Net deposition of mercury to the Antarctic Plateau enhanced by sea salt.

Photochemically driven mercury (Hg) exchange between the atmosphere and the Antarctic Plateau snowpack has been observed. An imbalance in bidirectional flux causes a fraction of Hg to remain in the snowpack perennially, but the factors that control the amount of Hg sequestered on the Antarctic Plateau are not fully understood. We analyzed sub-annual variations in total Hg (HgT) deposition to Dome Fuji over the period of 1986-2010 using cold vapor inductively coupled plasma mass spectrometry and compared concentrations with those of sea salt components (Na+ and Cl-). HgT ranged from 0.12 to 5.19pgg-1 (n=78) and was relatively high when the Na+ concentrations were high in the same or underlying snow layers. A significant correlation (r=0.7) was found between the annual deposition fluxes of HgT and Na+. Despite different origins and behavior of Hg and sea salt, the near-synchronous increases in the concentrations and correlation between the fluxes suggest that sea salt can intervene in the air-snow Hg exchange and promote the net deposition of Hg in the Antarctic Plateau.

Transcriptional regulation of glutathione biosynthesis genes, γ-glutamyl-cysteine ligase and glutathione synthetase in response to cadmium and nonylphenol in Chironomus riparius.

We characterized Chironomus riparius glutathione (GSH) biosynthesis genes, γ-glutamyl-cysteine ligase catalytic subunit (cr-gcl) and glutathione synthetase (cr-gs) and studied their expression after cadmium (Cd) and nonylphenol (NP) exposure. The full length cDNA of the Cr-GCL catalytic subunit was 2185 base pair (bp) in length containing an open reading frame of 1905bp, a 13bp 5' and 267bp 3' untranslated regions. The theoretical molecular mass of the deduced amino acid sequence (633) was 72.65kDa with an estimated pI of 5.42. The partial cDNA of Cr-GS was 739bp in length consisting 221 amino acids. The deduced amino acid sequence of Cr-GCL and Cr-GS cDNAs showed high conservation with homologs from other species. In phylogenetic analysis Cr-GCL and Cr-GS were grouped with equivalent genes from insects belonging to the dipteran order. The expression of cr-gcl and cr-gs was measured using quantitative real-time PCR after exposure to sub lethal concentrations of Cd (2, 10 and 20mg/L) and NP (10, 50 and 100µg/L) for 12, 24, 48 and 72h using real-time PCR methods. The mRNA expression of Cr-GCL and Cr-GS was significantly modulated after exposure to different concentrations of Cd and NP for different time periods. Total GSH levels showed a non-significant decrease after exposure to Cd for 24h. However, no change in GSH levels was observed after exposure to NP for 24h. These results suggest that Cr-GS and Cr-GCL expression is modulated by Cd and NP stress and may play an important role in detoxification of xenobiotics and antioxidant defense. We conclude that Cr-GS and Cr-GCL could be used as biomarkers of Cd and NP stress in aquatic environment for the studied species.