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(Recommended Approach)
 
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==Passive Sampling of Sediments==
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==Estimating PCE/TCE Abiotic First-Order Reductive Dechlorination Rate Constants in Clayey Soils Under Anoxic Conditions==  
"Passive sampling" refers to a group of methods used to quantify the availability of organic contaminants to move between different media and/or to react in environmental systems such as indoor air, lake waters, or contaminated sediment beds.  To do this, the passive sampling material is deployed in the environmental system and allowed to absorb chemicals of interest via diffusive transfers from the surroundings.  Upon recovery of the passive sampler, the accumulated contaminants are measured, and the concentrations in the sampler are interpreted to infer the chemical concentrations in specific surrounding media like porewater in a sediment bed. Such data are then useful inputs for site assessments such as those seeking to quantify fluxes from contaminated sediment beds to overlying waters or to evaluate the risk of significant uptake into benthic infauna and the larger food web.
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The U.S. Department of Defense (DoD) faces many challenges in restoring aquifers at contaminated sites, often due to back-diffusion of tetrachloroethene (PCE) and trichloroethene (TCE) from low-permeability clay zones. The uptake, storage, and subsequent long-term release of these dissolved contaminants from clays are key processes in understanding the longevity, intensity, and risks associated with many persistent chlorinated ethene groundwater plumes. Although naturally occurring abiotic and biotic dechlorination processes in clays may reduce stored contaminant mass and significantly aid natural attenuation, no standardized field method currently exists to verify or quantify these reactions. It is critical to remediation design efforts to demonstrate and validate a cost-effective in situ approach for assessing these dechlorination processes using first-order rate constants. An approach was developed and applied across eight DoD sites to support Remedial Project Managers (RPMs) and regulators in evaluating natural attenuation potential in clay-rich environments.
 
<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):'''
* [[Contaminated Sediments - Introduction]]
 
* [[In Situ Treatment of Contaminated Sediments with Activated Carbon]]
 
* [[Passive Sampling of Munitions Constituents]]
 
  
'''Contributor(s):''' [[Dr. Philip M. Gschwend]]
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*[[Monitored Natural Attenuation (MNA)]]
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*[[Monitored Natural Attenuation (MNA) of Chlorinated Solvents]]
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*[[Monitored Natural Attenuation - Transitioning from Active Remedies]]
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*[[Matrix Diffusion]]
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*[[REMChlor - MD]]
  
'''Key Resource(s):'''
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'''Contributors:''' Dani Tran, Dr. Charles Schaefer, Dr. Charles Werth
* Validating the Use of Performance Reference Compounds in Passive Samplers to Assess Porewater Concentrations in Sediment Beds<ref name ="Apell2014">Apell, J.N. and Gschwend, P.M., 2014. Validating the Use of Performance Reference Compounds in Passive Samplers to Assess Porewater Concentrations in Sediment Beds.  Environmental Science and Technology, 48(17), pp. 10301-10307.  [https://doi.org/10.1021/es502694g DOI: 10.1021/es502694g]</ref>
 
  
* ''In situ'' passive sampling of sediments in the Lower Duwamish Waterway Superfund site: Replicability, comparison with ''ex situ'' measurements, and use of data<ref name="Apell2016">Apell, J.N., and Gschwend, P.M., 2016. ''In situ'' passive sampling of sediments in the Lower Duwamish Waterway Superfund site: Replicability, comparison with ''ex situ'' measurements, and use of data. Environmental Pollution, 218, pp. 95-101. [https://doi.org/10.1016/j.envpol.2016.08.023 DOI: 10.1016/j.envpol.2016.08.023]&nbsp;&nbsp; [[Media: ApellGschwend2016.pdf | Authors’ Manuscript]]</ref>
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'''Key Resource:'''
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*Schaefer, C.E, Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils (3)
  
* Laboratory, Field, and Analytical Procedures for Using Passive Sampling in the Evaluation of Contaminated Sediments: User’s Manual<ref name="Burgess2017">Burgess, R.M., Kane Driscoll, S.B., Burton, A., Gschwend, P.M., Ghosh, U., Reible, D., Ahn, S., and Thompson, T., 2017. Laboratory, Field, and Analytical Procedures for Using Passive Sampling in the Evaluation of Contaminated Sediments: User’s Manual, EPA/600/R-16/357. SERDP/ESTCP and U.S. EPA, Office of Research and Development, Washington, DC 20460. [https://cfpub.epa.gov/si/si_public_record_report.cfm?Lab=NHEERL&dirEntryID=308731 Website]&nbsp;&nbsp; [[Media: EPA600R16357.pdf | Report.pdf]]</ref>
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==Introduction==
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Cost-effective methods are needed to verify the occurrence of natural dechlorination processes and quantify their dechlorination rates in clays under ambient in situ conditions in order to reliably predict their long-term influence on plume longevity and mass discharge. However, accurately determining these rates is challenging due to slow reaction kinetics, the transient nature of transformation products, and the interplay of biotic and abiotic mechanisms within the clay matrix or at clay-sand interfaces. Tools capable of quantifying these reactions and assessing their role in mitigating plume persistence would be a significant aid for long-term site management.
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For reductive abiotic dechlorination under anoxic conditions, a 1% hydrochloric acid (HCl) extraction of a sample of native clay coupled with X-ray diffraction (XRD) data can be used as a screening level tool to estimate reductive dechlorination rate constants. These rate constants can be inserted into fate and transport models such as [[REMChlor - MD]]<ref>Falta, R., 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]&nbsp; [[Media: FaltaWang2017.pdf | Open Access Manuscript]]</ref><ref>Kulkarni, P.R., Adamson, D.T., Popovic, J., Newell, C.J., 2022. Modeling a well-charactized perfluorooctane sulfate (PFOS) source and plume using the REMChlor-MD model to account for matrix diffusion. Journal of Contaminant Hydrology, 247, Article 103986. [https://doi.org/10.1016/j.jconhyd.2022.103986 doi: 10.1016/j.jconhyd.2022.103986]&nbsp; [[Media: KulkarniEtAl2022.pdf | Open Access Manuscript]]</ref> to quantify abiotic dechlorination impacts within clay aquitards on chlorinated solvent plumes. Thus, determination of the abiotic reductive dechlorination rate constant for a particular clayey soil can be readily utilized to provide a more accurate assessment of aquifer cleanup timeframes for groundwater plumes that are being sustained by contaminant back-diffusion.
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==Recommended Approach==
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[[File: TranFig1.png | thumb | 600 px | Figure 1: First-order rate constants for abiotic reductive dechlorination of TCE under anaerobic conditions (data from this study and prior research)]]
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[[File: TranFig2.png | thumb | 600 px | Figure 2: Flowchart diagram of field screening procedures]]
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The recommended approach builds upon the methodology and findings of a recent study<ref name="SchaeferEtAl2025">Schaefer, C.E., Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils. Groundwater Monitoring and Remediation, 45(2), pp. 31-39. [https://doi.org/10.1111/gwmr.12709 doi: 10.1111/gwmr.12709]</ref>, emphasizing field-based and analytical techniques to quantify abiotic first-order reductive dechlorination rate constants for PCE and TCE in clayey soils under anoxic conditions. Key components of this evaluation are listed below:
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#<u>Zone Identification:</u> The focus of the investigation should be to delineate clayey zones adjacent to hydraulically conductive zones.
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#<u>Ferrous Mineral Quantification:</u> Assess ferrous mineral context in clay via 1% HCl extraction at ambient temperature over a 10-minute interval.
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#<u>Mineralogical Characterization:</u> Conduct XRD analysis with the specific intent of identifying the presence of pyrite and biotite.  
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#<u>Reduced Gas Analysis:</u> Measurement of reduced gases such as acetylene, ethene, and ethane concentrations in clay samples. Gas-tight sampling devices (e.g., En Core® soil samplers by En Novative Technologies, Inc.)  should be used to ensure sample integrity during collection and transport. 
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Clay samples should be collected within a few centimeters of the high-permeability interface, with optional additional sampling further inward. For mineralogical analysis, a defined interval may be collected and subsequently subsampled. To preserve sample integrity, exposure to air should be minimized during collection, transport, and handling. Homogenization should occur within an anaerobic chamber, and if subsamples are required for external analysis, they must be shipped in gas-tight, anaerobic containers.
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Estimation of the abiotic reductive first-order rate constant for PCE and TCE is based on the “reactive” ferrous content in the clay. Reactive ferrous content (Fe(II)<sub>r</sub>) is estimated as shown in Equation 1:
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::'''Equation 1:'''&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <big>''Fe(II)<sub><small>r</small></sub> = DA + XRD<sub><small>pyr</small></sub> - XRD<sub><small>biotite</small></sub>''</big>
  
