Archive for Measurement

Cleaning up the dangerous contaminants — dry-cleaning fluids, solvents and petroleum hydrocarbons — found in underground water presents one of the most urgent challenges facing environmental science. A report issued January 30 by the U.S. Environmental Protection Agency (EPA) sheds light on a new way to monitor and improve the success of clean-up efforts using a technique developed at the University of Toronto.

“The most common method to clean-up groundwater is biodegradation — using microbes to consume the contaminants and break them down into more benign end products that are not harmful to the environment,” says U of T geochemist Barbara Sherwood Lollar, the scientist who initiated the concept and goals for the EPA report and is one of its five international authors.

The report outlines how this can be done using a novel technique called Compound Specific Isotope Analysis, developed in U of T’s Stable Isotope Laboratory. The elements of carbon that form the basis for the hydrocarbon contaminants actually come in two types called isotopes, explains Sherwood Lollar. “When microbes degrade contaminants, they prefer the lighter isotope carbon 12 over the heavier isotope carbon 13. The resulting change in the ratio of these isotopes in the contaminant itself is a dramatic and definitive indicator that the biodegradation is successfully taking place.”

Beginning in the 1990s, U of T’s Stable Isotope Laboratory has been an international pioneer in discovering how different carbon isotopes can be used to identify whether or not biodegradation is taking place. “Today, dozens of students in Canada have been trained in this method, drawn in by the fascinating combination of fundamental research that has important applications such as the clean-up of drinking water,” says Sherwood Lollar. Over the past decade, as the new technique has become more widespread, centres for research and education —- and even private companies — have blossomed worldwide.

“Much of the research on new methods of analyzing groundwater contamination has been published in scientific and professional journals but this report — written specifically for the practitioners in accessible language with clear procedural information and decision-making strategies — is a milestone,” says Sherwood Lollar.

“It is particularly gratifying to be able to take a technique out of the lab and to put it into the hands of the people working on this issue every day around the world,” she says.

The report can be found on the EPA website. It was funded by the International Atomic Energy Agency in Vienna, Austria, the EPA and the Natural Sciences and Engineering Research Council of Canada.

University of Toronto. “New Way To Monitor And Improve Clean-up Of Contaminated Groundwater.” ScienceDaily 1 February 2009. 3 February 2009 <http://www.sciencedaily.com­ /releases/2009/01/090130093405.htm>

Recent advances in laboratory methodologies made by USGS Toxics Hydrology Program scientists are providing improved capabilities for detecting large numbers of new and potentially harmful contaminants in our water resources at very low levels. There are many thousands of chemicals (including pesticides, human and veterinary medicines, personal care products, and other organic compounds) that enter our water resources by accidental spills, runoff from land applications, conventional waste-management practices and other mechanisms. Many of these compounds are known or suspected to have ecological or human health effects at very low concentrations. Development of capabilities to detect low concentrations in aquatic environments is important for several reasons: 1) many compounds are used in relatively small quantities and therefore concentrations in the environment are low; 2) many degrade or are transformed to other compounds, thereby reducing environmental concentrations; 3) compounds can partition among various environmental media such as soil or sediment particles; 4) the complex mix of natural and manufactured chemicals found in environmental waters can mask the detection of contaminants of concern, and 5) some classes of contaminants may have ecological health effects at low levels.

These new methods provide crucial tools that are enabling scientists to determine:

  • The levels and mixtures of compounds that occur in the environment,
  • The mechanisms by which these compounds enter the environment (source pathways), and
  • The processes that affect the transport, persistence, and fate of the compounds in the environment.

Toxics Program scientists have developed eight new methods during the past year that provide improved measurement capability for many tens of contaminants, including methyl mercury, surfactants, pesticides, and pharmaceuticals. Analytical method development is a continuing research topic for Toxics Program scientists.

