Environmental history: a piece in the puzzle for establishing plans for environmental management.

Establishment of plans for environmental planning and management requires that a number of natural and societal factors must be taken into consideration. Insights into the inherent dynamics of nature as well as the role that past human activities have played for establishing the current condition of the landscape and the natural environment in general are essential. Many natural and man-made changes occur over time scales of decades or centuries, and these are difficult to comprehend without a historical perspective. Such a perspective can be obtained using palaeoecological studies, i.e. by geochemical and biological analyses of lake sediment and peat deposits. To illustrate the long-term dynamics of nature and particularly the role of man, we present here five case studies from Sweden concerning pollution, lake acidification, lake eutrophication, biodiversity, and landscape dynamics and conservation--topics of broad interests--and discuss benefits of including a longer time perspective in environmental management.

Widespread waterborne pollution in central Swedish lakes and the Baltic Sea from pre-industrial mining and metallurgy.

Metal pollution is viewed as a modern problem that began in the 19th century and accelerated through the 20th century; however, in many parts of the globe this view is wrong. Here, we studied past waterborne metal pollution in lake sediments from the Bergslagen region in central Sweden, one of many historically important mining regions in Europe. With a focus on lead (including isotopes), we trace mining impacts from a local scale, through a 120-km-long river system draining into Mälaren--Sweden's third largest lake, and finally also the Baltic Sea. Comparison of sediment and peat records shows that pollution from Swedish mining was largely waterborne and that atmospheric deposition was dominated by long-range transport from other regions. Swedish ore lead is detectable from the 10th century, but the greatest impact occurred during the 16th-18th centuries with improvements occurring over recent centuries, i.e., historical pollution > modern industrial pollution.

Assessing the stability of mercury and methylmercury in a varved lake sediment deposit.

Using lake sediments to infer past total mercury and methylmercury loading to the environment requires that diagenetic processes within the sediment do not significantly affect the concentrations or net accumulation rates of the mercury species. Because carbon is lost during early sediment diagenesis, the close link between carbon and mercury raises the question of how reliable lake sediments are as archives of total mercury and methylmercury loading. In this study we used a series of freeze cores taken in a lake with varved (annually laminated) sediment to assess the stability of total mercury and methylmercury over time. By tracking material deposited in specific years in cores collected in different years, we found that despite a 20--25% loss of carbon in the first 10--15 years, there was no apparent loss of total mercury over time; hence, lake sediments can be considered as reliable archives. However, over the first 5--8 years after sedimentation, about 30--40% of the methylmercury was lost (a decrease of 0.025--0.030 microg MeHg m(-2) yr(-1)), suggesting that sediment profiles showing increasing methylmercury concentrations toward the sediment surface are in large part an artifact of diagenetic processes (net demethylation), rather than a record of changes in methylmercury loading.

Monitoring compared with paleolimnology: implications for the definition of reference condition in limed lakes in Sweden.

Surface water acidification was identified as a major environmental problem in the 1960s. Consequently, a liming program was launched in Sweden in the 1970s. The primary purpose of liming is to restore conditions that existed prior to acidification. To reach this goal, as well as achieve 'good status' (i.e. low levels of distortion resulting from human activity) in European freshwaters until 2016 under the European Union Water Framework Directive, lake data are required to define reference conditions. Here, we compare data from chemical/biological monitoring of 12 limed lakes with results of paleolimnological investigations, to address questions of reference conditions, acidification, and restoration by liming. Using diatom-based lake-water pH inferences, we found clear evidence of acidification in only five of the 12 lakes, which had all originally been classified as acidified according to monitoring data. After liming, measured and diatom-inferred pH agree well in seven lakes. The sediment record of three of the five remaining lakes gave ambiguous results, presumably due to sediment mixing or low sediment accumulation rates. It is difficult to determine whether liming restored the lakes to a good status, especially as some of the lakes were not acidified during the twentieth century. In addition to acid deposition, other factors, such as natural lake and catchment ontogeny or human impact through agricultural activity, influence lake acidity. This study shows that monitoring series are usually too short to define reference conditions for lakes, and that paleolimnological studies are useful to set appropriate goals for restoration and for evaluation of counter measures.

Mercury pollution trends in subarctic lakes in the northern Swedish mountains.

