The net exchange of methane with high Arctic landscapes during the summer growing season

High Arctic landscapes are essentially vast cold deserts interspersed with streams, ponds and wetlands. These landscapes may be important consumers and sources of the greenhouse gas methane (CH4), though few measurements exist from this region. To quantify the flux of CH4 (FCH4 ) between the atmosphere and high Arctic landscapes on northern Ellesmere Island, Canada, we made static chamber measurements over five and three growing seasons at a desert and wetland, respectively, and eddy covariance (EC) measurements at a wetland in 2012. Chamber measurements revealed that, during the growing season, desert soils consumed CH4 (-1.37±0.06 mg-CH4 m-2 d-1), whereas the wetland margin emitted CH4 (+0.22±0.14 mg-CH4 m-2 d-1). Desert CH4 consumption rates were positively associated with soil temperature among years, and were similar to temperate locations, likely because of suitable landscape conditions for soil gas diffusion. Wetland FCH 4 varied closely with stream discharge entering the wetland and hence e

Estimation and Mapping of Wet and Dry Mercury Deposition Across Northeastern North America

Whereas many ecosystem characteristics and processes influence mercury accumulation in higher trophic-level organisms, the mercury flux from the atmosphere to a lake and its watershed is a likely factor in potential risk to biota. Atmospheric deposition clearly affects mercury accumulation in soils and lake sediments. Thus, knowledge of spatial patterns in atmospheric deposition may provide information for assessing the relative risk for ecosystems to exhibit excessive biotic mercury contamination. Atmospheric mercury concentrations in aerosol, vapor, and liquid phases from four observation networks were used to estimate regional surface concentration fields. Statistical models were developed to relate sparsely measured mercury vapor and aerosol concentrations to the more commonly measured mercury concentration in precipitation. High spatial resolution deposition velocities for different phases (precipitation, cloud droplets, aerosols, and reactive gaseous mercury (RGM)) were computed using inferential models. An empirical model was developed to estimate gaseous elemental mercury (GEM) deposition. Spatial patterns of estimated total mercury deposition were complex. Generally, deposition was higher in the southwest and lower in the northeast. Elevation, land cover, and proximity to urban areas modified the general pattern. The estimated net GEM and RGM fluxes were each greater than or equal to wet deposition in many areas. Mercury assimilation by plant foliage may provide a substantial input of methyl-mercury (MeHg) to ecosystems.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/44443/1/10646_2004_Article_6259.pd

Net ecosystem exchange of CO2 with rapidly changing high Arctic landscapes

High Arctic landscapes are expansive and changing rapidly. However, our understanding of their functional responses and potential to mitigate or enhance anthropogenic climate change is limited by few measurements. We collected eddy covariance measurements to quantify the net ecosystem exchange (NEE) of CO2 with polar semidesert and meadow wetland landscapes at the highest latitude location measured to date (82°N). We coupled these rare data with ground and satellite vegetation production measurements (Normalized Difference Vegetation In

Atmospheric Concentrations and Wet/Dry Loadings of Mercury at the Remote Experimental Lakes Area, Northwestern Ontario, Canada

Mercury (Hg) is a global pollutant released from both natural and human sources. Here we compare long-term records of wet deposition loadings of total Hg (THg) in the open to dry deposition loadings of THg in throughfall and litterfall under four boreal mixedwood canopy types at the remote Experimental Lakes Area (ELA) in Northwestern Ontario, Canada. We also present long-term records of atmospheric concentrations of gaseous elemental (GEM), gaseous oxidized (GOM), and particle bound (PBM) Hg measured at the ELA. We show that dry THg loadings in throughfall and litterfall are 2.7 to 6.1 times greater than wet THg loadings in the open. GEM concentrations showed distinct monthly and daily patterns, correlating positively in spring and summer with rates of gross ecosystem productivity and respiration. GOM and PBM concentrations were less variable throughout the year but were highest in the winter, when concentrations of anthropogenically sourced particles and gases were also high. Forest fires, Arctic air masses, and road salt also impacted GEM, GOM, and PBM concentrations at the ELA. A nested GEOS-Chem simulation for the ELA region produced a dry/wet deposition ratio of >5, suggesting that the importance of dry deposition in forested regions can be reasonably modeled by existing schemes for trace gases

