Parts and functions of a compound microscope
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The document describes the main parts and functions of a compound microscope, including mechanical parts like the base and stage that support the microscope, magnifying parts like the objectives and ocular that enlarge specimens, and illuminating parts like the mirror and condenser that provide light. It also explains how to properly use a compound microscope, such as carrying and focusing it, as well as techniques for preparing slides including mounting, staining, and examining specimens.
Parts and functions of a compound microscope
- 1. Parts and Functions of a Compound Microscope
- 2. Light Microscope • Simple – uses a single lens • Compound – uses a set of lenses or lens systems
- 4. Compound Microscope • Mechanical Parts – Used to support and adjust the parts • Magnifying Parts – Used to enlarge the specimen • Illuminating Parts – Used to provide light
- 6. Mechanical Parts • Base – Bottommost portion that supports the entire/lower microscope • Pillar – Part above the base that supports the other parts • Inclination Joint – Allows for tilting of the microscope for convenience of the user
- 7. Inclination Joint Pillar Base
- 8. • Arm/Neck –Curved/slanted part which is held while carrying the microscope • Stage –Platform where object to be examined is placed • Stage Clips –Secures the specimen to the stage
- 9. • Stage Opening • Body Tube –Attached to the arm and bears the lenses • Draw Tube –Cylindrical structure on top of the body tube that holds the ocular lenses
- 10. Draw Tube Body Tube Arm / Neck Stage
- 11. • Revolving/Rotating Nosepiece –Rotating disc where the objectives are attached • Dust Shield –Lies atop the nosepiece and keeps dust from settling on the objectives
- 12. Dust Shield Revolving Nosepiece
- 13. • Coarse Adjustment Knob –Geared to the body tube which elevates or lowers when rotated bringing the object into approximate focus • Fine Adjustment Knob –A smaller knob for delicate focusing bringing the object into perfect focus
- 15. • Condenser Adjustment Knob –Elevates and lowers the condenser to regulate the intensity of light • Iris Diaphragm Lever –Lever in front of the condenser and which is moved horizontally to open/close the diaphragm
- 17. Illuminating Parts • Mirror – Located beneath the stage and has concave and plane surfaces to gather and direct light in order to illuminate the object • Electric Lamp – A built-in illuminator beneath the stage that may eb used if sunlight is not preferred or is not available
- 19. • Substage – Iris Diaphragm • Regualtes the amount of light necesaary to obtain a clearer view of the object – Condenser • A set of lenses between the mirror and the stage that concentrates light rays on the specimen.
- 21. MAGNIFYING PARTS • Ocular / Eyepiece – Another set of lens found on top of the body tube which functions to further magnify the image produced by the objective lenses. It usually ranges from 5x to 15x.
- 22. Ocular
- 23. MAGNIFYING PARTS • Objectives – Metal cylinders attached below the nosepiece and contains especially ground and polished lenses • LPO / Low Power Objective – Gives the lowest magnification, usually 10x • HPO / High Power Objective – Gives higher magnification usually 40x or 43x • OIO / Oil Immersion Objective – Gives the highest magnification, usually 97x or 100x, and is used wet either with cedar wood oil or synthetic oil
- 24. Objectives
- 25. Use of the Compound Microscope
- 26. • Make sure all backpacks are out of the aisles before you get a microscope! • Always carry the microscope with one hand on the Arm and one hand on the Base. Carry it close to your body.
- 27. • Be gentle. • Setting the microscope down on the table roughly could jar lenses and other parts loose.
- 28. • Always start and end with lowest powered objective.
- 29. • Place the slide on the microscope stage, with the specimen directly over the center of the glass circle on the stage (directly over the light).
- 30. • If you wear glasses, take them off; if you see only your eyelashes, move closer. • If you see a dark line that goes part way across the field of view, try turning the eyepiece.
- 31. • Use only the Fine adjustment knob when using the HIGH (long) POWER OBJECTIVE. • As much as possible, keep both eyes open to reduce eyestrain. Keep eye slightly above the eyepiece to reduce eyelash interference.
- 32. • If, and ONLY if, you are on LOW POWER, lower the objective lens to the lowest point, then focus using first the coarse knob, then the fine focus knob.
- 33. • Adjust the Diaphragm as you look through the Eyepiece, and you will see that MORE detail is visible when you allow in LESS light! • Too much light will give the specimen a washed-out appearance.
- 34. • Once you have it on High Power remember that you only use the fine focus knob! • The High Power Objective (40x) is very close to the slide. Use of the coarse focus knob will scratch the lens, and crack the slide.
- 35. MAGNIFICATION • The ratio of the original image to the “magnified” image.
- 38. RESOLUTION • limiting distance between two points at which they are perceived as distinct from one another.
- 40. Numerical Aperture • the amount of light that which enters the objective. • The larger the NA, the greater the resolving power of the objective.
- 41. Mounting • Glass Slide - thin flat piece of glass, typically 75 by 25 mm (3 by 1 inches) and about 1 mm thick, used to hold objects for examination under a microscope. • Cover Slip
- 42. Mounting • 1. Gather a thin slice/piece of whatever your specimen is. If your specimen is too thick, then the coverslip will wobble on top of the sample like a see-saw:
- 43. 2. Place ONE drop of water directly over the specimen.
- 44. • Place the coverslip at a 45 degree angle (approximately), with one edge touching the water drop, and let go.
- 46. Staining • A technique in microscopy that is used to enhance the image of the specimen. • To distinguish structures in cells and tissues
- 47. How to Stain a Slide 1. Place one drop of stain on one edge of the coverslip, and the flat edge of a piece of paper towel on the other edge of the coverslip. The paper towel will draw the water out from under the coverslip, and the cohesion of the water will draw the stain under the coverslip.
- 49. • As soon as the stain has covered the area containing the specimen you are finished. The stain does not need to be under the entire coverslip. If the stain does not cover the area needed, get a new piece of paper towel and add more stain until it does.
- 50. • 3. Be sure to wipe off the excess stain with a paper towel, so you don’t end up staining the objective lenses.
- 51. • 4. You are now ready to place the slide on the microscope stage. Be sure to follow all the instructions as to how to use the microscope.
- 52. • 5. When you have completed your drawings, be sure to wash and dry both the slide and the coverslip and return them to the correct places!
Editor's Notes
- #30: Then you have a 9 out of 10 chance of finding the specimen as soon as you look through the eyepiece!
- #33: The specimen will be in focus when the LOW POWER objective is close to the lowest point, so start there and focus by slowly raising the lens. If you can’t get it at all into focus using the coarse knob, then switch to the fine focus knob.
- #34: Once you have found the specimen on Low Power (100x), unless specifically asked to draw it on low power, center the specimen in your field of view, then, without changing the focus knobs, switch it to High Power. If you don’t center the specimen you will lose it when you switch to High Power (Yellow).
- #35: NEVER USE THE RED LENS. It is an oil immersion lens. Without the oil to lubricate the lens, you will destroy it!Also, the oil is needed to help gather enough light to actually see through the lens!
- #36: For example, if we looked at a 1 mm diameter dot with a magnifying glass we can measure the dot as it appears through the lens of the glass. If the dot after magnification is 2 mm, then the magnification is 2x
- #44: If you put too much water over the specimen, then the coverslip will float on top of the water, making it harder to draw the specimens as they float past the field of view!