write a 3 page double-spaced summary of the article"EMOTION"
Annu. Rev. Psychol. 1999. 50:191–214 Copyright © 1999 by Annual Reviews. All rights reserved
EMOTION
John T. Cacioppo Department of Psychology, The Ohio State University, Columbus, Ohio 43210-1222; e-mail: [email protected]
Wendi L. Gardner Department of Psychology, Northwestern University, Evanston, Illinois 60208-2710; e-mail: [email protected]
KEY WORDS: affect, evaluation, cognitive appraisal, positivity, negativity
ABSTRACT
We review recent trends and methodological issues in assessing and testing theories of emotion, and we review evidence that form follows function in the affect system. Physical limitations constrain behavioral expressions and incline behavioral predispositions toward a bipolar organization, but these limiting conditions appear to lose their power at the level of underlying mechanisms, where a bivalent approach may provide a more comprehensive account of the affect system.
CONTENTS INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 191
Methodological Issues in the Study of Emotion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 192
The Relation Between Emotion and Cognition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 194
The Relativity of Emotion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 196
THE AFFECT SYSTEM UNDERLYING EMOTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 198 Operating Characteristics of the Affect System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 199 Stages and Channels of Evaluative Processing. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 200
INTRODUCTION
Recent research on emotions is almost as vast and diverse as emotional life it-
self. A literature search limited to the term “emotion” using PsychInfo re-
0084-6570/99/0201-0191$08.00
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turned 5064 citations over the past five years, and a comparable search using
Medline returned 3542. A Handbook of Emotions appeared (Lewis & Havi-
land 1993) with a second edition already in preparation, journals are now de-
voted almost exclusively to the topic (e.g. Cognition and Emotion, Motivation
and Emotion), and numerous textbooks on the topic have surfaced. The swell
of interest in emotion continues to ascribe a large role to deliberation and civil
discourse. Humans have walked the surface of the earth for about 2,000,000
years, and for all but the last 2000–3000 years humans have been hunter-
gatherers. We nevertheless tend to see our distant past “through a reverse
telescope that compresses it: a short time as hunter-gatherers, a long time as
‘civilized’ people” (Ackerman 1990, p. 129). We begin by reviewing recent
developments in the study of human emotions. We then consider the general
features of an affect system, archaic in some respects, that can be conceived as
underlying emotion.
Methodological Developments in the Study of Emotion
The study of emotion has been aided in recent years by the development of
standardized stimulus materials and procedures for eliciting emotions, and this
continued to be an active area of inquiry in recent years (e.g. see Davidson &
Cacioppo 1992, Gerrards-Hesse et al 1994). New developments were seen in
stimulus sets consisting of pictures (Lang et al 1995), films (Gross & Levenson
1995, Philippot 1993, Westermann et al 1996), sounds (Bradley et al 1994),
words (Bradley et al 1997), and stories, imagery, or social interactions
(Westermann et al 1996, Gerrards-Hesse et al 1994). The measurement of emotions also remained a bustling research area. The
interplay among social, cognitive, and biological processes in emotion is be- coming increasingly tractable, and emotional phenomena are now fruitfully studied drawing upon theories and methodologies that require collaboration among social, cognitive, developmental, clinical, and neuroscientists. For in- stance, methods for stereogeometric functional brain imaging and comple- mentary methods for mapping the temporal dynamics of neural processing have become a reality over the past two decades. Positron emission tomogra- phy (PET) (e.g. Drevets & Raichle 1995, George et al 1995, Lane et al 1997, Paradiso et al 1997) and functional magnetic resonance imaging (fMRI) (e.g. Grodd et al 1995, Maddock & Buonocore 1997, Lang et al 1998) offer consid- erable promise in studies of affective processes (cf Fox & Woldorff 1994, Ku- tas & Federmeier 1998, Sarter et al 1996).
As Kutas & Federmeier note, the temporal resolution of the fMRI is still
limited by the fact that the blood flow response typically lags the actual electri-
cal signal by one to two seconds and does not track activity on a millisecond-
by-millisecond basis. The temporal resolution of PET is similarly limited. In
192 CACIOPPO & GARDNER
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studies in which higher temporal resolution is required, fMRI or PET studies
can be complemented by other measures. Indeed, advances in tracking phasic
aspects of emotion were seen in (a) event-related brain potential paradigms
(Cacioppo et al 1994, Crites et al 1995, Gardner & Cacioppo 1998); (b) startle
probe methods (Davis 1997, Lang 1995); (c) continuous self-report measures
(Stayman & Aaker 1993); (d) retrospective verbal protocols (Cacioppo et al
1997c, Davison et al 1997, Hurlburt 1997); (e) nonverbal pictorial assessment
techniques (Bradley & Lang 1994); (f) facial electromyography (Tassinary &
Cacioppo 1992, Witvliet & Vrana 1995); and (g) observational methods of in-
fants (Emde et al 1993) and interactants (Carroll & Russell 1997, Gottman
1993). Laboratory studies can afford impressive control over relevant variables, an
important feature when dissecting phenomena as complex and multiply deter-
mined as the emotions. The ecological and external validity of laboratory para-
digms and measures can sometimes be uncertain, however. Advances in elec-
tronics and statistics have improved the feasibility and methodological sophis-
tication of both ecological momentary assessments (e.g. Diener & Lucas 1998,
Larsen 1991, Suls et al 1998) and ambulatory monitoring of affective states
(e.g. Guyll & Contrada 1998, Kamarck et al 1998). These assessments intro-
duce their own set of statistical (cf Schwartz & Stone 1998) and methodologi-
cal problems (e.g. Litt et al 1998) but are noteworthy developments as they
should make it possible to identify which laboratory findings generalize to the
real world and to improve laboratory models of human emotions. Two addi-
tional developments that are needed are: (a) programmatic studies of emotion
that test specific conceptual hypotheses based on both the internal validity of
the laboratory and the external and ecological validity of field sampling
methods and ambulatory assessments; and (b) greater use of experimental ma-
nipulations (e.g. an intervention program) in conjunction with field sampling
methods and ambulatory assessments. There has been no shortage of debates over methods and measures, either.
Over the past couple years alone, discussions appeared on topics in a wide
range: (a) import of linguistic analyses of emotion (e.g. Wierzbicka 1995; cf
Forsyth & Eifert 1996); (b) the role and limits of self-reports in studies of emo-
tion (Lazarus 1995, Reisenzein 1995, Schwarz & Strack 1998) and moods (Ba-
gozzi 1993, Green et al 1993, Watson & Clark 1997); (c) the pancultural agree-
ment in emotion judgments (Ekman 1994, Rosenberg & Ekman 1995, Russell
1994); (d) the methodological nuances in research on cerebral asymmetries in
emotion (Davidson 1993, Hagemann et al 1998, Reid et al 1998); and (e) the
nature and existence of basic emotions (Ekman 1992, Izard 1992, Ortony &
Turner 1990, Panksepp 1992). Individual differences in emotional disposition (Davidson 1994, Depue
1996, Gray 1994, Rosenthal 1995, Tangney et al 1995), intensity (e.g. Keltner
EMOTION 193
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& Ekman 1996), and reactivity (e.g. Cacioppo et al 1992, Gilboa & Revelle
1994, Larsen et al 1996) continued to be popular areas of theory and research.
Explanations of the origins of the individual differences in emotion have
turned in part to studies of socioemotional development, work that now ex-
tends across the life span from infancy (e.g. Izard & Ackerman 1997, Nelson &
de Haan 1997, Walker-Andrews 1997) through adolescence (Flannery et al
1994) to old age (Carstensen et al 1997, Schulz & Heckhausen 1997). Related
reports of the genetic determinants of emotion (e.g. McGuire 1993, Plomin et
al 1993) and the universality of emotional expressions (e.g. Averill et al 1994,
Ekman & Keltner 1997, Izard 1994) were counterbalanced by studies of cul-
tural determinants (Mesquita et al 1997, Russell 1994). As this work attests,
emotion is a short label for a very broad category of experiential, behavioral,
sociodevelopmental, and biological phenomena.
The Relation Between Emotion and Cognition
An assumption by rationalists dating back to the ancient Greeks has been that higher forms of human existence—mentation, rationality, foresight, and deci- sion making—can be hijacked by the pirates of emotion. In accordance with the classic assumption that emotion wreaks havoc on human rationality, the emphasis for years in psychology has been on cognition and rationality, and on ways of diminishing the influence of subjectivity and emotion in decision making and behavior. Research with chimpanzees (Pan troglodytes) sup- ported the notion that symbolic representations (e.g. arabic numerals) evolved in part to lessen the primal grip of appetitive or aversive stimuli (e.g. candies) on decision making and behavior (Boysen et al 1996). However, emotions are much more than primitive reflexes. The notion that emotions are a disruptive force in rational thought and adaptive action was shown to be a gross oversim- plification (e.g. Berntson et al 1993). Although the obstacles of a civilized world still occasionally call forth blind rages, emotions are increasingly recog- nized for the constructive role they play in higher forms of human experience.
Consider the neurological case of Elliot reported by Damasio (1994). Elliot
was a businessman who developed a brain tumor that damaged his prefrontal
cortex. Although Elliot began behaving irrationally, testing of Elliot revealed
that his intelligence, attention, and memory remained unaffected by his illness.
Instead, Elliot had lost the ability to experience emotion; and the lack of emo-
tional guidance rendered decision making a dangerous game of roulette. The notion that emotion contributes not only to an intelligent but also to a
fulfilling life emerged most strikingly in the work on emotional intelligence.
The heightened ability to monitor one’s own and others’ emotions, to discrimi-
nate among them, and to use the information to guide one’s thinking and action
has proven to be as important a determinant of life success as traditional meas-
ures of intelligence such as IQ (Goleman 1995, Mayer & Salovey 1993).
