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<article article-type="research-article" xmlns:xlink="http://www.w3.org/1999/xlink">
 <front>
    <journal-meta>
	<journal-id journal-id-type="publisher-id">Jemr</journal-id>
      <journal-title-group>
        <journal-title>Journal of Eye Movement Research</journal-title>
      </journal-title-group>
      <issn pub-type="epub">1995-8692</issn>
	  <publisher>								
	  <publisher-name>Bern Open Publishing</publisher-name>
	  <publisher-loc>Bern, Switzerland</publisher-loc>
	</publisher>
    </journal-meta>
    <article-meta>
	<article-id pub-id-type="doi">10.16910/jemr.10.2.2</article-id> 
	  <article-categories>								
				<subj-group subj-group-type="heading">
					<subject>Research Article</subject>
				</subj-group>
		</article-categories>
      <title-group>
        <article-title>How a distractor influences fixations during the exploration of natural scenes</article-title>
      </title-group>
	   <contrib-group> 
				<contrib contrib-type="author">
					<name>
						<surname>Devillez</surname>
						<given-names>H&#xE9;l&#xE8;ne</given-names>
					</name>
					<xref ref-type="aff" rid="aff1">1</xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Gu&#xE9;rin-Dugu&#xE9;</surname>
						<given-names>Anne</given-names>
					</name>
					<xref ref-type="aff" rid="aff2">2</xref>
				</contrib>
				<contrib contrib-type="author">
					<name>
						<surname>Guyader</surname>
						<given-names>Nathalie</given-names>
					</name>
					<xref ref-type="aff" rid="aff2">2</xref>
				</contrib>
        <aff id="aff1">
		<institution>University of Colorado Boulder</institution>, <country>USA</country>
        </aff>
		<aff id="aff2">
		<institution>Universite&#x301; de Grenoble-Alpes</institution>, <country>France</country>
        </aff>
		</contrib-group>
     
	  <pub-date date-type="pub" publication-format="electronic"> 
		<day>10</day>  
		<month>4</month>
        <year>2017</year>
      </pub-date>
	  <pub-date date-type="collection" publication-format="electronic"> 
	  <year>2017</year>
	</pub-date>
      <volume>10</volume>
      <issue>2</issue>
	  <elocation-id>10.16910/jemr.10.2.2</elocation-id>
	<permissions> 
	<copyright-year>2017</copyright-year>
	<copyright-holder>Devillez et al.</copyright-holder>
	<license license-type="open-access">
  <license-p>This work is licensed under a Creative Commons Attribution 4.0 International License, 
  (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">
    https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use and redistribution provided that the original author and source are credited.</license-p>
</license>
	</permissions>
      <abstract>
        <p>The distractor effect is a well-established means of studying different aspects of fixation programming during the exploration of visual scenes. In this study, we present a taskirrelevant distractor to participants during the free exploration of natural scenes. We investigate the control and programming of fixations by analyzing fixation durations and locations, and the link between the two. We also propose a simple mixture model evaluated using the Expectation-Maximization algorithm to test the distractor effect on fixation locations, including fixations which did not land on the distractor. The model allows us to quantify the influence of a visual distractor on fixation location relative to scene saliency for all fixations, at distractor onset and during all subsequent exploration. The distractor effect is not just limited to the current fixation, it continues to influence fixations during subsequent exploration. An abrupt change in the stimulus not only increases the duration of the current fixation, it also influences the location of the fixation which occurs immediately afterwards and to some extent, in function of the length of the change, the duration and location of any subsequent fixations. Overall, results from the eye movement analysis and the statistical model suggest that fixation durations and locations are both controlled by direct and indirect mechanisms.</p>
      </abstract>
      <kwd-group>
        <kwd>Natural scenes</kwd>
        <kwd>Free exploration</kwd>
        <kwd>Eye Movement</kwd>
        <kwd>Distractor Effect</kwd>
        <kwd>Fixation control</kwd>
        <kwd>Saliency</kwd>
        <kwd>Statistical modeling</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>

    <sec id="S1">
      <title>Introduction</title>
	  
      <p>Human vision during visual perception is an active
process where observers select information relevant to
their exploration goal (
        <xref ref-type="bibr" rid="R5">5</xref>
        ). When viewing a visual scene,
we typically make three to four eye fixations per second.
At each fixation, decisions are made regarding the next
fixation, and the next saccade is programmed. This
programming involves the decision to terminate the current
fixation (when) and the choice of location for the next
fixation (where). Both characteristics have been widely
studied, most of the time separately, in order to gain
better understanding of saccade programming during
scene exploration (
        <xref ref-type="bibr" rid="R17 R30">17, 30</xref>
        ). The scene onset delay paradigm
has shown that fixation durations can be divided into two
populations: one population which comes under the direct
control of the scene and which increases in duration as
the delay is increased, and a second population, not under
the direct control of the current scene, whose duration
does not increase, irrespective of scene presence. These
results support a mixed eye movement control model (
        <xref ref-type="bibr" rid="R7 R8">7, 8</xref>
        ). Other paradigms have been proposed to study which
factor influences saccade programming and fixation
duration. The <italic>remote distractor effect</italic> is a well-known
phenomenon where saccadic responses to a visual target are
delayed if a distractor and the target are flashed
simultaneously. Results have clearly shown that remote
distractors modified not only saccade trajectory and landing
location (
        <xref ref-type="bibr" rid="R25 R11">25, 11</xref>
        ), but also saccade latency (
        <xref ref-type="bibr" rid="R29 R28 R16">29, 28, 16</xref>
        ). It has also
been shown that the time needed to select the next
fixation and to program the next saccade was impacted by the
distance of the distractor from the locations of the central
fixation and the saccade target (
        <xref ref-type="bibr" rid="R15">15</xref>
        ). Saccade amplitudes
can also be also impacted, as saccades tend to land at
intermediate locations between the saccade target and the
distractor location (
        <xref ref-type="bibr" rid="R29">29</xref>
        ).</p>
		
