Cadmium versus phosphate in the world ocean

Abstract

Cadmium (Cd) is one of the best studied trace metals in seawater and at individual stations exhibits a more or less linear relation with phosphate. The compilation of all data from all oceans taken from over 30 different published sources into one global dataset yields only a broad scatterplot of Cd versus phosphate. However, the smaller high-quality dataset obtained by rigorous selection of only those stations with uniform Cd PO 4 -ratio in the deep waters, provides a consistent global description of the deep (> 1000 m) waters. The deep Cd PO 4 -ratio increases from about 0.18 × 10 −3 in the subarctic North Atlantic to about 0.33–0.35 × 10 −3 in the northern Indian and Pacific Oceans, in accordance with increasing phosphate content, i.e. age, of the deep water. The increasing Cd PO 4 -ratio with age (and phosphate) of the deep water masses is a function of the coupling between biogeochemical cycling and deep water circulation. Changes in the latter, for example during a glacial period, inevitably lead to significant shifts in the Cd PO 4 relationship of seawater. There is a statistically significant bimodality of deep Atlantic versus deep Antarctic/Indo/Pacific waters, suggesting that the deep Atlantic is a distinct biogeochemical province for Cd cycling. This distinction is likely caused by the high inventories of both Cd and phosphate in Weddell Sea source waters. For each of both populations, a given concentration of phosphate yields a predicted value of Cd within ±100 pM (Atlantic) and ±200 pM (Antarctic/Indo/Pacific), respectively, at the 95% confidence level. If one ignores the bimodality, then for a given phosphate the corresponding Cd might be predicted within ±150 pM at the 95% confidence level; the validity of this is currently being verified by studies of South Atlantic waters which may or may not provide the missing link between both populations. Currently, the global distribution of the Cd PO 4 -ratio in surface, thermocline and deep waters is consistent with preferential biogeochemical removal of Cd versus phosphate from surface waters. The net result for Cd/PO 4 is not dissimilar to the preferential surface removal of 12C over 13C driving the deep distribution of the dissolved 12C 13C -ratio, although for Cd/PO 4 the underlying mechanism is obviously very different and not well understood.