Cadmium (Cd) is one of the best studied trace metals in seawater and a
t individual stations exhibits a more or less linear relation with pho
sphate. The compilation of all data from all oceans taken from over 30
different published sources into one global dataset yields only a bro
ad scatterplot of Cd versus phosphate. However, the smaller high-quali
ty dataset obtained by rigorous selection of only those stations with
uniform Cd/PO4-ratio in the deep waters, provides a consistent global
description of the deep (> 1000 m) waters. The deep Cd/PO4-ratio incre
ases from about 0.18 X 10(-3) in the subarctic North Atlantic to about
0.33-0.35 x 10(-3) in the northern Indian and Pacific Oceans, in acco
rdance with increasing phosphate content, i.e. age, of the deep water.
The increasing Cd/PO4-ratio with age (and phosphate) of the deep wate
r 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/PO4
relationship of seawater. There is a statistically significant bimodal
ity of deep Atlantic versus deep Antarctic/Indo/Pacific waters, sugges
ting 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 bot
h populations, a given concentration of phosphate yields a predicted v
alue of Cd within +/- 100 pM (Atlantic) and +/- 200 pM (Antarctic/Indo
/Pacific), respectively, at the 95% confidence level. If one ignores t
he bimodality, then for a given phosphate the corresponding Cd might b
e predicted within +/- 150 pM at the 95% confidence level; the validit
y of this is currently being verified by studies of South Atlantic wat
ers which may or may not provide the missing link between both populat
ions. Currently, the global distribution of the Cd/PO4-ratio in surfac
e, thermocline and deep waters is consistent with preferential biogeoc
hemical removal of Cd versus phosphate from surface waters. The net re
sult for Cd/PO4 is not dissimilar to the preferential surface removal
of C-12 over C-13 driving the deep distribution of the dissolved C-12/
C-13-ratio, although for Cd/PO4 the underlying mechanism is obviously
very different and not well understood.