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An Integrative Guide to Consumer Neuroscience
An Integrative Guide to
Consumer Neuroscience
S V EN B RAE UTIGAM AN D P ETER KEN N IN G
1
3
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DOI: 10.1093/oso/9780198789932.001.0001
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To Brigitte
To Maren
Contents
Preface ix
Abbreviations xi
Appendix 229
References 237
Index 265
Preface
These are complex and challenging times, but also extraordinarily interesting and
exciting times, at least from a scientific perspective. As never before, interdiscipli-
nary research is growing across the spectrum, blurring entrenched boundaries that
have existed for hundreds of years while simultaneously building new and diverse
avenues of exploration and thinking. This is perhaps most visible at the junction of
economics, neuroscience, and mathematics, where scholars and practitioners alike
draw on a vast array of theories and experimental approaches in order to understand
the mechanisms and hidden rules underlying and perhaps determining econom-
ically relevant behaviour. A critical, if not the most important, ingredient in these
endeavours are modern brain imaging technologies, which have become sufficiently
accessible and manageable to allow efficient cooperation of researchers coming from
varied backgrounds.
Out of these new developments, the ‘oldest’ academically advanced interdiscipline,
is neuroeconomics, which attempts to systematically integrate neuroscience and ec-
onomics, where the aim is a unified, biology-based theory of human behaviour. One
might be tempted to argue that the application of neuroimaging brings extra com-
plexity to the study of an already difficult problem. This, however, seems not to be
an issue, where growing evidence suggests that modern brain scanning facilitates a
better understanding of the mechanistic processes that subserve human behaviours
and interactions within an economic setting. Following this lead, the field of con-
sumer neuroscience is gaining momentum, and this is what this book is about.
The need for consumer neuroscience derives from the observation that the con-
sumption of goods and services is one of the main drivers of industrialized societies,
critically influencing the overall structure, wealth, and functioning of a nation.
The study of consumer behaviour is complex, ranging from individual to societal
aspects, from the outright commercial to issues of population health. Moreover, the
modern world faces challenges of possibly epic proportions, and humans will need
to address issues of sustainability (of consumption) along more than one dimension.
We strongly feel that any meaningful attempt to advance will necessarily be founded
on rigorous science, and we endeavour here to provide an integrative guide to con-
sumer neuroscience.
In this guide, we have made efforts to balance depth and breadth of material while
tracing the foundations, technologies and methodologies, applications, translational
aspects, and ethics of consumer neuroscience. Given the strong, albeit not exclu-
sive, reliance of the field on neurotechnologies, we have opted for a detailed exposi-
tion of the relevant technologies beyond the often short and sometimes simplifying
descriptions found in textbooks and articles. To this end, we have included a chapter
entirely dedicated to the mathematical concepts related to the measurement,
x Preface
AN anorexia nervosa
ANN artificial neural network
ANS autonomic nervous system
AW approach–withdrawal
BA Brodmann area
BOLD blood oxygenation level dependent
CBD compulsive buying disorder
CMRR common-mode rejection ratio
CNS central nervous system
COMT catechol- O-methyltransferase
CR conditioned response
CS conditioned stimulus
DCM dynamic causal modelling
DHT dihydrotestosterone
DM decision maker
DNA deoxyribonucleic acid
DOT diffuse optical tomography
EEG electroencephalography
EI emotional index
EPSP excitatory postsynaptic potential
FID free induction decay
fMRI functional magnetic resonance imaging
fNIRS functional near-infrared spectroscopy
FT Fair Trade
GABA gamma-aminobutyric acid
GLM general linear model
HMM hidden Markov model
HRF haemodynamic response function
ICA independent component analysis
IPSP inhibitory postsynaptic potential
LR logistic regression
MA mathematical anxiety
MEG magnetoencephalography
MR magnetic resonance
MRI magnetic resonance imaging
mRNA messenger ribonucleic acid
NIR near-infrared
NMR nuclear magnetic resonance
NMSBA Neuromarketing Science and Business Association
OPC oligodendrocyte progenitor cell
PCA principal component analysis
PLV phase locking value
PNS peripheral nervous system
xii Abbreviations
QZE quantum Zeno effect
RF radiofrequency
rTMS repeated transcranial magnetic stimulation
SHOP Savings Hold or Purchase
SMH somatic marker hypothesis
SNP single nucleotide polymorphism
S-O-R stimulus–organism–response
SQUID superconducting quantum interference device
S-R stimulus–response
SSVEP steady-state visually evoked potential
tACS transcranial alternating current stimulation
TD temporal difference
tDCS transcranial direct current stimulation
tES transcranial electric stimulation
TMS transcranial magnetic stimulation
TPJ temporoparietal junction
tRNS transcranial random noise stimulation
UCS unconditioned stimulus
WOM word of mouth
WTA willingness to accept
WTP willingness to pay
1
The Road to Consumer Neuroscience
Within perhaps the last 20 years, under the label of ‘consumer neuroscience’, a
new direction in consumer and marketing research emerged. The idea is to use
insights and methods from neuroscience to better understand consumer behaviour.
Assuming that the audience is mainly unfamiliar with this research direction, the
goal of this introduction is to provide an overview of the definition, the goal, and the
origin of consumer neuroscience. In addition, in this chapter we will briefly sketch
the structure of our comprehensive guide.
An Integrative Guide to Consumer Neuroscience. Sven Braeutigam and Peter Kenning, Oxford University Press. © Oxford University Press 2022.
DOI: 10.1093/oso/9780198789932.003.0001
2 An Integrative Guide to Consumer Neuroscience
was metaphorically regarded as a ‘black box’ (Smidts et al., 2014). The ongoing processes
therein were reconstructed theoretically (Howard and Sheth, 1969) and recorded indi-
rectly (e.g. through surveys). Today, however, modern techniques and procedures from
the fields of radiology and biology allow a direct view into the living brain (Kenning et
al., 2007a; Plassmann et al., 2015). Specifically, this holds for the so-called neuroimaging
techniques (Plassmann et al., 2007a; Riedl et al., 2010b).
