Peninsula Harbour Area of Concern Jellicoe Cove Thin-Layer Cap 2017 Long-Term Monitoring Assessment Tara George Ontario Ministry of the Environment, Conservation, and Parks November 2019 ISBN 978-1-4868-3850-9 ACKNOWLEGMENTS The author would like to acknowledge and thank Hans Biberhofer (ECCC), Lisa Richman (MECP), ECCC’s Dive Crew (Bruce Grey, Chris Duggan, Cory Treen, and Jeremy Hughes), MECP-EMRB Great Lakes Unit’s field crew (John Thibeau and Kyle McOuat), MECP-Northern Region (Curniss McGoldrick and Todd Kondrat), ECCC Sediment Remediation Group (Kay Kim, Matt Graham, and Roger Santiago), and TTU (Haley Schneider, Andrew Jackson, and Danny Reibel) for their support in study design, sample collection and processing, and instrument deployment and retrieval. Open hearts and open minds. The MECP Laboratory Services Branch is acknowledged and thanked for the sample analysis, as well as the MECP Geomatics Unit (Ela Lichblau) for creating the SWAC maps. Thank you to Lisa Richman, Dawn Talarico, Hans Biberhofer, Mark Chambers, Gurpreet Mangat, Danielle Milani, Jim Martherus, and Jennifer Winter for their review and comments on this report. EXECUTIVE SUMMARY Peninsula Harbour is located on the north shore of Lake Superior and is identified as an Area of Concern due to historical inputs from the former pulp mill and chlor-alkali plant, and historical log booming within the harbour. Over time these activities resulted in impaired fish and benthic communities, as well as elevated levels of contaminants in sediment and biota – specifically mercury (Hg), methyl-mercury (MeHg), and polychlorinated biphenyls (PCBs). The most heavily impacted area within Peninsula Harbour was Jellicoe Cove, a ninety-seven hectare embayment located adjacent to the mill and chlor-alkali plant. In 2008, an environmental risk assessment (ERA) and human health risk assessment (HHRA) addressed the risks of Hg and PCBs in the sediment and biota to receptors (ENVIRON 2008). The ERA concluded that hot spot management was the preferred remedial approach to manage the risks to fish and mink from exposure to sediment in Jellicoe Cove. Hot spots were defined as sediment with concentrations of total Hg equal to or greater than 3 µg/g. Overlap in the distribution of MeHg and total PCBs with the total Hg concentrations assured the management and reduction of those contaminants as well. To reduce the risks imposed by the contaminants, thin-layer capping was the selected sediment management option for Jellicoe Cove. The remedial action objectives of the thin-layer cap were to: reduce potential for offsite migration of Hg, MeHg, and PCBs from the hot spot area in Jellicoe Cove to the rest of Peninsula Harbour; and to reduce the potential for future exposure of MeHg and PCBs to receptors. In 2012 the thin-layer cap was constructed, and 15-20 cm of sand was placed over sediment exceeding the remedial target of 3 µg/g total Hg. In 2017, five-years post-cap, the first full long-term monitoring (LTM) assessment was completed with the goal of evaluating cap stability, cap effectiveness, and ecological recovery. Monitoring the cap against the remediation goals was a collaborative effort. The purpose of this report is to communicate the results of the LTM program as they relate to the work completed by the Ministry of the Environment, Conservation, and Parks (MECP): surficial sediment assessment, benthic invertebrate recolonization, and the assessment of fish tissue contaminants to determine the risks to fish and wildlife. Findings from additional survey monitoring components were reported by others, including: assessment of fish contaminant trends and fish consumption by humans (Drouillard 2019); submerged aquatic vegetation, and cap movement measurements and observations (Foster and Ratcliff 2018); passive samplers and sediment cores for sediment pore water analysis and determination of Hg flux through the cap (Rao et al. 2018); and high resolution multibeam sonar, and RoxAnn seabed classification and underwater video documentation (ECCC TBD). The pore water passive sampling survey was described and discussed in this report as it was integrated into the MECP’s survey design, and methodology was largely based on this component. Challenges were encountered with designing a sampling plan to address the LTM goals. The medium and coarse sands used to cap Jellicoe Cove were more coarse than the initial design, and therefore the traditional sample methods used to collect samples for the pre-cap baseline monitoring surveys were not feasible for the post-cap monitoring. Therefore, alternative technologies were employed to collect samples, and divers were used for most survey components. Divers collected sediment grabs (the surficial sediment that has deposited over the cap sand), sediment cores, deployed and retrieved passive samplers, and benthos with a benthic air lift. The first post-cap LTM survey has demonstrated that the thin-layer sediment cap is effective and met the goals and objectives of the remedial effort. Overall, the cap is stable (Foster and Ratcliff 2018), and the results from the analysis of passive samplers and sediment cores, have demonstrated that the cap has effectively reduced the flux of Hg to the overlying waters (Rao et al. 2018). Natural sedimentation has, and continues to, occur since the construction of the cap in 2012, and this surficial sediment was the focus of much of the MECP survey. The total Hg spatially-weighted average concentration (SWAC) (median SWAC 0.37 µg/g) in the surficial sediment was below the remedial target of 3 µg/g in the Jellicoe Cove capped area. As expected, the cap also effectively reduced the concentrations of MeHg and PCBs, albeit not to the same extent as the Hg reduction. Concentrations of some nutrients and metals in the cap surficial sediment exceeded their respective Provincial Sediment Quality Guidelines-Lowest Effect Limits (PSQG-LELs) at some sampling stations. However, concentrations of many parameters measured on the cap were similar to concentrations detected at the Peninsula Harbour reference station in Beatty Cove (MECP unpublished data, 2011). Biological surveys have indicated that the cap has been colonized with benthic invertebrates, the coverage of submerged aquatic vegetation continues to increase over time (Ratcliff and Foster 2018), and contaminant levels in fish tissue have decreased (Drouillard 2019). The abundance of benthos on the cap was low, but the diversity was fairly high and the taxa identified were similar to what was observed in the 2009 pre-cap baseline survey. It is expected that over time, as the sediment continues to deposit over the cap, the abundance of benthic invertebrates, as well as the abundance and distribution of macrophytes on the cap will continue to increase. The cap appears to have been effective in reducing the levels of Hg and PCBs in the fish tissue of Lake Trout and Lake Whitefish. A short-term temporal comparison (2012 to 2017) of contaminants in the fillet tissue of Lake Whitefish (50 – 55 cm) Lake Trout (45 – 55 cm) showed a decline of ≥ 26% in Hg and ≥84% in PCBs (Drouillard 2019). The assessment of estimated hazard quotients showed that the reproductive success of individual Longnose Sucker is predicted to be at risk from Hg exposure; however, the hazard quotients was 1 and should be assessed further. There was no potential for fish reproductive adverse effects from PCBs predicted at both the individual or population level. Current estimated concentrations of Hg in fish at specified consumption lengths were not at a level that was predicted to pose a risk to exposed bald eagles and mink. Likewise, the risk of mink consuming the estimated current levels of PCBs in 15 cm wholebodied fish was no longer predicted to be at risk. Recommendations for the next LTM survey (in 2022) are provided based on the sampling efforts and results of the MECP survey, as well as the aforementioned surveys. Generally, the next LTM survey should continue with the primary monitoring components (surficial sediment, benthic invertebrate collection, and fish and benthos tissue collection). Additionally, sediment traps should be deployed to further investigate the quality of sediment depositing on the cap, and the depositional patterns on the cap. The sampling effort should be increased over the coarse sand cap, where concentrations of total organic carbon (TOC) and many metals, including Hg and MeHg, are elevated, as well as in the north-east portion of the cap where PCB concentrations are elevated. TABLE OF CONTENTS 1. BACKGROUND ................................................................................................................... 1 2. SURVEY GOALS AND OBJECTIVES ............................................................................. 2 3. METHODOLOGY ............................................................................................................... 3 3.1. Station Locations .............................................................................................................. 3 3.2. Passive Samplers .............................................................................................................. 4 3.3. Surficial Sediment ............................................................................................................ 4 3.4. Sediment Cores ................................................................................................................. 5 3.5. Benthic Invertebrates ........................................................................................................ 5 3.6. Fish Tissue Contaminants ................................................................................................. 6 3.7. Other Sampling Components ............................................................................................ 6 3.7.1. Imaging .................................................................................................................... 6 3.7.2. Cap Movement and Submergent Aquatic Vegetation ............................................. 6 3.8. Order of Operation ............................................................................................................ 6 3.9. Laboratory Analysis .......................................................................................................... 7 3.9.1. Surficial Sediment ................................................................................................... 7 3.9.2. Porewater and Sediment Cores................................................................................ 8 3.9.3. Benthic Invertebrates ............................................................................................... 8 3.9.4. Fish Tissue Contaminants ....................................................................................... 8 3.10. Statistical Analysis and Data Interpretation ...................................................................... 