rrs^:? . ^-/^ » ^,-1 v(7\«» \N^x^\ UMASS/AMHERST 31,e0b(:i01bbDfl477 Report to the MASSACHUSETTS BAYS PROGRAM SOURCES AND LOADINGS OF POLLUTANTS TO THE MASSACHUSETTS BAYS •%. Prepared By: ^7 0 ^%' ''^^nzie-Cura & Associates, Inc. One Courthouse Lane, Suite Two Chelmsford, Massachusetts 01824 NOVEMBER, 1991 MBP-91-01 Funded by: The Massachusetts Environmental Trust The Massachusetts Bays Program Is a cooperative venture of Massachusetts Coastal Zone Management Office, U.S. Environmental Protection Agency, and Massachusetts Environmental Trust ^ -^^ /^a ^ ftnir**^ This research was made possible by funding from The Massachusetts Environmental Trust environmental philanthropy focussing on the Commonwealth's coastal resources. an ACKNOWLEDGEMENTS The primary authors of this document are Christine Werme and Charles A, Menzie. We were assisted by many people, some of whom authored specific sections of the report, and others of whom offered guidance or assistance. Bonnie Potocki and Jerome Cura assisted us in preparation of the sections on inputs from point sources and from rivers. The section on loadings in groundwater was written by Jon Freshman. Brian Field prepared the sections on loading from dredged material and in-place sediments. The section on loading associated with atmospheric deposition was prepared by William Galen. Kay Reddy prepared the section on the spatial distribution of hazardous waste sites near the coast and rivers. General admimstrative support and production of the final document was coordinated by Joan Pioli. Many of the data we used to estimate loadings from point sources were obtained from the U.S. Environmental Protection Agency Resource Information Center. Persoimel at the center assisted us by retrieving data from their permit compliance system (PCS) database. Michael Connor and Wendy Smith of the Massachusetts Water Resources Authority (MWRA) provided us with additional information to develop our estimates of inputs from point sources. The MWRA also supported a separate effort to estimate loadings to Boston Harbor. The estimates of loadings from runoff were made using data from the National Coastal Pollutant Discharge Inventory, which was developed and is maintained by the National Oceanic and Atmospheric Administration Ocean Assessment Division. Daniel Farrow of that office provided those data to us and assisted us in adapting the available information to our use. He also provided us with data on land use m the region and provided us with guidance for developing estimates of loads from point and nonpoint sources. Philip Shelly of EG&G also provided us with guidance for estimating inputs from point and nonpoint sources. He developed and reviewed our strategies poor to our preparation of this document. Warren Kimball of the Massachusetts Division of Water Pollution Control provided us with data and documents to assess water flow in the region. He also assisted us in dividing the system into drainage systems. Gordan Wallace of the University of Massachusetts at Boston provided guidance for use of data for estimating loads from rivers. Many of the data used to estimate loadings from atmospheric data were based upon regional estimates that were provided to us by Dhan Olmez of the Massachusetts Institute of Technology. We prepared this document under the direction of Diane Gould, Program Coordinator for the Massachusetts Bays Program, at the Massachusetts Executive Office of Environmental Affairs (EOEA). We thank Dr. Gould, as well as Judy Pederson and Jan Smith of EOEA, for their direction and support. We also thank Matthew Leibman, the Program Coordinator for the Massachusetts Bays Program at the U.S. Enviroimiental Protection Agency, Region I, Water Management Division. MASSACHUSETTS BAYS PROGRAM Massachusetts Executive Office of Environmental Affairs Coastal Zone Management 100 Cambridge St., Room 2006 Boston, Massachusetts 02202 (617) 727-9530 FOREWORD us Environmental ProteOion Ager»Cy Water Management Division John F. Kennedy Federal Building Boston, Massachusetts 02203 (617) 565-3514 The roots of the Massachusetts Bays Program extend back to 1 982, when the City of Ouincy filed suit against the Metropolitan District Commission and the Boston Water and Sewer Commission over the chronic pollution of Boston Harbor, Quincy Bay, and adjacent waters. Outdated and poorly maintained sewage treatment plants on Deer Island and Nut Island were being overwhelmed daily by sewage from the forty-three communities in the Metropolitan Boston area. Untreated and partially treated sewage were spilling into Boston Harbor. Litigation over the pollution of Boston Harbor culminated in 1 985 when the United States Attorney filed suit on behalf of the Environmental Protection Agency against the Commonwealth of Massachusetts for violations of the Federal Clean Water Act. The settlement of this suit resulted, in 1988, in the creation of the Massachusetts Water Resources Authority, the agency currently overseeing a multi-billion dollar project to repair and upgrade Metropolitan Boston's sewage treatment system. In addition, the settlement resulted in the establishment of the Massachusetts Environmental Trust - an environmental philanthropy dedicated to improving the Commonwealth s coastal and marine resources. $2 millon in settlement proceeds are administered by the Trust to support projects dedicated to the restoration and protection of Boston Harbor and Massachusetts Bay. The Trust provided $1 .6 million to establish the Massachusetts Bays Program, a collaborative effort of public officials, civic organizations, business leaders, and environmental groups to work towards improved coastal water quality. The funding was used to support both a program of public education and a scientific research program focussing on the sources, fate, transport and effects of contaminants in the Massachusetts and Cape Cod Bays ecosystem. To maximize the efficiency of limited research funding, the sponsored research program was developed in coordination with research funded by the MWRA, the United States Geological Survey, and the Massachusetts Institute of Technology Sea Grant Program. The study described in this report compares the relative magnitudes of point and nonpoint sources of pollution to the Bays system. This information will help to meet the Massachusetts Bays Program goal of producing an area- wide management plan for water quality enhancement and protection. In addition, the study provides a basis for identifying data gaps to be addressed in future research. In April, 1990, following a formal process of nomination, the Massachusetts Bays Program became part of the National Estuary Program. The additional funding provided as part of this joint program of the Environmental Protection Agency and the Commonwealth of Massachusetts is being used to continue a coordinated program of research in the Massachusetts Bays ecosystem, as well as supporting the development of a comprehensive conservation and management plan for the coastal and marine resources of Massachusetts and Cape Cod Bays. The information in this document has been subject to Massachusetts Bays Program peer and administrative review and has been accepted for publication as a Massachusetts Bays Program document. The contents of this document do not necessarily reflect the views and policies of the Management Conference. I ■ ■ TABLE OF CONTENTS EXECUTIVE SUMMARY ix 1.0 INTRODUCTION 1 1.1 Objectives 1 1.2 Report Organization 2 2.0 TECHNICAL APPROACH 3 2.1 General Approach 3 2.2 Selection ot Compounds and/or Biological Agents 3 2.3 Consideration of Spatial Scales 4 2.4 Quality Assurance 5 2.5 Integration with Other Programs 7 2.6 Uncertainty/Sensitivity Analysis 7 2.7 Source Types 7 3.0 WATERSHED CHARACTERIZATION 8 3.1 Drainage Areas 8 3.2 River Systems 12 4.0 POINT SOURCE INVENTORY 18 4.1 General 18 4.2 Identification of Point Sources 18 4.3 Point Source Loadings 22 4.3.1 Data Sources 22 4.3.2 Calculation of NPDES Loadings 27 4.3.3 Minor NPDES Dischargers 29 4.3.4 Anticipated Changes in Loadings Due to Upgrade of MWRA Effluents 71 4.3.5 Data Quality for Point Source Estimates 71 5.0 NONPOINT SOURCE INVTENTORY 75 5.1 General 75 5.2 Runoff from Urban and Nonurban Land Areas 75 5.2.1 Runoff to Drainage Areas 75 5.2.2 CSOs and Stormwater Discharges to Boston Harbor 84 5.3 Discharges from Coastal Rivers 89 5.3.1 Water Quality Data for Massachusetts Rivers 89 5.3.2 Estimates of Loadings via Major Rivers 100 5.4 Loadings in Groundwater 1 14 • 5.4.1 Methods 114 5.4.2 Results: Nitrogen Loadings to Cape Cod Bay via Groundwater 120 5.4.3 Results: Groundwater Loadings to Boston Harbor 127 5.5 Loadings Associated with Dredged Material Disposal 129 5.5.1 General Approach 129 5.5.2 Calculation of Loadings 129 5.6 Loadings Associated with Atmospheric Deposition 133 5.6.1 Nutrients 138 Phosphorus 139 5.6.2 Organic Compounds 140 5.6.3 Atmospheric loading of metals 143 5.7 Spatial Distribution of Hazardous Waste Sites Near the Coast and Rivers 161 5.7.1 Approach 161 5.7.2 Results 162 5.8 In-Place Sediments 164 5.8.1 North Shore 165 u 5.8.2 Boston Harbor System 180 5.8.3 The Bay 181 5.8.4 Data Quality and Quantity 183 6.0 CONTAMINANT LOADING AND ASSESSMENT 184 6.1 Comparison of pollutant sources 184 6. 1. 1 Freshwater Flow 185 6.1.2 Total Suspended Solids 188 6.1.3 Biochemical Oxygen Demand (BOD) 192 6.1.4 Total Nitrogen 196 6.1.5 Total Phosphorus 200 6.1.6 Oil and Grease 204 6.1.7 PAHs 208 6.1.8 PCBs 214 6.1.9 Metals 219 6.2 Identified Pollutant Problems in Nearshore Waters 243 6.3 Qualifications and Data Gaps 245 ui LIST OF TABLES Table 1. Drainage areas used in this study and their relationshrps to other designated drainage areas _ 8 Table 2. Land use within the various drainage areas (kin2) _ 12 Table 3. Estimated annual river discharge to Massachusetts Bays (m3/s) 13 Table 4. Names of NPDES permit holders depicted by number in Figure 8 20 Table 5. Compounds monitored for in major NPDES effluents: DMRs 23 Table 6. Contaminant:TSS ratios for selected parameters in sewage effluents of Massachusetts facilities ~ 29 Table 7. Estimated flows for major dischargers - 30 Table 8. Estimated point source loadings of solids -. 33 Table 9. Estimated point source loadings of biochemical oxygen demand (kg/yr) - 35 Table 10. Estimated point source loadings of nitrogen. ^ 37 Table 11. Estimated point source loadings of phosphorus _ 39 Table 12. Estimated point source loadings of oil and grease 41 Table 13. Estimated point source loadings of volatile organic compounds 43 Table 14. Estimated point source loadings of polynuclear aromatic hydrocarbons _ 45 Table 15. Estimated point source loadings of polychlorinated biphenyls (PCBs) _ 46 Table 16. Estimated point source loadings of phthalate esters 48 Table 17. Estimated point source loadings of cadmium based solely on DMR data _ 50 Table 18. Estimated point source loadings of cadmium based on DMR data as well as the CdiTSS Ratio _ 52 Table 19. Estimated point source loadings of chromium based solely on DMR data _ 54 Table 20. Estimated point source loadings of chromium based on DMR data as well as the Cr:TSS ratio _ 56 Table 21. Estimated point source loadings of copper -_ 58 Table 22. Estimated point source loadings of lead based soleh on the DMR data L 60 Table 23. Estimated point source loadings of lead based on the DMR data as well as the Pb:TSS ratio ^ 62 Table 24. Estimated point source loadings of nickel 64 Table 25. Estimated point source loadings of zinc 66 Table 26. Estimated point source loadings of mercury ^ 68 Table 27. Projected future loadings for MWRA effluents (kg/vr) 73 Table 28. Contaminant concentrations reported for MWRA CSOs and the NCPDI _ 77 Table 29. Contaminant concentrations in runoff. ^ 78 Table 30. Estimated loads for runoff within each drainage area. 80 Table 31. Estimated loads for runoff within 0.5 mile of coastline 82 Table 32. Stormwater and CSO annual load summary for northern Boston Harbor _ 85 Table 33. Summary of land use in the coastal drainage area around Boston Harbor _ 87 Table 34. Summary of annual loads to Boston Harbor using NURP data. 88 Table 35. Water quality data for total suspended soUds 91 Table 36. Water quality data for biochemical oxygen demand 92 Table 37. Water quality data for nitrogen -> 93 Table 38. Water quality data for phosphorous.. — 94 IV Table 39. Water quality data for cadmium 95 Table 40. Water quality data for chromium 96 Table 41. Water quality data for copper 97 Table 42. Water quality data for lead. 98 Table 43. Water quality data for zinc 99 Table 44. Literature values for ranges of concentrations of selected chemicals in river water 100 Table 45. Loadings of total suspended solids via rivers 101 Table 46. Loadings of biochemical oxygen demand via rivers 102 Table 47, Loadings of total nitrogen via rivers 103 Table 48. Loadings of total phosphorus via rivers 104 Table 49. Loadings of total PAHs via rivers 105 Table 50. Loadings of total PCBs via rivers 106 Table 51. Loadings of phthalates via rivers 107 Table 52. Loadings of arsenic via rivers 108 Table 53. Loadings of cadmium via rivers 109 Table 54. Loadings of chromium via rivers 110 Table 55. Loadings of copper via rivers Ill Table 56. Loadings of lead via rivers 112 Table 57. Loadings of zinc via rivers 113 Table 58. Recharge areas by town for Cape Cod 122 Table 59. Nitrogen loadings from Cape Cod Bay watershed 123 using discrete methods approach 123 Table 60. Loadings of nitrogen to Cape Cod Bay 125 using discrete ana groundwater measurements approach ,...125 Table 61. Summary of nitrate and ammonia concentrations used in the groundwater measurements approach 126 Table 62. Estimates of loadings via groundwater to Boston Harbor 128 Table 63. Loadings to Massachusetts Bay due to dredged material disposal 131 Table 64. Parameters used to estimate atmospheric loading 134 Table 65. Seasonal and annual rainfall (cm) in the Massachusetts Bays region measured at two sites in the National Atmospheric Deposition Program 136 Table 66. Areas of Massachusetts Bays 137 Table 67. Atmospheric loading (kg/>T) of nitrogen to Massachusetts Bays. Estimate includes wet and dry deposition 138 Table 68. Atmospheric loading (kg/yr) of phosphorus to Massachusetts Bays. Estimate includes dry and wet deposition 139 Table 69. Atmospheric loading (kg/yr) of PAHs to Massachusetts Bays (dry and wet) 141 Table 70. Atmospheric loading (kg/)rr) of PCBs to Massachusetts Bays. Estimates include dry and wet deposition 142 Table 71. Atmospheric loading ot antimony (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 144 Table 72. Atmospheric loading of arsenic (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 145 Table 73. Atmospheric loading ot cadmium (kg/yr) to Massachusetts Bays, Estimates include dry and wet deposition 146 Table 74. Atmospheric loading ot chromium (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 147 Table 75. Atmospheric loading ot cobalt (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 148 Table 76. Atmospheric loading ot copper (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 149 Table 77. Atmospheric loading of iron (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 150 Table 78. Atmospheric loading of lead (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 151 Table 79. Atmospheric loading ot manganese (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 152 Table 80. Atmospheric loading oi mercury (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 153 Table 81. Atmospheric loading ot molybdenum (kg/yr) to Massachusetts Bays. Estimates mclude only wet deposition 154 Table 82. Atmospheric loading of nickel (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 155 Table 83. Atmospheric loading of selenium (kg/yr) to Massachusetts Bays. Estimates include only dry deposition 156 Table 84. Atmosphenc loading of silver (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition 157 Table 85. Atmospheric loading of vanadium to Massachusetts Bays. Estimates include dry and wet deposition 158 Table 86. Atmospheric loading of zinc to Massachusetts Bays. Estimates include dry and wet deposition 159 Table 87. Atmospheric loading to the Massachusetts Bays (kg/yr) 160 Table 88. Distribution of sediment samples examined for this report 164 Table 89. Summary of sediment samples examined in the Boston Harbor system 180 Table 90. The distribution of high metals concentrations in the bay subarea. 182 Table 91. Freshwater inflow to Massachusetts Bay (m3/s) 186 Table 92. Suspended sediment load to Massachusetts Bay by source (kg/yr) 189 Table 93. BOD load to Massachusetts Bay by source (kg/yr) 193 Table 94. Nitrogen load to Massachusetts Bay by source (kg/yr) 197 Table 95. Phosphorus load to Massachusetts Bay by source (kg/y) 201 Table 96. Oil and grease load to Massachusetts Bay by source (kg/yr) 205 Table 97. Higher estimate of PAH loading by source (kg/yr) 209 Table 99. PCB load to Mass Bay by source (kg/yr) 216 Table 100. Cadmium load to Mass Bay by source (kg/yr) 220 Table 101. Chromium load to Mass Bay by source (kg/yr) 224 Table 102. Copper load to Mass Bay by source (kg/yr) 228 Table 103. Lead load to Mass Bay by source (kg/yr) 232 Table 104. Zinc load to Mass Bay by source (kg/yr) 236 Table 105. Mercury load to Mass Bay by source (kg/yr) 240 Table 106. Identified water quality problems in near-coastal areas 244 VI LIST OF FIGURES Figure 1. Drainage areas selected for this study 6 Figure 2. Drainage areas used by the Massachusetts 9 Department of Environmental Protection 9 Figure 3. USGS cataloguing units : 10 Figure 4. County boundaries 11 Figure 5. Seasonal pattern of flow in Merrimack River 15 Figure 6. Seasonal flow in Ipswich River ,. 16 Figure 7. Seasonal flow in Charles River 17 Figure 8. Lx)cations of major point sources on major rivers and along the coast 19 Figure 9. Groundwater divide on Cape Cod 121 Figure 10. Locations of DEP confirmed waste sites within 500 feet of the coast or Merrimack River 163 Figure 11. Locations of elevated levels of chromium in sediments of Massachusetts Bay 166 Figure 12. Locations of elevated levels of lead in sediments of Massachusetts Bay 167 Figure 13. Locations of elevated levels of total PAHs in sediments of Massachusetts Bay 168 Figure 14. Lead in sediments of Boston Inner Harbor 169 Figure 15. Cadmium in sediments of Boston Inner Harbor 170 Figure 16. Chromium in sediments of Boston Inner Harbor 171 Figure 17. Copper in sediments of Boston Inner Harbor 172 Figure 18. Mercuiy in sediments of Boston Inner Harbor 173 Figure 19. Nickel m sediments of Boston Inner Harbor 174 Figure 20. Zinc in sediments of Boston Inner Harbor , 175 Figure 21. PCBs in sediments of Boston Inner Harbor 176 Figure 22. Total PAHs in sediments of Boston Iimer Harbor 177 Figure 23. Carcinogenic PAHs in sediments of Boston Inner Harbor 178 Figure 24. Total phthalates in sediments of Boston Inner Harbor 179 Figure 25. Contribution of various sources to freshwater inflow 187 Figure 26. Suspended sediment load to Massachusetts Bay by source (mt/yr) 190 Figure 27. Relative contributions to suspended sediment load. 191 Figure 28. BOD load to Massachusetts Bay by source (mt/yr) 194 Figure 29. Relative contributions to BOD load 195 Figure 30. Nitrogen load to Massachusetts Bay by source (mt/yr) 198 Figure 31. Relative contributions to nitrogen load 199 Figure 32. Phosphorus load to Massachusetts Bay by source (mt/yr) 202 Figure 33. Relative contributions to Massachusetts Bay load of phosphorus 203 Figure 34. Oil and grease load to Massachusetts Bay by source (mt/yr) 206 Figure 35. Relative contributions to Massachusetts Bay load of oil and grease 207 igure 39. PCB load to Mass Bay by source (kg/yr) 217 Figure 40. Relative contributions to Mass Bay load of PCBs 218 Figure 41. Cadmium load to Mass Bay by source (kg/yr) 221 Figure 42. Relative contributions to cadmium load 222 Figure 43. Chromium load to Mass Bay by source (kg/yr) 225 Figure 44. Relative contributions to chromium load 226 Figure 45. Copper load to Mass Bay by source (kg/yr) 229 Figure 46. Relative contributions to copper load 230 Figure 47. Lead load to Mass Bay by source (kg/yr) .....233 vii i Figure 48. Relative contributions to lead load _ 234 Figure 49. Zinc load to Mass Bay by source (kg/yr) ^ 237 Figure 50. Relative contributions to zinc load ^ 238 Figure 51. Mercury load to Mass Bay by source (kg/yr) 241 Figure 52. Relative contributions to mercury load _ 242 ■ vm EXECUTIVE SUMMARY This report identifies and quantifies sources and loadings of pollutants to the Massachusetts Bays system and completes the objectives of Task 1 of the Massachusetts Bays Program (MBP). Information presented in this report is part of the MBP effort to develop a plan for conservation and management of the estuarine waters from the New Hampshire border to the tip of Cape Cod. The identification of sources and estimates of loadings of pollutants have been developed jfirom existing information and are viewed as part of an overall risk assessment framework for the bays. When linked with information on the fate and effects of contaminants, the results of this report can provide insight into the relative importance of contaminants and sources with regard to the natural resources of the bays' systems. Because environmental problems may be manifested at various spatial scales (i.e. local, regional, or bay-wide), information on sources and loadings has been developed with respect to individual point and non-point sources, specific rivers and drainage basins, and the Massachusetts Bays system as a whole. With regard to the "importance" of a source, care must be taken to consider the spatial scale of the natural resource of concern as well as that of the contaminant source. Most of the information on loadings has been organized and reported for six broad geographic areas. Five of these correspond to drainage areas and include: the Merrimack River to the Lowell Dam (abbreviated ME in Figures i through iv); tiie North Shore (NS); Boston Harbor (EH); South Shore (SS); and, Cape Cod (CC). In addition, loadings of materials that are introduced directiy into the bay (atmospheric deposition) or are moved from nearshore to offshore areas (dredged material), are presented as being introduced to the "Bay" and are not related to specific drainage basins. The general approach of this study was to identify important pollutants to the Massachusetts Bays system and, to the extent possible, quantify the point and nonpoint source loads of these chemicals and agents. We used the most recent available data . Where gaps in data occurred or where data were considered to be of low quality, we used estimates based upon typical values reported in the literature. Elements, compounds, and biological agents were selected for the study based upon several criteria: Potential to degrade the quality or impair the use of Massachusetts Bays water; Inherent toxicity to environmental receptors or humans; Potential to be bioaccumulated by marine organisms; Environmental persistence; Information indicating that Massachusetts Bays water or sediment is being "en- riched" as a result of loading. IX Based on these criteria, the following general categories of materials were initially selected for the study: Total suspended solids; Oxygen-consuming substances (biochemical oxygen demand or BOD;; Nutrients, including nitrogen and phosphorus; Oil and grease; Polynuclear aromatic hydrocarbons (PAHs); Pesticides and Polychlorinated Biphenyls (PCBs); Selected metals, including cadmium, chromium, copper, lead, zinc, mercury, arsenic, selenium, beryllium, silver and nickel; Pathogens (viruses and bacteria). Comparisons of sources and drainage areas were made for total suspended solids, BOD, nitrogen, phosphorus, oil and grease, PAHs, PCBs, cadmium, chromium, copper, lead, zinc and mercury. For some of the selected materials, data were insufficient to compare the relative magnitude of various sources. Comparisons were not made for pathogens or pathogen indicators, since they are a greater problem on a local rather than a bay-wide scale. However, based on surveys conducted by the Massachusetts Department of Environmental Protection, point and nonpoint sources are important contributors of pathogens at the local level. Few data are available on pesticides and other synthetic organic compounds, and their loads were not evaluated in detail in this report. Information on sources is presented for: 1. Point Sources - estimates were made for all major point sources throughout the drainage areas feeding the Massachusetts Bays system. For the Merrimack River, point sources were considered up to the Lowell Dam; 2. Coastal Point Sources - estimates were made for major point sources that discharge directly to coastal embay ments or to the open bay waters; 3. Rivers - estimates were made of loadings associated with 27 river systems; 4. Runoff from Drainage Basins - estimates were made of runoff in the five major drainage basins (ME, NS, BH, SS, and CC); 5. Groundwater Discharges - estimates were made for nutrients and toxics in Boston Harbor and nitrogen for Cape Cod; 6. Coastal Runoff - estimates were made of runoff directiy from the coast into open bay waters or embayments; this analysis considers a zone of 0.5 miles from the coast as contributing directiy as coastal runoff; 7. Locations of areas where sediments exhibit elevated levels of contaminants - these areas may indicate the presence of other sources and may, themselves, act as sources; 8. Locations of Hazardous Waste Sites within 500 Feet of a river or coastline - the presence of these sites indicates a potential for a release; however, no effort was made in this study to confirm if releases have occurred; 9. Ocean Disposal of Dredged Material - this results in movement of materials from near-shore embayments or channels to the offshore Massachusetts Bay Disposal Site (MBDS): While the contaminants are already "in-place" within the marine system and are the result of point and non-point sources, offshore disposal of dredged material provides a mechanism by which contaminants may be moved and introduced directiy to offshore areas. Therefore, within this document, dredged material is viewed as a source with regard to offshore areas; this is consistent with the approach taken in other coastal areas (e.g.. New York Bight); 10. Atmospheric Deposition - estimates are provided for the major areas of the bays (ME, NS, BH, SS, CC). It is estimated as direct input and does not attempt to determine what portion of run off is from atmospheric sources. Some of these sources of contaminants to the bays overlap. For example, estimates of runoff from entire drainage basins would include inputs to the bays from rivers. This overlap made it possible to calculate and compare loadings using more than one method. In this study, two approaches (A and B) were used to estimate loadings to Massachusetts Bay. These differed primarily in the way loadings from watersheds were considered. For Method A, loads were estimated as the sum of all discrete loadings to the drainage basins. This involved estimating loads by drainage basins as the sum of loads from (1) all major National Pollutant Discharge Elimination System (NPDES) discharges to the drainage basin; (2) all runoff from the drainage area; and (3) for selected parameters and areas for which data are available, groundwater flow from the drainage basin. Total load to Massachusetts Bay was estimated as the sum of these loadings, plus the loadings from atmospheric deposition onto the water surface and disposal of dredged material at the MBDS site. This will overestimate total load somewhat because the disposal of dredged material actually involves movement of contaminants that have already entered the system via various point and non-point sources. Note that contribution from inplace sediments is not included, leading to some underestimation of total loadings. For Method B, loads were estimated for each drainage area as the sum of (1) major NPDES discharges for only the coastal discharges; (2) river disch2Lrges; (3) runoff from coastal areas, defined as the area within 0.5 miles of shore (except for Cape Cod Bay for which total runoff was used); and (4) groundwater flow for the selected parameters and drainage basins. Similar to Method A, loads from atmospheric deposition and disposal of dredged material were added to this sum to provide an overall estimate of loadings to the Massachusetts Bays system. There is considerable uncertainty in the estimates and this is described in detail within the report. Loadings for most contaminants and sources are presented as ranges. For a number of contaminants and sources there were no available measurements or the available data were judged to be unreliable. When this was the case, concentrations and loads were estimated from literature values or from extrapolations from similar systems. Most data on runoff, for example, were obtained from the NO A A National Coastal Pollutant Discharge Inventory (NCPDI), a database that probably provides the best available estimates of runoff for the region but which relies on extrapolations from "typical" conditions. Data on loads from river flow were also frequently estimated from typical values reported in the literature rather than based upon actual data. FAtimates of Loadings The report should be consulted for details on estimates and the associated uncertainties. Here, we present summary information based on the upper estimates of loadings from the Merrimack River (ME), North Shore (NS), Boston Harbor (BH), South Shore (SS), Cape Cod (CC), and "directly" to the Bay (Figures i-iv). These figures present results using Method A only. In order to illustrate the data, loadings estimates are presented in "log" format in the figures. Thus, the "Y" axis increases by factors of 10 (e.g., 10, 100, l.CXX), etc.). A value that appears to be only a few times greater than another value, may actually be 10 to 1(X) times greater. Based on the analyses performed during this study, a few general observations can be made: • The Merrimack River, North Shore, and Boston Harbor drainage areas are the dominant sources of pollutants. They contain the greatest number of major NPDES discharges, riverine inputs, as well as the highest concentration of identified hazardous waste sites. Of these three drainage areas, Boston Harbor was generally the largest source; • NPDES discharges are the most important sources of nitrogen, phosphorous, and biochemical oxygen demand; • For drainage areas that are serviced predominately by septic systems (e.g., Cape Cod), groundwater can be the major source of nitrogen to nearshore waters; XII • For toxic organic compounds and metals, the relative importance of point and nonpoint sources depends on the compound. There is also considerable uncertainty in these estimates; • The atmosphere can be an important source of the toxic organic compounds PAHs and PCBs; • Sediments exhibiting elevated levels of organic compounds or metals occur as localized "patches" within some rivers and harbors. This has been observed in Boston and Salem Harbors; • Bacterial contamination, nutrient enrichment, and oxygen-related problems have been identified in a number of coastal and river environments. The localized occurrence of these conditions indicates the importance of local point and nonpoint sources of bacteria, nutrients, and oxygen-consuming substances and underscores the need to evaluate effects and sources at the right spatial scales. Freshwater Flow Freshwater flow to the bays was estimated. The total annual discharge from the Merrimack River accounted for 52% of the freshwater flow to the system based on the assumption that 100% of the flow enters Massachusetts Bay. Rainfall accounted for 28%. If the Merrimack River were excluded from calculations, rainfall would account for 58% of the total input of freshwater to the bays. While nonpoint sources dominated the inputs from most of the drainage basins, inputs from the Deer and Nut Island POTWs dominated the flow into Boston Harbor. Our estimates did not include estimates of inputs of freshwater from the Gulf of Maine. This source may in fact provide the greatest inputs of freshwater to the system, so its exclusion is significant. The estimates that we do provide are subject to uncertainty. Annual river flows were estimated using several techniques, depending upon whether gauge measurements were available. Seasonal and year-to-year variability in flow is also high. This variability will affect the input of contaminants as well as the amount of water to the system. Total Suspended Solids Fig. i Loadings of total suspended solids were calculated using both Methods A and B. No data were available to consider atmospheric inputs, but inputs from other sources ranged from 299,000-555,000 metric tons per year (mt/yr). Disposal of dredged material was a major source of solids, accounting for 31% of the Method A and 60% of the Method B estimate. XIII In the case of dredged material, the loading represents movement of sediments (solids; from nearshore areas to an offshore location. Biochemical Oxygen Demand (BOD) Fig. i Estimates of BOD loadings were almost identical using Methods A and B, about 180,000 mt/yr. Most of the loads were due to inputs from NPDES discharges. The Boston Harbor NPDES outfalls accounted for approximately one half of the coastal NPDES inputs to the bays. Total Nitrogen (N) Fig, i The NPDES discharges also accounted for major portions of the inputs of nitrogen to the system, 66% of 28,000 mt/yr for the Method A and 43% of 36,000 mt/yr for the Method B estimate. For Method A, runoff and atmospheric deposition were other important sources. For Method B, river discharges accounted for 37% of the inputs. Groundwater discharges were calculated only for Boston Harbor and Cape Cod Bay. For Cape Cod, groundwater appeared to be an important nearshore source for nitrogen and was ten times higher than the contribution from runoff. ToUd Phosphorus (P) Fig. i Approximately 3,880-4,100 mt/yr total phosphorus are introduced to the bays using Methods A and B. These estimates did not include inputs from dredged material. However dredged material accounted for only about 5% of the inputs of nitrogen, the other nutrient examined. NPDES discharges accounted for 82% of the Method A and 71% of the Method B estimate. Oil and Grease Fig. ii An estimate of 13,000 mt/yr oil and grease into the bays was obtained using Method A. Based upon the available information, nonpoint source runoff is probably the major source of oil and grease to the bays. Dredged material disposal is also important as a mechanism for movement of oil and grease from one location to another. XIV PAHs Fig, U We found considerable variability in the estimates of PAH loads to the system, largely because few measurements of PAH estimates have been made. Our estimates were therefore based upon ranges of values that we considered typical. Using our higher estimates, which assumed that municipal effluents contain average concentrations of PAHs of about 10 ug/1, Methods A and B resulted in approximately the same input, 13,100-13,700 kg/yr. The NPDES discharges to Boston Harbor dominated these estimates. Those values probably rq>resent an extreme worst-case high estimate. More recent, but preliminary, data, indicate that average concentrations of PAHs in municipal effluents are far lower than assumed by our high estimates, about 0. 1 ug/1. Even using an average concentration of 1 ug/1, the total loads were 1,819 kg/yr for Method A and 2,200 kg/yr for Method B. The NPDES discharges accounted for one third to one half of these estimates. Using the lower estimates, atmospheric deposition appeared to be an important source of PAHs to the system, 52% for Method A and 43% for Method B. PCBs Fig. U Total load of PCBs to the bays was approximately 2,600 kg/yr using both Methods A and B. The similarity of these estimates results from the dominance of our estimate by atmospheric deposition. This estimate was based upon data collected during the mid 1970s, and the current value may be less. Estimated inputs of PCBs from NPDES discharges ranged from 416-468 kg/yr, which is about 20% of the total load. However, there is uncertainty in these estimates because most measurements are reported as being below the detection limits. A value below the detection limit was selected for the purpose of developing an estimate. Recent, preliminary data indicate that the selected value may be high. Similar to PAHs, the estimates presented in this report for inputs from NPDES discharges represent an upper or worst case estimate. Cadmium (Cd) Fig, iU There is considerable uncertainty in the estimates of cadmium inputs to the bays, because few measurements have been made of cadmium in point sources. Using high estimates of these values, we calculated inputs of 8,020-14,700 kg/yr. NPDES discharges accounted for 34% of the Method A and 17% of the Method B estimates. Runoff accounted for 30% of the Method A estimate, and river discharge accounted for 66% of the Method B estimate, assuming an average concentration in rivers of 1 ug/1. XV Chromium (Cr) Fig, Hi Similarly, few data were available for chromium concentrations in NPDES discharges. Using high estimates for chromium in NPDES discharges for Methods A and B, 84,000- 120,000 kg/yr enter the bays. NPDES discharges accounted for 53% of the Method A estimate and 35% of the Method B estimate. Runoff accounted for 24% of the Method A estimate. Rivers accounted for 47% of the Method B estimate, assuming an average concentration of chromium in river waters of 6 ug/1. Copper (Cu) Fig, Hi Methods A and B provided similar estimates of copper inputs to the bay, 150,000 and 190,000 kg/yr. Point and nonpoint sources were both important contributors to the overall load. NPDES discharges accounted for 57% and 37% of the Methods A and B estimates, respectively. Runoff accounted for 25% of the Method A estimate, and rivers accounted for 50% of the Method B estimate, assuming an average concentration in river water of 10 ug/1. Lead (Pb) Fig. iU Lead inputs, however, were dominated by estimates of inputs from nonpoint sources. Based on Method A, an estimated 470,000 kg/yr enter the bays. Method B yields 540,000 kg/yr. NPDES discharges accounted for less than 10% of these estimates. Runoff accounted for 42% of the inputs, using Method A and assuming concentrations in CSOs of 92 ugA. Atmospheric deposition was also an important source of lead, accounting for 45% of the Method A and 39% of the Method B estimates. Zinc (Zn) Fig. iv Zinc inputs were estimated as 419,000-536,000 kg/yr using Methods A and B. NPDES discharges, runoff, and atmospheric deposition contributed approximately equally to these values. NPDES discharges accounted for about 35% of the total load. Assuming an average concentration of 30 ug/1, rivers accounted for 53% of the Method B estimate. Mercury (Hg) Ftg. iv Mercury inputs were estimated using only Method A. Point source loads were difficult to estimate, because the only available data were for the MWRA outfalls into Boston Harbor. Those data included only values that were below detection limits. Extrapolations from these limited data therefore represented a worst-case estimate. Using the limited available information, point sources were the major sources of mercury to the bays, accounting for about one half the total load. Runoff, dredged material, and atmospheric inputs also contributed to the mercury loads. XVI Qualifications and Data Gaps In addition to the uncertainties inherent in each of the estimates of pollutant inputs to the bays, there are other factors that affect interpretation or use of the information included in this report. For example, the fate and effects of contaminants entering the system will differ, dq)«iding upon the methods by which they are introduced. Atmospheric deposition, for example, is spread out over a wide area, while an NPDES discharge is located at a specific site. The horizontal and vertical (water depth) modes in which contaminants are introduced are important with regard to subsequent fate and effects. In order to understand the significance of a source, its location, spatial extent, and resultant exposure concentrations must be understood. Inputs also vary seasonally. River flow, nonpoint source runoff, and groundwater discharge are aU expected to vary seasonally. Stormwater runoff will vary not only seasonally, but periodically, when large rainfall events increase runoff from storm drains and CSOs. Also, seemingly constant inputs, such as those from the major NPDES discharges, may vary with the changes in the hydrodynamics of their receiving waters. Concentrations of contaminants in the receiving waters may be higher during periods of low flow than they are during periods of high flow when they are diluted by larger volumes of water. Several data gaps were identified during preparation of the report: • Few data were available on sources of PAHs. However, these are considered to be an important group of compounds in the Massachusetts Bay system. • Although heavily contaminated sediments have been identified in the report, it is unclear if they should be considered as sources. Resuspension of contaminants from the sediments has not been considwed in our comparison of relative magnitude of sources of contaminants to the bays. • Information on loadings is presented at various spatial scales. However, it is unclear how the different spatial scales affect the fate and effects of the contaminants. • Oil spills and other infrequent large-scale events were not considered in the estimates of sources. • Marine pumpout facilities and other discharges from marinas were not included; • Loadings of nitrogen from groundwater appears to be an important source of nutrients to embayments along the shores of Cape Cod. There is insufficient data to verify that this is the case. XVII ■ o 3 -• ■ a. a Si 3 o O Dl > z I t • m CO o a •* O Z CO m O S • D o c 3 a < 3 • 3 ^ O -« o o » -• o o o 5 -• o o o o " — o o o o o 2 I — I I I Turn — r i r iirtn — r i i Jinri — r-rrmw. — i i ttiiTX 3 a. m 3 o m ? 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D D) (O CD (^ 0 03 'IIIIIIIIIHtllHIHHIHIIIITimill' i ■ ■ ■ ■ ■ v> w o c 0* 3- (0 ar o 11 •• 3 a 3 0) o S 30 O O » ■o NC^^KCCC^C>S>^^X^K!^^CS»^^CS?C^ vVSSvVVM o o I kV\\\VV\\VSS\V\V\VN 'mMMM^M^^MM^^MM' s I CO c 3 < S r- =■ o SI a CD tJ ? u- (20 O c 1.0 INTRODUCTION This report identifies and quantifies sources and loadings of pollutants to the Massachusetts Bays system. This report provides the results of Task 1 of the Massachusetts Bays rrogram (MBP). The MBP is jointly administered by the U.S. Environmental Protection Agency (EPA) and Massachusetts Coastal Zone Management (CZM). The MBP is developing a plan for conservation and management of the estuarine waters from the New Hampshire border to Race Point on Cape Cod. The plan will cover Massachusetts and Cape Cod bays. 1.1 Objectives Over the past several years, investigators and regulators have approached marine pollution and waste management issues within a risk assessment/risk management framework (e.g., Bierman et al., 1985). The Massachusetts Bays Program embodies many of the key elements of this framework. In simple terms, the overall elements of any marine risk assessment/risk management program include the following: 1. Hazard Identification (what conditions are thought to pose a hazard) 2. Source Identification and Characterization 3. E?qposure Assessment - Fate and Transport studies - Estimates of Exposure Point Concentrations 4. Effects Assessment - Acute, subchronic, and chronic effects on marine organisms - Acute, subchronic, and chronic effects on humans using marine resources 5. Risk Characterization 6. Risk Management - Where can efforts be best spent to reduce risks? This report provides information related to the first elements of the risk assessment/risk management framework: 1. Hazard identification 2. Source identification and characterization The objectives are to identify and characterize the compounds or biological agents and estimate the loadings of these pollutants to the Massachusetts Bays system. This information has been developed to identify specific sources of the compounds. Such information is important for facilitating sound management decisions. In summary the proposed objectives for Task 1 of the MBP are: 1. Idemify chemical compounds and biological agents that may pose hazards to the Massachusetts bays system; 2. Identify and characterize point and nonpoint sources and loadings of these compounds and agents; 3. Gather and organize information to be compatible with fate and transport modeling efforts and with regulatory and research programs used to make decisions concerning the need for and efficacy of source controls; 4. Integrate information from the concurrent Massachusetts Water Resources Authority (MWRA) program and address data gaps as needed. 