Natural levels and photo-production rates of hydrogen peroxide (H2O2) in Andean Patagonian aquatic systems: Influence of the dissolved organic matter pool.

In aquatic environments the reactive oxygen species hydrogen peroxide (H2O2) is produced through photochemical reactions involving chromophoric dissolved organic matter (CDOM). Andean Patagonian freshwaters experience challenging underwater UV levels, which promote high levels of photochemical weathering. In this investigation, we study natural H2O2 levels and experimentally address the photochemical formation of H2O2 in stream and lake water with a range of dissolved organic matter (DOM) concentrations and quality. The screening of different pristine aquatic systems of Patagonia revealed that H2O2 concentration fluctuates between 8 and 60 nM. Laboratory incubation of different water types in PAR + UV showed photo-production of H2O2. The H2O2 formation rate increased linearly with dissolved organic carbon (DOC) in streams (13.5-20.5 nM h-1) and shallow lakes (25.7-37.8 nM h-1). In contrast, the H2O2 formation rate in deep lakes was much lower (2.1-7.1 nM h-1), and decreased with DOC. The natural potential for H2O2 formation was related to the concentration and quality of the DOM pool. At higher DOC levels, such as those present in shallow lakes, H2O2 production was directly related to DOC, whereas at low DOC levels in deep lakes and streams, two patterns were distinguished in relation to their DOM pool quality. Stream DOM, composed of high molecular weight/size humic compounds, proved to be a reactive substrate, as reflected by their high H2O2 formation rates. On the other hand, deep lake DOM, with its higher relative contribution of small and more processed compounds, was found to be a less reactive substrate, affording lower H2O2 formation rates.

Atmospheric mercury concentrations observed at ground-based monitoring sites globally distributed in the framework of the GMOS network.

Long-term monitoring of data of ambient mercury (Hg) on a global scale to assess its emission, transport, atmospheric chemistry, and deposition processes is vital to understanding the impact of Hg pollution on the environment. The Global Mercury Observation System (GMOS) project was funded by the European Commission (http://www.gmos.eu) and started in November 2010 with the overall goal to develop a coordinated global observing system to monitor Hg on a global scale, including a large network of ground-based monitoring stations, ad hoc periodic oceanographic cruises and measurement flights in the lower and upper troposphere as well as in the lower stratosphere. To date, more than 40 ground-based monitoring sites constitute the global network covering many regions where little to no observational data were available before GMOS. This work presents atmospheric Hg concentrations recorded worldwide in the framework of the GMOS project (2010-2015), analyzing Hg measurement results in terms of temporal trends, seasonality and comparability within the network. Major findings highlighted in this paper include a clear gradient of Hg concentrations between the Northern and Southern hemispheres, confirming that the gradient observed is mostly driven by local and regional sources, which can be anthropogenic, natural or a combination of both.