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Featured researches published by Teresia Svensson.


Geoderma | 2001

Organic and inorganic chlorine in Swedish spruce forest soil : influence of nitrogen

Emma Johansson; Gustav Ebenå; Per Sandén; Teresia Svensson; Gunilla Öberg

Concentrations of organic and inorganic chlorine were estimated in samples collected in forest soils in the southern part of Sweden, and changes were observed after the addition of nitrogen in incu ...


Environmental Science & Technology | 2012

Organic matter chlorination rates in different boreal soils: the role of soil organic matter content.

Malin Gustavsson; S. Karlsson; Gunilla Öberg; Per Sandén; Teresia Svensson; Salar Valinia; Yves Thiry; David Bastviken

Transformation of chloride (Cl(-)) to organic chlorine (Cl(org)) occurs naturally in soil but it is poorly understood how and why transformation rates vary among environments. There are still few measurements of chlorination rates in soils, even though formation of Cl(org) has been known for two decades. In the present study, we compare organic matter (OM) chlorination rates, measured by (36)Cl tracer experiments, in soils from eleven different locations (coniferous forest soils, pasture soils and agricultural soils) and discuss how various environmental factors effect chlorination. Chlorination rates were highest in the forest soils and strong correlations were seen with environmental variables such as soil OM content and Cl(-) concentration. Data presented support the hypothesis that OM levels give the framework for the soil chlorine cycling and that chlorination in more organic soils over time leads to a larger Cl(org) pool and in turn to a high internal supply of Cl(-) upon dechlorination. This provides unexpected indications that pore water Cl(-) levels may be controlled by supply from dechlorination processes and can explain why soil Cl(-) locally can be more closely related to soil OM content and the amount organically bound chlorine than to Cl(-) deposition.


Environmental Science & Technology | 2015

Experimental Evidence of Large Changes in Terrestrial Chlorine Cycling Following Altered Tree Species Composition

Malin Montelius; Yves Thiry; Laura Marang; Jacques Ranger; Jean-Thomas Cornélis; Teresia Svensson; David Bastviken

Organochlorine molecules (Clorg) are surprisingly abundant in soils and frequently exceed chloride (Cl(-)) levels. Despite the widespread abundance of Clorg and the common ability of microorganisms to produce Clorg, we lack fundamental knowledge about how overall chlorine cycling is regulated in forested ecosystems. Here we present data from a long-term reforestation experiment where native forest was cleared and replaced with five different tree species. Our results show that the abundance and residence times of Cl(-) and Clorg after 30 years were highly dependent on which tree species were planted on the nearby plots. Average Cl(-) and Clorg content in soil humus were higher, at experimental plots with coniferous trees than in those with deciduous trees. Plots with Norway spruce had the highest net accumulation of Cl(-) and Clorg over the experiment period, and showed a 10 and 4 times higher Cl(-) and Clorg storage (kg ha(-1)) in the biomass, respectively, and 7 and 9 times higher storage of Cl(-) and Clorg in the soil humus layer, compared to plots with oak. The results can explain why local soil chlorine levels are frequently independent of atmospheric deposition, and provide opportunities for improved modeling of chlorine distribution and cycling in terrestrial ecosystems.


Science of The Total Environment | 2016

Chlorination and dechlorination rates in a forest soil — A combined modelling and experimental approach

Malin Montelius; Teresia Svensson; Beatriz Lourino-Cabana; Yves Thiry; David Bastviken

Much of the total pool of chlorine (Cl) in soil consists of naturally produced organic chlorine (Clorg). The chlorination of bulk organic matter at substantial rates has been experimentally confirmed in various soil types. The subsequent fates of Clorg are important for ecosystem Cl cycling and residence times. As most previous research into dechlorination in soils has examined either single substances or specific groups of compounds, we lack information about overall bulk dechlorination rates. Here we assessed bulk organic matter chlorination and dechlorination rates in coniferous forest soil based on a radiotracer experiment conducted under various environmental conditions (additional water, labile organic matter, and ammonium nitrate). Experiment results were used to develop a model to estimate specific chlorination (i.e., fraction of Cl(-) transformed to Clorg per time unit) and specific dechlorination (i.e., fraction of Clorg transformed to Cl(-) per time unit) rates. The results indicate that chlorination and dechlorination occurred simultaneously under all tested environmental conditions. Specific chlorination rates ranged from 0.0005 to 0.01 d(-1) and were hampered by nitrogen fertilization but were otherwise similar among the treatments. Specific dechlorination rates were 0.01-0.03d(-1) and were similar among all treatments. This study finds that soil Clorg levels result from a dynamic equilibrium between the chlorination and rapid dechlorination of some Clorg compounds, while another Clorg pool is dechlorinated more slowly. Altogether, this study demonstrates a highly active Cl cycling in soils.


