Skip to main content
i-Perception logoLink to i-Perception
. 2021 May 27;12(3):20416695211018714. doi: 10.1177/20416695211018714

The Modulation of Exogenous Attention on Emotional Audiovisual Integration

Yueying Li 1,*, Zimo Li *, Aihui Deng, Hewu Zheng, Jianxin Chen 2, Yanna Ren 3, Weiping Yang 4,✉
PMCID: PMC8167015  PMID: 34104384

Abstract

Although emotional audiovisual integration has been investigated previously, whether emotional audiovisual integration is affected by the spatial allocation of visual attention is currently unknown. To examine this question, a variant of the exogenous spatial cueing paradigm was adopted, in which stimuli varying by facial expressions and nonverbal affective prosody were used to express six basic emotions (happiness, anger, disgust, sadness, fear, surprise) via a visual, an auditory, or an audiovisual modality. The emotional stimuli were preceded by an unpredictive cue that was used to attract participants’ visual attention. The results showed significantly higher accuracy and quicker response times in response to bimodal audiovisual stimuli than to unimodal visual or auditory stimuli for emotional perception under both valid and invalid cue conditions. The auditory facilitation effect was stronger than the visual facilitation effect under exogenous attention for the six emotions tested. Larger auditory enhancement was induced when the target was presented at the expected location than at the unexpected location. For emotional perception, happiness shared the biggest auditory enhancement among all six emotions. However, the influence of exogenous cueing effect on emotional perception seemed to be absent.

Keywords: emotion, exogenous attention, crossmodal integration, audiovisual stimuli


In real life, with the developments of technology, the question of whether exogenous attention can facilitate the emotional audiovisual integration has become increasingly more appealing. For example, to enhance the sense of engagement, many man–machine interfaces have begun to provide users with emotional audiovisual information. Specifically, video games give players not only auditory emotional feedback but also visual emotional feedback, and players combine this information into a coherent percept, thus enabling a deeper immersive experience than visual or auditory emotional feedback presented alone. Under such circumstances, the following question will arise: Can spatially allocated attention have an effect on emotional audiovisual integration? If the answer is yes, then the emotional audiovisual integration might be facilitated by setting an exogenous attentional cue in interface systems, therefore enhancing the emotional experience of users. Attention can be classified as either endogenous or exogenous. Endogenous attention, also called goal-driven or voluntary attention, involves a more purposeful orienting process driven by an individual’s goals and intentions (Doricchi et al., 2010), for example, orienting to a telephone booth in response to information that your friend is there waiting for you. In contrast, exogenous attention, also called stimulus-driven or involuntary attention, can be understood as the reorientation of endogenous attention to biologically salient events that occur outside of the current attentional focus (Collins & Schirillo, 2013); for example, audiences are attracted by the trick of a magician. In the classic exogenous cueing paradigm (Posner et al., 1980), a bright outline or a rapid flash of light across a potential target location presented on either the left or right side of a computer screen can serve as a peripheral cue to catch an individual’s attention. Improved task performance in terms of rapid detection or better accuracy at the correctly cued location than at the wrongly cued location or uncued location was found (Milliken et al., 2003).

As we pay attention to our social surroundings, information immersed continually in a complex stream of stimulations from multiple sensory channels includes not only unimodal (e.g., visual, auditory, tactile) information but also information from the integration of different modalities. By combining information from different sensory channels, multisensory integration can make better use of the available information and reduce interference in the sensory system (Stein & Meredith, 1990). Evidence shows one-way crossmodal dependence in exogenous orienting from audition to vision (Spence & Driver, 1997) as well as two-way crossmodal dependence in exogenous orienting, whereby audition and vision influence tactile sensation and vice versa (Spence et al., 1998). In addition to multimodal information input, emotional perception, which includes facial expression, gestures, and emotional vocalization, also serves as an inevitable part of human interactions. The integration of emotional signals from the human face and voice ensures the efficiency of emotional recognition and can result in the enhancement of perceptual sensitivity and behavioral responses (Brosch et al., 2008; Miller, 1986), in which the perception of an emotional facial expression can be biased toward the valence of simultaneously presented affective prosodic stimuli and vice versa (Föcker et al., 2011; Rigoulot & Pell, 2012). For instance, fearful and neutral faces were rated as being more fearful when accompanied by fearful sounds than by neutral sounds (Müller et al., 2011). Furthermore, there were evidence showing biases in spatial perception for emotional audiovisual integration (Bertelson & Radeau, 1981), in which visual events always modulate the perceived location of sounds, while sounds produce a much weaker influence on the perceived location of visual events (de Gelder et al., 1999).

However, studies on whether exogenous attention can have an impact on emotional audiovisual integration perception are limited. Most of the research has focused on the relationship between emotion and exogenous attention. In terms of the effects of emotions on exogenous attention, a study applied a color-flanker task to investigate the effects of emotion and color congruency on attentional allocation (Li et al., 2013). In the previous study, congruent processing conditions indicated that the flanker words and the target words had the same color, while incongruent processing conditions had different colors. This study confirmed the effects of emotion on attentional allocation, and such effects varied under different congruency conditions. Furthermore, our study manipulated attentional allocation by presenting a spatially congruent or incongruent cue. Thus, we proposed that the effects of emotion on attentional allocation may also vary in different spatial congruency conditions. Reduced attentional allocation was represented by an enhanced P200-related attentional response to negative stimuli compared to positive stimuli (Carretié et al., 2001). With respect to the modulation of exogenous attention to emotional information, previous studies have shown that exogenous attention can intensify the perception of emotional expressions, and elevated motivation leads to improved efficiency in orienting and reorienting exogenous spatial attention (Engelmann & Pessoa, 2014).

