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BOOK
EXCERPT Developing Ocular Motor and
Visual Perceptual Skills: An Activity Workbook Kenneth Lane OD, FCOVD
Chapter 3 Eye Movements and Reading
"The control of eye movements during reading
can be considered to involve temporal and spatial decisions" (Rayner,
1983)
Introduction
This chapter is one of the most important chapters in this
book. You must have a clear understanding on how ocular motor exercises help a
child with reading difficulties. This requires a good knowledge of eye
movements and reading.
We have already discussed the complexity of the human brain.
It is staggering to think that the cerebral cortex alone has about 10 billion
neurons and 1 million billion connections or synapses. Counting one synapse per
second, we would finish counting 32 million years from now. If we consider the
number of ways in which circuits or loops of connections would be stimulated,
we would be dealing with a 10 followed by at least a million zeros. There are
10 followed by 79 zeros, give or take a few, particles in the known universe
(Edelman, 1998). Considering how complex the brain is, one of its most complex
assignments is reading and one of the most important parts of reading is moving
the eyes across the page of print in perfect harmony to be able to encode
print. Encoding enables the brain to form a visual or nonvisual code of the
word and place it in working memory (Krueger, 1993). In decoding, the letter
components are accessed and compared against target letters in memory and the
word is remembered.
It is important to remember that the brain can't handle all
the visual information available to it. Three-quarters of the visual
information available to the brain when we read is ignored (Smith, 1994). When
we read, we don't take in large amounts of visual information. The eyes move
across the page in a series of quick movements called saccades and
pause to take in visual information called fixations (Figure 3-1)
(Ygge, 1994). Because only a small fraction of the retina has heightened
acuity, the point of fixation must constantly be moved about to allow detailed
visual processing. Moreover, this must be done so that each change of gaze
places the eye at convenient locations on the target (words). For example, in
reading, the eyes must accurately jump from word to word so that when each item
is fixated, it can be processed rapidly and the next eye movement can be
planned. This requires that each individual eye movement be guided by detailed
visual information obtained from locations peripheral to the current point of
fixation (Moore, 1999). As I mentioned before, we do not take in a large amount
of words as we move our eyes across the line of print (Figures 3-1 and 3-2).
The average good reader does not look at more than one word per fixation until
he is in the tenth grade (Morris, 1973). Even college students don't take in
more than 1.11 words per fixation. A child in first grade only takes in about
45% of a word (Vogel, 1995). The amount of visual information available to the
brain during the fixation is called the perceptual span or the
span of recognition. The perceptual span is the region around the
center of vision within which some aspect of visual detail of interest is used
in reading (Rayner, 1983). The perceptual span for letter information in words
lies asymmetric with respect to the fixation point and extends farther to the
right than the left. For Israeli readers, it is the opposite (Rayner, 1983). A
skilled reader has an average perceptual span of four characters to the left of
fixation and 15 characters to the right (Solan, 2001). Word recognition and
processing for comprehension occurs only seven to eight characters to the right
of fixation. Information from eight to 15 characters to the right of fixation
helps to direct subsequent saccades (Vogel, 1995). While the central foveal
areas are processing information for word recognition, parafoveal (peripheral)
retinal areas and their corresponding cerebral centers are analyzing word shape
and length information to help direct subsequent saccades (Vogel, 1995).
Regressive eye movements during reading occur 15% of the time. These are eye
movements in the opposite direction (to the left). Most are only a few
characters and typically reflect some text confusion or comprehension problem,
or perhaps a recheck or double check confirmation.
Children learning to read and poor readers make excessive numbers of
regressions (Figure 3-3). Normally, approximately 10% to 15% of all saccades
(or fixations) are actually regressive in nature. Uncommon words are refixated
more than common words (Ciuffreda, 1995). The average first grader makes 52
regressions per 100 words, while the average college student only makes 15
(Vogel, 1995).
