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2. Diaphragm (optics) - Wikipedia

   en.wikipedia.org/wiki/Diaphragm_(optics)

   Nine-blade iris Pentacon 2.8/135 lens with 15-blade iris Aperture mechanism of Canon 50mm f/1.8 II lens, with five blades In the human eye, the iris (light brown) acts as the diaphragm and continuously constricts and dilates its aperture (the pupil) A 750nm titanium-sapphire laser beam passing through an iris diaphragm, while opening and closing the iris.

3. Condenser (optics) - Wikipedia

   en.wikipedia.org/wiki/Condenser_(optics)

   The Arlow-Abbe condenser is a modified Abbe condenser that replaces the iris diaphragm, filter holder, lamp and lamp optics with a small OLED or LCD digital display unit. The display unit allows for digitally synthesised filters for dark-field, Rheinberg, oblique and dynamic (constantly changing) illumination under direct computer control.

4. Bright-field microscopy - Wikipedia

   en.wikipedia.org/wiki/Bright-field_microscopy

   A bright-field microscope has many important parts including; the condenser, the objective lens, the ocular lens, the diaphragm, and the aperture. Some other pieces of the microscope that are commonly known are the arm, the head, the illuminator, the base, the stage, the adjusters, and the brightness adjuster.

5. Slit lamp - Wikipedia

   en.wikipedia.org/wiki/Slit_lamp

   Eye examination with the aid of a slit lamp. Side view of a slit lamp machine. Cataract in human eye: magnified view seen on examination with the slit lamp. In ophthalmology and optometry, a slit lamp is an instrument consisting of a high-intensity light source that can be focused to shine a thin sheet of light into the eye.

6. Aperture - Wikipedia

   en.wikipedia.org/wiki/Aperture

   Different apertures of a lens In biology, the pupil (appearing as a black hole) of the eye is its aperture and the iris is its diaphragm. In humans, the pupil can constrict to as small as 2 mm (f / 8.3) and dilate to larger than 8 mm (f / 2.1) in some individuals.

7. Confocal microscopy - Wikipedia

   en.wikipedia.org/wiki/Confocal_microscopy

   Fluorescence and confocal microscopes operating principle. Confocal microscopy, most frequently confocal laser scanning microscopy (CLSM) or laser scanning confocal microscopy (LSCM), is an optical imaging technique for increasing optical resolution and contrast of a micrograph by means of using a spatial pinhole to block out-of-focus light in image formation. [1]