Sr-bearing marine barite [(Ba x , Sr 1−x )SO 4 ] cycling has been widely used to reconstruct geochemical evolutions of paleoenvironments. However, an understanding of barite precipitation in the ocean, which is globally undersaturated with respect to barite, is missing. Moreover, the reason for the occurrence of higher Sr content in marine barites than expected for classical crystal growth processes remains unknown. Field data analyses suggested that organic molecules may regulate the formation and composition of marine barites; however, the specific organic-mineral interactions are unclear. Using in situ grazing incidence small-angle X-ray scattering (GISAXS), size and total volume evolutions of barite precipitates on organic films were characterized. The results show that barite forms on organic films from undersaturated solutions. Moreover, from a single supersaturated solution with respect to barite, Sr-rich barite nanoparticles formed on organics, while micrometer-size Sr-poor barites formed in bulk solutions. Ion adsorption experiments showed that organic films can enrich cation concentrations in the adjacent solution, thus increasing the local supersaturation and promoting barite nucleation on organic films, even when the bulk solution was undersaturated. The Sr enrichment in barites formed on organic films was found to be controlled by solid-solution nucleation rates; instead, the Sr-poor barite formation in bulk solution was found to be controlled by solid-solution growth rates. This study provides a mechanistic explanation for Sr-rich marine barite formation and offers insights for understanding and controlling the compositions of solid solutions by separately tuning their nucleation and growth rates via the unique chemistry of solution-organic interfaces.Sr-rich marine barite | organic-mineral interactions | solid solution | nucleation and growth | paleoenvironments S r-bearing barite [(Ba x , Sr 1−x )SO 4 ] is an important marine authigenic mineral present in the seawater column and marine sediments (1-5). Marine barite formation, essential to the global cycles of organic carbon, sulfate, and oxygen, can be used to reconstruct the changes in geochemical cycles and paleoproductivity, and Sr incorporation may reflect the oceanographic conditions (2, 5-7). Despite the geochemical importance of marine (Ba x , Sr 1−x )SO 4 formation, two paradoxes still exist. First, the global oceans are undersaturated with respect to barite, while barite is extensively present in seawater column and marine sediments (5,7,8). Second, Sr-rich marine barite (>50 mol% strontium) formation (7, 9) is not thermodynamically favorable (7, 10), as the solubility of SrSO 4 (K sp,SrSO4 = 10 −6.63 ) is three orders of magnitude higher than BaSO 4 (K sp,BaSO4 = 10 −9.98 ) (3, 10). Field and laboratory studies provide evidence for the association of organics with both paradoxes (7, 11); however, the specific roles of organics in these thermodynamically unfavorable mineralization processes are not clear (7,11,12).Organic-mineral interac...