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==PFAS Sources==
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==Assessing Vapor Intrusion (VI) Impacts in Neighborhoods with Groundwater Contaminated by Chlorinated Volatile Organic Chemicals (CVOCs)==  
[[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)]] have been used in coatings for textiles, paper products, and cookware; in some firefighting foams; and have a range of applications in the aerospace, photographic imaging, semiconductor, automotive, construction, electronics, and aviation industries<ref name="ITRC2020">Interstate Technology and Regulatory Council (ITRC), 2020. Technical/Regulatory Guidance: Per- and Polyfluoroalkyl Substances (PFAS), PFAS-1. ITRC, PFAS Team, Washington DC. Website: https://pfas-1.itrcweb.org/ &nbsp;&nbsp; [https://pfas-1.itrcweb.org/wp-content/uploads/2020/04/ITRC_PFAS_TechReg_April2020.pdf  Free Download from ITRC].&nbsp;&nbsp; [[Media: ITRC_PFAS-1.pdf | Report.pdf]]</ref><ref name="KEMI2015">Swedish Chemicals Agency (KEMI), 2015. Occurrence and use of highly fluorinated substances and alternatives, Report 7/15. ISSN 0284-1185. Article number 361 164.  [[Media: KEMI2015.pdf | Report.pdf]]</ref><ref name="USEPA2021">US Environmental Protection Agency (USEPA), 2021. Basic Information on PFAS.  [https://www.epa.gov/pfas/basic-information-pfas#tab-1 Website]</ref>. Although PFAS and PFAS-containing products have been manufactured since the 1950s, PFAS were not widely documented in environmental samples until the early 2000s. Understanding PFAS manufacturing history, past and current uses, and waste management over the last six to seven decades is necessary for the identification of potential environmental sources of PFAS, possible release mechanisms, and associated pathway-receptor relationships.
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The VI Diagnosis Toolkit<ref name="JohnsonEtAl2020">Johnson, P.C., Guo, Y., Dahlen, P., 2020.  The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Mitigating Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent PlumesESTCP Project ER-201501, Final Report. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [[Media: ER-201501.pdf | Final Report.pdf]]</ref> is a set of tools that can be used individually or in combination to assess vapor intrusion (VI) impacts at one or more buildings overlying regional-scale dissolved chlorinated solvent-impacted groundwater plumes. The strategic use of these tools can lead to confident and efficient neighborhood-scale VI pathway assessments.
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<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
 
<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
  
 
'''Related Article(s):'''
 
'''Related Article(s):'''
  
* [[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)]]
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*[[Vapor Intrusion (VI)]]
* [[PFAS Transport and Fate]]
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*[[Vapor Intrusion – Sewers and Utility Tunnels as Preferential Pathways]]
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'''Contributor(s):'''
  
'''Contributor(s):''' [[Dr. Sheau-Yun (Dora) Chiang]] and [[Dr. Alexandra Salter-Blanc]]
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*Paul C. Johnson, Ph.D.
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*Paul Dahlen, Ph.D.
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*Yuanming Guo, Ph.D.
  
 
'''Key Resource(s):'''
 
'''Key Resource(s):'''
  
*[https://pfas-1.itrcweb.org/wp-content/uploads/2020/04/ITRC_PFAS_TechReg_April2020.pdf  Per- and Polyfluoroalkyl Substances (PFAS), PFAS-1. ITRC 2020.]<ref name="ITRC2020"/>
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*The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes, ESTCP Project ER-201501, Final Report<ref name="JohnsonEtAl2020"/>
 
 
==Introduction==
 
[[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)]] are a complex family of more than 3,000 manmade fluorinated organic chemicals<ref name="Wang2017">Wang, Z., DeWitt, J.C., Higgins, C.P., and Cousins, I.T., 2017. A Never-Ending Story of Per- and Poly-Fluoroalkyl Substances (PFASs)? Environmental Science and Technology, 51(5), pp. 2508-2518.  [https://doi.org/10.1021/acs.est.6b04806 DOI: 10.1021/acs.est.6b04806]&nbsp;&nbsp; [[Media: Wang2017.pdf | Open access article.]]</ref> although not all of these are currently in use or production. PFAS are produced using several different processes. Fluorosurfactants, which include perfluoroalkyl acids (PFAAs) (see [[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS) | PFAS]] article for nomenclature) and side-chain fluorinated polymers, have been manufactured using two major processes: [[Wikipedia: Electrochemical fluorination | electrochemical fluorination (ECF)]] and [[Wikipedia: Telomerization | telomerization]]<ref name="KEMI2015"/>. ECF was licensed by 3M in the 1940s<ref name="Banks1994">Banks, R.E., Smart, B.E. and Tatlow, J.C. eds., 1994. Organofluorine Chemistry: Principles and Commercial Applications. Springer Science and Business Media, New York, N. Y. [https://link.springer.com/book/10.1007/978-1-4899-1202-2 DOI: 10.1007/978-1-4899-1202-2]</ref> and used by 3M until 2001. ECF produces a mixture of even and odd numbered carbon chain lengths of approximately 70% linear and 30% branched substances<ref name="Concawe2016">Concawe (Conservation of Clean Air and Water in Europe), 2016.  Environmental fate and effects of poly- and perfluoroalkyl substances (PFAS).  Report No. 8/16. Brussels, Belgium. [[Media:Concawe2016.pdf | Report.pdf]]</ref>. Telomerization was developed in the 1970s<ref name="Benskin2012a">Benskin, J.P., Ahrens, L., Muir, D.C., Scott, B.F., Spencer, C., Rosenberg, B., Tomy, G., Kylin, H., Lohmann, R. and Martin, J.W., 2012. Manufacturing Origin of Perfluorooctanoate (PFOA) in Atlantic and Canadian Arctic Seawater. Environmental Science and Technology, 46(2), pp. 677-685.  [https://doi.org/10.1021/es202958p DOI: 10.1021/es202958p]</ref>, and yields mainly even numbered, straight carbon chain isomers<ref name="Kissa2001">Kissa, E., 2001. Fluorinated Surfactants and Repellents, Second Edition. Surfactant Science Series, Vol. 97. Marcel Dekker, Inc., CRC Press, New York. 640 pages. ISBN: 9780824704728</ref><ref name="Parsons2008">Parsons, J.R., Sáez, M., Dolfing, J. and De Voogt, P., 2008. Biodegradation of Perfluorinated Compounds. Reviews of Environmental Contamination and Toxicology, 196, pp. 53-71. Springer, New York, NY.  [https://doi.org/10.1007/978-0-387-78444-1_2 DOI: 10.1007/978-0-387-78444-1_2]&nbsp;&nbsp; Free download from: [https://www.researchgate.net/profile/Jan_Dolfing/publication/23489065_Biodegradation_of_Perfluorinated_Compounds/links/0912f5087a40c9d5df000000.pdf ResearchGate]</ref>.  PFAS manufacturers have provided PFAS to secondary manufacturers for production of a vast array of industrial and consumer products.
 
 
 
During manufacturing, PFAS may be released into the atmosphere then redeposited on land where they can also affect surface water and groundwater, or PFAS may be discharged without treatment to wastewater treatment plants or landfills, and eventually be released into the environment by treatment systems that are not designed to mitigate PFAS (see also [[PFAS Transport and Fate]]). Industrial discharges of PFAS were unregulated for many years, but that has begun to change. In January 2016, New York became the first state in the nation to regulate PFOA as a hazardous substance followed by the regulation of PFOS in April 2016. Consumer and industrial uses of PFAS-containing products can also end up releasing PFAS into landfills and into municipal wastewater, where it may accumulate undetected in biosolids which are typically treated by land application.
 
 
 
==Industrial Sources==
 
PFAS are used in many industrial and consumer applications, which may have released PFAS into the environment and impacted drinking water supplies in many areas of the United States<ref name="EWG2017">Environmental Working Group (EWG) and Northeastern University Social Science Environmental Health Research Institute, 2017. Mapping A Contamination Crisis. [https://www.ewg.org/research/mapping-contamination-crisis Website]</ref>. Both in the United States (US) and abroad, primary manufacturing facilities produce PFAS and secondary manufacturing facilities use PFAS to produce goods. Environmental release mechanisms associated with these facilities include air emission and dispersion, spills, and disposal of manufacturing wastes and wastewater. Potential impacts to air, soil, sediment, surface water, stormwater, and groundwater are present not only at primary release points but potentially over the surrounding area<ref name="Shin2011">Shin, H.M., Vieira, V.M., Ryan, P.B., Detwiler, R., Sanders, B., Steenland, K., and Bartell, S.M., 2011. Environmental Fate and Transport Modeling for Perfluorooctanoic Acid Emitted from the Washington Works Facility in West Virginia. Environmental Science and Technology, 45(4), pp. 1435-1442.  [https://doi.org/10.1021/es102769t DOI: 10.1021/es102769t]</ref>. Some of the potential primary and secondary sources of PFAS releases to the environment are listed here<ref name="ITRC2020"/>:
 
 
 
