| Abstract: | The analysis of ultraviolet (UV)-irradiated and untreated seawater samples has shown that the dissolved arsenic content of marine waters cannot be completely determined by hydride generation–atomic absorption spectrophotometry without sample pretreatment. Irradiation of water samples obtained during a survey of arsenic species in coastal waters during the summer of 1988 gave large increases in the measured speciation. Average increases in the measured speciation. Average increases in total arsenic, monomethylarsenic and dimethylarsenic were 0.29 μg As dm?3 (25%), 0.03 μg As dm?3 (47%) and 0.12 μg As dm?3 (79%), respectively. Overall, an average 25% increase in the concentration of dissolved arsenic was observed following irradiation. This additional arsenic may be derived from compounds related to algal arsenosugars or to their breakdown products. These do not readily yield volatile hydrides when treated with borohydride and are not therefore detected by the normal hydride generation technique. This has important repercussions as for many years this procedure, and other analytical procedures which are equally unlikely to respond to such compounds, have been accepted as giving a true representation of the dissolved arsenic speciation in estuarine and coastal waters. A gross underestimate may therefore have been made of biological involvement in arsenic cycling in the aquatic environment. |
