Methylmercury in arctic Alaskan mosquitoes: implications for impact of atmospheric mercury depletion events

2008 ◽  
Vol 5 (2) ◽  
pp. 127 ◽  
Author(s):  
Chad R. Hammerschmidt ◽  
William F. Fitzgerald

Environmental context. Recent research suggests that gross mercury deposition in the Arctic is increased significantly as a result of springtime Atmospheric Mercury Depletion Events (AMDE). A primary environmental and human health concern is whether mercury deposited with these events leads to enhanced production and uptake of the toxic methylmercury species in polar ecosystems. Here, we present an initial assessment of potential impact from AMDE utilising mosquitoes as bioindicators of methylmercury accumulation in freshwater and terrestrial food webs within 200 km of the Arctic Ocean. Abstract. Atmospheric Mercury Depletion Events (AMDE) – phenomena in which elemental Hg is oxidised and stripped from the atmosphere over an 8–12-week period following polar sunrise – appear to increase Hg deposition to environs near the Arctic Ocean with a lesser impact inland. A key concern is whether such events lead to enhanced production and uptake of the toxic methylmercury (MeHg) species into arctic food webs. Here, we used mosquitoes, which are sensitive and site-specific bioindicators of Hg loadings, to assess the impact of AMDE on ecosystem MeHg contamination along a 200-km transect between the Arctic Ocean coast and foothills of the Brooks Range, where gross atmospheric Hg deposition appears to be ~20-fold less than that near the coast. This preliminary survey revealed little variation and no gradient in mosquito MeHg levels, which suggests comparable ecosystem impact. This may also point to significant cycling and reemission (e.g. via photoreduction) of Hg deposited during AMDE from the snow and ice pack to the atmosphere.

2010 ◽  
Vol 7 (2) ◽  
pp. 133 ◽  
Author(s):  
R. W. Macdonald ◽  
L. L. Loseto

Environmental context. Mercury is a global contaminant that has entered Arctic food webs in sufficient quantity to put at risk the health of top predators and humans that consume them. Recent research has discovered a photochemical process unique to the Arctic that leads to mercury deposition on frozen surfaces after polar sunrise, but the connection between mercury deposition and entry into food webs remains tenuous and poorly understood. We propose here that the Arctic Ocean’s sensitivity to the global mercury cycle depends far more on neglected post-deposition processes that lead to methylation within the ice–ocean system, and the vulnerability of these processes to changes occurring in the cryosphere. Abstract. Emissions, atmospheric transport and deposition have formed the emphasis of recent research to understand Hg trends in Arctic marine biota, with the expressed objective of predicting how biotic trends might respond to emission controls. To answer the question of whether the Arctic Ocean might be especially vulnerable to global mercury (Hg) contamination and how biota might respond to emission controls requires a distinction between the supply of Hg from source regions and the processes within the Arctic Ocean that sequester and convert mercury to monomethyl Hg (MeHg). Atmospheric Mercury Depletion Events (AMDEs) provide a unique Hg deposition process in the Arctic; however, AMDEs have yet to be linked quantitatively with Hg uptake in marine food webs. The difficulty in implicating AMDEs or emissions to biotic trends lie in the ocean where several poorly understood processes lead to MeHg production and biomagnification. We propose that sensitivity of the Arctic Ocean’s ecosystem to Hg lies not so much in the deposition process as in methylation processes within the ocean, Hg inputs from large drainage basins, and the vulnerability these to climate change. Future research needs to be better balanced across the entire Hg cycle.


2012 ◽  
Vol 12 (1) ◽  
pp. 2647-2706 ◽  
Author(s):  
D. Durnford ◽  
A. Dastoor ◽  
A. Ryzhkov ◽  
L. Poissant ◽  
M. Pilote ◽  
...  