In general, consumer neuroscience can be seen as a subfield of neuroeconomics
(Plassmann et al., 2015). The aim of neuroeconomic research is the neurobiolog-
ical explanation of human behaviour and the development of a ‘unified theory of
human behaviour’ (Camerer et al., 2005; Foxall, 2008; Glimcher and Rustichini,
2004; Kenning and Plassmann, 2005). In this endeavour, consumer neuroscience
can explicitly be defined as the systematic integration of neuroscientific theories,
methods, and concepts into consumer research (Fugate, 2007; Grosenick et al.,
2008; Lee et al., 2007). In business practice, but even in academic research, the term
‘neuromarketing’ is often used to identify this development, but the label may be a
misnomer (Hubert and Kenning, 2008; Levalois, 2019; Lim, 2018). The term ‘mar-
keting’ is defined as market-orientated corporate management. Accordingly, the
term ‘retail marketing’ describes the concept of market-orientated management of
retailers. The branch of service marketing is concerned with the market-orientated
management of service companies. Given these exemplary uses for the term mar-
keting, the notion of neuromarketing poses an impractical ambiguity because,
strictly speaking, the term neuromarketing would be the market-oriented man-
agement of neurons. We therefore distinguish between consumer neuroscience as
the scientific basis of this approach, and neuromarketing as the application of the
findings from consumer neuroscience within the scope of managerial practice.
In order to present a guide to consumer neuroscience that is both integrative and
accessible to a wider audience, this book is conceptually organized in three parts,
although these are not explicitly declared. In the first part, comprising this and the
following two chapters, important biological, neurophysiological, cognitive, and
behavioural concepts are discussed. This first part makes only a limited number of
forward references to later chapters and is an essential read for anyone new to the
field of consumer neuroscience. The next three chapters cover, to a considerable
depth, relevant mathematical, physical, technological, and analytical concepts. This
part can be read independently of the rest of the book, but there are some moderate
dependencies: Chapter 4 → Chapter 5 → Chapter 6. Readers with little or no prior
exposure to science, technology, engineering, and mathematics (STEM) curricula
are encouraged to allocate some time and study this part in detail. Note that in this
part, relevant citations are provided as reading selections following each subsection
instead of inline (‘cite-as-you-write’) citations as in the rest of the book.
The following six chapters constitute the third part, discussing established applica-
tion domains, emergent research fields, translational aspects, and the ethics of con-
sumer neuroscience. The structure of these chapters recognizes the distinction made
in economics between decision theory and game theory, the practitioner’s intention
The Road to Consumer Neuroscience 3
to apply research results for business and/or sales purposes, and the observation that
consumer neuroscience both has an impact on and is influenced by other research
fields, such as organizational sciences, age research, and cultural analysis. Although
attempts have been made to reduce dependencies, the material covered in the third
part draws, at times heavily, on the preceding parts. Finally, a short outline of future
directions of consumer neuroscience in research and practice is presented in the last
chapter. Overall, the book adopts a primarily scientific and descriptive perspective
with the aim to provide the reader with a solid picture of the situations in which con-
sumer neuroscience can make a meaningful contribution to solving practical and/or
normative issues, thereby not negating the importance and appropriateness of clas-
sical approaches and concepts (Fugate, 2007; Lee et al., 2007).
experiment following the example of classical, exact natural sciences and many
psychologists cherished a hope to have found the components of behaviour from which
one can construct the colourful cosmos of behaviour. (Eibl-Eibesfeldt, 1997, p. 15)
The idea of behaviourism is ultimately based on John Locke’s1 assumption that the
human mind is a blank slate at birth and subsequently filled in by personal experience
1 An influential seventeenth-century English philosopher and physician. Note the term behaviourism was coined
derived from sense perception, implying that human behaviour can completely be
explained as reactions to external stimuli (Skinner, 1978). In this regard, humans
are assumed to be passively responding to the environment. Thus, it is possible to
condition human behaviour in the desired way with rewards and punishments. Even
then, the assumption of a given human nature ran the danger of being disqualified
from being a biological determinist or reductionist (Eibl-Eibesfeldt, 1997). At the
same time, in anthropology, a cultural relativism emerged that defined culture as
independent from biology and thus also disconnected culture from neurobiology.
In recent years, this approach found its antithesis in so-called cultural neuroscience
(Chiao et al., 2013), which is in turn confronted with collectivistic concepts and the-
ories (e.g. concept of distributed cognition).
The behaviourism investigated the coherence between environment (stimulus)
and observable behaviour (reaction) with the help of clearly defined experiments
(Plomin et al., 1990). The aim was to scientifically describe behaviour by exclu-
sively applying natural scientific methods. The organism was—according to
B.F. Skinner—regarded as a ‘black box’, because it was not possible to directly
observe internal psychological or physiological processes. Instead, behaviour
was considered as a function of a given stimulus (stimulus–response model (S-R
model)) (Kotler and Armstrong, 2010). It is obvious that due to methodological
constraints at this time, neurobiological methods and techniques did not have a
descriptive relevance.
An important concept of economic research was the idea that people always be-
have rationally. Thus, economic research assumed that, according to the model,
people behave in a reasonable way. Closely related to this assumption is the idea of
the Homo oeconomicus which has often been rebutted in recent years and which
was wrongly objurgated. It has often been ignored that it is a straw man argument.
In fact, the idea of the Homo oeconomicus can not only be applied on a descriptive
level, but rather on an ethical or practical-normative level. In this view, the predica-
tion is not how people actually behave, but how they should behave in certain situ-
ations from an economical point of view (Jacoby, 2002). Today this discussion can
be seen to be resolved. In this context the German marketing researchers Richard
Köhler and Manfred Bruhn come to the following postcritical result: ‘Even experi-
mental game theory moved away from the idea of the Homo oeconomicus. In this
regard, it would be desirable if critics of economic disciplines eventually register that
for decades the idea of the Homo oeconomicus is not object of economics anymore’
(Köhler and Bruhn, 2010, p. 5).
With the postulate of market-oriented management, consumer behaviour re-
search was more and more acknowledged to be an important theoretical basis of
marketing management. The idea spread quickly and can today be considered as
commonly accepted. In 1969, the Association for Consumer Research was founded,
and the first consumer behaviour textbooks and courses appeared in the late 1960s
(Engel et al., 1968; Kassarjian and Robertson, 1968). In these early days of con-
sumer research, the most important frameworks were comprehensive models of
The Road to Consumer Neuroscience 5
Intention
Overt Confidence
search
Attitude
Stimulus
ambiguity Choice Brand
Motives criteria comprehension
Perceptual
Attention bias Satisfaction
Flow of information
Feedback effects
concept formation. Fig. 1.2 depicts the intervening variables inside the organism.
Beside the input and the output variables there are exogenous variables that con-
struct the frame of the purchase process, but are not directly included in the model
(Howard and Sheth, 1969).
Another relevant total model of buying behaviour is the approach of Engel and
colleagues (Engel et al., 1978, 1995). They differentiated between extensive, lim-
ited, impulsive, and habituated buying-decision types that vary in the degree of in-
volvement and risk perception of the consumer. In this model, the decision-making
process can be classified into consecutive phases. The starting point is the need rec-
ognition defined as the difference between the target state and the actual condition.
