This
work quantified the accumulation efficiencies of Hg in cuttlefish,
depending on both organic (MeHg) and inorganic (Hg(II)) forms, under
increased pCO2 (1600 μatm). Cuttlefish
were fed with live shrimps injected with two Hg stable isotopic tracers
(Me202Hg and 199Hg(II)), which allowed for the
simultaneous quantification of internal Hg accumulation, Hg(II) methylation,
and MeHg demethylation rates in different organs. Results showed that pCO2 had no impact on Hg bioaccumulation and
organotropism, and both Hg and pCO2 did
not influence the microbiota diversity of gut and digestive gland.
However, the results also demonstrated that the digestive gland is
a key organ for in vivo MeHg demethylation. Consequently,
cuttlefish exposed to environmental levels of MeHg could exhibit in vivo MeHg demethylation. We hypothesize that in vivo MeHg demethylation could be due to biologically
induced reactions or to abiotic reactions. This has important implications
as to how some marine organisms may respond to future ocean change
and global mercury contamination.