As illustrated earlier, previous studies have demonstrated the interplay between exogenous attention and crossmodal integration, and the biases between different modalities as well as in spatial perception for emotional audiovisual integration. In the past, both scientists and layfolk have considered that the integration of facial and vocal emotional expressions is an automatic process that is independent of attention. This is because we often intuitively, effortlessly, and unconsciously integrate emotional audiovisual information, and previous studies seem to espouse this intuition (de Gelder & Vroomen, 2000; Vroomen et al., 2001). Under such circumstances, the early integration framework was proposed, stating that audiovisual integration is independent of attention (Koelewijn et al., 2010). If that is the case, emotional audiovisual processing should not be affected by the spatial allocation of visual attention. In contrast, the late integration framework asserts that attention is required for audiovisual integration to occur. Evidence challenging the early integration framework has emerged in recent studies, which suggests that the integration of emotional audiovisual information is not independent of attention (Chen et al., 2016; Ho et al., 2015). However, in the previous studies, subjects were instructed to attend to a certain modality while ignoring the other modality; that is, the influence of selective attention on emotional audiovisual integration was tested. Thus, these studies did not solve a critical question, which is whether emotional audiovisual processing can be affected by the spatial allocation of attention; that is, the influence of divided attention (subjects were required to attend to both visual and auditory modalities) on emotional audiovisual integration has not been tested. The current study attempted to address this issue by using a variant of exogenous spatial cueing paradigm, with an exogenous cue presented on the left or right side of the screen that is spatially congruent (valid) or incongruent (invalid) with the target’s location. Facial or vocal emotional target stimuli expressing six basic emotions (happiness, anger, disgust, sadness, fear, surprise) in the visual, auditory, or emotionally congruent audiovisual modality were presented randomly after the cue.

Materials and Methods

Participants

Fifty-four participants (20 men and 32 women; aged 18–23 years; mean age = 21.4 years), all right-handed and with normal or corrected-to-normal vision and hearing capabilities, participated in this experiment. To calculate the required sample size, a simple power analysis for a repeated-measures t test with a medium expected effect size of dz = 0.5 was performed. That analysis yielded a required sample size of N = 54. All participants provided written informed consent to participate in this study, which was previously approved by the Ethics Committee of Hubei University. All participants received payment for their time.

Stimuli

A black box (1.35 cm × 1.35 cm, with a visual signal of 0.86°) was used as an exogenous attention cue presented on the left or right side of the computer screen and was spatially congruent (valid) or incongruent (invalid) with the target location. Visual emotional stimuli were selected from the Chinese Facial Emotional Pictures collection (Gong et al., 2011). All facial pictures were black and white, 260 mm × 300 mm, and 24 bits. We selected pictures portraying six emotions, including happiness, sadness, disgust, surprise, fear, and anger. For each emotion, there were four pictures (two males and two females). The selection of visual stimuli was based on the dimensions of affective identity and affective intensity. The emotional pictures were chosen to have similar affective intensity scores (approximately 5) and a high identity rate (more than 70%). The rationale of choosing high identity rate pictures was to make sure the facial picture expressed the corresponding emotion, and the choice of similar intensity score pictures was to make sure a similar level of arousal was induced.

For auditory stimuli, students (two males and two females) who were performance artists from Sinan Troupe at Hubei University were asked to say six Chinese interjections (a, ai, ha, yo, ya, o) with happy, sad, disgusted, surprised, fearful, and angry facial expressions. While talking, the speakers were required to generate consistent facial expressions and imitate the expressions of emotional pictures to ensure the validity of the audio stimuli. Before the recording session, the speakers practiced until they could convey the specified emotion with simultaneous facial and vocal expressions. The recording session was conducted in a bright and quiet room, with a smart phone used to record the sound. The samples were standardized to 44.1 kHz, 32 bits, and stereo, with a duration of 500 ms using Adobe Audition CC.

For audiovisual stimuli, auditory stimuli were paired with the facial expressions for each emotion with the same valence and presented in the same direction (left or right). To avoid interactions of speaker sex and emotionality in stimulus pairs, only tokens from same-sex speakers were combined.

Evaluation Test

In the evaluation test, we tested the self-made auditory stimuli and the retested chosen visual stimuli on affective identity to ensure the validity of all the selected stimuli. Twenty-four college students were recruited to rate the affective identity of previous selected stimuli on a scale of 1 to 9. Each participant needed to complete a session for auditory stimuli evaluation as well as a session for visual stimuli evaluation. The sequence of the previous sessions was counterbalanced across participants. In both evaluation sessions, trials began with a fixation cross presented at the center of the screen for 500 ms; an emotional cue word (anger, disgust, fear, happiness, sadness, surprise) was then presented to suggest the type of emotion that the subsequent stimulus expressed. The duration of the emotional cue word was 1,000 ms, and the subsequent visual or auditory stimulus was presented for 500 ms. Participants needed to report the degree of consistency between the category shown on the screen and the type of emotion that visual or auditory stimuli expressed. Results were showed in Table S1 and Table S2. After collecting the consistency score of each stimulus, one-sample t tests were conducted to compare the value of the consistency score with 5. The result showed that the consistency score of all the selected stimuli was significantly higher than 5 (all ps < .05).

Procedure

For the experiment, a 2 cue (valid cue, invalid cue) × 6 emotion (anger, disgust, fear, happiness, sadness, surprise) × 3 modality (auditory, visual, audiovisual) within-group design was employed. The experiment was conducted in a quiet and bright room (Laboratory Room; Hubei University, China). Visual stimuli were generated and displayed with E-prime 2.0 and presented on a monitor (1,680 × 1,050 pixels; 60 Hz). The auditory stimuli were presented by means of two loudspeaker cones located on either side of the computer monitor. Participants sat at a distance of 50 cm from the screen and were asked to complete an emotional discrimination task to identify the emotion portrayed on each trial. At the beginning of each trial, a black fixation point appeared on a white background screen for 500 ms, and then a black box appeared (at a visual angle of 3.4° to the left or right of center) that was spatially congruent (valid) or incongruent (invalid) with the target’s location for 50 ms before target presentation (Figure 1). Then, participants were asked to press corresponding keys to make a judgment on the type of target with the buttons “a,” “s,” “d,” “j,” “k,” and “l,” matching anger, disgust, fear, happiness, sadness, and surprise, respectively. The buttons “a,” “s,” and “d” were pressed by the left hand, and the buttons “j,” “k,” and “l” were pressed by the right hand. A maximum of 1,800 ms was available for responding; after that time, the next trial started. There were 6 blocks, and every block consisted of 144 trials (48 auditory stimuli, 48 visual stimuli, 48 audiovisual stimuli). The proportion of valid and invalid cues was 50% in every modality. It took 40 minutes to perform the task blocks, and the three kinds of stimuli were presented at random to each participant in all blocks. Prior to the formal experiment, a practice experiment was conducted to ensure that the participants were familiar with the key responses.