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 Figure 3-1. The eyes move across the page in a series of
quick movements called saccades and pause to take in visual
information called fixations.
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 Figure 3-2. We do not take in a large amount of words as we
move our eyes across the line of print.
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 Figure 3-3. Children learning to read and poor readers make
excessive numbers of regressions.
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When we pause to take in information as we read, this is
called a fixation. The average child in first grade pauses 224 times per 100
words, while the average college student pauses 90 times per 100 words. The
average first grader has an average fixation time of .33 seconds, while the
average college student pauses for .24 seconds (Vogel, 1995). Because of this,
the limit that most people can read is 250 words per minute or about four words
per second (Smith 1994). In normal reading, fixations average about 250 msec.
During this short interval, visual information is extracted from the printed
material (Lovegrove, 1990). Fixation durations are influenced by properties of
the text such as word length (Hoffman, 1995). Other factors that can influence
longer fixation durations include: low-frequency words, technical words,
shorter words, certain grammatical elements, words at the beginning of a new
line, words that are misspelled, and regions of the text with important
information. Shorter durations of fixation are often caused by the final word
of a line, fixations before a regression, and in regions between sentences
(Garzia, 1994). The brain is very busy during the fixation. Not only must it
encode information but it must decide when to move the eyes and how far to move
them for the next fixation. To give you an idea of what happens during the
fixation, let's suppose the fixation lasts for 250 msec. We know that much of
the visual information necessary for reading can be acquired beginning at about
50 msec into the fixation (Vogel, 1995), leaving the remainder of the fixation
(200 msec) to complete programming the next eye movement and for higher level
linguistic processing (Rayner, 1983). Processing of information available
during the fixation is not completed by the end of the fixation and the onset
of the next fixation is not triggered by the completion of processing of
information (Rayner, 1983). In other words, the visual processing might be
completed but the brain is still digesting information from one fixation to the
next fixation. Language aspects of the text must begin having their influence
on processing within about 100 msec after the onset of the fixation. This is
called textual influence threshold. By about 100 msec, the brain has
an idea when the next saccade will start, and after 100 msec stimulus changes
will not affect when the next saccade will start. This is called the
saccade deadline. The time when the brain centers have become fully
committed to the time of the next saccade is called the point of no
return, and is estimated to occur at about 30 msec prior to the saccade
onset (Rayner, 1983). Contrary to what some people think, all the visual
information available to the foveal area is scanned and processed. Good readers
do not skip over parts of words when they read. If one letter in a child's
foveal vision is masked, his reading speed decreases by 50% (Stanovich, 1993).
Children must be taught to scan each letter in a word and every word when they
read.
We know that during the fixation the time of the next
saccade is determined, but how does the brain know how far to move the eyes for
the next fixation? The brain uses a combination of peripheral visual
information and knowledge of language patterns to know how far to move the eyes
(Rayner, 1983). Visual information such as word length patterns is acquired at
least 12 to 15 character positions to the right of the fixation point and
specific letter and word shape information no further than 10 character
positions to the right of the fixation point (Evans, 1990). There is an optimal
landing position for the eyes within a word (Fischer, 1993). The most likely
landing spot is near the center of a word. In fact, the location tends to be
between the middle and beginning of the word. The preferred viewing location in
a five letter word is the second letter and for a ten letter word, it is the
fourth (Rayner, 1983). The fixation is less likely to be of the word
the or on a blank area (Garzia, 1994). If the eyes miss the optimal
landing location in the word, the penalty is in the order of 20 msec slower
reading speed for every letter that the reader is away from his optimal
location (Richman, 1992). Accuracy in saccadic eye movement is obviously a very
important component in reading.
Laboratory studies have shown that after the presentation of
a visual stimulus, the stimulus continues to be seen for some time.
The visual response to a stimulus outlasts the actual duration of the stimulus.
This continuation of a response after the removal of a stimulus is known as
visible persistence and can last up to 300 msec. (Lovegrove, 1990). As you can
imagine, if this happened when we read, it would cause considerable problems.
