Observations and Measurement: The Microscope
dissecting microscope
eyepiece
ocular
body tube
revolving nosepiece
objective
stage
coarse adjustment
fine adjustment
substage condenser
iris
iris diaphragm
color aberration
arm
base
mechanical stage
stage clips
light source
scanning objective
low power objective
high power objective
oil immersion objective
phase-contrast
parfocal [par FOK ul]
resolution
magnification
light intensity
prepared or permanent slide
wet mount or temporary slide
glass slide
coverslip
stain
cyclosis [cy CLOSE siss]
plasmolysis [plaz MOLL eh siss]
protoslo
micrometer (sing.) [my CHROM eh tur]
lens paper
lens cleaner
chloroplast
central vacuole
nucleus
(1) 15X
(2) 115X
(3) 150X
(4) 1500X
(5) 15000X
(1) plasmolysis.
(2) crenolysis.
(3) hemolysis.
(4) cyclosis.
(5)turgor.
(1) Begin all microscope work with the scanning objective over the hole in the stage.
(2) Make sure the body tube is locked into the closest position to the objective.
(3) Make sure the iris diaphram is all the way closed.
(4) All of the above are correct.
(5) None of the above are correct.