==Introduction==
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where ''DA'' is the ferrous content from the dilute acid (1% HCl) extraction, ''XRD<sub><small>pyr</small></sub>'' is the pyrite content from XRD analysis, and ''XRD<sub><small>biotite</small></sub>'' is the biotite content from XRD analysis<ref name="SchaeferEtAl2025"/>.
[[File: Gschwend1w2fig1.png | thumb | 300px | Figure 1.  A representation of a clam living in a sediment bed that contains a chemical contaminant (depicted as red hexagons).  The contaminant is partly dissolved in the sediment porewater between the solid grains, and partly associated with solid phases, like natural organic matter and "black carbons" such as soots from diesel engines and chars emitted during forest fires.  All of these liquid and solid materials can exchange their contaminant loads with one another, with the distributions dependent on the chemical's relative affinity for each material.  When an animal like the clam moves into this system, the chemical is also accumulated into the animal, until the animal is also equilibrated with the other solids and liquid(s) present.]]
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Environmental media such as sediments typically contain many different materials or phases, including liquid solutions (e.g. water, [[Light Non-Aqueous Phase Liquids (LNAPLs)| nonaqueous phase liquids]]like spilled oils) and diverse solids (e.g., quartz, aluminosilicate clays, and combustion-derived soots).  Further, the chemical concentration in the porewater medium includes both molecules that are "truly dissolved" in the water and others that are associated with colloids in the porewater<ref name="Brownawell1986">Brownawell, B.J., and Farrington, J.W., 1986. Biogeochemistry of PCBs in interstitial waters of a coastal marine sediment. Geochimica et Cosmochimica Acta, 50(1), pp. 157-169.  [https://doi.org/10.1016/0016-7037(86)90061-X DOI: 10.1016/0016-7037(86)90061-X]&nbsp;&nbsp; Free download available from: [https://semspub.epa.gov/work/01/268631.pdf US EPA].</ref><ref name="Chin1992">Chin, Y.P., and Gschwend, P.M., 1992. Partitioning of Polycyclic Aromatic Hydrocarbons to Marine Porewater Organic Colloids. Environmental Science and Technology, 26(8), pp. 1621-1626.  [https://doi.org/10.1021/es00032a020 DOI: 10.1021/es00032a020]</ref><ref name="Achman1996">Achman, D.R., Brownawell, B.J., and Zhang, L., 1996. Exchange of Polychlorinated Biphenyls Between Sediment and Water in the Hudson River Estuary. Estuaries, 19(4), pp. 950-965.  [https://doi.org/10.2307/1352310 DOI: 10.2307/1352310]&nbsp;&nbsp; Free download available from: [https://www.academia.edu/download/55010335/135231020171114-2212-b93vic.pdf Academia.edu]</ref>. As a result, contaminant chemicals distribute among these diverse media (Figure 1) according to their affinity for each and the amount of each phase in the system<ref name="Gustafsson1996">Gustafsson, Ö., Haghseta, F., Chan, C., MacFarlane, J., and Gschwend, P.M., 1996. Quantification of the Dilute Sedimentary Soot Phase: Implications for PAH Speciation and Bioavailability. Environmental Science and Technology, 31(1), pp. 203-209.  [https://doi.org/10.1021/es960317s  DOI: 10.1021/es960317s]</ref><ref name="Luthy1997">Luthy, R.G., Aiken, G.R., Brusseau, M.L., Cunningham, S.D., Gschwend, P.M., Pignatello, J.J., Reinhard, M., Traina, S.J., Weber, W.J., and Westall, J.C., 1997. Sequestration of Hydrophobic Organic Contaminants by Geosorbents. Environmental Science and Technology, 31(12), pp. 3341-3347. [https://doi.org/10.1021/es970512m DOI: 10.1021/es970512m]</ref><ref name="Lohmann2005">Lohmann, R., MacFarlane, J.K., and Gschwend, P.M., 2005. Importance of Black Carbon to Sorption of Native PAHs, PCBs, and PCDDs in Boston and New York Harbor Sediments. Environmental Science and Technology, 39(1), pp.141-148. [https://doi.org/10.1021/es049424+  DOI: 10.1021/es049424+]</ref><ref name="Cornelissen2005">Cornelissen, G., Gustafsson, Ö., Bucheli, T.D., Jonker, M.T., Koelmans, A.A., and van Noort, P.C., 2005. Extensive Sorption of Organic Compounds to Black Carbon, Coal, and Kerogen in Sediments and Soils: Mechanisms and Consequences for Distribution, Bioaccumulation, and Biodegradation. Environmental Science and Technology, 39(18), pp. 6881-6895. [https://doi.org/10.1021/es050191b  DOI: 10.1021/es050191b]</ref><ref name="Koelmans2009">Koelmans, A.A., Kaag, K., Sneekes, A., and Peeters, E.T.H.M., 2009. Triple Domain in Situ Sorption Modeling of Organochlorine Pesticides, Polychlorobiphenyls, Polyaromatic Hydrocarbons, Polychlorinated Dibenzo-p-Dioxins, and Polychlorinated Dibenzofurans in Aquatic Sediments. Environmental Science and Technology, 43(23), pp. 8847-8853.  [https://doi.org/10.1021/es9021188 DOI: 10.1021/es9021188]</ref>. As such, the chemical concentration in any one medium (e.g., truly dissolved in porewater) in a multi-material system like sediment is very hard to know from measures of the total sediment concentration, which unfortunately is the information typically found by analyzing for chemicals in sediment samples.
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Abiotic dechlorination is unlikely to contribute to mitigating contaminant back-diffusion when reactive ferrous iron (Fe(II)<sub><small>r</small></sub>) concentrations are below 100 mg/kg (Figure 1). For Fe(II)<sub><small>r</small></sub> above 100 mg/kg, the first-order rate constant for PCE and TCE reductive dechlorination can be estimated using the correlation shown in Figure 1<ref name="SchaeferEtAl2018">Schaefer, C.E., Ho, P., Berns, E., Werth, C., 2018. Mechanisms for abiotic dechlorination of trichloroethene by ferrous minerals under oxic and anoxic conditions in natural sediments. Environmental Science and Technology, 52(23), pp.13747-13755. [https://doi.org/10.1021/acs.est.8b04108 doi: 10.1021/acs.est.8b04108]</ref><ref>Borden, R.C., Cha, K.Y., 2021. Evaluating the impact of back diffusion on groundwater cleanup time. Journal of Contaminant Hydrology, 243, Article 103889. [https://doi.org/10.1016/j.jconhyd.2021.103889 doi: 10.1016/j.jconhyd.2021]&nbsp; [[Media: BordenCha2021.pdf | Open Access Manuscript]]</ref>. The rate constant exhibits a strong positive correlation with the logarithm of reactive Fe(II) content (Pearson’s ''r'' = 0.82), with a slope of 4.7 × 10⁻⁸ L g⁻¹ d⁻¹ (log mg kg⁻¹)⁻¹.
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Figure 2 presents a decision flowchart designed to evaluate the significance and extent of abiotic reductive dechlorination. By applying Equation 1 to the dilute acid extractable Fe(II) plus measured mineral species data from clay samples, the reactive ferrous iron content (Fe(II)<sub><small>r</small></sub>) can be quantified, enabling a streamlined assessment of the extent to which abiotic processes are contributing to the mitigation of contaminant back-diffusion.
  
