Aperture IrisDiaphragmControl orReo-stat/LightIntensity KnobThe objectiveprojects a flatimage on theentire field ofview.Condenser10 X 100=1000X TMItincreasesor getsbetterOptimalIlluminationDecreasesa. Condenser is driven(moved) to its highestpointb. When you close thefield iris diagram the coneof light has crisp edgesc. When you remove theright eyepiece the lightconsumes 66% of thearea10,40,100Contaminated/fungalgrowthObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationGo back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmentCenteringScrewsslide upsidedown,objective notscrewed inplaceParcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightTheamount oflighting willbe altered.oculars,objectives,condeser,lenses in thebody tubeRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light sourcemagnification,resolution,contrast10powerObjectivesAperture IrisDiaphragm(on thecondenser)A kimwipeor kleenexscratchesoptical partsbulb, camelhair brush,lens cleaner,lens paperAperture IrisDiaphragmControl orReo-stat/LightIntensity KnobThe objectiveprojects a flatimage on theentire field ofview.Condenser10 X 100=1000X TMItincreasesor getsbetterOptimalIlluminationDecreasesa. Condenser is driven(moved) to its highestpointb. When you close thefield iris diagram the coneof light has crisp edgesc. When you remove theright eyepiece the lightconsumes 66% of thearea10,40,100Contaminated/fungalgrowthObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationGo back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmentCenteringScrewsslide upsidedown,objective notscrewed inplaceParcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightTheamount oflighting willbe altered.oculars,objectives,condeser,lenses in thebody tubeRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light sourcemagnification,resolution,contrast10powerObjectivesAperture IrisDiaphragm(on thecondenser)A kimwipeor kleenexscratchesoptical partsbulb, camelhair brush,lens cleaner,lens paper

Microscopy Bingo - Call List

(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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  1. Aperture Iris Diaphragm Control or Reo-stat/Light Intensity Knob
  2. The objective projects a flat image on the entire field of view.
  3. Condenser
  4. 10 X 100= 1000X TM
  5. It increases or gets better
  6. Optimal Illumination
  7. Decreases
  8. 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
  9. 10, 40,100
  10. Contaminated/fungal growth
  11. 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
  12. Go back to 10X objective & repeat the process of finding & clearly focussing with coarse adjustment
  13. Centering Screws
  14. slide upside down, objective not screwed in place
  15. Parcentric: specimen stay in field of view when magnification is increased Parfocal: specimen stays almost in focus when magnification is increased
  16. Resolution : the microsopes ability to separte small details crisp and clear Contrast: the specimen against the background ex. dark against light
  17. The amount of lighting will be altered.
  18. oculars, objectives, condeser, lenses in the body tube
  19. Rotating head, mechanical body tube, stage, rotating nosepiece, arm, coarse & fine adjustment, base, light source
  20. magnification, resolution, contrast
  21. 10 power
  22. Objectives Aperture Iris Diaphragm (on the condenser)
  23. A kimwipe or kleenex scratches optical parts
  24. bulb, camel hair brush, lens cleaner, lens paper