Contaminant biotransport by Pacific salmon to Lake Michigan tributaries

The Great Lakes are ideal systems for evaluating the synergistic components of environmental change, such as exotic species introductions and legacy pollutants. Introduced Pacific Salmon (Oncorhynchus spp.) represent an intersection of these drivers because they are non-native species of economic importance that bioaccumulate contaminants during the open water phase of their life cycle. Furthermore, Pacific salmon can deliver a significant pulse of contaminated tissue to tributaries during spawning and subsequent death. Thus, salmon represent a key pathway by which contaminants accumulated in Lake Michigan are transported inland to tributaries that otherwise lack point source pollution. Our research has revealed that salmon exhibit basin-specific persistent organic pollutant (POP) and mercury (Hg) concentrations reflecting pollutant inputs from both current and historic sources. Overall, Lake Michigan salmon were more contaminated with POPs and Hg than conspecifics from Lakes Huron or Superior. Consequently, Lake Michigan salmon pose a higher risk and magnitude of contaminant biotransport and transfer. Resident stream fish (e.g., brook trout) sampled from salmon spawning reaches had higher pollutant concentrations than fish sampled from upstream reaches lacking salmon, but the extent of fish contamination varied among lake basins and streams. In general, Lake Michigan tributaries were the most impacted, suggesting a direct relationship between the extent of salmon-derived contaminant inputs and resident fish contaminant levels. Within and among lake basins, contaminant biotransport by salmon is context dependent and likely reflects a suite of ecological characteristics such as species identity and trophic position, dynamics of the salmon run, watershed land-use, and instream geomorphology such as sediment size. We suggest that future management of salmon-mediated contaminant biotransport to stream communities in the Great Lakes basin should consider biological, chemical, and physical factors that constitute the environmental context

Contaminant biotransport by Pacific Salmon in Lake Michigan: analysis of salmon and stream-resident fish in Great Lakes tributaries

Pacific salmon (Oncorhynchus spp.) can deliver a significant pulse of biomass, including its bioaccumulated contaminants, to tributaries during spawning runs. Thus, salmon transport contaminants accumulated in the Great Lakes (e.g., persistent organic pollutants [POPs], total mercury [THg]) to tributaries that otherwise lack point source pollution. We used a combination of observational surveys, experimental manipulations, and modeling, to (1) assess the extent of salmon-mediated biotransport across the upper Great Lakes; (2) determine pathways by which stream fish become contaminated by salmon; and (3) forecast areas at significant risk from salmon biotransport. Resident stream fish (e.g., brook trout Salvelinus fontinalis) in salmon spawning reaches had higher POP concentrations than fish in upstream reaches lacking salmon, but the extent of contamination varied among lake basins and streams. In contrast, THg concentrations in the same fish did not differ between reaches with and without salmon spawners but exhibited considerable among-site variability. In general, resident fish in Lake Michigan tributaries were the most contaminated by POPs, suggesting a direct relationship between salmon-derived contaminant inputs and resident fish contaminant levels. Experimental exposure to salmon carcasses and eggs for 50 days increased brook trout POP concentrations by 50 times. Eggs are elevated in POPs but depleted in THg compared to whole salmon, suggesting that resident fish contaminant levels reflect direct consumption of eggs rather than indirect food web pathways. Our model suggests that salmon-mediated bioaccumulation is primarily influenced by the size and duration of salmon runs, and secondarily by factors including individual consumption rates, temperature regime, and background pollutant levels. Overall, our research provides increased understanding on the physical, chemical, and biological controls of salmon contaminant biotransport in the Great Lakes region. This research will help inform management decisions in this region with respect to legacy pollution, dam removal, stream connectivity, fish stocking, and non-native species in stream ecosystems

Oil and PCB interactions on the uptake and excretion in midges

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/47989/1/128_2005_Article_BF01625535.pd

Evaluation of multiple laboratory performance and variability in analysis of recreational freshwaters by a rapid Escherichia coli qPCR method (Draft Method C)

There is interest in the application of rapid quantitative polymerase chain reaction (qPCR) methods for recreational freshwater quality monitoring of the fecal indicator bacteria Escherichia coli (E. coli). In this study we determined the performance of 21 laboratories in meeting proposed, standardized data quality acceptance (QA) criteria and the variability of target gene copy estimates from these laboratories in analyses of 18 shared surface water samples by a draft qPCR method developed by the U.S. Environmental Protection Agency (EPA) for E. coli. The participating laboratories ranged from academic and government laboratories with more extensive qPCR experience to “new” water quality and public health laboratories with relatively little previous experience in most cases. Failures to meet QA criteria for the method were observed in 24% of the total 376 test sample analyses. Of these failures, 39% came from two of the “new” laboratories. Likely factors contributing to QA failures included deviations in recommended procedures for the storage and preparation of reference and control materials. A master standard curve calibration model was also found to give lower overall variability in log10 target gene copy estimates than the delta-delta Ct (ΔΔCt) calibration model used in previous EPA qPCR methods. However, differences between the mean estimates from the two models were not significant and variability between laboratories was the greatest contributor to overall method variability in either case. Study findings demonstrate the technical feasibility of multiple laboratories implementing this or other qPCR water quality monitoring methods with similar data quality acceptance criteria but suggest that additional practice and/or assistance may be valuable, even for some more generally experienced qPCR laboratories. Special attention should be placed on providing and following explicit guidance on the preparation, storage and handling of reference and control materials

Standardized data quality acceptance criteria for a rapid Escherichia coli qPCR method (Draft Method C) for water quality monitoring at recreational beaches

There is growing interest in the application of rapid quantitative polymerase chain reaction (qPCR) and other PCR-based methods for recreational water quality monitoring and management programs. This interest has strengthened given the publication of U.S. Environmental Protection Agency (EPA)-validated qPCR methods for enterococci fecal indicator bacteria (FIB) and has extended to similar methods for Escherichia coli (E. coli) FIB. Implementation of qPCR-based methods in monitoring programs can be facilitated by confidence in the quality of the data produced by these methods. Data quality can be determined through the establishment of a series of specifications that should reflect good laboratory practice. Ideally, these specifications will also account for the typical variability of data coming from multiple users of the method. This study developed proposed standardized data quality acceptance criteria that were established for important calibration model parameters and/or controls from a new qPCR method for E. coli (EPA Draft Method C) based upon data that was generated by 21 laboratories. Each laboratory followed a standardized protocol utilizing the same prescribed reagents and reference and control materials. After removal of outliers, statistical modeling based on a hierarchical Bayesian method was used to establish metrics for assay standard curve slope, intercept and lower limit of quantification that included between-laboratory, replicate testing within laboratory, and random error variability. A nested analysis of variance (ANOVA) was used to establish metrics for calibrator/positive control, negative control, and replicate sample analysis data. These data acceptance criteria should help those who may evaluate the technical quality of future findings from the method, as well as those who might use the method in the future. Furthermore, these benchmarks and the approaches described for determining them may be helpful to method users seeking to establish comparable laboratory-specific criteria if changes in the reference and/or control materials must be made