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Developmental psychology.pdf

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132 Modes of Awareness<br />

Figure 5.8<br />

Comparison of Place and Volley<br />

Theories. This table indicates that<br />

the theories explain pitch and<br />

loudness differently.<br />

Theory Pitch Loudness<br />

Place<br />

Volley<br />

place in the cochlea<br />

frequency of volleys<br />

spread of disturbance in the<br />

cochlea<br />

number of impulses per volley<br />

Theories of Hearing In hearing, just as in color vision, there are two major<br />

theoretical positions, one of which is place theory. According to place theory, different<br />

regions of hair cells in the cochlea are attuned to different frequencies of vibration,<br />

and the impulses aroused in different hair cells go to different regions of the auditory<br />

cortex. Pitch depends on the place in the cochlea that is most activated and also the<br />

place in the auditory cortex that receives the resulting nerve impulses. The assumption<br />

that there are precise cortical localizations for high-pitched and low-pitched sounds<br />

has yet to be verified, however.<br />

Loudness, according to this theory, depends on the spread of disturbance in<br />

either direction from the activated area of the cochlea. Two tones of the same pitch<br />

and loudness would activate the same fibers, but if the tones differ in intensity, the<br />

range of activated fibers would be greater for the louder sound.<br />

No single fiber in the auditory nerve can respond more frequently than 1,000<br />

times per second, however, which raises a complication in place theory. How can we<br />

readily hear sounds up to 4,000 hertz?<br />

The volley theory attempts to answer this question, suggesting that nerve fibers<br />

work in groups. One group of fibers is discharged by one sound wave, another<br />

group by the next. The first group, on account of the absolute refractory period of .001<br />

second, cannot respond to the second wave, but with different groups of fibers involved,<br />

there are always some fibers available to respond to any given wave. This group activity<br />

is the central concept in volley theory (Wever, 1949).<br />

For a tone of 4,000 hertz, a spurt of neural activity called a volley occurs in<br />

the auditory nerve every .004 second, with different groups of fibers contributing to<br />

different spurts. Also, some fibers, because of their greater excitability, contribute to<br />

more spurts than do other fibers. Pitch, according to volley theory, depends on the<br />

frequency of volleys rather than the frequency carried by the individual fibers.<br />

Loudness is thought to increase as more impulses occur in each volley, for an<br />

increase in the intensity of stimulation causes more fibers to respond. A large sound<br />

wave might activate 100 instead of 50 fibers, producing more impulses per volley without<br />

changing the frequency of the separate volleys (Figure 5.8).<br />

As in vision, the place and volley theories are not necessarily incompatible.<br />

The volley factor may play a major role in mediating frequencies up to 4,000 hertz,<br />

and the place factor may be more significant in higher frequencies. Recent research<br />

suggests that both phenomena may be involved in human hearing, to which the neural<br />

processes in the brain add further complexity.<br />

Sense of Smell<br />

In contrast to vision and hearing, the senses of smell, taste, and touch are the "lower<br />

senses" at the human level. This description does not mean that they are necessarily<br />

less acute, for it is impossible to make comparisons across the modalities. Rather, it<br />

means that they are generally less important in survival. The sense of smell does not<br />

alert us to predators, as it does with animals, although it puts us on guard when certain<br />

foods are unfit to eat and warns of such dangers as fire, gasoline, and ammonia. Smell<br />

might be of greater significance if we did not move in an upright position.

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