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Daniel J Simons

Publications and source records attributed to Daniel J Simons.

At least 19 recordsLinked to original sources

Angularly nonspecific response suppression in rat barrel cortex.

Response modulation by prior sensory stimulation is a common property of cortical neurons. The degree to which effects are specific to the adapting stimulus provides insights into properties of the underlying circuitry. Here, we examined the effects of an adapting whisker deflection's angle on the angular tuning of layer IV barrel neurons and their major input source, thalamic barreloid neurons. In both barrel regular-spike units (RSUs) and fast-spike units (FSUs), presumed excitatory and inhibitory neurons, prior whisker deflections suppressed subsequent test deflections in a largely angularly nonspecific manner, that is, adaptation in one direction reduced responses for test deflections of all angles. FSUs were poorly tuned for deflection angle and remained so after adaptation. In adapted RSUs, responses to suboptimal directions were suppressed most and angular preferences remained constant; tuning therefore became sharper. Adaptation effects in RSUs and FSUs do not appear to reflect corresponding changes in thalamic neurons. The angularly nonspecific suppression of barrel neurons is likely mediated by local intrabarrel suppressive interactions, such as broadly tuned inhibition and/or short-term synaptic depression of excitatory connections. The dominance of angularly nonspecific suppression suggests that barrel neurons interact largely in an angularly nonspecific manner to reinforce stimulus preferences encoded by their synchronously firing thalamic inputs.

Adaptation, Physiological↗

Spatial updating relies on an egocentric representation of space: effects of the number of objects.

Models of spatial updating attempt to explain how representations of spatial relationships between the actor and objects in the environment change as the actor moves. In allocentric models, object locations are encoded in an external reference frame, and only the actor's position and orientation in that reference frame need to be updated. Thus, spatial updating should be independent of the number of objects in the environment (set size). In egocentric updating models, object locations are encoded relative to the actor, so the location of each object relative to the actor must be updated as the actor moves. Thus, spatial updating efficiency should depend on set size. We examined which model better accounts for human spatial updating by having people reconstruct the locations of varying numbers of virtual objects either from the original study position or from a changed viewing position. In consistency with the egocentric updating model, object localization following a viewpoint change was affected by the number of objects in the environment.

Environment↗

Whisker trimming begun at birth or on postnatal day 12 affects excitatory and inhibitory receptive fields of layer IV barrel neurons.

In rats, whisker trimming during development leads to persistent alterations in the function of cortical barrel circuits and to behavioral deficits later in life. Here we examined how whisker trimming begun either at birth (P0) or on postnatal day 12 (P12), around the onset of whisking behavior, affects receptive fields of layer IV barrel neurons. All whiskers on the left face were trimmed for 40-45 days and then allowed to regrow fully. Extracellular single-unit recordings and controlled deflections of principal and adjacent whiskers (PW and AW, respectively), individually or in paired combinations, were used to assess excitatory and suppressive effects of neighboring whiskers on barrel neurons. Results indicate that whisker trimming both from P0 and P12 leads to enlarged excitatory and weakened inhibitory receptive fields in layer IV neurons. PW- and AW-evoked responses are larger in magnitude in trimmed than in control animals; AW-evoked responses are disproportionately affected, decreasing the spatial focus of barrel neurons. Deprivation after P12 accounts for approximately 50% of the total effect observed in P0 trimmed animals. Suppressive interactions, evoked by two whiskers deflected in succession, are weaker in trimmed than in control animals. Suppressive caudal/rostral and ventral/dorsal gradients, however, seem unaffected by sensory deprivation. Thus the developmental period during which experience persistently modifies maturing barrel circuitry extends up to and likely beyond the onset of whisking behavior. Sensory deprivation during this time affects development of both excitatory and inhibitory receptive fields of barrel neurons and likely impairs cortical integration of sensory information from multiple whiskers.

Action Potentials↗

The role of thalamic inputs in surround receptive fields of barrel neurons.

