Cecilia Agrell
Lund University
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Publication
Featured researches published by Cecilia Agrell.
Journal of Chemical Ecology | 2004
Jep Agrell; Peter Anderson; Wieslaw Oleszek; Anna Stochmal; Cecilia Agrell
We examined herbivore-induced responses of alfalfa (Medicago sativa) and cotton (Gossypium hirsutum) under different CO2 conditions. Plants were grown under ambient (350 ppm) or elevated (700 ppm) CO2 levels, and were either damaged or undamaged by Spodoptera littoralis larvae. At harvest, growth of undamaged (control) plants was determined, and foliar chemical composition of both undamaged and damaged plants was analyzed. Cotton grew faster overall and showed a greater increase in growth in response to CO2 enrichment than did alfalfa. Elevated CO2 levels increased starch and decreased nitrogen levels in damaged alfalfa and undamaged cotton plants. Alfalfa saponin levels were significantly increased by elevated CO2 and damage. Regarding specific saponins, medicagenic acid bidesmoside (3GlcA,28AraRhaXyl medicagenate) concentrations were reduced by high CO2, whereas zanhic acid tridesmoside (3GlcGlcGlc,23Ara,28AraRhaXylApi Za) levels were unaffected by the treatments. Soyasaponin I (3GlcAGalRha soyasapogenol B) was only detected in minute amounts. Alfalfa flavonoid analyses showed that total flavonoid levels were similar between treatments, although free apigenin increased and apigenin glucoside (7-O-[2-O-feruloyl-β-D-glucuronopyranozyl (1→2)-O-β-D-glucuronopyranozyl]-4′-O-β-D-glucuronopyranozide apigenin) decreased in CO2-enriched plants. In cotton, herbivore damage increased levels of total terpenoid aldehydes, gossypol, hemigossypolone, the heliocides H1 and H4, but not H2 and H3, whereas CO2 enrichment had no effect. These results demonstrate that combined effects of CO2 and herbivore damage vary between plant species, which has implications for the competitive balance within plant communities.
Atmospheric Environment | 2002
Cecilia Agrell; Per Larsson; Lennart Okla; Jep Agrell
Concentrations of PCB congeners were determined in precipitation and the annual and seasonal depositional fluxes were calculated for 16 (mostly rural) stations around the Baltic Sea during 1990-1993. The concentrations of individual congeners in precipitation were found to be influenced by atmospheric concentrations of PCBs, ambient temperature, precipitation volume and physico-chemical properties of the compounds. Median levels of PCBs in precipitation differed one order of magnitude between stations. When analyzing all data together to obtain regional trends, concentrations of PCBs in precipitation decreased with increasing temperature. This relationship was the same for all stations but differed in the magnitude of the slope for individual congeners. Low chlorinated PCB congeners showed steeper slopes for the temperature relationship than did high chlorinated congeners, a result explained by high atmospheric concentrations of the low chlorinated congeners during low temperatures. Annual wash out ratios were between 31 and 72 x 103 and tended to be higher for the high chlorinated congeners. Wash out ratios decreased with increasing temperature for all congeners except PCB-33. At snow scavenging events, the wash out ratio of PCBs increased with a factor of 2. Latitudinal trends for PCB concentrations in precipitation and deposition were generally not statistically significant. The calculated yearly deposition of PCBs to the Baltic Sea was 390 and 5-18 kg for individual congeners, with PCB-138 having the highest flux. Deposition of PCB congeners varied seasonally, with a factor between 2 and 3, and was generally highest during fall. Relatively higher deposition of low chlorinated congeners compared to high chlorinated congeners was found during winter
Science of The Total Environment | 2002
Cecilia Backe; Per Larsson; Cecilia Agrell
Spatial and temporal variations in polychlorinated biphenyl (PCB) concentrations were studied in precipitation at 11 sampling-sites over a period of 1 year and compared with PCB concentrations in the air. The study was carried out in a region of southern Sweden approximately 11 000 km2 in area. The PCB concentration in precipitation ranged between 1.18 and 81.4 ng l(-1). Two of the sampling sites showed concentrations that were approximately 30 times higher than at the rest of the sites. The variation in concentration between sites may be explained by location as well as by differences in weather conditions and particle content in the air. Wind direction played an important role for PCB concentration in precipitation in coastal areas, while at the inland sites this variable seemed to have a minor influence. We found no seasonal trends in PCB concentration in precipitation or any dependence on air temperature. To examine the intensity of precipitation scavenging, the total washout ratios (Wt) were calculated. There was a large variation in Wt over time, and the highest ratios were observed at the two sites where PCB concentration in the air was high. Furthermore, high concentrations of PCB in precipitation correlated with a high-chlorinated pattern, as shown by principal component analysis. For most of the sites there was a significantly negative relationship between PCB concentration and rain volume.
Archive | 2001
Frank Wania; Dag Broman; Johan Axelman; C. Näf; Cecilia Agrell
Persistent organic pollutants (POPs) such as polycyclic aromatic hydrocarbons and organochlorinated compounds reach lakes, estuaries and the oceans through direct discharge, riverine inflow or atmospheric deposition. These generally quite hydrophobic chemicals have a low affinity for the aqueous phase and tend to partition into the organic phases of suspended solids and bottom sediments or the lipid fraction of aquatic biota. Some POPs show a potential to biomagnify and the highest concentrations are often found in the upper trophic levels of aquatic food chains.
Environmental Science & Technology | 2004
Arnout ter Schure; Per Larsson; Cecilia Agrell; Jan P. Boon
Atmospheric Environment | 2004
Cecilia Agrell; Arnout ter Schure; Jeanette Sveder; Alma Bokenstrand; Per Larsson; Bart N. Zegers
Atmospheric Environment | 2004
Arnout ter Schure; Cecilia Agrell; Alma Bokenstrand; Jeanette Sveder; Per Larsson; Bart N. Zegers
Environmental Science & Technology | 1999
Cecilia Agrell; Lennart Okla; Per Larsson; Cecilia Backe; Frank Wania
Oikos | 2006
Jep Agrell; Peter Anderson; Wieslaw Oleszek; Anna Stochmal; Cecilia Agrell
Environmental Toxicology and Chemistry | 1999
Eric J. Willman; Jon B. Manchester-Neesvig; Cecilia Agrell; David E. Armstrong