Event-related potential correlates of the collective self-relevant effect.
ABSTRACT The present study investigated the electrophysiological correlates of the psychological processing of the collective self-relevant stimulus using a three-stimulus oddball paradigm. The results showed that P300 amplitude elicited by the collective self-relevant stimulus was larger than those elicited by familiar and unfamiliar stimuli. In addition, N250 and P300 amplitudes elicited by subjects' own names were larger than those elicited by other name stimuli. In terms of lateralization of P300, the collective self-relevant effect was largest in the left region sites and the individual self-relevant effect was largest in the right region sites. Therefore, the present study extended previous findings by showing that the collective self, similar to the famous individual self, was psychologically important to humans.
- SourceAvailable from: wisebrain.org[show abstract] [hide abstract]
ABSTRACT: Negative information tends to influence evaluations more strongly than comparably extreme positive information. To test whether this negativity bias operates at the evaluative categorization stage, the authors recorded event-related brain potentials (ERPs), which are more sensitive to the evaluative categorization than the response output stage, as participants viewed positive, negative, and neutral pictures. Results revealed larger amplitude late positive brain potentials during the evaluative categorization of (a) positive and negative stimuli as compared with neutral stimuli and (b) negative as compared with positive stimuli, even though both were equally probable, evaluatively extreme, and arousing. These results provide support for the hypothesis that the negativity bias in affective processing occurs as early as the initial categorization into valence classes.Journal of Personality and Social Psychology 11/1998; 75(4):887-900. · 5.08 Impact Factor
- [show abstract] [hide abstract]
ABSTRACT: Functional imaging studies consistently support the role of the medial prefrontal cortex to be a part of a functional network of reflective self-awareness. The current study introduces a new linguistic task which (1) directly compares self-reference and other-reference, and (2) separates pre-reflective from reflective aspects of self-awareness. Twenty-six healthy volunteers evaluated trait adjectives in reference to the self or a close friend while a continuous 30-channel EEG was recorded. Low-resolution brain electromagnetic tomography (LORETA) was used for statistical brain imaging. As expected, the direct comparison of self-reference to other-reference revealed the MPFC to be significant and strongly more active during the self-reference condition. Pre-reflective aspects of self seem to be implemented to a greater degree in the ventral, reflective aspects of the self in dorsal parts of the MPFC. In the pre-reflective self condition, brain areas that receive homeostatic afferents from somatic and visceral sensation of the body such as the insula and the somatosensory cortex were strongly activated as early as 134 ms after stimulus onset. The right inferior parietal lobe seems to be involved in self-referential processing in general.NeuroImage 08/2008; 42(1):437-49. · 6.25 Impact Factor
- [show abstract] [hide abstract]
ABSTRACT: On the bases of A. G. Greenwald and A. R. Pratkanis's (1984) distinction between private and collective aspects of the self and on H. C. Triandis's (see record 1989-36454-001) theory about individualistic and collectivistic cultures, 2 competing theories concerning the organization of self-cognitions were proposed. Findings from 2 experiments supported the notion that private and collective self-cognitions are stored in separate locations in memory. First, Ss from individualistic cultures retrieved more cognitions about the private self, and fewer about the collective self, than Ss from collectivistic cultures. Second, priming a particular aspect of the self increased the retrieval of self-cognitions pertaining to that aspect of the self. Finally, the probability of retrieving a self-cognition was greater if the same type of self-cognition had been previously retrieved than if a different type had been previously retrieved. (PsycINFO Database Record (c) 2012 APA, all rights reserved)Journal of Personality and Social Psychology 04/1991; 60(5):649-655. · 5.08 Impact Factor
Neuroscience Letters 445 (2008) 135–139
Contents lists available at ScienceDirect