* '''Textiles and leather:''' Factory or consumer applied coating to repel water, oil, and stains. Applications include protective clothing and outerwear, umbrellas, tents, sails, architectural materials, carpets, and upholstery<ref name="Rao1994">Rao, N.S., and Baker, B.E., 1994. Textile Finishes and Fluorosurfactants. In: Organofluorine Chemistry, Banks, R.E., Smart, B.E., and Tatlow, J.C., Eds. Springer, New York.  [https://doi.org/10.1007/978-1-4899-1202-2_15 DOI: 10.1007/978-1-4899-1202-2_15]</ref><ref name="Hekster2003">Hekster, F.M., Laane, R.W. and De Voogt, P., 2003. Environmental and Toxicity Effects of Perfluoroalkylated Substances. Reviews of Environmental Contamination and Toxicology, 179, pp. 99-121. Springer, New York, NY. [https://doi.org/10.1007/0-387-21731-2_4 DOI: 10.1007/0-387-21731-2_4]</ref><ref name="Brooke2004">Brooke, D., Footitt, A., and Nwaogu, T.A., 2004. Environmental Risk Evaluation Report: Perfluorooctanesulphonate (PFOS).  Environment Agency (UK), Science Group.  Free download from: [http://chm.pops.int/Portals/0/docs/from_old_website/documents/meetings/poprc/submissions/Comments_2006/sia/pfos.uk.risk.eval.report.2004.pdf The Stockholm Convention]&nbsp;&nbsp; [[Media:Brooke2004.pdf | Report.pdf]]</ref><ref name="Poulsen2005">Poulsen, P.B., Jensen, A.A., and Wallström, E., 2005. More environmentally friendly alternatives to PFOS-compounds and PFOA. Danish Environmental Protection Agency, Environmental Project 1013.  [[Media: Poulsen2005.pdf | Report.pdf]]</ref><ref name="Prevedouros2006">Prevedouros, K., Cousins, I.T., Buck, R.C. and Korzeniowski, S.H., 2006. Sources, Fate and Transport of Perfluorocarboxylates. Environmental Science and Technology, 40(1), pp. 32-44.  [https://doi.org/10.1021/es0512475 DOI: 10.1021/es0512475]&nbsp;&nbsp; Free download from: [https://www.academia.edu/download/39945519/Sources_Fate_and_Transport_of_Perfluoroc20151112-1647-19vcvbf.pdf Academia.edu]</ref><ref name="Walters2006">Walters, A., and Santillo, D., 2006. Technical Note 06/2006: Uses of Perfluorinated Substances. Greenpeace Research Laboratories. [http://www.greenpeace.to/publications/uses-of-perfluorinated-chemicals.pdf Website]&nbsp;&nbsp; [[Media: Walters2006.pdf | Report.pdf]]</ref><ref name="Trudel2008">Trudel, D., Horowitz, L., Wormuth, M., Scheringer, M., Cousins, I.T. and Hungerbühler, K., 2008. Estimating Consumer Exposure to PFOS and PFOA. Risk Analysis: An International Journal, 28(2), pp. 251-269.  [https://doi.org/10.1111/j.1539-6924.2008.01017.x DOI: 10.1111/j.1539-6924.2008.01017.x]</ref><ref name="Guo2009">Guo, Z., Liu, X., Krebs, K.A. and Roache, N.F., 2009. Perfluorocarboxylic Acid Content in 116 Articles of Commerce, EPA/600/R-09/033. National Risk Management Research Laboratory, US Environmental Protection Agency, Washington, DC.  Available from: [https://cfpub.epa.gov/si/si_public_record_report.cfm?Lab=NRMRL&dirEntryId=206124 US EPA.]&nbsp;&nbsp; [[Media: Guo2009.pdf | Report.pdf]]</ref><ref name="USEPA2009">US Environmental Protection Agency (USEPA), 2009. Long-Chain Perfluorinated Chemicals (PFCs), Action Plan.  [https://www.epa.gov/sites/production/files/2016-01/documents/pfcs_action_plan1230_09.pdf Website]&nbsp;&nbsp; [[Media: USEPA2009.pdf | Report.pdf]]</ref><ref name="Ahrens2011a">Ahrens, L., 2011. Polyfluoroalkyl compounds in the aquatic environment: a review of their occurrence and fate. Journal of Environmental Monitoring, 13(1), pp.20-31.
 
[http://dx.doi.org/10.1039/C0EM00373E DOI: 10.1039/C0EM00373E]. Free download available from: [https://www.researchgate.net/profile/Lutz_Ahrens/publication/47622154_Polyfluoroalkyl_compounds_in_the_aquatic_environment_A_review_of_their_occurrence_and_fate/links/00b7d53762cfedaf12000000/Polyfluoroalkyl-compounds-in-the-aquatic-environment-A-review-of-their-occurrence-and-fate.pdf ResearchGate]</ref><ref name="Buck2011">Buck, R.C., Franklin, J., Berger, U., Conder, J.M., Cousins, I.T., De Voogt, P., Jensen, A.A., Kannan, K., Mabury, S.A. and van Leeuwen, S.P., 2011. Perfluoroalkyl and Polyfluoroalkyl Substances in the Environment: Terminology, Classification, and Origins. Integrated Environmental Assessment and Management, 7(4), pp. 513-541. [https://doi.org/10.1002/ieam.258 DOI: 10.1002/ieam.258]&nbsp;&nbsp; [[Media:Buck2011.pdf | Open access article.]]</ref><ref name="UNEP2011">United Nations Environmental Programme (UNEP), 2011. Report of the persistent organic pollutants review committee on the work of its sixth meeting, Addendum, Guidance on alternatives to perfluorooctane sulfonic acid and its derivatives, UNEP/POPS/POPRC.6/13/Add.3/Rev.1 [http://www.pops.int/TheConvention/POPsReviewCommittee/Meetings/POPRC6/POPRC6Documents/tabid/783/ctl/Download/mid/3507/Default.aspx?id=125 Website]&nbsp;&nbsp; [[Media: UNEP2011.pdf | Report.pdf]]</ref><ref name="Herzke2012">Herzke, D., Olsson, E. and Posner, S., 2012. Perfluoroalkyl and polyfluoroalkyl substances (PFASs) in consumer products in Norway – A pilot study. Chemosphere, 88(8), pp. 980-987.  [https://doi.org/10.1016/j.chemosphere.2012.03.035 DOI: 10.1016/j.chemosphere.2012.03.035]</ref><ref name="Patagonia2016">Patagonia, Inc., 2016. An Update on Our DWR Problem.  [https://www.patagonia.com/stories/our-dwr-problem-updated/story-17673.html Website]&nbsp;&nbsp; [[Media: Patagonia2016.pdf | Report.pdf]]</ref><ref name="Kotthoff2015">Kotthoff, M., Müller, J., Jürling, H., Schlummer, M., and Fiedler, D., 2015. Perfluoroalkyl and polyfluoroalkyl substances in consumer products. Environmental Science and Pollution Research, 22(19), pp. 14546-14559.  [https://doi.org/10.1007/s11356-015-4202-7 DOI: 10.1007/s11356-015-4202-7]&nbsp;&nbsp; [[Media: Kotthoff2015.pdf | Open access article.]]</ref><ref name="ATSDR2018">Agency for Toxic Substances and Disease Registry (ATSDR), 2018. Toxicological Profile for Perfluoroalkyls, Draft for Public Comment. US Department of Health and Human Services. Free download from: [http://www.atsdr.cdc.gov/toxprofiles/tp200.pdf ATSDR]&nbsp;&nbsp; [[Media: ATSDR2018.pdf | Report.pdf]]</ref>.
 
 
 
* '''Paper products:''' Surface coatings to repel grease and moisture. Uses include non-food paper packaging (for example, cardboard, carbonless forms, masking papers) and food-contact materials (for example, pizza boxes, fast food wrappers, microwave popcorn bags, baking papers, pet food bags)<ref name="Rao1994"/><ref name="Kissa2001"/><ref name="Hekster2003"/><ref name="Poulsen2005"/><ref name="Trudel2008"/><ref name="Buck2011"/><ref name="UNEP2011"/><ref name="Kotthoff2015"/><ref name="Schaider2017">Schaider, L.A., Balan, S.A., Blum, A., Andrews, D.Q., Strynar, M.J., Dickinson, M.E., Lunderberg, D.M., Lang, J.R., and Peaslee, G.F., 2017. Fluorinated Compounds in US Fast Food Packaging. Environmental Science and Technology Letters, 4(3), pp. 105-111.  [https://doi.org/10.1021/acs.estlett.6b00435 DOI: 10.1021/acs.estlett.6b00435]&nbsp;&nbsp; [[Media: Schaider2017.pdf | Open access article.]]</ref>
 
