Abstract
The dorsal attentional network is known for its role in directing top-down visual attention toward task-relevant stimuli. This goal-directed nature of the dorsal network makes it a suitable candidate for processing and extracting predictive information from the visual environment. In this review we briefly summarize some of the findings that delineate the neural substrates that contribute to predictive learning at both levels within the dorsal attentional system: including the frontal eye field (FEF) and posterior parietal cortex (PPC). We also discuss the similarities and differences between these two regions when it comes to learning predictive information. The current findings from the literature suggest that the FEFs may be more involved in top-down spatial attention, whereas the parietal cortex is involved in processing task-relevant attentional influences driven by stimulus salience, both contribute to the processing of predictive cues at different time points.
Regularities in the visual environment are predictive of future events. Learning of such regularities may therefore help the visual system generate anticipatory activities (i.e., expectations) and reduce computational burden. Take traffic lights, for example; there is a serial order for which signals light up (temporal), as well as the color (feature based) and location (spatial) of each light, thus reflecting regularities in several domains of one's daily life. This information can be fully predictive of future events if they are always 100% valid, such as the traffic light. But even with partial predictive power (not always 100% valid), which we refer to as probabilistic, it remains advantageous to pick up such information, as the knowledge of any regularities can help the visual system reduce its computational load because future events can be anticipated and better managed in advance. This learning of predictive information is especially useful given that our ability to represent multiple objects within a scene at any given moment is rather limited (e.g., Buschman et al., ; Tsubomi et al., 2013). Indeed, many studies have already demonstrated the visual system's capability to learn and exhibit knowledge of regularities in the environment with and without subjective awareness (e.g., Chun and Jiang, ; Fiser and Aslin, ; Kristjánsson et al., ; Nakayama et al., 2004; Geng and Behrmann, ). Eye movement studies have also shown that people can direct their eyes and attention to highly probable locations faster than to low-probability locations without employing an explicit strategy to do so (e.g., Farrell et al., ). In this paper, we attempt to review evidence demonstrating the existence of predictive learning as well as their possible neural mechanism, such as the dorsal attentional network.
The dorsal attentional network is comprised of the frontal eye fields (FEF) and the posterior parietal cortex (PPC), where PPC includes the superior parietal lobule (SPL) and intraparietal sulcus (IPS). The dorsal network has been shown to be involved in voluntary top-down orienting of visual attention. This network shows strong activity when a spatial cue is presented, explicitly indicating where participants should direct their attention (Corbetta et al., ). However, it is important to note that even in the absence of a cue, contextual information, if predictive, can sometimes work in similar ways as a spatial cue in directing one's attention. For example, visual search with a repetitive and predictive distractor layout can promote implicit learning and efficient attentional orienting to the target location in observers over time, a phenomenon known as contextual cuing (Chun and Jiang, ). In this case, the contextual information (i.e., distractor configuration) is predictive of the target location, thus functioning like a probabilistic spatial cue in directing visual attention, and thereby activating the dorsal network (Manginelli et al., 2013). Therefore, the dorsal network has been suggested to mediate the processes of top-down attentional set, such as the expectation of a cue (Corbetta et al., ). This pre- and post-stimulus activation of the dorsal network can facilitate efficient selection of, and orienting toward, the stimuli of interest.