Figure 1.

Figure 1.

Design of the experimental paradigm.

Data Analysis

First, to investigate whether the factors (cue validity, emotion, and modality) had a general influence on accuracy (ACC) and response times (RTs), we performed a 2 × 6 × 3 repeated-measures analysis of variance in each presentation condition, with cue validity (valid, invalid); emotion (anger, disgust, fear, happiness, sadness, surprise); and modality (visual, auditory, audiovisual) serving as within-subject factors. Effect sizes are reported as partial eta-squared (ηp2). Analyses of variance were adjusted with the Greenhouse–Geisser nonsphericity correction for effects with more than one degree of freedom. Planned comparisons or post hoc Bonferroni tests were conducted to further explore the interactions between cue validity, channel, and emotion.

Second, to examine the benefit obtained from combining information from the two modalities, we computed both visual enhancement (VE), which reflects the benefit gained from adding an additional visual stimulus to an auditory stimulus, and auditory enhancement (AE), which reflects the benefit gained from adding an additional auditory stimulus to a visual stimulus. The measures of VE and AE have been widely used in investigation of audiovisual performance (Sommers et al., 2005; Sumby & Pollack, 1954; Tye-Murray et al., 2007; Winneke & Phillips, 2011). The formula for response accuracy data was as follows: VE/AE=ACC(visual/auditory)−ACC(audiovisual)ACC(audiovisual); and the formula for RT data was as follows: VE/AE=RT(visual/auditory)−RT(audiovisual)RT(audiovisual). By conducting the analysis, we could compare the visual contribution to emotional audiovisual integration with or without a valid visual cue, thus addressing the question of whether exogenous attention elicited by a visual cue could facilitate emotional audiovisual integration.

Finally, to examine whether the RTs obtained under the crossmodal condition exceeded the statistical facilitation predicted by the race model (Raab, 1962), the amount of race model violation was calculated under exogenously invalid and valid conditions. The race model is said to be violated when the probability (p) of a particular RT is higher in the multisensory condition than the joint probability of the unisensory responses, that is, p(AV) > p(A + V) – p(A*V), for that given RTs. Significant violations of the race model (i.e., RTAV < RT Race model) indicate multisensory integration.

Results

ACC and RTs

ACC and RTs for all conditions are presented in Table 1. The analysis revealed a significant main effect of modality on ACC, F(2, 106) = 517.889, p < .001, ηp2 = 0.925, and RTs, F(2, 106) = 187.661, p < .001, ηp2 = 0.878, indicating that participants responded more effectively under crossmodal condition than under either unimodal condition (all p < .001). Importantly, we found significant main effect of cue validity on ACC and RTs. Participants performed less accurately and more slowly under invalid cue than valid cue—72.7 ± 1.4% versus 73.8 ± 1.4%, F(1, 53) = 8.908, p = .004, ηp2 = 0.144 for ACC; 578.95 ± 20.27 ms versus 570.11 ± 19.78 ms, F(1, 53) = 18.348, p < .001, ηp2 = 0.257 for RTs—which showed the processing advantage of cue validity. There was a significant main effect of emotion on ACC, F(5, 265) = 22.265, p < .001, ηp2 = 0.296, and RTs, F(5, 265) = 12.308, p < .001, ηp2 = 0.557. Furthermore, main effects were accompanied by two-way interactions between modality and emotion on ACC, F(10, 530) = 25.921, p < .001, ηp2 = 0.855, and RTs, F(10, 530) = 21.938, p < .001, ηp2 = 0.833. No significant interactions were found between modality and cue validity on ACC, F(2, 106) = 0.550, p = 0.509, ηp2 = 0.010, and RTs, F(2, 106) = 1.495, p = 0.234, ηp2 = 0.054; between emotion and validity on ACC, F(5, 265) = 1.591, p = 0.163, ηp2 = 0.029, and RTs, F(5, 265) = 1.368, p = 0.253, ηp2 = 0.122; or between cue validity, modality, and emotion on ACC, F(10, 530) = 1.120, p = 0.345, ηp2 = 0.021, and RTs, F(10, 530) = 1.125, p = 0.341, ηp2 = 0.021. Post hoc comparisons (see Figure 2) further revealed significantly higher accuracy and faster RTs for bimodal audiovisual stimuli than for unimodal auditory stimuli and for unimodal visual stimuli than for unimodal auditory stimuli in six emotional conditions (all ps < .001). The accuracy for audiovisual stimuli was significantly higher than that for visual stimuli in anger (p < .001), disgust (p = .001), fear (p < .001), sadness (p < .001), and surprise (p = .001) emotional conditions. The RT for audiovisual stimuli was significantly faster than that for visual stimuli in anger (p < .001), disgust (p < .001), fear (p = .003), happiness (p < .001), and sadness (p < .001) emotional conditions. Happiness induced the highest accuracy and the fastest RTs for visual and audiovisual stimuli among all six emotions.

Table 1.

Mean Accuracy (%) and Response Times (ms) of Emotion Judgment Based on Visual, Auditory, and Audiovisual Stimulus Modalities Under Valid and Invalid Cue Conditions Across Emotion Categories.


Mean accuracy (%)
Anger Disgust Fear Happiness Sadness Surprise
Valid cue Visual 83.3 (1.7) 83.3 (1.6) 74.2 (2.2) 93.0 (1.1) 76.3 (2.6) 83.0 (1.8)
Auditory 65.6 (2.8) 37.9 (2.2) 53.7 (2.2) 35.6 (2.6) 58.7 (2.6) 67.3 (2.0)
Crossmodal 88.2 (1.6) 86.7 (1.8) 80.3 (2.1) 92.6 (1.5) 82.2 (2.0) 86.9 (1.6)
Invalid cue Visual 79.2 (1.9) 81.8 (1.8) 72.3 (2.5) 93.1 (1.5) 74.7 (2.6) 83.6 (1.7)
Auditory 66.6 (2.9) 85.9 (2.0) 52.6 (2.1) 34.4 (2.7) 57.0 (2.6) 66.9 (2.0)
Crossmodal 85.9 (1.7) 85.8 (1.9) 79.9 (1.9) 93.9 (0.9) 80.1 (2.0) 86.9 (1.8)

Response time (ms)