194 CACIOPPO & GARDNER
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Societal changes have also influenced the direction of research on emo-
tions. With rising health costs threatening to ravage families and finances, at-
tention has turned to the role of emotion in cancer progression (Andersen et al
1998, Spiegel 1997), cardiovascular disease (Brezinka & Kittel 1996, Carney
et al 1995), respiratory disease (Lehrer et al 1993), infectious illness (Cohen &
Rodriguez 1995, Leventhal et al 1997), and immune function (Herbert & Co-
hen 1993, Kiecolt-Glaser et al 1994, Sternberg 1997). A second societal trend,
the dawning of the information age and advances in computer vision, robotics,
and telecommunications, has placed a premium on speech and facial recogni-
tion and production software. For these programs to be realistic, they must
capture the emotion in the message. This need has fueled interest in the acous-
tic (Murray & Arnott 1993, Pittam & Scherer 1993) and rapid facial signals of
emotion (Ekman 1993, Russell & Fernandez-Dols 1997). Although these
represent relatively new areas of research, the economic stakes make these
likely areas of new developments. Research over the past two decades on cognition and emotion provides
further evidence for the ubiquity of emotion, with the influence of emotion ex-
tending to all aspects of cognition and behavior. Perhaps of particular note in
recent years are advances in our understanding of the role of emotions in atten-
tion and perception (Niedenthal & Kitayama 1994, Zajonc 1998); memory
(Bradley et al 1995, Cahill 1996, Phelps & Anderson 1997); psychological
defense (Paulhus et al 1997); subjective well-being (e.g. Diener & Suh 1998,
Myers 1993); attitudes and persuasion (Cacioppo et al 1992, Chen & Bargh
1998); reasoning and decision making (Forgas 1995, Schwarz & Clore 1996);
the meaning of expressive displays (Hess et al 1995, Rosenberg & Ekman
1994); emotional contagion (Hatfield et al 1994, Hietanen et al 1998); inter-
personal relationships (Gardner et al 1998, Reis & Patrick 1996); and political
information processing (Ottati et al 1992, Way & Masters 1996). Emotions are also physiological processes and cannot be understood fully
without considering the structural and functional aspects of the physical sub-
strates (cf LeDoux 1995). Physiological investigations not only delineate un-
derlying mechanisms but also contribute to better psychological theories by in-
spiring what is possible (e.g. implicit versus explicit knowledge representa-
tions) and by placing constraints on what is plausible (e.g. forward versus
backward propagation). The biological (e.g. Boiten et al 1994, Cacioppo et al
1997a, Davidson 1994, Levenson 1996), biochemical (e.g. Rubinow &
Schmidt 1996), and neural substrates of emotion (e.g. Damasio 1996, Davis
1997, LeDoux 1995, Neafsey et al 1993), as well as neuropsychological as-
pects of emotional expressions (Borod et al 1997), continued to be important
and active areas of research. For instance, Shizgal (1998), in summarizing re-
search using electrical brain stimulation to probe emotion, stated that in con-
trast to cognitive (i.e. perceptual and timing) channels, “the evaluative [affec-
EMOTION 195
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tive] channel operates without even a pretense of objectivity.” He noted that a
cool stimulus applied to the skin can be pleasant if one is overheated and un-
pleasant if one is hypothermic. The affective value of a stimulus, he concluded,
depends in part on the prevailing physiological and ecological conditions.
Shizgal’s (1998) physiological research implies that the brain is organized in
part as an affect system, and that the operation of the affect system is not con-
trolled in an absolute fashion by the objective features of a stimulus.
The Relativity of Emotion
The notion that there are absolute features that trigger emotional reactions was further undercut by new evidence that relativity governs the province of emotion. Kahneman and colleagues demonstrated that pain, long a bastion of absolutism, was preferred when its duration was extended while its intensity paled (Kahneman et al 1993). Kahneman and colleagues (e.g. Kahneman 1998) offered the intriguing hypothesis that the affective representation of a complex event varied as a function of the peak experience and the experience at the end of the event (i.e. the peak-end rule).
Schwarz & Strack (1998) noted that most objective life circumstances, even
when combined across a dozen domains of life, account for no more than 10%
of the variance in measures of subjective well-being. Indeed, they demon-
strated that the same event can increase or decrease judgments of subjective
well-being depending on its use in construing one’s life or its use as a standard.
Specifically, Schwarz & Strack (1998) suggested that a contrast effect is likely
to occur when an extreme (negative or positive) event is used as a standard
against which to compare a stimulus or one’s current state, whereas an assimi-
lation effect is more likely when the extreme event is included in the transient
representation of the affective event. For example, a moderately negative tar-
get stimulus (e.g. an argument with a spouse) is perceived more positively
when preceded by the experience of a rare, extremely negative event (e.g. a
death in the family) than when not preceded by such an event (Parducci 1995)
as long as the preceding event served as a comparison standard rather than as
part of the target event. Yet other ways were discovered in which the determinants of emotion are
relative. Brendl & Higgins (1995) reviewed evidence that an incentive is
greater when it is compatible with a person’s goal (see also Shah et al 1998).
Counterfactual thinking, or comparing objective outcomes with imagined
outcomes that “might have been,” was shown to leave bronze medalists at the
1992 Summer Olympics apparently happier than silver medalists (Medvec et
al 1995; see also Roese 1997) even though, by objective standards, an Olympic
silver medal is of higher value than a bronze medal. Similarly, stories or con-
fabulations that place an evocative event in a historical context were shown to
be as important a determinant of the emotions elicited by the event as the event
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itself (Harvey et al 1995, Kitayama & Masuda 1995, Traue & Pennebaker
1993). In addition to the perceived valuation of a stimulus or endstate, investi-
gators demonstrated that the rates of movement toward or away from the end-
state are important determinants of emotion in and of themselves (Carver &
Scheier 1990, Carver et al 1996, Hsee et al 1994). Research concerning cognitive appraisals represented an especially active
area of relativity research, complementing the research that emphasized the
features of the emotional eliciting stimulus by focusing upon the relativity of
the internal elicitors of the emotional experience. Indeed, more than 100 arti-
cles, various books (e.g. Lazarus 1991, Omdahl 1995), and special issues of
academic journals (e.g. Cognition and Emotion, Psychological Inquiry) were
devoted to the topic in recent years. The premise in cognitive appraisal theories
is that the appraisal of the significance of a stimulus involves “relational mean-
ing”—the import of an event in conjunction with the conditions present in the
environment and personal goals, beliefs, and adaptational resources (Lazarus
1994). Accordingly, universal antecedents are defined in terms of appraisal
dimensions rather than stimulus features (e.g. Ellsworth 1994, Frijda 1994).
Roseman et al (1996) argued that appraisals of unexpectedness, situational
state, motivational state, probability, control potential, problem source, and
agency differentiate 17 emotions, whereas in a cross-cultural study Scherer
(1997) found that fewer appraisal dimensions of the eliciting event provided a
reasonably good account of the major emotion categories (e.g. joy, sadness,
fear, anger, disgust, shame, and guilt) (see also Fitness & Fletcher 1993, Frijda
1993, Parkinson & Manstead 1993, Reisenzein & Hofmann 1993, Smith et al
1993). Importantly, suggestive evidence that the unfolding of cognitive ap-
praisals were themselves influenced by subcortical neural structures long asso-
ciated with emotion emerged from neuropsychological cases such as Scott et
al’s (1997) report of a patient with lesions of the left and right amygdala (see
also Bechara et al 1995, Damasio 1994, Scherer 1993). Cognitive appraisals may be more important for some types of emotional
elicitors than others. In an illustrative line of research summarized by Ohman
et al (1998), two types of emotional conditioning were identified. In one type
of conditioning, the knowledge that the conditioned stimulus (CS) and uncon-
ditioned stimulus (US) are associated in time is explicit (i.e. expectancy-based
learning)—that is, autonomic responses occur on the same trials on which sub-
jects develop the expectancy that the CS is followed by the US. This learning
does not require an aversive US (Hamm & Vaitl 1996), is accessible to con-
sciousness, and modifies responses related to orienting responses (LeDoux
1995, Ohman et al 1998). In a second type of visceral conditioning, the knowl-
edge that the CS and US are associated in time is implicit (Ohman et al 1998).
This learning appears most reliably when an aversive US is combined with a
fear-relevant CS (e.g. snake, angry facial display), results in an enhanced star-
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tle response and tachycardia, is relatively resistant to extinction, and, although not dependent on conscious awareness of the CS-US contingency, it modifies the perceived valence of the CS as revealed by ratings (Davey 1992, Schell et al 1991, see Ohman 1993). The hippocampus appears to be especially impor- tant in the explicit learning of emotional expectancies, whereas the amygdala appears especially important in the implicit emotional conditioning. For in- stance, Bechara et al (1995) found that two patients with bilateral lesions of the amygdala learned the conditioning contingencies but did not acquire condi- tioned skin conductance responses in aversive conditioning paradigms. Pa- tients with bilateral hippocampal damage, in contrast, failed to learn the condi- tioning contingencies but acquired conditioned skin conductance responses. Together, these studies suggest that cognitive appraisals may play a more im- portant causal role in human autonomic conditioning based on explicit than implicit knowledge (LeDoux 1995, Ohman et al 1998).
Classical conditioning has traditionally provided a valuable paradigm for studying behavioral preference in nonvertebrates and nonprimates, and more contemporaneously it has been used to examine the mechanisms underlying the learning and memory of affective associations. The evolutionary advan- tage is obvious; recognizing the neutral trappings of a predator as a danger signal allows organisms to avoid becoming a meal. Additional evidence for the special status accorded to motivationally significant stimuli can be found in research on orienting responses. Orienting responses to threat-related stimuli are found whether the stimuli are masked or not, whereas orienting responses to neutral stimuli are found for unmasked but not masked stimuli (Dimberg & Ohman 1996, Ohman 1993). According to Ohman’s theory of the orienting re- sponse, evolution has sculpted perceptual and attentional systems to provide preferential access to those classes of stimuli with adaptive significance for or- ganisms (Ohman et al 1998). Based on comparative data, Hunt & Campbell (1997) have further suggested that orienting responses to neutral stimuli may have evolved from earlier, more motivationally basic responses, answering the questions “Is it dangerous?” or “Is it food?” rather than the “What is it?” re- sponse posited by Pavlov.
