Trevor J. McDougall, P. Barker, R. Feistel, F. Roquet
{"title":"以绝对盐度、恒温和原位压力表示的海水热力学潜力","authors":"Trevor J. McDougall, P. Barker, R. Feistel, F. Roquet","doi":"10.5194/os-19-1719-2023","DOIUrl":null,"url":null,"abstract":"Abstract. A thermodynamic potential is derived for seawater as a function of Conservative Temperature, Absolute Salinity and pressure. From this thermodynamic potential, all the equilibrium thermodynamic properties of seawater can be found, just as all these thermodynamic properties can be found from the TEOS-10 (the International Thermodynamic Equation of Seawater – 2010; IOC et al., 2010) Gibbs function (which is a function of in situ temperature, Absolute Salinity, and pressure). Present oceanographic practice in the Gibbs SeaWater Oceanographic Toolbox uses a polynomial expression for specific volume (and enthalpy) in terms of Conservative Temperature (as well as of Absolute Salinity and pressure), whereas the relationship between in situ temperature and Conservative Temperature is based on the Gibbs function. This mixed practice introduces (numerically small) inconsistencies and superfluous conversions between variables. The proposed thermodynamic potential of seawater, being expressed as an explicit function of Conservative Temperature, overcomes these small numerical inconsistencies, and in addition, the new approach allows for greater computational efficiency in the evaluation of sea surface temperature from Conservative Temperature. It is also shown that when using Conservative Temperature, the thermodynamic information in enthalpy is independent of that contained in entropy. This contrasts with the cases where either in situ temperature or potential temperature is used. In these cases, a single thermodynamic potential serves the important purpose of avoiding having to impose a separate consistency requirement between the functional forms of enthalpy and entropy.\n","PeriodicalId":19535,"journal":{"name":"Ocean Science","volume":"56 10","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2023-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A thermodynamic potential of seawater in terms of Absolute Salinity, Conservative Temperature, and in situ pressure\",\"authors\":\"Trevor J. McDougall, P. Barker, R. Feistel, F. Roquet\",\"doi\":\"10.5194/os-19-1719-2023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Abstract. A thermodynamic potential is derived for seawater as a function of Conservative Temperature, Absolute Salinity and pressure. From this thermodynamic potential, all the equilibrium thermodynamic properties of seawater can be found, just as all these thermodynamic properties can be found from the TEOS-10 (the International Thermodynamic Equation of Seawater – 2010; IOC et al., 2010) Gibbs function (which is a function of in situ temperature, Absolute Salinity, and pressure). Present oceanographic practice in the Gibbs SeaWater Oceanographic Toolbox uses a polynomial expression for specific volume (and enthalpy) in terms of Conservative Temperature (as well as of Absolute Salinity and pressure), whereas the relationship between in situ temperature and Conservative Temperature is based on the Gibbs function. This mixed practice introduces (numerically small) inconsistencies and superfluous conversions between variables. The proposed thermodynamic potential of seawater, being expressed as an explicit function of Conservative Temperature, overcomes these small numerical inconsistencies, and in addition, the new approach allows for greater computational efficiency in the evaluation of sea surface temperature from Conservative Temperature. It is also shown that when using Conservative Temperature, the thermodynamic information in enthalpy is independent of that contained in entropy. This contrasts with the cases where either in situ temperature or potential temperature is used. In these cases, a single thermodynamic potential serves the important purpose of avoiding having to impose a separate consistency requirement between the functional forms of enthalpy and entropy.\\n\",\"PeriodicalId\":19535,\"journal\":{\"name\":\"Ocean Science\",\"volume\":\"56 10\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2023-12-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ocean Science\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.5194/os-19-1719-2023\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"METEOROLOGY & ATMOSPHERIC SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ocean Science","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.5194/os-19-1719-2023","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"METEOROLOGY & ATMOSPHERIC SCIENCES","Score":null,"Total":0}
A thermodynamic potential of seawater in terms of Absolute Salinity, Conservative Temperature, and in situ pressure
Abstract. A thermodynamic potential is derived for seawater as a function of Conservative Temperature, Absolute Salinity and pressure. From this thermodynamic potential, all the equilibrium thermodynamic properties of seawater can be found, just as all these thermodynamic properties can be found from the TEOS-10 (the International Thermodynamic Equation of Seawater – 2010; IOC et al., 2010) Gibbs function (which is a function of in situ temperature, Absolute Salinity, and pressure). Present oceanographic practice in the Gibbs SeaWater Oceanographic Toolbox uses a polynomial expression for specific volume (and enthalpy) in terms of Conservative Temperature (as well as of Absolute Salinity and pressure), whereas the relationship between in situ temperature and Conservative Temperature is based on the Gibbs function. This mixed practice introduces (numerically small) inconsistencies and superfluous conversions between variables. The proposed thermodynamic potential of seawater, being expressed as an explicit function of Conservative Temperature, overcomes these small numerical inconsistencies, and in addition, the new approach allows for greater computational efficiency in the evaluation of sea surface temperature from Conservative Temperature. It is also shown that when using Conservative Temperature, the thermodynamic information in enthalpy is independent of that contained in entropy. This contrasts with the cases where either in situ temperature or potential temperature is used. In these cases, a single thermodynamic potential serves the important purpose of avoiding having to impose a separate consistency requirement between the functional forms of enthalpy and entropy.
期刊介绍:
Ocean Science (OS) is a not-for-profit international open-access scientific journal dedicated to the publication and discussion of research articles, short communications, and review papers on all aspects of ocean science: experimental, theoretical, and laboratory. The primary objective is to publish a very high-quality scientific journal with free Internet-based access for researchers and other interested people throughout the world.
Electronic submission of articles is used to keep publication costs to a minimum. The costs will be covered by a moderate per-page charge paid by the authors. The peer-review process also makes use of the Internet. It includes an 8-week online discussion period with the original submitted manuscript and all comments. If accepted, the final revised paper will be published online.
Ocean Science covers the following fields: ocean physics (i.e. ocean structure, circulation, tides, and internal waves); ocean chemistry; biological oceanography; air–sea interactions; ocean models – physical, chemical, biological, and biochemical; coastal and shelf edge processes; paleooceanography.