The brain cannot allow the visual image of one fixation to continue into the
next. If this occurred, the two individual visual inputs may be seen but we
would not know which was from the first fixation and which was from the second
fixation (Lovegrove, 1990). This, of course, does not happen with most readers.
However, what does the brain do to overcome this? The answer is that there are
two parallel visual subsystems that operate from the retina to the visual
cortex. One is called the transient (M cells) and the other is called the
sustained (P cells) system.
Retinal images are sampled twice by the visual system
(Solan, 1994). It is sampled first by our peripheral vision to get the gross
overall view of an object or upcoming word in a sentence. It is then sampled
again to extract detailed information from the object or word. The two systems
originate in the retinal ganglion cells (Solan, 1994). The system that is
involved in the detailed analysis is called the sustained system (P
cells) and is also called the parvocellular system. This is active
during the fixation. The sustained system's role is an identification of shape,
patterns and the resolution of fine detail. P cells comprise 80% of the retinal
ganglion cells and are concentrated at the fovea. They have small receptive
fields and are more responsive to low temporal (slow movement) and high spatial
frequency (close together or detailed information) (Solan, 1994). Visual acuity
and color vision are principally sustained system's functions (Garzia, 1990).
The visual system that operates with the sustained system is
called the transient system (M cells). It is also called the
magnocellular system. M cells comprise 10% of the retinal ganglion
cells, are distributed evenly across the retina (Solan, 1994), and have large
receptive fields (Bassi, 1990). The transient system is thought to be involved
in the perception of motion, depth, brightness discrimination, the control of
eye movements, and the localization of targets in space. It seems to function
to accomplish a quick global analysis of a visual scene. It performs a global
analysis of the incoming stimulus, breaking the field into units and regions
and coding the position and movement of objects in space (Williams, 1990). Two
of the primary functions of the transient system is that it carries motion
detection and ocular motor control information (Garzia, 1990).
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 Figure 3-4. Visual information from one fixation smears into
the next fixation like an after image, making the text appear superimposed or
overlapping.
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The role of the transient system in reading is critical.
Previously, I have mentioned that the sustained system during the fixation is
processing detailed information about the text. It is during the fixation that
word encoding and decoding occur. The words are identified and the visual
information is used for comprehension. When we pause to fixate during reading,
both visual and cognitive information is used. Cognitive information is held in
our subconscious to help in word identification and comprehension. When we move
our eyes from one fixation to another by saccadic eye movement, the cognitive
information continues; however, the visual information is terminated. If it
isn't terminated at the end of the fixation, you will have visual information
from one fixation smearing into the next fixation like an after image, making
the text appear superimposed or overlapping (Lovegrove, 1990) (Figure 3-4).
This is called visible persistence and can greatly interfere with
reading. The reason why this does not happen is that the stimulation of the
transient system generated by the start of the saccade inhibits (suppresses)
the visible persistence of the sustained system from the pervious fixation
(Solan, 1998). A deficit that affects the timing of either system will
interfere with the processing of the second fixation and could lead to
superimposition of successive inputs (Solan, 1994). This is what often happens
with children with reading disabilities. In fact, over 75% of children with a
reading disability manifest a transient defect (Lovegrove, 1990). Since inputs
from successive fixations would be superimposed, disabled readers would do
better in reading that does not require eye movements.
Transient deficits can cause the following problems:
- Readers may only see parts of words.
- If they do not know which fixation the information came
from, they would know very little about the spatial arrangement of the letters
and this could lead to reading errors and word or letter reversals.
- It would be very difficult to learn any systematic
grapheme to phoneme (phonics) rule if the appearance of the graphemes was in
some way unstable.
- The disabled reader may make repeated errors in different
readings of the same word (Lovegrove, 1990).
- The disabled reader may experience perceptual grouping
deficits.
- Readers may suffer an inability to selectively
attend.