If the consumer recognized this difference as a problem, the next phase—the search
for information—begins. The decision-making process is completed with the last
phase—the evaluation of different alternatives.
A further approach to model consumer decision-making and to illuminate the
intervening variables is the decision-net approach of James Bettman (1974). This
model constructs networks that graphically depict consumer behaviour. To iden-
tify these networks, typically, an interviewer accompanies the purchase process of
a customer and records everything that the customer experiences and consciously
notices in order to create networks that reflect purchase behaviour. The aim is to
develop a theoretical structure of the black box by directly collecting empirical data
and to spontaneously record cognitive processes (Bettman, 1974).
The Road to Consumer Neuroscience 7
One goal . . . is, to understand and predict human behaviour. Psychologists have tradition-
ally used self-report measures and performance on laboratory tasks to achieve this end.
However, these measures are limited . . . We argue that current neuroscientific knowledge
has reached a point where it can complement other existing psychological measures in
predicting behaviour and other important outcomes.
Efforts to include biological components are not new in consumer research. In fact,
some prominent consumer researchers referred early on to the significance of neu-
roscience and its methodological possibilities (Kroeber-Riel, 1979). At that time,
physiological processes have been detected with different traditional measurement
methods. For example, the first studies to apply electroencephalography (EEG) to
marketing relevant subjects appeared in the 1970s (Krugman, 1971). However, in
general, consumer research has treated biological processes that determine con-
sumer behaviour only marginally for a very long time. Saad (2008) even talks about
a ‘collective amnesia of marketing scholars regarding consumers’ biological and evo-
lutionary roots’. Recent developments in the area of neuroeconomics and consumer
neuroscience prove that marketing research has succeeded in overcoming this am-
nesia (Camerer et al., 2005; Kenning et al., 2007a; Plassmann et al., 2015).
In neuroeconomics, one of the first economic and methodical relevant studies was
conducted by Alan Sanfey and colleagues and was concerned with neural processes
related to decisions during the ultimatum game (Sanfey et al., 2003). This study re-
vealed the potential of neuroeconomics to better explain economic behaviour. It
still has a high impact and has been cited more than 4000 times according to google
scholar.
The principle of the ultimatum game is the following scenario: two players are
asked to share a certain amount of money (e.g. 10€) by mutual agreement. In the
8 An Integrative Guide to Consumer Neuroscience
first step, player A starts by making a suggestion on how to divide the money. In the
second step, player B can either accept the offer or refuse the money. If player B does
not agree, both players get nothing. How should player A behave? His success does
not only depend on his own decision but on the behaviour of player B. According to
the axioms of traditional economic theory, player A behaves rationally if he tries to
maximize his gain. At the same time, player B should accept every amount greater
than zero, because from an isolated viewpoint it is better to receive a small amount
than nothing. However, in reality, this scenario almost never exists and shares that
strongly favour player A are often rejected indignantly by player B, irrespective of
the money loss.
Recent approaches explain this at-first-sight irrational behaviour with the idea
that people have an implicit preference for fairness and therefore often suggest 5€
for both players. But how is it possible to track this implicit preference? Is it observ-
able and how can the effect be measured? In order to answer these questions, Sanfey
et al. (2003) asked people to play the ultimatum game inside a magnetic resonance
(MR) scanner. One main finding was that a specific neural process was observable if
participants were confronted with unfair offers and refused these offers compared to
situations that were perceived as fair. An important role for the processing of unfair
offers plays the activity within the insula, a brain region which is often associated
with the processing of aversive emotions (Sanfey et al., 2003).
From the ground-breaking study of Sanfey et al. (2003) several relevant aspects
for neuroeconomic research and consumer neuroscience can be deduced, with re-
gard to both methodology and content. First, with regard to methodology, the study
showed for the first time that functional magnetic resonance imaging (fMRI) is able
to map processes relevant for economic and marketing research. It proved that the
spatial and temporal resolution of fMRI is sufficient to capture economically rel-
evant decision processes. Furthermore, it became clear that insights from specific
regions of the brain are adequate to enable a reasonable appreciation of fMRI results.
And third, the study showed that fMRI allows the simultaneous recording of making
a decision and measuring associated processes in the brain, thereby establishing a
link between neuronal activation and behaviour in an economically relevant, exper-
imental context.
With regard to content, the study provided evidence that people are able to
apply and integrate several decision-making processes in the same decision sit-
uation. This may be seen as the empirical proof for dual-process models that are
extensively discussed in the literature (Camerer et al., 2005; Strack and Deutsch,
2004). Furthermore, the study showed that unconscious emotions during the
perception of a certain stimulus can have a great impact on the decision-making
process by framing the decision. In this respect, the study also provided the first
insights for the neural mechanisms of the framing effect. Another important result
was that for the emergence of emotions and the perception of unfairness, the cor-
responding player was important. Every time the unfair offers were generated by a
The Road to Consumer Neuroscience 9
computer, people behaved in a more rational way and exhibited less activation in
the insula region. This result motivated further academic research in the field of
neuro-information-system (“Neuro-IS”), often in cooperation with partners from
industry (e.g. Riedl et al., 2011).
“. . . we learned is that the peak moments identified by the two diagnostics are not always
the same moments . . . [for] 36 commercials, brain wave measurement identified 113 peaks
of arousal and Picture Sorts identified 149, but only 61 of these moments, or roughly half,
were the same moments. What this tells us is that each approach has something to teach
the other about how the brain functions . . . Remember that with brain waves we are meas-
uring the audience response to the total multichannel experience of the commercial -the
pictures plus the words plus the music -while the Picture Sorts focus on the vision part of
the television commercial . . .” (Young and Sands, 2009)
At a descriptive level, one can distinguish between two fields of study: on the one
hand, the area of individual consumer neuroscience aims at explaining the behav-
iour of individual consumers on the bases of neuronal processes. For example, in-
dividual consumer neuroscience investigates how a consumer perceives marketing
relevant stimuli such as prices. On the other hand, the area of social neuroscience is
concerned with human behaviour in social contexts. In modern economies, coop-
eration with other companies and relationships with other people play an important
role in economic workaday life. Social neuroscience investigates, for example, in-
terpersonal trust building, fairness, altruism, and cooperation-relevant problems in
general.
10 An Integrative Guide to Consumer Neuroscience
The determination of cortical areas that are stimulated during consumer decision
processes by applying neurological methods offers various advantages over conven-
tional procedures:
To be a skilled consumer researcher may mean one has to be half neurophysiologist with
expertise in, for example, fMRI besides the latest in research design and statistical method.
