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1 AGENCY COMMENTS ON ERM PROPOSAL FOR HRMS REANALYSIS 28 April 2015 ERM has proposed that all samples of solid media (soil, sediment) collected from the inner PRIs in the Phase 1A/B investigation be analyzed for dioxins/furans/PCBs by Low Resolution Mass Spectroscopy (LRMS), and that, depending on the results of the LRMS analysis, a subset would be re-analyzed by High Resolution Mass Spectroscopy (HRMS). In accord with EPA suggestions, ERM has proposed a trigger for HRMS reanalysis that is intended to ensure that samples with HQ values for TEQ nearing a decision threshold would be identified for reanalysis. The specific rule proposed is that samples with OCDF concentrations lower than 40 ug/kg be reanalyzed by HRMS. Given typical concentration ratios of TEQ risk drivers to OCDF, ERM indicated that samples with 40 ug/kg or higher of OCDF would have detectable levels of most TEQ risk drivers, and HQ values for TEQ would be well above the level of concern. If so, results of the LRMS analysis would likely be adequate for risk assessment and risk management decision making. This approach is conceptually sound, but there is a potential problem. ERM evaluated the range of expected HQ values based on the lowest RBC available (0.00012 ug/kg). This might seem to be appropriate, but it is actually anti-conservative to focus on the lowest RBC. This is because the higher the RBC, the lower the HQ values, and the more samples that approach the grey zone(HQ values close to the decision threshold) for decision-making. In this regard, the RBCs for exposure of mammalian ecological receptors (fox, shrew) to TEQ derived during the refinement step are in the range of 0.02 to 0.3 ug/kg, substantially higher than the value of 0.00012 ug/kg used in ERM’s assessment. The RBC values for humans exposed to TEQ are likely to be even somewhat higher, depending on site-specific and PRI-specific exposure assumptions. The current default recommended by EPA headquarters 1 for an outdoor worker is 0.8 ug/kg. The basic problem is illustrated in Figure 1. Panel A plots HQ values based on mammalian 2 TEQ for the historic data using the proposed RBC of 0.00012 ug/kg, and Panel B plots the values using an RBC of 0.8 ug/kg. As seen, if the RBC were 0.00012, then HQ values at an OCDF trigger of 40 ug/kg would be well above the grey zone. However, if the RBC is 0.8 ug/kg, then most HQ values at the trigger are in the grey zone. Based on this, EPA believes the selection of a trigger for HRMS needs to be based on a consideration of the expected results using the highest, not the lowest, RBC value that is likely to be applicable. 1 http://epa-prgs.ornl.gov/cgi-bin/chemicals/csl_search 2 For avian receptors, TEQ is dominated by HCB. All TEQ values used in this discussion are based on mammalian TEFs.

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1

AGENCY COMMENTS ON ERM PROPOSAL FOR HRMS REANALYSIS

28 April 2015

ERM has proposed that all samples of solid media (soil, sediment) collected from the inner PRIs

in the Phase 1A/B investigation be analyzed for dioxins/furans/PCBs by Low Resolution Mass

Spectroscopy (LRMS), and that, depending on the results of the LRMS analysis, a subset would

be re-analyzed by High Resolution Mass Spectroscopy (HRMS). In accord with EPA

suggestions, ERM has proposed a trigger for HRMS reanalysis that is intended to ensure that

samples with HQ values for TEQ nearing a decision threshold would be identified for reanalysis.

The specific rule proposed is that samples with OCDF concentrations lower than 40 ug/kg be

reanalyzed by HRMS. Given typical concentration ratios of TEQ risk drivers to OCDF, ERM

indicated that samples with 40 ug/kg or higher of OCDF would have detectable levels of most

TEQ risk drivers, and HQ values for TEQ would be well above the level of concern. If so,

results of the LRMS analysis would likely be adequate for risk assessment and risk management

decision making.

This approach is conceptually sound, but there is a potential problem. ERM evaluated the range

of expected HQ values based on the lowest RBC available (0.00012 ug/kg). This might seem to

be appropriate, but it is actually anti-conservative to focus on the lowest RBC. This is because

the higher the RBC, the lower the HQ values, and the more samples that approach the “grey

zone” (HQ values close to the decision threshold) for decision-making. In this regard, the RBCs

for exposure of mammalian ecological receptors (fox, shrew) to TEQ derived during the

refinement step are in the range of 0.02 to 0.3 ug/kg, substantially higher than the value of

0.00012 ug/kg used in ERM’s assessment. The RBC values for humans exposed to TEQ are

likely to be even somewhat higher, depending on site-specific and PRI-specific exposure

assumptions. The current default recommended by EPA headquarters1 for an outdoor worker is

0.8 ug/kg.

