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History of The Light Microscope

The document provides a brief history of the development of the light microscope from its invention in the late 16th century through improvements in the 19th century. It describes key early microscopists including Jansen, Leeuwenhoek, and Hooke and their contributions. It also summarizes the development of tissue preparation techniques to make cellular structures visible under the microscope.

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Lorena Cionelo
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0% found this document useful (0 votes)
143 views6 pages

History of The Light Microscope

The document provides a brief history of the development of the light microscope from its invention in the late 16th century through improvements in the 19th century. It describes key early microscopists including Jansen, Leeuwenhoek, and Hooke and their contributions. It also summarizes the development of tissue preparation techniques to make cellular structures visible under the microscope.

Uploaded by

Lorena Cionelo
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd
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History of the Light Microscope Light microscopes date at least to 1595, when Zacharias Jansen (15801638) of Holland invented

a compound light microscope, one that used two lenses, with the second lens further magnifying the image produced by the first. His microscopes were collapsing tubes used like a telescope in reverse, and produced magnifications up to nine times (9x). Antony van Leeuwenhoek (16321723) invented a simple (one-lens) microscope around 1670 that magnified up to 200x and achieved twice the resolution of the best compound microscopes of his day, mainly because he crafted better lenses. While others were making lenses by such methods as squashing molten glass between pieces of wood, Leeuwenhoek made them by carefully grinding and polishing solid glass. He thus became the first to see individual cells, including bacteria, protozoans, muscle cells, and sperm. Englishman Robert Hooke (16351703) further refined the compound microscope, adding such features as a stage to hold the specimen, an illuminator, and coarse and fine focus controls. Until 1800, compound microscopes designed by Hooke and others were limited to magnifications of 30x to 50x, and their images exhibited blurry edges (spherical aberration) and rainbowlike distortions (chromatic aberration). The most significant improvement in microscope optics was achieved in the nineteenth century, when business partners Carl Zeiss (18161888) and Ernst Abbe (18401905) added the substage condenser and developed superior lenses that greatly reduced chromatic and spherical aberration, while permitting vastly improved resolution and higher magnification. Tissue Preparation The advancement of light microscopy also required methods for preserving plant and animal tissues and making their cellular details more visible, methods collectively called histotechnique (from histo, meaning "tissue"). In brief, classical histotechnique involves preserving a specimen in a fixative, such as formalin, to prevent decay; embedding it in a block of paraffin and slicing it very thinly with an instrument called a microtome; removing the paraffin with a solvent; and then staining the tissue, usually with two or more dyes. The slices of tissue, called histological sections, are typically thinner than a single cell. The colors of a prepared tissue are not natural colors, but they make the tissue's structural details more visible. A widely used stain combination called hematoxylin and eosin, for example, typically colors cell nuclei violet and the cytoplasm pink. Other methods of histotechnique have been developed for special purposes. One variation is to embed the tissue in special plastics (resins),

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