(Achrol and Kotler, 2012, p. 51)
Thus, it is not surprising that the subject has gained in relevance in the public view
and in academic contexts (Fugate, 2007; Hubert and Kenning, 2008; Lee et al., 2007;
Plassmann et al., 2007a). There are many conferences and journals dedicated to
the subject and the number of published studies and articles in leading marketing
journals is steadily increasing (Fig. 1.3). Moreover and notably, the renowned
Association of Consumer Research has established a new content area code for the
field to address novel research approaches.
1.0
0.8
Relative number of publications
0.6
0.4
0.2
0.0
2001 2002 2003 2004 2005 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 2020
Year
Fig. 1.3 Surge in publications related to consumer neuroscience. Shown is the relative
number of publications between 2001 and 2020. The data are based on a PubMed (https://
pubmed.ncbi.nlm.nih.gov) search using the (Title and/or Abstract) search string: (consumer
AND neuroscience) OR neuromarketing OR ((shopping OR purchase) AND (fmri OR eeg OR
meg)). Here, the total number of publications in 2020 was 47. Note different search strings
typically yield different absolute numbers of hits but the resulting pattern stays qualitatively
the same.
12 An Integrative Guide to Consumer Neuroscience
There are two phenomena that are particularly important for consumer neuroscience,
namely learning and memory. Both relate strongly to the formation, storage, and re-
trieval of knowledge and experience needed for adequate decision-making. For ex-
ample, customers who want to assess a product need to be able to remember alternative
prices for the comparison and retrieve them at the appropriate time. Another obvious
example are brand memories, typically formed through advertising, in the hope that
customers will thoroughly enshrine a given brand in their memory. The mechanisms
underlying memory and learning have been studied extensively in psychology and the
neurosciences, providing relevant models for consumer neuroscience.
Accordingly, memory and learning are assumed to reflect a coherent interaction
of several systems, each of which is associated, at least to some extent, with specific
activity in segregated brain regions. Thus, rather than being monolithic entities,
memory and learning are somewhat malleable systems, where the type of infor-
mation decrees storage location as well as encoding and retrieval processes (e.g.
Preilowski, 2009; Rolls, 2000). An important model was put forward by Squire,
which assumes that the medial aspects of the temporal lobes are primarily involved
in explicit, or declarative, memory (Fig. 2.1) (Squire, 2004). In contrast, implicit,
or non-declarative, memory comprises various aspects of perception and reflec-
tion. Note that implicit memory does not necessarily require conscious efforts (cf.
Preilowski, 2009, p. 568), making this form of memory of particular importance for
consumer neuroscience (e.g. buying on a whim).
As an illustrative example, when people rehearse a list of several words, one
can examine their explicit memory by asking them to repeat the words learned,
whereas implicit memory can be tested by presenting a few initial letters and asking
An Integrative Guide to Consumer Neuroscience. Sven Braeutigam and Peter Kenning, Oxford University Press. © Oxford University Press 2022.
DOI: 10.1093/oso/9780198789932.003.0002
14 An Integrative Guide to Consumer Neuroscience
Memory
Declarative Non-declarative
Emotional Skeletal
responses responses
the subjects to name the word which comes first to their mind (e.g. ‘ba’ in ‘bath es-
sence’; see Thompson, 2001, p. 407). Note the two types of memory are similar to the
concepts of supported and unsupported degree of awareness in market and adver-
tising research (e.g. Trommsdorff and Teichert, 2011).
In more detail, explicit memory encodes information about episodic, semantic,
and factual knowledge (e.g. the typical price of a 400 mL jar of Nutella®). The
content attributed to this type of memory is based on primarily conscious cog-
nitive processes and can be retrieved through a deliberate act of remembering.
As mentioned previously, the medial portions of the temporal lobes are critical,
where the hippocampus (Richardson, 2004; Strange et al., 1999) and the cortical
structures associated with it (e.g. parts of the para-hippocampus) as well as the
amygdala play important roles in the case of emotionally influenced memories (cf.
Richardson, 2004; see also Preilowski, 2009). Damage to these areas only interferes
with the storage of new information and not pre-existing memories, and it is com-
monly assumed that the hippocampus (whose name derives from the Latin term
for seahorse) is only a short-term store for contents of long-term memory stored
somewhere else (e.g. Kandel et al., 1995).
In contrast, implicit memory is more reflexive and of an automatic nature. It forms
slowly (e.g. through practice) and manifests itself in a better accomplishment of the
Cognitive Processes and Behaviours 15
without the UCS. The organism then forgets the linking again. This process of ex-
tinction represents an extremely important adaptive mechanism. At the same time,
it should be noted that the organism does not simply forget the linking, but learns a
new association (Kandel et al., 1995, p. 676). This observation is important regarding
the hypothesis of somatic markers that will be discussed below.
In contrast, operant conditioning is based on trial and error. Occasionally, this
principle is also referred to as learning from success (Eibl-Eibesfeldt, 1997, p. 114).
In contrast to classical conditioning, in which the characteristics of specific reflec-
tive responses to certain stimuli are changed, operant conditioning changes the
frequency of behavioural patterns. One therefore also speaks more aptly of the fact
that operant behaviour is released rather than created (Kandel et al., 1995, p. 678).
In more general terms, reward-associated behaviours tend to be repeated (more
often) at the expense of other, less rewarding, behaviours. In contrast, unpleasant
behaviours are not repeated. This simple model, known in literature as the law of
effects, explains a large part of the behaviour (e.g. Thorndike and Gates, 1930). It has
found its specification in many different theories of buyer and consumer behaviour,
for example, in research on approach-avoidance conflicts (Elliot and Thrash, 2010).
Generally speaking, operant learning has occurred when a certain subsequent stim-
ulus or the removal of a negative stimulus has reliably increased or decreased the
probability of occurrence of a behaviour above the operant level.
Even though at first sight the two types of conditioning appear to be different, it
is assumed that the underlying neural mechanisms are similar. Thus, in both types
temporal aspects play an important role. Advocates of the theory of contiguity
even assume that everything that coincides in time and space relates to each other
(Winkel et al., 2006, p. 95ff.). If, for example, a finger is held in a flame, pain imme-
diately occurs and the finger is pulled back (Thompson, 2001, p. 377). The next time
we see a candle, a corresponding neural reaction occurs. The temporal connection
is called contiguity. It is an indispensable prerequisite for associative learning. The
example of food aversion still to be described shows, however, that other types of
linkage are also possible.
For both types of conditioning, however, there is an optimal time interval for
learning success. If this interval is too short or too long, it has a negative impact on
the learning effect. In addition, it gradually became clear that certain (neuro-)bi-
ologically induced factors could have an influence on learning success, so that the
basic assumption that humans had the characteristics of a ‘blank slate’ could not be
maintained. This finding also has implications for consumer and purchasing behav-
iour research, because it illustrates once again that inherited or acquired biolog-
ical determinants can also influence specific forms of behaviour and could thus be
considered in corresponding management concepts.