Anger

Disgust

Fear

Happiness

Sadness

Surprise
Valid cue Visual 541.0 (21.4) 527.3 (24.1) 600.9 (30.9) 345.6 (18.1) 565.3 (26.9) 542.9 (29.2)
Auditory 633.3 (25.6) 758.8 (33.7) 724.2 (28.5) 733.0 (26.8) 622.4 (19.2) 704.3 (23.9)
Crossmodal 494.5 (25.2) 486.8 (22.2) 540.4 (27.6) 372.8 (17.4) 515.8 (22.8) 552.3 (27.2)
Invalid cue Visual 567.8 (24.9) 563.9 (27.7) 604.6 (28.4) 361.9 (15.5) 574.6 (26.8) 585.9 (29.4)
Auditory 613.3 (26.1) 773.5 (29.9) 709.3 (28.1) 785.7 (31.8) 621.8 (21.5) 696.1 (25.2)
Crossmodal 497.9 (23.3) 514.1 (24.7) 581.4 (25.6) 420.9 (15.9) 529.6 (23.0) 580.6 (28.4)

Note. Standard errors are given in parentheses.

Figure 2.

Figure 2.

Response times and accuracy for each emotion category with respect to visual, auditory, and audiovisual modality. Error bars represent the standard error (SE). Asterisks indicate significant differences between presentation conditions (**p < .01, ***p < .001).

VE and AE

To demonstrate the level of crossmodal enhancement for accuracy and RTs under exogenous attention conditions, VE and AE were calculated separately. We found significant main effect of modality on ACC, F(1, 53) = 405.762, p < .001, ηp2 = 0.884, and RTs, F(1, 53) = 188.043, p < .001, ηp2 = 0.78, which indicated larger enhancement for auditory than visual stimuli. Importantly, we found significant main effect of cue validity on RTs, F(1, 53) = 8.004, p = .007, ηp2 = 0.131, but not on ACC, F(1, 53) = 1.822, p = .183, ηp2 = 0.033. Larger enhancement was induced when the target was presented at the expected location than at the unexpected location. There was a significant main effect of emotion on ACC, F(5, 265) = 35.410, p < .001, ηp2 = 0.783, and RTs, F(5, 265) = 16.723, p < .001, ηp2 = 0.631. Furthermore, there were significant interactions between modality and emotion on ACC, F(5, 265) = 53.691, p < .001, ηp2 = 0.503, and RTs, F(5, 265) =33.709, p < .001, ηp2 = 0.775; between modality and cue validity on RTs, F(1, 53) = 8.216, p = 0.006, ηp2 = 0.134. No significant interactions were found between modality and cue validity on ACC, F(1, 53) = 0.500, p = .775, ηp2 = 0.049, and RTs, F(1, 53) = 0.500, p = .775, ηp2 = 0.049; between emotion and validity on ACC, F(5, 265) = 1.591, p = .163, ηp2 = 0.029, and RTs, F(5, 260) = 1.69, p = .137, ηp2 = 0.031; or between cue validity, modality, and emotion on ACC, F(5, 260) = 0.895, p = .492, ηp2 = 0.084, and RTs, F(5, 265) = 0.586, p = .711, ηp2 = 0.011. Post hoc comparisons results showed significantly stronger AE than VE for all six emotions for ACC (all ps < .05; Figure 3A) and RTs (all ps < .05; Figure 3B). Moreover, valid cue can induce stronger AE than invalid cue (0.534 vs. 0.431, p = .002; Figure 4). In addition, happiness showed the biggest AE for RT (all ps < .001) and ACC (all ps < .001).

Figure 3.

Figure 3.

Enhancement scores in accuracy and RTs under each emotion category. Error bars represent the SE. Asterisks indicate significant differences between presentation conditions (**p < .01, ***p < .001).

Figure 4.

Figure 4.

Enhancement scores in RTs with respect to cue validity for all emotion categories. Error bars represent the SE. Asterisks indicate significant differences between presentation conditions (**p < .01).

Race Model Analysis

To test whether race model predictions are met or violated, the RT data were plotted as cumulative distribution functions (CDFs). We divided the RT interval from 90 ms to 1,800 ms into 10 ms bins and calculated the likelihood that a response occurred at a given RT or faster. The CDFs under valid cue conditions and invalid cue conditions are plotted in Figure 5. These data were analyzed by conducting paired t tests at each time bin to determine whether the observed audiovisual RT probabilities, p(AV), were higher than the joint probability of the unisensory responses, p(A + V) – p(A * V). The CDF values for RTs to audiovisual conditions were significantly larger (p < .05) than the CDF values of the joint probability of the unisensory responses for each time bin from 110 ms to 130 ms under invalid conditions and from 100 ms to 120 ms under validly conditions, which indicated audiovisual integration.

Figure 5.

Figure 5.

Test for the violation of race model inequality under valid cue conditions (A) and invalid cue conditions (B). The figure illustrates the cumulative probability curves of the RT under the visual, auditory, and audiovisual conditions. The summed probability for the visual and auditory responses is depicted by the race model curve. Note that the crossmodal responses are faster than the race model prediction from 110 ms to 130 ms under invalid conditions and from 100 ms to 120 ms under valid conditions (all p < .05).

Discussion

The purpose of the present study was to investigate whether exogenous attention was able to affect emotional audiovisual integration. Visual (facial expressions), auditory (nonverbal affective prosody), and audiovisual (simultaneous, congruent facial, and vocal affective expressions) stimuli expressing six basic emotions (anger, disgust, fear, happiness, sadness, and surprise) were adopted to examine the multisensory nature of emotion processing under exogenous attention. In this study, our results have shown the processing advantage of audiovisual modality over unimodal visual and auditory modalities. We also found higher accuracy and a shorter RT in categorizing emotional stimuli when an onset cue correctly predicts the following target location. Moreover, larger AE was induced when the target was presented at the expected location than at the unexpected location. For emotional perception, happiness indicated the biggest AE among all six emotions. However, exogenous attention and emotional perception seemed to work independently and showed no interactions. One potential limitation of the current study is that the cue we used to attract participants’ attention was a visual cue (a black square); it is possible that the cue worked more effectively for attracting visual attention. Thus, it would be helpful to perform a similar study with an auditory cue in the future. Combination of electroencephalogram or functional magnetic resonance imaging could also be used to further establish the corresponding neural correlates of these effects.

