Microscopy


Microscopy

Microscopy is the technical field of using microscopes to view samples and objects that cannot be seen with the unaided eye (objects that are not within the resolution range of the normal eye). There are three well-known branches of microscopy, optical, electron, and scanning probe microscopy.

Optical and electron microscopy involve the diffraction, reflection, or refraction of electromagnetic radiation/electron beams interacting with the specimen, and the subsequent collection of this scattered radiation or another signal in order to create an image. This process may be carried out by wide-field irradiation of the sample (for example standard light microscopy and transmission electron microscopy) or by scanning of a fine beam over the sample (for example confocal laser scanning microscopy and scanning electron microscopy). Scanning probe microscopy involves the interaction of a scanning probe with the surface of the object of interest. The development of microscopy revolutionized biology and remains an essential technique in the life and physical sciences.

Contents

Optical microscopy

Stereo microscope

Optical or light microscopy involves passing visible light transmitted through or reflected from the sample through a single or multiple lenses to allow a magnified view of the sample.[1] The resulting image can be detected directly by the eye, imaged on a photographic plate or captured digitally. The single lens with its attachments, or the system of lenses and imaging equipment, along with the appropriate lighting equipment, sample stage and support, makes up the basic light microscope. The most recent development is the digital microscope, which uses a CCD camera to focus on the exhibit of interest. The image is shown on a computer screen, so eye-pieces are unnecessary.

Limitations

Limitations of standard optical microscopy (bright field microscopy) lie in three areas;

  • The technique can only image dark or strongly refracting objects effectively.
  • Diffraction limits resolution to approximately 0.2 micrometres (see: microscope).
  • Out of focus light from points outside the focal plane reduces image clarity.

Live cells in particular generally lack sufficient contrast to be studied successfully, internal structures of the cell are colourless and transparent. The most common way to increase contrast is to stain the different structures with selective dyes, but this involves killing and fixing the sample. Staining may also introduce artifacts, apparent structural details that are caused by the processing of the specimen and are thus not a legitimate feature of the specimen.

These limitations have all been overcome to some extent by specific microscopy techniques that can non-invasively increase the contrast of the image. In general, these techniques make use of differences in the refractive index of cell structures. It is comparable to looking through a glass window: you (bright field microscopy) don't see the glass but merely the dirt on the glass. There is however a difference as glass is a denser material, and this creates a difference in phase of the light passing through. The human eye is not sensitive to this difference in phase but clever optical solutions have been thought out to change this difference in phase into a difference in amplitude (light intensity).

Techniques

In order to improve specimen contrast or highlight certain structures in a sample special techniques must be used. A huge selection of microscopy techniques are available to increase contrast or label a sample.

Bright field

Bright field microscopy is the simplest of all the light microscopy techniques. Sample illumination is via transmitted white light, i.e. illuminated from below and observed from above. Limitations include low contrast of most biological samples and low apparent resolution due to the blur of out of focus material. The simplicity of the technique and the minimal sample preparation required are significant advantages.

Oblique illumination

The use of oblique (from the side) illumination gives the image a 3-dimensional appearance and can highlight otherwise invisible features. A more recent technique based on this method is Hoffmann's modulation contrast, a system found on inverted microscopes for use in cell culture. Oblique illumination suffers from the same limitations as bright field microscopy (low contrast of many biological samples; low apparent resolution due to out of focus objects), but may highlight otherwise invisible structures.

Dark field

Dark field microscopy is a technique for improving the contrast of unstained, transparent specimens.[2] Dark field illumination uses a carefully aligned light source to minimize the quantity of directly-transmitted (unscattered) light entering the image plane, collecting only the light scattered by the sample. Darkfield can dramatically improve image contrast—especially of transparent objects – while requiring little equipment setup or sample preparation. However, the technique does suffer from low light intensity in final image of many biological samples, and continues to be affected by low apparent resolution.

Rheinberg illumination is a special variant of dark field illumination in which transparent, colored filters are inserted just before the condenser so that light rays at high aperture are differently colored than those at low aperture (i.e. the background to the specimen may be blue while the object appears self-luminous yellow). Other color combinations are possible but their effectiveness is quite variable.[3]

Dispersion staining

Dispersion staining is an optical technique that results in a colored image of a colorless object. This is an optical staining technique and requires no stains or dyes to produce a color effect. There are five different microscope configurations used in the broader technique of dispersion staining. They include brightfield Becke` line, oblique, darkfield, phase contrast, and objective stop dispersion staining.

