In two recent studies (Tian et al., Deep-Sea Res. I 43 (1996) 723-738; Camp
os et al., Deep-Sea Res. II 43 (1996) 455-466), in order to explain the obs
erved temporal variations in the distributions of the dissolved iodine spec
ies at the time-series stations in the Mediterranean Sea, the North Atlanti
c and the North Pacific, diverse assumptions were invoked on the relationsh
ips between changes in the speciation of dissolved iodine in the surface oc
eans and biological production such that the surface enrichment of I- was l
inked to both regenerated production and primary production while the surfa
ce depletion of [IO3- + I-] was linked to "new" production. However, while
some of the major conclusions in these studies are critically dependent on
these assumptions, the validity of the assumptions has yet to be verified w
ith experimental evidence. On the other hand, while there are still signifi
cant unknowns in the understanding of the cycling among dissolved iodine sp
ecies in the surface oceans, presently available data from laboratory cultu
res and field observations are consistent with an alternative conceptual mo
del in which IO3- and NO3- are taken up at some ratio to each other during
NO3- uptake and almost all of the IO3- taken up is exuded as I-. Thus, the
depletion of IO3- and the enrichment of I- in the surface water are linked
to NO3- uptake. This alternative model is also consistent with the data set
s presented by Tian et al. (1996) and Campos et al. (1996). By linking the
surface depletion of IO3- to NO3- uptake, significantly different biogeoche
mical behavior of the marine dissolved iodine system may be inferred. The e
xtent to which I- may be oxidized to IO3- within the euphotic zone during t
he residence time of the water in the surface ocean is still an open questi
on. (C) 2001 Elsevier Science Ltd. All rights reserved.