If an animal moves into this system, it will also accumulate the chemical in its tissues from the loads in all the other materials (Figure 1). This is important if one is concerned with exposures of the chemical to other organisms, including humans, who may eat such shellfish. Predicting the quantity of contaminant in the clam requires knowledge of the relative affinities of the chemical for the clam versus the sediment materials. For example, if one knew the chemical's truly dissolved concentration in the porewater and could reasonably assume the chemical of interest in the clams has mostly accumulated in its lipids (as is often the case for very hydrophobic compounds), then one could estimate the chemical concentration in the clam (''C<sub><small>clam</small></sub>'', typically in units of &mu;g/kg clam wet weight) using a lipid-water [[Wikipedia: Partition coefficient | partition coefficient]], ''K<sub><small>lipid-water</small></sub>'', typically in units of (&mu;g/kg lipid)'''/'''(&mu;g/L water), and the porewater concentration of the chemical (''C<sub><small>porewater</small></sub>'', in &mu;g/L) with Equation 1.
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==Study Design Considerations==
{|
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===Diagnostic Resin Treatments===
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Several commercially available resins have been verified for use in the iTIE system. Investigators can select resins based on stressor classes of interest at each site. Each resin selectively removes a CoC class from site water prior to organism exposure.
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*[https://www.dupont.com/products/ambersorb560.html DuPont Ambersorb 560] for removal of 1,4-dioxane and other organic chemicals<ref>Woodard, S., Mohr, T., Nickelsen, M.G., 2014. Synthetic media: A promising new treatment technology for 1,4-dioxane. Remediation Journal, 24(4), pp. 27-40. [https://doi.org/10.1002/rem.21402 doi: 10.1002/rem.21402]</ref>
| || Equation 1.
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*C18 for nonpolar organic chemicals
| style="text-align:center;"| <big>'''''C<sub><small>clam</small></sub> '''=''' f<sub><small>lipid</small></sub> '''x''' K<sub><small>lipid-water</small></sub> '''x''' C<sub><small>porewater</small></sub>'''''</big>
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*[https://www.bio-rad.com/en-us Bio-Rad] [https://www.bio-rad.com/en-us/product/chelex-100-resin?ID=6448ab3e-b96a-4162-9124-7b7d2330288e Chelex] for metals
|-
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*Granular activated carbon for metals, general organic chemicals, sulfide<ref>Lemos, B.R.S., Teixeira, I.F., de Mesquita, J.P., Ribeiro, R.R., Donnici, C.L., Lago, R.M., 2012. Use of modified activated carbon for the oxidation of aqueous sulfide. Carbon, 50(3), pp. 1386-1393. [https://doi.org/10.1016/j.carbon.2011.11.011 doi: 10.1016/j.carbon.2011.11.011]</ref>
| where:
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*[https://www.waters.com/nextgen/us/en.html Waters] [https://www.waters.com/nextgen/us/en/search.html?category=Shop&isocode=en_US&keyword=oasis%20hlb&multiselect=true&page=1&rows=12&sort=best-sellers&xcid=ppc-ppc_23916&gad_source=1&gad_campaignid=14746094146&gbraid=0AAAAAD_uR00nhlNwrhhegNh06pBODTgiN&gclid=CjwKCAiAtLvMBhB_EiwA1u6_PsppE0raci2IhvGnAAe5ijciNcetLaGZo5qA3g3r4Z_La7YAPJtzShoC6LoQAvD_BwE Oasis HLB] for general organic chemicals<ref name="SteigmeyerEtAl2017"/>
|-
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*[https://www.waters.com/nextgen/us/en.html Waters] [https://www.waters.com/nextgen/us/en/search.html?category=All&enableHL=true&isocode=en_US&keyword=Oasis%20WAX%20&multiselect=true&page=1&rows=12&sort=most-relevant Oasis WAX] for PFAS, organic chemicals of mixed polarity<ref>Iannone, A., Carriera, F., Di Fiore, C., Avino, P., 2024. Poly- and Perfluoroalkyl Substance (PFAS) Analysis in Environmental Matrices: An Overview of the Extraction and Chromatographic Detection Methods. Analytica, 5(2), pp. 187-202. [https://doi.org/10.3390/analytica5020012 doi: 10.3390/analytica5020012]&nbsp; [[Media: IannoneEtAl2024.pdf | Open Access Article]]</ref>
| || ''f<sub><small>lipid</small></sub>'' || is the fraction lipids contribute to the total wet weight of a clam (kg lipid/kg clam wet weight), and
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*Zeolite for ammonia, other organic chemicals
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| || ''C<sub><small>porewater</small></sub>'' || is the freely dissolved contaminant concentration in the porewater surrounding the clam.
 
|}
 
  
While there is a great deal of information on the values of ''K<sub><small>lipid-water</small></sub>'' for many chemicals<ref name="Schwarzenbach2017">Schwarzenbach, R.P., Gschwend, P.M., and Imboden, D.M., 2017.  Environmental Organic Chemistry, 3rd edition. Ch. 16: Equilibrium Partitioning from Water and Air to Biota, pp. 469-521. John Wiley and Sons.  ISBN: 978-1-118-76723-8</ref>, it is often very inaccurate to estimate truly dissolved porewater concentrations from total sediment concentrations using assumptions about the affinity of those chemicals for the solids in the system<ref name="Gustafsson1996"/>. Further, it is difficult to isolate porewater without colloids and/or measure the very low truly dissolved concentrations of hydrophobic contaminants of concern like [[Polycyclic Aromatic Hydrocarbons (PAHs) | polycyclic aromatic hydrocarbons (PAHs)]], [[Wikipedia: Polychlorinated biphenyl | polychlorinated biphenyls (PCBs)]], nonionic pesticides like [[Wikipedia: DDT | dichlorodiphenyltrichloroethane (DDT)]], and [[Wikipedia: Polychlorinated dibenzodioxins | polychlorinated dibenzo-p-dioxins (PCDDs)]]/[[Wikipedia: Polychlorinated dibenzofurans | dibenzofurans (PCDFs)]]<ref name="Hawthorne2005">Hawthorne, S.B., Grabanski, C.B., Miller, D.J., and Kreitinger, J.P., 2005. Solid-Phase Microextraction Measurement of Parent and Alkyl Polycyclic Aromatic Hydrocarbons in Milliliter Sediment Pore Water Samples and Determination of K<sub><small>DOC</small></sub> Values. Environmental Science and Technology, 39(8), pp. 2795-2803.  [https://doi.org/10.1021/es0405171 DOI: 10.1021/es0405171]</ref>.
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Resins must be adequately conditioned prior to use. Otherwise, they may inadequately adsorb toxicants or cause stress to organisms. New resins should be tested for efficacy and toxicity before being used in an iTIE system.  
  
