Parcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedAperture IrisDiaphragmControl orReo-stat/LightIntensity KnobA kimwipeor kleenexscratchesoptical partsCondenserItincreasesor getsbetteroculars,objectives,condeser,lenses in thebody tubeOptimalIllumination10powermagnification,resolution,contrast10,40,100The objectiveprojects a flatimage on theentire field ofview.Go back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmenta. 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 theareaObjectivesAperture IrisDiaphragm(on thecondenser)Theamount oflighting willbe altered.slide upsidedown,objective notscrewed inplaceCenteringScrewsResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightDecreasesContaminated/fungalgrowthObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationbulb, camelhair brush,lens cleaner,lens paper10 X 100=1000X TMRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light sourceParcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedAperture IrisDiaphragmControl orReo-stat/LightIntensity KnobA kimwipeor kleenexscratchesoptical partsCondenserItincreasesor getsbetteroculars,objectives,condeser,lenses in thebody tubeOptimalIllumination10powermagnification,resolution,contrast10,40,100The objectiveprojects a flatimage on theentire field ofview.Go back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmenta. 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 theareaObjectivesAperture IrisDiaphragm(on thecondenser)Theamount oflighting willbe altered.slide upsidedown,objective notscrewed inplaceCenteringScrewsResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightDecreasesContaminated/fungalgrowthObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationbulb, camelhair brush,lens cleaner,lens paper10 X 100=1000X TMRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light source

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