Phase contrast

Phase-contrast image of uncalcified matrix (top) and calcified matrix (bottom).
In electron microscopy: Phase-contrast imaging

More sophisticated techniques will show proportional differences in optical density . Phase contrast is a widely used technique that shows differences in refractive index as difference in contrast. It was developed by the Dutch physicist Frits Zernike in the 1930s (for which he was awarded the Nobel Prize in 1953). The nucleus in a cell for example will show up darkly against the surrounding cytoplasm. Contrast is excellent; however it is not for use with thick objects. Frequently, a halo is formed even around small objects, which obscures detail. The system consists of a circular annulus in the condenser, which produces a cone of light. This cone is superimposed on a similar sized ring within the phase-objective. Every objective has a different size ring, so for every objective another condenser setting has to be chosen. The ring in the objective has special optical properties: it first of all reduces the direct light in intensity, but more importantly, it creates an artificial phase difference of about a quarter wavelength. As the physical properties of this direct light have changed, interference with the diffracted light occurs, resulting in the phase contrast image.

one disadvantge of phasecontrast microscopy is halo formation ( halo-light ring)

Differential interference contrast

Superior and much more expensive is the use of interference contrast. Differences in optical density will show up as differences in relief. A nucleus within a cell will actually show up as a globule in the most often used differential interference contrast system according to Georges Nomarski. However, it has to be kept in mind that this is an optical effect, and the relief does not necessarily resemble the true shape. Contrast is very good and the condenser aperture can be used fully open, thereby reducing the depth of field and maximizing resolution.

The system consists of a special prism (Nomarski prism, Wollaston prism) in the condenser that splits light in an ordinary and an extraordinary beam. The spatial difference between the two beams is minimal (less than the maximum resolution of the objective). After passage through the specimen, the beams are reunited by a similar prism in the objective.

In a homogeneous specimen, there is no difference between the two beams, and no contrast is being generated. However, near a refractive boundary (say a nucleus within the cytoplasm), the difference between the ordinary and the extraordinary beam will generate a relief in the image. Differential interference contrast requires a polarized light source to function; two polarizing filters have to be fitted in the light path, one below the condenser (the polarizer), and the other above the objective (the analyzer).

Note: In cases where the optical design of a microscope produces an appreciable lateral separation of the two beams we have the case of classical interference microscopy, which does not result in relief images, but can nevertheless be used for the quantitative determination of mass-thicknesses of microscopic objects.

Interference reflection microscopy

An additional technique using interference is interference reflection microscopy (also known as reflected interference contrast, or RIC). It is used to examine the adhesion of cells to a glass surface, using polarized light of a narrow range of wavelengths to be reflected whenever there is an interface between two substances with different refractive indices. Whenever a cell is attached to the glass surface, reflected light from the glass and from the attached cell will interfere, while if there is no cell attached to the glass, there will be no interference.

Interference reflection microscopy can be obtained by using the same elements used by DIC, but without the prisms. Also, the light that is being detected is reflected and not transmitted as it is when DIC is employed.

Fluorescence

When certain compounds are illuminated with high energy light, they then emit light of a different, lower frequency. This effect is known as fluorescence. Often specimens show their own characteristic autofluorescence image, based on their chemical makeup.

This method is of critical importance in the modern life sciences, as it can be extremely sensitive, allowing the detection of single molecules. Many different fluorescent dyes can be used to stain different structures or chemical compounds. One particularly powerful method is the combination of antibodies coupled to a fluorophore as in immunostaining. Examples of commonly used fluorophores are fluorescein or rhodamine. The antibodies can be made tailored specifically for a chemical compound. For example, one strategy often in use is the artificial production of proteins, based on the genetic code (DNA). These proteins can then be used to immunize rabbits, which then form antibodies which bind to the protein. The antibodies are then coupled chemically to a fluorophore and then used to trace the proteins in the cells under study.

Highly-efficient fluorescent proteins such as the green fluorescent protein (GFP) have been developed using the molecular biology technique of gene fusion, a process that links the expression of the fluorescent compound to that of the target protein. This combined fluorescent protein is, in general, non-toxic to the organism and rarely interferes with the function of the protein under study. Genetically modified cells or organisms directly express the fluorescently-tagged proteins, which enables the study of the function of the original protein in vivo.

