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Phosphorus and its solubility in aerosols from continental and marine sources in the sea areas near China: Results from a 40-day cruise mission in late spring.
Liu, Yatong; Guan, Yang; Shi, Jinhui; Gao, Huiwang; Yao, Xiaohong; Zhang, Daizhou.
Affiliation
  • Liu Y; Key Laboratory of Marine Environmental Science and Ecology, Ocean University of China, Ministry of Education of China, Qingdao 266100, China.
  • Guan Y; Key Laboratory of Marine Environmental Science and Ecology, Ocean University of China, Ministry of Education of China, Qingdao 266100, China.
  • Shi J; Key Laboratory of Marine Environmental Science and Ecology, Ocean University of China, Ministry of Education of China, Qingdao 266100, China; Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China. Electronic addr
  • Gao H; Key Laboratory of Marine Environmental Science and Ecology, Ocean University of China, Ministry of Education of China, Qingdao 266100, China; Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.
  • Yao X; Key Laboratory of Marine Environmental Science and Ecology, Ocean University of China, Ministry of Education of China, Qingdao 266100, China; Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China.
  • Zhang D; Faculty of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, Kumamoto 862-8502, Japan.
Sci Total Environ ; 875: 162655, 2023 Jun 01.
Article in En | MEDLINE | ID: mdl-36894079
Accurate assessments of soluble phosphorus (P) in aerosol particles are essential to understand the atmospheric nutrients supply to the marine ecosystem. We quantified total P (TP) and dissolved P (DP) in the aerosol particles collected in the sea areas near China in a cruise mission from May 1 to June 11, 2016. The overall concentrations of TP and DP were 3.5-99.9 ng m-3 and 2.5-27.0 ng m-3, respectively. When the air originating from the desert areas, TP and DP were 28.7-99.9 ng m-3 and 10.8-27.0 ng m-3, respectively, and P solubility was 24.1-54.6 %. When the air influenced mainly by anthropogenic emissions from eastern China, TP and DP were 11.7-12.3 ng m-3 and 5.7-6.3 ng m-3, respectively, and P solubility was 46.0-53.7 %. More than half of the TP and more than 70 % of the DP were from pyrogenic particles, with a considerable DP converted via aerosol acidification after the particles met humid marine air. On average, aerosol acidification promoted the fractional solubility of dissolved inorganic P (DIP) to TP from 22 % to 43 %. When the air originating from the marine areas, TP and DP were 3.5-22.0 ng m-3 and 2.5-8.4 ng m-3, respectively, and P solubility was 34.6-93.6 %. About one-third of the DP was from biological emissions in organic forms (DOP), leading to higher solubility than in the particles from continental sources. These results reveal the dominance of inorganic P in TP and DP from the desert and anthropogenic mineral dust and the significant contribution of organic P from marine sources. The results also indicate the necessity to treat aerosol P carefully according to different sources of the aerosol particles and atmospheric processes the particles experience in assessing aerosol P input to seawater.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Sci Total Environ Year: 2023 Document type: Article Affiliation country: China Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Sci Total Environ Year: 2023 Document type: Article Affiliation country: China Country of publication: Países Bajos