      <p>The effect of a distractor has also been studied using
more ecological paradigms during which observers
explored natural scenes. This effect is called the <italic>distractor
effect</italic>. Authors using these paradigms deal with fixation
durations rather than saccade latencies because there is no
explicit saccade target. Brockmole and Henderson (
        <xref ref-type="bibr" rid="R1">1</xref>
        )
found that an object, which appeared after 500 ms of
exploration, captured the attention immediately, and
suggested that transient motion captures attention in a
bottom-up manner.</p>

      <p>In a series of experiments, Pannasch and colleagues
used digitized paintings and a gaze contingent irrelevant
distractor onset (
        <xref ref-type="bibr" rid="R20 R19 R18">20, 19, 18</xref>
        ). They showed that any visual
change prolongs the current fixation duration in
comparison to previous and subsequent fixations. This result
suggests that fixation durations are under the direct
control of stimulus information (
        <xref ref-type="bibr" rid="R19">19</xref>
        ). The distractor effect on
fixation duration was analyzed in relation to a number of
different factors. The authors tested different stimulus
onset asynchronies and showed similar distractor effects
for each of these asynchronies. They also measured the
influence of the distractor on fixation durations in relation
to the amplitude of the preceding saccade, and showed
that visual distractors had significantly more influence if
the amplitude of the previous saccade was less than 5&#xB0;
(
        <xref ref-type="bibr" rid="R20">20</xref>
        ). In addition, they found that the effect of the
distractor on fixation duration was stronger when it was close to
the current fixation (
        <xref ref-type="bibr" rid="R18">18</xref>
        ).</p>
		
      <p>However, while the effect of a distractor on the
duration of a current fixation has been widely studied, the
influence of the distractor on subsequent fixations has
been relatively neglected. The question of whether
distractor onset, known to increase the duration of the
current fixation, also influence the programming of the next
saccade has yet to be investigated. It has been shown that
a distractor flashed during a fixation increases the
duration of the fixation. We also know that the next fixation is
programmed during the current fixation. We therefore
wondered if the distractor location would become a
potential target location for the next fixation. In our data
analysis, we explored the link between the increase in the
duration of the current fixation and the programming of
the next saccade, leading to the next fixation location, in
function of distractor duration. We asked if a distractor
that strongly increases fixation duration had a greater
chance of being gazed at in subsequent fixations, and for
how long a distractor needed to be displayed in order to
be targeted during subsequent fixations. In this study, we
aimed to investigate the control and programming of
successive fixations during the exploration of natural
scenes through the appearance of an irrelevant distractor.
A Gabor patch was flashed at the onset of a fixation
which occurred at the beginning of exploration. Three
different durations were used for the distractor: the
distractor appeared and disappeared within the fixation; the
distractor was present during the whole fixation; or the
distractor never disappeared. These three conditions were
compared to a control condition during which no
distractor was flashed.</p>

      <p>We began by studying the distractor effect on
classical eye movement parameters (fixation durations and
fixation locations). This allowed us to validate the
proposed protocol by replicating the distractor effect during
the free exploration of natural scenes. We measured how
the distractor modified the fixations that followed its
onset, and the link between the distractor effect on the
current fixation duration and the location of subsequent
fixations. We hypothesized that if the distractor had an
effect on the current fixation, measured by an increase in
duration, it would be gazed at more often during
subsequent fixations. We already know that the next fixation
location is chosen during the current fixation. We might
suppose that the increase in duration of the current
fixation is due to the fact that the distractor attracts visual
attention, and therefore becomes a potential target
location for the next fixation. We tested our hypothesis using
several distractor durations. One could legitimately
hypothesize that when a distractor is presented for a longer
duration, the visual system has more time to encode its
precise location. If this was the case, we would observe a
greater impact on fixation locations which followed, with
more fixations landing on the distractor.</p>

      <p>Secondly, we proposed a simple statistical model to
evaluate the contribution of a distractor to fixation
locations observed, relative to scene saliency. It is already
well known that fixations are driven, at least in part, by
the saliency of the scene, which is defined by the
locations that attract observers&#x2019; gaze (
        <xref ref-type="bibr" rid="R14 R23 R13">14, 23, 13</xref>
        ). The model also
allowed us to evaluate the distractor effect on fixations
other than those that landed on the distractor location.
The proposed model assumes that recorded fixations
might be explained by a linear combination of two
guiding factors represented by 2D spatial maps: (1) the region
of interest of the scene evaluated by experiment saliency
maps and (2) the influence of the distractor evaluated by
a localized Gaussian function. The influence of each
factor was evaluated using the Expectation-Maximization
(EM) algorithm. This algorithm has been successfully
applied in visual attention models (
        <xref ref-type="bibr" rid="R27 R9 R2 R6 R3">27, 9, 2, 6, 3</xref>
        ).</p>
    </sec>
	
    <sec id="S2">
      <title>Material and methods</title>
      <sec id="S2a">
        <title>Stimuli</title>
		
        <p>We used 156 real-world images representing a large
variety of scenes (landscapes, buildings, indoor scenes)
(Figure 1). Scenes were presented in grayscale and had a
resolution of 768 by 1024 pixels and were presented in
full screen subtending a visual angle of 30&#xB0; &#xD7; 40&#xB0;. All
scenes were equalized to an average luminance of 127
(luminance values were between 0 and 255).</p>

