Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013 Dec 17:7:851.
doi: 10.3389/fnhum.2013.00851. eCollection 2013.

Brain regions concerned with the identification of deceptive soccer moves by higher-skilled and lower-skilled players

Affiliations

Brain regions concerned with the identification of deceptive soccer moves by higher-skilled and lower-skilled players

Michael J Wright et al. Front Hum Neurosci. .

Abstract

Expert soccer players are able to utilize their opponents' early body kinematics to predict the direction in which the opponent will move. We have previously demonstrated enhanced fMRI activation in experts in the motor components of an action observation network (AON) during sports anticipation tasks. Soccer players often need to prevent opponents from successfully predicting their line of attack, and consequently may try to deceive them; for example, by performing a step-over. We examined how AON activations and expertise effects are modified by the presence of deception. Three groups of participants; higher-skilled males, lower-skilled males, and lower-skilled females, viewed video clips in point-light format, from a defender's perspective, of a player approaching and turning with the ball. The observer's task in the scanner was to determine whether the move was normal or deceptive (involving a step-over), while whole-brain functional images were acquired. In a second counterbalanced block with identical stimuli the task was to predict the direction of the ball. Activations of AON for identification of deception overlapped with activations from the direction identification task. Higher-skilled players showed significantly greater activation than lower-skilled players in a subset of AON areas; and lower-skilled males in turn showed greater activation than lower-skilled females, but females showed more activation in visual cortex. Activation was greater for deception identification than for direction identification in dorsolateral prefrontal cortex, medial frontal cortex, anterior insula, cingulate gyrus, and premotor cortex. Conversely, greater activation for direction than deception identification was found in anterior cingulate cortex and caudate nucleus. Results are consistent with the view that explicit identification of deceptive moves entails cognitive effort and also activates limbic structures associated with social cognition and affective responses.

