ARAM. NE PAMOS Corr, * Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, 5-7 June 1989 Disposal Area Monitoring System DAMOS oe ae BY JEP Ge ee ol g rc ay a eA Pa 20 cm. Boundary Meters Figure 1-2. Location of grab samples taken at MBDS, June 1989. MDA buoy is the active disposal point; "A" buoy was an historic disposal location. Dredged material footprint from bathymetric survey of 1990 (Germano et al. 1994). Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 «A 2.0 METHODS 2.1 Field Procedures Samples were collected aboard the US Environmental Protection Agency’s (EPA) vessel O.S.V. Anderson by the NED during 5-7 June 1989. LORAN-C, calibrated to a fixed reference point, was used for navigational control. Water depths at the sample stations ranged from approximately 60 to 90 meters. Three replicate grab samples were taken at twenty-six stations located within or adjacent to the western half of the MBDS (Figure 1-2). Replicate grabs are collected in order to average out local sediment variation. Contaminant concentrations are, in general, highly dependent upon local sediment redox conditions, and dredged materials are characterized by high variability (Morton and Karp 1980). Results are presented for each approximate station location rather than for each replicate (Figure 2-1). Two reference areas (18-17 and FG-23), located south of the site (Figure 1-1), were also sampled in triplicate. Two additional replicates were collected from 18-17 from the same grab sample as a measure of field sampling replicability. Each station sample replicate was analyzed for a suite of metals and total organic carbon (TOC) by the NED laboratory. Samples from the three replicate grabs were composited at each station for analysis of a suite of semivolatiles. Replicate samples from station 18-17 were analyzed individually for semivolatile compounds. Grab samples were taken at each station using a Smith-MclIntyre grab sampler. One core was taken from each grab sample using polycarbonate tubes which had been rinsed with seawater by the NED laboratory prior to the cruise; stainless steel spoons were used to stabilize lifting the core from the grab sampler. The grab sampler and the stainless steel spoons were thoroughly rinsed with seawater between each station. The replicate samples at reference station 18-17 were taken without the use of stainless steel spoons. Cores were taken from the center of each grab to avoid contamination. Samples were stored at approximately 4° C in plastic sample bags and then transported to the NED laboratory where they were stored again at approximately 4° C until analysis. 2.2 Laboratory Procedures Samples were analyzed for both metal and organic constituents (Table 2-1). Metals, including chromium (Cr), nickel (Ni), copper (Cu), zinc (Zn), cadmium (Cd), mercury (Hg), and lead (Pb), were analyzed using the EPA’s Test Methods for Evaluating Solid Waste (SW-846) procedures (Table 2-1; EPA 1986). Sediment samples were acid digested (Method 3050) and analyzed using direct aspiration atomic absorption (AA) except for mercury (Hg) analysis (Method 7471). Mercury was analyzed using cold vapor atomic absorption Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 MBDS STATION LOCATIONS © = Station Location 70°33.00' W 42°26.00'N Disposal Site Boundary O 18-17 Meters Figure 2-1. Approximate station locations averaged from three replicate grabs, MBDS, June 1989 Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 Table 2-1 Summary of Laboratory Analytical Methods ANALYTE SW-846 TEST METHOD NO. INSTRUMENTATION LABORATORY Metals Sample Prep Analytical NED Cadmium 3050 7130 AA Chromium 3050 7190 AA Copper 3050 7210. AA Lead 3050 7420 AA Mercury = 7471 CVAA Nickel 3050 7520 AA Zinc 3050 7950 AA BNA 3550 8270 GC/MS Chemrox Pesticides/PCBs 3540 8080 GC/ECD NED Total Organic Carbon 9060 NED Instrumentation: AA - Direct Aspiration Atomic Absorption CVAA Cold Vapor Atomic Absorption ECD Electron Capture Detector GC Gas Chromatograph MS Mass Spectrometer Analytes: BNA Basic, Neutral, and Acidic Semivolatiles PCB Polychlorinated Biphenyl Laboratories: NED US Army Corps of Engineers, New England Division Laboratory Chemrox Chemrox Laboratory Services All methods from EPA SW-846 (EPA 1986). Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 (CVAA). AA determinations are completed as single element analyses which allow for low detection limit thresholds (the direct aspiration method is not as sensitive as graphite furnace AA). TOC was measured using protocols described in SW-846 Method 9060 (EPA 1986). Organic carbon in the samples was converted by the analyzer to carbon dioxide (CO,), which was subsequently measured by an infrared detector. The amount of CO, is directly proportional to the concentration of carbonaceous material in the sample. Inorganic forms of carbon (carbonate and bicarbonate) are not included as part of the reported total organic carbon value. Total organic carbon is a measurement of organic matter (both labile and refractory) in sediments. Composited MBDS samples were analyzed for semivolatile organics using SW-846 Method 8080 (pesticides and PCBs) by the NED laboratory, and Method 8270 (basic, neutral, and acidic semivolatiles or BNA) by Chemrox Laboratory Services in Shelton, Connecticut. BNA compounds include a full suite of polynuclear aromatic hydrocarbons (PAHs; Table 2-2). Method 8080 measures the concentrations of several chlorinated pesticides and PCBs from a sample extract using a gas chromatograph with an electron capture detector. Method 8270 measures the concentration of semivolatile organic compounds soluble in methylene chloride using a gas chromatograph with a mass spectrometer detector (GC/MS). Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 Co Table 2-2 Organic Compound Method Detection Limits Organic Compound Method Detection Limits Pesticides (Method 8080) DL (ppb) |Base Neutrals/Acid, continued DL (ppb) 4-Chloroaniline 1300 4-Chlorophenyl-phenylether 660 4-Methylphenol 660 4-Nitroaniline 3300 4-Nitrophenol 3300 Acenaphthene 660 Acenaphthylene 660 Anthracene 660 Benzo(a)anthracene 660 Benzo(a)pyrene 660 Benzo(b)fluoranthene 660 Benzo(g,h,i)perylene 660 Benzo(k)fluoranthene 660 Benzoic acid 3300 Benzyl alcohol 1300 Bis(2-chloroethoxy methane 660 Bis(2-chloroethy1)ether 660 Bis(2-chloroisopropy|)ether 660 Bis(2-ethy lhexyl)phthalate 660 Butylbenzylphthalate 660 Chrysene 660 Di-n-butylphthalate 660 Di-n-octy! phthalate 660 Dibenzo(a,h)anthracene 660 Dibenzofuran 660 Diethy|phthalate 660 Dimethy!phthalate 660 Fluoranthene 660 Fluorene 660 Hexachlorobenzene 660 Hexachlorocyclopentadiene 660 Hexachlorobutadiene 660 Hexachloroethane 660 Indeno(1,2,3-cd)pyrene 660 Isophrone X 660 N-Nitroso-di-n-propylamine 660 N-Nitrosodiphenylamine 660 Napthalene 660 Nitrobenzene 660 Pentachlorophenol 3300 Phenanthrene 660 Phenol 660 Pyrene lEndosulfan I lEndosulfan II 1.0 lEndosulfan Sulfate Endrin Aldehyde 2.0 lgamma-BHC (Lindane) 0.5 [Heptachlor Epoxide 0.5 IMethoxychlor 1.0 ‘otal PCBs (Method 8080) ase Neutrals/Acid (Method 8270) 1,2,4-Trichlorobenzene 660 1,2-Dichlorobenzene 660 1,3-Dichlorophenol 660 1,4-Dichlorobenzene 660 2 ,4,5-Trichlorophenol 660 2 ,4,6-Trichlorophenol 660 2 ,4-Dichlorophenol 660 2 ,4-Dimethylphenol 660 2 ,4-Dinitrophenol 3300 2 .4-Dinitrotoluene 660 2 ,6-Dinitrotoluene 660 2-Chloronaphthalene 660 2-Chlorophenol 2-Methylphenol 660 2-Nitroaniline 3300 2-Nitrophenol 660 B ,3-Dichlorobenzidine 1300 3-Nitroaniline 3300 4_6-Dinitro-2-methylphenol 3300 4-Bromophenyl-phenylether 660 4-Chloro-3-methylphenol Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 ‘Oo 3.0 RESULTS 3.1 Data Quality Analysis Results submitted by the NED laboratory and Chemrox were found to be acceptable and supported by appropriate documentation, with some data qualified as discussed below. Sample data were evaluated using protocols developed by the EPA (EPA 1988a, 1988b), including a review of laboratory detection limits, sample holding times, and laboratory quality control (QC) samples. QC samples consisted of method blanks, matrix spikes, and duplicate samples. No QC sample results were submitted with the TOC data; consequently, all TOC data were qualified “J” as estimated. Data qualified as estimated are acceptable, but a greater degree of uncertainty is associated with these values than with unqualified data. Method detection limits (MDLs) are the minimum concentrations of a substance that can be measured and reported with 99% confidence that the analyte concentration is greater than zero. The MDL incorporates all of the analytical operations. All MDLs were acceptable as proscribed by each method (Table 2-2) for all sample results, except for two basic, neutral, acidic semivolatile (BNA) results for samples 8-5 and 9-8. These samples were diluted tenfold which resulted in detection limits an order of magnitude higher than the other samples. Samples are diluted either because the presence of high concentrations of a measured compound can interfere with accurate quantification of chromatographic peaks, or because the sediment matrix itself causes interference. All compounds were below detection in these samples except for one estimated value of di-n-octyl phthalate (1900 ppb). The result of this dilution is that the potential presence of PAHs at concentrations above the normal detection limit at these two stations cannot be determined. This uncertainty was taken into account in discussing the MBDS chemical results (Section 4.1). The EPA recommends a limit to the amount of time samples can be stored before analysis; this period is called the holding time. There are no formal