxidation of Guangzhou.</p><p>&#160;</p>