Fecal Colform Bacteria Contamination during Rain Events in Sayler’s Creek, Virginia Blake N.
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Fecal Colform Bacteria Contamination during Rain Events in Sayler’s Creek, Virginia Blake N. Robertson Senior Honors Research Under the Supervision of Dr. David Buckalew Natural Science Department Longwood University Categories of River and Stream Impairment: • • • • • • Suspended Sediments Biochemical Oxygen Demand Nutrients Toxic Chemicals Heavy metals Fecal Coliform Bacteria Magnitude of Impairment • 13,218 miles of streams and rivers monitored in Virginia by Virginia’s Department of Environmental Quality • 52% or 6,301 of those miles were determined to be impaired (DEQ 2004 303(d) and 305 (b)) Why Focus on Bacterial Pollutants? “Agricultural to be one of the primary sources Contributing to the bacteria standards violations (DEQ)” TMDL plans •The Clean Water Act requires states to establish water quality standards •Water quality is determined by ability to support specific uses •If water quality is not sufficient, then a Total Maximum Daily Load plan is created •In Virginia, TMDL plans are optional •However, some aid exists Uses and their corresponding fecal coliform bacteria standard Drinking Water 1 colony forming unit (CFU) per 100 ml Total body contact 200 CFU/100ml Partial Body contact 1000 CFU/100ml Treated sewage effluent <200 CFU/100ml Why Focus on Sayler’s Creek? • Impaired headwater of the Appomattox River • Drains into the heavily depended upon Chesapeake Bay • Public Health – Local and Regional • Eutrophication is accelerated leading to anoxia • Lack of data Past and Ongoing Studies • Clean Virginia Waterways ARWQMP samples monthly at four locations in the Sayler’s Creek watershed • Virginia’s DEQ monitors monthly where the two tributaries in the watershed meet • Scarcity of research existing for the area • Excellent place for such a study Objectives Objective: To quantify fecal coliform bacterial contamination entering the stream during rain events Secondary Objective: To measure differences between testing methods for fecal coliform bacteria in water samples collected during rain events Experimental Hypotheses Hypotheses: H0: An increase in streamflow will not cause fecal coliform contamination to increase HA: An increase in streamflow will cause fecal coliform contamination to increase Hypotheses: H0: There is no difference in coliform contamination between sampled sites Hypotheses: H0: Measures of coliform bacteria do not differ between testing methods HA: There is a difference in coliform contamination between sampled sites HA: Measures of coliform bacteria differ between testing methods Field Data Collection Sample Collection • Water samples collected before (baseline), during, and after rain events • Duplicate water samples taken randomly Site Characterization • • • • • Precipitation for event period Water velocity Water temperature Water depth Information not collected in every instance Determining Stream Profile Establishing a Transect Surveying the Stream Profile Measuring Streamflow Stream Profile Example Salyer 7 Stream Profile 1 98 0 97 -1 96 -2 95 Distance from left bankfull (Feet) 18 17 16 15 13 11 9 7 5 3. 3 2 -3 94 0 Depth (Feet) 2 99 Discharge Calculation Discharge or Q (ft3/sec) = velocity (ft/sec) X stream area (ft2) Example: Stream Area = 5.558 ft2 Water Velocity = 0.713 ft/sec Discharge = 3.964 ft3/sec Sample Collection • Samples were collected according to published guidelines of the Standard Methods for the Examination of Water and Wastewater, 20th ed. • Samples were collected in sterile 18oz. Whirl-Pak Bags • Stored in a cooler with ice packs • Transported to the lab for processing within 6 hours of sample collection Sample Collection Samples Transported for Processing Membrane Filtration • Samples diluted to 1% and passed through a 0.45 micron Millipore filter • Incubated at 44.5 +/- 0.5°C for 24 +/- 2 hours. Apparatus mFC Agar Defined Substrate • Water sample is combined with two substrates (ONPG and MUG) • Incubated at 44.5 +/- 0.5°C for 24 +/- 2 hours. • Coliforms use ß-galactosidase to metabolize ONPG and change the cell to a yellow color • E. Coli uses ß-glucuronidase to metabolize MUG and create fluorescence Site Identification Little Sayler’s