1.2 Report Organization The technical approach used in the study is presented in Chapter 2. A discussion of the various watersheds that feed the Massachusetts Bays system is provided in Chapter 3 and provides a basis for organizing data on point and nonpoint sources. The locations and magnitudes of point and nonpoint sources are described in Chapters 4 and 5 respectively. An overview of contaminant loadings and an assessment of these foadings is given in Chapter 6. This chapter also identifies sources of uncertainty and data gaps in the estimates of loadings. 2.0 TECHNICAL APPROACH 2.1 General Approach The approach employed in this study was to identify important poUutants being discharged to the Massachusetts Bays system, quantify to the extent possible the point and nonpoint source loads of these chemicals, and organize this information at several spatial scales. An effort was made to obtain the most recent data available. In some cases, where data gaps or data of poor quadity existed, estimates were made based on available data in the literature or based on extrapolation from similar systems. An example is the loading of lead via National Pollutant EHscharge Elimination System (NPDES) outMls. We recognize that lead will probably be present in virtually all Publicly Owned Treatment Works (POTW) effluents. However, it is not measured in all effluents (i.e., it is not reported in their Discharge Monitoring Reports). To obtain an estimate of loadings, we developed a ratio of lead to total suspended solids (TSS) for other POTWs in the system and applied this ratio to the TSS levels measured at the POTWs for which there were no lead data. Wherever possible we have identified uncertainties associated with the data. We have also included an annotated bibliography of data sources as Appendix A of this document. This bibliography provides additional information on tne data bases and also provides some basis for evaluating the quality of underlying data. 2.2 Selection of Compounds and/or Biological Agents The assessment considered a specific set of compounds and/or biological agents judged to have the potential for posing a hazard to the Massachusetts Bays System. The selection of these compounds was a critical part of the program because it provides the framework for subsequent data collection and analysis efforts. Several criteria were considered in selecting the compounds and/or biological agents to be included in the analysis. The primary cnteria are the following: • The potential for the compounds to degrade the quality or impair the use of Massachusetts Bays water; • The inherent toxicity of the chemical to environmental receptors or humans; • The potential for the chemical to be bioaccumulated by marine organisms; • The environmental persistence of the compounds; • Information indicating that Massachusetts Bays water or sediment is being "enriched" as a result of the loading of the compound. Based on the criteria provided above the following general categories of materials were selected for the analyses: • Total suspended soHds • Polynuclear aromatic hydrocarbons (PAHs); • Environmentally persistent chlorinated organic compounds (e.g., PCBs, pesticides); • Selected metals including lead, cadmium, chromium, mercury, copper, arsenic, selenium, beryllium, silver and nickel; • Oxygen consuming substances (BOD); • Nutrients; • Pathogens (viruses/bacteria in wastewater). 2.3 Consideration of Spatial Scales Loadings to Massachusetts Bays are estimated at several spatial scales. This has been done in recognition of the fact that environmental problems may be manifested at various spatial scales and to provide a basis for identifying which sources or which regions are most "important" with regard to loadings to Massachusetts Bays. The spatial scales included in the analyses are as follows: 1. Point Sources - estimates are provided individually for all major point sources throughout the drainage areas feeding the Massachusetts Bays system; 2. Coastal Point Sources - estimates are provided individually for major point sources that discharge directly to coastal embayments or to the open bay waters; 3. Rivers - estimates are provided for point sources by river and for total loadings associated with each major river discharge to the bays; twenty- seven river systems are considered in the analysis; 4. Drainage Basins - estimates are provided for point sources, runoff, and, in few cases, groundwater discharges; the system has been broken up into five drainage basins for the purpose of this analysis: Merrimack, North Shore, Boston Harbor, South Shore, and Cape Cod (Figure 1); 5. Coastal Runoff - estimates are provided for runoff directly from the coast into open bay waters or embavrnents; this analysis considers a zone of 0.5 miles from the coast as contributing directly as coastal runoff; these estimates are made for each drainage basin; 6. Locations of In-place Sediments and Hazardous Waste Sites within 500 Feet of a Surface Waterbody Draining to Massachusetts Bays - this information is presented in terms of the locations of such sediments or waste sites; 7. Ocean Disposal of Dredged Material - this is considered as a direct input to the bays and occurs at the DAMOS site; 8. Inputs of Atmospheric Deposition - these estimates are provided for the major areas of the bays. Source information organized within these various spatial scales should help provide linkage between the fate and effects of chemicals in the bays and specific sources. 2.4 Quality Assurance The analysis presented in this report relies upon data obtained from a variety of sources which may differ in quality and level of documentation. To provide some basis for evaluating the quality of the underlying data each data source is described in Appendix A along with comments related to the apparent quality of the data. A detailed review of these data was beyond the scope of this program. Nevertheless, the probable ranges and values of data were assessed using appropriate "reality checks". Where data were suspect we nevertheless used it, but provided qualifications regarding its usefulness. Data judged to be unrehable are not used in Chapter 6 where an assessment is made of overdl loadings of pollutants to the Bays. The effort involved entry of many data points into spreadsheets and calculations of loadings using these spreadsheets. Quality Assurance included a review of data entry and generally several reviews of calculations. -^ timmMiimi MERRIMACK NORTH SHORE BOSTON HARi30R SOUTH SHORE CAPE COD T"" 0 s 10 muM FIGURE 1 BROT C9d C9n*tvi* ■nr ' Catry Banttkm* a^^ar ^DR.\[!^-\GE BASINS --■■ '**— -^-> - '^1 nrir nJ 2.5 Integration with Other Programs Members of the study team participated in exchanges of information with other MBP Project teams. In addition, information gathered as part of meetings with citizen's groups was utilized to define and/or supplement data gathering efforts. 2.6 Uncertainty/Sensitivity Analysis This project yields a variety of estimates of loadings. Underlying these estimates are various statistical distributions and assumptions. Therefore, there is a certain amount of uncertainty associated with each estimate. In most cases we have provided ranges for estimates and have checked estimates in several ways. Underlying assumptions are identified in Chapters 4 and 5 of this report. 2.7 Source Types The Water Quality Act of 1987 (PL 100-4) and its predecessor legislation identifies two categories of water discharges: point and nonpoint sources. However, it is generally convenient to consider them in the following way: • Traditional point sources: discharges from POTWs and industrial wastewater discharges. • Nontraditional point sources: discharges that are defined as point sources under the act but that are driven by additional considerations such as meteorological conditions, e.g., separate municipal storm sewers, combined sewer overflows. • Nonpoint sources: everytin^ else, including runoff from nonurban areas, atmospheric deposition, interflow and groundwater inputs, inplace sediments, and seeps. We used these definitions because while the nontraditional point sources are treated as point sources under the law, they behave in fact liJce nonpoint sources, and similar methodological approaches are needed to assess them. 3.0 WATERSHED CHARACTERIZATION 3.1 Drainage Areas The Massachusetts Bays system was organized into five drainage basins within which twenty-seven major rivers were identified (Figure 1). These drainage basins can be compared to those established by the Massachusetts Department of Environmental Protection (DEP) (Figure 2). Tne drainage basins selected for this analysis (Figure 1) were established based on the extent of information available on land use in the National Oceanic and Atmospheric Administrations (NOAA) National Coastal Pollutant Discharge Inventory (NCPDI) file. The United States Geological Survey (USGS) and County boundaries are shown in Figures 3 and 4 respectively. Data in the NCPDI were reported by drainage basins denned by the USGS cataloging units, counties, and units called HUCOs, unique areas made up by overlaying county lines upon the lines defined by the USGS cataloging units. Because the areal resolution or the USGS units was too coarse to mimic the five drainage areas, HUCOs or Portions of HUCOs were attributed to each drainage area. The spatial relationships etween the drainage areas selected for this study and those used by DEP, NOAA, and USGS are summarized in Table 1. In one instance, Cape Cod Bay, the drainage area was a portion of the DEP drainage area. Table 1 . Drainage areas used In this study and their relationships to other designated drainage areas. Drainage Area Merrimack River (1,527 km2) Massachusetts DEP Coastal Drainage Area 84 (1,960 km2) NOAA HUCO (County x USGS Cataloging Unit) 30, 32, 33, 34 North Shore (1,553 km2) 91, 92, 93 (1,060 km2) 29,31,(40%)35, (25%)37 Boston Harbor (1,425 km2) 71, 72, 73, 74 (1,560 km2) (60%) 35, 36, (75%) 37, 38,42 South Shore (636 km2) 94 (681 km2) 39, (60%) 43 Cape Cod Bay (117 km2) Part of 96 (30%) 45 8 Figure 2. Drainage areas used by the Massachusetts Department of Environmental Protection 2 >^*<9 1 S •• ■ QBiSO X i ? S M 9 5«ia<» i S S S & S S«ae««S*«ae 8^ w S . « s K ;( 8 8 S S X ? 9 8 S S 9 8 « « « FCF ■jgsaaas^ 01070005 P*rr w 10 MiU* 3 FIGURE 3 iwum CoW Corwpfa T^ 0^•«k«*«l Cary DonafVii4\ B-«^ix»r to«^«- ||« & jiat»cialm iwg h.-^^ Land-use characteristics were developed for each of the five drainage areas using information presented in the NCPDI. Seven categories of urban environment were used as well as nonurban (Table 2). The total study area for the five drainage areas is 5,270 km^. The largest drainage area is the North Shore (1,550 km^) and the smallest is Cape Cod (118 km^). The drainage area with the highest percentage of urban environment is Boston Harbor (51%) and the area with the lowest percentage is the South Shore (17%). Table 2. Land use within the various drainage areas (km^). l^ndUse ReskJentlal Merrimack 317(73%) North Shore 3//(68%) Boston Harbor 516(71%) South Shore 82.3(76%) Cape Cod 23.4(67%) Total 1316(71%) Commercial 67.4 (16%) 81.9(15%) 107(15%) 6.0(6%) 3.9(11%) 266(14%) Industrial 3.7(1%) 14.0(3%) 13.8(2%) 0.9(1%) 0.3(1%) 32.7(2%) Transport. 17.2 (4%) 25.4(5%) 29.8(4%) 9.3 (9%) 1.2(3%) 82.9(4%) Industrial /Commercial 0.6 1.5 2.7 0.2 0.3 5.3 Mixed Urban 3.2(1%) 0.2 2.1 2.5 0.9(3%) 8.9 Total Urban 433 (28%) 553(36%) 727(51%) 108(17%) 35(30%) 1856(35%) Non-Urban 1104(72%) 1000 (64%) 698 (49%) 528 (83%) 83 (70%) 3413 (65%) Total 1537 1553 1425 636 118 5270 3.2 River Systems Twenty-seven rivers were considered in this analysis (Table 3). Annual flows for each nver were estimated from a combination oi gauge measurements and estimates of river discharge for drainage areas. For rivers with gauges, statistical summaries of stream flow data were employed to estimate average flow. All USGS flow data are reported in units of cubic feet per second. For our loading analysis, flows were converted to cubic meters per second. 12 Table 3. Estimated annual river discharge to Massachusetts Bays (m3/,) M UJ V u m ' c 1 3 O) E e ^ CH c m < 21 c ■o E « 3, 2 « 3 »«. <~> f^ «* /Vl l"^ />\ /~S f"^ «-N ^^ <«N/VI<*^*n,A#AaA d d ^' 1-^ d o d ^ U5 H CM 00 CM 8f- ^ CO U5 ^ d d d d O CM CM ^ ,ft "«• o> -^ in »« O) o> g g ^^88S S§^^ S?S8S88j^§S o> CM CM 00 CM O § 8 .A lA in CM CO CM f- ^CM ^ ^ CM " SgS CM in "V ^ h- CO d CO S.SSffl «> Oi 5 lO II - cc > o ■=1 ^lij o oc QC 0) ^ o ^ -"531351 = 5 65 S£ r « o • g • 1 |i jQ A at in 9 o 2 d — « to t5 S ^ if CO c II « £ ll If -I CO ^ si 3 Si l~ il ll UJ 5 ^ CM 13 When available, flow data from gauginc stations near the mouths of the coastal rivers were used. Otherwise, flow data from other stream gauges within the river drainage basin and nearest the mouth as possible were used, we calculate total flow as: Total Flow = Flow at Gauge X Total Drainage Area Drainage Area Above Gauge Most minor coastal rivers which drain to Massachusetts Bays system do not have USGS gauges and many of the major rivers have gauges that capture only part of the tot5 drainage area. Therefore, flows were estimated using another method. Throudi information provided in the USGS gazetteers, the drainage areas of minor as well as major coastal rivers were estimated by multiplying the conversion factor, 1.7 cfs per square mile, by the river's discharge area. Tliis value was calculated as being typical for such rivers. Total estimated average annual freshwater flow to Massachusetts Bays via river discharges is 300 m^/s including the Merrimack and about 60 m^/s excluding the Merrimack. Flows trom rivers vary seasonally as well as among years. To illustrate recent variability in river flow to the Massachusetts Bays system, monthly mean flow values (cfs) are presented in Figures 5 through 7 for the Merrimack, Ipswich, and Charles Rivers tor 1987 to 1989. The overall seasonal pattern of flow was similar for these three rivers. Flow tended to be higher in March throu^ May period and lowest in July through October. Year-to-year variation is clearly evident. For example, the flow in April 1987 is substantially greater than the flows observed in 1988 and 1989. 14 u. <1> o o 2 c > CO tt CO v* 0) -g CO § u5| CO c (0 0) fe €0 3 2 w D>^ H u. *« O 1 o 0) CO 0) CO CO 0> CO 0) I o Q. cc a I I > CO CO o CO s 3 o CO 15 o u. Q> (0 CO ^ Q- (Q 5 0) £ > o -^ CO QC CO _ CO -g . ^ — 3 O) u. €0 ^ o o o 0> 00 CO GO GO 0> I o a a I • > CO 00 o CO • o CO 16 o LL O (0 (0 k. c ^ o > CO cc CO <1> CO CO o v« CO O ^B 3 O) LL o o (O 0> CO 0> a> I o I o o o o ca o o o o o 00 o o (O o o o o CM • > CO 09 o 00 • o 00 17 I 4.0 POINT SOURCE INVENTORY 4.1 General This section describes the inventory of point source contributions to Massachusetts Bays and the potential loadings of contaminants from these point sources within coastal drainage basins to Massachusetts Bays. Under the Water Quality Act of 1987, point sources are identified as discharges from publicly-owned treatment works (POTWs) and industrial wastewater discharges. Those major point sources which contribute directly to Massachusetts Bays were identified as well as those which contribute to rivers, streams, estuaries or near coastal environments which enter or exchange with the Massachusetts Bays system. Estimates of loadings are provided for individual dischargers as well as the five major drainage areas. Estimates of point source contribution to Massachusetts Bays were made by: • Indentifying and characterizing the point sources within each watershed. Emphasis was placed upon obtaining information on the compounds ana biological agents that are the subject of the analysis. However, other parameters monitored for thes emuemts were characterized when available. • Providing qualitative characterization and, where possible, quantitative estimates of the contaminant contributions from these sources. • Estimating (by extrapolation from other similar discharges) the concentrations and loadings for sources for which data may be lacking. 4.2 identification of Point Sources All major point source discharges within the five drainage basins were identified and located on USGS maps. The locations of the major point source dischargers are shown in Figure 8. Annotated USGS maps are being provided separately to CZM. Major NPDES outfalls which discharge to tributaries of the major coastal rivers are not displayed on Figure 8. These tributaries include Mill Brook, Concord River, Assabet River, Sudbury River, Hop River, French Stream and River Meadow River. The names of the dischargers depicted by number in Figure 8 are provided in Table 4. 18 Table 4. Names of NPDES permit holders depicted by number In Figure 8. MAP-ID. NPDES-# Facility Name 1 101745 AMESBURY 2 102873 SALISBURY 3 101427 NEWBURYPORT 4 100145 ROCKPORT MTP 5 281 GOULD INC. 6 100625 GLOUCESTER 7 100501 SOUTH ESSEX SEWAGE DIST. 8 100871 MANCHESTER WTP 9 5096 NEW ENGLAND POWER 10 101907 SWAMPSCOTT 11 100552 LYNN SEWER MAIN OUTFALL 11A 100552 LYNN SEWER MAIN 2ND OUTFALL 12 3905 GENERAL ELECTRIC-A.F. PLT 29 13 28193 REFUSE ENERGY SYS! EMS CO. 14 100609 IPSWICH 15 101621 HAVERHILL WPAF 16 100447 GREATER LAWRENCE SO 17 1261 AT&T NORTH ANDOVER 18 100633 LOWELL MSS 19 2225 EXXONC) 20 809 MONSANTO EVERb 1 1 PLANT 21 4740 BOSTON EDISON MYSTIC STATION 22 833 EXXON OIL ISLAND END 23 4731 BOSTON EDISON CO-NEW BOSTON STATION 24 101192 BOSTON WATER & SEWER COMMISSIONC) 25 4898 CAMBRIDGE ELEC.-KENDAI 1 SO. 26 101231 HULL 27 101737 MARSHFIELD 28 100587 PLYMOUTH 29 3557 BOSTON EDISON PYLGRIM PLANT 30 4928 CANAL ELECTRIC PLANT-1 31 102351 MWRA DEER ISLAND OUTFALL 32 102361 MWRA SLUDGE OUTFALL 33 1023S2 MWRA NUT ISLAND OU I FALL 34 281 BOSTIC CHEMICAL GROUP 35 7 MWRA TROPOSED" OUTFALL (•)= REFER TO TEXT RED = INDUSTRIAL DISCHARGERS BLUE= MUNICIPAL; DISCHARGERS 20 Point source discharges include NPDES-permitted outfalls. The NPDES permits include industrial as well as municipal facilities. Wastewater discharges to all surface waters in the Commonwealth are regulated by permits which co-issued by EPA and DEP. This system sets levels of effluent quahty to be maintained by the POTWs and the industrial dischargers and designates implementation schedules for meeting effluent limits for discharges that contribute to water quality standards violations. NPDES permits are usually reviewed and reissued every five years. NPDES facilities are either designated as major or minor dischargers. The major NPDES facilities are closely monitored by the regulatory agencies. Tlie discharges from the niajor facilities must meet more effluent limits than the discharges fi^om the minor NPDES facilities. There are several factors that determine whether a facility should be listed as a major or minor NPDES discharger. If a facility is a steam electric power plant with a power output of 500 MW or greater (not using a cooling pond or lake) and/or has a cooling water discharge greater than 25% of the receiving water body's seven-day, ten-year mean low-flow rate, then the facility is automatically listed as a major NPDES discharger. When the facility does not fall under this category, then a series of parameters must be evaluated for the facility. For instance, the NPDES regulatory permit writers take into account the quantity and type of wastewater discharge from the facility. The permit writer scores the facihty for not only the quantity and type of wastewater discharged, but also its relationship to the receivmg stream low flow. The wastewater type is determined based on the relative volumes of noncontact cooling water, process wastewater (resulting from most manufacturing processes, contact cooling water, and contaminated simace water run-off), and other wastewaters in the total combined discharge from the facility. The SIC code or codes of a fadlity is another parameter which must be evaluated by the NPDES permit writer. The SIC code represents the activity at the facility and indicates the toxic pollutant potential of its discharges. For example, a large metal finishing plant which discharges a large quantity of process wastewater could be potentiSly discharging toxic concentrations of metals into a river. Once a NPDES facility has been assigned a major or minor designation, then its permit information is mcluded in the Permit Compliance System (PCS) computer data base. In support of the current project, the EPA Region I Resource Information Center conducted two kinds of computer searches and provided summarized data to Menzie-Cura for each Massachusetts major NPDES discharger within the selected drainage areas. The resultant reports included: • An Effluent Statistical Summary Report, which summarizes effluent data on an annual basis for 1988, 1989, and 1990; • A Facnity Information Report, which provides general information on the facility (discharger). 21 These data were used to estimate loadings and to map the locations of the major outfalls. For some discharges, telephone calls were made to local communities to determine the approximate locations of the outfalls. 4.3 Point Source Loadings 4.3.1 Data Sources Estimates of loadings were made for major point source dischargers using the following data sources: Computer searches conducted by EPA Region I; NPDES permit applications; Discharge Monitoring Reports (DMRs); 301(h) studies; Massachusetts Division of Water Pollution Control survey reports. The DMRs were used as the primary source of information on discharge flow and on the concentrations of pollutants. However, NPDES dischargers are required to monitor for a hmited number of parameters and, thus, there are data gaps in the available information. Table 5 provides a summary of which compounds are monitored at each of the effluents. Often the data did not include toxic components, but only conventional pollutants. We extraaed and tabulated the available effluent monitoring data from the DMRs for all existing point sources. r> «0 a o • • 5 % 0) Ul Q o. z o E o i c o E «o TS C 3 i E o o lO CD O o. fl X < a. o 8 I I 8 I I (0 XX < 8 < 8 < o < IL 8 i I I o (0 < 8 8 o UJ lU I I J 1 < 8 (0 I Ui 23 I 3 J t. a. o o ¥ 3 1 O E 3 1 O < o < < 8 < 8 I t I 1 t < o < u. I t < 8 I < 8 CO I I ■ f 8 I u. r f s < 8 < I 3 < 8 ?%l ■fi! O COi * X s • < UJ ntact cooftng water Very Fme Inc. 001 1 2033 2.77E-02 1.27E-02 30 SIC Maximum Minimum Facility Code Flow (m3/8) Flow (m3/8) North Shore Drainage Basin Ipswich Rlv0r Bostic Chemical Group 001 A 2821 2.54E-02 1.05E-03 Bostic Chemical Grcxjp 0010 2821 6.22E-02 8.76E-03 Bostic Chemical Group 003A 2821 7.10E-O4 1.97E-04 Bostic Chemical Group 0036 2821 Bostic Chemical Group 004A 2821 3.15E-03 1.18E-03 Bostic Chemical Group 004B 2821 Bostic Chemical Group 005A 2821 2.53E-03 4.82E-04 Rockport MTP 4962 2.79E-02 2.41 E-02 Ipswich Public 4952 6.41 E-02 3.03E-02 North Shon South Essex SD outfall 001 A 4952 1.19E+00 9.15E-01 New Englarxj Power outfall 001 A 4911 1.87E+01 1.75E+01 New England Power outfall 005A 4911 New England Power outfall 006B 4911 9.19E-03 4.49E-04 New England Power outfall 007A 4911 New England Power outfall 008A 4911 1.31E-03 1.31E-03 New England Power outfall 01 OA 4911 1.31E-03 1.31 E-03 New England Power outfall 01 4A 4911 Gloucester 001 A 4952 1.61E-01 1.10E-01 Lynn Water & Sewer 001 A 4952 3.68E+00 1.25E+00 Lynn Water & Sewer 002A 4952 4.17E-02 2.63E-04 Manchester WTP FACA 4952 3.00E-02 1.76E-02 Swampscott WPCP FACA 4952 4.16E-02 4.16E-02 Swampscott WPCP 001 A 4952 1.26E-01 3.72E-02 General Electric 001 A 3511 4.38E-04 2.92E-04 General Electric 003A 3511 3.50E-02 2.33E-02 General Electric 005A 3511 8.76E-04 5.84E-04 General Electric 007A 3511 4.91 E-02 3.27E-02 General Electric 009A 3511 3.11E-03 2.07E-03 General Electric 01 OA 3511 1.S8E-01 1.05E-01 General Electric 01 2A 3511 General Electric 01 3A 3511 1.53E-02 1.02E-02 General Electric 01 4A 3511 1.10E+00 6.84E-01 General Electric 01 5A 3511 1.10E-03 7.30E-04 General Electric 01 7A 3511 2.19E-04 1.46E-04 General Electric 01 8A 3511 1.10E+00 7.30E-01 General Electric 01 9A 3511 1.53E-02 1.02E-02 General Electric 020A 3511 7.36E^)1 2.96E-01 General Electric 021 A 3511 1.58E-01 1.05E-01 General Electric 027A 3511 4.38E-02 2.92E-02 General Electric 028A 3511 3.29E-03 2.19E-03 General Electric 029A 3511 9.46E-01 9.46E-02 General Electric 030A 3511 2.19E-03 2.19E-03 Gerteral Electric 031 A 3511 3.90E-02 3.90E-02 Refuse Energy Systems 001 A 4923 2.37E+00 2.37E+00 31 SIC Maximum Minimum Facility Code Flow (m3/s) Flow (m3/s) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 4952 1.40E+01 1.40E-t-01 MWRA - Nut Island 4952 6.00E+00 6.00E+00 MWRA - Nut Island Sludge Outfall 4952 Mystic River Boston Edison (Boston) 01 1 A 4911 1.58E-02 6.57E-03 Boston Edison (Boston) 01 2A 4911 Boston Edison (Boston) 01 3A 4911 Boston Edison (Boston) 01 4A 4911 Monsanto 001 A 2819 8.76E-03 2.92E-03 Exxon Oil * Island End Terminal 5172 2.71 E-02 3.69E-04 Boston Edison (Everett) 002A 4911 2.41 E-02 1.26E-02 Boston Edison (Everett) 003A 4911 1.75E-02 1.75E-02 Cambridge Electric 001 A 4911 2.11E+00 1.91E+00 Cambridge Electric 002A 4911 2.11E+00 1.91E+00 Cambridge Electric 003A 4911 2.81 E-01 1.02E-01 Charles River Norfolk- Walpole 001 A 9223 1.37E-02 1.34E-02 Norfolk-WalpoleOOIB 9223 1 .39E-02 1.39E-02 Charles River PCD 01 1 4952 1.68E-01 1.14E-01 Charles River PCD 012 4952 1.60E-01 1.60E-01 Charles River PCD 013 4952 1.48E-01 1.48E-01 Charles River PCD 014 4952 1.17E-01 1.17E-01 MedflekJ WWTP FACA 4952 3.33E-02 3.33E-02 MedfieWWWTPOOIA 4952 4.00E-02 3.57E-02 Neponset River Plymouth Rubber Co. 2821 2.01 E-01 1.31 E-01 Foxboro Co. Neponset 001 A 3471 2.88E-03 2.88E-03 Foxboro Co. Neponset 001 B 3471 3.23E-03 4.04E-04 South Shore Drainage Basin HullWTPOOIA 4952 6.57E-02 5.61 E-02 Plymouth 001 A 4952 1.10E-01 1.02E-01 MarshfiekJWTPOOIA 4952 4.24E-02 4.04E-02 Boston Edison-Pilgrim PI.001 1 4911 1.70E+01 7.71 E+00 Boston Edison-Pilgrim PI.0021 4911 1.09E+00 6.13E-02 Boston Edison-Pilgrim PI.003A 4911 4.42E-02 1.26E-02 Boston Edison-Pilgrim PI.010A 4911 3.02E-01 1.61 E-01 Boston Edison-Pilgrim PI.001 1 A 4911 2.48E-05 2.23E-05 Rockland V\n-P 001 C 4952 1.12E-01 6.18E-02 Rockland WTP 001 B 4952 1.07E-01 8.51 E-02 Cape Cod Drainage Basin Canal Electric-PI.#1 001 A 4911 1.52E+01 6.40E-KO0 Canal Electric-PI.#1 002A 4911 1.10E-01 1.10E-01 Canal Electric-PI.#1 Oil A 4911 6.44E-03 5.39E-03 Canal Electric-PI.#1 01 2A 4911 1.88E-03 1.62E-03 32 Table 8. Estimated point source loadings of solids. ^int Sources Lower Higher Total Suspended Solids Estimate (kg/yr) Estimate (kg/yr) Merriniack River Drainage Basin Concord Rlvr Westborough WTP 1.30E+04 3.90E+04 Billerica-Letchworth WTP FACA 1.30E+04 3.90E+04 Marlborough STP 1.50E+04 4.50E+04 Hudson WWTF FACA 2.60E+04 6.40E+04 Marlborough Westerly WTF 3.20E+04 5.60E+04 Maynard STP 1.80E+04 3.60E+04 Raytheon Corporation 1.80E+01 2.80E+02 Concord 1.30E+03 4.00E+04 Silicon Transistor 4.20E+02 3.40E+03 Raytheon Co.-Wayland 1.80E+02 3.90E+02 NYES Japenamelac WWTP 1.30E+05 6.70E+05 Merrimaci( River Amesbury Haverhill WPAF 2.90E+04 3.60E+05 AT&T 7.70E+03 8.10E+03 Gould Inc. FACA Greater Lawrence SD 3.40E+05 7.10E+05 Newburyport WPCF 1.20E+04 3.10E+04 Salisbury Sewer Comm. 2.30E+02 1.90E+03 Exxon Company O.OOE+00 O.OOE+00 Lowell MSS 3.60E-I-03 3.60E+03 Very Fine Inc. 3.90E+07 4.00E+07 Subtotal 3.96E+07 4.21 E+07 North Shore Drainage Basin Ipswich Rivw Bostic Chemical Group 9.30E+03 9.30E+03 Rockport MTP 2.70E+03 7.80E+03 Ipswich Public 5.10E+03 3.50E+04 North Shon South Essex SD 1.00E+06 6.20E+06 New England Power 2.20E+03 2.20E+03 Gloucester 2.30E+05 4.40E+05 Lynn Water & Sewer 2.20E+06 8.30E+06 Manchester WTP FACA 9.40E+03 3.80E+04 Swampscott WPCP 1.10E+05 3.80E+05 General Electric O.OOE+00 O.OOE+00 Refuse Energy Systems O.OOE+00 O.OOE+00 Subtotal 3.57E+06 1.54E+07 33 ^oint Sources Lower HighM- Total Susp«nd«d Solids Estln^to (kg/yr) Estlmat* (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 4.30E+07 4.30E+07 MWRA - Nut Island 1.90E+07 1 .90E+07 MWRA - Nut Island Sludge Outfall 2.30E+07 2.30E+07 MysHc RIvr Boston Edison (Boston) Monsanto Exxon Oil • Island End Terminal 3.50E+02 1.90E+04 Boston Edison (Everett) 1.70E+04 5.70E+04 Cambridge Electric Charles RIvr Norfolk-Walpoie 4.70E+03 5.90E+03 Charles River PCD 2.00E+06 3.10E+06 Medfield WWTP 8.00E+03 l.OOE+04 Neponset River Plynrwuth Ruk)ber Co. Foxboro Co. Neponset 3.10E+03 3.10E+01 Subtotal 8.70E+07 8.82E+07 South Shore Drainage Basin Hull WTP 2.20E+04 1.30E+05 Plymouth 8.60E+04 1.20E+05 Marshfiekj WTP Boston Edison-Pilgrim PI. Rockland WTP 3.60E+04 3.60E+04 Subtotal 1.44E+05 2.86E+05 Cape Cod Drainage Basin Canal Electric-PI. 5.60E+03 6.60E+03 Subtotal 5.60E+03 6.60E-K03 TOTAL 1.30E+08 1 .46E+08 Table 9. Estimated point source toadinas of biochemical oxygen demand (kg/yr). Lower Higher ^ Biochemicai Oxygen Demand Estimate Estimate Merrimack River Drainage Basin Concord RIvr Westborough WTP 1.20E+04 3.40E+04 Billerica-Letchworth WTP FACA 3.90E+04 2.30E+05 Marlborough SIR 4.70E+03 3.00E+04 Hudson WWTF FACA 4.00E+04 7.10E+04 Marlborough Westerly WTF 2.30E+04 4.50E+04 Maynard STP 2.50E+04 7.30E+04 Raytheon Corporation Concord 3.30E+03 2.80E+04 Silicon Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merriniack River Amesbury 1.00E+05 1.00E+05 Haverhill WPAF 2.20E+05 7.30E+05 AT&T 4.60E+04 5.90E+04 Gould Inc. FACA Greater Lawrence SD 3.40E+06 1.10E+06 Newburyport WPCF Salisbury Sewer Comm. 9.30E+02 1.10E+03 Exxon Company Lowell MSS 2.40E+05 7.20E+05 Very Fine Inc. 9.00E+03 2.00E+04 Subtotal 1.10E+06 3.24E+06 North Shore Drainage Basin Ipswich Riv9r Bostic Chemical Group 2.30E+03 2.30E+03 Rockport MTP 8.40E+03 1.00E+04 Ipswich Public 1.20E+04 3.00E+04 North Shore South Essex SD 2.30E+07 2.00E+07 New England Power 7.20E+01 7.20E+01 Gloucester 7.50E+05 7.50E+05 Lynn Water & Sewer 5.30E-J-06 1.40E+07 Manchester WTP FACA 1.30E+04 4.60E+04 Swampscott WPCP 8.60E>06 3.50E+07 General Electric Refuse Energy Systems Subtotal 3.77E+07 6.98E+07 35 Biochemical Oxygen Demand .ower Estinr«te Higher Estimate Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island MWRA - Nut Island MWRA - Nut Island Sludge Outfall Mystic RIvr Boston Edison (Boston) Monsanto Exxon Oil * Island End Terminal Boston Edison (Everett) Cambridge Electric Charfos Rivar Norfolk-Walpole Charies River PCD MedfiekJ WWTP Neponsat Rlvor Plynrwuth Rubber Co. Foxboro Co. Neponset 5.40E+07 2.20E+07 1.5OE+07 5.40E+07 2.20E-t-07 1.50E+07 Subtotal 9.10E+07 9.10E+07 South Shore Drainage Basin Hull WTP 2.50E+04 3.80E+04 Plymouth 7.60E+04 1.00E+05 MarshfiekJ WTP Boston Edison-Pilgrim PI. Rockland WTP 2.40E+04 6.00E+04 Subtotal 1.25E+05 1.98E+05 Cape Cod Drainage Basin Canal Electric-Pl. Subtotal O.OOE+00 O.OOE+00 TOTAL 1.30E+08 1.64E+08 36 Table 10. Estimated point source loadings of nitrogen. »oint Sourcot Nitrogen .ow«r Higher Estlmatt (kg/yr) Eitimaf (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP Billerica-Letchworth WTP FACA Marlborough STP Hudson WWTF FACA Marlborough Westerly WTF Mayr»rd STP Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merrimack RtvBr Amesbury Haverhill WPAF AT&T Gould Inc. FACA Greater Lawrence SD Newburyport WPCF Salisbury Sewer Comm. Exxon Company Lowell MSS Very Fine Inc. Subtotal North Shore Drainage Basin Ipswich Rlv9r Bostic Chemical Group Rockport MTP Ipswich Public North Shon South Essex SD New England Power Gloucester Lynn Water & Sewer Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal 1.70E+03 8.40E+04 1.40E+0S 1.40E+05 5.90E+02 7.50E+04 8.30E+04 8.30E+04 8.10E+04 8.10E+04 2.50E+02 6.40E+02 7.10E+03 4.00E+04 2.10E+03 7.90E+04 3.20E+05 6.00E+05 4.30E+04 4.30E+04 1.20E+05 1.20E+05 2.50E+04 3.70E+04 7.80E+05 8.70E+05 5.20E+04 5.20E+04 1.50E+03 2.90E+03 4.20E+05 4.60E+05 1.10E+00 8.40E+01 2.08E+06 2.77E+06 1.10E+03 1.10E+03 3.90E+04 3.90E+04 3.90E+06 3.90E+06 1.40E+05 1.40E+05 1.20E+04 1.20E+04 4.09E+06 4.09E-I-06 37 Point Sources Lowof Higher NItrogon Estimate (kg/yr) Estimatt (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 7.00E+06 7.00E-K06 MWRA - Nut Island 3.30E+06 3.30E-»^ I^WRA - Nut Island Sludge Outfall 1.10E+06 1.10E+06 Mystic Rivsr Boston Edison (Boston) Monsanto 3.20E+02 3.20E-^O2 Exxon Oil • Island End Terminal 5.60E-»-03 5.60E+03 Boston Edison (Everett) 4.80E+03 4.80E-^O3 Cambridge Electric Chariss RIvar Norfolk-Walpole 5.80E+04 6.50E+04 Charies River PCD 1.20E+04 3.10E+04 MedfieW WWTP Neponset Rlvar Plyrnouth Rubber Co. Foxboro Co. Neponset 3.90E+04 3.90E+04 Subtotal 1.15E+07 1.15E+07 South Shore Drainage Basin Hull WTP 7.90E+04 7.90E+04 Plymouth MarshfieW WTP Boston Edison-Pilgrim PI. Rockland WTP 1.20E+03 5.20E+03 Subtotal 8.02E+04 8.42E+04 Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL 1.78E+07 1.85E+07 38 Table 11. Estimated point source loadings of phosphorus. Low«r Higher Estimata (kg/yr) Estimato (Icg/yr) Merriniacic River Drainage Basin Concord Rivr Westborough WTP Billerica-Letchworth WTP FACA Marlborough STP Hudson WWTF FACA Marlborough Westerly WTF Mayriard STP Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merrimack RIvr Amesbury Haverhill WPAF AT&T Gould Inc. FACA Greater Lawrence SD Newburyport WPCF Salisbury Sewer Comm. Exxon Company Lowell MSS Very Fine Inc. Subtotal 2.15E+04 2.15E+04 1.82E+04 1.82E+04 4.78E+04 4.78E+04 1.61E+04 1.61 E+04 2.75E+04 2.75E+04 1.11E+04 1.11 E+04 2.04E+03 7.43E+03 2.40E-i^ 2.40E+02 3.07E+02 3.07E+02 1.69E+04 1.69E+04 1.17E+04 1.17E+04 1.38E+03 2.36E+03 6.23E+04 9.32E+04 7.56E+03 7.56E+03 2.45E+05 2.82E+05 North Shore Drainage Basin Ipswich Riv9r Bostic Chemical Group Rockport MTP Ipswich Public North Shon South Essex SD New England Power Gloucester Lynn Water & Sewer Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal 2.93E+05 2.93E+05 1.53E+04 1.53E+04 1.63E+03 1.63E+03 3.10E+05 3.10E+05 39 ^oint sources Phosphorus Lowsr Higher Estimats (kg/yr) Estimato (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA • Deer Island MWRA - Nut Island MWRA - Nut Island Sludge Outfall Mystic RIvr Boston Edison (Boston) Monsanto Exxon Oil * Island End Terminal Boston Edison (Everett) Cambridge Electric Charles RIvar Norfdk-Walpole Charles River PCD MedfieW WWTP Naponsat Rlvar Plymouth Rubber Co. Foxt)oro Co. Neponset Subtotal South Shore Drainage Basin Hull WTP Plymouth MarshfiekJ WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal 1.75E+06 1.75E+06 7.50E+05 7.50E+05 7.(X)E+04 7.00E+04 3.76E+02 1.18E+03 4.58E+03 9.76E+03 5.81 E+02 8.65E+02 9.08E+01 9.08E+01 2.58E+06 2.58E+06 1.14E+04 1.14E+04 1.41 E+00 2.(X)E+00 1.14E+04 1.14E+04 Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL 3.14E+06 3.19E+06 40 Table 12. Estimated point source loadings of oil and grease. Point SourcM Lower Higher Oil and GrMM Estimate (Icg/yr) Estimata (Icg/yr) Merrimack River Drainage Basin Concord RIvr NOTE: THIS TABLE NEEDS A QA CHECK Westborough WTP Billerica-Letchworth WTP FACA Mariborough SIR Hudson WWTF FACA Marlborough Westerly WTF Maynard STP Raytheon Corporation Concord Silicon Transistor 1.27E+03 7.36E+03 Raytheon Co.-Wayland 2.56E+01 2.67E+02 NYES Japenametec WWTP 1.72E+01 1.24E+02 Merrimack Rlvw Amesbury Haverhill WPAF AT&T 4.59E+04 5.98E+04 Goukj Inc. FACA Greater Lawrence SD 2.97E+02 3.09E+02 Newburyport WPCF Salisbury Sewer Comm. Exxon Company Lowell MSS Very Fine Inc. 3.30E+02 1.81E+03 Subtotal 4.79E+04 6.97E+04 North Shore Drainage Basin Ipswhh RIvr Bostic Chemical Group 1.20E+03 7.37E+03 Rockport MTP 1.20E+03 7.37E+03 Ipswich Public North $hor9 South Essex SD 5.95E+04 8.75E+05 New England Power 6.59E+02 2.27E+03 Gloucester 2.90E+04 2.69E+05 Lynn Water & Sewer 1.12E+06 1.99E+06 Manchester WTP FACA Swanpscott WPCP General Electric 2.60E-i>04 2.08E+05 Refuse Energy Systems Subtotal 1.24E+06 3.36E+06 41 Point Sources Lower High>er Oil and GrMM Estimate (kg/yr) Estinruit« (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 1.39E-^04 1.39E+04 MWRA • Nut Island 6.95E-J.03 5.95E-^03 MWRA - Nut Island Sludge Outfall Mystic RIvr Boston Edison (Boston) Monsanto 1.23E+02 5.81 E+02 Exxon Oil * Island End Terminal 2.83E+01 5.66E+03 Boston Edison (Everett) 9.52E+01 7.35E+02 Cambridge Electric Chartss RIvr Norfolk-Walpole Charies River PCD Medflekj WWTP Neponsat RIvar Plymouth Rul)ber Co. 9.67E+03 3.36E+04 Foxtx>ro Co. Neponset 1.87E+02 6.68E+02 Subtotal 2.99E+04 6.11E+04 South Shore Drainage Basin Hull WTP 8.77E+03 1.17E+04 Plynnouth Marshfiekj WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal 8.77E+03 1.17E+04 Cape Cod Drainage Basin Canal Electric-Pi. Subtotal TOTAL 1.32E+06 3.50E+06 42 Table 13. Estimated point source loadings of volatile organic compounds. Point Sources Lower Higher Volatile Organic Compounds Estimate Estimate Merrimack River Drainage Basin Concord River Westborough WTP 1.24E+02 1.24E+02 Billerica-Letchworth WTP FACA Marlborough STP Hudson WWTF FACA 7.03E+00 7.03E+00 Marlborough Westerly WTF 6.51 E+01 6.51 E+01 Maynard STP 9.84E+00 9.84E+00 Raytheon Corporation Concord 8.26E+00 8.26E+00 Silicon Transistor 6.23E+01 7.51 E+03 Raytheon Co.-Wayland NYES Japenamelac WWTP 1.86E-01 1.86E-01 Merrimack River Amesbury 7.34E+01 7.34E+01 Haverhill WPAF 2.35E+03 2.35E+03 AT&T Gould Inc. FACA 1.86E-01 1.86E-01 Greater Lawrence SD 1.15E+02 1.15E+02 Newburyport WPCF Salisbury Sewer Comm. Exxon Company 8.82E+03 8.82E+03 Lowell MSS 1.37E+02 4.03E+02 Very Fine Inc. 7.33E+00 7.45E+03 Subtotal 1.18E+04 2.69E+04 North Shore Drainage Basin Ipswich River Bostic Chemical Group 1.37E+04 1.37E+04 Rockport MTP Ipswich Public North Shore South Essex SD 4.66E+03 8.79E+06 New England Power 1.14E+00 1.14E+00 Gloucester Lynn Water & Sewer 1.14E+00 1.14E+00 Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal 1.84E+04 8.81 E+06 43 Point Sources Lower Higher Volatile Organic Compounds Estimate Estimate Boston Harbor Drainage Basin Boston Harbor MWRA- Deer Island (1) 1.53E+05 1.53E+05 MWRA- Nut Island (1) 6.57E+04 6.57E+04 MWRA - Nut Island Sludge Outfall: benzene only 3.00E+00 3.00E+00 Mystic River Boston Edison (Boston) Monsanto Exxon OJI * Island End Terminal Boston Edison (Everett) Cambridge Electric Charles River Norfoll<-Walpole Charles River PCD Medfield WWTP Neponset River Plymouth Rubber Co. Foxboro Co. Neponset Subtotal 2.19E+05 2.19E+05 South Shore Drainage Basin Hull WTP 2.32E+04 2.32E+04 Plymouth Marshfield WTP Boston Edison- Pilgrim PI. Rockland WTP Subtotal 2.32E+04 2.32E+04 Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL 2.72E+05 9.08E+06 1. VOCs for MWRA efluents are from Table 3.3.1-1 of the Secondary Treatment Facilities Plan Volume V, Appendix A and includes the following: benzene, bromomethane. chloroform, ethylbenzene, methylene chloride, styrene, tetrachtoroethylene, trichloroethylene, acetone, 2-butanone, cartwn disulfide, chlorobenzene, dichloroethylene, methylpentanone. .trichloroethane. tetrachloroethane, toluene, and xylenes 44 Table 14. Estimated point source loadings of polynuclear aromatic hydrocarbons. PAH PAH Point SourcM Load Load PAH Loadings MIn. Flow Max Flow at Cone, of at Cone, of (1ug/l) (10ug/l) Merrimack River Drainage WestboroughWTPOOIA 3.41 E+OO 6.15E+01 Blllerica-Letchworth WTP FACA 3.18E+00 3.93E+01 Marlborough STP 2.63E+00 4.98E+01 Hudson WWTF FACA 2.49E+00 3.60E+01 Marlborough Westerty WTF 001 A 2.07E+00 2.46E+01 MaynardSTPOOIA 1.27E+00 1.73E+01 Greater Lawrence SD 001 A 5.00E+01 5.46E+02 NewburyportWPCFOOIA 2.68E+00 3.72E+01 Salisbury SewerComm. 001A 4.36E-01 4.75E+00 6.81 E+01 8.16E+02 North Shore Drainage Basin Ipswich River Rockport MTP 7.61 E-01 8.80E+00 Ipswich Public 9.58E-01 2.03E+01 North $hor9 South Essex SD outfall 001 A 2.89E+01 3.76E+02 Gloucester 001 A 3.48E+00 5.09E+01 Lynn Water & Sewer 001 A 3.95E+01 1.16E+03 Lynn Water & Sewer 002A 8.31 E-03 1.32E+01 Manchester WTP FACA 5.55E-01 9.49E-t-00 Swampscott WPCP FACA 1.32E+00 1.32E+01 Swampscott WPCP 001 A 1.18E+00 3.97E+01 7.66E+01 1.70E+03 Boston Harbor Drainage Basin Boston Harbor MWRA- Deer Island 4.36E+02 4.36E+03 MWRA - Nut Island 1.87E+02 1.87E+03 MWRA - Nut Island Sludge Outfall 4.60E+01 2.16E+03 Charles Rivar Medf ieW WWTP FACA 1.05E+00 1.05E+01 MedfieldWWTPOOIA 1.13E+00 1.26E+01 6.71 E+02 8.41 E+03 South Shore Drainage Basin Hull WTP 001 A 1.77E+00 2.08E+01 Plynxxjth 001A 3.21 E+OO 3.49E+01 MarshfieldWTPOOIA 1.28E+00 1.34E+01 Rockland WTP 001C 1.95E+00 3.53F+01 RocWandWTPOOIB 2.69E+00 3.39E+01 1.09E+01 1.38E+02 Cape Cod Drainage Basin Totals 8.27E+02 1.11E+04 45 Table 15. Estimated point source loadings of polychiorinated biphenyls (PCBs). l>OTW Point SourcM Low*r Higher PCBs Ettinrwit* (kg/yr) Estlmatt (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP 5.20E-02 1.56E-01 Billerica-Letchworth WTP FACA 5.20E-02 1.56E-01 Marlborough STP 6.00E-02 1.80E-01 Hudson WWTF FACA 1.04E-01 2.56E-01 Marlborough Westerly WTF 1.28E-01 2.24E-01 Maynard STP 7.20E-02 1.44E-01 Raytheon Corporation Concord 5.20E-03 1.60E-01 Silicon Transistor 1.68E-03 1.36E-02 Raytheon Co.