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Microbiology Chapter 7 Quiz
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Microbiology Chapter 7 Quiz

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Questions and Answers

What should be done when inoculating to avoid cross-contamination?

  • Open plates to ensure they are not contaminated.
  • Perform inoculations away from plate 1. (correct)
  • Label all plates before inoculation.
  • Inoculate plates 1 and 2 simultaneously.
  • At what temperature should plates 3, 4, 5, 6, and 7 be incubated?

  • 20°C
  • 25°C
  • 30°C
  • 37°C (correct)
  • What information is required when labeling the base of each plate?

  • The cost of materials used.
  • The date and type of exposure. (correct)
  • The laboratory procedure followed.
  • The estimated growth time.
  • How long should plates be incubated for?

    <p>24 to 48 hours.</p> Signup and view all the answers

    When preparing to observe colonies, what drawing details should be included?

    <p>Drawings should include side views of colonies.</p> Signup and view all the answers

    What is the function of Kohler illumination in microscopy?

    <p>To uniform the light source on the specimen</p> Signup and view all the answers

    What adjustment should be made if the field appears unevenly illuminated?

    <p>Adjust the condenser height to focus the edges of the diaphragm</p> Signup and view all the answers

    What happens when the field diaphragm is closed?

    <p>The amount of light entering the objective lens decreases</p> Signup and view all the answers

    How can the light in the field of view be centered?

    <p>By using the condenser centering screws</p> Signup and view all the answers

    Why is it necessary to adjust the condenser in microscopy?

    <p>To ensure uniform illumination across the field</p> Signup and view all the answers

    How many ocular units correspond to a distance of 1,500 µm?

    <p>47 ocular units</p> Signup and view all the answers

    What is the calibration value for one ocular unit (OU) based on the provided information?

    <p>32 µm/OU</p> Signup and view all the answers

    Which objective lens has a total magnification of 400X?

    <p>High-Dry Power</p> Signup and view all the answers

    What should be done if the calculated ocular unit values differ when measuring?

    <p>Take the arithmetic mean of the values</p> Signup and view all the answers

    Using the information given, what is the distance measurement associated with 25 ocular units?

    <p>800 µm</p> Signup and view all the answers

    If using the scanning objective at 40X magnification, what is the calibration in µm per ocular unit?

    <p>32 µm/OU</p> Signup and view all the answers

    Which total magnification corresponds to the low power objective?

    <p>100X</p> Signup and view all the answers

    What is the correct relationship between ocular units and the stage micrometer distance?

    <p>Ocular units can be calculated by dividing distance by units</p> Signup and view all the answers

    How many ocular units does 800 µm span?

    <p>25 ocular units</p> Signup and view all the answers

    Which of the following is true about measuring specimens with an ocular micrometer?

    <p>It must be calibrated for each objective</p> Signup and view all the answers

    Study Notes

    Inoculation Procedure

    • Inoculate away from plate 1 to prevent cross-contamination.
    • Plates 7 and 8 should remain covered and not be opened.
    • Label the base of each plate with the date, exposure type, and group name or number.
    • Invert all plates during incubation for consistency.

    Incubation Conditions

    • Incubate plates 1, 2, and 8 at 25°C.
    • Incubate plates 3, 4, 5, 6, and 7 at 37°C.
    • Incubation time ranges from 24 to 48 hours for optimal microbial growth.

    Observations and Drawings

    • Use provided circles as Petri dishes for drawing colony observations.
    • Choose two different colonies from each plate for detailed illustrations.
    • Label drawings with incubation time, temperature, and inoculum source, including colony color and abundance.

    Microscope Techniques

    • Kohler illumination improves uniform lighting when focusing on specimens.
    • The field diaphragm can be adjusted to enhance light quality for clearer visibility.
    • Adjust condenser height and centering for optimal field diaphragm visibility.

    Ocular Micrometer Calibration

    • Total magnifications vary across objectives: Scanning (40X), Low Power (100X), High-Dry Power (400X), Oil Immersion (1000X).
    • Use ocular micrometer to measure specimens by calculating ocular unit values based on stage micrometer measurements.

    Bacterial Emulsion Preparation

    • Prepare smears of different organisms on slides without mixing to avoid cross-contamination.
    • Heat-fix slides by passing through a flame but avoid overheating to minimize aerosol production.
    • Follow staining protocols for consistent results, with specific times for crystal violet and safranin.

    Safety and Disposal Practices

    • Dispose of used pipette and emulsion slides in designated disinfectant jars or sharps containers to ensure biohazard safety.
    • Use sterile tools, such as inoculating needles, especially for BSL-2 organisms, and properly disinfect after use.

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    Related Documents

    micro lab ch2&3.pdf

    Description

    Test your knowledge with this quiz based on Chapter 7 of Bailey & Scott's Diagnostic Microbiology. Focus on important practices for inoculation and contamination prevention techniques. Perfect for students learning about microbiological methods and laboratory safety.

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