Wetlands were found to be important sources of methyl mercury to the boreal forest ecosystem. Yields of methyl mercury were about 26–79 times higher from wetland portions of catchments (1.84–5.55 mg∙ha−1∙yr−1) than from purely upland areas (0.07 mg∙ha−1∙yr−1). Mass-balance estimates using methyl mercury inputs in wet deposition and outputs in runoff water indicated that purely upland catchments and lakes were sites of methyl mercury retention or demethylation, while catchments with wetland areas were sites of net methyl mercury production. These observations may explain the high concentrations of mercury in fish taken from lakes that are high in colour because they receive water from wetlands. There was no relationship between the concentration of total mercury and the concentration of methyl mercury in runoff water. Total mercury yields were low from a wetland-dominated catchment, higher from a combination upland/riparian wetland catchment, and highest from a purely upland catchment. The opposite was true for methyl mercury yields from these same catchments. This indicates that environmental factors other than total mercury concentration are controlling the production and loss of methyl mercury from catchments.
Previous methods of performing aquatic acetylene-reduction assays are described and several problems associated with them are discussed. A refinement of these older techniques is introduced and problems that it overcomes are also discussed. A depth profile of nitrogen fixation (C2H4 production), obtained by the refined technique, is shown for a fertilized Canadian Shield lake in the Experimental Lakes Area of northwestern Ontario.
During summer stratification methane‐oxidizing bacteria in Lake 227 are confined to a narrow zone within the thermocline because of their sensitivity to high epilimnetic oxygen concentrations. This oxygen sensitivity is based on the dependence of the oxidizers on an oxygen‐sensitive nitrogen fixation process. Thus epilimnetic methane oxidation is absent during periods of nitrogen limitation, since high epilimnetic oxygen concentrations prevent nitrogen fixation. During periods of overturn and throughout the winter, the methane oxidizers become oxygen insensitive and oxidation occurs rapidly throughout the water column. This oxygen insensitivity likely occurs as a result of high in situ concentrations of dissolved inorganic nitrogen, which replaces nitrogen fixation as a source for fixed nitrogen. Under ice‐cover, rapid methane oxidation throughout the water column can be a major cause of total anoxia.
Four terrestrial boreal forest catchments containing different types of wetlands were studied to determine their strength as sources or sinks of methylmercury (MeHg) and total mercury (THg) to downstream ecosystems and to determine if patterns seen in one year were consistent over several years. All catchments were sinks for THg. The wetland type, percentage wetland area (0−25%), or annual water yield did not appear to have a consistent effect on the magnitude of this retention. Wetland areas of the catchments were always net sources of MeHg. Unlike for THg, there were large and consistent differences in the source strength among wetland types for MeHg. These differences appeared to be related to differences in the internal hydrology of the wetlands. All types of wetlands were greater sources of MeHg during years of high water yield, but even during years of low flow all wetland types were sources of MeHg. Thus, we conclude that wetlands are important sites of MeHg production in boreal ecosystems on the long term. Upland areas of catchments were consistently sinks for MeHg, and so whole catchment sink/source values were strongly affected by the percentage of wetland areas within a catchment. Mass balance estimates of MeHg input from wetland areas to a lake indicate that the annual input of MeHg from wetlands is larger than the annual uptake of Hg by fish and is similar to the amount of MeHg produced in the lake. Because of the predictable patterns between terrestrial catch ments in their strength as sources or sinks of MeHg, it is possible to model inputs of MeHg from lake catchments with knowledge of the percentage wetland area in a catchment, the type of wetland contained in a catchment, and the annual water yield of a catchment.
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