Visualization without
eye movements is the only visual meditation
technique conducive to Samadhy
Dinu-Stefan Teodorescu
Tromsø University
Three different perception styles, Free Vision,
Fixation and Unfocused or Holistic Vision, have been investigated in
twelve participants, divided in three experimental groups by recording their
eye movements while they viewed and visualized eight irregularly-checkered
diagrams. The same eye movement patterns were observed during viewing the
stimulus and during the imaging of the stimulus. Vividness and accuracy tests
were used to quantify the differences between the three perception styles.
Contrary to previous findings (Neisser, 1967), the most vivid imagery was found
in the Holistic Visual group. Greater accuracy in recall was found in the Free
Vision group. The flexibility of the attention window was hypothesized to
account for the different perception styles and the findings propose an enlargement of the imagery theory
of Kosslyn (1994). Strong evidence that scanpaths during perception are encoded
in a kinesthethic memory was found from the repetition of the same eye movement
patterns during retrieval in the visual imagery condition. It is proposed that
only the Holistic Vision and Fixation
styles in perception are conductive to an absence of eye movements,
stabilization of image and achieving Samadhy during meditative visualization.
INTRODUCTION
Key words: holistic perception, attention window, stabilization of
image.
Visualization of sacred objects, like mandalas (Kværne, 1995; Tucci,
1969), yantras (Rao, 1988; Khanna,
1997; Bru-sgom rGyal-ba g.yung-drung, 1996; Johari, 1987), icons ( Laeng, 1980; Dancu, 1982), and kasinas (
Buddhaghossa, 1975), have been kept in high esteem from the world mystical
traditions, used for attaining of one or another types of Samadhy ( Patanjali,
1990). The metaphor that the eyes are the window of the soul have been taken
literally by transpersonal researchers in the studies of eye movements, all
trying to decode the unseen Kognitive (
Wilber, 1999) processes. Vision has certainly a privileged place in the human
cognition, since most areas of the brain appear to be involved in visual
processing. Indeed; it is since Aristotle that thought is supposed to be also
visual, and after the apparition of transpersonal psychology, visualization
have been enthroned again as an important area of research. The present
research have been done in the spirit of the
new integral psychology ( Wilber,in press) using the tools from the
third quadrant to account for changes in the first quadrant ( Wilber, 1995),
trying to establish a new tradition for research in the Transpersonal.
It is possible and desirable to use
all the tools we have in order to validate the
information of different quadrants, so that the Transpersonal science
may become really holistic, an all quadrant research.
The present study was done in order
to clarify the subject of visualization techniques that have a broad following,
especially in the indian tantric
traditions (Feurstein, 1998; Johari, 1986 ) , tibetan tantric traditions
( Tucci,1967; Kværne, 1995) and to add to the researched data of Transpersonal Psychology.
Visual perception have been taken more or less to be of only one kind,
namely the normal scanning of the visual field, following a “ hypothesis
testing” strategy (Gregory, 1998), when the information is extracted during the
fixations and integrated during the
scanpaths ( Neisser, 1967; Hebb; 1967; Stark, 1971 ). The visual perception
styles have been not so much researched, but the practical implications of
“special “ perceptual styles has probably always been appreciated in human
areas such as sports, e.g. basket, martial arts ( Herigell, 1974; Deshimaru,
1983 ) and mysticism (Bankei,1984;
Buddhaghosa, 1970 ). The visualization practices used for meditation purposes,
has as its main point the stillness of mind using an image, first using visual
perception and afterwards imagery. The apparition of deeper brain waves , such
as alpha, theta and delta are used to indicate the achievement of a meditative
state (Motoyama, 1978; Hirai, 1994; Tart, 1980; Shapiro & Walsh, 1985
).
Eye movements are associated with beta waves, and hence a meditative
state is excluded, which is associated with alpha, theta and delta brain waves.
It is therefore claimed that there is a clear difference between a normal
visual perception and a holistic visual perception, which in essence could be
captured by the difference between a serial cognitive processing ( as in the normal scanning visual
perception ) and a parallel cognitive processing (supposedly used in holistic
visual perception ). Although we cannot measure directly these different mental
processes, by using eye movements as the target of analysis, we might infer
correctly the presence of these different processes during visual cognition and
imagery. Several studies have acknowledged vaguely the implication for a
parallel visual processing, for example, that vivid imager can perceive
literally ( Sheehan, 1967 ), eidetic imagers have a different encoding strategy
( Luria, 1978; Haber & Haber, 1964 ) and Norton and Stark ( !971 ) noticed
that in recognition studies, the participants seemed to recognize the image
even before they scan the whole image. Paivio ( 1986, 1991 ) in his dual-code
theory, has proposed the simultaneous encoding of pictures in the visual code,
as opposed to verbal information that uses a sequential processing (
Goldenberg, 1987 ), this clearly pointing out a parallel processing system.