THE AFFECT SYSTEM UNDERLYING EMOTION
Evolutionary forces do not value knowledge or truth per se but species sur-
vival. Hunt & Campbell’s provocative proposition underscores the primeval
importance of a system that differentiates between hostile and hospitable
stimuli (1997). The human brain and body have been shaped by natural selec-
tion to perform this affective categorization and to respond accordingly. Af-
fective categorizations and responses are so critical that organisms have rudi-
mentary reflexes for categorizing and approaching or withdrawing from cer-
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tain classes of stimuli and for providing metabolic support for these actions
(Davis 1997, LeDoux 1995). These rudimentary processes are evident in hu-
mans as well, but a remarkable feature of humans is the extent to which the af-
fective categorizations are shaped by learning and cognition (Berntson et al
1993, Kahneman et al 1998). As various authors have noted, an additional
adaptive advantage is conferred to species whose individual members have the
capacity to learn based on the unique environmental contingencies to which
they are exposed, to represent and predict events in their environment, to ma-
nipulate and plan based on representations, and to exert some control over their
attentional and cognitive resources. Zajonc’s influential paper “Preferences Need No Inferences” underscored
the utility of the affect system as an object of study (1980). Evidence that the neural circuitry involved in computing the affective significance of a stimulus (i.e. evaluative processing) diverges at least in part from the circuitry involved in identification and discrimination (i.e. nonevaluative processing) was pro- vided by Shizgal (1998) in a series of studies involving brain stimulation in rats and by Cacioppo and colleagues (Cacioppo et al 1996, Crites & Cacioppo 1996) in a series of studies of ERP topographies in humans. For instance, in- vestigations of the spatial distribution of late positive potentials across the scalp have revealed a relatively symmetrical distribution during nonaffective categorizations, whereas the spatial distribution of the late positive potentials associated with affective categorizations were more right lateralized (Ca- cioppo et al 1996). This asymmetrical activation is consistent with the impor- tance of the right hemisphere in emotion (see Tucker & Frederick 1989). Fur- thermore, the similarities in ERP topographies indicate that affective and non- affective appraisals are not entirely different but rather rely on a number of common information-processing operations.
In the last chapter on emotion in the Annual Review of Psychology, LeDoux covered in detail some of the neural substrates of the affect system (1995). Here, therefore, we focus on the structure and operating characteristics of the affect system.
Operating Characteristics of the Affect System
Stimuli and events in the world are diverse, complex, multidimensional—in
short, seemingly incomparable. Yet each perceptual system has evolved to be
tuned to specific features, resulting in the expression of these stimuli on a com-
mon metric (Tooby & Cosmides 1990). Seemingly incomparable stimuli and
events can also be conceived as being expressed on common motivational met-
rics (Cacioppo & Berntson 1994, Lang 1995, Shizgal 1998). As Ohman et al
note, “Evolution has primed organisms to be responsive to stimuli that more or
less directly are related to the overall task of promoting one’s genes to prosper
in subsequent generations. . .. Stimuli of these types are embedded within emo-
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tional systems that help regulate behavior within critical functional domain”
(Ohman et al 1998). Information is lost in translating a multidimensional representation of a
stimulus onto a common motivational metric (i.e. a currency function). How- ever, as Shizgal states, “the information lost due to the collapsing of multiple dimensions is essential for identifying the stimulus and distinguishing it from others. . ..The circuitry that computes instantaneous utility must diverge from the perceptual circuitry subserving identification and discrimination” (Shizgal 1998). As noted above, there is now considerable evidence for differences in the circuitry in affective processing versus the processes of identification and discrimination.
From classical learning theory came the principle that motivational strength increases as the distance from a desired or undesired endstate decreases. Cur- rency functions, in essence, represent the activation function for motivational strength. Perceptual activation functions tend to be negatively accelerating, and this appears to describe the activation function for emotion as well (Boy- sen et al 1996, Kemp et al 1995). For example, Boysen et al (1996) demon- strated that, for chimpanzees judging the differential incentive values of candy arrays, the relative effectiveness of a given increment in payoff diminished as the base size of the payoff increased. The activation function for affective re- sponses is thus reminiscent of microeconomic marginal utility functions.
Stages and Channels of Evaluative Processing
One distinction Shizgal (1998) made between the evaluative (affective) and
perceptual channels is that the former is constructed not to return objective
properties of the stimulus but to provide a subjective estimate of the current
significance of these properties. How many evaluative channels are there?
Most have posited one in which subjective, valent information is derived from
the flow of sensation (e.g. Green et al 1993). Studies of the conceptual organi-
zation of emotion, for instance, suggest that people’s knowledge about emo-
tions is hierarchically organized and that a superordinate division is between
positivity and negativity (e.g. Lang et al 1990). One reason underlying this superordinate division in emotional knowledge
may be that physical constraints restrict behavioral manifestations to bivalent actions (approach/withdrawal). Evolution favors the organism that can learn, represent, and access rapidly whether approach or withdrawal is adaptive when confronted by a stimulus. Accordingly, mental guides for one’s actions in future encounters with the target stimuli—attitudes (e.g. Cacioppo & Bernt- son 1994), preferences (e.g. Kahneman 1998), and conceptual organizations of emotion (e.g. Ortony et al 1988)—also tend to be more expected and stable when organized in terms of a bipolar evaluative dimension (ranging from very good and not at all bad to very bad and not at all good).
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Physical limitations may constrain behavioral expressions and incline be-
havioral guides toward bipolar (good/bad; approach/withdraw) dispositions,
but these constraints do not have the same force at the level of underlying
mechanism. That is, the fact that approach and withdrawal tend to be recipro-
cally activated behavioral manifestations does not mean that they were derived
from a single bipolar evaluative channel; it only means that the outputs of all of
the evaluative processors comprising the affect system are combined in order
to compute preference and organize action. Various theorists have posited
that the module in the affect system that computes attitudes, preferences, and
actions derives input from at least two specialized evaluative channels that
process information in parallel—one in which threat-related (i.e. negative) in-
formation is derived from the flow of sensation and a second in which safety
and appetitive (i.e. positive) information is derived (e.g. Cacioppo et al 1998a,
Gilbert 1993, Lang et al 1990, Marcus & Mackuen 1993, Watson & Clark
1992, Zautra et al 1997). According to the model of evaluative space (Cacioppo & Berntson 1994,
Cacioppo et al 1997b), the common metric governing approach/withdrawal is
a single dimension at response stages but is the consequence of two interven-
ing metrics (i.e. evaluative channels)—the activation function for positivity
and the activation function for negativity—at the inaugural affective process-
ing stages. Further, multiple modes of activation are posited to exist for the two
evaluative channels: (a) reciprocal activation occurs when a stimulus has op-
posing effects on the activation of positivity and negativity; (b) uncoupled ac-
tivation occurs when a stimulus affects only positive or only negative evalua-
tive activation; and (c) nonreciprocal activation occurs when a stimulus in-
creases (or decreases) the activation of both positivity and negativity. This
model thus does not reject the reciprocal activation that is assumed in subjec-
tive reports of affect, and demanded in behavioral manifestations of affect, but
rather subsumes it as one of the possible modes of activation and explores the
antecedents for each mode of evaluative activation. Evidence for the existence of multiple modes of evaluative activation has
been observed across all levels of analysis (cf Cacioppo & Berntson 1994). For
instance, Hoebel (1998) reviewed evidence that whereas morphine has recipro-
cal effects on neurochemical processes underlying approach and withdrawal be-
havior, food restriction alters neurochemical effects underlying approach behav-
ior in an uncoupled fashion. At the verbal level, Goldstein & Strube (1994)
demonstrated the uncoupled activation of positivity and negativity in affective
reports collected from students at the beginning and end of three consecutive
class periods. The intensity of positive and negative reactions on any particular
day were found to be uncorrelated. Moreover, exam feedback activated positiv-
ity and negativity differently. Students who performed well on an exam showed
an increase in positive affect relative to their beginning-of-class level, whereas
EMOTION 201
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their level of negative affect remained unchanged; and students who performed
poorly showed an increase in negative affect but no change in positive affect. Such distinctions between positive and negative affective processes have
also been observed in (a) uplifts and hassles (Gannon et al 1992, Zautra et al
1990); (b) mood states (Lawton et al 1992, Zautra et al 1997); (c) organization
of self-knowledge (e.g. Showers 1995, Showers & Kling 1996); (d) self-
regulatory focus (e.g. Higgins 1997); (e) self-efficacy (Zautra et al 1997); (f)
personality processes (Robinson-Whelen et al 1997, Rusting & Larsen 1998,
Watson et al 1992); (g) achievement motivations (Elliot & Church 1997, Elliot
& Harackiewicz 1996); (h) attitudes and persuasion (Cacioppo & Berntson
1994); (i) emotional expressivity (Gross & John 1997); (j) social interactions
(Berry & Hansen 1996, Cacioppo et al 1997b); (k) affect toward political lead-
ers (Marcus & Mackuen 1993); and (l) intergroup discrimination (Blanz et al
1997, Brewer 1996). However, Green et al (1993) questioned the notion that positive and nega-
tive affect were separable on methodological grounds (see also Bagozzi 1993,
Marsh 1996). Specifically, they argued that measures of affect typically rely
on similarly worded scales with identical endpoints. This feature, they argued,
can lead to positively correlated measurement error effectively suppressing the
magnitude of the true negative correlation between positive and negative af-
fective states. Thompson et al (1995), in contrast, suggested that methodologi-
cal artifacts (e.g. carryover between unipolar positive and negative rating
scales) could instead inflate the negative correlation between positive and
negative rating scales, and they recommended segregating self-report meas-
ures of positive and negative affect to avoid self-presentational biases. A recent investigation by Nelson (1998) addressed these methodological
concerns and found evidence for the operation of multiple modes of evaluative
activation. Nelson (1998) used a structural modeling approach to examine the
structure of affect toward two different social categories—African Americans
and the poor—while accounting for correlated measurement error among the
observed variables. Nelson’s analyses of the structure of the emotional re-
sponses toward the poor revealed substantial independence between positive
and negative factors. This two-factor model was significantly better than the
bipolar model even when the effects of correlated measurement error were
extracted. This result is precisely what would be expected if positive and nega-
tive affect were separate dimensions at a basic level. Nelson’s analyses of the
structure of students’ emotional responses toward African Americans, how-
ever, revealed a bipolar model to be sufficient when the effects of correlated
measurement error were considered. This latter result illustrates that affect is
not invariably organized in a bipolar or a bivariate structure but rather the
structure of affective response is influenced by the mode of evaluative activa-
tion elicited by the stimulus (Cacioppo & Berntson 1994).
202 CACIOPPO & GARDNER
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Methodological issues are important to consider, but assuming that the af-
fect system consists only of a single bipolar evaluative channel can also be
costly in terms of the fertile avenues of research it precludes. Brain imaging
studies, for instance, have tended to contrast positive and negative states, a
procedure that impedes the differentiation of the conditions in which positive
and negative processes are separable. This may be unwise because, although
preliminary at this juncture, some brain imaging studies suggest that different
neural structures may be involved in positive and negative hedonic processes.