-Wayland 7.20E-04 1.56E-03 NYES Japenamelac WWTP 5.20E-01 2.68E+00 Merrimacic River Amesbury Haverhill WPAF 1.16E-01 1.44E+00 AT&T Gould Inc. FACA Greater Lawrence SD 4.00E-06 4.00E-06 Newburyport WPCF 4.00E-06 4.00E-06 Salisbury Sewer Comm. 4.00E-06 4.00E-06 Exxon Company Lowell MSS Very Fine Inc. Subtotal 1.11 E+00 5.41 E+00 North Stiore Drainage Basin Ipswich RIvw Bostic Chemical Group Rockport MTP 1.08E-02 3.12E-02 Ipswich Public 2.04E-02 1.40E-01 North Shon South Essex SD 4.00E+00 2.48E+01 New England Power Gloucester 9.20E-01 1.76E+00 Lynn Water & Sewer 8.80E+00 3.32E+01 Manchester WTP FACA 3.76E-02 1.52E-01 Swampscott WPCP 4.40E-01 1.52E+00 General Electric Refuse Energy Systems Subtotal 1.42E+01 6.16E+01 46 POTW Point Sources Lower Higher RGBs Estimate (kg/yr) Estimate (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA • Deer Island 1.75E+02 1.75E+02 MWRA - Nut Island 7.50E+01 7.50E+01 MWRA - Nut Island Sludge Outfall 1.50E+02 1.50E+02 Mystic Rivr Boston Edison (Boston) Monsanto Exxon OH • Island End Tenninal Boston Edison (Everett) ■ Cambndge Electric Charlos Rlvr Norfolk-Walpole 1.88E-02 2.36E-02 Chartes River PCD Medfield WWTP 3.20E-02 4.00E-02 Neponset River Plymouth Rubber Co. Foxboro Co. Neponset Subtotal 4.00E+02 4.00E+02 South Shore Drainage Basin Hull WTP 8.80E-02 5.20E-01 Plymouth 3.44E-01 4.80E-01 Marshfiekj WTP Boston Edison-Pilgrim PI. Rockland WTP 1.44E-01 1.44E-01 Subtotal 5.76E-01 1.14E+00 Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL O.OOE+OO 4.16E+02 O.OOE+OO 4.68E+02 47 Table 16. Estimated point source loadings of phthalate esters . ToVN Point SourcM Low*r Higher Phthalata Ett»rt Estlmat* {kg/yi) Estimat* (kg/yr) Merrinnack River Drainage Basin Concord RIvr Westborough WTP 1.43E+00 4.29E-^00 Billerica-Letchwofth WTP FACA 1.43E+00 4.29E+00 Marlborough STP 1.65E+00 4.95E+00 Hudson WWTF FACA 2.86E+00 7.04E+00 Marlborough Westerly WTF 3.52E+00 6.16E+00 Maynard STP 1.98E+00 3.96E+00 Raytheon Corporation Concord 1.43E-01 4.40E+00 Silicon Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merrimack River Amesbury Haverhill WPAF 3.19E+00 3.96E+01 AT&T Gould Inc. FACA Greater Lawrence SO 3.74E+01 7.81 E+01 Newburyport WPCF 1.32E+00 3.41 E+00 Salisbury Sewer Comm. 2.53E-02 2.09E-01 Exxon Company Lowell MSS Very Fine Inc. Subtotal 5.49E+01 1.56E+02 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP 2.97E-01 8.58E-01 Ipswich Public 5.61 E-01 3.85E+CX) Nortli Shore South Essex SD 1.10E+02 6.82E-K02 New England Power Gloucester 2.53E+01 4.84E+01 Lynn Water & Sewer 2.42E+02 9.13E+02 Manchester WTP FACA 1.03E+00 4.18E+00 Swampscott WPCP 1.21E+01 4.18E-K01 General Electric Refuse Energy Systems Subtotal 3.91 E-»^ 1.69E+03 A9 POTW Point Sources Lower Higher Phthalato Esters Estimate (kg/yr) Estimate (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA- Deer island 4.90E+03 4.90E+03 MWRA - Nut Island 2.10E+03 2.10E+03 MWRA - Nut Island Sludge Outfall 1.80E+03 1.80E+03 Mystic Rlvw Boston Edison (Boston) Monsanto Exxon Oil * island End Terminal Boston Edison (Everett) Cambridge Electric Charles RIvar Norfolk-Waipole 5.17E-01 6.49E-01 Charles River PCD MedfiekJWWTP 8.80E-01 1.10E+00 Neponset River Plymouth Rut^ber Co. Foxtx)ro Co. Neponset Subtotal 8.80E+03 8.80E+03 South Shore Drainage Basin Hull WTP 2.42E+00 1.43E+01 Piynwuth 9.46E+00 1.32E+01 Marshfield WTP Boston Edison-Pilgrim PI. Rockland WTP 3.96E-I-00 3.96E+00 Subtotal 1.58E+01 3.15E+01 Cape Cod Drainage Basin Canal Electric-Pi. Subtotal TOTAL O.OOE+00 9.26E+03 O.OOE+00 1.07E+04 49 Table 17. Estimated point source loadings of cadmium based solely on DMR data. Point Sources Lowir High«f Cadmium: DMRs Estlmaf (kg/yr) E«t]m«t» (kg/yr) Merrimack River Drainage Basin Concord Rlvr Westborough WTP Billerica-Letchworth WTP FACA Marlborough STP Hudson WWTF FACA Marlborough Westerly WTF Maynard STP Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Waytand NYES Japenamelac WWTP Merrimack River Amesbury Haverhill WPAF AT&T 3.20E+00 3.20E+00 Gould Inc. FACA Greater Lawrence SD Newburyport WPCF (considered high) 4.40E+03 2.30E+04 Salisbury Sewer Comm. Exxon Company Lowell MSS 7.40E+01 7.40E+01 Very Fine Inc. Subtotal 4.48E+03 2.31 E+04 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP ipswich Public North Shore South Essex SD New England Power Gloucester Lynn Water & Sewer Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal O.OOE+00 O.OOE+00 Point Sources Lower HighM^ Cadmium: OMRs Estimate (Icg/yr) Estimate (kgAyr) Boston Harbor Drainage Basin Boston Harbor MWRA- Deer island 1.20E+03 1.20E+03 MWRA- Nut Island 5.00E+02 5.00E+02 I^WRA - Nut Island Sludge Outfall 3.70E+02 3.70E+02 Mystic Rivar Boston Edison (Boston) Monsanto Fxxon Oil * Island End Temiinal Boston Edison (Everett) Cambridge Electric Charles Rivar Norfolic-Walpoie Charies River PCD Medflekj WWTP Neponset River PlynfK>utii Rubber Co. Foxboro Co. Neponset 2.40E+01 5.50E+01 Subtotal 2.09E+03 2.13E+03 South Shore Drainage Basin Hull WTP Piynx>utii Marshf lew WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal O.OOE+00 O.OOE+00 Cape Cod Drainage Basin Canal Eiectric-PI. O.OOE+00 O.OOE+00 Subtotal O.OOE+00 O.OOE+00 TOTAL 6.57E+03 2.52E+04 51 Table 18. Estimated point source loadings of cadmium based on DMR data as well as the Cd:TSS Ratio. ^oint Sources Cadmium: DMRt and Cd:TSS Ratios for POTWt .owar Ettlmaf (kg/yr) — m^ — Estlmata (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP Billerica-Letchworth WTP FACA Mailborough STP Hudson WWTF FACA Marlborough Westerty WTF Maynard STP Raytheon Corporation Concord Silkx>n Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merrimack River Anr>esbury Haverhill WPAF AT&T GouW Inc. FACA Greater Lawrence SD Newburyport WPCF Salisbury Sewer Comm. Exxon Company Lowell MSS Very Fine Inc. Subtotal 3.63E-01 3.63E-01 4.19E-01 7.26E-01 8.93E-01 5.02E-01 8.09E-01 3.20E+00 9.49E+00 3.35E-01 6.42E-03 7.40E+01 9.11E+01 1.09E^-00 1.09E-(-00 1 .26E+00 1.79E-t-00 1.56E-K00 1 .OOE+00 1.00E+01 3.20E-»-00 1.98E+01 8.65E-01 5.30E-02 7.40E+01 1.16E+02 North Shore Drainage Basin Ipswich River BosXic Chemnal Group Rockport MTP Ipswich Public North Shore South Essex SD New England Power Gk>ucester Lynn Water & Sewer Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal 7.53E-02 2.18E-01 1.42E-01 9.77E-01 2.79E+01 1.73E^^ 6.42E+00 1.23E+01 6.14E+01 2.32E+02 2.62E-01 1.06E+00 3.07E+00 1.06E+01 9.93E+01 4.30E+02 52 Point Sources Lower Higher Cadmium: DMRs and Cd:TSS Ratios for POTWs Estimate (kg/yr) Estimate (Icg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 1.20E+03 1.20E+03 MWRA • Nut Island 5.00E+02 5.00E+02 MWRA • Nut Island Sludge Outfall 3.70E+02 3.70E+02 Mysth Rlv9r Boston Edison (Boston) Monsanto Exxon Oil • Island End Terminal Boston Edison (Everett) Cambridge Electric Charl08 Rivr Noffolic-Walpole Charles River PCD Medfiekj WWTP 2.23E-01 2.79E-01 NeponsBt Rlvsr Plynxxith Rubber Co. Foxboro Co. Neponset Subtotal 2.07E+03 2.07E+03 South Shore Drainage Basin Hull WTP 6.14E-01 3.63E+00 Plymouth 2.40E+00 3.35E+00 Marshf ieid WTP Boston Edison-Pilgrim PI. Rocldand WTP 1.00E+00 1.00E+00 Subtotal 4.02E+00 7.98E+00 Cape Cod Drainage Basin Canal Eiectric-PI. Subtotal O.OOE+00 O.OOE+00 TOTAL 2.26E+03 2.62E+03 S3 Table 19. Estimated point source loadings of chromium based solely on DMR data. Toint SourcM Low^r WflK^ ^ Chromium: DMRs Estimate (kg/yr) Estimate (kgAyr) Merrimack River Drainage Basin Concord RIvBr Westborough WTP Billerica-Letchworth WTP FACA 2.30E+02 2.30E+02 Marlt)orough STP Hudson WWTF FACA Marlborough Westerly WTF 1.20E+02 1.20E+02 Maynard STP Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Wayland 1.20E+00 1.70E+00 NYES Japenamelac WWTP 3.90E+00 1.10E-K01 Merrimack Rlv9r Amesbury 4.20E+01 1.10E+02 Haverhill WPAF AT&T 8.40E+01 4.30E+02 Gould Inc. FACA Greater Lawrence SD 1 .30E+02 1.30E+02 Newburyport WPCF 2.70E+01 6.70E+01 Salisbury Sewer Comm. Exxon Company Lowell MSS 1.80E+02 1.80E+02 Very Fine Inc. Subtotal 8.18E+02 1.28E+03 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP Ipswich Public North Shore South Essex SD New England Power 3.30E+03 3.30E+03 Gloucester Lynn Water & Sewer Manchester WTP FACA 5.50E+01 5.50E+01 Swampscott WPCP General Electric Refuse Energy Systems Subtotal 3.36E+03 3.36E+03 54 Point SourcM Lower Higher Chromium: DIMRs Estimate (kg/yr) Estimate (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 8.40E+03 8.40E+03 MWRA - Nut Island 3.60E+03 3.60E+03 MWRA - Nut Island Sludge Outfall 3.70E+03 3.70E+03 Mystic Rivsr Boston Edison (Boston) Monsanto Exxon Oil • Island End Terminal Boston Edison (Everett) 2.90E+01 2.90E+01 Cambridge Electric Chariss Rivar Norfolk-Walpole Charies River PCD Medfleld WWTP Neponset Rivar Plynx>uth Rubber Co. Foxboro Co. Neponset 3.10E-05 3.10E-05 Subtotal 1.57E+04 1.57E+04 South Shore Drainage Basin Hull WTP Plynrx>uth Marshfiekj WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal O.OOE+00 O.OOE+00 Cape Cod Drainage Basin Canal Electric-PI. Subtotal O.OOE+00 TOTAL 1.99E+04 2.04E+04 55 Table 20. Estimated point source loadings of chromium based on DMR data as well as the CriTSS ratio. Point SourcM Chromium: DMRs and CrTSS Ratios for POTWs .owr E8tlmat«(kg/yT) Estimate (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP Billerica-Letchworth WTP FACA Marlborough STP Hudson WWTF FACA Marllx)rough Westerly WTF Maynard STP Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Wayland NYES Japenamelac WWTP Merrimack River Amesbury Haverhill WPAF AT&T Gould Inc. FACA Greater Lawrence SD Newburyport WPCF Salisbury Sewer Comm. Exxon Company Lowell MSS Very Fine Inc. Subtotal 1.95E+01 2.30E+02 2.25E+01 3.90E+01 1.20E+02 2.70E+01 1.20E+00 3.90E+00 4.20E+01 4.35E+01 8.40E+01 1.30E+02 2.70E+01 3.45E-01 1.80E+02 9.70E+02 5.85E+01 2.30E+02 6.75E+01 9.60E+01 1.20E+02 5.40E+01 1.70E+00 1.10E+01 1.10E+02 5.40E+02 4.30E+02 1.30E+02 6.70E+01 2.85E+00 1.80E+02 2.10E+03 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP Ipswich Public North Shore South Essex SD New England Power Gk)ucester Lynn Water & Sewer Manchester WTP FACA Swampscott WPCP General Electric Refuse Energy Systems Subtotal 4.05E+00 1.17E+01 7.65E+00 5.25E+01 1.50E+03 9.30E+03 3.30E+03 3.30E+03 3.45E+02 6.60E+02 3.30E+03 1.25E+04 5.50E+01 5.50E+01 1.65E+02 5.70E+02 8.68E+03 2.64E+04 56 Point Sources Low«r Chromium: DMRs and Cr:TSS Ratios for POTWt Estimaf (kg/yr) Highar Estlmata (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island MWRA - Nut Island MWRA - Nut Island Sludge Outfall Mystic RIvBr Boston Edison (Boston) Mortsanto Exxon Oil * Island End Terminal Boston Edison (Everett) Cambridge Electric Chari9s RIvar Norfolk-Walpoie Charles River PCD 8.40E+03 8.40E+03 3.60E+03 3.60E+03 3.70E+03 3.70E+03 2.90E+01 2.90E+01 Medfiekj WWTP 1.20E+01 1.50E+01 Neponset River Plymouth Rubber Co. Foxboro Co. Neponset 3.10E-05 3.10E-05 Subtotal 1.57E+04 1.57E+04 South Shore Drainage Basin Hull WTP 3.30E+01 1.95E+02 Plymouth 1.29E+02 1.80E+02 MarshfieW WTP Boston Edison-Pilgrim PI. Rockland WTP 5.40E+01 5.40E+01 Subtotal 2.16E+02 4.29E+02 Cape Cod Drainage Basin Canal Electric-PI. O.OOE+00 O.OOE+00 Subtotal O.OOE+00 TOTAL 57 Table 21. Estimated point source loadings of copper. Point SourcM Low«r MlgU Copp«r: DMRt Estlmat* (kg/yr) E«tlm«t« (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP 3.00E+02 3.00E+02 Billerica-Letchworth WTP FACA Marlborough STP 1.10E+02 1.10E-K02 Hudson WWTF FACA 2.70E+02 2.70E+02 Marlborough Westerly WTF 8.30E+01 8.30E+01 Maynard STP 4.10E+00 1.70E.^02 Raytheon Corporation Concord 7.80E+00 1.40E+02 Silicon Transistor 1.90E-fOO 6.10E-J-00 Raytheon Co.-Wayiand 1.70E+00 2.40E+01 NYES Japenamelac WWTP 4.10E-01 4.10E-01 Merrimack River Amesbury 6.30E+01 1.70E'^03 Haverhill WPAF 2.20E+03 2.20E+03 AT&T 2.20E+03 7.90E+03 Goukj Inc. FACA Greater Lawrence SD 9.90E+02 3.30E-K03 Newburyport WPCF (considered high) 2.70E+01 2.30E+02 Salisbury Sewer Comm. Exxon Company Lowell MSS 1.20E+03 1.30E+03 Very Fine Inc. 9.40E+00 1.10E+01 Subtotal 7.47E+03 1.77E+04 North Shore Drainage Basin ipswicti River Bostic Chemical Group Rockport MTP Ipswich Public North Shore South Essex SD 2.50E+03 2.50E+03 New England Power 4.40E-01 4.20E+01 Gloucester 1.00E+02 1.00E+02 Lynn Water & Sewer Manchester WTP FACA 4.40E+01 4.40E+01 Swampscott WPCP General Electric Refuse Energy Systems Subtotal 2.64E+03 2.69E-K03 58 Point Sources Lower Higher Copper: DMRs Estimate (kg/yr) Estimate (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer island 3.10E+04 3.10E+04 MWRA - Nut Island 1.30E+04 1.30E+04 MWRA - Nut Island Sludge Outfall 2.20E+04 2.20E+04 Mystic River Boston Edison (Boston) 6.00E+00 6.20E+00 Monsanto Exxon Oil * Island End Terminal Boston Edison (Everett) 2.80E+01 5.70E+01 Cambridge Electric Ctiaries River Norfolk-Walpole Charles River PCD Medf iekj WWTP Neponset River Plymouth Rubber Co. Foxboro Co. Neponset Subtotal 6.60E+04 6.61 E+04 South Shore Drainage Basin Hull WTP 1.50E+02 1.50E+02 Plymouth MarshfiekJ WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal 1.50E+02 1.50E+02 Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL 2.60E+01 3.00E+01 2.60E+01 3.00E+01 7.63E+04 8.67E+04 59 Table 22. Estimated point source loadings of lead based soieiy on the DMR data. Point Sources Low^r Higher LMd: DMRs Estlmat* (kg/yr) Estlmat* (kg/yr) Merrinnack River Drainage Basin Concord Rlv0r Westborough WTP Billerica-Letchworth WTP FACA 4.60E-».03 4.60E^-03 Mariborough STP Hudson WWTF FACA Mariborough Westerly WTF Maynard STP 4.80E+00 7.60E-^00 Raytheon Corporation Concord Silicon Transistor 4.40E+00 5.70E+00 Raytheon Co.-Wayland 4.80E+00 6.10E+00 NYES Japenamelac WWTP Merrimack River Amesbury 2.10E+01 5.70E+01 Haverhill WPAF AT&T 8.60E+01 7.70E+02 Gould Inc. FACA Greater Lawrence SD 1.00E+02 1.00E*02 Newburyport WPCF (considered high) 5.30E+01 1.20E+02 Salisbury Sewer Comm. Exxon Company Lowell MSS 3.80E+02 3.80E+02 Very Fine Inc. 1.40E+00 2.20E+00 Subtotal 5.26E+03 6.05E+03 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP Ipswich Pul:>lic North Shore South Essex SD 1.90E+03 1.90E+03 New England Power Gloucester Lynn Water & Sewer Manchester WTP FACA 2.90E+02 2.90E+02 Swampscott WPCP General Electric Refuse Energy Systems Subtotal 2.19E+03 2.19E+03 60 Point SourcM Lower Higher LMd: DMRs Estimate (kg/yr) Estimate (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island 7.70E+03 7.70E+03 MWRA • Nut Island 3.30E+03 3.30E+03 MWRA - Nut Island Sludge Outfall 3.30E+03 3.30E+03 Mystic Rivw Boston Edison (Boston) Monsanto Exxon Oil * Island End Terminal Boston Edison (Everett) 4.80E+01 4.80E+01 Cambridge Electric Charles River Norfolk-Walpole Charies River PCD MedfieW WWTP Neponset River Plymouth Rubber Co. Foxboro Co. Neponset 1.10E+01 1.10E+01 Subtotal 1.44E+04 1.44E+04 South Shore Drainage Basin Hull WTP Plymouth Marshf ield WTP Boston Edison-Pilgrim PI. Rockland WTP Subtotal Cape Cod Drainage Basin Canal Eledric-PI. Subtotal TOTAL 2.18E+04 2.26E+04 61 Table 23. Estimated point source loadings of lead based on the DMR data as well as the Pb:TSS ratio. Point Sources Low*r Hlgh«f LMd : DMRs and Pb:TSS Ratios for POTWt Estimate (kg/yr) Estlmatt (kg/yr) Merrimack River Drainage Basin Concord RIvtr Westbofough WTP 2.34E+01 7.02E-»-01 Billerica-Letchworth WTP FACA 4.60E+03 4.60E-K03 Mariborough STP 2.70E+01 8.10E+01 Hudson WWTF FACA 4.68E+01 1.15E+02 Marlborough Westerly WTF 5.76E+01 1.01E-^02 Maynard STP 4.80E+00 7.60E-^00 Raytheon Corporation Concord Silicon Transistor 4.40E+00 5.70E+O0 Raytheon Co.-Wayland 4.80E+00 6.10E+00 NYES Japenamelac WWTP Menimack Rlvor Amesbury 2.10E+01 5.70E+01 Haverhill WPAF 5.??E+01 6.48E+02 AT&T 8.60E+01 7.70E+02 Gould Inc. FACA Greater Lawrence SD 1 .OOE+02 1. OOE+02 Newburyport WPCF 5.30E+01 1.20E+02 Salisbury Sewer Comm. 4.14E-01 3.42E+00 Exxon Company Lowell MSS 3.80E+02 3.80E+02 Very Fine Inc. 1.40E+00 2.20E+00 Subtotal 5.46E+03 7.07E+03 North Shore Drainage Basin Ipswich RivQr Bostic Chemical Group Rockport MTP 4.86E+00 1.40E+01 Ipswich Public 9.18E+(X) 6.30E-K01 North Short South Essex SD 1.90E+03 1.90E4CD 7.70E+03 3.30E+03 3.30E+03 7.70E+03 3.30E+03 3.30E+03 4.80E+01 4.80E+01 Medfiekj WWTP 1.44E+01 1.80E+01 Neponsat Rivsr PlynKHJth Rubber Co. Foxboro Co. Neponset 1.10E+01 1.10E+01 Subtotal 1.44E+04 1.44E+04 South Shore Drainage Basin Hun WTP 3.96E+01 2.34E+02 Plymouth 1.55E+02 2.16E+02 MarshfieldWTP Boston Edison-Pilgrim PI. Rocldand WTP 6.48E+01 6.48E+01 Subtotal Cape Cod Drainage Basin Canal Electric-PI. Subtotal TOTAL 63 Table 24. Estimated point source loadings of nickel. Point Sources Lower [higher Nickel: OMRs Estimate (kg/yr) Estimate (kg/yr) Merrlnnack River Drainage Basin Concord Rlvr Westborough WTP Billerica-Letchworth WTP FACA Martborough STP Hudson WWTF FACA Martborough Westerty WTF 1.41E+03 1.41E+03 Maynard STP Raytheon Corporation Concord Sliicon Transistor Raytheon Co.-Waytand NYES Japenamelac WWTP Merrimack Rlvr Amesbury 6.31 E+01 1.38E+02 Havertiili WPAF AT&T 2.36E+02 7.49E+03 Gouid Inc. FACA Greater l_awrence SD 3.13E+02 3.13E+02 Newburyport WPCF (considered high) 4.43E+01 2.43E+02 Salisbury Sewer Comm. Exxon Company Lowell MSS 3.32E+02 1.25E+03 Very Fine Inc. Subtotal 2.40E+03 1 .08E+04 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rocl02 Raytheon Corporation 5.50E+00 5.5OE+O0 Concord 2.90E+01 8.60E+01 Silicon Transistor 2.40E+00 2.40E+00 Raytheon Co.-Wayland 1.10E+01 1.10E+01 NYES Japenamelac WWTP 3.70E-01 3.70E-01 Merrimack River Amesbury 2.50E+02 2.50E+02 Haverhill WPAF 1.10E+03 1.10E+03 AT&T 3.00E+02 3.00E+02 Gould Inc. FACA Greater Lawrence SD 1.90E+03 3.10E+03 Newburypoft WPCF (considered high) 1.30E+02 2.10E+02 Salisbury Sewer Comm. Exxon Company Lowell MSS 2.50E+03 3.90E+03 Very Fine Inc. 1.50E+01 3.10E+01 Subtotal 7.46E+03 1.03E+04 North Shore Drainage Basin Ipswich River Bostic Chemical Group Rockport MTP Ipswich Public North Shore South Essex SD 5.30E+03 5.30E+03 New England Power 5.70E-01 3.20E+01 Gloucester 2.40E+02 2.40E+02 Lynn Water & Sewer Manchester WTP FACA 8.30E+02 8.30E+02 Swampscott WPCP General Electric Refuse Energy Systems Subtotal 6.37E+03 6.40E-K03 66 Lowtr Estimato (kg/yr) HighM* Estlmaf (kgAyr) Boston Harbor Drainage Basin Boston Hsrbor MWRA - Deer island MWRA • Nut Island MWRA - Nut Island Sludge Outfall Mystic RIvr Boston Edison (Boston) Monsanto Exxon Oil * Island End Tenninal Boston Edison (Everett) Cambridge Electric Chsrtss RIvr Norfoik-Walpoie Charies River PCD MedTiekJ WWTP Neportset River Plymouth Rubber Co. Foxboro Co. Neponset Subtotal 5.11E+04 2.19E-i-04 4.70E+04 1.80E+01 1.90E+01 1.90E+01 5.11E+04 2.19E+04 4.70E+04 9.40E+01 1.90E+01 8.00E+01 1.20E+05 1.20E+05 South Shore Drainage Basin HullWTP Plymouth Marshfiekj WTP Boston Edison-Pilgrim PI. RocWand WTP 1.10E+04 1.10E+04 Subtotal 1.10E+04 1.10E+04 Cape Cod Drainage Basin Canal Electric-PI. Subtotal O.OOE+00 O.OOE+00 TOTAL 1.45E+05 1.48E+05 67 Table 26. Estimated point source ioadings of mercury. Point Sourcet =s Mercury Low(kg/yr High (kg/yr) Merrimack River Drainage Basin Concord RIvr Westborough WTP 2.30E-02 6.90E-02 Blllerica-Letchwoith WTP FACA 2.30E-02 6.90E-02 Marlborough STP 2.66E-02 7.97E-02 Hudson WWTF FACA 4.60E-02 1.13E-01 Marlborough Westerly WTF 5.66E-02 9.91 E-02 Maynard STP 3.19E-02 6.37E-02 Raytheon Corporation Concord Silicon Transistor Raytheon Co.-Wayland HiES Japenamelac WWTP 2.30E-01 1.19E + 00 Merrimack River Amesbury Haverhill WPAF 5.13E-02 6.37E-01 AT&T Gould Inc. FACA Greater Lawrence SD 6.02E-01 1.26E + 00 Newburyport WPCF 2.12E-02 5.49E-02 Salisbury Sewer Comm. 4.07E-04 3.36E-03 Exxon Company Lowell MSS 6.37E-03 6.37E-03 Very Fine Inc. Subtotal 1.12E+00 3.64E + 00 Nortti Shore Drainage Basin Ipswich Rivr Bostic Chemical Group RockportMTP 4.78E-03 1.38E-02 Ipswich Publk: 9.03E-03 6.20E-02 North Shorn O.OOE+00 O.OOE + 00 South Essex SD 1.77E+00 1.10E+01 New England Power Gloucester 4.07E-01 7.79E-01 Lynn Water & Sewer 3.89E+00 1.47E+01 Manchester WTP FACA 1.66E-02 6.73E-02 SwampscottWPCP 1.95E-01 6.73E-01 General Electric Refuse Energy Systems Subtotal 6.30E+00 2.73E+01 68 Point Sources Mercury Low(kg/yr High (kg/yr) Boston Harbor Drainage Basin Boston Harbor MWRA - Deer Island MWRA- Nut Island MWRA - Nut Island Sludge Outfall Mystic River Boston Edison (Boston) Monsanto Exxon Oil * Island End Terminal Boston Edison (Everett) Cambridge Electric Charles River 1.10E+02 1.10E+02 110 110 Norfdk-Walpole 8.32E-03 1.04E-02 Charies River PCD 3.54E+00 5.49E+00 Medfield WWTP 1.42E-02 1.77E-02 Neponset River Plymouth Rubber Co. Foxboro Co. Neponset Subtotal 2.24E+02 2.26E+02 South Shore Drainage Basin Hull wrp 3.89E^2 2.30E-01 Plymouth 1.52E-01 2.12E-01 Marshfieid WTP Boston Edison-Pilgrim PI. Rockland WTP 6.37E-02 6.37E-02 Subtotal 2.55E-01 5.06E-01 Cape Cod Drainage Basin Canal Electric-Pl. Subtotal TOTAL 2.31 E +02 2.57E+02 69 A PCS retrieval was performed to identify the Massachusetts minor dischargers. The minor dischargers were aggregated by two major drainage basins: Merrimack River basin and Massachusetts Coastal basin. The Merrimack basin included 88 minor point sources south of the Pawtucket dam in Lx)well, MA. There were 225 minor dischargers within the Massachusetts Coastal River basin. TTie minor dischargers were further subdivided according to the minor river subbasins within one of the two major river basins. A key identified all minor dischargers by facility name and NPDES ID number. A general facility report and 1989 effluent statistical summary also was requested from the PCS retrieval system for each identified minor discharger. If no general facility information and/or effluent summary statistics were available, then we reviewed selected hard copy permit files of Massachusetts minor dischargers. These files are maintained at the EPA Region I offices in Boston. We reviewed approximately 30 permit files for minor dischargers to establish the general nature of these discharges; this is approximately 10% of the minor point sources discharging to the drainage areas for which there are permits. The permitted minor discharges reviewed by us were found to consist of stormwater runoff from drainage systems, sanitary waste water, boiler blowdown, noncontaa cooling water from air compressor units, refrigeration units and heat exchange pumps. The permitted storm drainage systems typically contained oil/water separators. Occasionally, permits for groundwater recovery wells were found. The groundwater discharge permits required that the treated effluent must meet drinking water standarcis before being released into a receiving water body. Accordmg to EPA personnel, there are approximately "a couple hundred" of these permittedgroundwater remediation systems within the state of Massachusetts. Because of the nature of the minor discharges (i.e. stormwater runoff), the discharges may only occur periodically, unlike the discharges from the major NPDES facilities which are often continuous. Parameters that are typically monitored within the effluents from minor NPDES facilities are temperature, oil & grease, conductivity, total suspended and settleable solids. Cobalt, phthalate esters, chromium and residual chlonne were among the parameters measured occasionally. For a given effluent limit, daily maximum or average monthly are usually reported based on the analysis of grab samples. From our investigation of minor permits, the flow from the outfalls of the minor NPDES facilities ranged from 400 to 42,000,000 GPD per outfall. The wide range of effluent flows and limited effluent data for the minor NTDES dischargers prevented the estimation of pollutant loads for this particular group of point sources. Most of the permits are for stormwater outfalls and, to some, extent, we have taken these into account under nonpoint sources in Section 5. Another major category of minor dischargers included noncontact cooling water discharges. It is likely that these dischargers will not contain high concentrations of contaminants. Small sanitary wastewater discharges are also included among the minor point sources and will contribute to the loadings of nutrients and other pollutants. These loadings may be important at the local level. 70 4.3.4 Anticipated Changes in Loadings Due to Upgrade of MWRA Effluents Current MWRA effluents include the discharge of sludges from Nut and Deer Island, primary treated wastewater from these two facilities, and CSO discharges. Upgraae of the system will involve removal of the sludge discharges and abatement of^CSOs via enhancing the capability of the system to handle stormwater. In addition, increased treatment of the wastewater will reduce loadings of conventional as well as toxic pollutants. Here, we provide estimates of the reduction in loadings associated with the additional treatment of wastewater (Table 27). Loads associated with complete secondary treatment are shown. Depending on the pollutant, load reductions range from a few percent to over 95%. Thus, elimination of sludge and complete secondary treatment should have a relatively large impact on overall point source loads to Massachusetts Bay. It is anticipated that the treatment of MWRA effluents may involve several phases which include some combination of enhanced primary and secondaiy treatment. At this writing, the schedules for these activities is still not clear. Thus, we project that future loadings from MWRA effluents will be within the range shown in Table 27. 4.3.5 Data Quality for Point Source Estimates There are several sources of uncertainty in estimating loadings for point sources. One of the major sources of uncertainty is that discharge monitoring is performed on only a subset of nutrients, organic compounds, or metals at any one facility and, therefore, there are a number of data gaps. Discharge monitoring may occur in a manner that is aperiodic or uneven. In the case of major stormwater outfalls, monitoring is event oriented. In the case of minor dischargers, the overall availability of data may be limited. Loadings developed on a drainage area basin may not reflect the loadings received by Massachusetts Bays. A number of chemical and physical processes (e.g., volatilization, biodegradation, sedimentation) will affect the fate and transport of materials discharged from point sources within the drainage areas. To provide a lower bound for direct point source loadings, we have made a separate estimate for major "coastal" dischargers located within the Massachusetts coastal zone. These estimates exclude all the dischargers on the Merrimack Drainage Area, include all those for the North Shore and South Shore and the Boston Harbor effluents. Data quality for one set of compounds, PAHs, is especially uncertain, because few data are available. Because the concentrations that we estimated in effluents may be too high, we checked our total loads for the MWRA outfalls using the ratio of PAH:TSS in the MWRA sludge. If 23,000 mt solids/yr are discharged in the sludge, and 62,000 mt are discharged m the effluent, then the effluent discharges approximately 2.7 times more solids than the sludge. Using this ratio and our data for inputs from sludge, PAH discharges from MWTIA effluent would range from 124-5,830 kg/yr. This range is approximately the same as the 624-6,230 kg/yr that we calculated. We also checked PAH data using a more recent estimate from the MWRA (personal communication, M. Connor, MWRA) that sludge inputs account for 71 approximately 365 kg/yr. Using the same PAH:TSS ratio, MWRA effluents would contribute 986 kg PAHs/yr, a value just slightly higher than our lower estimates. 72 Table 27. Projected future loadings for MWRA effluents (kg/yr). MWRA WMt«watM' Primary Secondary pv—nX and futur* EfflUMlt Effluwit Parcant Load Load Reduction Constituant (kflAyr) (kgAyr) (%) Conv^ntlonMl Pollutants total suspended solids 6.20E+07 2.91 E+O/ 53% biochemicai oxygen demand 7.70E+07 1.99E+06 1.19E+06 53% Volatlh Organic Compounds acetone 6.96E+04 3.48E403 95% benzene 2.74E+03 1.36E+02 95% bromomethane 1.03E+04 5.17E+02 95% 2-butanone 1.70E+04 1.70E4C3 90% cartx>n disulfide 5.68E+03 2.84E402 95% chiorobenzene 5.60E+03 5.61 E+02 90% chloroform 3.69E+03 3.69E+02 90% trans- 1 ,2-dichloroethylene 3.17E+03 4.95E+02 84% ethytbenzene 5.54E+03 2.78E+02 95% methyierte chloride 1.99E+04 9.97E+02 95% 4-methy!-2-pentanone 1.33E+04 1.33E+03 90% styrene 6.22E+03 6.21 E+02 90% 1 .1 ,2.2-tetrachioroethane 5.68E-»-03 5.68E+02 90% tetrachtoroethylene 1.02E+04 1.02E+03 90% toluene 1.18E+04 1.18E+03 90% 1,1,1-trichloroethane 4.94E+03 4.10E+02 92% trichloroethylene 5.78E+03 3.63E+02 94% xylenes 1.77E+04 8.86E+02 95% Volatlla Acid Extractable and Basa Neutral Compounds benzoic acid 5.56E+04 5.56E+03 90% benzyl alcohol 1.43E+04 1.43E+03 90% bis(2-ethylhexyOphthalate 1.30E+04 1.30E+03 90% butyibenzyl phthalate 1.06EH-04 5.27E+02 95% di-n-butyi phthalate 1.13E+04 1.13E+03 90% 1,2-dichlorobenzene 1.24E+04 1.24E+03 90% diethyl phthalate 1.12E+04 1.12E+03 90% dimethyl phthalate 1.01E+04 6.6SE4C2 93% di-n-octyl phthalate 1.09E+O4 1.09E403 90% fluorene 2.72E+03 2.71 E+02 90% 2-methylnaphthalene 1.02E+04 1.02E+03 90% 2-methylphenol 1.46E'i04 1.46E+03 90% 4-methylphenol 1.26E-f04 1.26E+08 90% naphthalene 8.70E+O3 4.35F+0e 95% n-nitro6odiphenylamine 1.43E+04 4.43E+03 69% phenol 8.51 E+03 5.33F+02 94% 2.4.54rlchlorophenol 6.65E404 6.64E+03 90% 73 If WRA Wastewater Primary S«cor>dary prasent and futura Effluant Effluant Parcant Load Load Radudion Constltuant (kg/yr) (kgW (%) ifaea/s antimony 1 .88E+03 1 .08E+03 43% arsenic 9.46E+02 6.31 E+02 33% cadmium 1.19E+03 6.97E+02 41% chromium 8.80E+03 3.52E+03 60% copper 4.31 E+04 1.19E+04 72% lead 6.22E+03 4.95E+03 20% mercury 6.40E+02 2.06E+02 68% fnolytxienum 3.18E+03 1.77E+03 44% nickel 1.11 E+04 8.91 E+03 20% selenium 7.94E+03 4.42E+03 44% silver 2.08E+03 2.96E+02 86% zinc 8.61 E+04 3.44E+04 60% Posticki9 and Ottwr Compounds akjrin 1.10E+02 1.10E+01 90% 4.4-DDT 2.68E+01 2.68E+00 90% dieldrin 1.17E+01 1.17E+0C 90% heptachlor 1.26E+02 1 .39E+01 89% boron 2.55E+05 2.47E+05 3% cyanide 1.67E+04 7.42E+03 56% PCBs 5.27E+02 4.10E+01 92% 1 . Current loadings of conventional pollutants are from Menzie-Cura 1 991 ; current and future loadings of toxics are calculated from Table 3.3.1(1-4) of Volume V, Appendix A of Secondary Treatment Facilities Plan; future loadings of conventional pollutants are calculated for average high groundwater days from the Trailer Pilot Plant report prepared by Metcalf and Eddy (1 990). 74 5.0 NONPOINT SOURCE INVENTORY 5.1 General Several categories of nonpoint sources were evaluated. These induded ruaoff from urban and nonurban areas for the entire drainage areas as well as for a 0.5 mile area along he coastal shoreline, direct discharge of coastal rivers, ocean disposal of dredged material, atmospheric loadings, and groundwater discharees oi seleaed S)Ilutants for selected drainage areas. In addition, an inventory of DEP Confirmed azardous Waste Sites located within 500 feet of a surface water body draining to the Massachusetts Bays was compUed. Sediment data for harbors and the bays were reviewed in an effort to identify locations where levels of contaminants were elevated and could represent in-place sediment contaminant sources. 5.2 Runoff from Urban and Nonurban Land Areas Estimates of loadings have been made for each of the five drainage areas. In addition additional calculations are presented for Boston Harbor. These calculations are based on the Menzie-Cura (1991) report prepared for the NfWRA. S.2.1 Runoff to Drainage Areas Estimates of urban and nonurban runoff were developed for the areas delineated for each of the five drainage areas. The bases for these areas are provided in Section 3 of this report. Estimates of the concentrations of pollutants in the runoff were taken from NOAA's National Coastal Pollutant Discharge Inventory (NCPDI) and are based on data gathered as part of the Nationwide Urban Runoff Program (NURP). Nonpoint source categories in the NCPDI data base included urban storm runoff (CSO and non-CSO), runoff from cropland, runoff from pastures and brushland, and runoff from deciduous, coniferous, and mixed forests with good and poor cover. Although the NCPDI relies on extrapolation rather than upon direct measurements, it is probably the best source of information necessary to estimate runoff in the region. Data in the NCPDI were reported by drainage basins defined by U.S. Geological Survey (USGS) cataloging units, counties, and unique areas made up by overlaying county lines upon the USGS cataloging units. As described in Section 3, we assigned each of these areas (caUedHUCOs) to one of our five drainage areas: Merrimack River, North Shore, Boston Harbor, South Shore, or Cape Cod Bay. In some cases, a HUCO straddled the line of our drainage basins. In those instances, we visually estimated the aerial proportion of the HUCO included in each drainage basin. In subsequent calculations, we assumed that runoff was uniform throughout the HUCO. Therefore, we adjusted data on runoff to reflect the pn^wrtion of that HUCO included within the drainage area. Adjusting data proportional^ isprobably a reasonable approach for estimating most runoff. For areas tnat include CoOs, however, runoff may be disproportionate between the drainage areas. Specifically, for HUCOs that straddled the North 75 Shore and Boston Harbor drainage areas, the methods would probably attribute more runoff from CSOs to the North Shore than actually occurs. The NCPDI used separate methods to calculate runoff from urban and nonurban land-use areas. For urban land, runoff was calculated separately for areas with CSOs and areas without CSOs. For areas with CSOs, estimates of flow were based on the capacity of the wastewater treatment plant. The estimates accounted for design capacity, the age and condition of the system, and the amount of the capacity used to treat sanitary sewage. The estimates did not, however, include actual measurements. MWRA has measured CSO flow and calculated 7.9 x 10^ gallons per year from their entire system. The MWRA value is about one third of the value estimated by the NCPDI for Boston Harbor and about one quarter the NCPDI estimate for Boston Harbor and the North Shore combined. Therefore, the loads calculated for CSOs using flow data from the NCPDI are probably over estimates. Despite this shortcoming, we used the NCPDI data for flow. The NCPDI calculated pollutant loads by multiplying total flow by typical concentrations of pollutants in CSOs. For most contaminants, data were also available for CSOs from the MWRA system (MWRA, 1989; Wallace et al., 1990) (Table 28). For these data, we recalculated loads, using the NCPDI data for flow and the MWRA data for contaminant concentration. . For areas without CSOs, the NCPDI sunmied daily precipitation for each land-use type. The total annual precipitation for each land-use type was multiplied by a land- use-specific runoff coefficient, and these values were summed. Loads were calculated using mean urban runoff concentrations for different types of land use compiled for the NCPDI from NURP (EPA, 1983) and Stenstrom et al. (1984) in Table 29. Nonurban runoff was calculated using the Simulator for Water Resources for Rural Basins (SWRRB) which was developed by the U.S. Department of Agriculture's Agricultural Research Service (USDA ARS). SWRRB simulations were performed for each HUCO that contained nonurban land-use types (all HUCOs except the one comprising Suffolk County). 76 Table 28. Contaminant concentrations reported for MWRA CSOs and the NCPDI. Concentrations in CSOt Pollutant Units NCPCX MWRA Total Suspended Solids mg/l 310 240 Biochemical Oxygen Demand mg/1 47.5 110 Total Nitrogen mg/l 5.08 5.8 Total Phosphorus mg/l 1.07 2.7 Fecal Collfomi cells/100 ml 2.13E+05 Oil and Grease mg/l 13.8 Iron ug/l 10.5 Arsenic ug/l 9.82 Cadmium ug/l 8.09 3.5 Chromium ug/l 103 22 Copper ug/I 100 74 Lead ug/l 474 92 Mercury ug/I 0.673 Zinc ug/l 264 217 PCBs ug/l 0.42 77 % c 3 10 C o «5 o c o ID C O o 2 c o J I E e u z E 8 m *. £ ? = e 3 CE e m 3 O 1 c 1. 00 ^ CM CM E cvi csi 8 CSi CNJ "^ E s ? in ca CO c\i CO Z, o d d CO d E E ss + + UJ UJ o o "•- CM K CO + + UJ LU O O t- CNJ 1^ CO SS + + UJ UJ o o h*: CO ss + + LU HI o o 1- ca N: CO SS + + UJ UJ o o t- CM f^ CO E E 88 11 o o u u 00 CO E CO CM CO CM CO cvi O 5 CM S U) V r*. 00 m oi CM 00 T" h* d CM CO CM f3 CM d CM ^ S U3 ^ N. 00 U3 o> CM 00 h* U3 d CO o CM U3 CM S U) d CM lA d CO CM CO CO (A T* 1^ CM CO CM '^ S kO ^ h^ 00 in d CM d h- d cri - CM lA CM S wn .fm. r^ 00 lA d CM d 1^ r^ lA d CO csi Si 2 ^ E E 3 E S o 2 2 N (S o 0. 78 Following the recommendation of USDA ARS (1976), runoff of total nitrogen and total phosphorus from nonurban areas was based solely upon inputs from fertilizers. The procedure employed by NCPDI was as follows: For each county, determine the tons of nitrogen and phosphorus applied per season. Compute the total cropland in each HUGO. Compute the amount of nitrogen and phosphorus appbed in each HUCO by weighting the amounts according to area of cropland. Determine the percent of cropland in each HUCO that is in conservation tillage. Compute the runoff of nitrogen and phosphorus discharged in each HUCO by applying different loss rates from conservation and conventional tillage. Nonurban runoff of metals was calculated using data on concentrations of metals in soils (Shacklette and Boemgen, 1984 for arsemc, chromiurn, copper, iron, lead, mercury, and zinc; Helsel, 1978 and Lorenz, 1978 for cadmium). The quantity of soil eroded in each HUCO for each season, calculated by SWRRB, ^-as multiplied by the most frequently occurring concentration reported at the closest sampling points to the HUCO. Loads calculated using the NCPDI are presented in Table 30. To estimate runoff from areas that drain directly into coastal waters, we arbitrarily assumed that such runoff occurred from land within 0.5 mi of the shore. We estimated the percentage of area within each drainage area that occurred within 0.5 mi of the shore as 0.3% for Merrimack River, 3% for North Shore, 2% for Boston Harbor, 8% for South Shore, and 60% for Cape Cod Bay. Assuming that runoff is uniform, we used these percentages of the values for total runoff to estimate runoff from coastal areas. This procedure ignored differences in land-use practices along the shoreline from those of the entire drainage areas. It also resulted in underestimating inputs from CSOs that drain into coastal waters. These estimates are provided in Table 31. Because we did not estimate river discharges from Cape Cod to Cape Cod Bay, our summary information on flow and runoff from the Cape Cod Drainage Area is based on the entire drainage area and not on the 0.5 mile region from shore. 79 s c si 6| 3l j| 2 i r a. 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Op ^ o 00 CM CD in CM ^-^ T-^ CM CM is! 888S8S + + + + + ♦ LU LU LU UJ LU Ui h^ in CM cp o> u> CM CM in in to CM T^ ^* CO ▼^ ^ d in in (o in 9 CD o o o o o 5 + + + + + ♦ LU LU LU LU LU UJ SO) in CO CM (D CM CO O ▼- K r*.' ih ^ ^" CO ei ^^88S + + + + + o + LU UJ LU LU LU UJ ^ ▼- in o ^ in 00 o h* •»- g> fli d ^' 1^ K ^' «-^ ^ (o h> m in N o o o o o p + + + + + ♦ LU LU LU LU UJ UI m 0> 00 Q p 01 ▼- CO CM in w ^ -^ ^* T-' "^ -^ CM CO ^ «^ 01 1-^ d *-^ CM w «» I CO c ^O «-?£ ^ 80 Loads via Runoff F« Pb Hg Zn Oil PCBs Total Drainage Areas kg/yr kg/yr kg/yr kg/yr kg/yr kg/yr Area/Source CSO Inputs Merrimack River 1.72E+05 1.51E+03 1.11E+01 3.56E+03 2.26E+05 6.83E+00 North Shore 2.71 E+05 2.38E+03 1.74E+01 5.62E+03 3.57E+05 1.08E*01 Boston Hartx>r 8.58E+05 7.54E+03 5.50E+01 1.78E+04 1.13E+06 3.41 E+01 South Shore O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 Cape Cod Bay O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 O.OOE+00 TOTAL 1.30E+06 1.14E+04 8.35E+01 2.70E+04 1.71 E+06 5.17E+01 NonCSO Inputs Merrimacl< River 5.78E+05 3.23E+04 1.78E+01 3.59E+04 1 .42E+06 O.OOE+00 North Shore 4.09E+05 2.30E+04 1.26E+01 2.54E+04 1.01 E+06 O.OOE+00 Boston Hartx)r 1.01 E+06 5.67E+04 3.11E+01 6.30E+04 2.50E+06 O.OOE+00 South Shore 1.22E+05 6.82E+03 3.75E+00 7.57E+03 2.93E+05 O.OOE+00 Cape Cod 3.52E+04 1.98E+03 1.09E+00 2.19E+03 8.18E+04 O.OOE+00 TOTAL 2.16E+06 1.21 E+05 6.64E+01 1.34E+05 5.30E+06 O.OOE+00 NonUrban Merrimacic River 6.60E+05 4.82E+02 3.22E-03 1.45E+03 O.OOE+00 O.OOE+00 North Shore 3.34E+05 1.68E+02 1.12E-03 5.03E+02 O.OOE+00 O.OOE+OO Boston Hartx)r 2.53E+04 2.44E+01 1.69E-04 7.58E+01 O.OOE+00 O.OOE+00 South Shore 5.20E+03 3.46E+00 3.46E-05 1.56E+01 O.OOE+00 O.OOE+00 Cape Cod Bay 1.15E+02 7.65E-02 3.82E-07 1.30E-01 O.OOE+00 O.OOE+00 TOTAL 1.02E+06 6.78E+02 4.54E-03 2.04E+03 O.OOE+00 O.OOE+00 Total Merrimack River 1.41 E+06 3.43E+04 2.88E+01 4.09E+04 1.64E+06 6.83E+00 North Shore 1.01 E+06 2.55E+04 3.00E+01 3.16E+04 1.37E+06 1.08E+01 Boston Hartx>r 1.90E+06 6.42E+04 8.62E+01 8.08E+04 3.63E+06 3.41 E+01 South Shore 1.27E+05 6.83E+03 3.75E+00 7.59E+03 2.93E+05 O.OOE+00 Cape Cod 3.53E+04 1.98E+03 1.09E+00 2.19E+03 8.18E+04 O.OOE+00 TOTAL 4.48E+06 1.33E+05 1.50E+02 1.63E+05 7.02E+O6 5.17E+01 81 (0 CO o o B 9 1 • O C ^ ? «D o 1 (0 Ul CO 9 5 oS ol si 2I s II Z a f Ss LU UJ LU LU LU tlJ a CO O CO CD p CO csi CO -r^ cvi ^ ?????? LU Lli LU HI 111 Ul 8 S ? S 8 S T^ K o> C«i (O M !????? UJ LU LU HI HI U T- ^ "*- <0 '- ^ f ????? LU LU LU LU UJ UJ » t; li: 2 CJ U) <0 CSJ CO M csi ■^-^ cvi CO* ^ h» fllll! o LU UJ o ca cj LU LU lU Ul u) CO CO p U) « T- h» • • • * ▼- T- m ^ ^ mil? LU LU LU UJ LU UJ ^ CM to Q £i ^ CM CO 10 © CO *^ ^ T-* CM CO 1^ 10 ^ U5 U5 ^ ^ Ift T- ^- ^ ▼- ^ *" + + + + + + LU UJ LU lU LU Ul CO 10 J «D S CM T^ CM I/) C4 ^ o> • LU LU LU LU lU Ul rs. fx^ p CO rr M 00 o> t^ o> ▼- o CM CM T- CM ^ 82 ffi ^ O* 't 888888 + + + ■♦■ + ♦ LU Uil LU LU UJ Ul 888888 d d ^ d d ^ + + + + + + 111 LJ 111 UJ lit 111 CO O <0 5 ^ ^ O) '" CNJ CO O) 0> 'd^ '^^ 1^ CNJ •^* ^-J ^S| 8g8S + + + LU 111 HI LU m UJ CO h* cj r«* CM ^ CM <^ <0 O CO (D • ••••• ^ o> •»- (O o> O o T^ eo 833SS$ ++++++ liJ UJ LU UJ CO CM "^ CO CO T-" LU LU SO) ^ r^ o CM 1^ 83 5.2.2 CSOs and Stormwater Discharges to Boston Harbor This section of the report presents calculations made by Menzie-Cura (1991) for the MWRA. We estimated urban runoff to Boston Harbor in two ways: The first involved using information developed for MWRA by CH2M Hill (1989). The second involved applying the NURP model to the Boston Harbor area. For Quincy Bay, recently discovered problems with storm-drain contamination may result in loadings being underestimated. CH2M Hill Studv Estimates of pollutant loading to Boston Harbor from CSOs and storm drains are from the Facilities Plan (CH2M Hill, 1989). The study area for the Facilities Plan includes the Dorchester Bay Basin, the Neponset Estuary Basin, the Inner Harbor Basin, and the Quincy Bay /Outer Harbor Basin, which comprise the North Harbor as defined for tne present analysis. The Alewife/Mystic Basin, the Upper Charles River Basin, and the Lower Charles River Basin are other basins for which loadings were estimated by CH2M HiU; these are not included in the estimates of direct loading to Boston Harbor since their contribution is included as tributary sources. None of the CSO or storm drain load in these estimates directly enters the South Harbor. Annual pollutant loadings due to CSOs and storm drains were calculated by CH2M Hill using a sewer model that was calibrated with measured concentrations and flow rates taken during wet and dry conditions during the spring and summer of 1988 (CH2M HILL Tech. Mem. 3-10). The Facilities Plan provides estimates of dry weather overflow (DWO), and wet weather overflow from CSOs and storm drains (SWO). The DWO estimate was subtracted from the sum of the CSO and SWO estimates to obtain the net discharge associated with storm events. Estimates of loads via CSOs and stormwater to the northern Boston Harbor are provided in Table 32. These estimates were taken from the facilities plan authored by CH2M Hill and are presented according to their selected basins: Dorchester Bay, Neponset Estuary, Inner Harbor, and Quincy Bay/Outer Harbor. All these basins are contained within North Harbor as defined for the present analysis. No estimates of CSO loadings were available for the South Harbor. Total annual loading to North Harbor is estimated to be 8,855 mt total suspended solids, 3,905 mt BOD, 20 kg TKN, 96 kg phosphorus, 4,278 kg copper, 354 kg lead, 854 kg zinc, and 4.92E+ 16 counts fecal coliform. 84 c o»| N J »n ^ «n ♦ + + LU LU LU 9 c^ in m aS ^ CNJ CNJ CNJ "»- 00 X) at a. ^ o CD E E 3 «0 TJ CO 2^ Z O CQ A i« iz «c (/> CO C CD w O CD E o 2 |2 3 I (L OB I- 5H I" I 5^ CM fy. U) u> -»- u> 52 « ca CNJ I s U) <0 («> uj CNi S U) ca " csi E 3 o hs e O CO o -s 2 ico "♦■ -f + LU LU LU S J8 S? 00 00 h«^ ^ ▼-■ cj ^ fc s eg CNJ CO CM 0> T- CO "S Q U) lA ^ -r- C4 ^ -^ -^ O U) U) -_ CNJ CO CM CNJ o> S2$§ o> o> o '•- CM (0 (A <0 T T ^ LU LU LU ^' CO ^ i CO . CM o> P is CO i in 00 -t- m i/i n o> CO »- ^ CM eg ^ LU CM !8 CM* in* CO CM f^ CM ° m T- to ••- »- CM CM c» 2 CO $ CM O) in m 00 00* o> o S CM »- CO m o CO* I O s « c CO o ^ I o S 6 9 C 9 5 & i« « c o i « 3 CO 2 "5 8S We estimated pollutant loading to Boston Harbor due to direct urban runoff from the cities and towns within the coastal drainage basin using the methodology adopted by the EPA Nonpoint Source Branch (described in the National IJrban Runoff Program Report available from EPA Office Of Water). The NURP methodology is a stochastic approach. It models the episodic rainfall events which cause urban runoff, in the model, pollutant concentration in runoff derives from land use category and rainfall event statistics. The NURP approach calculates loadings from total rainfall and the area within each land use category. Event statistics were calculated from long-term, hourly rainfall records from four gauging stations in eastern Massachusetts. Mean and coefficient of variation for storm duration, intensity, volume, and time between storms were calculated using SYNOP, a computer program developed specifically to provide input for the NURP analysis. Pollutant concentration and runoff coefficient for each land use type were taken from the NURP report based on the event statistics provided by SYNOP. The area of each land-use category within the cities and towns bordering Boston Harbor was from Hruby et al. (1988) and is based on the land use maps of MacCoimell et al. (1985). These areas include only the portion of cities and towns within the coastal drainage basin (Table 33). Pollutant loadings by land-use category were calculated by multiplvine the mean concentration by the runoff coefficient and an armual rainfall or 44 inches. Total loading was calculated by summing over land-use categories. Loadings are estimated for total suspended solids, BOD and COD combined, total phosphorous, total nitrogen, TkN, copper, lead, and zinc (Table 34). Estimates of loadings for other pollutants are not validated sufficiently using the NURP methodology to allow their presentation.The estimated loadings for lead, 6,585 kg for North Harbor and 1927 kg for South Harbor, may be higher than present loadings due to decreased use of leaded gasoline since the time the >fURP methodology was developed. The NURP estimate is much lower than the estimated lead loading reported by Hruby et al. (1988), which is roughly 60,000 kg/yr to North and South Harbors combined. Hruby et al. relied on the methodology of Midwest Research Institute (McElroy et al., 1976), using lead loadings which are likely outdated. 