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Recent Publications

  • Babiarz, C.L., Hurley, J.P., Krabbenhoft, D.P., Gilmour, C., and Branfireun, B.A., 2003, Application of ultrafiltration and stable isotopic amendments to field studies of mercury partitioning to filterable carbon in lake water and overland runoff :The Science of the Total Environment, v. 304, p. 295-303.
  • DeWild, J.F., Olson, M.L., and Olund , S.D. , 2002, Determination of methyl mercury by aqueous phase ethylation, followed by gas chromatographic separation with cold vapor atomic fluorescence detection : U.S. Geological Survey Open-File Report 01-445, 14 p.
  • Ferrer, I., Schroeder, H.F., and Furlong, E.T., 2003, LC/MS analyses of cationic surfactants–Methods and applications, in: Knepper, T.P., Barcelo, D., and de Voogt, P., eds., Analysis and fate of surfactants in the aquatic environment: Amsterdam, Elsevier, Comprehensive Analytical Chemistry Series, v. XL, p. 353-383.
  • Ferrer, Imma, Furlong, E.T., and Thurman, E.M., 2003, Identification of Homologue Unknowns in Wastewater by Ion Trap MS: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, p. 376-393.
  • Ferrer, Imma and Thurman, E.M., 2003, Analysis of Emerging Contaminants: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, Ferrer and Thurman, eds, Chapter 1, p. 2-13.
  • Furlong, E.T., Ferrer, I. , Gates, P.M., Cahill, J.D., and Thurman, E.M., 2003, Identification of Labile Polar Organic Contaminants by Atmospheric-Pressure Ionization Tandem Mass Spectrometry, in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850 p. 175-187.
  • Lee, E.A., Strahan, A.P., and Thurman, E.M., 2002, Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group – Determination of glyphosate, aminomethylphosphonic acid, and glufosinate in water using online solid-phase extraction and high-performance liquid chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 01-454, 13 p.
  • Lee, E.A., Zimmerman, L.R., Bhullar, B.S., and Thurman, E.M., 2002, Linker-assisted immunoassay and liquid chromatography/mass spectrometry for the analysis of glyphosate : Analytical Chemistry, v. 74, no. 19, p. 4937-4943.
  • Lee, E.A., Kish , J.L., Zimmerman, L.R., and Thurman, E.M., 2001,Methods of analysis by the U.S. Geological Survey Organic Geochemistry Research Group–Update and additions to the determination of chloroacetanilide herbicide degradation compounds in water using high-performance liquid chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 01-10, 17 p.
  • Leenheer, J.A., Furlong, E.T., Ferrer, I. , and Rostad C.E., 2003, Charge Characteristics and Fragmentation of Polycarboxylic Acids by Electrospray Ionization/Multistage Tandem Mass Spectrometry (ESI/MS/MS), in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850; p. 312-324.
  • Lindsey , M.E. , Meyer, M.T., and Thurman, E.M., 2001, Analysis of trace levels of sulfonamide and tetracycline antimicrobials in groundwater and surface water using solid-phase extraction and liquid chromatography/mass spectrometry : Analytical Chemistry, v. 73, no. 19, p. 4640-4646.
  • Thurman, E.M., and Ferrer, Imma, 2003, Comparison of Quadrupole-Time-of-Flight, Triple Quadrupole, and Ion-Trap Mass Spectrometry/Mass Spectrometry for the Analysis of Emerging Contaminants, ACS Symposium, volume 850.
  • Thurman, E.M. and Ferrer, Imma, 2003, Comparison of Quadrupole Time-of-Flight, Triple Quadrupole, and Ion-Trap Mass Spectrometry/Mass Spectrometry for the Analysis of Emerging Contaminants: in Liquid Chromatography/Mass Spectrometry, MS/MS and Time-of-Flight MS: Analysis of Emerging Contaminants. American Chemical Society Symposium 850, p. 14-31.
  • Thurman, E.M., Ferrer, I. , and Furlong E.T., 2003, TOF/MS and Quadrupole Ion Trap MS/MS for the Discovery of Herbicide Degradates in Groundwater, in: LC/MS/MS and TOF/MS: Analysis of Emerging Contaminants (eds. I Ferrer and E.M. Thurman) American Chemical Society Symposium Series Number 850 p. 128-144.
  • Zimmerman, L.R., Schneider, R.J., and Thurman, E.M., 2002, Analysis and detection of the herbicides dimethanamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water: Journal of Agricultural and Food Chemistry, v. 50, no. 5, p. 1045-1052.
  • Zimmerman, L.R., Ziegler, A.C., and Thurman, E.M., 2002, Method of analysis and quality-assurance practices by U.S. Geological Survey Organic Geochemistry Research Group–Determination of geosmin and methylisoborneol in water using solid-phase microextraction and gas chromatography/mass spectrometry: U.S. Geological Survey Open-File Report 02-337, 12 p.
  • Zimmerman, L.R., Schneider, R.J., and Thurman, E.M., 2002, Analysis and detection of the herbicides dimethanamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water : Journal of Agricultural and Food Chemistry, v. 50, no. 5, p. 1045-1052.

[Source: http://toxics.usgs.gov]