A particularly interesting phenomenon in this context is food aversion. If, for
example, a certain substance is added to a certain food, which leads to immediate
or later nausea, the corresponding taste stimuli are also permanently associated
with nausea. This is evolutionary very meaningful, since the organism might
Cognitive Processes and Behaviours 17
otherwise die from poisoning. If, on the other hand, the impression of taste is
merely followed by pain stimuli (e.g. if we eat an ice cream that is too cold or a soup
that is too hot), there are no permanent aversive reactions. The choice of a suit-
able reinforcer therefore depends essentially on the type of reaction to be learned
(Kandel et al., 1995).
Arousal
Difficult task Easy task
The upward (left) part of the inverted U can be thought of as an energizing, or motivating,
effect of arousal, whereas the downward part reflects negative effects of arousal (or stress)
on cognitive processes, such as attention (e.g. tunnel vision), memory, and problem-solving.
The inverted U should be seen as reflecting the concept ‘neither too little nor too much is
good’ rather than describing a precise mathematical relationship between arousal and per-
formance. The proposition that optimal task performance occurs at an intermediate level of
arousal holds typically in the case of difficult tasks. For easy tasks, the peak may occur at
lower levels of arousal, or there is no peak at all and performance increases monotonically as
a function of arousal up to a certain level.
2.3 Motivation
Instinct
Drive or Desire
Motive Self-actualisation
Social
Monetary incentive
Economic Performance
Fairness
Fig. 2.2 Overview of the different motives that are used to explain motivated and goal-directed
behaviour.
agreed upon, the scheme shown in Fig. 2.2 is most conducive to consumer neurosci-
ence. Note that other, rather general classifications of motivation exist that partially
straddle the dimensions of this scheme. The most important are inherent versus
learned motives, and intrinsic versus extrinsic motivation. Inherent motives are in-
born and central to survival, as can be seen in instincts and drives directed towards
fulfilling biological needs (James, 1890). Hunger is a typical inherent motive. In
contrast, learned motives are formed through experience and depend on social and
cultural influences (White and Lehman, 2005; Zimbardo, 2007). For example, the
desire to become rich is typically a learned motive (Opsahl and Dunnette, 1966).
Extrinsic motivation involves rewards awarded by some external entity, where the
reward can be tangible, such as money, or non-tangible, such as positive feedback.
In contrast, intrinsic motivation leads to behaviour that on its own is individually
pleasurable or gratifying (Deci et al., 1999). Retail therapy, defined as buying with
the sole purpose of improving one’s mood or disposition, is an example of intrinsic
motivation. A brief exposition of the motives presented in Fig. 2.2 is provided in the
remainder of this section.
Instincts are biologically determined, exist in all species, and are innate drivers of
behaviour (James, 1890; Kubie, 1948; Sherrington, 1916). Instincts as motives typ-
ically yield reflexive, rigid, and predictable patterns of behaviour that are not ac-
quired by learning (Davis et al., 1948; James, 1890). Although humans can react to
environmental stimuli automatically, some instincts are not immutable and can be
voluntarily overridden (Maslow, 1954).
A drive or desire is a state of arousal or tension triggered by physiological or bio-
logical needs, such as food, water, or sex. According to the drive-reduction theory,
drives are thought to arise from physiological needs created by a deviation from ho-
meostasis, that is, the tendency to maintain a balance, or an optimal level, within
Cognitive Processes and Behaviours 21
a biological system (Hull, 1952). So-called secondary drives are associated with
(primary) drives through experiences or conditioning procedures (Pavlov, 1941).
For example, the desire to receive money, which helps to pay for the satisfaction of
primary drives like food and shelter (Mowrer, 1951; Olds, 1953). Drive is an eco-
logically valid concept; however, one has to be careful when modelling behaviour
because drive-reduction theory largely fails to explain both the role of secondary
reinforcers in regulating tension, and behaviour that is not intended to reduce any
tension, such as a person eating even if not hungry (Cellura, 1969).
Operant conditioning refers to the association of a spontaneous behaviour with
a specific incentive (Flora, 2004; Skinner, 2011), thereby extending the concept of
classical conditioning relying on the presence of a given stimulus that exhibits a nat-
ural reaction (Skinner, 1938). Analogous to drive-reduction theory, one can distin-
guish between primary reinforcers (stimuli provoking a specific response without a
specific association) and the secondary reinforcers often acquired to fulfil the pri-
mary reinforcers, as in the case of gaining money to buy food.
The operant/reinforcement approach as a model for motivation assumes that all
behaviour needs to happen at least once, accidentally or voluntarily, before it can be
modulated or altered, that is, conditioned (Chomsky, 1959; Wiest, 1967). However,
this is not necessarily the case in real life, where an animal might face large and pos-
sible singular choice sets and where there are multiple links between performance
and the outcome (Hsee et al., 2003). Thus, operant conditioning as a motive can be a
useful model on occasion but may provide an incomplete and/or inadequate expla-
nation in complex real-life scenarios.
The arousal theory of motivation suggests that people execute a specific behaviour
in order to maintain an ‘optimum’ level of individual physiological arousal, which
may vary with age but is in general independent of the balance needed to main-
tain biological homeostasis (Keller, 1981; Mitchell, 1982). There is some conceptual
similarity with drive-reduction theory, although the goal here is to maintain arousal
instead of reducing tension. In general, the postulated optimum level is quantifi-
able; however, its existence would be consistent with a variety of so-called inverted-
U phenomena, where the outcome is a non-linear function of some variable (see, e.g.
the Yerkes–Dodson law, mentioned earlier).
Self-determination as a motive for goal-directed behaviour is based on the
premise that the organism is an active system with an inherent propensity for growth
and resolution of inconsistencies (Deci and Ryan, 2000, 2004; Ryan, 2012). Growth
is an essential element of this type of motivation, which distinguishes it from drive-
reduction and arousal theories. Here, motivation is assumed to comprise three
main aspects: competence (capability of producing positive while avoiding negative
outcomes), relatedness (emotionally secure and stimulating proximity to others),
and autonomy (ability to act independently in accordance with one’s own sense of
self (Markland, 1999)). Self-determination as motivation is a useful concept to dif-
ferentiate between personalities; however, the model fails to provide clear-cut meas-
ures to assess and/or predict behaviours.
22 An Integrative Guide to Consumer Neuroscience
associated with the processing of subjective value, which might give hints as to why
incentive effects can be non-linear (Strombach et al., 2015).