The perceptual learning
theory ( Hebb, 1968; Hochberg, 1970 ) proposed that thoroughly scanning which
brings parts of a stimulus serially into the foveatic vision is the only way to
effectively encode visual stimuli. All other kind of vision, for example
peripheral visual perception was able only to distinguish vague, gross features
such as brightness or contour. However, several studies have shown that the
peropheral vision can be quite accurate ( Maurer & Lewis; 1981, Cohen, 1981
) although one of its roles is to guide the foveal perception ( Irwin, 1992;
Finke, 1985, Rayner et al.,1978;
Yarbus, 1967 ) towards the “interesting” targets ( Gibson, 1998 ).
The representation in
the brain of visual information while scanning an image have been proposed to
be encoded in two separate representational systems: one encoding the visual
information and the other encoding the kinesthetic information ( Hochberg,
1970; Kosslyn, 1990; Gauthier et al., 1990; Henderson, 1994; Schneider, 1995; Demarais & Cohen, 1998
)
Scanpath and visual attention theories
The prevailing paradigm in eye movement research (Rayner et al.,1978) is the scannpaths theory
which proposes that visual information
is integrated across fixations of the eyes.
This theory was also formally proposed by Norton and Stark (1971), based on
the research of Yarbus (1967) as well as some theoretical insights of Hebb
(1968). The theory proposed a «feature
ring» , later expanded into a «feature network» which is an integration of
sensory and motor elements which guide the saccades of the eye for each visual
image. The feature network is supposed to use serial encoding, and at retrieval
during a recognition task, the same scannpaths is supposed to be reenacted. The
theory was acknowledged to include many problems even from the beginning
(Norton & Stark,1971). In later revisions
(Stark & Ellis, 1981; Brandt
& Stark, 1997), the theory is still wanting because of the dismissal of the
role of peripheral vision in the
generation of the scanpaths (Brandt & Stark,1997). One proposal is that
there is a transsaccadic memory that is limited up to four tokens or object
files (Irwin,1998), a memory type close to short -term visual memory. The
transsaccadic memory theory have been further developed and renamed as
«object-file» theory of transsaccadic memory (Irwin,1996), using the
theoretical framework for object perception proposed by Kahneman and Treisman
(1984). Specifically, Irwin (1998) used for the development of his theory, the
VAM-Visual Attention Theory proposed by Schneider (1995). .
VAM theory claims that, because
motor action (e.g. looking or fixating) can be directed only to one item, in
order to program a saccade to a target, attention is required to be redirected
to that location in space, but not all the tokens to be formed can be
remembered because of the limited capacity of the short-term memory.
In short, VAM propose that
attention shifts will determine what information is encoded into transsaccadic
memory and hence remembered across eye movements. Attention is shifted around
the visual field before the eye movements, this indicating that information
from regions surrounding that of each fixation is encoded and remembered
through a peripheral perception.
Kosslyn (1994,1995) has also
proposed an attention shift subsystem which is guided by stimulus
impulses that may be detected by the peripheral vision, even “in the corner of
one’s eye”(Kosslyn,1994).
Visual perception and imagery common structures
and mechanisms
Perception and imagery share many common structural features, and this
have been demonstrated by the interference phenomenon (Perky,1910),
electrophysiological measurements (Farah,1988) and from positron emission
tomography studies (Kosslyn,1994).
Finke (1985) have reviewed
the existing theories relating perception to visual imagery, and he have
identified three categories of such theories: structural theories that propose
identical spatial and pictorial properties for perceived and imaged objects,
represented by Kosslyn (1980),
functional theories which propose formation and transformation of mental images
contribute to object recognition and comparison, represented by Shephard & Cooper (1982), and interactive
theories which propose that imagery contributes directly to ongoing perceptual
processes, represented by Finke (1971) and Peterson & Graham (1974). This
experiment have followed a structural approach and the theory of perception and
imagery proposed by Kosslyn (1995), have been used as guide line.
Kosslyn’s computational approach model to
perception and imagery
Kosslyn have proposed a retinotopically visual buffer, that is an
integrated “image” is projected in the
visual buffer. The visual buffer contains an attention window, that allows the
attention to select the needed information present in the visual buffer, and
because the visual buffer contains much more information that can be processed
at a time, the attention window selects , only a part of the visual buffer at a
time. For shifting the attention it is proposed a special subsystem that
function both ways, both from top-down commands and from bottom-up or
stimulus-based impulses. Thus the attention window is adjusted on one side by
the stimulus-based attention-shifting subsystem and on the other side by the
higher cortical commands zones. The output from the attention window is sent to
a recognition system which allows shapes to be matched. The encoding of the
visual information is understood to contain a visual component as well as a
motor component, in order to identify the image and its location in space. It
is conceived in Kosslyn’s model that the visual buffer and the attention window
play similar roles in both perception and imagery, and the properties of each,
affect both sorts of processes. It is proposed that imagery is a part of the
perception itself, and that the shared structures are a support for this. In
the experiment there have been considered only
the visual buffer, the attention window and the spatiotopic map
construction from Kosslyn’s theory.