Growth of protein crystals results in both protein and salt crystals. Both are colorless and microscopic. Recovery of the protein crystals requires imaging which can be done by the intrinsic fluorescence of the protein or by using transmission microscopy. Both methods require a ultraviolet microscope as protein absorbs light at 280 nm. Protein will also fluorescence at approximately 353 nm when excited with 280 nm light.[4]

Since fluorescence emission differs in wavelength (color) from the excitation light, an ideal fluorescent image shows only the structure of interest that was labeled with the fluorescent dye. This high specificity led to the widespread use of fluorescence light microscopy in biomedical research. Different fluorescent dyes can be used to stain different biological structures, which can then be detected simultaneously, while still being specific due to the individual color of the dye.

To block the excitation light from reaching the observer or the detector, filter sets of high quality are needed. These typically consist of an excitation filter selecting the range of excitation wavelengths, a dichroic mirror, and an emission filter blocking the excitation light. Most fluorescence microscopes are operated in the Epi-illumination mode (illumination and detection from one side of the sample) to further decrease the amount of excitation light entering the detector.

See also total internal reflection fluorescence microscope.

Confocal

Using a scanning point of light instead of full sample illumination confocal microscopy gives slightly higher resolution, and significant improvements in optical sectioning . Confocal microscopy is, therefore, commonly used where 3D structure is important.

Single plane illumination microscopy and Light sheet florescence microscopy

Using a plane of light formed by focusing light through a cylindrical lens at a narrow angle or by scanning a line of light in a plane perpendicular to the axis of objective, high resolution optical sections can be taken.[5] Single plane illumination is also accomplished using beam shaping techniques incorporating multiple-prism beam expanders.[6] The images are captured by CCDs. These variants allow very fast and high signal to noise ratio image capture.

Deconvolution

Fluorescence microscopy is extremely powerful due to its ability to show specifically labeled structures within a complex environment and also because of its inherent ability to provide three-dimensional information of biological structures. However, this information is blurred by the fact that, upon illumination, all fluorescently labeled structures emit light no matter whether they are in focus or not. This means that an image of a certain structure is always blurred by the contribution of light from structures that are out of focus. This phenomenon becomes apparent as a loss of contrast especially when using objectives with a high resolving power, typically oil immersion objectives with a high numerical aperture.

However, this phenomenon is not caused by random processes such as light scattering but can be relatively well defined by the optical properties of the image formation in the microscope imaging system. If one considers a small fluorescent light source (essentially a bright spot), light coming from this spot spreads out the further out of focus one is. Under ideal conditions, this produces a sort of "hourglass" shape of this point source in the third (axial) dimension. This shape is called the point spread function (PSF) of the microscope imaging system. Since any fluorescence image is made up of a large number of such small fluorescent light sources, the image is said to be "convolved by the point spread function".

Knowing this point spread function[7] means that it is possible to reverse this process to a certain extent by computer-based methods commonly known as deconvolution microscopy.[8] There are various algorithms available for 2D or 3D deconvolution. They can be roughly classified in nonrestorative and restorative methods. While the nonrestorative methods can improve contrast by removing out-of-focus light from focal planes, only the restorative methods can actually reassign light to its proper place of origin. This can be an advantage over other types of 3D microscopy such as confocal microscopy, because light is not thrown away but reused. For 3D deconvolution, one typically provides a series of images derived from different focal planes (called a Z-stack) plus the knowledge of the PSF, which can be derived either experimentally or theoretically from knowing all contributing parameters of the microscope.

Sub-diffraction techniques

A multitude of super-resolution microscopy techniques has been developed in recent times which circumvent the diffraction barrier. This is mostly achieved by imaging a sufficiently static sample multiple times and either modifying the excitation light or observing stochastical changes in the image. Knowledge of and chemical control over fluorophore photophysics is at the core of these techniques, by which resolutions of ~20 nanometers are regularly obtained.[9]

Serial time-encoded amplified microscopy (STEAM)

Serial time encoded amplified microscopy (STEAM) is an imaging method that provides ultrafast shutter speed and frame rate, by using optical image amplification to circumvent the fundamental trade-off between sensitivity and speed, and a single-pixel photodetector to eliminate the need for a detector array and readout time limitations [10] The method is at least 1000 times faster than the state-of-the-art CCD and CMOS cameras. Consequently, it is potentially useful for a broad range of scientific, industrial, and biomedical applications that require high image acquisition rates, including real-time diagnosis and evaluation of shockwaves, microfluidics, MEMS, and laser surgery.[citation needed]

Extensions

Most modern instruments provide simple solutions for micro-photography and image recording electronically. However such capabilities are not always present and the more experienced microscopist will, in many cases, still prefer a hand drawn image rather than a photograph. This is because a microscopist with knowledge of the subject can accurately convert a three dimensional image into a precise two dimensional drawing . In a photograph or other image capture system however, only one thin plane is ever in good focus.