Fairness is arguably one of the most important of interpersonal (or ‘other-re-
garding’) preferences (Camerer and Hogarth, 1999; Falk et al., 1999; Fehr and Falk,
2002). Other-regarding preferences are one of the core concepts in behavioural eco-
nomics postulating that self-regarding preferences are not sufficient to explain and
motivate behaviour of economic man. By implication, humans in general do not
value their own reward in isolation, but they also compare their own set-point with
reference to others, where, for example, monetary incentives are less effective when
offers are perceived as unfair in some sense (Sanfey, 2007).
Clearly, motivation is complex and often dependent on the situation and context.
In real life, an individual is likely to be motivated by a variety of mechanisms that
operate neither entirely sequentially nor in parallel. This can be seen, for example,
in some developing societies, where people, unfortunately, may suffer from hunger
or are exposed to life-threatening situations on a regular basis, that is, their basal
motives cannot be fulfilled, but nevertheless show motivated behaviours in other
domains.
2.4 Reward
role in the formation of product preference. Second, the orbitofrontal cortex, which
is part of the prefrontal cortices, is commonly thought to represent emotion and
reward in decision-making, thereby establishing a link between reward and subse-
quent behaviour. In particular, the orbitofrontal cortex is also involved in the repre-
sentation of loss and punishment, which makes it an interesting target region for the
study of consumer responses to unfair or over-priced offers.
• Trading rewards against risks (Foxall, 2008; McClure et al., 2004c; Mohr et al.,
2010).
• Handling uncertainty, risk, and ambiguity (Huettel et al., 2005; Krain et al.,
2006).
• Solving conflicts of goals (Camerer, 2003).
Several studies provide evidence that for decision-making the prefrontal cortex,
and especially the orbitofrontal and dorsolateral prefrontal cortex, plays a decisive
role (e.g. Mohr et al., 2010). This brain region receives information from many other
parts of the brain and interacts with the insula and subcortical structures such as
the striatum (Ernst and Paulus, 2005). In general, the prefrontal cortex is associated
with processing rationally marked stimuli whereas emotionally marked elements
are generated in subcortical structures (e.g. striatum) (Mohr et al., 2010).
It is noteworthy that the prefrontal cortex and especially the VMPFC plays a cen-
tral role for the integration of subconscious emotional elements in the decision-
making process. There is evidence that the dorsolateral prefrontal cortex is important
for decision-making under risk (Mohr et al., 2010). Additionally, Hsu et al. (2005)
show that the effort to make decisions is correlated with activity changes in the orbit-
ofrontal cortex and the amygdala.
Related to the construct of cognitive decision-making is the construct of cog-
nitive processing which is particularly important in neuropsychological liter-
ature. Cognitive processing is the way the brain processes cognitive information.
Cognitive Processes and Behaviours 25
According to dual process models, the brain seems to distinguish between cognitive
and emotional information. Therefore, each decision-making process is composed
of emotional-affective-reflexive elements on the one hand and rational-cognitive-
reflective elements on the other hand. Ferstl et al. (2005) showed that cognitive
information is primarily processed in the lateral prefrontal cortex whereas emo-
tional information primarily activates the dorsal frontomedial cortex (Ferstl et
al., 2005). Cognitive efforts, elements of short-term memory, and processing of
real-time information are associated with activity changes in the dorsolateral pre-
frontal cortex (Braver et al., 1997; Linden et al., 2003; Owen et al., 2005; Rypma and
D’Esposito, 1999).
Fig. 2.3 The Iowa Gambling Task. The subjects are presented with a number of virtual decks
(typically four) of cards on a computer screen. The decks differ from each other in the balance
of reward (good decks) versus penalty (bad decks) cards, that is, some decks will tend to reward
the player more often than other decks. The goal of the game is to win as much (game) money
as possible, and healthy volunteers typically need to sample a total of 40–50 cards from the
decks in order to identify the good decks.
Data from Bechara et al., 1994.
Gambling Task (Fig. 2.3), which has been employed in several hundred studies of
patients with frontal lobe damage and healthy volunteers.
A common finding in patients with frontal lobe dysfunction is that they, in con-
trast to healthy volunteers, continue to persevere with the bad decks, even when
realizing that they lose money overall. Concurrent measurements of the galvanic
skin response show that patients usually lack a ‘stress’ reaction observed in healthy
controls when hovering over the bad decks, long before conscious sensation that the
decks are bad. Moreover, patients with VMPFC damage choose outcomes that yield
high immediate gains in spite of higher losses in the future.
Despite the overarching importance of the VMPFC, many other brain regions
are critically involved in the processing of somatic markers and decision-making.
The complexity of the resultant network can be conceptualized in terms of two re-
action schemata known as the ‘body loop’ and the ‘as-if body loop’ (Bechara and
Damasio, 2005). The former facilitates the default mechanism, where activation and
possibly reactivation of somatic markers cause various alterations, both physiolog-
ical and neuronal, which in turn affect cognition and behaviour (Fig. 2.4). The latter
facilitates mechanisms where decisions are accompanied by neuronal processes nor-
mally associated with somatic maker activation, although real activation of somatic
states is absent. Thus, somatic states are somehow emulated that influence behaviour
and decision-making analogous to body loop mechanisms.
Cognitive Processes and Behaviours 27
Amygdala Amygdala
Brainstem Brainstem
Body Body
Fig. 2.4 Body loop and as-if body loop. SMC, sensorimotor cortex; VMPFC, ventromedial
prefrontal cortex.
Adapted from Bechara, Damasio (2005).
Over the years, the SMH has become an important tool that has identified many
of the brain areas involved in decision-making as well as the neuronal representa-
tion of emotions and body states. The model, however, has failed to demonstrate
how these processes interact at a psychological and evolutionary level. More specifi-
cally, conceptual weaknesses of the Iowa Gambling Task have been pointed out, and
incompatible results have been reported. Nevertheless, the model has reasonably
good ecological validity and will continue to exert its influence on neuroscience. It is
clearly of interest for consumer neuroscience because of the emphasis on emotions
in the decision-making process, making it possible to address concepts like ‘gut
feeling’ or ‘buying on a whim’ rigorously, at least to some extent. In essence, SMH is a
powerful way of holistically approaching many of the mechanisms presented in this
chapter.
The concept of theory of mind (ToM) was introduced by Premack and Woodruff
(1978, p. 515) as follows: ‘An individual has a theory of mind if he imputes mental
states to himself and others’. In essence, ToM explains how people put themselves in
the position of others and how behaviours such as empathy and compassion emerge
(Fletcher et al., 1995; Singer, 2009). Thus, ToM (sometimes loosely referred to as
28 An Integrative Guide to Consumer Neuroscience
Fig. 2.5 Example of the application of the mirror neurons concept in advertising.