<fig id="fig01" fig-type="figure" position="float">
					<label>Figure 1</label>
					<caption>
						<p>Examples of scenes without (left column) and with the distractor (right column); distractors always appeared 4° from the scene center.</p>
					</caption>
					<graphic id="graph01" xlink:href="jemr-10-02-b-figure-01.png"/>
				</fig>
      </sec>
	  
      <sec id="S2b">
        <title>Distractor</title>
		
        <p>The distractor, a Gabor patch, was inserted into the
scene. The patch had a radius R<sub>d</sub> of 2.2&#xB0; (i.e. 56.4 pixels)
with maximal luminance contrast. The distractor shape
corresponded to a 2D Gaussian function modulated by a
vertical sinusoid with a spatial frequency of 2.2 cycles
per degree. It appeared at the onset of the second detected
fixation<xref ref-type="fn" rid="FN1">1</xref>. Note that &#x201C;fixation 1&#x201D; refers to the first fixation
that occurred after scene onset (and not the fixation that
started before scene onset). To speed up the display of the
scene with the distractor at the second fixation, this scene
was computed before the experiment. For each scene,
four different locations for the distractor were chosen
randomly on a 4&#xB0; radius-centered circle.</p>
      </sec>
	  
      <sec id="S2c">
        <title>Apparatus</title>
		
        <p>Eye movements were recorded using the SR Research
Eyelink II (500 Hz) infrared eye tracking system. Stimuli
were presented on a 20-inch ViewSonic CRT monitor,
with a resolution of 768 by 1024 pixels, a refresh rate of
85 Hz, at a viewing distance of 57 cm. Experiments were
run using SoftEye (
        <xref ref-type="bibr" rid="R10">10</xref>
		).</p>
      </sec>
	  
      <sec id="S2d">
        <title>Protocol</title>
		
        <p>Each trial started with a white fixation cross presented
for 1 s on a gray screen. This fixation cross was located
on the screen diagonals 5&#xB0; from the center. After 1 s, and
if gaze had stabilized for 100 ms (gaze contingent
display), the scene was displayed. If the participant did not
gaze at the cross, the scene was still displayed after 5 s,
but the trial was considered invalid and recorded data
were not analyzed.</p>

        <p>In the control condition, the scene was displayed for
2.5 s. Three distractor conditions were used. The
distractor always appeared at the onset of fixation 2, an early
fixation known to be mainly guided by the visual
properties of the scene. As already mentioned, the starting point
of exploration was on the screen diagonals 5&#xB0; from the
center of the screen. The probability that fixation 1 would
appear on the scene center was therefore very high, due
to the &#x201C;central bias&#x201D; observed during eye movement
experiments (
          <xref ref-type="bibr" rid="R24">24</xref>
          ). The distractor was displayed for 50 ms
(Short Presentation Time: SPT), 210 ms (Medium
Presentation Time: MPT) or until the end of the
exploration (Long Presentation Time: LPT). The duration of
scene presentation was therefore different in these three
distractor conditions. In the SPT condition, scenes
containing a distractor were displayed for 50 ms, and then,
scenes with no distractor were shown for 2250 ms. In the
MPT condition, a scene featuring the distractor was
displayed for 210 ms and followed by the same scene
without the distractor for 2090 ms. In the LPT condition, a
scene with the distractor was displayed for 2300 ms.
Distractor onset was synchronized with the onset of
fixation 2 for each scene and each observer. On average, it
appeared 580 ms after scene onset. Finally, at the end of
the trial, a gray screen appeared for 1 s (Figure 2).</p>

<fig id="fig02" fig-type="figure" position="float">
					<label>Figure 2</label>
					<caption>
						<p>Trial sequence with distractor onset triggered on fixation 2. In the control condition, scenes were displayed without the distractor for 2.5 sec. In distractor conditions, the distractor was displayed for three different durations: 50 ms (Short Presentation Time), 210 ms (Medium Presentation Time) and during the whole exploration (Long Presentation Time).</p>
					</caption>
					<graphic id="graph02" xlink:href="jemr-10-02-b-figure-02.png"/>
				</fig>

        <p>Observers were asked to look carefully at scenes in
preparation for a questionnaire on scene content. The
questionnaire was never actually given. A 9-point
calibration routine was completed and repeated every 50 trials
or if the drift correction, completed every ten trials,
detected an error above 0.5&#xB0;.</p>
      </sec>
	  
      <sec id="S2e">
        <title>Participants</title>
		
        <p>Forty-eight na&#xEF;ve healthy volunteers with normal or
corrected-to-normal vision took part in the experiment
(17 female; age range: 21-27, M=24.12, SD=2.46).
Participants were assigned randomly to one of four
experimental conditions: the control condition (without the
distractor) or one of the three distractor conditions (SPT,
MPT or LPT). In the control condition, participants
viewed all 156 scenes. In the distractor conditions, each
participant viewed only 52 of the 156 scenes. In the MPT
and LPT conditions, all participants reported perceiving
the distractor. However, in the SPT condition only 10 out
of 12 reported it. We analyzed only the data from these
10 participants in order to maintain consistency. Analyses
indicated that the two observers who did not notice the
distractor differed from the other participants in their eye
movement patterns but showed no increase in fixation
durations.</p>
      </sec>
	  
      <sec id="S2f">
        <title>Data analysis</title>
		
        <p>Raw eye-movement data were preprocessed by
removing fixations that occurred around eye blinks or
outside the presentation screen. Fixations whose duration
was shorter than 50 ms or longer than 1000 ms were
excluded. In total, less than 10% of the data was
removed, including invalid trials.</p>