86 a i2 m Sssa 00 f- 3 P (0 s 9 C S CO O o oO CO CO 3 O o CO E E 3 I o I. m e e I- O Q O O O ssssf 00 o J^ o o> Oi CO "t- T- O C5 O 00 ^ CVJ B i2 E 5 I w ll lis « o S; <=> ® o 0> Q CNJ (O O ^ (A (O ca c « 2 o 5) CO la. o o @ CD w e I* e Ri-S lo a a c c < o i E 3 CO CO CM -Is 5 CM CO" <0 CM h- 00 CO h* CO CO CO 1- O U5 -^ 1- ^ O) 0> CO CO O CO 00 y- CM ^ ■* CO o CM CM CM CO CO CM S co" "^" CO CM O) 0> CO a> CO ^ ^ r^ 0> ^ O CM h* T-" CM* r^ ir> CO CM r>» u) CO r^ CO CM CO CO r^ T- o) ST- g CM -^ 00 00 ^ r^ -»- T- ^ It o> ^ CO o ? CM 1- 00 ^ in CO ■«»■ Ui CO CO O) r». "^ CM OJ O) h*. o> o 00 T- CO 00 r»- O" lO co" o>" h-" r>." co" K T-" o CO CO CM CM O) 00 o h". CM "T- in o> CO CM « CO h^ w a> CM CO O CO U5 CO r^ 00 00 oo U5_ CO o "t -*" cm" ^ oo" co" co" ^ co" of " " 00 h- U) •* 5 ■* CO CM CO CM CO "*r Q in in ■^ 00 00 CM CM O ^ UJ ■«t r>. CO CO -»- co" ▼-" co" ■^ '" 1-" '^* O) o O) •^ CM o> r^ f- in h- o T- CO o> O) CM s 00 0> CO ▼" 00 CM CM \Xi T- CO o h* CO o) CO in in in m CO CO N» CO CO T- ^- cm" a KB • « c & O c S=l (0 9 "?= to 5 « 2 > o Z CD O LLI ^ h- CB CD E Q I I I o.e (0 _ c 2k75 O > I- 88 5.3 Discharges from Coastal Rivers The major coastal rivers discharging to Massachusetts Bay are presented in Section 6 along with estimates of annual flow. We have estimated loaclings associated with these rivers as another method for estimating loading^ associated with point and nonpoint sources within the various drainage areas. The approach involved developing estimates of pollutant concentrations near the mouths of the rivers and multiplying these estimates by aimual river flows presented in Section 3 of this report. Estimates of pollutant concentrations were developed using a combination of measurements made by the Massachusetts DWPC along with literature vsilues on typical levels of chemicals in river water. The latter data were used in several cases where the measurements did not seem to be correa in our opinion or where data were lacking. S.3.1 Water Quality Data for Massachusetts Rivers Water quality data were available at or near the mouths of several rivers within the Massacnusetts Bay drainage areas: • Merrimack River. Data were available for two stations sampled in 1986, one at the Routes 1 and lA bridge in Newburyport (River Mile 3.0) and one near the Essex-Merrimack Bridge in Amesbury (River Mile 5.2). Data were also available for 1989, but the farthest downstream station was at the Route 25 bridge in Haverhill (River Mile 18.5). • Ipswich River. Data were available for two stations sampled in 1985, one at Green Street in Ipswich (River Mile 4:2) and one at the GTE- Sylvania Dam in Ipswich (River Mile 4^). • Parker River. Data were available for one station sampled in 1984, the Route 1 bridge in Newburyport (River Mile 4.9). • Mystic River. Data were available for one station sampled in 1983- 1986, near the confluence with the Island End River. • Chelsea River. Data were available for one station sampled in 1983- 1986, at Meridian Street (River Mile 02). • Qiarles River. Data were available for one station sample in 1982- 1986, just downstream of the Charlestown Bridge. • Neponset River. Data were available for one station sampled in 1984- 1986, just upstream from the Neponset Bridge in BostoiL • North River. Data were available for one station san^led in 1989, at the Bridge Street bridge in Norwell (River Mile 42). Only conventional parameters were measured. 89 Summaries of the water quality data for the rivers are provided in Tables 35 through 43. 90 Table 35. Water quality data for total suspended solids. River Water Quality TSS Concentraticns (mg/l) Number Number Number River Stations Years Obeerv. Mewi MIn Max References Merrimack Drainage Merrimack River 3 2 10 6.80 3.50 19.00 DEQE,1988.DEP, 1990a North Shore Drainage Ipswich River 2 1 5 3.70 3.00 6.50 DEQE.1986a Essex River Rowley River Parker River 1 1 2 17.00 14.00 20.00 DEQE.1986b Annisquam River Bass River htorth River Danvers River Crane River Pines River Saugus River * Boston Harbor Drainage Mystic River 1 5 30 15.10 1.00 46.00 DEQE,1982,19e3. 1984, 1986c. 1987 Chelsea River 1 3 21 13.37 4.00 56.x DEQE. 1984,1986c, 1987 Charles River 1 5 31 11.26 0.00 30.00 DEQE. 1982,1983,1984, 1986C.1987 Neponset River 1 3 18 16.61 <2 31.00 DEQE,1984,1986c,1987 Weymouth Fore River Weymouth Back River Weir River South Shore Drainage South River North River 1 1 3 3.00 2.00 4.50 DEP.1990b Green Hartxx River Jor>es River Town Brook Eel River Herring River Beaver Brook Dam Mean for rivers 10.86 Mean for all measurenients 12.59 91 Table 36. Water quality data for biochemical oxygen demand. River WatM' OiMriity ' BOD Concentrations (mg/1) Number Number Number River Stations Years Observ. Mean IMin IMax References Merrimack Drainage MeTTimack River 3 North Shore Drainage Ipswich River 2 Essex River Rowley River Parker River 1 Annisquam River Bass River North River Danvers River Crar>e River Pir^es River Saugus River Boston Hart>or Drainage Mystic River Chelsea River 1 Charles River Neponset River Weymouth Fore River Weymouth Back River Weir River 1.61 0.00 2.40 DEQE.1988:DEP.1990a 2.64 0.90 4.80 DEQE, 1986a 3.10 1.20 5.00 DEQE,1986b 4.58 1.20 8.70 DEQE, 1982, 1983 South Shore Drainage South River North River Green Hartxx River Jones River Town Brook Eel River Herring River Beaver Brook Dam DEP,1990b Mean for rivers Mean for all measurements 3.98 3.00 92 Table 37. Water quality data for nitrogen. River Water Quality Nitrogen Concentrations (mg/l) Nunnt>er Numl>er Number River Stations Years Observ. Mean iyiin Max Reference* Merrimack Drainage Mwnmack River North Shore Drainage Ipswich River Essex River Rowley River Parker River Annisquam River Bass River North River Danvers River Crarte River Pines River Saugus River Boston Harbor Drainage Mystic River Chelsea River Charles River Neponset River Weymouth Fore River Weymouth Back River Weir River 1.44 0.87 2.03 DEQE.1988;DEP. 1990a 1.49 0.97 3 00 DEQE, 1986a 2.01 1.51 2.50 DEQE, 1986b 5 31 1.59 0.50 2.80 3 22 2.85 1.07 6.61 S 31 1.63 0.44 3.11 3 19 1.77 0.72 4.11 DEQE, 1982.1983, 1984. 1986c.19e7 DEQE, 1984. 1986c, 1987 DEQE , 1 982, 1 983. 1 984 , 1 986c 1 987 DEQE, 1984, 1986c. 1987 South Shore Drainage South River North River Green Hartxx River Jones River Town Brook Eei River Herring River Beaver Brook Dam 1.71 1.53 1.90 DEP, 1990b Mean for rivers Mean for all measurements 1.81 1.86 93 Table 38. Water quality data for phosphorous. River Watar QuaHty PhosphofiM Concentrations (mg/l) Number Number Number River Stationa Years Observ. Mean MIn Max References Merrimack Drainage Merrimack River North Shore Drainage Ipswich River Essex River Rowley River Parker River Annisquam River Bass River North River Danvers River Crane River Pines River Saugus River Boston Harbor Drainage Mystic River Chelsea River Charles River Neponset River Weymouth Fore River Weymouth Back River Weir River 11 0.14 0.09 0.20 DEQE.1988;DEP,1990a 0.09 0.07 0.11 DEQE. 1986a 0.15 0.14 0.16 DEQE,1986b 5 31 0.17 0.04 0.29 DEQE.1982,1983,1984.1986C,1987 3 27 0.20 0.08 0.36 DEQE.1984.1986c.1987 5 31 0.17 0.06 0.39 DEQE. 1 982. 1 983. 1 984. 1 986c. 1 987 3 19 0.18 0.11 0.28 DEQE.1984.1986c.1987 South Shore Drainage South River North River Green Hartxx River Jor>es River Town Brook Eel River Herring River Beaver Brook Dam 0.15 0.13 0.17 DEP.1990b Mean for rivers Mean for all measurements 0.16 0.18 94 r Table 39. Water quality data for cadmium. River Water Qu^tty Cadmium Concentrations (mg/l) Number Number Number River Stations Years Observ. Mean MIn Max Refer an c«« Merrimack Drainage Merrimack River North Shore Drainage Ipswich River Essex River Rowley River Parker River Annisquam River Bass River North River Danvers River Crane River Pines River Saugus River Boston Harbor Drainage Mystk: River Chelsea River Charles River Neponset River Weymouth Fore River Weymouth Back River Weir River 10 0.001 0.000 0.004 DEQE,1988:DEP, 1990a 0.000 0.000 0.000 DEQE, 1986a 0.000 0.000 0.000 DEQE. 1986b 4 2 4 2 20 0.020 0.000 0.070 DEQE, 1 982, 1 983. 1 984, 1 986c 13 0.020 0.000 0.060 DEQE. 1984, 1986c 21 0.018 0.000 0.070 DEQE, 1982.1983, 1984. 1986c 12 0.021 0.000 0.060 DEQE, 1984. 1986c South Shore Drainage South River North River Green Harbor River Jones River Town Brook Eel River Herring River Beaver Brook Dam DEP. 1990b Mean for rivers Mean for all measurements 0.011 0.017 Values entered as 0 are less than detection limits of .001 -.02 mg/1 95 Table 40. Water quality data for chromium. Water OuaMy Chromium Concantraflons (mg/l) Numbar Numbar Numbar RIvar Stattona Yay Ob—r^. Maan MIn Max Referancaa Merrimack Drainage Merrimack Rivar 2 1 4 0.00 0.00 0.00 DEQE,1988;DEP.1990a North Shore Drainage Ipswich Rivar 11 1 0.00 0.00 0.00 DEOE.1986a Essax Rivar Rowiay Rfvar Parltar Rivar 1 1 1 0.01 0.01 0.01 DEQE,1986b Annisquam Rivar Bass Rivar NorlhRivar Danvars Rivar Crane River Pines River Saugus River Boston Harbor Drainage Mystic River 1 4 Chelsea River 1 2 Charles River 1 4 Neponset River 1 2 Weymouth Fore River Weymouth Bacic River Weir River South Shore Drainage South River North River DEP.1990b Qreen Harbor River Jones River TownBrooic Eel River Herring River Beaver Brook Dam Mean for rivers o.oi Mean for all measurements 0.02 23 0.03 0.00 0.06 DEQE,1982,1983,1984.19e6c 14 0.02 0.00 0.03 DEQE.1984,1986C 23 0.02 0.00 0.06 DEQE,1982.1983,1984.1986C 13 0.02 0.00 0.04 DEQE. 1984, 1986c Values entered as 0 are less Ihan the detection limtt of 0.02 mgd 96 Table 41 . Water quality data for copper. Water Oiuriity Coppar Conoantratfofw (rngfti Numbar Rivar Stationa Nmnbar Obaarv. yin Max Rafarencaa Merrimack Drainage Marrimack Rtvar 3 North Shora Dralnaga Ipswich Rivar 1 Easax Rivar Rowiay Rivar ParKar Rivar 1 Annisquam Rivar Basa Rivar North Rivar Danvars Rivar Crana Rivar Pinas Rivar Saugus Rivar Boston Hart>or Drainage Mystic Rivar 1 Chalsaa Rivar 1 Chartas Rivar 1 Naporisat Rivar 1 Waymouth Fore Rivar Waymouth Back Rivar Wair Rivar 11 0.002 <0.002 0.000 <0.002 0.019 DEQE.1968,DEP,1»0a <0.002 <0.002 DEQE.1986a 0.000 0.000 DEQE. 19666 4 2 4 2 23 0.070 <0.02 0.150 14 0.068 <0.02 0.250 23 0.054 <0.02 0.240 14 0.069 <0.02 0.260 DEQE. 1 982. 1 963. 1 964. 1 9e6c DEOE. 1984. 1966c DEQE. 1982, 1963, 1964 19660 DEQE. 1984. 19660 South Shore Drainage South Rivar North Rivar Qraan Hartxx Rivar Jonas Rivar Town Brook Eal Rivar luring Rivar Baavar Brook Dam DEP.1990b Mean for rivers Mean for all measurements 0.129 0.056 97 Table 42. Water quality data for lead. River Water Quality Lead Concentrations (mg/l) Number Numl}er Numljer River Stations Years OI>8erv. iMean IMin Max References Merrimack Drainage Merrimack River North Shore Drainage Ipswich River Essex River Rowley River Parker River Annisquam River Bass River North River Danvers River Crarw River Pines River Saugus River Boston Harbor Drainage Mystic River Chelsea River Charles River Neportset River Weymouth Rxe River Weymouth Back River Weir River 11 0.01 <0.02 0.06 <0.02 <0.02 0.06 0.03 DEQE.1988;DEP.1990a <0.02 DEQE, 1986a 0.06 DEQE, 1986b 4 2 4 2 23 0.22 <0.04 0.40 DEQE,1982,1983,1984,1986c 14 0.19 <0.04 0.46 DEQE. 1984, 1986c 23 0.17 <0.04 0.33 DEQE, 1 982, 1 983, 1 984, 1 986c 13 0.19 <0.04 0.37 DEQE,1984,1986c South Shore Drainage South River North River Green Harbor River Jones River Town Brook Eel River Herring River Beaver Brook Dam Mean for rivers Mean for all measurements 0.12 0.168 98 Table 43. Water quality data for zinc. Rlw YiaHmr Quality Zinc Concentrations (mg/l) NumtMr Number Number River Stations Years Ot>serv. Mean Min Max References Merrimack Drainage Merrimack River 3 2 11 0.004 0.000 0.023 DEQE.19d8,DEP. 1990a North Shore Drainage Ipswich River 1 1 1 0.000 0.000 0.000 DEOE. 1986a Essex River Rowley River Parker River 1 1 2 0.040 0.020 0.060 DEQE.l986b Annisquam River Bass River North River Danvers River Crane River Pines River Saugus River Boston Harbor Drainage Mystk: River 1 Chelsea River 1 Charles River 1 Neponset River 1 Weymouth Fore River Weymouth Back River Weir River South Shore Drainage South River North River DEP. 1990b Green Hart)or River Jortes River Town Brook Eel River Herring River Beaver Brook Dam Mean for rivers o.03i Mean for all nieasurements ooss Values entered as 0 are less than detection linvts ol 0.03-0.03 mgd 4 23 0.037 0.000 0.100 DEQE, 1 982, 1 983, 1 984, 1 986c 2 14 0.021 0.000 0.070 DEQE. 1984. 1986c 4 23 0.048 0.000 0.450 DEQE.1982.1983.1984.1966C 2 13 0.069 0.000 0.210 DEQE. 1984, 1986c 99 S.3.2 Estimates of Loadings via Major Rivers Based on an evaluation of the reliability of the data in Tables 35 through 43, we judged that the following water quality parameters could be relied upon for making estimates of loadings from the available measurement data: total suspended solids, biochemical oxygen demand, nitrogen, and phosphorus. The data for metals were not considered entirely reliable because some ot the values greatly exceeded levels reported for urban riverine environments and also differed with more recent data gathered by Gordon Wallace of University of Massachusetts at Boston. No data were available for the levels of PAHs in Massachusetts river water. Based on a review of the literature on metals and PAH levels in rivers of the United States, ranges were developed for estimating loadings of these chemical compounds to Massachusetts Bays via rivers (Table 44). Primary sources of data were Neff (1979), Forstner and Wittman (1981), USGS (1985), USEPA (1983, 1986), Atlas et al. (1986), USPHS (1987), and Menzie et al. (1991). Table 44. Literature values for ranges of concentrations of selected chemicals In river water. Chemicals Range from Literature Value Used Review Arsenic 90% < 10 ug/1 10 ug/1 Cadmium 0.01 - 7 1 ug/1 Chromium 1 - 30 ug/1 6 ug/1 Copper 10 ug/1 Lead 1-890 1-30 ug/1 Zinc 2 -50,000 ug/1 1-30 ug/1 PAHs 10-lOOng/l 50ng/l PCBs 0.1 - 20 ng/1 1 ng/1 Phthalates 50 - 10.000 ng/1 IQQ flg/l Using either the measured values or the ranges in literature values, estimates were made of the loadings via major rivers are provided in Tables 45 through 57. 100 Table 45. Loadings of total suspended solids via rivers. Riv«r Loads Annual Cone. Ussd suspended solids flow rats Avg In Loadings Estlmatsd (m3/ssc) Ysarsof Cone Estimats Loadings Data (mg/I) (mgA) (Kg/Yr) lltonimack Drainags Merrimaclc River 243.84 3 7.58 7.58 Subtotal = 5.83E-»-07 5.83E-^07 North Shots Drainags Ipswich River 6.46 1 3.25 3.25 6.62E-^05 Essex River 0.45 10.SO 1.49E-K05 Rowley River 0.48 10.50 1.59E-.^)6 Parker River 2.86 2 16.58 16.58 1.50E^06 Annisquam River 0.11 10JO 3.64E*04 Bass River 0.07 10.50 2.32E-»-04 North River 10.50 0.0OE*O0 Danvers River 0.59 10.50 1.95E-»^)5 Crane River 0.28 10.50 9.27E+04 Pines River 0.48 10.50 1.59E-K05 Saugus River 2.32 10JO Subtotal = 3.74E^-06 7.68E-K05 Boston Hart>or Drainags Mystic River 3.18 5 11.97 11.97 1.20E.K06 Chelsea River 5 15.47 15.47 O.OOE+00 Charles River 15.35 5 10.16 10.16 4.92E*06 Neponset River 5.58 6 21.92 21.92 3.86E+06 Weymouth Fore River 6.28 1 5.60 5.60 1.11E-K06 Weymouth Back River 4.38 1 9.10 9.10 1.26E+06 Weir River 1.25 1 9.10 9.10 Subtotals 1.27E-^07 3.59E+05 South Shore Drainage 1.15 10JO South River 3.81E-^05 North River 3.90 1 5.00 5.00 6.15E.K)5 Green Harbor River 0.35 10J0 1.16E+05 Jones River 1.71 10J0 5.65E.K06 Town Brook 0.31 10.50 1.03E+O5 Eel River 0.51 10S0 1.69E+06 Herring River 0.37 10J0 1.23E+06 Beaver Brook Dam 0.18 10.50 Subtotals 2.13E+06 5.96E<*^ Maximum: 21.92 TOTAL. 7.69E+07 Minimum s 3.25 Average s 10.52 i ^Memr7»ck = 76% 101 Table 46. Loadings of biochemical oxygen demand via rivers. Riv«r Loads Annual Wochamical oxygan flow rata damand (m3/8ac) Yaarsof Data Avfl Cone ssssn Cone. Usad In Loadings Estimata (mg/Q Estimatad Loadings Marrimack Drainaga Merrimack River 243.84 2 1.61E+00 1.61 E+00 Subtotals 1.24E+07 1.24E+07 North Shore Drainaga Ipswich River 6.46 1 2.64E+00 2.64E-«or Drainaga Mystic River 3.18 3.00E+00 3.01 E+05 Chelsea River 1 4.58E+00 4.58E+00 O.OOE+00 Charles River 15.35 3.00E+00 1.45E+06 Neponset River 5.58 3.00E+00 5.28E+05 Weymouth Fore River 6.28 3.00E+00 5.94E+05 Weymouth Back River 4.38 3.00E+00 4.14E+05 Weir River 1.25 3.00E+00 Subtotal = 3.41 E+06 1.18E+05 South Shore Drainage 1.15 3.00E+00 1.09E+05 South River North River 3.90 3.00E+00 3.69E+05 Green Hartx>r River 0.35 3.00E-tgt Ettlmatad {vn3/99c) Yaartof Cone Estimata Loadings Data (mgn) (mg/I) (Kg/Yr) Manimack Drainaga 243.84 3 1.44E+00 1.44E+00 Merrimack River 1.11 E*07 Subtotal- 1.11E+07 North Shora Drainaga Ipswich River 6.46 1 1.20E+00 1.20E400 2.43E*05 Essex River 0.45 1.39E+00 1.97E-^04 Rowley River 0.48 1.39E+00 2.10E-K04 Parker River 2.86 1 2.01 E+00 2.01 E+00 1.81E+05 Annisquam River 0.11 1 9.13E-01 9.13E-01 3.17E-»^ Bass River 0.07 1.39E+00 3.07E*03 North River 1.39E+00 O.OOE+00 Danvers River 0.59 1.39E.^00 2.S9E*04 Crane River 0.28 1.39E+00 1.23E+04 Pines River 0.48 1.39E+00 2.10E-^04 Saugus River 2.32 1.39E+00 Subtotals 6.32E+06 1.02E-.-05 Boston Harbor Drainaga Mystic River 3.18 5 1.56E+00 1.56E-h00 1.56E<^05 Chelsea River 6 1.45E-»^ 1.46E.^00 O.OOE^OO Charies River 15.35 6 1.57E+00 1.57E-MX) 7.60E-»^ Neponset River 5.58 8 1.82E+00 1.82E-»^ 3.21E.K05 WeynxHJth Fore River 6.28 2 7.16E-01 1.39E+00 2.7SE+05 WeynrxHJth Back River 4.38 1.39E+00 1.92E+05 Weir River 1.25 1 1.43E+00 1.39E+00 Subtotals 1.76E+06 5.48E-^04 South Shora Drainaga 1.15 1.39E+00 South River 5.04E-^04 North River 3.90 1 1.17E+00 1.17E+00 1.44E^^ Green Harbor River 0.35 1.39E+00 1.53E-K04 Jones River 1.71 1.39E+00 7.48E+04 Town Brook 0.31 1.39E+00 1.36E-K>4 Eel River 0.51 1.39E+00 2.24E+04 Herring River 0.37 1.39E-^00 1.62E*04 Beaver Brook Dam 0.18 1.39E+00 Subtotals 3.45E+06 7.89E+03 Maximum: 2.01 E+00 TOTAL. 1.38E+07 Minimum = 7.16E-01 Average X 1.39E+00 % Merrimack s 80% 103 Table 48. Loadings of total phosphorus vfa rivers. Riv^r Loads Annual Cone. Used total phosphorus flow rate Avg in Loadings Estimated (m3/sec) Years of Cone Estimate Loadings Data (mg/l) (mg/l) (Kg/Yr) Merrimack Drainage Merrimacic River 243.84 3 1.40E-01 1.40E-01 Subtotals 1.08E+06 1.08E+06 f4orth Shore Drainage Ipswich River 6.46 1 1.00E-01 1.00E-01 2.04E+04 Essex River 0.46 1.47E-01 2.09E+03 Rowley River 0.48 1.47E-01 2.23E+03 Parker River 2.86 1.47E-01 1.33E+04 Annisquam River 0.11 2 1.30E-01 1.30E-01 4.51 E+02 Bass River 0.07 1.47E-01 3.25E+02 North River 1.47E-01 O.OOE+00 Danvers River 0.59 1.47E-01 2.74E+03 Crane River 0.28 1.47E-01 1.30E+03 Pines River 0.48 1.47E-01 2.23E+03 Saugus River 2.32 1.47E-01 Subtotal s 5.57E+04 1.08E+04 Boston Harbor Drainage Mystic River 3.18 5 1.90E-01 1.90E-01 1.91 E+04 Chelsea River 6 1.80E-01 1.80E-01 O.OOE+00 Charles River 15.35 6 1.80E-01 1.80E-01 8.71E-I-04 Neponset River 5.58 8 1.90E-01 1.90E-01 3.34E+04 Weynxxith Fore River 6.28 2 8.00E-02 8.00E-02 1.58E+04 Weymouth Back River 4.38 1 1.10E-01 1.10E-01 1.52E+04 Weir River 1.25 1.47E-01 Subtotals 1.76E+05 5.79E+03 South Shore Drainage South River 1.15 1.47E-01 5.33E+03 North River 3.90 1 1.70E-01 1.70E-01 2.09E+04 Green l-lartx>r River 0.35 1.47E-01 1.62E+03 Jones River 1.71 1.47E-01 7.92E+03 Town Brook 0.31 1.47E-01 1.44E+03 Eel River 0.51 1.47E-01 2.36E+03 Hening River 0.37 1.47E-01 1.72E+03 Beaver Brook Dam 0.18 1.47E-01 Subtotals 4.21 E+04 8.34E+02 Maximum: 1.90E-01 TOTAL « 1.35E+06 Minimum s 8.00E-02 Averages 1.47E-01 4 )^ Merrimack s 80% 104 Table 49. Loadings of total PAHs via rtvert. Riv«r Loads Annual ConcUsad Lowar total PAHs flow rata in Loadings EstJmatad (m3/sac) Estimate (1) (mg/l) Loadings (Kg/Yr) Merrimaclc Drainaga Merrimaclc River 243.84 5.00E-05 Subtotal =: 3.84E+02 3.84E+02 North Shora Drainaga Ipswich River 6.46 5.00E-05 1.02E+01 Essex River 0.45 5.00E-05 7.10E-01 Rowley River 0.48 5.00E-05 7.57E-01 Parker River 2.86 5.00E-05 4.51E-t.00 Annisquam River 0.11 5.00E-05 1.73E-01 Bass River 0.07 5.00E-05 1.10E-01 North River 5.00E-05 O.OOE+00 Danvers River 0.59 5.00E-05 9.30E-01 Crane River 0.28 5.00E-05 4.42E-01 Pines River 0.48 5.00E-05 7.57E-01 Saugus River 2.32 5.00E-05 Subtotal = 2.22E-M)1 3.66E+00 Boston Harbor Drainaga Mystic River 3.18 5.00E-05 5.01 E+00 Chelsea River 5.00E-05 O.OOE+OO Charles River 15.35 5.00E-05 2.42E+01 Neponset River 5.58 5.00E-05 8.80E+00 WeynxHJth Fore River 6.28 5.00E-05 9.90E+00 Weymouth Back River 4.38 5.00E-05 6.91 E+00 Weir River 1.25 5.00E-05 Subtotal = 5.68E+01 1.97E+00 South Shora Drainaga South River 1.15 5.00E-05 1.81 E+00 North River 3.90 5.00E-05 6.15E+00 Green Hartx>r River 0.35 5.00E-05 5.52E-01 Jor>es River 1.71 5.00E-05 2.69E+00 Town Brook 0.31 5.00E-O5 4.89E-01 Eel River 0.51 5.00E-O5 8.04E-01 Herring River 0.37 5.00E-O5 5.83E-01 Beaver Brook Dam 0.18 5.00E-05 Subtotals 1.34E+01 TOTAL- % Merrimack = 2.84E-01 : 4.77E+02 81% 1. A vahje of 50 ng/l was selected for PAH concentratk>n in surface water. This vakie falla within the range of 10 to 100 ng^ reported by Menzie (1990) for urban river systems. IDS Table 50. Loadings of total PCBs via rivers. RivM* Loads Annual Cone. Used Lower PCBs flow rate In Loadings Estimated (m3/sec) Estimate (1) « Loadings (mg/1) (Kg/Yr) Merrimack Dralnags Merrimack River 243.84 1.00E-06 7.69E+00 Subtotal = 7.69E+00 North Shore Drainage Ipswich River 6.46 1.00E-06 2.04E-01 Essex River 0.45 1.00E-06 1.42E-02 Rowley River 0.48 1.00E-06 1.51 E-02 Parker River 2.86 1.00E-06 9.02E-02 Annisquam River 0.11 1.00E-06 3.47E-03 Bass River 0.07 1.00E-06 2.21 E-03 North River 1.00E-06 O.OOE+00 Danvers River 0.59 1.00E-06 1.86E-02 Crane River 0.28 1.00E-06 8.83E-03 Pines River 0.48 1.00E-06 1.51 E-02 Saugus River 2.32 1.00E-06 7.32E-02 Subtotal =: 4.45E-01 Boston Harbor Drainage Mystk; River 3.18 1.00E-06 1.00E-01 Chelsea River 1.00E-06 O.OOE+00 Chartes River 15.35 1.00E-06 4.84E-01 Neponset River 5.58 1.00E-06 1.76E-01 Weymouth Fore River 6.28 1.00E-06 1.98E-01 Weymouth Back River 4.38 1.00E-06 1.38E-01 Weir River 1.25 1.00E-06 3.94E-02 Subtotal - 1.14E+00 South Shore Drainage South River 1.15 1.00E-06 3.63E-02 North River 3.90 1.00E-06 1.23E-01 Green Hart)or River 0.35 1.00E-06 1.10E-02 Jones River 1.71 1.00E-06 5.38E-02 Town Brook 0.31 1.00E-06 9.78E-03 Eel River 0.51 1.00E-06 1.61 E-02 Hening River 0.37 1.00E-06 1.17E-02 Beaver Brook Dam 0.18 1.00E-06 5.68E-03 Subtotal = 2.67E-01 TOTALS 9.54E+00 % Merrimack :r 81% 1 . A value of 1ng/l was selected for PCB concentratkxi in surface water. This value is conskjered by Atlas et al. (1986) to be a 'reasonable upper Rmit' for PCBs in average river water. 106 Table 51. Loadings of phthalates via rivers. Rivw Loads Annual Cone. Used Lower phthalatts flow rate in Loadings Estimated (m3/8ec) Estimate (1) (mg/i) Loadings (Kg/Yr) Merrimack Drainaga Merrimack River 243.84 1.00E-04 Subtotal = 7.69E+02 7.69E+02 North Shore Drainage Ipswich River 6.46 1.00E-04 2.04E+01 Essex River 0.45 1.00E-04 1.42E+00 Rowtey River 0.48 i.ooe-04 1.51E+00 Parker River 2.86 1.00E-04 9.02E+00 Anr>isquam River 0.11 1.00E-04 3.47E-01 Bass River 0.07 1.00E-04 2.21 E-01 North River i.ooe-04 O.OOE+00 Danvers River 0.59 1.00E-04 1.86E+00 Crane River 0.28 I.ooe-04 8.83E-01 Pines River 0.48 1.00E-04 1.51E+00 Saugus River 2.32 1.00E-04 Subtotals 4.45E+01 7.32E+00 Boston Harbor Drainage Mystic River 3.18 I.OOE-04 1.00E+01 Cheisea River I.OOE-04 O.OOE+00 Chartes River 15.35 1.0OE-O4 4.84E-K01 Neponset River 5.58 I.OOE-04 1.76E-K01 Weymouth Fore River 6.28 I.OOE-04 1.98E-^1 Weymouth Back River 4.38 I.OOE-04 1.38E-K01 Weir River 1.25 I.OOE-04 Subtotals 1.14E+02 3.94E+00 South Shore Drainage South River 1.15 I.OOE-04 3.63E+00 North River 3.90 I.OOE-04 1.23E+01 Green Hartxx Rh^er 0.35 I.OOE-04 1.10E+00 Jones River 1.71 I.OOE-04 5.38E+00 Town Brook 0.31 I.OOE-04 9.78E-01 Eel River 0.51 I.OOE-04 1.61E+00 Herring River 0.37 I.OOE-04 1.1/E+OO Beaver Brook Dam 0.18 I.OOE-04 Subtotals 2.67E+01 TOTAL = %Menimack = 5.68E-01 ; 9.54E+02 81% 107 Table 52. Loadings of araenic via rivers. Riv«r Loads Annual ConcUsad arssnic flow rata Avg in Loadings Estlmatad (m3/sac) Yaarsof Cone Estlmata Loadings Data (mg/0 (mg/0 (Kg/Yr) Merrimack Dralnaga Merrimack River 243.84 1.00E-02 Subtotals 7.69E+04 7.69E+04 North Shore Dralnaga Ipswich River 6.46 1.00E-02 2.04E+03 Essex River 0.45 1.00E-02 1.42E+02 Rowley River 0.48 1.00E-02 1.51E+02 Parker River 2.86 1 1.00E-03 1.00E-03 9.02E+01 Annisquam River 0.11 1.00E-02 3.47E+01 Bass River 0.07 1.00E-02 2.21 E+01 North River 1.00E-02 O.OOE-kOO Danvers River 0.59 1.00E-02 1.86E+02 Crane River 0.28 1.00E-02 8.83E+01 Pines River 0.48 1.00E-02 1.61 E+02 Saugus River 2.32 1.00E-02 Subtotals 3.63E+03 7.32E+02 Boston Hart>or Drainage Mystic River 3.18 5.00E-03 5.00E-03 5.01 E+02 Chelsea River 6.30E-02 6.30E-02 O.OOE+00 Charles River 15.35 5.40E-02 5.40E-02 2.61 E+04 Neponset River 5.58 1.18E-01 1.18E-01 2.08E+04 Weymouth Fore River 6.28 1.00E-02 1.98E+03 Weymouth Back River 4.38 1.00E-02 1.38E+03 Weir River 1.25 1.00E-02 Subtotal s 5.12E+04 3.94E+02 South Shore Drainage South River 1.15 1.00E-02 3.63E+02 hiorth River 3.90 1.00E-02 1.23E+03 Green Hartx>r River 0.35 1.00E-02 1.10E+02 Jones River 1.71 1.00E-02 5.38E+02 Town Brook 0.31 1.00E-02 9.78E+01 Eel River 0.51 1.00E-02 1.61 E+02 Herring River 0.37 1.00E-02 1.17E+02 Beaver Brook Dam 0.18 1.00E-02 Subtotals 2.67E+03 5.68E+01 Maximum: 1.18E-01 TOTAL. 1.34E+05 Minimum - 1.00E-03 Averages 4.82E-02 % Merrimack s 57% 1 . A value of 0.01 mg^ is used for rivers for which we have no measuremerts. This value is selected as representative of typical maximum values in the United States rivers. 106 Table 53. Loadings of cadmium via rtvers. Rlv^r Loads Annual Estimated cadmium flow rate Loadings (m3/sec) (Kg/Yr) Cd Cones 0.001 mg/1 Merrimack Drainaga 243.84 Subtotals ^ 7.69E+03 Merrimack River 7.69E-h03 North Shore Drainage 6.46 2.04E+02 Ipswfch River 0.45 1.42E+01 Essex River 0.48 1.51E+01 Rowley River 2.86 9.02E+01 Parker River 0.11 3.47E+00 Annisquam River 0.07 2.21 E+00 Bass River O.OOE+00 North River 0.59 1.86E+01 Danvers River 0.28 8.83E+00 Crane River 0.48 1.51E+01 Pines River 2.32 Subtotals = 7.32E+01 Saugus River 4.45E+02 Boston Hartx>r Drainage 3.18 1.00E+02 O.OOE^^ Mystic River 15.35 4.84E-K02 Chelsea River 5.58 1.76E+02 Charies River 6.28 1.98E+02 Neponset River 4.38 1.38E+02 Weymouth Fore River 1.25 Subtotals = 3.94E-^01 Weymouth Back River 1.14E+03 Weir River South Shore Drainage 1.15 3.63E-K01 3.90 1.23E+02 South River 0.35 1.10E+01 North River 1.71 5.38E+01 Green Hartx>r River 0.31 9.78E"fO0 Jones River 0.51 1.61E+01 Town Brook 0.37 1.17E-^01 Eel River 0.18 Subtotals s 5.68E^^ Herring River 2.67E+02 Beaver Brook Dam TOTAL. 9.54E+03 %MerTirnacks 81% 109 Table 54. Loadings of chromium via rivers. Rlv^r Loads Annual Estimated chromium flow rate Loadings {n\3f99c) (Kgnrr) Or Cone « 0.006 mg/l IMttiTlmacIc Drainagt Merrimack River 243.84 4.61 E+04 Subtotals s 4.61 E+04 North Short Drainaga Ipswich River 6.46 1.22E+03 Essex River 0.46 8.61 E+01 Rowley River 0.48 9.08E-t^1 Paricer River 2.86 5.41 E+02 Annisquam River 0.11 2.08E+01 Bass River 0.07 1.32E+01 HorXh River O.OOE+00 Danvers River 0.59 1.12E+02 Crane River 0.28 5.30E+01 Pines River 0.48 9.08E+01 Saugus River 2.32 4.39E+02 Subtotals s 2.67E+03 Boston Harbor Drainage • Mystic River 3.18 6.02E+02 Chelsea River O.OOE+00 Charles River 15.36 2.90E+03 Neponset River 6.58 1.06E+03 Weymouth Fore River 6.28 1.19E+03 Weymouth Back River 4.38 8.29E+02 Weir River 1.25 2.37E+02 Subtotals = 6.82E+03 South Shore Drainage South River 1.15 2.18E+02 North River 3.90 7.38E+02 Green Hartx>r River 0.36 6.62E+01 Jories River 1.71 3.23E+02 Town Brook 0.31 6.87E+01 Eel River 0.51 9.66E+01 Herring River 0.37 7.00E+01 Beaver Brook Dam 0.18 3.41 E+01 Subtotals » 1.60E+03 TOTAL* 5.72E+04 %Merrimacks 81% 110 Table 55. Loadings of copper via rfvert. Riv«r Loads Annual Estimated copp«r flow rate Loadings (m3/sec) (Kgnrr) Cu Concz 0.01 rr>g/l Merrimack Drainaga Merrimack River 243.84 7.69E+04 SU}totals = 7.69E+04 ^k>rth Shore Drainaga Ipswich River 6.46 2.04E-»'03 Essex River 0.45 1.42E-^02 RowJey River 0.48 1.51 E+02 Parker River 2.86 9.02E+02 Annisquam River 0.11 3.47E-»^1 Bass River 0.07 2.21 E^1 North River O.OOEt^ Danvers River 0.59 1.86E+02 Crane River 0.28 8.a3E+01 Pines River 0.48 1.51 E+02 Saugus River 2.32 7.32E+02 Subtotals = 4.45E+03 Boston Harbor Drainage Mystic River 3.18 1.00E+03 Chelsea River C.OOE-t^ Charles River 15.35 4.84E-^03 Neponset River 5.58 1.76Et-03 Weymouth Fore River 6.28 1.98E.^ Weymouth Back River 4.38 1.38E-»^ Weir River 1.25 3.94E-K02 Subtotals = 1.14E-K04 South Shore Drainage South River 1.15 3.63E+02 North River 3.90 123E+03 Green Hartx>r River 0.35 1.10E-K02 Jones River 1.71 5.38E.K02 Town Brook 0.31 9.78E«M)1 Eei River 0.51 1.61 E+02 Herring River 0.37 1.17E+02 Beaver Brook Dam 0.18 5.68E+01 Subtotals = ^67E+03 TOTAL « 9.54E+04 %Mdntiiack« 81% lU Table 56. Loadings of lead via rivers. Riv»r Loads Annual Estimated Estimated iMd flow rate Loadings Loadings (m3/sec) (Kg/Yr) (Kg/Yr) Pb Cones 0.001 mg/1 0.03 mg/l Merrimack Drainaga Merrimack River 243.84 7.69E+03 2.31 E+05 Subtotals s 7.69E+03 2.31 E+05 North Shora Drainage lpswk:h River 6.46 2.04E+02 6.11E+03 Essex River 0.45 1.42E+01 4.26E+02 Rowley River 0.48 1.51E+01 4.54E+02 Parker River 2.86 9.02E-(>01 2.71 E+03 Annisquam River 0.11 3.47E+00 1.04E+02 Bass River 0.07 2.21 E+00 6.62E+01 North River O.OOE+00 O.OOE+00 Danvers River 0.59 1.86E+01 5.58E+02 Crane River 0.28 8.83E+00 2.65E+02 Pines River 0.48 1.51E+01 4.54E+02 Saugus River 2.32 7.32E+01 2.19E+03 Subtotals = 4.45E-t-02 1.33E+04 Boston Harbor Drainage Mystic River 3.18 1.00E+02 3.01 E+03 Chelsea River O.OOE+00 O.OOE+00 Charles River 15.35 4.84E-i^ 1.45E+04 Neponset River 5.58 1.76E+02 5.28E+03 WeynxHJth Fore River 6.28 1.98E+02 5.94E+03 Weymouth Back River 4.38 1.38E+02 4.14E+03 Weir River 1.25 3.94E+01 1.18E+03 Subtotals s 1.14E+03 3.41 E+04 South Shore Drainage South River 1.15 3.63E+01 1.09E+03 North River 3.90 1.23E+02 3.69E+03 Green Hartx>r River 0.35 1.10E+01 3.31 E+02 Jor>es River 1.71 5.38E-t-01 1.62E+03 Town Brook 0.31 9.78E+00 2.93E+02 Eel River 0.51 1.61E+01 4.83E+02 Herring River 0.37 1.17E+01 3.50E+02 Beaver Brook Dam 0.18 5.68E+00 1.70E+02 Subtotals =r' 2.67E+02 8.02E+03 TOTAL. 9.54E+03 2.86E+05 % Merrimack s 81% 81% 112 Table 57. Loadings of zinc via rtvert. Rlv*r Loads Annual Estimated Estimated zinc flow rata Loadings Loadings (m3/sac) (Kgnrr) (KgTfr) Zn Concz 0.001 mgl 0.03 mg/1 IM«nimacl( Dnilnag« Merrimack River 243.84 7.69E+03 2.31 E+05 Subtotals =' 7.69E+03 2.31 E+05 North Shore Drairmge Ipswich River 6.46 2.04E+02 6.11E+03 Essex River 0.45 1.42E+01 4.26E*02 Rowley River 0.48 1.51E+01 4.54E-M)2 Partner River 2.86 9.02E+O1 2.71E-^03 Annlsquam River 0.11 3.47E+00 1.04E-K02 Bass River 0.07 2.21 E+00 6.62E+01 ^4orth River O.OOE-^00 O.OOE-J-00 Danvers River 0.59 1.86E+01 5.58E+02 Crane River 0.28 8.83E+00 2.65E+02 Pines River 0.48 1.51E+01 4.54E+02 Saugus River 2.32 7.32E+01 2.19E+03 Subtotals s 4.45E+02 1.33E+04 Boston Harbor Drainage Mystic River 3.18 1.00E-^Q2 3.01 E+03 Chelsea River O.OOE+00 O.OOE+00 Charles River 15.35 4.84E+02 1.45E+04 Neponset River 5.58 1.76E+02 5.28E+03 Weymouth Fore River 6.28 1.98E+02 5.94E+03 Weymouth Back River 4.38 1.38E+02 4.14E+03 Weir River 1.25 3.94E-^01 1.18E-^03 Subtotals = ' 1.14E+03 3.41 E+04 South Shore Drainage • South River 1.15 3.63E+01 1.09E+03 North River 3.90 1.23E+02 3.69E+03 Green Hartx>r River 0.35 1.10E+01 3.31 E+02 Jones River 1.71 5.38E+01 1.62E-K03 Town Brook 0.31 9.78E+00 2.93E-K02 Eel River 0.51 1.61E+01 4.83E^^ Herring River 0.37 1.17E+01 3.50E+02 Beaver Brook Dam 0.18 5.68E-^00 1.70E-K02 Subtotals =:' 2.67E+02 e.OZE-^OS TOTAL. 9.54E-^03 2.86E+05 %Menimack« 81% 81% 113 5.4 Loadings In Groundwater Loads in groundwater were made only for selected watersheds and contaminants for which data were available. 5.4.1 Methods Nitrogen Loading to Cape Cod Bay We used two methods to estimate nitrogen loading into Cape Cod Bay and the watershed. The first method estimated nitrogen loadings into both Cape Cod Bay and its watershed (i.e., inputs to both the water and onto the land) by identifying significant inputs of nitrogen. The second method considered nitrogen loading just into Cape Cod Bay, including flow from groundwater. This second method required an estimate of both groundwater flow and nitrogen groundwater concentration. Note that here the term "Cape Cod Bay watershed" refers specifically to that area whose groundwater discharges into Cape Cod Bay. We assumed that all groundwater in the Cape Cod Bay watershed discharges directly into Cape Cod Bay, thereby ignoring streams, springs, or other surface water. We also assumed steady-state conditions for the flow, concentration, and loading data. In addition, we assumed a contiguous groundwater divide exists, such that groundwater discharges on one side into Cape Q)d Bay, on the other, into Buzzards Bay, Vineyard Sound, Nantucket Sound, and the Atlantic Ocean. To estimate the location of the ^oundwater divide, we used a method similar to M. Frimpter (personal communication, M. Frimpter. We assumed that regionally the water table coincides with piezometric head. Orthogonal lines to groundwater contours therefore represent the migration of groundwater from a higher to lower fluid potential (i.e., the general directions of groundwater flow.) By determining the general directions of flow, the groundwater divide can be found. We used the USGS groundwater atlas for Cape Cod (USGS Atlas HA-692, 1986) to obtain our groundwater profile. The atlas displays six discrete cells in which the water-table altitude is generally higher near the center of the cells, and lower near the coast. Thus groundwater generally flows from the center of the Cape to the coastlines. After approximating the groundwater divide for each cell, we connected them to create a contiguous divide for the Cape Cod region. Much of this groundwater divide comcides with Route 6, which in turn tends to coincide with topographic highs. Only land lying within the Cape Cod Bay watershed was included in the analysis. For each town, this area was measured by digitizing the groundwater divide and town boundaries into ARC/INFO computer mappmg system. Towns which have land lying within the watershed include Barnstable, Yarmouth, Sandwich, Dennis, Brewster, Orleans, Eastham, Provincetown, Wellfleet, and Truro. Note that Bourne was not included in the analysis, since we assessed that almost all of its nitrogen sources discharge into Buzzards Bay. 114 Estimates of Nitrogen Loading Using Method A: Discrete Loadings to Cape Cod Watershed The first method identifies discrete sources of nitrogen introduced into the watershed. For each source, we calculated a respective nitrogen loading; we then summed these to obtain the total nitrogen loading. Sources of nitrogen considered are precipitation; septic systems; and lawn, agricultural, and ^olf course fertilizers. We Ignored package treatment plants as a potential source smce onJy a few are located withm the Cape Cod Bay watershed. Precipitation We calculated a nitrogen loading to the watershed via precipitation by estimating an annual volume of precipitation and its associated nitrogen concentration. We calculated a mean preapitation rate of 1.1 m/year, based upon 1947 to 1976 data (USGS Atlas HA 692, 1986) for stations located within the Cape Cod Bay watershed. The annual volume of precipitation was found by multiplying the annual precipitation rate by the area of the watershed. We used a mean concentration of dissolved inorganic nitrogen (DIN) in precipitation of 22.4 uM, measured in Buttermilk Bay, an embayment of Cape Cod, by Valiela, et al., 1988. The nitrogen loading due to precipitation was calculated by multiplying the annual precipitation volume by the mean DIN concentration. Domestic Fertilizer To obtain a lawn fertilizer loading for the watershed, we first obtained the number of combined housing units for each town of concern (personal communications, towns' assessors). We define one combined housing unit as any residential building, regardless of the number of families residing there. Therefore, a four family home equals only one combined housing unit. Usmg approximations made by USGS (Frimpter, et al., July 1988), we assumed each housing unit possessed a lawn area of 5000 square feet. In addition, we assumed that the percentage of both a town's land and its residential units within the watershed were identical. For example, if 30 percent of a town's land lies within the watershed, then 30 percent of its lawns do as well. Street maps of each town were used to assess the validity of this assumption. USGS (Frimpter, et al., July 1988) also provides a typical application rate of^2 lb/ 1000 square ft/year of nitrogen to the soil. To calculate the nitrogen loading due to lawn fertilizer, we multiplied the mean lawn size by the number of lawns to obtain total lawn land use. We multiplied this area by the mean fertilizer application rate to obtain a mean total nitrogen loading. Septic Systems We calculated septic system loading for the Cape Cod Bay watershed based upon the number of residents per town. However, Barnstable County has disparate winter and summer populations. We therefore assumed nine months of a year only permanent residents would be present; the remaining three months of peak summer tourism, a substantially larger population was considered. We obtained each town's winter population through town clerks (personal communications, towns' clerks. In addition, some town clerks provided an estimate of their summer population. If no estimate on the sunmier population was available, winter population was tripled as a rough estimate (Fersky, 1986). Similar to our assumption concerning housing 115 distributions, we assumed that the percentage of a town's area within the watershed would hold an identical percentage of the town's population. We used a septic system infusion rate of 3.8 kg/DIN /person/year, based upon Valiela et al. (1988). We multiplied this rate by winter and summer populations within the watershed to obtain winter and summer loadings, respectivefy. Once weighted and summed (i.e. [9/12 winter population + 3/12 summer populationjinfusion rate ), we obtained a total nitrogen loading due to septic systems. Other Fertilizers The most significant source of agricultural fertilizer on Cape Cod is cranberry production; we used 1980 cranberry bog land-use data for each town of concern from MacConnell, et al., 1984. Similar to our previous assumptions, we assumed that the percentage of a town's land within the watershed is identical to the percentage of the town's cranberry bog land use within the watershed. In addition, Valiela et al. (1988) provide a typical cranberry fertilizer application rate of 22.5 kg DEN/ha/yr. We multiplied these data together to obtain a nitrogen loading estimate for the watershed. Finally, the nitrogen loading due to golf course fertilizer was estimated. This method is identical to that mentioned previously for agricultural fertilizer: land use data by town (MacConnell, et al., 1984), the percent area within the watershed, and a typical golf course fertilizer application rate of 99 DIN/acre/yr were used to calculate a loading. The application rate was obtained by taking the mean of application rates on several Cape Cod golf course fairways and roughs (Cape Cod Planning and Economic Development Commission, 1989). Total Estimates These individual estimates, when summed together, yield the nitrogen loading for the Cape Cod Bay watershed. From these estimates we calculated a nitrogen loading into Cape Cod Bay itself via groundwater. Estimate of Loadings Using Method A: Discrete Loadings to Cape Cod Bay The modeling previously applied to the Cape Cod Bay watershed can also be applied to Cape Cod Bay sdone. This is accomplished by: (1) predicting the amount of nitrogen in the watershed which leaches into the groundwater; (2) assuming all of the mtrogen introduced into groundwater will discharge into Cape Cod Bay; (3) assuming the annual recharge into the Cape Cod Bay watershed dictates the annual discharge into Cape Cod Bay. Precipitation After DIN enters the watershed via precipitation, a portion of this nitrogen leaches from the zone of aeration into the groundwater. Since the nitrogen is dissolved, the area's recharge determines the amount of nitrogen to reach the groundwater. Once an annual estimate of recharge is found, a method identical to mat used for precipitation loading into the watershed is used. Our recharge data (USGS Atlas HA 692, 1986), based upon the mean annual precipitations used in Section 5.1 were estimated by USuS using the Thomthwaite and Mather (1957) method. The annual volume of recharge was then found by multiplying the annual recharge by the area of the Cape Cod Bay watershed. Again, 116 we used the mean concentration of DIN in precipitation (22.4 uM). We a.ssumed that all recharge discharges to the ocean and neglected minor discharges into canals or streams (USGS Atlas HA-692, 1986). Thus the nitrogen loading into the Bay was calculated by multiplying the annual recharge volume by the mean DIN concentration. Septic Systems Since septic systems are typically located at least four feet below topsoil, we assumea that none of its mtrogen will be available to plants for uptake. In addition, as Valiela et al. (1988) point out, denitrification in porous sand or groundwater are probably not significant, since the low amounts of dissolved inorganic carbon present here disallow microbial activity. Instead, we assumed that all of the nitrogen leaches directly into the groundwater, where it is eventually discharged into Cape Cod Bay. Thus, Cape Cod Bay and its watershed have identical estimates for mtrogen loading due to septic systems. Fertilizers We assessed what portion of fertilizer (and therefore nitrogen) would leach into groundwater, as opposed to plant uptake or denitrification. USGS (Frimpter, et al., 1988) states that typically, for the Cape Cod region, 45 to 50 percent of lawn fertilizer leaches into the groundwater. (The leachable portion of fertilizer depends on many factors including application rate, type of vegetation, and soil characteristics.) Similar estimates have been made for golf course fertilizer leachability, while no estimates could be obtained as cranberry fertilizer leachability. For simplicity, we assumed that for all of the previously mentioned fertilizers, the leachable to total fertilizer ratio is 0.5. Estimate of Loadings to Cape Cod Bav Using Method B: Groundwater Measurements and Discharge Rates We assumed in the second approach that a typical nitrogen concentration in groundwater exists, along with a typical groundwater flow rate. Although both nitrogen concentrations and flow in groundwater can vary widely locally, they are probably adequate to quantify a regional estimate for Cape Cod Bay. This method simply multiplies a representative nitrogen concentration by a representative flow in groundwater to obtain a nitrogen loading due to groundwater for Cape Cod Bay. A data base of nitrate levels from private wells in Cape Cod was obtained through the Barnstable County Health Department. Each data base record had to meet the following criteria: (1) sample measured on or after 1 January 1989; and (2) sample taken from an area within the Cai>e Cod Bay watershed. Once these records were selected from the data base, various statistics were calculated in an attempt to obtain a representative nitrate concentration. It should be noted that this data set may contain an inherent bias: older homes (whose owners suspeaed possible water quality problems) were probably sampled most frequently. In some cases, however, sampling was conducteci for real estate transactions or general information purposes. No ammonia concentrations for groundwater were available from this data base. Other sources of summary nitrate and ammonia concentrations for Cape Cod include two USGS publications to be discussed in Section 5.4.2. We assumed that an amount of groundwater equal to the annual recharge in the Cape Cod Bay watershed would discharge aimually into Cape Cod Bay. We used this value as our representative flow into Cape Cod Bay. Thus we could calculate a 117 second estimate of nitrogen loading into Cape Cod Bay by calculating the groundwater flow by its associated concentration. Groundwater Discharges to Boston Harbor Estimates of loadings associated with groundwater discharges were made for the harbor as a whole by making estimates of possible groundwater discharge and estimating the concentrations of substances in groundwater. An estimate of groundwater discharge to the harbor was made indirectly from the application of the NURP methodology. It was assumed that the areas considered for the purpose of runoff calculations in Menzie-Cura (1991) for M WRA were the same areas that would provide recharge to the harbor. Areas further landward were presumed to discharge groundwater to the major tributaries (e.g., Charles, Mystic, Neponset Rivers) and not directly to the harbor. The NURP methodology provided an estimate of the amount of rainfall that becomes runoff and enters the harbor. By difference, the remaining rainfall either is lost to the atmosphere via evapotranspiration or recharges the shallow groundwater aquifers underlying the land masses considered in our analysis. Based on discussions with the USGS at Boston and Arlington, Virginia, it appears that approximately 50% of the rainfall that does not runoff would become groundwater and would eventually discharge to Boston Harbor. This is the basis of our flow estimate. The concentrations of substances in the groundwater were estimated based on a review of the literature and an examination of groundwater data for several sites around Boston. 