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Lab #3 Titlle: Water Sampling Testing and Statistical Application

Dr. Javier Arce

       From this laboratory, I learned the basics of taking water samples. The procedure

consists of first, letting water run for 2 to 3 minutes to clean the pipes. To take the water

sample you need a 100ml sterilized bottle. As soon as possible, put the water in a cooler

at 40 ° C and then take it to the refrigerator in the laboratory. An important tip is to

measure the temperature instantly after taking the water sample. This is done to

determine if the sample has the appropriate conditions for organism to live. When

analyzing samples, there are several steps too. First, use a substrate that interacts with E.

coli and another that interacts with Total Coliforms (you can also use a substrate that

interacts with both of them). Pour 100ml of water in the Quanty- Tray and label time,

number of sample, and date. After that, place the Quanty- Tray in the Quanty-Tray sealer.

Now, it is ready for placement in the incubator for 24 hours at 35° Celsius. We can

conclude that Sample #2 was positive to Total Coliforms and to E. coli. The Total

Coliforms are 231MPN and the E.coli is 2MPN. As a continuation of the lab, we used

Excel to analyze data given by Dr. Arce and create charts. This includes calculating the

mean, average, standard deviation or variance.

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Water Sampling Lab Statistical Analysis

  • 1. Lab #3 Titlle: Water Sampling Testing and Statistical Application Dr. Javier Arce From this laboratory, I learned the basics of taking water samples. The procedure consists of first, letting water run for 2 to 3 minutes to clean the pipes. To take the water sample you need a 100ml sterilized bottle. As soon as possible, put the water in a cooler at 40 ° C and then take it to the refrigerator in the laboratory. An important tip is to measure the temperature instantly after taking the water sample. This is done to determine if the sample has the appropriate conditions for organism to live. When analyzing samples, there are several steps too. First, use a substrate that interacts with E. coli and another that interacts with Total Coliforms (you can also use a substrate that interacts with both of them). Pour 100ml of water in the Quanty- Tray and label time, number of sample, and date. After that, place the Quanty- Tray in the Quanty-Tray sealer. Now, it is ready for placement in the incubator for 24 hours at 35° Celsius. We can conclude that Sample #2 was positive to Total Coliforms and to E. coli. The Total Coliforms are 231MPN and the E.coli is 2MPN. As a continuation of the lab, we used Excel to analyze data given by Dr. Arce and create charts. This includes calculating the mean, average, standard deviation or variance.