==Passive Samplers==
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===Test Organism Species and Life Stages===
One approach to address this problem for contaminated sediments is to insert organic polymers like low density polyethylene (LDPE), polydimethylsiloxane (PDMS), or polyoxymethylene (POM) that can absorb such chemicals in the sediment<ref name="Mayer2000">Mayer, P., Vaes, W.H., Wijnker, F., Legierse, K.C., Kraaij, R., Tolls, J., and Hermens, J.L., 2000. Sensing Dissolved Sediment Porewater Concentrations of Persistent and Bioaccumulative Pollutants Using Disposable Solid-Phase Microextraction Fibers. Environmental Science and Technology, 34(24), pp. 5177-5183.  [https://doi.org/10.1021/es001179g DOI: 10.1021/es001179g]</ref><ref name="Booij2003">Booij, K., Hoedemaker, J.R., and Bakker, J.F., 2003. Dissolved PCBs, PAHs, and HCB in Pore Waters and Overlying Waters of Contaminated Harbor Sediments. Environmental Science and Technology, 37(18), pp. 4213-4220.  [https://doi.org/10.1021/es034147c DOI: 10.1021/es034147c]</ref><ref name="Cornelissen2008">Cornelissen, G., Pettersen, A., Broman, D., Mayer, P., and Breedveld, G.D., 2008. Field testing of equilibrium passive samplers to determine freely dissolved native polycyclic aromatic hydrocarbon concentrations. Environmental Toxicology and Chemistry, 27(3), pp. 499-508.  [https://doi.org/10.1897/07-253.1 DOI: 10.1897/07-253.1]</ref><ref name="Tomaszewski2008">Tomaszewski, J.E., and Luthy, R.G., 2008. Field Deployment of Polyethylene Devices to Measure PCB Concentrations in Pore Water of Contaminated Sediment. Environmental Science and Technology, 42(16), pp. 6086-6091.  [https://doi.org/10.1021/es800582a DOI: 10.1021/es800582a]</ref><ref name="Fernandez2009">Fernandez, L.A., MacFarlane, J.K., Tcaciuc, A.P., and Gschwend, P.M., 2009. Measurement of Freely Dissolved PAH Concentrations in Sediment Beds Using Passive Sampling with Low-Density Polyethylene Strips. Environmental Science and Technology, 43(5), pp. 1430-1436. [https://doi.org/10.1021/es802288w DOI: 10.1021/es802288w]</ref><ref name="Arp2015">Arp, H.P.H., Hale, S.E., Elmquist Kruså, M., Cornelissen, G., Grabanski, C.B., Miller, D.J., and Hawthorne, S.B., 2015. Review of polyoxymethylene passive sampling methods for quantifying freely dissolved porewater concentrations of hydrophobic organic contaminants. Environmental Toxicology and Chemistry, 34(4), pp. 710-720.  [https://doi.org/10.1002/etc.2864 DOI: 10.1002/etc.2864]&nbsp;&nbsp;  [https://setac.onlinelibrary.wiley.com/doi/epdf/10.1002/etc.2864 Free access article.]&nbsp;&nbsp; [[Media: Arp2015.pdf | Report.pdf]]</ref><ref name="Apell2016"/>. In this approach, the polymer is inserted in the sediment bed where it absorbs some of the contaminant load via the contaminant's diffusion into the polymer from the surroundings. When the polymer achieves sorptive equilibration with the sediments, the chemical concentration in the polymer, ''C<sub><small>polymer</small></sub>'' (&mu;g/kg polymer), can be used to find the corresponding concentration in the porewater,  ''C<sub><small>porewater</small></sub>'' (&mu;g/L), using a polymer-water partition coefficient, ''K<sub><small>polymer-water</small></sub>'' ((&mu;g/kg polymer)'''/'''(&mu;g/L water)), that has previously been found in laboratory testing<ref name="Lohmann2012">Lohmann, R., 2012. Critical Review of Low-Density Polyethylene’s Partitioning and Diffusion Coefficients for Trace Organic Contaminants and Implications for Its Use as a Passive Sampler. Environmental Science and Technology, 46(2), pp. 606-618.  [https://doi.org/10.1021/es202702y DOI: 10.1021/es202702y]</ref><ref name="Ghosh2014">Ghosh, U., Kane Driscoll, S., Burgess, R.M., Jonker, M.T., Reible, D., Gobas, F., Choi, Y., Apitz, S.E., Maruya, K.A., Gala, W.R., Mortimer, M., and Beegan, C., 2014. Passive Sampling Methods for Contaminated Sediments: Practical Guidance for Selection, Calibration, and Implementation. Integrated Environmental Assessment and Management, 10(2), pp. 210-223.  [https://doi.org/10.1002/ieam.1507 DOI: 10.1002/ieam.1507]&nbsp;&nbsp; [https://setac.onlinelibrary.wiley.com/doi/epdf/10.1002/ieam.1507 Free access article.]&nbsp;&nbsp; [[Media: Ghosh2014.pdf | Report.pdf]]</ref>, as shown in Equation 2.
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Practitioners can also select different organism species and life stages for use in the iTIE system, depending on site characteristics and study goals. The iTIE system can accommodate various small test organisms, including embryo-stage fish and most macroinvertebrates. The following common toxicity tests can be adapted for application within iTIE systems<ref>U.S. Environmental Protection Agency, Office of Solid Waste and Emergency Response, 1994. Catalogue of Standard Toxicity Tests for Ecological Risk Assessment. ECO Update, 2(2), 4 pages. Publication No. 9345.0.05I [https://www.epa.gov/sites/default/files/2015-09/documents/v2no2.pdf Free Download]&nbsp; [[Media: usepa1994.pdf | Report.pdf]]</ref>.
{|
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<ul><u>Freshwater acute toxicity:</u></ul>
|
+
*[[Wikipedia: Daphnia magna | ''Daphnia magna'']] or [[Wikipedia: Daphnia pulex | ''Daphnia pulex'']] 24-, 48-, and 96-hour survival
|-
+
<ul><u>Freshwater chronic toxicity:</u></ul>
|&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;|| Equation&nbsp;2.
+
*[[Wikipedia: Ceriodaphnia dubia | ''Ceriodaphnia dubia'']]  7-day survival and reproduction
| style="width:600px; text-align:center;" | <big>'''''C<sub><small>porewater</small></sub> '''=''' C<sub><small>polymer</small></sub> '''/''' K<sub><small>polymer-water</small></sub>'''''</big>
+
*''D. magna'' 7-day survival and reproduction
|}
+
*[[Wikipedia: Fathead minnow | ''Pimephales promelas'']] 7-day embryo-larval survival and teratogenicity
 +
*[[Wikipedia: Hyalella azteca | ''Hyalella Azteca'']] 10- or 30-day survival and reproduction
 +
<ul><u>Marine acute toxicity:</u></ul>
 +
*[[Wikipedia: Americamysis bahia | ''Americamysis bahia'']] 24- and 48-hour survival
 +
<ul><u>Marine chronic toxicity:</u></ul>
 +
*''Americamysis'' survival, growth and fecundity
 +
*[[Wikipedia: Topsmelt silverside | ''Atherinops affinis'']] embryo-larval survival and growth
  
Such “passive uptake” by the polymer also reflects the availability of the chemicals for transport to adjacent systems (e.g., overlying surface waters) and for uptake into organisms (e.g., [[Wikipedia: Bioaccumulation | bioaccumulation]]).  Thus, one can use the porewater concentrations to estimate the biotic accumulation of the chemicals, too.  For example, for the concentration in the clam equilibrated with the sediment, ''C<sub><small>clam</small></sub>'' (&mu;g/kg clam), would be found by combining Equations 1 and 2 to get Equation 3.
+
Acute toxicity is quantifiable via organism survival rates immediately following the termination of an iTIE system field deployment. Chronic toxicity can be quantified by continuing to culture and observe test organisms in-lab. Common chronic endpoints include stunted growth, altered development such as teratogenicity in larval fish, decreased reproduction rates, and changes in gene expression.  
{|
 
|
 
|-
 
|&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;|| Equation&nbsp;3.
 