        <p>Because the distributions of fixation durations were
skewed, median values were used for each subject per
condition. Eye fixation locations were also extracted and
the proportion of fixations that landed on the distractor
was computed. In order to test if the proportions of
fixations that landed on the distractor location were greater in
the distractor conditions than in the control condition, we
calculated the proportion of fixations recorded at the
distractor location in the control condition (with no
distractor). Fixations were represented by a circle of 1&#xB0;
around the fixation location and classified as being on the
distractor if there was an intersection between the circle
with a radius of 2.2&#xB0; representing the distractor and the
circle with a radius of 1&#xB0; representing the fixation.</p>

        <p>For each scene, we computed a map highlighting all
the regions of interest. These maps were called empirical
saliency maps. They were created using fixations
recorded during the control condition. Empirical saliency maps
were obtained for each scene by summing a 2D Gaussian
with a standard deviation of 1&#xB0; centered on fixations. The
size of Gaussians was chosen in relation to foveal size
and eye-tracker accuracy. It should be noted that only
fixations 2 to 8 were used; we did not use fixation 1,
mainly due to central bias (
          <xref ref-type="bibr" rid="R24">24</xref>
          ). Empirical saliency maps
were then converted into binary maps using a threshold
of 0.2 (for eye movement analysis) or normalized to 1 to
correspond to probability density function (for the
modeling part). These maps obtained using the eye fixations of
several observers predict the fixations of other observers
about as well as the best saliency models do. Even if
individual differences do exist between observers,
consistency between the fixations of several observers has
been reported, making the prediction of fixation locations
of one observer by using the fixations of other observers
efficient (
          <xref ref-type="bibr" rid="R26 R12">26, 12</xref>
          ).</p>
      </sec>
    </sec>
	
    <sec id="S3">
      <title>Results: Eye movements</title>
	  
      <p>The distractor effect was measured on both fixation
durations and locations based on the fixation order in
scene exploration. Analysis of the distractor effect also
took into account the saliency of the scene, computed by
empirical saliency maps.</p>

      <p>Analyses were conducted using a repeated measures
Analysis of Variance (ANOVA).</p>

      <sec id="S3a">
        <title>Fixation duration</title>
		
        <p>A repeated-measure ANOVA was conducted with
Fixation (fixation 1 to 8) as a within-subjects factor and
Condition (control/SPT/MPT/LPT) as a between-subjects
factor. We found main effects of <italic>Condition</italic>, F(3,41) =
9.65, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.41, and Fixation, F(7,287) = 10.59,
p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.20. The interaction Condition &#xD7; Fixation
was also significant, F(21,287) = 2.47, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; =
0.15 (Figure 3). Multiple comparisons of distractor
conditions to the control condition were assessed with Dunnett
post-hoc tests. The distractor effect was particularly
noticeable at fixation 2, during which the distractor
appeared. Its duration significantly increased in the three
distractor conditions compared to the control condition (p
&lt; .05 &#x2013; marginal effect for LPT, p = 0.06). We observed
an equal increase of the duration of fixation 2 in the three
distractor conditions. The fixation following distractor
onset (fixation 3) also increased in duration compared to
the control condition in the MPT and LPT conditions (p &lt;
.05). Moreover, in the LPT condition, fixations 4 to 8
were longer than in the control condition (p &lt; .05).
Finally, the fixation preceding distractor onset (fixation 1) was
more prolonged in the LPT condition than in the control
condition (p &lt; .05).</p>

<fig id="fig03" fig-type="figure" position="float">
					<label>Figure 3</label>
					<caption>
						<p>Mean fixation duration in milliseconds as a function of fixation order (fixations 1 to 8) for the control condition and the three distractor conditions (SPT, MPT and LPT). Error bars represent standard error.</p>
					</caption>
					<graphic id="graph03" xlink:href="jemr-10-02-b-figure-03.png"/>
				</fig>
      </sec>
	  
      <sec id="S3b">
        <title>Fixation location</title>
		
        <p>A repeated-measure ANOVA was conducted with
Fixation (fixation 2 to 8) as a within-subjects factor and
Condition (control/SPT/MPT/LPT) as a between-subjects
factor. The analysis revealed main effects of Condition,
F(3,41) = 9.55, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.41, and Fixation,
F(6,246) = 37.82, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.48. The interaction
Condition &#xD7; Fixation was also significant, F(18,246) =
6.78, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.33 (Figure 4). Multiple
comparisons of distractor conditions to the control condition were
assessed with Dunnett post-hoc tests. The proportion of
fixation 3s on the distractor, i.e. the fixation immediately
following distractor onset, was higher in all distractor
conditions compared to the control condition (p &lt; .01).
The proportion of fixation 4s on distractor location was
also higher for MPT and LPT than in the control
condition (p &lt; .01). In the LPT condition, the proportion of
fixations 5 to 7 that landed on the distractor was again
higher than in the control condition (p &lt; .05).</p>

<fig id="fig04" fig-type="figure" position="float">
					<label>Figure 4</label>
					<caption>
						<p>Mean proportion of fixations on the distractor location as a function of fixation order (fixations 2 to 8) for the control condition and the three distractor conditions (SPT, MPT and LPT). Error bars represent standard error.</p>
					</caption>
					<graphic id="graph04" xlink:href="jemr-10-02-b-figure-04.png"/>
				</fig>

        <p>Results on fixation durations and fixation locations were
coherent: the current fixation increased in duration and
the following fixation had a high probability of landing
on the distractor location. The following analysis directly
tested the link between the distractor effect on the
duration of fixation 2 and the location of fixation 3.</p>