The creation of careful and accurate micrographs requires a microscopical technique using a monocular eyepiece. It is essential that both eyes are open and that the eye that is not observing down the microscope is instead concentrated on a sheet of paper on the bench besides the microscope. With practice, and without moving the head or eyes, it is possible to accurately record the observed details by tracing round the observed shapes by simultaneously "seeing" the pencil point in the microscopical image.

Practicing this technique also establishes good general microscopical technique. It is always less tiring to observe with the microscope focused so that the image is seen at infinity and with both eyes open at all times.

Other enhancements

Microspectroscopy:spectroscopy with a microscope

X-ray

As resolution depends on the wavelength of the light. Electron microscopy has been developed since the 1930s that use electron beams instead of light. Because of the much smaller wavelength of the electron beam, resolution is far higher.

Though less common, X-ray microscopy has also been developed since the late 1940s. The resolution of X-ray microscopy lies between that of light microscopy and electron microscopy.

Electron microscopy

Until the invention of sub-diffraction microscopy, the wavelength of the light limited the resolution of traditional microscopy to around 0.2 micrometers. In order to gain higher resolution, the use of an electron beam with a far smaller wavelength is used in electron microscopes.

  • Transmission electron microscopy (TEM) is quite similar to the compound light microscope, by sending an electron beam through a very thin slice of the specimen. The resolution limit in 2005 was around 0.05 nanometer and has not increased appreciably since that time.
  • Scanning electron microscopy (SEM) visualizes details on the surfaces of cells and particles and gives a very nice 3D view. It gives results much like those of the stereo light microscope, and, akin to that, its most useful magnification is in the lower range than that of the transmission electron microscope.

Scanning probe microscopy

This is a sub-diffraction technique. Examples of scanning probe microscopes are the atomic force microscope (AFM), the Scanning tunneling microscope and the photonic force microscope. All such methods imply a solid probe tip in the vicinity (near field) of an object, which is supposed to be almost flat.

Ultrasonic force

Ultrasonic Force Microscopy (UFM) has been developed in order to improve the details and image contrast on "flat" areas of interest where the AFM images are limited in contrast. The combination of AFM-UFM allows a near field acoustic microscopic image to be generated. The AFM tip is used to detect the ultrasonic waves and overcomes the limitation of wavelength that occurs in acoustic microscopy. By using the elastic changes under the AFM tip, an image of much greater detail than the AFM topography can be generated.

Ultrasonic force microscopy allows the local mapping of elasticity in atomic force microscopy by the application of ultrasonic vibration to the cantilever or sample. In an attempt to analyze the results of ultrasonic force microscopy in a quantitative fashion, a force-distance curve measurement is done with ultrasonic vibration applied to the cantilever base, and the results are compared with a model of the cantilever dynamics and tip-sample interaction based on the finite-difference technique.

Ultraviolet microscopy

Ultraviolet microscopes have two main purposes. The first is to utilize the shorter wavelength of ultraviolet electromagnetic energy in order to improve the image resolution beyond that of the diffraction limit of standard optical microscopes. This technique is used for non-destructive inspection of devices with very small features such as those found in modern semiconductors. The second application for UV microscopes is contrast enhancement where the response of individual samples is enhanced, relative to their surrounding, due to the interaction of light with the molecules within the sample itself. One example is in the growth of protein crystals. Protein crystals are formed in salt solutions. As both salt and protein crystals are both formed in the growth process, and both are commonly transparent to the human eye, they cannot be differentiated with a standard optical microscope. As the tryptophan of protein absorbs light at 280 nm, whereas salt does not, imaging with a UV microscope with 280 nm bandpass filters makes it simple to differentiate between the two types of crystals as the protein crystals appear dark while the salt crystals are transparent.