Working definitions and hypothesis
Three groups have been selected
for this experiment, and each group was
defined using the window attention equivalent from Kosslyn’s theory. The first
group, named Free Vision, was defined
by a ”mobile” attention
window but limited to a certain resolution degree area, the area supposed to
be selected for further processes. The second group, named Central Fixation ,
was defined by a “ fixed and
contracted” attention window, where the contraction was to its utmost limit,
equivalent with a point seen at a distance of 60 cm. The third group, named
Unfocused, was defined by a “ fixed and
expanded “ attention window where the
expansion was to its utmost limit, equivalent with the entire visual
field. It was conceptualized that in order to demonstrate the existence of a
particular visual perception style, there should be clear differences in the
encoding processes , clear differences in the retrieval process, and clear
differences in accuracy and vividness.
The first goal was to test the flexibility of the attention window and
to identify a Holistic Visual perception style with its implications for
achieving a meditative state.
Theoretically, the Holistic Vision could be characterized as having the
attention window expanded ad infinitum which may force the visual system into a parallel cognitive
processing. The second goal, was to replicate an early experiment of Brandt
& Stark (1997), used as a accepted standard for the normal visual
perception. The Free Vision group was considered as a control group for the
other two groups, the Central Fixation and
the Unfocused, or the Holistic Visual perception .
The
hypothesis for this study was:
If during the visual perception
task, a particular eye movement pattern shall be observed, than during the
imagery task, the same eye movement pattern shall be observed.
The predictions for this experiment
were: 1) the Central Fixation group shall keep the eyes fixed in the
same place during the imagery task as in the visual perception task, and
their encoding shall be limited to the fixation point. The vividness shall also
be expected to be higher than proposed by earlier studies (Neiser,1967, Sheehan & Neiser,1969). 2)
the Unfocused group shall keep the eyes fixed in the the same region during the
imagery task as in the visual perception task, and their encoding and vividness
in imagery shall be the best from all groups. 3) the Free Vision group shall
follow the same scanpaths during imagery task, as during the visual perception
task, with a high accuracy in retrieval and a moderate vividness in the imagery
task.
In order to test the hypothesis, an
experiment was designed, composed by two conditions, one visual perception task
and an imagery task in which the independent variable was
perceptual style. It was expected that a manipulation of the visual perception
style would influence the imagery style, directly reflected by the eye movement
patterns , accuracy of recall and vividness of the imagery. A vividness
questionnaire was also used in order to measure the so-called vividness IQ of each participant (that is, an
imagery ability that is thought to be stable and general trait of a particular
individual), and to assign them
randomly to three balanced groups. It was also expected that the visual
perceptual style would influence the accuracy of retrieval from long-term
memory, and for this reason, a memory test was conducted at the end of the
imagery task.
METHODS
Participants
Twelve University of Tromsø. students, nine females and three males,
volunteered to participate as paid participants to this experiment which was
conducted in the cognitive neuropsychology laboratory at the Psychology
Institute of Tromsø. All participants reported having normal or corrected to
normal vision (with contact lenses)
and their age was between twenty three to forty one. The participants were told
that the experiment intended to test the influence of “inspirational” landscape
pictures on the memory for geometric figures. All the participants were naive
about the true purpose of the experiment, and during the debriefing session at
the end of the experiment, this was confirmed.
Apparatus and Materials
Eye movements were recorded by means of a remote eyetracking device
using infrared light. The Remote Eye Tracking Device, R.E.D. built by
SMI-SensoMotoric Instruments from Teltow-Germany, which uses iView-software. The R.E.D.-II can operate at a
distance of 0,5 - 1,5m, the
recording eye tracking sample rate is
50/60 Hz., and the resolution is better than 0,1 degree. The eyetracking device
is operating by determining the positions of two elements of the eye: the
center of the pupil and the center of the corneal reflection. The sensor, a
video camera views the left eye of the participant using infrared light and the
video signal is processed to extract the features of interest: the center of
the pupil and the center of the corneal reflection. The coordinates of all the
boundary points are fed to a computer that, in turn, determines the centroids
of the two elements. The vectorial difference between the two centroids is the
“raw” computed eye position. There was electric light in the room during the
experiment, which was not interfering with the recording capabilities of the
apparatus.
“Vividness of Visual Imagery Questionnaire”, or in short, VVIQ Survey questionnaire
developed by Mark (1973) was used to determine a vividness of imagery estimate of each participant. The
questionnaire consists of sixteen questions, asking the participant first to
image a scene and then to rate the vividness of the mental image on a
five-point rating scale. Here is an example of a question from the questionnaire:”
Think of some relative or friend whom you frequently see (but who is not with
you at present), and consider carefully the picture that comes before your
mind’s eye. 1-The exact contour of the face, head, shoulders, and body.” The
rating scale was ranging from one (“No image at all, you only “know” that you
are thinking of the object”), through three (“Moderately clear and
vivid”), to five (“Perfectly clear and
vivid as normal vision”).