journal homepage: www.elsevier.com/locate/neulet
Music-induced mood modulates the strength of emotional negativity bias:
An ERP study
Jie Chena,b, Jiajin Yuana,b, He Huanga,b, Changming Chena,b, Hong Lia,b,∗
aKey Laboratory of Cognition and Personality (SWU), Ministry of Education, Southwest University, Chongqing 400715, China
bSchool of Psychology, Southwest University, Chongqing 400715, China
a r t i c l e i n f o
Received 21 May 2008
Received in revised form 1 August 2008
Accepted 25 August 2008
Emotional negativity bias
a b s t r a c t
The present study investigated the effect of music-elicited moods on the subsequent affective processing
through a music-primed valence categorization task. Event-related potentials were recorded for positive
and negative emotional pictures that were primed by happy or sad music excerpts. The reaction time
data revealed longer reaction times (RTs) for pictures following negative versus positive music pieces,
irrespective of the valence of the picture. Additionally, positive pictures elicited faster response latencies
than negative pictures, irrespective of the valence of the musical prime. Moreover, the main effect of
and for the averaged amplitudes at 500–700ms interval. Negative pictures elicited smaller P2 amplitudes
than positive pictures, and the amplitude differences between negative and positive pictures were larger
with negative musical primes than with positive musical primes. Similarly, compared to positive pictures,
negative pictures elicited more negative deflections during the 500–700ms interval across prime types.
positive music primes at this interval. Therefore, the present study observed a clear emotional negativity
bias during either prime condition, and extended the previous findings by showing increased strength of
the negative bias under negative mood primes. This suggests that the neural sensitivity of the brain to
negative stimuli varies with individuals’ mood states, and this bias is particularly intensified by negative
© 2008 Elsevier Ireland Ltd. All rights reserved.
Considerable studies revealed the existence of negativity bias
in emotional processing that people are particularly sensitive
to emotionally negative events, such that negative events are
often preferentially processed compared to neutral and positive
events [9,16,17,20,27]. Behavioral studies have suggested that neg-
ative traits are given greater weight in overall evaluations than
are positive traits , and a greater weight paid for negative
information than for positive information was manifested in risk-
taking research . Moreover, a growing body of event-related
brain potential studies documents a bias towards negative over
positive information [16,20,23,27]. For instance, it was reported
that larger P1 amplitudes were elicited by rare negative stim-
uli than rare positive stimuli as early as 110ms after stimulus
onset . In addition, at approximately 170ms after stimulus
onset, smaller P2 amplitudes were observed for highly nega-
tive stimuli than for moderately negative and neutral stimuli
∗Corresponding author at: School of Psychology, Southwest University, Beibei,
Chongqing 400715, China. Tel.: +86 23 6825 4337; fax: +86 23 6825 2309.
E-mail address: email@example.com (H. Li).
[20,27]. More recently, it was further demonstrated that the
emotional negativity bias also occurred in reaction readiness
As described above, it is clear that the emotional negativity bias
occurs at each step of the information-processing stream. Never-
ative stimuli [7,8]. According to Bower’s network model of emotion
and cognition [7,8], negatively distorted thinking influences judg-
ment of events and situations, and the perception of emotional
information are colored by the underlying emotional state. In this
view, it is predictable that variations in mood will modulate the
occurrence or features of the negativity bias during human emo-
tional processing. It has been shown that subjects perceived more
sadness in ambiguous faces and less happiness in clear faces dur-
ing the depressive mood induction than during the elation mood
induction. This result suggested a depression-related negative bias
in the perception of facial affects . More recently, some behav-
ioral as well as neuroimaging studies consistently demonstrated
that depressive and anxious patients, as compared to healthy indi-
viduals, displayed increased strength of emotional negativity bias
0304-3940/$ – see front matter © 2008 Elsevier Ireland Ltd. All rights reserved.