8 3.10.1. Surficial Sediment ................................................................................................... 8 3.10.1.1. Spatially-Weighted Average Concentrations .............................................. 9 3.10.1.2. Data Comparison ......................................................................................... 9 3.10.2. Benthic Invertebrates ............................................................................................. 10 3.10.3. Fish Tissue Contaminants ..................................................................................... 10 3.10.3.1 Fish ............................................................................................................ 11 3.10.3.2 Wildlife ..................................................................................................... 12 4. RESULTS ............................................................................................................................ 12 4.1. Surficial Sediment .......................................................................................................... 12 4.1.1. Characteristics ....................................................................................................... 12 4.1.2. Nutrients ................................................................................................................ 13 4.1.2.1. Total Organic Carbon ................................................................................ 13 4.1.2.2. Total Phosphorus ....................................................................................... 13 4.1.2.3. Total Nitrogen ........................................................................................... 13 4.1.2.4. Historical Comparisons ............................................................................. 14 4.1.3. Metals .................................................................................................................... 14 4.1.3.1. Trace Metals .............................................................................................. 14 4.1.3.2. Specific Ions .............................................................................................. 16 4.1.3.3. Total Mercury ............................................................................................ 16 4.1.3.4. Methyl-Mercury......................................................................................... 17 4.1.4. PCBs ...................................................................................................................... 18 4.1.5. Surficial Sediment Discussion .............................................................................. 19 4.2. Benthic Invertebrates ...................................................................................................... 19 4.2.1. Pre-cap Baseline Comparison ............................................................................... 20 4.3. Fish Tissue ...................................................................................................................... 21 4.3.1. Trend Analysis ...................................................................................................... 21 4.3.2. Human Fish Consumption ..................................................................................... 21 4.3.3. Risks to Fish .......................................................................................................... 22 4.3.4. Risks to Mammals and Birds ................................................................................ 22 4.4. Passive Samplers and Sediment Cores ........................................................................... 23 4.4.1. Passive Samplers ................................................................................................... 23 4.4.1.1. Peepers ....................................................................................................... 23 4.4.1.2. Horizontal Flux Chambers ........................................................................ 23 4.4.2. Sediment Cores ..................................................................................................... 23 5. CONCLUSIONS ................................................................................................................. 24 5.1. Performance Monitoring Goal ........................................................................................ 24 5.1.1. Objective 1a - Cap Placement ............................................................................... 24 5.1.2. Objective 1b - Surficial Sediment Evaluation ....................................................... 24 5.1.3. Overall Conclusion of Performance Monitoring Goals ........................................ 25 5.2. Remedial Monitoring Goal ............................................................................................. 25 5.3. Ecological Recovery Goal .............................................................................................. 25 5.3.1. Objective 3a – Benthic Invertebrate Re-Colonization........................................... 26 5.3.2. Objective 3b – Tissue Contamination ................................................................... 26 5.3.2.1. Benthic Invertebrates ................................................................................. 26 5.3.2.2. Fish ............................................................................................................ 26 5.3.3. Objective 3c – Submerged Aquatic Vegetation and Re-Colonization .................. 27 5.3.4. Objective 3d – Habitat for Benthic Invertebrates .................................................. 27 5.4. Overall Conclusions........................................................................................................ 27 6. RECOMMENDATIONS.................................................................................................... 28 7. REFERENCES .................................................................................................................... 30 LIST OF TABLES Table 1. Monitoring goals, objectives, and monitoring components to fulfil the Jellicoe-Cove thin-layer cap Long Term Monitoring program. ........................................................................... 33 Table 2. Sampling station locations for survey components (presented in directional order from SE to NW). .................................................................................................................................... 35 Table 3. Particle size (median and range) of surficial sediment collected in individual deployment and retrieval surveys, and a combination of both surveys. ........................................................... 36 Table 4. Nutrient concentrations (median and range) in surficial sediment collected in individual deployment and retrieval surveys, and a combination of both surveys......................................... 37 Table 5. Concentrations (median and range) of select metals in surficial sediment collected in individual deployment and retrieval surveys, and a combination of both surveys. ...................... 38 Table 6. Concentrations (median and range) of selected ions in surficial sediment collected in individual deployment and retrieval surveys, and a combination of both surveys. ...................... 41 Table 7. Total mercury concentrations (median and range) in surficial sediment on the thin-layer cap and at cap reference station 25. Sediment was from all surveys and all jars. ........................ 43 Table 8. Concentrations (median and range) of methyl-mercury, mercury, and total organic carbon in surficial sediment collected in individual deployment and retrieval surveys, and a combination of both surveys. All analysis conducted on sediment from MeHg jar. ................... 44 Table 9. Total PCBs in surficial sediment overlying the thin-layer cap and at cap reference 25. 45 Table 10. Average density of benthic invertebrate taxa in the surficial sediment on the thin-layer cap and cap reference station 25. .................................................................................................. 46 Table 11. Percent dominant benthic invertebrate taxa in the surficial sediment on the thin-layer cap and cap reference station 25. .................................................................................................. 46 Table 12. Indices, based on genus and species benthic invertebrate density in the surficial sediment on the thin-layer cap and cap reference station 25......................................................... 46 Table 13. Indices, based on family benthic invertebrate density in the surficial sediment on the thin-layer cap and cap reference station 25 in 2017, and pre-cap (2009) baseline stations on the cap footprint and at reference station 289 in Beatty Cove. ........................................................... 47 Table 14. Risk estimation of fish collected from Peninsula Harbour, 2017. ................................ 48 Table 15. Summary of hazard quotients for wildlife consuming fish in Peninsula Harbour. ....... 48 LIST OF FIGURES Figure 1. Peninsula Harbour Area of Concern, Lake Superior. .................................................... 49 Figure 2. Capped area with 100 m grid lines (Figure source: Public Works and Government Services Canada, 2012). ................................................................................................................ 50 Figure 3. Jellicoe Cove thin-layer sand cap and 2017 sampling station locations. ....................... 51 Figure 4. Design and placement configuration of vertical passive sampler (peeper). .................. 52 Figure 5. Design and placement configuration of the horizontal passive sampler. ...................... 53 Figure 6. Sediment core collected from sampling station on the thin-layer cap. .......................... 54 Figure 7. Optimal spacing and sampling design for monitoring components. ............................. 55 Figure 8. Spatially-weighted area average concentration of total organic carbon (mg/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. .......................................................................................... 56 Figure 9. Spatially-weighted area average concentration (SWAC) of total organic carbon (mg/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). ....................................................................................................................................................... 57 Figure 10. Median concentrations of select metals in surficial sediment at each station on the cap and cap reference station 25. The relative concentration on the y-axis is due to Al, Fe, and Mn being divided by factors of 10 in order to fit the scale so that trends could be easily compared. . 