Publisher Correction: Pelagic barite precipitation at micromolar ambient sulfate.

The original version of this Article contained an error in the barite saturation state equation in the fourth paragraph of the Introduction and incorrectly read 'Ωbarite=({134Ba2+}⋅{SO42-})/Ksp)'. The correct version removes the superscript 134 next to 'Ba2+'. This error has now been corrected in both the PDF and HTML versions of the Article.

Pelagic barite precipitation at micromolar ambient sulfate.

Geochemical analyses of sedimentary barites (barium sulfates) in the geological record have yielded fundamental insights into the chemistry of the Archean environment and evolutionary origin of microbial metabolisms. However, the question of how barites were able to precipitate from a contemporary ocean that contained only trace amounts of sulfate remains controversial. Here we report dissolved and particulate multi-element and barium-isotopic data from Lake Superior that evidence pelagic barite precipitation at micromolar ambient sulfate. These pelagic barites likely precipitate within particle-associated microenvironments supplied with additional barium and sulfate ions derived from heterotrophic remineralization of organic matter. If active during the Archean, pelagic precipitation and subsequent sedimentation may account for the genesis of enigmatic barite deposits. Indeed, barium-isotopic analyses of barites from the Paleoarchean Dresser Formation are consistent with a pelagic mechanism of precipitation, which altogether offers a new paradigm for interpreting the temporal occurrence of barites in the geological record.