First, we observed higher accuracy and shorter RTs in categorizing audiovisual emotional stimuli than in categorizing unimodal visual or auditory stimuli. Analysis of the race model revealed violations under exogenously invalid conditions (110–130 ms) and valid conditions (100–120 ms), which indicated that the faster responses during audiovisual conditions were likely due to an interaction of the two unisensory information channels and not simply the result of two redundant signals (Gondan & Minakata, 2016; Otto & Mamassian, 2017). The assumptions of independent race model were based on statistical independence between two unisensory signals and context invariance. Compared to unimodal information input, the combination of congruent emotional information from different channels could induce higher response efficiency, which reveals crossmodal integration (Spence & Driver, 1997; Spence et al., 1998). Our results align with previous findings, indicating that emotional judgment tend to improve when more than one source of congruent information about the intended emotion is available (de Gelder & Vroomen, 2000; Massaro & Egan, 1996). The fact that similar results were found by discriminating between fear and disgust emotion expressions displayed auditorily, visually, or audiovisually via short dynamic facial and nonlinguistic vocal clips (Collignon et al., 2008), as well as by presenting stimuli with different combinations of facial, semantic, and prosodic cues conveying five basic emotions (anger, disgust, sad, happy, pleasant surprise; Paulmann & Pell, 2011) provide supportive evidences for the multisensory nature of emotion processing. We then calculate the crossmodal enhancement, which is considered a behavioral marker for crossmodal integration (Calvert et al., 2001), and it features shorter RTs and higher accuracy when participants are confronted with congruent bimodal stimuli than when they are faced with unimodal ones. Our results indicated a stronger AE, as opposed to a VE, under exogenous attention for the six emotions tested, which was in line with previous findings (Maurage et al., 2007), showing that emotion recognition was easier in response to facial stimuli than vocal stimuli (Hunter et al., 2010). As have been illustrated with the visual dominance effect (Colavita, 1974), visual stimuli yielded faster RTs than auditory stimuli. The responses of participants are often driven by the visual stimulus, thus indicating faster RT for visual (e.g., facial expressions, semantic contents conveyed via text) than auditory stimuli (e.g., prosody; Koppen & Spence, 2007; Paulmann & Pell, 2011; Stefanou et al., 2019). Moreover, happiness showed the biggest AE of all six emotions. There is robust evidence that people have attentional bias toward negative emotions (Cisler et al., 2009; Van Bockstaele et al., 2014; Yiend, 2010), which could be regarded as facilitated processing of negative alerting (Asmundson & Stein, 1994; Hope et al., 1990) or difficulty in disengaging attention from negative events (Yiend & Mathews, 2001). In our study, the observed faster RT for happiness under visual and audiovisual stimuli confirms the latter point of view and is in line with previous findings (Laurence et al., 2015) but contrasts with studies (Pell & Kotz, 2011; Rigoulot et al., 2013) using verbal emotional stimuli. It might suggest that nonverbal affective vocalizations are processed at different rates. Researchers have argued that auditory emotion expressions are perceived categorically but in a probabilistic manner over time (Juslin & Laukka, 2003). During emotional communication, auditory and visual events may activate different emotional-related concepts. The physical features which signify emotions in the facial channel can be processed instantaneously and are known to demonstrate strong category boundaries in perception. In contrast, the emotional expressions conveyed through prosody are inherently dynamic and their meanings are unfolded over a protracted time period (Etcoff & Magee, 1992).

Furthermore, we observed faster behavioral responses and higher accuracy for target emotional discrimination in valid than invalid conditions for all manipulations, demonstrating that the allocation of visual attention can be successfully manipulated by an onset visual cue (a black square). Our results indicated the existence of an exogenous cueing effect during the perception of peripheral information and was in accordance with that of Armony and Dolan (2002), who used threaten-related fear stimuli. As suggested by the Posner effect, by shifting exogenous attention to the cue location, the task-irrelevant spatial location of the cue can affect the processing of the subsequent target and modulate the perception of the target (Posner, 1980). If the cue predicts the target validly, there is a benefit in the RT and accuracy. However, if the cue is invalid, a cost occurs in the RT and accuracy (Eimer, 1993). A simple explanation for this effect could be that the valid cue automatically attracts subjects’ visual attention to the location of the target, while the invalid cue attracts their attention to the location of the nontarget areas. Because the ratio of valid cues to invalid cues was 1:1, the effects of expectations were well controlled. In addition, valid cues can augment the significance of spatial orientation to reduce the necessity of spatial orientation to audiovisual targets, thus allowing faster behavioral responses to multisensory stimuli (Brosch et al., 2011). Moreover, the proportion of valid cue conditions can modulate attention in a linear manner; namely, the higher the proportion of valid cue conditions is, the faster the RTs and higher accuracy with valid cue conditions relative to invalid cue conditions (Risko et al., 2008), which is a promising question awaiting future research. In addition to the holistic exogenous cueing effect, we also found stronger AE under valid cues than under invalid cues. Posner (1987) suggested that the presentation of a cue increases alertness and directs attention to that spatial location and enhances the processing of targets in this location. Visual cues can enhance visual target performance, thus making the reaction to visual targets faster than that to auditory targets and inducing stronger AE in audiovisual perception (Ngo & Spence, 2010). Visual exogenous cues that are presented for a short duration give rise to stronger facilitating responding to target stimuli on valid trials than invalid trials and showed the crossmodal facilitation of visual cues to AE. However, the impact of exogenous cueing effect seems to be absent for emotional recognition. Exogenous attention, a bottom-up sensory-driven mechanism that biases selection of stimuli, is thought to operate by involuntarily or exogenously shifting attention to salient stimuli (Collins & Schirillo, 2013). Emotional stimuli are another class of stimuli believed to have the ability to capture attention involuntarily (Ohman & Mineka, 2001). Previous studies indicated that emotional attention and exogenous attention reflect different sources of modulations on sensory processing that operate independently of one another (Brosch et al., 2011). The involuntary capture of attention by emotion-related information involves amygdala (Vuilleumier, 2005), and thus might be at least partly separable from exogenous-attention-related frontoparietal modulation of visual processing (Vuilleumier & Driver, 2007). Although both emotional stimuli and bottom-up exogenously shifting can capture attention involuntarily (Ohman & Mineka, 2001), they may work independently in different brain regions and show no interaction. In addition, by following an involuntary manner, emotion recognition processes may incorporate all available emotion cues, possibly leading to systematically higher accuracy rates as observed here.