58 Figure 11. Median (max and min) of total mercury (µg/g) concentrations in surficial sediment on cap stations and cap reference station 25. Horizontal line depicts the PSQG – Lowest Effect Level (LEL) of 0.2 µg/g. ............................................................................................................... 59 Figure 12. Spatially-weighted area average concentration of total mercury (µg/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. ................................................................................................................ 60 Figure 13. Median (and max and min) of total mercury concentrations (bulk chemistry and TOCnormalized concentrations) measured in the post-cap 2017 survey, and pre-cap/historical surveys conducted in 2000, 2002, 2009, and 2011. ................................................................................... 61 Figure 14. Spatially-weighted area average concentration (SWAC) of total mercury (µg/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). ....................................................................................................................................................... 62 Figure 15. Median (and max and min) of methyl-mercury (ng/g) concentrations in surficial sediment on cap stations and cap reference station 25.................................................................. 63 Figure 16. Spatially-weighted area average concentration of methyl-mercury (ng/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. .......................................................................................... 64 Figure 17.Spatially-weighted area average concentration (SWAC) of methyl-mercury (ng/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). ....................................................................................................................................................... 65 Figure 18. Median and range MeHg concentration (bulk chemistry and TOC-normalized concentrations) measured in the post-cap 2017 survey, and pre-cap surveys conducted in 2000, 2002, 2009, and 2011. ................................................................................................................... 66 Figure 19. Spatially-weighted area average concentration of PCBs (ng/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum and minimum concentrations detected at each station. ................................................................................................................ 67 Figure 20. Spatially-weighted area average concentration (SWAC) of PCBs (ng/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (minimum of replicates at each station); B) 2017 (maximum of replicates at each station; and C) 2011 (single replicates at each station). ... 68 Figure 21. Proportion of PCB congeners in surficial sediment on the thin-layer cap................... 69 Figure 22. Average density of benthic invertebrates collected from the surficial sediment at the cap stations and reference station 25............................................................................................. 70 Figure 23. Percent dominant benthic invertebrate taxa in the surficial sediment at the cap stations and reference station 25. ............................................................................................................... 71 1. BACKGROUND Peninsula Harbour is located on the north shore of Lake Superior, adjacent to the town of Marathon, Ontario (Figure 1). The Harbour is identified as an Area of Concern (AOC) due to historical inputs from the pulp mill and chlor-alkali plant, and historical log booming. Over several decades, these activities resulted in impaired fish and benthic communities, elevated levels of contaminants in sediment and biota, and degraded aesthetics (Peninsula Harbour RAP Team, 1991). There have been efforts over time to reduce contaminant loads through regulatory change, upgrades to effluent treatment facilities, and cessation of logging practices etc.; however, contamination of the sediment continued to be a concern, specifically with regard to mercury (Hg) and polychlorinated biphenyls (PCBs). In 2008, an environmental risk assessment (ERA) and human health risk assessment (HHRA) were conducted to estimate the potential risks of Hg and PCBs in the sediment and biota to AOC receptors (ENVIRON 2008a). Results of the risk assessments were:  Hg was predicted to cause impaired reproduction in Lake Trout, Walleye, Lake Whitefish, and Longnose Suckers;  Reproductive success was predicted to be reduced in individual Bald Eagles (and other raptors) exposed to Hg in fish;  Longnose Suckers exposed to the PCBs in the assessed area were predicted to reproductively impaired;  The concentration of PCBs in the fish tissue was predicted to reduce the reproductive success in mink and other piscivorous mammals; and  The HHRA showed only PCBs in fish tissue were predicted to present a significant risk to both adult anglers and more sensitive consumers such as children and adolescents. The most heavily impacted area within Peninsula Harbour was Jellicoe Cove, a ninety-seven hectare embayment located adjacent to the mill site (Figure 1). The risk assessment calculated spatially weighted average concentrations (SWAC) of methyl-Hg (MeHg) and PCBs in both Jellicoe Cove and in Peninsula Harbour as a whole. The SWAC for MeHg in Peninsula Harbour and Jellicoe Cove were 1.9 ng/g and 5.1 ng/g, respectively. The PCB contamination was not as widespread as Hg concentrations, but the areas of contamination did overlap. The SWAC for PCBs in Peninsula Harbour and Jellicoe Cove were 120 ng/g and 140 ng/g, respectively (ENVIRON 2008a). Hot spot management was the preferred remedial approach to manage the risks to fish and mink from exposure to contaminated sediment in Jellicoe Cove (ENVIRON 2008). The risk assessment identified other management approaches (i.e., guideline based, background based, and risk based); however, there were cost and feasibility constraints to considering the additional options. Hot spots were defined as sediment with concentrations of total Hg equal to or greater than 3 µg/g. Total Hg was selected as the remedial parameter as it is a source of MeHg, and it is more cost effective to measure than MeHg. In addition, the overlap in the distribution of MeHg and total PCBs with the total Hg concentrations assured the management and reduction of those 1 contaminants as well. Thin-layer capping was the selected sediment management option for the hot spot in Jellicoe Cove. This decision was based on an informative assessment of the risks, benefits, costs, and community acceptance. The average net deposition rate in Jellicoe Cove is very low (1 to 2 mm of sediment being deposited per year), and as such, it was calculated that the placement of a 1520 cm sand cap would be equivalent to seventy-five years of sedimentation, thereby enhancing the natural recovery of the site (ENVIRON 2008b). The remedial action objectives of the thinlayer cap were to:  reduce potential for offsite migration of Hg, MeHg, and PCBs from the hot spot area in Jellicoe Cove to the rest of Peninsula Harbour; and  reduce the potential for future exposure of MeHg and PCBs to receptors (ENVIRON 2008b). In 2012, a 15-20 cm thin-layer cap – at a cost of $7.3 million – was placed over Jellicoe Cove. The cap was constructed from two different sand types: medium-grade and coarse-grade. The coarse-grade sand, which was sourced from Manitoulin Island, was placed on the south side, nearshore area of the delineated contaminated area; ultimately making up 33% of the total cap. Since energy was higher in the nearshore areas, it was anticipated that the course sand would be able to withstand storm events and prevailing currents. The medium-grade sand was sourced from a local quarry and was used over the remainder of the cap footprint. A long-term monitoring (LTM) plan was developed by AECOM (2011) to assess the success of the cap over a twenty-year time frame. The first full assessment – presented in this report – was completed five years post-cap construction. Initially, the intention of the LTM was to follow the methodology used to collect samples in the pre-cap baselines studies conducted in 2009 and 2011 by AECOM and ECCC, respectively (ECCC unpublished data). However, the sand used to cap was more coarse than the initial design specification, and therefore collecting and analyzing samples from the cap could not be completed using the pre-cap survey methodologies. In addition, there were concerns over the ability to penetrate the coarse cap, particularly due to the high limestone content in the Manitoulin Island sourced material (J. Biberhofer per comm. 2013). These challenges were addressed by introducing secondary sampling strategies, such as the use of passive samplers to measure Hg levels in porewater, a benthic airlift to collect benthos, and divers to collect surficial sediment. 2. SURVEY GOALS AND OBJECTIVES The LTM program outlined three main goals: performance monitoring, remedial goal monitoring, and assessment of ecological recovery (AECOM 2011). Table 1 outlines the LTM goals and objectives, with the associated primary and secondary monitoring components. The primary monitoring components are those that were reflected in the original LTM plan (AECOM 2011). Secondary monitoring components were elements added to this LTM survey to address 2 the challenges with monitoring the more course sand cap; these secondary components may not necessarily be repeated in future LTM surveys. The question that each goal and objective was intended to address were also included in Table 1. The purpose of this report is to communicate the results of the LTM program as they relate to the work completed by the Ministry of the Environment, Conservation, and Parks (MECP): surficial sediment assessment and benthic invertebrate recolonization. Findings from additional survey monitoring components were reported by others, including: fish contaminant levels (Drouillard 2019), submerged aquatic vegetation, and cap movement measurements and observations (Foster and Ratcliff 2018); passive samplers for sediment pore water analysis (Rao et al. 2018); and high resolution multibeam sonar, and RoxAnn seabed classification and underwater video documentation (TBD). To some extent the pore water passive sampling survey will be described and discussed here as it was integrated into the MECP’s surveys and was largely considered in survey design and methodology. Additionally, the risk of fish contaminant levels to avian and mammalian receptors was assessed in this report. 