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Page 1: Nearshore Habitat & Water Quality

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About the Authors

Shawn Bland

Shawn Bland was born in 1985 and raised in Saint John, New Brunswick where he graduated with Honours from Harbour View High School in 2003. In 2013, after gaining 10 years of experience in various work settings, he decided to further his education and follow his passion for the sciences by enrolling in the NBCC Saint John Chemical Technology Program.

Jacob Lewis

Jacob was born in 1992 and graduated with Honours from Harbourview High Schoolin 2010.Unclear as to which career path to

follow, he ultimately decided that the NBCC Chemical Technology program was a natural fit in an industrial area like Saint John.

‘’Life can only be enjoyed through understanding, and science is the

language’’.

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Executive Summary Marsh Creek, which is the largest watershed in greater Saint John, has been the recipient of centuries of untreated municipal wastewater deposition. Offensive odours, unsightly sanitary products and the threat

posed by various human pathogens, resulting largely from the ~50 sewage outfalls in the lower reaches of Marsh Creek and the Saint John Harbour have caused most residents to abandon the wellness of the

watercourse. ACAP Saint John, a community-based ENGO and champion of the Harbour Cleanup project, has been conducting water quality monitoring and fish community surveys in the watershed since 1993 with

the view towards someday restoring the ecological integrity of this underutilised natural asset.

Analyses conducted by the Atlantic Coastal Action Program (ACAP) Saint John have indicated substantial improvements to the quality of water in Marsh Creek in 2014. The most notable change was the decrease in faecal coliform bacteria, which are used as an indicator for the potential presence of other disease causing

pathogens such as amoebic dysentery and Hepatitis. Sampling conducted during 2014 along the lowest 400 m of the creek - which has historically received the greatest volume of untreated municipal wastewater - has

shown decreases in faecal bacteria counts ranging from 95 to 99%, as compared to results from 2013.

While the levels of bacteria still remain on average above the federal recreational water safety guidelines of 200 counts/100 ml at all sites tested, the substantial improvements in water quality are very encouraging,

suggesting that the City of Saint John’s ongoing efforts to complete Harbour Cleanup are beginning to pay dividends. ACAP staff have also noted that, in addition to observed improvements in the clarity of the water in Marsh Creek, there have been no calls received from the public complaining about the offensive odours

that have historically plagued this area of the city.

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Acknowledgements

The 2014 ‘Impact of Harbour Cleanup on Nearshore Habitat and Water Quality in Saint John, New Brunswick’ project represents the third consecutive year of intensive sampling and analyses directed at

documenting the ecological implications of recent (2014) improvements in municipal wastewater treatment and discharge in Saint John, New Brunswick. Funding for the 2014 installment of this Marsh Creek project was provided by Environment Canada’s Atlantic Ecosystem Initiative and

Service Canada’s Canada Summer Jobs (CSJ) program. Technical and laboratory support was [once again] generously provided by the Chemical Technology program of the New Brunswick

Community College (Saint John).

It must be noted that this report builds directly upon the 2013 ACAP Saint John report “LeBlanc, M. and Z. Sears. 2013. The Re-Birth of Marsh Creek: Chronicling the benefits of Harbour Cleanup on the Marsh Creek watershed of Saint John, New Brunswick, Canada. 49 pages.” Given that much of the text is taken verbatim, this acknowledgement will serve as the only reference indicating the

direct duplication of some content.

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Table of Contents Subject Page About the Authors i Executive Summary ii Acknowledgements iii Table of Contents iv 1.0  Background 1 1.1 Overview of the Marsh Creek Watershed 1 1.2 History 1 2.0 Methodology 2 2.1 Water Quality Analyses 2 2.1.1 Comparative Historical Data 2 2.1.2 Sampling Stations Analysis A 3 2.1.3 Sampling Stations Analysis B 3 2.1.4 Water Quality Parameters 5 2.2 Water Quality Procedures 6 2.2.1Field pH 6 2.2.2Dissolved Oxygen 6 2.2.3Salinity 7 2.2.4Orthophosphates 7 2.2.5Total Suspended Solids 8 2.2.6Fecal Coliform 9 2.2.7 Lab pH 10 2.3 Sampling of Fish 11 2.3.1 Electrofishing 11 2.3.2 Fyke Nets 12 2.3.3 Beach Seines 12 2.3.4 Reporting of Fish Collected 13 2.4 Other Observations 13 3.0 Results 14 3.1 Water Quality Parameters 14 3.1.1 Analysis A Water Quality Parameters 14 3.1.2 Analysis B Water Quality Parameters 15 3.1.3. Water Quality Parameters of Additional Site 19

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3.2 Fish Collection 20 3.2.1 Lower Marsh Creek 20 3.2.2 Ashburn Lake 20 3.2.2 Ashburn Creek 21 3.3 Other Observations 21 3.3.1 European Green Crab 21 3.3.2 Canada Post Retaining Wall: Creosote 22 4.0 Discussion 23 4.1 Water Quality Parameters Analysis A 23 4.2 Water Quality Parameters Analysis B 24 4.3 Fish Communities 25 5.0 Conclusion 25 6.0 References 26

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1.0 Background

1.1 Overview of the Marsh Creek Watershed The Marsh Creek watershed is a 4,200 hectare feature located in the eastern quadrant of Saint John, New Brunswick, Canada, that drains directly into the Bay of Fundy (Figure 1.1). The watershed consists of six primary watercourses, eighteen lakes and countless wetlands, including a brackish semi-tidal wetland at its terminus. Marsh Creek, which served as a valuable natural asset for early settlers, became an internationally recognized environmental concern due in large part to its receipt of untreated municipal wastewater and the existence of heavy creosote contamination in the sediments of its lower reaches. Locally, the creek is also subject to extreme flooding resulting from its low-lying drainage basin, commercial and residential developments in and around its floodplain and the cumulative effects of crustal subsidence and watercourse channel and wetland infilling.

1.2 History

Saint John, New Brunswick, as one of the most rapidly changing urban environments in Atlantic Canada, is currently undertaking several once-in-a-lifetime alterations that have the potential to significantly improve the water quality of inland and near-shore environments. The most noteworthy of these alterations is the 2014 completion of the Saint John Harbour Cleanup project, which will result in the cessation of the centuries old practice of discharging raw sewage into its urban waterways, including Marsh Creek, Courtenay Bay, Saint John Harbour, and ultimately the Bay of Fundy.

Harbour Cleanup, which has come aboutlargely from two decades of dedicated community engagement by ACAP Saint John, represents the single greatest opportunity in recent history to restore the recipient near-shore water quality of Saint John, thereby improving the habitat needed to increase (and potentially even restore) the diversity of flora and fauna. As such, the information acquired in

Figure  1.1:  The  Marsh  Creek  Watershed  (outlined  in  red)  in  Saint  John,  New  Brunswick  

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this project represents one of the last opportunities in Canadian history to acquire the baseline metrics needed to measure and document any changes that occur in the associated biodiversity following the cessation of untreated municipal wastewater discharges into near-shore environments.

The objectives of this project were to acquire the firstbaseline (post-wastewater treatment) water quality measurements and fish community assemblages within the estuarine and aquatic habitats of Marsh Creek and the Courtenay Bay Forebay. The scope of this report included the recipient waters as well as those immediately above (upstream of) the historic zone of influence. This project was designed to acquire data and present information in a format that will enable comparable data to be collected and analysedin subsequent years. It must also be noted that field staff were instructed to be vigilant and take note of any other conditions that could increase our understanding of the current status of this ecosystem.

2.0 Methodology 2.1 Water Quality Analyses

2.1.1 Comparative Historical Data

This project conducted two separate water quality analyses in the Marsh Creek watershed to enable comparisons with two distinct historical data sets. Analysis A involved a simple upstream (U)/downstream (D) comparison relative to the area receiving wastewater discharges (Figure 2.1.A). These sample stations have now acquired data in various years between 1993 and 2014.

Analysis B consisted of five sample stations in the last 2 km of Marsh Creek used to conduct a more defined concentration gradient analyses within the wastewater discharge zone (Figure 2.1.A). These sample stations were first established in the 2012 Marsh Creek study

2.1.2 Sample Stations Analysis A

Figure   2.1.A:  Water   Quality  Monitoring   Stations   used   for  the  Marsh  Creek  Watershed  in  2014  

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The stations used in Analysis A included a Downstream Site (45° 16' 32", 66° 00' 00")located on the downstream side of the access road/rail crossing which contains three metal culverts (Figure 2.1 B(left)); and an Upstream Site (45° 16' 59", 66°03'02")located on the downstream side of the small bridge on Glen Road near MacKay Street (Figure 2.1 B (right)).

Figure   2.1.B:   Downstream   (left)   and   Upstream   (right)  Sampling  Stations  used  in  water  quality  monitoring  in  Marsh  Creek  between  1993  and  2014  

2.1.3 Sample Stations Analysis B

Analysis B, which has acquired water quality measurements since 2012,incorporated five sampling stations located approximately 500 m apart within the last 2km of Marsh Creek (Figure 2.1 C). The stations included two sites in the Courtenay Forebay and three sites above the three culvert station used as the Downstream Sampling Station in Analysis A (Section 2.1.2). The characteristics of the five individual Sampling Stations used in Analysis B are provided in Table 2.1 and in Figures 2.1D and 2.1E.

Figure  2.1.C:  Map  showing  the  location  of  the  five  Sampling  Stations  used  in  Marsh  Creek   water   quality   Analysis   B   (2012-­‐2014)  

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 Table  2.1:  Characteristics  of  Sampling  Stations  used  in  Marsh  Creek  water  quality  Analysis  B  in  2012  through  2014.  

Site Number GPS Coordinates Site Description

1 45.277506, -66.047122

Located on the upstream side of the Courtenay tide gates at the terminus of Marsh Creek.

2 45.281560, -66.048694

Located approximately 500 m upstream from Site 1, just upstream of where Dutchman’s Creek enters Marsh Creek.

