Research
The primary aim of our research is to obtain a mechanistic understanding of the effects of chemicals and additional stressors on aquatic organisms in order to support a knowledge-based risk assessment. To achieve this aim we are studying:
- the exposure of aquatic organisms to chemical stressors (e.g., organic chemicals, heavy metals, and synthetic nanoparticles) and the effect of chemical speciation on uptake and bioavailability
- the dynamic responses of aquatic organisms to fluctuating concentrations of chemicals and chemical mixtures
- the mode of action of multiple chemical and physical stressors and the capacity of aquatic organisms to detoxify chemicals and/or recover from exposure to stressors
This fundamental understanding serves as the basis for the
development of models to aid in the prediction of risks and of effect-directed
analytical tools for the environmental risk assessment of chemicals and the
ecotoxicological assessment of aquatic ecosystems.
Research Topics
- Internal Exposure and Effects
- Multiple Stressors
- Linking effects across biological levels
- Environmental Risk Assessment
- Nanoecotoxicology
- Advancing experimental models
Research Models
| in vivo/in vitro | in silico |
| Algae | biogeochemical models |
| Daphnids | TK-TD models |
| Gammarids | QSAR models |
| Fish/fish cells | cellular network models |
| mammalian cell | Mixture toxicity prediction models |
Research Methods
| Tools | Equipment/Methods |
| bio-analytical | Combined algae test |
| Bacterial bioluminescence inhibition test | |
| EROD assay | |
| E-Screen assay | |
| YES-assay | |
| Synchronous algae toxicity test | |
| chemical-analytical | Enrichment: passive samplers (POCIS, SDB, DGT), SPE |
| Separation: HPLC, IC, CE, GC | |
|
Mass Spectrometery: HRSF ICP-MS, (nano)ESI/MS,
MALDI high resolution MS, MS/MS, MSn |
|
| Spectroscopy: ICP OES, UVvis, Fluorescence, Chemiluminescence | |
| Determination of liposome-water partition coefficients | |
| mathematical modeling | Equilibrium Speciation Calculations |
| Bioconcentration models | |
| Quantitative structure activity relationships (QSARs) | |
| Toxikokinetic-toxicodynamic models | |
| Parameter estimation methods (classical least squares, MCMC) | |
| Dynamic simulation of effects and associated uncertainty | |
| Models for toxicity of mixtures | |
| proteomics tools | OMSSA, X!Tandem |
| molecular | conventional and real-time PCR |
| bioanalyzer | |
| Silencing techniques (morpholinos) | |
| In-situ hybridization | |
| nano-analytical | DLS |
| electrophoretic mobility | |
| TEM |

