Sophia V. Hansson
Umeå University
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Featured researches published by Sophia V. Hansson.
The Holocene | 2013
Sophia V. Hansson; Johan Rydberg; Malin E. Kylander; Kerry Gallagher; Richard Bindler
The past decade has seen a rapid increase in interest in the biogeochemical record preserved in peat, particularly as it relates to carbon dynamics and environmental change. Importantly, recent studies show that carbon dynamics, that is, organic matter decomposition, can influence the record of atmospherically derived elements such as halogens and mercury. Most commonly, bulk density, light transmission, or carbon/nitrogen (C/N) ratios are used as a proxy to qualitatively infer the degree of decomposition in peat, but do these three proxies reflect the same patterns? Furthermore, how do each of these proxies relate to other geochemical data? To address these questions, we analyzed bulk density, light transmission, and C/N ratios, as well as multielement geochemistry (wavelength-dispersive x-ray fluorescence (WD-XRF)), in three hummock cores (70 cm in length, c. 500 years) from an ombrotrophic Swedish bog. To compare the proxies, we applied principal component analysis (PCA) to identify how the proxies relate to and interact with the geochemical matrix. This was coupled with changepoint modeling to identify and compare statistically significant changes for each proxy. Our results show differences between the proxies within and between cores, indicating each responds to a different part of the decomposition process. This is supported by the PCA, where the three proxies fall on different principal components. Changepoint analysis also showed that the inferred number of changepoints and their depths vary for each proxy and core. This suggests that decomposition is not fully captured by any one of these commonly used proxies, and thus, more than one proxy should be included.
Environmental Science & Technology | 2012
Richard Bindler; Ruilian Yu; Sophia V. Hansson; Neele Classen; Jon Karlsson
In Central Sweden an estimated 80% of the lakes contain fish exceeding health guidelines for mercury. This area overlaps extensively with the Bergslagen ore region, where intensive mining of iron ores and massive sulfide ores occurred over the past millennium. Although only a few mines still operate today, thousands of mineral occurrences and mining sites are documented in the region. Here, we present data on long-term mercury pollution in 16 sediment records from 15 lakes, which indicate that direct release of mercury to lakes and watercourses was already significant prior to industrialization (<AD 1800). Thirteen of our lakes show increases in mercury from 3-fold-equivalent to the enrichment factor in many remote lakes today-to as much as 60-fold already during the period AD 1500-1800, with the highest values in the three lakes most closely connected to major mines. Although the timing and magnitude of the historical increases in mercury are heterogeneous among lakes, the data provide unambiguous evidence for an incidental release of mercury along with other mining metals to lakes and watercourses, which suggests that the present-day problem of elevated mercury concentrations in the Bergslagen region can trace its roots back to historical mining.
Scientific Reports | 2015
Erik J. Lundin; Jonatan Klaminder; David Bastviken; Carolina Olid; Sophia V. Hansson; Jan Karlsson
Lakes play an important role in the global carbon (C) cycle by burying C in sediments and emitting CO2 and CH4 to the atmosphere. The strengths and control of these fundamentally different pathways are therefore of interest when assessing the continental C balance and its response to environmental change. In this study, based on new high-resolution estimates in combination with literature data, we show that annual emission:burial ratios are generally ten times higher in boreal compared to subarctic – arctic lakes. These results suggest major differences in lake C cycling between biomes, as lakes in warmer boreal regions emit more and store relatively less C than lakes in colder arctic regions. Such effects are of major importance for understanding climatic feedbacks on the continental C sink – source function at high latitudes. If predictions of global warming and northward expansion of the boreal biome are correct, it is likely that increasing C emissions from high latitude lakes will partly counteract the presumed increasing terrestrial C sink capacity at high latitudes.
