ObjectivesAperture IrisDiaphragm(on thecondenser)10poweroculars,objectives,condeser,lenses in thebody tubebulb, camelhair brush,lens cleaner,lens paperCenteringScrewsObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationOptimalIlluminationCondenserA kimwipeor kleenexscratchesoptical partsThe objectiveprojects a flatimage on theentire field ofview.a. 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 theareaParcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedGo back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmentslide upsidedown,objective notscrewed inplaceAperture IrisDiaphragmControl orReo-stat/LightIntensity Knob10,40,100magnification,resolution,contrastResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light sourceDecreases10 X 100=1000X TMItincreasesor getsbetterContaminated/fungalgrowthTheamount oflighting willbe altered.ObjectivesAperture IrisDiaphragm(on thecondenser)10poweroculars,objectives,condeser,lenses in thebody tubebulb, camelhair brush,lens cleaner,lens paperCenteringScrewsObjectives not parfocal;slide is upside down;rotate the fine focusadjustment knob in theopposite directionReturn to 10X & refocusw/ coarse adjustmentknob then increasemaginificationOptimalIlluminationCondenserA kimwipeor kleenexscratchesoptical partsThe objectiveprojects a flatimage on theentire field ofview.a. 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 theareaParcentric: specimenstay in field of viewwhen magnification isincreasedParfocal: specimenstays almost in focuswhen magnification isincreasedGo back to 10Xobjective & repeatthe process offinding & clearlyfocussing withcoarse adjustmentslide upsidedown,objective notscrewed inplaceAperture IrisDiaphragmControl orReo-stat/LightIntensity Knob10,40,100magnification,resolution,contrastResolution : themicrosopes ability toseparte small detailscrisp and clearContrast: the specimenagainst the backgroundex. dark against lightRotating head,mechanical bodytube, stage, rotatingnosepiece, arm,coarse & fineadjustment, base,light sourceDecreases10 X 100=1000X TMItincreasesor getsbetterContaminated/fungalgrowthTheamount oflighting willbe altered.

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