George et al, for instance, used PET during the recall of happy, sad, or neutral
memories while viewing congruent happy, sad, or neutral faces (George et al
1995). Comparisons between the sadness-minus-neutral and the happy-minus-
neutral conditions revealed that, rather than reciprocal changes in blood flow
to the same brain regions, a change from sad to happy affective state produced
increased cerebral blood flow to distinguishable brain regions (see also Lane et
al 1997). Research on cortical asymmetry is also consistent with the notion of spe-
cialized evaluative channels for the processing of positive and negative infor-
mation that are subsequently integrated in the production of an affective re-
sponse (e.g. Davidson 1993, Davidson et al 1990). In a study by Sutton &
Davidson, for instance, resting EEG asymmetries were compared with scores
on Carver & White’s Behavioral Approach System/Behavioral Inhibition Sys-
tem measure, a self-report instrument designed to assess individual differences
in the tendency to approach or withdraw and to experience concomitant affec-
tive states (Sutton & Davidson 1997, Carver & White 1994). Consistent with
the notion that positivity and negativity are separable systems differentially as-
sociated with left and right hemispheric activation, respectively, greater rela-
tive left asymmetry at midfrontal electrode sites was positively correlated with
behavioral activation system scores and negatively correlated with behavioral
inhibition system scores. Similarly, studies using computerized tomography
to investigate the relationship between the location of stroke-related lesions
and affective symptoms showed that the severity of post-stroke depression was
positively related to lesion proximity to the left frontal pole but negatively re-
lated to lesion proximity to the right frontal pole (Robinson & Downhill 1995).
Robinson and colleagues further observed that patients with right lateralized
infarctions were more likely than their left-hemisphere–lesioned counterparts
to display inappropriate cheerfulness. The evidence for the separability of positive and negative evaluative pro-
cesses becomes more controversial when one turns to the literature on the
conceptual organization of moods, affect, and emotion. Among the best
known research bearing on the centrality of people’s net positive and negative
feelings is Osgood et al’s classic work on the measurement of meaning (1957).
In multiple studies and cultures, evaluative bipolar word pairs (e.g. pleasant-
EMOTION 203
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unpleasant) were found to comprise a fundamental dimension underlying peo-
ple’s understanding of the world. Conceptually similar results have been found
in crosscultural, multidimensional scaling studies of emotional feelings (e.g.
Bradley & Lang 1994, Larsen & Diener 1992) and in crosscultural ratings of
emotionally evocative pictures (e.g. Lang et al 1995). Thus, the two-
dimensional representation that best represents people’s conceptual organiza-
tion of affect and emotion may tend to be positive/negative X active/inactive
rather than positive/nonpositive X negative/non-negative. Given that psycho-
logical states such as conflict, ambivalence, and inconsistency among beliefs
about an attitude object tend to be unexpected, nonharmonious, and unstable,
people’s conceptual organization of evaluative processes and affective states
(e.g. moods) may tend toward a bipolar structure because of the operation of
motives to maintain a simple and psychologically consistent representation of
the world. In sum, the common metric governing approach/withdrawal can perhaps be
best conceptualized as a single dimension at response stages with the bivalent
affective response the consequence of two intervening evaluative channels,
one for positivity (appetition) and one for negativity (aversion). Consistent
with the notion that input from these evaluative channels is combined with an-
tagonistic effects on action dispositions and behavior, a bivalent organization
of affect is more likely to be observed as one moves down the neuraxis (see
Berntson et al 1993, Cacioppo et al 1998). For instance, relative to neutral
states, negative states tend to potentiate startle eyeblink whereas positive states
tend to inhibit it (see reviews by Filion et al 1998, Lang et al 1990) because of
the modulating effects of the amygdala (Davis 1997, Lang 1995). The value of considering the additional complexities introduced by multi-
ple evaluative channels and modes of evaluative activation derives not only
from the data it explains but also from the questions it generates and the
bridges it builds across data previously thought to be separate. Research in ar-
eas of inquiry as distinct as coping in chronic pain patients (Zautra et al 1995),
classroom performance and academic motivation (Elliot & Church 1997), fre-
quency and quality of social interactions (Berry & Hansen 1996), blood and
organ donation (Cacioppo & Gardner 1993), and racial prejudice (Schofield
1991) all support the wisdom of considering the two motivational systems as
functionally separable. The partial segregation of the positive and negative evaluative channels in
the affect system not only confers an additional flexibility of orchestrating ap-
petitive and aversive motivational forces via modes of evaluative activation,
but also affords evolution the opportunity to sculpt distinctive activation (i.e.
currency) functions for positivity and negativity. Interest in differences in the
effects of positive versus negative information has grown substantially in re-
cent years. Not only have numerous articles and several major reviews on the
204 CACIOPPO & GARDNER
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topic appeared (e.g. Cacioppo & Berntson 1994, Levy 1992, Peeters &
Czapinski 1990, Skowronski & Carlston 1989, Taylor 1991) but two issues of
the European Journal of Social Psychology are devoted to the topic. The ex-
tant data suggest at least two differences in these currency functions: (a) a
positivity offset—the output of positivity is higher than the output of nega-
tivity at very low levels of affective input; and (b) a negativity bias—the in-
crease in output per quantum of input is greater for negativity than positivity
(see Cacioppo et al 1998).
POSITIVITY OFFSET The positivity offset is the tendency for there to be a weak positive (approach) motivational output at zero input, an intercept differ- ence in the affective system. As a consequence of the positivity offset, the mo- tivation to approach is stronger than the motivation to avoid at low levels of evaluative activation (e.g. at distances far from a goal). What might be the pos- sible evolutionary significance of the positivity offset? Without a positivity offset, an organism in a neutral environment may be unmotivated to approach novel objects, stimuli, or contexts. Such organisms would learn little about novel or neutral-appearing environments and their potential value or threat. With a positivity offset, however, an organism facing neutral or unfamiliar stimuli would be weakly motivated to engage in exploratory behavior. Such a tendency may have important survival value, at least at the level of a species.
How might this evolutionarily endowed tendency manifest itself in the
present day? One line of evidence may be the prevalence of “unrealistic opti-
mism,” the tendency to expect generally positive outcomes for unknown fu-
ture events (Brinthaupt et al 1991, Hoorens & Buunk 1993, Pulford & Colman
1996, Regan et al 1995). A second line of evidence may be the robust “positiv-
ity bias” found in impressions of neutral, unknown, or ambiguous human and
nonhuman targets (Klar & Giladi 1997, Sears 1983, Peeters 1991). Finally,
research concerning the “mere exposure” effect demonstrates that affectively
neutral stimuli may be evaluated positively even when presented outside of
conscious awareness (Bornstein 1989, Harmon-Jones & Allan 1998). These
lines of research support the existence of a positivity offset in a myriad of do-
mains; when asked to evaluate stimuli or situations that by objective standards
should be affectively neutral (e.g. the unknowable future, the “average” per-
son, an unfamiliar Chinese idiogram), people show a consistent tendency to re-
spond in a mildly positive fashion.
NEGATIVITY BIAS Exploratory behavior can provide useful information about an organism’s environment, but exploration can also place an organism in proximity to hostile stimuli. Because it is more difficult to reverse the conse- quences of an injurious or fatal assault than those of an opportunity unpursued, the process of natural selection may also have resulted in the propensity to re-
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act more strongly to negative than to positive stimuli. Termed the negativity bias, this heightened sensitivity to negative information is a robust psychologi- cal phenomenon (see reviews by Cacioppo & Berntson 1994, Cacioppo et al 1997b, Peeters & Czapinski 1990, Taylor 1991).
Miller’s research on rodent behavior provided some of the earliest evidence for a negativity bias through determining that the slope for the avoidance gra- dient was steeper than the slope for the approach gradient (Miller 1961). Forty years later, evidence supporting a negativity bias has been found in domains as varied as impression formation (e.g. Skowronski & Carlston 1989), person memory (e.g. Ybarra & Stephan 1996), blood and organ donation (e.g. Ca- cioppo & Gardner 1993), hiring decisions (e.g. Rowe 1989), personnel evalua- tions (e.g. Ganzach 1995), and voting behavior (e.g. Klein 1991, 1996). It has been found to characterize the judgments of children as well as adults (e.g. Aloise 1993, Robinson-Whelen et al 1997). Taylor summarized a wide range of evidence showing that negative events in a context evoke stronger and more rapid physiological, cognitive, emotional, and social responses than neutral or positive events (Taylor 1991; see also Westermann et al 1996). As further evidence, Ito et al (1998) have recently uncovered ERP evidence consistent with a negativity bias in the affect system.
In sum, negative emotion has been depicted previously as playing a funda- mental role in calibrating psychological systems; it serves as a call for mental or behavioral adjustment. Positive emotion, in contrast, serves as a cue to stay the course or as a cue to explore the environment. This characterization may help account for evolutionary forces sculpting distinctive activation functions for positive and negative affect; the separable activation functions serve as complementary, adaptive motivational organization. Species with a positivity offset and a negativity bias enjoy the benefits of exploratory behavior and the self-preservative benefits of a predisposition to avoid or withdraw from threat- ening events. The features reviewed in this section represent only the rudimen- tary operations of an affect system, however. Work on the relativity of emotion shows that cognitive factors and physiological states affect the extent to which appetitive or defensive motivations are aroused, and recent work suggests that self-regulatory focus also influences approach and withdrawal gradients (Carver & Scheier 1990, Higgins 1997, Shah et al 1998). The organization of the affect system warrants further study as a reflection of our evolutionary heritage and as a continued force in the shaping of even our most civilized re- sponses.
Visit the Annual Reviews home page at
http://www.AnnualReviews.org.