118 The following groundwater concentrations were used for our estimates for Boston Harbor: Nitrogen A concentration range of 0.1 to 1.0 mg/l is used. TTie lower end of this ranee is considered representative of coastal areas and the higher end may provide an upper bound of average groundwater conditions. The Maximum Contaminant Level (MCL) for nitrate in groundwater is 10 mg/1. Levels at and exceeding the MCL can typically be tound in the immediate vicinity of subsurface sewage disposal systems and in agricultural areas. Phosphorous Phosphorous occurs in low concentrations in groundwater. Jones and Lee (1977) report a range of 0.01 to 0.06 ug/1 nationwide. This range was used to estimate loadings. Metals Metals in groundwater can exhibit wide ranges in values (i.e., over several orders of magnitude). In developing ranges for groundwater discharging to Boston Harbor, we examined the groundwater monitoring results for three study sites in the Boston area, considered other information on the general levels of metals in groundwater and considered the existing MCL values for metals. The ranges we provided are probably on the high side for average natural groundwater conditions but are intended to give some indication of the implications of discharging slightly contaminated groundwater to the harbor: • Cadmium: A range of 2 to 20 ug/1 was selected. Groundwater levels of 2 to 29 ug/1 and 6 to 20 ug/1 were reponed for studies at the Monsanto site in Everett and the Quincy Shipyard, respectively. The MCL for cadmium in drinking water is 10 ug/1 (proposed value is 5 ug/1). • Chromium: A range of 10 to 100 ug/1 was selected. Groundwater levels of 3 to 1,900 ug/1 were reported for the Quincy Shipyard. Typical values for chromium appear to be at or less than 10 ug/1. The MCL for chromium is 50 ug/1 (proposed level is 100 ug/1. • Copper: A range of 10 to 100 ug/1 was selected. Groundwater levels of 7 to 28 ug/1 and 20 to 1,000 ug/1 were reported for the Monsanto Plant in Everett and the Qumcy Shipyard, respectively. The MCL for copper is 1,3000 ug/l. • Lead: A range of 1 to 100 ug/1 was selected. Groundwater levels of 1 to 200 ug/1 were reported for the Quincy Shipyard. The MCL for lead in raw drinking water is 5 ug/1. • Nickel: A range of 10 to 100 was seleaed. Groundwater levels of 25 to 120 ue/1, 1 10 to 230 ug/1, and 20 to 165 ug/1 were reported for the Monsanto, Parcel 18, and Quincy Shipyard sites, respectively. The MCL for nickel is 100 ug/1. 119 Zinc: A range of 10 to 100 ug/1 was selected. Groundwater levels of 17 to 230 ug/1, 6 to 11 ug/1, and 12 to 30,500 ug/1 were reported for the Monsanto, Parcel 18,and Quincy Shipyard sites. Polycyclic Aromatic Hydrocarbons (PAHs) A range of 1 to 10 ng/1 was selected based on the literature review carried out by Menzie et al. (1991). The proposed MCL for the PAH compound Benzo(a)pyrene is 200 ng/1. Volatile Organic Compounds Volatile organic compounds such as benzene, toluene, and xylene are mobile in groundwater and also are the substances that are most likely to be transported away from locations of petroleum spills or leaks of underground storage tanks. Based on our knowledge of the levels that occur in contaminated groundwaters (10s to 1,000s of ug/1), we have selected a range of 1 to 10 ug/1 to represent average conditions for groundwater entering Boston Harbor. 5.4.2 Results: Nitrogen Loadings to Cape Cod Bav via Groundwater Groundwater Divide The estimated location of the groundwater divide for Cape Cod is presented in Figure 9. Areas to the north (and west for the arm of the Cape) or the divide are assumed to discharge groundwater into Cape Cod Bay. Using ARC/INFO to calculate areas with respect to the groundwater divide, we estimated that 25 percent of Barnstable County discharges into Cape Cod Bay. This estimate is broken down by town in Table 58. Watershed Estimate The resulting estimates of nitrogen loading into the watershed are presented in Table 58. We estimated the total nitrogen loading to the Cape Cod Bay watershed to be 447 metric tons/year. Just under half of this estimate is predicted to originate from septic systems, while lawn fertilizer and precipitation account for most of the remaimng inputs. Golf course and agricultural fertilizers together accounted for only six percent of the total nitrogen mputs. Table 58 summarizes each input's loading, as well as its percent contribution to total inputs. 120 CRQUNDVArER DrVEDC TOVN BQARICKS 10 MiUa =3 FIGURE 9 ^•"■ajK-ty^ • *i*nfm * icw>» ic J^ !^3SSS^L &i>1» 'efc-N».-T, .. LW. it-.^- Table 58. Recharge areas by town for C^>e Cod. Source Year Nitrate Statistic An¥nonta Statistic Measured (ug/l) (u^) Frimpter, et al. 1979 0.12 median 0.01 median Persky(1) 1980-1984 1.54 weighted average 0.24 weighted average Barnstable County r Health Department 1989-1990 1.51 average NA ■ '1989-1990 0.6 median NA ■ '1989-1990 0.9 geometric mean NA NA = Not Available 1 . These values were calculated from histograms of nitrate arxj ammonia measured throughout Cape Cod. 122 1^ z 88 8 O CD Ob m CM 5 1 ^ ^ 5 c ±i ifi .1 m The largest nitrogen input, septic systems, resulted in a loading of 206 metric tons DIN /year, which accounts for 46 percent of the total loading into the watershed. Valiela et al. (1988) estimated that 43 percent of the total loading into Buttermilk Bay watershed was due to septic systems. Cape Cod has undergone major housing developments in the past 15 years, thus drastically increasing the septage produced. Since, as Persky (1986) points out, Barnstable County's population is expected to continue its rapia increase, septic systems should continue to contribute a majority of the input into the watershed well into the next century. Domestic fertilizers account for the next most significant input of nitrogen into the watershed. We calculated a DE^ loading of 125 metric tons/year, accounting for 28 percent of our total loading, while Valiela et al. (1988) estimated lawn fertilizers contribute to 17 percent to Buttermilk Bay watershed. Precipitation accounted for 20 percent of our total, as compared to 34 percent for Buttermilk Bay. Golf course fertilizer accounted for only 22 metric tons DlN/year; agricultural fertilizer, 4 metric tons. Cape Cod Bay Estimates Groundwater is probably the most significant mechanism of transport of nitrogen into Cape Cod Bay. Vauela et al. estimate that 85 to 95 percent of all nitrogen input into Buttennilk Bay originates from groundwater transport We have two results in which we estimated nitrogen transport via eroundv^ter: our discrete inputs approach yielded 322 metric tons DD^I/year vmile groundwater measurements predicted a slightly lower result of 224 metric tons DIN/year. By comparing the watershed loading to both the discrete inputs and groundwater measurement methods, we estimate between 50 and 72 percent of the nitrogen in the watershed discharges into the Bay. Discrete Input Results We estimate that 64 percent of nitrogen in groundwater is due to septic system loading; this results not only because septic systems were the largest input into the watershed, but also because nitrogen from septage does not typically experience denitrification or uptake from plants. Lawn fertilizer contributes 20 percent of the loading into the Bay while precipitation and golf and agricultural fertilizers make up the remaining 16 percent of inputs into the Bay. Table 60 summarizes each loading lo Cape Cod Bay. Groundwater Measurement Results Table 60 provides a summary of representative measurements of nitrate and ammonia in groundwater on Cape Cod. The nitrate records selected from the Barnstable Q)unty Health Department private well data base (498 samples) were found to have neither a normal nor a lognormal distribution. This suggests that the median nitrate level would be more appropriate to represent the data set than the mean or geometric mean. The median nitrate concentration, 0.6 ug/1, is less than half of the mean, 1.51 ug/1. The Barnstable County nitrate data were used since they contained only recent measurements (1989 to 1990), selected only for the Cape Cod Bay watershed. Other sources include Frimpter, et al^ (data from 1979) and Persky (data from 1980 to 1984). 124 Table 60. Loadings of nitrogen to Cape Cod Bay using discrete and groundwater measurements approach. Nitrogen Loading via Prtclpitatfon Mean Recharge Recharge Concentration Town Area within Watershed Volume of Recharge PncipHation Loading Nitrogen Loading via Septic Systems Septic System Infusion Rate Winter Population within Watershed Winter Septic System Loading Summer Population within Watershed Summer Septic System Loading Septic SystBm Total Loading Nitrogen Loading via Domestic Fertilizer Mean Lawn Area/Unit Mean Nitrogen Application Rate Combined Residential Units within Watershed Leachabie/Total Nitrogen Ratio Lawn Fartllizar Total Loading Nitrogen Loading via Agricultural Fertilizer Cranberry Fertilizer Application Rate Cranberry Bog Land Use within Watershed Leachable/Totai Nitrogen Ratio Cranbarry Fartillzor Total Loading Nitrogen Loading via Golf Course Fertilizer Application Rate Golf Course Land Use within Watershed Leachabie/Total Nitrogen Ratio Golf Coursa Fartillzar Total Loading 0.49 nVyvar 22.4 uM DIN 101.00 sq. miles 1.28E+11 Itteifyear 40.216 kgDINAyear 3.8 leg DIN/person/yr 35.643 # of persons 101.583 kgDIN^season 110.310 Estimates 104.795 kgDIN/season 206.377 kgDIN^ear 5,000 sqfl 2 lb/1000 sq ft/yr 27.643 reskiential unit 0.5 62.694 kgDiN/year 22.5 kg DIN/ha/yr 378 acrts 0.5 1.723 kgDIN/year 99 lb 0IN/acr«/yr 481 acres 0.5 10.809 kgDINAyear Cape Cod Bay Watershed Nitrogen Loading: 321.819 kgDIN/year Percent Contribution to Total Loading Septb Systems 64% Domestic Fertilizers 19% Precipitation 12% Other Fertilizers 4% 125 I s ri vi t( le H '8 —■ V «rf «>" o IS •"a «? 8 8 « n 8 A ..-- Mf ^ rsT rf 8[ ^s •^ Mf ^ Co SS O IB is • S c • • E II II S e» i| CO I ij I 8 3 8 8 8 !^ 10 Si li I - I I ys5 8 = 8 1 M • f^' «f n -■ -• -■ 9S M ^:' K K V §S§2S 5lf§5 • V la V • M cv M # lUll S;:8£8 O K> ^ (X ^ 2 S 8 S S % a 3 I 1 I I J f M 'ill H Hiih §1 SS 2 fc 8 s 8 ; SB •5 §1 111 2 I K 10 I I ii i! I 1 Jill «8 'S 8= S| a 9a 8 52S| I II SS ?3 ?S • 8 2 s 5 3 } f liij I s r 5 1 I I J I 126 Persly presented histograms of nitrate and ammonia concentrations (number of samples for each class and range of each class), from which mean concentrations were calculated. The nitrate and ammonia data reported by Frimpter, et al. is significantly less than those calculated from Persky (0.12 vs. 1.54 ug/1 nitrate and 0.01 vs. 0.24 ug/1 ammonia). Presumably, this difference over a few years is due to rapid population increases and a housing boom. Since ammonia concentrations were not available from the Barnstable County data base, the ammonia concentration calculated from the Persky report was used. Since this was an average ammonia concentration, we used the average nitrate concentration of 1.51 ug/1 from the Barnstable Health data base in lieu of the median. This choice permitted us to sum the two values to obtain an average nitrogen concentration. Using the average concentration is probably an overestimate due to the non-normality of the nitrate database. The representative flow of groundwater in the watershed was estimated using the annual recharge. We assumed that whatever recharge enters the watersheds' aquifers, an equal amount of groundwater would be discharged. Thus, a flow rate of 1.28E+ 11 liters groundwater/year was assumed to discharge into Cape Cod Bay. We then obtain a nitrogen loading into Cape Cod Bay via groundwater of 224 metric tons/year. 5.4.3 Results: Groundwater Loadings to Boston Harbor Groundwater flow to the North and South Harbors was estimated to be approximately 1 m^/sec. The estimated loadings of substances associated with the discharge of groundwater are provided in Table 62. 127 Table 62. Estimates of loadings via groundwater to Boston Harbor. Constituent Low High Estimate Estimate Total Flow (m3/s) > 1 m3/s Conventionais (mt/yr) Total BOD not determined Total Nitrogen 1.6 15.7 Total Phosphorus 1.6E-04 9.5E-04 Total Solids not determined Total Conforms not determined • Metais (kg/yr) Cadmium 32 320 Chromium 160 1600 Copper 160 1600 Lead 16 1600 Mercury not determined Nickel 160 1600 Zinc 160 1600 Organic Compounds (kg/yr) PCBs not determined PAHs 0.02 0.2 Phthalates not determined Volatile Organic Cmpds 16 160 128 5.5 Loadings Associated with Dredged Material Disposal 5.5.1 General Approach This section of the report provides estimates of pollutant loadings resulting from the ocean disposal of dredged material at the ocean disposal site in Massachusetts Bay (Figure 2). The continuous effort to dredge and maintain the waterways and shipping channels of Massachusetts Bay results in the creation of large amounts of dredged material for disposal. This material, because it comes from waterways located in urban and inclustrial areas, may be contaminated with various pollutants. Dredged material disposal is regulated by the U.S. Army Corps of Engineers (USAGE) and EPA. Disposal taJces place at two locations within the bay. The first of these is the Massachusetts Bay Disposal Site, located at the Northeastern edge of the Stellwagen Basin. The second site is located in Cape Cod Bay, and, is used only for the dispos2il of clean sandy materials from the dredging of the Cape Cod Canal. Prior to disposal the USACE requires that sediments be analyzed for the following metals: mercury, cadmium, lead, chromium, copper, nickel, zinc and arsenic. In addition concentrations of PCBs, volatile organics and oils are measured. PAHs are not measured in materials destined for ocean disposal. However, data on levels of these compounds in coastal marine sediments can be used to provide an estimate of loadings. Using data showing the volume of materials disposed of at the Massachusetts Bay Disposal Site from 1976 through 1987 and concentrations of contaminants in the sediments (Hubbard, Penko and Fleming, 1988), we have calculated the loadings of these materials to the bay. 5.5.2 Calculation of Loadings. The USACE data are presented in terms of barge volumes of sediment in cubic meters per year. We multiplied these volumes by a factor of 0.65 to convert barge volume to in-place sediment volume as suggested by Tavalaro (1985). Metals data are presented as weighted annual averages, in parts per million dry weight. The water content of sediment samples vary widely and is dependent on the grain-size and distribution. Based on discussions with Glenn Jones at Woods Hole Oceanographic Institution, we estimated that 1 cubic meter of wet sediment contains approximately 1 metric ton of sediment on a dry weight basis. 129 The following formula was used to calculate the loading of a particular metal: Metal (mt) = Sediment (mt) x Metal Concentration (mg/kg) 1,000,000 (conversion factor) The results of the calculations are presented in Table 63. There are several sources of uncertainty in the calculations. Based on conversations with Mr. Fredette of the USAGE, we assumed that the material at the Cape Cod Bay disposal site is clean and therefore did not contribute to pollutant loadings. Thus, the estimates are for those materials that are dumped at the ocean disposal site in Massachusetts Bay alone. Weighted, averaged data are used in the estimates, and it must be recognized that there is variability among samples. For example the weighted average for mercury was 0.68 ppm, while the standard deviation was 0.9 ppm. Some uncertainty is introduced when converting from wet weight to dry weight. We estimated that a cubic meter of wet in-place sediment would contain approximately one metric ton of dry solids. However, the range, depending on bulk density could fall between 0.6 to 1.2 metric tons of dry sediment per cubic meter of in-place wet sediment. In addition, the factor for conversion from barge estimates to in place sediment volumes will varies with the amount of water entrained in the sediments during the dredging process. 130 {« Is • o (0 E o o> n S O 3 c S c N • O Iz % o o ? o o i CO CO i2 A CO CO o CO c CO 2 A A A (Ol -I < I- Ui • o Q. "S o » I- 5 t5 o S •- X ^ o §1 5|E ^ 3 Sst lis Q 2 >- r^ c\j T— op o> CO ■r- 0> CO CNJ u5 o o> CO T-: d d d d ■»- 00 CNJ CNJ CO lf> ^ r>. ^ fs. .^ f^ T-' uj -r^ T-: T-^ T-" d *^. CJOOflOOj'^^P^^^R CVJ^^'^'^CMh^CMr-caf-T- co cvj o r^ o> « in" d d "»- 00 (O U) N. ^ o> "^ r^ **/ >*» _^ 1"^ ■>* W< ^*^ l"~ CNJt^^. -.-T-OJCJ-r- 2T-csiooo>2l5:r'!>r:fcco «*5^^ftifi;co<3>i^i^cs4q;;ii '^ h- o) cr> in fc o 1^ o> ® ojcocviirid^g^^C^^r^ CM CM S ^ COh-lft'^CMCO^CMeOO^h". ^OO^O^CM'«rCO^CO"r- dddddd-r^ddcicici (Dh-^T-iocpuSincocMcoo 0»-^eoQOoo®h»^h»^ i-OOOOt-CMOOOOO dddddddddddd §88 lA d 00 r*^ CO lO fo- o) 'sr CO ■^* CD U5 CM T- '^ 8 U) 8 S 18 8 o CM o ^CMCOCbCM-^fcM-vi QOLOCOOOLOCOS! ococotoioflortg U) :S o CM 'ii^^^^^m 88888SS88 8 88 CO O CO CM CM r»> lo CO CM U) 8 CM"*^'^'^CM^r<^f>.t^oooooo. 0>0>0>0>0>0>0>0>0>0)0>0> S5 in CO h- 00 00 CO 00 (O 8 d (O CM CM CM CM CM o 55 d o lA I 8 < —I Dl Oil Metric Tons PCB MT 0.2 mg/kg • PAHs PAH 10 mg/kg P o z < o o PAHs MT 'd 0.1 mg/kg Dredged Materials Year s CO "^ d cvj o> tX) h«- lO CO O) T- lO T- o •*- o o> CO r^ c\j ;o ^' d CO 1^ (^ _. O) o> o) U5 in 0> CJ> CO 00 -^ CSJ 00 C\J CM CNJ C\J »- s in in CO Q r>o in in rt o T- 'jr cvj o o o o o o o d d d d d d d s >o-«-co(Oino) incj-r-5Qinc\j^i-co^in oooooooooooo o o o o o o o o o o cor-cooo-r-csjco^incDf^ s•^>•^^s•ooQOoooooocooooo CM ® 00 <5> "^ Q o ^ o> in CO CO CM CM CM ^ O O O O O in O O O O O o T- Q in q CO in 00 c o CM in u §5 o 0 O) in ^ i- CO T - m T~ CO o d 132 5.6 Loadings Associated with Atmospheric Deposition The atmospheric loading of selected nutrients, organic compounds and metals to the Massachusetts Bays is estimated in this section. Tne listed metals, except for iron, have been identified as toxic or potentially toxic by Wood (1974). Iron is included in the loading analysis because it is listed as a pollutant in the NCPDI (Farrow et al., 1986). Beryllium, although listed as toxic by Wood (1974), is not analyzed because of the lack of data pertaining to the Massachusetts Bays region. The limited data available on the aerosol concentration of beryllium (Measures et aL, 1984) indicates that atmospheric loading to the western North Atlantic is not significant. Atmospheric deposition of beryllium to the Massachusetts Bays therefore is not likely to be sigmficant. The atmospheric loading of the orgamc pollutants PAH and PCB are also estimated in this section as are the nutrients nitrogen and phosphorus. Atmospheric loading was calculated as the sum of dry and wet depositional flux integrated over the entire area of the Massachusetts Bays. Dry deposition is the direct settling of aerosol-bound pollutants. Dry flux is calculated by multiplying the measured aerosol concentration by an estimated deposition velocity. Wet deposition results from the scavenging of aerosol- bound pollutants by rain and snow. Concentration in precipitation has been measured directly for some pollutants. Where such measurements were available, the concentration was multiplied by the precipitation rate per unit area to estimate wet depositional flux. WTiere wet concentration has not been measured directly, it was estmiated by multiplying the dry concentration by a scavenging or "washout" ratio, i.e., the ratio of measured wet and dry concentrations, as reported in refereed literature. The combined dry flux and wet flux are multiplied by the surface area of the Massachusetts Bays to obtain the loading from atmospheric deposition. Atmospheric concentration data were found in refereed literature that pertain specifically to the Massachusetts Bays region for all chemicals except mercury and phosphorus (Table 64). Loadings were estimated for these chemicals based on regional concentrations or concentrations represented as characteristic of urban areas. The data sources for each chemical are discussed in detail in subsections 5.3.1 through 5.3.3. Some of the most relevant data were provided by Dhan Olmez of the Massachusetts Institute of Technology. The estimate of atmospheric flux is assumed to apply equally to all the Massachusetts Bays, regardless of distance from the measurement location. The spatial sampling of aerosol concentration is generally inadequate to estimate concentration gradients, so a point estimate of flux is used to calculate loadings. Tliis approach may introduce a bias towards higher loadings since many of the measurements have been made in urban areas and almost none have been made in the marine atmosphere. This potential bias is minimized by restricting the concentration data to submicron-sized 133 Table 64. Parameters used to estimate atmospheric ioading. Deposition Washout Atmospheric Velocity, Vd (cm/s) Ratio, Concentration Chemical W (ng/m3) Metals Sb 0.1 — 9.1 As 0.22 110 0.8 Cd 0.45 125 3 Cr 0.5 150 3.4 Co 0.3 — 1 Cu 0.5 140 16.1 Fe 1.1 250 75.7 Pb 0.3 76 326 Mn 0.56 370 3.6 Hg — — — Mo — — 0,14 to 2 Ni 0.7 gw 1?,S 8.6 Se 0.1 — _ 0.6 Ag 0.24 — 0.5 V 0.29 110 25 Zn 0.62 179 38.7 Organic Compounds PAH 0.53 1.5 to 2 PCB 0.16 86 1.4 to 3.9 Nutrients t-N 0.4 1700 to 5500 t-P — — ... 134 particles which have a higher likelihood of dispersing over the entire study area than coarser particles. In order to represent the variability in the concentration measurements, the 10th and 90th percentiles of the frequency distribution are used as bounds on the range of concentration in the study area. Tliese estimates are based on a log-norm5 distribution. Loadings are estimated on an annual basis only. The seasonal variation of atmospheric concentration has not been measured for most of the pollutants in this study. Rainfall, affecting the amount of wet deposition, does not have a strong seasonal dependence as described further below. Dry deposition flux is calculated by multiplying the atmospheric concentration, C, by a characteristic deposition velocity, Vd: Fd = Vd . C (1) which is the approach used by Hicks et al. (1988) and other investigators. Deposition velocities are reported for metals by McMahon (1979), Sehmel (1980), McVeety and Hites (1988), for organics by McVeety and Hites (1988), and for nutrients (nitrogen) by Galloway et al. (1987). Wet deposition flux is calculated by multiplying the atmospheric concentration by the precipitation rate, P, and the volumetric washout ratio, Wv, for each specific chemical: Fw = Wv . P . C (2) The volumetric washout ratio is defined as the ratio of concentration in precipitation to the concentration in unscavenged air: (ug/l)^ain Wv = (ng/m3),air (3) Washout ratios for metals were reported by McMahon (1979) and by Jaffrezo and Colin (1988), and for organic compounds by Ligocki et al. (1985 a,b). Washout ratios are not available for antimony, mercury, molybdenum, selenium, silver, nitrogen or phosphorus. (Wet deposition flux of mercury, molybdenum, sUver, nitrogen and phosphorus was determined directly from estimates of concentration in rainfall). Precipitation in the Massachusetts Bays region was measured on Cape Cod and in a Boston suburb as part of the National Atmospheric Deposition Program (Table 65). Annual precipitation is about 1.1 m/yr. Preapitation rates show little seasonal variation. Wet concentration is presented in units of ug/1 and wet deposition flux in units of mg/m2/yr. 135 Table 65. Seasonal and annual rainfall (cm) in the Massachusetts Bays region measured at two sites in the National Atmospheric Deposition Program. North Atlantic Coastal Lab Barnstable County MA TOTAL FALL WINILK SPRING SL^ME R 1982 134.12 35.01 28.60 27.38 42.70 1983 160.47 38.28 31.09 56.97 28.99 1984 134.52 24.38 34.53 44.39 36.68 1985 121.00 23.04 17.12 31.05 54.75 1986 118.93 27.38 21.63 21.36 34.18 1987 58.01 16.10 49.40 — 1988 96.36 36.18 30.02 17.67 1738 East Middlesex County MA 1982 96.14 20.07 4.75 21.97 46.46 1983 133.65 35.99 24.39 47.32 14.47 1984 122.53 17.64 39.47 32.84 39.50 1985 92.13 30.94 13.26 20.15 33.15 1986 107.55 23.10 17.53 16.76 33.71 1987 102.81 30.83 37.16 31.37 16.27 \m 92.88 28.34 19.66 23.66 24.58 The flux determined from analysis of dry and wet deposition are multiplied by the area of each of the Massachusetts Bays (Table 66). These bays were identified and their areas were estimated at the MIT Collegium, 1989. The total area of the Massachusetts Bays closely matches that of Long Island Sound, 3,350 kin2 (Connecticut Department of Environmental Protection, 1987), which is used for comparison of some of the loading estimates. Summaries by land use (i.e., urban, rural, marine) such as Galloway et al. (1982) for wet deposition and such as the Gas Research Institute for PAH data are also used for comparison purposes. 136 Table 66. Areas of Massachusetts Bays. Location Area kin2 Massachusetts Bay 2200 Cape Cod Bay 1300 Broad Sound 66 North Harbor 41 Quincy Bay Inner Harbor 38 10 Hingham Bay 19 Total 3700 137 Annual loadings of metals, organic pollutants and nutrients are presented in the following subsections. 5.6.1 Nutrients Nitrogen Atmospheric concentration of nitrogen is reported to be 1700 ng N/m^ as measured 50 km east of Boston (Galloway et al., 1987), and 5500 ng N/m^ for the nonheastern U.S. (Galloway et al., 1984). TTiese concentrations are used as the lower and upper range limits, respectively, for the present analysis. Deposition velocity of nitrogen (as NOx) is reported to be 0.4 cm/s by Galloway et al. (1987); deposition velocity of N03 + HN03 is 0.8 cm/s. The deposition velocitv used for nitrogen in the present analysis is 0.4 cm/s. This deposition velocity results in a dry deposition flux of 214 to 694 mg/m2/yr. No data are available on the washout ratio of nitrogen. Wet deposition is calculated directly from measurements of nitrogen concentration in precipitation at stations on Cape Cod and in a suburb of Boston (NADP, 1989). These concentrations ranged from 200 to 479 ug/1, a combination of N03 and NH4. These data exhibited seasonal variation, largest concentrations in summer, smaDest in winter. The estimate of atmospheric loading of nitrogen to the Massachusetts Bays is presented in Table 67. Total annual loading of nitrogen is estimated to be 1759 to 4944 tons/yr. Table 67. Atmospheric loading (^g/yr) of nitrogen to Massachusetts Bays. Estimate includes wet and dry deposition. Area Low Estimate High Estimate Mass Bay Cape Cod Bay Broad Sound 955779 564778 28673 2685522 1586900 80566 North Harbor 17812 50048 Quincy Bay Inner Harbor 16509 4344 46386 12207 Hingham Bay 8254 23193 Total 1596150 4484822 138 Phosphorus Graham and Duce (1982) measured the concentration of phosphorus off Cape Cod to be 19 ng/m3 t-P. Deposition velocity was estimated to be 0.4(0.2) cm/s. TTie resulting dry deposition flux is then 1.2 mg/m2/yr. Wet concentrations of 2 ug/1 and 11.6 ug/1 were measured by Graham and Duce (1982) in the western Atlantic near the study area. This results in a wet deposition flux of 12 to 70 mg/m2/yr for the study area. The wet deposition flux for Long Island Sound (Connecticut Department of Environmental Protection, 1987), as measured by USGS, is 11.1 mg/m2/yr, indicating that the lower estimates are probably more representative. The estimate of atmospheric loading of phosphorus to the Massachusetts Bays is presented in Table 68. Total annual loading of phosphorus is estimated to be 14 to 290 tons/yr. Table 68. Atmospheric loading (kg/yr) of phosphorus to Massachusetts Bays. Estimate includes dry and wet deposition. Area Low High Mass Bay Cape Cod Bay Broad Sound North Harbor Quincy Bay Inner Harbor Hingham Bay Total 124S6 512g3 7476 30708 4418 18146 224 921 139 572 129 530 34 140 65 265 139 5.6.2 Organic Compounds Atmospheric loadings of PAH and PCB to Massachusetts Bays are estimated in this subsection. PAH loading to Massachusetts Bays is of concern because of the carcinogenjc potential of some PAH compounds. Kertesz-Saringer et al. (1971), for instance, identify benzo[alpyrene as a very dangerous carcinogen. Tlie atmospheric concentration or B[a]P has been momtored by the EPA at stations in Boston and in Chelsea. Dry deposition flux is determined from these concentrations and an estimate of deposition velocity. Wet deposition flux is determined from these concentrations and an estimate of the washout ratio. Extrapolation to total PAH from the estimates for B[a]P is based on the relative abundances of PAH compounds measured in sediments in Boston Harbor. This approach to estimating t-PAH suffers from variabilities among the PAH compounds in particle size distribution, aerosol-vapor partitioning, and washout ratios for aerosol and vapor phases. PCB loading to Massachusetts Bays is calculated on the basis of regional measurements of atmospheric concentration of PCB as Aroclor 12d4. Deposition velocity and washout ratios for Aroclor 1254 are used to estimate dry and wet deposition fluxes and total atmospheric loading. This approach neglects other congeners, but loading of t-PCB is likely to be dominatea by Aroclor 1254. PAH Atmospheric concentration of B[a]P is reported to be 0.2 ng/m3 (U.S. EPA AIRS, 1990). These concentrations are similar to those for the low range of urban areas by the Gas Research Institute (Atlantic Environmental Services, 1988). No data are available on the atmospheric concentration of other PAH compounds in the Massachusetts Bays region. The relative abundance of PAH compounds measured in sediments from Boston Harbor and remote sites along the N'ew England coast may reflect to some extent the composition in atmospheric deposition and is used here to derive total PAH inputs from data on B[a]P. A limitation on using these data as a basis for estimating total PAH inputs is that PAH compounds seem to be apportioned among different particle sizes based on their molecular weight. High molecular weight compounds, such as B[a]P, are associated with submicron-sized particles on which diey were emitted while lo^- molecular weight compounds, such as fluoranthene, can migrate to larger particles (DeWiest, 1978).) Gshwend and Kites (1981) found that B[a]P comprised 10% of the total PAH in sediments from Boston Harbor and at a remote site off the coast of Maine; Shiaris and Jambord-Sweet (1986) reported B[a]P concentrations that average 13% of t- PAH (variability was large, 2 to 40%). Assuming that B[a]P comprised 10 to 13% of the total PAH in air, the concentration of t-PAH in air was 1.5 to 2 ng/m3. This estimate is similar to the mean urban concentration, 3 ng/m3, reported by the Gas Research Institute (Atlantic Environmental Services, 1988). Deposition velocity of PAH is reported to be 0.53 cm/s for combined vapor and aerosol by McVeety and Hite (1988). This deposition velocity was used for PAH in 140 the present analysis and results in a dry deposition flux of 0.25 to 0.33 mg/ni2/yr. This estimate is similar to the total deposition flux, 0.2 m^/m2/yr, measured at a remote site by Gschwend and Hites (1981). Wet deposition was estimated from the concentration of t-PAH in air and the scavenging ratio. Ligocki et al. (1985 a,b) have measured the scavenging ratio for gas phase and particle phase PAH in coastal and urban Oregon. Particulate washout is important only for tne higher molecular weight compounds, e.g., benzo[a]pyrene. Lower molecular weight compounds, e.g. ghenanthrene, have predominantly gas phase washout. B[a]P and phenanthrene ux were determined to be about the same by Gschwend and Hites (1981), 0.17 and 0.24 mg/m2/yr. This result may indicate that B[a]P scavenging is representative of total PAH scavenging, even though most PAH compounds are scavenged through their gas phase. Based on the measured concentration of B[a]P, 0.2 ng/m3, anda particulate washout ratio of 1700, the concentration in rain is estimated as 0.34 ng/1. Extrapolating from B[a]P to t-PAH results in estimates of 2.6 to 3.4 ng t-PAH/1. This estimate is about the same as the estimate of wet deposition made by Gschwend & Hites (1981) based on concentration in rain at the Great Lakes by Eisenreich et al. (1981). The estimate of atmospheric loading of total PAH to the Massachusetts Bays is presented in Table 69. Total annual loading of PAH is on the order of 1 metric ton/yr. Dry deposition dominates the loading, which may be expected because of the low efficiency of scavenging submicron-sized particles (Gschwend & Hites, 1981). It is approximately the same as the estimate of atmospheric loading made by Gschwend and Hites (1981), but is low by a factor of 2 to 10 compared with estimates presented at the MIT Collegium (1989). Table 69. Atmospheric loading (l(g/yr) of PAHs to Massachusetts Bays (dry and wet). Area Low Estimate High Estimate 571 755 337 446 17 23 11 14 10 13 3 3 5 7 Mass Bay Cape Cod Bay Broad Sound North Harbor Quincy Bay Inner Harbor Hingham Bay JsM 252 1260 1 141 PCB Atmospheric concentration of PCB (as Aroclor 1254) is reported to be 1.4 n2/m3 at Georges Bank and 3.9 ng/m3 at Vineyard Sound (Harvey and Steinhauer, 1974). These concentrations are used as the lower and upper range limits, respectively, for the present analysis. Deposition velocity of PCB (Aroclor 1254) is reported to be 0.16 cm/s by McVeety and Hites (1988); deposition velocity oft- PCB is 0.13 cm/s and for PCB aerosol is 0.91 cm/s. The deposition velocity used for PCB in the present analysis is 0.16 cm/s. This deposition velocity results in a dry deposition flux of 0.07 to 9.20 mg/m2/yr. The washout ratio for PCB is 86, according to Mackay et al. (1986). This results in a wet deposition flux of 0.12 to 0.34 mg/m2/yr. The dryiwet ratio calculated in the present analysis (1:2) is in moderate agreement with the ratio for the Great Lakes (1:3) reported by Swackhamer et al. (1988). The estimate of atmospheric loading of PCB to the Massachusetts Bays is presented in Table 70. Total annual loading of PCB is estimated to be 1 to 2 metric tons/yr. Table 70. Atmospheric loading (kg/yr) of PCBs to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 446 1256 Cape Cod Bay 263 742 Broad Sound 13 38 North Harbor 8 23 Quincy Bay 8 22 Inner Harbor 2 6 Hingham Bay 4 11 JsM 245 2097 142 5.6.3 Atmospheric loading of metals. The principal data sources for atmospheric metal concentrations are Zoller and Gordon (1970), Gladney et al. (1974), Hopke et al. (1976), Fogg and Fitzgerald (1979), Rahn (1981), Rahn and Lowenthal (1984), Thurston and Spengler (1985), and Olmez (1990). Zoller and Gordon (1970) analyzed samples collected at MIT and other locations in the Boston area. Instrumental neutron activation analysis provided results for a large suite of metals. Gladney et al. (1974) analyzed samples collected from two sites at MIT: the roof of the Nuclear Chemistry Building and the roof of the Green Building (100 m above ground level) and from one site west of Route 128 in Wellesley. Size distribution was also determined. Zoller and Gordon (1970) and Gladney et al. (1974) both used instrumental neutron activation analysis. Hopke et al. (1976) analyzed samples taken from locations around the perimeter of Boston Harbor (Hull, Long Island, Massachusetts General Hospital, Boston Naval Shipyard, Lx)gan International Airport) and at Wellesley. They used INAA on 90 total samples. Fogg and Fitzgerald (1979) measured the concentration of mercury in rainwater at a site on Cape Cod (Centerville, MA) during September and Oaober, 1975. Rahn (1981) measured the concentration of manganese and vanadium at a rural site in Narragansett, RI for the purpose of establishing regional tracers. Rahn and Lowenthal (1984) measured arsenic, antimony, selenium, vanadium, zinc, manganese, and indium at Narragansett. They isolated measurements obtained during winds from the Boston area in order to identify a Boston signature. Data used for comparison purposes were found in Scudlark and Church (1988), Galloway et al. (1982), ancl Connecticut Department of Environmental Protection (1987). Scudlark and Church measured arsenic concentration at a remote site at Lewes, DE. Galloway et al. (1982) summarized reports of metal concentration in precipitation, categorized by urban, rural, and manne areas or by specific areas in some cases. Connecticut Department of Environmental Protection estimated atmospheric loadings to Long Island Sound by extrapolating measurements from Chesapeake Bay and the Great Lakes, and using local measurements reported in the literature and made by USGS for the DEP as part of the National Estuary Program. Concentrations of metals are provided as means; standard deviations are shown in parentheses in the following sections. 