The basic problem is illustrated in Figure 1. Panel A plots HQ values based on mammalian2

TEQ for the historic data using the proposed RBC of 0.00012 ug/kg, and Panel B plots the values

using an RBC of 0.8 ug/kg. As seen, if the RBC were 0.00012, then HQ values at an OCDF

trigger of 40 ug/kg would be well above the grey zone. However, if the RBC is 0.8 ug/kg, then

most HQ values at the trigger are in the grey zone. Based on this, EPA believes the selection of

a trigger for HRMS needs to be based on a consideration of the expected results using the

highest, not the lowest, RBC value that is likely to be applicable.

1 http://epa-prgs.ornl.gov/cgi-bin/chemicals/csl_search 2 For avian receptors, TEQ is dominated by HCB. All TEQ values used in this discussion are based on

mammalian TEFs.

2

Granted that the RBC value is based on the highest reasonably expected, the next critical step is

deciding how to recognize a sample when a reanalysis is needed. EPA proposes that the basic

rule is: reanalysis is needed when the difference between LRMS and HRMS becomes

significant for decision-making (i.e., LRMS yields a different decision than HRMS). Based on

this, EPA feels the most informative data that are presently available are the set of 8 samples that

were analyzed by both LRMS and HRMS as part of the DMA. The basic approach is to plot the

HQ value for workers (RBC = 0.8 ug/kg TEQ) based on both LRMS and HRMS as a function of

OCDF, and see where the difference between the two becomes large enough that the LRMS

would not be considered optimal and HRMS would be needed.

This, in turn, raises a question as to how ND congeners in the LRMS analysis will be treated in

the calculation of TEQ. For simplicity, substitution of ND=1/2DL has been used to date3.

The results are shown in Figure 2. Although a data set of only 8 samples is too small to be

highly confident, the main conclusions seem to be:

1. At high values of OCDF (e.g., above 5,000 ug/kg), there is not much difference between

LRMS and HRMS, and LRMS results will likely be adequate.

2. As OCDF levels decrease, a difference begins to emerge, with the LRMS samples

tending to yield higher TEQ and HQ values than the HRMS.

3. The concentration at which the difference begins to become important is difficult to judge

with such a limited data set, but it seems likely it is in the range of 500 to 5,000 ug/kg

OCDF. Above this range, risk conclusions are likely to be the same by both methods,

while below this range, risk conclusions based on LRMS TEQ would likely be biased

high.

Based on this, EPA has concluded that an OCDF trigger of about 500-1000 ug/kg is needed to

prevent substantial overestimation of hazard from samples in the low end of the risk range.

3 EPA Region 8 has also briefly investigated the use of EPA’s KM TEQ calculator spreadsheet

tool, but it appears the results are generally similar to the ND=1/2DL approach.

3

FIGURE 1

HQ vs OCDF FOR LOW AND HIGH RBC VALUES

BASED ON HISTORIC DATA

Panel A: RBC = 0.00012 ug/kg

Panel B: RBC = 0.8 ug/kg

0.01

0.1

1

10

100

1000

10000

100000

1000000

0.01 0.1 1 10 100 1000 10000

HQ

OCDF (ug/kg)

0.01

0.1

1

10

100

1000

10000

100000

0.01 0.1 1 10 100 1000 10000

HQ

OCDF (ug/kg)

OCDF = 40

OCDF = 40

4

FIGURE 2

COMPARISON BETWEEN LRMS AND HRMS ESTIMATES OF HQ

BASED ON PAIRED SAMPLES FROM THE DMA

0.1

1

10

100

10 100 1000 10000

HQ

OCDF (ug/kg)

LRMS ND=1/2DL

HRMS ND = 1/2DL

OCDF = 500OCDF = 40

1

AGENCY COMMENTS ON ERM PROPOSAL FOR HRMS REANALYSIS

28 April 2015

ERM has proposed that all samples of solid media (soil, sediment) collected from the inner PRIs

in the Phase 1A/B investigation be analyzed for dioxins/furans/PCBs by Low Resolution Mass

Spectroscopy (LRMS), and that, depending on the results of the LRMS analysis, a subset would

be re-analyzed by High Resolution Mass Spectroscopy (HRMS). In accord with EPA

suggestions, ERM has proposed a trigger for HRMS reanalysis that is intended to ensure that

samples with HQ values for TEQ nearing a decision threshold would be identified for reanalysis.

The specific rule proposed is that samples with OCDF concentrations lower than 40 ug/kg be

reanalyzed by HRMS. Given typical concentration ratios of TEQ risk drivers to OCDF, ERM

indicated that samples with 40 ug/kg or higher of OCDF would have detectable levels of most

TEQ risk drivers, and HQ values for TEQ would be well above the level of concern. If so,

results of the LRMS analysis would likely be adequate for risk assessment and risk management

decision making.