- Readers may require larger time intervals to make
accurate temporal judgments.
- They may require more time to alleviate attention across
visual space without eye movements.
- Readers may skip lines during reading.
- Readers may have to use a finger to help keep place
during reading.
- They may complain of words appearing to move on the page
(Garzia, 1993).
It is important that we understand the relationship between
the sustained and transient systems. It gives us a much better understanding as
to why we do certain activities. This will become clearer when you follow the
pathways of the two systems in the brain. For this description, I will use P
cells to describe the sustained system and M cells to describe the transient
system. These two parallel processing pathways in the visual system are
relatively independent. These pathways transmit information from the retina to
the dorsal lateral geniculate nucleus to the visual cortex and then to higher
cortical levels with little or no cross-talk between them (Steinman, 1996).
Although the principle function of the lateral geniculate nucleus is to relay
ganglion cell information to the visual cortex, less than 20% of the synaptic
input to the lateral geniculate nucleus is retinal in origin. The majority of
the afferent neurons is extraretinal, midbrain, and brain stem; therefore, M
and P ganglion cell information is influenced by nonvisual inputs (Solan,
1994). This is another reason why we do a lot of nonvisual activities that
involve lower brain areas, such as motor activities.
Information travels faster along large, highly myelinated
axons, causing information from the M pathway to reach the visual cortex faster
than information from the P pathway (Steinman, 1996). Receiving information
first from the M system and then from the P system allows the visual system
first to quickly locate objects and then identify them (Steinman, 1996).
It seems obvious from the previous discussions that the
proper functioning of the transient system is critical for normal reading
skills. It also seems obvious that anything that can improve the transient
system would be beneficial. Research has shown that the transient system is
sensitive to short wavelengths (e. g., blue) (Solan, 1994) and may perform more
efficiently when stimulated by this wavelength. One research paper showed that
blue overlays significantly improved reading comprehension in 70% of children
identified as reading disabled (Solan, 1998). Positive results were obtained by
gray overlays but they were not as successful as the blue overlays (Solan,
1998). It has also been shown that while blue enhances transient function, red
reduces it (Richman, 1992). Does this mean that the Scotopic Sensitivity
Syndrome exists? Also called the Irlen Syndrome, this claims that some children
have difficulty processing full-spectrum light efficiency and that certain
colored tints may improve their reading efficiency. This syndrome consists of
eyestrain, photophobia (preference to reading in dim light), problems in visual
resolution (blurred print, unstable text), restricted span of focus (only small
areas of print seen), difficulties with sustained focusing (print blurs unless
the reader puts a lot of effort into keeping it clear), problems in depth
perception (difficulty judging distances), and handwriting (Garzia, 1990). The
problem is there is no scientific evidence of a Scotopic Sensitivity Syndrome.
All of the symptoms of this syndrome listed above are usually caused by visual
problems such as ocular motor, convergence, or accommodation. What is important
to know is that there does seem to be improvement in some children with a blue
tint, but not necessarily other tints.
This chapter was devoted to eye movements and reading. It is
extremely important that you have an understanding of eye movements and reading
and also the sustained and transient systems. This enables you to understand
how some visual procedures improve a child's overall reading efficiency.
Tips for a Successful
Activities Program
There are no exercises that have been proven to enhance the
transient system. Because of this, I recommend that we do exercises that affect
the functions of the transient system and hope by doing this that the transient
system is improved. Therefore, I recommend the following:
- Do activities that work with the peripheral visual
system.
- Do a lot of visual scanning activities.
- Do figure-ground activities; for example, hidden
pictures, etc.
- Try a light blue filter and see if this helps the child's
reading performance. This can be obtained from an office supply store, usually
as a page separator or file cover.
- Do a lot of ocular motor activities.
References
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visual pathways. Journal of the American Optometric Association,
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Ciuffreda, K. J. (1995). Eye movement basics for the
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Edelman, G. M. (1998). Building a picture of the brain.
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