1. Module 1

1.30. Page 5

Lesson 5

Module 1—The Nervous System

Rods and Cones Initiate Nerve Impulses

 

A diagram comparing the structure of a cone and a rod. The diagram on the left is a cone. Both types of cells have a similar base composed of synaptic ending, synaptic vesicles, nucleus, and an inner segment. The outer segment of the cone is composed of membranous discs containing the pigment photopsin, but these stacked discs have unequal sizes, and form the shape of a cone, with smaller disks at its upper end. The membranous discs of the rod are all equally sized and contain the pigments photopsin and rhodopsin.

Inquiry into Biology (Whitby, ON: McGraw-Hill Ryerson, 2007), 415, fig. 12.15. Reproduced by permission.

Rods and cones contain pigments called photopsins, which absorb light and start chemical changes. Cones contain three different pigments called iodopsins. Rods have only one type of pigment called rhodopsin. When rhodopsin absorbs light, it is bleached and breaks down into opsin, a colourless protein, and a derivative of Vitamin A called retinal. This chemical change in the rods initiates a nerve impulse in the bipolar cells, which transfers the impulse to the ganglions. The ganglions, which make up the optic nerve, then transmit the impulse to the occipital lobe of the cerebrum to be processed.

 

Your eye then restores opsin and retinal to rhodopsin, but this takes energy. As you will recall from Biology 20, this energy is in the form of ATP. This reverse reaction also requires Vitamin A. Knowing this, can you explain why your eyes get strained in poor lighting, why night blindness is caused by Vitamin A deficiency, and why you should eat your carrots?



iodopsin: the general name of any of the three visual pigments found in cone cells that is stimulated by light to initiate a nerve impulse

 

rhodopsin: a visual pigment found in rod cells that is decomposed by light into opsin and retinal

 

The change from rhodopsin to opsin and retinal initiates a nerve impulse.

 

opsin: a protein that is the result of the decomposition of rhodopsin

 

retinal: a derivative of Vitamin A (retinol) that is the result of the decomposition of rhodopsin and is instrumental in initiating a nerve impulse



A photo of a constricted pupil, producing a small central dark area in the centre of the eye.

© Gilmanshin/shutterstock

A photograph of a dilated pupil, producing a large central black area in the centre of the eye.

© Johanna Goodyear/shutterstock



Light and Dark Adaptation

 

adaptation: the process by which the iris adjusts the diameter of the pupil based on light conditions, thus controlling the amount of light that enters the eye and strikes the retina

Rhodopsin is extremely sensitive to light. Even starlight causes some molecules of rhodopsin to become bleached. In high-intensity light, rhodopsin is broken down almost as fast as it is remade. In such a situation, the rods become nonfunctional and the cones take over completely. For example, think about what happens when the lights are turned on after a movie. You are momentarily “blinded,” and all you see is white light. Your pupils constrict as a reflex to protect your retina from the bright light. Within a minute or so, the cones become sufficiently stimulated to take over once again. Over the next few minutes, visual acuity and colour vision improve. On the other hand, adaptation to low light occurs when you go from a well-lit area into a dark one. At first you see nothing but velvety darkness because your cones have stopped functioning due to lack of light, and your rods are not functioning because they have been bleached out by the bright light. Once in the dark, rhodopsin is remade and accumulates so that low-intensity light can again stimulate the rods. During adaptation to both light and dark, reflexive changes occur in the pupil.

 

The Pathway to the Brain

 

Try This

 

TR 5. Did you know that each eye sees thing differently? Each eye has its own area of “blindness,” the blind spot. To find your blind spot, try the activity shown in “Figure 12.17” on page 416 of your textbook.

 

The information you receive from each eye is communicated through the optic nerve to the brain. Your brain processes this information into one image without gaps or blind spots. The optic nerves enter the optic chiasm on the ventral, front of the brain (see Lesson 2). In the X-shaped optic chiasma, some axons from each eye cross over to the opposite side of the brain, while others continue to their own side of the brain. The crossing over of about half of the sensory fibres ensures that each half of the occipital lobe receives the same image or part of the visual field viewed by each eye. However, keep in mind that each eye will see the image from a slightly different angle. Study the illustration provided below very carefully in order to better understand visual interpretation by the brain.

 

depth perception: the ability to see in three dimensions

Depth perception is possible due to the “fusing” or superimposing of the slightly different images from the two eyes by the visual cortex. This creates a three-dimensional image. Thus, by working together, the eyes provide slightly different angles of view that allow the brain to estimate distance.

 

The image that was reversed and inverted in the lens is at this point interpreted correctly.

 

A diagram of the eyes, optic nerves, and parts of the human brain involved in sight is shown. Evident in the diagram is the optic chiasm, where the optic nerves from each eye meet, and information from the right eye is transferred to the left half of the brain, and information from the left eye is transferred to the right half of the brain. The components in the brain that form structures involved in the transfer of information from the chiasm are the optic tract and the lateral geniculate nucleus. The nerves from the geniculate nucleus terminate in the occipital lobe of the cerebrum (also called the visual cortex).

Inquiry into Biology (Whitby, ON: McGraw-Hill Ryerson, 2007), 416, fig. 12.18. Reproduced by permission.