This approach is conceptually sound, but there is a potential problem. ERM evaluated the range

of expected HQ values based on the lowest RBC available (0.00012 ug/kg). This might seem to

be appropriate, but it is actually anti-conservative to focus on the lowest RBC. This is because

the higher the RBC, the lower the HQ values, and the more samples that approach the “grey

zone” (HQ values close to the decision threshold) for decision-making. In this regard, the RBCs

for exposure of mammalian ecological receptors (fox, shrew) to TEQ derived during the

refinement step are in the range of 0.02 to 0.3 ug/kg, substantially higher than the value of

0.00012 ug/kg used in ERM’s assessment. The RBC values for humans exposed to TEQ are

likely to be even somewhat higher, depending on site-specific and PRI-specific exposure

assumptions. The current default recommended by EPA headquarters1 for an outdoor worker is

0.8 ug/kg.

The basic problem is illustrated in Figure 1. Panel A plots HQ values based on mammalian2

TEQ for the historic data using the proposed RBC of 0.00012 ug/kg, and Panel B plots the values

using an RBC of 0.8 ug/kg. As seen, if the RBC were 0.00012, then HQ values at an OCDF

trigger of 40 ug/kg would be well above the grey zone. However, if the RBC is 0.8 ug/kg, then

most HQ values at the trigger are in the grey zone. Based on this, EPA believes the selection of

a trigger for HRMS needs to be based on a consideration of the expected results using the

highest, not the lowest, RBC value that is likely to be applicable.

1 http://epa-prgs.ornl.gov/cgi-bin/chemicals/csl_search 2 For avian receptors, TEQ is dominated by HCB. All TEQ values used in this discussion are based on

mammalian TEFs.

2

Granted that the RBC value is based on the highest reasonably expected, the next critical step is

deciding how to recognize a sample when a reanalysis is needed. EPA proposes that the basic

rule is: reanalysis is needed when the difference between LRMS and HRMS becomes

significant for decision-making (i.e., LRMS yields a different decision than HRMS). Based on

this, EPA feels the most informative data that are presently available are the set of 8 samples that

were analyzed by both LRMS and HRMS as part of the DMA. The basic approach is to plot the

HQ value for workers (RBC = 0.8 ug/kg TEQ) based on both LRMS and HRMS as a function of

OCDF, and see where the difference between the two becomes large enough that the LRMS

would not be considered optimal and HRMS would be needed.

This, in turn, raises a question as to how ND congeners in the LRMS analysis will be treated in

the calculation of TEQ. For simplicity, substitution of ND=1/2DL has been used to date3.

The results are shown in Figure 2. Although a data set of only 8 samples is too small to be

highly confident, the main conclusions seem to be:

1. At high values of OCDF (e.g., above 5,000 ug/kg), there is not much difference between

LRMS and HRMS, and LRMS results will likely be adequate.

2. As OCDF levels decrease, a difference begins to emerge, with the LRMS samples

tending to yield higher TEQ and HQ values than the HRMS.

3. The concentration at which the difference begins to become important is difficult to judge

with such a limited data set, but it seems likely it is in the range of 500 to 5,000 ug/kg

OCDF. Above this range, risk conclusions are likely to be the same by both methods,

while below this range, risk conclusions based on LRMS TEQ would likely be biased

high.

Based on this, EPA has concluded that an OCDF trigger of about 500-1000 ug/kg is needed to

prevent substantial overestimation of hazard from samples in the low end of the risk range.

3 EPA Region 8 has also briefly investigated the use of EPA’s KM TEQ calculator spreadsheet

tool, but it appears the results are generally similar to the ND=1/2DL approach.

3

FIGURE 1

HQ vs OCDF FOR LOW AND HIGH RBC VALUES

BASED ON HISTORIC DATA

Panel A: RBC = 0.00012 ug/kg

Panel B: RBC = 0.8 ug/kg

0.01

0.1

1

10

100

1000

10000

100000

1000000

0.01 0.1 1 10 100 1000 10000

HQ

OCDF (ug/kg)

0.01

0.1

1

10

100

1000

10000

100000

0.01 0.1 1 10 100 1000 10000

HQ

OCDF (ug/kg)

OCDF = 40

OCDF = 40

4

FIGURE 2

COMPARISON BETWEEN LRMS AND HRMS ESTIMATES OF HQ

BASED ON PAIRED SAMPLES FROM THE DMA

0.1

1

10

100

10 100 1000 10000

HQ

OCDF (ug/kg)

LRMS ND=1/2DL

HRMS ND = 1/2DL

OCDF = 500OCDF = 40