krit.club logo

Microscope and Microscopy - A Quick historical Journey of Microscopes-advanced

Grade 9CBSE

Review the key concepts, formulae, and examples before starting your quiz.

🔑Concepts

•

The journey of microscopy began in the late 16th century (circa 15901590) with Zacharias Janssen and his father Hans, who created the first compound microscope using two convex lenses.

•

Robert Hooke (16651665) used a primitive compound microscope to observe thin slices of cork and coined the term 'cell'. His observations were published in the famous book 'Micrographia'.

•

Antonie van Leeuwenhoek (1670s1670s) developed high-quality single-lens (simple) microscopes with magnifications up to 270×270\times. He was the first to observe living cells, which he called 'animalcules', including bacteria and protozoa.

•

Magnification (MM) is the process of enlarging the apparent size of an object. Total magnification in a compound microscope is the product of the magnification of the objective lens and the ocular (eyepiece) lens.

•

Resolving Power is the ability of an optical instrument to distinguish two closely placed objects as separate entities. It is inversely proportional to the limit of resolution (dd).

•

Ernst Abbe (18731873) formulated the physical laws governing image formation, introducing the concept of Numerical Aperture (NANA). He proved that resolution is limited by the wavelength of light (λ\lambda).

•

The Electron Microscope was co-invented by Ernst Ruska and Max Knoll in 19311931. It uses a beam of electrons instead of light. Since the wavelength of electrons is significantly smaller than that of visible light, it achieves much higher resolution (up to 0.1 nm0.1\ nm).

•

Modern microscopy includes specialized techniques like Phase-Contrast Microscopy (to see living, unstained cells), Scanning Electron Microscopy (SEM) for 3D surface imaging, and Transmission Electron Microscopy (TEM) for internal cell structure.

📐Formulae

Mtotal=Mobjective×MeyepieceM_{total} = M_{objective} \times M_{eyepiece}

NA=nsin⁡θNA = n \sin \theta

d=0.61λNAd = \frac{0.61 \lambda}{NA}

Resolving Power=1d=nsin⁡θ0.61λResolving\ Power = \frac{1}{d} = \frac{n \sin \theta}{0.61 \lambda}

💡Examples

Problem 1:

A student uses a compound microscope with an eyepiece marked 15×15\times and an objective lens marked 45×45\times. Calculate the total magnification of the specimen being observed.

Solution:

Given: Magnification of eyepiece (MeM_e) = 15×15\times Magnification of objective (MoM_o) = 45×45\times Using the formula: Mtotal=Me×MoM_{total} = M_e \times M_o Mtotal=15×45=675M_{total} = 15 \times 45 = 675 The total magnification is 675×675\times.

Explanation:

In a compound microscope, the image formed by the objective lens acts as the object for the eyepiece lens, resulting in a multiplicative effect on the final magnification.

Problem 2:

Why does an electron microscope have a higher resolving power than a light microscope? Use the concept of wavelength (λ\lambda).

Solution:

The limit of resolution (dd) is given by d=0.61λNAd = \frac{0.61 \lambda}{NA}.

  1. For visible light, λ\lambda ranges from 400 nm400\ nm to 700 nm700\ nm.
  2. For an electron beam, the de Broglie wavelength can be as small as 0.005 nm0.005\ nm. Since d∝λd \propto \lambda, a smaller wavelength results in a smaller dd (better resolution).

Explanation:

Because the wavelength of electrons is thousands of times smaller than that of visible light, the electron microscope can distinguish features that are much closer together, which would appear as a single blur under a light microscope.