        <sec id="S3ba">
          <title>Relation between fixation 2 duration and fixation 3 location</title>
		  
          <p>Three separated chi-square tests were conducted to
test the independence of fixation 2 duration (Short/Long)
and fixation 3 location (In/Out). Fixation 2 duration was
divided into two groups according to the duration of
fixation 2 during the Control condition (Short: &lt; 223 ms;
Long: &gt; 223 ms). There was a dependence link between
fixation 2 duration and fixation 3 location for MPT,  &#x3C7;<sup>2</sup> =
9.44, p &lt; 0.01, and LPT,  &#x3C7;<sup>2</sup> = 34.49, p &lt; 0.001. For these
conditions, trials with long fixation 2s also showed more
fixation 3s inside the distractor location. No dependency
link between fixation 2 duration and fixation 3 location
was observed for SPT,  &#x3C7;<sup>2</sup> = 0.29, p = 0.86 ns.</p>
        </sec>
		
        <sec id="S3bb">
          <title>Fixation 3 location and saliency</title>
		  
          <p>A repeated-measure ANOVA was conducted on
fixation 3 location, with <italic>Saliency</italic> (Salient/Non salient
distractor) as a within-subjects factor and <italic>Condition</italic>
(SPT/MPT/LPT) as a between-subjects factor. Statistical
analysis revealed a main effect of <italic>Saliency</italic>, F(1,31) =
22.53, p &lt; .001, &#x3B7;<sub>p</sub>&#x00B2; = 0.42. No effect of <italic>Condition</italic>,
F(2,31) = 1.95, p = .16 ns, &#x3B7;<sub>p</sub>&#x00B2; = 0.11, was observed and
the interaction <italic>Saliency &#xD7; Condition</italic> was not significant,
F(2,31) = .47, p = .63 ns, &#x3B7;<sub>p</sub>&#x00B2; = 0.03. Multiple
comparisons were assessed with Bonferroni post-hoc tests. For
MPT and LPT, the proportion of fixation 3s on the
distractor was higher when the distractor location was
salient (p &lt; .05).</p>
        </sec>
      </sec>
	  
      <sec id="S3c">
        <title>Interim summary</title>
		
        <p>In line with previous studies (
          <xref ref-type="bibr" rid="R12 R13">12, 13</xref>
          ), an increase in
the mean duration of fixation 2s and a high probability of
observing fixation 3s on the distractor location, were
observed. These parameters were linked when the
distractor was presented for longer durations: more fixation 3s
were observed inside the distractor location when fixation
2s were of longer duration. Although the effect of the
distractor was the same on the duration of fixation 2 in
the three distractor conditions, we observed differences
on subsequent fixations. Distractors of longer duration
had a greater impact on the location and even on the
duration of subsequent fixations. Finally, the distractor
effect was influenced by scene saliency at the distractor
location: a stronger distractor effect was observed with an
increase in the proportion of fixation 3s on the distractor
location, when the distractor appeared in a salient
location. We measured the distractor effect only on fixations
that landed on the distractor location with these eye
movement analyses. Furthermore, the analysis presented
did not allow us to quantify the contribution of the
distractor in relation to scene saliency, which is known to
drive fixation location during the exploration of scenes.</p>
      </sec>
    </sec>
	
    <sec id="S4">
      <title>Statistical modeling</title>
	  
      <p>In this section, we proposed a mixture model to
quantify the relative importance of scene saliency and the
presence of the distractor on fixation locations. This
model focused only on fixation locations and did not take
into account fixation durations. One important property
of the model was its capacity to capture the influence of
the distractor on all fixations, including fixations which
did not land on the distractor location. Furthermore, the
model evaluated the effect of the distractor at onset and
on subsequent fixations.</p>

      <sec id="S4a">
        <title>The proposed model</title>
		
        <p>The proposed statistical model explains the
distribution of recorded eye fixation locations using a linear
weighted summation of three possible guiding factors.
We used the Expectation-Maximization (EM) algorithm,
a statistical method using the recorded eye movements to
calculate the relative contribution of each guiding factor
in order to maximize the global likelihood of the mixture
model (
          <xref ref-type="bibr" rid="R21">21</xref>
          ).</p>
		  
        <p>The first factor known to guide eye movement during
scene exploration is the saliency of a scene. We used the
experiment saliency map: S<sub>m</sub>(p), with  p=(x,y) the 2D
fixation position.</p>

        <p>The second factor in the model was the impact of
distractor<xref ref-type="fn" rid="FN2">2</xref> appearance on a given position. In line with
previous results showing the attractiveness of the distractor,
this factor was modeled by a 2D Gaussian function:
 &#x39D;(p;&#x3BC;(t),&#x3C3;(t)). In other words,  &#x3BC;(t) (mean) was the
spatial position and the parameter  &#x3C3;(t) (standard
deviation) represented the size of the Gaussian. The parameters
 &#x3BC;(t) and  &#x3C3;(t) were estimated for each fixation order  .
This factor acted as a &#x201C;localizer Gaussian&#x201D; and indicated
that fixation locations were gathered on a particular
spatial location modeled by the Gaussian. The ability of this
factor to reflect the influence of the distractor on fixation
locations was related to the parameters  &#x3BC;(t),  &#x3C3;(t) of the
Gaussian function. For this reason we named this second
factor the &#x201C;Gaussian&#x201D; and not the &#x201C;distractor&#x201D; factor.</p>

        <p>Finally, even if the saliency of the scene and the
distractor were the two main factors which explained eye
movements, a third factor was added to cover any other
non-controlled processes which may have influenced eye
movements. This third factor was a noise factor, and
explains any fixations that were not explained by the two
other factors. The lower the weight of this factor was, the
better the other factors explained the data. It was simply
modeled by a uniform spatial distribution on the whole
image:  U(p) and was called &#x201C;noise factor&#x201D; for simplicity.</p>

