Abstract:The level of marine environmental management is a key factor in the successful implementation of marine power strategies. The improvement in management levels of marine environments requires innovation in marine management. In other words, the transformation of marine environmental management into marine ecological environment management must be done in order to achieve sustainable development of the marine economy. As an environmental economic policy that combines both administrative and market measures, ecological compensation mechanisms have significant advantages in marine ecological environment management. Based on the study of the current development of ecological compensation mechanisms in China, through the analysis of the connotation of marine ecological civilization, existing marine ecological protection practices and marine environmental management methods, this paper posits that the current marine ecological environment management in China should be established on the basis of ecological compensation mechanisms. At present, a lack of laws and regulations for overall marine ecological environment management is the key factor restricting the practice of marine ecological environment management. Therefore, it is necessary to explore the current path of marine ecological environment management in China from the perspective of the construction of legal system of ecological compensation law, the establishment of ecological compensation fees, ecological taxes and ecological compensation fund systems, and the clear status for a marine ecological management and supervision body.

No abstract

Identifying the health risk of PM 2.5 is essential for urban air pollution control. In 2013, China announced the ever-strict national Air Pollution Prevention and Control Action Plan, and its health benefit should be evaluated to provide reference for future policymaking. In this study, we conducted a seven-year (2014−2020) continuous observation of PM 2.5 in Shenzhen, the third largest city in China, which has relatively good air quality. The results showed that the annual mean PM 2.5 and total concentration of 21 associated metals dropped from 37.7 to 18.5 μg/m 3 and from 2.4 to 1.1 μg/m 3 , respectively. Combining methods for source apportionment and health risk assessment, we found that the total carcinogenic risk (CR) of five hazardous metals (Cd, Cr, Ni, Co, and Pb) showed a clear decreasing trend. However, the total CR (1.8 × 10 −6 ) in 2020 still exceeded the widely acceptable risk level (i.e., 1 × 10 −6 ), with the primary contributor changing from industrial emissions (61%) to vehicle emissions (63%). Further analysis indicated that the CR of vehicles mainly came from Cr and Ni released by braking and tire wearing and has fluctuated in recent years, highlighting a great challenge of controlling nonexhaust emissions of vehicles (including electric cars) in the future.

Tropospheric ozone (O3) is a harmful gas compound to humans and vegetation, and it also serves as a climate change forcer. O3 is formed in the reactions of nitrogen oxides and volatile organic compounds (VOCs) with light. In this study, an O3 pollution episode encountered in Shenzhen, South China in 2018 was investigated to illustrate the influence of aerosols on local O3 production. We used a box model with comprehensive heterogeneous mechanisms and empirical prediction of photolysis rates to reproduce the O3 episode. Results demonstrate that the aerosol light extinction and NO2 heterogeneous reactions showed comparable influence but opposite signs on the O3 production. Hence, the influence of aerosols from different processes is largely counteracted. Sensitivity tests suggest that O3 production increases with further reduction in aerosols in this study, while the continued NO x reduction finally shifts O3 production to an NO x -limited regime with respect to traditional O3–NO x -VOC sensitivity. Our results shed light on the role of NO x reduction on O3 production and highlight further mitigation in NO x not only limiting the production of O3 but also helping to ease particulate nitrate, as a path for cocontrol of O3 and fine particle pollution.

Abstract. The ambient radical concentrations were measured continuously by laser-induced fluorescence during the STORM (STudy of the Ozone foRmation Mechanism) campaign at the Shenzhen site, located in the Pearl River Delta in China, in the autumn of 2018. The diurnal maxima were 4.5×106 cm−3 for OH radicals and 4.2×108 cm−3 for HO2 radicals (including an estimated interference of 23 %–28 % from RO2 radicals during the daytime), respectively. The state-of-the-art chemical mechanism underestimated the observed OH concentration, similar to the other warm-season campaigns in China. The OH underestimation was attributable to the missing OH sources, which can be explained by the X mechanism. Good agreement between the observed and modeled OH concentrations was achieved when an additional numerical X equivalent to 0.1 ppb NO concentrations was added into the base model. The isomerization mechanism of RO2 derived from isoprene contributed approximately 7 % to the missing OH production rate, and the oxidation of isoprene oxidation products (MACR and MVK) had no significant impact on the missing OH sources, demonstrating further exploration of unknown OH sources is necessary. A significant HO2 heterogeneous uptake was found in this study, with an effective uptake coefficient of 0.3. The model with the HO2 heterogeneous uptake can simultaneously reproduce the OH and HO2 concentrations when the amount of X changed from 0.1 to 0.25 ppb. The ROx primary production rate was dominated by photolysis reactions, in which the HONO, O3, HCHO, and carbonyls photolysis accounted for 29 %, 16 %, 16 %, and 11 % during the daytime, respectively. The ROx termination rate was dominated by the reaction of OH+NO2 in the morning, and thereafter the radical self-combination gradually became the major sink of ROx in the afternoon. As the sum of the respective oxidation rates of the pollutants via reactions with oxidants, the atmospheric oxidation capacity was evaluated, with a peak of 11.8 ppb h−1 around noontime. The ratio of P(O3)net to AOCVOCs, which indicates the yield of net ozone production from VOC oxidation, trended to increase and then decrease as the NO concentration increased. The median ratios ranged within 1.0–4.5, with the maximum existing when the NO concentration was approximately 1 ppb. The nonlinear relationship between the yield of net ozone production from VOC oxidation and NO concentrations demonstrated that optimizing the NOx and VOC control strategies is critical to controlling ozone pollution effectively in the future.