Ad
related to: how to calculate magnification and resolution of lens in microscopeglobalindustrial.com has been visited by 100K+ users in the past month
Search results
Results from the WOW.Com Content Network
In microscopy, NA is important because it indicates the resolving power of a lens. The size of the finest detail that can be resolved (the resolution) is proportional to λ / 2NA , where λ is the wavelength of the light. A lens with a larger numerical aperture will be able to visualize finer details than a lens with a smaller numerical ...
With any telescope, microscope or lens, a maximum magnification exists beyond which the image looks bigger but shows no more detail. It occurs when the finest detail the instrument can resolve is magnified to match the finest detail the eye can see. Magnification beyond this maximum is sometimes called "empty magnification".
A USAF 1951 resolution chart in PDF format is provided by Yoshihiko Takinami. This chart should be printed such that the side of the square of the 1st element of the group -2 should be 10 mm long. USAF 1951 Resolution Target Further explanations and examples; Koren 2003: Norman Koren's updated resolution chart better suited for computer analysis
In a dry objective or condenser, this gives a maximum NA of 0.95. In a high-resolution oil immersion lens, the maximum NA is typically 1.45, when using immersion oil with a refractive index of 1.52. Due to these limitations, the resolution limit of a light microscope using visible light is about 200 nm.
The ability of a lens to resolve detail is usually determined by the quality of the lens, but is ultimately limited by diffraction.Light coming from a point source in the object diffracts through the lens aperture such that it forms a diffraction pattern in the image, which has a central spot and surrounding bright rings, separated by dark nulls; this pattern is known as an Airy pattern, and ...
where N is the uncorrected f-number, NA i is the image-space numerical aperture of the lens, | | is the absolute value of the lens's magnification for an object a particular distance away, and P is the pupil magnification. Since the pupil magnification is seldom known it is often assumed to be 1, which is the correct value for all symmetric lenses.
With no modification to the microscope, i.e. with a simple wide field light microscope, the quality of optical sectioning is governed by the same physics as the depth of field effect in photography. For a high numerical aperture lens, equivalent to a wide aperture, the depth of field is small (shallow focus) and gives
Memorial in Jena, Germany to Ernst Karl Abbe, who approximated the diffraction limit of a microscope as = , where d is the resolvable feature size, λ is the wavelength of light, n is the index of refraction of the medium being imaged in, and θ (depicted as α in the inscription) is the half-angle subtended by the optical objective lens (representing the numerical aperture).
Ad
related to: how to calculate magnification and resolution of lens in microscopeglobalindustrial.com has been visited by 100K+ users in the past month