143 Antimony Atmospheric concentration of antimony is reported to be 0.5 n£/m3 by ZoUer and Gordon (1970), 9.1(11) ng/m3 bv Hopke et al. (1976) and 0.83^0.41) ng/m3 by Rahn et al. (1984). Analysis of (fata reported by Olmez (1990) results in an estimate of 1.1(2.2) ng/m3. The concentration used for antimony in the present analysis is 1.1(2.2) ng/m3 based on the data of Olmez (1990). It is the roost recent and most extensive data set available. Except for the data of Hopke et al., it is the most representative of the study area. Antimony is associated with emissions from coal combustion, incineration, and antimony roasting (Keeler and Samson, 1989). Hopke et al. (1976) identify an incinerator in Somerville as a possible source of pollution to Boston Harbor. Deposition velocity of antimony is reported to be 0.06 to <0.4 cm/s by Sehmel (1980). The deposition velocity of metals reported by McMabon (1979) is usually at the lower end of the range reported by Sehmel (1980). Since McMahon does not report a deposition velocity for antimony, it is estimated to be 0.1 cm/s. No data are available on the concentration of antimony in precipitation or on the washout ratio of antimony. Wet depositional flux is therefore not estimated. The estimate of atmospheric loading of antimony to the Massachusetts Bays is presented in Table 71. Dry depositional flux is estimated to be 0.01 to 0.09 mg/m2/yr using the 10th and 90th percentiles of aerosol concentration. Total annual loading of antimony is estimated to be < < (much less than) 1 metric ton/yr (46 to 333 kg^), based on dry deposition alone. Table 71 . Atmospheric loading of antimony (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Arga Low Estimate High Estimate Mass Bay 28 200 Cape Cod Bay 16 118 Broad Sound 1 6 North Harbor 1 4 Quincy Bay Inner Harbor 0 0 3 1 Hingham Bay 0 2 Total 46 333 144 Arsenic Atmospheric concentration of arsenic is reported to be 0.5(2.1) ng/m3 by Olmez (1990). Rahn et al. (1984) measured concentrations of 0.49(0.15) ng/m3 and Walsh et al. (1979) measured concentrations of 1.9 ng/m3. Both these measurements were made in Rhode Island, the former in a rural area and the latter in an urban area (Providence). Scudlark and Church measured arsenic concentrations of 1.05 ng/m3 at Lewes, DE. The major source of arsenic is the upper Ohio River Valley andthe Sudbury region of Ontario, Canada (Keeler and Samson, 1989). Arsenic is therefore not a local source and the concentration across the Massachusetts Bays is likely to be uniform. The concentration of 0.5(2.1) ng/m3 by Olmez was used in the present analysis. The 10th and 90th percentile are 0.2 and 1.3 ng/m3. Deposition velociw of arsenic is reported to be 0.22 cm/s by McMahon (1979) and to be <0.1 to < 0.6 cm/s by Sehmel (1980). The deposition velocity used for arsenic in the present analysis is 0.22 cm/s. The resulting dry deposition flux is 0.01 to 0.09 mg/m2/yr. The washout ratio for arsenic is 110, according to McMahon (1979). This results in a wet deposition flux of 0.02 to 0.16 mg/m2/yr. The arsenic concentration in precipitation is 0.02 to 0.16 ug/1; this is much smaller than the 0.58 ug/1 that Galloway et al. (1982) report tor generic urban areas. The estimate of atmospheric loading of arsenic to the Massachusetts Bays is presented in Table 72. Total annual loading of arsenic is estimated to be about < 1 metric ton per year. Table 72. Atmospheric loading of arsenic (l(g/yr) to Massachusetts Bays. Estimates Include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 87 557 Cape Cod Bay 51 329 Broad Sounds 17 North Harbor 2 10 Quincy Bay 2 10 Inner Harbor 0 3 Hingham Bay 1 5 Total 145 930 145 Cadmium Very few data are available on the atmospheric concentration of cadmium in the northeast U.S. Olmez (1990) reported nine measurements, roost of which are below detection. The lowest detectable concentration that he reports is 2.4 ng/m3, which was used in the present analysis as the high end of the range of concentration. Deposition velocity of cadmium is reported to be 0.45 cm/s b> McMahon (1979) and to be <0.4 to >8 cm/s by Sehmel (1980). The deposition velocity used for cadmium in the present analysis is 0.45 cm/s. Dry de|X>sition flux is estimated to be 0.34 mg/m2/yr. The washout ratio for cadmium is 125, according to McMahon (1979), resulting in a wet concentration of 0.30 ug/l using the Olmez data. Concentration of cadmium in rainfall was measured to be 0.31 ug/l at Woods Hole, Massachusetts. Reported wet concentrations of 2.3 ug/l by Galloway et al. (1982) for a generic urban area are too high to be representative of the study area. Wet deposition based on the above concentrations are 0.34 mg/m2/yr. The estimate of atmospheric loading of cadmium to the Massachusetts Bays is presented in Table 73. Total annual loading of cadmium is estimated to be 3 metric tons/yr. Table 73. Atmospheric loading of cadmium (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 0 1499 Cape Cod Bay 0 886 Broad Sound 0 45 North Harbor 0 28 Quincy Bay 0 26 Inner Harbor 0 7 Hingham Bay 0 13 Total Q 2504 146 Chromium Atmospheric concentration of chromium is reported to be 3.4(5^) ng/m3 by Hopke et al. (1976). Analysis of the data provided by Olmez (1990) results m 0.7(4.0) ng/m3. The estimates from the Olmez data set is used in the present analysis with 10th and 90th percentiles of 0.1 and 4.3 ng/m3 respectively. Deposition velocity of chromium is reported to be 0.5 cm/s by McMahon (1979) and to be 0.6 to 6.8 cm/s by Sehmel (1980). The deposition velocity used for chromium in the present analysis is 0.5 cm/s. This results in a dry deposition flux of 0.02 to 0.68 mg/m2/yr. The washout ratio for chromium is 150, according to McMahon (1979). This results in a wet deposition flux of 0.02 to 0.71 m§/m2/yr. This flux corresponds to the low end of the range of urban wet concentrations reported by Galloway et sH. (1982), 0.51tol5ug/l. The estimate of atmospheric loading of chromium to the Massachusetts Bays is presented in Table 74. Total annual loading of chromium is estimated to be < 6 metric tons/yr. Table 74. Atmospheric loading of chromium (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Est Mass Bay 87 Cape Cod Bay 51 Broad Sound 3 North Harbor 2 Quincy Bay 1 Inner Harbor 0 Hingham Bay 1 High Estimate 3062 1810 92 57 53 14 14 Total 145 511L 147 Cobalt Atmospheric concentration of cobalt is reported to be 0.2 ng/ni3 by Zoller and Gordon (1970), 0.62 to 2.3 ng/m3 by Gladney et al. (1974) and 1.00 (0.70) ng/m3 by Hopke et al. (1976). Analysis of the data provided by Olmez (1990) results in estimates of 0.3(3.1) ng/m3. The 10th and 90th percentiles of the Olmez data, 0.08 and 1.5 ng/m3, are used. Deposition velocit>^ of cobalt is reported to be to be 0.3 to 1.9 cm/s by Sehmel (1980). The deposition velocity used for cobalt in the present analysis is 0.3 cm/s, consistent with the deposition velocity selected for other metals which are at the low end of the range reported by Sehmel (1980). This deposition velocity results in a dry deposition flux of 0.01 to 0.14 mg/m2/yr. No data are available on the washout ratio of cobalt. The wet deposition of cobalt is estimated from the urban concentration of cobalt in precipitation reported by Galloway et al. (1982), 1.8 ug/1. This results in a wet depositional flux of 1.98 mg/m2/yr. The estimate of atmospheric loading of cobalt to the Massachusetts Bays is presented in Table 75. Total arniual loading of cobalt is estimated to be 8 to 9 metric tons/yr. Most of this loading is due to wet deposition, which is based on summary data for urban areas and do not include data specific to eastern Massachusetts. Dry deposition is based on data from the Boston area, and constitutes < 1 metric ton/year of loading, which is probably a more representative estimate. Table 75. Atmospheric loading of cobalt (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 4373 4662 Cape Cod Bay 2584 2755 Broad Sound 131 140 North Harbor 82 87 Quincy Bay 76 81 Imier Harbor 20 21 Hingham Bay 38 40 Total 7303 7786 148 Copper Atmospheric concentration of copper is reported to be 50 ng/m3 by Zoller and Gordon (1970) according to their own measurements; they 3so repon a value of 1 10 ng/m3 as measured by the U.S. Public Health Service in SomerviUe. Thurston and Spengler (1985) measured fine and coarse concentrations of copper of 16.1 and 10.4 ng/nfi, respectively. The fine concentration measured by Thurston and Spengler (1985), 16.1 ng/m3, is used. Deposition velocity of copper is reported to be 0.5 cm/s by McMahon (1979) and to be <0.6 to 1.1 cm/s by Sehmel (1980). The deposition velocity used for copper in the present analysis is 0.5 cm/s. This results in a dry deposition flux of 2.5 to 8.4 mg/m2/yr. The washout ratio for copper is 140, according to McMahon (1979). This results in a wet deposition flux of 2.5 mg/m2/yr. This flux is lower than the low end of the range of urban wet concentrations reported by Galloway et al. (1982), 6.8 to 120 ugA The estimate of atmospheric loading of copper to the Massachusetts Bays is presented in Table 76. Total aimuaT loading of copper is estimated to be 20 metric tons/yr, lower than estimates for Long Island Sound (29 to 78 metric tons/yr; Cormecticut Department of Environmental Protection, 1987). Table 76. Atmospheric loading of copper (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 11040 Cape Cod Bay 6523 Broad Sound 331 North Harbor 206 Quincy Bay 191 Inner Harbor 50 Hingham Bay 95 Total m}6 149 Iron Atmospheric concentration of iron is reported to be 1000 to 1300 ng/ni3 by Zoller and Gordon (1970) and to be 1090(1000) ng/m3 by Hopke et al. (1974). Thurston and Spengler (1985) report 74.7 and 281 ng/m3 for the fine and coarse fractions, respectively. Analysis of the data provided by Olmez (1990) results in a mean of 1 1 1 ng/m3 with 10th and 90th percentiles of 53 and 231 ng/m3. These estimates are used in the present analysis. Deposition velocity of iron is reported to be 1.1 cm/s by McMahon (1979) and to be 1.0 to 2.5 cm/s by Sehmel (1980). The deposition velocity used for iron in the present analysis is 1.1 cm/s. This results in a dry deposition flux of 18.5 to 80.4 mg/m2/yr. The washout ratio for iron is 250, according to McMahon (1979). Jaffrezo and Colin (1988) report a scavenging ratio which is equivalent to a washout ratio of 330, as defined by McMahon (19/9). A washout ratio of 250 is used in the present analysis. This results in a wet deposition flux of 14.6 to 63.7 mg/ni2/yr. The estimate of atmospheric loading of iron to the Massachusetts Bays is presented in Table 77. Total aimual loading of iron is estimated to be 134 to 584 metric tons/yr. The iron loading estimated for Long Island Sound, an area comparable in size to the Massachusetts Bays, is 1110 metric tons/yr (Connecticut Department of Environmental Protection). Table 77. Atmospheric loading of iron (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 72804 316977 Cape Cod Bay Broad Sound 43021 2184 187304 9509 North Harbor 1357 5907 Quincy Bay Iimer Harbor 1258 331 5475 1441 Hingham Bay Total 629 121584 2738 529^51 150 Lead Atmospheric concentration of lead is reported to be 326(13.2) ng/m3 for the fine fraction and 75.6(4.57) ng/m3 for the coarse fraction by Thurston and Spengler (1985). The fine concentration is used in the present analysis. Deposition velocity of lead is reported to be 0.3 cm/s by McMahon (1979). This deposition velocity is used in the present analysis. This results in a dry deposition flux of 30.8 mg/m2/yr. The washout ratio for lead is 76, according to McMahon (1979). This results in a wet deposition flux of 27 mg/m2/yr. The estimate of atmospheric loading of lead to the Massachusetts Bays is presented in Table 78. The annual loading of lead is estimated to be 235 metric tons/yr. ITie lead loading estimated for Long Island Sound is 628 metric tons/yr (Connecticut Department of Environmental Protection), much higher than the estimate for Massachusetts Bays. Connecticut also reports a wet depositional loading of 30 metric tons/yr, measured by USGS. The wet loading to Massachusetts Bays is estimated to be 110 tons/yr. This comparison suggests that the estimates for Massachusetts Bays may be low. Other data sources for the atmospheric concentration of lead and for the washout ratio for lead should be sought to resolve this question. Table 78. Atmospheric loading of lead (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 127811 Cape Cod Bay 75525 Broad Sound 3834 North Harbor 2382 Quincy Bay 2208 Inner Harbor 581 Hingham Bay 1104 Total 213444 151 Manganese Atmospheric concentration of manganese is reported to be 10 to 50 ng/ni3 by Zoller and Gordon (1970) and 27(19) ng/m3 by Hopke et al. (1974). Thurston and Spengler (1985) report 3.61 ajnd 5.81 ng/m3 for the fine and coarse size fraaions, respectively. Rahn and Lowenthal (1984) report non-crustaJ manganese concentrations of 4.2(0.8) ng/m3 at Narragansett during winds from the direction of Boston. The data provided by Olmez (1990) results in a mean of 3.7 ng/m3 with 10th and 90th percentiles of 1.8 and 7.3 ng/m3, respectively. These estimates are used in the present analysis. Deposition velocity of manganese is reported to be 0.56 cm/s by McMahon (1979) and to be 0.4 to 0.9 cm/s by Sehmel (1980). The deposition velocity used for manganese in the present analysis is 0.56 cm/s. This results in a dry deposition flux of 0.§ to 1.3 mg/n^/yr. The washout ratio for manganese is 370, according to McMahon (1979). This results in a wet deposition flux of 0.7 to 3.0 mg/m2/yr. This flux corresponds to the low end of the range of urban wet concentrations reported by Galloway et al. (1982), 1.9to80ug/l. The estimate of atmospheric loading of manganese to the Massachusetts Bays is presented in Table 79. Total annual loading of manganese is estimated to be 4 to 17 metric tons/yr. The total manganese loading estimated for Lone Island Sound is 22.2 metric tons/yr (Cormecticut Department of Environmental Protection, 1987). Table 79. Atmospheric loading of manganese (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. ■■■■■' ■■ t. '- JJ-' ' ■ ?■■-- 1 "-■■■'-' ■'■-■■' - ■ * ■' ' ■ » ^^-^— I ■ ■■ — y ■■!■ Area Low Estimate High Estimate Mass Bay 2338 9433 Cape Cod Bay 1382 5580 Broad Sound 70 283 North Harbor 44 176 QuincyBay Inner Harbor 40 11 163 43 Hingham Bay 20 82 Total 3905 15770 152 Mercury No data are available for the atmospheric concentration of mercury in the Massachusetts Bays region. No data are available on the deposition velocity of mercury. No data are available on the washout ratio of mercury. The concentration of mercury in precipitation was measured directly by Fogg and Fitzgerald (1979), 6 to 18ng/l. The estimate of atmospheric loading of mercury to the Massachusetts Bays is presented in Table 80 and in the Appendix. Total annual loading of mercury is estimated to be 24 to 73 kg/yr. Table 80. Atmospheric loading of mercury (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 15 44 Cape Cod Bay 9 26 Broad Sound 0 1 North Harbor 0 1 QuincyBay 0 1 Inner Harbor 0 0 Hingham Bay 0 0 JjM 24 22_ 153 Molybdenum TTie data provided by Olmez (1990) result in a mean concentration of 0.6 ng/ni3 with 10th and 90th percentiles of 0.2 and 1.8 ng/m3, respectively. However, no data are available on the deposition velocity of molybdenum, therefore no estimate is made for dry deposition loading of molybdenum. No data is available on the washout ratio of molybdenum. The concentration of molybdenum in precipitation is taken from the summary of Galloway et al. (1982) for urban areas, 0.2 ug/1. This results in a wet deposition flux of 0.22 mg/m2/yr. The estimate of atmospheric loading of molybdenum to the Massachusetts Bays is presented in Table 81. Total annual loading of molybdenum is estimated to be < 1 metric ton/yr, based on wet deposition alone. Table 81. Atmospheric loading of molybdenum (kg/yr) to Massachusetts Bays. Estimates include only wet deposition. Area Low Estimate High Estimate Mass Bay 484 Cape Cod Bay 286 Broad Sound 15 North Harbor 9 Quincy Bay 8 Iimer Harbor 2 Hingham Bay 4 Total 808 154 J Nickel Atmospheric concentration of nickel is reported to be 52 ng/m3 by Zoller and Gordon (1970). Thurston and Spengler (1985) report 8.57(0.39) and 2.44(0.13) ng/m3 for the fine and coarse fractions, respectively. The fine fraction concentration measured by Thurston and Spengler (1985), 8,57 ng/m3, is used in the present analysis. Deposition velocity of nickel is reported to be 0.45 cm/s by McMahon (1979) and to be 0.7 to <2 cm/s by Sehmel (1980). The deposition velocity used for nickel in the present analysis is 0.7 cm/s. This results in a dry deposition flux of 1.9 mg/m2/yr. The washout ratio for nickel is 125, according to McMahon (1979). This results in a wet deposition flux of 1.2 mg/m2/yr. The estimate of atmospheric loading of nickel to the Massachusetts Bays is presented in Table 82 and in the Appendix. The total annual loading of nickel is estimated to be 12 metric tons/yr, 5 metric tons/yr for wet deposition. The loading from wet deposition estimated for Lonp Island Sound is 8 tons/yr (Connecticut Department of Environmental Protection, 1987), slightly below the estimate for Massachusetts Bays. Table 82. Atmospheric loading of nickel (kg/yr) to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay Cape Cod Bay Broad Sound North Harbor Quincy Bay Inner Harbor Hingham Bay Total 6754 3991 203 126 117 31 58 11280 155 Selenium Atmospheric concentration of selenium is reported to be 0.6 ng./m3 bv Zoller and Gordon (1970), 1.4 to 4.9 ng/m3 by Gladney et al. (1974) and 123(1.13) ng/ni3 by Hopke et al. (1974). Thurston and Spengler (1985) report 0.595(0.46) for the fine size fraction; no coarse fraction was detected. Rahn and Lowenihal (1984) report selenium concentrations of 1.00(0.60) ng/m3 at Narragansett, Rhode Island during winds from the direction of Boston. The data provided by Olmez (1990) results in an estimated mean concentration of 0.7 ng/m3 with 10th and 90th percentiles of 0.2 and 2.6 ng/m3, respectively. These values are used in the present analysis. The data from Rahn and Lowenthal (1984), suggest that these values are Likely representative of the entire study area. Deposition velocity of selenium is reported to be 0.1 to 0.6 cm/s by Sehmel (1980). The deposition velocity used for selenium in the present analysis is 0.1 cm/s; this is consistent with the selection of deposition velocity for other metals, i.e. choosing from the lower limit reported by Sehmel (1980). This deposition velocity results in a dry deposition flux of <0.01 to 0.08 mg/m2/yr. No data is available on the washout ratio of selenium. No data is available on the concentration of selenium in wet deposition, either specifically for the Massachusetts Bays region or for generic urban, rural, or marme regions. No wet deposition can be estimated for selenium in the present analysis. The estimate of atmospheric loading of selenium to the Massachusetts Bays is presented in Table 83. Total aimuaJ loading of selenium is estimated to be < < 1 metric ton/yr. This estimate is based on dty deposition only. Table 83. Atmospheric loading of selenium (kg/yr) to Massachusetts Bays. Estimates include only dry deposition. Area Low Estimate High Estimate Mass Bay Cape Cod Bay Broad Sound 14 8 0 182 108 North Harbor 0 3 Quincy Bay Inner Harbor 0 0 3 1 Hingham Bay Total 0 23 2 305 156 Silver Very few aerosol data are available for silver. Olmez (1990) reports a maximum concentration of 1 ng/m3 for silver; most samples were below cfetection. A concentration of 0.2 ng/m3 is used, based on Olmez data. Deposition velocity of silver is reported to be 0.24 cm/s by McVeety and Hites (1988) and 0.1 to 0.6 cm/s by Sehmel (1980). The deposition velocity assumed for silver in the present analysis is 0.24 cm/s. This results in a dry depositional flux of 0.02 mg/m2/yr. No data are available on the washout ratio of silver. The concentration of silver in precipitation is taken from the summary of Galloway et al. f 1982) for urban areas, 3.2 ug/1. This results in a wet deposition flux of 3.5 mg/m2/yr. This estimate may not be representative of the study area. The estimate of atmospheric loading of silver to the Massachusetts Bays is presented in Table 84 and in the Appendix. Total annual loading of silver is estimated to be 14 metric tons/yr. This estimate is dominated by the wet con- centration of silver in generic urban areas, not on data specific to the Massachusetts Bays region. The total silver loading estimated for Long Island Sound is 5.23 metric tons/yr (Connecticut Department or Environmental Protection, 1987), which may indicate that the estimate of silver loading for Massachusetts Bays is too high. Table 84. Atmospheric loading of silver (kg/yr) to Massachusetts Bays. Estimates Include dry and wet deposition. Area Low Estimate High Estimate Mass Bay Cape Cod Bay Broad Sound North Harbor Quincy Bay Inner Harbor Hingham Bay Total 7777 4596 233 145 134 35 67 12988 157 Vanadium Atmospheric concentration of vanadium is reported to be 13.18 n2/m3 by Rahn (1981) and 35(6) ng/m3 by Rahn and Lowenthal (1984) measured at Narragansett, RI during winds from the Boston direction. Thurston and Spengler (1985) reported concentrations of 22.1(1.10) and 3.34(0.33) ng/m3 for the fine and coarse size fractions respectively. Data provided by Olmez (1990) have a mean concentration of 12.1 ng/rn3 with 10th and 90th percentiles of 4.1 and 35.7 ng/m3, respeaively. These values are used in the present analysis. Measurements of atmospheric concentration of vanadium made in the 1960's and early 1970's (Gladney et al., 1974; Hopke et al. 1976) were as hi^ as 2000 n2/m3. The source of this vanadium was local combustion of residual oil. Rahn (1981) notes that this is no longer an important source and that urban concentrations are generally under 100 ng/m3. The older reports of extremely high vanadium concentrations are no longer representative of present conditions. Deposition velocity of vanadium is reported to be 0.29 cm/s by McMahon (1979) and 0.2 to <0.7 cm/s by Sehmel (1980). The deposition velocity used for vanadium in the present analysis is 0.29 cm/s. This deposition velocity results in a dry deposition flux of 0.4 to 3.3 mg/m2/yr. The washout ratio for vanadium is 110, accordineto McMahon (1979). This results in a wet deposition flux of 0.4 to 4.3 mg/ni2/yr. This flux corresponds to a wet deposition concentration well below the range reported by Galloway et al. (1982), 16 to 68 ug/1. The older measurements reported in the review article by Galloway are probably not representative of present conditions. The estimate of atmospheric loading of vanadium to the Massachusetts Bays is presented in Table 85. Total annualloading of vanadium is estimated to be 4 to 31 metric tons/yr. Table 85. Atmospheric loading of vanadium to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 1909 16668 Cape Cod Bay 1128 9850 Broad Sound 57 500 North Harbor 36 311 Quincy Bay 33 288 Inner Harbor 9 76 Hingham Bay 16 144 Total 3188 27836 L58 Zinc Atmospheric concentration of zinc is reported to be 100 to 210 ng/m3 by Zoller and Gordon (1970), 100 to 340 ng/m3 by Gladney et al. (1974) and 190(220) ng/m3 by Hopke et al. (1974). Thurston and Spengler (1985) report 26.5(1.05) and 12.2(0.64) ng/m3 for the fine and coarse size fractions, respectively. The data provided by Olmez (1990) has a mean concentration of 14.6 ng/ni3 with 10th and 90th percentiles of 3.7 and 58.3 ng/m3, respectively. Tnese values are used in the present analysis. The concentrations reported by Thurston and Spengler (1985) and the measurements of Rahn and Ijowenthal (1984) at Narragansett during winds from the direction of Boston are similar to the data of Olmez (1990), suggesting that these data are temporally and spatially representative of the entire study area. Deposition velocity of zinc is reported to be 0.62 cm/s by McMahon (1979) and 0.4 to 4.5 cm/s by Sehmel (1980). The deposition velocity used for zinc in the present analysis is 0.62 cm/s. This deposition velocity results in a dry deposition flux of 0.7 to 11.4 ms/m2/yr. The washout ratio for zinc is 179, accordmg to McMahon (1979). This results in a wet deposition flux of 0.7 to 11.5 mg/m2/yr. The estimate of atmospheric loading of zinc to the Massachusetts Bays is presented in Table 86. Total annual loading of zinc is estimated to be 6 to 93 metric tons/yr. TTie total zinc loading estimated for Long Island Sound is 480 metric tons/yr (Connecticut Department of Environmental Protection, 1987), much larger than the estimate for Massachusetts Bays. Table 86. Atmospheric loading of zinc to Massachusetts Bays. Estimates include dry and wet deposition. Area Low Estimate High Estimate Mass Bay 3153 50325 Cape Cod Bay 1863 29738 Broad Sound 95 1510 North Harbor 59 938 Quincy Bay 54 869 Inner Harbor 14 229 Hingham Bay 27 435 Total 5265 88043 159 Summary of atmospheric loading Ranges in atmospheric loadings of chemicals to Massachusetts Bays are presented in Table 87. Table 87. Atmospheric loading to the Massachusetts Bays (kg/yr). Chemical Total References Nutrients Nitrogen 1596150-4484822 M7M8 Phosphorus 12486-51283 R6 Organics PAHs 953 - 1260 M6 PCB 745 - 2097 R5 Metals Sb 46- 333 M1M2M8R1 As 145 - 930 M8R1R2 Cd 2504 M8R3 Cr 145-5114 M2M8 Co 7303 - 7786 M1M2M3M8 Cu 18436 M1M4 Fe 121584-529351 Ml M2 M4 M8 Pb 213444 M4 Mn 3905 - 15770 Ml M2 M4 M8 Hg 24-73 M5 Mo 808 M8G1 Ni 11280 M4 Rl R4 Se 23-305 M1M2M3M4M8 Rl Ag 12988 M8G1 V 3188 - 88043 M4M8R1R2 Zn 5265 - 88043 Ml M2 M3 M4 M8 Rl References by area. Massachusetts Bays: Ml (Zoller & Gordon, 1970); M2 (Hopke et al., 1976); M3 (Gladney et al., 1974); M4 (Thurston & Spengler, 1985); M5 (Fogg & Fitzgerald, 1974); M6 (US EPA AIRS, 1990); M7 (Galloway et al., 1987); M8 (NADP, 1989); M8 (Olmez, 1990). New England Regional: Rl (Rahn & Lowenthal, 1984); R2 (Walsh et al., 1979): R3 (Galloway et al., 1982); R4 (Rahn, 1981); R5 (Harvey & Steinhauer, 1974); R6 (Conn. Dept. Environ. Protect., 1987). Generic Urban Areas: Gl (Galloway, et al., 1982). 160 5.7 Spatial Distribution of Hazardous Waste Sites Near the Coast and Rivers This section identifies DEP Confirmed Waste Disposal Sites and Locations To Be Investigated within 500 feet of Massachusetts coastal waters and the Merrimack River to Pawtucket Dam, 5.7.1 Approach The following approach was used to identify the sites: 1. Streets and roadways within 500 feet of surface water bodies were identified using the "Universal Atlas of Metropolitan Boston and Eastern Massachusetts", 23rd Edition published in 1990 by Universal Publishing Company, Stoughton, MA and the "Universal Atlas of Cape Cod and Southeastern Massachusetts," 1st Edition published in 19»8 by Universal Publishing Company. 2. The October 15, 1990 and November 1990 Northeast Region Sites database was reviewed. This is a DEP inhouse database of all Environmental Site Assessment Reports on file with the Northeast Office of the DE in Wobum, MA. Properties located within 500 feet of coastal or Merrimack River surface waters were identified. 3. The September, 1990 and December 1990 Southeast Region Sites Database were reviewed. This inventory is maintained at the Southeast Office of the DEP in Lakeville, MA. Properties within 500 feet of surface waters were identified. 4. The July 15, 1990 and January 15, 1991 "List of Confirmed Disposal Sites and Locations To Be Investigated" was reviewed for possible additional sites. 5. Pertinent reports at the Northeast and Southeast Region Offices of the DEP were reviewed in order to determine the exact locations of properties for plotting on USGS maps. 6. Site visits were made to certain locations in Newburyport, Methuen, Amesbury, Andover, North Andover, Lowell, and Lawrence, MA, in order to determine if selected properties were located within 500 feet of Massachusetts coastal waters or tributaries. 7. Sites were classified in the following ways: (A) Former Coal Gasification Plants; (B) Tanneries and Factories; (C) Gasoline Stations and Miscellaneous Unknown Usage (Commercial Sites). 8. All sites were classified by town, by drainage basin, and by contaminant (H-hazardous materials, P-petroleum, UNK-unknown, not specified). 161 9. All sites identified within 500 feet of coastal surface waters or the Merrimack River were plotted on USGS maps and also on a computer-aided design (CAD) drawing of coastal Massachusetts, 5.7.2 Results Sites identified within 500 feet of coastal waters or the Merrimack River illustrated on Figure 10. Figure 10 shows how the sites are grouf>ed along the Merrimack River, in the greater Boston area, and in several smaller clusters. Details about the sites are presented in Appendix C, Within Appendix C, drainage basins are identified as follows: ME: Merrimack River WF: Weymouth Fore NS: North Shore Coastal WB: Weymouth Back IP: Ipswich River MB: Massachusetts Bay SS: South Shore Coastal MS: Mystic River Some municipalities were found to be free of sites within 500 feet of Massachusetts coastal water ways and along the Merrimack River. The abbreviation N/A (not applicable) is reierenced in Appendix B for each of these. A total of 239 Confirmed Waste Sites were found to be located v^ithin 500 feet of the coast or Merrimack River. Most of these are located in the northern part of the state. Relatively few sites were found along the South Shore drainage area or on Cape Cod. Sites were dominated by commercial facilities including gasoline stations. Tanneries and factories made up the next most prevalent category. Finally, there were four sites identified as former coal gasification facilities. Petroleum-related contamination was identified at 177 sites and hazardous materials were identified at 65 sites. 162 ! ! +; u cs -H u ■■ a Lu If Q! U c L <3 — ■ Oi ^ 0 £ 3 i. c u. ei 5.8 In-Piace Sediments This section describes the status of knowledge about the quality of the sediments in Massachusetts Bay. TTie data are the results of core and grab sample analyses reported in various sources including both the scientific and the gray literature. Many of the coastal data were derived from regulation-driven sampling relating to the sites of sewage treatment plants or dredging activity. TTie samples taken were analyzed for various chemical constituents depending on the purpose of the study, thus, results for any subarea will tend to be weighted by a panicularly heavy sampling effort due to a specific study. These data sources are described in Appendix B. The nature of the data are, therefore, not representative of the sediments throughout any particular system. Since the majority of sampling within the bay has been driven by the search for answers to environmental questions, the data may indicate that the extent of contamination is greater than reality. To facilitate analysis and discussion of the data we have divided the study area by drainage basin and added two further subareas, the harbor and the bay. Data included in the drainage basin subarea is for coastal sampling stations. Table 88 shows the distribution of samples within each subarea. Table 88. Distribution of sediment samples examined for this report. Subarea Number of Samples (Drainage Basin) North Shore 20 Boston Harbor 193 Bay (including Cape Cod) 101 TOTAL ai4 Each subarea will be discussed in a sub-section of this report. Each subsection will contain a description of the area, sample availability and sources, metals, organics, PCB and pesticides. For metals,the sediments will be discussed in terms of the Massachusetts Criteria for Classification of Dredged or Fill Material (314 CMR 9.00, Certification for Dredging, Dredged Material Disposal and Filling in Waters). Three categories are provideo, category I being the least contaminated, category III being most contaminated. Sediments will be classified in terms of FCB, pesticide and PAH content. With regard to total PAH concentrations, three levels were identified for classification purposes: < 10 mg/kg, 10 mg/kg to 100 mg/kg, greater than 100 mg/kg. The locations of sediments exhibiting elevated levels of chromium, lead, and P.AHs throughout the system are illustrated in Figures 11 to Figure 13. These figures are somewhat qualitative in nature but are intended to show those areas where bulk concentrations of compounds are generally elevated. Such areas may be considered to represent potential "hot spots". Based on our review of available data there appeared to be locations within the Boston Inner Harbor and Mystic River s>-stem 164 N^ here elevated levels of contaminants occurred. These data are summarized in Figures 14 through 24. 5.8.1 North Shore Description The North Shore Drainage Basin extends from Castle Neck in the North East to Swampscott in the South West. The major coastal centers of population and industry are Gloucester, Beverly, Salem and Marblehead. The available data for this sub- area are presented in Appendix C. Metals Of the twenty samples collected, eleven were classified as category III, sue as category II, and the remaining three samples as category I. Several of the Salem Harbor samples contained high levels of chromium, this metal is associated with the hide tanning industry which was important in Salem's early industrial history. Organic Compounds PAHs were analyzed in only one sample set, the Salem Harbor Tier II Chemical evaluation report. PAHs were analyzed for samples from eight stations. Two of these exhibited PAH levels in excess of 10 mg/kg; none exceeded 100 mg/kg. Pesticides Pesticides were not measured in any of the samples taken. PCBs were measured in sixteen samples, of these the highest concentration was 0.03 mg/kg. Pesticides were measured in nine samples, but none were detected. 165 ^1 * CHROMIUM CATEGORY PPM 1 = <100 2 = 100-300 >*i# 3 = >300 <» • /O JK2m I 1 =1 FIGURE 11 CW* CvnfT^}* Cory i^09%*^»M ^.n^ * &««■ ^ rf.r-^A., Jnc iW "W-vfcn ? t**; B^n IZZI LEAD CATEGORY PPM 1 = <100 f I 2 = 100-200 3 = >200 >»ir. 5 =1= /O MUam 3 FIGURE 12 ^ Ob* Ovnt-rjtt (r«yy •act ' X ^ fnvmrnvu POLYAROMATIC HYDROCARBONS CATEGORY PPM 1 = <10 W ! 2 = 10-100 3 = >100 IMf 0 S to MUm 1 I 1 FIGURE 13 Ob4 Cvn^^U JU'^fm. * «.-» A M Bte« '.a»vM tfti^ A^c fc.^ ew^-. < ,4fc ■>_^ ^ 169 *% 170 171 n II [I ii I I m , 8 1 o * ?l m t It B « i\hlU c Z\°ZH' i € • :!l si «0 c 1 •• ft- & a o o • ▼■ fi 3 a» i I I I I i I p II 172 I 173 SB J ;s 174 ■ ■ ■ ■ ■ • » • • l» » 175 i 176 I 177 178 179 5.8.2 Boston Harbor System The Boston Harbor system is highly developed and includes many industries. Major tributaries are the Mystic, Charles, Neponsctt, and Weymouth Rivers. The available data for this subarea are presented in Appendix B and summarized in Table 89. Table 89. Summary of sediment samples examined In the Boston Harbor system. Northern Percent Southern Percent Harbor of Total Harbor of Total Total Metals #Sampies 161 # Samples 32 Class 11 Metals 47 29.19% 10 31.25% Class ill 98 60.87% 2 6.25% Metals Total PAH 25 8 PAH 13 52.00% 0 0.00% >10mg/kg PAH 6 24.00% 0 0.00% >100mg/kg Total PCS 37 10 PCS 16 43.24% 4 40.00% >1 mg/kg PCS 1 2.70% 0 0.00% > 10 mg/kg Metals The northern Boston Harbor area (north and northwest of Long Island) exhibited higher bulk metal contamination of sediments than did the southern harbor. Over 80% of the samples collected in the northern harbor and tributaries exceeded either Categoiy II or Category III sediment criteria used for judging disposal of dredged material. Less than 40% exceeded either of these criteria in the southern harbor. Highest concentrations tended to occur in the Inner Harbor and Mystic River drainage. Organic Compounds Organic compounds were found in elevated concentrations at a number of stations. PAJIs were analyzed at 25 stations in the northern harbor and over 70% of these exhibited concentrations in excess of 10 mg/kg; most of these stations were located in the Inner Harbor and Mystic River system. None of the stations analyzed in the southern harbor exceeded 10 mg/kg total PAH. PCBs were analyzed at 37 stations in the northern harbor and 10 stations in the southern harbor. The percentage of locations at which PCB concentrations exceeded 1 mg/kg was about the same (40%). Only one station, in the northern harbor, exhibited a PCB concentration in excess of 10 mg/kg. 180 i i ■I ■I M •I H 9 ■f V P * 5.8.3 The Bav Description The bay is bounded on the east by a line from Cape Ann in the north to Provincetown at the tip of Cape Cod. On the east it is bound by the Massachusetts Coast and a line from Winthrop to Hull. Data are particularly sparse for Cape Cod Bay and the coast south of the Weymouth River Basin. We were, however, able to obtain some data for Wellfleet Harbor from the USACE. These data are presented in Appendix B along with the data for the bay. Metals One hundred and one samples were collected in the bay. Of these fifty-six were classified as category III, forty-two were classified as category II and thirteen as category I. There was a concentration of contaminated sediments at the Massachusetts Bay Disposal Site as weU as at the mouth of Boston Harbor. The highest concentration of each measured metal and its sample location is given in Table 90. 181 Table 90. The distribution of liigh metais concentrations in the bay subarea. Metal Number of Maximum Location Samples Concentration rmg/kg> Ag 7 8 Mouth of Boston Harbor An 6 3 Mouth of Boston Harbor As 21 17 Mass Bay Disposal Site Be 7 7 Mass Bay Disposal Site Cd 78 4 Mass Bay Disposal Site Co 2 22 Mouth of Boston Harbor Cr 81 134 Mass Bay Disposal Site Cu 81 75 Mass Bay Disposal Site Hg 67 1 Cape Cod Bay Mo 2 4 Mouth of Boston Harbor Ni 79 56 Mass Bay Disposal Site Pb 81 161 Mass Bay Disposal Site Se 6 7 Mouth of Boston Harbor Th 6 16 Middle of bay Va 6 99 Mouth of Boston Harbor Zn 79 3121 Middle of bay 182 Organic Compounds Sixteen PAH samples were taken in the Bay. The highest concentration of PAH, 14 mg/kg, was found outside the mouth of Boston Harbor. This \fc-as the onJy sample with a concentration of PAH exceeding 10 mg/kg. PCB and Pesticides No pesticide samples were taken in the Bay, but 86 PCB samples were taken. S.8.4 Data Quality and Quantity Uncertainty Sediment sampling programs conducted throughout the Massachusetts Bays systems have had varied objectives and have been conducted across several years. Thus, some of the data may be out of date. Also, there is considerable variability in the degree to which samples represent conditions. Much of the sampling is biased toward examining conditions thought to be contaminated or located near sources of pollutants (e.g., outfalls). Therefore, the data and statistics derived from them should not be viewed as representative of the system as a whole. Their value is in providing broad overviews of conditions in selected areas and in providing a basis tor identifying potential sources of in-place sediment contamination. The identiiScation of such areas is consistent with the generally biased nature of the sampling performed to date in the system. A second source of variability and uncertainty in the data is the fact that we have collected the results of a large number of studies and the techniques used for sampling and analysis will differ. Such differences can result in differences in apparent contaminant concentrations from samples taken in the same area. Finally, the level of effort among sampling areas varies greatly. Thus, there are many more samples in some areas than in others. The probability of locating in- place sediment contamination is related to some degree to the amount of efmrt expended. Because some harbors and near-shore areas have been sampled more extensively than others, there is a greater likelihood of identifying contamination in those areas. 183 6.0 CONTAMINANT LOADING AND ASSESSMENT This section of the report provides a tabular and graphical comparison of the relative magnitude ot the pollutant loadings from all sources. Implications of the data, qualifications of the data, and data gaps are also identified and discussed m this section. 6.1 Comparison of pollutant sources The following are compared for various sources to the Massachusetts Bays: freshwater flow, total suspended solids, biochemical oxygen demand, total nitrogen, total phosphorus, oil and grease, PAHs, PCBs, cadmium, copper, chromium, lead, zinc, and mercury. In several cases, we have used two approaches for estimating and comparing overall loadings. The main difference between the methods is in the way inland discharges are handled. One method (A) estimates loads as the sum of all discrete loadings to the drainage basins. The other (B), estimates loads as a combination of discrete sources discharging directly to coastal waters and river loads which presumably reflect inland loadings. These two approaches provide a rough basis for checking estimates. Method A involves estimating loads by drainage area as the sum of (1) all NPDES discharge loadings to the drainage area, (2) all runoff to the drainage area, and (3) groundwater discharge to the drainage area (estimated for selected parameters for Cape Cod and Boston Harbor). Atmospheric loadings and disposal of dredged material are added to the loadings calculated from Method A to provide overall loadings to the Massachusetts Bay system. Method B involves estimating loads by drainage area as the sum of (1) NPDES discharge loadings for coastal facilities only within each drainage area, (2) river/tributary discharge within each drainage area, (3) runoff from the coastline (within 0.5 miles of shore) except for Cape Cod for which total runoff was used because no river discharge is calculated, and (4) groundwater discharge as described above. As with Method A, atmospheric loading and dredged material disposal are added in to provide an overall estimate. Estimates for each of the components are presented in tabular form. In addition a series of bar and pie charts are used to illustrate the data. 184 6.1.1 Freshwater Flow Freshwater flow to Massachusetts Bay was calculated using Method B (Table 91). Groundwater flow estimates are presented for two of the drainage areas: Boston Harbor and Cape Cod. POTWs were judged to dominate the coastal dischargers and are used to estimate freshwater input from point sources. Many of the coastal industrial NPDES permits are for cooling water systems, llie total freshwater flow to Massachusetts Bay from the sources identified in Table 91 averages 462 m3/s. Much of this flow includes that of the Merrimack River (244 m3/s). The i>ercent distribution of freshwater flow by drainage area is depicted in Figure 41 both with and without inclusion of the Merrimack River dramage area. The Merrimack River drainage area could account for 52% of the freshwater flow to the system. Rainfall accounts for 28% if the Merrimack is included and 58% if the Merrimack is excluded from the estimate. Nonpoint sources dominate the freshwater inflow for aU drainage areas except the boston Harbor system which is dominated by the NPDES outfalls from the Deer and Nut Island POTWs. If the Merrimack River is excluded the Boston Harbor drainage area accounts for 27% of the freshwater flow to the bay. Groundwater also appears to be important. Estimates were made for the Boston Harbor and Cape Cod drainage areas. For the latter, total groundwater inflow to Cape Cod Bay is estimated to amount to 4.1 m3/s. This discharge dominates over runoff for Cape Cod and is equivalent to one-half the riverine inputs estimated for the South Shore Drainage Area. Our estimates did not include estimates of freshwater inputs from the Gulf of Maine. This source may in fact provide the greatest inputs of freshwater to the system, so this exclusion is significant. Even for this most basic measurement, data are subject to uncertainties. Annual river flows were estimated by several methods, depending upon whether gauge measurements were available. Seasonal and year-to-year variability is also high for flow. Where seasonal variability was measured, flow tended to be high during March-May than in other months. Annual variability can also be substantial. This variability affects not only the measurements of flow but the measurements of inputs of the pollutants. 185 (0 CO g >> (0 CQ (A 3 O CD (0 « CD I CD (0 9 2 ' ' ■■■ ■""■ ■^" ■■^" ' ' ,f- Q CM y-\ , CVJ O Q o a o O i o lO O + + + LU O 00 + + + . i 0) LU LU LU LU LU LU « 3 g CM CO 88 O CM CO CO oi CO |0,0 I 8 CMi ICM, 1 o ;o + + + ^ LU UJ 'LU Q. X 8 O) o> IT 2 CM |CM D 5 1 o "^ -! 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Q) ■♦■^ C H— o O O lO CO CM O CD 3 igur O CO u. 03 o CO > ® ® o D O CO 187 i i i I 6A2 Total Suspended Solids Lx)adines of total suspended solids are presented in Table 92 and Figures 26 and 27. Methods A and B yielded loadings estimates of 555,000 mt/yr and 299,000 rai/yr respectively. Atmospheric loadings are not included. The disposal of dredged material was a major contributor to loadings and accounted for 31% of the Method A estimate and 60% of the Method B estimate. These solids are added to one site within the system and would not be expected to affect the system in the same way as loadings from discharges and runoff. NPDES discharges accounted for 27% of the Method A estimate with Boston Harbor discharges comprising 60% of this source of loadings. Loadings delivered to the system via runoff amounted to 41% of the Method A estimate. Loadings associated with rivers accounted for 26% of the Method B estimate. Because suspended solids are expected to settle out to some extent within the drainage basins, the nonpoint source loadings provided in Method B (primarily direct river discharge) may be a better estimate than those in Method A. 1S& 3 O "O, « o c E •o e CO s s g 8 ^ S & g 8 8 8 + + ^ ^ + + + + + + + • UJ ID UJ UJ LU LU LU UJ lU LU UJ 1 « S 8 IS OO S 8 8 S i2 • esj o CO CO CO f^ o '- O ■^ s 8 8 v.- 8 8 + + + \ + + i LU UJ UJ . UJ UJ 8 8 00 ' 00 g s o o T- "^ •^ s 8 s 1 8 8 8 8 8 + ^ + + f LU + + + LU UJ UJ UJ UJ UJ lU UJ s § • s 00 • 00 A • 00 • in (A csi s 8 8 s s 8 8 8 8 + + + + + + + + + _c e (0 lU lU UJ UJ LU UJ LU UJ UJ 8 CNJ s CO csi in CM - CO CM II < X II CO I & o s & s & o j 8 o 1 + + + + + + + + + LU LU UJ UJ LU lU UJ LU LU 9 o < a k ;s U) 8 U) fx. CM U) CM < < o 1 • X 00 f^ U) CM h- r«- 1*". o o C 00 00 iT" CVi ^ ▼- CO ^~ CO cc a. 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I o a CO o E ce E E ^^ OB eo c *^ O <8 190 CO c • O "O • m^ (0 _o JLJ .,_, i3 c C 0 o E o • ^^ "D Q) 0 > (0 ca 73 Rei nde a 0 r^ a CM CO D 0) CO s^ D O) U- © Q. > O D O C/3 o c GC 191 6.1.3 Biochemical Oxvgen Demand (BOD) Loadings of BOD to the Massachusetts Bay system are summarized in Table 93 and Figures 28 and 29. The estimates do not mclude inputs from the atmosphere, dredged material disposal or groundwater. Methods A and B gave almost identical total loadincs of BOD to Massachusetts Bay at approximately 180,000 mt/yr. Most of this (90%) was due to NPDES dischargers witn approximately 10% due to runoff or riverine inflow. The Boston Harbor m*DES outtsQls accounted for approximately 56% of the coastal NPDES BOD inputs to the bay. 192 o CO >» n n ffl I (0 3 O (0 « (0 S CO o o O CO i2 00 o o 8 00 o 00 o in o o 8 § 8 8 + + + + + + + + + + + (0 LU LU UJ UJ LU LU UJ UJ LU LU LU 5 ;s s s ^ 1 CO CO CO CO CO CO 00 1^ o o ■^ T- '" ■^ T- ^ ■^ ■^ lA in in in s in in ' in in O o o o o o o o + + + + + + + + + ^ S o LU LU LU LU LU LU LU LU LU 3 00 s oo § 8 3 ?2 00 GO S (0 "^ II < II CQ N. 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Q. iS 1 (0 "5 3 O 9 a c I II i2 "5 • CD c 1 II iS a (0 3 3 z cc o P D 3 O O cr O H o < O H- H 193 194 c o o T3 o CO o d) ativ Q O CO 3 8 s s g 1 8 8 8 + + + + ^ + ^^'' + + ^ 1 LU UJ UJ Ui UI UJ UJ WyMi UI s 00 s < z § 00 CO < z tn -^ §-• f 00 • Si • II < I II CD & s s & & s 8 S & & & 2 + + + + + + + + + ' + + 5^ LU UJ UJ UJ UJ UJ UJ UJ UJ UJ UI ^ < c ^ ^ ^ in -^ o> (O 1** CM vn CM < .^ 0 1 • X C>i 1^ CO (O I^ U) CO CO CO o u # C s s '" CO ■^ '" CM ■*" ^" '" *" ^^ Q. Q. < X tr Q. < X S o s s 8 8 s 8 8 8 8 + + + + + + + + + »- h- ^ e i (0 UJ UJ UJ UJ UI UJ UJ UJ UJ CO 1 2 8 < z 8 o s> < z s • 8 •** Jtf 8 s 8 s ^ ^ - 8 ^ CD JE + + + + + + + + C/> f/) S UJ UJ UJ UJ UJ UJ ' UJ UJ C/) f/) c f^ r; ^ lA ▼» ^ , "^ T~ ^ < 1 q < CVJ CO CM CM • < ^ CO T" 2 2 S z z a O UL s, ^ -J C o e o i f ? S 3 u C 8 < CD o o 1- ti 3 2 CO O J i < 1 C i (0 UJ o z O (0 5 I < • I n 1 e 5 D CO UJ o Q. z CO 3 1 s M a 1 GC 2 3 1 s S 5c 1 1 t 1 f 1 1 1 it 1 z 1 2 • c c i 1 iS 1 N 1 197 (0 m (0 CO (0 CO E c o o ^ CO o CO O) • ■IB U- (0 CD o o CO c o O CO CO 0) o o CO CD CO O CO o o c 3 cc 9 (0 :e ® 0) CO <0 LU Q Q. 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CO O O CO cvi CO (0 a> > 3 CL O) CO • aiB c u. o o E (0 CD O O CO CO 0) o D o CO CD CO z LU 03 q; JC Q «9 O E < CO O CO o o c GC CO LU O a. z o *5 1 L 03 w ^ O "D "^ C o o ^■! CO S B • « E s °» o£ Z "O 202 CO o ■D CO *^ o 3 CO ^ D +^ CI o o o Q. ive hos CO a CD >» CC CO ■ m CO CO CO CO CO o s 3 C3) o ■ ^^ ^^ U- CD ® < ® CD C "cD Q CD CO o £1 CO a O CO .