This manuscript describes the development and characterization of a high-density microarray calibration standard, manufactured in-house and designed to overcome the limitations in precision, accuracy, and throughput of current calibration approaches for the quantification of elemental concentrations on the cellular level using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICPMS). As a case study, the accumulation of Cu in the model organism Scrippsiella trochoidea resulting from transition metal exposure (ranging from 0.5 to 100 μg/L) was evaluated. After the Cu exposure, cells of this photosynthetic dinoflagellate were treated with a critical point drying protocol, transferred to a carbon stub, and sputter-coated with a Au layer for scanning electron microscopy (SEM) analysis. In subsequent LA-ICPMS analysis, approximately 100 cells of each population were individually ablated. This approach permitted the evaluation of the mean concentration of Cu in the cell population across different exposure levels and also allowed the examination of the cellular distribution of Cu within the populations. In a cross-validation exercise, subcellular LA-ICPMS imaging was demonstrated to corroborate synchrotron radiation confocal X-ray fluorescence (SR-XRF) microimaging of single cells investigated under in vivo conditions.

Predicting copper (Cu) toxicity in marine and estuarine environments is challenging because of the influence of anions on Cu speciation, competition between Cu(2+) and other cations at the biotic ligand and the effect of salinity on the physiology of the organism. In the present study the combined effect of salinity and dissolved organic carbon (DOC) on Cu toxicity to larvae of Mytilus galloprovincialis was assessed. Two statistical models were developed and used to elucidate the relationship between Cu toxicity, salinity, and DOC. All models based on dissolved Cu indicate a decrease in Cu toxicity with increasing DOC concentrations, which can partly be explained by complexation of Cu(2+) ions with DOC. These models also indicate an increase in Cu toxicity (modeled with dissolved Cu or Cu(2+) activity) with increasing salinity, suggesting a salinity-induced alteration in the physiology of the mussel larvae. When based on Cu body burdens, neither of the models indicates an effect of salinity or DOC. This shows that the Cu body burden is a more constant predictor of Cu toxicity, regardless of the water chemistry influencing Cu speciation or competition and possible physiological alterations or changes in Cu speciation or competition.

The development of a novel and straightforward procedure for the preparation of matrix-matched calibration standards for the quantitative imaging of iron (Fe) in biological tissues by laser ablation (LA)-ICP-MS with on-tissue internal standard addition is described. This simple approach enabled on-tissue addition of Rh as internal standard to samples (with heterogeneous Fe distribution) and calibrants (with homogeneous Fe distribution). This is achieved without altering the original Fe distribution of the sample. Calibration standards were prepared by full horizontal immersion of slides with mounted homogenised sheep brain tissue section into the corresponding solution containing 0.5, 0.75, 1, 5, 10 and 20 mg kg(-1) Fe (each also containing 250 mu g kg(-1) Rh as IS) in pure methanol for 30 minutes (6 immersions, each for 5 minutes). Subsequent air-drying (bench drying at room temperature) for approximately 5 minutes was undertaken in between consecutive immersions, to prevent long-term exposure of the tissue to lipid degradation. Tissue-matched standards were characterised in-house for Fe composition, homogeneity and stability (at storage temperatures of -80 degrees C, -20 degrees C, 4 degrees C and 25 degrees C for up to 2 months) in order to investigate their suitability as calibrants for quantitative LA-ICP-MS. The homogeneity data suggested that the materials are homogeneous in terms of Fe and Rh distribution with RSDs (n = 30) of 8.3% and 4.7%, respectively. The Fe measurement precision was improved by approximately a factor of 2 when normalising Fe-56 intensities to Rh-103 intensities; the RSD (n = 30) for Fe-56/Rh-103 was 3.6%. The produced calibration standards were found to be stable when stored at room temperature for approximately 50 days, suggesting that they can be reused for multiple batches. Using LA coupled to double-focusing sector field ICP-MS in medium resolution mode (m/Delta m = 4000), linear calibration over a range of 107 to 1519 mg kg(-1) Fe (R-2 = 0.99) was achieved with a limit of detection of 1.84 mg kg(-1) Fe. Assessment of the accuracy of the method for the quantitative imaging of Fe in tissues was undertaken by comparison of the LA-ICP-MS data with that obtained by micro-XRF; the average Fe concentrations in selected tissue regions obtained by using XRF fell within the window defined by the LA-ICP-MS values and their associated standard deviations