The minimum resolvable separation distance of a light microscope depends on the wavelength of illumination and the numerical aperature. Because the electron beam has a far smaller wavelength than light used in light microscopy, it achieves far better resolution and it doesn't even involve the NE.
Coupling efficiency = NA2 such that if you have an initial power output P0 you get P=P0*NA2
It depends on poo
The ability to distinguish close objects is called resolution or resolving power.It is important in microscopy as well as in other fields involving optical instruments, such as photography.A light microscope, using a high-power objective with oil immersion, can achieve a resolution of about 0.2 μm (micrometers). An electron microscope has, in practice, a resolving power about 100 times that, namely 1 to 2 nm (nanometers).
mas density
As power = work done/time, power depends upon magnitude of w.d. and time required.
You also need to know the wavelength :)
In a light microscope when magnifiaction increases resolution decreases and the object will apear blurred. It can be removed by putting immersion oil on slides or object which increase the refractive index and cause to increase the numerical aperture which ultimately cause the better resolution as resolution power depends on numerical aperture of lens. The immersion oil used can be cedar oil.
Use the Equation, Resolving Power=lambda/2(Numerical Aperture). So, given the values for Numerical Aperture(NA): If NA=0, then R=0, NA=0.2, then R=1500, NA=0.4, then R=750, etc. Simply solve the equation substituting the provided Numerical Aperture (NA) values in.
By using immersion oil
In a light microscope the resolution of the image it can project is limited by the distance each photon travels in its wavelength. Beneath this minimum distance, the "noise" of the photon's movement along its path overwhelms any resolution the light source may otherwise provide.
To find resolution power of optical microscopes.
Coupling efficiency = NA2 such that if you have an initial power output P0 you get P=P0*NA2
Resolving power = 0.5x wavelength/ numerical aperture (n sin theta)n sin theta in most microscope have value = 1.2 and 1.4therefore:R. P. = 0.5x500nm/ 1.25 = 200nm = 0.2 microns.(conv. 1000nm = 1micron).
The "resolving power" of a telescope is a measure of the ability of a telescope to distinguish between two separate objects that appear to be very close together in the sky.
The limit of resolving power of a microscope is described by the Abbe criterion: d=wl/NA d being the minimal resolvable distance between two spots of the object wl being the wavelength of the light used NA being the numerical aperture of the microscope, which is equal to n*sin(a) with n being the refraction index of the immersion liquid between object and objective a being the aperture angle because sin(a) is always smaller than 1 and n cannot rise above 1.7, the maximal resolving power of a microscope is about d=wl/2 and thus only depends on the wavelength of the light used, which normally will be about 600 nm.
The question is about the resolving power of optical instruments like telescope and microscope.It is the ability of the instrument to resolve the images of two points that are close to each other. If dθ is the angular separation, resolving power is given by the formulaR = 1/dθ = D/1.22 λ where Dis the aperture of the objective; λ is the wavelength of the light .
346.7nm's