        <p>The guiding factors that explain fixation locations
after distractor onset could be confounded: when the
distractor appeared in a salient location, the contributions of
the scene saliency and the distractor could not be
distinguished. Consequently, only trials where the distractor
was not in a salient location were used in the proposed
model. 49% of the trials were therefore used. This also
allowed us to avoid instability in the convergence of the
parameters of the model.</p>

        <p>The density function  f(p,t) of the fixation position 
p=(x,y) at each fixation order t was expressed in terms
of an additive mixture of the three spatial maps, each
associated with a given prior probability or weight
&#x3B1;<sub>i</sub>(t),i = 1,2,3:</p>

        <p>f(p,t)=&#x3B1;&#x2081;(t)&#xD7;S<sub>m</sub>(p)+ &#x3B1;&#x2081;(t)&#xD7;&#x39D;(p;&#x3BC;(t),&#x3C3;(t))+&#x3B1;&#x2083;(t)&#xD7;U(p)</p>

        <p>with p=(x,y) the 2D fixation position, f(p,t) the eye
fixation map for one distractor condition (SPT, MPT, or
LPT) at each fixation order t (t= 2:8) and &#x3B1;<sub>i</sub>(t) the
estimated weights of the factor  with &#x3B1;&#x2081;(t)+&#x3B1;&#x2081;(t)+&#x3B1;&#x2083;(t) = 1. 
&#x3B1;&#x2081;(t) represented the weight of the saliency
map, &#x3B1;&#x2081;(t) the weight of the Gaussian factor and &#x3B1;&#x2083;(t)
the weight of the &#x201C;noise factor&#x201D;.</p>

        <p>The EM algorithm was used for each distractor
condition, for each fixation order, to calculate unknown
parameters. To deal with the sensitivity of the estimated
parameters to initial conditions, ten randomly chosen
values for the initialization were used.</p>

        <p>The parameters &#x3BC;(t) and &#x3C3;(t) of the Gaussian factor,
which were free parameters across fixation order, were
calculated. For each fixation order  , and each distractor
condition, the number of estimated parameters was six
(&#x3B1;&#x2081;(t),&#x3B1;&#x2081;(t),&#x3B1;&#x2083;(t),&#x3BC;<sub>x</sub>(t),&#x3BC;<sub>y</sub>(t) 
and &#x3C3;(t) with &#x3C3;<sub>x</sub>(t)=&#x3C3;<sub>y</sub>(t)=&#x3C3;(t)), and five degrees 
of freedom (&#x3B1;&#x2081;(t)+&#x3B1;&#x2081;(t)+&#x3B1;&#x2083;(t)=1). 
The attractiveness of the distractor was analyzed by both the weight, and the spatial
parameters (&#x3BC;(t),&#x3C3;(t)) at the convergence. Consequently,
interpretation of this factor as a guiding factor during the
exploration could be carried out only once estimated
parameters had been obtained at the EM convergence.
More precisely, the interpretation of this &#x201C;localized
Gaussian&#x201D; factor as the &#x201C;distractor factor&#x201D; was only
justified when the mean corresponded to the physical position
of the distractor. To evaluate it, the Euclidean distance
d<sub>&#x3BC;</sub>(t)=d<sub>E</sub>(&#x3BC;(t),D&#x2080;) between &#x3BC;(t) and the spatial
location D&#x2080; of the distractor, was computed, in function of the
fixation order t. If this distance was different from zero,
the nature of this factor changed. In other words, its
interpretation depends on the distance d<sub>&#x3BC;</sub>(t). If the distance
is high, this Gaussian factor does not represent the
distractor accurately, but rather indicates that fixation
locations are gathered at a particular spatial location modeled
by the Gaussian function. That is why we chose to call
this guiding factor the &#x201C;localized Gaussian&#x201D; factor.</p>
      </sec>
	  
      <sec id="S4b">
        <title>Results</title>
		
        <p>The saliency map weight &#x3B1;&#x2081;(t) was the highest for all
fixations and distractor conditions (Figure 5). Although
the scene saliency map had the highest weight, the weight
of the Gaussian factor was not negligible. As expected,
the temporal evolution of the Gaussian factor (&#x3C3;(t) and d<sub>&#x3BC;</sub>(t) 
was different in the various distractor conditions
(Figure 7).</p>

<fig id="fig05" fig-type="figure" position="float">
					<label>Figure 5</label>
					<caption>
						<p>Contributions (weights) of the three factors for the three distractor conditions SPT, MPT and LPT as a function of fixation order. Mean estimations across initializations and corresponding standard errors are plotted. Note that standard error bars are really small.</p>
					</caption>
					<graphic id="graph05" xlink:href="jemr-10-02-b-figure-05.png"/>
				</fig>
				
<fig id="fig07" fig-type="figure" position="float">
					<label>Figure 7</label>
					<caption>
						<p>Evolution of &#x3C3;(t) (<bold>A</bold>) and d<sub>&#x3BC;</sub>(t) (<bold>B</bold>), in degrees, for the three distractor conditions SPT, MPT and LPT as a function of fixation order. Mean estimations across initialization and corresponding standard errors are plotted. The dark blue line shows the radius R<sub>d</sub>=2.2&#xB0; of the distractor (<bold>A</bold>) and the distance 𝐷&#x2080; of the distractor from the image center (<bold>B</bold>).</p>
					</caption>
					<graphic id="graph07" xlink:href="jemr-10-02-b-figure-07.png"/>
				</fig>				