  
* '''Metal Plating & Etching:''' Corrosion prevention, mechanical wear reduction, aesthetic enhancement, surfactant, wetting agent/fume suppressant for chrome, copper, nickel and tin electroplating, and post-plating cleaner<ref name="USEPA1996">US Environmental Protection Agency (USEPA), 1996. Emission Factor Documentation for AP-42, Section 12.20. Office of Air Quality Planning and Standards, Emission Factor and Inventory Group, Research Triangle Park, NC.  [[Media: USEPA1996.pdf | Report.pdf]]</ref><ref name="Riordan1998">Riordan, B.J., Karamchandanl, R.T., Zitko, L.J., and Cushnie Jr., G.C., 1998Capsule Report: Hard Chrome Fume Suppressants and Control Technologies. Center for Environmental Research Information, National Risk Management Research Laboratory, Office of Research and Development. EPA/625/R-98/002  [https://cfpub.epa.gov/si/si_public_record_Report.cfm?Lab=NRMRL&dirEntryID=115419 Website]&nbsp;&nbsp; [[Media: Riordan1998.pdf | Report.pdf]]</ref><ref name="Kissa2001"/><ref name="Prevedouros2006"/><ref name="USEPA2009a">US Environmental Protection Agency (USEPA), 2009. PFOS Chromium Electroplater Study. US EPA – Region 5, Chicago, IL.  [[Media: USEPA2009a.pdf | Report.pdf]]</ref><ref name="UNEP2011"/><ref name="OSHA2013">Occupational Safety and Health Agency (OSHA), 2013. Fact Sheet: Controlling Hexavalent Chromium Exposures during Electroplating. United States Department of Labor.  [[Media: OSHA2013.pdf | Report.pdf]]</ref><ref name="KEMI2015"/><ref name="DEPA2015">Danish Environmental Protection Agency, 2015. Alternatives to perfluoroalkyl and polyfluoroalkyl substances (PFAS) in textiles. [[Media: DEPA2015.pdf | Report.pdf]]</ref>  
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*CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment, ESTCP Project ER-201501, Technical Report<ref name="JohnsonEtAl2021">Johnson, P.C., Guo, Y., Dahlen, P., 2021CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment. ESTCP ER-201501, Technical Report. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [[Media: ER-201501_Technical_Report.pdf | Technical_Report.pdf]]</ref>    
  
* '''Wire Manufacturing:''' Coating and insulation<ref name="Kissa2001"/><ref name="vanderPutte2010">van der Putte, I., Murin, M., van Velthoven, M., and Affourtit, F., 2010. Analysis of the risks arising from the industrial use of Perfluorooctanoic acid (PFOA) and Ammonium Perfluorooctanoate (APFO) and from their use in consumer articles. Evaluation of the risk reduction measures for potential restrictions on the manufacture, placing on the market and use of PFOA and APFO. RPS Advies, Delft, The Netherlands for European Commission Enterprise and Industry Directorate-General.  [https://ec.europa.eu/docsroom/documents/13037/attachments/1/translations/en/renditions/pdf Website]&nbsp;&nbsp; [[Media: vanderPutte2010.pdf | Report.pdf]]</ref><ref name="ASTSWMO2015">Association of State and Territorial Solid Waste Management Officials (ASTSWMO), 2015. Perfluorinated Chemicals (PFCs): Perfluorooctanoic Acid (PFOA) and Perfluorooctane Sulfonate (PFOS) Information Paper. Remediation and Reuse Focus Group, Federal Facilities Research Center, Washington, D.C. Free download from: [https://clu-in.org/download/contaminantfocus/pops/POPs-ASTSWMO-PFCs-2015.pdf US EPA]&nbsp;&nbsp; [[Media:ASTSWMO2015.pdf | Report.pdf]]</ref>  
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*VI Diagnosis Toolkit User Guide, ESTCP Project ER-201501<ref name="JohnsonEtAl2022">Johnson, P.C., Guo, Y., and Dahlen, P., 2022. VI Diagnosis Toolkit User Guide, ESTCP ER-201501, User Guide. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [[Media: ER-201501_User_Guide.pdf | User_Guide.pdf]]</ref>
  
* '''Industrial Surfactants, Resins, Molds, Plastics:''' Manufacture of plastics and fluoropolymers, rubber, and compression mold release coatings; plumbing fluxing agents; fluoroplastic coatings, composite resins, and flame retardant for polycarbonate<ref name="Kissa2001"/><ref name="Renner2001">Renner, R., 2001. Growing Concern Over Perfluorinated Chemicals. Environmental Science and Technology, 35(7), pp. 154A-160A. [https://doi.org/10.1021/es012317k DOI: 10.1021/es012317k]&nbsp;&nbsp; [[Media: Renner2001.pdf | Open access article.]]</ref><ref name="Poulsen2005"/><ref name="Fricke2005">Fricke, M. and Lahl, U., 2005. Risk Evaluation of Perfluorinated Surfactants as Contribution to the current Debate on the EU Commission’s REACH Document. Umweltwissenschaften und Schadstoff-Forschung (UWSF), 17(1), pp. 36-49. [https://doi.org/10.1007/BF03038694 DOI: 10.1007/BF03038694]</ref><ref name="Prevedouros2006"/><ref name="Skutlarek2006">Skutlarek, D., Exner, M. and Färber, H., 2006. Perfluorinated Surfactants in Surface and Drinking Waters. Environmental Science and Pollution Research International, 13(5), pp. 299-307. [https://doi.org/10.1065/espr2006.07.326 DOI: 10.1065/espr2006.07.326]&nbsp;&nbsp; Free download from: [https://www.researchgate.net/profile/Dirk_Skutlarek/publication/6729263_Perfluorinated_surfactants_in_surface_and_drinking_waters/links/0deec52049b9cba2e4000000.pdf ResearchGate]</ref><ref name="vanderPutte2010"/><ref name="Buck2011"/><ref name="Herzke2012"/><ref name="Kotthoff2015"/><ref name="Chemours2010">Chemours, 2010. The History of Teflon Fluoropolymers. [https://www.teflon.com/en/news-events/history Website]</ref>
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==Background==
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[[File:ChangFig2.png | thumb | 400px| Figure 1. Example of instrumentation used for OPTICS monitoring.]]
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[[File:ChangFig1.png | thumb | 400px| Figure 2. Schematic diagram illustrating the OPTICS methodology. High resolution in-situ data are integrated with traditional discrete sample analytical data using partial least-square regression to derive high resolution chemical contaminant concentration data series.]]
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Nationwide, the liability due to contaminated sediments is estimated in the trillions of dollars. Stakeholders are assessing and developing remedial strategies for contaminated sediment sites in major harbors and waterways throughout the U.S. The mobility of contaminants in surface water is a primary transport and risk mechanism<ref>Thibodeaux, L.J., 1996. Environmental Chemodynamics: Movement of Chemicals in Air, Water, and Soil, 2nd Edition, Volume 110 of Environmental Science and Technology: A Wiley-Interscience Series of Texts and Monographs. John Wiley & Sons, Inc. 624 pages. ISBN: 0-471-61295-2</ref><ref>United States Environmental Protection Agency (USEPA), 2005. Contaminated Sediment Remediation Guidance for Hazardous Waste Sites. Office of Superfund Remediation and Technology Innovation Report, EPA-540-R-05-012. [[Media: 2005-USEPA-Contaminated_Sediment_Remediation_Guidance.pdf | Report.pdf]]</ref><ref>Lick, W., 2008. Sediment and Contaminant Transport in Surface Waters. CRC Press. 416 pages. [https://doi.org/10.1201/9781420059885 doi: 10.1201/9781420059885]</ref>; therefore, long-term monitoring of both particulate- and dissolved-phase contaminant concentration prior to, during, and following remedial action is necessary to document remedy effectiveness. Source control and total maximum daily load (TMDL) actions generally require costly manual monitoring of dissolved and particulate contaminant concentrations in surface water. The magnitude of cost for these actions is a strong motivation to implement efficient methods for long-term source control and remedial monitoring.  
  
* '''Photolithography, Semiconductor Industry:''' Photoresists, top anti-reflective coatings, bottom anti-reflective coatings, and etchants, with other uses including surfactants, wetting agents, and photo-acid generation<ref name="Choi2005">Choi, D.G., Jeong, J.H., Sim, Y.S., Lee, E.S., Kim, W.S. and Bae, B.S., 2005. Fluorinated Organic− Inorganic Hybrid Mold as a New Stamp for Nanoimprint and Soft Lithography. Langmuir, 21(21), pp. 9390-9392. [https://doi.org/10.1021/la0513205 DOI: 10.1021/la0513205]</ref><ref name="Rolland2004">Rolland, J.P., Van Dam, R.M., Schorzman, D.A., Quake, S.R., and DeSimone, J.M., 2004. Solvent-Resistant Photocurable “Liquid Teflon” for Microfluidic Device Fabrication. Journal of the American Chemical Society, 126(8), pp. 2322-2323.  [https://doi.org/10.1021/ja031657y DOI: 10.1021/ja031657y]</ref><ref name="Brooke2004"/><ref name="vanderPutte2010"/><ref name="UNEP2011"/><ref name="Herzke2012"/>
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Traditional surface water monitoring requires mobilization of field teams to manually collect discrete water samples, send samples to laboratories, and await laboratory analysis so that a site evaluation can be conducted. These traditional methods are well known to have inherent cost and safety concerns and are of limited use (due to safety concerns and standby requirements for resources) in capturing the effects of episodic events (e.g., storms) that are important to consider in site risk assessment and remedy selection. Automated water samplers are commercially available but still require significant field support and costly laboratory analysis. Further, automated samplers may not be suitable for analytes with short hold-times and temperature requirements.  
  