|style="width:700px; text-align:center;" |<big>'''''C<sub><small>clam</small></sub> '''=''' f<sub><small>lipid</small></sub> '''x''' K<sub><small>lipid-water</small></sub> '''x''' C<sub><small>polymer</small></sub> '''/''' K<sub><small>polymer-water</small></sub>'''''</big>
 
|}
 
[[File: Gschwend1w2fig2a.png | thumb | 300px | Figure 2a.  Plot of the initial concentrations of a PRC (green lines) in a polyethylene (PE) sheet inserted in a sediment showing constant concentration across the PE and zero concentration outside the PE. At the same time, a target contaminant of interest (red lines) initially has a constant concentration in the sediment outside the PE and zero concentration inside the PE.]][[File: Gschwend1w2fig2b.png | thumb | 300px | Figure 2b.  After the PE has been deployed for a time, the PRC is depleted from the PE (green lines), especially near the surfaces contacting the sediment, and its concentration is building up outside the PE and diffusing away into the sediment.  Meanwhile, the target chemical leaves the sediment and begins to diffuse into the PE (red lines).  The "jumps" in concentration  at the PE-sediment boundary reflect the equilibrium paritioning coefficient, ''K<sub>PE-sed</sub> = C<sub>PE</sub>/C<sub>sediment</sub>''.]]
 
  
==Performance Reference Compounds (PRCs)==
+
Several gene expression endpoints have been detectable in bioassays following an iTIE system deployment and in-lab culturing period. Steigmeyer ''et al.''<ref name="SteigmeyerEtAl2017"/> were able to detect changes in the expression of two genes in ''D. magna'' after a 24-hour exposure to bisphenol A. In a separate study, Nichols<ref>Nichols, E., 2023. Methods for Identification and Prioritization of Stressors at Impaired Sites. Masters thesis, University of Michigan. University of Michigan Library Deep Blue Documents. [https://deepblue.lib.umich.edu/bitstream/handle/2027.42/176142/Nichols_Elizabeth_thesis.pdf?sequence=1 Free Download]&nbsp; [[Media: Nichols2023.pdf | Report.pdf]]</ref> found a significant decline in acetylcholinesterase activity in ''H. azteca'' after a 24-hour exposure to chlorpyrifos. These results indicate a potential to adapt other gene expression bioassays for use in conjunction with iTIE system field exposures to prove stressor-causality linkages.
Perhaps unsurprisingly, pollutants with low water solubility like PAHs, PCBs, etc. do not diffuse quickly through sediment beds.  As a result, their accumulation in polymeric materials in sediments can take a long time to achieve equilibration<ref name="Fernandez2009b">Fernandez, L. A., Harvey, C.F., and Gschwend, P.M., 2009. Using Performance Reference Compounds in Polyethylene Passive Samplers to Deduce Sediment Porewater Concentrations for Numerous Target Chemicals. Environmental Science and Technology, 43(23), pp. 8888-8894. [https://doi.org/10.1021/es901877a DOI: 10.1021/es901877a]</ref><ref name="Lampert2015">Lampert, D.J., Thomas, C., and Reible, D.D., 2015. Internal and external transport significance for predicting contaminant uptake rates in passive samplers. Chemosphere, 119, pp. 910-916. [https://doi.org/10.1016/j.chemosphere.2014.08.063 DOI: 10.1016/j.chemosphere.2014.08.063]&nbsp;&nbsp; Free download available from: [https://www.academia.edu/download/44146586/chemosphere_2014.pdf Academia.edu]</ref><ref name="Apell2016b">Apell, J.N., Tcaciuc, A.P., and Gschwend, P.M., 2016. Understanding the rates of nonpolar organic chemical accumulation into passive samplers deployed in the environment: Guidance for passive sampler deployments. Integrated Environmental Assessment and Management, 12(3), pp. 486-492.  [https://doi.org/10.1002/ieam.1697 DOI: 10.1002/ieam.1697]</ref>. This problem was recognized previously for passive samplers called [[Wikipedia: Semipermeable membrane devices | semipermeable membrane devices]] (SPMDs, e.g. polyethylene bags filled with triolein<ref name="Huckins2002">Huckins, J.N., Petty, J.D., Lebo, J.A., Almeida, F.V., Booij, K., Alvarez, D.A., Cranor, W.L., Clark, R.C., and Mogensen, B.B., 2002. Development of the Permeability/Performance Reference Compound Approach for In Situ Calibration of Semipermeable Membrane Devices. Environmental Science and Technology, 36(1), pp. 85-91.  [https://doi.org/10.1021/es010991w DOI: 10.1021/es010991w]</ref>) that were deployed in surface waters. As a result, representative chemicals called performance reference compound (PRCs) were dosed inside the samplers before their deployment in the environment, and the PRCs' diffusive losses out of the SPMD could be used to quantify the fractional approach toward sampler-environmental surroundings equilibration<ref name="Booij2002">Booij, K., Smedes, F., and van Weerlee, E.M., 2002. Spiking of performance reference compounds in low density polyethylene and silicone passive water samplers. Chemosphere 46(8), pp.1157-1161. [https://doi.org/10.1016/S0045-6535(01)00200-4 DOI: 10.1016/S0045-6535(01)00200-4]</ref><ref name="Huckins2002"/>. A similar approach can be used for polymers inserted in sediment beds<ref name="Fernandez2009b"/><ref name="Apell2014"/>. Commonly, isotopically labeled forms of the compounds of interest such as deuterated or <sup>13</sup>C-labelled PAHs or PCBs are homogeneously impregnated into the polymers before their deployments.  Upon insertion of the polymer into the sediment bed (or overlying waters or even air), the initially evenly distributed PRCs begin to diffuse out of the sampling polymer and  into the sediment (Figure 2).  
 
  
Assuming the contaminants of interest undergo the same mass transfer restrictions limiting their rates of uptake into the polymer (e.g., diffusion through the sedimentary porous medium) that are also limiting transfers of the PRCs out of the polymer<ref name="Fernandez2009b"/><ref name="Apell2014"/>, then fractional losses of the PRCs during a particular deployment can be used to adjust the accumulated contaminant loads to what they would have been at equilibrium with their surroundings with Equation 4.
+
===Cost Effectiveness Study===
{|
+
Burton ''et al.''<ref name="BurtonEtAl2020"/> conducted a cost effectiveness study comparing the iTIE technology with the traditional US EPA Phase 1 TIE method. Comparisons were based on the estimated time required to complete various sub-tasks within each method. Sub-tasks included organism care, equipment preparation, mobilization and deployment, test maintenance, test termination, demobilization, and test termination analyses. It was ultimately estimated that the iTIE protocol requires 47% less time (67 fewer hours) to complete than the Phase 1 TIE method, with the largest time differences in equipment preparation, deployment, test maintenance, and demobilization. It is important to note that the iTIE method may require additional initial costs for equipment and training.
|
 
|-
 
| || Equation 4.
 
