How to Control Image Resolution with Numerical Aperture
The resolving power of an objective determines the size of the formed Airy diffraction pattern: The radius of the central disk is determined by the combined numerical apertures of the objective and condenser. When condenser and objective have equivalent numerical apertures or the objective acts also as the condenser like in an inverted fluorescence microscope, the Airy pattern radius from the central peak to the first minimum is given by the equation:
r(Airy) = 1.22λ/2NA(Obj)(1)
r(Airy) is the Airy radius, λ is the wavelength of the illuminating light, and NA(Obj) is the objective´s numerical aperture (objective aperture = condenser aperture). The numerical aperture depends on the aperture angle of the illumination entering the objective aperture, as well as the refractive index of the imaging medium:
NA(Obj) = n(sin(θ))(2)
θ is the objective’s angular aperture and n is the refractive index of the medium (air, water, or oil) between the objective and the specimen.
The image resolution (D) is defined by this equation and hence corresponds to the Airy radius:
D = 0.61λ/NA(3)
Resolution is clearly influenced by the objective’s numerical aperture. Note that lower values of D indicate higher resolution. In the tutorial, the Numerical Aperture slider is used to control how the image structure evolves as the objective’s numerical aperture is increased. At the lowest numerical aperture value (0.20), the image details visible in the microscope are poorly defined and surrounded by diffraction fringes. As the slider is moved to higher numerical aperture values (0.50-0.80), the structural outline of the image becomes sharper and higher-order diffraction rings begin to emerge. At the highest numerical apertures (1.00-1.30), the diffraction disks are resolved individually as discrete luminous points surrounded by alternating series of bright and dark higher-order diffraction rings of decreasing intensity.