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Optically-based characterization of surface water contaminants is a cost-effective alternative to traditional discrete water sampling methods. Unlike discrete water sampling, which typically results in sparse data at low resolution, and therefore, is of limited use in determining mass loading, OPTICS (OPTically-based In-situ Characterization System) provides continuous data and allows for a complete understanding of water quality and contaminant transport in response to natural processes and human impacts<ref name="ChangEtAl2019"/><ref name="ChangEtAl2018"/><ref name="ChangEtAl2024"/><ref>Bergamaschi, B.A., Fleck, J.A., Downing, B.D., Boss, E., Pellerin, B., Ganju, N.K., Schoellhamer, D.H., Byington, A.A., Heim, W.A., Stephenson, M., Fujii, R., 2011. Methyl mercury dynamics in a tidal wetland quantified using in situ optical measurements. Limnology and Oceanography, 56(4), pp. 1355-1371. [https://doi.org/10.4319/lo.2011.56.4.1355 doi: 10.4319/lo.2011.56.4.1355]&nbsp;&nbsp; [[Media: BergamaschiEtAl2011.pdf | Open Access Article]]</ref><ref>Bergamaschi, B.A., Fleck, J.A., Downing, B.D., Boss, E., Pellerin, B.A., Ganju, N.K., Schoellhamer, D.H., Byington, A.A., Heim, W.A., Stephenson, M., Fujii, R., 2012. Mercury Dynamics in a San Francisco Estuary Tidal Wetland: Assessing Dynamics Using In Situ Measurements. Estuaries and Coasts, 35, pp. 1036-1048. [https://doi.org/10.1007/s12237-012-9501-3 doi: 10.1007/s12237-012-9501-3]&nbsp;&nbsp; [[Media: BergamaschiEtAl2012a.pdf | Open Access Article]]</ref><ref>Bergamaschi, B.A., Krabbenhoft, D.P., Aiken, G.R., Patino, E., Rumbold, D.G., Orem, W.H., 2012. Tidally driven export of dissolved organic carbon, total mercury, and methylmercury from a mangrove-dominated estuary. Environmental Science and Technology, 46(3), pp. 1371-1378. [https://doi.org/10.1021/es2029137 doi: 10.1021/es2029137]&nbsp;&nbsp; [[Media: BergamaschiEtAl2012b.pdf | Open Access Article]]</ref>. The OPTICS tool integrates commercial off-the-shelf ''in situ'' aquatic sensors (Figure 1), periodic discrete surface water sample collection, and a multi-parameter statistical prediction model<ref name="deJong1993">de Jong, S., 1993. SIMPLS: an alternative approach to partial least squares regression. Chemometrics and Intelligent Laboratory Systems, 18(3), pp. 251-263. [https://doi.org/10.1016/0169-7439(93)85002-X doi: 10.1016/0169-7439(93)85002-X]</ref><ref name="RosipalKramer2006">Rosipal, R. and Krämer, N., 2006. Overview and Recent Advances in Partial Least Squares, In: Subspace, Latent Structure, and Feature Selection: Statistical and Optimization Perspectives Workshop, Revised Selected Papers (Lecture Notes in Computer Science, Volume 3940), Springer-Verlag, Berlin, Germany. pp. 34-51. [https://doi.org/10.1007/11752790_2 doi: 10.1007/11752790_2]</ref> to provide high temporal and/or spatial resolution characterization of surface water chemicals of potential concern (COPCs) (Figure 2).
  
 +
==Technology Overview==
 +
The principle behind OPTICS is based on the relationship between optical properties of natural waters and the particles and dissolved material contained within them<ref>Boss, E. and Pegau, W.S., 2001. Relationship of light scattering at an angle in the backward direction to the backscattering coefficient. Applied Optics, 40(30), pp. 5503-5507. [https://doi.org/10.1364/AO.40.005503 doi: 10.1364/AO.40.005503]</ref><ref>Boss, E., Twardowski, M.S., Herring, S., 2001. Shape of the particulate beam spectrum and its inversion to obtain the shape of the particle size distribution. Applied Optics, 40(27), pp. 4884-4893. [https://doi.org/10.1364/AO.40.004885 doi:10/1364/AO.40.004885]</ref><ref>Babin, M., Morel, A., Fournier-Sicre, V., Fell, F., Stramski, D., 2003. Light scattering properties of marine particles in coastal and open ocean waters as related to the particle mass concentration. Limnology and Oceanography, 48(2), pp. 843-859. [https://doi.org/10.4319/lo.2003.48.2.0843 doi: 10.4319/lo.2003.48.2.0843]&nbsp;&nbsp; [[Media: BabinEtAl2003.pdf | Open Access Article]]</ref><ref>Coble, P., Hu, C., Gould, R., Chang, G., Wood, M., 2004. Colored dissolved organic matter in the coastal ocean: An optical tool for coastal zone environmental assessment and management. Oceanography, 17(2), pp. 50-59. [https://doi.org/10.5670/oceanog.2004.47 doi: 10.5670/oceanog.2004.47]&nbsp;&nbsp; [[Media: CobleEtAl2004.pdf | Open Access Article]]</ref><ref>Sullivan, J.M., Twardowski, M.S., Donaghay, P.L., Freeman, S.A., 2005. Use of optical scattering to discriminate particle types in coastal waters. Applied Optics, 44(9), pp. 1667–1680. [https://doi.org/10.1364/AO.44.001667 doi: 10.1364/AO.44.001667]</ref><ref>Twardowski, M.S., Boss, E., Macdonald, J.B., Pegau, W.S., Barnard, A.H., Zaneveld, J.R.V., 2001. A model for estimating bulk refractive index from the optical backscattering ratio and the implications for understanding particle composition in case I and case II waters. Journal of Geophysical Research: Oceans, 106(C7), pp. 14,129-14,142. [https://doi.org/10.1029/2000JC000404 doi: 10/1029/2000JC000404]&nbsp;&nbsp; [[Media: TwardowskiEtAl2001.pdf | Open Access Article]]</ref><ref>Chang, G.C., Barnard, A.H., McLean, S., Egli, P.J., Moore, C., Zaneveld, J.R.V., Dickey, T.D., Hanson, A., 2006. In situ optical variability and relationships in the Santa Barbara Channel: implications for remote sensing. Applied Optics, 45(15), pp. 3593–3604. [https://doi.org/10.1364/AO.45.003593 doi: 10.1364/AO.45.003593]</ref><ref>Slade, W.H. and Boss, E., 2015. Spectral attenuation and backscattering as indicators of average particle size. Applied Optics, 54(24), pp. 7264-7277. [https://doi.org/10.1364/AO.54.007264 doi: 10/1364/AO.54.007264]&nbsp;&nbsp; [[Media: SladeBoss2015.pdf | Open Access Article]]</ref>. Surface water COPCs such as heavy metals and polychlorinated biphenyls (PCBs) are hydrophobic in nature and tend to sorb to materials in the water column, which have unique optical signatures that can be measured at high-resolution using ''in situ'', commercially available aquatic sensors<ref>Agrawal, Y.C. and Pottsmith, H.C., 2000. Instruments for particle size and settling velocity observations in sediment transport. Marine Geology, 168(1-4), pp. 89-114. [https://doi.org/10.1016/S0025-3227(00)00044-X doi: 10.1016/S0025-3227(00)00044-X]</ref><ref>Boss, E., Pegau, W.S., Gardner, W.D., Zaneveld, J.R.V., Barnard, A.H., Twardowski, M.S., Chang, G.C., Dickey, T.D., 2001. Spectral particulate attenuation and particle size distribution in the bottom boundary layer of a continental shelf. Journal of Geophysical Research: Oceans, 106(C5), pp. 9509-9516. [https://doi.org/10.1029/2000JC900077  doi: 10.1029/2000JC900077]&nbsp;&nbsp; [[Media: BossEtAl2001.pdf | Open Access Article]]</ref><ref>Boss, E., Pegau, W.S., Lee, M., Twardowski, M., Shybanov, E., Korotaev, G. Baratange, F., 2004. Particulate backscattering ratio at LEO 15 and its use to study particle composition and distribution. Journal of Geophysical Research: Oceans, 109(C1), Article C01014. [https://doi.org/10.1029/2002JC001514 doi: 10.1029/2002JC001514]&nbsp;&nbsp; [[Media: BossEtAl2004.pdf | Open Access Article]]</ref><ref>Briggs, N.T., Slade, W.H., Boss, E., Perry, M.J., 2013. Method for estimating mean particle size from high-frequency fluctuations in beam attenuation or scattering measurement. Applied Optics, 52(27), pp. 6710-6725. [https://doi.org/10.1364/AO.52.006710 doi: 10.1364/AO.52.006710]&nbsp;&nbsp; [[Media: BriggsEtAl2013.pdf | Open Access Article]]</ref>. Therefore, high-resolution concentrations of COPCs can be accurately and robustly derived from ''in situ'' measurements using statistical methods.
  
 +
The OPTICS method is analogous to the commonly used empirical derivation of total suspended solids concentration (TSS) from optical turbidity using linear regression<ref>Rasmussen, P.P., Gray, J.R., Glysson, G.D., Ziegler, A.C., 2009. Guidelines and procedures for computing time-series suspended-sediment concentrations and loads from in-stream turbidity-sensor and streamflow data. In: Techniques and Methods, Book 3: Applications of Hydraulics, Section C: Sediment and Erosion Techniques, Ch. 4. 52 pages. U.S. Geological Survey.&nbsp;&nbsp; [[Media: RasmussenEtAl2009.pdf | Open Access Article]]</ref>. However, rather than deriving one response variable (TSS) from one predictor variable (turbidity), OPTICS involves derivation of one response variable (e.g., PCB concentration) from a suite of predictor variables (e.g., turbidity, temperature, salinity, and fluorescence of chlorophyll-a) using multi-parameter statistical regression. OPTICS is based on statistical correlation – similar to the turbidity-to-TSS regression technique. The method does not rely on interpolation or extrapolation. 
  
