Hydrogen peroxide photocycling in the Gulf of Aqaba, Red Sea.

The dynamics of hydrogen peroxide (H(2)O(2)) was investigated from December 2007 to October 2008 in the Gulf of Aqaba, which in the absence of H(2)O(2) contribution from biological production, rain and runoff, turned out to be a unique natural photochemical laboratory. A distinct seasonal pattern emerged, with highest midday surface H(2)O(2) concentrations in spring-summer (30-90 nM) as compared to winter (10-30 nM). Similarly, irradiation normalized net H(2)O(2) formation rates obtained in concurrent ship-board experiments were faster in spring-summer than in winter. These seasonal patterns were attributed to changes in water characteristics, namely elevated spring-summer chromophoric dissolved organic matter (CDOM). The role of trace elements in H(2)O(2) photoformation was studied by simultaneously measuring superoxide (O(2)(-)), Fe(II), and H(2)O(2) formation and loss in ambient seawater and in the presence of superoxide dismutase, iron and copper. O(2)(-) was found to decay fast in the Gulf water, with a half-life of 15-28 s, primarily due to catalytic reactions with trace metals (predominantly copper). Hence, H(2)O(2) formation in the Gulf involves metal-catalyzed O(2)(-) disproptionation. Added iron moderately lowered net H(2)O(2) photoformation, probably due to its participation in Fe(II) oxidation, a process that may also modify H(2)O(2) formation in situ.