Controversy exists regarding the relative roles of thalamic versus intracortical inputs in shaping the response properties of cortical neurons. In the whisker-barrel system, this controversy centers on the mechanisms determining the receptive fields of layer IV (barrel) neurons. Whereas principal whisker-evoked responses are determined by thalamic inputs, the mechanisms responsible for adjacent whisker (AW) responses are in dispute. Here, we took advantage of the fact that lesions of the spinal trigeminal nucleus interpolaris (SpVi) significantly reduce the receptive field size of neurons in the ventroposterior thalamus. We reasoned that if AW responses are established by these thalamic inputs, brainstem lesions would significantly reduce the receptive field sizes of barrel neurons. We obtained extracellular single unit recordings from barrel neurons in response to whisker deflections from control rats and from rats that sustained SpVi lesions. After SpVi lesions, the receptive field of both excitatory and inhibitory barrel neurons decreased significantly in size, whereas offset/onset response ratios increased. Response magnitude decreased only for inhibitory neurons. All of these findings are consistent with the hypothesis that AW responses are determined primarily by direct thalamic inputs and not by intracortical interactions.

Animals↗

Change blindness: past, present, and future.

Change blindness is the striking failure to see large changes that normally would be noticed easily. Over the past decade this phenomenon has greatly contributed to our understanding of attention, perception, and even consciousness. The surprising extent of change blindness explains its broad appeal, but its counterintuitive nature has also engendered confusions about the kinds of inferences that legitimately follow from it. Here we discuss the legitimate and the erroneous inferences that have been drawn, and offer a set of requirements to help separate them. In doing so, we clarify the genuine contributions of change blindness research to our understanding of visual perception and awareness, and provide a glimpse of some ways in which change blindness might shape future research.

Attention↗

What you see is what you set: sustained inattentional blindness and the capture of awareness.

This article reports a theoretical and experimental attempt to relate and contrast 2 traditionally separate research programs: inattentional blindness and attention capture. Inattentional blindness refers to failures to notice unexpected objects and events when attention is otherwise engaged. Attention capture research has traditionally used implicit indices (e.g., response times) to investigate automatic shifts of attention. Because attention capture usually measures performance whereas inattentional blindness measures awareness, the 2 fields have existed side by side with no shared theoretical framework. Here, the authors propose a theoretical unification, adapting several important effects from the attention capture literature to the context of sustained inattentional blindness. Although some stimulus properties can influence noticing of unexpected objects, the most influential factor affecting noticing is a person's own attentional goals. The authors conclude that many--but not all--aspects of attention capture apply to inattentional blindness but that these 2 classes of phenomena remain importantly distinct.

Adult↗

Imaging implicit perception: promise and pitfalls.

The study of implicit perception - perception in the absence of awareness - has a long history. Decades of behavioural work have identified crucial theoretical and methodological issues that must be considered when evaluating claims of implicit perception. Neuroimaging methods provide an important new avenue for illuminating our understanding of perception both with and without awareness, but most imaging experiments have not met the rigorous conditions that the behavioural work has shown are necessary for inferring implicit perception. Here, we review the literature of both behavioural and neuroimaging studies, and note the pitfalls of studying implicit perception as well as the promise that neuroimaging studies have for providing insights about implicit perception when combined with appropriately rigorous behavioural measures of awareness.

Animals↗

Do new objects capture attention?

The visual system relies on several heuristics to direct attention to important locations and objects. One of these mechanisms directs attention to sudden changes in the environment. Although a substantial body of research suggests that this capture of attention occurs only for the abrupt appearance of a new perceptual object, more recent evidence shows that some luminance-based transients (e.g., motion and looming) and some types of brightness change also capture attention. These findings show that new objects are not necessary for attention capture. The present study tested whether they are even sufficient. That is, does a new object attract attention because the visual system is sensitive to new objects or because it is sensitive to the transients that new objects create? In two experiments using a visual search task, new objects did not capture attention unless they created a strong local luminance transient.

Attention↗

Visual sensing IS seeing: why "mindsight," in hindsight, is blind.

Faced with the surprising failure to notice large changes to visual scenes (change blindness), many researchers have sought evidence for alternative, nonattentional routes to change detection. A recent article in Psychological Science (Rensink, 2004) proposed a new, nonsensory "mindsight" mechanism to explain the finding that some subjects on some trials reported sensing the presence of a recurring change before they could explicitly identify it and without having a localizable visual experience of change. This mechanism would constitute a previously unknown mode of seeing that, as Rensink suggested, might be akin to a sixth sense. Its existence would have radical implications for the mechanisms underlying conscious visual experience. Provocative claims merit rigorous scrutiny. We rebut the existence of a mindsight mechanism by supporting a more mundane explanation: Some subjects take time to verify their initial conscious detection of changes.