 +
The OPTICS technique utilizes partial least-squares (PLS) regression to determine a combination of physical, optical, and water quality properties that best predicts chemical contaminant concentrations with high variance. PLS regression is a statistically based method combining multiple linear regression and principal component analysis (PCA), where multiple linear regression finds a combination of predictors that best fit a response and PCA finds combinations of predictors with large variance<ref name="deJong1993"/><ref name="RosipalKramer2006"/>. Therefore, PLS identifies combinations of multi-collinear predictors (''in situ'', high-resolution physical, optical, and water quality measurements) that have large covariance with the response values (discrete surface water chemical contaminant concentration data from samples that are collected periodically, coincident with ''in situ'' measurements). PLS combines information about the variances of both the predictors and the responses, while also considering the correlations among them. PLS therefore provides a model with reliable predictive power.
  
+
OPTICS ''in situ'' measurement parameters include, but are not limited to current velocity, conductivity, temperature, depth, turbidity, dissolved oxygen, and fluorescence of chlorophyll-a and dissolved organic matter. Instrumentation for these measurements is commercially available, robust, deployable in a wide variety of configurations (e.g., moored, vessel-mounted, etc.), powered by batteries, and records data internally and/or transmits data in real-time. The physical, optical, and water quality instrumentation is compact and self-contained. The modularity and automated nature of the OPTICS measurement system enables robust, long-term, autonomous data collection for near-continuous monitoring.
  
 +
[[File:ChangFig3.png | thumb | 400px| Figure 3. OPTICS to characterize COPC variability in the context of site processes at BCSA. (A) Tidal oscillations (Elev.<sub>MSL</sub>) and precipitation (Precip.). (B) – (D) OPTICS-derived particulate mercury (PHg) and methylmercury (PMeHg) and total PCBs (TPCBs). Open circles represent discrete water sample data.]] OPTICS measurements are provided at a significantly reduced cost relative to traditional monitoring techniques used within the environmental industry. Cost performance analysis shows that monitoring costs are reduced by more than 85% while significantly increasing the temporal and spatial resolution of sampling. The reduced cost of monitoring makes this technology suitable for a number of environmental applications including, but not limited to site baseline characterization, source control evaluation, dredge or stormflow plume characterization, and remedy performance monitoring. OPTICS has been successfully demonstrated for characterizing a wide variety of COPCs: mercury, methylmercury, copper, lead, PCBs, dichlorodiphenyltrichloroethane (DDT) and its related compounds (collectively, DDX), and 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD or dioxin) in a number of different environmental systems ranging from inland lakes and rivers to the coastal ocean. To date, OPTICS has been limited to surface water applications. Additional applications (e.g., groundwater) would require further research and development.
  
[[File:NewellMatrixDiffFig1.PNG | thumb |500px| Figure 1. Diffusion of a dissolved solute (chlorinated solvent) into lower ''K'' zones during loading period, followed by diffusion back out into higher ''K'' zones once the source is removed <ref name="Sale2007">Sale, T.C., Illangasekare, T.H., Zimbron, J., Rodriguez, D., Wilking, B., and Marinelli, F., 2007. AFCEE Source Zone Initiative. Air Force Center for Environmental Excellence, Brooks City-Base, San Antonio, TX. [https://www.enviro.wiki/images/0/08/AFCEE-2007-Sale.pdf Report.pdf]</ref>]]
+
==Applications==
 +
[[File:ChangFig4.png | thumb | 400px| Figure 4. OPTICS reveals baseflow daily cycling and confirms storm-induced particle-bound COPC resuspension and mobilization through bank interaction. (A) Flow rate (Q) and precipitation (Precip). (B) – (C) OPTICS-derived particulate mercury (PHg) and methylmercury (PMeHg). Open circles represent discrete water sample data.]]
 +
[[File:ChangFig5.png | thumb | 400px| Figure 5. Three-dimensional volume plot of high spatial resolution OPTICS-derived PCBs in exceedance of baseline showing that PCBs were discharged from the outfall (yellow arrow), remained in suspension, and dispersed elsewhere before settling.]]
 +
An OPTICS study was conducted at Berry’s Creek Study Area (BCSA), New Jersey in 2014 and 2015 to understand COPC sources and transport mechanisms for development of an effective remediation plan. OPTICS successfully extended periodic discrete surface water samples to continuous, high-resolution measurements of PCBs, mercury, and methylmercury to elucidate COPC sources and transport throughout the BCSA tidal estuary system. OPTICS provided data at resolution sufficient to investigate COC variability in the context of physical processes. The results (Figure 3) facilitated focused and effective site remediation and management decisions that could not be determined based on periodic discrete samples alone, despite over seven years of monitoring at different locations throughout the system over a range of different seasons, tidal phases, and environmental conditions. The BCSA OPTICS methodology and its results have undergone official peer review overseen by the U.S. Environmental Protection Agency (USEPA), and those results have been published in peer-reviewed literature<ref name="ChangEtAl2019"/>.
  
 +
OPTICS was applied at the South River, Virginia in 2016 to quantify sources of legacy mercury in the system that are contributing to recontamination and continued elevated mercury concentrations in fish tissue. OPTICS provided information necessary to identify mechanisms for COPC redistribution and to quantify the relative contribution of each mechanism to total mass transport of mercury and methylmercury in the system. Continuous, high-resolution COPC data afforded by OPTICS helped resolve baseflow daily cycling that had never before been observed at the South River (Figure 4) and provided data at temporal resolution necessary to verify storm-induced particle-bound COC resuspension and mobilization through bank interaction. The results informed source control and remedy design and monitoring efforts. Methodology and results from the South River have been published in peer-reviewed literature<ref name="ChangEtAl2018"/>.
  
[[File: GreenTank.mp4 | thumb |500px| Figure 2. Video of dye tank simulation of matrix diffusion]]
+
The U.S. Department of Defense’s Environmental Security Technology Certification Program (ESTCP) supported an OPTICS demonstration study at the Pearl Harbor Sediment Site, Hawaii, to determine whether stormwater from Oscar 1 Pier outfall is a contributing source of PCBs to Decision Unit (DU) N-2 (ESTCP Project ER21-5021). High spatial resolution results afforded by ship-based, mobile OPTICS monitoring suggested that PCBs were discharged from the outfall, remained in suspension, and dispersed elsewhere before settling (Figure 5). More details regarding this study were presented by Chang et al. in 2024<ref name="ChangEtAl2024"/>.
  
One other implication of matrix diffusion is that plume migration is attenuated by the loss of contaminants into low permeability zones, leading to slower plume migration compared to a case where no matrix diffusion occurs.  This phenomena was observed as far back as 1985 when Sudicky et al. observed that “A second consequence of the solute-storage effect offered by transverse diffusion into low-permeability layers is a rate of migration of the frontal portion of a contaminant in the permeable layers that is less than the groundwater velocity.”<ref name="Sudicky1985"> Sudicky, E.A., Gillham, R.W., and Frind, E.O., 1985. Experimental Investigation of Solute Transport in Stratified Porous Media: 1. The Nonreactive Case. Water Resources Research, 21(7), pp. 1035-1041. [https://doi.org/10.1029/WR021i007p01035 DOI: 10.1029/WR021i007p01035]</ref>  In cases where there is an attenuating source, matrix diffusion can also reduce the peak concentrations observed in downgradient monitoring wells.  The attenuation caused by matrix diffusion may be particularly important for implementing [[Monitored Natural Attenuation (MNA)]] for contaminants that do not completely degrade, such as [[Metal and Metalloid Contaminants | heavy metals]] and [[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)]].
+
==Summary==
 +
OPTICS provides:
 +
*High resolution surface water chemical contaminant characterization
 +
*Cost-effective monitoring and assessment
 +
*Versatile and modular monitoring with capability for real-time telemetry
 +
*Data necessary for development and validation of conceptual site models
 +
*A key line of evidence for designing and evaluating remedies.
  
