{"title":"Quantifying Lithogenic Inputs to the Ocean From the GEOTRACES Thorium Transects in a Data-Assimilation Model","authors":"Hairong Xu, Thomas Weber","doi":"10.1029/2024GB008485","DOIUrl":null,"url":null,"abstract":"<p>The primordial thorium (Th) isotope <sup>232</sup>Th is delivered to global ocean waters by lithogenic material dissolution, originating from dust deposition on the ocean surface and seafloor sediments around continental margins. Radiogenic <sup>230</sup>Th shares the same particle-scavenging removal processes as <sup>232</sup>Th but has a simpler source from uniform <sup>234</sup>U decay. The <sup>232</sup>Th–<sup>230</sup>Th isotope system is therefore widely used to jointly constrain source and sink processes and infer lithogenic trace element inputs but has not been leveraged systematically at the global scale. This study utilizes data-assimilation models of the <sup>230</sup>Th and <sup>232</sup>Th cycles to draw global insights from GEOTRACES section data. Optimization of <sup>230</sup>Th model reveals that scavenging onto biogenic particles is the largest Th removal mechanism globally, but regional-scale losses are dominated by scavenging onto metal oxides near hydrothermal vents, nepheloid layer particles along deep margins, and lithogenic particles beneath dust plumes. Together with large-scale ocean circulation, these processes shape the global distribution of <sup>230</sup>Th. A subsequent ensemble of <sup>232</sup>Th model optimizations reveals that the observed <sup>232</sup>Th distribution is consistent with a global source of 2.8 ± 0.54 Mmol/yr from dust dissolution, and implies a higher and more homogeneous solubility of <sup>232</sup>Th relative to other lithogenic trace elements. An additional source of 5.25 ± 0.86 Mmol/yr from lithogenic sediment dissolution is required to match observed <sup>232</sup>Th, with a distribution controlled by sediment lithology and accumulation rate. This translates to an oceanic Fe source of 5–50 Gmol/yr, highlighting the need to resolve this process in Fe cycle models that often only consider a reductive sedimentary source.</p>","PeriodicalId":12729,"journal":{"name":"Global Biogeochemical Cycles","volume":"39 6","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1029/2024GB008485","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Global Biogeochemical Cycles","FirstCategoryId":"89","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1029/2024GB008485","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The primordial thorium (Th) isotope 232Th is delivered to global ocean waters by lithogenic material dissolution, originating from dust deposition on the ocean surface and seafloor sediments around continental margins. Radiogenic 230Th shares the same particle-scavenging removal processes as 232Th but has a simpler source from uniform 234U decay. The 232Th–230Th isotope system is therefore widely used to jointly constrain source and sink processes and infer lithogenic trace element inputs but has not been leveraged systematically at the global scale. This study utilizes data-assimilation models of the 230Th and 232Th cycles to draw global insights from GEOTRACES section data. Optimization of 230Th model reveals that scavenging onto biogenic particles is the largest Th removal mechanism globally, but regional-scale losses are dominated by scavenging onto metal oxides near hydrothermal vents, nepheloid layer particles along deep margins, and lithogenic particles beneath dust plumes. Together with large-scale ocean circulation, these processes shape the global distribution of 230Th. A subsequent ensemble of 232Th model optimizations reveals that the observed 232Th distribution is consistent with a global source of 2.8 ± 0.54 Mmol/yr from dust dissolution, and implies a higher and more homogeneous solubility of 232Th relative to other lithogenic trace elements. An additional source of 5.25 ± 0.86 Mmol/yr from lithogenic sediment dissolution is required to match observed 232Th, with a distribution controlled by sediment lithology and accumulation rate. This translates to an oceanic Fe source of 5–50 Gmol/yr, highlighting the need to resolve this process in Fe cycle models that often only consider a reductive sedimentary source.
期刊介绍:
Global Biogeochemical Cycles (GBC) features research on regional to global biogeochemical interactions, as well as more local studies that demonstrate fundamental implications for biogeochemical processing at regional or global scales. Published papers draw on a wide array of methods and knowledge and extend in time from the deep geologic past to recent historical and potential future interactions. This broad scope includes studies that elucidate human activities as interactive components of biogeochemical cycles and physical Earth Systems including climate. Authors are required to make their work accessible to a broad interdisciplinary range of scientists.