3. METHODOLOGY This LTM survey – to assess the Jellicoe Cove thin-layer cap – was split into two sampling efforts to accommodate the time the passive samplers needed to be deployed in/on the sediment, and then retrieved once they reached equilibrium. The first sampling effort, herein known as the deployment survey, corresponded to the deployment of the passive samplers on July 12 – 14, 2017. The second sampling effort, herein known as the retrieval survey, was completed August 10 – 13, 2017 and corresponded with the retrieval of the passive samplers. The methodology will be presented according to the matrix investigated during the surveys. 3.1. Station Locations Information on the sampling stations and the samples collected at each station is shown in Table 2. A 100 m x 100 m grid over the cap footprint, as depicted in Figure 2, was used as the basis of selecting station locations. The grid captured a gradient of water depth and total Hg concentrations in native sediment, while capturing adequate spatial coverage of the cap. As a starting point, a sampling station was placed in the centre of each square on the grid. Where historical sampling stations were within 50 m of the sampling station placed in the centre of the grid, the historical station location was selected as a surrogate so that pre-cap/historical comparisons could be made. Ultimately, sampling locations were selected and distributed on the cap according to substrate types (course or medium-grade sand) and water depth (<5m, 5-12 m, and >12 m). Eighteen (18) stations were identified in total for this survey; twelve (12) on the medium sand cap, four (4) on the course sand cap, and two (2) reference stations located off the cap (Table 2, Figure 3). Reference stations were selected mainly for the passive sampling pore water 3 assessment and were selected primarily based on lower total Hg concentrations and approximate water depth. Consideration was also given to physical characteristics of the sediment (i.e., attempting to match native capped sediment characteristics with reference sediment characteristics); however, this proved to be difficult. 3.2. Passive Samplers Texas Tech University (TTU) was engaged to advise on the use of passive samplers on the cap to assess pore water Hg concentrations, assist with construction, deployment, and retrieval of the samplers, analyze the collected samples, and provide interpretation of analytical results. A full report of the passive sampler survey was provided by Rao et al. (2018), and a brief overview is provided in this report. Passive samplers were used to determine the migration of total Hg from the underlying contaminated sediment through the thin-layer cap. Two types of passive samplers were used: vertical diffusion samplers (peepers) (Figure 4), and horizontal surface flux chambers (Figure 5). For the vertical peeper, the ECCC Machine Shop fabricated a unique stainless steel casing so that the peeper could withstand the force required to insert it into the sand cap. Environment and Climate Change, in consultation with TTU designed the horizontal flux chambers, and the ECCC Machine Shop fabricated them. Details of design of both the vertical peepers and the horizontal flux chambers are provided in Rao et al. (2018). Every station had at least one (1) passive sampler deployed. Vertical peepers were placed in the medium sand cap at twelve (12) sites, one (1) in the course sand cap, and one (1) at each of the two (2) reference stations. The horizontal surface flux chambers were designed to accommodate the coarse sand area of the cap and were placed at four (4) sites. The horizontal surface flux chambers were also co-located at three (3) vertical peeper sites, as well as one (1) of the reference locations (Table 2). The passive samplers were assembled on-shore, transported out to the divers, and deployed within one hour of assembly. The vertical peepers were inserted in the cap, ensuring that one chamber penetrated the native sediment, and one chamber was above the surface water-sediment (cap) interface (Figure 4). The horizontal flux chamber was placed directly over the surface sediment (Figure 5). The passive samplers were deployed for 28 days. 3.3. Surficial Sediment Surficial sediment was collected during both the passive sampler deployment and retrieval surveys to assess the effectiveness of the cap to meet the remedial goal of an area average of < 3 µg/g total Hg. The surficial sediment that overlaid the medium and coarse sand cap was the target substrate. Given the low quantities of the surficial sediment (generally 1 mm to 3 cm thick), the number of sediment sample replicates varied between stations. For each parameter measured, one to three replicates were collected at select stations. Surficial sediment was not collected from all stations. 4 Due to the challenges associated with the cap grain size and the limited amount of surficial sediment overlying the cap, sediment was collected by ECCC divers by use of a stainless steel spatula or wafting the fine surficial sediment into the sampling jar. Each replicate for each specified parameter(s) was collected in a separate jar. The parameter allocation was as such:    PET jar: particle size, total organic carbon (TOC), metals, Hg, total nitrogen (TN); 5P jar: PCBs; and 250 ml polyethylene jar: MeHg (and subsequently Hg and TOC) At stations 9 and 17, where it was not possible to collect the minimal mass of sediment required for analysis for multiple replicates, substrate from replicate jars were combined and homogenized to create a single sample. Sampling jars were brought to the surface by the divers and placed upright until the overlying water was clear of suspended particulates and could be decanted. All sampling jars were kept cool, in a dark location, until submitted for chemical analysis. Sediment that was collected for MeHg analysis was frozen. 3.4. Sediment Cores The purpose of the sediment core collection was twofold: (1) to determine the thickness of the cap prior to the vertical peeper deployment; and (2) to measure Hg concentrations in different horizons within the cap and native sediment. During the deployment survey, sediment cores were collected from ten (10) selected stations, which included one (1) reference station, one (1) coarse sand cap station, and eight (8) medium sand cap stations. Sediment cores were collected using cellulose acetate butyrate core tubes (1 m long, with a 10 cm internal diameter). The tubes were hand pushed into the top layer of the cap and driven through the remainder of the cap and into the native sediment with a 3 lb sledge hammer by the divers. Once collected, the core tubes were put on ice until they could be processed. On shore, water was decanted from the core tubes, and the tubes were split with a circular saw. Several sediment samples were collected from the core for analysis, including: top surficial sediment overlying the cap; top portion of the sand cap (approximate top 3 cm); bottom portion of the sand cap (approximate the bottom 3 cm); and top 3 cm of native sediment, as well as other definitive horizons in the native sediment (Rao et al. 2018) (Figure 6). Samples were collected from the centre of the core to limit the effect of smearing and handling. Each sample was placed in a separate 40 ml autosampling vial and stored in a dark cool location. 3.5. Benthic Invertebrates Benthic invertebrates were collected using a benthic airlift provided by ECCC. The benthic airlift was a 1.1 m long aluminum tube with a 37.5 mm inside diameter. The air used to ‘vacuum’ up the samples was supplied by an eighty cubic foot dive tank regulated to airflow rates of 120-130 5 psi. Airflow rate, which was controlled by the diver operated ball valve, dictated suction/water flow rates for sample collection. Once an acceptable airflow rate was established on the first station, all subsequent stations were set to the same flowrate. A 243 µm mesh drawstring closure bag on the airlift allowed the air and water to pass through, while retaining benthic invertebrates ≥ 243 µm for enumeration. The divers collected benthos samples from an area defined by a 50 cm x 50 cm (0.25 m 2 area) quadrat at eight selected stations (Table 2). Sampling locations at each site were randomly selected within a specified target area (described in section 3.7). Triplicate replicate samples were collected within 5 m of each other and no less than 1 m apart. Once sieved, each sample was placed in 500 ml polyethylene jar and preserved with 10% formalin buffered with sodium borate until they were identified and enumerated. 3.6. Fish Tissue Contaminants Longnose Suckers, Lake Trout, and Lake Whitefish were collected from the Peninsula Harbour AOC by the Ministry of Natural Resources and Forestry, Upper Great Lakes Management Unit as part of the fish community index program. The species type, weight, length, and sex of each fish was recorded prior to obtaining boneless skinless dorsal tissue. The fillets were processed and stored according to the methods outlined in the MECP’s protocol for collecting sport fish samples (MOE 2014). Young-of-the-year (YOY) Round Whitefish were collected from the boat launch in Jellicoe Cove by MECP-Biomonitoring Unit field staff in the fall of 2017. Fish were captured by seine nets, measured for weight and length, and frozen on dry ice in the field. Each sample (four in total) was a composite of whole-bodied fish equalling to a combined weight of approximately 10g (requirement for routine monitoring) (MECP, unpublished methods). 3.7. Other Sampling Components 3.7.1. Imaging Environment and Climate Change Canada conducted a high resolution multibeam sonar, and RoxAnn seabed classification; both of which were supported by an underwater video. The data generated from these initiatives will be reported separately. 3.7.2. Cap Movement and Submergent Aquatic Vegetation A cap movement and submergent aquatic vegetation survey was conducted and reported on by an external consultant, Northern Bioscience (Foster and Ratcliff 2018). 3.8. Order of Operation The divers were instructed to collect the various samples according to spacing depicted in Figure 7. The final coordinates for the station were defined by the placement of the passive sampler during deployment. 6 Prior to deploying the passive samplers, the top sediment layer was collected within a 5 m radius from the centre point, defined by the location of the passive sampler. Next, at approximately 5 to 10 m from the passive sampler centre point, a sediment core was collected and used to determine depth of the cap to inform and guide the placement of the vertical peeper, and to provide sediment samples for TTU. Following the collection of the sediment and cores, the passive samplers were deployed at the centre point location. If the station had both a horizontal surface flux chamber and a peeper, the flux chamber was placed approximately 50 cm from the vertical peeper. The main objective of this collection and deployment strategy was to minimize disturbance of both samplers. Upon retrieval, the passive samplers were removed, ensuring that the area outside the 5 m radius passive sampler footprint was not disturbed. Within the area of target substrate, but away from previously disturbed core site, a footprint of 5 m x 5 m was established to air lift the benthos. Benthic invertebrate samples were collected according to the methodology described in section 3.5. Outside of all the disturbed areas, but not to exceed a 20 m x 20 m footprint, surficial sediment was collected. 