{"title":"一般环流模式与对流层化学模式耦合得到的OH浓度","authors":"Gerhard W. Gross, M.A.K. Khalil","doi":"10.1016/S1465-9972(99)00054-9","DOIUrl":null,"url":null,"abstract":"<div><p>A comprehensive general circulation model has been coupled with a tropospheric chemistry model (TCM) using “on-line” actinic flux calculation. The three-dimensional global distribution of OH was calculated and is presented in some detail. A 2-year integration generated a volume- and pressure-weighted global, tropospheric, annual mean OH concentration of 8.4×10<sup>5</sup> molecules/cm<sup>3</sup>. Over 70 gas phase reactions involving 28 chemical species were solved, using a two-step backward differentiation formula (BDF) combined with Gauss–Seidel iteration. The set of chemical equations was solved every model hour. “On-line” actinic flux calculation allows for photo-radiation feedback between the two model components. Local changes in clouds and radiatively active gas concentrations directly affect the availability of actinic flux which has a direct impact on photochemistry through the photolysis rate constant. The actinic flux was efficiently calculated in each grid cell every model hour by the delta-Eddington radiation scheme of the general circulation model. The spectral resolution of the radiation scheme was 5 nm between 200 and 400 nm, 2 nm between 245 and 350 nm, and 25 nm between 350 and 700 nm. This provided for accurate calculations in the photolytically active spectral regions of O<sub>3</sub> and NO<sub>2</sub>.</p></div>","PeriodicalId":100235,"journal":{"name":"Chemosphere - Global Change Science","volume":"2 2","pages":"Pages 191-206"},"PeriodicalIF":0.0000,"publicationDate":"2000-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1465-9972(99)00054-9","citationCount":"7","resultStr":"{\"title\":\"OH concentrations from a general circulation model coupled with a tropospheric chemistry model\",\"authors\":\"Gerhard W. Gross, M.A.K. Khalil\",\"doi\":\"10.1016/S1465-9972(99)00054-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A comprehensive general circulation model has been coupled with a tropospheric chemistry model (TCM) using “on-line” actinic flux calculation. The three-dimensional global distribution of OH was calculated and is presented in some detail. A 2-year integration generated a volume- and pressure-weighted global, tropospheric, annual mean OH concentration of 8.4×10<sup>5</sup> molecules/cm<sup>3</sup>. Over 70 gas phase reactions involving 28 chemical species were solved, using a two-step backward differentiation formula (BDF) combined with Gauss–Seidel iteration. The set of chemical equations was solved every model hour. “On-line” actinic flux calculation allows for photo-radiation feedback between the two model components. Local changes in clouds and radiatively active gas concentrations directly affect the availability of actinic flux which has a direct impact on photochemistry through the photolysis rate constant. The actinic flux was efficiently calculated in each grid cell every model hour by the delta-Eddington radiation scheme of the general circulation model. The spectral resolution of the radiation scheme was 5 nm between 200 and 400 nm, 2 nm between 245 and 350 nm, and 25 nm between 350 and 700 nm. This provided for accurate calculations in the photolytically active spectral regions of O<sub>3</sub> and NO<sub>2</sub>.</p></div>\",\"PeriodicalId\":100235,\"journal\":{\"name\":\"Chemosphere - Global Change Science\",\"volume\":\"2 2\",\"pages\":\"Pages 191-206\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1465-9972(99)00054-9\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemosphere - Global Change Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1465997299000549\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemosphere - Global Change Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1465997299000549","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
OH concentrations from a general circulation model coupled with a tropospheric chemistry model
A comprehensive general circulation model has been coupled with a tropospheric chemistry model (TCM) using “on-line” actinic flux calculation. The three-dimensional global distribution of OH was calculated and is presented in some detail. A 2-year integration generated a volume- and pressure-weighted global, tropospheric, annual mean OH concentration of 8.4×105 molecules/cm3. Over 70 gas phase reactions involving 28 chemical species were solved, using a two-step backward differentiation formula (BDF) combined with Gauss–Seidel iteration. The set of chemical equations was solved every model hour. “On-line” actinic flux calculation allows for photo-radiation feedback between the two model components. Local changes in clouds and radiatively active gas concentrations directly affect the availability of actinic flux which has a direct impact on photochemistry through the photolysis rate constant. The actinic flux was efficiently calculated in each grid cell every model hour by the delta-Eddington radiation scheme of the general circulation model. The spectral resolution of the radiation scheme was 5 nm between 200 and 400 nm, 2 nm between 245 and 350 nm, and 25 nm between 350 and 700 nm. This provided for accurate calculations in the photolytically active spectral regions of O3 and NO2.