Abstract. An unknown fraction of mercury that is deposited onto snowpacks is revolatilized to the atmosphere. Determining the revolatilized fraction is important since mercury that enters the snowpack meltwater may be converted to highly toxic bioaccumulating methylmercury. In this study, we present a new dynamic physically-based snowpack/meltwater model for mercury that is suitable for large-scale atmospheric models for mercury. It represents the primary physical and chemical processes that determine the fate of mercury deposited onto snowpacks. The snowpack/meltwater model was implemented in Environment Canada's atmospheric mercury model GRAHM. For the first time, observed snowpack-related mercury concentrations are used to evaluate and constrain an atmospheric mercury model. We find that simulated concentrations of mercury in both snowpacks and the atmosphere's surface layer agree closely with observations. The simulated concentration of mercury in both in the top 30 cm and the top 150 cm of the snowpack, averaged over 2005–2009, is predominantly below 6 ng l−1 over land south of 66.5° N but exceeds 18 ng l−1 over sea ice in extensive areas of the Arctic Ocean and Hudson Bay. The average simulated concentration of mercury in snowpack meltwater runoff tends to be higher on the Russian/European side (>20 ng l−1) of the Arctic Ocean than on the Canadian side (<10 ng l−1). The correlation coefficient between observed and simulated monthly mean atmospheric surface-level GEM concentrations increased significantly with the inclusion of the new snowpack/meltwater model at two of the three stations (midlatitude, subarctic) studied and remained constant at the third (arctic). Oceanic emissions are postulated to produce the observed summertime maximum in concentrations of surface-level atmospheric GEM at Alert in the Canadian Arctic and to generate the summertime volatility observed in these concentrations at both Alert and Kuujjuarapik on subarctic Hudson Bay, Canada. We find that the fraction of deposited mercury that is revolatilized from snowpacks increases with latitude from 28% between 30 and 45° N, to 51% from 45 to 66.5° N, to 70% polewards of 66.5° N on an annual basis. Combining this latitudinal gradient with the latitudinally increasing coverage of snowpacks causes yearly net deposition as a fraction of gross deposition to decrease from 98% between 30 and 45° N to 85% between 45 and 66.5° N to 44% within the Arctic Circle. The yearly net deposition and net accumulation of mercury at the surface within the Arctic Circle north of 66.5° N are estimated at 153 and 117 Mg, respectively. We calculate that 63 and 45 Mg of mercury are deposited annually to the Arctic Ocean directly and indirectly via melting snowpacks, respectively. For terrestrial surfaces within the Arctic Circle, we find that 24 and 21 Mg of mercury are deposited annually directly and indirectly via melting snowpacks, respectively. Within the Arctic Circle, multi-season snowpacks gained an estimated average of 136 kg of mercury annually on land but lost an average of 133 kg annually over sea ice, possibly as a result of increased melting caused by rising temperatures. The developed snowpack/meltwater model can be used for investigating the impact of climate change on the snowpack/atmosphere exchange of mercury.


2012 ◽  
Vol 12 (19) ◽  
pp. 9251-9274 ◽  
Author(s):  
D. Durnford ◽  
A. Dastoor ◽  
A. Ryzhkov ◽  
L. Poissant ◽  
M. Pilote ◽  
...  