| style="text-align:center;"| <big>'''''C(<sub>&infin;</sub>)<sub><small>polymer</small></sub> '''=''' C(<small>t</small>)<sub><small>polymer</small></sub> '''/''' f<sub><small>PRC lost</small></sub>'''''</big>
 
|-
 
| where:
 
|-
 
| || ''f<sub><small>PRC lost</small></sub>'' || is the fraction of the PRC lost to outward diffusion,  
 
|-
 
| || ''C(<sub>&infin;</sub>)<sub><small>polymer</small></sub>'' || is the concentration of the contaminant in the polymer at equilibrium, and
 
|-
 
| || ''C(<small>t</small>)<sub><small>polymer</small></sub>'' || is the concentration of the contaminant in the polymer after deployment time, t.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
 
|}
 
  
Since investigators are commonly interested in many chemicals at the same time, it is impractical to have a PRC for each contaminant of interest. Instead, a representative set of PRCs is used to characterize the rates of polymer-environment exchange as a function of the PRCs' properties (e.g., diffusivities, partition coefficients), the sediments characteristics (e.g., porosity), and the nature of the polymer used (e.g., film thickness, affinity for the chemicals)<ref name="Fernandez2009b"/><ref name="Lampert2015"/>. The resulting mass transfer model fit can then be used to estimate the fractional approaches to equilibrium for many other contaminants, whose diffusive and partitioning properties are also known. And these fractions can be used to adjust the target chemical concentrations that have accumulated from the sediment into the same polymeric sampler to find the equilibrated results<ref name="Apell2014"/>. Finally, these equilibrated concentrations can be used in Eq. 2 to estimate truly dissolved contaminant concentrations in the sediment's porewater.
+
==Field Application==
 +
[[File: CraneFig6.png | thumb | left | 400px | Figure 6. iTIES deployment at the Rouge River, Detroit, MI.  In the foreground is the iTIE Cooler Sub-System, which contains iTIE resin treatments and test organism groups, as well as the oxygenation coil and sample collection bottles. Next to the iTIE Cooler are the two pump cases. The Trident can be seen above the pump cases, installed in the river channel near shore.]]
 +
The&nbsp;iTIE&nbsp;system&nbsp;has&nbsp;been successfully deployed at a variety of marine and freshwater sites during the proof-of-concept phase of prototype development. One example is the 2024 iTIE system deployment completed near the mouth of the Rouge River in Detroit, MI (Figure 6). The Rouge River watershed has a long history of industrialization, with a legacy of chemical dumping, channelization, damming, and urban runoff<ref>Ridgway, J., Cave, K., DeMaria, A., O’Meara, J., Hartig, J. H., 2018. The Rouge River Area of Concern—A multi-year, multi-level successful approach to restoration of Impaired Beneficial Uses. Aquatic Ecosystem Health and Management, 21(4), pp. 398-408. [https://doi.org/10.1080/14634988.2018.1528816 doi: 10.1080/14634988.2018.1528816]</ref>. This has led to degraded environmental conditions, with previous detections of a wide range of chemicals including heavy metals and various organics.
  
==Field Applications==
+
[[File: CraneFig7.png | thumb | 300px | Figure 7. Survival and healthy development of ''P. promelas'' embryos and larvae following a 48-hour iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater as embryos for 48 hours and cultured post-exposure for an additional 5 days.]]
[[File: Gschwend1w2fig3.png | thumb | 300px | Figure 3. Passive sampler system made of polyethylene sheet loaded into an aluminum sheet metal frame, before (left), during (middle), and after (right) deployment in sediment.]]
+
[[File: CraneFig8.png | thumb | 300px | Figure 8. Survival of ''C. dilutus'' larvae after an iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater for 48 hours and cultured post-exposure for an additional 5 days. Error bars show standard deviation.]]
Polymeric materials can be deployed in sediment in various ways<ref name="Burgess2017"/>. PDMS coatings on silica rods, called SPMEs (solid phase micro extraction devices), can be incorporated into slotted rods, while thin sheets of polymers like LDPE or POM can be incorporated into sheet metal frames.  In both cases, such hardware is used to insert the polymers into sediment beds (Figure 3).
+
An&nbsp;iTIE&nbsp;system&nbsp;deployment&nbsp;was designed and completed to determine which chemical classes are most responsible for causing toxicity at the site. Resin treatments included glass wool (inert, non-fractionating substance), Chelex (metals sorption), Oasis HLB (general organics sorption), and Oasis WAX (organics sorption, with a high affinity for PFAS). The study utilized fathead minnow (''P. promelas'') embryos, due to their relative sensitivity to metals and PAHs, as well as second-instar midge ([[Wikipedia: Chironomus |''Chironomus dilutus'']]) larvae due to their relative sensitivity to PFAS.  
  
Deployment of the assembled passive samplers can be done via poles from a boat<ref name="Apell2014"/>, by divers<ref name="Apell2016"/>, or by attaching the samplers to a sampling platform lowered off a vessel<ref name="Fernandez2012">Fernandez, L.A., Lao, W., Maruya, K.A., White, C., Burgess, R.M., 2012. Passive Sampling to Measure Baseline Dissolved Persistent Organic Pollutant Concentrations in the Water Column of the Palos Verdes Shelf Superfund Site. Environmental Science and Technology, 46(21), pp. 11937-11947.  [https://doi.org/10.1021/es302139y DOI: 10.1021/es302139y]</ref>. Typically, the method used depends on the water depth.  Small buoys on short lines, sometimes with associated water-sampling polymeric materials in mesh bags (see right panel of Figure 3), are attached to the samplers to facilitate the sampler recoveries.  After recovery, the samplers are wiped to remove any adhering sediment, biofilm, or precipitates and returned to the laboratory for PRC and target contaminant analyses. The resulting measurements of the accumulated target chemical concentrations can be adjusted using the observed PRC losses and publicly available software programs<ref name="Gschwend2014">Gschwend, P.M., Tcaciuc, A.P., and Apell, J.N., 2014. Guidance Document: Passive PE Sampling in Support of In Situ Remediation of Contaminated Sediments – Passive Sampler PRC Calculation Software User’s Guide, US Department of Defense, Environmental Security Technology Certification Program Project ER-200915. Available from: [https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Sediments/Bioavailability/ER-200915 ESTCP].</ref><ref name="Thompson2015">Thompson, J.M., Hsieh, C.H. and Luthy, R.G., 2015. Modeling Uptake of Hydrophobic Organic Contaminants into Polyethylene Passive Samplers. Environmental Science and Technology, 49(4), pp. 2270-2277.  [https://doi.org/10.1021/es504442s DOI: 10.1021/es504442s]</ref>.
+
The test organisms were exposed to fractionated porewater ''in situ'' for 48 hours. Following exposure, organisms were cultured for an additional five days, and survival was recorded (Figures 7 and 8). Moderate declines in survival were seen in both species in the glass wool treatment, indicating toxicity at the site. For ''P. promelas'', the highest proportion of healthy development occurred in the Chelex treatment, supporting the hypothesis that metals are a dominant cause of toxicity. ''C. dilutus'' had the greatest survival in the Oasis WAX treatment, suggesting that an organic stressor class like PFAS is also present at harmful concentrations in the river.
  