Sourced from Nespresso
As pointed out previously, many different forms of learning (rote, meaningful, in-
formal, etc.) have been identified and the underlying mechanisms studied. So-
called reward-based learning is the most relevant to consumer neuroscience and
is discussed in more detail in this section. Reward-based learning is a form of re-
inforcement learning that, as the name implies, facilitates the acquisition of a new
behaviour, knowledge, or skill through rewarding the desired learning outcome.
From a conceptual perspective, reward plays an important role in the consumer’s
world, where reward can become manifest directly through reward schemes, or less
directly and often multifacetedly through customer satisfaction.
The latter is of particular importance because research has conclusively shown that
customer satisfaction plays a central role in building customer loyalty—the state of
satisfaction causes some form of learning that can positively influence brand image
and future purchasing behaviour. From a more technical perspective, a rich set of
robust and validated mathematical algorithms exists to model learning through re-
ward, where, to some extent, the model parameters both correspond with concepts
of consumer research and can be mapped to neuronal systems.
30 An Integrative Guide to Consumer Neuroscience
where V denotes a suitable state value function with states st, rewards (or,
outcomes) Rt, a learning rate α, and a scale factor γ. The states and rewards are
indexed by some quantity t, which is usually but not necessarily interpreted as
time. In words, the model describes an iterative update process continuously re-
fining the estimates of the value function, where only the current and the immedi-
ately following state are taken into account (hence the term TD). The process starts
by assigning an initial value V to each state, acting as the initial estimates of the
returns obtained when transitioning from one state to the next according to some
policy associated with a given model. Each step yields a target based on the reward
provided by the environment, which is used to update the value of the starting
state according to the formula given (which implies bootstrapping for α ≠ 1). The
term Vtarget – V is known as the one-step TD error (a type of prediction error).
The process continues thereby gradually updating the value function at each state
towards increasingly accurate estimates. Under fairly general assumptions, it can
be shown that TD models converge to an optimal measure of the value function
at each state. An example illustrating one episode of TD learning is shown in Tab.
2.1, where the policy is given by a particular sequence of actions performed to pre-
pare a subject for a combined magnetoencephalography (MEG) and EEG scan.
The initial state values can come from a variety of sources, such as guessing or pre-
vious experience.
In the most general sense, TD models relate to the observation that humans learn
by comparing pre-exiting expectations and actual experiences. As such, the models
are naturally aligned with the confirmation/disconfirmation models of consumer
and marketing research. Moreover, the scale factor γ can be interpreted as some
form of temporal discounting, that is, TD allows the effectiveness of immediate
versus delayed rewards to be studied. Finally, the learning rate allows the degree to
which individuals or groups of individuals respond to (prediction) errors in a given
situation (α =0 implies errors are being ignored) to be modelled.
From a neuroscience perspective, several studies have suggested that dopamin-
ergic activity in subcortical areas such as the ventral segmental area (specifically,
the ventral striatum and the nucleus accumbens) and the midbrain reflect the pro-
cessing of prediction errors (Delgado et al., 2005; McClure et al., 2004a; O’Doherty
et al., 2003; Schultz et al., 1997). Moreover, there is evidence that neuronal activa-
tion of the reward system is stronger if a reward is received immediately compared
to a delayed reward (McClure et al., 2004a; Read et al., 2005; note delay is rel-
ative dependent on the situation), which corroborates the notion that temporal
discounting is associated with specific brain mechanism and therefore amenable
to modelling.
Cognitive Processes and Behaviours 31
Table 2.1 Preparing for a combined MEG and EEG scan. State values
(V) denote minutes of remaining preparation time and rewards (R;
here, outcomes) denote times between states. For simplicity, both
the learning rate (α) and scale factor (γ) have been set to 1. Thus, the
transition equation reads: V ( st ) = Rt +1 + V ( st +1 ) . The total preparation
time in this example is 52 minutes (=∑ R)
EOG, electro-oculography.
Note this example is conceptually similar to the famous ‘Driving Home’ example (Sutton
and Barto, 2018, chap. 6) cited in many books and lectures.
The human brain is an organ of extraordinary complexity that has attracted the in-
terest of scholars, philosophers, and scientist for aeons. Arguably, the early Greek
physician Alcmaeon of Croton (sixth century bc) was the first to postulate that the
human brain is the central instance of sensation and thought. The intimate cou-
pling between physical reality and cognitive process implied by Alcmaeon’s claims,
however, was challenged in the centuries to come. Most notably, French polymath
René Descartes (1596–1650) proposed a dualistic system in which the brain is
viewed rather like a machine acting separately from an immaterial mind that ac-
counts for higher mental faculties. Ultimately, it is modern neuroscience, the ad-
vent of which is commonly credited to Spanish anatomist Santiago Ramón y Cajal
(1852–1934) and Italian biologist Camillo Golgi (1843–1926), advanced through
innumerable contributions from all areas of science over time, that makes us argue
that the brain is the central structure of the human nervous system, controlling a
vast range of activities and functions, including but not restricted to motor con-
trol, sensory perception, autonomic and hormonal regulation, language, emotion,
reasoning, and cognition. Such control, however, is a highly dynamic process con-
tingent upon genetic, anatomical, metabolic, and physiological factors, all of which
operate on partly dissociable temporal and spatial scales and interact which each
other in a context-dependent fashion. At present, there is no unifying theory that
can explain the complex functioning of neuronal systems. Acknowledging that the
human brain can only be fully understood in a holistic fashion encompassing all
aspects at all scales, the remainder of this chapter provides an overview of the main
aspects in isolation.
3.1 Neuroanatomy
The human nervous system consists of two main parts: the peripheral nervous system
(PNS) and the central nervous system (CNS). The former contains nerves and a va-
riety of supporting cells that branch throughout the body and communicate with the
CNS. The PNS includes 12 pairs of cranial nerves that emerge directly from structures
within the cranium and not from segments of the spinal cord as all other nerves
do. Three of these cranial nerves (olfactory, optic, and trigeminal) are located en-
tirely within the cranium and are more accurately considered part of the CNS from
a structural perspective. An important division of the PNS is known as the auto-
nomic nervous system (ANS), which acts largely unconsciously and regulates various
An Integrative Guide to Consumer Neuroscience. Sven Braeutigam and Peter Kenning, Oxford University Press. © Oxford University Press
2022. DOI: 10.1093/oso/9780198789932.003.0003
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Dense Stars
The agreement of the observational points with the curve is
remarkably close, considering the rough nature of the observational
measurements; and it seems to afford a rather strong confirmation of
the theory. But there is one awful confession to make—we have
compared the theory with the wrong stars. At least when the
comparison was first made at the beginning of 1924 no one
entertained any doubt that they were the wrong stars.
