Abstract
AbstractThe chemistry of copper (Cu) in seawater is well known to be dominated by complexation with organic ligands. The prevailing paradigm is that Cu forms strong but labile complexes. Recently, a novel procedure revealed that only a small fraction of dissolved Cu exists as labile complexes. The majority is present as a fraction that is relatively inert on timescales of weeks or more and probably does not participate in coordination exchange reactions, including biologically mediated processes. Samples collected from the 2018 GEOTRACES GP15 cruise show that throughout the interior of the Pacific Ocean, this inert fraction comprises about 90% of the dissolved Cu. Labile Cu accumulates in surface waters, probably arising from photochemical decomposition of the inert fraction. There is also a modest accumulation of labile Cu near deep sea sediments and along the Alaskan shelf and slope. The results have important implications for Cu transport and biological availability. Inert Cu may influence Cu transport throughout the water column and contribute to the linear increase in Cu with depth, a distribution which is hard to explain for a biologically active trace metal. The origins of inert Cu are unknown. It may be produced slowly within the water column on the timescale of meridional overturning circulation. In the Columbia River, between 92% and 98% of the dissolved Cu is in the inert fraction, suggesting a possible terrestrial source of inert Cu to the ocean.
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