3 45.284844, -66.052393

Located 500 m upstream from Site 2 immediately (2m) upstream of the raw sewage outfall adjacent to the Sunbury parking lot.

4 45.288143, -66.048764

Located 500 m upstream from Site 3immediately upstream of another raw sewage outfall.

5 45.290998, -66.043606

Located upstream of the raw sewage outfalls, approximately 2 km from the outlet of Marsh Creek at the tide gates (Site 1). This sampling station was located beneath the train bridge adjacent to Rothesay Avenue.

Figure  2.1.E:  Images  of  Sample  Site  3  (left),  4  (middle)  and  5  (right)  used  in  Water  Quality  Analysis  B  conducted  in  Marsh  Creek  in  2012  through  2014  

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2.1.4 Water Quality Parameters

Water quality parameters measured in 2014 included dissolved oxygen, salinity, pH, orthophosphates, total suspended solids, and fecal coliform. Historically, ammonia concentration, nitrates, and turbidity were parameters that had also been recorded for the upstream and downstream (Analysis A) sampling locations. Ammonia and turbidity tests were last performed during the 2007 testing period while nitrates were only measured during the 2003 testing period. Dissolved oxygen (DO) refers to the amount of oxygen that is dissolved in water and is usually represented in parts per million (ppm) or percent saturation. Oxygen is introduced into a watercourse via the atmosphere and photosysthesis. Moving water will see typically higher concentrations of disolved oxygen (at any given temperature) due to its churning. Oxygen is removed from the watercourse by the respiration of aquatic life, decomposition, and chemical reactions that consume oxygen. Sewage water often contains organic materials that are decomposed by micro-organisms which use oxygen in the proccess. DO is also sensitive to temperature with colder water typically holding more oxygen than warmer water. When more oxygen is being consumed than produced, the DO levels will decline and cause some of the more sensitive animals to leave, weaken or die. DO is constantly fluctuating seasonally as well as day to day (EPA). The pH scale is a logarithmic function that represents the concentration of hydrogen ions in a solution. The pH scale is expressed as follows; a pH of 0 represents maximum acidity, 7 is neutral, and 14 is the maximum limit for bases. Being a logarithmic scale, every pH level under 7 is 10 times more acidic than the previous one. The same can be said for bases; every pH level above 7 is 10 times more basic than the previous one (EPA). A healthy watercourse should have a pH between 6 and 8. As a stream acidifies and reaches 5 or lower, unwanted species of plankton and mosses will start to appear while fish populations start to disappear. As the pH drops below 4.5, the stream will become devoid of fish life. High pH levels can damage the outer surfaces of fish like the gills and eyes and can even cause death. High pH can also increase the toxicity of other chemicals such as ammonia which becomes 10 times greater when a pH value of 7 increases to 8 (Lenntech). Salinity represents the amount of dissolved salts that are present in water. The types of salt ions that are predominant in surface watersinclude sodium, chloride, magnesium, calcium, and sulfate. Surface waters have varying levels of salinity. For example, fresh snow melting is pure water and contains no salts, therefore having a theoretical value of zero for salinity. This can be compared to the salinity in the oceans where the water contains an abundance of salt ions(Encyclopaedia Britannica Inc.) with typically oceanic salinitiesbeing 32 – 36 ppt (grams salt per litre). Phosphorus and nitrogen are essential plant and animal nutrients; phosphate is the form of phosphorus used by aquatic plants. In aquatic ecosystems nitrogen is generally readily available; however, phosphate is most often the limiting reagent for growth. Therefore when abnormal amounts of phosphates are introduced to aquatic ecosystems, it can rapidly cause increases in the biological activity of certain organisms and disrupt the ecological balance of the waterway. Some sources of phosphates are agricultural runoff (fertilizer), biological waste (sewage, manure), and industrial waste (NCSU).

The term Total Suspended Solids (TSS) refers to the measurement of the dry-weight of the particles trapped by a filter through a filtration process. The solids are a mixture of organic (algae or bacteria) and inorganic (clay or silt) components. These suspended particles, which will scatter light as it tries

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to pass through the water, will affect the turbidity or cloudiness of a water body and can be represented in nephelometric turbidity units (NTU). However, TSS is most commonly expressed in mg/L. Some sources of the organic and inorganic components which contribute to TSS and turbidity are eroding soil, microscopic organisms, industrial and municipal effluent, and suspended bottom sediment. From early spring to early fall there is an increase in turbidity and TSS due to spring runoff, microscopic organisms, and algae blooms. Due to these changes, throughout the seasons, the amount of sunlight that algae and other aquatic life can absorb will increase and decrease significantly as well. Fecal coliform bacteria are largely found in the intestinal tracts of warm-blooded animals including humans. Increased levels of fecal coliformscan be indicative of a failure in wastewater treatment, a break in the integrity of the distribution system, or possible pathogenic contamination. Fecal coliforms can also enter a water body through direct waste from mammals, birds, agricultural runoff, storm runoff, and human sewage. Since fecal coliform are an indication that other pathogens may be present, any water body that contains elevated levels of fecal coliforms has the potential to transmit diseases. Testing for fecal coliform is inexpensive, reliable and fast (1-day incubation). Observing the fecal coliform levels and fluctuations can provide an estimation of the relative amounts of pathogenic contamination within a water body. The standard for recreational water quality limit (contact such as wading, swimming and, fishing) is 200 fecal coliform per 100 mL of water (10% not >400) (Task Force). 2.2 Water Quality Procedures 2.2.1 Field pH A handheld pH meter (Fisher Scientific, Accumet AP 63, Handheld pH/mV/Ion Meter) was used to test the pH in the field. The meter was standardized prior to testing using pH buffers 4 and 7. The probe of the meter was then immersed in the creek and moved in a small circular motion. This was continued until the value stabilized on the pH meter and that value was then recorded. This same procedure was repeated at each sampling site. 2.2.2 Dissolved Oxygen Testing the Dissolved Oxygen (D.O.) was also conducted in the field using a handheld meter (YSI EcoSense DO200, Field/Lab, Dissolved Oxygen and Temperature Instrument).Calibration of this meter required knowing the approximate atmospheric pressure in mBars and the salinity concentration in ppt. Salinity was assumed to be approximately 35 ppt in sea water and 0 ppt for fresh water. The probe of the meter was then immersed in the creek and moved in a small circular motion until the reading stabilized. This reading was then recorded and the method was repeated at every site. 2.2.3 Salinity Salinity was measured in the labvia a handheld conductivity meter. The Accumet AP 65 conductivity meter was prepared by setting the cell constant to 10.0 cm-1 for an optimal conductivity range of 1,000 to 200,000 µS/cm. The probe was then dipped in the water 3 times to completely wet the surface. The temperature and conductivity of the water were obtained by using the AP 65meter along with the atmospheric pressure for that time of day which was retrieved from the weather network website. These values were then computed into a salinity calculator which was created using Microsoft Excel

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in order to convert conductivity at a particular temperature and pressure to salinity in parts per thousand (PPT) 2.2.4 Orthophosphates The phosphate concentration was determined using the ascorbic acid method. The process involved mixing 25 mL of each sample and 2-3 drops of phenolphthalein indicator with 4 mL of a previously mixed combined reagent. The combined reagent was composed of 50mL of 5N Sulfuric acid, 5mL of Potassium Antimonyl Tartrate solution, 15mL Ammonium Molybdate solution, and 30 mL of Absorbic acid solution. After the mixing was completed the samples were left to sit for at least 10 minutes but no more than 30 minutes and then placed in the spectrophotometer(Spectronic 21 in weeks 1-3 and Thermo Scientific Genesys 20 in the remaining weeks). The transmittance and absorbance were then measured using the spectrophotometer and recorded. A calibration curve was constructed to represent the phosphate concentration in mg/L by first dissolving 0.11g of KH2PO4 into a 250 mL volumetric flask containing distilled water. Using an eppendorf pipette, 2 mL of this solution was then transferred to another 250 mL volumetric flask that was then topped off using distilled water. Using the diluted stock solution, standards of approximately 0.04, 0.08, 0.12, 0.16, 0.20, 0.24, 0.28, 0.32, and 0.36 mg/L were created. This was done by pipetting 5, 10, 15, 20, 25, 30, 35, 40, and 45 mL of the stock solution into separately labelled 150 mL beakers. Deionised water was added to each beaker so that the total volume in each beaker was 50 mL. A 10th 150 mL beaker was also prepared with 50 mL of distilled water to later be used as a blank sample. Next, 8 mL of the reagent was then added to all 10 beakers. The beakers were then swirled to ensure proper mixing, and then between 10 and 30 minutes (max) were allowed for color development.(The absorbance and transmittance were then recorded for all 10 beakers. The absorbance and the known mg/L were then plottedand, using Microsoft Excel to generate a best fit line from the plotted graph (Appendix B), the absorbance values that were recorded from the Marsh Creek water sample were then converted into mg/L.

Figure  2.2.A:  Photograph  showing  the  results  of  20  minutes  of  colour  development  for  all  10  beakers  used  in  the  colour  development  procedure  of  the  Orthophosphate  Calibration  Curve  

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2.2.5 Total Suspended Solids Total suspended solids (TSS) were measured using the vacuum filtration method. A glass fibre filter disk (Whatman Grade 934-AH Circles 55mm) was washed by rinsing 20 mL of distilled water and allowing it to be filtered out through a vacuum filtration, this was then repeated twice. The filter was then placed into an aluminum weighing dish and transferred into an oven that was set at 105 degrees Celsius for approximately one hour. The filter and aluminum weighing dish were then removed from the oven and transferred into a desiccator were they were cooled to room temperature. They were then weighed using an analytical balance, the mass was recorded and they were, again, returned to the oven for at least another 20 minutes. Following this, the filter and aluminum weighing dish were once again placed into a desiccator prior to being weighed. After weighing them, if the two weights were within ± 0.0003 g, they were considered to have reached a constant weight.A predetermined sample size of 100 mL was slowly poured onto the filter, after which the apparatus was rinsed three times with distilled water to ensure that the entire sample had been filtered and none was left on the walls of the apparatus (Figure 2.2.B). Once the filtration was completed, the same constant weight procedure was followed. TSS in milligrams per litre was then calculated by subtracting the initial constant weight value from the final weight (Appendix A, Sample Calculation A-3). All results were then recorded.