Despite many years of research about mercury pollution, data concerning high-latitude regions of Europe are limited, particularly studies of long-term temporal trends. It is not clear whether the mercury load at high latitudes follows the recent decreasing trends in European mercury emissions or whether the load is still high because of continuing global emissions. In this study we use sediments from 12 lakes, located above the Arctic Circle in the Swedish mountains, to assess the past and recent mercury pollution situation, especially for the last 200 y. The mercury load increased clearly in sediment deposited from the late 19th or early 20th century to a peak between 1960 and 1990. This peak represents an enrichment of 1.4 to 4.2 times over background concentrations. This enrichment is comparable with enrichments in sediments from lower latitudes as well as other Arctic regions. Since the 1990s mercury concentration has declined in 8 of the 12 lakes, i.e., similar to emission trends in Europe.

Near-infrared spectroscopy (NIRS) of epilithic material in streams has a potential for monitoring impact from mining.

There is an increasing demand for cost-effective methods for environmental monitoring, and here we assess the potential of near-infrared spectroscopy (NIRS) on epilithic material from streams (material covering submerged stones) as a new method for monitoring the impact of pollution from mining and mining-related industries. NIRS, a routine technique in industry, registers the chemical properties of organic material on a molecular level and can detect minute alterations in the composition of epilithic material. Epilithic samples from 65 stream sites (42 uncontaminated and 23 contaminated) in northern Sweden were analyzed. The NIRS approach was evaluated by comparing it with the results of chemical analyses and diatom analyses of the same samples. Based on Principal Component Analysis, the NIRS data distinguished contaminated from uncontaminated sites and performed slightly betterthan chemical analyses and clearly betterthan diatom analyses. Of the streams designated a priori as contaminated, 74% were identified as contaminated by NIRS, 65% were identified by chemical analysis, and 26% were identified by diatom analysis. Unlike chemical analyses of water samples, NIRS data reflect biological impacts in the streams, and the epilithic material integrates impact over time. Given that, and the simplicity of NIRS-analyses, further studies to assess the use of NIRS of epilithic material as an inexpensive environmental monitoring method are justified.

Flux rates of atmospheric lead pollution within soils of a small catchment in northern Sweden and their implications for future stream water quality.

It is not well-known how the accumulated pool of atmospheric lead pollution in the boreal forest soil will affect the groundwater and surface water chemistry in the future as this lead migrates through the soil profile. This study uses stable lead isotopes (206Pb/207Pb and 208Pb/ 207Pb ratios) to trace the transport of atmospheric lead pollution within the soil of a small catchment and predict future lead level changes in a stream draining the catchment. Low 206Pb/207Pb and 208Pb/207Pb ratios for the lead in the soil water (1.16 +/- 0.02; 2.43 +/- 0.03) and streamwater (1.18 +/- 0.03; 2.42 +/- 0.03) in comparison to that of the mineral soil (>1.4; >2.5) suggest that atmospheric pollution contributes by about 90% (65-100%) to the lead pool found in these matrixes. Calculated transport rates of atmospheric lead along a soil transect indicate that the mean residence time of lead in organic and mineral soil layers is at a centennial to millennial time scale. A maximum release of the present pool of lead pollution in the soil to the stream is predicted to occur within 200-800 years. Even though the uncertainty of the prediction is large, it emphasizes the magnitude of the time lag between the accumulation of atmospheric lead pollution in soils and the subsequent response in streamwater quality.

Natural fluctuations of mercury and lead in Greenland lake sediments.

Given the current scenario of increasing global temperatures, it is valuable to assess the potential influence of changing climate on pollution distribution and deposition. In this study we use long-term sediment records from three lakes (spanning ca. 1000, 4800, and 8000 years, respectively) from the Greenland west coast to assess recent and long-term variations in mercury (Hg) and lead (Pb), including stable Pb isotopes (206Pb and 207Pb), in terms of pollution and climate influences. The temporal trends in sediment deposited from about the mid-19th century and forward are in general agreement with the history of industrial emissions at lower latitudes. Therefore, in recent sediment a possible influence from changing climate is difficult to assess. However, by using deeper sediment layers we show that changes in Greenland climate caused changes in the lake influx of material from regional aeolian activity, which resulted in large fluctuations in Hg and Pb concentrations and 206Pb/207Pb ratios. The aeolian material is primarily derived from glacio-fluvial material with low Hg and Pb concentrations and a different isotopic composition. For one of the lakes, the fluctuations in Hg concentrations (10 to 70 ng g(-1)) prior to the 19th century are equal to the anthropogenic increase in the uppermost layers, suggesting that when studying recent concentrations and time trends of pollution in relatively low-contaminated areas such as the Arctic, the early natural fluctuations must be considered.

