Staffan Åkerblom

The Effects of Forestry on Hg Bioaccumulation in Nemoral/Boreal Waters and Recommendations for Good Silvicultural Practice

Abstract Mercury (Hg) levels are alarmingly high in fish from lakes across Fennoscandia and northern North America. The few published studies on the ways in which silviculture practices influence this problem indicate that forest operations increase Hg in downstream aquatic ecosystems. From these studies, we estimate that between one-tenth and one-quarter of the Hg in the fish of high-latitude, managed forest landscapes can be attributed to harvesting. Forestry, however, did not create the elevated Hg levels in the soils, and waterborne Hg/MeHg concentrations downstream from harvested areas are similar to those from wetlands. Given the current understanding of the way in which silviculture impacts Hg cycling, most of the recommendations for good forest practice in Sweden appear to be appropriate for high-latitude regions, e.g., leaving riparian buffer zones, as well as reducing disturbance at stream crossings and in moist areas. The recommendation to restore wetlands and reduce drainage, however, will likely increase Hg/MeHg loadings to aquatic ecosystems.

Temporal change estimation of mercury concentrations in northern pike (Esox lucius L.) in Swedish lakes

Adequate temporal trend analysis of mercury (Hg) in freshwater ecosystems is critical to evaluate if actions from the human society have affected Hg concentrations ([Hg]) in fresh water biota. This study examined temporal change in [Hg] in Northern pike (Esox lucius L.) in Swedish freshwater lakes between 1994 and 2006. To achieve this were lake-specific, multiple-linear-regression models used to estimate pike [Hg], including indicator variables representing time and fish weight and their interactions. This approach permitted estimation of the direction and magnitude of temporal changes in 25 lakes selected from the Swedish national database on Hg in freshwater biota. A significant increase was found in 36% of the studied lakes with an average increase in pike [Hg] of 3.7±6.7% per year that was found to be positively correlated with total organic carbon. For lakes with a significant temporal change the dataset was based on a mean of 30 fish, while for lakes with no temporal change it was based on a mean of 13 fish.

Terrestrial discharges mediate trophic shifts and enhance methylmercury accumulation in estuarine biota

Terrestrial discharge can cause pelagic zone trophic shifts and enhance methylmercury accumulation in plankton three- to sixfold. The input of mercury (Hg) to ecosystems is estimated to have increased two- to fivefold during the industrial era, and Hg accumulates in aquatic biota as neurotoxic methylmercury (MeHg). Escalating anthropogenic land use and climate change are expected to alter the input rates of terrestrial natural organic matter (NOM) and nutrients to aquatic ecosystems. For example, climate change has been projected to induce 10 to 50% runoff increases for large coastal regions globally. A major knowledge gap is the potential effects on MeHg exposure to biota following these ecosystem changes. We monitored the fate of five enriched Hg isotope tracers added to mesocosm scale estuarine model ecosystems subjected to varying loading rates of nutrients and terrestrial NOM. We demonstrate that increased terrestrial NOM input to the pelagic zone can enhance the MeHg bioaccumulation factor in zooplankton by a factor of 2 to 7 by inducing a shift in the pelagic food web from autotrophic to heterotrophic. The terrestrial NOM input also enhanced the retention of MeHg in the water column by up to a factor of 2, resulting in further increased MeHg exposure to pelagic biota. Using mercury mass balance calculations, we predict that MeHg concentration in zooplankton can increase by a factor of 3 to 6 in coastal areas following scenarios with 15 to 30% increased terrestrial runoff. The results demonstrate the importance of incorporating the impact of climate-induced changes in food web structure on MeHg bioaccumulation in future biogeochemical cycling models and risk assessments of Hg.

The Influence of Sulphate Deposition on the Seasonal Variation of Peat Pore Water Methyl Hg in a Boreal Mire