J. Chen et al. / Neuroscience Letters 445 (2008) 135–139
Fig. 1. Grand average ERPs at Fz, FCz, CZand CPZfor NN (thick solid lines), NP (thin solid lines), PN (thick dotted lines), and PP (thin dotted lines).
during the perception of emotional words, images as well as faces
Nevertheless, whether the processing bias of the brain for neg-
ative stimuli is modulated by mood changes in normal individuals
iological mechanism that accounts for, this phenomenon needs to
be determined. With high temporal resolution, ERP measures are
advantageous to our investigation of the time course of the poten-
tial modulation effect of the negative bias by mood primes. Based
on these considerations, the present study focused on the effects
of music-induced moods (sadness or happiness) on the strength of
negativity bias in emotional processing via ERP measures. Specifi-
cally, as predicted by the established emotional negativity bias, we
hypothesized that the neural responses to negative images would
be more intense than to positive images, irrespective of music
primes. Moreover, based on prior studies [6,10,14,21], it was pre-
dicted that the strength of emotional negativity bias, as indexed
by difference ERPs between negative and positive images, would
be increased with negative music prime than with positive music
The present study used an affective priming paradigm. Negative
(sad) and positive (happy) music pieces, which were believed to
ing stimuli to induce negative (sad) and positive (happy) moods
[5,18,19]. Emotional pictures were used as the task-relevant target
tem (IAPS) has been reported in Chinese subjects , the pictures
selected to elicit emotional responses in the present study were
mood-inducing musical pieces were selected from Chinese classi-
cal music pool that were more familiar to Chinese participants, so
as to guarantee the effectiveness of mood inducement.
As paid volunteers, 12 native Chinese students (7 women and
5 men) aged 20–25 years (mean age, 22.8 years) participated in
the study. All subjects were healthy, right-handed, with normal or
corrected to normal vision and audition, and reported no history of
affective disorder. Each subject signed an informed consent form
with the ethical principles of the 1964 Declaration of Helsinki .
The stimulus material consisted of 7 blocks of 232 prime–target
pairs, in which music excerpts served as primes and pictures as
targets, and these pairs were divided into four experimental condi-
target), 58 NP trials (negative music as prime and positive picture
as target), 58 PP trails (positive music as prime and positive picture
Summary of results of the 2 (music category: negative and positive)×2 (picture category: negative and positive)×3 (laterality: left, midline and right sites)×4 (frontality:
front, front-central, central and central-parietal) ANOVAs for the 500–550, 550–600, 600–650 and 650–700ms time windows
Time (ms) Music Picture LateralityFrontalityMusic×picture
J. Chen et al. / Neuroscience Letters 445 (2008) 135–139
as target), and 58 PN trials (positive music as prime and negative
picture as target).
Picture targets consisted of 116 emotionally negative pictures
and 116 emotionally positive pictures selected from the CAPS. The
negative pictures were divided into two groups and each con-
tains 58 pictures. There were no significant difference in valence
[t(39)=−0.37, p=0.71] and arousal [t(39)=−0.7, p=0.94] between
two groups. In the same way, the positive pictures were divided
into two groups and each contains 58 pictures. There were also no
significant difference in valence [t(39)=−0.17, p=0.87] and arousal
[t(39)=−0.11, p=0.92] between two groups. In addition, the lumi-
nance level of the pictures was matched in the four conditions,
and the contrast of the monitor was set to a constant value across
Prime stimulus consisted of 75 negative (sad) music and 75
positive (happy) music from the Chinese classical music. All were
instrumental and rated by 40 non-musician college students (20
women and 20 men). These excerpts were rated for valence
on a nine-point scale (1=‘extremely sad’ whereas 9=‘extremely
happy’). All excerpts were also rated for arousal on a 9-point scale
(1=‘not arousing at all’ to 9=‘extremely arousing’). Finally, a total
of 116 excerpts were selected for the EEG experiment: 58 negative
music and 58 positive music, with the valence significantly differ-
ent (t=−36.34, p<0.001) whereas the arousal similar (t=−0.687,
p=0.5) between the two music groups (the averaged valence were
3.01 for sad music and 6.99 for happy music, whereas the mean
arousal for sad and happy excerpts were 5.72 and 5.8, respectively).