        <p>In the three distractor conditions, at fixation 2, the
standard deviation  &#x3C3;(2) was larger and the distance
d<sub>&#x3BC;</sub>(2) close to zero, showing a mode close to the image
center (Figure 6). At this fixation, the distractor had not
yet been displayed. The fact that this mode was close to
the scene center illustrated the central bias currently
observed in eye movement data (
          <xref ref-type="bibr" rid="R24">24</xref>
          ).</p>
		  
<fig id="fig06" fig-type="figure" position="float">
					<label>Figure 6</label>
					<caption>
						<p>Spatial representation of the evolution of the Gaussian factor, for the three distractor conditions SPT, MPT and LPT as a function of fixation order. The colored circles show the estimated Gaussian factor and are located at the spatial position (&#x3BC;<sub>x</sub>(t),&#x3BC;<sub>y</sub>(t)) and with a size &#x3C3;(t); these parameters were evaluated by the model.. The black circle shows the distractor location with it size R<sub>d</sub>.</p>
					</caption>
					<graphic id="graph06" xlink:href="jemr-10-02-b-figure-06.png"/>
				</fig>		  
		  
        <p>For SPT and MPT conditions, the evolution of &#x3C3;(t)
and d<sub>&#x3BC;</sub>(t) was divided into three phases. Firstly, between
fixations 2 and 3, the Gaussian weight &#x3B1;&#x2081;(t) increased
slightly (Figure 5). At the same time, the deviation &#x3C3;(t)
decreased and became smaller than the size R<sub>d</sub> of the
distractor. Secondly, after fixation 3, d<sub>&#x3BC;</sub>(t) decreased to
almost zero and &#x3C3;(t) was slightly larger than R<sub>d</sub> (Figure
7). In the MPT condition, the Gaussian factor was more
attractive, as we can see for fixations 3 and 4. We
observed smaller values for &#x3C3;(3) and &#x3C3;(4), which in turn
were even smaller than R<sub>d</sub> (Figure 7A). The mean &#x3BC; was
at the location of the distractor (Figure 6). From fixations
4 to 6, &#x3C3;(t) and d<sub>&#x3BC;</sub>(t) increased, resulting in the Gaussian
factor moving towards the image center (Figure 6).
Finally, from fixation 6, all parameters were stabilized.</p>

        <p>For the LPT condition, the Gaussian factor weight
&#x3B1;&#x2081;(t increased from fixation 2 to fixation 3, until it was
almost equal to the weight &#x3B1;&#x2081;(3) of the saliency mode.
The contribution of saliency remained stable, while from
fixation 3, the contribution of the distractor decreased,
and the &#x201C;noise factor&#x201D; weight &#x3B1;&#x2083; increased (Figure 5).
From fixation 3, we also observed a decrease in the
parameter &#x3C3;(t) and a decrease in the distance d<sub>&#x3BC;</sub>(t) (Figure
7). &#x3C3;(t) which was twice as small as  R<sub>d</sub> from fixation 4
to the end of the exploration. Contributions of this factor
and of the &#x201C;noise factor&#x201D; were similar from fixation 6.
Furthermore, the position of the Gaussian mode
converged at the spatial location D&#x2080; of the distractor (Figure
6).</p>

        <p>Interestingly, when comparing the three distractor
conditions, we observed that the larger distractor effect
on eye movements observed in LPT than in MPT and in
MPT than in SPT was illustrated by the results of the
model. The influence of the distractor on fixation 3,
&#x3B1;&#x2081;(3), was higher in LPT than in MPT, which in its turn
was slightly higher than in SPT.</p>
      </sec>
    </sec>
	
    <sec id="S5">
      <title>General Discussion</title>
	  
      <p>The present study demonstrates that presenting a
taskirrelevant distractor during the exploration of natural
scenes prolongs not only the duration of the current
fixation but also modifies both the duration and location of
subsequent fixations. After a brief summary of the
results, we discuss our findings relative to the programming
of eye movements during scene viewing.</p>

      <p>Firstly, we replicated previous results which showed
an increase in current fixation duration due to distractor
onset (
        <xref ref-type="bibr" rid="R19">19</xref>
        ). More interestingly, we analyzed the effect of
the distractor on the duration and location of subsequent
fixations, using three durations of distractor. We reported
different effects of the distractor depending on its
duration. For SPT, only the current fixation duration was
impacted, while for MPT, the fixation directly following
distractor onset was also lengthened even if the distractor
was no longer present. The duration of all fixations
increased in the LPT condition compared to the control
condition, with larger increases for the two fixations
directly following distractor onset.</p>

      <p>Secondly, analysis of fixation locations following
distractor onset revealed that the distractor spatially attracted
fixations. As observed for fixation durations, the
attractiveness of the distractor was again stronger when the
distractor was presented for a longer duration.
Furthermore, we observed that fixations had a greater tendency
to land on the distractor location when this location was
salient. In order to evaluate the influence of the distractor
while taking into account scene saliency, we used a
mixture model and the Expectation-Maximization algorithm
to calculate the relative importance of these two factors
(attractiveness of the distractor, and of salient regions) for
eye fixations, when the distractor was not located in a
salient region. If we had not done so, it would have been
difficult to distinguish the effects of the two factors.
Results first showed that fixation locations in the experiment
were mainly driven by the saliency of the scene (
        <xref ref-type="bibr" rid="R21">21</xref>
        ).
This was an expected result which supported the
validation of our model. In addition to the analysis of fixation
locations, the modeling results also showed a strong
attractiveness of the distractor (even when it was no longer
present) not only for the fixation directly following its
onset but also for the one after that. Therefore, even if
fixations did not land directly on the distractor location,
the results from the statistical model showed that they
were still attracted by it for at least two fixations.
Distractor attraction was also dependent on duration of
presentation: it was stronger in MPT than in SPT. The LPT can be
seen here as a control condition, since the distractor
remained present for the whole exploration. In this case, the
irrelevant distractor attracted fixations for all fixations
after its onset.</p>

