Chromium biogeochemistry and stable isotope distribution in the Southern Ocean. (1st October 2019)

• Record Type: Journal Article
• Authors: Rickli, Jörg; Janssen, David J.; Hassler, Christel; Ellwood, Michael J.; Jaccard, Samuel L.
• Is Part Of: Geochimica et cosmochimica acta. Volume 262(2019)
• Page Start: 188
• Page End: 206
• Publication Date: 2019-10-01
• Subjects: Seawater -- Chromium isotopes -- Southern Ocean; Geochemistry -- Periodicals; Meteorites -- Periodicals; Géochimie -- Périodiques; Météorites -- Périodiques; Geochemie; Astrochemie; Electronic journals; 551.905
• DOI: 10.1016/j.gca.2019.07.033
• Languages: English
• ISSNs: 0016-7037

Abstract

Abstract: Despite the potential of stable chromium (Cr) isotope compositions as a proxy for past changes in oceanic redox conditions, a detailed understanding of the processes that govern their spatial distribution in the modern ocean is still lacking. Here, we report seawater Cr isotope compositions and concentrations from the uppermost 1000 m of the water column in the Southern Ocean. The survey includes a cross-frontal transect from Tasmania to Antarctica, sites near the Antarctic ice-edge and in the vicinity of the Balleny Islands, as well as sites in the Drake Passage. Although a coastal influence is clearly visible in the silicon-nitrate relationship at the stations neighbouring the Balleny Islands, close to the Mertz Glacier and adjacent to the western Antarctic Peninsula, seawater δ 53 Cr and Cr concentrations remain largely unaffected. As for the coastal sites, Cr depletion and isotopic shifts are also virtually absent in Antarctic and Subantarctic surface waters of the open ocean. Biological uptake of Cr and/or scavenging of Cr onto sinking particles are apparently not strong enough to induce water column variability. Contrasting with the small variations in δ 53 Cr and Cr concentrations at each site, there are, however, systematic meridional changes. The seawater samples show an increase in Cr concentrations and a parallel decrease in δ 53 Cr southwards from the Subantarctic across the Polar Frontal into the Antarctic Zone. Chromium concentrations and δ 53 Cr are, however, uniform at all stations south of the Polar Front. The spatial pattern is consistent with the mixing of Southern Ocean sourced Cr with an isotopically heavier Cr pool from northward of the studied area, as evidenced by strong correlations of Cr and δ 53 Cr with salinity at the level of Subantarctic Mode Water and at shallower levels. The heavy δ 53 Cr signature of the northerly Cr pool could either result from Cr cycling in the subtropical gyre or originate in oxygen minimum zones. On a regional scale, δ 53 Cr is strongly correlated with phosphate concentrations, which may hint at a time-integrated effect of major nutrient drawdown on δ 53 Cr. Southern Ocean data support previous work demonstrating a strong relationship between seawater Cr concentrations and δ 53 Cr. At the studied sites, this relationship reflects mixing of isotopically distinct Cr pools. The end-members observed in the studied area are, however, consistent with the previously described closed-system Rayleigh type fractionation of Cr in seawater characterized by a single fractionation factor. The underlying processes, which produce the observed fractionation, are not fully constrained to date.