Musical excerpts were matched for length. Happy excerpts lasted
on average 11.72s and sad excerpts lasted on average 11.93s. All
Subjects were seated in a quiet room at approximately 150cm
from a computer screen with the horizontal and vertical visual
angles below 5◦. In order to familiarize participants with the task,
experiment started with 12 practice trials, with 3 trials under each
condition. Each trial was initiated by a 300ms presentation of a
small white cross on the black computer screen; then, the auditory
presentation of a musical excerpt via an earphone was followed
by the visual presentation of target emotional image (presenta-
tion time for targets was 1000ms). The interstimulus interval (ISI)
between prime and target was 200ms. Half of the subjects were
instructed to press the “F” key on the key board (as accurately and
quickly as possible) if the pleasant images appeared, and to press
the “J” key if the unpleasant images appeared. For the remaining
subjects the response pattern was reversed. The stimulus picture
was terminated by a key pressing, or was terminated when it
elapsed for 1000ms. Therefore, each subject was informed that
their responses must be made under 1000ms. Each response was
followed by 2000ms of a blank screen. Trails were presented ran-
domly and distributed over seven blocks.
Electroencephalography (EEG) was recorded from 64 scalp sites
on the medial frontal aspect. Eye movements were monitored with
canthi. Electrode impedance was maintained below 5k?. EEG and
EOG activity was amplified with a dc∼100Hz bandpass and con-
tinuously sampled at 500Hz/channel. EEG data were corrected to
a 200ms baseline prior to the onset of the target. Artifact-free EEG
segments to trials with correct responses were averaged separately
for each experimental condition. ERP averages were computed off-
line; trials with EOG artifacts (mean EOG voltage exceeding ±80V),
amplifier clipping artifacts, or peak-to-peak deflection exceeding
±80V were excluded from averaging.
EEG activity for correct response in each valence condition
was overlapped and averaged separately. ERP waveforms were
time-locked to the onset of pictures and the average epoch was
ERPs grand averaged waveforms and topographical map, negative
tures, irrespective of the prime types. Moreover, these differences
were largest at left frontal sites. In order to test the lateralization,
the following 12 electrode sites were selected for statistical analy-
sis: F3, FC3, C3, CP3(four left sites); Fz, FCz, CZ, CPZ(four midline
sites); F4, FC4, C4, CP4(four right sites). The latencies and peak
500–700ms were measured. A four-way repeated measures anal-
ysis of variance (ANOVA) was conducted for the amplitude and
latency of each component. ANOVA factors were music (negative
ity (left, midline and right sites) and frontality (front, front-central,
central and central-parietal sites). The degrees of freedom of the F-
ratio were corrected according to the Greenhouse-Geisser method.
A two-way repeated measure ANOVA, with music and image
valence as factors, was performed for mean reaction time (RT)
and accuracy rates (ACC). Analysis of RT revealed a signif-
icant main effects for music [F(1, 11)=48.63, p<0.001] and
picture [F(1, 11)=29.98, p<0.001], but no significant interac-
tion effect between music and picture valence [F(1, 11)=0.9,
p=0.363]. Longer RTs were recorded for images following nega-
tive (M=640.78ms, S.E.=23.26ms) versus positive music pieces
(M=614.16ms, S.E.=24.17ms), irrespective of the valence of the
picture. Moreover, the behavioral responses for negative pictures
(M=668.61ms, S.E.=26.45ms) were delayed compared to posi-
tive pictures (M=586.34ms, S.E.=23.04ms), irrespective of the
valence of the musical prime. In addition, false responses were
rare, mean accuracy rates for the NN, NP, PP and PN condi-
tions were 94%(S.E.=0.012), 95%(S.E.=0.016), 96.4%(S.E.=0.014),
effects observed for mean ACC.