Subsequently, since the passive sampling reveals the concentrations of contaminants in a sediment bed's porewater and the overlying bottom water<ref name="Booij2003"/>, the data can be used to estimate bed-to-water column diffusive fluxes of contaminants<ref name="Koelmans2010">Koelmans, A.A., Poot, A., De Lange, H.J., Velzeboer, I., Harmsen, J., and van Noort, P.C.M., 2010. Estimation of In Situ Sediment-to-Water Fluxes of Polycyclic Aromatic Hydrocarbons, Polychlorobiphenyls and Polybrominated Diphenylethers. Environmental Science and Technology, 44(8), pp. 3014-3020.  [https://doi.org/10.1021/es903938z DOI: 10.1021/es903938z]</ref><ref name="Fernandez2012"/> and bioirrigation-affected fluxes<ref name="Apell2018">Apell, J.N., Shull, D.H., Hoyt, A.M., and Gschwend, P.M., 2018. Investigating the Effect of Bioirrigation on In Situ Porewater Concentrations and Fluxes of Polychlorinated Biphenyls Using Passive Samplers.  Environmental Science and Technology, 52(8), pp. 4565-4573.  [https://doi.org/10.1021/acs.est.7b05809 DOI: 10.1021/acs.est.7b05809]</ref>. The data are also useful for assessing the tendency of the contaminants to accumulate in benthic organisms<ref name="Vinturella2004">Vinturella, A.E., Burgess, R.M., Coull, B.A., Thompson, K.M., and Shine, J.P., 2004. Use of Passive Samplers to Mimic Uptake of Polycyclic Aromatic Hydrocarbons by Benthic Polychaetes. Environmental Science and Technology, 38(4), pp. 1154-1160.  [https://doi.org/10.1021/es034706f DOI: 10.1021/es034706f]</ref><ref name="Yates2011">Yates, K., Pollard, P., Davies, I.M., Webster, L., and Moffat, C.F., 2011. Application of silicone rubber passive samplers to investigate the bioaccumulation of PAHs by Nereis virens from marine sediments. Environmental Pollution, 159(12), pp. 3351-3356.  [https://doi.org/10.1016/j.envpol.2011.08.038 DOI: 10.1016/j.envpol.2011.08.038]</ref><ref name="Fernandez2015">Fernandez, L.A. and Gschwend, P.M., 2015.  Predicting bioaccumulation of polycyclic aromatic hydrocarbons in soft-shelled clams  (Mya arenaria) using field deployments of polyethylene passive samplers.  Environmental Toxicology and Chemistry, 34(5), pp. 993-1000.  [https://doi.org/10.1002/etc.2892 DOI: 10.1002/etc.2892]</ref>, and by extension into food webs that include such benthic species<ref name="vonStackelberg2017">von Stackelberg, K., Williams, M.A., Clough, J., and Johnson, M.S., 2017. Spatially explicit bioaccumulation modeling in aquatic environments: Results from 2 demonstration sites. Integrated Environmental Assessment and Management, 13(6), pp. 1023-1037.  [https://doi.org/10.1002/ieam.1927 DOI: 10.1002/ieam.1927]</ref>. Furthermore, recent efforts have found that passive sampling observations can be used to infer ''in situ'' transformations of substances like nitro aromatic compounds<ref name="Belles2016">Belles, A., Alary, C., Criquet, J., and Billon, G., 2016. A new application of passive samplers as indicators of in-situ biodegradation processes. Chemosphere, 164, pp. 347-354.  [https://doi.org/10.1016/j.chemosphere.2016.08.111 DOI: 10.1016/j.chemosphere.2016.08.111]</ref> and DDT<ref name="Tcaciuc2018">Tcaciuc, A.P., Borrelli, R., Zaninetta, L.M., and Gschwend, P.M., 2018. Passive sampling of DDT, DDE and DDD in sediments: accounting for degradation processes with reaction–diffusion modeling. Environmental Science: Processes and Impacts, 20(1), pp. 220-231.  [https://doi.org/10.1039/C7EM00501F DOI: 10.1039/C7EM00501F]&nbsp;&nbsp; Open access article available from: [https://pubs.rsc.org/--/content/articlehtml/2018/em/c7em00501f Royal Society of Chemistry].</ref>.
+
Water chemical analyses of fractionated and unfractionated water samples were completed to support biological results. Analyses were conducted for a range of stressor classes including metals, PAHs, PCBs, an organophosphate pesticide (chlorpyrifos), a PFAS compound (PFOS) and a pyrethroid insecticide (permethrin). Of these analytes, only heavy metals and PFOS were detected. Some chemical classes including PAHs and PCBs were not detected at the site.
 +
To reach similar conclusions using traditional Phase 1 TIE methods, one would need to complete the following tests: baseline toxicity, filtration, aeration, EDTA, C18 SPE, and methanol elution of C18 SPE. The iTIE method allows the same conclusions to be drawn with significantly less time and effort required.
  
<br clear="left" />
+
==Summary==
 +
The ''in situ'' Toxicity Identification Evaluation technology and protocol is a powerful tool that investigators can use to strengthen causal linkages between chemical stressors and ecological toxicity. By fractionating sampled water and exposing test organisms ''in situ'', investigators can gather toxicity response data while minimizing sample manipulation and accurately representing environmental conditions.
 +
<br clear="right"/>
  
 
==References==
 
==References==
 
<references />
 
<references />
 +
 
==See Also==
 
==See Also==

Latest revision as of 15:58, 14 April 2026

Estimating PCE/TCE Abiotic First-Order Reductive Dechlorination Rate Constants in Clayey Soils Under Anoxic Conditions

The U.S. Department of Defense (DoD) faces many challenges in restoring aquifers at contaminated sites, often due to back-diffusion of tetrachloroethene (PCE) and trichloroethene (TCE) from low-permeability clay zones. The uptake, storage, and subsequent long-term release of these dissolved contaminants from clays are key processes in understanding the longevity, intensity, and risks associated with many persistent chlorinated ethene groundwater plumes. Although naturally occurring abiotic and biotic dechlorination processes in clays may reduce stored contaminant mass and significantly aid natural attenuation, no standardized field method currently exists to verify or quantify these reactions. It is critical to remediation design efforts to demonstrate and validate a cost-effective in situ approach for assessing these dechlorination processes using first-order rate constants. An approach was developed and applied across eight DoD sites to support Remedial Project Managers (RPMs) and regulators in evaluating natural attenuation potential in clay-rich environments.

Related Article(s):

Contributors: Dani Tran, Dr. Charles Schaefer, Dr. Charles Werth

Key Resource:

  • Schaefer, C.E, Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils (3)

Introduction

Cost-effective methods are needed to verify the occurrence of natural dechlorination processes and quantify their dechlorination rates in clays under ambient in situ conditions in order to reliably predict their long-term influence on plume longevity and mass discharge. However, accurately determining these rates is challenging due to slow reaction kinetics, the transient nature of transformation products, and the interplay of biotic and abiotic mechanisms within the clay matrix or at clay-sand interfaces. Tools capable of quantifying these reactions and assessing their role in mitigating plume persistence would be a significant aid for long-term site management.

For reductive abiotic dechlorination under anoxic conditions, a 1% hydrochloric acid (HCl) extraction of a sample of native clay coupled with X-ray diffraction (XRD) data can be used as a screening level tool to estimate reductive dechlorination rate constants. These rate constants can be inserted into fate and transport models such as REMChlor - MD[1][2] to quantify abiotic dechlorination impacts within clay aquitards on chlorinated solvent plumes. Thus, determination of the abiotic reductive dechlorination rate constant for a particular clayey soil can be readily utilized to provide a more accurate assessment of aquifer cleanup timeframes for groundwater plumes that are being sustained by contaminant back-diffusion.

Recommended Approach

File:TranFig1.png
Figure 1: First-order rate constants for abiotic reductive dechlorination of TCE under anaerobic conditions (data from this study and prior research)
File:TranFig2.png
Figure 2: Flowchart diagram of field screening procedures

The recommended approach builds upon the methodology and findings of a recent study[3], emphasizing field-based and analytical techniques to quantify abiotic first-order reductive dechlorination rate constants for PCE and TCE in clayey soils under anoxic conditions. Key components of this evaluation are listed below:

  1. Zone Identification: The focus of the investigation should be to delineate clayey zones adjacent to hydraulically conductive zones.
  2. Ferrous Mineral Quantification: Assess ferrous mineral context in clay via 1% HCl extraction at ambient temperature over a 10-minute interval.
  3. Mineralogical Characterization: Conduct XRD analysis with the specific intent of identifying the presence of pyrite and biotite.
  4. Reduced Gas Analysis: Measurement of reduced gases such as acetylene, ethene, and ethane concentrations in clay samples. Gas-tight sampling devices (e.g., En Core® soil samplers by En Novative Technologies, Inc.) should be used to ensure sample integrity during collection and transport.

Clay samples should be collected within a few centimeters of the high-permeability interface, with optional additional sampling further inward. For mineralogical analysis, a defined interval may be collected and subsequently subsampled. To preserve sample integrity, exposure to air should be minimized during collection, transport, and handling. Homogenization should occur within an anaerobic chamber, and if subsamples are required for external analysis, they must be shipped in gas-tight, anaerobic containers.