==SERPD/ESTCP Research==
+
Because OPTICS monitoring involves deployment of autonomous sampling instrumentation, a substantially greater volume of data can be collected using this technique compared to traditional sampling, and at a far lower cost. A large volume of data supports evaluation of chemical contaminant concentrations over a range of spatial and temporal scales, and the system can be customized for a variety of environmental applications. OPTICS helps quantify contaminant mass flux and the relative contribution of local transport and source areas to net contaminant transport. OPTICS delivers a strong line of evidence for evaluating contaminant sources, fate, and transport, and for supporting the design of a remedy tailored to address site-specific, risk-driving conditions. The improved understanding of site processes aids in the development of mitigation measures that minimize site risks.  
{|
 
The SERDP/ESTCP programs have funded several projects focusing on how matrix diffusion can impede progress towards reaching site closure, including:
 
|-
 
|
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-1740 SERDP Management of Contaminants Stored in Low Permeability Zones, A State-of-the-Science Review] <ref name="Sale2013"/>
 
|-
 
|
 
*[https://www.serdp-estcp.org/Tools-and-Training/Environmental-Restoration/Groundwater-Plume-Treatment/Matrix-Diffusion-Tool-Kit ESTCP Matrix Diffusion Toolkit]<ref name="Farhat2012">Farhat, S.K., Newell, C.J., Seyedabbasi, M.A., McDade, J.M., Mahler, N.T., Sale, T.C., Dandy, D.S. and Wahlberg, J.J., 2012. Matrix Diffusion Toolkit. Environmental Security Technology Certification Program (ESTCP) Project ER-201126.  [[Media:Farhat2012ER-201126UsersManual.pdf | User’s Manual.pdf]]  Website: [https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201126 ER-201126]</ref>
 
|-
 
|
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-200530 ESTCP Decision Guide]<ref>Sale, T. and Newell, C., 2011. A Guide for Selecting Remedies for Subsurface Releases of Chlorinated Solvents. Environmental Security Technology Certification Program (ESTCP) Project ER-200530. [[Media: Sale2011ER-200530.pdf | Report.pdf]]  Website: [https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-200530 ER-200530]</ref>
 
|-
 
|
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201426 ESTCP REMChlor-MD: the USEPA’s REMChlor model with a new matrix diffusion term for the plume]<ref name="Farhat2018">Farhat, S. K., Newell, C. J., Falta, R. W., and Lynch, K., 2018. A Practical Approach for Modeling Matrix Diffusion Effects in REMChlor. Environmental Security Technology Certification Program (ESTCP) Project ER-201426.  [https://enviro.wiki/images/0/0b/2018-Falta-REMChlor_Modeling_Matrix_Diffusion_Effects.pdf  User’s Manual.pdf]  Website: [https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201426 ER-201426]</ref>
 
|}
 
[[File:ADRFig3.png | thumb| left |400px| Figure 3.  Comparison of tracer breakthrough (upper graph) and cleanup curves (lower graph) from advection-dispersion based (gray lines) and advection-diffusion based (black lines) solute transport<ref name="ITRC2011">Interstate Technology and Regulatory Council (ITRC), 2011. Integrated DNAPL Site Strategy (IDSS-1),  Integrated DNAPL Site Strategy Team, ITRC, Washington, DC. [https://www.enviro.wiki/images/d/d9/ITRC-2011-Integrated_DNAPL.pdf Report.pdf]  Free download from: [https://itrcweb.org/GuidanceDocuments/IntegratedDNAPLStrategy_IDSSDoc/IDSS-1.pdf ITRC]</ref>.]]
 
 
 
==Transport Modeling==
 
Several different modeling approaches have been developed to simulate the diffusive transport of dissolved solutes into and out of lower ''K'' zones<ref>Falta, R.W., and Wang, W., 2017. A semi-analytical method for simulating matrix diffusion in numerical transport models. Journal of Contaminant Hydrology, 197, pp. 39-49.  [https://doi.org/10.1016/j.jconhyd.2016.12.007 DOI: 10.1016/j.jconhyd.2016.12.007]</ref><ref>Muskus, N. and Falta, R.W., 2018. Semi-analytical method for matrix diffusion in heterogeneous and fractured systems with parent-daughter reactions. Journal of Contaminant Hydrology, 218, pp. 94-109.  [https://doi.org/10.1016/j.jconhyd.2018.10.002 DOI: 10.1016/j.jconhyd.2018.10.002]</ref>.  The [https://www.serdp-estcp.org/Tools-and-Training/Environmental-Restoration/Groundwater-Plume-Treatment/Matrix-Diffusion-Tool-Kit Matrix Diffusion Toolkit]<ref name="Farhat2012"/> is a Microsoft Excel based tool for simulating forward and back diffusion using two different analytical models<ref name="Parker1994">Parker, B.L., Gillham, R.W., and Cherry, J.A., 1994. Diffusive Disappearance of Immiscible Phase Organic Liquids in Fractured Geologic Media. Groundwater, 32(5), pp. 805-820. [https://doi.org/10.1111/j.1745-6584.1994.tb00922.x DOI: 10.1111/j.1745-6584.1994.tb00922.x]</ref><ref>Sale, T.C., Zimbron, J.A., and Dandy, D.S., 2008. Effects of reduced contaminant loading on downgradient water quality in an idealized two-layer granular porous media. Journal of Contaminant Hydrology, 102(1), pp. 72-85. [https://doi.org/10.1016/j.jconhyd.2008.08.002 DOI: 10.1016/j.jconhyd.2008.08.002]</ref>.  Numerical models including [https://en.wikipedia.org/wiki/MODFLOW MODFLOW]/[https://xmswiki.com/wiki/GMS:MT3DMS MT3DMS]<ref name="Zheng1999">Zheng, C. and Wang, P.P., 1999. MT3DMS: A Modular Three-Dimensional Multispecies Transport Model for Simulation of Advection, Dispersion, and Chemical Reactions of Contaminants in Groundwater Systems; Documentation and User’s Guide. Contract Report SERDP-99-1 U.S. Army Engineer Research and Development Center, Vicksburg, MS. [https://www.enviro.wiki/images/3/32/Mt3dmanual.pdf User’s Guide.pdf]  [https://xmswiki.com/wiki/GMS:MT3DMS MT3DMS website]</ref> have been shown to be effective in simulating back diffusion processes and can accurately predict concentration changes over 3 orders-of-magnitude in heterogeneous sand tank experiments<ref>Chapman, S.W., Parker, B.L., Sale, T.C., Doner, L.A., 2012. Testing high resolution numerical models for analysis of contaminant storage and release from low permeability zones. Journal of Contaminant Hydrology, 136, pp. 106-116. [https://doi.org/10.1016/j.jconhyd.2012.04.006 DOI: 10.1016/j.jconhyd.2012.04.006]</ref>. However, numerical models require a fine vertical discretization with short time steps to accurately simulate back diffusion, greatly increasing computation times<ref>Farhat, S.K., Adamson, D.T., Gavaskar, A.R., Lee, S.A., Falta, R.W. and Newell, C.J., 2020. Vertical Discretization Impact in Numerical Modeling of Matrix Diffusion in Contaminated Groundwater. Groundwater Monitoring and Remediation, 40(2), pp. 52-64. [https://doi.org/10.1111/gwmr.12373 DOI: 10.1111/gwmr.12373]</ref>.  These issues can be addressed by incorporating a local 1-D model domain within a general 3D numerical model<ref>Carey, G.R., Chapman, S.W., Parker, B.L. and McGregor, R., 2015. Application of an Adapted Version of MT3DMS for Modeling Back‐Diffusion Remediation Timeframes. Remediation, 25(4), pp. 55-79. [https://doi.org/10.1002/rem.21440 DOI: 10.1002/rem.21440]</ref>.
 
 
 
The [[REMChlor - MD]] toolkit is capable of simulating matrix diffusion in groundwater contaminant plumes by using a semi-analytical method for estimating mass transfer between high and low permeability zones that provides computationally accurate predictions, with much shorter run times than traditional fine grid numerical models<ref name="Farhat2018"/>.
 
 
 
==Impacts on Breakthrough Curves==
 
 
 
The impacts of matrix diffusion on the initial breakthrough of the solute plume and on later cleanup are illustrated in Figure 3<ref name="ITRC2011"/>. Using a traditional advection-dispersion model, the breakthrough curve for a pulse tracer injection appears as a bell-shaped ([[wikipedia:Gaussian function |Gaussian]]) curve (gray line on the right side of the upper graph) where the peak arrival time corresponds to the average groundwater velocity.  Using an advection-diffusion approach, the breakthrough curve for a pulse injection is asymmetric (solid black line) with the peak tracer concentration arriving earlier than would be expected based on the average groundwater velocity, but with a long extended tail to the flushout curve.
 
 
 
The lower graph shows the predicted cleanup concentration profiles following complete elimination of a source area.  The advection-dispersion model (gray line) predicts a clean-water front arriving at a time corresponding to the average groundwater velocity. The advection-diffusion model (black line) predicts that concentrations will start to decline more rapidly than expected (based on the average groundwater velocity) as clean water rapidly migrates through the highest-permeability strata. However, low but significant contaminant concentrations linger much longer (tailing) due to diffusive contaminant mass exchange between zones of high and low permeability. A similar response to source remediation is seen in models such as the sand tank experiment shown in Figure 2, and also in field observations of plume contaminant concentrations in heterogeneous aquifers.
 