^» o e o ' < c 3 ^ "^^^^ Source ype 203 6.1.6 Oil and Grease Loadings of oil and grease to Massachusetts Bay are summarized in Table 96 and Figures 34 and 35. No estimates have been developed for atmospheric loadings. Total loadings are estimated to be 13,000 metric tons usine Method A and 6,100 metric tons using Method B. The reason for the two-fold oiffercnce is that no estimate was developed for river discharges in Method B. Method B is therefore considered an incomplete estimate. Based on the available estimates, it appears that nonpoint source runoff dominates the loading of oil and ^ease. Inputs from CSOs are estimated as 1,700 , and nonCSO inputs are estimated as 5,300 metric tons annually. Unfortunately, we have no measurements of variability or uncertainty in these estimates. Dredged material disposal is also a maior source for this poUutant category and accounts for 19% of tne load estimated using Method A. 204 o 3 O CO fO CD CO CO 3 (0 . o o CO cs c CO s 2 8 8 8 o 8 o 8 8 8 8 8 + + + + + + + + + + + « UJ UJ LU LU LU LU UJ LU UJ LU LU 5 o CO 8 Z 5? 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O ^v^ O CO o CO o o c 3 CTD cr 207 iLLZ_EAHs The loadings of PAHs to Massachusetts Bay arc provided in TaWes 97 and 98 and in Figures 36 to 38 Loadings estimates for PAHs are provided for several cases involving Methods A anoB and higher and lower estimates. We present this range to illustrate the kind of variability (i.c^ range) there exists in the estimates. Because of uncertainty in the data we used and the estimates we made, the lower and higher values should not be considered a complete range. For the NPDES discharges, our higher estimates assume that concentrations of PAHs in municipal effluents average 10 ug/1, and the lower estimates assume average concentrations of 1 ue/1. In fact, average concentrations may be even lower. Prehminaiy analysis of one grab sample from Deer Island effluent and one from Nut Island effluent has indicated that no individual PAH compound is present in concentrations greater than 10 ng/1 (personal communication, D. Shea, BatteUe). MWRA plans greater, representative sampling and analysis of effluents to confirm these data. Estimates for loads in runoff and rivers were also estimated, based on assumed concentrations of 0.1 and 1 mg/1 in runoff and 50 ne/l in river water. The low estimate for runoff is based on Menzie et al. (1991 J. The higher estimate was selected as moderate but still low. This level is lower than v5ues found in typical urban soils but may be considered representative of levels that occur in open field or suburban areas. As a basis for comparison, the levels of PAHs in road dust can typically be on the order of 100s of mg/kg. Thus, even though our calculations do not indicate that runoff is a dominant or important source ofloadings, had we used somewhat higher values for runoff (i.e., typical or urban areas), runoff estimates could have been a substantial fraction of tne total. These value for rivers was selected as typical, assuming that 10-100 ng/1 are typical concentrations of PAHs in urban river systems (Menzie et al., 1991). Using the higher estimates. Methods A and B give approximately the same result, 13,700 and 13,100 kg/yr. These higher estimates are dominated by NPDES dischaj^es (81%) and the discharges to the Boston Harbor drainage area account for 76% of the NPDES load. Using the higher estimates, atmospheric inputs and dredge material disposal are about an order of magnitude less than the NPDES inputs. If the lower estimates are used the following results are obtained (Table Error! Bookmark not defined.). The total estimated loads are 1,810 kg/yr for Method A and 2,200 kc/yr for Method B. NPDES discharges account for 45% (Method A) and 34% (Method B) of the total load. The potential importance of the atmosphere as the dominant source emerges when lower estimates are employed: 52% of tne load for Method A and 43% for Method B. 208 J^ o o 3 O (0 12 c CO o X < a. o E to o o o 2 CO s g O s z 8 g o 5 CO o CO o + + III + + + + LU 8 + + + « LU LU LU LU UJ LU LU LU LU LU 1 S 8 CO s ^ o CM < o> • o> CO CO o o ■^ z ^" ^ Z ■^ ■^ ■^ ■^ ■^ CSJ s CM CM ^. ^. CM CM CM O O o o o O o O + + + + UJ + + + + J^ o (A lU LU LU LU UJ LU LU LU 3 & ^ < z S ^ < z • LA s? II < II CD CO ^ T- CO CO 8 ^ .^. 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Z (0 Tn 3 1 3 cr o b 1 M 3 O W 2 1 1 JZ Its n ^■'"* ^"^ ^^Mi CO T— ^r- CO CM y- CM ,_ """" 8 cm:-»- o o o o O o 0 0 0 0 1 + + 1 + + + 1 + ■♦• + « LU liJ LJJ UJ LU LU LU LU LU LU UJ in o ^ 8 ^ •^ ^ CO 8 CO 2 CO o CM CM ^ O) CO ^ CM '- o> '- 8 8 CM 0 0 s s + + + + r/^' + + 1 Q LU LU LU LU := LU LU 8 d 8 2 1.16 9.65 in CO ^_ .r- .^~ ^. W^ ^. V. CO CO o o o 0 #■:-' 0 ' 0 ' 00 ? LU (0 < UJ LU CO O) < LU O) + + + + LU UJ LU LU g 00 00 , in r^ O O z z <<>>,'■ ^^ --; y^ ^ ,_ y^ CM y. y^ ^. o o o o o 0 0 ?;»:■;■ 0 0 + 1 + + + + !:;::-■:; + + jj o lU LU UJ UJ LU UJ LU X LU LU s 00 § in CM 00 ^ s :. in Wy CM 2 j; - S;:;-.;::: n! r*. iCC CC a e s CD z il;! U. E s 1 CM o 8 s 8 0 0 3 11 § 8 iiii s + + + + m 0 CM + + ;sa:^;^ + + Il-IK r 2 o LU UJ < Z UJ LU UJ SI CM < z LU K: :: LU UJ 0503 c 0 I < JX g 8 3 CO 0 s 8 ym: CM S CD CD Je + + + LU 8 CM + + ffm^ + + 05103 Q. c lU LU LU UJ UJ ;;r LU'LU en en a 1 8 < in • CO < CO in CO < < IS S F S z 0 iO U. LL 0 CO ^ —1 0 r p a < < c o o GD S CB s 1- K 00 .2 A CB 3 u « 8 < 0 CD 0 t- t- (0 c 0 1 1 1 • • m X < 3 < 1 c 03 lU Q CO O (0 O 1 3 3 2 « • S C CO UJ Q Q. z 05 0 1 3 CC 2 0 Q 1 0 5 C0 § 3 s 1 - 1 1 3 1^ CO 05 a> E 3 1 1 i o o CB c S II iS s o o « c g « II (0 ■5 otals with otals with Q. ^ (0 3 3 Z cc O h- ° 5 o 0 QC 0 K 0 < Q \-\\- "^ 210 (0 ffl CO ,0'^ 0) ^■4 a> CO CO E 3 ■«■■ ach CO (1) CO 4^ CO 0) CO ^ IE o o ■» klB > "O ^>^ CO O) o ^ ■^" ^*— ^ X 0) < o £ D • o CO CO CO 0) iD X (0 CD O O CO CO 0 O D O CO OQ CO illl I UJ CO c 3 O O CO O CO O o c 3 (0 V. 0> CO 9 o> a> CO UJ o a CO o E CO i 2 < I O o o o o 211 < Q. o CO 0) (0 (0 c E o ■ w^at a Mi^ ■4>^ *-» CO 3 Q> Si a an^ 0 C JZ o O) o ■ ^^ Q> c > a ^a^ o ^^ <0 TJ o 0 cc (0 CO • ^ CO T5 CO 0) O 3 D) U. CD CD < 0 CD CD C 'cD Q (D Q. CD O Z5 O CO 212 ID < Q. O 0) +"^ O ima • ai^B •4-^ 3 CO ^ 0) • ^BiB ^_ o o o Q) CO "D Rel 0 CO CO ■ ^ 00 CO ■D CO 0) o O) •o CO ® 5 < CD CD CD C "cD Q O c 213 6.1.8 PCBs Loadings of PCBs to Massachusetts Bay are summarized in Table 99 and Figures 39 and 40. Total loadings are estimated to be approximately 2,600 kg/yr for both Method A and B. The reason that Methods A and B give almost identical results is that the loading is dominated by atmospheric inputs which account for about 85% of the total load. The estimates of atmospheric load are based on data collected during the mid 1970s, and, therefore, may be substantially higher than current levels. Because production of PCBs declined in the late 1970s, it is likely that concentrations of these compounds are declining. Still, Atlas et al. (1986) point out that the atmosphere is the major source of PCBs to the oceans and they estimate that 98% of the PCBs entering the oceans is currently being deposited from the atmosphere. For the oceans as a whole their estimate is 1,700,000 kg/vr or about three orders of magnitude greater than our estimate for Massachusetts Bay. Our estimates of inputs from NPDES discharges ranged from 416-468 kg/yr. Using the higher of these estimates, point sources accounted for about 20% of the inputs to the bays. These estimates are probably too high however, because they are based upon data that were below detection limits. These estimates are likely to decline, when the MWRA completes analyses of additional effluent samples. Preliminary data from the MWRA mdicates that no individual PCB compound is present in effluent at concentrations greater than 10 ng/1. 214 THIS PAGE INTENTIONALLY LEFT BLANK 215 g o 8 s g o n o 8 + o + ? 8 + 1 ^ ? 9 8 ■f 8 O t» UJ UJ UJ UJ UJ UJ UJ UJ UJ UJ UJ a s f>. 8 o s 8 ^ 8 f^f o s i2 •^ lA o \n "^ '- t^ ca •^ CNJ CVI 8 8 8 o m 8 8 + + + + li -^ ■♦' 1 s UJ UJ UJ UJ m\n UJ 8 d 8 d o J8 W W CVI eg 8 8 8 8 88 + + WM + + + -f ut UJ ^UJ UJ UJ UJ 5 2 < z 8 d < Z 8 d £ %^{:- 8 d 8 to CO Csj CVJ s 8 8 s 8 8 8 + + + ( + i^'.? + + _c s i 0) LU UJ UJ LU 8 d UJ !>/' UJ UJ s s •^ < z ^ 'a- t in ^ U) a < I O H CD I O Ml 3 O S 3 8 s o 8 8 8 1 + LU + UJ + UJ + UJ + UJ UJ 1 UJ UJ UJ UJ < e o 1 « 8 T— •^ JS 8 8 8 8 o ^ O t g • e i ■^ C3 < z -^ •^ T— "^ cvi -^ ^ "^ CC Q. % I CC Q. < X O O o O S o O o + + + + 1 + f + •f h- H r e o (0 (6 UJ 00 o < z UJ 1^ UJ d LU 8 < z UJ d UJ UJ d > ^ 5 J« 8 + 8 + UJ o + UJ 8 + UJ 8 + UJ o + 8 UJ CD CD C/5 "1 1 • o < SI • rs.' < o o < 2 < 2 S z z CL £ CL O U. t -J ^ c c « < < o o ffi K K S 5 o ^ o • 8 « S < m o o 3 « m ro o 9 9 1 < 1 S C (0 UJ Q 0. S [J 3 I ID 1 oa c m (fi UJ o Q. z 2 o 3 1 a 1 • 3 2 9 1 « f 1 f 1 « CD O k i • CO c 1 H • c 1 a U If 1 JS5 (0 Q. f 3 D z (I o H 3 o o CC CD h- o < Q K •- 216 (0 CD €0 €0 (0 • :e > o v^ ** ^ "D ^ CO ■"^^ O 0) ^■~ o CD D O O Q. CO 39. > a> 3 O) u. (0 o CD O CL O) iiini i I liiiii liili (0 CD O O ^ 2 CO CO m o o> CO CO o o o o o o o o o III O CQ CO 2 i S o I CL a CO £ 2 < o a I o a 75 o c E UJ 217 o CO c o •^ CO z a. So o "cc > • CO O CO ^ CO a> O) CO CO o LU CO Q O CL '"^ Z «^ ^ o .^fl c ^^H 3 A ^^^H CL A ^ CD O a> •D 0) CO (D < CD O) CO c 'co Q (D d CD O O CO 218 6.1.9 Metab We selected the followingmctals for presentation: cadmium, chromium, copper, lead, zinc, and mercuiy. These appear to be six of the more important metals from a human health and/or ecological standpoint in the system and have been observed at elevated levels in the Massachusetts oay system. Cadmium Loadings of cadmium are summarized in Table 100 and in Figures 41 and 42. There is considerable uncertainty in the cadmium estimates because there are few measurements for point sources. We have addressed this lack of data, in part, by estimatinecadmium concentrations for various POTWs based upon the cadmiumrrSS ratio in Deer Island efQuent We feel this is reasonable because Deer Island effluent integrates a wide variet}^ of inputs. TSS is generally measured for these effluents. WitB the TSS-based estimates, the our estmiates of cadmium entering the bays ranged from 2,260-2,620 kg/yr. Using the higher estimates for all sources we obtain cadmium loadings of 8,020 kg/yr and 14,700 kg/yr for Methods A and B respectively. NPDES discharges account for 34% and 17% of the Method A and B estimates. Most of this load is associated with the Boston Harbor drainage area (78% of the Method A NPDES load). Nonpoint sources appear to be relatively important sources. Runoff in Method A accounts for 30% ot the load and river discharge in Method B accounts for 66% of the load. The runoff estimate was made using the NCPDI, with values for CSO inputs corrected for concentrations measured by the MWRA. CSOs accoimted for most of the cadmium inputs. Our estimate of inputs from rivers assumed an average concentration in river water of 1 ug/1. Values reported in the literature ranged from 0.01-7 ug/1, so our estimates of total contribution for rivers would vary substantially if we selected a different value. The atmosphere contributes 31% for Method A and 17% for Method B. Very few data were available upon which to base the estimate of atmospheric inputs, and our estimate, the only one we made, is considered to be high. Groundwater discharge to Boston Harbor was estimated to be about 15% of the point source load, using our higher estimate of 320 kg/yr. Our lower estimate was only 10% that value. 219 o 3 O 10 <0 CO (0 o E 3 E (0 O I 2 |2 ^^^ """"* CO CO CM CO CO y- CO 8 3 CO -.- : i o o O o o o o o o + + + + + + + + + + + « Hi LU LU LU LU LU LU LU LU LU LU 1 ^ O O CNJ CNJ u5 O s 8 oj OOO LOCO i2 csj csi CO iri CNJ CO O) d '-' CNi|r^ 8 8 CO -.- ,•;-<■ COiCO OIO o o -♦- + + + + + 1 LU lU LU LU LU LU 8 8 O 00 00 00 in ] 00 in in o d d CNJ r». CVICNJI y^ y^ ^- 8 ^ •r- f- CO •^l o o o o OiO o O + + + + + + + 4- + UJ LU LU lU LU LU LU LU LU 1 8 CNJ < Z 8 CNJ 8 CNJ 8 d < Z 8 csi 2.00 2.00 8.02 1.47 8 O o 8 8 g CNJ o •.-CNJ OiO + + + + + + + + 1 + ^ s LXJ LU LU LU LU LU LU LUiLU *; O O O) O 8 (d h* ^ Oi.-r- 3 O o> 1^ CJ> < (0 1^' to CNJ < z 00 CNJ 00 Csi II n CO CO CNJ CO CO ^r- CO CO CO CO < mi 1 o o o O O o O o O O XX + + + + + + + + LU LU LU LU LU LU LU LU < c o 1 "* CNJ O CNJ ?2 o o -^ CO CNJ r^ CNJ; lO O 9 ^ CNJ T^ CO CO CNJ T-' t-' CO CO CO ice cc « o « < IQ. Q. c & m X z ' ■ a. Q- < < CNJ CNJ CNJ CNJ CNJ CNJ y- CNJ CNJ O O O O O o O o O Oi i i + + + + + + + + + 1- 1- S o (0 LU LU LU LU LU LU LU LU LU =: =: O CO CO < z 00 1^ O CO 8 in < z in 00 od 00 in ^5 2 5 ^ ^ Jte s s g 8 8 § 3E + + + + + + + + i C/J C/5 S lU LU LU LU LU LU LU 111' ^*rf . >** LU : rn fo ;o < 00 8 C3> (0 < CO s z z I ' O O 5. LL U.| -J _j c c « < < o o CD !l— h- s C0 O O s 3 o « 2 < CD u >- t- 3 O v> O 5 J 1 c LU Q 0. <0 o C/3 O 1 3 a> 1 "S 3 2 "5 o CD s CD •a o £ S m c « CO LU Q Q. Z 2 to g 03 O 5 s m 3 O (0 1 2 o a o "5 i i2 (D "5 s 1 E 3 E I: 3 O • « c S II (0 "5 • CB 1 II iS (0 f .•tr a "5 o ^ (0 3 3 Z cc CD K D 3 o u QC K Q 3 03 E "D O OJ ZL o 42. o CO ^ cvj cvi CVJ |cr cc CB o CB • Q. Q. c S Q ffi X a. Q. < < I I s 8 5 s o CO o z 3 3 + + + + + + + + + 'K H ^ S o HI LU LU UJ LU LU LU LU LU > > 8 Csj cvi < z 00 cvi s cvi s cvj 00 cvi CO cvi 00 cvi J£ CO o CO o 8 O 5 3 §iSi ,ss X + + + + + + + + itn cfi\ S ID LU LU UJ UJ LU UJ LU' 'o5 cri\ • o Csj in < 8 (0 Jo CO fO < < s z m^ u. u. t _l _J c c CB '.< 51 o o m H el S5 f0 1 I O O S S «0 «B s < o ffi 1- 1- 3 O 3 O CO O UJ U E 3 E 1 5 J 1 < 9 o> (B C s < o § s c W LU Q Q- O w o 1 1 2 1 m 1 • s c w LU Q 0. Z (0 « CO o 1 3 cc 15 «5 s 9 5 1 1 o C0 § 3 1 9 3 O II 0) (0 "5 • (B C S H o « 0> CO « £ S loo 1 o^ ^ (0 5_ D Z DC_ o_ h- p D o o^ 5^ o ^ 5 < Q IH Hi II 224 225 226 CQppgr leadings of copper (higher estimates) are provided in Table 102 and Figures 45 and 46. Because we had data for many of the POTWs for copper, we elected not to estimate loadings for those few for which data were lacking. Methods A and B gave good a^eement for total loadings with 150,000 kg/yr and 190,000 kg/yr respectively. Pomt and nonpoint sources were both important contributors to the overall loads. NPDES dischargers accounted for 57% and 37% of the loads for Methods A and B respectively. The Boston Harbor Drainage Area accounted for about 76% of the NPDES load under Method A. Our estimates of total copper inputs ranged from 76,300 to 86,700 kg/yr. Runoff amounted to 25% of the load for Method A while riverine inputs amounted to 50% of the load under Method B. NonCSO urban runoff accounted for most of the inputs from runoff. Our estimate of inputs from rivers assumed an average concentration in river water of 10 ug/1. The atmosphere contributed to 12% and 9% of the load for the two methods, using our estimate of about 20,000 kg/yr. Dredged material contributed 4% of the load under Method A. We have no range of estimates for these inputs. 227 3 O (0 (0 OQ (0 CO (0 S a •a (0 o o Q. Q. O o o o n CO I- s. S 8 o 3 C\J o s 8 in o 5iS, 1 1 i 1 1 + + + + + + + + + + •¥ «) LU LU LU UJ LU LU UJ LU LU UJ LU ?s in CO 2 8 in CM § 3 8 in s CO i^ 00 CO o -^ o "^ "^ i csi o s S o s S 3 3 S S + + + + + + ^<^ + + + •f LU LU LU LU LU LU ^ UJ LU' LU LU 8. o 8 8 to 8 s «; , <0 O O 1 CO ■^ -* m "* "<^ m ^1^! ^^ C\J CO CO CM CVJ CO CO CO CO o o o o o o o K? O'Oi , , 1 + + + + + + + #• + + .e £ LU UJ LU LU UJ UJ LU i$:: LU LU «■« O CVJ r- s o 1^ in M?i r^ U) 3 O (0 o 0) iq (£> CO == c\i 5o s 8 in CO p? eo CO CD CO CD Ji! S 8 5 o z z z H + + + + + + '"' + + C/} CO S LU lU UJ UJ UJ LU UJ LU fO CO 1 • 1^ c\i o csi "O O) CO ^ o ^-^ CL O o CO C3) H ■■<■■»■■■ WlllM>W—WWWltlHH«WiWlWWttlllH>—»WH»WIWWW (0 00 o o (0 o 3 o C9 O O o o o o o o o o o o o o CO o ♦* O 10 CO 2 O >* -o 0) «^ o» o T3 5 £ oc o b 5 » I CO i 2 < I o ^^ C CO a> CO "O CO .E o CO $ ii ujO 229 c o £1 o to o o > 0 '^ a (0 a U- CO ® CO < U) CO c 'co a> CB sz ■D a CO o o e r ^ ype 230 Loadings of lead are provided in Table 103 and Figures 47 and 48. In the case of NPDES dischargers we have made estimates for a number of the POTWs by applying a Pb:TSS factor derived from averaging data for several other POTWs in the Massachusetts Bay system. Estimates for Methods A and B agreed fairly well yielding loads of 470,000 kg/yr and 540,000 kg/yr respectively. Loads were dominated by nonpoint sources. CSOs and other urban runoff accounted for most of the estimate of inputs from runoff. These values were calculated using the NCPDL Concentrations of lead in CSO discharges were assumed to be 92 ug/1, as measured by the MWRA, rather than the 474 ug/1 used in the NCPDL NPDES discharges accounted for less than 10% of the loads using either Method A or B. Runoff accounted for 42% of the load under Method A and river discharge accounted for 54% of the load under Method B. The estimate for river discharge assumes an average concentration of lead in rivers of 30 ug/1. Had an average concentration of 1 ug/1 been used, lead inputs from rivers would total 9,540 kg/yr, or only 4% of the total inputs. Atmospheric inputs were also found to be a major contributor to the total load and accounted for 45% of the Method A estimate and 39% of the Method B estimate, using our estimate of lead deposition, 213,000 kg/vr. Higher estimates of lead deposition have been made for Long Island Sound, so our values may be low. 231 O) 9 2 3 O m (0 CO s o CO o •a n o o s in o CO o in o 5 CO o in o 8 in o ;in CO 1 iO;Ol 1,1 1 + + + + + + + + + + + « ID LU LU LU LU LU UJ LU LU UJ UJ s CO O 8 5 cvj o s 8 el CO .2 cri cvi -^ Csj CO cvj eg d CO cvi n: 8 1 — 8 in o 8 in in o o 1 + + + + ./ ■♦■ + i LU LU LU LU '- LU LU 8 8 CO ^ eg C^ 5 d ^___ d ej 1^' '■■//?:■ ■■ eg eg ' 1 m CO CO CO CO CO in in o o o o #>/<=> o o o + + + + m- + + + -t- LLl LU LU UJ '«'-'' LU LU ' LU LU s. 00 00 00 00 00 00 r^ -^ ^3 o> O) o> o> % Oi Oi <£) -rt m O 5 T— w^ ▼» ^" TT inl .,_ 00 CO T- eg CO CO CO CO o o o o o o o O O + + + + + + + + + £ o LU LU UJ LU LU UJ LU LUiLU 3 4^ O in 00 00 O in CO eg o 2 05:C0 001(0 O (0 v^ <6 "«r ^ "^ S. S. o 1 "^ 00 "^ eg 5 o> O) o o ts r^ o> t-' I-' W 1-' CO •^ T^ -^ CCiCC a o OS '"', Q.IQ. c CD I '{M, C^ CL 1 Q < < z S 5 5 s 5 z zz + + + + + + + + + , »- »- ^ o LU LU LU LU UJ UJ LU LU UJ| :::= = l CO in O 00 in 1^ ^ eg CO CO in CO ^ 5 CO CO >- > < < CD CD Jtf § z s s S § 5 in O' B + + + + + + + + 1 ^ to s LU UJ LU UJ UJ LU LLI.LU c/5 CO c O CO "^ CO y— '"T — ZJ-Z<\ "E • r^ eg <6 o CO cvi eg (b Si 2 2 s I CC cc o o « U_ LL —1 —1 c c • < < o o m J- h- w OiO S a (0 < CD o i-'k 3 U 3 O s S 1 ! 1 1 S i < 1 s c CO UJ Q V) O O 1 3 1 3 2 1 m 1 s Ol c (/) LU Q Q. Z CO ■ 1 3 2 5 « 3 O (0 i 2 o a 1 f f (0 2 o 1 I 0) 2 ! i 1 1 3 0 o CO c s II « "5 « a c S II 0) 2 o -£ iT (0 a D Z cc o H D D o _CJ cc_ o K 5 O) -o J^ €0 ^-^ o 0 o -o CO D o o CO 0) O) (0 CL Ji ' — ■— ■■, (0 CD O O CD 0 O) CO CO UJ iiiim milllH^IIIIIIIB^IIIIIIIBHI c 3 0 C5 O CO o •1- 0 c 3 c 0 Q. k. 0 1 « CO (0 o •a Q « c CO 0 E < 1 L o o o o o o o o o o o o o o o o o o o o o ▼- c >. o c a o ii c CD :^ a> ~ Is Is is :;: o o» ^ UJ o 233 CO c o 3 ^ 4»^ c ■ o 73 o (0 o 0 > ■ ■■■ "D lat (0 j; (0 ^ r^ < z ^ (d 00 < z ^ ^ II ' II in z in in CO z in in in <;m i o o o o o o + + + + + + + + liJ LU LU LU LU LU LU LU < c k o O T- O o o s V- ^ i5^ o 1 C\J ▼- O CM <£> -^ o ini iO O 9 ^ y- 00 C\J ^— f- CO f- CM ^ icc:cc c 2 Q s Z < z < z [^..CL 8 z z § s z z Z\Z ,1 X + + + + + + + + + 11- 1- ^ 2 o LU LU LU LU LU LU LU LU Lu' '^ =; O O eg CO < z CO O <6 s o CO < z z cvi CO CM >- >• 1 — ' — < :< Z oi iCDiCD iC 5 z z s in o in o as + + + + + + + + i^kn S LU LU LU UJ UJ LU LU LU! :C0 CO 1 • 9 O < CO iri o CO o CO cvi < 8 CM CO in ^! ill s z z (X CL o 1<^ 1 5. LL -J -J n c (B i 1 0) s o o c 1 3 O O O) cc c S i 3 2 II (0 (C "6 • « c S II s o N i? 0) 3 3 Z cr O K D s o o oc o h- Q o <0 c Q) N cc O o lO o =} O) u. o o en CO CO CD < (D O) CO c "co Q 0 Q. CD O O CO o c 238 Mercury leadings of mercury are provided in Table 105 and Figures 48 and 49. Because so few data were available for mercury, we calculated loading using only Method A. Our calculations indicate that NPDES discharges account for about one half the mercury entering the system. There were no data for mercury concentrations in NPDES discharges, except for values that were below detection limits for MWRA effluent and sludge. We therefore developed worst-case estimates, based upon the detection limits for effluent and the TSS content of other POTWs discharging into the system. Our estimates of total mercury entering the system from point sources, 231 and 257 kg/yr, are almost certainly high. Runoff accounts for 27% of our estimate of mercury loading. This estimate was based entirely upon data from the NCPDI. Estimates of inputs from the atmosphere ranged from 24 to 73 kg/yr. However, there are no data on the concentration of mercury in the region, the deposition velocity of mercury, or its washout ratio. Therefore, these values are very uncertain. 239 O) o o %m 3 O (0 JQ (0 OQ (0 (0 CO CO o o S id o 2 CO i to (0 o + LU r- IT) csj CsJ o + LU 8 + LU 8 d 1 LU 8 Si -♦- LU 8 d 8 + UJ 8 d 8 + UJ 8 d 8 LU 8 d 8 + UJ 8 d O + LU O + UJ i b •1 s 8 + LU 8 d 8 + LU 8 d o LU O CO LU' 00 00 • 1 •WS CM o UJ CM CM LU' CM wo O o 8 + LU 8 + LU o> O 8 + UJ 8 d 88 + + UJ LU 88 -r^ d UJ in < Z x: 5 2 C/3 o lij 8 8 + LU in CO 8 + LU CVJ 8 + LU 8 d 88 + + UJ LU CVJiO ^ d N < I o < o GC Q. Q. << N i < • « c S Q c o 1 ffi 8 + lU csi o + LU < CD (0 CO < cc o LL < o o g + LU c6 o + LU 00 00 cvj o + UJ CVJ CO 8 + LU 8 o ;|i O + UJ Si CO 8 + lU 8 d c o c o 1 s s o m 3 o < 1 1 1 3 u CO D < o o S Oi c M D CO LU Q Q. 2 o CO O 1 3 DC (B C 2 D II iS (0 5 ex CO < 1 G £1 % CO « o flO O 1- 240 > CO m CO CO CO ^ s > ^v. o O) *^ J^ ^^^^ "D CO 0 o O ^_ O) I 3 O CO • > iO ^ O D O) u. (0 C?) X CO 00 mil I I I CO LU liilLLL O O o o o CO O CO O 3 oc (0 CO LU o Q. z a CO £ 2 < ID 241 242 6.2 Identified Poilutant Problems in Nearshore Waters The Massachusetts Division of Water Pollution Control (DWPC, 1988) has published information on the environmental conditions of rivers and coastal areas of the state. This information is included in the DWPC (1988) Appendix HI - Basin/Segment Information, Commonwealth of Massachusetts Summary of Water Quality for 1988. The data presented by DWPC was examined as part of this study near the mouths of rivers (within 10 miles) and along the coast for the five drainage areas. This material is presented in Appendix D for 85 locations identified in these areas. A summary of the DWPC data for the 85 coastal and river mouth locations is provided in Table 106. High coliform bacteria levels was the most common problem identified, with 86% of the areas exhibiting these conditions. Shellfish bed closures were identified as problems for 21% of the areas and low dissolved oxygen was identified as a problem in 19% of the areas. Sediment contamination by metals and organic compounds was reported as a problem in 21% and 10.6% of the areas respectively. Eutrophication/nutrient problems were identified in 9.4% of the areas. A broad range of nonpoint and point sources was identified as sources of the problems in coastal areas and within river mouths (Appendix D). In many cases the source of the observed problems was unknown but in others the sources have been identified along with specific abatement needs. In many locations additional studies are recommended. The information presented in Appendix D underscores the importance of examining local sources of pollutants in assessing pollutant abatement needs. The material also indicates that there are a number of water quality problem areas along the Massachusetts coastline and within the mouths of estuaries and rivers. 243 (0 (0 a> Is (0 M (0 o V (0 CO E o o. 9 (0 B CO s < O O Is •2 UJ •» « c N £ 1' IS 0) o -I o 2 8 |< z o i < OH C s CO CO CNi CD «2 '«t f- ca CM CM ■»- -^ i 4C « e Q s o CO E Q I a X c o o CD O) « c & O S o t/i I o CO CM X<¥. CM CO g f~ CM R fill o o 244 6.3 Qualifications and Data Gaps This report provides estimates of loadings from a broad range of sources and at a range of spatial scales. However, several factors must be considered with regard to using the data presented in this report for risk assessment or risk management purposes: 1. There are many uncertainties associated with estimates. These stem from lack of data. In many cases we estimated loadings based on literature values or by extrapolating from similar systems. These estimates provide an overview of the relative magnitudes of sources and provide insights into the potential for discriminating among sources. However, the ranges in estimates are broad and thus, the estimates provided in this report should not be viewed as precise. 2. The fate and effects of chemicals or biological agents in the environment will depend on where and how the materials are introduced to the system. The loadings presented in this report differ in their "delivery systems". For example, atmospheric deposition is spread out over a large area and represents a large but diffuse source. On the other hand, an NPDES discharge is locahzed, as is the disposal of dredged material. The manner in which chemicals are introduced is especially important with regard to potential receptors. For example, atmospheric deposition will occur directly to the sea surface and may directly affect the sea surface microlayer. Subsurface diffusers from outfalls are typically located on or near the bottom and are initially mixed with seawater or river water upon discharge; groundwater discharges to nearshore regions and may be important sources at near shore local scales. Inasmuch as delivery systems are a critical part of exposure assessment for marine risk assessment, compansons of ma^tudes of sources should not be the sole basis for evaluating the relative importance of the sources. 3. Sources will vary somewhat based on seasonal factors. We identify two kinds of seasonal variability. First, there are sources that vary because of natural periodicity. Examples include river flow, nonpoint source runoff, and groundwater discharge. These vary both seasonally and as a result of storm events. TTius loads associated with these dischargers will be higher during certain times of the year and may be relatively "more important" at those times. Straight comparisons of aimual means does not provide a complete picture of the characteristics of these loads. In the case of stormwater runoff, short term events are especially important if there is the potential for short- term acute effects resulting from suspended sediment, nutrient, or chemical loads. Second, relatively constant sources such as the major NPDES outfalls will result in short-term and seasonal variability in receiving waters as a result in natural variations in the hydrodynamics of the receiving water. Thus, concentrations of materials discharged from an outfall may be higher in receiving waters during low river flow periods as 245 compared to high flow periods. This "apparent" temporal variability is important in evaluating the loadings from point sources. Data Gaps Many data gaps emerged during the course of this study. However, the occurrence of data gaps ooes not necessarily mean that studies are needed to address them. We suggest that data gaps be addressed as part of the risk assessment. This would involve (1) identifying the those marine resources that represent "receptors" ; (2) identifying the water quality conditions that are thought to pose hazards to the receptors; (3) quantifying the magnitudes of the exposure conditions; (4) assessing risks; and (5) identifying sources that may be contributing to the exposure conditions on a local, regional (drainage oasin), or bay-wide basis. Once this framework is in place and an initial effort has been made to assess risks, it should be possible to identify which "data gaps" are most important to address from a risk assessment and management basis. We have not attempted to generate an exhaustive list of data gaps. However, there are several areas that have emerged which should be considered on a preliminary basis: • Sources of PAHs to the marine environment - few data were available on PAHs. • Elevated levels of contaminants in sediments. Although heavily contaminated sediments have been identified in the report, and we have summarized available data, we have not determined how to consider them as sources. Resuspension from the sediments has not been considered in our comparison of relative magnitude of sources of contaminants to the bays. • Varying spatial scales. We assessed loads from sources that vary in spatial scale. However, we have not determined appropriate how the different spatial scales affect the fate and effects of various contaminants. • Oil spills. Oil spills and other infrequent, large-scale events were not considered. • Marine pump-out facilities. We did not consider pump-out facilities or other discharges from marinas. • Groundwater. Loadings of nitrogen from groundwater appears to be an important source of nutrients to embayments alon^ the snores of Cape Cod. Concentrations of nutrients should be measured within these embayments to verify this source. • Synthetic organic compounds. Few data are available on pesticides and other synthetic organic compounds, and their loads were not evaluated in this report. 246 APPENDIX A BIBLIOGRAPHY 247 POINT SOURCE REFERENCES TITLE; EPA Permit Compliance System, NPDES permitted Dischargers in Massachusetts. (Includes Effluent Data Statistics for 1988-1990 and Facility Reports . ) DATE; May 30, 1990 AUTHOR; A database maintained by United States Environmental Protection Agency DATA; Wastewater discharges to all surface waters in the Oonmonwealth, are regulated by permits v^ch co- issued by U.S. EPA and MA DEP in accordance with guidelines established by National Pollutant Discharge Elimination System. This system sets levels of effluent quality to be maintained by the POTWs and the industrial dischargers and designates implementation schedules for meeting effluent limits for discharges that contribute to water quality standards violations. NPDES permits are usually reviewed and reissued every five years. EPA Region I Resource Information Center performed a retrieval from PCS. This retrieval cc«sisted of two reports for each Massachusetts Major NPDES discharger; an effluent Statistical Surmary Report v^di sumnarizes effluent data on an annual basis for 1988, 1989, and 1990;and a Facility Informatioi Report, v^ch provides general permit informaticxi cai the facility (the discharger) . TITLE; Massachusetts River Basin Water Quality and Wastewater Discharge Data Survey Reports DATE; 1983-1990 depending on the year that river basin was surveyed. AUTHOR; Massachusetts Department of Environmental Protection, Division of Water Pollution Control DATA; The Massachusetts Divisicai of Vfeter Pollution Ccmtrol provides wastewater discharge data for streams and rivers. The wastewater discharge data are presented in survey reports for a designated river basin. Often these reports include data on the effluent discharge characteristics of the industrial and municipal discharges in that particular river basin. Data were available for 1986 to 1990 for sane NPDES outfalls depending hew often the drainage basin was surveyed. Typically, the Massachusetts Division of Water Pollution Control surveys report results fran grab sanples taken at vcirious outfalls within a particular River Basin. Massachusetts DEP Division of Water Polluticn Control periodically analyzes wastewater discharges for contaminants that are not specified in the NPDES outfell s permit in addition to typically miiHiitored pollutants . As part of duties and responsibilities of the Massachusetts Divisicxi of W^ter Pollutioi Control, periodic examinaticns of the water quality of various coastal v^aters, rivers, streams and ponds of the OoniroTwealth are required. The water quality surveys are conducted periodically within the various coastal river basins. Typically, the Massachusetts Division of Wciter Pollution Control surveys report results fran grab sanples taken within a peirticular River Basin. These surveys are used to develop state surface water standards and devise water quality management plans for a particular river basin. Water quality parameters v^ch are comoily analyzed for, are dissolved oxygen, pB, dissolved metals, alkalinity, biochemical oxygen demand, total phosphorus and total Kjeldahl Nitrogen, etc. TITLE: U.S. Geological Survey Gazetteers of Hydro logic Qiaracteristics of Streains in Massachusetts- Coastal River Basins of the Itorth Shore, Massachusetts Bay, South Shore, Buzzards Bay, and Merrimack River Basin DATE; 1984 ALTTHOR; United States Geological Survey lATA; Daily stream flew records are inaintained for all US Geological Service gaging stations and the data are available by the gage number. In 1984, the US Geological Service prepared three Gazetteers of hydrologic characteristics of Massachusetts streams categorized by Coastal River Basins in the South Shore and Buzzards Bay, Merrimack River Basin, and the North Shore in cooperation >fessachusetts Division of Vfeter Pollution Control. TITLE; Metal distribution in a major urban estuary (Bostoi Harbor) iirpacted by ocean disposal. Chapter 7 in Wolfe, D.A. and T.P. O Gcnnor (eds.)/ Urban Waste in Coastal Marine EInvironments , Volune 5 of Oceanic Processes in f-laririe BDllution. Kreiger, Malibar FL. DATE: 1988 AUTHOR: Wallace, G.T., J.H. Waugh and K.A. Gamer. C>ATA: Water quality saitples fran Mystic, Chelsea, Nepcnset, and Weymouth Fbre River. Collection of sanples were made at lev/ tide on 17 and 18 of August and at high tide 6 days later on 23 and 24 of August. Sanples were collected at a depth of 10 an and 13 feet. Water quality analysis included dissolved metals and trace □etals in particulate form. TITLE: Draft Final Report: Assessment of the Chemical Outiipositiai of The Pox Point CSO Effluent and Associated Subtidal and Intertidal Eiivironments : Analysis of CSO Effluents and Surficial Sediments for Trace Metals Prior to CSO ^t)dification and. Assessment of the Chemical Conposition of the Pox Point CSO Elf fluent and Associated Subtidal and Intertidal Envircranents : Analysis of Water Cblumn Sairples for Trace Metals Prior to CSO Modif icaticn . Massachusetts Department of Environmental Protectioi DATE; January 9, 1990 AUTHDR; Vfellace, G.T. et al. DATA; Water samples and surface sediment were collecteod at the mouth of tfepcxiset River (intertidal area). Concentrations of dissolved and particulate metal concentrations were determined. TITLE: Storet DATE: December 1990 ALflHDR; A database maintained by United States Environmental Protection Pqency (EPA) Office of Water DtYTA: STORET, located at EPA s National Computer Center in Research Triangle Park stores, retrieves, and analyzes v;ater quality information. STORET assists state and EPA officials in making pollution control decisiois. Itie retrieval consisted of water quality data which was collected at the mouths of the various coastal rivers of Massachusetts Bay. Data collected within the last 5 years \<.ere retrieved . TrTT.K: U.S. Geological Survey Vfeter Resources Data Massachusetts and FQiode Island Vfeter Annual Reports DAZE; 1986, 1987, 1988, 1989 ALTIHOR; United States Geological Survey DAZA; These annual reports include records of stage discharge, and water quality of streams. The individual gaging station informaticxi includes its location (latitude and longitude); drainage area; period of reocard; gage description; average disciharge; extremes for the period of discharge; extremes for period of record; extremes outside period of record; extremes for current year and monthy mean discharge values for that year. Additional water data are collected at various sites, not involved in the systonatic data-collection program and are published as miscellaneous discharge measurements. Water quality parameters included dissolved oxygen, tenperature, specific conductance cind pH. TITLE; National Estuarine Inventory Data Atlas DATE: January 1987 AUTHOR; National Oceanic and Atmospheric Administration, National Ocean Service DATA; A summary of land use from the USGS Land Use Data Analysis (LUDA) system and the USDA Soil Conservation Service 1082 National Resource Inventory (NRI) . LUDA provided the basic delineation of land-use types. NRI data were used to disaggregate the LUDA agricultural acreage into cropland and pasture, to distinguish between irrigated and nonirrigated cropland, and to determine the specific crops. NRI data were also used to subdivide forest land into areas with good and poor cover. Data were reported by USGS cataloging unit and by county. (Additional, unpublished information was provided by NOAA which compiled some data by cataloging unit x county.) TITLE: Ground-Water Resources of Cape Cod, Massachusetts. USGS Atlas HA-692 DATE: 1986 AUTHOR: LeBlanc, D. R. , J. H. Guswa, M. H. Frimpter, and C. J. Londguist. DATA: Recharge, precipitation and stream flow measured throughout Barnstable County. Contains the general flow system of groundwater for Cape Cod, broken up into six cells. TITLE: Eutrophication of Buttermilk Bay, a Cape Cod Coastal Emt>ayinent : Concentrations of Nutrients and Watershed Nutrient Budgets DATE: 1988 AUTHOR: Valiela, I., J. E. Costa DATA: Assessment of nutrient concentration and loading data into Buttermilk Bay. Nitrate and ammonia levels were measured in precipitation, groundwater, streams and surface runoff. Contributions from different input sources were calculated, such as septic system input. TITLE: Universal Atlas of Cape Cod & Southern Massachusetts DATE: 1988 AUTHOR: Universal Publishing Company DATA: Barnstable County town areas TITLE : none DATE: 1989 AUTHOR: Personal communication, Cape Cod Planning and Economic Development Commission DATA: Nitrogen application rates for golf courses. TITLE: Land Use Update for Cape Cod and the Islands with Area Statistics for 1951, 1971 and 1980 DATE: February 1984 AUTHOR: MacConnell, W. , D. Swartout, J. Stone DATA: Land use data broken down by town. Categories used include golf course and cranberry bog land use data for 1980. TITLE: None DATE: October 1990 AUTHOR: Phone conversations with town clerks and assessors. DATA: Number of residential units and winter (and estimated summer) to%m populations for the following Cape Cod towns: Sandwich, Barnstable, Yarmouth, Dennis, Brewster, Orleans, Eastham, Well fleet, Truro, Provincetown, and Bourne. TITLE: Mass-Balance Nitrate Model for Predicting the Effects of Land Use on Groundwater Quality in Municipal Wellhead Protection Areas. DATE: July, 1988 AUTHOR: Frimpter, M. H. , J. J. Donohue, IV, and M. V, Rapacz DATA: Estimates of nitrate leachability, average lawn size, and typical lawn fertilizer use. TITLE: The Relation of Ground-Water Quality to Housing Density, Cape Cod, Massachusetts DATE: 1986 AUTHOR: Perskey, J. H. DATA: Summary statistics of nitrate and ammonia groundwater samples from private wells throughout Barnstable County. These samples were taken between 1980 and 1984, some by Barnstable County Health Department, and the remainder by DEQE. The sampling may contain a slight bias, since some samples were taken in new housing developments, where septic systems have not affected groundwater yet. Still other samples are collected when an owner suspects a private well to be contaminated. TITLE; Ten- Year Bostcxi Harbor MDnitoring Program First Report March 1987 - July 1989 DATE: August 15, 1990 ?iJJBDR: New England Aquarium DATA; Water sanples were taken at the mouths of Chelsea River (depth of 12 m) , the Weymouth Pore River ( 7 m) and the Neponset River (7m). Total nitrogen and tjotal phosphorus coicentratiais, averaged for 15-17 samples taken over 2 years (1987-1988). Nitrogen was measured as amnonia, nitrate and nitrite. All three -were primarily measured as the dissolved inorganic ion. Total phosphorus was also measured. The data was reported in units of umoles/liter. For our purposes, «s converted the units to mg/ liter. TITLE; List of Confirmed Disposal Sites and Locations to be Investigated DATE; 1990 AUTHOR; Massachusetts Department of Environmental Protection Bureau of Waste Site Cleanup DATA; Includes an index of all 4,148 locations and disposal sites that have been identified in Massachusetts. The document identifies the 1,486 sites where releases of oil and/or hazardous substances have been confirmed. The list of both confirmed sites and sites to be investigated was used to identify sites within 500 ft of Massachusetts coastal waterways and the Merrimack River (to Pawtucket Dam) . TITLE; National Estuarine Inventory Data Atlas DATE; January 1987 AUTHOR; National Oceanic and Atmospheric Administration, National Ocean Service DATA; A summary of land use from the USGS Land Use Data Analysis (LUDA) system and the USDA Soil Conservation Service 1082 National Resource Inventory (NRI) . LUDA provided the basic delineation of land-use types. NRI data were used to disaggregate the LUDA agricultural acreage into cropland and pasture, to distinguish between irrigated and nonirrigated cropland, and to determine the specific crops. NRI data were also used to subdivide forest land into areas with good and poor cover. Data were reported by USGS cataloging unit and by county. (Additional, unpublished information was provided by NOAA which compiled some data by cataloging unit x county.) TITLE: National Coastal Pollutant Discharge Inventory (NCPDI) DATE; 1987 AUTHOR; A database and computational framework developed by the National Oceanic and Atmospheric Administration (NOAA) Strategic Assessment Branch. DATA; The NCPDI calculates runoff by separate methods for urban and nonurban land-use types. For urban land, runoff was calculated separately for areas with CSOs and areas without CSOs. For areas with CSOs, estimates of flow were based on the capacity of the wastewater treatment plant. Pollutant loads were calculated by multiplying total flow by typical concentrations of pollutants in CSOs. For areas without CSOs, daily precipitation was summed for each land-us type. The total annual precipitation for each land- use type was multiplied by a land-use-specific runoff coefficient, and these values were summed. Loads were calculated using mean urban runoff concentrations by land use compiled by the National Urban Runoff Program (NURP) (EPA, 1983) and Stenstrom et al. (1984) . Nonurban runoff was calculated using the Simulator Model for Water Resources for Urban Basins (SWRRB) which was developed by the U.S. Department of Agriculture Agricultural Research Service (USDA ARS) . ADOITIOMMi REFERENCES ARS. 1976. Control of Water Pollution form Cropland. Volume 1, A Manual for Guideline Development, and Volume 2, An Overview. U.S. Department of Agriculture. Agricultural Research Services. CH2MHill. 1989. Combined sewer overflow facilities plan. Prepared for the Massachusetts Water Resources Authority. EPA. 1983. Results of the National Urban Runoff Program. Executive Summary and 2 Volumes. U.S. Environmental Protection Agency. Monitoring and Data Support Division. NTIS Nos. PB84-185545, PB84-185552, PB84-185560. Forstner, U. and G.T.W. Wittmann. Metal pollution in the aquatic environment. With contributions by F. Prosi and J.H. van der Lierde. Second Revised Edition. Springer-Verlag. Helsel, D.R. 1978. Land Use Influences on Heavy Metals in an Urban Reservoir System. Department of Commerce. NTIS No. PB-296724. Hruby, T. , S. Cotter, and K. Barnes. 1988. Land use in the coastal drainage area in and around Boston Harbor. Prepared for the Massachusetts Audubon Society. Lorenz, W.D., Jr. 1978. Heavy Metal Partitioning in a Stream Receiving Urban Runoff. U.S. Department of Commerce. NTIS No. PB-296725. McElroy, A.D., S.Y. Chiu, J.W. Nebgen, A. Aleti, and E. Vandergrift. 1975. Water pollution from non-point sources. Water Res. 9: 675-681. Metcalf and Eddy. 1990. Facilities Plan. Prepared for the Massachusetts Water Resources Authority. Menzie-Cura Associates Inc. 1991. Boston Harbor: Estimates of loading. Prepared for the Massachusetts Water Resources Authority . Neff, J.M. Polycyclic aromatic hydrocarbons in the aquatic environment: Sources, fates, and biological effects. Applied Science Publishers Ltd. NOAA. 1987a. The National Coastal Pollutant Discharge Inventory. Urban Runoff Methods Document. National Oceanic and Atmospheric Administration. Strategic Assessments Branch . NOAA. 1987b. The National Coastal Pollutant Discharge Inventory. Nonurban Runoff Methods Document. National Oceanic and Atmospheric Administration. Strategic Assessments Branch. Shacklette, H.T. and J.G. Boerngen. 