Chapter 2: The Cell as the Basic Unit of Life Flashcards
*Molecules of life, Biomolecules excluded (included in Ch.5 Food Substances and Molecules of Life)
State the Cell Theory.
- All organisms are made up of 1 or more cells.
- The cell is the basic unit of life; it is the smallest unit that shows all the characteristics of life.
- All cells come from pre-existing cells.
Definition of unicellular organisms and multicellular organisms.
Unicellular organisms:
- Organisms made up of only 1 cell (e.g. bacteria, Amoeba).
Multicellular organisms:
- Organisms made up of > 1 cells (e.g. plants, animals).
What are some major events in cell biology and the development of microscopes?
1590: The first light microscope was invented (by Hans Janssen & his son).
1665: “Cells” (cell walls) were discovered (by Robert Hooke with his microscope).
1674: Living cells were observed (by Antoni van Leeuwenhoek with his microscope).
1831: The nucleus was discovered (by Robert Brown).
1839: The Cell Theory was proposed (by Theodor Schwann & Matthias Jakob Schleiden).
1886: The mitochondrion was discovered.
1933: The first electron microscope was made.
1950: The ribosome was discovered.
What are the aspects of nature of science (NOS) are demonstrated in the discovery of cells and the development of the Cell Theory?
- Scientific knowledge is based on and derived from observations of the natural world.
- Science is affected by the technology and the types of equipment available at the time.
- Scientists build on the work of other scientists.
Comparison of different types of microscopes.
(Refer to document)
What are the differences between higher resolution and higher magnification?
Higher resolution:
- Clearer and more details of the image observed
Higher magnification:
- The specimen is enlarged to a larger extent
What are the structures of a light microscope and their uses?
(Setup: refer to notes p.11)
- Eyepiece: Magnifying lens → magnify specimens
- Nosepiece: Holds different objectives (of different magnifications); Can be rotated
- Objectives: Magnifying lens → magnify specimens
- Stage: Where the microscope slide is clipped for observation; Have hole → light can pass through; Can be raised or lowered to focus
- Condenser: Focuses light onto the specimen
- Diaphragm: Control the amount of light shone onto the condenser
- Coarse adjustment knob: Rotated to raise or lower the stage to obtain a rough focus; Causes a larger movement of the stage
- Fine adjustment knob: Rotated to raise or lower the stage to obtain a sharp focus; Causes a smaller movement of the stage
- Base: Foundation to support the whole microscope
- Arm: For holding the microscope
- Body tube: Connects the eyepiece and nosepiece
- Mirror: Reflects light from an external light source onto the specimen
- Light source: Provides light for viewing the specimen
What are the steps for using a light microscope?
- Insert a low-power eyepiece (e.g. 5X) into the body tube. Select a low-power objective (e.g. 4X) by rotating the nosepiece.
- Turn on the light source, adjust the the diaphragm until the light is sufficient.
- Clip the microscope slide with specimen onto the stage, with the specimen directly over the hole of the stage.
- Steps for focusing on the specimen:
(a) Look at the stage at eye level. Raise the stage (or lower the body tube) by turning the coarse adjustment knob until the objective almost touches the microscope slide.
(b) Look through the eyepiece. Lower the stage (or raise the body tube) slowly by turning the coarse adjustment knob until the image of the specimen is in rough focus.
(c) Turn the fine adjustment knob to get a sharp focus. - Search the field and move the region to be observed to the centre of the field of view.
- Select a high-power objective (e.g. 40X) by rotating the nosepiece.
- Turn the fine adjustment knob to get a sharp focus again.
- Brighten the view by adjusting the diaphragm if needed. (Why? Higher power magnification → dimmer)
Describe the image observed through a light microscope?
The image observed is magnified and inverted:
- Moving the slide right → Image moves left.
- Moving the slide away from the observer → Image moves towards the observer.
Comparison of image observed through low-power magnification and high-power magnification.
^Area of field of view, Details of specimen, Brightness of image
Area of field of view:
- Low-power magnification: Larger (More cells are observed)
- High-power magnification: Smaller (Fewer cells are observed)
Details of specimen:
- Low-power magnification: Less
- High-power magnification: More
Brightness of image:
- Low-power magnification: Brighter
- High-power magnification: Dimmer
Definition of magnification.
Magnification represents how many times an image is larger than the object.
What are the two equations for calculating the total magnification of a microscope?
^Reverse, Units
Total magnification = Power of eyepiece x Power of objective
Total magnification = Size of the image / Size of the object
Unit:
- 1cm = 10^-2m
- 1μm (micrometer/micron) = 10^-6m
- 1nm (nanometer) = 10^-9m
How do we prepare temporary mounts of ox corneal cells?
^Animal cells
Ox corneal cells:
- Touch the ox cornea gently with the middle of a clean slide.
- Add a drop of methylene blue solution to the touched area to stain the cells.
- Use a pair of forceps to place a cover slip over the cells.
How do we prepare temporary mounts of onion epidermis, banana tissue?
^Plants cells that are mount with iodine solution
Diagram: Refer to book p.31
Onion epidermis
- Peel off the inner epidermis of the fleshy layer of an onion.
- Cut out a small piece of epidermis.
- Mount it with a drop of iodine solution.
Banana tissue
- Take a small amount of tissue from the soft white middle part of a banana.
- Put the tissue into a drop of water on a slide.
- Separate the cells with a toothpicks.
- Mount the cells with a drop of iodine solution.
How do we prepare temporary mounts of hydrilla leaf, onion root tip cells?
^Plants cells that are mount with water
Hydrilla leaf
- Mount a hydrilla leaf with a drop of water.
Onion root tip cells
- Put small pieces of onion root tips into freshly prepared macerating fluid (浸離液) for 2 to 3 days to soften the root tips.
- Pour the content into a watch glass. Tear the tissue apart.
- Filter off the macerating fluid. Wash the macerated onion root tip gently with water.
- Mount the macerated onion root tip with a drop of water.
How do we prepare temporary mount of pollen grains?
^Plants cells that does not require a mounting medium
Pollen grains
- Touch a piece of sticky tape with the anther of a flower (e.g. a Gladiolus flower or a lily flower).
- Stick the tape onto a slide.
How do we place a cover slip on temporary mount of a specimen?
- Let the edge of a cover slip touch the mounting medium.
- Slowly lower the cover slip. Make sure no air bubbles are trapped (adding sufficient mounting medium can help minimize the chance of trapping air bubbles).
- Use tissue paper to soak up any excess mounting medium.
What is the purpose of sectioning the specimen?
^ Cut the specimen into a thin (1-cell thick) section
- Allow light to pass through the specimen
- Obtain a thin section for clearer observation