Bioavailability of nanoscale metal oxides TiO(2), CeO(2), and ZnO to fish.

Nanoparticles (NPs) are reported to be a potential environmental health hazard. For organisms living in the aquatic environment, there is uncertainty on exposure because of a lack of understanding and data regarding the fate, behavior, and bioavailability of the nanomaterials in the water column. This paper reports on a series of integrative biological and physicochemical studies on the uptake of unmodified commercial nanoscale metal oxides, zinc oxide (ZnO), cerium dioxide (CeO(2)), and titanium dioxide (TiO(2)), from the water and diet to determine their potential ecotoxicological impacts on fish as a function of concentration. Particle characterizations were performed and tissue concentrations were measured by a wide range of analytical methods. Definitive uptake from the water column and localization of TiO(2) NPs in gills was demonstrated for the first time by use of coherent anti-Stokes Raman scattering (CARS) microscopy. Significant uptake of nanomaterials was found only for cerium in the liver of zebrafish exposed via the water and ionic titanium in the gut of trout exposed via the diet. For the aqueous exposures undertaken, formation of large NP aggregates (up to 3 mum) occurred and it is likely that this resulted in limited bioavailability of the unmodified metal oxide NPs in fish.

Spatial inhomogeneity of metals in particulate matter on ambient air filters determined by LA-ICP-MS and comparison with acid digestion ICP-MS.

Laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) has been used to examine the spatial distribution of metals in particulate matter on ambient air filters. The implications of the inhomogeneous distribution observed for the sub-sampling of such filters for multiple analyses have been discussed. It has been shown that large biases in measured values may occur unless the position and size of the sub-sample are chosen judiciously. Additionally, LA-ICP-MS has been compared against acid digestion ICP-MS as an alternative method for the determination of metals in particulate matter. It has been shown that the majority of variation in the LA-ICP-MS sensitivity accrues from small differences in the positioning of samples.