Figure  2.2.B:  Image  showing  the  residue  left  on  the  filter  paper  after  filtration  was  completed  during  the  Total  Suspended  Solids  procedure.  

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2.2.6 Fecal Coliform The membrane filtration technique was used for the testing of fecal coliform bacteria. An m-FC agar containing 1% rosolic acid was prepared and placed into sterile Petri dishes. A Millipore (EZ Pak membrane; white, gridded, 0.45µm pore size, 47mm) filter was added to a Microanalysis Filter Holder and centered accurately on the support screen. Multiple dilutions of the same sample were prepared and then slowly added to the apparatus, a vacuum was then applied. Once the filtration process was completed the membrane filter was removed from the apparatus and placed into a previously prepared petri dish. The petri dishes were then incubated upside down at 44.5°C (±0.2°C) for 24 hours. After 24 hours, the petri dishes were removed from the incubator. Only the blue colonies on the petri dishes were counted. When choosing which plate to count, plates between 20 and 60 colonies were preferred. If all plates were above 60 colonies, the data had to be represented as > 60. If some of the plates had a count under 20, the additional steps had to be taken to determine the fecal concentration (refer to Appendix A sample calculation A-1). Using the dilution ratio of the sample used for the specific petri dishes, the colony forming units (CFU) per 100 mL of water were calculated and recorded. The accepted way of expressing fecal coliform level in water is in terms of the number of colony forming units per 100 millilitres of water (CFU/100 mL). Despite the assumed decline of fecal coliforms in Marsh Creek caused by the cessation of the dumping of raw sewage, all sampling sites (Analysis A and Analysis B) were diluted to 1/10, 1/100, 1/1000, 1/10000, and 1/100000 for the first 2 weeks of testing. This was done to ensure that the number of fecal coliforms are indeed declining, as well as accurate counts, and to compare the results found at high and low tide. After completing the first two weeks of sampling, the dilutions were adjusted as needed. The following dilutions were prepared for the Downstream Site and sites 1, 2, and 3 for all of the remaining sampling days: 1/10, 1/100, 1/1000 and 1/10 000. The dilutions for the Downstream site and sites 4 and 5 were also permanently changed to: 1/10,1/100, and1/1000.

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Figure  2.2.C:  Image  showing  the  Coliform  Forming  Units  (CFU)  per  100  mL  water  sample  taken  from  Analysis  B  Site  3  in  Marsh  Creek.  The  sample  dilutions  were  (from  left  to  right)  1/1  (no  dilution),  1/10,  1/100,  1/1000,  and  1/10000.  

2.2.7 Lab pH The pH level was also tested in the labby standardizing the pH meter with the 4, 7, and 10 pH buffers. The probe was then immersed into a beaker containing the desired sample. When the pH measurement stabilized, the value was recorded and the probe was then rinsed thoroughly with distilled water. The procedure was then repeated for the remaining samples.

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2.3 Sampling of Fish

2.3.1 Electrofishing Electrofishing was conducted in the Ashburn Creek tributary of Marsh Creek on July 26, 2014. Electrofishing activities were conducted using a battery-powered Smith-Root LR-24 electrofisher (Figure 2.3.A). The certified operators were Tim Vickers and Graeme Stewart-Robertson of ACAP Saint John. The settings used were varied depending on the substrate, water conductivity and the effect they were having on fish. In most cases, the built-in quick setup option was used and minor adjustments (typically to the voltage) were made as necessary. The 'on time' and settings were noted upon completion of each site. Dip nets were used to capture fish which were then transferred to a 5 gallon bucket of water until they could be measured and released back to their original environment as quickly as possible.

Figure  2.3.A:  Image  showing  ACAP  staff  calibrating  a  Smith  Root  LR-­‐24  electrofisher  used  to  sample  fish  in  Marsh  Creek.  

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2.3.2 Fyke nets Two Fyke nets were used to collect fish in the lower reaches of Marsh Creek on May 31, June 13, 20 & 27, and September 26 (Figure 2.3.B). On each occasion one net was set in the riverine section located approximately 250m upstream of the tide gates located within the Courtenay Bay Causeway, and the second net was set in the Marsh Creek channel in the Courtenay Bay estuary approximately 50m below the tide gates. The nets were set during low tide and checked during a subsequent low tide either 12 or 24 hours after the set. Tide heights were closely monitored to prevent the nets from becoming completely emergent during any period so as to maintain the submergence of any trapped fish within the holding end. Fish were removed from nets, placed in a 5 gallon pail, identified, measured, counted, and then immediately returned to the watershed.

Figure  2.3.B:  Fyke  nets  set  in  Marsh  Creek  (Courtenay  Bay)  on  June  5,  2014.    

2.3.3 Beach Seine Beach seining was conducted in Ashburn Lake on August 6, 2014 using a 10m x 1.5m seine (Figure 2.3.C). Three substrate types were sampled (sandy, mixed organic& rock, and organic) and were in keeping with historical sample locations conducted in each of the past five years. Sampling was conducted as part of an ongoing youth education program, and as a presence/absence study conducted by ACAP Saint John. Fish parameters (i.e. length, abundance, etc.) were not collected so as to maintain the health of the fish. Figure  2.3.C:  Beach  seining  in  Ashburn  Lake,  July  

3,  2013.  

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2.3.3 Reporting of Fish Collected

The lengths of all fish recorded herein were measured as total lengths to the nearest millimetre. The common names of fishes mentioned this report can be referenced to their scientific names (Table 2.3.A).

Table  2.3.A:  A  list  of  common  fish  names  and  their  corresponding  scientific  names  used  in  ACAP  Saint  John  reports.  Common Name Scientific Name Alewife Alosa pseudoharengus American eel Anguilla rostrata Atlantic salmon Salmo salar Atlantic tomcod Microgadus tomcod Blacknose dace Rhinichthys atratulus Brook trout Salvelinus fontinalis Brown bullhead Ictalurus nebulosus Brown trout Salmo trutta Chain pickerel Esox niger Creek chub Semotilus atromaculatus Four spine stickleback Apeltes quadracus Golden shiner Notemigonus crysoleucas Mummichog Fundulus heterclitus Nine spine stickleback Pungitius pungitius Northern Redbelly dace Chrosomus eos Pearl dace Semotilus margarita Pumpkinseed sunfish Lepomis gibbosus Rainbow smelt Osmerus mordax Three spine stickleback Gasterosteus aculeatus White perch Morone americana White sucker Catostomus commersoni Winter flounder Psuedopleuronectes americanus Yellow perch Perca flavescens

2.4 Other Observations ACAP Saint John instructed its staff to be vigilant in observing any other parameters that could influence the current or future integrity of the Marsh Creek ecosystem. While these other parameters were not measured during this project, they were documented and included in this report due to their relevance to the long term management objectives of the Marsh Creek watershed, a principle upon which this project was founded.

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3.0 Results

3.1 Water Quality Parameters

Confirmation that municipal wastewater outfalls had been diverted from Marsh Creek prior to the first water samples acquired on June 10, 2014 was obtained by way of a personal conversation with Graeme Huddleston, the Operations Manager for Environmental Protection at City of Saint John. Mr. Huddleston noted that while the municipal wastewater system was technically ‘online’, it was still viewed as being in its commissioning stage which is subject to necessary adjustments and fine tuning. As such, there may have been temporary occurrences where discharges into Marsh Creek could have occurred during one or two of our sampling periods. If any such discharges had occurred during our sampling, they would only have had the potential to affect the results obtained for the Downstream sample station of Analysis A, as well Analysis B stations 1 and 2. Given that the results presented herein reflect average values from at each of the sampling station taken on five different sample periods, the authors are confident that any such discharges would be unlikely to greatly affect the interpretation of any overall trends.

3.1.1 Analysis A Water Quality Parameters

Water quality parameters averaged across five sample periods in 2014(Appendix C; Tables C-1 through C-6)showed marked differences in dissolved oxygen, fecal coliforms, total phosphates, total suspended solids and salinity between the upstream and downstream sites (Table 3.1.A). Temperatures were comparable (21.50C for both upstream and downstream),with small standard deviations in all parameters except fecal coliforms, Downstream TSS, and %Transmittance (Table 3.1.B).The deviation in %Transmittance is believed to be caused from the use of two different spectrophotometers, as the original one became damaged, and therefore resulted in the use of 2 separate calibration curves. Despite this, the results for total phosphates are still reliable due to the equations used were specific to the spectrophotometer used to calculate them.

Due to the materials required to calculate salinity not being available during the first two weeks of testing, the average values of salinity (Table 3.1.A) is representative of the values obtained during the remaining sample periods (Appendix C; Tables C-3through C-6).

Due to Tropical Storm Arthur, the results for fecal coliforms, total suspended solids, and total phosphates from weeks 3 and 4 are not consistent with the other sample periods due to the increase of water in Marsh Creek.

Table  3.1.A:  Calculated  averages  of  water  quality  parameters  measured  for  Marsh  Creek  Analysis  A  (upstream/downstream)  from  five  sample  periods  in  2014.  

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Table  3.1.B:  Standard  deviations  for  calculated  averages  of  water  quality  parameters  measured  for  Marsh  Creek  Analysis  A  (upstream/downstream)  from  five  sample  periods  in  2014.  

Figure  3.1.A:  Fecal  coliforms  (CFU/100  mL  sample)  measured  in  Marsh  Creek  Upstream  and  Downstream  sample  stations  from  1995-­‐2014.    The  logarithmic  scale  does  not  permit  the  “zero  CFU”  values  obtained  in  the  2005  and  2006   Upstream   site   to   be   plotted.   Values   were   not   obtained   in   years   2008,   2009,   2010   and   2012   and   are  represented  only  as  a  trend  line  for  these  years.  