In this paper we investigate the hypothesis that long-term sulphate (SO4 2−) deposition has made peatlands a larger source of methyl mercury (MeHg) to remote boreal lakes. This was done on experimental plots at a boreal, low sedge mire where the effect of long-term addition of SO4 2− on peat pore water MeHg concentrations was observed weekly throughout the snow-free portion of 1999. The additions of SO4 2− started in 1995. The seasonal mean of the pore water MeHg concentrations on the plots with 17 kg ha−1 yr−1 of sulphur (S) addition (1.3±0.08 ng L−1, SE; n = 44) was significantly (p<0.0001) higher than the mean MeHg concentration on the plots with 3 kg ha−1 yr−1 of ambient S deposition (0.6±0.02 ng L−1, SE; n = 44). The temporal variation in pore water MeHg concentrations during the snow free season was larger in the S-addition plots, with an amplitude of >2 ng L−1 compared to +/−0.5 ng L−1 in the ambient S deposition plots. The concentrations of pore water MeHg in the S-addition plots were positively correlated (r2 = 0.21; p = 0.001) to the groundwater level, with the lowest concentrations of MeHg during the period with the lowest groundwater levels. The pore water MeHg concentrations were not correlated to total Hg, DOC concentration or pH. The results from this study indicate that the persistently higher pore water concentrations of MeHg in the S-addition plots are caused by the long-term additions of SO4 2− to the mire surface. Since these waters are an important source of runoff, the results support the hypothesis that SO4 2− deposition has increased the contribution of peatlands to MeHg in downstream aquatic systems. This would mean that the increased deposition of SO4 2− in acid rain has contributed to the modern increase in the MeHg burdens of remote lakes hydrologically connected to peatlands.

Organic matter control of mercury and lead toxicity in mor layers

This study evaluated the effect of organic matter composition on Hg and Pb toxicity for heterotrophic respiration in mor layers in long-term in vitro dose-response experiments. Pb proved to be a more potent toxin than Hg at comparable metal additions. The degree of litter decomposition and fragmentation and background Hg concentration levels were key factors determining metal toxicity. Higher sensitivity to metal additions in the fermentation layer than in litter and humification layers was corroborated. The role of organic matter composition was further examined in litter after structural disintegration by milling, which significantly increased the sensitivity of heterotrophic respiration to metal additions. A threshold value causing 5% reduction in heterotrophic respiration was estimated at 800 microg Hg kg(-1). In boreal forests in the northern hemisphere, the mean regional Hg concentrations in mor layers amount to approximately half this threshold value.

Long-term changes (1990–2015) in the atmospheric deposition and runoff water chemistry of sulphate, inorganic nitrogen and acidity for forested catchments in Europe in relation to changes in emissions and hydrometeorological conditions

The international Long-Term Ecological Research Network (ILTER) encompasses hundreds of long-term research/monitoring sites located in a wide array of ecosystems that can help us understand environmental change across the globe. We evaluated long-term trends (1990-2015) for bulk deposition, throughfall and runoff water chemistry and fluxes, and climatic variables in 25 forested catchments in Europe belonging to the UNECE International Cooperative Programme on Integrated Monitoring of Air Pollution Effects on Ecosystems (ICP IM). Many of the IM sites form part of the monitoring infrastructures of this larger ILTER network. Trends were evaluated for monthly concentrations of non-marine (anthropogenic fraction, denoted as x) sulphate (xSO4) and base cations x(Ca+Mg), hydrogen ion (H+), inorganic N (NO3 and NH4) and ANC (Acid Neutralising Capacity) and their respective fluxes into and out of the catchments and for monthly precipitation, runoff and air temperature. A significant decrease of xSO4 deposition resulted in decreases in concentrations and fluxes of xSO4 in runoff, being significant at 90% and 60% of the sites, respectively. Bulk deposition of NO3 and NH4 decreased significantly at 60-80% (concentrations) and 40-60% (fluxes) of the sites. Concentrations and fluxes of NO3 in runoff decreased at 73% and 63% of the sites, respectively, and NO3 concentrations decreased significantly at 50% of the sites. Thus, the LTER/ICP IM network confirms the positive effects of the emission reductions in Europe. Air temperature increased significantly at 61% of the sites, while trends for precipitation and runoff were rarely significant. The site-specific variation of xSO4 concentrations in runoff was most strongly explained by deposition. Climatic variables and deposition explained the variation of inorganic N concentrations in runoff at single sites poorly, and as yet there are no clear signs of a consistent deposition-driven or climate-driven increase in inorganic N exports in the catchments.