Estimation of the abiotic reductive first-order rate constant for PCE and TCE is based on the “reactive” ferrous content in the clay. Reactive ferrous content (Fe(II)r) is estimated as shown in Equation 1:

Equation 1:       Fe(II)r = DA + XRDpyr - XRDbiotite

where DA is the ferrous content from the dilute acid (1% HCl) extraction, XRDpyr is the pyrite content from XRD analysis, and XRDbiotite is the biotite content from XRD analysis[3].

Abiotic dechlorination is unlikely to contribute to mitigating contaminant back-diffusion when reactive ferrous iron (Fe(II)r) concentrations are below 100 mg/kg (Figure 1). For Fe(II)r above 100 mg/kg, the first-order rate constant for PCE and TCE reductive dechlorination can be estimated using the correlation shown in Figure 1[4][5]. The rate constant exhibits a strong positive correlation with the logarithm of reactive Fe(II) content (Pearson’s r = 0.82), with a slope of 4.7 × 10⁻⁸ L g⁻¹ d⁻¹ (log mg kg⁻¹)⁻¹.

Figure 2 presents a decision flowchart designed to evaluate the significance and extent of abiotic reductive dechlorination. By applying Equation 1 to the dilute acid extractable Fe(II) plus measured mineral species data from clay samples, the reactive ferrous iron content (Fe(II)r) can be quantified, enabling a streamlined assessment of the extent to which abiotic processes are contributing to the mitigation of contaminant back-diffusion.

Study Design Considerations

Diagnostic Resin Treatments

Several commercially available resins have been verified for use in the iTIE system. Investigators can select resins based on stressor classes of interest at each site. Each resin selectively removes a CoC class from site water prior to organism exposure.

  • DuPont Ambersorb 560 for removal of 1,4-dioxane and other organic chemicals[6]
  • C18 for nonpolar organic chemicals
  • Bio-Rad Chelex for metals
  • Granular activated carbon for metals, general organic chemicals, sulfide[7]
  • Waters Oasis HLB for general organic chemicals[8]
  • Waters Oasis WAX for PFAS, organic chemicals of mixed polarity[9]
  • Zeolite for ammonia, other organic chemicals

Resins must be adequately conditioned prior to use. Otherwise, they may inadequately adsorb toxicants or cause stress to organisms. New resins should be tested for efficacy and toxicity before being used in an iTIE system.

Test Organism Species and Life Stages

Practitioners can also select different organism species and life stages for use in the iTIE system, depending on site characteristics and study goals. The iTIE system can accommodate various small test organisms, including embryo-stage fish and most macroinvertebrates. The following common toxicity tests can be adapted for application within iTIE systems[10].

    Freshwater acute toxicity:
    Freshwater chronic toxicity:
    Marine acute toxicity:
    Marine chronic toxicity:
  • Americamysis survival, growth and fecundity
  • Atherinops affinis embryo-larval survival and growth

Acute toxicity is quantifiable via organism survival rates immediately following the termination of an iTIE system field deployment. Chronic toxicity can be quantified by continuing to culture and observe test organisms in-lab. Common chronic endpoints include stunted growth, altered development such as teratogenicity in larval fish, decreased reproduction rates, and changes in gene expression.

Several gene expression endpoints have been detectable in bioassays following an iTIE system deployment and in-lab culturing period. Steigmeyer et al.[8] were able to detect changes in the expression of two genes in D. magna after a 24-hour exposure to bisphenol A. In a separate study, Nichols[11] found a significant decline in acetylcholinesterase activity in H. azteca after a 24-hour exposure to chlorpyrifos. These results indicate a potential to adapt other gene expression bioassays for use in conjunction with iTIE system field exposures to prove stressor-causality linkages.

Cost Effectiveness Study

Burton et al.[12] conducted a cost effectiveness study comparing the iTIE technology with the traditional US EPA Phase 1 TIE method. Comparisons were based on the estimated time required to complete various sub-tasks within each method. Sub-tasks included organism care, equipment preparation, mobilization and deployment, test maintenance, test termination, demobilization, and test termination analyses. It was ultimately estimated that the iTIE protocol requires 47% less time (67 fewer hours) to complete than the Phase 1 TIE method, with the largest time differences in equipment preparation, deployment, test maintenance, and demobilization. It is important to note that the iTIE method may require additional initial costs for equipment and training.

Field Application

Figure 6. iTIES deployment at the Rouge River, Detroit, MI. In the foreground is the iTIE Cooler Sub-System, which contains iTIE resin treatments and test organism groups, as well as the oxygenation coil and sample collection bottles. Next to the iTIE Cooler are the two pump cases. The Trident can be seen above the pump cases, installed in the river channel near shore.

The iTIE system has been successfully deployed at a variety of marine and freshwater sites during the proof-of-concept phase of prototype development. One example is the 2024 iTIE system deployment completed near the mouth of the Rouge River in Detroit, MI (Figure 6). The Rouge River watershed has a long history of industrialization, with a legacy of chemical dumping, channelization, damming, and urban runoff[13]. This has led to degraded environmental conditions, with previous detections of a wide range of chemicals including heavy metals and various organics.

Figure 7. Survival and healthy development of P. promelas embryos and larvae following a 48-hour iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater as embryos for 48 hours and cultured post-exposure for an additional 5 days.
Figure 8. Survival of C. dilutus larvae after an iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater for 48 hours and cultured post-exposure for an additional 5 days. Error bars show standard deviation.

An iTIE system deployment was designed and completed to determine which chemical classes are most responsible for causing toxicity at the site. Resin treatments included glass wool (inert, non-fractionating substance), Chelex (metals sorption), Oasis HLB (general organics sorption), and Oasis WAX (organics sorption, with a high affinity for PFAS). The study utilized fathead minnow (P. promelas) embryos, due to their relative sensitivity to metals and PAHs, as well as second-instar midge (Chironomus dilutus) larvae due to their relative sensitivity to PFAS.

The test organisms were exposed to fractionated porewater in situ for 48 hours. Following exposure, organisms were cultured for an additional five days, and survival was recorded (Figures 7 and 8). Moderate declines in survival were seen in both species in the glass wool treatment, indicating toxicity at the site. For P. promelas, the highest proportion of healthy development occurred in the Chelex treatment, supporting the hypothesis that metals are a dominant cause of toxicity. C. dilutus had the greatest survival in the Oasis WAX treatment, suggesting that an organic stressor class like PFAS is also present at harmful concentrations in the river.

Water chemical analyses of fractionated and unfractionated water samples were completed to support biological results. Analyses were conducted for a range of stressor classes including metals, PAHs, PCBs, an organophosphate pesticide (chlorpyrifos), a PFAS compound (PFOS) and a pyrethroid insecticide (permethrin). Of these analytes, only heavy metals and PFOS were detected. Some chemical classes including PAHs and PCBs were not detected at the site. To reach similar conclusions using traditional Phase 1 TIE methods, one would need to complete the following tests: baseline toxicity, filtration, aeration, EDTA, C18 SPE, and methanol elution of C18 SPE. The iTIE method allows the same conclusions to be drawn with significantly less time and effort required.

Summary

The in situ Toxicity Identification Evaluation technology and protocol is a powerful tool that investigators can use to strengthen causal linkages between chemical stressors and ecological toxicity. By fractionating sampled water and exposing test organisms in situ, investigators can gather toxicity response data while minimizing sample manipulation and accurately representing environmental conditions.

References

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  13. ^ Ridgway, J., Cave, K., DeMaria, A., O’Meara, J., Hartig, J. H., 2018. The Rouge River Area of Concern—A multi-year, multi-level successful approach to restoration of Impaired Beneficial Uses. Aquatic Ecosystem Health and Management, 21(4), pp. 398-408. doi: 10.1080/14634988.2018.1528816

See Also