Poly- and perfluoroalkyl
substances (PFAS) are contaminants of
emerging Arctic concern and are present in the marine environments
of the polar regions. Their input to and fate within the marine cryosphere
are poorly understood. We conducted a series of laboratory experiments
to investigate the uptake, distribution, and release of 10 PFAS of
varying carbon chain length (C
4
–C
12
)
in young sea ice grown from artificial seawater (NaClsolution). We
show that PFAS are incorporated into bulk sea ice during ice formation
and regression analyses for individual PFAS concentrations in bulk
sea ice were linearly related to salinity (
r
2
= 0.30 to 0.88,
n
= 18,
p
< 0.05). This shows that their distribution is strongly governed
by the presence and dynamics of brine (high salinity water) within
the sea ice. Furthermore, long-chain PFAS (C
8
–C
12
), were enriched in bulk ice up to 3-fold more than short-chain
PFAS (C
4
–C
7
) and NaCl. This suggests
that chemical partitioning of PFAS between the different phases of
sea ice also plays a role in their uptake during its formation. During
sea ice melt, initial meltwater fractions were highly saline and predominantly
contained short-chain PFAS, whereas the later, fresher meltwater fractions
predominantly contained long-chain PFAS. Our results demonstrate that
in highly saline parts of sea ice (near the upper and lower interfaces
and in brine channels) significant chemical enrichment (ε) of
PFAS can occur with concentrations in brine channels greatly exceeding
those in seawater from which it forms (e.g., for PFOA, ε
brine
= 10 ± 4). This observation has implications for
biological exposure to PFAS present in brine channels, a common feature
of first-year sea ice which is the dominant ice type in a warming
Arctic.