Tree rings as Pb pollution archives? A comparison of 206Pb/207Pb isotope ratios in pine and other environmental media.

Tree rings, if validated as an environmental archive for pollution, would provide a convenient, geographically widespread archive for studying the temporal and spatial distribution of atmospheric pollutants. We collected tree-ring records from Scots pine (Pinus sylvestris L.), ranging in age from 100 to 300 years and from one spruce (Picea abies), from sites in southern and northern Sweden and analyzed their stable lead isotopic composition (206Pb/207Pb). These results are compared to the Pb isotopic composition in soil profiles from each of the sites and temporal changes in the 206Pb/207Pb ratio in peat and lake sediment deposits in Sweden. The mineral soils at each site are characterized by high 206Pb/207Pb ratios (> 1.35), while the ratios in the mor layer are low (1.14-1.16) and characterized by atmospheric lead pollution. The 206Pb/207Pb ratios of the tree rings, typically approximately 1.18-1.20, indicate a significant (10-30%) contribution of Pb derived from the underlying mineral soil. While peat and lake sediment records show that the 206Pb/207Pb ratio of atmospheric deposition has varied over time, with a pronounced trough between approximately 1930 and 1990, the tree rings show no similar trend. Further comparison of published Pb isotope data from other tree-ring records with time series from peat bogs and herbarium samples also shows poor agreement, and indicates that tree rings always contain a mixture of pollution Pb and Pb from the underlying mineral soil. The majority of Pb in the wood is derived from atmospheric pollution either directly, through aerial interception, or indirectly, through uptake from the large pool of accumulated pollution Pb in the soil. Since the Pb isotope ratios of the wood indicate that some natural Pb is taken up into the tree, then it must also be concluded that some fraction of the pollution Pb in the wood is likewise taken up from the forest soil. Based on the Pb isotope analyses, we can only conclude that dendrochemical records are not useful in temporal studies of metal pollution.

Time trends of selected persistent organic pollutants in lake sediments from Greenland.

Sediments from seven lakes in West Greenland were used as natural archives to study past and present levels of PCBs (polychlorinated biphenyls, tri- to decachlorinated), tetra-BDE #47 (2,2',4,4'-bromodiphenyl ether), chlordane (cis- and trans-octachlordane) and HxCBz (hexachlorobenzene). The concentrations found are lower than or comparable to concentrations found in sediments from other Arctic regions and one to 2 orders of magnitude lower than concentrations typically found in sediments at lower latitudes. The observed temporal trends (direct and indirect dating) show a decreasing total PCB concentration. Even though local contamination sources exist, the POP deposition in the studied area is most likely a result from long-range transport. The hypothesis about "cold condensation" suggests a latitudinal fractionation to occur between different volatile compounds during the transport toward the pole. In this study a time delay in the deposition for the low-chlorinated PCBs (tri- and tetrachlorinated), compared to their emission histories and compared to higher chlorinated PCBs, was indicated. Although very low tetra-BDE #47 concentrations are observed in this study, there are indications for an increasing concentration in recent sediment layers that may reflect increasing environmental concentrations at lower latitudes. The investigated pesticides are still in use at lower latitudes, however neither chlordane nor HxCBz show any distinct temporal trend of increasing or decreasing concentration toward the sediment surface.

Pre-industrial atmospheric pollution: was it important for the pH of acid-sensitive Swedish lakes?

Acid rain has caused extensive surface water acidification in Sweden since the mid-20th century. Sulfur emissions from fossil-fuel burning and metal production were the main sources of acid deposition. In the public consciousness, acid deposition is strongly associated with the industrial period, in particular the last 50 years. However, studies of lake-water pH development and atmospheric pollution, based on analyses of lake sediment deposits, have shown the importance of a long-term perspective. Here, we present a conceptual argument, using the sediment record, that large-scale atmospheric acid deposition has impacted the environment since at least Medieval times. Sulfur sources were the pre-industrial mining and metal industries that produced silver, lead and other metals from sulfide ores. This early excess sulfur deposition in southern Sweden did not cause surface water acidification; on the contrary, it contributed to alkalization, i.e. increased pH and productivity of the lakes. Suggested mechanisms are that the excess sulfur caused enhanced cation exchange in catchment soils, and that it altered iron-phosphorus cycling in the lakes, which released phosphorus and increased lake productivity.