Posterior parietal cortex
The idea that one's visual attention is efficiently oriented toward the predictive and salient cue in the environment is plausible, because one of the functions of PPC is indeed attentional orienting and capture. Specifically, the right (hemisphere) PPC has been associated with a variety of functions in visual attention (Behrmann et al., ; Rushworth and Taylor, 2006), including attentional control (Nobre et al., 1997; Ellison and Cowey, ; Morris et al., 2007), updating spatial mapping (Andersen et al., ; Merriam et al., 2003; Morris et al., 2007), and shifting spatial attention (Ellison et al., ; Chambers et al., ; Constantinidis and Steinmetz, ; Mevorach et al., 2006; Schenkluhn et al., 2008). Damage to the right PPC may lead to hemifield neglect, where patients become unaware of the contralateral visual space although their visual acuity is not affected (Heilman and Van Den Abell, ; Mesulam, 1981). In the contextual cuing example above, it is important to note that the predictive context is facilitative by efficiently directing eye gazes toward the target location (Neider and Zelinsky, 2006; also see Kunar et al., 2007; for an effect in response selection). Indeed, Peterson and Kramer (2001) monitored participants' eye movements and found that fewer saccades were made when context was repeated, suggesting a more efficient allocation of attention to the old condition. Thus, predictive contextual information, even with uneven probability (Tseng et al., 2011), can have a direct impact on visual attention and eye movements, suggesting a critical involvement of the dorsal attentional network that is also heavily involved in oculomotor control. Indeed, Schankin and Schubo (2009) measured event-related potentials (ERP) using this paradigm and found greater negativity in the posterior parietal region around 200 ms after display onset. This component is known as the N2pc component (Luck and Hillyard, 1994), which reflects the allocation of visual attention in the parietal region that is contralateral to the visual field of the attended stimulus. This physiological evidence demonstrates an important correlation between attentional allocation and PPC. In contextual cuing, however, there exists a confound between distractor saliency and predictability, thus the exact role of PPC remains unclear. That is, it is unclear whether the activation of PPC was due to the bottom-up salience of the distractors, or because of their predictive nature that matched the top-down task set. To dissociate these two factors, one needs a situation where salient but non-predictive distractors compete with the target and therefore need to be suppressed. To answer this question, one important study by Geng and Mangun () used a visual search paradigm, where the search target appeared either with a low-contrast (low competition) or high-contrast (high competition) distractor. These authors found that target-induced aIPS (part of PPC) activation scaled linearly with increasing RT, especially when the distractor was salient. Thus, PPC activation seemed to be coupled with salient distractors at the perceptual level. Subsequent study by Mazaheri et al. (2011) recorded EEG activity using the same paradigm. Critically, in the 1-s pre-stimulus time window before each high-competition trial, these authors found higher alpha activity from PPC on trials where the target was correctly identified by the first saccade. Based on the wealth of literature that suggests alpha activity as an indication of cortical inhibition (e.g., see Klimesch, for a review), the results suggest that PPC alpha was indicative of suppression of salient distractors, consistent with the conclusion by Geng and Mangun () that PPC is involved in processing salient perceptual information.
Using brain stimulation, another direct test of such idea was carried out by Chao et al. (), with the use of transcranial magnetic stimulation (TMS) coupled with a similar 1-target and 1-distractor visual orienting paradigm (see also Hodsoll et al., ) that is preceded by either a spatially-predictive or neutral cue. In this study, saccade curvatures, along with saccade latency and accuracy, were recorded as they have been shown to be indicative of the active excitation and suppression processes that the visual system must resolve between the target and the distractor (e.g., Walker et al., 2006; McSorley et al., 2009). Not surprisingly, people could saccade faster and with more precision and smaller curvature (less “pulling” effect from the distractors) when the target location was predictable. The pattern becomes interesting when TMS was applied over the right PPC. When target location was predictable, PPC TMS had no significant effect on saccade curvature. However, when target location was unpredictable, TMS over the right PPC decreased saccade curvature toward the distractor such that impaired PPC functioning actually strengthened distractor suppression (Figure 1). These results suggest that PPC plays an important role in attentional capture (thus why PPC TMS would decrease attentional capture toward the distractor), and subsequent study has shown that such effect took place at modulating the torque of each eye movements (Liang and Juan, 2012). Together, the alpha inhibition and TMS suppression of PPC from Mazaheri et al. (2011) and Chao et al. () demonstrate that PPC is sensitive to salient distractors, and is indirectly sensitive to predictive information when predictability also becomes a salient feature.
Figure 1
Without a salient distractor, is PPC still involved in predictive processing? As mentioned, research has shown that as long as predictability is a relevant aspect of the task, PPC should also play an important role in processing targets and predictive information. For example, a TMS study by Ellison et al. () found that TMS over PPC disrupted performance in visual search when participants had to decide whether a single item presented was a target or not. This impairment effect, however, was only present when target location was unpredictable. Further support comes from an fMRI study by Kristjánsson et al. (), who found decreased PPC activation when target form or location is known ahead of time via priming, suggesting that PPC is sensitive to predictability and unpredictability beyond salience competition between target and distractors.
