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{{short description|Laboratory technique}}{{refimprove|date=March 2017}}(File:Red blood cells by darkfield microscopy.jpg|right|thumb|Red blood cells as seen by darkfield microscopy x 1000)File:Dark field and phase contrast microscopies.ogg|thumb|Operating principle of dark-field and phase-contrast microscopies]]Dark-field microscopy (also called dark-ground microscopy) describes microscopy methods, in both light and electron microscopy, which exclude the unscattered beam from the image. Consequently, the field around the specimen (i.e., where there is no specimen to scatter the beam) is generally dark.In optical microscopes a darkfield condenser lens must be used, which directs a cone of light away from the objective lens. To maximize the scattered light-gathering power of the objective lens, oil immersion is used and the numerical aperture (NA) of the objective lens must be less than 1.0. Objective lenses with a higher NA can be used but only if they have an adjustable diaphragm, which reduces the NA. Often these objective lenses have a NA that is variable from 0.7 to 1.25.Nikon: Darkfield Illumination

Light microscopy applications

In optical microscopy, dark-field describes an illumination technique used to enhance the contrast in unstained samples. It works by illuminating the sample with light that will not be collected by the objective lens and thus will not form part of the image. This produces the classic appearance of a dark, almost black, background with bright objects on it.

The light’s path

The steps are illustrated in the figure where an inverted microscope is used.(File:Dark Field Microscope.png|thumb|Diagram illustrating the light path through a dark-field microscope)

1. Light enters the microscope for illumination of the sample.
2. A specially sized disc, the patch stop (see figure), blocks some light from the light source, leaving an outer ring of illumination. A wide phase annulus can also be reasonably substituted at low magnification.
3. The condenser lens focuses the light towards the sample.
4. The light enters the sample. Most is directly transmitted, while some is scattered from the sample.
5. The scattered light enters the objective lens, while the directly transmitted light simply misses the lens and is not collected due to a direct-illumination block (see figure).
6. Only the scattered light goes on to produce the image, while the directly transmitted light is omitted.

Advantages and disadvantages

Dark-field microscopy is a very simple yet effective technique and well suited for uses involving live and unstained biological samples, such as a smear from a tissue culture or individual, water-borne, single-celled organisms. Considering the simplicity of the setup, the quality of images obtained from this technique is impressive.One limitation of dark-field microscopy is the low light levels seen in the final image. This means that the sample must be very strongly illuminated, which can cause damage to the sample. Dark-field microscopy techniques are almost entirely free of halo or relief-style artifacts typical of DIC and phase-contrast imaging. This comes at the expense of sensitivity to phase information. The interpretation of dark-field images must be done with great care, as common dark features of bright-field microscopy images may be invisible, and vice versa. In general the dark-field image lacks the low spatial frequencies associated with the bright-field image, making the image a high-passed version of the underlying structure. While the dark-field image may first appear to be a negative of the bright-field image, different effects are visible in each. In bright-field microscopy, features are visible where either a shadow is cast on the surface by the incident light or a part of the surface is less reflective, possibly by the presence of pits or scratches. Raised features that are too smooth to cast shadows will not appear in bright-field images, but the light that reflects off the sides of the feature will be visible in the dark-field images.Image:Paper_Micrograph_Dark.png|Dark-field illumination, sample contrast comes from light scattered by the sampleImage:Paper_Micrograph_Bright.png|Bright-field illumination, sample contrast comes from attenuation of light in the sampleImage:Paper_Micrograph_Cross-Polarised.png|Cross-polarized light illumination, sample contrast comes from rotation of polarized light through the sampleImage:Paper_Micrograph_Phase.png|Phase-contrast illumination, sample contrast comes from interference of different path lengths of light through the sample

Use in computing

Dark-field microscopy has recently been applied in computer mouse pointing devices to allow the mouse to work on transparent glass by imaging microscopic flaws and dust on the glass’s surface.

Dark-field microscopy combined with hyperspectral imaging

When coupled to hyperspectral imaging, dark-field microscopy becomes a powerful tool for the characterization of nanomaterials embedded in cells. In a recent publication, Patskovsky et al. used this technique to study the attachment of gold nanoparticles (AuNPs) targeting CD44+ cancer cells.JOURNAL, S. Patskovsky, Wide-field hyperspectral 3D imaging of functionalized gold nanoparticles targeting cancer cells by reflected light microscopy, Journal of Biophotonics, 8, 5, 1–7, 2014, 10.1002/jbio.201400025, 24961507, etal,

Transmission electron microscope applications

File:NuclearTrackPaper02chromiteA.jpg|right|thumb|300px|Weak-beam DF of strain around nuclear track cores ]]Dark-field studies in transmission electron microscopy play a powerful role in the study of crystals and crystal defects, as well as in the imaging of individual atoms.

Conventional dark-field imaging

Briefly, imagingP. Hirsch, A. Howie, R. Nicholson, D. W. Pashley and M. J. Whelan (1965/1977) Electron microscopy of thin crystals (Butterworths/Krieger, London/Malabar FL) {{ISBN|0-88275-376-2}}. involves tilting the incident illumination until a diffracted, rather than the incident, beam passes through a small objective aperture in the objective lens back focal plane. Dark-field images, under these conditions, allow one to map the diffracted intensity coming from a single collection of diffracting planes as a function of projected position on the specimen and as a function of specimen tilt.In single-crystal specimens, single-reflection dark-field images of a specimen tilted just off the (Bragg condition]] allow one to “light up” only those lattice defects, like dislocations or precipitates, that bend a single set of lattice planes in their neighborhood. Analysis of intensities in such images may then be used to estimate the amount of that bending. In polycrystalline specimens, on the other hand, dark-field images serve to light up only that subset of crystals that are Bragg-reflecting at a given orientation.{| class=“toccolours collapsible collapsed” width=“60%” style="text-align:left“!Animation: dark-field imaging of crystals

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center|Digital dark-field simulation of 2 nm metal particles on a nano-cylinder) This animation illustrates movement of an aperture (centered in the orange figure at left) over the power spectrum (a digital substitute for the back focal-plane’s optical diffraction pattern) shown with the DC peak (or unscattered beam) below center. Only nanocrystals with projected periodicities that diffract into the aperture light up in the dark-field image at right. The aperture is moving by 1.25° increments around the ring associated with diffraction from gold 2.3 Ã… (111) lattice spacings.

Weak-beam imaging

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