Infrared microscopy

The term infrared microscope covers two main types of diffraction-limited microscopy. The first provides optical visualization plus IR spectroscopic data collection. The second (more recent and more advanced) technique employs focal plane array detection for infrared chemical imaging, where the image contrast is determined by the response of individual sample regions to particular IR wavelengths selected by the user.

IR versions of sub-diffraction microscopy (see above) exist also. These include IR NSOM [11] and photothermal microspectroscopy.

Digital holographic microscopy

Human cells imaged by DHM phase shift (left) and phase contrast microscopy (right).

In digital holographic microscopy (DHM), interfering wave fronts from a coherent (monochromatic) light-source are recorded on a sensor. The image is digitally reconstructed by a computer from the recorded hologram. Besides the ordinary bright field image, a phase shift image is created as well.

DHM can operate both in reflection and transmission mode. In reflection mode, the phase shift image provides a relative distance measurement and thus represents a topography map of the reflecting surface. In transmission mode, the phase shift image provides a label-free quantitative measurement of the optical thickness of the specimen. Phase shift images of biological cells are very similar to images of stained cells and have successfully been analyzed by high content analysis software.

A unique feature of DHM is the ability to adjust focus after the image is recorded, since all focus planes are recorded simultaneously by the hologram. This feature makes it possible to image moving particles in a volume or to rapidly scan a surface. Another attractive feature is DHM’s ability to use low cost optics by correcting optical aberrations by software.

Digital Pathology (virtual microscopy)

Digital Pathology is an image-based information environment enabled by computer technology that allows for the management of information generated from a digital slide. Digital pathology is enabled in part by virtual microscopy, which is the practice of converting glass slides into digital slides that can be viewed, managed, and analyzed.

Laser microscopy

Laser microscopy is a rapidly growing field that uses laser illumination sources in various forms of microscopy. For instance, laser microscopy focused on biological applications uses ultrashort pulse lasers, or femtosecond lasers, in a number of techniques labeled as nonlinear microscopy, saturation microscopy, and multiphoton fluorescence microscopy.[12]

Amateur microscopy

Amateur Microscopy is the investigation and observation of biological and non-biological specimens for recreational purposes. Collectors of minerals, insects, seashells, and plants may use microscopes as tools to uncover features that help them classify their collected items. Other amateurs may be interested in observing the life found in pond water and of other samples. Microscopes may also prove useful for the water quality assessment for people that keep a home aquarium. Photographic documentation and drawing of the microscopic images are additional tasks that augment the spectrum of tasks of the amateur. There are even competitions for photomicrograph art. Participants of this pastime either may use commercially prepared microscopic slides or may engage in the task of specimen preparation.

While microscopy is a central tool in the documentation of biological specimens, it is, in general, insufficient to justify the description of a new species based on microscopic investigations alone. Often genetic and biochemical tests are necessary to confirm the discovery of a new species. A laboratory and access to academic literature is a necessity, which is specialized and, in general, not available to amateurs. There is, however, one huge advantage that amateurs have above professionals: time to explore their surroundings. Often, advanced amateurs team up with professionals to validate their findings and (possibly) describe new species.

In the late 1800s, amateur microscopy became a popular hobby in the United States and Europe. Several 'professional amateurs' were being paid for their sampling trips and microscopic explorations by philanthropists, to keep them amused on the Sunday afternoon (e.g., the diatom specialist A. Grunow, being paid by (among others) a Belgian industrialist). Professor John Phin published "Practical Hints on the Selection and Use of the Microscope (Second Edition, 1878)," and was also the editor of the “American Journal of Microscopy.”

In 1995, a loose group of amateur microscopists, drawn from several organizations in the UK and US, founded a site for microscopy based on the knowledge and input of amateur (perhaps better referred to as 'enthusiast') microscopists. This was the first attempt to establish 'amateur' microscopy as a serious subject[citation needed]in the then-emerging new media of the Internet. Today, it remains as a powerful established international resource for all ages, to input their findings and share information. It is a nonprofit-making web presence dedicated to the pursuit of science and understanding of the small-scale world: [1]

Examples of amateur microscopy images:

See also

References

  1. ^ Abramowitz M, Davidson MW (2007). "Introduction to Microscopy". Molecular Expressions. http://micro.magnet.fsu.edu/primer/anatomy/introduction.html. Retrieved 2007-08-22. 
  2. ^ Abramowitz M, Davidson MW (2003-08-01). "Darkfield Illumination". http://micro.magnet.fsu.edu/primer/techniques/darkfield.html. Retrieved 2008-10-21. 
  3. ^ Abramowitz M, Davidson MW (2003-08-01). "Rheinberg Illumination". http://micro.magnet.fsu.edu/primer/techniques/rheinberg.html. Retrieved 2008-10-21. 
  4. ^ Gill, Harindarpal (January 2010). "Evaluating the efficacy of tryptophan fluorescence and absorbance as a selection tool for identifying protein crystals". Acta Crystallographica F66: 364–372. 
  5. ^ Greger, K.; J. Swoger, E. H. K. Stelzer (2007). "Basic building units and properties of a fluorescence single plane illumination microscope". Review of Scientific Instruments 78: 023705. doi:10.1063/1.2428277. ISSN 00346748. http://link.aip.org/link/RSINAK/v78/i2/p023705/s1&Agg=doi. Retrieved 2011-10-16. 
  6. ^ Duarte FJ (1993), Electro-optical interferometric microdensitometer system, US Patent 5255069.
  7. ^ Nasse M. J., Woehl J. C. (2010). "Realistic modeling of the illumination point spread function in confocal scanning optical microscopy". J. Opt. Soc. Am. A 27 (2): 295–302. doi:10.1364/JOSAA.27.000295. 
  8. ^ Wallace W, Schaefer LH, Swedlow JR (2001). "A workingperson's guide to deconvolution in light microscopy". BioTechniques 31 (5): 1076–8, 1080, 1082 passim. PMID 11730015. 
  9. ^ van de Linde S., Wolter S.,Sauer S. (2011). "Single-molecule Photoswitching and Localization". Aust. J. Chem. (64): 503­-511. doi:http://dx.doi.org/10.1071/CH10284. 
  10. ^ K. Goda, K. K. Tsia, and B. Jalali (2009). "Serial time-encoded amplified imaging for real-time observation of fast dynamic phenomena". Nature 458 (7242): 1145. Bibcode 2009Natur.458.1145G. doi:10.1038/nature07980. 
  11. ^ H M Pollock and D A Smith, The use of near-field probes for vibrational spectroscopy and photothermal imaging, in Handbook of vibrational spectroscopy, J.M. Chalmers and P.R. Griffiths (eds), John Wiley & Sons Ltd, Vol. 2, pp. 1472 - 1492 (2002)
  12. ^ Thomas JL; Rudolph W (2008). "Biological Microscopy with Ultrashort Laser Pulses". In Duarte FJ. Tunable Laser Applications (2nd ed.). Boca Raton: CRC Press. pp. 245–80. ISBN 1-4200-6009-0. 

Further reading

  • Advanced Light Microscopy vol. 1 Principles and Basic Properties by Maksymilian Pluta, Elsevier (1988)
  • Advanced Light Microscopy vol. 2 Specialised Methods by Maksymilian Pluta, Elsevier (1989)
  • Introduction to Light Microscopy by S. Bradbury, B. Bracegirdle, BIOS Scientific Publishers (1998)
  • Video Microscopy by Shinya Inoue, Plenum Press (1986)
  • [2] 1978: Theoretical basis of super resolution 4Pi microscopy & design of a confocal laser scanning fluorescence microscope
  • Portraits of life, one molecule at a time, a feature article on sub-diffraction microscopy from the March 1, 2007 issue of Analytical Chemistry

External links

General

Techniques

Organizations


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  • Microscopy — Mi*cros co*py, n. The use of the microscope; investigation with the microscope. [1913 Webster] …   The Collaborative International Dictionary of English

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  • microscopy — mikroskopija statusas T sritis fizika atitikmenys: angl. microscopy vok. Mikroskopie, f rus. микроскопия, f pranc. microscopie, f …   Fizikos terminų žodynas

  • microscopy — noun Date: circa 1665 the use of or investigation with a microscope • microscopist noun …   New Collegiate Dictionary

  • microscopy — microscopist /muy kros keuh pist, muy kreuh skoh pist/, n. /muy kros keuh pee, muy kreuh skoh pee/, n. 1. the use of the microscope. 2. microscopic investigation. [1655 65; MICROSCOPE + Y3] * * * …   Universalium


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