(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.
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The objective projects a flat image on the entire field of view.
magnification, resolution, contrast
The amount of lighting will be altered.
oculars, objectives, condeser, lenses in the body tube
Go back to 10X objective & repeat the process of finding & clearly focussing with coarse adjustment
Rotating head, mechanical body tube, stage, rotating nosepiece, arm, coarse & fine adjustment, base, light source
slide upside down, objective not screwed in place
Objectives
Aperture Iris Diaphragm (on the condenser)
Decreases
Objectives not parfocal; slide is upside down; rotate the fine focus adjustment knob in the opposite direction
Return to 10X & refocus w/ coarse adjustment knob then increase maginification
a. Condenser is driven (moved) to its highest point
b. When you close the field iris diagram the cone of light has crisp edges
c. When you remove the right eyepiece the light consumes 66% of the area
It increases or gets better
Optimal Illumination
Condenser
Resolution : the microsopes ability to separte small details crisp and clear
Contrast: the specimen against the background
ex. dark against light
bulb, camel hair brush, lens cleaner, lens paper
A kimwipe or kleenex scratches optical parts
10 X 100= 1000X TM
10 power
Centering Screws
Contaminated/fungal growth
Parcentric: specimen stay in field of view when magnification is increased
Parfocal: specimen stays almost in focus when magnification is increased
Aperture Iris Diaphragm Control or Reo-stat/Light Intensity Knob