Humans↗

The dynamic events that capture visual attention: A reply to Abrams and Christ (2005).

We recently demonstrated that, contrary to previous findings, some types of irrelevant motion are capable of capturing our attention (Franconeri & Simons, 2003). Strikingly, whereas sitmulated looming (a dynamic increase in object size) captured attention, simulated receding (a decrease in object size) did not. Abrams and Christ (2003, 2005) have provided a different interpretation of this evidence, arguing that in each case attention was captured by the onset of motion rather than by motion per se. They argued that the only published finding inconsistent with their motion onset account is our evidence that simulated receding motion failed to capture attention. Abrams and Christ (2005) presented a receding object stereoscopically and found that it did capture attention, leading them to conclude that the motion onset account explains existing data more parsimoniously than our account does. Our reply has three parts. First, we argue that evidence of capture by receding motion is interesting but irrelevant to the debate over whether capture by motion requires a motion onset. Second, we show that the original empirical evidence in support of the motion onset claim (Abrams & Christ, 2003) put the motion-only condition at a critical disadvantage. We present a new experiment that demonstrates strong capture by motion in the absence of a motion onset, showing that motion onsets are not necessary for attention capture by dynamic events. Finally, we outline what is known about the set of dynamic events that capture attention.

Attention↗

Attention capture is modulated in dual-task situations.

Because some features affect the efficiency of visual search even when they are irrelevant to the task, they are thought to capture attention in a stimulus-driven manner. If such attention shifts are stimulus driven, they should be unaffected by reduced resources. We added a concurrent auditory task to a traditional attention capture paradigm and found that capture by an irrelevant, abruptly appearing stimulus (i.e., an onset) was eliminated. In contrast, prioritization of an irrelevant color singleton--a stimulus that at most receives only mild prioritization in this paradigm--was increased under dual-task conditions. These results challenge the hypothesis that attention capture by irrelevant features is stimulus driven. Instead, prioritization depends on and is modulated by the availability of resources.

Attention↗

Robust temporal coding in the trigeminal system.

The ability of rats to use their whiskers for fine tactile discrimination rivals that of humans using their fingertips. Rats perform discriminations rapidly and accurately while palpating the environment with their whiskers. This suggests that whisker deflections produce a robust and reliable neural code. Whisker primary afferents respond with highly reproducible temporal spike patterns to transient stimuli. Here we show that, with the use of a linear kernel, any of these reproducible response trains recorded from an individual neuron can reliably predict complex whisker deflections. These predictions are significantly improved by integrating responses from neurons with opposite angular preferences.

Acoustic Stimulation↗

Precise temporal responses in whisker trigeminal neurons.

The ability of rats using their whiskers to perform fine tactile discrimination rivals that of humans using their fingertips. Rats must perform these discriminations rapidly and accurately while palpating the environment with their whiskers. This suggests that whisker-derived inputs produce a robust and reliable code, capable of capturing complex, high-frequency information. The first neural representation of whisker-derived stimulus information is in primary afferent neurons of the trigeminal ganglion. Here we demonstrate that there is a continuum of direction-dependent response profiles in trigeminal neurons and provide the first quantitative analysis of the encoding of complex stimuli by these neurons. We show that all classes of trigeminal ganglion neurons respond with highly reproducible temporal spike patterns to transient stimuli. Such a robust coding mechanism may allow rapid perception of complex tactile features.

Action Potentials↗

Functional topography of corticothalamic feedback enhances thalamic spatial response tuning in the somatosensory whisker/barrel system.