Creek •Sayler’s 6 - 37 17’ 22’’ N and 78 16’ 22 W •More human land use upstream Big Sayler’s Creek • Sayler’s 7 – 37 18’ 29’’ N and 78 13’ 41’’ W • More forested land upstream •Both are 2nd order streams (Headwaters) •Drain a similar amount of land •Similar bottom substrate and riparian buffer at each site Statistical tests • To determine if any statistical differences exist – Confidence Level = 95% • Normality was tested for each data set – Bacterial assays – Assay method • Tests used include: – A paired-sample t-test was used to compare methods of measuring fecal coliform bacteria – A nonparametric, related samples test to compare baseflow bacterial counts with those of peak flow – A Wilcoxon Rank Sum test was used to compare flow and bacterial counts between the two different sites Results: Site Characteristics Location Saylers 6 Sayler 7 Temperature Avg (Sd, n) Velocity Avg (ft/ sec) Discharge Avg (ft3/sec) 62.45 F° (2.27, 42) 63.39 F° (2.47, 42) 1.23 10.71 1.23 9.65 •Precipitation data was not used for rain events 4 through 7 Results ra in 7 6 5 4 3 2 1 12000 10000 8000 6000 4000 2000 0 ev en t CFU's per 100ml Mean Contamination of Rain Events Mean Bacterial Counts for Sampled Rain Events Sayler 6 Sayler 7 Saylers 6 had a greater mean bacterial count over the 7 rain events Rain Event at Sayler 6 30000 3.5 3 2.5 Velocity (ft/sec) 20000 2 15000 1.5 10000 1 5000 • Sampled rain event: September 4th to 8th 0.5 0 0 10 20 30 40 Total Hours Elapsed •At sampled times, contamination appears to increase and decrease with streamflow at both sites •Similar trend appears for each rain event Rain Event at Sayler 7 30000 3 25000 2.5 20000 2 15000 1.5 10000 1 5000 0.5 0 0 0 10 20 Total Hours Elapsed 30 40 Velocity (ft/sec) 0 CFU's per 100/ml CFU's per 100ml 25000 Streamflow and Bacterial Count Statistical Results Variable Sig. Result P<0.002 Reject H0 Velocity P>0.88 Fail to reject H0 Discharge P>0.28 Fail to reject H0 Fecal Coliform P<0.005 Reject H0 Site Comparison Fecal Coliform Peak and Baseline Comparison Summary of Statistics Conclude that there was no difference between velocity and discharge at the two sites during sampled rain events. Conclude that the two sites differed in bacterial counts. Conclude that there was a significant difference between peak and baseline bacterial counts during sampled rain events. Duration Since Last Rain Event • At Sayler 6, on Little Sayler’s Creek, a rain events with similar amounts of rain yielded different concentrations of fecal coliform bacteria. Rain Event Number 1 3 Peak Stream Flow (ft/sec) >3.0 >3.9 Time since last rain event 14 days 4 days Peak Contamination (CFU’s per 100ml) 28,500 4,800 Total precipitation (in) 2.35 2.5 Method Comparison Variable Sig. Result Method Difference in fecal P>0.9 Fail to reject 7 H0 comparison Coliform measurements Summary of Statistics Conclude that there was no difference between the methods for measuring fecal coliform bacteria during rain events at the two sampled sites. Summary of Results • There is a difference in bacterial counts between sites sampled. – Sayler 6 is more heavily contaminated • When both sites were included, there was a difference between peak flow and baseflow fecal coliform contamination. • A trend between streamflow and fecal coliform contamination exists. • There was no difference in the methods used to test for fecal coliform bacteria. Future Studies and Recommendations • The DEQ had listed the cause of fecal coliform pollutants as agricultural, but the source is now listed as ‘unknown’. – Stresses the importance of bacterial source tracking • Adopt a TMDL plan. • Determine if the area upstream of Sayler 6 that drains into Little Sayler’s Creek is more developed than the area above Big Sayler’s Creek and how that is affecting bacteria counts. • Investigate the effect of varying times between rain events. • The Sayler’s Creek watershed is an excellent outdoor classroom. Acknowledgements •I would first like to acknowledge and thank Dr. David Buckalew for the supervision and guidance he provided. I learned a great deal this year and owe much of it to him. •Thank you to Mrs. Alecia Daves of the Piedmont Soil and Water Conservation District for her surveying assistance. •This research was funded by the Dean’s Fund for Undergraduate Research