RISK e Learning Bioavailability – Metals, Organics, and Use at Hazardous Waste Sites June 11 th, 2008 Session 2: “Bioavailability of Organic Compounds:

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RISK e Learning Bioavailability – Metals, Organics, and Use at Hazardous Waste Sites June 11 th, 2008 Session 2: “Bioavailability of Organic Compounds: Methods and Case Studies” Dr. Edward Neuhauser, National Grid Determining True PAH Bioavailability in Sediments Using Solid-Phase Microextraction (SPME) Dr. Danny Reible, University of Texas at Austin Defining the Availability and Mobility of Contaminants in Sediments 1

Determining True PAH Bioavailability in Sediments Using Solid-Phase Microextraction (SPME) Ed Neuhauser, PhD National Grid June 11,

Traditional Management Approaches Use NOAA Sediment Screening Criteria TEC – Threshold Effect Concentration 1.6 PEC – Probable Effect Concentration22.8 MacDonald et. al. (2000) - Freshwater Total PAH 16 (mg/kg) Long et. al. (1998) - Marine ERL – Effects Range Low 4.0 ERM – Effects Range Median44.8 3

Total [PAH 16 ] Sediment Screening Approach Toxicity Not Expected Toxicity Uncertain Toxicity Expected (MacDonald et. al. 2000) 4

Pore Water [PAH 34 ] Provides True Bioavailability –Porewater is “the most accurate indicator of bioavailable exposure concentration” (USEPA 2007) –Solid-Phase Microextraction (SPME) Applied to >240 sediment samples (precise) Rapid – 60 minute cycle time Small sample size: ~ 20 ml of sediment ~ 1.5 ml of pore water Low detection limit: ~ pg/mL (ppt) (sensitive) (Hawthorne et. al. 2005) 5

SCBA Approach Builds Upon Existing EPA Framework Convert Bioavailable PAH Concentrations to Toxic Units Measure 34 PAHs in Sediment (NOAA PAH 34 ) Use Equilibrium Partitioning to Estimate Bioavailable PAH Concentrations Sum PAH Toxic Units (TU 34 ) If TU 34 > 1, Toxicity is Expected SPME pore water PAH 34 concentration U.S. EPA (2007 Draft) Evaluating ecological risk to invertebrate receptors from PAHs in sediments at hazardous waste sites 6

K oc Values Vary 1,000-fold in Sediments Lower Bioavailability PAHs NAP ACEY ACE FLU PHE ANT FLUA PYR BAA CHR BbkF BEP BAP PER IND DAH BGP Log 10 K OC EPA log 10 Koc Value (4.5) = 31,200 U.S. EPA 2003 log 10 K oc Value (4.5) = 31,200 Measured Mean log 10 Koc Value (5.3) = 182,000 Measured Mean log 10 K oc Value (5.3) = 182,000 N=114 (Hawthorneet al.2006) Log 10 K OC 7

Urban River Sediments Contain Natural and Anthropogenic Carbon oxidized coal charcoal coke coal tar pitch cenosphere bituminous coal soot carbon anthracite coal lignitewood PAH binding (K oc ) is very different for different types of carbon. Quantity and type of carbon are important! (U. Ghosh et al. 2003) 8

Low and Mid-MW PAHs Account for the Vast Majority of Pore Water TUs 2-, 3-, and 4-ring PAHs 5- and 6-ring PAHs % of SPME Pore Water TU 34 95% of toxicity is from 2-, 3-, and 4-ring PAHS N = 97 9

Alkylated PAHs Account for ~75% of Pore Water TUs % of SPME Pore Water TU 34 N = 97 10

Alcoa ESTCP NiSource NGA (Marine) Sediment Contaminant Bioavailability Alliance (SCBA) To date: 18 sites >250 samples 11

Toxic Nontoxic National Grid – Hudson, NY 27 samples H. azteca 28-day toxicity SPME Pore Water PAHs 27 samples H. azteca 28-day toxicity SPME Pore Water PAHs 12

Hudson Site-Specific Dose-Response Provides an Accurate Characterization Tool N=27 <20 TU 34 >35 TU 34 13

PAH 16 >1.6 mg/kg PAH 16 >22.8 mg/kg >35 TU 34 <20 TU 34 SPECIFICITY – Focused on Measured Toxicity Provides accurate characterization tool 14

Total [PAH 16 ] DOES NOT Predict Toxicity 15

SCBA [PAH 34 ] Method Allows Better Decisions < 5 TU > 40 TU 16

SPME Pore Water Prediction Efficiency is Better 17

No Equilibrium Partitioning Model Hydrocarbon Narcosis Model (NOAA PAH 34 ) SPME TU 34 > 5 ? Biota Exposure Sediment Concentration Improved Site-Specific Information Bioavailable PAHs (SPME Pore Water) Procedures for the Derivation of Sediment Benchmarks: PAH Mixtures (U.S. EPA 2003) PAH Mixtures (U.S. EPA 2003) Yes No Further Action Significantly Toxic to Benthic Test Organisms? No Yes Further Action Required 18

Summary: Possible Approach for Using SPME Data SPME TU 34 < 5 Sediment non-toxic Biological testing not required SPME TU 34 > 40 Sediment toxic Biological testing not required 5 < SPME TU 34 < 40 Biological testing required 19