The fecal coliform counts obtained in 2014 (Table 3.1.A) were included in the historical (2005 – 2011) data set for these sampling stations (Appendix E).The2014 results were consistent with those obtained in previous years where the Upstream fecal coliform values were substantially lower than those for the Downstream site (Figure 3.1.A).However, due to the cessation of the dumping of raw sewage into Marsh Creek, the Downstream Site is at its lowest fecal coliform count in 10 years.

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3.1.2 Analysis B Water Quality Parameters Water samples were acquired in 2014 from five sample periods, each three days in duration, which included June10-12, July 2-4, July 9-11, July 16-18, July 23-25,and July 29-31, 2014(Appendix F; Tables F-1 through F-6). The average values for water quality parameters acquired in five sample periods indicated a general trend of increasing salinity and total suspended solids, and decreasing water temperatureas one moves from the most upstream site (Site 5) to the most downstream site (Site 1) (Table 3.1.C). It must be noted that due to the required materials not being immediately available, salinity was not recorded during the first two weeks of sampling. The average values of salinity (Table 3.1.C), are representative of the values obtained during the remaining sample periods (Appendix F; Tables F-3 through F-6). Due to Tropical Storm Arthur, the results for fecal coliforms, total suspended solids, and total phosphates from weeks 3 and 4 are not consistent with the other sample periods due to the increase of water in Marsh Creek. During the July 23-25, 2014 sampling period (Appendix F; Table F-5), it was found that Site 3 had a significantly higher fecal coliform count than any other site that week. This is believed to be due to creosote being disturbed while the samples were being taken. The wide range of values obtained within a single sample site amongst the five sample dates resulted in a considerable degree of within site variation in some parameters, especially fecal coliforms, %Transmittance for the reasons stated in Analysis A, and total suspended solids. (Table 3.1.D).

Table  3.1.C:  Calculated  averages  of  water  quality  parameters  measured  for  Marsh  Creek  Analysis  B  (five  sample  sites  in  the  last  2  km  of  the  watercourse)  from  five  sample  periods  in  2014.  

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Table  3.1.D:  Standard  deviations  for  calculated  averages  of  water  quality  parameters  measured  for  Marsh  Creek  Analysis  B  (five  sample  sites  in  the  last  2  km  of  the  watercourse)  from  five  sample  periods  in  2014.  

Fecal coliform levels (CFU/100mL) were plotted amongst the five sample stations for 2012,2013,and 2014 (Figure 3.1.B). The results did not indicate a strong consistent trend amongst the five sites between 2012 and 2013; however, both years did indicate a trend towards declining fecal coliform concentrations as one moved both upstream and downstream from Site 3 (Figure 3.1.B).This is evident due to the 95-99% decrease of fecal bacteria from 2013-2014 with the largest decrease is located at Site 1.The anomaly of high fecal coliforms at Site 3 may be able to be contributed to the water fowl that nest in and around that section of Marsh Creekand also the possibility of outflow from the duck pond located at Lily Lake.Site threes anomaly may be due amount of bird life in marsh creek and the surrounding areas. The section of site 3 has a runoff from the lily lake duck pond which may lead to finding of high levels of fecal coliforms. Without performing DNA testing at that site ,If the results are due to human’s or birds are unknown

Total suspended solids (mg TSS/L) were plotted amongst the five sample stations for 2012, 2013, and 2014 (Figure 3.1.C). The results indicated a consistent trend amongst the five sites between 2012 and 2014 with slightincreases in TSS as one moved from the most upstream Station 5 to the downstream Station 1. While the TSS tread to increase in downstream sites was consistent, the degree to which this increase occurred was not consistent amongst years with 2012 values being 58.9 times higher in Site 1 than Site 5, verso an 8.4 times increase in 2013, and a 3.8 times increase in 2014(Figure 3.1.C). Absolute TSS values were also considerably higher in 2012 and 2013versus 2014 Total phosphates (measured as orthophosphate in mg/L) were plotted amongst the five sample stations for 2012, 2013, and 2014 (Figure 3.1.D). The results indicated a consistent trend between 2012 and 2013 with increased phosphate concentrations as one moved downstream from Site 4, however, the results from 2014 showed no such trend. Sample stations 1 and 2 showed moderate increases in total phosphates in 2014 when compared to 2013 at 1.3 and 2.5 times greater respectively, while sample stations 3, 4, and 5 showed large increases of 7.1, 6.1, and 10.4 times greater than 2013 (Figure 3.1.D).

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Figure  3.1.B:  Fecal  Coliforms  (CFU/100  mL  sample)  measured  in  five  sites  in  Lower  Marsh  Creek  (Analysis  B)  from  2012-­‐2014.  The  2012  Site  4  sample  was  discarded  and  no  data  was  acquired.  

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Figure  3.1.C:  Total  Suspended  Solids  (mgTSS/L)  measured  in  five  sites  in  Lower  Marsh  Creek  (Analysis  B)  from  2012-­‐2014.  The  2012  Site  4  sample  was  discarded  and  no  data  was  acquired.  

Figure  3.1.D:  Orthophosphates  (mgPO4/L)  measured  in  five  sites  in  Lower  Marsh  Creek  (Analysis  B)  from  2012-­‐2014.  

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Salinity, measured across the five sample sites in 2014, indicated a distinct decrease in salt concentration as one moved upstream from Site 1 (Figure 3.1.E). Salinity varied little upstream of Site 2, with Sites 3, 4 & 5 having salinities of 0.38, 0.29, and 0.26 ppt, respectively (Table 3.1.C).

Figure  3.1.E:  Salinity  (part  per  thousand  0/00)  measured  in  five  sites  in  Lower  Marsh  Creek  in  2013  and  2014.  

3.1.3. Water Quality Parameters of Additional Site

ACAP staff added a new site in week 5 (July 23-25, 2014) to test the water quality in the area. The site is located beside Avenue Animal Hospital at 507 Rothesay Avenue and was subject to the same tests as all the sites in Analysis A and B and is approximately halfway between the Upstream and Downstream Sites (Table 3.1.E).

It should be noted that due to insufficient filters to perform the Total Suspended Solids test during the July 23-25, 2014 test period no value was recorded at this site. Also, during the July 29-31, 2014 test period, the battery in the field pH meter died and no value was recorded at this site.

Table  3.1.E:  Water  quality  parameters  measured  for  Marsh  Creek  located  beside  Avenue  Animal  Hospital  during  the  test  periods  of  July  23-­‐25  &  July  29-­‐31,  2014.  

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3.2 Fish Collection

3.2.1 Lower Marsh Creek Fyke Nets A total of 52 fish comprised of 11 different species were collected from ten separate hauls between May 31 and September 26, 2013 (Table 3.2.A). The fyke net catch in the upstream site (Courtenay Forebay above tide gates) contained only four species and was dominated by Pumpkinseed sunfish (52.9%) and Mummichog (35.3%). A single Golden shiner (5.9%) and 4-spine stickleback (5.9%) comprised the remaining two species. The downstream site (Courtenay Bay below tide gates) resulted in the capture of 32 fish of five different species, and was dominated by Tomcod at 70.6% (Table 3.2.B). Rainbow smelt and Pumpkinseed sunfish were the second most-frequently captured fish (11.8% each), with a single American eel and Brown bullhead each comprising 2.9% of the remaining total catch.

Table  3.2.A:  Fish  species  composition  caught  in  fyke  nets  in  the  Courtenay  Forebay,  2013.  Species Number Caught % of Total Catch Range (TL in mm) 4 spine stickleback 1 5.9 71 Golden shiner 1 5.9 97 Mummichog 6 35.3 78 - 104 Pumpkinseed sunfish 9 52.9 78 - 110

Table  3.2.B:  Fish  species  composition  caught  in  fyke  nets  in  Courtenay  Bay,  2013.  Species Number Caught % of Total Catch Range (TL in mm) Tomcod 24 70.6 106 - 250 Rainbow smelt 4 11.8 162 – 242 Pumpkinseed sunfish 4 11.8 75 – 100 American eel 1 2.9 510 Brown bullhead 1 2.9 265

3.2.2 Ashburn Lake Fyke Nets Two fyke nets were set in Ashburn Lake on each of July 3, July 31 and August 23, 2013. The nets were part of an outdoor youth education program conducted each year at the Glen Carpenter Centre. The nets performed poorly, yielding only two fish for the effort; an American eel and a White sucker.

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Beach Seine Beach seining was used to collect fish from Ashburn Lake, on three different occasions (July 3, July 31 and August 23, 2013). Fish were neither measured nor counted due to warmer water temperatures, and because the intent of this sampling to serve as an educational medium for youth and as an annual presence / absence monitoring protocol for ACAP. Fish collected in 2013 included White sucker, age 0+ Brown trout, Pearl dace, Northern Redbelly dace, Blacknose dace, Creek chub and Mummichog.

3.2.3 Ashburn Creek Electrofishing was conducted on June 19, 2013 to determine fish species composition in Ashburn Creek as well as to conduct an initial ‘fin marking’ procedure to assess the success of a pending removal of a barrier to the upstream passage of fish. Sixteen fish were captured which were comprised of five different species (Table 3.2.C). Lower caudal fin clips were given to the two Brown trout prevent re-counting at a later date and to determine upstream/downstream, mobility.

Table  3.2.C:  Fish  captured  by  electroseining  in  lower  Ashburn  Creek  on  June  19,  2013.  Species Number Captured Total length (mm) Brown trout 2 61, 122 Brook trout 1 22 Blacknosed dace 6 61, 63, 70, 73, 75, 85 American eel 5 140 - 160

3.3 Other Observations 3.3.1:European Green Crab ACAP staff captured (in a fyke net set on September 25-26, 2013) and recorded what is believed to be the first documented occurrence of the invasive Green crab (Carcinus maenus) in the Courtenay Forebay. The specimen was captured at a location approximately 200m upstream of the tide gates located within the Courtenay Causeway. The green crab was easily identified by the five sharp spines on either side of its eyes, and the three rounded spines between its eyes (Figure 3.3.A).

