Åsa Arrhenius
University of Gothenburg
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Featured researches published by Åsa Arrhenius.
Ecotoxicology and Environmental Safety | 2003
Marco Vighi; Rolf Altenburger; Åsa Arrhenius; Thomas Backhaus; Wolfgang Bödeker; Hans Blanck; F Consolaro; Michael Faust; Antonio Finizio; K. Froehner; Paola Gramatica; L.H. Grimme; Frederick Grönvall; V Hamer; Martin Scholze; Helge Walter
The need to develop water quality objectives not only for single substances but also for mixtures of chemicals seems evident. For that purpose, the conceptual basis could be the use of the two existing biometric models: concentration addition (CA) and independent action (IA), which is also called response addition. Both may allow calculation of the toxicity of mixtures of chemicals with similar modes of action (CA) or dissimilar modes of action (IA), respectively. The joint research project Prediction and Assessment of the Aquatic Toxicity of Mixtures of Chemicals (PREDICT) within the framework of the IVth Environment and Climate Programme of the European Commission, provided the opportunity to address (a) chemometric and QSAR criteria to classify substances as supposedly similarly or dissimilarly acting; (b) the predictive values of both models for the toxicity of mixtures at low, statistically nonsignificant effect concentrations of the individual components; and (c) the predictability of mixture toxicity at higher levels of biological complexity. In this article, the general outline, methodological approach, and some preliminary findings of PREDICT are presented. A procedure for classifying chemicals in relation to their structural and toxicological similarities has been developed. The predictive capabilities of CA and IA models have been demonstrated for single species and, to some extent, for multispecies testing. The role of very low effect concentrations in multiple mixtures has been evaluated. Problems and perspectives concerning the development of water quality objectives for mixtures are discussed.
Environmental Toxicology and Chemistry | 2011
Thomas Backhaus; Tobias Porsbring; Åsa Arrhenius; Sara Brosché; Per Johansson; Hans Blanck
The single-substance and mixture toxicity of five pharmaceuticals and personal care products (fluoxetine, propranolol, triclosan, zinc-pyrithione, and clotrimazole) to marine microalgal communities (periphyton) was investigated. All compounds proved to be toxic, with median effective concentration values (EC50s) between 1,800 nmol/L (triclosan) and 7.2 nmol/L (Zn-pyrithione). With an EC50 of 356 nmol/L, the toxicity of the mixture falls into this span, indicating the absence of strong synergisms or antagonisms. In fact, a comparison with mixture toxicity predictions by the classical mixture concepts of concentration addition and independent action showed a good predictability in the upper effect range. However, the mixture provoked stimulating effects (hormesis) in the lower effect range, hampering the application of either concept. An independent repetition of the mixture experiment resulted in a principally similar concentration-response curve, again with clear hormesis effects in the lower range of test concentrations. However, the curve was shifted toward higher effect concentrations (EC50 1,070 nmol/L), which likely is due to changes in the initial species composition. Clear mixture effects were observed even when all five components were present only at their individual no-observed-effect concentrations (NOECs). These results show that, even with respect to mixtures of chemically and functionally dissimilar compounds, such as the five pharmaceuticals and personal care products investigated, environmental quality standards must take possible mixture effects from low-effect concentrations of individual compounds into consideration.
Marine Pollution Bulletin | 2014
Åsa Arrhenius; Thomas Backhaus; Annelie Hilvarsson; Ida Wendt; Aleksandra Zgrundo; Hans Blanck
This paper presents a novel assay that allows a quick and robust assessment of the effects of biocides on the initial settling and establishment of marine photoautotrophic biofilms including the multitude of indigenous fouling organisms. Briefly, biofilms are established in the field, sampled, comminuted and re-settled on clean surfaces, after 72h chlorophyll a is measured as an integrating endpoint to reflect both settling and growth. Eight antifoulants were used to evaluate the assay. Efficacy ranking, based on EC98 values from most to least efficacious compound is: copper pyrithione>TPBP>DCOIT>tolylfluanid>zinc pyrithione>medetomidine>copper (Cu(2+)), while ecotoxicological ranking (based on EC10 values) is irgarol, copper pyrithione>zinc pyrithione>TPBP>tolylfluanid>DCOIT>copper (Cu(2+))>medetomidine. The algaecide irgarol did not cause full inhibition. Instead the inhibition leveled out at 95% effect at 30 nmoll(-)(1), a concentration that was clearly lower than for any other of the tested biocides.