      <p>Several studies have suggested that fixation duration
can come under direct or indirect control mechanisms
(
        <xref ref-type="bibr" rid="R22">22</xref>
        ). Direct control theories suppose that decisions about
fixations are made during the current fixation and so
individual fixations are controlled by visual and cognitive
factors associated with the scene region currently under
fixation. On the contrary, indirect control theories
suppose that the current fixation is influenced by other
factors. In our study, we tested whether the duration and
location of a fixation also reflected the processing
demands of the previous fixation i.e. whether fixation 3s
and fixations which followed were impacted by the
distractor which appeared during fixation 2s. If mechanisms
that control fixations were direct, the onset of the
distractor would not have modified the following fixations. If,
on the contrary, mechanisms were indirect, the fixation
following distractor onset could potentially be influenced
by the distractor and its perceptual trace. Interestingly,
distractor onset increased the current fixation duration
equally, irrespective of the duration of distractor
presentation. These results confirmed that it was the transient
motion signal itself which captured attention in a
bottomup manner. However, the duration of an irrelevant
distractor differentially impacted subsequent exploration.
Surprisingly, when the distractor was presented for a
longer duration (in the MPT condition), it also impacted
the duration of subsequent fixations. Even though it had
already disappeared, the distractor remained as a
perceptual trace. This was true only when the distractor was
flashed for a certain duration, suggesting that when
flashed for a short period of time, its onset and the
transient motion associated impacted only the current fixation
duration. For a longer duration, we might suppose that
more information was processed during the current
fixation. This information was retained and indirectly
increased the next fixation duration. We also observed that
a greater number of fixations inside the distractor location
when the duration of the previous fixation had been more
greatly increased by the distractor. The programming of
fixation locations was linked to events which occurred
previously in the exploration, and any abrupt and
timelimited visual change such as distractor onset modified
the subsequent exploration of the scene. Overall, these
results suggest that fixation durations and fixation
locations are controlled by both direct and indirect
mechanisms. Direct control on the current fixation was reflected
by the increase in duration and by the location of the next
fixation, strongly attracted by the distractor. Indirect
control was shown by the residual influence of the
distractor on both fixation duration and fixation location, for
several fixations after distractor onset and offset.</p>

      <p>Our data also support the theory of parallel
programming of saccades during scene viewing. The increase in
the duration of the current fixation can be seen as a delay
in the programming of the subsequent saccade, due to
processes involved in cancelling the ongoing saccade and
programming the new saccade toward the distractor.
These results are also consistent with the assumption of
the CRISP model which shows that saccade
programming is completed in two stages: an initial, labile stage
that is subject to cancellation and a subsequent,
nonlabile stage (
        <xref ref-type="bibr" rid="R17">17</xref>
        ). In our experiment, the distractor probably
appeared during the labile stage, at the beginning of a
fixation. This is supported by results showing that this
subsequent fixation was mainly attracted by distractor
location and happened to land exactly in the location of
the distractor, in a large number of trials.</p>

      <p>Our results could have important implications for
understanding how fixations are controlled during the
exploration of a complex visual scene. While substantial
research has been devoted to investigating the temporal
control of fixations separately from the spatial control of
fixations, our present study provides evidence on the
spatial and temporal aspects of fixation control during the
exploration of natural scenes. Furthermore, a statistical
model such as the one proposed in the study has several
advantages: it is parsimonious, easy to use, and the
interpretation of results is straightforward. It uses simple and
unrestricted numbers of hypotheses concerning the visual
factors that could influence fixation, and quantifies these
contributions for all fixations involved in the exploration.
Different factors might be included in such a simple
model. For example, central bias could be included as a
factor or a face saliency map could be added as a possible
guiding factor to explain eye fixations. Another
possibility is the inclusion of maps depicting specific regions of
interest, for example, to quantify the relative importance
of a specific object compared to scene saliency. Our
study provides a complementary approach to the classical
analysis of fixation locations as it allows for the study of
all fixations, even those which did not land on the
distractor in our particular case. As such, it has the potential to
be useful in visual attention research to help gain better
understanding of the control and programming of
fixations during scene viewing.</p>
    </sec>
	
    <sec id="S6">
      <title>Acknowledgements</title>
	  
      <p>The authors would like to thank Sebastian Pannasch
for his enlightening comments on the manuscript. This
work was supported by a grant from the <italic>French Minist&#xE8;re
de la Recherche et de l&#x2019;Enseignement Sup&#xE9;rieur</italic> funding
the doctorate work of H&#xE9;l&#xE8;ne Devillez. The software
development was performed by Gelu Ionescu.</p>
    </sec>
	
  </body>
  
	
	  
  
  <back>
  <fn-group>
  <fn id="FN1">
  <p>There was a delay of 33 ms between fixation onset and the appearance of the distractor.</p>
  </fn>
  <fn id="FN2">
  <p>Due to the protocol, the distractor appeared at a random location, 4° from the center of the screen. Because in the model, the distractor was modeled by a unique spatial mode, we performed a rotation of the data to place the distractor on the right side of the center, still at 4°. Thus, the distractor was always at the same reference position for all trials and all scenes. We analyzed the corresponding fixation locations in relation to this location.</p>
  </fn>  
  </fn-group>
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