Here it is important to emphasize again the goal-directed nature of the dorsal network when interpreting these results regarding PPC. Specifically, PPC does not respond to all perceptually-salient distrators, but only those that are relevant to the current task set. One important fMRI study by Downar et al. () instructed participants to monitor a change either in visual or auditory modality. These authors observed increased activation in right PPC when a change occurred, but only when the change happened in the modality that is relevant to participants' current behavior. Indeed, monkey neurophysiology has already shown that lateral intraparietal cortex (LIP, equivalent to the vicinity of human PPC) encodes behaviorally salient objects (Gottlieb et al., ), desirable actions (Dorris and Glimcher, ), and the color of a cue if it is associated with an eye movement (Toth and Assad, 2002). In addition, target predictability, when leading to reward (i.e., behaviorally salient), can have a significant effect in modulating LIP activity as it can represent predictive information such as the weighted likelihood of certain shape combinations (Konen et al., ; Yang and Shadlen, 2007). Together, it is plausible to conclude from these studies that all manipulations of various psychological constructs such as salience (Geng and Mangun, ), predictability (Chao et al., ), reward (Yang and Shadlen, 2007), desirability (Dorris and Glimcher, ), and behavioral relevance (Toth and Assad, 2002; Muggleton et al., 2011), are all essentially similar in nature. That is, PPC activation is observed as long as a stimulus, be it a target or distractor, is closely matched with one's current task/goal. This idea may help generalize the nature of PPC activation across different contexts. And as such, PPC is not only crucial to spatial attention, but can also be involved in processing predictive information when such information is perceptually or behaviorally relevant, or salient.
Frontal eye fields
On the other end of the dorsal attentional network is FEF. As its name implies, much of the work on FEF have been devoted to the oculomotor control of eye movements and visual attention, although studies have begun to document FEF involvement in other domains of cognition such as inhibitory control (e.g., Muggleton et al., 2010). Early studies such as Miller (1988) studied the effects of absolute and relative target position. A target letter was to be detected in a sequence of four letters in which one location had a higher probability of containing the target. The letter sequence was occasionally offset in horizontal position to probe whether the effects of high probability was dependent on absolute position or the position in the sequence (relative position). It was found that target location probability benefited from both types of spatial relationship. Subsequent study by Kingstone and Klein () also demonstrated that people can be sensitive to the likelihood that a specific stimulus form would appear in a particular spatial location.
More recently, Geng and Behrmann () investigated the role of targets' spatial probabilities in a visual conjunction search task, combined with endogenous and exogenous cues. These authors found that spatial probability indeed induced an implicit facilitation to attentional orienting. But most importantly, the facilitation from spatial probability is additive to the explicit endogenous cue (the effect was purely additive) and interacted with the salient exogenous cue. Thus, the effect of probability in visual selection seems to occur early at the stage where salient exogenous cues are processed. To further investigate this issue, Liu et al. (2010) used a similar setup while recording participants' eye movements. In this version of the task, participants responded with pro- and antisaccade eye movements, which refers to eye movements toward (pro) and away from (anti) the target (Figure 2A). Prosaccades have been consistently found to have shorter and longer RT due to the extra stages of suppression in antisaccades (termed the antisaccade cost; Everling and Fischer, ; Kristjansson, ; Kristjánsson et al., ; Kristjansson et al., ; Olk and Kingstone, 2003; Munoz and Everling, 2004), and therefore the magnitude of the antisaccade cost provides a suitable measure of the modulating effect that probability may have on oculomotor control. These authors found that under these conditions, prosaccades to the probabilistically-salient location became faster. The sizes of the antisaccade cost also changed to compliment the magnitude of prosaccade probability. Most important, the saccade RTs followed the magnitude of probability saliency such that the RTs decreased gradually as the probability of a certain location increased, and vice versa (Figure 2B). Together, these results suggest that the oculomotor system is sensitive to multiple levels of spatial probability. It is important to note that both studies by Geng and Behrmann () and Liu et al. (2010) accounted for the effect of repetition priming by taking trial-to-trial RT facilitation into account. While the effect of repetition priming is undoubtedly present, the effect of spatial probability is independent of such effect.