Science of The Total Environment | 2014
Sophia V. Hansson; James M. Kaste; Carolina Olid; Richard Bindler
Accurate dating of peat accumulation is essential for quantitatively reconstructing past changes in atmospheric metal deposition and carbon burial. By analyzing fallout radionuclides (210)Pb, (137)Cs, (241)Am, and (7)Be, and total Pb and Hg in 5 cores from two Swedish peatlands we addressed the consequence of estimating accumulation rates due to downwashing of atmospherically supplied elements within peat. The detection of (7)Be down to 18-20 cm for some cores, and the broad vertical distribution of (241)Am without a well-defined peak, suggest some downward transport by percolating rainwater and smearing of atmospherically deposited elements in the uppermost peat layers. Application of the CRS age-depth model leads to unrealistic peat mass accumulation rates (400-600 g m(-2) yr(-1)), and inaccurate estimates of past Pb and Hg deposition rates and trends, based on comparisons to deposition monitoring data (forest moss biomonitoring and wet deposition). After applying a newly proposed IP-CRS model that assumes a potential downward transport of (210)Pb through the uppermost peat layers, recent peat accumulation rates (200-300 g m(-2) yr(-1)) comparable to published values were obtained. Furthermore, the rates and temporal trends in Pb and Hg accumulation correspond more closely to monitoring data, although some off-set is still evident. We suggest that downwashing can be successfully traced using (7)Be, and if this information is incorporated into age-depth models, better calibration of peat records with monitoring data and better quantitative estimates of peat accumulation and past deposition are possible, although more work is needed to characterize how downwashing may vary between seasons or years.
Scientific Reports | 2018
Malin E. Kylander; Antonio Martínez-Cortizas; Richard Bindler; Joeri Kaal; Jenny Sjöström; Sophia V. Hansson; Noemí Silva-Sánchez; Sarah L. Greenwood; Kerry Gallagher; Johan Rydberg; Carl-Magnus Mörth; Sebastien Rauch
Peatlands in northern latitudes sequester one third of the world’s soil organic carbon. Mineral dusts can affect the primary productivity of terrestrial systems through nutrient transport but this process has not yet been documented in these peat-rich regions. Here we analysed organic and inorganic fractions of an 8900-year-old sequence from Store Mosse (the “Great Bog”) in southern Sweden. Between 5420 and 4550 cal yr BP, we observe a seven-fold increase in net peat-accumulation rates corresponding to a maximum carbon-burial rate of 150 g C m−2 yr−1 – more than six times the global average. This high peat accumulation event occurs in parallel with a distinct change in the character of the dust deposited on the bog, which moves from being dominated by clay minerals to less weathered, phosphate and feldspar minerals. We hypothesize that this shift boosted nutrient input to the bog and stimulated ecosystem productivity. This study shows that diffuse sources and dust dynamics in northern temperate latitudes, often overlooked by the dust community in favour of arid and semi-arid regions, can be important drivers of peatland carbon accumulation and by extension, global climate, warranting further consideration in predictions of future climate variability.
Environmental Science & Technology | 2018
Sophia V. Hansson; Michael Bank
Exposure in Aquatic Ecosystems Sophia V. Hansson*,† and Michael S. Bank‡,§ †Department of Bioscience − Arctic Research Centre, Aarhus University, Frederiksborgvej 399, Roskilde DK-4000, Denmark ‡Department of Contaminants and Biohazards, Institute of Marine Research, Bergen, Norway Department of Environmental Conservation, University of Massachusetts Amherst, 160 Holdsworth Way, Amherst, Massachusetts 01003, United States
Journal of Archaeological Science | 2011
Richard Bindler; Ulf Segerström; Ing-Marie Pettersson-Jensen; Anna Berg; Sophia V. Hansson; Harald Holmström; Karin Olsson; Ingemar Renberg
Biogeochemistry | 2014
Sophia V. Hansson; James M. Kaste; Keyao Chen; Richard Bindler
Science of The Total Environment | 2015
Sophia V. Hansson; Julie Tolu; Richard Bindler
Archive | 2014
Erik J. Lundin; Jonatan Klaminder; David Bastviken; Carolina Olid; Sophia V. Hansson; Jan Karlsson