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Chapter 3 Observing Microorganisms Through a Microscope

Total questions: 25

Worksheet time: 13mins

Name
Class
Date
1.

What does the term resolution (resolving power) refer to in microscopy?

a)

The ability to magnify an image

b)

Minimum distance between two objects where you can still see them as separate entities

c)

The ability to change the color of an image

d)

The ability to focus light on a specimen

2.

How does wavelength affect the resolving power of a microscope?

a)

Longer wavelengths increase resolution

b)

Shorter wavelengths decrease resolution

c)

Shorter wavelengths increase resolution (higher energy)

d)

Wavelength has no effect on resolution

3.

Which of the following are types of light microscopes?

a)

Electron, Scanning Probe, Atomic Force, Bright-field, Fluorescence

b)

X-ray, Infrared, Bright-field, Confocal, Dark-field

c)

Bright-field, Phase-contrast, Differential Interference Contrast, Dark-field, Fluorescence, Confocal

d)

Bright-field, Transmission Electron, Scanning Electron, Fluorescence, Confocal

4.

What is the most common type of light microscope, which uses two lenses and is known as a compound microscope?

a)

Dark-field microscope

b)

Phase-contrast microscope

c)

Bright-field microscope

d)

Fluorescence microscope

5.

What is the maximum magnification and resolution capability of a bright-field microscope?

a)

1000X magnification; 0.5 µm resolution

b)

2000X magnification; 0.2 µm resolution

c)

1500X magnification; 0.3 µm resolution

d)

2500X magnification; 0.1 µm resolution

6.

What is the primary function of a phase-contrast microscope?

a)

It uses fluorescence to highlight structures in a specimen

b)

It enhances the difference in refractive index of the sample and its surrounding

c)

It uses electron beams to create high-resolution images

d)

It provides a three-dimensional view of the specimen

7.

How does a specimen appear when viewed under a phase-contrast microscope?

a)

Brighter than the surrounding

b)

The same brightness as the surrounding

c)

Darker than the surrounding

d)

Fluorescent against a dark background

8.

What is the key characteristic of a Differential Interference Contrast microscope?

a)

It uses fluorescence to highlight specific structures in a specimen

b)

Passes two beams (split light) through a specimen and then recombine out of phase 

c)

It uses electron beams to produce high-resolution images

d)

It provides a dark background to enhance specimen visibility

9.

How does a specimen appear when viewed under a Differential Interference Contrast microscope?

a)

Fluorescent against a dark background

b)

Darker than its surroundings

c)

Colored with a 3D appearance

d)

Transparent with no visible contrast

10.

How does a Dark-Field Microscope create contrast?

a)

It amplifies differences in refractive index

b)

It passes light through a specimen at an angle so only refracted light enters the objective

c)

It separates light into two beams and recombines them out of phase

d)

 It uses a fluorescent tag to highlight the specimen

11.

What is the function of a fluorescent tag in Fluorescence Microscopy?

a)

It absorbs UV light and becomes transparent

b)

It emits light of a specific wavelength when hit with UV light

c)

It scatters visible light to increase contrast

d)

It creates a three-dimensional colored image

12.

What is a Fluorescence Microscope?

a)

A microscope that uses angled light to create a dark background and bright specimen

b)

A microscope that uses a fluorescent tag and UV light to make specific structures visible

c)

A microscope that separates light into two beams to create a 3D image

d)

A microscope that enhances contrast by amplifying differences in refractive index

13.

What is the primary function of a Confocal Microscope?

a)

To create a dark background while illuminating the specimen

b)

To amplify differences in refractive index for contrast

c)

To scan vertical sections of a specimen and reconstruct a 3D image

d)

To use fluorescent tags to highlight specific structures

14.

How does a Confocal Microscope achieve high-resolution imaging?

a)

By using a special filter to capture specific wavelengths of light

b)

By scanning vertical slices of a specimen with lasers and mirrors

c)

By reflecting light off the specimen at an angle

d)

By amplifying phase differences within the specimen

15.

What role does the computer play in Confocal Microscopy?

a)

It enhances magnification beyond 2000X

b)

It reassembles scanned slices to create a 3D image (CAT scan for cells)

c)

It filters out unwanted light to improve fluorescence visibility

d)

It amplifies the brightness of the specimen against a dark background

16.

Why does Electron Microscopy achieve much greater resolution than Light Microscopy?

a)

It uses a fluorescent tag to highlight structures

b)

Electrons have a much shorter wavelength than visible light

c)

It amplifies differences in refractive index

d)

It separates light into two beams and recombines them out of phase

17.

What is the approximate resolving power of an Electron Microscope?

a)

2 µm

b)

2.5 nm

c)

10 nm

d)

1.5 µm

18.

What is the maximum magnification of an Electron Microscope?

a)

2,000X

b)

10,000X

c)

50,000X

d)

100,000X

19.

How does a Transmission Electron Microscope (TEM) create an image?

a)

By passing electrons through a thin sample onto a fluorescent screen or photographic plate

b)

By scanning the surface of a specimen with electron beams

c)

By using phase shifts to enhance contrast

d)

By separating light into two beams and recombining them out of phase

20.

What is the magnification range of a TEM?

a)

2,000X - 10,000X

b)

10,000X - 100,000X

c)

100X - 1,000X

d)

500,000X - 1,000,000X

21.

What type of image does an SEM produce?

a)

A 1D internal structure image

b)

A 3D surface detail image

c)

A fluorescent-tagged image

d)

A thin-section electron transmission image

22.

Why is a specimen coated with heavy metal in SEM?

a)

To make it fluorescent under UV light

b)

To prevent artifacts from forming

c)

To allow electrons to reflect back for imaging

d)

To allow electrons to pass through the specimen

23.

What is the primary advantage of Scanned-Probe Microscopy?

a)

It can view live specimens at high resolution

b)

It can resolve features 1/100 the size of an atom

c)

It uses fluorescence to highlight specific molecules

d)

It creates 3D images by reflecting electrons off a specimen

24.

How does a Scanning Tunneling Microscope (STM) generate an image?

a)

By passing electrons through a thin sample

b)

By detecting the reflection of electrons from a surface

c)

By scanning across a surface and creating a map

d)

By using fluorescent dyes to label molecules

25.

What is the difference between a Scanning Tunneling Microscope (STM) and an Atomic Force Microscope (AFM)?

a)

STM creates a map, while AFM creates a 3D map

b)

STM uses fluorescence, while AFM uses electron beams

c)

STM only works with biological specimens, while AFM only works with metals

d)

There is no difference; they are the same instrument