Dark field microscopy

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Dark field microscopy (dark ground microscopy) describes microscopy methods, in both light and electron microscopy, which exclude the unscattered beam from the image. As a result, the field around the specimen (i.e. where there is no specimen to scatter the beam) is generally dark.

Contents 1 Light Microscopy Applications 1.1 The light's path 1.2 Advantages and disadvantages 2 Transmission Electron Microscope Applications 2.1 Conventional darkfield imaging 2.2 Weak beam imaging 2.3 Low and high angle annular darkfield imaging 3 See Also 4 External links and references 5 Footnotes

[edit] Light Microscopy Applications

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

[edit] The light's path

The steps are illustrated in the figure where an upright microscope is used.

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.
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.

this is the only common factor

[edit] 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.

The main limitation of dark field microscopy is the low light levels seen in the final image. This means the sample must be very strongly illuminated, which can cause damage to the sample.

Dark field microscopy techniques are almost entirely free of artifacts, due to the nature of the process. However 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.

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.

[edit] Transmission Electron Microscope Applications

Main article: Transmission Electron Microscope

Darkfield 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.

[edit] Conventional darkfield imaging

Briefly, conventional darkfield imaging^[1] 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. Darkfield 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 darkfield images of a specimen tilted just off the Bragg condition allow one to "light up" only those lattice defects, like dislocations or preciptates, which 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, darkfield images serve to light up only that subset of crystals which is Bragg reflecting at a given orientation.

Animation: darkfield imaging of crystals

Digital darkfield simulation of 2nm 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 nanocystals with projected periodicities that diffract into the aperture light up in the darkfield image at right. The aperture is moving by 1.25 degree increments around the ring associated with diffraction from gold 2.3 Ångstrom (111) lattice spacings.

[edit] Weak beam imaging

Weak beam imaging involves optics similar to conventional darkfield, but use of a diffracted beam harmonic rather than the diffracted beam itself. Much higher resolution of strained regions around defects can be obtained in this way.

[edit] Low and high angle annular darkfield imaging

Annular darkfield imaging requires one to form images with electrons diffracted into an annular aperture centered on, but not including, the unscattered beam. For large scattering angles in a scanning transmission electron microscope, this is sometimes called Z-contrast imaging because of the enhanced scattering from high atomic number atoms.

[edit] See Also

• Annular dark-field imaging
• Wavelets

[edit] External links and references

• http://www.darkfieldtraining.com
• http://www.microscopyu.com/articles/stereomicroscopy/stereodarkfield.html
• Live blood photos under a Darkfield Microscope
• Molecular Expressions:
• Darkfield Illumination Primer

[edit] Footnotes

v • d • e Optical microscopy illumination techniques Bright field – Dark field – Differential interference contrast – Fluorescence – Phase contrast