Stimuli
The pictures used as stimuli were derived from a study by Brandt and
Stark (1997) . The stimuli consisted of eight , 6x6 grid
irregularly-checkered diagrams, each containing five black squares . The five
black squares were spread in all the directions on the diagram, with no
identical patterns. The stimuli 10x10 cm.,
we presented on the full screen of a flat screen, color monitor with a
diameter of 49 cm, in the middle of a
sky-blue screen . The stimuli presentation was done using software ACDSee
32v2.4. The participant was seated in the front of the monitor at 60 cm., and
with the head placed in a chin-and-forehead rest apparatus to minimize head
movements, to maintain the viewing distance and the 3x3 degrees
(horizontally/vertically) visual angle field of the diagram.
Figure 1. Stimulus prototype

Procedures
The participants were randomly divided between three experimental
groups, four in each group. The first group was the Free Vision condition, the
second group was the Central Fixation condition and the third was the Unfocused
condition. Before the experiment, each participant was asked to read the
instructions for the experiment, the first part consisting of general
instructions common to all groups while the second part were specific
instructions for each group. The experiment was divided in two tasks, one
perception task and one imagery task and two ratings for vividness of visual
memory and accuracy of memory. The
instructions for the Free Vision group for the perception task were: ”Look
carefully at the figure that shall appear on the monitor and try to remember it
as precisely as possible.” The instructions for the Central Fixation
group in the perception task were: “Look, and keep your eyes focused in the
center of the diagram, and try to remember the whole figure as precisely as
possible.” The instructions for the Unfocused group for the perception task
were: “Look straight ahead, unfocused and keep an even look at the whole
surface and try to remember the whole figure as good as you can.” The
instructions for the imagery task were common for all the groups: “ Try to
imagine the figure you just saw while keeping the eyes open.” There was no instruction about how to keep
the gaze in the imagery task. After reading the experiment’s instructions, each
participant was seated comfortably on a chair with his or her head placed in a
chin-and-forehead rest apparatus. The eye movements were recorded twice, for 20 sec in the perception task and for
another 20 sec in the imagery task, for each of the eight experiment stimuli.
The experimental protocol
After the calibration of the apparatus , the experimental session was
starting immediately, asking the participant to keep the head unmoved in the support.
Each trial consisted of the following sequence of events: 1) six nature landscape pictures were
presented followed by a prototype of the stimuli and an empty diagram used for
the imagery task. The pictures were shown to all groups, but the “unfocused”
group have received five minutes
training on them to learn how to look
unfocused. All the groups were then
familiarized with the stimulus prototype and with the empty diagram which they
would see while doing the imagery task.
2) the first stimulus diagram was presented for perception for a
duration of 20 sec.3) an empty screen
was presented on the monitor for 40 sec, or for a duration of repeating the
instructions for the imagery task, and in order to prevent the afterimages and
to ensure the encoding of the stimulus in the long-term memory. 4) the empty diagram was presented for another
20 sec and the participant was instructed to image the stimulus presented
before, while keeping the eyes open. 5) a diagram with numbers in all its
squares was presented on the screen for the memory test. 6) the participants
were asked to rate the vividness of the image in the imagery task, using a
rating scale from one to five, similarly to the VVIQ Survey’s ratings, used
before, which were recorded by the experimenter in a protocol. 7) the
participants were asked to indicate verbally, the numbers corresponding to the
black squares they remembered from the stimulus, while the experimenter was
recording the answers in a protocol. 8)
the next stimulus was presented for the perception task. The whole experimental
session consisted of eight stimuli.9) in the end of each session, a new
calibration session was conducted, in order to ensure the reliability of the
collected data. 10) a debriefing session was conducted at the end of the
experiment, to ensure that the participant was “naive”, that he was not aware
of the true purpose of the experiment, and to make sure that the experiment
have not harmed the participant.
Figure 2. Diagram of experimental procedure.

Perception
Field
Report Field
Imagery Field

Masking Field
Perception Field
Calibration and eye movement analysis
Before and after each experimental session a calibration routine was
recorded using a nine calibration points(a plus sign) dividing the monitor in
three equal rows and colons. The calibration was over a matrix of 3x3 points,
each 10 degrees apart while the viewing distance was 60 cm. The participant was
instructed to fixate each location which was sampled at a rate of 1000Hz for
100msec near the middle of this interval. These recordings served to calibrate
the output of the eyetracker device against spatial position, and to analyze
the eye movement trajectories for fixation points and sequence of fixation
points. The calibrations of all the participants shown no changes in the head
position during the experimental trial, and the quality of the recorded data
was thus not affected. The calibration procedure was repeated at the end of
each experiment while recording the eye-movements in order to get a visual
record of the precision of the calibration procedure.