Abstract. An unknown fraction of mercury that is deposited onto snowpacks is revolatilized to the atmosphere. Determining the revolatilized fraction is important since mercury that enters the snowpack meltwater may be converted to highly toxic bioaccumulating methylmercury. In this study, we present a new dynamic physically-based snowpack/meltwater model for mercury that is suitable for large-scale atmospheric models for mercury. It represents the primary physical and chemical processes that determine the fate of mercury deposited onto snowpacks. The snowpack/meltwater model was implemented in Environment Canada's atmospheric mercury model GRAHM. For the first time, observed snowpack-related mercury concentrations are used to evaluate and constrain an atmospheric mercury model. We find that simulated concentrations of mercury in both snowpacks and the atmosphere's surface layer agree closely with observations. The simulated concentration of mercury in both in the top 30 cm and the top 150 cm of the snowpack, averaged over 2005–2009, is predominantly below 6 ng L−1 over land south of 66.5° N but exceeds 18 ng L−1 over sea ice in extensive areas of the Arctic Ocean and Hudson Bay. The average simulated concentration of mercury in snowpack meltwater runoff tends to be higher on the Russian/European side (>20 ng L−1) of the Arctic Ocean than on the Canadian side (<10 ng L−1). The correlation coefficient between observed and simulated monthly mean atmospheric surface-level gaseous elemental mercury (GEM) concentrations increased significantly with the inclusion of the new snowpack/meltwater model at two of the three stations (midlatitude, subarctic) studied and remained constant at the third (arctic). Oceanic emissions are postulated to produce the observed summertime maximum in concentrations of surface-level atmospheric GEM at Alert in the Canadian Arctic and to generate the summertime volatility observed in these concentrations at both Alert and Kuujjuarapik on subarctic Hudson Bay, Canada. We find that the fraction of deposited mercury that is revolatilized from snowpacks increases with latitude from 39% between 30 and 45° N, to 57% from 45 to 60° N, 67% from 60 to 66.5° N, and 75% polewards of 66.5° N on an annual basis. Combining this latitudinal gradient with the latitudinally increasing coverage of snowpacks causes yearly net deposition as a fraction of gross deposition to decrease from 98% between 30 and 45° N to 89% between 45 and 60° N, 73% between 60 and 66.5° N, and 44% within the Arctic Circle. The yearly net deposition and net accumulation of mercury at the surface within the Arctic Circle north of 66.5° N are estimated at 153 and 117 Mg, respectively. We calculate that 58 and 50 Mg of mercury are deposited annually to the Arctic Ocean directly and indirectly via melting snowpacks, respectively. For terrestrial surfaces within the Arctic Circle, we find that 29 and 16 Mg of mercury are deposited annually directly and indirectly via melting snowpacks, respectively. Within the Arctic Circle, multi-season snowpacks on land and over sea ice gained, on average, an estimated 0.1 and 0.4 Mg yr−1 mercury, respectively, from 2000–2005. The developed snowpack/meltwater model can be used for investigating the impact of climate change on the snowpack/atmosphere exchange of mercury.


2021 ◽  
Vol 34 (10) ◽  
pp. 3799-3819
Author(s):  
Hyung-Gyu Lim ◽  
Jong-Yeon Park ◽  
John P. Dunne ◽  
Charles A. Stock ◽  
Sung-Ho Kang ◽  
...  

AbstractHuman activities such as fossil fuel combustion, land-use change, nitrogen (N) fertilizer use, emission of livestock, and waste excretion accelerate the transformation of reactive N and its impact on the marine environment. This study elucidates that anthropogenic N fluxes (ANFs) from atmospheric and river deposition exacerbate Arctic warming and sea ice loss via physical–biological feedback. The impact of physical–biological feedback is quantified through a suite of experiments using a coupled climate–ocean–biogeochemical model (GFDL-CM2.1-TOPAZ) by prescribing the preindustrial and contemporary amounts of riverine and atmospheric N fluxes into the Arctic Ocean. The experiment forced by ANFs represents the increase in ocean N inventory and chlorophyll concentrations in present and projected future Arctic Ocean relative to the experiment forced by preindustrial N flux inputs. The enhanced chlorophyll concentrations by ANFs reinforce shortwave attenuation in the upper ocean, generating additional warming in the Arctic Ocean. The strongest responses are simulated in the Eurasian shelf seas (Kara, Barents, and Laptev Seas; 65°–90°N, 20°–160°E) due to increased N fluxes, where the annual mean surface temperature increase by 12% and the annual mean sea ice concentration decrease by 17% relative to the future projection, forced by preindustrial N inputs.


2014 ◽  
Vol 11 (2) ◽  
pp. 293-308 ◽  
Author(s):  
E. E. Popova ◽  
A. Yool ◽  
Y. Aksenov ◽  
A. C. Coward ◽  
T. R. Anderson