Supplemental Material

sj-pdf-1-ipe-10.1177_20416695211018714 - Supplemental material for The Modulation of Exogenous Attention on Emotional Audiovisual Integration

Supplemental material, sj-pdf-1-ipe-10.1177_20416695211018714 for The Modulation of Exogenous Attention on Emotional Audiovisual Integration by Yueying Li, Zimo Li, Aihui Deng, Hewu Zheng, Jianxin Chen, Yanna Ren and Weiping Yang in i-Perception

Acknowledgements

The authors would like to thank the individuals who participated in our study.

Footnotes

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by the National Natural Science Foundation of China (31700973, 31800932), the Humanity and Social Science Youth Foundation of Ministry of Education of China (16YJC190025, 18XJC190003), the Humanity and Social Science Youth Foundation of the Education Bureau of Hubei Province of China (16Q030), Natural Science Foundation of Hubei Province of China (2017CFB704), the Doctor Scientific Research Staring Foundation of Guizhou University of Chinese Medicine (043180020), and Youth Project of National Education Science Program (CBA160187).

Ethical Standard: All procedures performed in this study were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Informed Consent: Informed consent was obtained from all individual participants included in the study.

Supplemental Material: Supplemental material for this article is available online at: http://journals.sagepub.com/doi/suppl/10.1177/20416695211018714.

Contributor Information

Yueying Li, Department of Psychology, Faculty of Education, Hubei University, Wuhan, China; Graduate School of Humanities, Kobe University, Japan.

Jianxin Chen, Department of Psychology, Faculty of Education, Hubei University, Wuhan, China.

Yanna Ren, Department of Psychology, Medical Humanities College, Guiyang College of Traditional Chinese Medicine, Guiyang, China.

Weiping Yang, Department of Psychology, Faculty of Education, Hubei University, Wuhan, China; Brain and Cognition Research Center (BCRC), Faculty of Education, Hubei University, Wuhan, China.