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EMOTION 207
Literature Cited
Ackerman D. 1990. A Natural History of the Senses. New York: Vintage Books
Aloise PA. 1993. Trait confirmation and dis- confirmation: the development of attribu- tion biases. J. Exp. Child Psychol. 55: 177–93
Andersen BL, Farrar WB, Golden-Kreutz D, Kutz LA, MacCallum R, et al. 1998. Stress and immune responses after surgical treat- ment for regional breast cancer. J. Natl. Cancer Inst. 90:30–36
Averill JR, Ekman P, Ellsworth PC, Frijda NH, Lazarus R, et al. 1994. How is Evi- dence of Universals in Antecedents of Emotion Explained? New York: Oxford Univ. Press
Bagozzi RP. 1993. An examination of the psy- chometric properties of measures of nega- tive affect in the PANAS-X scales. J. Pers. Soc. Psychol. 65:836–51
Bechara A, Tranel D, Damasio H, Adolphs R, Rockland C, Damasio AR. 1995. Double dissociation of conditioning and declara- tive knowledge relative to the amygdala and hippocampus in humans. Science 269: 1115–18
Berntson GG, Boysen ST, Cacioppo JT. 1993. Neurobehavioral organization and the car- dinal principle of evaluative bivalence. Ann. NY Acad. Sci. 702:75–102
Berry DS, Hansen JS. 1996. Positive affect, negative affect, and social interaction. J. Pers. Soc. Psychol. 71:796–809
Blanz M, Mummendey A, Otten S. 1997. Nor- mative evaluations and frequency expecta- tions regarding positive versus negative outcome allocations between groups. Eur. J. Soc. Psychol. 27:165–76
Boiten FA, Frijda NH, Wientjes CJE. 1994. Emotions and respiratory patterns: review and critical analysis. Int. J. Psychophys. 17:103–28
Bornstein RF. 1989. Exposure and affect: overview and meta-analysis of research, 1968–1987. Psychol. Bull. 106:265–89
Borod JC, Haywood CS, Koff E. 1997. Neu- ropsychological aspects of facial asymme- try during emotional expression: a review of the normal adult literature. Neuropsy- chol. Rev. 7:41–60
Boysen ST, Berntson GG, Hannan MB, Ca- cioppo JT. 1996. Quantity-based choices: interference and symbolic representations in chimpanzees (Pan troglodytes). J. Exp. Psychol. Anim. Behav. Proc. 22:76–86
Bradley BP, Mogg K, Williams R. 1995. Im- plicit and explicit memory for emotion- congruent information in clinical depres-
sion and anxiety. Behav. Res. Ther. 33: 755–70
Bradley MM, Lang PJ. 1994. Measuring emo- tion: the self-assessment manikin and the semantic differential. J. Behav. Ther. Exp. Psychiatry 25:49–59
Bradley MM, Lang PJ, Cuthbert BN. 1997. Af- fective Norms for English Words (ANEW). NIMH Cent. Stud. Emot. Atten., Univ. FL
Bradley MM, Zack J, Lang PJ. 1994. Cries, screams, and shouts of joy: affective re- sponses to environmental sounds. Psycho- physiology 31:S29
Brendl CM, Higgins ET. 1995. Principles of judging valence: what makes events posi- tive or negative? Adv. Exp. Soc. Psychol. 28:95–160
Brewer MB. 1996. In–group favoritism: the subtle side of intergroup discrimination. In Codes of Conduct: Behavioral Research Into Business Ethics, ed. DM Messick, AE Tenbrunsel, pp. 160–70. New York: Rus- sell Sage Found.
Brezinka V, Kittel F. 1996. Psychosocial fac- tors of coronary heart disease in women: a review. Soc. Sci. Med. 42:1351–65
Brinthaupt LJ, Moreland RL, Levine JM. 1991. Sources of optimism among pro- spective group members. Pers. Soc. Psy- chol. Bull. 17:36–43
Cacioppo JT, Berntson GG. 1994. Relation- ship between attitudes and evaluative space: a critical review, with emphasis on the separability of positive and negative substrates. Psychol. Bull. 115:401–23
Cacioppo JT, Berntson GG, Klein DJ, Poehl- mann KM. 1997a. The psychophysiology of emotion across the lifespan. Annu. Rev. Gerontol. Geriatr. 17:27–74
Cacioppo JT, Crites SL Jr, Gardner WL. 1996. Attitudes to the right: evaluative process- ing is associated with lateralized late posi- tive event-related brain potentials. Pers. Soc. Psychol. Bull. 22:1205–19
Cacioppo JT, Crites SL Jr, Gardner WL, Berntson GG. 1994. Bioelectrical echoes from evaluative categorizations. I. A late positive brain potential that varies as a function of trait negativity and extremity. J. Pers. Soc. Psychol. 67:115–25
Cacioppo JT, Gardner WL. 1993. What under- lies medical donor attitudes and behavior? Health Psychol. 12:269–71
Cacioppo JT, Gardner WL, Berntson GG. 1997b. Beyond bipolar conceptualizations and measures: the case of attitudes and evaluative space. Pers. Soc. Psychol. Rev. 1:3–25
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
208 CACIOPPO & GARDNER
Cacioppo JT, Gardner WL, Berntson GG. 1998a. The affect system: form follows function. J. Pers. Soc. Psychol. In press
Cacioppo JT, Marshall-Goodell BS, Tassinary LG, Petty RE. 1992. Rudimentary determi- nants of attitudes: classical conditioning is more effective when prior knowledge about the attitude stimulus is low than high. J. Exp. Soc. Psychol. 28:207–33
Cacioppo JT, Tassinary LG, Berntson GG, ed 1998b. The Handbook of Psychophysiol- ogy. New York: Cambridge Univ. Press. In press
Cacioppo JT, Uchino BN, Crites SL Jr, Sny- dersmith MA, Smith G, et al. 1992. Rela- tionship between facial expressiveness and sympathetic activation in emotion: a criti- cal review, with emphasis on modeling underlying mechanisms and individual differences. J. Pers. Soc. Psychol. 62: 110–28
Cacioppo JT, von Hippel W, Ernst JM. 1997c. Mapping cognitive structures and pro- cesses through verbal content: the thought- listing technique. J. Consult. Clin. Psy- chol. 65:928–40
Cahill L. 1996. Neurobiology of memory for emotional events: converging evidence from infra-human and human studies. Cold Spring Harbor Symp. Quant. Biol. 61:259–64
Carney RM, Rich MW, Jaffe AS. 1995. De- pression as a risk factor for cardiac events in established coronary heart disease: a re- view of possible mechanisms. Ann. Behav. Med. 17:142–49
Carroll JM, Russell JA. 1997. Facial expres- sions in Hollywood’s portrayal of emo- tion. J. Pers. Soc. Psychol. 72:164–76
Carstensen L, Gross J, Fung H. 1997. The so- cial context of emotional experience. Annu. Rev. Gerontol. Geriatr. 17:325–52
Carver CS, Scheier MF. 1990. Origins and functions of positive and negative affect: a control-process view. Psychol. Rev. 97: 19–35
Carver CS, Lawrence JW, Scheier ME. 1996. A control-process perspective on the ori- gins of affect. In Striving and Feeling: In- teractions Among Goals, Affect, and Self- Regulation, ed. LL Martin, A Tesser, pp. 11–52. Mahwah, NJ: Erlbaum
Carver CS, White TL. 1994. Behavioral inhi- bition, behavioral activation, and affective responses to impending reward and pun- ishment: the BIS/BAS scales. J. Pers. Soc. Psychol. 67:319–33
Chen M, Bargh JA. 1998. Motivational and emotional consequences of automatic eval- uation. Pers. Soc. Psychol. Bull. In press
Cohen S, Rodriguez MS. 1995. Pathways link-
ing affective disturbances and physical disorders. Health Psychol. 14:374–80
Crites SL Jr, Cacioppo JT. 1996. Electrocorti- cal differentiation of evaluative and non- evaluative categorizations. Psychol. Sci. 7: 318–21
Crites SL Jr, Cacioppo JT, Gardner WL, Berntson GG. 1995. Bioelectrical echoes from evaluative categorizations. II. A late positive brain potential that varies as a function of attitude registration rather than attitude report. J. Pers. Soc. Psychol. 68: 997–1013
Damasio AR. 1994. Descartes’ Error: Emo- tion, Reason, and the Human Brain. New York: Grossett/Putnam & Sons
Damasio AR. 1996. The somatic marker hy- pothesis and the possible functions of the prefrontal cortex. Philos. Trans. R. Soc. London Ser. B 351:1413–20
Davey GC. 1992. An expectancy model of laboratory preparedness effects. J. Exp. Psychol. Gen. 121:24–40
Davidson RJ. 1993. Parsing affective space: perspectives from neuropsychology and psychophysiology. Neuropsychology 7: 464–75
Davidson RJ. 1994. Honoring biology in the study of affective style. See Ekman & Davidson 1994, pp. 321–28
Davidson RJ. 1998. Anterior electrophysio- logical asymmetries, emotion and depres- sion: conceptual and methodological co- nundrums. Psychophysiology. In press
Davidson RJ, Cacioppo JT. 1992. New devel- opments in the scientific study of emotion. Psychol. Sci. 3:21–22
Davidson RJ, Ekman P, Saron CD, Senulis JA, Friesen WV. 1990. Approach-withdrawal and cerebral asymmetry: emotional ex- pression and brain physiology. J. Pers. Soc. Psychol. 58:330–41
Davis M. 1997. The neurophysiological basis of acoustic startle modulation: research on fear motivation and sensory gating. In At- tention and Orienting, ed. PJ Lang, RF Si- mons, M Balaban, pp. 69–96. Mahwah, NJ: Erlbaum
Davison GC, Vogel RS, Coffman SG. 1997. Think-aloud approaches to cognitive as- sessment and the articulated thoughts in simulated situations paradigm. J. Consult. Clin. Psychol. 65:950–58
Depue RA. 1996. A neurobiological frame- work for the structure of personality and emotion: implications for personality disorders. In Major Theories of Personal- ity Disorder, ed. JF Clarkin, MF Len- zenweger, pp. 347–90. New York: Guil- ford
Diener E, Lucas RE. 1998. Personality and
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
EMOTION 209
subjective well-being. See Kahneman et al 1998. In press
Diener E, Suh E. 1998. National differences in subjective well-being. See Kahneman et al 1998. In press
Dimberg U, Ohman A. 1996. Behold the wrath: psychophysiological responses to facial stimuli. Motiv. Emot. 20:149–82
Drevets WC, Raichle ME. 1995. Positron emission tomographic imaging studies of human emotional disorders. In The Cog- nitive Neurosciences, ed. MS Gazzan- iga, pp. 1153–64. Cambridge, MA: MIT Press
Ekman P. 1992. Are there basic emotions? Psychol. Rev. 99:550–53
Ekman P. 1993. Facial expression and emo- tion. Am. Psychol. 48:384–92
Ekman P. 1994. Strong evidence for univer- sals in facial expressions: a reply to Rus- sell’s mistaken critique. Psychol. Bull. 115:268–87
Ekman P, Davidson RJ, eds. 1994. The Nature of Emotion: Fundamental Questions. New York: Oxford Univ. Press
Ekman P, Keltner D. 1997. Universal facial expressions of emotion: an old controversy and new findings. In Nonverbal Communi- cation: Where Nature Meets Culture. ed. UC Segerstrale, P Molnar, pp. 27–46. Mahwah, NJ: Erlbaum