3.9. Laboratory Analysis 3.9.1. Surficial Sediment Surficial sediment samples were analysed according to established methods by the Ontario MECP’s Laboratory Services Branch (LSB), Etobicoke, ON. Sediment samples were analysed for: metals by method E3470 (including Al, Sb, As, Ba, Be, B, Ca, Cd, Cr, Co, Cu, Fe, Pb, Mg, Mn, Mo, Ni, K, P, Se, Ag, Na, Sr, S, Tl, Sn, Ti, V, and Zn); particle size by method E3328A; total organic carbon (TOC) by method CARB3529; total nitrogen (TN) by method TN3529, polychlorinated biphenyls (PCBs) by method E3487; and total mercury (Hg) by method E3059A. Value qualifier factors (VQF) were assigned to the sediment data provided by MECP-LSB (and shown in the raw data appendices). The qualifier ‘W’ is the standard deviation of replicate measurements of low-level spiked blank matrix samples, rounded down to the nearest 1, 2, or 5. This value indicates the baseline response of the instrument and the smallest amount of the analyte that can be measured by the procedure. A qualifier of ‘≤W’ is interpreted as no measurable response. The qualifier ‘T’ is a factor of ‘W’; the factor is dependent upon the parameter measured. Results quantified by ‘ 1 indicates that estimated exposures exceeds effect levels, while a HQ < 1 indicates the exposures are less than effect levels. As described by ENVIRON’s ERA (ENVIRON 2008a), the mean HQ is a central tendency estimate and therefore a mean HQ > 1 suggests that adverse effects in that fish species may propagate to population-level effects. The 11 95th percentile HQ is used to predict risks to individuals, as it is based on the most highly exposed fish. 3.10.3.2 Wildlife To calculate the HQs for mammalian and avian piscivorous receptors, dietary intakes (DI) were calculated for use as the effect parameter (HQ = DI / TRV). The DI variable was based on whole-bodied fish at a length that would be consumed by the receptor of interest. The fish collected in 2017 had lengths ranging from 46 – 90 cm for Lake Trout, 34 – 55 cm for Lake Whitefish, and 31 – 49 cm for Longnose Suckers. As such, whole-bodied fish concentrations (as calculated above) were size-normalized to the median length of fish the avian or mammalian receptor would consume. Young-of-year Round Whitefish were not size-normalized, as they were less than the target lengths for each receptor. The ERA (ENVIRON 2008a) provided exponential power regressions for both PCB and Hg to model the relationship between fish length and whole-bodied fish concentration for each fish species. The regression equations were used to predict the concentration of Hg and PCB in whole-bodied fish at 15 cm (for mink assessment) and 30 cm (for bald eagle assessment) in length. The average and 95% upper confidence limit of the predicted concentrations for each target length were used to calculate the DIs, and subsequently the HQs. 4. RESULTS 4.1. Surficial Sediment 4.1.1. Characteristics A fine layer of surficial sediment overlaying the sediment cap was observed both by the divers, and in the cores that were collected for TTU. The divers described this layer of surficial sediment to have a depth that ranged from 1 mm to 3 cm, and at some stations the surficial sediment appeared to have a wavy-like pattern, with the formation of troughs. As expected, the particle size of the surficial sediment overlying the cap was sandy; the majority of stations were >54% sand in the 62-2000 µm range (Table 3). With the exception of stations 15 and 16 (which had CVs of 43% and 45%, respectively), the variability both within and between surveys for particle size (% sand) was <20%. A one-way ANOVA indicated that there were statistical (p<0.001) differences between stations for particle size; however, the variability in replicates at stations 15 and 16 did not allow for a post-hoc test to indicate the differences. By removing stations 15 and 16 from the statistical test (which had the lowest median % sand on the cap), statistically significant (p<0.05) differences were noted between the stations with the most sand content in the sediment (23, 17, 14, and 9) from stations 10 and 12, with the least amount of sand. 12 4.1.2. Nutrients 4.1.2.1. Total Organic Carbon The median SWAC for TOC in the surficial sediment on the cap was 21.2 mg/g (min: 14.7 mg/g, max: 26.2 mg/g), which exceeded the PSQG-LEL (10 mg/g) (Table 4, Figure 8). Individually, the only stations that did not exceed the PSQG-LEL were stations 17 and 23 in the northwest area of the cap. The highest median concentrations, ranging from 31 mg/g to 45 mg/g, were measured at the course sand cap stations 19, 16, and 21. Statistically the TOC concentration at the coarse cap stations differed (p<0.05) from the remainder of the medium cap stations, which had median TOC concentrations ranging from 5.7 mg/g to 28 mg/g. Comparatively, the index station in McKellar Harbour and the reference station in Beatty Cove – which had mostly silty sediment – had median TOC concentrations in 2011 of 21 mg/g and 20 mg/g, respectively. There was no relationship between TOC and particle size (% sand) (r 2 = 0.03, p = 0.275, power = 0.19) on the cap; log-transforming the data did not strengthen the relationship. 4.1.2.2. Total Phosphorus The median TP concentrations in the surficial sediment on the cap ranged from 270 µg/g to 665 µg/g (Table 4). The highest and lowest median concentrations detected were at the reference station 25 and the coarse cap stations (19, 16, 21), respectively. As a point of comparison, the TP concentrations at the more silty index station in McKellar Harbour and the reference station in Beatty Cove were 800 µg/g and 700 µg/g, respectively. Concentrations of TP were evenly distributed across the remainder of the cap (p<0.05), with only slight elevations above the PSQGLEL (600 µg/g) at cap stations 9, 20, 12, 10, and 23. There was little variability between measurements taken at each station during the two surveys (CV <24%). 4.1.2.3. Total Nitrogen The median TN concentrations in the surficial sediment on the cap ranged from 0.10 mg/g to 1.31 mg/g (based on one replicate) (Table 4). Comparatively, the TN concentrations measured at the index station in McKellar Harbour and the reference station in Beatty Cove were 1.1 mg/g and 0.9 mg/g, respectively. When the TN cap data from the two surveys were combined, the CVs ranged from 55 – 153%, which was due to significant (p<0.001) differences observed in concentrations measured between the deployment and retrieval surveys. Generally, samples collected during the deployment survey had higher TN concentrations (ranging from 0.93 to 1.63 mg/g) than samples collected during the retrieval survey (ranging from 0.05 to 0.46 mg/g). With the exception of station 19, the median concentrations of TN in surficial sediment collected from all the cap stations during the deployment survey exceeded the PSQG-LEL (0.55 mg/g). In the retrieval survey, station 10 was the only station with a median concentration that exceeded the PSQG-LEL. Due to the differences observed between the surveys, data was assessed as separate surveys, with results showing no significant (p<0.05) differences in concentrations across the cap. 13 4.1.2.4. Historical Comparisons Prior to conducting historical comparisons, regression analyses were conducted to establish if a relationship existed between TP and TN with TOC, and whether the TP and TN cap data could be TOC-normalized. There was a significant negative (r2 = 0.59, p<0.001, power = 1.0) relationship between TOC and TP when all the 2017 cap data was considered. Given this unusual relationship, the TOC-normalized TP data was not assessed. There did not appear to be a relationship (r2 = 0.037, p = 0.194, power = 0.25) between TN and TOC concentrations in the surficial sediment on the cap; TN-normalized data was also not assessed. The SWAC determined for the pre-cap baseline 2009 and 2011 measurements for TOC over the cap footprint was 27.1 mg/g and 30.2 mg/g, respectively (Figure 9). These pre-cap values were comparable to the 2017 maximum SWAC (26.2 mg/g). Given the results of the 2017 study, and the differences noted between the coarse and medium sand cap areas, the current and historic data were separated into two groups: one that reflected that area over the coarse sand cap, and one which encompassed the remainder of the cap over the medium sand. Over the coarse sand cap footprint there was no change in TOC concentrations over time. However, poor replication, as well as variability in the historic data, resulted in a statistical test with low power (0.35), and this conclusion is cautioned. For the remainder of the cap, the TOC concentrations observed in 2017 were significantly (p>0.05) lower than measured in all of the historic surveys. Similar to TOC, the current and historical TP data was separated into two groups: coarse sand cap stations and medium sand cap stations. Over the coarse cap footprint, concentrations of TP significantly (p<0.05) declined since the 2002 survey (no significant difference from the TP concentrations measured in 2000). Contrary to the coarse cap, the stations over the medium cap displayed no significant (p<0.05) difference since the 2002 survey. Historical comparison for TN could only be made to the 2000 (Milani and Grapentine 2005) and 2002 (Grapentine 2005) datasets, as TN was not analysed in the 2009 and 2011 pre-cap baseline surveys (TKN was measured). Given the variability observed in the post-cap data, historical comparisons were made based on the deployment and retrieval surveys individually. The concentrations of TN observed during the deployment survey was not significantly (p<0.05) different from the historical surveys, while concentrations measured in the retrieval survey were significantly (p<0.05) less. 4.1.3. Metals 4.1.3.1. Trace Metals Concentrations of select trace metals in the surficial sediment overlying the cap are presented in Table 5. The variability (CV) between the replicates was reasonable, ranging from 22 to 47%. Metal concentrations in the surficial sediment on the cap were compared to concentrations measured in 2011 at reference station in Beatty Cove and the index station in McKellar harbour. Again, it is recognized that the surficial sediment at the reference and index stations had a higher 14 percentage of silt and clay; however, based on bulk chemistry alone, the concentrations of metals observed on the cap were generally similar or less (with a few exceptions) than measurements taken at the index and reference stations. The lowest concentrations of metals were detected over the coarse cap stations 19 