References

  1. Armony J. L., Dolan R. J. (2002). Modulation of spatial attention by fear-conditioned stimuli: An event-related fMRI study. Neuropsychologia, 40, 817–826. 10.1016/S0028-3932(01)00178-6 [DOI] [PubMed] [Google Scholar]
  2. Asmundson J. G., Stein M. B. (1994). Selective processing of social threat in patients with generalized social phobia: Evaluation using a dot-probe paradigm. Journal of Anxiety Disorders, 8, 107–117. 10.1016/0887-6185(94)90009-4 [DOI] [Google Scholar]
  3. Bertelson P., Radeau M. (1981). Cross-modal bias and perceptual fusion with auditory-visual spatial discordance. Perception and Psychophysics, 29, 578–584. 10.3758/bf03207374 [DOI] [PubMed] [Google Scholar]
  4. Brosch T., Grandjean D., Sander D., Scherer K. (2008). Behold the voice of wrath: Cross-modal modulation of visual attention by anger prosody. Cognition, 106, 1497–1503. 10.1016/j.cognition.2007.05.011 [DOI] [PubMed] [Google Scholar]
  5. Brosch T., Pourtois G., Sander D., Vuilleumier P. (2011). Additive effects of emotional, endogenous, and exogenous attention: Behavioral and electrophysiological evidence. Neuropsychologia, 49, 1779–1787. 10.1016/j.neuropsychologia.2011.02.056 [DOI] [PubMed] [Google Scholar]
  6. Calvert G., Hansen P. C., Iversen S. D., Brammer M. (2001). Detection of audio-visual integration sites in humans by application of electrophysiological criteria to the BOLD effect. Neurolmage, 14, 427–438. 10.1006/nimg.2001.0812 [DOI] [PubMed] [Google Scholar]
  7. Carretié L., Mercado F., Tapia M., Hinojosa J. A. (2001). Emotion, attention, and the ‘negativity bias’, studied through event-related potentials. International Journal of Psychophysiology Official Journal of the International Organization of Psychophysiology, 41, 75–85. 10.1016/S0167-8760(00)00195-1 [DOI] [PubMed] [Google Scholar]
  8. Chen X., Han L., Pan Z., Luo Y., Wang P. (2016). Influence of attention on bimodal integration during emotional change decoding: ERP evidence. International Journal of Psychophysiology, 106, 14–20. 10.1016/j.ijpsycho.2016.05.009 [DOI] [PubMed] [Google Scholar]
  9. Cisler J. M., Bacon A. K., Williams N. L. (2009). Phenomenological characteristics of attentional biases towards threat: A critical review. Cognitive Therapy and Research, 33, 221–234. 10.1007/s10608-007-9161-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Colavita F. B. (1974). Human sensory dominance. Attention Perception & Psychophysics, 16, 409–412. 10.3758/BF03203962 [DOI] [Google Scholar]
  11. Collignon O., Girard S., Gosselin F., Roy S., Saint-Amour D., Lassonde M., Lepore F. (2008). Audio-visual integration of emotion expression. Brain Research, 1242, 126–135. 10.1016/j.brainres.2008.04.023 [DOI] [PubMed] [Google Scholar]
  12. Collins L., Schirillo J. (2013). Attention to endogenous and exogenous cues affects auditory localization. Experimental Brain Research, 231, 13–18. 10.1007/s00221-013-3663-5 [DOI] [PubMed] [Google Scholar]
  13. de Gelder B., Böcker K., Tuomainen J., Hensen M., Vroomen J. (1999). The combined perception of emotion from voice and face: Early interaction revealed by human electric brain responses. Neuroscience Letters, 260, 133–136. 10.1016/S0304-3940(98)00963-X [DOI] [PubMed] [Google Scholar]
  14. de Gelder B., Vroomen J. (2000). The perception of emotions by ear and by eye. Cognition & Emotion, 14, 289–311. 10.1080/026999300378824 [DOI] [Google Scholar]
  15. Doricchi F., Macci E., Silvetti M., Macaluso E. (2010). Neural correlates of the spatial and expectancy components of endogenous and stimulus-driven orienting of attention in the Posner task. Cerebral Cortex, 20, 1574–1585. 10.1093/cercor/bhp215 [DOI] [PubMed] [Google Scholar]
  16. Eimer M. (1993). Spatial cueing, sensory gating and selective response preparation: An ERP study on visuo-spatial orienting. Electroencephalography & Clinical Neurophysiology, 88, 408–420. 10.1016/0168-5597(93)90017-J [DOI] [PubMed] [Google Scholar]
  17. Engelmann J. B., Pessoa L. (2014). Motivation sharpens exogenous spatial attention. Motivation Science, 1, 64–72. 10.1037/2333-8113.1.S.64 [DOI] [PubMed] [Google Scholar]
  18. Etcoff N. L., Magee J. J. (1992). Categorical perception of facial expressions. Cognition, 44, 227–240. 10.1016/0010-0277(92)90002-Y [DOI] [PubMed] [Google Scholar]
  19. Föcker J., Gondan M., Röder B. (2011). Preattentive processing of audio-visual emotional signals. Acta Psychologica, 137, 36–47. 10.1016/j.actpsy.2011.02.004 [DOI] [PubMed] [Google Scholar]
  20. Gondan M., Minakata K. (2016). A tutorial on testing the race model inequality. Attention, Perception, & Psychophysics, 78, 723–735. 10.3758/s13414-015-1018-y [DOI] [PubMed] [Google Scholar]
  21. Gong, X., Huang, Y. X., Wang, Y., & Luo, Y. J. (2011). Revision of the Chinese facial affective picture system (in Chinese). Chinese Mental Health Journal, 25, 40–46. https://doi: 10.3969/j.issn.1000-6729.2011.01.011 [Google Scholar]
  22. Ho H. T., Schroger E., Kotz S. A. (2015). Selective attention modulates early human evoked potentials during emotional face-voice processing. Journal of Cognitive Neuroscience, 27, 798–818. 10.1162/jocn_a_00734 [DOI] [PubMed] [Google Scholar]
  23. Hope D. A., Rapee R. A., Heimberg R. G., Dombeck M. J. (1990). Representations of the self in social phobia: Vulnerability to social threat. Cognitive Therapy and Research, 14, 177–189. 10.1007/BF01176208 [DOI] [Google Scholar]
  24. Hunter E. M., Phillips L. H., MacPherson S. E. (2010). Effects of age oncross-modal emotion perception. Psychology and Aging, 25, 779–787. 10.1037/a0020528 [DOI] [PubMed] [Google Scholar]
  25. Juslin P., Laukka P. (2003). Communication of emotions in vocal expression and music performance: Different channels, same code? Psychological Bulletin, 129, 770–814. 10.1037/0033-2909.129.5.770 [DOI] [PubMed] [Google Scholar]
  26. Koelewijn T., Bronkhorst A., Theeuwes J. (2010). Attention and the multiple stages of multisensory integration: A review of audiovisual studies. Acta Psychologica (Amst), 134, 372–384. 10.1016/j.actpsy.2010.03.010 [DOI] [PubMed] [Google Scholar]
  27. Koppen C., Spence C. (2007). Audiovisual asynchrony modulates the Colavita visual dominance effect. Brain Research, 1186, 224–232. 10.1016/j.brainres.2007.09.076 [DOI] [PubMed] [Google Scholar]
  28. Laurence C., Luherne-Du B. V., Mohamed C., Monique P. (2015). Compensating for age limits through emotional crossmodal integration. Frontiers in Psychology, 6, 691–702. 10.3389/fpsyg.2015.00691 [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Li W., Jiang Z., Liu Y., Wu Q., Zhou Z., Jorgensen N., Li X., Li C. (2013). Positive and negative emotions modulate attention allocation in color-flanker task processing: Evidence from event-related-potentials. Motivation & Emotion, 38, 451–461. 10.1007/s11031-013-9387-9 [DOI] [Google Scholar]
  30. Massaro D. W., Egan P. B. (1996). Perceiving affect from the voice and the face. Psychonomic Bulletin Review, 3, 215–221. 10.3758/BF03212421 [DOI] [PubMed] [Google Scholar]
  31. Maurage P., Campanella S., Philippot P., Pham T. H., Joassin F. (2007). The crossmodal facilitation effect is disrupted in alcoholism: A study with emotional stimulus. Alcohol and Alcoholism, 42, 552–559. 10.1093/alcalc/agm134 [DOI] [PubMed] [Google Scholar]