Design
A 3 (perception style: free vision / central fixation / unfocused) X 2
(Visual Task: perception / imagery ) design was used.
For the latter factor, the 6 X 6 grid was divided in 9 equal parts
corresponding to separate square regions of the diagram, which for
experimental reasons it was named
region one through nine.
Figure 3 Regions of calculus
|
1 |
2 |
3 |
|
4 |
5 |
6 |
|
7 |
8 |
9 |
Data analysis
In order to calculate the fixation times on the different locations on
the stimulus, we have subdivided the stimulus in 3 X 3 matrix of areas of
interest, and called them Region 1 to 9.
Simple regressions and repeated-measures analysis of variance (ANOVA)
were performed for each dependent
measure. A probability level of .05 was used for all statistical tests; tests
with a probability level greater than .10 are not reported.
RESULTS
Relationship between perception and imagery
For each participant the eye
movement rate (EMR) was calculated for the viewing and imaging tasks. The
EMR is
defined as the percentage of time, for each item’s
recording in the perception or imagery conditions, spent on each defined region
(N=9). Consequently, three simple
regression analyses were performed between the percent of time spent in each
region in the perception condition (the regressor) and in the imagery condition
(the dependent variable). in each of the 9 defined regions of the stimulus
checkerboard in order to assess whether the variables of perception and imagery
were related. The regression analysis for the Free Vision condition showed a
clear linear relationship between EMRs in the perception task and in the
imagery task (THE DATA IS ERASSED !!!)The regression plot is shown in Figure 4.
Figure 4. Free Vision: Linear regression of EMRs for
perception and imagery tasks

The regression analysis for the
Central Fixation also showed a linear relationship between EMRs in the
perception task and in the imagery task (THE DATA IS ERRASED!!!)The regression
plot is shown in Figure 5.
Figure 5. Fixation: Linear regression of EMRs for perception
and imagery tasks

The regression analysis for the
Unfocussed condition showed again a clear linear relationship between EMRs in
the perception task and in the imagery task (THE DATA IS ERASSED!!!) The
regression plot is shown in Figure 6.
Figure 6. Unfocussed: Linear regression of EMRs for perception
and imagery tasks

Table 1shows the percent of time in
each region for the perception and
imagery condition for each group and the respective R values .
Table 1.Means,
standard deviations and correlation for EMR times for the three groups in perception and imagery tasks
( THE TABLE IS ERASSED !!!!)
In addition, a repeated-measures 3
by 2 ANOVA was performed with Perception Style ( free vision, central fixation,
unfocused) as the between-subjects factor, Regions (1-9) as the within-subject
factor and EMR in the imagery condition as the dependent variable. The
goal of this analysis was to reveal whether each Perceptual Style would affect
differently the EMR during the imagery task. Importantly, a reliable interaction
effect was found between Perceptual Style and Regions,(THE DATA IS ERRASED!!!).
This interactive effect is shown in Figure 7. Figure 7. Interaction plot
between Perceptual Styles and the EMR
in the 9 Regions

In the table 2 there is a presentation of the numeric values of the means for EMR times across the 9 Regions
for all the three groups during the perception and imagery tasks. The numbers
indicate clearly, the near- identical EMRs times during the two tasks.
Table 2.Means for
EMR times across the 9 Regions for the three groups in perception and imagery
tasks
(THE TABLE IS ERRASED!!!)
In the Figure 8, the EMR recordings from the three conditions
during both perception and imagery
are shown to better illustate the close correlation between the
two.

Accuracy of recall
A repeated-measures ANOVA was
performed with Perceptual Style (Free Vision, Central Fixation, Unfocussed)
with accuracy of recall as the dependent variable. This analysis showed that
the Free Vision (THE DATA IS
ERASSED!!!) and Central Fixation (THE
DATA IS ERASSED!!!) groups were equally accurate, whereas teh Unfocussed group
was significantly less accurate than these two
(THE DATA IS ERASSED!!!), as also confirmed by post-hoc Scheffe’s tests
(p < 0.01 in both cases). The means and
SDs of the accuracy rates in
each condition are shown in the table 3.
Table 3 Means and
standard deviations for total correct answers for the three groups
(THE TABLE IS ERRASED!!!)
A percentage rating have also been calculated, showing that the most
accurate group was the Central Fixation with (THE DATA IS ERASSED!!!)total
correct answers, followed by the Free Vision group with (THE DATA IS
ERASSED!!!)total correct answers and on the last place the Unfocused group with
(The data is erased!!!)total correct answers.
Vividness
The scores for vividness of the imagery for each trial were analyzed in
an ANOVA with Perceptual Style as the between-subjects factor. This analysis
revealed no significant difference between the three groups in this «global» measure of vividness (F<
1).