Danny Reible Civil, Architectural and Environmental Engineering The University of Texas at Austin Work supported by ESTCP/EPA/NIEHS 20

 Relationship between sediment contaminants and potential for exposure and risk  Contaminants- Hydrophobic organics  PAHs and PCBs  Metric – Accumulation in benthic organisms  Benthic organisms often control contaminant exposure to higher organisms through food chain transfer and direct release (via bioturbation)  Accumulation provides a dose proportionate response 21

 Bulk sediment concentration  Relatively easily measured  If equilibrium partioning to porewater bulk sediment is also indicates porewater/mobile phase concentrations  In the absence of direct partitioning information  Reality – porewater concentration typically much less than predicted by this equation due to desorption resistant phenomena 22

 Test organism  Deposit-feeding freshwater tubificide oligochaete  Ilyodrilus templetoni  Ease to culture  High tolerance to contaminants and handling stress  Intense sediment processing environment (overcome mass transfer resistances?)  Measure of bioavailability  steady state biota-sediment accumulation factor, BSAF Where C t is contaminant concentration accumulated in organisms’ tissue (  g/g ) f lip is organisms’ lipid content (g lipid/g dry worm) C s is the sediment concentration (  g/g dry sediment) f oc is total organic carbon content of the sediment (g TOC/g dry sediment). 23

Anacostia River PAHs/PCBs 24

Assuming K lipid =K oc Anacostia River Porewater Anacostia River PAHs/PCBs 25

In sediments and in deposit feeding organism (porewater not route of exposure) Freshwater oligochaetes PAHs and PCBs Anacostia River sediments R 2 =

Freshwater oligochaetes PAHs and PCBs Sequentially diluted New Bedford Harbor sediments R 2 =

Saltwater/Freshwater sediments & organisms, PAHs and PCBs 28

 Strongly sorptive phases cause desorption resistance and decreased porewater concentration  Slow transport processes in porewater results in achievement of apparent equilibrium  Rapid transport processes would yield kinetic limited desorption and ultimately complete release of sorbed contaminants  No unavailable fraction – assumed to be strictly a kinetic phenomena  Deposit feeding benthic organisms rapidly equilibrate with local solid phases  Route of exposure controls dynamics of uptake  Extent of uptake controlled by apparent equilibrium 29

 Solid Phase MicroExtraction  Sorbent Polymer PDMS (poly-dimethylsiloxane)  Thickness of glass core: µ m  Thickness of PDMS coating: µ m  Volume of coating: (±0.02) µ L PDMS per meter of fiber  Easily capable of measuring ng/L concentrations  Field deployable system under development  ng/L detection with 1 cm resolution  May require days to equilibrate  Recent work with thin coating  10 µ m on 230 µ m core  9 times faster dynamics  ~ 7 µ L PDMS per meter of fiber x 30

Outer slotted tube 31

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 Deployment for ~10-30 days (or shorter for nonequilibrium deployment or for light PAHs)  In-situ  when sediment cannot be removed without compromising porewater integrity  when porewater chemical gradients must be retained or to assess field migration processes  Ex-situ  Box cores can be collected and maintained  Field deployment is hazardous (e.g. divers in chemically or physically hazardous environments)  Retrieval and sectioning for desired resolution  Extraction  Analysis 35

(ng/L) Bulk sediment concentration does not reflect high gradient near surface 36

 Lumbriculus – freshwater deposit feeder  Preliminary Data  Variety of uncontrolled factors  Still promising correlation  Additional field demonstration planned Summer

 Thin layer sand capping (10-15 cm) often used to provide clean surface over dredging residuals  Assessed via bioaccumulation experiments with deposit feeding organism with layers of varying thickness  Thin (0.5 cm) of fine grained sediment above thin layer sand cap to simulate deposition of new sediment (allowing recolonization by deposit feeders)  Porewater and bioaccumulation testing after 28/ 56 days  No porewater advection  Objectives  Can a thin layer sand cap reduce bioaccumulation?  Can porewater concentrations indicate bioaccumulation? 38

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Thin Layer Capping to Manage Residuals Overlying Water 40

Thin Layer Capping to Manage Residuals Overlying Water 41

Unit slope is BSF estimated by K ow 42

 Interstitial water concentration indicative of available and mobile contaminants  Typically much lower than predicted by W s / (Koc foc) due to desorption resistance  Interstitial water concentration indicative of bioaccumulation in deposit feeding organisms  Not indicative of route of exposure but of ss accumulation  PAHs and PCBs (although less data for PCBs)  BCF useful in-situ for deposit feeders as well as for passive uptake in organisms in overlying water  SPME a useful tool for measuring interstitial water concentration  Field deployable tool useful for indicating interstitial water concentration and gradients to understand chemical migration 43

Register now for the third presentations of the Bioavailability series: “Use of Bioavailability Information at Hazardous Waste Sites” – June 18 th by following the registration link on the Risk e Learning web page.Risk e Learning For more information and archives of this and other Risk e Learning web seminars please refer to the Superfund Basic Research Program Risk e Learning web page:Risk e Learning 44

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