Abstract. The Arctic Ocean is a region that is particularly vulnerable to the impact of ocean acidification driven by rising atmospheric CO2, with potentially negative consequences for calcifying organisms such as coccolithophorids and foraminiferans. In this study, we use an ocean-only general circulation model, with embedded biogeochemistry and a comprehensive description of the ocean carbon cycle, to study the response of pH and saturation states of calcite and aragonite to rising atmospheric pCO2 and changing climate in the Arctic Ocean. Particular attention is paid to the strong regional variability within the Arctic, and, for comparison, simulation results are contrasted with those for the global ocean. Simulations were run to year 2099 using the RCP8.5 (an Intergovernmental Panel on Climate Change (IPCC) Fifth Assessment Report (AR5) scenario with the highest concentrations of atmospheric CO2). The separate impacts of the direct increase in atmospheric CO2 and indirect effects via impact of climate change (changing temperature, stratification, primary production and freshwater fluxes) were examined by undertaking two simulations, one with the full system and the other in which atmospheric CO2 was prevented from increasing beyond its preindustrial level (year 1860). Results indicate that the impact of climate change, and spatial heterogeneity thereof, plays a strong role in the declines in pH and carbonate saturation (Ω) seen in the Arctic. The central Arctic, Canadian Arctic Archipelago and Baffin Bay show greatest rates of acidification and Ω decline as a result of melting sea ice. In contrast, areas affected by Atlantic inflow including the Greenland Sea and outer shelves of the Barents, Kara and Laptev seas, had minimal decreases in pH and Ω because diminishing ice cover led to greater vertical mixing and primary production. As a consequence, the projected onset of undersaturation in respect to aragonite is highly variable regionally within the Arctic, occurring during the decade of 2000–2010 in the Siberian shelves and Canadian Arctic Archipelago, but as late as the 2080s in the Barents and Norwegian seas. We conclude that, for future projections of acidification and carbonate saturation state in the Arctic, regional variability is significant and needs to be adequately resolved, with particular emphasis on reliable projections of the rates of retreat of the sea ice, which are a major source of uncertainty.


2018 ◽  
Vol 32 (1) ◽  
pp. 15-32 ◽  
Author(s):  
Qiang Wang ◽  
Claudia Wekerle ◽  
Sergey Danilov ◽  
Dmitry Sidorenko ◽  
Nikolay Koldunov ◽  
...  

Abstract The freshwater stored in the Arctic Ocean is an important component of the global climate system. Currently the Arctic liquid freshwater content (FWC) has reached a record high since the beginning of the last century. In this study we use numerical simulations to investigate the impact of sea ice decline on the Arctic liquid FWC and its spatial distribution. The global unstructured-mesh ocean general circulation model Finite Element Sea Ice–Ocean Model (FESOM) with 4.5-km horizontal resolution in the Arctic region is applied. The simulations show that sea ice decline increases the FWC by freshening the ocean through sea ice meltwater and modifies upper ocean circulation at the same time. The two effects together significantly increase the freshwater stored in the Amerasian basin and reduce its amount in the Eurasian basin. The salinification of the upper Eurasian basin is mainly caused by the reduction in the proportion of Pacific Water and the increase in that of Atlantic Water (AW). Consequently, the sea ice decline did not significantly contribute to the observed rapid increase in the Arctic total liquid FWC. However, the changes in the Arctic freshwater spatial distribution indicate that the influence of sea ice decline on the ocean environment is remarkable. Sea ice decline increases the amount of Barents Sea branch AW in the upper Arctic Ocean, thus reducing its supply to the deeper Arctic layers. This study suggests that all the dynamical processes sensitive to sea ice decline should be taken into account when understanding and predicting Arctic changes.


1984 ◽  
Vol 5 ◽  
pp. 61-68 ◽  
Author(s):  
T. Holt ◽  
P. M. Kelly ◽  
B. S. G. Cherry

Soviet plans to divert water from rivers flowing into the Arctic Ocean have led to research into the impact of a reduction in discharge on Arctic sea ice. We consider the mechanisms by which discharge reductions might affect sea-ice cover and then test various hypotheses related to these mechanisms. We find several large areas over which sea-ice concentration correlates significantly with variations in river discharge, supporting two particular hypotheses. The first hypothesis concerns the area where the initial impacts are likely to which is the Kara Sea. Reduced riverflow is associated occur, with decreased sea-ice concentration in October, at the time of ice formation. This is believed to be the result of decreased freshening of the surface layer. The second hypothesis concerns possible effects on the large-scale current system of the Arctic Ocean and, in particular, on the inflow of Atlantic and Pacific water. These effects occur as a result of changes in the strength of northward-flowing gradient currents associated with variations in river discharge. Although it is still not certain that substantial transfers of riverflow will take place, it is concluded that the possibility of significant cryospheric effects and, hence, large-scale climate impact should not be neglected.