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3.3.2.Canada Post Retaining Wall: Creosote A ~200m section of Marsh Creek adjacent to the Canada Post property on Rothesay Avenue is contaminated with creosote resultant from the wood preservative operations of the Likely Lumber Mill that existed on the banks of Marsh Creek from approximately 1930-1970 (ACAP Saint John 2003). A Phase I Environmental Assessment on the site in 1996 precipitated a Phase I and Phase IIEnvironmental Assessment on the Canada Post property, after which a steel retaining wall was inserted along the base of the property below a wooden retaining wall (Figure 3.3.B) adjacent to Marsh Creek to reduce the migration of creosote from the property into the watercourse (ACAP Saint John 2005).

Figure   3.3.A:   Photo   of   the  (believed)   first   confirmed  occurrence   of   the   invasive  European   Green   crab  (Carcinus   maenus)   in   the  Courtenay  Forebay  of  Marsh  Creek;  September  26,  2013.  

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ACAP staff observed that (in late November 2013) the structural integrity of a section of the wooden retaining wall had failed (Figure 3.3.B - bottom) and that the remaining wall sections (upstream and downstream of the collapse) were at risk of similar failures in structural integrity (Figure 3.3.C.). ACAP’s Executive Director reported the event to the Regional Office of the NB Department of Environment and to Mr. Dan Hurley, Saint John Operations Manager of Canada Post Corporation. Mr. Hurley provided a quick response indicating that they were aware of the situation and that they had an engineering firm as well as a property management firm taking the necessary actions to prevent exacerbating the situation. Unfortunately, upon observationin 2014, the walls condition seemed to slightly worsen and no preventable measures were implicated.

Figure  3.3.B:  Images  showing  the  state  of  Canada  Post’s  wooden  retaining  wall  in  the  bank  of  Marsh  Creek  prior  to  collapse  (top)  and  immediately  after  collapse  in  late  November  2013  (bottom).  

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4.0  Discussion

4.1 Water Quality Parameters Analysis A

The greater Marsh Creek watershed has been the subject of water quality monitoring since 1993. Appendix D and E, represents a data compilation of all the parameters that were recorded at the upstream and downstream location since 1993. The data recorded from the summer of 2014 consisted of identical tests as those performed in 2013. This was done to continue to monitor the water quality under the same parameters and to demonstrate the affect of the cessation of the outflow of raw sewage into Marsh Creek, which took place in July 2014. As seen in Table 3.1.A, fecal coliform, orthophosphates, and TSS were all present in higher concentrations at the downstream site compared to upstream. The downstream site recorded approximately a 6 time greater concentration of fecal coliforms. Downstream also showed 1.5 times the concentrations of phosphates compared to its upstream counterpart. Another trend that was observed and behaved expectedly was salinity. The downstream site which was located approximately 1.3 km from the tide gate did experience higher salinity values. Dissolved oxygen and pH levels at both sites were also well within the desired range. Fecal coliforms, despite maintaining approximately the same concentration at the Upstream site as 2013, saw a drastic decrease of 99% at the Downstream site due to raw sewage no longer flowing into Marsh Creek and the quality of the water is already beginning to show great improvement.

4.2Water Quality Parameters Analysis B

The water quality monitoring of the Lower Marsh Creek had the objective of monitoring certain parameters over the summers of 2012, 2013, and 2014. This year saw a dramatic decrease in fecal

Figure  3.3.C:   Image   indicating   the   state   of  Canada  Post’s  wooden   retaining  wall   in   the  bank   of  Marsh  Creek  immediately  upstream  of  the  section  that  collapsed  in  late  November  2013.  

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counts at a majority of the sample stations. While none of the sites are, on average, below the Canadian guide lines over 200 CFU/100 mL (Task Force), as can be seen in Table 3.1.C, Site 3 saw no real increase/decrease if fecal counts which is believed to be due to the outflow from the Lily Lake Duck Pond, which has seen high activity this year and fecal matter from various forms of wildlife can affect the counts. Also this year, there were several occurrences where the fecal counts were under the Canadian guidelines for recreational water that particular week as well as the first time that some sites returned with 0 CFU/100 mL in the 1/1 dilution (Appendix F).

The Marsh Creek portion that was tested was considered non-salmonid waters, meaning, the dissolved oxygen levels needed are much lower. The Canadian water quality guidelines indicate that the desired dissolved oxygen levels are to be greater than 6.5 ppm. A moderate impairment is experienced by these fishes at 4 ppm and death at 3.5 ppm (Task Force, 3-14). As seen in Appendix H; Table H-1, on average, sites 1 through 4 were much lower than the desired guidelines and site 3 was at a level were fishes could not survive. The average dissolved oxygen levels for 2013 were a drastic improvement with only site 1 not at the desired level. Average dissolved oxygen levels for 2014 displayed further improvement from 2013 with all sites above the desired levels allowed for no fish impairment.

From 2012-2014, total phosphates have been increasing as time goes on. In 2012, total phosphates were at the desired level of between 0.01-0.02 mgPO4/L. While the results from the 2013 study displayed an moderate increase in total phosphates at all sites with only two sites outside of the desired range, 2014 displayed large increases at all sites ranging from 3-6 times greater than the desired level. This could be the result of increased rainfall causing large amounts of sediment to be introduced to the water via runoff during sampling periods.

Because the raw sewage has ceased entering Marsh Creek, toilette paper and other toiletry debris can no longer be seen floating down Marsh Creek. By testing for total suspended solids, it was possible to determine the mg/L value of the remaining floating debris. Although, it should be noted that some of the larger debris could not be sampled and measured, for this reason the suspended solids are actually at a greater concentration than recorded. The Canadian water quality guidelines indicated that TSS would have had no harmful effect if values were > 25 mg/L, 80-400 mg/L is not ideal for fish life (Task Force, 3-42). Table 3.1.C. shows that average TSS for 2014 was under 80.0 mg/L at all sites with the highest TSS counts found at site 1 with the average reading 25.63 mg/L.

Throughout the 3 years of sampling, the average pH has been between 6 and 8 which are the recommended guidelines. None of the results from 2014 produced any pH values that were below 6 or above 8.

The Marsh Creek watershed experienced salinity intrusion through the tide gates of the Courtenay Bay Causeway. As seen in Figure 3.1.E., the samples taken showed much higher values for salinity near the tide gates than at any other site. This was expected due to the heavy tide influence experienced by Marsh Creek.

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5.0  Conclusion

In conclusion, the data recovered during the water quality monitoring of the lower Marsh Creek watershed study was successful in compiling and recording data prior to the completion of harbour clean up. The data collected for the water quality monitoring of the greater Marsh Creek watershed study was compiled and added to a 20 year-long study The lower parts of Marsh Creek were highly contaminated with fecal coliforms in 2013 and also tested high for other sewage related parameters In 2014 the data found for theses parameters were from 95%-99% lower than the previous year. This indicating Marsh Creek is on its way to recovery.

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6.0 References

Atlantic Coastal Action Program (ACAP) Saint John Inc. 2013.“The Rebirth of Marsh Creek, 2013”. www.acapsj.com/reports.

Atlantic Coastal Action Program (ACAP) Saint John Inc. 2003. “The 2004 Marsh Creek Remediation Technology Demonstration Project”.www.acapsj.com/reports

Atlantic Coastal Action Program (ACAP) Saint John Inc. 2003. “2003 Marsh Creek Passive Recovery Project”. www.acapsj.com/reports

Dohrman, Paul. "How to convert conductivity to salinity." n.d. eHow.http://www.ehow.com/how_5911746_convert-conductivity-salinity.html. 12 June 2014.

Encyclopædia Britannica, Inc. "Biosphere." 2013. Encyclopædia Britannica. http://www.britannica.com/EBchecked/topic/66191/biosphere/70878/Salinity. 20 June 2013.

Environment, Task Force on water Quality Guidelines of the Canadian Council of Ministers of the. Canadian Water Quality Guidelines. Ottawa, 1994. Book.

EPA. "5.2 Dissolved Oxygen and Biochemical Oxygen Demand." 6 March 2012. Water: Monitoring & Assessment . http://water.epa.gov/type/rsl/monitoring/vms52.cfm. 3 July 2013.

. http://www.water.ncsu.edu/watershedss/info/phos.html. 3 July 2013.

James, William E. Yake and Robert K. "Setting Effluent Ammonia Limits to Meet In-Stream Toxicity Criteria." Journal (Water Pollution Control Federation Vol. 55, No. 3, Part I. Water Environment Federation, 1983. 303-309. http://www.jstor.org/discover/10.2307/25041852?uid=3739416&uid=2&uid=3737720&uid=4&sid=21102555970873.

Johnson, T.R. "Water Quality Criteria for Microbiological Indicators ." 7 August 2001. Government of British Columbia. http://www.env.gov.bc.ca/wat/wq/BCguidelines/microbiology/microbiology.html. July 2013.

Lenntech. "Acids & alkalis in freshwater." 2012. Water Treatment Solutions. http://www.lenntech.com/aquatic/acids-alkalis.htm. June 2013.

Microbiology, Environmental Health. Total and Fecal coliform and E. coli Analyses by Membrane Filter Methods. 2006. http://webcache.googleusercontent.com/search?q=cache:3Kc4aWhzGzIJ:www.unc.edu/courses/2006spring/envr/133/001/ENVR133_Lab2_2006.doc+why+must+u+count+betwe

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en+2060+fecal+coliforms+on+mfc+agar&cd=4&hl=en&ct=clnk&gl=cahttp://webcache.googleusercontent.com/sea. 15 August 2013. <http://webcache.googleusercontent.com/search?q=cache:3Kc4aWhzGzIJ:www.unc.edu/courses/2006spring/envr/133/001/ENVR133_Lab2_2006.doc+why+must+u+count+between+2060+fecal+coliforms+on+mfc+agar&cd=4&hl=en&ct=clnk&gl=cahttp://webcache.googleusercontent.com/sea>.