A simple regression analysis between
the vividness score at the VVIQ Survey questionnaire and the mean vividness
ratings during the imagery task, found only a low positive regression(the data
is erased!!!) but the correlation was extremely low(THE DATA IS
ERASSED!!!). Means and standard deviations for vividness ratings in the imagery task is shown in the table 4.
Table 4 Means and
standard deviations for vividness ratings during the imagery task
(THE TABLE IS ERRASED!!!)
Accuracy related to vividness
Both measures of vividness were
expected to predict accuracy for the visual memory, therefore two simple
regression analyses (collapsed across Perceptual Style groups) between these
two measures was performed. Surprisingly, a regression analysis between VVIQ
and accuracy showed no clear positive relation was found between these two variables (THE DATA IS
ERASSED!!!). Similarly, a positive
relation but too small was shown by the regression analysis of vividness in
each imagery trial and accuracy (THE DATA IS ERRASED !!!!).
However, when separate regression
analyses were performed for each Perceptual Style group it became clear that
the Free Vision group indeed showed a clearly positive relation between
vividness in imagery and accuracy variables (THE DATA IS ERASSED!!!!).
DISCUSSION
The purpose of this study was to
investigate how the differences in the visual perception styles influences
the visual imagery styles. Towards this end, EMRs were
recorded, an accuracy for recall test and vividness in imagery
ratings were administered. The
hypothesis was confirmed: the same eye
movement patterns during visual perception in each group were observed during
the visual imagery task. In addition, the experiment did
replicate the findings of an earlier study by Brandt & Stark (1997), by showing that
the scanpaths during imagery are the same as in direct visual perception.
The
first prediction, that the Central Fixation group shall keep the eyes fixed in
the same place during the imagery task as in the visual perception task, and
their encoding shall be limited to the fixation point was confirmed partially.
What was confirmed, was that the eye
movement pattern was identical during the perception and imagery being in fact,
fixed on the same spot. This involuntary
fixation of the gaze during imagery, has not been reported in other
studies. An explanation for this phenomena has been proposed by Kosslyn
(personal communication) for this experiment,
suggesting that efferent commands to shift attention may be stored along
the representation, during encoding, they can be also retrieved during recall.
Gauthier and colleagues (1990) have proposed the active role of the ocular
muscle proprioception in both afferent and efferent signals in controlling
the vision. Bridgeman and Stark (1991) have replicated the study
done by Gauthier and colleagues (1990), but could find only a week extraretinal proprioceptive
information provided by the muscle spindles. There have been a long dispute between the inflow theory, or
proprioception proposed by Sherrington
(Gregory, 1998) and the outflow theory proposed by Helmholtz (Gregory,1998),
each proposing a different direction of
the fed back signals from the eye muscles for visual location of
targets. The current position of Gauthier and colleagues (1990) and of Steinbach (1987), is that there is a double
fed back signals from the eye muscles; the major component of the
eye-position-coding signal is derived from both eye muscle activation and
ocular muscle proprioception that may account up to 32% (Gauthier et.al., 1990). Therefore, it might be
safe to advance an inference based on the findings of this study, that indeed,
the kinesthetic information is parallel encoded with the visual information,
and at retrieval this may be reenacted as a specific eye movement pattern. The prediction for this group concerning the
limited encoding caused by the narrowing of the gaze area supposedly followed
by the attention window was not confirmed. This fact, clearly points towards
the bad coordination, between the fixation of the gaze and the adjustment of
the attention window on the spot of the gaze. It has been proposed that the
attention window follows the eye gaze (
Schneider, 1995), but it can also
detect external stimuli from the peripheral vision ( Kosslyn, 1994). According
to this logic, if the attention window is there to select the amount of information for processing , than it should control the flow
of information also in a restrictive way, by inhibiting other areas in the
visual buffer that are not attended to.
This is clear not the case here, the participants remember all too much, and even if their attention
window was supposed to be restricted to near zero. But, the fault, so far, is
not with the cognitive mechanism, but with the participants’ attentional
mastery skills that needs to be trained. Mahabharata epic from the indian
cultural tradition, offer an
illustration of this point when it is told that the master archer Arjuna could
see only the eye of the bird to be pointed at, and not other parts of the
bird’s body. Herigell (1974) reports of similar results in his training in the
art of japanese archery. It can be that
the participants could not maintain their attention window to the limited area of the fixation point
because of lack of visual perceptual
skill. It seems that even if you have the cognitive structure, this doesn’t
become operative, unless you develop it consciously. Even if the evidence from
this study in this condition is pointing against the presence of the attention
window, it is believed that the fault may stay with the participants who were
unable to follow the experimental instructions.
The vividness predicted for the Central Fixation group was to be good, against the findings of previous studies. Vividness for
the Central Fixation group was second
in the ratings between the three groups, supporting thus the prediction,
even if several studies have proposed a
high rate for eye movements in order to obtain a vivid image (Neisser, 1967;
Sheehan & Neisser, 1969).