Figure 2
The neural mechanism behind such spatial probability learning in oculomotor behaviors likely involves FEF, as it tends to produce pretarget-related neural activity during saccade selection and saccade preparation, respectively (Schall et al., 1995; Thompson et al., 1996, 1997; Schall, 1997; Bichot and Schall, ; Sato and Schall, 2003; Juan et al., , ). Note that, however, the bilateral FEF both have distinctive functions in mediating oculomotor control. Studies have shown that the left FEF behaves much like the right PPC, where it is mostly involved when target location is unpredictable. One notable study by Lane et al. (2012) manipulated spatial predictability via spatial priming in a visual search task while applying TMS over either left FEF, right FEF, or right PPC. These authors found that when target location was predictable, TMS only increased reaction time when it was applied over the right FEF, and not the left FEF or the right PPC. Their findings suggest that left FEF and right PPC are only involved when target location is unpredictable (also see Campana et al., ), whereas the right FEF is more involved in top-down visual attention that treats predictability in a task-driven manner. In addition, using the same orienting paradigm and manipulation of probability as their previous study (Liu et al., 2010), Liu and colleagues (2011) applied theta burst TMS over participants' right FEF or supplementary eye fields (SEF) for 20 s (Figure 3A) and found that FEF TMS, but not SEF, successfully disrupted the effect of probability such that high-probability prosaccades became slower when TMS was applied. These results suggest that right FEF, but not SEF, is critical to the learning of spatial probabilities1 in this orienting paradigm (Figure 3B). Furthermore, when a target becomes less predictable, the top-down effort in search of the new target also requires heavy FEF involvement, presumably because the neuronal buildup has to start over toward a new target that is either located at a new location or defined by one or more new features. As such, TMS over rFEF when target suddenly becomes unpredictable (Muggleton et al., 2003) or is no longer defined by an old set of features (Muggleton et al., 2011) will also impair saccade latency. Together, these studies suggest that rFEF is critical to the processes of target selection either via pretarget neuronal buildup (when target is predictable) or top-down attentional orienting (when target is unpredictable). Indeed, TMS over rFEF at early and late time points during an antisaccade task revealed that FEF involvement occurs at early (target selection) and late (endpoint selection) stages (Figure 4), both of which are necessary component for mediating the effect of probability (Juan et al., ). In addition, preparatory-related activities can be found in FEF with trained monkeys in an antisaccade task, where the endpoints of the probable saccade type enjoys a lower threshold or early neural activity buildup (Dorris and Munoz, ; Dorris et al., ; Everling and Munoz, ; Connolly et al., ) and speeds up the process of saccade preparation and thus decrease saccade latency. fMRI data also showed that rFEF activity can be used to predict saccadic reaction time (SRT) in humans (Connolly et al., ). Thus, these findings suggest that the effect of location probability on SRT could be reflective of the neural firing rate within a subpopulation of neurons in the rFEF. This may account for the role of rFEF in mediating the effects of location probability because both target and endpoint selections are necessary for the benefit of location probability to surface.
Figure 3
Figure 4
Comparing FEF and PPC
If FEF and PPC both process predictive and probabilistic cues in the environment, how do they differ from each other in terms of timing and function? Several neuroimaging and stimulation studies that compares FEF and PPC involvement using the same paradigm may provide some clues to this question. First, in a non-predictive visual search array, Kalla et al. () applied TMS over either FEF or PPC at various timings and found that FEF involvement took place early (0–40 ms) while PPC is late (120–160 ms). But as previously mentioned, FEF involvement in oculomotor control can occur both early and late (under the right conditions), covering both stages of target selection and endpoint selection. Indeed, in the aforementioned study by Lane et al. (2012), they found that TMS over right FEF impaired visual search in both primed (predictable) and non-primed (unpredictable) condition, suggesting a general search mechanism that is mediated by right FEF. Stimulation over PPC had no effect when the target was at a predictable location, which is in line with the results from the Chao et al. () study, who also found that PPC TMS is effective in saccade curvature only when target location is unpredictable. An fMRI study using a cuing paradigm also found that PPC activation was modulated by the perceptual salience of the stimuli (target and distractor alike), whereas FEF activation was associated with the location of spatial attention (Geng and Mangun, ). This suggests that FEF may be more involved in top-down spatial attention, whereas PPC is involved in processing task-relevant attentional influences driven by stimulus salience, both of which can be utilized in processing predictive cues in the environment.