and 21, and highest concentrations mainly in the northern section of the cap at station 12, 11, 20, 10, as well as stations 23 and 15 in the northwest cap area (Table 5). There were exceptions to this generalization, specifically with As, Sb, B, Mo, Se, Sn, Sr, and Tl. However, other than B and Sr, the concentrations of these metals were less than the method detection limit at the stations on the medium cap, and only slightly above on the coarse cap, so there is a hesitation to draw any conclusions on their distribution pattern. It should be noted that the levels of Sn in the retrieval and deployment surveys at many stations were significantly different, and this metal should be re-assessed in the next LTM survey. Based on the index and reference data, the sediment is naturally enriched with Cu, Ni, and Cr. Elevated concentrations of Cu and Ni are explained by the Coldwell Complex (Ecometrix 2012), and Cr likely by the presence of mafic to ultramafic rocks in the Complex (M. Puumala, per. comm., 2019). As expected, based on the elevated naturally occurring concentrations, these metals exceeded the PSQG-LELs (Cu: 16 µg/g, Ni: 16 µg/g, Cr: 26 µg/g) at various stations on the cap (Table 5). The median concentrations of Ni and Cr exceeded their respective LELs at all stations except 16, 19, and 21 (Cr also exceeded at station 25). As described previously, generally the lowest concentrations were measured at the coarse stations 19 and 21, and the highest at stations located in the north and northwest portion of the cap (Figure 10). For sake of completion, metals from the surficial sediment over the cap were compared to precap measurements. Prior to historical comparisons, metals were normalized to Al, as there was no correlation between particle size and Al over the cap. As discussed previously, this finding was likely an indication of the mixing of the surficial sediment and sand from the cap. In general, most of the metals correlated well with Al (except B and Cu). An assessment of the bulk metals data from the cap surficial sediment against the pre-cap baseline bulk data indicated that concentrations of metals in the surficial sediment increased after the placement of the cap. However, normalizing the current and historical data to Al, indicated that metal concentrations were actually less than the pre-cap survey measurements. Exceptions to this trend were: Mn, which had concentrations post-cap that were significantly (p<0.05) greater than pre-cap measurements; Cu, which had concentrations that did not changed; and Ti, which had concentrations that were similar to concentrations measured in 2011. The assessment of bulk data at individual stations showed that metals decreased at the coarse sand stations 16 and 19, and stayed the same or increased at the remainder of the medium sand stations; there were some exceptions (Mn and Zn), but this was the general pattern. Again, normalizing the metals and individual stations to Al showed that the concentrations of many metals had decreased postcap, with similar exceptions as the whole cap for Mn, Sr, and Ti. Metals (Sb, As, Cd, Mo, Ag, and Sn) that were detected at less than the method detection limit, or had an elevated detection limit (on account of another parameter at a higher concentration), in both the pre-cap surveys and the current survey were not assessed further. 15 4.1.3.2. Specific Ions The anions and cations Ca, Mg, K, Na, and S were measured on the cap as part of the metals scan (Table 6). Elevated concentrations of Ca and Mg on the coarse sand stations 16, 19, and 21 can likely be attributed to the coarse sand which was sourced from Manitoulin Island and primarily consists of limestone and marbles, in which Ca and Mg carbonates are naturally elevated (R. Purdon, per comm. 2019). The material for the medium sand cap was sourced locally, and therefore concentrations of Mg and Ca were consistent to what was measured at the reference and index stations. Levels of S were also higher at the coarse sand cap stations and north-central stations 12 and 10, although concentrations were not as high as concentrations observed in sediment adjacent to other kraft mills (MECP unpublished data). Generally, the distribution of S over the majority of the cap could be considered even, as the coarse cap and north-central stations were only significantly (p<0.05) different from station 17. Bulk concentrations of K were highest at stations 12, 20, 15, and 23; however, when normalized to Al, the coarse cap stations were shown to be enriched compared to the remainder of the cap. Reasons for this observation are unknown. Generally bulk concentrations of Na followed a trend similar to K, but due to a weak relationship with particle size and Al, normalized data was not assessed. Given that the level of these specific ions seemed to be attributed mainly to the source of the sand material, historical comparisons were not completed. 4.1.3.3. Total Mercury The median concentrations of total Hg in the cap surficial sediment ranged from 0.07 µg/g to 1.10 µg/g, with a median SWAC of 0.37 µg/g (min: 0.23 µg/g, max: 0.61 µg/g) (Table 7, Figure 11). The CV for this data ranged from 27 to 53%, which was reasonable given that the data was derived from the two surveys, and two separate jars for each survey (one jar collected for metals scan and another for MeHg analysis). The median Hg concentration of the surficial sediment at the cap reference station 25 was 0.53 µg/g (range 0.21 µg/g), which was higher than the concentration of Hg at all stations except 16 and 19. The distribution of total Hg over the cap is depicted in the Figure 12. The greatest median (range) concentrations of Hg were observed over the coarse cap stations 16 (1.10 µg/g, range 1.05 µg/g) and 19 (1.00 µg/g, range 1.36 µg/g). A statistical comparison showed Hg concentrations at stations 16 and 19 to be significantly (p<0.05) higher than Hg concentrations detected in the northwest corner of the cap (stations 23, 17, and 14). A regression analysis indicated that logTOC explained 61% of the variance in log-Hg concentrations (p<0.001, power = 1.0). As such, Hg concentrations were TOC-normalized and assessed, showing no significant (p<0.05) difference between stations on the cap. Considering the cap as a whole, the median SWAC (0.37 µg/g) was approximately eight times less than the remedial target concentration (3 µg/g) (Figure 12). As a point of comparison, the cap median SWAC was the same as median concentration measured at the index station in Beatty Cove in 2011. At the reference station in McKellar Harbour, outside of Peninsula Harbour AOC, 16 the median concentration measured was 0.04 µg/g. The PSQG-LEL (0.2 µg/g) was exceeded at all individual stations, except the northwest stations 15, 23, 14, 17, and 21. A comparison of the 2017 dataset to the pre-cap data sets (both bulk and TOC-normalized concentrations) indicated that Hg concentrations in the surficial sediment on the cap were significantly less (p<0.05) than the concentrations measured in each historic survey (Figure 13). The SWACs calculated for the 2009 and 2011 pre-cap baseline dataset were 7.69 µg/g and 6.37 µg/g, respectively (Figure 14). Given the relatively elevated concentrations of Hg detected at stations 16 and 19 in 2017, these two stations (data combined) were compared to the pre-cap baseline data (2009 and 2011) for stations over the coarse cap footprint. The comparison indicated Hg concentrations in surficial sediment over the coarse cap footprint were significantly (p<0.05) less than in the sediment collected pre-cap over the same general area. 4.1.3.4. Methyl-Mercury The median surficial sediment concentrations of MeHg on the cap ranged from 0.42 ng/g to 12.14 ng/g (single replicate), with a median SWAC of 3.02 ng/g (min: 2.54 ng/g, max: 4.61 ng/g) (Table 8, Figure 15). The MeHg concentration detected in the surficial sediment at the cap reference station 25 was 1.33 ng/g (range 0.74 ng/g). The variability (CV) among the replicates between surveys ranged from 0.4 to 80%. Excluding the variability observed at stations 16 and 12, the CV for the remainder of the stations did not exceed 49%. The distribution of MeHg on the cap is depicted in Figure 16. Similar to the cap Hg analysis, the highest concentrations were detected at station 16 (median 4.63 ng/g, range 14.20 ng/g) and station 19 (12.14 ng/g, single replicate). The median MeHg concentration of the surficial sediment at reference station 25 was 1.33 ng/g (range 0.74 ng/g), which was higher than the concentration of MeHg in the northwest portion of the cap. Due to the lack of replication of samples at several stations, the MeHg data was assessed according to groups based on a combination of observed concentrations and location on the cap: <1 ng/g (stations 17 and 23 in the northwest area of the cap); 1.1-1.9 ng/g (stations 21, 14, and 20, located mid-cap); and >2 ng/g (stations 16, 19, 11, 12, and 10, located in the southeast area of the cap). A comparison of the groups using a one-way ANOVA showed the lowest concentration (<1 ng/g) group and the highest concentration (>2 ng/g) group to be significantly (p<0.05) different. Given the significant relationship between log-TOC and log-MeHg (r2= 0.69, p<0.001, power = 1.0), TOCnormalized MeHg data was assessed according to the predetermined groups. The result of the MeHg-TOC normalized comparison was the same as the bulk data comparison – there was a significant (p<0.05) difference between the high and low concentration group. Methyl-mercury concentrations were compared to the Peninsula Harbour ERA risk-based sediment management goal of 2.0 ng/g for the protection of fish (ENVIRON 2008a); there is no provincial sediment guideline for MeHg. Specifically, sediment at stations 10, 12, 11, 16 and 19 (located in the southeast area of the cap) had concentrations of MeHg that exceeded the goal (Table 8, Figure 15). The median SWAC of 3.02 ng/g exceeded the risk-based goal by a factor of 1.5. However, there was a decrease compared to SWACs derived from pre-cap assessments: 17 5.1 ng/g, as provided in the ERA and calculated using theissen polygons from data from multiple years (ENVIRON 2008a); 7.78 ng/g in 2009; and 5.11 ng/g in 2011 (Figure 17). The decrease observed post-cap in both the bulk and TOC-normalized concentrations were statistically significant (p<0.05), with the exception of the comparison of 2011 and 2017 TOC-normalized MeHg concentrations. 4.1.4. PCBs The total PCB concentrations in the surficial sediment overlying the thin-layer cap in both the deployment and retrieval surveys ranged from 10 (indicating less than method detection limit (1m Benthic footprint centre point for placement of passive sampler area of each air-lifted benthic lift replicate (3 reps no less than 1m apart in a 5x5 m area) area for collection of core surficial sediment collected in a 20x20 m area, based on centre point Figure 7. Optimal spacing and sampling design for monitoring components. 