Assessment of radium-226 bioavailability and bioaccumulation downstream of decommissioned uranium operations, using the caged oligochaete (Lumbriculus variegatus).

The present study investigated the integrated effects of several geochemical processes that control radium-226 ((226) Ra) mobility in the aquatic environment and bioaccumulation in in situ caged benthic invertebrates. Radium-226 bioaccumulation from sediment and water was evaluated using caged oligochaetes (Lumbriculus variegatus) deployed for 10 d in 6 areas downstream of decommissioned uranium operations in Ontario and Saskatchewan, Canada. Measured (226) Ra radioactivity levels in the retrieved oligochaetes did not relate directly to water and sediment exposure levels.

Exposure histories derived from selenium in otoliths of three cold-water fish species captured downstream from coal mining activity.

Establishing exposure to contaminants within a given environment is often difficult for fish species with large home ranges. Chemical analyses of muscle or visceral tissue are useful indicators of recent exposure, but depuration, metabolic transformation, and tissue redistributions can alter temporal resolution. Otoliths are metabolically stable and thus provide complete chemical records within their calcified tissues that, when coupled to the annular structure, can provide temporal resolution for exposure to trace metals.

Food chain transfer of selenium in lentic and lotic habitats of a western Canadian watershed.

Selenium (Se) is an essential micronutrient, exhibiting a narrow margin between nutritionally optimal and potentially toxic concentrations. Egg-laying vertebrates at the top of aquatic food chains are most at risk in environments with elevated aqueous Se concentrations. The Elk River watershed in British Columbia, Canada receives effluents containing Se from five coal mine operations.

Results of a cytomegalovirus (CMV)-specific CD8+/interferon- gamma+ cytokine flow cytometry assay correlate with clinical evidence of protective immunity in patients with AIDS with CMV retinitis.

To evaluate the potential clinical utility of a cytomegalovirus (CMV)-specific CD8+/interferon (IFN)- gamma+ cytokine flow cytometry (CFC) assay for patients with CMV retinitis (CMVR), stored peripheral blood mononuclear cell specimens were obtained from patients with active CMVR (i.e., having clinical evidence of absent CMV-protective immunity), as well as from highly active antiretroviral therapy-treated patients with CMVR who were able to discontinue anti-CMV therapy without subsequent progression of retinitis (i.

Performance of plate-based cytokine flow cytometry with automated data analysis.

Background: Cytokine flow cytometry (CFC) provides a multiparameter alternative to ELISPOT assays for rapid quantitation of antigen-specific T cells. To increase the throughput of CFC assays, we have optimized methods for stimulating, staining, and acquiring whole blood or PBMC samples in 96-well or 24-well plates.

Results: We have developed a protocol for whole blood stimulation and processing in deep-well 24- or 96-well plates, and fresh or cryopreserved peripheral blood mononuclear cell (PBMC) stimulation and processing in conventional 96-well round-bottom plates.