Conclusion
In this paper we have briefly reviewed how predictive information in the environment can powerfully modulate human visual attention and oculomotor control. Importantly, neurophysiological studies suggest that such learning requires a dynamic interplay between regions within the dorsal attentional network, which includes PPC and FEF. Specifically, FEF is responsive to predictive information via its top-down early preparatory neural activity buildup that biases the processes of target selection and saccade preparation; whereas PPC responds to salient bottom-up stimuli that carry predictive information, even if they are not targets, if such information matches one's current behavioral goal. Much of the work until now has emphasized the individual contributions of these regions to mediate probability learning. Future studies that disentangle the timing, roles, functional connectivities, and interactions between these regions will provide exciting new insights into how the visual system strategically adapts to the environment.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Statements
Acknowledgments
We are grateful to Neil G. Muggleton and Chang-Mao Chao for their constructive suggestions to earlier versions of the manuscript. This work was sponsored by the National Science Council, Taiwan (101-2628-H-008-001-MY4, 102-2420-H-008-001-MY3, 99-2410-H-008-022-MY3, 97-2511-S-008-008-MY5). Philip Tseng is supported by NSC (101-2811-H-008-014).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Footnotes
1.^It is worth mentioning that due to the nature of brain stimulation, one alternative account to this pattern of result is that perhaps TMS is affecting the connections between brain regions, instead of the neural locus itself. Therefore, it remains possible that some of the stimulation results reviewed here is due to a connectivity issue of FEF or PPC's communication with other areas.
References
1
AndersenR. A.EssickG. K.SiegelR. M. (1985). Encoding of spatial location by posterior parietal neurons. Science230, 456–458. 10.1126/science.4048942
2
BehrmannM.GengJ. J.ShomsteinS. (2004). Parietal cortex and attention. Curr. Opin. Neurobiol. 14, 212–217. 10.1016/j.conb.2004.03.012
3
BichotN. P.SchallJ. D. (2002). Priming in macaque frontal cortex during popout visual search: feature-based facilitation and location-based inhibition of return. J. Neurosci. 22, 4675–4685.
4
BuschmanT. J.SiegelM.RoyJ. E.MillerE. K. (2011) Neural substrates of cognitive capacity limitations. Proc. Natl. Acad. Sci. U.S.A. 108, 112252–111255.
5
CampanaG.CoweyA.CascoC.OudsenI.WalshV. (2007) Left frontal eye field remembers “where” but not “what”. Neuropsychologia45, 2340–2345.
6
ChambersC. D.PayneJ. M.StokesM. G.MattingleyJ. B. (2004). Fast and slow parietal pathways mediate spatial attention. Nat. Neurosci. 7, 217–218. 10.1038/nn1203
7
ChaoC. M.TsengP.HsuT. Y.SuJ. H.TzengO. J. L.HungD. L.et al. (2011). Predictability of saccadic behaviors is modified by transcranial magnetic stimulation over human posterior parietal cortex. Hum. Brain Mapp. 32, 1961–1972. 10.1002/hbm.21162
8
ChunM. M.JiangY. (1998). Contextual cueing: implicit learning and memory of visual context guides spatial attention. Cogn. Psychol., 36, 28–71. 10.1006/cogp.1998.0681
9
ConnollyJ. D.GoodaleM. A.GoltzH. C.MunozD. P. (2005). fMRI activation in the human frontal eye field is correlated with saccadic reaction time. J. Neurophysiol. 94, 605–611. 10.1152/jn.00830.2004
10
ConstantinidisC.SteinmetzM. A. (2005). Posterior parietal cortex automatically encodes the location of salient stimuli. J. Neurosci. 25, 233–238. 10.1523/JNEUROSCI.3379-04.2005
11
CorbettaM.PatelG.ShulmanG. L. (2008). The reorienting system of the human brain: from environment to theory of mind. Neuron58, 306–324. 10.1016/j.neuron.2008.04.017
12
DorrisM. C.GlimcherP. W. (2004). Activity in posterior parietal cortex is correlated with the relative subjective desirability of action. Neuron44, 365–378. 10.1016/j.neuron.2004.09.009
13
DorrisM. C.MunozD. P. (1998). Saccadic probability influences motor preparation signals and time to saccadic initiation. J. Neurosci. 18, 7015–7026.
14
DorrisM. C.PareM.MunozD. P. (2000). Immediate neural plasticity shapes motor performance. J. Neurosci. 20, RC52.
15
DownarJ.CrawleyA. P.MikulisD. J.DavisK. D. (2001) The effect of task relevance on the cortical response to changes in visual and auditory stimuli: An event-related fMRI study. Neuroimage14, 1256–1267.