55 Figure 8. Spatially-weighted area average concentration of total organic carbon (mg/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. 56 Figure 9. Spatially-weighted area average concentration (SWAC) of total organic carbon (mg/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). 57 100 Al Cr Cu Fe Mn Ni Zn Relative Concentration 80 60 40 20 0 25 19 16 21 9 11 10 12 20 14 17 23 15 Station Number Figure 10. Median concentrations of select metals in surficial sediment at each station on the cap and cap reference station 25. The relative concentration on the y-axis is due to Al, Fe, and Mn being divided by factors of 10 in order to fit the scale so that trends could be easily compared. 58 2.5 2.0 Total Mercury (ug/g dw) 1.5 1.0 0.5 LEL 0.0 25 19 9 16 20 11 21 12 10 17 14 23 15 Station Number Figure 11. Median (max and min) of total mercury (µg/g) concentrations in surficial sediment on cap stations and cap reference station 25. Horizontal line depicts the PSQG – Lowest Effect Level (LEL) of 0.2 µg/g. 59 Figure 12. Spatially-weighted area average concentration of total mercury (µg/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. 60 35 Bulk Chemistry TOC-Normalized Chemistry 30 Total Mercury (ug/g dw) 800 25 600 20 15 400 10 200 5 0 0 2000 2002 2009 2011 2017 Survey Year Figure 13. Median (and max and min) of total mercury concentrations (bulk chemistry and TOC-normalized concentrations) measured in the post-cap 2017 survey, and pre-cap/historical surveys conducted in 2000, 2002, 2009, and 2011. 61 TOC-Normalized Total Mercury (ug/g TOC dw) 1000 Figure 14. Spatially-weighted area average concentration (SWAC) of total mercury (µg/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). 62 18 16 Methyl-mercury (ng/g dw) 12 10 8 6 4 2 0 25 16 19 21 20 11 12 10 17 14 23 Station Number Figure 15. Median (and max and min) of methyl-mercury (ng/g) concentrations in surficial sediment on cap stations and cap reference station 25. 63 Figure 16. Spatially-weighted area average concentration of methyl-mercury (ng/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum concentration detected at each station, the median of replicates from both surveys, and the minimum concentration detected at each station. 64 Figure 17.Spatially-weighted area average concentration (SWAC) of methyl-mercury (ng/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (median of replicates at each station); B) 2011 (single replicates at each station); and C) 2009 (single replicate at each station). 65 25 1200 1000 20 MeHg (ng/g) 800 15 600 10 400 5 200 0 0 2000 2002 2009 2011 2017 Survey Year Figure 18. Median and range MeHg concentration (bulk chemistry and TOC-normalized concentrations) measured in the post-cap 2017 survey, and pre-cap surveys conducted in 2000, 2002, 2009, and 2011. 66 TOC-Normalized MeHg (ng/g TOC) Bulk Chemistry TOC-Normalized Chemistry Figure 19. Spatially-weighted area average concentration of PCBs (ng/g) in the surficial sediment on the thin-layer cap. SWACs were derived using the maximum and minimum concentrations detected at each station. 67 Figure 20. Spatially-weighted area average concentration (SWAC) of PCBs (ng/g) in the surficial sediment on the thin-layer cap collected in: A) 2017 (minimum of replicates at each station); B) 2017 (maximum of replicates at each station; and C) 2011 (single replicates at each station). 68 20 18 16 12 10 8 6 4 2 PCB Congener Figure 21. Proportion of PCB congeners in surficial sediment on the thin-layer cap. 69 210 200 190 180 170 160 150 140 130 120 110 100 90 80 70 60 50 40 30 20 10 0 0 Proportion 14 5000 Insecta Oligochaeta Gastropoda Malacostraca Bivalvia Arachnida Other Average Density (no./m2) 4000 3000 2000 1000 0 25 19 16 20 10 17 14 23 Station Number Figure 22. Average density of benthic invertebrates collected from the surficial sediment at the cap stations and reference station 25. 70 100 Dominant Taxa (%) 80 Insecta Oligochaeta Gastropoda Malacostraca Bivalvia Arachnida Other 60 40 20 0 25 19 16 20 10 17 14 23 Station Number Figure 23. Percent dominant benthic invertebrate taxa in the surficial sediment at the cap stations and reference station 25. 71 Appendix Table 1a. Particle size of surficial sediment on the thin-layer cap and cap reference station 25 – deployment survey. Data provided by MECP-LSB. Station No. Sample ID 100170009 100170010 100170011 100170014 100170015 100170016 100170016 100170016 100170017 100170019 100170019 100170019 100170020 100170021 100170023 100170023 100170023 100170025 100170025 GL171305 GL171306 GL171308 GL171309 GL171310 GL171311 GL171312 GL171313 GL171316 GL171317 GL171318 GL171319 GL171320 GL171321 GL171322 GL171323 GL171324 GL171325 GL171326 <2.63 um >0.10 um % vol. qualifier 1.2 3.5 2.9 0.9 1.7 8.2 8.8 3.5 1.3 1.5 1.6 2.5 1.7 4.3 1.6 1 1.6 2.3 2.8 - <62 um >2.63 um % vol. qualifier 6.5 40.5 19.3 7.3 15.7 66.3 67 26.7 13.8 12.2 12.9 19.6 16.5 34.5 13.7 7.4 13.2 14.7 20.3 - 72 <1000 um >62 um % vol. qualifier 71.4 50.2 75.7 55.1 68.7 25.5 24.2 47.9 60.9 57.6 63.6 58.4 63.6 54 56.9 60.4 59.8 83 76.9 - 1000-2000 um % vol. qualifier 21 6 2 36.5 14 0.5 <=W 0.5 <=W 22 24 28.5 22 19.5 18 7 28 31 25.5 0.5 <=W 0.5 <=W Appendix Table 1b. Particle size of surficial sediment on the thin-layer cap and cap reference station 25 – retrieval survey. Data provided by MECP-LSB. Station No. Sample ID 100170019 100170019 100170019 100170016 100170016 100170016 100170020 100170020 100170020 100170012 100170012 100170012 100170025 100170025 100170025 100170021 100170021 100170021 100170010 100170010 100170010 100170011 100170011 100170011 100170014 100170014 100170014 100170017 100170017 100170023 100170015 100170015 100170015 GL172261 GL172262 GL172263 GL172264 GL172265 GL172266 GL172267 GL172268 GL172269 GL172270 GL172271 GL172272 GL172273 GL172274 GL172275 GL172276 GL172277 GL172278 GL172279 GL172280 GL172281 GL172282 GL172283 GL172284 GL172285 GL172286 GL172287 GL172288 GL172289 GL172291 GL172294 GL172295 GL172296 <2.63 um >0.10 um % vol qualifier 2.8 2.6 2.8 3.4 1.7 2.1 2.2 1.6 1.7 3.9 3.3 2.3 2.5 2.2 1.9 2.4 2.8 1.6 2.9 2.6 3.1 2.6 2.6 2.9 1.5 1.5 1.6 1.4 1 1.1 2.9 7.5 6.7 - <62 um >2.63 um % vol qualifier 25.1 22 28.5 32.6 13.9 19.5 23.8 15.9 13.9 40.2 32.7 21.9 16.4 15.4 9.7 21.5 25.5 12.6 27.3 26.6 31.6 22.9 29.4 24.5 13.8 14.3 14.7 11.5 8.7 7.7 25.9 58.4 56.1 - 73 <1000 um >62 um % vol qualifier 49.4 49.3 48.9 50.7 55.8 55.2 58.6 61.1 53.4 54 58.4 64 81.1 81.2 88.4 55.7 60.1 63.1 57.9 57.7 60.8 71.3 65.5 70.2 55.7 55.2 56.8 70.7 60.3 62.9 61.5 34.1 37.2 - 1000-2000 um % vol qualifier 22.5 26 20 13.5 28.5 23 15.5 21.5 31 2 5.5 12 0.5 <=W 1 TAXA Hydra Mesenchytraeus Tubificinae - imm. with hairs Tubificinae - imm. without hairs Amphichaeta leidyi Arcteonais lomondi Aulodrilus americanus Aulodrilus pluriseta Chaetogaster diaphanus Chaetogaster diastrophus Limnodrilus hoffmeisteri Nais Nais behningi Nais communis Nais simplex Piguetiella blanci Rhyacodrilus Slavina appendiculata Specaria josinae Spirosperma ferox Stylaria lacustris Tasserkidrilus superiorensis Uncinais uncinata Vejdovskyella comata Vejdovskyella intermedia Lumbriculus variegatus complex Stylodrilus herringianus Glossiphonia complanata Gloiobdella elongata Hydrolimax grisea Musculium Musculium securis TSRC1 TSRC3 TSRC4 100 TSRC2 0019 100 100 2 0 86 2 0 1 1 18 0 0 0 0 0 0 2 8 0 3 0 16 0 0 1 0 0 1 0 0 0 7 0 0 8 0 11 0 0 1 0 0 0 0 0 0 0 0 0 5 0 1 0 9 0 0 0 0 0 0 0 0 0 1 0 0 8 0 453 29 0 7 60 72 0 0 0 0 0 0 2 11 0 1 1 2 0 0 5 0 0 0 0 0 0 10 0 0 108 TSRC6 TSRC7 100 TSRC5 0016 100 TSRC9 TSRC10 100 TSRC8 0020 100 100 1 0 45 0 0 0 0 19 0 0 0 0 0 0 0 2 0 0 1 11 0 0 1 0 0 0 0 0 0 0 0 0 4 0 1696 31 3 30 0 209 0 0 2 0 0 5 1 27 4 13 85 175 0 24 8 4 19 1 0 0 0 3 0 0 0 2 29 1 0 15 0 8 0 0 0 0 0 0 0 9 1 0 1 14 0 2 5 0 0 0 0 0 0 3 0 0 TSRC12 100 TSRC11 0025 100 100 5 0 33 0 0 3 0 1 0 0 0 0 0 0 0 2 0 0 0 3 2 0 1 0 0 0 0 0 0 0 0 0 0 0 21 0 0 13 1 2 0 0 0 0 0 0 0 2 0 0 0 16 0 0 6 0 0 1 0 0 0 1 0 0 3 0 35 0 0 10 0 1 0 0 0 0 0 1 2 2 0 0 0 7 0 0 2 0 0 1 0 0 0 0 0 0 2 8 12 0 0 10 0 0 1 6 0 0 0 0 5 13 0 0 0 1 0 0 8 0 0 6 0 1 1 1 1 0 0 1 6 0 0 3 0 0 0 2 0 0 0 0 0 16 0 0 0 3 0 0 8 0 0 0 2 0 0 0 0 0 1 9 35 1 0 10 0 0 0 6 0 1 0 0 18 23 0 0 2 2 0 0 17 0 0 0 8 0 0 0 0 0 100 Pisidiidae Pisidiidae Pisididae Pisidiidae Pisidiidae Pisidiidae Lymnaeidae Lymnaeidae Lymnaeidae Physidae Planorbidae Planorbidae Planorbidae Planorbidae Planorbidae Planorbidae Valvatidae Valvatidae Valvatidae Valvatidae Hydrobiidae Leptoceridae Leptoceridae Leptoceridae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Pisidium Pisidium casertanum Pisidium ferrugineum Pisidium henslowanum Pisidium nitidum Pisidium ventricosum Unknown specimens Fossaria Pseudosuccinea columella Physa Unknown specimens Gryaulus Gyraulus circumstriatus Gyraulus deflectus Gyraulus parvus Helisoma anceps Valvata Valvata lewisi Valvata piscinalis Valvata tricarinata Pyrgulopsis lacustrica Mystacides sepulchralis Oecetis Oecetis nocturna Chironominae Orthocladiinae Ablabesmyia janta Chironomus Cladotanytarsus Conchapelopia Cricotopus Cryptochironomus blarina Demicryptochironomus cuneatus Heterotrissocladius Heterotrissocladius changi Heterotrissocladius marcidus Larsia canadensis Mesocricotopus 0 37 0 8 0 0 0 0 0 0 0 0 0 0 0 0 0 5 7 4 5 1 1 6 1 0 0 22 23 0 0 0 0 0 1 0 0 0 109 0 2 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 1 0 4 0 0 0 2 0 0 0 1 10 0 0 0 0 0 5 0 0 0 0 57 0 7 0 6 0 0 0 4 0 6 0 0 1 6 0 10 3 5 2 2 0 1 1 3 0 4 14 1 0 1 0 0 3 0 0 1 0 3 0 0 0 1 0 0 0 0 0 0 0 0 0 1 0 13 3 0 0 0 0 4 1 0 0 2 1 0 0 0 0 0 3 0 0 0 0 21 0 4 0 4 0 0 0 1 0 2 0 0 0 2 0 30 1 3 1 0 0 22 1 0 0 32 2 0 0 0 1 0 5 1 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 8 3 1 1 0 0 6 0 0 0 3 6 0 0 0 0 0 6 5 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 2 2 0 0 0 0 0 0 0 0 2 0 0 0 0 0 1 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 2 0 9 3 8 2 0 0 2 0 0 0 0 1 0 0 0 0 0 2 6 0 0 0 1 0 0 0 0 0 0 0 0 0 2 0 0 3 6 23 13 9 12 1 0 0 5 1 0 0 0 6 0 0 0 0 0 2 1 0 0 0 3 1 0 9 0 4 2 0 0 1 0 0 0 0 0 11 9 1 5 6 0 0 1 0 0 0 1 126 0 0 0 0 4 18 5 0 0 3 0 0 1 11 0 2 0 0 0 0 0 0 0 0 1 7 5 1 1 6 1 0 3 0 2 0 0 88 0 1 0 0 0 7 6 0 0 1 0 0 0 24 0 2 0 0 0 0 0 0 0 0 0 14 5 0 1 4 0 0 1 1 0 0 0 101 0 0 0 0 1 6 8 0 0 Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Gammaridae Pontoporeiidae Asellidae Aturidae Hygrobatidae Lebertiidae Limnesiidae Oxidae Oxidae Pionidae Pionidae Halicaridae Halicaridae Hydrozetidae Micropsectra Microtendipes pedellus group Monodiamesa tuberculata Orthocladius Orthocladius annectens Parachronomus potamogeti Paracladopelma Paracladopelma winnelli Parakiefferiella Paratanytarsus Paratendipes Phaenopsectra Polypedilum lateum group Polypedilum scalaenum group Potthastia Procladius Protanypus Psectrocladius Pseudochironomus Stempellina Stempellinella Tanytarsus Thienemannimyia norena Gammarus pseudolimnaeus Pontoporeia hoyi Caecidotea Unknown specimens Aturus Hygrobates