 
 
<br clear="left" />
 
  
 
==References==
 
==References==
 
 
<references />
 
<references />
  
 
==See Also==
 
==See Also==
 
*[http://www.gsi-net.com/en/publications/useful-groundwater-resources/colorado-state-matrix-diffusion-video.html Matrix Diffusion Movie]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-1737 Impact of Clay-DNAPL Interactions on Transport and Storage of Chlorinated Solvents in Low Permeability Zones]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-200320 Prediction of Groundwater Quality Improvement Down-Gradient of ''In Situ'' Permeable Treatment Barriers and Fully Remediated Source Zones]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201032 Determining Source Attenuation History to Support Closure by Natural Attenuation]
 
*[https://www.coursera.org/learn/natural-attenuation-of-groundwater-contaminants/lecture/2R7yh/matrix-diffusion-principles Coursera Matrix Diffusion Online Lecture]
 

Latest revision as of 20:39, 15 July 2024

Assessing Vapor Intrusion (VI) Impacts in Neighborhoods with Groundwater Contaminated by Chlorinated Volatile Organic Chemicals (CVOCs)

The VI Diagnosis Toolkit[1] is a set of tools that can be used individually or in combination to assess vapor intrusion (VI) impacts at one or more buildings overlying regional-scale dissolved chlorinated solvent-impacted groundwater plumes. The strategic use of these tools can lead to confident and efficient neighborhood-scale VI pathway assessments.

Related Article(s):

Contributor(s):

  • Paul C. Johnson, Ph.D.
  • Paul Dahlen, Ph.D.
  • Yuanming Guo, Ph.D.

Key Resource(s):

  • The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes, ESTCP Project ER-201501, Final Report[1]
  • CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment, ESTCP Project ER-201501, Technical Report[2]
  • VI Diagnosis Toolkit User Guide, ESTCP Project ER-201501[3]

Background

Figure 1. Example of instrumentation used for OPTICS monitoring.
Figure 2. Schematic diagram illustrating the OPTICS methodology. High resolution in-situ data are integrated with traditional discrete sample analytical data using partial least-square regression to derive high resolution chemical contaminant concentration data series.

Nationwide, the liability due to contaminated sediments is estimated in the trillions of dollars. Stakeholders are assessing and developing remedial strategies for contaminated sediment sites in major harbors and waterways throughout the U.S. The mobility of contaminants in surface water is a primary transport and risk mechanism[4][5][6]; therefore, long-term monitoring of both particulate- and dissolved-phase contaminant concentration prior to, during, and following remedial action is necessary to document remedy effectiveness. Source control and total maximum daily load (TMDL) actions generally require costly manual monitoring of dissolved and particulate contaminant concentrations in surface water. The magnitude of cost for these actions is a strong motivation to implement efficient methods for long-term source control and remedial monitoring.

Traditional surface water monitoring requires mobilization of field teams to manually collect discrete water samples, send samples to laboratories, and await laboratory analysis so that a site evaluation can be conducted. These traditional methods are well known to have inherent cost and safety concerns and are of limited use (due to safety concerns and standby requirements for resources) in capturing the effects of episodic events (e.g., storms) that are important to consider in site risk assessment and remedy selection. Automated water samplers are commercially available but still require significant field support and costly laboratory analysis. Further, automated samplers may not be suitable for analytes with short hold-times and temperature requirements.

Optically-based characterization of surface water contaminants is a cost-effective alternative to traditional discrete water sampling methods. Unlike discrete water sampling, which typically results in sparse data at low resolution, and therefore, is of limited use in determining mass loading, OPTICS (OPTically-based In-situ Characterization System) provides continuous data and allows for a complete understanding of water quality and contaminant transport in response to natural processes and human impacts[7][8][9][10][11][12]. The OPTICS tool integrates commercial off-the-shelf in situ aquatic sensors (Figure 1), periodic discrete surface water sample collection, and a multi-parameter statistical prediction model[13][14] to provide high temporal and/or spatial resolution characterization of surface water chemicals of potential concern (COPCs) (Figure 2).

Technology Overview

The principle behind OPTICS is based on the relationship between optical properties of natural waters and the particles and dissolved material contained within them[15][16][17][18][19][20][21][22]. Surface water COPCs such as heavy metals and polychlorinated biphenyls (PCBs) are hydrophobic in nature and tend to sorb to materials in the water column, which have unique optical signatures that can be measured at high-resolution using in situ, commercially available aquatic sensors[23][24][25][26]. Therefore, high-resolution concentrations of COPCs can be accurately and robustly derived from in situ measurements using statistical methods.

The OPTICS method is analogous to the commonly used empirical derivation of total suspended solids concentration (TSS) from optical turbidity using linear regression[27]. However, rather than deriving one response variable (TSS) from one predictor variable (turbidity), OPTICS involves derivation of one response variable (e.g., PCB concentration) from a suite of predictor variables (e.g., turbidity, temperature, salinity, and fluorescence of chlorophyll-a) using multi-parameter statistical regression. OPTICS is based on statistical correlation – similar to the turbidity-to-TSS regression technique. The method does not rely on interpolation or extrapolation.

The OPTICS technique utilizes partial least-squares (PLS) regression to determine a combination of physical, optical, and water quality properties that best predicts chemical contaminant concentrations with high variance. PLS regression is a statistically based method combining multiple linear regression and principal component analysis (PCA), where multiple linear regression finds a combination of predictors that best fit a response and PCA finds combinations of predictors with large variance[13][14]. Therefore, PLS identifies combinations of multi-collinear predictors (in situ, high-resolution physical, optical, and water quality measurements) that have large covariance with the response values (discrete surface water chemical contaminant concentration data from samples that are collected periodically, coincident with in situ measurements). PLS combines information about the variances of both the predictors and the responses, while also considering the correlations among them. PLS therefore provides a model with reliable predictive power.

OPTICS in situ measurement parameters include, but are not limited to current velocity, conductivity, temperature, depth, turbidity, dissolved oxygen, and fluorescence of chlorophyll-a and dissolved organic matter. Instrumentation for these measurements is commercially available, robust, deployable in a wide variety of configurations (e.g., moored, vessel-mounted, etc.), powered by batteries, and records data internally and/or transmits data in real-time. The physical, optical, and water quality instrumentation is compact and self-contained. The modularity and automated nature of the OPTICS measurement system enables robust, long-term, autonomous data collection for near-continuous monitoring.

Figure 3. OPTICS to characterize COPC variability in the context of site processes at BCSA. (A) Tidal oscillations (Elev.MSL) and precipitation (Precip.). (B) – (D) OPTICS-derived particulate mercury (PHg) and methylmercury (PMeHg) and total PCBs (TPCBs). Open circles represent discrete water sample data.

OPTICS measurements are provided at a significantly reduced cost relative to traditional monitoring techniques used within the environmental industry. Cost performance analysis shows that monitoring costs are reduced by more than 85% while significantly increasing the temporal and spatial resolution of sampling. The reduced cost of monitoring makes this technology suitable for a number of environmental applications including, but not limited to site baseline characterization, source control evaluation, dredge or stormflow plume characterization, and remedy performance monitoring. OPTICS has been successfully demonstrated for characterizing a wide variety of COPCs: mercury, methylmercury, copper, lead, PCBs, dichlorodiphenyltrichloroethane (DDT) and its related compounds (collectively, DDX), and 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD or dioxin) in a number of different environmental systems ranging from inland lakes and rivers to the coastal ocean. To date, OPTICS has been limited to surface water applications. Additional applications (e.g., groundwater) would require further research and development.

Applications

Figure 4. OPTICS reveals baseflow daily cycling and confirms storm-induced particle-bound COPC resuspension and mobilization through bank interaction. (A) Flow rate (Q) and precipitation (Precip). (B) – (C) OPTICS-derived particulate mercury (PHg) and methylmercury (PMeHg). Open circles represent discrete water sample data.
Figure 5. Three-dimensional volume plot of high spatial resolution OPTICS-derived PCBs in exceedance of baseline showing that PCBs were discharged from the outfall (yellow arrow), remained in suspension, and dispersed elsewhere before settling.

An OPTICS study was conducted at Berry’s Creek Study Area (BCSA), New Jersey in 2014 and 2015 to understand COPC sources and transport mechanisms for development of an effective remediation plan. OPTICS successfully extended periodic discrete surface water samples to continuous, high-resolution measurements of PCBs, mercury, and methylmercury to elucidate COPC sources and transport throughout the BCSA tidal estuary system. OPTICS provided data at resolution sufficient to investigate COC variability in the context of physical processes. The results (Figure 3) facilitated focused and effective site remediation and management decisions that could not be determined based on periodic discrete samples alone, despite over seven years of monitoring at different locations throughout the system over a range of different seasons, tidal phases, and environmental conditions. The BCSA OPTICS methodology and its results have undergone official peer review overseen by the U.S. Environmental Protection Agency (USEPA), and those results have been published in peer-reviewed literature[7].

OPTICS was applied at the South River, Virginia in 2016 to quantify sources of legacy mercury in the system that are contributing to recontamination and continued elevated mercury concentrations in fish tissue. OPTICS provided information necessary to identify mechanisms for COPC redistribution and to quantify the relative contribution of each mechanism to total mass transport of mercury and methylmercury in the system. Continuous, high-resolution COPC data afforded by OPTICS helped resolve baseflow daily cycling that had never before been observed at the South River (Figure 4) and provided data at temporal resolution necessary to verify storm-induced particle-bound COC resuspension and mobilization through bank interaction. The results informed source control and remedy design and monitoring efforts. Methodology and results from the South River have been published in peer-reviewed literature[8].