16
EllisonA.CoweyA. (2006). TMS can reveal contrasting functions of the dorsal and ventral visual processing streams. Exp. Brain Res. 175, 618–625. 10.1007/s00221-006-0582-8
17
EllisonA.RushworthM.WalshV. (2003). The parietal cortex in visual search: a visuomotor hypothesis. Suppl. Clin. Neurophysiol. 56, 321–330. 10.1016/S1567-424X(09)70236-3
18
EverlingS.FischerB. (1998). The antisaccade, a review of basic research and clinical studies. Neuropsychologia36, 885–899. 10.1016/S0028-3932(98)00020-7
19
EverlingS.MunozD. P. (2000). Neuronal correlates for preparatory set associated with pro-saccades and anti-saccades in the primate frontal eye field. J. Neurosci. 20, 387–400.
20
FarrellS.LudwigC. J.EllisL. A.GilchristI. D. (2009). Influence of environmental statistics on inhibition of saccadic return. Proc. Natl. Acad. Sci. U.S.A. 107, 929–934.
21
FiserJ.AslinR. N. (2001). Unsupervised statistical learning of higher-order spatial structures from visual scenes. Psychol. Sci. 12, 499–504. 10.1111/1467-9280.00392
22
GengJ. J.BehrmannM. (2005). Spatial probability as an attentional cue in visual search. Percept. Psychophys. 67, 1252–1268. 10.3758/BF03193557
23
GengJ. J.MangunG. R. (2008). Anterior intraparietal sulcus is sensitive to bottom-up attention driven by stimulus salience. J. Cogn. Neurosci. 21, 1584–1601. 10.1162/jocn.2009.21103
24
GottliebJ. P.KusunokiM.GoldbergM. E. (1998). The representation of visual salience in monkey parietal cortex. Nature391, 481–484. 10.1038/35135
25
HeilmanK. M.Van Den AbellT. (1980). Right hemisphere dominance for attention: the mechanism underlying hemispheric asymmetries of inattention (neglect). Neurology30, 327–330. 10.1212/WNL.30.3.327
26
HodsollJ.MevorachC.HumphreysG. W. (2009). Driven to less dis-traction: rTMS of the right parietal cortex reduces attentional capture in visual search. Cereb. Cortex19, 106–114.
27
JuanC. H.MuggletonN. G.TzengO. J. L.HungD. L.CoweyA.WalshV. (2008). Segregation of visual selection and saccades in human frontal eye fields. Cereb. Cortex18, 2410–2415. 10.1093/cercor/bhn001
28
JuanC. H.Shorter-JacobiS. M.SchallJ. D. (2004). Dissociation of spatial attention and saccade preparation. Proc. Natl. Acad. Sci. U.S.A. 101, 15541–15544. 10.1073/pnas.0403507101
29
KallaR.MuggletonN. G.JuanC. H.CoweyA.WalshV. (2008). The timing of the involvement of the frontal eye fields and posterior parietal cortex in visual search. Neuroreport19, 1067–1071. 10.1097/WNR.0b013e328304d9c4
30
KingstoneA.KleinR. (1991). Combining shape and position expectancies: hierarchical processing and selective inhibition. J. Exp. Psychol. Hum. Percept. Perform. 17, 512–519. 10.1037/0096-1523.17.2.512
31
KlimeschW. (2012). Alpha-band oscillations, attention, and controlled access to stored information. Trends Cogn. Sci. 16, 606–617. 10.1016/j.tics.2012.10.007
32
KonenC. S.KleiserR.WittsackH. J.BremmerF.SeitzR. J. (2004). The encoding of saccadic eye movements within human posterior parietal cortex. Neuroimage22, 304–314. 10.1016/j.neuroimage.2003.12.039
33
KristjanssonA. (2007). Saccade landing point selection and the competition account of pro- and antisaccade generation: the involvement of visual attention–a review. Scand. J. Psychol. 48, 97–113. 10.1111/j.1467-9450.2007.00537.x
34
KristjánssonA.ChenY.NakayamaK. (2001). Less attention is more in the preparation of antisaccades, but not prosaccades. Nat. Neurosci. 4, 1037–1042. 10.1038/nn723
35
KristjanssonA.VandenbrouckeM. W.DriverJ. (2004). When pros become cons for anti- versus prosaccades: factors with opposite or common effects on different saccade types. Exp. Brain Res. 155, 231–244. 10.1007/s00221-003-1717-9
36
KristjánssonA.VuilleumierP.SchwartzS.MacalusoE.DriverJ. (2007). Neural basis for priming of pop-out during visual search revealed with fMRI. Cereb. Cortex17, 1612–1624. 10.1093/cercor/bhl072
37
KunarM. A.FlusbergS.HorowitzT. S.WolfeJ. M. (2007). Does contextual cuing guide the deployment of attention?J. Exp. Psychol. Hum. Percept. Perform. 33, 816–828.