NEOGEN. "m-FC Agar (7397)." July 2008. Acumedia. http://www.neogen.com/Acumedia/pdf/ProdInfo/7397_PI.pdf. June 2013.

Thursby, Glen, Don Miller, Sherry Poucher, Laura Coiro, Wayne Munns, and Timothy Gleason. "Ambient Aquatic Life Water Quality Criteria for Dissolved Oxygen (Saltwater): Cape Cod to Cape Hatteras." November 2000. EPA. http://water.epa.gov/scitech/swguidance/standards/upload/2007_03_01_criteria_dissolved_docriteria.pdf. July 2013.

USGS. "Fecal Indicator Bacteria and Sanitary Water Quality." 21 December 2007. USGS: science for a changing world. http://mi.water.usgs.gov/h2oqual/BactHOWeb.html. June 2013.

Wenner, E., M. Thompson, and D. Sanger. "Water Quality." n.d. NOAA.http://nerrs.noaa.gov/doc/siteprofile/acebasin/html/envicond/watqual/wqintro.htm. July 2013.

Environment Canada. “Erosion & Sedimentation.” https://www.ec.gc.ca/eau-water/ default.asp?lang=En&n=32121A74-1. Government of Canada, February 15, 2011. Web. August 11, 2014

Health Canada. “Guidelines for Canadian Recreational Water Quality.” http://www.hc-sc.gc.ca/ewh- semt/pubs/water-eau/guide_water-2012-guide_eau/index-eng.php. Health Canada, April 2012. Web. August 11, 2014.

http://www.health.gov.bc.ca/public-health/pdf/Water_Quality_Recreational_Water-Evidence_Review.pdf

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC91772/

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Appendix A: Sample Calculations used to determine water quality parameters in Marsh Creek in 2013.

A-1: Fecal coliforms:

In determining the total amount of fecal coliforms in a 100mL of sample a plate count between 20 – 60 coliform bacteria must be counted from a 10mL sample.

Counted fecal coliforms = Counted bacteria *Dilution

Where:

Counted bacteria = are the bacteria counted in agar plate from a 10mL sample.

Dilution = is the dilution of bacteria counted in the agar plate

𝑇𝑜𝑡𝑎𝑙  𝐹𝑒𝑐𝑎𝑙  𝐶𝑜𝑙𝑖𝑓𝑜𝑟𝑚𝑠 = 𝐶𝑜𝑢𝑛𝑡𝑒𝑑  𝑓𝑒𝑐𝑎𝑙  𝑐𝑜𝑙𝑖𝑓𝑜𝑟𝑚𝑠 ∗ 10

Where:

Total Fecal Coliforms = the total amount of fecal coliforms from a 100mL sample

Counted fecal coliforms = the amount of coliform bacteria counted

If all plates were less than 20:

789:;  <8;8=>  <8?=9@789:;  A8;?BC  DE;9CFCG

× 100

http://www2.vernier.com/sample_labs/WQV-09-COMP-fecal_coliform.pdf

Sample Calculation

Counted fecal coliforms = 45HIJKLBM

*100 = 4,500HIJKLBM

𝑇𝑜𝑡𝑎𝑙  𝐹𝑒𝑐𝑎𝑙  𝐶𝑜𝑙𝑖𝑓𝑜𝑟𝑚𝑠 = 4,500   HIJKLBM

∗ 10  = 45,000 HIJKLLBM

If all plates were less than 20:

KQ×KL S(U×KLL)UL  BM

× 100 = 1,950HIJKLLBM

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A-2: Orthophosphates:

To determine the amount of phosphates in a litre sample of water the equation from the calibration graph must be used.

Refer to Appendix

Y = 0.953 * X [Spectronic 21] ; Y = 1.377 * X [Genesys 20]

X = W

L.QYZ[Spectonic 21] ; X =

WK.Z[[

[Genesys 20]

Where:

Y = absorbance value from spectrophotometer

X = total phosphates in mg/L

Sample Calculation

X = L.LQ[L.QYZ

= 0.102B]M

[Spectronic 21] ; X = L.LUUK.Z[[

= 0.016B]M

[Genesys 20]

A-3: Total Suspended Solids:

In order to determine how much total suspended solids are in a litre of sample a calculation was made by using 100mL of sample.

tss = filter after – filter prior

Where:

tss = the total suspended solids in 100mL sample measured in g/100mL

filter after = the weight of the filter and aluminum foil container after the sample was poured

filter prior = the weight of the filter and aluminum foil container before the pouring of the sample.

TSS = tss*1000B]K  ]

*10

Where:

TSS = the total suspended solids in 1 litre sample measured in mg/L

Sample Calculation

tss = 1.4593 ]

KLLBM - 1.4591

]KLLBM

= 2.0*10-4 ]KLLBM

TSS = 2.0*10-4 ]KLLBM

* 1000B]K  ]

*10 = 2.0B]M

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A-4: Average pH

In calculation an average pH value from a given number of pH values, you must first convert the pH value into a hydrogen ion concentration

pH = -log[H+]

[H¸+] = 10^ (-pH)

Where:

pH = the measurement value

H+ = is the hydrogen concentration in units of molarity (M)

Next you take the average of the H+ values and then convert that average back into a pH to get your average pH value.

Avg H+ = ( HS) K`

Avg pH = -log (Avg H+)

Where:

n = number of terms of H+

Avg H+ = the average hydrogen concentrations in units of molarity (M)

Avg pH = the average pH value

Sample Calculation

[H+] = 10^ (-7.25) = 5.62E-08 M

Avg H+ = (5.62𝐸 − 08 + 5.13𝐸 − 08 + 4.57𝐸 − 08 + 6.46𝐸 − 08 + 9.12𝐸 − 08 + 1.12𝐸 − 07 +1.12𝐸 − 07) K

[= 7.62𝐸 − 08  𝑀

Avg pH = -log (7.62𝐸 − 08)  =  7.12

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A-5: Salinity Equation:

In calculating the salinity an equation to find conductivity ratio (R) must first be calculated

R =

ijklminoponq(rsit)uvvvv

w.UQKw st R =

xyx.u  rsituvvvv

w.UQKw st = 0.00800

Next the r-sub-t must be calculated which is a function of temperature:

𝑟 − 𝑠𝑢𝑏 − 𝑡 = 𝐶0 + 𝐶1 ∗ 𝑡 + 𝐶2 ∗ (𝑡)^2 + 𝐶3 ∗ (𝑡)^3 + 𝐶4 ∗ (𝑡)^4

Where:

t =temperature (degrees Celsius)

C0 = 6.77E-01

C1 = 2.01E-02

C2 = 1.10E-04

C3 = -7E-07

C4 = 1.00E-09

𝑟 − 𝑠𝑢𝑏 − 𝑡 = 6.77𝐸 − 01 + 2.01𝐸 − 02 ∗ 21.3 + 1.10𝐸 − 04 ∗ (21.3)^2 + −7𝐸 − 07 ∗ (21.3)^3+ 1.00𝐸 − 09 ∗ (21.3)^4

r-sub-t = 1.15

A function of pressure and temperature called R-sub-p must now be calculated as follows:

𝑅 − 𝑠𝑢𝑏 − 𝑝   = 1 + 𝑝 ∗ (𝐸0 + 𝐸1 ∗ 𝑝 + 𝐸2 ∗ (𝑝)^2)/(1 + 𝐷0 ∗ 𝑡 + 𝐷1 ∗ (𝑡)^2 + (𝐷2 + 𝐷3 ∗ 𝑡) ∗ 𝑅)

Where:

t = temperature (degrees Celsius)

p = pressure (in decibars)

R = previous calculation

E0 = 2.07E-05

E1 = -6.37E-10

Page 40: Nearshore Habitat & Water Quality

E2 = 3.99E-15

D0 = 3.43E-02

D1 = 4.46E-04

D2 = 4.22E-01

D3 = -3.11E-03

Page 41: Nearshore Habitat & Water Quality

𝑅 − 𝑠𝑢𝑏 − 𝑝   = 1 + 10.12 ∗ (2.07𝐸 − 05 ± 6.37𝐸 − 10 ∗ 10.12 +3.99E-15

∗ (10.12)^2)/(1 + 3.43𝐸 − 02 ∗ 21.3 + 4.46𝐸 − 04 ∗ (21.3)^2 + (4.22𝐸 − 01 + −3.11𝐸 − 03∗ 21.3) ∗ 0.00800)

R-sub-p = 0.517

Next R-sub-t must be calculated as a function of R, r-sub-t, and R-sub-p as follows:

𝑅 − 𝑠𝑢𝑏 − 𝑡   =𝑅

𝑅 − 𝑠𝑢𝑏 − 𝑝 ∗ 𝑟 − 𝑠𝑢𝑏 − 𝑡

𝑅 − 𝑠𝑢𝑏 − 𝑡   = L.LL�LLK.KY∗L.YK[

=0.135

An equation for S must now be calculated as follows:

𝑆   =𝑡 − 15

(1 + 𝑘 ∗ (𝑡 − 15))∗ (𝐵0 + 𝐵1 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^(1/2) + 𝐵2 ∗ 𝑅 − 𝑠𝑢𝑏 − 𝑡 + 𝐵3 ∗ (𝑅 − 𝑠𝑢𝑏

− 𝑡)^(3/2) + 𝐵4 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^2 +𝐵5 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^(5/2))

Where:

t = temperature (degrees Celsius)