The second prediction,
that the Unfocused group shall keep an
immobility of the gaze, steady maintained on a particular spot
during both the visual perception and
the imagery tasks have also been confirmed. This involuntary, steady fixation
on the same spot during both visual perception and imagery task, has not been
investigated in other studies. An explanation for this kinesthetic phenomena,
might be linked to the previous research from the literature ( Gaauthier et al.,1990; Steinbach, 1987). In the Central Fixation condition, the
attention window was expected to contract to a resolution degree near to zero,
but in the Unfocused condition, the attention window was expected to expand its
resolution degree to the entire visual field. If we can equate the direction of
the gaze with the attention window during imagery, than we might infer that in
the case of the Unfocused or holistic
visual perception, the cognitive processing must be parallel. In this
condition, there is no evidence for any scanpaths , which might imply a serial
processing, while the participants remember well the encoded information from a
large resolution degree. Their visual attention was equally spread over the
entire visual field, with the experimental stimulus covering only a tiny part
of it, so, their accuracy of recall must be seen in the context of the whole
range of information in the visual field, and by this standard, their accuracy
was very high. Several other studies have indicated that a recognition of an
image was prior to the scanning the image (Norton & Stark, 1971), which
might indicate that cognitive parallel process are involved. From the studies
of eidetic memory, there is evidence that there are no eye movements, and that
the image is processes in its entirety (Hebb,1968; Haber & Haber; 1964,
Luria, 1968). The attention window, which is supposed to be limited in
resolution, as proposed by Kosslyn (1980,1994,1995) doesn’t support the
findings for the Unfocused group which could perceive simultaneously the entire
visual field. The experimental
instruction for the Unfocused group was
just to keep an equal spread attention over the entire visual field and to not
fixate on anything in particular. During the memory test for the
irregularly-checkered diagram, the five black squares were chosen out of a 200
degree of resolution , implying that
the participants must have encoded the entire field in order to search after
the supposed targets. In consequence, it is proposed an adjustable quality for
the attention window, contrary with the current theories of visual attention (
Kosslyn, 1994; Schneider, 1995).
In order to use efficient the attention window expanded to the
entire visual field, it is proposed the necessity for training of this cognitive skill. There is anecdotal evidence
(Bankei,1984; Deshimaru, 1983), about the availability of this skills in
perception, perception are not only restricted
to visual perception, but to all perception senses. The test for visual memory for this group, found, contrary to expectations, that the
retrieval was poor, which might be
interpreted either as a less effective encoding style or a lack of appropriate cognitive skills. It may
also be interpreted in support for the view
that a normal size of the attention window is important for the efficient
encoding in memory.
One prediction that was supported by the finding, was the
vividness in the Unfocused group was the highest of all groups. This might be
explained by the supposed used of parallel processes during both encoding and
retrieving. The spread activation of parallel processes might exceed in power
simple serial activation, and this may explain the increased in vividness of
the imagery. It is proposed that the vividness is connected with the power of
the brain activated during an imagery task, than with the number of eye
movements which was supposed to contribute to the increase of vividness
(Neisser,1968). Absence of eye movements have been linked to a vividness for
visual images (Marks,1973), so it may be the quality of the cognitive
processes, namely parallel processing, than the simple eye movements per see,
which may contribute to the generation of a vivid image.
The proposed holistic
visual perception, might be identified as a visual perceptual style that uses
the expansion of attention window
to the entire visual field, which can
be monitored, and processed with accuracy. The proposed holistic visual perception is supposed to include parallel processing, which might increase
the power of the mind during imagery, with consequent increasing in vividness
quality. There is increased need for developing of new cognitive skills, and
the proposed visual holistic perception might be one of them . Further research
must consider the possibility of the training of these skills, to learn to
concentrate the attention window on the spot of the gaze, skill that may
require years of hard practice, but as annedoctical evidence suggests, these skills are worth the effort.
The third prediction, that the Free
Vision group shall make the same scanpaths during the visual perception and
imagery tasks was confirmed. This was a replication of an earlier experiment
done by Brandt and Stark (1997). In addition to the replicated study, there
have been introduced two extra variables, accuracy and vividness, with the
prediction that a high accuracy in retrieval and a moderate vividness were
expected. The findings confirmed the
predictions of accuracy and vividness. The literature (Neisser, 1967; Sheehan, & Neisser, 1969) propose a high
vividness for Free Vision group, but the present experiment haven’t found this.
The vividness have been proposed to be dependent of the “power of the mind”
involved in the encoding and recall, and not a condition of the eye movement
patterns. And again, the eye movement patterns have been proposed by this
experiment to represent retrieved kinesthetic information, that have been encoded
together with the visual information, this
being the case in simple
retrieval of encoded visual information.