holding times for sediment matrix samples. Samples were extracted for organic analyses less than forty-five days after sampling, and analyzed less than thirty-eight days after extraction. No organics or metals samples were qualified based on excessive holding times (EPA 1988a, 1988b). Method blanks are laboratory QC samples processed with the samples but containing only reagents, and are used to test for contamination which may have been contributed by the laboratory during sample preparation. An acceptable number of method blanks were analyzed with all sample sets except that there were no method blanks for Hg or total organic carbon (TOC) analyses. TOC results were already qualified, so no further qualification was necessary. Mercury results were also qualified as estimated. Method blanks were below detection for all pesticides, PCBs, and metals except Hg. BNA compounds were also undetected in the associated method blanks with the exception of bis(2-ethylhexyl)phthalate which was detected in three of the four BNA method blanks at estimated concentrations Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 10 below the MDL. Phthalates are common constituents of plastic and may have been introduced in the laboratory sample preparation process. All sample detections of bis(2-ethylhexyl)phthalate were qualified with a “J” because of the laboratory method blank detections. Detected phthalates in MBDS samples may have been introduced in the laboratory; in addition, samples may have been contaminated with phthalates from the plastic storage bags. All phthalate detections were qualified due to the uncertainty. There was no apparent difference between replicate samples taken with and without the use of the stainless steel spoon in the field. Matrix spike samples are spiked with a known concentration of a particular inorganic or organic analyte. The percent recovery of the spiked compound indicates the efficiency and effectiveness of sample preparation and analysis procedures, and how tightly bound a compound is to the sample matrix. One sample and sample duplicate (10-7) were spiked with six pesticide compounds; percent recoveries were within acceptance ranges (EPA 1988a). No samples were spiked with PCBs. Two matrix spike duplicate pairs were analyzed for eleven BNA compounds; all recoveries were within acceptance limits. Pesticide, PCB, and BNA samples were also spiked with surrogate compounds, which are artificial compounds not normally found in environmental samples. Surrogate recovery is also used to indicate the efficiency and effectiveness of sample preparation and analysis procedures. Pesticide and PCB samples were spiked with the surrogate TCMX, and BNA samples were spiked with six surrogate compounds. Percentage recoveries of surrogates indicated acceptable laboratory sample extraction. Laboratory duplicate samples indicate precision (replicability) of laboratory procedures. Calculation of the relative percent difference (RPD) between the duplicate samples is the common method to compare duplicate results as a measure of laboratory precision. Matrix spike duplicate samples were analyzed for pesticide, PCB, and BNA analyses, and eight duplicate sample pairs were analyzed for all of the metals analyzed in the MBDS samples. RPDs for all duplicate analyses were acceptable within EPA required limits (EPA 1988a, 1988b), indicating acceptable laboratory precision. Field replicate analysis is an indicator of field precision as well as degrees of difference between individual samples. The pesticide 4,4’-DDE (DDE) was the only compound detected in the two field replicates collected at Station 18-18. Measured concentrations were 2.81 ppb and 1.16 ppb with a resulting RPD of 83%. Since only one trace compound was detected, this information is not sufficient to comment on the precision of field sampling. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 I] See Trace Metal Results The results from the three replicates were averaged for each station (Table 3-1). Almost all of the metals concentrations were within the “low” category of contaminated sediments as classified by the New England River Basin Commission (Oceanic Society 1982). Exceptions, which fell in the moderately contaminated category, include four (out of twenty- eight) Cr results, five Pb results, and one Zn result. Cadmium concentrations were below detection (<2 ppm) in all samples except for one replicate from Station 8-7 (4 ppm). Average Cr concentrations ranged from 38 ppm (16-9) to 123 ppm (10-9). Nickel concentrations were below detection (< 14 to <16 ppm) at several stations, and reached a maximum of 35 ppm at Station 8-3 (Table 3-1). Copper concentrations ranged from 19 ppm (8-9) to 78 ppm (Station 12-3). The lowest Zn concentration was also measured at Station 8-9 (66 ppm), and the highest, 221 ppm, was again found at Station 12-3. Mercury was below detection limits (<0.05 ppm) in all replicates at Station 8-7, and in two out of three replicates at Stations 8-3 and 8-5. The highest Hg concentration was measured at Station 12-3 (0.47 ppm), followed closely by Station 14-9 (0.45 ppm), which is the station located by the “MDA” buoy (Figure 2-1). Finally, Pb concentrations ranged from 29 ppm at Stations 16-7 and 16-9 to 155 ppm at Station 9-6 (Table 3-1). 