38
LaneA. R.SmithD. T.SchenkT.EllisonA. (2012) The involvement of posterior parietal cortex and frontal eye fields in spatially primed visual search. Brain Stimul. 5, 11–17.
39
LiangW. K.JuanC. H. (2012). Modulation of motor control in saccadic behaviors by TMS over the posterior parietal cortex. J. Neurophysiol. 108, 741–752. 10.1152/jn.01135.2011
40
LiuC. L.ChiauH. Y.TsengP.HungD. L.TzengO. J. L.MuggletonN. G.et al. (2010). The antisaccade cost is modulated by contextual experience of location probability. J. Neurophysiol. 103, 1438–1447. 10.1152/jn.00815.2009
41
LiuC. L.TsengP.ChiauH. Y.LiangW. K.HungD. L.TzengO. J. L.et al. (2011). The location probability effects of saccade reaction times are modulated in the frontal eye fields but not in the supplementary eye field. Cereb. Cortex21, 1416–1425. 10.1093/cercor/bhq222
42
LuckS. J.HillyardS. A. (1994). Electrophysiological correlates of feature analysis during visual search. Psychophysiology31, 291–308. 10.1111/j.1469-8986.1994.tb02218.x
43
ManginelliA. A.BaumgartnerF.PollmannS. (2013). Dorsal and ventral working memory-related brain areas support distinct processes in contextual cueing. Neuroimage67, 363–374. 10.1016/j.neuroimage.2012.11.025
44
MazaheriA.DiQuattroN. E.BengsonJ.GengJ. J. (2011). Pre-stimulus activity predicts the winner of top-down vs. bottom-up attentional selection. PLoS ONE6:e16243. 10.1371/journal.pone.0016243
45
McSorleyE.HaggardP.WalkerR. (2009). The spatial and temporal shape of oculomotor inhibition. Vision Res. 49, 608–614. 10.1016/j.visres.2009.01.015
46
MerriamE. P.GenoveseC. R.ColbyC. L. (2003). Spatial updating in human parietal cortex. Neuron39, 361–373. 10.1016/S0896-6273(03)00393-3
47
MesulamM. M. (1981). A cortical network for directed attention and unilateral neglect. Ann. Neurol. 10, 309–325. 10.1002/ana.410100402
48
MevorachC.HumphreysG. W.ShalevL. (2006). Opposite biases in salience-based selection for the left and right posterior parietal cortex. Nat. Neurosci. 9, 740–742. 10.1038/nn1709
49
MillerJ. (1988). Components of the location probability effect in visual search tasks. J. Exp. Psychol. Hum. Percept. Perform. 14, 453–471. 10.1037/0096-1523.14.3.453
50
MorrisA. P.ChambersC. D.MattingleyJ. B. (2007). Parietal stimulation destabilizes spatial updating across saccadic eye movements. Proc. Natl. Acad. Sci. U.S.A. 104, 9069–9074. 10.1073/pnas.0610508104
51
MuggletonN. G.ChenC. Y.TzengO. J. L.HungD. L.JuanC. H. (2010). Inhibitory control and the frontal eye fields. J. Cogn. Neurosci. 22, 2804–2812. 10.1162/jocn.2010.21416
52
MuggletonN. G.KallaR.JuanC. H.WalshV. (2011) Dissociating the contributions of human frontal eye fields and posterior parietal cortex to visual search. J. Neurophysiol. 105, 2891–2896.
53
MuggletonN. G.JuanC. H.CoweyA.WalshV. (2003). Human frontal eye fields and visual search. J. Neurophysiol. 89, 3340–3343. 10.1152/jn.01086.2002
54
MunozD. P.EverlingS. (2004). Look away: the anti-saccade task and the voluntary control of eye movement. Nat. Rev. Neurosci. 5, 218–228. 10.1038/nrn1345
55
NakayamaK.MaljkovicV.KristjanssonA. (2004). Short-term memory for the rapid deployment of visual attention, in The Cognitive Neurosciences III, ed GazzanigaM. S. (Cambridge, MA: MIT Press), 397–408.