As shown in Fig. 1, P2 component was elicited by all four con-
ditions. A four-way repeated measures ANOVA on P2 amplitudes
demonstrated a significant music by picture valence interaction
effect [F(1, 11)=6.58, p=0.026]. To break down this interaction,
we performed a simple-effect analysis with which P2s elicited
by positive and negative pictures were compared within each
priming condition. Negative images elicited smaller P2 amplitudes
than positive pictures in both positive music priming condition
[Mnegative pictures=3.33, S.E.=0.88; Mpositive pictures=4.04, S.E.=1.03;
F(1, 11)=18.51, p=0.001] and negative music priming condi-
tion [Mnegative pictures=3.1, S.E.=0.99; Mpositive pictures=4.33, S.E.=1;
F(1, 11)=48.14, p<0.001]. More importantly, the ERP difference
between negative and positive pictures was larger with negative
musical primes than with positive musical primes [F(1, 11)=6.58,
p=0.026]. In addition, the interaction effect between laterality and
and picture valence [F(3, 11)=4.27, p=0.038] were both significant.
The amplitude differences during negative and positive conditions
significant main, or interaction effects observed at the P2 latencies.
A four-way repeated measure ANOVA on the average ampli-
tudes showed significant music by picture valence interaction
effects at each 50ms of the 500–700ms interval (Table 1). To
break down this interaction, we compared the average ampli-
tudes elicited by positive and negative pictures for negative and
positive priming conditions, respectively. Negative images elicited
more negative deflections than positive images with the pos-
itive musical primes during the time interval of 500–550ms
[F(1, 11)=12.19, p=0.005], 550–600ms [F(1, 11)=15.44, p=0.002],
J. Chen et al. / Neuroscience Letters 445 (2008) 135–139
Fig. 2. Top: the negative picture minus positive picture difference wave in the negative musical condition (solid line) and in the positive musical condition (dotted line) at
FCzand CZ. Left-bottom: topographical maps of voltage amplitudes for the negative picture minus positive picture difference wave in the positive musical condition at each
50ms interval from 500 to 700ms. Right-bottom: topographical maps of voltage amplitudes for the negative picture minus positive picture difference wave in the negative
musical condition at each 50ms interval from 500 to 700ms.
600–650ms [F(1, 11)=29.48, p<0.001] and 650–700ms [F(1,
11)=22.87, p=0.001]. Furthermore, negative images elicited more
negative deflections than positive images with the negative musi-
cal primes during the time interval of 500–550ms [F(1, 11)=50.08,
11)=55.94, p<0.001] and 650–700ms [F(1, 11)=38.52, p<0.001].
More importantly, the ERP difference between negative and pos-
itive images was larger with negative musical primes than with
positive musical primes during the time interval of 500–550ms
[F(1, 11)=8.77, p=0.013), 550–600ms (F(1, 11)=24.2, p<0.001),
600–650ms (F(1, 11)=23.04, p=0.001) and 650–700ms [F(1,
11)=9.41, p=0.011] (see Fig. 2). In addition, there were significant
laterality by picture valence interaction effect as well as site by
picture valence interaction effect (see Table 1), and the amplitude
differences between negative and positive pictures were largest at
left frontal sites (see Fig. 2).
As for behavioral data, longer RTs were observed for negative
trigger extensive and time-consuming cognitive analysis , and
this might be manifested in longer categorization times of neg-
ative than positive stimulus in valence categorization task .
Thus, these behavioral data were consistent with previous studies
and the predictions based on emotional negativity bias, indexed an
enhanced processing for information of negative emotions, espe-
cially when following the negative primes.
At approximately 170ms after stimulus onset, obvious P2 activ-
ity was elicited in all four conditions, and smaller P2 amplitudes
were detected for negative images than for positive images, irre-
spective the musical prime. Frontal P2 activation within 200ms
is indicative of rapid detection of typical stimulus features .
for positive images is likely indicative of a rapid feature detection
process. This is consistent with previous studies which observed
erately negative and neutral stimuli [20,27]. Because information
processing within 200ms probably occurs subconsciously, and the
frontal P2 activity within 200ms is modulated by the valence
of emotional images across musical primes, the present study
hypothesized a subconscious process that attends to the emotional
salience of picture stimuli rapidly. Interestingly, the amplitude dif-
ferences between negative and positive images were larger with
negative musical primes than with positive musical primes, which
ulated by music-primed mood even at the early processing stages
in the present study, and the bias of the brain for negative images
is intensified by the negative mood induced by the sadness music.