Elliot AJ, Church MA. 1997. A hierarchical model of approach and avoidance achieve- ment motivation. J. Pers. Soc. Psychol. 72:218–32
Elliot AJ, Harackiewicz JM. 1996. Approach and avoidance achievement goals and in- trinsic motivation: a mediational analysis. J. Pers. Soc. Psychol. 70:461–75
Ellsworth PC. 1994. Some reasons to expect universal antecedents of emotion. See Ek- man & Davidson 1994, pp. 150–54
Emde RN, Osofsky JD, Butterfield PM. 1993. The IFEEL Pictures: A New Instrument for Interpreting Emotions. Madison, CT: In- ternational Univ. Press
Filion DL, Dawson ME, Schell AM. 1998. The psychological significance of human star- tle eyeblink modification: a review. Biol. Psychol. 47:1–43
Fitness J, Fletcher G. 1993. Love, hate, anger, and jealousy in close relationships: a pro- totype and cognitive appraisal analysis. J. Pers. Soc. Psychol. 65:942–58
Flannery DJ, Torquati JC, Lindemeier L. 1994. The method and meaning of emo- tional expression and experience during adolescence. J. Adoles. Res. 9:8–27
Forgas JP. 1995. Mood and judgment: the af- fect intrusion model (AIM). Psychol. Bull. 117:39–66
Forsyth JP, Eifert GH. 1996. The language of feeling and the feeling of anxiety: contri- butions of the behaviorisms toward under- standing the function-altering effects of language. Psychol. Rec. 46:607–49
Fox PT, Woldorff MG. 1994. Integrating hu- man brain maps. Curr. Opin. Neurobiol. 4:151–56
Frijda NH. 1993. The place of appraisal in emotion. Cogn. Emot. 7:357–87
Frijda NH. 1994. Universal antecedents exist, and are interesting. See Ekman & David- son 1994, pp. 155–62
Gannon L, Vaux A, Rhodes K, Luchetta T. 1992. A two-domain model of well-being: everyday events, social support, and gender-related personality factors. J. Res. Pers. 26:288–301
Ganzach Y. 1995. Negativity (and positivity) in performance evaluation: three field studies. J. Appl. Psychol. 80:491–99
Gardner WL, Cacioppo JT. 1998. A brain based index of evaluative processing: a late positive brain potential reflects indi- vidual differences in the extremity of a negative evaluation. Soc. Cogn. In press
Gardner WL, Gabriel S, Diekman A. 1998. In- terpersonal processes. See Cacioppo et al 1998. In press
George MS, Ketter TA, Parekh PI, Horwitz B, Herscovitch P, Post RM. 1995. Brain ac- tivity during transient sadness and happi- ness in healthy women. Am. J. Psychiatry 152:341–51
Gerrards-Hesse A, Spies K, Hesse FW. 1994. Experimental inductions of emotional states and their effectiveness: a review. Br. J. Psychol. 85:55–78
Gilbert P. 1993. Defence and safety: their function in social behaviour and psychopa- thology. Br. J. Clin. Psychol. 32:131–53
Gilboa E, Revelle W. 1994. Personality and the structure of affective responses. In Emotions: Essays on Emotion Theory, ed. SHM van Goozen, NE Van de Poll, JA Sergeant, pp. 135–59. Hillsdale, NJ: Erl- baum
Goldstein MD, Strube MJ. 1994. Independ- ence revisited: the relation between posi- tive and negative affect in a naturalistic setting. Pers. Soc. Psychol. Bull. 20:57–64
Goleman D. 1995. Emotional Intelligence. New York: Bantam
Gottman JM. 1993. Studying emotion in social interaction. See Lewis & Haviland 1993, pp. 475–87
Gray JA. 1994. Personality dimensions and emotion systems. See Ekman & Davidson 1994, pp. 329–31
Green DP, Goldman SL, Salovey P. 1993. Measurement error masks bipolarity in af-
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
210 CACIOPPO & GARDNER
fect ratings. J. Pers. Soc. Psychol. 64: 1029–41
Grodd W, Scheider F, Klose U, Nagele T. 1995. Functional magnetic resonance to- mography of psychological functions ex- emplified by experimentally induced emo- tions. Radiologe 35:283–89
Gross JJ, John OP. 1997. Revealing feelings: facets of emotional expressivity in self- reports, peer ratings, and behavior. J. Pers. Soc. Psychol. 72:435–48
Gross JJ, Levenson RW. 1995. Emotion elici- tation using films. Cogn. Emot. 9:87–108
Guyll M, Contrada RJ. 1998. Trait hostility and ambulatory cardiovascular activity: responses to social interaction. Health Psychol. 17:30–39
Hamm AO, Vaitl D. 1996. Affective learning: awareness and aversion. Psychophysiol- ogy 33:698–710
Harmon-Jones E, Allan JB. 1998. Probing the mere exposure effect with psychophysio- logical indices of affect. Psychol. Sci. In press
Hagemann D, Naumann E, Becker G, Maier S, Bartussek D. 1998. Frontal brain asymme- try and affective style: a conceptual repli- cation. Psychophysiology. In press
Harvey JH, Stein SK, Scott PK. 1995. Fifty years of grief: accounts and reported psy- chological reactions of Normandy inva- sion veterans. J. Narrat. Life Hist. 5: 315–32
Hatfield E, Cacioppo JT, Rapson RL. 1994. Emotional Contagion. New York: Cam- bridge Univ. Press
Herbert TB, Cohen S. 1993. Depression and immunity: a meta-analytic review. Psy- chol. Bull. 113:472–86
Hess U, Banse R, Kappas A. 1995. The inten- sity of facial expression is determined by underlying affective state and social situa- tion. J. Pers. Soc. Psychol. 69:280–88
Hietanen J, Surakka V, Linnankoski I. 1998. Facial electromyographic responses to vo- cal affect expressions. Psychophysiology. In press
Higgins ET. 1997. Beyond pleasure and pain. Am. Psychol. 52:1280–1300
Hoebel BG. 1998. Neural systems for rein- forcement and inhibition of behavior: rele- vance to eating, addiction and depression. See Kahneman et al 1998. In press
Hoorens V, Buunk BP. 1993. Social compari- son of health risks: locus of control, the person-positivity bias, and unrealistic op- timism. J. Appl. Soc. Psychol. 23: 291–302
Hsee CK, Salovey P, Abelson RP. 1994. The quasi-acceleration reaction: satisfaction as a function of the change of velocity of out-
come over time. J. Exp. Soc. Psychol. 30: 96–111
Hunt PS, Campbell BA. 1997. Autonomic and behavioral correlates of appetitive condi- tioning in rats. Behav. Neurosci. 111: 494–502
Hurlburt RT. 1997. Randomly sampling think- ing in the natural environment. J. Consult. Clin. Psychol. 65:941–49
Ito TA, Cacioppo JT, Lang PJ. 1998. Eliciting affect using the International Affective Picture System: trajectories through evaluative space. Pers. Soc. Psychol. Bull. In press
Ito TA, Larsen JT, Smith NK, Cacioppo JT. 1998. Negative information weighs more heavily on the brain: the negativity bias in evaluative categorizations. J. Pers. Soc. Psychol. In press
Izard CE. 1992. Basic emotions, relations among emotions, and emotion-cognition relations. Psychol. Rev. 99:561–65
Izard CE. 1994. Innate and universal facial ex- pressions: evidence from developmental and cross-cultural research. Psychol. Bull. 115:288–99
Izard CE, Ackerman BP. 1997. Emotions and self-concepts across the life span. Annu. Rev. Gerontol. Geriatr. 17:1–26
Kahneman D. 1998. Objective happiness. See Kahneman et al 1998. In press
Kahneman D, Diener E, Schwarz N, eds. 1998. Hedonic Psychology: Scientific Perspec- tives on Enjoyment, Suffering, and Well- Being. New York: Cambridge Univ. Press. In press
Kahneman D, Fredrickson BL, Schreiber CA, Redelmeier DA. 1993. When more pain is preferred to less: adding a better end. Psy- chol. Sci. 4:401–5
Kamarck TW, Shiffman SM, Smithline L, Goodie JL, Paty JA, et al. 1998. Effects of task strain, social conflict, and emotional activation on ambulatory cardiovascular activity: daily life consequences of recur- ring stress in a multiethnic adult sample. Health Psychol. 17:17–29
Keltner D, Ekman P. 1996. Affective intensity and emotional responses. Cogn. Emot. 10: 323–28
Kemp S, Lea SEG, Fussell S. 1995. Experi- ments on rating the utility of consumer goods: evidence supporting microeco- nomic theory. J. Econ. Psychol. 16:543–61
Kiecolt-Glaser JK, Malarkey W, Cacioppo JT, Glaser R. 1994. Stressful personal rela- tionships: endocrine and immune function. In Handbook of Human Stress and Immu- nity, ed. R Glaser, JK Kiecolt-Glaser, pp. 321–39. San Diego: Academic
Kitayama S, Masuda M. 1995. Reappraising
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
EMOTION 211
cognitive appraisal from a cultural per- spective. Psychol. Inq. 6:217–23
Klar Y, Giladi EE. 1997. No one in my group can be below the group’s average: a robust positivity bias in favor of anonymous peers. J. Pers. Soc. Psychol. 73:885–901
Klein JG. 1991. Negativity effects in impres- sion formation: a test in the political arena. Pers. Soc. Psychol. Bull. 17:412–18
Klein JG. 1996. Negativity in impressions of presidential candidates revisited: the 1992 election. Pers. Soc. Psychol. Bull. 22: 288–95
Kutas M, Federmeier KD. 1998. Minding the body. Psychophysiology 35:135–50
Lane RD, Reiman EM, Ahern GL, Schwartz GE. 1997. Neuroanatomical correlates of happiness, sadness, and disgust. Am. J. Psychiatry 154:926–33
Lang PJ. 1995. The emotion probe: studies of motivation and attention. Am. Psychol. 50: 372–85
Lang PJ, Bradley MM, Cuthbert BN. 1990. Emotion, attention, and the startle reflex. Psychol. Rev. 97:377–95
Lang PJ, Bradley MM, Cuthbert BN. 1995. In- ternational Affective Picture System (IAPS): Technical Manual and Affective Ratings. NIMH Cent. Study Emot. Atten., Univ. FL
Lang PJ, Bradley M, Fitzsimmons J, Cuthbert B, Scott J, et al. 1998. Emotional arousal and activation of the visual cortex: an fMRI analysis. Psychophysiology 35: 199–210
Larsen RJ. 1991. Day-to-day physical symp- toms: individual differences in occurrence, duration, and emotional concomitants of minor daily illnesses. J. Pers. 59:387–423
Larsen RJ, Billings DW, Cutler SE. 1996. Af- fect intensity and individual differences in informational style. J. Pers. 64:185–207
Larsen RJ, Diener E. 1992. Promises and prob- lems with the circumplex model of emo- tion. Rev. Pers. Soc. Psychol. 13:25–59
Lawton MP, Kleban MH, Dean J, Rajogopal D, Parmelee PA. 1992. The factorial gen- erality of brief positive and negative affect measures. J. Gerontol. 47:228–37
Lazarus R. 1991. Emotions and Adaptation. New York: Oxford Univ. Press
Lazarus R. 1994. Universal antecedents of the emotions. See Ekman & Davidson 1994, pp. 163–71
Lazarus RS. 1995. Vexing research problems inherent in cognitive-mediational theories of emotion—and some solutions. Psychol. Inq. 6:183–96
LeDoux JE. 1995. Emotion: clues from the brain. Annu. Rev. Psychol. 46:209–35
Lehrer PM, Isenberg S, Hochron SM. 1993.