3.3 TOC, Pesticides, and PCB Results All of the samples collected in the June 1989 survey were analyzed for TOC. Average TOC values ranged from 0.44% at Station 10-7 to 2.2% at Station 18-17 (Table 3-2). Composited samples, and two replicates of 18-17, were analyzed for pesticides and PCBs. Most of the analyzed pesticides were below detection limits in all of the samples. The most commonly detected pesticide was 4,4’-DDE (DDE), which was detected in seventeen of the thirty samples at concentrations ranging from 0.65 (Station 10-7) to 10.5 ppb (Station 18-17; Table 3-2). The only other pesticides detected, including endrin, dieldrin, and 4,4’-DDD, were all at Station 10-7 (Table 3-2). PCBs were not detected (<20 ppb) in any sample except in the composite sample from Station 16-9, at barely above the detection limit (20 ppb; Table 3-2). 3.4 BNA Results Composited samples were analyzed for BNA compounds including PAHs. Many of the PAH sample results were qualified (“J”) as estimated when they were less than the MDL but were able to be quantified from the chromatographic peaks (above the practical Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 12 Z Ob S “OL 686 ‘Wuul| UOHOEJap ayeLdoudde au) (>) UeY) ssa] Se pajsi| ue yw) UONOSJap poujawW ay} Mojaq sanje/ NOILVIS SGSW [ sung ‘sajdures yuounpas SQ_W Jo Si[Nsay seal T-€ 9IqeL ‘uONeUe|dXxa JO} 1x9} BES ‘payljenb ase sanjea Aunoeyy Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 13 8-LL OL 6-01 l OL S OL € “‘Wuul| UODa}ap ayeudosdde ayy (>) UeU) Sse] Se Pa}s!| ae JWI] UONDaJap poyyaw au} MOjaq Sanje/ OL [eeases SNOILVIS SGEW (1U09) T-€ 219421, Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 14 Table 3-2 Pesticides and TOC Results of MBDS Sediment Samples, June 1989 Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 quantitation limit; Table 3-3). Two types of BNA compounds were detected in MBDS samples: phthalate esters and PAHs. Almost all of the samples contained bis(2- ethylhexy])phthalate (including three of four method blanks), and ten out of thirty samples contained di-n-octyl phthalate (Table 3-4). Samples containing bis(2-ethylhexyl)phthalate were qualified due to method blank contamination. About one-third of the MBDS stations were below detection limits in all PAH compounds, including the reference area 18-17. FG-23 contained an estimated concentration of pyrene (130 ppb). PAH results were separated into low molecular weight (LMW) and high molecular weight (HMW) compounds (Table 3-3). Total LMW PAH concentrations ranged from 100 to 510 ppb, except for a maximum LMW PAH concentration measured at Station 12-3 (1500 ppb). Phenanthrene was the most commonly detected LMW PAH compound; naphthalene was detected only at Station 12-3. Eight HMW PAH compounds were detected, and total HMW concentrations ranged from 130 to 6520 ppb (Station 12-3) (Table 3-3). Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 16 “SOIfEI Papfoq UI sanyeA Joy yda0x9 (TQI>) payewinso ose eyep [TV ‘qdd 099 st spunodwioo {je Joy (TQ) HUN] UoNsa}9p poyjeur ‘UMoYs oFe SUONeNUIDU0 punodulod paysajap AJUQ uoqses0JpAH oNeWOrY Jesjonudjog = HVd OST O€1 009 O€S O€b O9EZ OBLT OSL OSZ 0S9 O97 O7S9 OGE SOEI O61 O86I OZIE OFOI OPI OTE eee nna 061 suarAd(po-¢°Z" | Jouapu] OZ auayArad(1‘y “3 ozuag OLY Ole auoJAd(e)ozusg 096 002 ors auoyjuesoNG(q )ozuag ost 076 061 Ore Oth auasAIy orl 028 Stl Of OP ausovsyjuE(e )oZuag OSE OSE 08% OS~ OSh 09% OO8T OST O8b O61 008 O78 aualAg Osc =(O8T 081 002 OOIT OI 062 OIs 009 sustjUBION]] YBIaM Je[NoajoW] Yyst ost _0zI ON0Sta : | MATEO] 081 Oocl O1l Ose auarpueUay auayeundeny WYSII AA Je[NIaTOVY MO 6-91 L-9l S-91 6-bI Lvl S-hl €bl OE GCI LI S-Zl €-7l BIl O9Il 6-Ol S-Ol £01 96 LB LY SNOILVLS SGdN 6861 sung ‘sadureg quouNpeg Sa JO siINsoy HVd €-€ FGF L Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 ee ee — a Table 3-4 Phthalate Results of MBDS Sediment Samples, June 1989 Stations Di-n-octyl Bis(2-ethylhexyl) phthalate phthalate 6-5 6-7 610 J 8-3 8-7 8-9 9-8 9-6 10-3 10-5 10-7 11-6 11-8 12-3 12-5 12-7 12-9 13-6 14-3 14-5 14-7 14-9 16-5 16-7 16-9 18-17 FG-23 Qualified data ("J") are estimated. Only detected compounds are shown. Units are all ppb. 1200 J 5000 J 2200 J 2300 J 790 J 1200 J 1400 J 580 J 660 J 4800 J 1900 J 570 J 2100 J 2600 J 1100 J 2600 J 830 J 1600 J 2400 J 570 J 15073 200 J 640 J Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 18 4.0 DISCUSSION Since 1985, the majority of dredged material has been disposed in the southwestern quarter of MBDS near the MDA buoy (Figure 2-1; Germano et al. 1994). The distribution of metals and organics was examined in order to determine the nature and extent of contaminants in the western half of MBDS, and to identify areas that should be capped with material suitable for open ocean disposal. Sediment samples have been collected at MBDS and at the MBDS reference areas several times since 1985. Sample results from the 1989 survey were compared both with these historical MBDS data, and with sediment chemistry data from coastal Massachusetts collected by the National Oceanic and Atmospheric Administration (NOAA) through the National Status and Trends (NS&T) Program. 4.1. Spatial Distribution of Chemical Constituents Historical disposal activity north and west of the current disposal point may have influenced the present distribution of sediment contaminants; the distribution of each metal shows a similar pattern. The ranges of trace metal concentrations were limited. A contour plot of Cu concentrations shows a band of higher concentrations in the center of western MBDS (along Stations 12-3, 11-6, and 11-8; Figure 4-1). Station 12-3, located on the far western edge of MBDS, had the highest measured concentrations of Cr (139 ppm), Cu (78 ppm), Zn (221 ppm), and Hg (0.47 ppm). The distribution of DDE is relatively random, with two distinct highs at Stations 12-9 and 18-17 (> 10 ppb). The spatial distribution of PAHs is even more indicative of an offsite concentration to the west (Figure 4-2). Although PAH concentrations are questionable at Stations 9-8 and 8-5 due to elevated detection limits, the contoured pattern suggests that these samples were taken in an area of relatively lower PAH concentrations (Figure 4-2). 4.2 Comparative Analysis of MBDS Sediment Chemistry Data 4.2.1 Historical MBDS Data Reference area concentrations of trace metals were near or below the average of MBDS stations sampled in the 1989 survey. Concentrations of trace metals at both reference areas have remained relatively constant since reference area 18-17 was first sampled in 1985 (SAIC 1987; Table 4-1). Concentrations of trace metals detected at a few isolated stations at MBDS, when compared with reference area results, indicated no significant accumulation of trace metals, relative to the reference areas. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 MBDS SEDIMENT COPPER CONCENTRATIONS (ppm) 42°26.00'N 42°25.00'N Disposal Site Boundary O 37 Meters Figure 4-1. Contour map of copper concentrations (ppm) Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 MBDS SEDIMENT TOTAL HMW PAH CONCENTRATIONS (ppb) ND = Not Detected 42°26.00' N Disposal Site Boundary Ownp Meters Figure 4-2. Contour map of total high molecular weight PAH concentrations (ppb) Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 21 Table 4-1 Historical MBDS Reference Station Metal Data Sample Dat 70 95 4] 33 18 64 110 97 12 24 50 95 47 33 22 Reference Station 18-17 June 85 18-17 January 86 18-17 October 87 18-17 June 89 83 135 62 26 37 FG-23 October 87 40 95 40 33 19 *Data include all stations sampled in June 1989 except for reference stations. Pesticides were present (DDE) at both reference areas, including the maximum measured concentration of 10.5 ppb at 18-17. The two replicate samples from 18-17 contained less than 3 ppb of the same compound, indicating that the elevated concentration of DDE measured in the composite sample from 18-17 was not distributed across the entire reference area. As will be discussed in Section 4.2.2, pesticides are fairly common in Massachusetts Bay sediments in concentrations similar to those measured at most of the MBDS stations (NOAA 1991). PAHs and pesticides generally have been undetected in previous surveys. Pesticide detection limits were higher in the past, so the trace detections of DDE may have been missed. The HMW PAH fluoranthene was detected prior to the June 1989 survey (510 ppb at Station 14-9; SAIC 1990). Although all but one PCB replicate sample from MBDS were below detection, PCBs have been detected in sediments at MBDS prior to the June 1989 survey. In September 1985, replicate samples were taken at Stations 18-17 and 9-8. Average concentrations of PCBs were 75 and 1240 ppb, respectively. Sampling was duplicated at Stations 18-17 and 9- 8 in January of 1986 with lower results (48 and 329 ppb, respectively; all from SAIC 1987). The 1985 sampling was repeated in 1986 with similar, although slightly lower, results, which increases the validity of the historical data. The 1989 PCBs data were accompanied by Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 22 reasonable surrogate and matrix spike