2020 ◽  
Vol 117 (42) ◽  
pp. 26069-26075
Author(s):  
Anne de Vernal ◽  
Claude Hillaire-Marcel ◽  
Cynthia Le Duc ◽  
Philippe Roberge ◽  
Camille Brice ◽  
...  

The impact of the ongoing anthropogenic warming on the Arctic Ocean sea ice is ascertained and closely monitored. However, its long-term fate remains an open question as its natural variability on centennial to millennial timescales is not well documented. Here, we use marine sedimentary records to reconstruct Arctic sea-ice fluctuations. Cores collected along the Lomonosov Ridge that extends across the Arctic Ocean from northern Greenland to the Laptev Sea were radiocarbon dated and analyzed for their micropaleontological and palynological contents, both bearing information on the past sea-ice cover. Results demonstrate that multiyear pack ice remained a robust feature of the western and central Lomonosov Ridge and that perennial sea ice remained present throughout the present interglacial, even during the climate optimum of the middle Holocene that globally peaked ∼6,500 y ago. In contradistinction, the southeastern Lomonosov Ridge area experienced seasonally sea-ice-free conditions, at least, sporadically, until about 4,000 y ago. They were marked by relatively high phytoplanktonic productivity and organic carbon fluxes at the seafloor resulting in low biogenic carbonate preservation. These results point to contrasted west–east surface ocean conditions in the Arctic Ocean, not unlike those of the Arctic dipole linked to the recent loss of Arctic sea ice. Hence, our data suggest that seasonally ice-free conditions in the southeastern Arctic Ocean with a dominant Arctic dipolar pattern, may be a recurrent feature under “warm world” climate.


Polar Biology ◽  
2010 ◽  
Vol 33 (12) ◽  
pp. 1683-1694 ◽  
Author(s):  
Maria Montserrat Sala ◽  
Jesús M. Arrieta ◽  
Julia A. Boras ◽  
Carlos M. Duarte ◽  
Dolors Vaqué

Author(s):  
Irina Panyushkina ◽  
David M Meko ◽  
Alexander Shiklomanov ◽  
Richard D Thaxton ◽  
Vladimyr Myglan ◽  
...  

Abstract The Yenisei River is the largest contributor of freshwater and energy fluxes among all rivers draining to the Arctic Ocean. Modeling long-term variability of Eurasian runoff to the Arctic Ocean is complicated by the considerable variability of river discharge in time and space, and the monitoring constraints imposed by a sparse gauged-flow network and paucity of satellite data. We quantify tree growth response to river discharge at the upper reaches of the Yenisei River in Tuva, South Siberia. Two regression models built from eight tree-ring width chronologies of Larix sibirica are applied to reconstruct winter (Nov–Apr) discharge for the period 1784-1997 (214 years), and annual (Oct–Sept) discharge for the period 1701–2000 (300 years). The Nov–Apr model explains 52% of the discharge variance whereas Oct–Sept explains 26% for the calibration intervals 1927–1997 and 1927-2000, respectively. This new hydrological archive doubles the length of the instrumental discharge record at the Kyzyl gauge and resets the temporal background of discharge variability back to 1784. The reconstruction finds a remarkable 80% upsurge in winter flow over the last 25 years, which is unprecedented in the last 214 years. In contrast, annual discharge fluctuated normally for this system, with only a 7% increase over the last 25 years. Water balance modeling with CRU data manifests a significant discrepancy between decadal variability of the gauged flow and climate data after 1960. We discuss the impact on the baseflow rate change of both the accelerating permafrost warming in the discontinuous zone of South Siberia and widespread forest fires. The winter discharge accounts for only one-third of the annual flow, yet the persistent 25-year upsurge is alarming. This trend is likely caused by Arctic Amplification, which can be further magnified by increased winter flow delivering significantly more freshwater to the Kara Sea during the cold season.


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