Abstract. Comprehensive observations of hydroxyl (OH) and hydroperoxy (HO2) radicals were conducted in October 2019 at a coastal continental site in the Pearl River Delta (YMK site, 22.55° N, 114.60° E). The average daily maximum OH and HO2 concentrations were (4.7–9.5) × 106 cm−3 and (4.2–8.1) × 108 cm−3, respectively. The synchronized air mass transport from the northern cities and the South China Sea exerted a time-varying influence on atmospheric oxidation. Under a typical ocean-atmosphere (OCM), reasonable measurement model agreement was achieved for both OH and HO2 using a 0-D chemical box model incorporating the regional atmospheric chemistry mechanism version 2-Leuven isoprene mechanism (RACM2-LIM1). Land mass (LAM) influence promoted more active photochemical processes, with daily averages of 7.1 × 106 cm−3 and 5.2 × 108 cm−3 for OH and HO2, respectively. Intensive photochemistry occurred after precursor accumulation, allowing local net ozone production comparable with surrounding suburban environments (5.52 ppb/h during the LAM period). The rapid oxidation process was accompanied by a higher diurnal nitrous acid (HONO) concentration (> 400 ppt). After a sensitivity test, HONO-related chemistry elevated the ozone production rate by 33 % and 39 % during the LAM and OCM periods, respectively, while the nitric acid and sulfuric acid formation rates were 52 % and 35 % higher, respectively. The simulated daytime HONO and ozone concentrations were reduced to a low level (~70 ppt and ~35 ppb) without the HONO constraint. This work challenges the conventional recognition of the MBL in a complex atmosphere. For coastal cities, the particularity of the HONO chemistry in the MBL tends to influence the ozone-sensitive system and eventually magnifies the background ozone. Therefore, the promotion of oxidation by elevated precursor concentrations is worth considering when formulating emission reduction policies.