Variation in peak growing season net ecosystem production across the Canadian arctic

Tundra ecosystems store vast amounts of soil organic carbon, which may be sensitive to climatic change. Net ecosystem production, NEP, is the net exchange of carbon dioxide (CO2) between landscapes and the atmosphere, and represents the balance between CO2 uptake by photosynthesis and release by decomposition and autotrophic respiration. Here we examine CO 2 exchange across seven sites in the Canadian low and high Arctic during the peak growing season (July) in summer 2008. All sites were net sinks for atmospheric CO2 (NEP ranged from 5 to 67 g C m-2), with low Arctic sites being substantially larger CO2 sinks. The spatial difference in NEP between low and high Arctic sites was determined more by CO2 uptake via gross ecosystem production than by CO2 release via ecosystem respiration. Maximum gross ecosystem production at the low Arctic sites (average 8.6 μmol m-2 s-1) was about 4 times larger than for high Arctic sites (average 2.4 μmol m-2 s-1). NEP decreased with increasing temperature at all low Arctic sites, driven largely by the ecosystem respiration response. No consistent temperature response was found for the high Arctic sites. The results of this study clearly indicate there are large differences in tundra CO2 exchange between high and low Arctic environments and this difference should be a central consideration in studies of Arctic carbon balance and climate change

The role of terrestrial vegetation in atmospheric Hg deposition: Pools and fluxes of spike and ambient Hg from the METAALICUS experiment

As part of the Mercury Experiment to Assess Atmospheric Loading in Canada and the U.S. (METAALICUS), different stable Hg(II) isotope spikes were applied to the upland and wetland areas of a boreal catchment between 2001 and 2006 to examine retention of newly deposited Hg(II). In the present study, a Geographical Information Systems (GIS)-based approach was used to quantify canopy and ground vegetation pools of experimentally applied upland and wetland spike Hg within the METAALICUS watershed over the terrestrial loading phase of the experiment. A chemical kinetic model was also used to describe the changes in spike Hg concentrations of canopy and ground vegetation over time. An examination of the fate of spike Hg initially present on canopy vegetation using a mass balance approach indicated that the largest percentage flux from the canopy over one year post-spray was emission to the atmosphere (upland: 45%; wetland: 71%), followed by litterfall (upland: 14%; wetland: 10%) and throughfall fluxes (upland: 12%; wetland: 9%) and longer term retention of spike in the forest canopy (11% for both upland and wetland). Average half-lives (t 1/2) of spike on deciduous (110 30days) and coniferous (180 40days) canopy and ground vegetation (890 620days) indicated that retention of new atmospheric Hg(II

Some like it cold: microbial transformations of mercury in polar regions

The contamination of polar regions with mercury that is transported from lower latitudes as inorganic mercury has resulted in the accumulation of methylmercury (MeHg) in food chains, risking the health of humans and wildlife. While production of MeHg has been documented in polar marine and terrestrial environments, little is known about the responsible transformations and transport pathways and the processes that control them. We posit that as in temperate environments, microbial transformations play a key role in mercury geochemical cycling in polar regions by: (1) methylating mercury by one of four proposed pathways, some not previously described; (2) degrading MeHg by activities of mercury resistant and other bacteria; and (3) carrying out redox transformations that control the supply of the mercuric ion, the substrate of methylation reactions. Recent analyses have identified a high potential for mercury-resistant microbes that express the enzyme mercuric reductase to affect the production of gaseous elemental mercury when and where daylight is limited. The integration of microbially mediated processes in the paradigms that describe mercury geochemical cycling is therefore of high priority especially in light of concerns regarding the effect of global warming and permafrost thawing on input of MeHg to polar regions