  32. Miller J. (1986). Timecourse of coactivation in bimodal divided attention. Perception & Psychophysics, 40, 331–343. 10.3758/BF03203025 [DOI] [PubMed] [Google Scholar]
  33. Milliken B., Lupiáñez J., Roberts M., Stevanovski B. (2003). Orienting in space and time: Joint contributions to exogenous spatial cueing effects. Psychonomic Bulletin & Review, 10, 877–883. 10.3758/bf03196547 [DOI] [PubMed] [Google Scholar]
  34. Müller V. I., Habel U., Derntl B., Schneider F., Zilles K., Turetsky B. I., Eickhoff S. B. (2011). Incongruence effects in crossmodal emotional integration. NeuroImage, 54, 2257–2266. 10.1016/j.neuroimage [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Ngo M. K., Spence C. (2010). Crossmodal facilitation of masked visual target identification. Attention Perception & Psychophysics, 72, 1938–1947. 10.3758/app.72.7.1938 [DOI] [PubMed] [Google Scholar]
  36. Ohman A., Mineka S. (2001). Fears, phobias, and preparedness: Toward an evolved module of fear and fear learning. Psychological Review, 108, 483–522. 10.1037//0033-295X.108.3.483 [DOI] [PubMed] [Google Scholar]
  37. Otto T. U., Mamassian P. (2017). Multisensory decisions: The test of a race model, its logic, and power. Multisensory Research, 30, 1–24. 10.1163/22134808-00002541 [DOI] [Google Scholar]
  38. Paulmann S., Pell M. D. (2011). Is there an advantage for recognizing multi-modal emotional stimuli? Motivation and Emotion, 35, 192–201. 10.1007/s11031-011-9206-0 [DOI] [Google Scholar]
  39. Pell M. D., Kotz S. A. (2011). On the time course of vocal emotion recognition. PLoS One, 6, e27256. 10.1371/journal.pone.0027256 [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Posner M. I. (1980). Orienting of attention. The Quarterly Journal of Experimental Psychology, 32, 3–25. 10.1080/00335558008248231 [DOI] [PubMed] [Google Scholar]
  41. Posner M. I., Inhoff A. W., Friedrich F. J., Cohen A. (1987). Isolating attentional systems: A cognitive-anatomical analysis. Psychobiology, 15, 107–121. 10.3758/BF03333099 [DOI] [Google Scholar]
  42. Posner M. I., Snyder C. R., Davidson B. J. (1980). Attention and the detection of signals. Journal of Experimental Psychology General, 109, 160–174. 10.1037/0096-3445.109.2.160 [DOI] [PubMed] [Google Scholar]
  43. Raab D. H. (1962). Statistical facilitation of simple reaction times. Transactions of the New York Academy of Sciences, 24, 574–590. [DOI] [PubMed] [Google Scholar]
  44. Rigoulot S., Pell M. D. (2012). Seeing emotion with your ears: Emotional prosody implicitly guides visual attention to faces. PLoS One, 7, e30740. 10.1371/journal.pone.0030740 [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Rigoulot S., Wassiliwizky E., Pell M. D. (2013). Feeling backwards? How temporal order in speech affects the time course of vocal emotion recognition. Frontiers in Psychology, 4, 367. 10.3389/fpsyg.2013.00367 [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Risko E. F., Blais C., Stolz J. A., Besner D. (2008). Covert orienting: A compound-cue account of the proportion cued effect. Psychonomic Bulletin & Review, 15, 123–127. 10.3758/PBR [DOI] [PubMed] [Google Scholar]
  47. Sommers M. S., Tye-Murray N., Spehar B. (2005). Auditory-visual speech perception and auditory-visual enhancement in normal-hearing younger and older adults. Ear and Hearing, 26, 263–275. 10.1097/00003446-200506000-00003 [DOI] [PubMed] [Google Scholar]
  48. Spence C., Driver J. (1997). Audiovisual links in exogenous covert spatial orienting. Perception & Psychophysics, 59, 1–22. 10.3758/bf03206843 [DOI] [PubMed] [Google Scholar]
  49. Spence C., Nicholls M. E. R., Gillespie N., Driver J. (1998). Cross-modal links in exogenous covert spatial orienting between touch, audition, and vision. Perception & Psychophysics, 60, 544–557. 10.3758/bf03206045 [DOI] [PubMed] [Google Scholar]
  50. Stein B. E., Meredith M. A. (1990). Multisensory integration. Annals of the New York Academy of Sciences, 608, 51–70. 10.1111/j.1749-6632.1990.tb48891.x [DOI] [PubMed] [Google Scholar]
  51. Stefanou M. E., Dundon N. M., Bestelmeyer P. E. G., Koldewyn K., Saville C. W. N., Fleischhaker C., Feige B., Biscaldi M., Smyrnis N., Klein C. (2019). Electro-cortical correlates of multisensory integration using ecologically valid emotional stimuli: Differential effects for fear and disgust. Biological Psychology, 142, 132–139. 10.1016/j.biopsycho.2019.01.011 [DOI] [PubMed] [Google Scholar]
  52. Sumby W. H., Pollack I. (1954). Visual contribution to speech intelligibility in noise. The Journal of the Acoustical Society of America, 26, 212–215. 10.1121/1.1907309 [DOI] [Google Scholar]
  53. Tye-Murray N., Sommers M. S., Spehar B. (2007). Audiovisual integration and lipreading abilities of older adults with normal and impaired hearing. Ear and Hearing, 28, 656–668. 10.1097/AUD.0b013e31812f7185 [DOI] [PubMed] [Google Scholar]
  54. Van Bockstaele B., Verschuere B., Tibboel H., De Houwer J., Crombez G., Koster E. H. (2014). A review of current evidence for the causal impact of attentional bias on fear and anxiety. Psychological Bulletin, 140, 682–721. 10.1037/a0034834 [DOI] [PubMed] [Google Scholar]
  55. Vroomen J., Driver J., de Gelder B. (2001). Is cross-modal integration of emotional expressions independent of attentional resources? Cognitive, Affective, & Behavioral Neuroscience, 1, 382–387. 10.3758/cabn.1.4.382 [DOI] [PubMed] [Google Scholar]
  56. Vuilleumier P. (2005). Howbrains beware: Neural mechanisms of emotional attention. Trends in Cognitive Sciences, 9, 585–594. 10.1016/j.tics.2005.10.011 [DOI] [PubMed] [Google Scholar]
  57. Vuilleumier P., Driver J. (2007). Modulation of visual processing by attention and emotion: Windows on causal interactions between human brain regions. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 362, 837–855. 10.1098/rstb.2007.2092 [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Winneke A. H., Phillips N. A. (2011). Does audiovisual speech offer a fountain of youth for old ears? An event-related brain potential study of age differences in audiovisual speech perception. Psychology and Aging, 26, 427–438. 10.1037/a0021683 [DOI] [PubMed] [Google Scholar]
  59. Yiend J. (2010). The effects of emotion on attention: A review of attentional processing of emotional information. Cognition & Emotion, 24, 3–47. 10.1080/02699930903205698 [DOI] [Google Scholar]
  60. Yiend J., Mathews A. (2001). Anxiety and attention to threatening pictures. The Quarterly Journal of Experimental Psychology, 54A, 665–681. 10.1080/713755991 [DOI] [PubMed] [Google Scholar]

How to cite this article

  1. Li Y., Li Z., Deng A., Zheng H., Chen J., Ren Y., Yang W. (2021). The modulation of exogenous attention on emotional audiovisual integration. i-Perception, 12(3), 1–16. 10.1177/20416695211018714 [DOI] [PMC free article] [PubMed]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

sj-pdf-1-ipe-10.1177_20416695211018714 - Supplemental material for The Modulation of Exogenous Attention on Emotional Audiovisual Integration

Supplemental material, sj-pdf-1-ipe-10.1177_20416695211018714 for The Modulation of Exogenous Attention on Emotional Audiovisual Integration by Yueying Li, Zimo Li, Aihui Deng, Hewu Zheng, Jianxin Chen, Yanna Ren and Weiping Yang in i-Perception


Articles from i-Perception are provided here courtesy of SAGE Publications

RESOURCES