Presentation is loading. Please wait.

Presentation is loading. Please wait.

MAGNIFICATION versus RESOLUTION of a Microscope GEOL 3213, Micropaleontology.

Similar presentations


Presentation on theme: "MAGNIFICATION versus RESOLUTION of a Microscope GEOL 3213, Micropaleontology."— Presentation transcript:

1 MAGNIFICATION versus RESOLUTION of a Microscope GEOL 3213, Micropaleontology

2 Low-Power Dissecting Light Microscopy Low to moderate resolution is usually adequate for forams, ostracodes, and other microfossils around a tenth to a few mm in size. Some additional information with moderate enlargement

3 Transmitted Light, Polarizing Microscopy Whole specimen mounts Low-power objective used with NA = 0.10 Magnification does not seem to improve visibility, so resolution is low

4 Transmitted Light, Polarizing Microscopy Higher power objective used with a larger NA More details visible with magnification, so the resolution is high.

5 Magnifying Low-Resolution Microscopy If resolution is low =NA, for example, is low “Empty magnification” = no additional information Just a larger fuzzy image of a fuzzy image

6 SEM SEM = Scanning electron microscopy Resolution is about 10 times the best light microscope

7 Magnification Ratio of apparent enlarged image size to object viewed apparent size = magnification actual size In terms of lenses: ( objective lens power) X (ocular lens power) = magnification For a light microscope, maximum useful magnification, assuming a NA for a very good lens to be 1.4-1.5, ~1000 X 1.4 = 1400 times Usually highest magnification is ~1000X. “Empty magnification” above this because a fuzzy image enlarged is just a larger fuzzy image

8 Stopped Here on Friday

9 Resolution (r) Minimum distance apart that 2 points can be distinguished Smaller the value, the better is the resolution Maximum r for a light microscope is about 0.2 µ m. This is 200 nm. Note: 1 µ m = 1 000 nm 1 µ m = 10 -6 m 1 nm = 10 -9 m Abbe’s relationship: 0.61  r = n sin  n sin  is also called the numerical aperture (NA)  = wavelength or average wavelength of light used n is the refractive index of medium between objective lens and specimen. n is 1.0 for air (& about 1.4 for immersion oil)  is the aperture angle of lens. Good lenses have larger angles to accept more light. For a good lens it is about 70 degrees.

10 Resolution (r) For a very good lens: NA = n sin  = (1) sin 70° = 1 x 0.9397 = 0.94 With white light, average  = ~550 nm, so for a good lens: r = (0.61 x 550) / (0.94) = 360 nm = 0.36 um With a good lens & blue light (  = ~450 nm): r = (0.61 x 450) / (0.94) = 292 nm = 0.292 um = ~0.3 um Repeat above with oil-immersion lens (n = 1.4): r = (0.61 x 450) / (1.4 x 0.94) = 209 nm = 0.209 um = ~0.2 um If UV (  = ~350 nm) used, then r = ~ 0.1 um, but must photo.

11 Homework #1 Solve the numerical problems on the handout sheet.

12 END OF FILE


Download ppt "MAGNIFICATION versus RESOLUTION of a Microscope GEOL 3213, Micropaleontology."

Similar presentations


Ads by Google