56
NeiderM. B.ZelinskyG. J. (2006). Scene context guides eye movements during visual search. Vision Res. 46, 614–621. 10.1016/j.visres.2005.08.025
57
NobreA. C.SebestyenG. N.GitelmanD. R.MesulamM. M.FrackowiakR. S.FrithC. D. (1997). Functional localization of the system for visuospatial attention using positron emission tomography. Brain120, 515–533. 10.1093/brain/120.3.515
58
OlkB.KingstoneA. (2003). Why are antisaccades slower than prosaccades? A novel finding using a new paradigm. Neuroreport14, 151–155. 10.1097/00001756-200301200-00028
59
PetersonM. S.KramerA. F. (2001). Attentional guidance of the eyes by contextual information and abrupt onsets. Percept. Psychophys. 63, 1239–1249. 10.3758/BF03194537
60
RushworthM. F.TaylorP. C. (2006) TMS in the parietal cortex: updating representations for attention and action. Neuropsychologia44, 2700–2716.
61
SatoT. R.SchallJ. D. (2003). Effects of stimulus-response compatibility on neural selection in frontal eye field. Neuron38, 637–648. 10.1016/S0896-6273(03)00237-X
62
SchallJ. D. (1997). Visuomotor areas of the frontal lobe, in extrastriatc cortex of primates, in Cerebral Cortex, 1st Edn., Vol. 12, eds RocklandK.PetersA.KaasJ. (New York, NY: Plenum Press), 527–638.
63
SchallJ. D.HanesD. P.ThompsonK. G.KingD. J. (1995) Saccade target selection in frontal eye field of macaque. I. Visual and premovement activation. J. Neurosci. 15, 6905–6918.
64
SchankinA.SchuboA. (2009). Cognitive processes facilitated by contextual cueing: Evidence from event-related brain potentials. Psychophysiology46, 668–679. 10.1111/j.1469-8986.2009.00807.x
65
SchenkluhnB.RuffC. C.HeinenK.ChambersC. D. (2008). Parietal stimulation decouples spatial and feature-based attention. J. Neurosci., 2811106–11110. 10.1523/JNEUROSCI.3591-08.2008
66
ThompsonK. G.BichotN. P.SchallJ. D. (1997) Dissociation of visual discrimination from saccade programming in macaque frontal eye field. J. Neurophysiol. 77, 1046–1050.
67
ThompsonK. G.HanesD. P.BichotN. P.SchallJ. D. (1996) Perceptual and motor processing stages identified in the activity of macaque frontal eye field neurons during visual search. J. Neurophysiol. 76, 4040–4055.
68
TothL. J.AssadJ. A. (2002). Dynamic coding of behaviourally relevant stimuli in parietal cortex. Nature415, 165–168. 10.1038/415165a
69
TsengP.HsuT. Y.TzengO. J. L.HungD. L.JuanC. H. (2011). Probabilities in implicit learning. Perception40, 822–829. 10.1068/p6833
70
TsubomiH.FukudaK.WatanabeK.VogelE. K. (2013). Neural limits to representing objects still within view. J. Neurosci. 33, 8257–8263. 10.1523/JNEUROSCI.5348-12.2013
71
WalkerR.McSorleyE.HaggardP. (2006). The control of saccade trajectories: direction of curvature depends on prior knowledge of target location and saccade latency. Percept. Psychophys. 68, 129–138. 10.3758/BF03193663
72
YangT.ShadlenM. N. (2007). Probabilistic reasoning by neurons. Nature447, 1075–1080. 10.1038/nature05852
Summary
Keywords
probability, predictability, visual attention, eye movements, TMS, transcranial magnetic stimulation
Citation
Tseng P, Chang C-F, Chiau H-Y, Liang W-K, Liu C-L, Hsu T-Y, Hung DL, Tzeng OJL and Juan C-H (2013) The dorsal attentional system in oculomotor learning of predictive information. Front. Hum. Neurosci. 7:404. doi: 10.3389/fnhum.2013.00404
Received
24 May 2013
Accepted
09 July 2013
Published
02 August 2013
Volume
7 - 2013
Edited by
Joy Geng, University of California Davis, USA
Reviewed by
Britt Anderson, Brown University, USA; Amanda Ellison, Durham University, UK
Copyright
© 2013 Tseng, Chang, Chiau, Liang, Liu, Hsu, Hung, Tzeng and Juan.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chi-Hung Juan, Institute of Cognitive Neuroscience, National Central University, No.300, Jhongda Rd. Jhongli City 320, Taiwan e-mail: chijuan@cc.ncu.edu.tw
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.