We must recall that the theory was developed for stars in the
condition of a perfect gas. In the right half of Fig. 7 the stars
represented are all diffuse stars; Capella with a mean density about
equal to that of the air in this room may be taken as typical. Material
of this tenuity is evidently a true gas, and in so far as these stars
agree with the curve the theory is confirmed. But in the left half of the
diagram we have the Sun whose material is denser than water,
Krueger 60 denser than iron, and many other stars of the density
usually associated with solid or liquid matter. What business have
they on the curve reserved for a perfect gas? When these stars were
put into the diagram it was not with any expectation that they would
agree with the curve; in fact, the agreement was most annoying.
Something very different was being sought for. The idea was that the
theory might perhaps be trusted on its own merits with such
confirmation as the diffuse stars had already afforded; then by
measuring how far these dense stars fell below the curve we should
have definite information as to how great a deviation from a perfect
gas occurred at any given density. According to current ideas it was
expected that the sun would fall three or four magnitudes below the
curve, and the still denser Krueger 60 should be nearly ten
magnitudes below.[8] You see that the expectation was entirely
unfulfilled.
The shock was even greater than I can well indicate to you,
because the great drop in brightness when the star is too dense to
behave as a true gas was a fundamental tenet in our conception of
stellar evolution. On the strength of it the stars had been divided into
two groups known as giants and dwarfs, the former being the
gaseous stars and the latter the dense stars.
Two alternatives now lie before us. The first is to assume that
something must have gone wrong with our theory; that the true curve
for gaseous stars is not as we have drawn it, but runs high up on the
left of the diagram so that the Sun, Krueger 60, &c., are at the
appropriate distances below it. In short, our imaginary critic was
right; Nature had hidden something unexpected inside the star and
so frustrated our calculations. Well, if this were so, it would be
something to have found it out by our investigations.
The other alternative is to consider this question—Is it impossible
that a perfect gas should have the density of iron? The answer is
rather surprising. There is no earthly reason why a perfect gas
should not have a density far exceeding iron. Or it would be more
accurate to say, the reason why it should not is earthly and does not
apply to the stars.
The sun’s material, in spite of being denser than water, really is a
perfect gas. It sounds incredible, but it must be so. The feature of a
true gas is that there is plenty of room between the separate
particles—a gas contains very little substance and lots of emptiness.
Consequently when you squeeze it you do not have to squeeze the
substance; you just squeeze out some of the waste space. But if you
go on squeezing, there comes a time when you have squeezed out
all the empty space; the atoms are then jammed in contact and any
further compression means squeezing the substance itself, which is
quite a different proposition. So as you approach that density the
compressibility characteristic of a gas is lost and the matter is no
longer a proper gas. In a liquid the atoms are nearly in contact; that
will give you an idea of the density at which the gas loses its
characteristic compressibility.
The big terrestrial atoms which begin to jam at a density near that
of the liquid state do not exist in the stars. The stellar atoms have
been trimmed down by the breaking off of all their outer electrons.
The lighter atoms are stripped to the bare nucleus—of quite
insignificant size. The heavier atoms retain a few of the closer
electrons, but have not much more than a hundredth of the diameter
of a fully arrayed atom. Consequently we can go on squeezing ever
so much more before these tiny atoms or ions jam in contact. At the
density of water or even of platinum there is still any amount of room
between the trimmed atoms; and waste space remains to be
squeezed out as in a perfect gas.
Our mistake was that in estimating the congestion in the stellar
ball-room we had forgotten that crinolines are no longer in fashion.
It was, I suppose, very blind of us not to have foreseen this result,
considering how much attention we had been paying to the
mutilation of the atoms in other branches of the investigation. By a
roundabout route we have reached a conclusion which is really very
obvious. And so we conclude that the stars on the left of the diagram
are after all not the ‘wrong’ stars. The sun and other dense stars are
on the perfect gas curve because their material is perfect gas.
Careful investigation has shown that in the small stars on the
extreme left of Fig. 7 the electric charges of the atoms and electrons
bring about a slight deviation from the ordinary laws of a gas; it has
been shown by R. H. Fowler that the effect is to make the gas not
imperfect but superperfect—it is more easily compressed than an
ordinary gas. You will notice that on the average the stars run a little
above the curve on the left of Fig. 7. It is probable that the deviation
is genuine and is partly due to superperfection of the gas; we have
already seen that imperfection would have brought them below the
curve.
Even at the density of platinum there is plenty of waste space, so
that in the stars we might go on squeezing stellar matter to a density
transcending anything known on the earth. But that’s another story—
I will tell it later on.
The general agreement between the observed and predicted
brightness of the stars of various masses is the main test of the
correctness of our theories of their internal constitution. The
incidence of their masses in a range which is especially critical for
radiation pressure is also valuable confirmation. It would be an
exaggeration to claim that this limited success is a proof that we
have reached the truth about the stellar interior. It is not a proof, but
it is an encouragement to work farther along the line of thought
which we have been pursuing. The tangle is beginning to loosen.
The more optimistic may assume that it is now straightened out; the
more cautious will make ready for the next knot. The one reason for
thinking that the real truth cannot be so very far away is that in the
interior of a star, if anywhere, the problem of matter is reduced to its
utmost simplicity; and the astronomer is engaged on what is
essentially a less ambitious problem than that of the terrestrial
physicist to whom matter always appears in the guise of electron
systems of the most complex organization.
We have taken the present-day theories of physics and pressed
them to their remotest conclusions. There is no dogmatic intention in
this; it is the best means we have of testing them and revealing their
weaknesses if any.
In ancient days two aviators procured to themselves wings.
Daedalus flew safely through the middle air and was duly honoured
on his landing. Icarus soared upwards to the sun till the wax melted
which bound his wings and his flight ended in fiasco. In weighing
their achievements, there is something to be said for Icarus. The
classical authorities tell us that he was only ‘doing a stunt’, but I
prefer to think of him as the man who brought to light a serious
constructional defect in the flying-machines of his day. So, too, in
Science. Cautious Daedalus will apply his theories where he feels
confident they will safely go; but by his excess of caution their hidden
weaknesses remain undiscovered. Icarus will strain his theories to
the breaking-point till the weak joints gape. For the mere adventure?
Perhaps partly; that is human nature. But if he is destined not yet to
reach the sun and solve finally the riddle of its constitution, we may
at least hope to learn from his journey some hints to build a better
machine.
LECTURE II
SOME RECENT INVESTIGATIONS