A prior ERP study conducted for anxious subjects suggested that
the amplitudes of the early contingent negative variation (CNV)
were larger when anxious subjects were vigilant towards nega-
tive affective stimuli than towards positive affective stimuli. In
contrast, this bias was absent in non-anxious subjects . It has
been indicated that the amplitude of early CNV is directly related
to vigilance-related attention . Consistent with this view, it
was most likely that, in the present study, the sadness music pro-
vided a negative emotional context, in which the neural sensitivity
and the vigilance of the brain to negative stimuli was enhanced
compared to that in the positive music context. This probably con-
tributed to the increased intensity of the early negative bias with
J. Chen et al. / Neuroscience Letters 445 (2008) 135–139
sadness versus happiness primes during the processing of emo-
ative images elicited increased negativity as compared to positive
images, independent of the type of music prime (Fig. 1). These
differences were largest across the left frontal scalp regions, and
ity in the negative-positive difference waveforms (Fig. 2). There
was some evidence suggesting that the SNW is an index for the
memory-related processes . In particular, it was indicated that
the emotional processing reflected by SNW activity involves a ref-
erence to emotional experiences stored in long-term memory, and
stimuli with increased saliency would evoke greater SNW activ-
ity compared to stimuli of lesser saliency . Therefore, the SNW
activity could be interpreted as reflecting richer associations of
emotional memories evoked by negative stimuli than by positive
Negative stimuli were of greater adaptive importance for indi-
viduals, as they typically represent a salient threat to survival,
which was absent in positive stimuli. Therefore, negative images
in the present study were given enhanced resources for later
cognitive-related processing than were positive stimuli. More
importantly, the negative bias during memory-related stages, as
primes, which suggested that the neural sensitivity of the human
brain to negative stimuli was enhanced under negative mood than
under positive mood. This is similar to prior evidence indicating a
memory tasks [4,12]. Therefore, it seems that the later memory-
related negative bias, as indexed by the larger SNW activity for
negative pictures, would be intensified within a negative mood
Therefore, the processing bias of the brain for negative stimuli,
as termed as emotional negativity bias, occurred in both negative
and positive mood conditions in the present study. This suggests
that the existence of emotional negativity bias, to some extent, is
stable across mood states , despite the variability of its strength
in different emotional contexts. On the other hand, in addition to
repeated reports of the existence of the negativity bias during the
processing of emotional stimuli [9,16,17,20,27], there were still a
body of studies that reported a conspicuous modulation effect of
[10,14,21]. This suggests that individuals different in mental health
may be distinct in emotional processing and may influence the
strength of the processing bias for emotionally negative stimuli.
In fact, there exist noticeable individual differences during the pro-
cessing of emotional stimuli. Difference in sex, as well as that in
personality traits such as neuroticism and extroversion that closely
relate to emotional processing [11,20,22], all contribute a large part
to individual differences in emotional processing, in particular, in
ations within the same individual also influence the strength of
the processing biases for negative stimuli, in addition to the estab-
lished influences of subject variables on emotional activity. Thus,
the present study concluded that the processing bias for negative
over positive stimuli, as termed as emotional negativity bias, exists
stably under different emotional contexts, and the strength of bias
might be influenced by individuals’ mood states.
In conclusion, the current findings provide evidence that the
emotional negativity bias occurs not only at early stage of features
detection, but also in later cognitive and memory-related stages,
of this bias is modulated by individuals’ mood states at each step of
the information-processing stream, and negative mood intensifies
the neural sensitivity of the brain to emotionally negative stimuli.
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