Asthma and emotion: a review. J. Asthma 30:5–21
Levenson RW. 1996. Biological substrates of empathy and facial modulation of emo- tion: two facets of the scientific legacy of John Lanzetta. Motiv. Emot. 20:185–204
Leventhal H, Patrick-Miller L, Leventhal E, Burns E. 1997. Does stress-emotion cause illness in elderly people? Annu. Rev. Ger- ontol. Geriatr. 17:138–84
Levy JS. 1992. An introduction to prospect theory. Polit. Psychol. 13:171–86
Lewis M, Haviland JM, eds. 1993. Handbook of Emotions. New York: Guilford
Litt MD, Cooney NL, Morse P. 1998. Ecologi- cal momentary assessment (EMA) with treated alcoholics: methodological prob- lems and potential solutions. Health Psy- chol. 17:48–52
Maddock RJ, Buonocore MH. 1997. Activa- tion of left posterior cingulate gyrus by the auditory presentation of threat-related words: an fMRI study. Psychiatry Res. 75: 1–14
Marcus GE, Mackuen MB. 1993. Anxiety, en- thusiasm, and the vote: the emotional un- derpinnings of learning and involvement during presidential campaigns. Am. Polit. Sci. Rev. 87:672–85
Marsh HW. 1996. Positive and negative global self-esteem: a substantively meaningful distinction of artifactors? J. Pers. Soc. Psy- chol. 70:810–19
Mayer JD, Salovey P. 1993. The intelligence of emotional intelligence. Intelligence 17: 433–42
McGuire TR. 1993. Emotion and Behavior Genetics in Vertebrates and Invertebrates. New York: Guilford
Medvec VH, Madey SF, Gilovich T. 1995. When less is more: counterfactual thinking and satisfaction among Olympic medal- ists. J. Pers. Soc. Psychol. 69:603–10
Mesquita B, Frijda NH, Scherer KR. 1997. Culture and Emotion. Boston: Allyn & Ba- con
Miller NE. 1961. Some recent studies on con- flict behavior and drugs. Am. Psychol. 16: 12–24
Murray IR, Arnott JL. 1993. Toward the simu- lation of emotion in synthetic speech: a re- view of the literature on human vocal emo- tion. J. Acoust. Soc. Am. 93:1097–108
Myers DG. 1993. The Pursuit of Happiness. London: Aquarian
Neafsey EJ, Terreberry RR, Hurley KM, Ruit KG, Frysztak RJ. 1993. Anterior Cingu- late Cortex in Rodents: Connections, Vis- ceral Control Functions, and Implications for Emotion. Boston: Birkhauser
Nelson CA, de Haan M. 1997. A Neurobehav-
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
212 CACIOPPO & GARDNER
ioral Approach to the Recognition of Fa- cial Expressions in Infancy. New York: Cambridge Univ. Press
Nelson TE. 1998. Group affect and attribution in social policy opinion. J. Politics. In press
Niedenthal PM, Kitayama S. 1994. The Heart’s Eye: Emotional Influences in Per- ception and Attention. San Diego, CA: Academic
Ohman A. 1993. Fear and anxiety as emo- tional phenomena: clinical phenomenol- ogy, evolutionary perspectives, and infor- mation-processing mechanisms. See Lewis & Haviland 1993, pp. 511–36
Ohman A, Hamm A, Hugdahl K. 1998. Cogni- tion and the autonomic nervous system: orienting, anticipation, and conditioning. See Cacioppo et al 1998. In press
Omdahl BL. 1995. Cognitive Appraisal, Emo- tion, and Empathy. Mahwah, NJ: Erlbaum
Ortony A, Clore GL, Collins A. 1988. The Cognitive Structure of Emotions. Cam- bridge: Cambridge Univ. Press
Ortony A, Turner TJ. 1990. What’s basic about basic emotions? Psychol. Rev. 97: 315–31
Osgood CE, Suci GJ, Tannenbaum PH. 1957. The Measurement of Meaning. Urbana, IL: Univ. Ill. Press
Ottati VC, Steenbergen MR, Riggle E. 1992. The cognitive and affective components of political attitudes: measuring the determi- nants of candidate evaluations. Polit. Be- hav. 14:423–42
Panksepp J. 1992. A critical role for “affective neuroscience” in resolving what is basic about basic emotions. Psychol. Rev. 99: 554–60
Paradiso S, Robinson RG, Andreasen NC, Downhill JE, Davidson RJ, Kirchner PT, et al. 1997. Emotional activation of limbic circuitry in elderly normal subjects in a PET study. Am. J. Psychiatry 154:384–89
Parducci A. 1995. Happiness, Pleasure, and Judgment: The Contextual Theory and Its Applications. Hillsdale, NJ: Erlbaum
Parkinson B, Manstead A. 1993. Making sense of emotion in stories and social life. Cogn. Emot. 7:295–323
Paulhus DL, Fridhandler B, Hayes S. 1997. Psychological Defense: Contemporary Theory and Research. San Diego, CA: Academic
Peeters G. 1991. Evaluative influence in social cognition: the roles of direct versus indi- rect evaluation and positive-negative asymmetry. Eur. J. Soc. Psychol. 21: 131–46
Peeters G, Czapinski J. 1990. Positive- negative asymmetry in evaluations: the distinction between affective and informa-
tional negativity effects. In Eur. Rev. Soc. Psychol. 1:33–60. New York: Wiley
Phelps EA, Anderson AK. 1997. Emotional memory: what does the amygdala do? Curr. Biol. 7:R311–14
Philippot P. 1993. Inducing and assessing dif- ferentiated emotion-feeling states in the laboratory. Cogn. Emot. 7:171–93
Pittam J, Scherer KR. 1993. Vocal expression and communication of emotion. See Lewis & Haviland 1993, pp. 185–97
Plomin R, Emde RN, Braungart JM, Campos J, Corley R, et al. 1993. Genetic change and continuity from fourteen to twenty months: the MacArthur Longitudinal Twin Study. Child Dev. 64: 1354–76
Pulford BD, Colman AM. 1996. Overconfi- dence, base rates and outcome positiv- ity/negativity of predicted events. Br. J. Psychol. 87:431–45
Regan PC, Snyder M, Kassin SM. 1995. Unre- alistic optimism: self-enhancement or per- son positivity? Pers. Soc. Psychol. Bull. 21:1073–82
Reid SA, Duke LM, Allen JJB. 1998. Resting frontal electroencephalographic asymme- try in depression: inconsistencies suggest the need to identify mediating factors. Psy- chophysiology. In press
Reis HT, Patrick BC. 1996. Attachment and intimacy: component processes. In Social Psychology: Handbook of Basic Princi- ples, ed. ET Higgins, AW Kruglanski, pp. 523–63. New York: Guilford
Reisenzein R. 1995. On appraisals as causes of emotions. Psychol. Inq. 6:233–37
Reisenzein R, Hofmann T. 1993. Discriminat- ing emotions from appraisal-relevant situational information: baseline data for structural models of cognitive appraisals. Cogn. Emot. 7:271–93
Robinson RG, Downhill JE. 1995. Lateraliza- tion of psychopathology in response to fo- cal brain injury. In Brain Asymmetry, ed. RJ Davidson, K Hugdahl, pp. 693–711. Cambridge, MA: MIT Press
Robinson-Whelen S, Kim C, MacCallum RC, Kiecolt-Glaser JK. 1997. Distinguishing optimism from pessimism in older adults: is it more important to be optimistic or not to be pessimistic? J. Pers. Soc. Psychol. 73:1345–53
Roese NJ. 1997. Counterfactual thinking. Psy- chol. Bull. 121:133–48
Roseman IJ, Antoniou AA, Jose PE. 1996. Ap- praisal determinants of emotions: con- structing a more accurate and comprehen- sive theory. Cogn. Emot. 10:241–77
Rosenberg EL, Ekman P. 1994. Coherence be- tween expressive and experiential systems in emotion. Cogn. Emot. 8:201–29
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
EMOTION 213
Rosenberg EL, Ekman P. 1995. Conceptual and methodological issues in the judgment of facial expressions of emotion. Motiv. Emot. 19:111–38
Rosenthal J. 1995. Galen’s Prophecy: Tem- perament in Human Nature. New York: Basic Books
Rowe PM. 1989. Unfavorable information and interview decisions. In The Employment Interview: Theory, Research, and Prac- tice, ed. RW Eder, GR Ferris, pp. 77–89. Newbury Park, CA: Sage
Rubinow DR, Schmidt PJ. 1996. Androgens, brain, and behavior. Am. J. Psychiatry 153: 974–84
Russell JA. 1994. Is there universal recogni- tion of emotion from facial expressions? A review of the cross-cultural studies. Psy- chol. Bull. 115:102–41
Russell JA, Fernandez-Dols JM. 1997. The Psychology of Facial Expression. New York: Cambridge Univ. Press
Rusting CL, Larsen RJ. 1998. Personality and cognitive processing of affective informa- tion. Pers. Soc. Psychol. Bull. 24:200–13
Sarter M, Berntson GG, Cacioppo JT. 1996. Brain imaging and cognitive neuroscience: towards strong inference in attributing function to structure. Am. Psychol. 51: 13–21
Schell AM, Dawson ME, Marinkovic K. 1991. Effects of potentially phobic conditioned stimuli on retention, reconditioning, and extinction of the conditioned skin conduc- tance response. Psychophysiology 28: 140–53
Scherer KR. 1993. Neuroscience projections to current debates in emotion psychology. Cogn. Emot. 7:1–41
Scherer KR. 1997. Profiles of emotion- antecedent appraisal: testing theoretical predictions across cultures. Cogn. Emot. 11:113–50
Schofield JW. 1991. School desegregation and intergroup relations. In Rev. Res. Educ., 17:335–409. Washington, DC: Am. Educ. Res. Assoc.