recoveries, which also indicates that these data are valid. Therefore, the decrease in PCB concentrations in MBDS sediment is apparently real. Commercial production of PCBs ceased in 1977 (Kennish 1992). These compounds persist in estuarine and marine sediments and have a half-life in environmental samples from 8 to 15 years (Kennish 1992). They may be nearly undetectable in the water column, but tend to accumulate in biota (Pequegnat et al. 1990). The observed decreases in PCB concentrations may be related to a lower environmental input than in the past. Reduced inputs through better management have now allowed reductions to occur over the past 5-10 years or more. Subsequent burial or dilution with newer deposited (natural) sediments containing lower levels of PCBs seems the most likely explanation. 4.2.2 Regional Data Comparison Samples from coastal and estuarine sediment data from 300 sites in the United States have been collected and analyzed during NOAA's NS&T since 1984. Several sites along the coast of Massachusetts and in Boston Harbor were sampled from 1984 to 1989 (NOAA 1991). Stations closest to MBDS, including Cape Ann, Duxbury Bay, Salem Harbor, and Quincy Bay, were compared to the MBDS results. None of the NS&T stations were located as far offshore as MBDS. However, since much of the material sampled at MBDS was presumably material dredged from Massachusetts harbors, the comparison is appropriate to place the chemistry data in a relative context. In comparing the MBDS results with NS&T data, several qualifiers must be made. The analytical methods vary somewhat between the two; NS&T methods were developed for very low detection limits. For example, although many PAHs were lower than the MDL in MBDS samples, detection limits were higher than those of the NS&T data, so the two datasets are not directly comparable. Individual concentrations of detected PAHs (rather than total HMW or LMW PAHs) were compared with NS&T data, because of the uncertainty of summing values which are below detection. PCBs are analyzed by NS&T methods as individual isomers, and are not comparable with the total PCB measurement obtained by the NED laboratory. Metals. MBDS metals data were compiled, and several ranges of values were compared both with regional Massachusetts and national NS&T data. The maximum and minimum metals values, and the statistical range of values (mean + one standard deviation) were reported for MBDS data, and compared with four regional sites and the values reported by NS&T for national mean and ‘high” values (greater than one standard deviation above the national mean; NOAA 1991). The four regional areas used for comparison are: Cape Ann-Gap Head (CAGH), Salem Harbor (SAL), Quincy Bay (QUI), and Duxbury Bay-Clarks Island (DBCI; Figure 1-1). Data over several years were averaged from each of these sites. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 23 SAL and QUI are reported to have “high” concentrations of many metals (Cr, Cu, Hg, Pb); CAGH has “high” concentrations of Pb only; and DBCI is a sandy site without any reported “high” concentrations of any metal or organic contaminant (NOAA 1991). In general, CAGH and DBCI have lower concentrations of all metals than SAL and QUI (Table 4-2). The maximum measured concentration of Ni, Pb, and Zn in MBDS samples was higher than both QUI and SAL. However, the statistical ranges of all metals concentrations from MBDS samples were intermediate between the two highest metals sites (SAL and QUI), and the two lowest metals sites (CAGH and DBCI). One exception was the maximum Pb value, which was greater than that measured at QUI (Table 4-2). Relative to national values, the mean values of MBDS metals concentrations were less than the national mean for all metals except Cu, Hg, and Pb (Table 4-2). All of the Cu and Hg concentrations measured at MBDS were less than the value classified as “high” by NS&T, but the statistical maximum value of Pb measured at MBDS was higher than this “high” value. In general, Ni values are lower in the entire Massachusetts Bay region, including the MBDS, relative to national concentrations. Table 4-2 MBDS Trace Metal Data Relative to Regional Massachusetts Bay MBDS Maximum MBDS Minimum MBDS Mean Statistical Range“ NS&T National Mean NS&T National "High" NS&T = National Status and Trends (NOAA 1991). Pesticides and PAHs. All organic data for both MBDS and the NS&T sites were normalized to TOC. Natural variations in sedimentary parameters can influence the concentration of trace metal and organic constituents measured in the laboratory. For example, an increase in the fine-grained fraction and in TOC are both positively correlated Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 24 with metal and organic concentrations (e.g., NOAA 1991). Consequently, MBDS