1984. Element Concentrations in Soils and Other Surficial Materials in the Coterminous United States. U.S. Geological Services Professional Paper 1270. Stenstrom, M. and others. 1984. Oil and Grease in Urban Stormwaters. J. Environmental Engineering 110:58-72. Alpert, D J. and P.K. Hopke. 1980. A quantitative determination of sources in the Boston urban aerosol. Atmos. Environ., 14: 1137-1146. Applied target transformation factor analysis to the data of Hopke et al. (1976) to apportion the observed aerosol concentrations to various sources. 90% or V was attributed to oil combustion and 90% of Pb and Br was attributed to auto emissions. Atlantic Environmental Services. 1988. Management of Manufactured Gas Plant Sites. Vol III. Risk Assessment. Provides a compilation of PAH concentration levels in air by compound and by environment (i.e., residential, rural, urban and specific locations and seasons). Connecticut Department of Environmental Protection. 1987. Report on Long Island Sound Study Activities (Draft)~III. Pollutant leadings to Long Island Sound, pp. 25-54. Connecticut Department of Environmental Protection, Water Compliance Unit. Estimated atmospheric loadings of nutrients and heavy metals to Long Island Sound based on local measurements and on the scaling, by area ratios, of loading estimates for Chesapeake Bay and the Great Lakes. DeWiest, F. 1978. Any factors influencing the dispersion and the transport of heavy hydrocarbons associated with airborne particles. Atmos. Environ., 12: 1705-1711. 44% of aerosol-bound fluoranthene was associated with particles > lum while no benzopyrenes were associated with that size fi-action; the cause mav be redistribution of volatile compounds to larger ambient particles, while the less volatile remain on the particles on which they were emitted. Doskey, P.V. and A-W. Andren. 1981. Modeling the flux of atmospheric polychlorinated biphenyls across the air/water mterface. Environ. Sci. Technol.. 15: 705-711. Aerosol deposition velocity of PCBs is estimated as 0.5 cm/s. Vapor phase, defined as fraction passing 0.3 um filter, may actually be bound to submicron particles. Other measurement difficulties: desorption of PCBs fi'om filter, adsorbents are less efficient for the more volatile congeners, usual analytical chemical methods are inadequate to identify and quantitate compounds. Fogg, T.R. and W.F. Fitzgerald. 1979. Mercuiy in southern New England coastal rains. J. Geophys. Res., 84: 6987-6989. Hg concentration in rain was measured at Centervdlle, MA (Cape Cod) during Sep/Oct 1975; notes the complex nature of scavenging of Hg by rain, that Hg behaves as a vapor rather than as an aerosol. Galloway, J.N. and D.M. Whelpdale. 1987. WATOX-86 overview and western North Atlantic Ocean S and N atmospheric budgets. Global Biogeochem. Cycles, 1(4): 261-281. Provides estimates of deposition velocity of NOx, N03, and HN03 and N concentration measured by aircraft 50 km east of Boston. GaUoway, J.N., D.M. Whelpdale and G.T.Wolff. 1984. The flux of S and N eastward from North America. Atmos. Environ., 18: 2595- 2607. NOx concentration for the east coast is reported as a function of latitude range. 248 Galloway, J.N., J.D. Thornton, S.A. Norton, H.L. Volchok and R.A.N. McLean. 1982. Trace metals in atmospheric deposition: A review and assessment- Atmos. Environ., 16: 1677-1700. Summaries of toxic metal concentration in wet deposition for urban and rural areas. No studies for Be, Se, Sn, Te, Tl. Gladney, E.S., W.H. Zoller, A,G. Jones and G.E. Gordon. 1974. Composition and size distributions of atmospheric particulate matter in the Boston area. Environ. Sci. Technol., 8: 551-559. Estimated the concentration of heavy metals in aerosols as a function of aerosol size for two locations in the Boston area, using instrumental neutron activation analysis. Graham, W.F. and R.A. Ehice. 1982. The atmospheric transport of phosphorus to the western North Atlantic. Atmos. Environ., lo: 1089-1097. Atmospheric phosphorus concentrations were measured off the eastern coast of North America, with one station located near Cape Cod. Concentration decayed exponentially with distance from the coast; this relationship was used to estimate a total deposition velocity which includes both wet and dry fallout Gschwend, P.M., and R.A- Hites. 1981. Fluxes of polycyclic aromatic hydrocarbons to marine and lacustrine sediments in the northeastern United States. Geochim. Cosmochim. Acta 45: 2359- 2367. PAH flux in Boston Harbor (off Calf Island, an urban area) and at remote areas off the coast of Maine was estimated based on concentrations in core samples and *210Pb activity. Flux reached a maximum in 1950 (5 to 10 times that in 1980), attri- buted to coal combustion. No temporal resolution for Boston Harbor due to bioturbation of core samples. Greater concentrations in urban areas is attributed to nmoff. Harvey, G.R. and W.G. Steinhauer. 1974. Atmospheric transport of Polychlorobiphenyls to the North Atlantic. Atmos. Environ., 8: 777-782. CB concentration in aerosols and in the vapor phase was measured at Vineyard Sound, Georges Bank, Bermuda, and the Grand Banks. Hites, R.A. and K. Bieman. 1972. Water pollution: Organic compounds in the Charles River, Bostoa Science, 178: 158-160. Water samples collected weekly from the Harvard Bridge were analyzed for naphthalene. Concentrations were successfully fitted to a runoff model which assumes an exponential dependence on rainfall. A likely source of this naphthalene is auto exhaust condensate washed directly from streets into the Charles River. Hopke, P.K., E.S. Gladney, G.E. Gordon, W.H. Zoller and AJB. Jones. 1976. The use of multivariate analysis to identify sources of selected elements in the Boston urban aerosol. Atmos.Environ., 10: 1015-1025. Concentration of trace metals in aerosols from samples collected in 1970 from locations around Boston Harbor were analyzed using instrumental neutron activation. Identified an incinerator in Somerville, auto emissions, and oil-fueled power plants in East Cambridge and Charlestown as sources. Jaffrezo, J.-L. and J.-L. Colin. 1988. Rain-aerosol coupling in urban area: Scavenging ratio measurements and identification of some transfer processes. Atmos. Environ., 22(5): 929-935. Washout ratios of Zn, Fe and other elements were calculated firom measurements taken in Paris. Power law relates concentration in rain to concentration in air. 249 Keeler, G J. and P J. Samson. 1989. Spatial representativeness of trace element ratios. Environ. Sci. Techno!., 23(11): 1358-1364. Quantitative transport bias analysis was used to infer the source areas for trace elements measured in aerosol samples taken at six locations in the northeastern United States during August, 1983. The nearest location to Massachusetts Bay was Narragansett, RI. Se and Zn were associated with coal combustion in the Midwest; Zn was also associated with incineration, smelters, and the iron-steel industry. V was associated with oil combustion in the northeast. As was associated with the Midwest and with smelters in the Sudbury region of Canada, Sb was associated with coal combustion, incineration and antimony roasting along the east coast firom Washington, D.C. to Connecticut. Kertesz-Saringer, M., E. Meszaros and T. Varkonyi. 1971. On the size distribution of benzo[a]pyrene containing particles in urban air. Atmos. Environ., 5: 429-431. Half of B[a]P measured in Budapest is in the size range < 03 um (median diameter); distribution may be bmiodal, extending to 12-14 um diameter. ligocki, M.P., C. Leuenberger and J.F. Pankow. 1985a, Trace organic compounds in rain-n. Gas scavenging of neutral organic compounds. Atmos. Environ., 19: 1609- 1617. Table of gas scavenging ratios is presented for PAHs. Ligocki, M.P., C. Leuenberger and J.F. Pankow. 1985b. Trace organic compounds in ram~in. Particle scavenging of neutral organic compounds. Atmos. Environ., 19: 1619-1626. Table of particle scavenging ratios is presented for PAHs. Lowenthal, D.H., K.A. Rahn, G.D. Thurston and J.D. Spengler. 1987. A cjuantitative assessment of source contributions to inhalable particulate matter pollution in metropolitan Boston. Discussion. Atmos. Environ., 21(1): 257-265. Discussion between L/R and T/S regarding apportionment of observed aerosol concentrations to sources. Mackay, D., S. Patterson, W.H. Schroeder. 1986. Model describing the rates of transfer processes of organic chemicals between atmosphere and water. Environ. Sci. TechnoL, 20: 810-816. Fugacity model for PCBs is presented which includes volatilization, absorption, dry deposition of particles, wet deposition (washout) and dissolution in rain. Observed washout ratios for PGBs are given. McMahon, Tj\- and P. Dennison. 1979. Empirical atmospheric deposition parameters-A survey. Atmos. Environ., 13: 571-585. Particle velocities and washout ratios for trace metals from Gatz (1973), Cawse (1974) and Chamberiain (1960). McVeety, B.D. and RA. Hites. 1988. Atmospheric deposition of polycyclic aromatic hydrocarbons to water surfaces: A mass balance approach. Atmos. Environ,, 22: 511-536. Estimates aerosol deposition velocity for PAHs based on measurements taken in the region of northern Lake Superior. Gives ratio of dry to wet deposition. 250 Measures, C.I., B. Grant, M. Khadem, D.S. Lee and J.M. Edraond. 1984. Distribution of Be, Al, Se, and Bi in surface waters of western North Atlantic and Caribbean. Earth Planet. Sci. Lett., 71: 1-12. Enrichment of Be in North Atlantic waters with respect to North Pacific appears dominated by fluvial sources; atmospheric deposition is negligible. Misanchuk, B.A-, D.R. Hastie and H.L Schiff. 1987. The distribution of nitrogen oxides off the east coast of North America, Global Biogeochem, Cycles, 1(4): 345- 355. Measured the concentration of NOx from an aircraft located 50 km east of Boston. National Atmospheric Deposition Program. 1989. Annual and seasonal deposition totals for Barnstable County, MA and Middlesex Coimty, MA. Personal communication, W. Gary Williams. Measurements of nutrient wet deposition by season and by year for the period 1981 through 1988. Nicholson, K,W. 1988. The dry deposition of small particles: A review of experimental measurements. Atmos. Environ., 22(12): 2653-2666. Notes an unaccceptable disagreement in the measured values of the depositional velocity of small particles. One confounding influence is high humidity. Rahn, KA. 1981. The Mn/V ratio as a tracer of large-scale sources of pollution aerosol for the arctic. Atmos. Environ., 15: 1457-1464. Measured concentration of total and non-crustal Mn and V at a rural site at Narragansett, RI. Rahn, KA. and D.H. Lowenthal. 1984. Elemental tracers of distant regional pollution aerosols. Science, 223: 132-139. Monitored remote site at Narragansett, RI for arsenic, antimony, selenium, non- crustal vanadium, zinc, non-crustal manganese and indium. Boston source aerosol was measured during favorable winds. Scudlark, J.R. and T.M. (Thurch. 1988. The atmospheric deposition of arsenic and association with acid precipitation. Atmos. Environ., 22(5): 937-943. As flux (dry and wet deposition) was measured at Lewes, DE. As identified as a tracer ot coal combustion. Sehmel, GJi. 1980. Particle and gas dry deposition: A review. Atmos. Environ., 14: 983-1011. Compilation of deposition velocities for an extensive list of elements. In many cases the range of Vd given is very large. Shiaris, M.P. and D. Jambard-Sweet. 1986. Polycyclic aromatic hydrocarbons in surficial sediments of Boston Harbor, Massachusetts, USA Mar. Pol. Bui., 17: 469- 472. Measured PAH concentration in core samples taken from 24 locations within and near to Boston Harbor. Areas of highest concentration were the Inner Harbor, and offshore of Logan Airport and Moon Island. Urban runoff is attributed as the source for the first two areas, sewage overflow for the third. Swackhamer, D.L^ B.M. McVeety and RA Hites. 1988. Deposition and evaporation of polychlorobiphenyl congeners to and from Sisldwit Lake, Isle Royale, Lake Supenor. Environ. Sd. Technol., 22: 664-672. 251 Measured concentration of PCBs in air, rain, snow, water and sediments during winter and summer. Dry deposition velocity was given. Wet deposition is 3X greater than dry, dominated by particle washout. PCBs are associated with submicron particles in air. Thurston, G.D. and J.D. Spender. 1985. A quantitative assessment of source contributions to inhalable particulate matter pollution in metTopolitan Boston. Atmos. Environ., 19: 9-25. Measurements of trace metals in Watertown, MA for fine (<2.5um) and coarse (2.5 to 15um) fractions. Absolute Principal Component Scores plus regression were used to estimate sources: Soil (Si, Fe, Ca); Auto emissions (Br, Fb); Coal combustion, non-local (Se, S); Residual oil (Ni, V); Salt (CI). Se is associated with As, traceable to Ohio Valley. U.S. Environmental Protection Agency. 1990. Aerometric Information Retrieval System, Air Quality Subsystem, Quick Lx>ok Report. Personal communication, Ms. Bonnie Potocki. Data table of concentration of Benzo[a]pyrene measured at locations in the Boston area. Wallace, G.T. Jr., G. Hoffinan, and R.A. Duce. 1977. The influence of organic matter and atmospheric deposition on the particulate trace metal concentration of northwest Atlantic surface seawater. Mar. Chem., 5: 143-170. Major mass of Cu, Zn, Pb, Cd is associated with particles of < lum. A single estimate of dry deposition velocity is provided for these elements. Walsh, P.R., R A. Duce and J.L. Fasching. 1979. Tropospheric arsenic over marine and continental regions. J. Geophys. Res., 84: 1710-1718. Measurements at Providence (urban), 1.7(1.7) ng/m3 particulate and 0.21(0.23) ng/m3 vapor; Narragansett (rural coast); and Bermuda, Oahu, Samoa (marine). (Sn't distinguish natural and anthropomorphic sources. Windsor, J.G. and RA.Hites. 1979. Poly^clic aromatic hydrocarbons in Gulf of Maine sediments and Nova Scotia soils. Geochem. Cosmochim. Acta, 43: 27-33. Sediment samples collected along a line trendingNE from Boston Harbor showed an exponential decrease in PAH concentration. The source of PAH in concentrations >50 ppb is attributed to urban runoff of large particulates which settle rapidly. Low level concentrations are due to long- range aeolian transport of smaller particulates. Size distribution of PAH aerosols was noted to be bimodal, with modes at 1 um and > 10 van. Whitby, K.T., R.E. Charlson, W.E. Wilson and R.K. Stevens. 1974. The size of suspended particle matter in air. Science, 183: 1098- 1100. Discussion. Whitby et al. (1972^ showed atmospheric aerosols to have a bimodal, rather than a unimodal, mass distribution. One mode is < lum, another in the 5 to 15 um range; each mode has different sources. Wood, J.M. 1974. Biological cycles for toxic elements in the environment Science, 183: 1049-1052. Identified toxic or potentially toxic metals. Zoller, W.H., and G.E. Gordon. 1970. Instrumental neutron activation analysis of atmospheric pollutants utilizing Ge(Li) gamma- ray detectors. Analyt Chem., 42: 257-265. 252 Concentration of trace elements in aerosols was analyzed in samples collected in Cambridge, Boston, and Wellesley. V was observed in very high concentrations, perhaps resulting from the burning of residual oil. 2S3 APPENDIX B SEDIMENT DATA FOR MASSACHUSETTS BAYS KJorihfihofo GLOUCESTER HARBOR, personal communication Dr. Alan Michael State Stall Sed Class 1 1 Arsenic 2.10 2.80 Cadmium 0.48 0.28 Chromium 0.22 11.00 Copper 10.00 11.00 Lead 18.00 8.60 Mercury 0.091 0.032 Nickel 6.70 5i0 Zinc 35.00 19.00 All measurements in mg/Kg wet weight SALEM HARBOR from Tier II - Chemical Evaluation Report 1 991 BW1 BW2 BW3 BW4 BW6 S2 S3 S6 Sed Class 3 1 1 1 1 3 3 3 Arsenic 12.00 6.00 1.00 3.00 3.00 4.00 5.00 7.00 Cadmium 2.80 0.60 0.04 0.04 0.60 0.05 2.00 2.20 Chromium 87.00 36.00 16.00 9.00 14.00 320.00 660.00 770.00 Copper 170.00 11.00 21.00 4.00 5.00 31.00 64.00 110.00 Lead 520.00 16.00 95.00 4.00 6.00 59.00 110.00 260.00 Mercury 2.40 0.04 0.12 0.04 0.04 0.25 0.54 1.00 Nickel 24.00 21.00 8.00 7.00 12.00 16.00 2.30 24.00 Zinc 340.00 50.00 69.00 14.00 21.00 65.00 110.00 200.00 Total PAH 32.00 0.00 4.60 0.30 0.70 4.90 7.60 22.60 Total PCS BDL BDL BDL BDL BDL BDL BDL BDL All data in Ug/g dry weight BDL - Below Detection Limits. NATIONAL STATUS AND TRENDS PR0GRAM,1 98? Rne sediments STATION SAL CASI Sed dass 3 3 Ag 2.83 0.32 As 19.24 20.91 Cd 9.79 0.51 Ct 3373.98 103.42 Cu 125.67 33.38 Hg 1.68 0.25 Ni 46.03 41.79 Pb 260.1 108.9 Sb 5 7.03 Se 1.48 0 Sn 19.14 8.61 Zn 342 155 METALS IN ug/g DRY WEIGHT Pagel North Shore DISTRIBUTION OF POLiUTED MATERIALS IN MASS BAY, NE A, 1 97B Stations CIA aB C2A C2B C3A 038 05A C5B sed dass 2 3 3 2 3 3 3 2 Cd 0.89 1.05 1.52 1.88 2.25 2.82 0.65 0.69 Cr 73 87 382 157 1042 545 96 68 Cu 32.8 34.3 18.3 16.3 26.7 55.2 36.7 20.4 Hg 98 227 203 146 150 135 184 58 Ni 9.8 8.2 2 9.2 11.9 36 38.7 16 Pb 0.55 55 45 23 71 76 35 21 Zn 78 70 42 34 117 161 113 44 METALS IN ppm dry -weight PCBppb 22.5 16.1 23 6.6 26.1 30.5 21.6 22 Page2 Myeiic NATIONAL STATUS AND TRENDS PROGRAMS 98J Fine sediments STATION BHDI Sed dass 2 Ag 4.64 As 11.62 Cd 1.68 Cr 284.99 Cu 155.27 Hg 1.05 Ni 41.23 Pb 166.44 Sb 10.01 Se 0.87 Sn 22.56 Zn 213 METALS IN ug/g DRY WEIGHT ORGANICDATA IN NQ/G DRY WEIGHT Tot DDT 36.59 Tot Chip 17.88 TotPCB 357.24 Tot PAH 6546 BOSTON HARBOR SURVEY, MASS DEP, 1 990 1987 SURVEY 1986 SURVEY 1985 SURVEY Station BH01 Station BH01 BH01A Station BH01 sed dass 3 sed dass 2 3 3 Al 10800 Ag 1.6 1.2 Ag 1 Cd 2.3 Cd 2 5.2 As 12 Cr 140 Cr 52 156 Cd 1 Cu 320 Cu 85 400 Cr 40 Ni 24 Hg 0.36 1.176 Cu 90 Pb 220 Ni 19 60 Ni 17 2n 360 Pb 172 440 Pb 230 Zn 212 640 Zn 235 METALS IN mgrtcgDPY WEIGHT TotPCB 0.44 TotPCB 1.04 2.98 Tot PAH 67.54 TotPAH 54.51 8.26 TotPCB 0.63 ORGANICS IN ug/g DRY WEIGHT ORGANIC POUHTAI^ BIOGEOCHEMISTRY STUDIES, BATTEU£,1 984 Stations 6H-2 Total PAH (ug/g) 880 Total PC8(ng/g) 139 Pagel MysHc APPUCATION FOR WAIVER 301 (hi NUT & DEER ISUNDS,1984, METCAU & EDDY FROM DWPC 1972 Station 96 97 sed dass 2 3 Cd 1.5 3.2 Cr 68 38 Cu 63 170 Hg 1.45 1.2 Ni 24 38 Pb 140 640 Zn 130 650 Units mg/kg dry weight SAMPUNG,1979 Sampling '82 Station 1 4 6 7 Stations DIA DIG DIB DGA 3 2 2 2 sed dass 1 2 2 2 Ag 13.7 7.8 4.7 7.3 Ag 0.1 001 0.1 1.6 Od 11.1 4.5 3.5 3.8 An 2 2 2 3 0 0.257 0.292 0.224 0.21 As 4 3 4 4 Cu 0.367 0.134 0.116 0.139 Be 5.1 3.9 3.1 8.1 Hg 4.9 5.9 8 4.7 Cd 0.6 4.1 3.5 2.6 Pb 0.7 0.123 0.115 0.122 Cr 35.9 101 84 216 Zn 0.803 0.233 0.194 0.216 Cu 29 331 259 142 Units mg/g dry weight Hg 0.45 1.2 0.63 0.82 Station 1 6 7Ni 9.9 19.5 25.5 269 PCBs(ng/g) 889 137 94 Pb 2 69 87 3 Se 2 2 2 3 Th 3 3 3 5 Zn 67.4 224 190 207 Units ug/g SAMPUNG'8^ 1 Stations 3 4 5 sed dass 2 3 2 Ag 0.4 1.3 0.2 An 7.7 26 4.8 As 11.5 38.9 7.2 Be 6.9 26.4 2.2 Cd 1.5 10.4 2.6 Cr 188 852 71.4 Cu 92.7 397 129 Hg 1.24 4.5 0.49 Ni 23 87 11.3 Pb 77 130 72 . Se 1.9 6.5 1.2 Th 15.3 51.9 9.6 Zn 156 758 281 IMsug/g Page2 Mystic htrsnc, MALDEN AND ISLAND END RIVERS, DEQE Metals in ug/g dry weight STATION 28 23 44 39 41 34 seddass 3 3 3 3 3 3 AntJnf)ony 6.9 13 3.9 6.8 8.1 7 Arsenic 27 340 2.7 44 25 12 Berylliunf) 0.57 1.1 0.32 0.57 0.67 0.58 Cadmium 11 12 1.2 9.5 6.5 2.1 Chromium 97 150 9.4 140 49 34 Copper 150 200 24 250 150 55 Lead 270 390 130 220 380 350 Mercury 0.41 0.777 0.121 0.982 0.605 0.244 Nickel 45 64 13 77 37 23 Selenium 6.1 11 3.2 5.8 6.5 6 Silver 1.1 2.2 0.65 1.1 6.3 1.2 Thallium 0.61 1.1 0.32 0.58 0.57 0.6 Zinc 850 1700 95 430 870 250 TOTPAH ug/kg 23000 2000 68000 44000 463000 35000 PCB ug/g 6.7 4.3 1.6 1.8 0.3 STATION 6 5 4 7 17 3 seddass 3 3 3 3 3 3 Antimony 9.6 4.9 7.4 14 15 6.1 Arsenic 26 37 25 26 130 26 Beryllium 0.8 0.41 0.62 1.2 1.2 0.91 Cadmium 8.5 5.8 3.9 16 12 4.4 Chromium 96 61 70 130 96 72 Copper 330 84 120 740 560 67 Lead 790 89 170 1400 350 160 Mercury 1.78 1.02 0.892 1.71 1.25 0.521 Nid^l 35 18 25 56 110 0.2 Selenium 2.6 1 1.2 2.4 2.9 1.2 Silver 5 0.82 1.2 7.7 7 1 Thallium 1.6 0.81 1.2 2.4 2.4 1 Zinc 630 310 230 1400 660 250 TOTPAH ugrt^g 1610000 4000 42000 789000 561000 110000 PCB ug/g 3.3 NO 0.66 4.7 2.2 1.1 Page3 Mystc TRACE METAL ANALYSIS OF BOSTON HARBOR WATER SEDIMEMTSJ 972 Surface concentrations in ppnr). DF2 DF3 DF4 3 3 OUTER HARBOR STATION DF1 sed dass 3 Cadmium 13.4 Chromium 165 CobaK 11 Copper 108 Lead 102 Mercury 0.9 Molybden 3.5 Nickel 25 Vanadium 49 3.3 2.5 Zinc 171 DF5 DF6 IH2 IH1 IH3 3 2 3 3 0 J J 7.6 08 48 10 33 78 402 109 179 144 174 18 29 9 13.9 13.6 6.8 206 63 105 310 226 357 151 44 91 675 161 411 2.4 03 4 1.5 0.92 233 9.4 4.7 9 12.3 5 75 38 65 23 45 44 87 111 74 52 510 416 1110 400 126 188 1230 445 985 Page4 Charla« NATIONAL STATUS AND TRENDS PROGRAM,! 988 Fine sediments STATION BOS Sed dass 3 Ag 11.65 As 16.98 Cd 3.24 Or 419.32 Cu 256.13 Hg 1.7 Ni 53.9 Pb 207.37 Sb 12.32 Se 1.29 Sn 42.86 Zn 452 METALS in ug/g DRY WEIGHT ORGANICS in ng/g DRYWEIGKT Tot DDT 34 TotChP 47.87 TotPCB 11218.76 Tot PAH 57778 BOSTON HARBOR SURVEY, MASS DEP, 1990 1986 SURVEY 1985 SURVEY Station BH04A Station BH04 BH05 i 1 3H06 sed dass 3 3 . 3 3 Ag 1.2 Ag 1.5 2 1.5 Cd 4.4 Ai 21100 Cr 220 As 9.3 19 22 Cu 296 cd 8 6 2.5 Hg 1.288 0 115 245 210 Ni 0.39 Cu 295 265 160 Pb 300 Ni 40 38 30 Zn 392 Pb 250 305 110 Zn 550 330 220 METALS IN mq/kq DRY WEIGHT ORGANICS in ug/g DRY WEIGHT 05-S ( )6-S Tot PCS 2.57 TotPCB 7 0.68 0.27 Tot PAH 10.83 Tot PAH 16.6 24 ORGANIC POUUTAKT BIOGEOCHEMISTRY STUDIES, BATTEUf ,1 984 Stations BH-1 Total PAH (ug/g) 2.7 Total PCS (ng/gj 70.4 Pagel Chartes APPUCATION FOR WAIVER 301 (hL NLTT & DEER ISL^NDS,1 984, METCALf & EDDY HHOM DWPC 1 972 SAMPUNG 79, M&E. SAMPUNG '84 Station 98 Station 2 3 Stations 1 2 sed class 3 sed dass 3 2 sed dass 3 3 Cd 6Ag 9.2 0.133 Ag 3.5 1.9 Cr 240 Cd 8.8 0.081 An 6 6.4 Cu 220 Cr 0.418 0.16 As 8.8 9.6 Hg 2.2 Cu 0.339 0.084 Be 8.85 8.9 Ni 37 Hg 6.3 7.5 Cd 5.3 3.2 Pb 260 Pb 0.402 2.8 Cr 350 274 Zn 350 Zn 0.506 6.8 Cu 287 188 Units mg/kg dry weight Units mg/g dry weight Hg 1.79 1.58 Ni 41.5 31.1 Pb 235 128 Se 1.5 1.6 Th 12 12.8 Zn 406 252 UNITS ug/g DRY WEIGHT PCBsfng/ 414 170 POST DREDGING STUDIES ATTHE CHARLES RIVERDAM SrTE,^EA 1973 Station 1 2 3 4 5 6 sed dass 3 3 1 3 3 3 Cd 2.4 20.1 1.1 4.1 4 4.8 Cu 279 449.2 74.3 369.2 299.5 252.3 Hg 0.99 2.84 0.48 1.59 2 3.52 Pb 1051.8 1024 58.4 465.6 410.6 409.3 Zn 497.8 1189.4 95.4 416.6 751.1 628.3 Units ppm dry weight COI^AMINANT LEVELS IN BOSTON HARBOR, ZDANOWICZ STATION BT1 BT2 sed dass 1 2 Cadmium 0.95 3.31 Chromium 43 227 Copper 37.6 134 Lead 37.8 107 All measurements in ug/g dry weight Page 2 Charles PROGRESS REPORT BOSTON HARBOR STUDY OF SOURCES.,1 990 Data Pram Core X, Inner Harbor. Date in ug/g. sed dass 3 Aluminum 69.34 From top .5 cm. Cadmium 2.27 Chromium 325.46 Copper 284.03 Iron 49.17 mg/g Lead 485.94 Manganese 420.02 mg/g Nickel 48.11 Zinc 345.92 TRACE METALANALYSIS OF BOSTON HARBOR WATER SEDIh€NTS,1 972 STATION IH4 sed dass 3 Cadmium 29 Chromium 116 CobaR 17.5 Copper 494 Lead 595 Mercury 5.7 Molybdenur 14 Nid^l 75 Vanadium 600 Zinc 1360 Page 3 Neponset NATIONAL STATUS AND TRENDS WOGRAM,! 988 STATION BHDB Sed dass 2 Ag As 16.71 Cd 1.87 Cr 265.25 Cu 157.39 Hg 1.09 Ni 40.28 Pb 175.8 Sb 9.43 Se 0.7 Sn 20.87 Zn 242 METALS IN ug/g DRY WEIGHT ORGANIC DATA IN NGA3 DRY WEIGHT Tot DDT 62.39 Tot Chip 31.06 TotPCB 876.67 Tot PAH 8901 BOSTON HARBOR SURVEY, MASS DEP, 1 990 1987 SURVEY 1986 SURVEY 1985SURVE>' Station BH10A 6H10B 6H10S Station BH09 BHIOA BHIOB Station BHK ) sed dass 3 2 3 sed dass 2 2 3 2 Al 10400 7700 6400 Ag 2.4 1.6 1.6 Ag 2 Cd 2.2 2.9 ICd 1.6 2.8 2.8 As 12 Cr 150 140 70 Cr 100 132 92 Cd 2 Cu 540 130 150 Cu 96 128 96 Cr 124 Ni 22 16 15 Hg 0.784 0.856 0.44 Cu 128 Pb 180 200 420 Ni 19 20 17 Hg 1.3 Zn 330 260 130 Pb 120 196 204 Ni 22 Zn 148 220 212 Pb 160 METALS IN mgfl(g DRY SNtlGHT Zn 192 TotPCB 0.85 2.4 1.12 TotPCB 0.83 0.86 5.47 TotPCB 1.7 PCB'S IN ug/g DRY WEIGHT Tot PAH 1.16 ^47 5.82 Tot PAH 3.43 Page1 Neponset AFRICATION FOR WAIVER 301 (hi NUT & DEER ISLANDS,1 984, METCALF & EDDY F TOM DWPC 1972 FROM DWPC 1972 Sta&on 153 154 155 156 157 158 159 160 161 3 3 3 3 3 2 1 3 3 Cd 4.1 1.8 1.4 2.2 2.2 1.7 0.3 6.8 7.1 Cr 220 48 160 190 130 69 14 230 210 Cu 170 38 120 150 120 82 14 180 180 Hg 3 1.1 1.8 2.1 1.9 1.2 0.14 2.3 2.4 Ni 46 20 38 44 38 25 12 47 43 Pb 200 58 170 170 150 150 34 160 330 Zn 340 490 220 750 210 300 190 280 290 Units mg/kg dry weight Station 162 163 164 165 166 sed dass 3 3 3 3 3 Cd 3.1 2.4 3.6 9.3 6.9 Cr 130 38 95 190 66 Cu 110 92 80 150 270 Hg 2.1 0.95 1.5 2.7 1 Ni 35 17 27 38 25 Pb 160 400 120 220 1000 Zn 180 240 170 270 570 COM 79 Survey Station A B C D E sed dass 3 1 33 1 Cd 32 22 2 Cr 79.1 72 73110 36 Cu 123 59.5 64115 31.5 Hg 0.75 0.34 1.6 0.78 0.36 Ni 27 23 23 37 24 Pb 280 96 100 200 78 Zn 220 84.5 75195 80 Units mg/kg dry weigtrt Station F G H J K L M sed dass 3 3 33 3 3 3 Cd 43 59 8 9 7 Cr 230 205 170 96 155 13 260 Cu 210175 170 255 190 200 230 Hg 1.5 1.3 0.65 1.5 1.3 1.7 Ni 45 43 8156 40 39 52 Pb 300 280 280 1950 500 260 320 Zn 300 240 405 830 345 250 265 Units mg/kg dry weight Page 2 Neponset SAMRJNG,1979 Stabon 11 17 24 25 29 sed dass 2 2 1 1 2 Ag 5.1 4.6 7 3.1 9.2 Cd 1.4 31 1.8 1.3 2.16 Cr 0.184 0.129 0.07 0.068 0.113 Cu 0.121 0.102 0.057 0.046 0.087 Hg 4.7 5 3.7 1.7 4.53 Pb 0.144 0.144 0.059 0.065 0.125 Zn 0.173 0.198 0.105 0.085 0.171 Units mg/g dry weight Station 11 PC8s(ng/ 243 SAMPLING'S^ 1 Stations 12 13 14 15 16 17 18 sed dass 2 1 2 2 2 3 2 Ag 0.1 0.1 0.1 0.2 0.3 2.4 0.3 An 2 2 1 2 6 7.9 3 As 3.2 2.4 2 4.2 8 11.9 2.2 Be 6.58 5 5.08 7.21 9.29 14.9 8.94 Cd 1.4 0.4 0.9 0.6 1.4 4 1.1 0 167 62.6 98.5 73.2 217 358 20.3 Cu 87.9 39.1 67.9 50.6 154 292 126 Hg 0.76 0.4 1 0.57 0.56 2.64 1.45 Ni 19.9 12.2 17.6 17.7 28.4 46.2 24.8 Pb 92 55 11 73 142 237 142 Se 0.6 0.5 0.4 0.6 1.4 2 0.8 Th 5 4 3 5 11 15.8 6 Zn 146 79.2 140 105 214 427 177 Units ug/g ASSESMENTTOFTHE CHEMICAL COMPOSmON OFTHE FOXPOINT„,1990 STATION Savin Hill Cove Thonfipson Island Neponset River sed dass 3 3 2 Mir Max Min Max Mir 1 Max Aluminum 51.6 83.5 58.3 88.6 52.8 91.6 CadnrHum 1.96 2.6 0.43 4.55 0.69 1.4 Chromium 196.7 247.9 63.4 308.7 64.8 121.9 Copper 163.5 206.3 43.2 257.9 32.3 76.6 Iron 39.2 55.4 33.5 45 23.2 34.9 Lead 202.7 279.6 63 234.7 66.5 121.4 Mangane* 0.521 0981 0.415 0.796 0.433 0.58 Nid(el 31.1 42.9 21.9 41.9 15.7 28.4 Zinc 213.1 338.8 42 279.6 34.4 210.2 Min max data expressed in ug/g for top .5cm of core. Page 3 Neponset TRACE METAL ANALYSIS OF BOSTON HARBOR WATER SEDIMENTS,! 972 OLfTER HARBOR Surface concentrations in ppm. STATION Ul T12 TL3 U4 TL5£ I T15B TL6 sed dass 3 3 3 3 3 3 3TL8 QB1 Cadmium 5 5.4 2 3 Chromium 145 141 229 3.6 11.2 Cobalt 15 12 92 433 Copper 117 129 265 12 37 Lead 116 199 153 35 363 Mercury 2.8 4.1 3.5 2.3 1.8 1.8 3.8 52 256 Moiybden 8 4.6 6.7 1.4 3.9 Nickel 31 9 38 8.9 4.9 Vanadium 57 40 38 36 57 Zinc 258 427 336 79 205 48 455 STATK)N QB2 Q63 QB4 Q65 DB1 0B2 DB3 sed dass 2 3 2 2 2 3 2DB4 Cadmium 2.4 2.7 1 2.9 2.7 14.9 2 Chromium 4 312 254 57 122 125 2.7 Cobalt 0.2 24 1 18 9 15 19 Copper 48 212 57 35 120 88 4 Lead 20 241 72 56 60 128 24 Mercury 1.1 3.5 0.9 0.8 0.2 1.2 21 Moiybden 4.8 8 4 7.3 3.9 1.9 0.5 Nid' weight Hg 0.59 0.46 0.92 Hg 1.1 Ni 7.3 10.4 14.9 Ni 224 Pb 2 2 2Pb 94 Se 2 2 2Se 08 Th 3 4 4Th 6.3 Station 14 Zn 53.7 94 82.4 Zn 183 PCBs{ng/ 365 Units ug/g TRACE METAL ANALYSIS OF BOSTON HARBOR WATER SEDIMENTS,1 972 STATION 01 1 012 013 014 015 016 017 seddass 3 3 3 2 2 2 1 Cadmium 7.9 2.6 2.1 4.8 4.8 2 Chromium 167 31 109 108 150 256 26 Cobalt 10 12 8 27 28 17 Copper 360 39 70 48 73 116 16 Lead 112 82 89 87 42 168 18 Mercury 2.3 2 1.6 0.4 0.8 1.1 0.3 Molybden 0.5 10.2 11.4 1.9 1.8 3 0.8 Nid^el 40 25 8 18 27 44 32 Vanadium 48 31 56 37 43 80 25 Zinc 200 188 191 107 157 218 63 * Pagel Bay STTE EVALUATION STUDIES OFTHE MASS BAY DISPOSAL SFTE, U.S. ARMY CORPS OF ENGINEERS 1 988 Station REF REF OF ON ON JUN85 JAN86 SEP85 SEP85 SEP85 seddass 2 2 2 2 2 As 11.3 12.1 10 12 13.3 Cd 3 3 3 4 3 Or 70.3 84 72 134 102 Cu 18 27 23 75 84 Hg 0.1 0.01 Ni 33.3 24 24 31 26 Pb 41.3 97 58 151 161 Zn 95.3 110 105 233 206 METALS IN ppm dry weight PAH,ppm 3 PCBppb 75 48 495 1240 ' 329 DISTRBUnON OF POLLLJTED MATERIALS IN MASS BAY, NE A, 1 976 Offshore Stations Stations 1A IB 2A 2B 3A 3B 4A 4B 5A 5B sed dass 2 1 1 2 2 2 2 2 3 3 Cd 0.45 0.37 0.29 0.45 0.95 1.21 0.46 3.59 0.34 0.65 Cr 0.41 35 15 17 48 82 29 49 64 122 Cu 7.2 8.1 2.6 3.4 14.2 19.8 4 6.1 10 14.3 Hg 112 23 76 85 105 57 102 319 310 Ni 13.5 13.4 8.1 7.2 21.2 24.3 10.6 12.5 22.4 Pb 0.18 16 9 10 31 40 14 21 36 29 Zn 43 24 20 162 95 41 42 101 METALS IN ppm dry weight PCBppb 2.4 2.7 02 4.4 1.8 2.7 0.3 2.3 3.3 1.8 Stations 6A 66 8A 8B 9A 9B 10A 10B 11A 11B SedGass 1 1 3 3 3 3 2 3 3 3 Cd 0.31 0.29 1.08 1.01 1.99 1.03 0.28 1.19 0.49 Cr 10 28 121 82 126 55 97 93 85 69 Cu 1.9 4.9 29.1 16.2 27 16.3 14.9 36 17.9 16.2 Hg 22 457 196 172 288 89 264 162 177 Ni 8.1 9.9 32.4 11.9 26.8 44.5 14 55.9 34.7 17.8 Pb 6 12 50.03 71.92 44.27 73.49 34 49 51 91 Zn 26 28 2495 51 108 216 97 110 541 68 METALS IN ppm dry weight PCBppb 1 3.1 3.6 2.1 1.2 0.32 1.3 2.3 4.7 7 Pagel Bay Stations 12A 12B 13A 13B 14A 14B 15A seddass 3 2 1 3 2 3 Cd 0.12 0.19 2.14 0.6 0.38 0.9 Cr 94 91 104 83 26 15 Cu 21 10.4 24.5 19 114 14.6 Hg 323 107 132 409 111 167 Ni 29.6 31.3 45.6 35.6 28.9 15.4 Pb 38 44 65 106 33 14 Zn 119 80 110 116 332 304 METALS IN ppm dry weight PCBppb 11.8 11.8 5.8 15.2 0.9 1.1 15B 16A 16B 2 37 11.5 50 16.7 16 68 0.9 2 0.29 46 9.8 121 23.1 46 245 1.4 017 74 157 168 8.4 35 20 18 3 0.64 51 99 236 144 46 84 15.1 Stations 17A 17B 18A 18B I9A 19B 20A 20B 21 A 21 B sed dass 3 3 3 2 1 3 3 2 3 2 Cd 1.05 0.47 1.13 1.77 0.57 1.66 0.26 0.46 045 072 0 105 39 73 92 71 61 70 74 91 87 Cu 20.6 9.9 19.8 21.1 14.2 9.9 15.9 15.5 23.6 m Hg 262 294 151 71 33 568 341 125 161 126 Ni 29.4 15.9 27.9 46.1 ??1 40.1 15.7 17.9 38.8 29.1 Pb 71 24 50 61 43 34 52 67 149 38 Zn 146 23 131 131 96 108 29 123 172 151 METALS IN ppm dry weight PCBppb 3.1 0.9 2.1 2.1 3.3 6.5 7.9 12.8 Stations 22A 22B 23A 23B 24A 24B 25A 25B 26A 288 sed dass 3 3 2 3 3 2 2 2 3 2 Cd 0.13 0.79 0.66 0.32 0.14 0.74 0.45 0.38 0.35 0.43 Cr 57 90 47 46 45 45 59 18 76 32 Cu 20.3 19.1 13.7 10.3 10.5 17.5 9.6 7.2 16.9 39 Hg 4240 544 130 333 273 101 129 109 108 88 Ni 32.4 26.7 23.9 19.9 14.8 21 14 9.3 22.3 5.5 Pb 38 35 32 28 22 38 41 16 41 22 Zn 88 106 78 189 62 65 51 103 3131 10 METALS IN ppm dry weight PCBppb 10.7 17.7 Ul 1.6 3.3 13.9 2.5 0.8 0.31 Stations 27A 27B 28A 28B 29A 29B 30A 30B 31 A 31B sed dass 2 1 3 2 2 2 3 2 3 3 Cd 0.69 0.54 0.79 0.94 0.76 0.1 0.1 0.59 097 Cr 42 41 48 41 66 44 37 48 66 58 Cu 18.4 16.4 8.5 9.6 16.5 10.7 10 1^5 163 15-2 Hg 80 42 186 80 103 94 159 53 160 172 Ni 15.8 16.8 15.3 13.3 225 19.3 15 11i 32 23.5 Pb 37 27 29 38 41 25 31 35 62 34 Zn 48 78 124 60 195 248 110 96 271 270 METALS IN ppm dry weight PCBppb 0.7 4.9 0.37 5.6 2.1 11 3.5 7 P8ge2 Bay Stations 32A 32B seddass 3 - 3 Cd 1.3 0.93 Cr 0.73 66 Cu 14.6 21.7 Hg 234 156 Ni 24.6 26.3 Pb 52 45 Zn 390 324 METALS IN ppm dry weight PCBppb 4.3 4.8 ORGANIC POLLUTANT BiOGEOCHEMISTFY STUDIES, BATTELLE,1 984 Stations BH-7 MB-1 MB^ MB^ MM MB-7 MM MB-9 MB-10 Total PAH (ug/g) 0.8 14.3 2.3 0.6 3.5 1.3 0.3 0.2 1.5 Total PCB(ng/g) 14.5 39.3 21 4.6 82.9 24.7 23.4 2.3 25.3 Stations MB-11 MB-13 MB-14 MB-16 CC-1 CO-2 Total PAH (ug/g) 1.9 0.5 0.7 0.6 1 1.4 Total PC8 (ng/gj 7 6.7 10.3 5.1 31.3 26.9 APRXATION FOR WAIVER 301 (hi NUT & DEER ISLANDS,1 984, METCAU^ & EDDY SAMRJNai979 Sanripling '82 SAMPUNG'84 Station 9Stafions CS PD Stations 6 7A 8 24 seddass 1 1 2seddass 12 11 Ag 2.4 Ag 8 5.9 Ag 0.1 0.07 0.1 0.1 Cd 0.7 An 0.062 0.56 An 2 12 3 Cr 0.018 As 0.1 0.1 As 4 2 7 4 Cu 0.014 Be 0.1 0.1 Be 5.59 3.24 4.82 6.97 Hg 3.7 Cd 2 2 Cd 0.1 0.1 0.1 0.1 Pb 0.011 Ct 2 2Cr 11 16.6 12.3 25.3 Zn 0.043 Cu 2 2 Cu 4.6 2.4 1.5 2.8 Units mg/g dry weigh Hg 48.7 89.4 Hg 0.15 0.71 0.05 0.14 Ni 4 4Ni 5.3 3.2 9.1 15.5 Pb 3 3Pb 19 7.1 20 15 Se. 6.5 4.1 Se 0.9 0.4 0.5 0.7 Ttl 11.7 16Th 5 3 4 6 Zn 27 22.6 Zn 26.5 37 37.3 53.1 Units ug/g Page 3 Bay DISPOSAL AFE A MONfTORJNG, USACOE, 1 990 Station 1 5 3FG2: t FG9 SE sed dass 2 2 2 2 2 2 Arsenic 16.7 13.3 15 13 16.3 14.3 Chromium 16.7 Copper 21.7 29 23.7 18.7 23.3 19 Lead 46.2 62.4 51.8 40 46.7 46.3 Nickel 32.7 31 30.7 32.7 29.7 31.3 Zinc 94.9 104.6 93.2 95 94.3 84.7 PCB 0.05 0.22 0.06 0,04 0.08 0.04 All measurements in ppm. Means for top 2cm of cores. RNAL EIR FOR THE IDENTIFICATION OF DFEDGED MATERIAL DISPOSAL SfTES IN CAPE COD BAY. 1 990 SfTI B C D E sed dass 2 2 2 2 Arsenic 14 16 15 15 Cadmium 0.7 0.9 0.9 0.8 Chromium 43 48 39 30 Copper 18 20 20 16 Lead 40 36 38 31 Mercury 0.3 0.4 0.6 0.6 Nidcel 22 27 26.92 22.78 Varmdium 92 98 20 16 Zinc 84 88 108 87 All measurements in ug/g dry weight and averaged from four stations. TRACE METAL ANALYSIS OF BOSTON HARBOR WATER SEDIMENTS,1 972 Surface concentrations in ppm. STATION 018 019 sed dass 1 1 Cadmium 3.3 2.4 Chromium 74 63 Cobalt 22 12 Copper 36 40 Lead 16 40 Mercury 0.2 0.2 Molytjden 1.9 4 Nid(el 39 16 Vanadium 99 42 Zinc 110 99 Page4 Qay WelHIeetHarbc )r Dredging Project 1 987, U.S. A.C.O.I Station 1 2 3 5 Sed Class 2 3 3 1 As 17.8 23.6 27.3 8.5 Cd 4 4 9 3 Cu 28 31 69 17 Hg 0.3 0.2 0.71 0.2 Ni 18 18 49 11 Pb 37 4B 126 26 Zn 107 114 306 66 Metals in ppm PC8 13 13 13 13 PCBinppb Pages APPENDIX C CONFIRMED HAZARDOUS WASTE SITES WITHIN 500' OF COASTAL WATERS OR THE MERRIMACK RTVER M»nzi»-Cun &A)9octuts, Inc. KF FMdy, inc. Project No. 90108-B Much 9. 1991 P»9t$or39 2.0 Sites Within SOOFeet Of Massachusetts Coastal Waterways And The Merr/madt River To Pawtucket Dam 2.1 Coastal Amesbury OEPSit« DEPNMoand Number Stta Ltcalion Sili H-H«zMil DrainM* Manzit-Ciirt CtaM P-PtI Batin Amm. SileNe. 3-02M B^ey$ Pond Parcel Memmeck It Beacon Sb C H ME 3-0528 Former Merrimack Halt Merrimack l( Beacon Ste 6 H ME M615 Property Merrimack Street H ME Salisbury DEPSite DEPNtnawd Nwnbar Stta Ltcatian Site H-HazIM OffiinM» MMizle-Cm Otss P-Pet Basin Aiaac. SitaNa. 3-1181 Exxon Station 591 No. End Blvd. NS 218 Newburyport DEPSita DEPNMiaand Nunbar Stta Lacatlan Sila H-Haz Mat Drainaf a Manzia-Cart P-Pat Baaki Aaaac. SRa Na. 3-2837 Bank of Nev England 345MefflmackSt H&P ME 2t3 3-2947 FormerCa^DOICo. 115 VMer Street HaiP ME 214 Menzle-Cura S( Assoctatas, Inc. KF FWddy. Inc Pro)»cl No 9010e-B MarcM 1991 Newburyport (continued) DEPSHt DEPNanewid Number Stte Locdien Cl4M P-Ptt bukn AMM.SAiNt. 3-2425 Gould Asaociat 63 374Men1iTUCkSt B ME 217 3-1295 Motor Shop 37 Liberty a \MK ME 3-1771 Property(Gas Station) 189Me(Timac)(St ME 3-1965 Property MenlmeckatKentSts C ME 3-0919 Tovr^eSHverCo 260MerHrrAckSt B iMK ME 216 3-2883 WEAtkirwonCo 27W8^efStreef B ME 21S RowUy DEPSttt DEPNMietfitf Sit H-HttkM DnlrMi* Uenzit-Curt Number SReLecatien CItst P-Pek B«sin Amm. Sllf Ne N/A N/A N/A N/A UIA NVA Ipswich DEPSRe Number DEPNMieani SReLecaUen SRe H4taz P-Pet Dnintfe ytrude-Cun Aseec. SReNe. N/A N/A N/A N/A hVA N/A M*nzt»-Cun & Assodat*). Inc. KF FWddy, Inc. Project No. 9O10e-B Mvcn5,1991 P»9*7cr99 Newbury DEPSttt Numbtr DEPNamstfid Stto Localion Sttt H-HttlMt Dfyntft Mtnzie-Cwi CltM P-Ptt Bttin A«9M. SRo Nq. N/A N/A N/A N/A N^A N/A Essex OEP SHe Number DEP Name and Site LocatiMi Sttf H-H«ziyM DrainMt Mtnzit-Cwi CItM P-Pet Bttin Assoc. SRe No. N/A N/A N/A N/A f«A N/A Gloucester DEPSile Number DEPNomemi SttoLociUon Stto CliM 3-0752 >^ eric old 159 E»Mn Street B 3-0753 Mietfeoid 69Roger9St 6 3-0134 C&pe>knn Forge WhittemoreSt B 3-2130 Exxon Station IHoRySt C 3-0841 FormerGae Station 134ViteNngtonSt C H-fiez iuW DfiiiMmo Monzio^iiiio P-Pit BiHn Atow.SRoNo. UNK UNK H NS NS NS IP IP 172 173 10 12 174 3-2890 QoucesterHerborCove 27 Rogers Street C 3-2172 Qouceeter Marine ReiKi«y9 9HarborLoop C NS NS 175 9 Merut»-Cura & Assodalts, Inc. KF R»ddy, Inc Project No. 90106-8 P»9»«of39 Gloucester (continued) Number 3-3017 3-2305 3-1152 3-2678 OEPHtmttni SHe LoceUtn SItt Clesa H4U2M^ P-Pet OrainM* Betin AestC. SAtNt L 0 b$t er C ove Mkt a^ Marlrta 33RiverR(MK) C IP 11 Mass Electric 26Rog6f9St C NS 176 Mobil Station Rogere&MdnSt C NS 7 Propwty 8 School Street C NS 8 Rockport DEPSHe DEP Name and Nufflber Site LaeaMon Sita Ctaaa 3-1090 Cape^^nnTool Pigeon Co>/e B 3-1091 TerrSchool School Street C Manchester DEPSRe DEPNMieane Nwabtr Silt LteiHtfi SKt CItM 3-3248 Marine Storage Asen 1 2 AsNend Avenue c H-HazIM DralnMe Mtnzle^vt P-Pat Beam Aaaac.StteNa H&P N5 NS tHtazltel Dr^naff 13 H NS y*nzJe10of}3 Beverly (continued) DEP SiU DEP Name tf)4 SHe H-Ha2iMlil Dramaie Utnat-Cure Number Site Lecttien Cleee P-Pet B«iln AMec.StteNe 3-1585 Shore Saies 97Riv«rStrert C P IP 233 Salem DEPSite Number DEPNiaeend SiteLecatien Site Clau 3-1709 Boston Gas-Sdem Lng Ptt RerceAve&VMtSt A 3-1212 DarbioLandinoMahna lOWWeSt C 3-2135 FwrnarTanlcFanTi S7Whafa C 3-04 2S Grit & Grease Chambers 50 Fort Avenue C 3-0433 GTES>4v«rM 71 Lorino Avenue B 3-0918 Jeff'aAutoSefvtta 65 Bridge St C 3-2898 MassBedric Derby 3iH«»8 Much 5, 1991 P»9»1$of33 Everett DEPStte Nymber DEP Name end SHe LocaUen Stte CtMf 3-0308 Bo9t on G» Plant Rover St C 3-0309 FofmcrCod GflMftofltion Fecity Market ^BeahanSts A 3-1395 bidependant Cam^ CofnmsicWSt C Somerville \ DEPStte Nynber DEPNametfid StteLecitlen Stte Claee H-Haz Mi CMntf e Menzie-Ceri P-Pet Betin Aeaec. Stte Ne. UNK H H H^tezIM P-Pal MB MB MB 146 H7 148 Oriinafa Menzie-Cm Baain Aaaac. SReNe. 3-0434 3-0951 Cambridge Mac hina Prod 100 Foley St 6 <3ffrityOSCo 100Sturtr»«ntSt 6 HAP MS MS 30 31 3-0S49 3-1096 HKPortarCo 74 Foley St PannOiCo St urt event St B MS MS 29 32 Chartestown (Boston) DEPSRa DEPNanawii Nanbar Stte Lec^an Stta H-HazMal IMnt|a Manzie-Cm P-Pat Baain Aaaae.SieNe. 3-0923 Boston Ed^ilyatic Sta 176 /Word St HaiP MB 40 Menzi»-ajrai & Assodalts, Inc. KF n*4rordSt a NavChar1eatov«n Pump Station MordSt c WMmoreVAight 62>WordSt 6 H-HtzIM CMnM* Mtnadt-Cwi P-PtI Btain AMtc.SitNa. H H Hit,? H H«cP UNK MB HB HB MB MB MB MB MB MB MB 33 37 41 42 34 39 36 35 36 43 M»nzi»-Cun & Assodaits, inc. Much 5, 1991 i(FR«Jdy,tncPTO)tctNo.9010e-B Pa9»17of33 East Boston OEPStte DEPNametntf Site H-HaziuM Dninage Manzia-Cara Number Stte Locatian Clate P-Pat Baain Aeaac.StteNe. 3-1935 AvwRantACar 375McaelianHvy C P MB 114 3-1577 BetcherNev England vjH I orniinei McOdiflnHvy C P MB 115 3-2841 Constnictlon Lot 480McaeiaiHvy C P MB 116 3-1486 CovenA Service Co 73Addi3onSt B H MB 110 3-3068 EeetBoetonCentniPier OydeSt C P MB 106 3-0700 FoiTnerAT^oco 470MeHdlenSt C P MB 117 3-0177 Loef:pottMeni^6Ctuflng 99RCondorSt B UN< MB 111 3-1116 M4d$port 256Mergin8fSt C P MB 109 3-1558 MotdOaCorp 580Chel3eaSt C P MB 112 3-0528 Old Natvy Fuel Depot McOeienHwy C P MB 119 3-1923 Property 175McQel8nHvy C P MB 118 3-1906 Servtee SteUon 52MeHdlen C P MB 107 M9nzt»-Cura & Assodatos, Inc. KF Rtddy, Inc. Projta No. 901 06-B MirctiS 1991 P»9»ieof39 Boston DEPStta Nmnbtr DEPNMieani Sttt Location Silo ClOM P-Pot Oroina|t BMin M»n2ft-Cva Amoc. SRiNo 3-2297 Colunbus P«1( Columbus Pflfk c p MB 119 3-0248 PornierMoM Station 425 Summer St c p MB 123 3-2809 Harbor G0tev«y hduathalPark Drydock Avenue B p MB 122 3-1819 Property 324MarQinaiSt C UNK MB 121 3-2S74 Property 285McaelianHVfy c P MB 120 3-2169 USNftv/ BoatonNavBiSNpyard B&D H MB 124 Dordiestar (Boston) DEPSRe Nimbor DEPNmoani SMoLocaUon Sio CtaM H-Htt P-Ptt 3-0152 BIW Cable Systems 65 Bay Street 6 H 3-2656 Boston Globe 135Mo(TtoseyBtvd 6 H«iP 3-2706 Commercial Property 725Mom$sey6ivd C P 3-2478 Merinfli 24Bi(sonSt C P IMnM* Monzle-Cvt Amoc. SNiNo. 138 MB MB MB MB 139 140 141 M»nz)t-Cun & A$)odii»s, inc. KF Rtftery c M443 Property 57^593 Southern c M7D4 Property 542ESquantum c 3-3222 OuJncyOPW Garage 55 Sea Street c 3-0117 Quinoilnduetried 726 Southern >ktery c 3-1291 StopNShop 495 Southern >Wefy c 3-0005 Suioco Station 555 Southern Mery c H4taz Mit Dreintie Mtnzit^iri ?'?9K toin AMoc.SitNt. MB 93 MB 94 MB 95 H&P MB 96 MB 97 HliP MB 69 MB 86 UNK MB 98 MB 84 MB 88 H MB 85 MB 67 Men2l»-Cura & AssodiMs, Inc. KF RwJdy, Inc. Pn\/KA No. 90106-B Braintree OEPSHt Number DEPNMitand Site Location Site CItoe H-haziM P-Pot DniriMO Btttln MtnzJe-Ciirt Aeeoc.StteNe 3-2893 444QuirtcyAve C P WF 150 3-2389 3-1799 Arrow Rivet Co G en ereil C h 6rnic8d C 0 60CoiumbiaTetT B B H H WF WF 151 151 3-0260 ^0529 CKgo Breintree Iwrind a een Herb ore, Inc. 385QuJncyAye C C HAP HliP WF WF 153 153 3-1605 PHbotte'sAutoSeivaQe ColumbiaTerraiCif St C P WF 154 3-2085 MetropotttfiYechtOub 30 Vinedde St C P WF 155 3-0145 PlyvoodRench 288 Quincy Avenue c P WF 156 3-2010 Property 431-441 Quincy Ave c P WF 157 Weymouth DEPSAo DEPNMomtf Number SRe Loc«tien SRo H-Hazyat Dnlnaie yonzio-Cun P-Po( Duski A890C.9ReNe. 3-tS71 3-2387 Best Petroleum 520 Bridge St BoetonEdtoon Edgar Stetion 1 Bridge St WF W6 152 159 M»nzt^Cun & AS)odat«$, inc. KF R^Jdy, Inc. ProfKi No. 90106-6 Mucn$.1991 P*9*29 0O3 Weymouth (continued) DEPSilt OEPNMietnd Number Sfta Locition Silt H-HizMtl Clttt P-Pti Drtintft Mtnzit-Ciri Bttin Aaaoc. Stta Nt. 3-1314 3-3146 3-3227 3-1547 Propwty 770-780 BHdge St Shel Station ShHI Station 351 Bridge Street Short Stop Auto 525 Bridge St B WF WF WF 161 162 163 Hingham DEPSttt Number DEP Nine and SRe Lec^en 3-0037 BeareCoveViaoe BeeTdCoveRd 3-1310 Former Sunoco 223 Lincoln St 3-0648 Lincoln Plaza LincolnliBeelSte ^2788 MotiStttlon 24 Summer St 3-0570 Property IIOBealSt 3-1513 ShavSaab 425 Lincoln St Stte H-HizMat DnlnMt Menzle-Cura aase P-Pet Besin Aseec. StteNe. HkP H WB WB WB WB WB WB 158 164 165 168 167 168 MBn2t»-Cun & Assoclitos, Inc. KF n^tty, Inc. Pio)Kl No. 9010$-B Hull DEP Site Number DEP Name and Site Location Silo CItoo 3-1767 Hull Fire Dept 671Ntn(e9ket C 3-0337 HutlMunUohtino Plant EdgevBier Avenue C 3-0661 NeeTs Service 268AAtlenticAve c 3-302S Property 7-1 31/2 Nentesket Ave c 3-3114 Property 6 A Street c 3-3153 Wftveiend Marina 7 A Street c 3-0907 Waveland Service Station 663 Nantasket Avenue c H-HazMat Drainafo Mtnzie-Cvt P-Pot Btoln Aaeoc.SAeNe. UNK UNK MB MB MB MB MB MB MB 76 32 7i 79 60 77 61 Cohasset DEP Sito DEPNainomd Sito Nunbof Sito Location Claoo 3-1814 Old State Houae 40 Border St c M478 Realdence 52JeruMiemRd c 3-2552 ReatauTMi 44 Border St c H^ltzlkltt Drynaso Monzio-Cwi P-Po( Baoin Aoooc. SiteNe. 169 SS SS SS 170 171 Monzi»-Cun & A$)odMs, Inc. KF R^ddy, Inc Proftct No 90106-8 Much 5, 1991 Scituate DEPStte DEPNMietnd Nwnbtr Silt Location Stto H-HozIhM Dnim%$ Monzio-Curt Cku P-Pot Btiin Aootc. SiloNo. N/A N/A N/A N/A N/A N/A Marshfield DEPSito OEPNonoond Numkor Stto Location Sito H-HaikW Drakiaio Monzlo-Cm CloM P-Pol Daoin Aaaoc. SlloNo. 4-0466 Green HarbofMaflna Route 139 SS 160 4-0378 Tft^orMailneCorp 95 Central St SS 179 Duxbury DEPSito OEPNanoand Nimbor SRo LocoUon Silo H^lazMal Drilnaio Monzlo^m Oaao P-Pot Baiin Aaaoc. SRo No. N/A N/A N/A N/A N/A N/A Plymouth Nanbor 4-0445 4-0140 4-0293 DEP Mmio and SRo LocoUon SRo Claaa H4la2iMW P-Pat Drainaio Baam Uofizio-Cara Aaaac. SRaNa Bradley Automotive 23 Sennzl»-Cura & AssoctMs, Inc. KF R*dd/, Inc. Project No. 9010(-B MVCf)5,1W1 P»9»2eo03 Plymouth (continued) DEP 3tt9 NiMBber DEP Name and Site Ltc^ion sua CJaas 4-0272 Eagle Snacks SendriDr&HedgeRd C 4-0539 GettyGas SUtion 724 Stdte Road C 4-0446 102 Court Street c 4-0600 Property 115S«idMi«e BayMotel 53 South Street C H4tezMiA Drainafa Uanzia-Carm P4>at Baain Aaaac. SttaNa. 235 UNK HtA UlA 236 M»nzt»-Cun & Associatts, inc. m Cand Street B 3-1013 C>rOiCo. 1 00 VMter Street C 3-2420 FrstMutud Benk of Boston 360Men1mack9reet C H-HazU^ DrrinMt Utfuit^wm P-Pet Btiln AMtc.SlttNi. Hk? ME ME 206 227 H ME 228 3-3140 Qbco-ureTechnoiOQies 421 Merrtmeck Street 8 ME 229 3-2934 L«yrerx;e Pumpe 37 ]M«1( at Street B H&P ME 232 3-0935 Propefty 3 IMeirimttk Street C UNK ME 230 Andover DEPSttt Nmber DEPNtaaw^ Silt LocaUtn Silt H-HttIM P-PtI DrUntit Bttin Mtnzlt* en Avenue C 3-0601 Jetllne-Geochem 283Hor!rdSb'eet C 3-2609 WnnyjTexBCO 262 Pa^lAucket St. c 3-1610 Property Rtverby Street c 3-2066 Property 160 Martin Street e 3-1809 Property 1 29 Mflrtin Street c ^2928 St. John's Property E Merrimack JcNesmfth c 3-0852 Staff Reaty Property 43LakeMev^tv/enue c Tewksbury DEPSite Number DEP Nflne ani Site Laeatitn SRe diet H-Htz luUt IMntf e Menzie^en P-Pet Bttin Ateec.SfteNe. 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II M BREDPORT 75 EA. 4/92, P850971