Schulz R, Heckhausen J. 1997. Emotion and control: a life-span perspective. Annu. Rev. Gerontol. Geriatr. 17:185–205
Schwartz JE, Stone AA. 1998. Strategies for analyzing ecological momentary assess- ment data. Health Psychol. 17:6–16
Schwarz N, Clore GL. 1996. Feelings and Phenomenal Experiences. New York: Guilford
Schwarz N, Strack F. 1998. Reports of subjec- tive well-being: judgmental processes and their methodological implications. See Kahneman et al 1998. In press
Scott SK, Young AW, Calder AJ, Hellawell
DJ, Aggleton JP, Johnson M. 1997. Im- paired auditory recognition of fear and an- ger following bilateral amygdala lesions. Nature 385:254–57
Sears DO. 1983. The person positivity bias. J. Pers. Soc. Psychol. 44:233–49
Shah J, Higgins ET, Friedman RS. 1998. Per- formance incentives and means: how regu- latory focus influences goal attainment. J. Pers. Soc. Psychol. 74:285–93
Shizgal P. 1998. On the neural computation of utility: implications from studies of brain stimulation reward. See Kahneman et al 1998. In press
Showers CJ. 1995. The evaluative organiza- tion of self-knowledge: origins, processes, and implications for self-esteem. In Effi- cacy, Agency, and Self-Esteem, ed. M Ker- nis, pp. 101–20. New York: Plenum
Showers CJ, Kling KC. 1996. Organization of self-knowledge: implications for recovery from sad mood. J. Pers. Soc. Psychol. 70: 578–90
Skowronski JJ, Carlston DE. 1989. Negativity and extremity biases in impression forma- tion: a review of explanations. Psychol. Bull. 105:131–42
Smith CA, Haynes KN, Lazarus RS, Pope LK. 1993. In search of the “hot” cogni- tions: attributions, appraisals, and their re- lation to emotion. J. Pers. Soc. Psychol. 65:916–29
Spiegel D. 1997. Psychosocial aspects of breast cancer treatment. Semin. Oncol. 24: S136–47
Stayman DM, Aaker DA. 1993. Continuous measurement of self-report of emotional response. Psychol. Mark. 10:199–214
Sternberg EM. 1997. Emotions and disease: from balance of humors to balance of molecules. Nat. Med. 3:264–67
Suls J, Green P, Hillis S. 1998. Emotional re- activity to everyday problems, affective inertia, and neuroticism. Pers. Soc. Psy- chol. Bull. 24:127–36
Sutton SK, Davidson RJ. 1997. Prefrontal brain asymmetry: a biological substrate of the behavioral approach and inhibition systems. Psychol. Sci. 8:204–10
Tangney JP, Burggraf SA, Wagner PE. 1995. Shame-proneness, guilt-proneness, and psychological symptoms. In Self- Conscious Emotions: The Psychology of Shame, Guilt, Embarrassment, and Pride, ed. JP Tangney, KW Fischer, pp. 343–67. New York: Guilford
Tassinary LG, Cacioppo JT. 1992. Unobserv- able facial actions and emotion. Psychol. Sci. 3:28–34
Taylor SE. 1991. Asymmetrical effects of positive and negative events: the mobili-
A nn
u. R
ev . P
sy ch
ol . 1
99 9.
50 :1
91 -2
14 . D
ow nl
oa de
d fr
om w
w w
.a nn
ua lr
ev ie
w s.
or g
by C
al if
or ni
a St
at e
U ni
ve rs
ity -
F ul
le rt
on o
n 04
/2 8/
14 . F
or p
er so
na l u
se o
nl y.
214 CACIOPPO & GARDNER
zation-minimization hypothesis. Psychol. Bull. 110:67–85
Thompson MM, Zanna MP, Griffin DW. 1995. Let’s not be indifferent about (attitu- dinal) ambivalence. In Attitude Strength: Antecedents and Consequences, ed. RE Petty, JA Krosnick, pp. 361–86. Hillsdale, NJ: Erlbaum
Tooby J, Cosmides L. 1990. On the universal- ity of human nature and the uniqueness of the individual: the role of genetics and ad- aptation. J. Pers. 58:17–67
Traue HC, Pennebaker JW. 1993. Emotion In- hibition and Health. Gottingen, Germany: Hogrefe & Huber
Tucker DM, Frederick SL. 1989. Emotion and brain lateralization. In Handbook of Social Psychophysiology, ed. H Wagner, A Man- stead, pp. 27–70. Chichester: Wiley
Walker-Andrews AS. 1997. Infants’ percep- tion of expressive behaviors: differentia- tion of multimodal information. Psychol. Bull. 121:437–56
Watson D, Clark LA. 1992. Affects separable and inseparable: on the hierarchical ar- rangement of the negative affects. J. Pers. Soc. Psychol. 62:489–505
Watson D, Clark LA. 1997. Measurement and mismeasurement of mood: recurrent and emergent issues. J. Pers. Assess. 68: 267–96
Watson D, Clark LA, McIntyre CW, Hamaker S. 1992. Affect, personality and social ac- tivity. J. Pers. Soc. Psychol. 63:1011–25
Way BM, Masters RD. 1996. Political atti- tudes: interactions of cognition and affect. Motiv. Emot. 20:205–36
Westermann R, Spies K, Stahl G, Hesse FW. 1996. Relative effectiveness and validity of mood induction procedures: a meta- analysis. Eur. J. Soc. Psychol. 26:557–80
Wierzbicka A. 1995. The relevance of lan- guage to the study of emotions. Psychol. Inq. 6:248–52
Witvliet C, Vrana SR. 1995. Psychophysio- logical responses as indices of affective di- mensions. Psychophysiology 32:436–43
Ybarra O, Stephan WG. 1996. Misanthropic person memory. J. Pers. Soc. Psychol. 70: 691–700
Zajonc RB. 1980. Feeling and thinking: pref- erences need no inferences. Am. Psychol. 35:157–93
Zajonc RB. 1998. Emotions. In Handbook of Social Psychology, ed. DT Gilbert, ST Fiske, L Gardner, pp. 591–634. New York: Oxford Univ. Press
Zautra AJ, Burleson MH, Smith CA, Blalock SJ, Wallston KF, et al. 1995. Arthritis and perceptions of quality of life: an examina- tion of positive and negative affect in rheu- matoid arthritis patients. Health Psychol. 14:399–408
Zautra AJ, Potter PT, Reich JW. 1997. The in- dependence of affects is context- dependent: an integrative model of the re- lationship between positive and negative affect. Annu. Rev. Gerontol. Geriatr. 17: 75–103
Zautra AJ, Reich JW, Gaurnaccia CA. 1990. The everyday consequences of disability and bereavement for older adults. J. Pers. Soc. Psychol. 59:550–61
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Annual Review of Psychology Volume 50, 1999
CONTENTS On Knowing a Word, George A. Miller 1 Cognitive Development: Children's Knowledge About the Mind, John H. Flavell 21
Conflict in Marriage: Implications for Working with Couples, Frank D. Fincham, Steven R. H. Beach 47
Psychopathology: Description and Classification, P. E. Nathan, J. W. Langenbucher 79
Deductive Reasoning, P. N. Johnson-Laird 109 Health Psychology: Mapping Biobehaviorial Contributions to Health and Illness, Andrew Baum, Donna M. Posluszny 137
Interventions for Couples, A. Christensen, C. L. Heavey 165 Emotion, John T. Cacioppo, Wendi L. Gardner 191 Quantifying the Information Value of Clinical Assessments with Signal Detection Theory, John T. Cacioppo, Wendi L. Gardner 215
High-Level Scene Perception, John M. Henderson, Andrew Hollingworth 243
Interpersonal Processes: The Interplay of Cognitive, Motivational, and Behavioral Activities in Social Interaction, Mark Snyder, Arthur A. Stukas Jr.
273
Somesthesis, James C. Craig, Gary B. Rollman 305 Peer Relationships and Social Competence During Early and Middle Childhood, Gary W. Ladd 333
Organizational Change and Development, Karl E. Weick, Robert E. Quinn 361
Social, Community, and Preventive Interventions, N. D. Reppucci, J. L. Woolard, C. S. Fried 387
The Suggestibility of Children's Memory, Maggie Bruck, Stephen J. Ceci 419
Individual Psychotherapy Outcome and Process Research: Challenges to Greater Turmoil or a Positive Transition?, S. Mark Kopta, Robert J. Lueger, Stephen M. Saunders, Kenneth I. Howard
441
Lifespan Psychology: Theory and Application to Intellectual Functioning, Paul B. Baltes, Ursula M. Staudinger, Ulman Lindenberger 471
Influences on Infant Speech Processing: Toward a New Synthesis, Janet F. Werker, Richard C. Tees 509
Survey Research, Jon A. Krosnick 537 Trust and Distrust in Organizations: Emerging Perspectives, Enduring Questions, Roderick M. Kramer 569
Single-Gene Influences of Brain and Behavior, D. Wahlsten 599 The Psychological Underpinnings of Democracy: A Selective Review of Research on Political Tolerance, Interpersonal Trust, J. L. Sullivan, J. E. Transue
625
Neuroethology of Spatial Learning: The Birds and the Bees, E. A. Capaldi, G. E. Robinson, S. E. Fahrbach 651
Current Issues and Emerging Theories in Animal Cognition, S. T. Boysen, G. T. Himes 683
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