organics data were normalized and compared with the same regional Massachusetts sites (CAGH, SAL, QUI, and DBCI; Figure 1-1). Data over several years were averaged from each of these sites and divided by the TOC concentration (Table 4-3). After normalizing pesticide concentrations to TOC, the DDE concentration of Station 18-17 falls within the ranges of other values measured at MBDS. In general, DDE concentrations are similar to those measured at the NS&T sites. This factor, and the lack of any spatial distribution of DDE concentrations, indicates that the detections of DDE at MBDS are representative of background concentrations in Massachusetts Bay. SAL and QUI are reported to have “high” concentrations (greater than one standard deviation from the national mean) of total LMW and HMW PAHs, and total DDT pesticides (NOAA 1991). CAGH also is reported to have “high” concentrations of total HMW PAHs, and actually has higher concentrations in individual HMW PAHs than the other regional Massachusetts sites examined here (Table 4-3). About one-third of the MBDS stations were below detection for all PAHs measured, and only two LMW PAH compounds and eight HMW compounds were detected in any sample. Both reference areas were below detection in all PAHs except for an estimated value of pyrene at FG-23. Many of the detected and estimated concentrations of individual PAHs in MBDS sediment were in the same range or higher than those measured at all of the NS&T sites used in the comparison (Table 4-3). A degree of uncertainty exists in comparing the MBDS estimated PAH concentrations, which are below the MDL and estimated from the chromatograms. This uncertainty is compounded by the different methods used by NS&T. All of the PAHs detected (not estimated) at Station 12-3 were above the MDL and higher than all of the NS&T sites, which indicates clearly that the sediment near this station is anomalously high in HMW PAHs relative to both the NS&T stations and the national average. The distribution of HMW PAHs at MBDS indicates that the highest values are concentrated in the far western edge of MBDS, and are influenced by historical disposal of dredged and perhaps other waste materials (Figure 4-2). HMW PAHs were detected at many MBDS stations, including those near the current disposal buoy, in concentrations similar to coastal measurements made in the NS&T program (Table 4-3). HMW PAHs have long residence times in the aquatic environment, even relative to LMW PAHs, and are generally derived from fossil fuel combustion (Kennish 1992). It is currently thought that pyrogenic PAHs (HMW) are more tightly bound to particles than petroleum source (LMW) PAHs (McGroddy et al. 1992). Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 25 JOqMeyH wales Keg Aouino BIS] Se|o - Aeg Aingxnq) an Se ae : ae —zldg WIE Aeg syasnyoessep] [RUOIsoy 0} VANeJoY SUONeIUIDUOD HVWd Puke aplonseg pazi[euLION DOL €-p AGeL Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 26 5.0 CONCLUSIONS AND RECOMMENDATIONS Sediment chemistry results from the MBDS survey of June 1989 indicate that the distribution of both organic and inorganic constituents reflects a difference in disposal practices from the past to the present with lower contaminant concentrations observed in the area of active disposal. Conversely, the highest concentrations of contaminants, especially PAHs, are located along the western edge of MBDS where disposal in earlier decades was concentrated. Relatively low trace metal concentrations and the spatial consistency of trace metal data indicate no specific anthropogenic point sources of trace metals; maximum measured concentrations of all metals are at stations north of the present disposal buoy. In general, the data suggest no accumulation of elevated concentrations of trace metals at MBDS. Metal concentrations are within MBDS reference area values. Overall, Pb concentrations are the highest relative to both regional and national comparisons. Detected HMW PAHs clearly show the highest concentrations near Station 12-3, located near the approximate center of the historical disposal site (1 nmi west of present center). Approximately two-thirds of the stations at MBDS contained HMW PAHs at concentrations within the range of values measured along coastal Massachusetts by the National Status and Trends Program, and a trace of pyrene was detected (estimated) at reference area FG-23. These factors indicate that the presence of PAHs at MBDS is influenced by both background concentrations of PAHs in the Massachusetts Bay region and historic disposal. The detection of 4,4'-DDE in many samples is consistent with the fairly common presence of pesticides in Massachusetts Bay sediments. PCBs, previously reported at the same stations measured in the 1989 survey at concentrations of up to 1 ppm, were virtually undetected; subsequent burial seems the most likely explanation. ° The presence of relatively high concentrations of HMW PAHs along the western edge of MBDS indicates that this area should be considered to receive new capping material suitable for unconfined disposal. ° Future chemical sampling at MBDS should focus on the distribution of PAHs at MBDS, including the eastern half of the site, in order to document background concentrations of PAHs in the Massachusetts Bay region. Concentrations of PAHs at MBDS are similar to coastal background, but are likely not as low as background levels found in the Stellwagen Basin. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 27 6.0 REFERENCES EPA. 1986. Test methods for evaluating solid waste (SW-846): physical/chemical methods. US Environmental Protection Agency, Office of Solid Waste, Washington, D.C. EPA. 1988a. Laboratory data validation: functional guidelines for evaluating organics analyses. US Environmental Protection Agency, Office of Emergency and Remedial Response, Washington, D.C. EPA. 1988b. Laboratory data validation: functional guidelines for evaluating inorganics analyses. US Environmental Protection Agency, Office of Emergency and Remedial Response, Washington, D.C. Fredette, T. J. 1990. Cruise report for O.S.V. Anderson, sediment chemistry and benthic body burden surveys at the Massachusetts Bay Disposal Site, 5-7 June 1989. US Army Corps of Engineers, New England Division, Waltham, MA. Germano, J.; Parker, J.; Charles, J. C. 1994. Monitoring cruise at the Massachusetts Bay Disposal Site, August 1990. (SAIC Report No. SAIC-90/7599&C90). Submitted to the US Army Corps of Engineers, New England Division, Waltham, MA. Kennish, M. J. 1992. Ecology of estuaries: anthropogenic effects. Boca Raton, Fl: CRC Press, Inc. McGroddy, S. E.; Farrington, J. W.; Phinney, C. S.; Johnson, C. G. 1992. Partitioning of polycyclic aromatic hydrocarbons between sediments and porewaters from Boston Harbor, MA. Seventh Annual Boston Harbor/Mass. Bay Symposium Proceeding, Mass. Bay Marine Studies Consortium, P.O. Box 660, Boston, MA 02125-0005 (Abstract). Morton, R. W.; Karp, C. A. 1980. DAMOS annual report 1980. Volume 1 Physical Measurements. DAMOS Contribution No. 17. Science Applications Inc. Submitted to US Army Corps of Engineers, New England Division, Waltham, MA. NOAA. 1991. Second summary of data on chemical contaminants in sediments from the National Status and Trends Program. NOAA Tech. Mem. NOS OMA 59. National Oceanic and Atmospheric Administration, Rockville, MD. Oceanic Society. 1982. Dredging and dredged material management in the Long Island Sound regions. The Oceanic Society, Stamford, CT. New England Governors Conference, Boston, MA. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 28 Pequegnat, W. E.; Galloway, B. J.; Wright, T. D. 1990. Revised procedural guide for designation surveys of ocean dredged material disposal sites. Final report. Technical Report D-90-8. Prepared for the Department of the Army, US Army Corps of Engineers, Washington, D.C. SAIC. 1987. Environmental information in support of site designation documents for the Foul Area Disposal Site. SAIC Report No. SAIC-85/7528&93. US Army Corps of Engineers, New England Division, Waltham, MA. SAIC. 1988. Monitoring surveys at the Foul Area Disposal Site, February 1987. DAMOS Contribution No. 64 (SAIC Report No. SAIC-87/7516&C64). US Army Corps of Engineers, New England Division, Waltham, MA. SAIC. 1990. Analysis of sediment chemistry and body burden data obtained at the Foul Area Disposal Site, October 1987. DAMOS Contribution No. 75 (SAIC Report No. SAIC- 88/7535&C73). US Army Corps of Engineers, New England Division, Waltham, MA. Chemical Analyses of Sediment Sampling at the Massachusetts Bay Disposal Site, June 1989 INDEX atomic absorption spectrophotometry 4, 6 benthos 27 body burden 27, 28 buoy 1, 3, 11, 18, 24, 26 disposal 1, 24, 26 capping v, 26 contaminant v, 4, 18, 23, 26, 27 deposition 22 organics 1, 7, 9, 18, 24, 27 polyaromatic hydrocarbon (PAH) iii, iv, v, 1, 7, 9, 11, 15, 16, 18, 20-26 polychlorinated biphenyl (PCB) v, 1, 6, 7, 9-11, 21, 22, 26 total organic carbon 1, 4, 6, 7, 9 reference area 4, 15, 18, 21, 22, 26 REMOTS® redox potential discontinuity (RPD) 10 RPD REMOTSS®; redox potential discontinuity (RPD) 10 RPDs REMOTSS®; redox potential discontinuity (RPD) 10 sandy 23 sediment chemistry v, 18, 26-28 sediment sampling 1 cores 4 grabs iv, 3-5 spectrophotometry atomic absorption 4, 6 statistical testing 22, 23 survey bathymetry 3 trace metals iii, v, 1, 4, 6, 9-12, 18, 21-24, 26 cadmium (Cd) 4, 6, 11 chromium (Cr) 4, 6, 11, 18, 23 copper (Cu) iv, 4, 6, 11, 18, 19, 23 mercury (Hg) 4, 6, 9, 11, 18, 23 nickel (Ni) 4, 6, 11, 23 zinc (Zn) 4, 6, 11, 18, 23 waste v, 1, 4, 24, 27 industrial v, 1 ui i