The U.S. Department of Defense’s Environmental Security Technology Certification Program (ESTCP) supported an OPTICS demonstration study at the Pearl Harbor Sediment Site, Hawaii, to determine whether stormwater from Oscar 1 Pier outfall is a contributing source of PCBs to Decision Unit (DU) N-2 (ESTCP Project ER21-5021). High spatial resolution results afforded by ship-based, mobile OPTICS monitoring suggested that PCBs were discharged from the outfall, remained in suspension, and dispersed elsewhere before settling (Figure 5). More details regarding this study were presented by Chang et al. in 2024[9].

Summary

OPTICS provides:

  • High resolution surface water chemical contaminant characterization
  • Cost-effective monitoring and assessment
  • Versatile and modular monitoring with capability for real-time telemetry
  • Data necessary for development and validation of conceptual site models
  • A key line of evidence for designing and evaluating remedies.

Because OPTICS monitoring involves deployment of autonomous sampling instrumentation, a substantially greater volume of data can be collected using this technique compared to traditional sampling, and at a far lower cost. A large volume of data supports evaluation of chemical contaminant concentrations over a range of spatial and temporal scales, and the system can be customized for a variety of environmental applications. OPTICS helps quantify contaminant mass flux and the relative contribution of local transport and source areas to net contaminant transport. OPTICS delivers a strong line of evidence for evaluating contaminant sources, fate, and transport, and for supporting the design of a remedy tailored to address site-specific, risk-driving conditions. The improved understanding of site processes aids in the development of mitigation measures that minimize site risks.

References

  1. ^ 1.0 1.1 Johnson, P.C., Guo, Y., Dahlen, P., 2020. The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Mitigating Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes. ESTCP Project ER-201501, Final Report. Project Website   Final Report.pdf
  2. ^ Johnson, P.C., Guo, Y., Dahlen, P., 2021. CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment. ESTCP ER-201501, Technical Report. Project Website   Technical_Report.pdf
  3. ^ Johnson, P.C., Guo, Y., and Dahlen, P., 2022. VI Diagnosis Toolkit User Guide, ESTCP ER-201501, User Guide. Project Website   User_Guide.pdf
  4. ^ Thibodeaux, L.J., 1996. Environmental Chemodynamics: Movement of Chemicals in Air, Water, and Soil, 2nd Edition, Volume 110 of Environmental Science and Technology: A Wiley-Interscience Series of Texts and Monographs. John Wiley & Sons, Inc. 624 pages. ISBN: 0-471-61295-2
  5. ^ United States Environmental Protection Agency (USEPA), 2005. Contaminated Sediment Remediation Guidance for Hazardous Waste Sites. Office of Superfund Remediation and Technology Innovation Report, EPA-540-R-05-012. Report.pdf
  6. ^ Lick, W., 2008. Sediment and Contaminant Transport in Surface Waters. CRC Press. 416 pages. doi: 10.1201/9781420059885
  7. ^ 7.0 7.1 Cite error: Invalid <ref> tag; no text was provided for refs named ChangEtAl2019
  8. ^ 8.0 8.1 Cite error: Invalid <ref> tag; no text was provided for refs named ChangEtAl2018
  9. ^ 9.0 9.1 Cite error: Invalid <ref> tag; no text was provided for refs named ChangEtAl2024
  10. ^ Bergamaschi, B.A., Fleck, J.A., Downing, B.D., Boss, E., Pellerin, B., Ganju, N.K., Schoellhamer, D.H., Byington, A.A., Heim, W.A., Stephenson, M., Fujii, R., 2011. Methyl mercury dynamics in a tidal wetland quantified using in situ optical measurements. Limnology and Oceanography, 56(4), pp. 1355-1371. doi: 10.4319/lo.2011.56.4.1355   Open Access Article
  11. ^ Bergamaschi, B.A., Fleck, J.A., Downing, B.D., Boss, E., Pellerin, B.A., Ganju, N.K., Schoellhamer, D.H., Byington, A.A., Heim, W.A., Stephenson, M., Fujii, R., 2012. Mercury Dynamics in a San Francisco Estuary Tidal Wetland: Assessing Dynamics Using In Situ Measurements. Estuaries and Coasts, 35, pp. 1036-1048. doi: 10.1007/s12237-012-9501-3   Open Access Article
  12. ^ Bergamaschi, B.A., Krabbenhoft, D.P., Aiken, G.R., Patino, E., Rumbold, D.G., Orem, W.H., 2012. Tidally driven export of dissolved organic carbon, total mercury, and methylmercury from a mangrove-dominated estuary. Environmental Science and Technology, 46(3), pp. 1371-1378. doi: 10.1021/es2029137   Open Access Article
  13. ^ 13.0 13.1 de Jong, S., 1993. SIMPLS: an alternative approach to partial least squares regression. Chemometrics and Intelligent Laboratory Systems, 18(3), pp. 251-263. doi: 10.1016/0169-7439(93)85002-X
  14. ^ 14.0 14.1 Rosipal, R. and Krämer, N., 2006. Overview and Recent Advances in Partial Least Squares, In: Subspace, Latent Structure, and Feature Selection: Statistical and Optimization Perspectives Workshop, Revised Selected Papers (Lecture Notes in Computer Science, Volume 3940), Springer-Verlag, Berlin, Germany. pp. 34-51. doi: 10.1007/11752790_2
  15. ^ Boss, E. and Pegau, W.S., 2001. Relationship of light scattering at an angle in the backward direction to the backscattering coefficient. Applied Optics, 40(30), pp. 5503-5507. doi: 10.1364/AO.40.005503
  16. ^ Boss, E., Twardowski, M.S., Herring, S., 2001. Shape of the particulate beam spectrum and its inversion to obtain the shape of the particle size distribution. Applied Optics, 40(27), pp. 4884-4893. doi:10/1364/AO.40.004885
  17. ^ Babin, M., Morel, A., Fournier-Sicre, V., Fell, F., Stramski, D., 2003. Light scattering properties of marine particles in coastal and open ocean waters as related to the particle mass concentration. Limnology and Oceanography, 48(2), pp. 843-859. doi: 10.4319/lo.2003.48.2.0843   Open Access Article
  18. ^ Coble, P., Hu, C., Gould, R., Chang, G., Wood, M., 2004. Colored dissolved organic matter in the coastal ocean: An optical tool for coastal zone environmental assessment and management. Oceanography, 17(2), pp. 50-59. doi: 10.5670/oceanog.2004.47   Open Access Article
  19. ^ Sullivan, J.M., Twardowski, M.S., Donaghay, P.L., Freeman, S.A., 2005. Use of optical scattering to discriminate particle types in coastal waters. Applied Optics, 44(9), pp. 1667–1680. doi: 10.1364/AO.44.001667
  20. ^ Twardowski, M.S., Boss, E., Macdonald, J.B., Pegau, W.S., Barnard, A.H., Zaneveld, J.R.V., 2001. A model for estimating bulk refractive index from the optical backscattering ratio and the implications for understanding particle composition in case I and case II waters. Journal of Geophysical Research: Oceans, 106(C7), pp. 14,129-14,142. doi: 10/1029/2000JC000404   Open Access Article
  21. ^ Chang, G.C., Barnard, A.H., McLean, S., Egli, P.J., Moore, C., Zaneveld, J.R.V., Dickey, T.D., Hanson, A., 2006. In situ optical variability and relationships in the Santa Barbara Channel: implications for remote sensing. Applied Optics, 45(15), pp. 3593–3604. doi: 10.1364/AO.45.003593
  22. ^ Slade, W.H. and Boss, E., 2015. Spectral attenuation and backscattering as indicators of average particle size. Applied Optics, 54(24), pp. 7264-7277. doi: 10/1364/AO.54.007264   Open Access Article
  23. ^ Agrawal, Y.C. and Pottsmith, H.C., 2000. Instruments for particle size and settling velocity observations in sediment transport. Marine Geology, 168(1-4), pp. 89-114. doi: 10.1016/S0025-3227(00)00044-X
  24. ^ Boss, E., Pegau, W.S., Gardner, W.D., Zaneveld, J.R.V., Barnard, A.H., Twardowski, M.S., Chang, G.C., Dickey, T.D., 2001. Spectral particulate attenuation and particle size distribution in the bottom boundary layer of a continental shelf. Journal of Geophysical Research: Oceans, 106(C5), pp. 9509-9516. doi: 10.1029/2000JC900077   Open Access Article
  25. ^ Boss, E., Pegau, W.S., Lee, M., Twardowski, M., Shybanov, E., Korotaev, G. Baratange, F., 2004. Particulate backscattering ratio at LEO 15 and its use to study particle composition and distribution. Journal of Geophysical Research: Oceans, 109(C1), Article C01014. doi: 10.1029/2002JC001514   Open Access Article
  26. ^ Briggs, N.T., Slade, W.H., Boss, E., Perry, M.J., 2013. Method for estimating mean particle size from high-frequency fluctuations in beam attenuation or scattering measurement. Applied Optics, 52(27), pp. 6710-6725. doi: 10.1364/AO.52.006710   Open Access Article
  27. ^ Rasmussen, P.P., Gray, J.R., Glysson, G.D., Ziegler, A.C., 2009. Guidelines and procedures for computing time-series suspended-sediment concentrations and loads from in-stream turbidity-sensor and streamflow data. In: Techniques and Methods, Book 3: Applications of Hydraulics, Section C: Sediment and Erosion Techniques, Ch. 4. 52 pages. U.S. Geological Survey.   Open Access Article

See Also