Mercury evasion from a boreal peatland shortens the timeline for recovery from legacy pollution

Peatlands are a major source of methylmercury that contaminates downstream aquatic food webs. The large store of mercury (Hg) in peatlands could be a source of Hg for over a century even if deposition is dramatically reduced. However, the reliability of Hg mass balances can be questioned due to missing long-term land-atmosphere flux measurements. We used a novel micrometeorological system for continuous measurement of Hg peatland-atmosphere exchange to derive the first annual Hg budget for a peatland. The evasion of Hg (9.4 µg m−2 yr−1) over the course of a year was seven times greater than stream Hg export, and over two times greater than wet bulk deposition to the boreal peatland. Measurements of dissolved gaseous Hg in the peat pore water also indicate Hg evasion. The net efflux may result from recent declines in atmospheric Hg concentrations that have turned the peatland from a net sink into a source of atmospheric Hg. This net Hg loss suggests that open boreal peatlands and downstream ecosystems can recover more rapidly from past atmospheric Hg deposition than previously assumed. This has important implications for future levels of methylmercury in boreal freshwater fish and the estimation of historical Hg accumulation rates from peat profiles.

The importance of bioconcentration into the pelagic food web base for methylmercury biomagnification: A meta-analysis

Methylmercury (MeHg) transfer from water into the base of the food web (bioconcentration) and subsequent biomagnification in the aquatic food web leads to most of the MeHg in fish. But how important is bioconcentration compared to biomagnification in predicting MeHg in fish? To answer this question we reviewed articles in which MeHg concentrations in water, plankton (seston and/or zooplankton), as well as fish (planktivorous and small omnivorous fish) were reported. This yielded 32 journal articles with data from 59 aquatic ecosystems at 22 sites around the world. Although there are many case studies of particular aquatic habitats and specific geographic areas that have examined MeHg bioconcentration and biomagnification, we performed a meta-analysis of such studies. Aqueous MeHg was not a significant predictor of MeHg in fish, but MeHg in seston i.e., the base of the aquatic food web, predicted 63% of the variability in fish MeHg. The MeHg bioconcentration factors (i.e., transfer of MeHg from water to seston; BCFw-s) varied from 3 to 7 orders of magnitude across sites and correlated significantly with MeHg in fish. The MeHg biomagnification factors from zooplankton to fish varied much less (logBMFz-f, 0.75 ± 0.31), and did not significantly correlate with fish MeHg, suggesting that zooplanktivory is not as important as bioconcentration in the biomagnification of fish MeHg across the range of ecosystems represented in our meta-analysis. Partial least square (PLS) and linear regression analyses identified several environmental factors associated with increased BCF, including low dissolved organic carbon, low pH, and oligotrophy. Our study reveals the widespread importance of MeHg bioconcentration into the base of the aquatic food web for MeHg at higher trophic levels in aquatic food webs, as well as the major influences on the variability in this bioconcentration.

Does forest harvest increase the mercury concentrations in fish? : Evidence from Swedish lakes

A number of studies have evaluated the effects of forest harvest on mercury (Hg) concentrations and exports in surface waters, but few studies have tested the effect from forest harvest on the change in fish Hg concentrations over the course of several years after harvest. To address this question, mercury (Hg) concentrations in perch (Perca fluviatilis) muscle tissue from five lakes were analyzed for two years before (2010-2011) and three years after (2013-2015) forest harvest conducted in 2012. Fish Hg concentrations in the clear-cut catchments (n=1373 fish specimens) were related to temporal changes of fish Hg in reference lakes (n=1099 fish specimen) from 19 lakes in the Swedish National Environmental Monitoring Programme. Small (length<100mm) and large perch (length≥100mm) were analyzed separately, due to changing feeding habitats of fish over growing size. There was considerable year-to-year and lake-to-lake variation in fish Hg concentrations (-14%-121%) after forest harvest in the clearcut lakes, according to our first statistical model that count for fish Hg changes. While the effect ascribed to forest harvest varied between years, after three years (in 2015), a significant increase of 26% (p<0.0001) in Hg concentrations of large fish was identified in our second statistical model that pooled all 5 clearcut lakes. The large fish Hg concentrations in the 19 reference lakes also varied, and in 2015 had decreased by 7% (p=0.03) relative to the concentrations in 2010-2011. The majority of the annual changes in fish Hg concentrations in the clearcut lakes after harvest were in the lower range of earlier predictions for high-latitude lakes extrapolated primarily from the effects of forest harvest operations on Hg concentrations in water. Since the risk of forest harvest impacts on Hg extends to fish and not just surface water concentrations, there is even more reason to consider Hg effects in forestry planning, alongside other ecosystem effects.