The role of eye movements in visual meditation
The most common type of visual meditation contains two stages: the
visual perception stage and second, the imagery or visualization stage. The
present experiment have demonstrated the influence of the visual perception
style on the imagery, proposing that there is a strict sequence of visual
perceptual skills to be followed. For the first stage of visual meditation with
mandalas and yantras, David Fontana (1991,pp.86,88) suggests:
“Try not to move the
eyes, but to take in the whole pattern from the one point of vision.”
“ If you are working with a mandala
or a yantra, try after a time to commit it to visual memory so completely that
you see it in your mind’s eye as clearly as if it hangs on the wall in front of
you.”
“Gaze at it steadily, without making
any attempt to commit it to memory. Then suddenly snap the eyes shut, and hold
the image behind your closed eyelids, almost as if you have taken a photograph
of it.”
The second stage in visual
meditation is the imagery or visualization stage that is directly influenced by
the perception style during the visual perception. After development of visual
skills, the meditation can start directly with the stage two as described by
Fontana (1995,pp.88):
“Before very long, you will find
that you are able to visualize the shape at will as soon as you close your
eyes, even without first gazing at it.”
The aim of visual meditation is the stabilization of the image effect,
which makes the image disappear completely living only a “blank- out” or an
awareness of sheer emptiness
In order to achieve a stabilization of an image, the stimulus must fall
constantly in the same place on the retina. To achieve a perfect stabilization
of image in direct visual perception, complex devices are needed ( Yarbus,
1967), but to achieve it in imagery it is much more easy. This is why, all the
mystical traditions, use the imagery techniques in order to achieve the stabilization
of image effect in the internal space (Kosslyn, 1994).
The function of the eye movements in
imagery is not clear, but the present study points toward a close connection of
the attention window with the oculomotor muscles. In order to achieve a
stabilization of the image in imagery, it is important that the image is kept
constant in the internal space and this is done by the attention window
directly connected with the oculomotor muscles.
Any saccadic movements that may
appear in imagery may disrupt the stabilization of the image and forsake the
goal of meditation, namely, achieving a state free of visual perceptual
stimuli.
In order to don’t have eye movements
during imagery, it is necessary to encode the visualized object using either
Fixation or Unfocussed visual perception styles. The proposed connection
between the attention window and the oculomotor muscles, makes impossible to
retrieve an image without being accompanied by eye movements, if it was encoded
using Free Vision with saccades. The optical nystagmus in visual perception
affects the stabilization of the image, but in imagery, the effect is low.
Stabilization of image effects on
the brain waves activity have been investigated by Lehmann and colleagues
(1967) who observed an increase of alpha rhythm, when the image disappeared.
The same effect have been reported also from the studies on “ganzfelt” defined
as a homogenous visual imput(Cohen & Cadwallader, 1958; Broughton, 1992).
EEG alpha activity have been
found to be influenced by emotions, mental effort, orienting reaction,
attention level and actual oculomotor activity ( Mulholland & Evans, 1966;
Zikmund, 1972 ). The reason for alpha blocking could be attributed to
mechanisms controlling alertness ( Oswald, 1957).
The EEG studies on alpha rhythm
during imagery, have been rather confusing, some finding a suppression or
blocking of the EEG alpha rhythm during visual imagery (Mundy- Castle, 1957 ),
others finding no blocking of the alpha rhythm ( Barratt, 1956; Zikmund, 1972).
For example, Zikmund (1972) found that effortless visual imagery is accompanied
by EEG alpha rhythm.
The easiest meditation
experiment on the habituation effect in the visual system is to keep the eyes
open and to stare straight ahead in a completely obscure room. After some
minutes, the person shall lose the control over the position of the eyes, not
knowing if the eyes are open or shut and a meditative state shall be reach.
The importance of this
experiment to the meditation research is that it has identified that the eye
movement patterns are encoded together with the image and at retrieval during
imagery of the image, the same eye movement patterns are present. We have
inferred that the phenomenon of stabilizing of image in the visual perception
can be extended to imagery, suggesting an easier process, only in the
situations when the encoding of the visualized image have been without
saccades. The visual perceptual styles, such as Fixation and Unfocused are
proposed to be the only possible encoding strategies in visual meditation that
includes imagery. The normal visual perception, or Free Vision perception
style, encodes together with the image also the saccades, which at retrieval
are reenacted. The eye movements disrupts the stabilization of image during
imagery, and this makes the attaining of meditative absorption- Samadhy,
impossible.
The ultimate aim of
meditation is a direct experience of the Reality, the transcendence of
perceptual phenomena (Naranjo & Ornstein, 1974).
When during visualization, the contemplated image disappears because of
the stabilization effect, what remains is the pure experience of awareness of
what IS. This experience must not be interpreted, reductionistic, in the
tradition of cognitive science, which equates the brain with mind, but in a
transpersonal perspective which acknowledge a mind that use a brain for its
purposes ( Eccles, 1994).
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