Corticothalamic (CT) projections are approximately 10 times more numerous than thalamocortical projections, yet their function in sensory processing is poorly understood. In particular, the functional significance of the topographic precision of CT feedback is unknown. We addressed these issues in the rodent somatosensory whisker/barrel system by deflecting individual whiskers and pharmacologically enhancing activity in layer VI of single whisker-related cortical columns. Enhancement of corticothalamic activity in a cortical column facilitated whisker-evoked responses in topographically aligned thalamic barreloid neurons, while activation of an adjacent column weakly suppressed activity at the same thalamic site. Both effects were more pronounced when stimulating the preferred, or principal, whisker than for adjacent whiskers. Thus, facilitation by homologous CT feedback sharpens thalamic receptive field focus, while suppression by nonhomologous feedback diminishes it. Our findings demonstrate that somatosensory cortex can selectively regulate thalamic spatial response tuning by engaging topographically specific excitatory and inhibitory mechanisms in the thalamus.

Action Potentials↗

Nothing compares 2 views: change blindness can occur despite preserved access to the changed information.

Change blindness, the failure to detect visual changes that occur during a disruption, has increasingly been used to infer the nature of internal representations. If every change were detected, detailed representations of the world would have to be stored and accessible. However, because many changes are not detected, visual representations might not be complete, and access to them might be limited. Using change detection to infer the completeness of visual representations requires an understanding of the reasons for change blindness. This article provides empirical support for one such reason: change blindness resulting from the failure to compare retained representations of both the pre- and postchange information. Even when unaware of changes, observers still retained information about both the pre- and postchange objects on the same trial.

Awareness↗

Searching for stimulus-driven shifts of attention.

Several types of dynamic cues (e.g., abrupt onsets, motion) draw attention in visual search tasks even when they are irrelevant. Although these stimuli appear to capture attention in a stimulus-driven fashion, typical visual search tasks might induce an intentional strategy to focus on dynamic events. Because observers can only begin their search when the search display suddenly appears, they might orient to any dynamic display change (Folk, Remington, & Johnston, 1992; Gibson & Kelsey, 1998). If so, the appearance of capture might result from task-induced biases rather than from the properties of the stimulus. In fact, such biases can even create the appearance of stimulus-driven capture by stimuli that typically do not capture attention (Gibson & Kelsey, 1998). The possibility of task-induced, top-down biases plagues the interpretation of all previous studies claiming stimulus-driven attention capture by dynamic stimuli. In two experiments, we attempt to eliminate potential task-induced biases by removing any need to monitor for display changes. In the first experiment, search displays did not change on most trials. In the second experiment, although new search displays appeared on each trial, we ensured that observers never saw the changes, by making them during large saccades. In both cases, dynamic events still received search priority, suggesting that some dynamic stimuli capture attention in a stimulus-driven fashion.

Attention↗

Thalamocortical angular tuning domains within individual barrels of rat somatosensory cortex.

In the rodent somatosensory cortex, whisker-related barrels in layer IV are morphological counterparts of functional cortical columns that extend throughout the cortical depth. We used microelectrode recordings and spike-triggered averaging of field potentials evoked by single thalamic barreloid neurons to investigate functional thalamocortical microcircuits. The function of such circuits was probed by deflecting the principal whisker of a barrel in different angular directions. We found that individual barrels contain minicolumns of neurons preferring the same deflection angle. Angular tuning domains are established by convergent inputs from thalamocortical cells with corresponding angular preferences. Processing within such domains may depend on local connectivity among vertically aligned barrel neurons.

Action Potentials↗

Angular tuning and velocity sensitivity in different neuron classes within layer 4 of rat barrel cortex.

Local circuitry within layer IV whisker-related barrels is preferentially sensitive to thalamic population firing synchrony, and neurons respond most vigorously to stimuli, such as high-velocity whisker deflections, that evoke it. Field potential recordings suggest that thalamic barreloid neurons having similar angular preferences fire synchronously. To examine whether angular tuning of cortical neurons might also be affected by thalamic firing synchrony, we characterized responses of layer IV units to whisker deflections that varied in angular direction and velocity. Barrel regular-spike units (RSUs) became more tuned for deflection angle with slower whisker movements. Deflection amplitude had no affect. Barrel fast-spike units (FSUs) were poorly tuned for deflection angle, and their responses remained constant with different deflection velocity. The dependence of angular tuning on deflection velocity among barrel RSUs appears to reflect the same underlying response dynamics that determine their velocity sensitivity and receptive field focus. Unexpectedly, septal RSUs and FSUs are largely similar to their barrel counterparts despite available evidence suggesting that they receive different afferent inputs and are embedded within different local circuits.

Afferent Pathways↗