individual congeners to 2,3,7,8-TCDD, for which the most toxicologicalinformation is available. This procedure is commonly referred to as the TEQapproach and was presented and described in USEPA (1987, 2008b) and Van denBerg et al. (1998, 2006). Although refinements and updates to application <strong>of</strong> thisprocedure have occurred, the basic premise has stayed the same and continues tobe used by the USEPA.The term "dioxins" refers to the 17 tetra- through octa-chlorinated dioxin andfuran and 12 tetra- through hexa-chlorinated biphenyl compounds assigned TEFvalues by the WHO. Dioxins and furans are formed as unintended by-products <strong>of</strong>specialty chemical processes or combustion <strong>of</strong> chlorine-containing substances.Furans and dioxin-like PCBs occur in various proportions in commercial PCBsunder various trade names. These compounds are highly hydrophobic. Whenreleased into the environment, dioxins, furans and dioxin-like PCBs bind to solidsand are typically found in the highest concentrations in soil or sediment. Highvolume water sampling <strong>of</strong> surface, ground and pore waters using EPA Methods1613B and 1668A/B can detect and quantify these congeners in suspended solidsand in the dissolved state (USEPA 1994c and 1999c). Biological matrices can beroutinely characterized as well. Testing for dioxin is relatively expensive;therefore, dioxin testing is warranted only under certain site conditions. Someexamples are as follows: when site history indicates manufacturing (e.g., synthesis, blending or storage)or application <strong>of</strong> chlorophenolic or pesticide and herbicide compounds, whichare known to lead to formation <strong>of</strong> chlorinated dioxins and furans. Thesechemicals were identified by USEPA (1980) as Class I and II chemicals relatedto dioxin formation and Class I and II pesticides related to dioxin formation,respectively; when site history indicates bleach-kraft pulp and paper mill processes involvingthe use <strong>of</strong> chlorine and chlorine derivatives; when site history indicates PCB contamination (e.g., contaminated oils or othermaterials containing a high percentage <strong>of</strong> chlorine-containing substances) thatmay have been involved in a fire, including building interior fires; when site history indicates burning <strong>of</strong> plastics or other materials containingchlorine-containing compounds (e.g., burning <strong>of</strong> plastic coated wiring forprecious metals recovery, miscellaneous burning <strong>of</strong> refuse with high percentage<strong>of</strong> plastic or vinyl-like materials); when site history indicates chlor-alkali plant manufacturing processes usingcarbon electrodes.As described in Section 5.3, sampling and analysis may be conducted in a phasedmanner with soil samples from source areas prioritized for analysis, followed bysampling in contaminant migration pathways and ESNRs. Dioxin source areasinclude areas <strong>of</strong> spills, discharges, burning grounds, and ash or waste disposal.Soil and sediment sampling depth intervals are determined site-specifically;however, because dioxin binds strongly to particulate matter, it is most <strong>of</strong>tenfound in surface or shallow depth soil and sediment intervals, and these intervalsshould be targeted for sampling. The exception to this is when site information<strong>Ecological</strong> <strong>Evaluation</strong> <strong>Technical</strong> <strong>Guidance</strong> Document 77Version 1.2 8/29/12
indicates burial <strong>of</strong> potential dioxin-impacted soil and sediment (or ash), such asthrough landfilling operations, soil re-working activities on site, or long-termaccretion <strong>of</strong> clean sediments. In these situations, alternate depths are targetedbased on site information and conditions. For fly ash or combustion wastesources, sample intervals may be guided by visual evidence <strong>of</strong> the ash.Depending on historic site operations, best pr<strong>of</strong>essional judgment should be usedregarding the decision to limit the field sampling and analysis plan and the TEQprocess to only dioxin and furans or only dioxin-like PCB congeners, or toevaluate both contaminant classes.Detailed specifics regarding the TEQ approach can be found in Appendix I.6.4.9 Historic Fill Material and Dredged MaterialCertain areas <strong>of</strong> sites and ESNRs associated with sites may have, over time,received industrial fill material or dredged materials. This practice was likely tohave been more common at sites adjacent to water bodies where fill was used tocreate upland or to improve grade, and where low-lying areas provided for easydeposition <strong>of</strong> dredged materials. During the SI, COPECs may be found in soil,surface water, and sediment collected from these areas, yet the source <strong>of</strong> thesechemicals may have little or no link to past or present site operations. Theidentification <strong>of</strong> historic fill and dredged materials and management options forthese areas should be evaluated during the SI and RI in accordance with N.J.A.C.7:26E–3.12 & 4.7 and the Historic Fill <strong>Guidance</strong> document. Examples <strong>of</strong> tools toaid in the identification <strong>of</strong> historic fill and dredged materials include review <strong>of</strong>historical documentation and the inclusion <strong>of</strong> soil or sediment assessmenttechniques, such as grain size, TOC, and various soils parameters (e.g., redoxpotential) with sample analyses from areas suspected to have received fill ordredged materials.For ecological purposes, areas <strong>of</strong> historic fill and dredged materials should beconsidered as potential contaminant sources to ESNRs and should be investigatedpursuant to N.J.A.C. 7:26E-1.16 and 4.8. Regardless <strong>of</strong> whether the contaminantsare considered site-related, if adverse ecological effects from the historic fill ordredged materials are documented, remediation may be required. Capping is apresumptive remedy for historic fill or dredged materials in upland (non-ESNR)areas. Alternative remedies should be considered if capping would result inadverse impacts to the ESNR.6.4.10 Acid-Volatile Sulfides/Simultaneously Extracted MetalsBioavailability and associated toxicity <strong>of</strong> some divalent metals found in anoxicsediment has been linked to the presence <strong>of</strong> acid-volatile sulfides (AVS) and theirrelationship to simultaneously extracted metals (SEM). The USEPA hasrecommended the use <strong>of</strong> the AVS/SEM ratio as a predictor <strong>of</strong> the bioavailability<strong>of</strong> these metals in sediment (USEPA, 2005b).The AVS component <strong>of</strong> sediment is comprised <strong>of</strong> a variety <strong>of</strong> reduced sulfurcompounds, quantified using a cold acid extraction. The SEM componentincludes the reactive metal fraction (including cadmium, copper, lead, nickel,<strong>Ecological</strong> <strong>Evaluation</strong> <strong>Technical</strong> <strong>Guidance</strong> Document 78Version 1.2 8/29/12
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Ecological EvaluationTechnical Guid
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6.2.1.3 Biological Sampling of Fish
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Acronyms and AbbreviationsADDAETAFA
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Executive SummaryThis document prov
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environmentally sensitive areas pur
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Figure 3-1: Flow diagram to describ
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assessment may also include evaluat
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“Hazard quotient” or “HQ” m
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“Site investigation” means the
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parameters as specified in ERAGS (i
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71 0Sampling pointsSampling transec
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Data PresentationTabular presentati