Keywords: action observation; deception; expertise; fMRI; football; mirror neuron system; soccer; sport.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Mean percentage accuracy on normal and deceptive trials in scanner sessions where the task was to identify of the type of move (normal or deceptive) and in sessions where the task was to identify the direction of play (left or right). Error bars are ±1 s.e.m. Difference between deception identification and direction identification (bracketed bars) is significant at **p < 0.005.
Figure 2
Figure 2
Mean values for d-prime (d′); perceptual sensitivity, and Beta (β); likelihood ratio or response bias, for all experimental conditions. (A) d′, 0 ms occlusion; (B) d′, −160 ms occlusion; (C) β, 0 ms occlusion (D) β, −160 ms occlusion. Error bars are ±1 s.e.m. Asterisks for Beta values represent mean values significantly different from 1 (one sample t-test, two-tailed p < 0.5* < 0.005**). All d′ were significantly different from zero (one sample t-test, two-tailed).
Figure 3
Figure 3
Higher-skilled males. Second-level fMRI activations (p < 0.005, FWE corrected, 25 voxels minimum cluster size) to deception identification (cyan) and direction identification (magenta) in point-light soccer video clips, relative to stimulus-matched non-biological motion (NBM) controls. Overlapping areas responding to both identification tasks appear purple. Activations above threshold (blobs) are displayed in co-registration with an individual normalized structural brain image and sampled in horizontal sections 10 mm apart from z = 60 to z = −20. In darker blue areas, activation to deception identification exceeds activation to direction identification; and in red areas, activation to direction identification exceeds activation to deception identification (at p < 0.001 uncorrected). Key: a: premotor, BA6; b: parietal, BA40; c: medial frontal, BA6; d: anterior cingulate, BA32; e: posterior cingulate, BA23; f: dorsolateral prefrontal, BA46; g: caudate nucleus; h: superior temporal gyrus, BA37; i: anterior insula/frontal operculum, BA13/45; j: cerebellum; k: superior parietal lobule, BA7.
Figure 4
Figure 4
Lower-skilled males. Second-level fMRI activations (p < 0.005, FWE corrected, 25 voxels minimum cluster size) to deception identification (cyan) and direction identification (magenta) in point-light soccer video clips, relative to stimulus-matched non-biological motion (NBM) controls. Overlapping areas responding to both identification tasks appear purple. Activations above threshold (blobs) are displayed in co-registration with an individual normalized structural brain image and sampled in horizontal sections 10 mm apart from z = 60 to z = −20. In darker blue areas, activation to deception identification exceeds activation to direction identification; and in red areas, activation to direction identification exceeds activation to deception identification (at p < 0.001 uncorrected). Key: a: premotor, BA6; b: parietal, BA40; c: medial frontal, BA6; d: anterior cingulate, BA32; e: posterior cingulate, BA23; f: dorsolateral prefrontal, BA46; g: caudate nucleus; h: superior temporal gyrus, BA37; i: anterior insula/frontal operculum, BA13/45; j: cerebellum; k: superior parietal lobule, BA7.
Figure 5
Figure 5
Lower-skilled females. Second-level fMRI activations (p < 0.005, FWE corrected, 25 voxels minimum cluster size) to deception identification (cyan) and direction identification (magenta) in point-light soccer video clips, relative to stimulus-matched non-biological motion (NBM) controls. Overlapping areas responding to both identification tasks appear purple. Activations above threshold (blobs) are displayed in co-registration with an individual normalized structural brain image and sampled in horizontal sections 10 mm apart from z = 60 to z = −20. In darker blue areas, activation to deception identification exceeds activation to direction identification; and in red areas, activation to direction identification exceeds activation to deception identification (at p < 0.001 uncorrected). Key: a: premotor, BA6; b: parietal, BA40; c: medial frontal, BA6; d: anterior cingulate, BA32; e: posterior cingulate, BA23; f: dorsolateral prefrontal, BA46; g: caudate nucleus; h: superior temporal gyrus, BA37; i: anterior insula/frontal operculum, BA13/45; j: cerebellum; k: superior parietal lobule, BA7; m: medial occipital cortex, BA18; n: anterior cingulate.
Figure 6
Figure 6
Blue colored voxels indicate regions where activation is significantly greater for deception identification than for direction identification, and red voxels indicate regions that respond more to direction identification than deception identification. z = 50; medial frontal, z = 28; dorsolateral prefrontal cortex and posterior cingulate cortex, z = 1; blue: left and right anterior insula, red: left caudate nucleus. z = −2.4; blue: left and right anterior insula; red: anterior cingulate cortex. Data are combined across participant groups and occlusion levels.
Figure 7
Figure 7
Activation differences between higher- and lower-skilled males (red) and between lower-skilled males and females (green) in soccer action identification tasks at p < 0.05 FWE corrected, minimum cluster size = 5 voxels. Data are combined across task types (deception identification and direction identification) and occlusion levels (0 ms, −160 ms). Second-level group analysis is based on first-level contrasts between identification tasks and NBM controls.

References

    1. Abernethy B., Gill D., Parks S. L., Packer S. T. (2001). Expertise and the perception of kinematic and situational probability information. Perception 30, 233–252 10.1068/p2872 - DOI - PubMed
    1. Abernethy B., Russell D. G. (1984). Advance cue utilisation by skilled cricket batsmen. Austr. J. Sci. Med. Sport 16, 2–10
    1. Abernethy B., Zawi K., Jackson R. (2008). Expertise and attunement to kinematic constraints. Perception 37, 931–948 10.1068/p5340 - DOI - PubMed
    1. Abernethy B., Russell D. G. (1987). Expert-novice differences in an applied selective attention task. J. Sport Psychol. 9, 326–245
    1. Aglioti S. M., Cesari P., Romani M., Urgesi C. (2008). Action anticipation and motor resonance in elite basketball players. Nat. Neurosci. 11, 1109–1116 10.1038/nn.2182 - DOI - PubMed

LinkOut - more resources