R-sub-t = previously calculated

k = 0.0162

B0 = 0.0005

B1 = -0.006

B2 = -0.007

B3 = -0.038

B4 = 0.0636

B5 = -0.014

Page 42: Nearshore Habitat & Water Quality

𝑆   =21.3 − 15

(1 + 0.0162 ∗ (21.3 − 15))∗ (0.0005 +∗ −0.006(0.135)^(1/2) +  −0.007 ∗ 0.135 +

 −0.038 ∗ (0.135)^(3/2) +  0.0636 ∗ (0.135)^2 + −0.014 ∗ (0.135)^(5/2))

S = -0.00194

Finally to calculate Salinity in units of ppt the following equation must be used:

𝑆𝑎𝑙𝑖𝑛𝑖𝑡𝑦   =  𝐴0 + 𝐴1 ∗ 𝑅 − 𝑠𝑢𝑏 − 𝑡u� + 𝐴2 ∗ 𝑅 − 𝑠𝑢𝑏 − 𝑡 + 𝐴3 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^(3/2) +

𝐴4 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^2 + 𝐴5 ∗ (𝑅 − 𝑠𝑢𝑏 − 𝑡)^(5/2) + 𝑆

Where:

S = previous calculation

A0 = 0.008

A1 = -0.169

A2 = 25.385

A3 = 14.094

A4 = -7.026

A5 = 2.7081

𝑆𝑎𝑙𝑖𝑛𝑖𝑡𝑦   =  0.008 + −0.169 ∗ 0.135u� + 25.385 ∗ 0.135 + 14.094 ∗ (0.135)^(3/2) +

−7.026 ∗ (0.135)^2 +  2.7081 ∗ (0.135)^(5/2) + −0.00194

Salinity = 0.35 ppt

Page 43: Nearshore Habitat & Water Quality

Appendix B. Calibration curve of Absorbance vs Total Phosphates

y = 0.9536xR² = 0.9798

0.00

0.05

0.10

0.15

0.20

0.25

0.30

0.35

0.40

0.00 0.04 0.08 0.12 0.16 0.20 0.24 0.28 0.32 0.36 0.40

Abs

orba

nce

Total Phosphates (mg/L)

Absorbance as a function of Total Phosphates (mg/L) [Spectronic 21]

Page 44: Nearshore Habitat & Water Quality

y = 1.3777x - 0.0002R² = 0.99976

0.00

0.05

0.10

0.15

0.20

0.25

0.30

0.35

0.40

0.45

0.50

0.55

0.00 0.04 0.08 0.12 0.16 0.20 0.24 0.28 0.32 0.36 0.40

Abs

orba

nce

Total Phosphates (mg/L)

Absorbance as a function of Total Phosphates (mg/L) [Genesys 20]

Page 45: Nearshore Habitat & Water Quality

Appendix C. Water quality parameters measured for Marsh Creek Analysis A (Upstream/Downstream) in 2014.

Table C-1: Summary of water quality parameters for Marsh Creek Analysis A for June 10-12, 2014

Table C-2: Summary of water quality parameters for Marsh Creek Analysis A for July 2-4, 2014

Table C-3: Summary of water quality parameters for Marsh Creek Analysis A for July 9-11, 2014

Table C-4: Summary of water quality parameters for Marsh Creek Analysis A for July 16-18, 2014

Page 46: Nearshore Habitat & Water Quality

Table C-5: Summary of water quality parameters for Marsh Creek Analysis A for July 23-25, 2014

Table C-6: Summary of water quality parameters for Marsh Creek Analysis A for July 29-31, 2014

Page 47: Nearshore Habitat & Water Quality

Appendix D. Water quality parameters measured for Marsh Creek Analysis A (Upstream/Downstream) in 2013.

Table D-1: Summary of water quality parameters for Marsh Creek Analysis Afor June 24-26, 2013

Table D-2: Summary of water quality parameters for Marsh Creek Analysis Afor July 9-11, 2013

Table D-3: Summary of water quality parameters for Marsh Creek Analysis Afor July 23-25, 2013

Table D-4: Summary of water quality parameters for Marsh Creek Analysis Afor July 29-31, 2013

Table D-5: Summary of water quality parameters for Marsh Creek Analysis Afor August 6-8, 2013

%Transmittance Absorbance Total  Upstream 1 Low 18.4 6.62 9.63  >6000   98.0 0.009 0.004 6.25 0.0 0.07

Downstream 1 Low 17.6 7.69 10.71                                  1,200,000   75.4 0.123 0.049 8.09 5.0 0.89

OrthophosphatesField  pH D.O.  (ppm) Fecal  Coliforms  (CFU/100mL)

Date:  June  25  -­‐  26,  2013

Samples Tides Temp  (°C)

Salinity  (ppt)Lab  pH

TSS  (mg/L)

%Transmittance Absorbance Total  Upstream 1 Low 17.8 -­‐ 9.85                                                1,400   98.0 0.009 0.004 6.79 0.0 0.05

Downstream 1 Low 18.8 -­‐ 9.38                                        525,000   65.0 0.187 0.075 7.77 3.0 0.30

Date:  July  9  -­‐  11,  2013

Samples Tides Temp  (°C)

D.O.  (ppm)Field  pH Fecal  Coliforms  (CFU/100mL)

Lab  pH

TSS  (mg/L)

Salinity  (ppt)Orthophosphates

%Transmittance Absorbance Total  Upstream 1 Low  -­‐  Mid 16.6 -­‐ 8.85                                                      550   98.2 0.008 0.003 6.48 5.0 0.06

Downstream 1 Low  -­‐  Mid 16.2 -­‐ 6.30                                                              -­‐   85.6 0.067 0.027 6.95 10.0 0.24

D.O.  (ppm) Fecal  Coliforms  (CFU/100mL)

Lab  pH

TSS  (mg/L)

Salinity  (ppt)OrthophosphatesDate:  July  23  -­‐  25,  2013

Samples Tides Temp  (°C)

Field  pH

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Upstream 1 High  -­‐  Mid 19.4 -­‐ 8.27                                                      280   99.8 0.001 0.000 6.65 0.0 0.06Downstream 1 High  -­‐  Mid 18.4 -­‐ 5.41                                            85,000   73.2 0.136 0.055 6.91 0.0 0.19

D.O.  (ppm)Fecal  Coliforms  (CFU/100mL)

Lab  pH

TSS  (mg/L) Salinity  (ppt)

OrthophosphatesDate:  July  29  -­‐  

31,  2013 Samples TidesTemp  (°C) Field  pH

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Upstream 1 Low  -­‐  Mid 16.2 -­‐ 9.24                                                      550   99.2 0.004 0.002 6.51 0.0 0.06Downstream 1 Low  -­‐  Mid 18.1 -­‐ 6.23                                        167,500   76.8 0.115 0.046 7.23 10.0 0.30

Field  pHTemp  (°C)TidesSamples

Date:  August  6  -­‐  8,  2013 Salinity  (ppt)

TSS  (mg/L)

Lab  pH

Fecal  Coliforms  (CFU/100mL)D.O.  (ppm)

Orthophosphates

Page 48: Nearshore Habitat & Water Quality

Appendix E. Water quality parameters measured for Marsh Creek Analysis A (Upstream (top) and Downstream (bottom)) for years 1995 through 2014.

Page 49: Nearshore Habitat & Water Quality

Appendix F. Water quality parameters measured for Marsh Creek Analysis B (five locations in the last 2 km stretch) in 2014.

Table F-1: Summary of water quality parameters for Marsh Creek Analysis B for June 10-12, 2014

Table F-2: Summary of water quality parameters for Marsh Creek Analysis B for July 2-4, 2014

Table F-3: Summary of water quality parameters for Marsh Creek Analysis B for July 9-11, 2014

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Table F-4: Summary of water quality parameters for Marsh Creek Analysis B for July 16-18, 2014

Table F-5: Summary of water quality parameters for Marsh Creek Analysis B for July 23-25, 2014

Page 51: Nearshore Habitat & Water Quality

Table F-6: Summary of water quality parameters for Marsh Creek Analysis B for July 29-31, 2014

Appendix G. Water quality parameters measured for Marsh Creek Analysis B (five locations in the last 2 km stretch) in 2013.

Table G-1: Summary of water quality parameters for Marsh Creek Analysis Bfor June 24-26, 2013

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

1 Low 14.4 7.01 5.27                                        130,000   80.2 0.096 0.039 7.25 2.0 13.742 Low 14.4 6.99 5.50                                        110,000   79.0 0.103 0.041 7.29 5.0 17.133 Low 14.9 6.49 5.56                                            25,000   77.0 0.113 0.045 7.34 4.0 17.25

Site  2 1 Low 17.1 6.99 9.10                                        105,000   75.2 0.123 0.049 7.74 6.0 1.90Site  3 1 Low 18.9 8.52 14.94                                        105,000   93.8 0.028 0.011 8.82 1.0 0.20Site  4 1 Low 18.9 8.42 14.83                                                3,500   93.0 0.031 0.012 8.61 8.0 0.20Site  5 1 Low 18.5 7.54 10.01                                                          50   92.2 0.036 0.014 7.16 0.0 0.20

Lab  pH TSS  (mg/L)

Site  1

Temp  (°C)

Fecal  Coliforms  (CFU/100mL)

Date:  June  24  -­‐  26,  2013

Samples Tides

Orthophosphates

Field  pH D.O.  (ppm) Salinity  (ppt)

Page 52: Nearshore Habitat & Water Quality

Table G-2: Summary of water quality parameters for Marsh Creek Analysis Bfor July 9-11, 2013

Table G-3: Summary of water quality parameters for Marsh Creek Analysis Bfor July 23-25, 2013

Table G-4: Summary of water quality parameters for Marsh Creek Analysis Bfor July 29-31, 2013

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Site  1 1 Low 16.9 -­‐ 5.08                                  1,150,000   66.2 0.072 0.072 7.19 4.0 11.301 Low 18.3 -­‐ 7.76                                        215,000   73.0 0.055 0.055 7.41 1.0 1.062 Low 18.4 -­‐ 7.84                                        175,000   67.6 0.068 0.068 7.42 4.0 1.093 Low 18.5 -­‐ 8.08                                        155,000   70.2 0.062 0.062 7.50 1.0 1.11