Environmental Science & Technology | 2013

Portable chamber system for measuring chloroform fluxes from terrestrial environments--methodological challenges.

Lauren Pickering; T. Andrew Black; Chanelle Gilbert; Matthew Jeronimo; Zoran Nesic; Juergen Pilz; Teresia Svensson; Gunilla Öberg

This study describes a system designed to measure chloroform flux from terrestrial systems, providing a reliable first assessment of the spatial variability of flux over an area. The study takes into account that the variability of ambient air concentrations is unknown. It includes quality assurance procedures, sensitivity assessments, and testing of materials used to ensure that the flux equation used to extrapolate from concentrations to fluxes is sound and that the system does not act as a sink or a source of chloroform. The results show that many materials and components commonly used in sampling systems designed for CO2, CH4, and N2O emit chloroform and other volatile chlorinated compounds (VOCls) and are thus unsuitable in systems designed for studies of such compounds. To handle the above-mentioned challenges, we designed a system with a non-steady-state chamber and a closed-loop air-circulation unit returning scrubbed air to the chamber. Based on empirical observations, the concentration increase during a deployment was assumed to be linear. Four samples were collected consecutively and a line was fitted to the measured concentrations. The slope of the fitted line and the y-axis intercept were input variables in the equation used to transform concentration change data to flux estimates. The soundness of the flux equation and the underlying assumptions were tested and found to be reliable by comparing modeled and measured concentrations. Fluxes of chloroform in a forest clear-cut on the east coast of Vancouver Island, BC, during the year were found to vary from -130 to 620 ng m(-2) h(-1). The study shows that the method can reliably detect differences of approximately 50 ng m(-2) h(-1) in chloroform fluxes. The statistical power of the method is still comparatively strong down to differences of 35 ng m(-2) h(-1), but for smaller differences, the results should be interpreted with caution.


Environmental Science & Technology | 2017

Influence of Multiple Environmental Factors on Organic Matter Chlorination in Podsol Soil

Teresia Svensson; Malin Montelius; Malin Andersson; Cecilia Lindberg; Henrik Reyier; Karolina Rietz; Åsa Danielsson; David Bastviken

Natural chlorination of organic matter is common in soils. The abundance of chlorinated organic compounds frequently exceeds chloride in surface soils, and the ability to chlorinate soil organic matter (SOM) appears widespread among microorganisms. Yet, the environmental control of chlorination is unclear. Laboratory incubations with 36Cl as a Cl tracer were performed to test how combinations of environmental factors, including levels of soil moisture, nitrate, chloride, and labile organic carbon, influenced chlorination of SOM from a boreal forest. Total chlorination was hampered by addition of nitrate or by nitrate in combination with water but enhanced by addition of chloride or most additions including labile organic matter (glucose and maltose). The greatest chlorination was observed after 15 days when nitrate and water were added together with labile organic matter. The effect that labile organic matter strongly stimulated the chlorination rates was confirmed by a second independent experiment showing higher stimulation at increased availability of labile organic matter. Our results highlight cause-effect links between chlorination and the studied environmental variables in podsol soil-with consistent stimulation by labile organic matter that did overrule the negative effects of nitrate.


Geochimica et Cosmochimica Acta | 2007

Chloride retention in forest soil by microbial uptake and by natural chlorination of organic matter

David Bastviken; Frida Thomsen; Teresia Svensson; S. Karlsson; Per Sandén; G. Shaw; Miroslav Matucha; Gunilla Öberg


Environmental Science & Technology | 2006

Chloride Retention and Release in a Boreal Forest Soil: Effects of Soil Water Residence Time and Nitrogen and Chloride Loads

David Bastviken; Per Sandén; Teresia Svensson; Carina Ståhlberg; Malin Magounakis; Gunilla Öberg


Biogeochemistry | 2012

Is chloride a conservative ion in forest ecosystems

Teresia Svensson; Gary M. Lovett; Gene E. Likens


Environmental Science & Technology | 2009

Temperature sensitivity indicates that chlorination of organic matter in forest soil is primarily biotic.

David Bastviken; Teresia Svensson; S. Karlsson; Per Sandén; Gunilla Öberg

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Gunilla Öberg

University of British Columbia

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Christian Wiencke

Alfred Wegener Institute for Polar and Marine Research

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Matti Parikka

Swedish University of Agricultural Sciences

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