Lebertia Limnesia Frontipoda americana Oxus Unknown specimens Piona Unknown specimens Parasoldanellonyx parviscutatus Hydrozetes 5 0 0 0 0 0 0 3 0 0 1 1 0 0 0 67 6 1 0 6 1 9 0 0 1 0 0 0 1 5 0 0 0 1 3 0 0 0 110 0 0 0 0 0 0 0 0 3 0 0 0 0 0 0 22 1 1 0 3 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 4 0 0 1 0 1 0 0 13 0 6 21 0 3 0 96 7 1 0 4 0 22 0 4 4 0 0 0 5 4 0 0 2 0 7 0 0 0 0 0 0 0 0 0 0 0 2 0 0 0 0 0 0 6 1 0 0 5 0 5 0 0 3 0 0 0 0 0 0 0 0 0 0 1 0 0 143 2 0 0 1 0 2 0 1 0 60 86 0 29 0 135 2 0 0 5 0 51 0 0 6 2 0 0 0 4 0 0 0 0 0 3 0 0 0 0 4 0 0 0 0 0 1 0 0 0 0 0 0 16 0 0 0 9 0 5 0 0 4 0 0 0 0 4 0 0 3 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 15 0 0 0 2 0 3 0 0 5 0 0 0 0 0 0 0 2 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 11 0 0 0 0 0 1 0 0 3 0 0 0 0 0 0 0 0 0 0 4 0 0 1 0 2 0 0 0 0 0 1 0 0 1 0 0 0 13 1 0 0 6 0 8 0 1 1 0 0 0 0 1 0 0 0 0 0 2 0 0 8 0 2 1 0 0 0 3 10 2 0 0 0 0 0 25 1 3 0 3 0 53 1 23 7 0 0 0 6 3 0 0 2 0 11 0 0 1 2 0 1 1 0 0 0 2 2 0 0 0 0 3 0 14 0 1 1 3 0 29 0 14 23 1 0 2 7 1 0 1 0 0 4 0 0 0 10 0 0 2 0 0 0 3 6 1 0 0 0 2 0 29 0 3 0 1 0 20 0 19 29 5 0 0 5 4 0 1 1 0 0 0 0 2 Malaconothricidae Chydoridae Daphniidae Holopediidae Cyclopidae Candonidae Candonidae Candonidae Cyprididae Cyprididae Cyprididae Cyprididae Lymnocythereidae Unknown specimens Unknown specimens Unknown specimens Unknown specimens Holopedium gibberum Unknown specimens Unknown specimens Unknown specimens Unknown specimens Unknown specimens Candona Fabaeformiscandona Cyclocypris Cypria Cypridopsis Pelocypris Limnocythere 0 0 280 12 0 5 385 14 42 0 112 36 307 4 0 378 104 111 0 0 111 35 0 11 136 16 13 0 78 17 159 4 0 0 40 0 0 299 28 0 0 444 56 52 0 133 57 267 6 0 319 142 0 0 17 9 0 18 158 26 2 0 17 10 21 4 0 192 5 0 100 50 7 0 6 130 973 22 0 165 63 20 37 0 254 61 0 3 18 2 0 2 106 23 3 0 94 10 48 0 0 191 12 1 1 35 17 0 9 131 43 7 0 74 19 59 1 0 252 23 0 0 26 31 0 14 153 25 4 0 77 15 91 0 0 251 18 0 4 30 35 0 5 193 48 13 0 85 50 154 3 0 283 24 0 0 3316 5 18 5 1046 115 308 0 622 1 41 2 0 415 30 1 20 2712 1 23 11 860 27 210 0 405 0 16 0 22 532 20 0 34 1567 0 19 9 823 106 359 0 589 0 23 0 30 550 35 Appendix Table 8 cont’d. Benthic invertebrate counts on the thin-layer cap and cap reference station. 25. Each replicate is 0.25m2. Data provided by Craig Logan. Family Hydridae Enchytraeidae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Naididae Lumbriculidae Lumbriculidae Glossiphoniidae Glossiphoniidae Plagiostomidae Pisidiidae SAMPLE CODE STATION NO. #cells picked out of 100 --> TAXA Hydra Mesenchytraeus Tubificinae - imm. with hairs Tubificinae - imm. without hairs Amphichaeta leidyi Arcteonais lomondi Aulodrilus americanus Aulodrilus pluriseta Chaetogaster diaphanus Chaetogaster diastrophus Limnodrilus hoffmeisteri Nais Nais behningi Nais communis Nais simplex Piguetiella blanci Rhyacodrilus Slavina appendiculata Specaria josinae Spirosperma ferox Stylaria lacustris Tasserkidrilus superiorensis Uncinais uncinata Vejdovskyella comata Vejdovskyella intermedia Lumbriculus variegatus complex Stylodrilus herringianus Glossiphonia complanata Gloiobdella elongata Hydrolimax grisea Musculium TSRC13 100 18 0 4 0 0 0 0 1 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 2 0 0 0 0 0 0 112 TSRC14 0010 100 TSRC15 TSRC16 100 100 10 1 76 0 0 2 0 2 0 0 0 0 0 0 0 1 0 2 0 6 0 0 0 0 1 0 0 0 0 2 0 8 1 115 3 0 13 0 15 0 0 0 0 0 0 0 29 0 1 10 13 0 0 1 0 15 0 3 0 0 1 0 8 0 9 0 0 5 0 0 0 0 0 1 3 0 0 0 0 7 0 3 0 0 1 0 15 0 0 0 0 0 1 TSRC17 0014 100 TSRC18 TSRC19 100 100 7 1 5 0 0 10 0 1 0 0 0 2 0 10 0 10 0 12 0 9 0 0 3 0 16 0 2 0 0 0 0 6 0 1 0 0 4 0 0 0 0 0 0 0 2 0 0 0 14 0 4 0 0 1 0 16 0 1 0 0 1 0 1 0 1 0 0 9 0 0 0 0 0 0 0 2 0 3 0 0 0 6 0 0 2 0 16 3 0 0 0 2 0 TSRC20 0017 100 TSRC21 TSRC22 100 100 1 0 68 2 0 19 0 1 0 0 0 1 0 2 0 9 2 0 0 29 0 0 2 0 17 5 0 0 0 0 0 0 2 11 2 0 7 1 1 0 0 0 0 0 0 0 2 0 0 0 7 0 0 2 0 1 10 0 0 0 1 0 2 1 0 0 0 0 0 0 0 0 0 0 0 0 1 2 0 0 0 12 0 0 1 0 49 5 0 0 0 2 0 TSRC23 0023 100 2 1 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 0 0 15 0 0 2 0 44 1 0 0 0 0 0 TSRC24 100 0 0 0 0 0 4 0 0 0 0 0 0 0 0 0 0 0 0 0 18 0 0 1 0 31 4 0 0 0 0 0 Pisidiidae Pisidiidae Pisidiidae Pisididae Pisidiidae Pisidiidae Pisidiidae Lymnaeidae Lymnaeidae Lymnaeidae Physidae Planorbidae Planorbidae Planorbidae Planorbidae Planorbidae Planorbidae Valvatidae Valvatidae Valvatidae Valvatidae Hydrobiidae Leptoceridae Leptoceridae Leptoceridae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Musculium securis Pisidium Pisidium casertanum Pisidium ferrugineum Pisidium henslowanum Pisidium nitidum Pisidium ventricosum Unknown specimens Fossaria Pseudosuccinea columella Physa Unknown specimens Gryaulus Gyraulus circumstriatus Gyraulus deflectus Gyraulus parvus Helisoma anceps Valvata Valvata lewisi Valvata piscinalis Valvata tricarinata Pyrgulopsis lacustrica Mystacides sepulchralis Oecetis Oecetis nocturna Chironominae Orthocladiinae Ablabesmyia janta Chironomus Cladotanytarsus Conchapelopia Cricotopus Cryptochironomus blarina Demicryptochironomus cuneatus Heterotrissocladius Heterotrissocladius changi Heterotrissocladius marcidus Larsia canadensis 0 1 0 0 0 2 0 0 0 0 0 2 0 0 0 0 0 3 10 2 5 0 1 1 3 0 0 0 0 0 0 0 0 0 0 1 2 0 113 1 3 0 0 0 4 2 1 0 0 0 0 0 0 0 0 1 6 11 1 4 0 0 0 3 0 4 0 2 3 0 0 0 0 5 4 1 0 1 4 13 0 0 1 1 0 0 0 0 0 0 0 0 1 4 1 25 0 4 1 0 0 6 0 0 0 1 16 0 0 0 0 0 4 3 0 0 0 0 0 0 1 0 1 0 0 0 0 0 1 0 0 0 0 17 4 5 1 0 0 3 5 0 3 0 1 0 0 0 0 0 2 1 0 0 0 0 0 0 1 0 0 0 0 0 0 0 1 0 0 0 5 20 0 9 1 0 0 2 1 1 0 4 6 0 0 0 0 1 4 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 21 1 1 0 1 2 0 0 0 1 0 2 0 0 0 0 0 3 0 1 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 0 0 11 4 4 0 0 0 0 0 0 0 1 5 0 0 0 0 1 3 1 0 0 0 1 1 0 0 2 0 0 0 0 0 0 2 0 0 1 0 21 2 2 2 0 0 1 1 0 0 0 12 0 0 0 0 0 6 5 0 0 0 0 0 0 1 1 0 0 0 0 0 0 0 0 0 0 10 20 6 6 0 0 0 0 0 0 0 0 7 0 0 0 0 0 2 7 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 2 6 2 0 0 0 0 0 0 1 0 0 1 0 0 0 0 0 2 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 3 1 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 7 1 0 0 1 0 0 0 0 0 0 0 0 0 0 0 1 0 0 3 1 10 0 0 0 0 0 1 0 0 0 2 0 0 0 0 0 2 0 0 Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Chironomidae Gammaridae Pontoporeiidae Asellidae Aturidae Hygrobatidae Lebertiidae Limnesiidae Oxidae Oxidae Pionidae Pionidae Halicaridae Halicaridae Mesocricotopus Micropsectra Microtendipes pedellus group Monodiamesa tuberculata Orthocladius Orthocladius annectens Parachronomus potamogeti Paracladopelma Paracladopelma winnelli Parakiefferiella Paratanytarsus Paratendipes Phaenopsectra Polypedilum lateum group Polypedilum scalaenum group Potthastia Procladius Protanypus Psectrocladius Pseudochironomus Stempellina Stempellinella Tanytarsus Thienemannimyia norena Gammarus pseudolimnaeus Pontoporeia hoyi Caecidotea Unknown specimens Aturus Hygrobates Lebertia Limnesia Frontipoda americana Oxus Unknown specimens Piona Unknown specimens Parasoldanellonyx parviscutatus 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 3 0 0 0 4 0 1 0 8 1 5 0 0 4 1 1 0 0 0 1 0 0 114 0 0 0 1 0 0 0 0 0 3 0 2 0 0 4 0 17 1 0 0 0 0 4 0 2 11 6 0 0 3 0 0 0 0 0 0 0 0 0 2 0 1 1 0 0 0 2 7 0 0 0 0 2 1 58 3 0 0 12 0 7 0 9 13 6 0 0 3 0 0 2 0 0 1 2 0 0 1 0 0 1 0 0 0 0 1 0 0 0 0 0 0 3 0 0 0 18 0 6 0 1 1 0 0 0 1 2 0 0 0 0 0 1 0 0 2 0 2 0 0 0 0 0 2 0 0 0 0 0 0 16 0 0 0 10 0 2 0 3 3 0 0 0 1 0 0 0 2 0 2 4 0 0 1 0 0 0 0 0 0 0 3 0 0 0 0 0 0 9 0 0 0 4 0 2 0 3 0 0 0 0 3 1 0 0 1 0 0 3 0 0 0 0 0 0 0 0 1 0 2 0 0 0 0 0 0 11 0 0 0 9 0 2 0 0 2 0 0 0 1 2 0 0 0 0 1 7 0 0 1 0 1 0 0 0 0 2 4 0 0 0 1 0 0 10 0 0 0 17 0 12 0 0 8 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 8 1 0 0 8 0 0 0 1 6 0 0 0 2 0 0 0 0 0 0 5 0 0 1 0 0 0 0 0 0 0 2 0 0 0 0 0 1 0 0 0 0 12 0 12 0 0 3 0 0 0 0 0 0 0 0 0 1 4 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 8 0 2 0 0 2 0 0 0 0 0 0 0 0 0 0 0 1 0 1 0 0 1 0 0 0 1 2 0 0 0 0 0 0 4 0 0 0 28 0 5 0 0 1 1 0 0 0 0 0 0 0 0 0 4 0 Hydrozetidae Malaconothricidae Chydoridae Daphniidae Holopediidae Cyclopidae Candonidae Candonidae Candonidae Cyprididae Cyprididae Cyprididae Cyprididae Lymnocythereidae Hydrozetes Unknown specimens Unknown specimens Unknown specimens Unknown specimens Holopedium gibberum Unknown specimens Unknown specimens Unknown specimens Unknown specimens Unknown specimens Candona Fabaeformiscandona Cyclocypris Cypria Cypridopsis Pelocypris Limnocythere 1 0 0 61 53 26 7 159 49 5 4 21 5 112 3 1 236 10 115 0 0 5 28 26 2 5 202 123 16 0 51 15 93 9 0 149 9 0 1 0 38 43 4 5 273 568 27 0 76 12 142 8 9 223 43 0 0 0 18 13 0 21 323 96 13 0 82 6 140 0 0 143 29 1 0 1 30 19 0 69 363 71 9 0 93 8 95 1 0 231 26 0 0 0 35 10 8 60 241 121 17 0 65 11 87 3 0 112 12 0 0 0 34 7 1 152 328 39 10 0 50 4 24 1 0 256 38 1 0 20 23 9 0 48 106 73 7 0 46 6 37 0 0 256 28 0 0 4 0 0 1 37 136 23 0 0 36 0 41 0 0 200 15 0 0 23 22 0 0 73 84 7 6 0 72 1 33 0 0 511 38 0 0 12 11 2 1 27 39 2 0 0 13 0 15 0 0 249 15 0 0 9 32 4 4 101 74 1 4 0 39 3 31 0 0 695 16 Appendix Table 9. Mercury, total PCBs, and DLPCB congener concentrations in dorsal fillet tissue of Lake Trout, Lake Whitefish, and Longnose Suckers, and whole-body composites of young-of-year Round Whitefish collected in Peninsula Harbour. Data provided by MECP-LSB. Species Name Length Weight Sex M ercury Total PCB Lipid PCB 77 PCB 81 PCB105 PCB114 PCB118 PCB123 PCB126 PCB156 PCB157 PCB167 PCB169 PCB189 ug/g ww ng/g ww % pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww pg/g ww Lake Trout 90.3 7900 M 1.3 6600 5 81 5.6 23000 1500 81000 1000 250 42000 3800 15000 66 9700 Lake Trout 67.2 2605 M 0.38 1400 7.1 21 2 2600 140 9200 110 34 4200 360 1500 9 940 Lake Trout 61.3 2135 M 0.19 160 4.4 33 2.5 1700 82 5300 80 29 1700 200 840 8.7 360 Lake Trout 59.7 1960 M 0.36 600 5 38 2.8 4100 230 14000 200 52 6400 540 2400 12 1400 Lake Trout 54.3 1295 M 0.14 78 2.4 Lake Trout 54.2 1100 M 0.11 210 4.5 Lake Trout 52.4 1135 F 0.1 45 3.6 Lake Trout 51.7 1220 M 0.15 310 9.8 Lake Trout 45.8 685 F 0.13 70 2.5 7.1 <0.79 430 22 1400 20 7.4 470 51 180 2.7 100 Lake Trout 61 2240 F 0.2 230 5.7 Lake Whitefish 54.8 1265 M 0.11 39 4 Lake Whitefish 51.5 1125 M 0.11 20 1.8 3.5 <0.38 89 4.2 250 5.1 2.5 56 9.4 27 <0.64 11 Lake Whitefish 49.8 1140 F 0.09 25 4.3 5.5 <0.48 190 9.8 530 12 4.1 130 22 70 1.5 27 Lake Whitefish 40.5 465 F 0.09 27 2.1 Lake Whitefish 34.5 330 F 0.07 20 2.2 Lake Whitefish 34.3 340 M 0.07 20 2.7 <1.6 <0.51 88 4.4 260 5.2 <1.5 52 9.8 31 <0.45 11 Longnose Sucker 48.5 1090 F 0.67 1100 5 Longnose Sucker 47.3 860 F 0.5 1400 2.4 Longnose Sucker 47.2 1025 F 0.23 130 1.9 Longnose Sucker 45.6 955 F 0.21 360 2.1 Longnose Sucker 44.1 800 0.3 480 2.8 Longnose Sucker 42 755 F 0.25 200 1.3 Longnose Sucker 39.4 625 M 0.32 650 2.5 Longnose Sucker 37.8 550 M 0.43 2700 3.7 Longnose Sucker 34.2 350 F 0.17 150 1.4 31.2 285 F Longnose Sucker 0.15 130 1.6 1 9.9 0.07 590 2.0 Round Whitefish1 9.8 0.07 590 2.0 Round Whitefish1 9.6 0.06 590 1.5 Round Whitefish1 9.5 0.06 590 1.6 Round Whitefish 1young-of-year whole-body composites 116