Environmental Toxicology and Chemistry | 2015
K. Martin Eriksson; C. Henrik Johansson; Viktor Fihlman; Alexander Grehn; Kemal Sanli; Mats X. Andersson; Hans Blanck; Åsa Arrhenius; Triranta Sircar; Thomas Backhaus
Triclosan is a widely used antibacterial agent that has become a ubiquitous contaminant in freshwater, estuary, and marine environments. Concerns about potential adverse effects of triclosan have been described in several recent risk assessments. Its effects on freshwater microbial communities have been well studied, but studies addressing effects on marine microbial communities are scarce. In the present study, the authors describe short- and long-term effects of triclosan on marine periphyton (microbial biofilm) communities. Short-term effects on photosynthesis were estimated after 60 min to 210 min of exposure. Long-term effects on photosynthesis, chlorophyll a fluorescence, pigment content, community tolerance, and bacterial carbon utilization were studied after exposing periphyton for 17 d in flow-through microcosms to 0.316 nM to 10,000 nM triclosan. Results from the short-term studies show that triclosan is toxic to periphyton photosynthesis. Half maximal effective concentration (EC50) values of 1080 nM and 3000 nM were estimated using (14)CO2-incorporation and pulse amplitude modulation (PAM) fluorescence measurements, respectively. After long-term triclosan exposure in flow-through microcosms, photosynthesis estimated using PAM fluorometry was not inhibited by triclosan concentrations up to 1000 nM but instead increased with increasing triclosan concentration. Similarly, at exposure concentrations of 31.6 nM and higher, triclosan caused an increase in photosynthetic pigments. At 316 nM triclosan, the pigment amounts were increased by a factor of 1.4 to 1.9 compared with the control level. Pollution-induced community tolerance was observed for algae and cyanobacteria at 100 nM triclosan and higher. Despite the widespread use of triclosan as an antibacterial agent, the compound did not have any effects on bacterial carbon utilization after long-term exposure.
Marine Pollution Bulletin | 2013
Ida Wendt; Åsa Arrhenius; Thomas Backhaus; Annelie Hilvarsson; Kristina Holm; Katherine Langford; Timur Tunovic; Hans Blanck
The herbicide irgarol 1051 is commonly used on ship hulls to prevent growth of algae, but as a component of self-eroding paints it can also spread in the surrounding waters and affect non-target organisms. The effect of irgarol on settlement and growth of zoospores from the marine macro algae Ulva lactuca from the Gullmar fjord on the Swedish west coast was investigated in the present study. The zoospores were allowed to settle and grow in the presence of irgarol, but neither settlement - nor growth inhibition was observed at concentrations of up to 2000 nmol l(-1). This is between 10 and 100 times higher than effect concentrations reported earlier for algae. Irgarol also induced the greening effect (4-fold increase in chlorophyll a content) in the settled zoospore/germling population, typical for photosystem II inhibitors like irgarol. This study support previous findings that irgarol constitutes a selection pressure in the marine environment.
Environmental Science & Technology | 2004
Thomas Backhaus; Åsa Arrhenius; Hans Blanck
Continental Shelf Research | 2003
Thomas Backhaus; Rolf Altenburger; Åsa Arrhenius; Hans Blanck; Michael Faust; Antonio Finizio; Paola Gramatica; Matthias Grote; Marion Junghans; Wiebke Meyer; Manuela Pavan; Tobias Porsbring; Martin Scholze; Roberto Todeschini; Marco Vighi; Helge Walter; L. Horst Grimme
Aquatic Toxicology | 2004
Åsa Arrhenius; Frederick Grönvall; Martin Scholze; Thomas Backhaus; Hans Blanck
Archives of Environmental Contamination and Toxicology | 2006
Åsa Arrhenius; Thomas Backhaus; Frederick Grönvall; Marion Junghans; Martin Scholze; Hans Blanck
Journal of Experimental Marine Biology and Ecology | 2007
Tobias Porsbring; Åsa Arrhenius; Thomas Backhaus; Mats Kuylenstierna; Martin Scholze; Hans Blanck