Site  3 1 Low 19.5 -­‐ 12.46                                            23,000   87.6 0.023 0.023 8.34 0.0 0.20Site  4 1 Low 19.5 -­‐ 10.68  >60000   88.2 0.022 0.022 7.73 0.0 0.20Site  5 1 Low 19.4 -­‐ 9.06                                                      300   95.6 0.008 0.008 7.65 0.0 0.20

Site  2

Lab  pH TSS  (mg/L)

Salinity  (ppt)Fecal  Coliforms  (CFU/100mL)

OrthophosphatesDate:  July  9  -­‐11,  

2013Samples Tides Temp  

(°C)Field  pH D.O.  (ppm)

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Site  1 1 Low  -­‐  Mid 16.1 -­‐ 5.25                                        240,000   79.8 0.098 0.039 7.04 12.0 3.93Site  2 1 Low  -­‐  Mid 16.2 -­‐ 6.03                                        105,000   86.4 0.063 0.025 7.11 9.0 0.24

1 Low  -­‐  Mid 16.2 -­‐ 6.57                                        112,500   89.4 0.048 0.019 6.82 5.0 0.162 Low  -­‐  Mid 16.1 -­‐ 6.47                                            15,500   89.4 0.049 0.020 6.94 3.0 0.153 Low  -­‐  Mid 16.1 -­‐ 6.49                                            21,000   92.8 0.032 0.013 7.04 7.0 0.21

Site  4 1 Low  -­‐  Mid 16.2 -­‐ 6.32                                        120,000   92.2 0.035 0.014 6.75 2.0 0.15Site  5 1 Low  -­‐  Mid 15.8 -­‐ 6.14                                                2,700   95.0 0.022 0.009 6.61 0.0 0.16

Site  3

Lab  pH TSS  (mg/L)

Salinity  (ppt)

OrthophosphatesDate:  July  23  -­‐  

25,  2013Samples Tides Temp  

(°C)Field  pH D.O.  (ppm) Fecal  Coliforms  

(CFU/100mL)

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Site  1 1 High  -­‐  Mid 18.0 -­‐ 5.37                                            19,500   94.6 0.025 0.010 6.95 0.0 1.45Site  2 1 High  -­‐  Mid 17.9 -­‐ 5.23  >60000   76.6 0.116 0.047 6.95 0.0 1.21Site  3 1 High  -­‐  Mid 18.6 -­‐ 6.17  -­‐   94.0 0.027 0.011 6.87 0.0 0.17

1 High  -­‐  Mid 18.6 -­‐ 5.72  >60000   92.2 0.035 0.014 6.73 0.0 0.142 High  -­‐  Mid 18.5 -­‐ 5.94                                            27,500   94.0 0.027 0.011 6.79 0.0 0.163 High  -­‐  Mid 18.5 -­‐ 5.86                                                4,250   91.6 0.038 0.015 6.83 5.0 0.13

Site  5 1 High  -­‐  Mid 18.5 -­‐ 5.95                                                5,250   94.6 0.024 0.010 6.65 5.0 0.13

Site  4

TSS  (mg/L) Salinity  (ppt)

Date:  July  29  -­‐  31,  2013

OrthophosphatesFecal  Coliforms  (CFU/100mL)Samples Tides

Temp  (°C) Field  pH D.O.  (ppm) Lab  pH

Page 53: Nearshore Habitat & Water Quality

Table G-5: Summary of water quality parameters for Marsh Creek Analysis Bfor August 6-8, 2013

Appendix H. Water quality parameters measured for Marsh Creek Analysis B (five locations in the last 2 km stretch) in 2012.

Table H-1: The Average of the Data Tables of Sites 1 through 5 During 2012

Averages for 2012

Site Field pH D.O (ppm) Orthophosphates

Lab pH mg TTS/L Fecal Coliform (CFU/100 mL) %T Absorb. mg/L

1 6.83 5.24 90.8 0.043 0.017 7.23 221.0 > 8325 2 6.68 3.63 91.1 0.040 0.016 7.05 72.5 > 95825 3 6.70 2.30 89.9 0.047 0.019 7.11 12.5 > 20825 4 6.55 / 25.4 0.021 0.008 7.13 ND - 5 6.78 6.51 94.0 0.028 0.011 7.33 3.75 > 8325

%Transmittance AbsorbanceTotal  

phosphates  (mg/L)

Site  1 1 Low  -­‐  Mid 16.9 -­‐ 3.97                                        105,000   73.8 0.132 0.053 6.95 14.0 6.35Site  2 1 Low  -­‐  Mid 17.9 -­‐ 5.26                                            45,000   77.2 0.112 0.045 7.20 8.0 0.41Site  3 1 Low  -­‐  Mid 18.9 -­‐ 7.85                                            13,500   95.0 0.023 0.009 7.24 0.0 0.18Site  4 1 Low  -­‐  Mid 18.8 -­‐ 7.59                                        115,000   93.6 0.029 0.012 7.25 0.0 0.16

1 Low  -­‐  Mid 18.0 -­‐ 5.61                                                1,425   95.2 0.021 0.008 6.70 0.0 0.182 Low  -­‐  Mid 18.1 -­‐ 5.98                                                      400   93.0 0.031 0.012 6.83 0.0 0.183 Low  -­‐  Mid 18.1 -­‐ 6.08                                                      450   97.4 0.011 0.004 6.90 0.0 0.18

Site  5

Lab  pHTSS  

(mg/L) Salinity  (ppt)Fecal  Coliforms  (CFU/100mL)D.O.  (ppm)

Orthophosphates

Field  pHTemp  (°C)TidesSamples

Date:  August  6  -­‐  8,  2013

Page 54: Nearshore Habitat & Water Quality

Table H-2: Summary table of results for August 1, 2012

Table H-3: Summary table of results for August 8, 2012

%T Absorb.Sample  1 >300 80.8 0.092 6.83 937.5Sample  2 >300 80.4 0.095 6.84 380.0Sample  3 >300 81.4 0.089 6.90 ND

6.72 /

Week  1

Site  1

Site  2

Site  3

Site  4

Site  5

Tide Temp. Field  pH D.O  (ppm) Total  Fecal  Coliforms  (CFU/100mL)

OrthophosphatesLab  pH mg  TSS/L

High/Middle  Tide

High/Middle  Tide

High/Middle  Tide

High/Middle  Tide

High/Middle  Tide

6.52 / >300

6.55 / >300

22°C

Sample  1

Sample1

Sample1

Sample1 / / >300 83.6 0.078 7.10 ND

25.4 0.021 7.13 ND

90.0 0.046 6.87 ND

6.40 / >300 89.0 0.051 6.94 ND

%T Absorb.Sample  1 >3000 90.4 0.043 7.23 2.5

>3000>3000

91.891.092.2

0.037 7.01 ND6.72 6.4

Site  1

Site  2

Site  3

Site  4

Going  out

Going  out

6.88 2.5 >3000

6.96 /

Sample  1 >3000

Site  5 7.01 6.06 >3000 97.0 0.012 7.10 5.0Coming  InSample1

Sample1

Sample1

/

Coming  In 22°C 88.4 0.054 7.12 10.0

/ / -­‐ / / / /

Week  2

Tide Temp. Field  pH D.O  (ppm) Total  Fecal  Coliforms  (CFU/100mL)

OrthophosphatesLab  pH mg  TSS/L

Page 55: Nearshore Habitat & Water Quality

Table H-4: Summary table of results for August 14, 2012

Table H-5: Summary table of results for August 16, 2012

%T Absorb.

Sample1 >30000 81.8 0.088 6.99 12.5Sample2 >30000 89.0 0.051 7.10 NDSample3 >30000 89.8 0.047 7.17 ND

6.62 2.5

Week  3

Tide Temp. Field  pH D.O  (ppm) Total  Fecal  Coliforms  (CFU/100mL)

OrthophosphatesLab  pH mg  TSS/L

/ / -­‐ / / / /

6.54 6.5 >30000 98.6 0.006 7.48 ND

High

High

High

High

High

Site  1

Site  2

Site  3

Site  4

Site  5

20.4°C

Sample  1

Sample  1

Sample1

Sample1

>30000 93.8 0.027 7.26 2.5

7.18 5.24 >30000 97.8 0.010 7.45 2.5

6.81 2.66

%T Absorb.

Sample1 -­‐ 95.8 0.018 7.69 2.5Sample2 -­‐ 97.4 0.012 7.61 NDSample3 -­‐ 97.4 0.012 7.61 ND

/ 6.98

Tide Temp. Field  pH D.O  (ppm) Total  Fecal  Coliforms  (CFU/100mL)

OrthophosphatesLab  pH mg  TSS/L

Site  5

Middle  (Coming  In)

Middle  (Coming  In)

Middle  (Coming  In)

Middle  (Coming  In)

Middle  (Coming  In)

Week  4

22.8°C

Sample  1

Sample  1

Sample1

Sample1

Site  1

Site  2

Site  3

Site  4 /

1.84 >700000 89.0 0.051 7.05 7.5

1.91 >100000 95.4 0.020 7.27 15.0

/ / -­‐ 94.0 0.028 7.37 220.0

/

/

/ -­‐ / / / /

Page 56: Nearshore Habitat & Water Quality

Appendix I

Salinity of the Lower Marsh Creek Watershed

Figure E-1: Salinity Readings for Lower Marsh Creek

Page 57: Nearshore Habitat & Water Quality

The data that was plotted in Figure 3.0.A was taken from appendix A, table A-4 and A-9. This was done to compare fecal coliform from 2012 – 2013.

Figure 3.0.A: Fecal Coliform Counts Compared from 2012 to 2013 at Sites 1 through 5

0

100000

200000

300000

400000

500000

600000

700000

800000

1 2 3 4 5

Fecal  Colifo

rms  (CFU/100mL)

Sample  Sites

Fecal  Coliforms  for  2012

Fecal  Coliforms  for  2013