Introduction to Psychology – Interim exam 1

Introduction to Psychology – Interim exam 1

This bundle contains everything you need to know for the first interim exam of Introduction to Psychology for the University of Amsterdam. It uses the book "Psychology by P. Gray and D. F., Bjorkland (eight edition)". The bundle contains the following chapters:

- 2, 3, 4, 5, 7, 8, 9.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 2

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 2

Science is the attempt to answer questions through the systematic collection and analysis of objective, observable data.

Clever Hans was a horse, which had received an education and seemed to be able to answer a lot of questions, including arithmetic questions. This was, in fact, not true. The horse was able to recognize visual signals to which he responded. The story of Clever Hans shows that the result of an experiment (e.g: asking a horse what 9+10 is) can be influenced by the observers (they give unintended visual signals). This is phenomenon is known as the observer-expectancy effect.

A theory is an idea or conceptual model, that is designed to explain existing facts and make predictions about new facts that might be discovered. A hypothesis is a prediction about new facts based on the theory.

Scepticism leads to more mundane explanations instead of a highly unlikely one because scepticism leads us to test, rather than accept a bizarre theory. A theory has to be parsimonious. The simpler, more sober theories are preferred over complex theories. A theory also has to be falsifiable. Experiments should be conducted in a controlled environment because the observer (and other things) can (unintentionally) influence the outcome of the experiment. It is important that the researcher controls the conditions, to make sure that no unaccounted conditions influence the outcome of the research and to exclude alternative explanations. Besides that, researchers should beware of the observer-expectancy effects.

There are several types of research determined by:

  • Research Design
    Experimental research, correlational research and descriptive research
  • Research Setting
    Field and laboratory
  • Data-collection method
    Self-report and observation

Experimental research is used to determine a cause-effect relationship between two variables. An experiment is a procedure in which a researcher systematically manipulates one or more independent variables and looks for changes in one or more dependent variable while keeping all other variables constant. There are two types of variables in a cause-effect relationship. An independent variable is a variable that is determined and controlled by the researcher. A dependent variable is a variable that (hopefully) is affected by the independent variable. There are two basic types of experiments. A within-subject experiment, in which the participant is exposed to each of the conditions of the independent variables and is repeatedly tested. It is a within-subject experiment if there multiple conditions of the independent variable are applied to the same subject. A between-subjects experiment, in which the participant is only tested in one condition of the independent variable and there are multiple participant groups, a group for each of the conditions of the independent variable.

A correlational study is used when you cannot conduct experimental research, such as when researching personal variables that can´t be manipulated, such as divorce. A correlational study is a study in which the researcher does not manipulate any variable, but observes or measures two or more already existing variables to find a relation between them.

It is not possible to get a cause and effect relation between two variables through a correlational study, because it is never certain that the two variables affect each other the way you might think they do. It is possible that A affects B, but also possible that B affects A, or that C affects A or B and because of this it is not possible to get a cause-effect relation by conducting correlational research. Correlation does not imply causality.

A descriptive study describes the behaviour of an individual or a set of individuals without assessing relationships between variables. A descriptive study can be very similar to a correlational study, especially when a descriptive study uses numbers (e.g: the amount of mental disorders in a community), but when the goal is to describe the situation and not to correlate two variables then it is a descriptive study.

A laboratory study is any study in which the participants are brought to a specifically designated area that has been set up to facilitate the researcher’s collection of data or control over environmental conditions. A laboratory study can be anywhere, as long as the researcher has control over the experiences the participants have at that time. A field study is any research study in which the researcher does not have control over the experiences a participant has.

A laboratory study allows the researcher to collect data under more controlled conditions than in the field, but an artificial environment can cause different behaviour than usual and the one the researcher wants to study. E.g: parent-child interactions may be different in a controlled environment than when at home.

A field experiment is possible when a researcher manipulates a variable but has no control over the other variables. (e.g: putting signs somewhere and observing what happens. The researcher has control over the variable signs, but has no control over the other variables, while he wants to research the behaviour the signs cause)

There are two broad dimensions of data-collection methods. The first one is the self-report. Self-report methods are procedures in which people are asked to rate or to describe their behaviour or mental state in some way. One form of self-report is introspection: the personal observations of one’s thoughts, perceptions and feelings. Introspection is subjective, but not unreal. Another form of self-report is when someone is asked to assessments of other people. (e.g: teacher being asked to evaluate children in terms of aggression).

Observational research includes all procedures by which observe and record the behaviour of interest rather than relying on the participant’s self-report. It is possible to test behaviour or to have a naturalistic observation in which the observer doesn’t do anything but observe. Naturalistic observation has one important disadvantage to it. People may change their behaviour if they know they are being observed. This is called the Hawthorne effect. There are two ways to minimise the Hawthorne effect. The first is called habituation. If a stimulus is repeatedly or continuously present, the participants might habituate to the presence. Another way to minimise the Hawthorne effect is hiding.

Statistics are needed to determine that the likelihood that observed patterns in data are simply the result of chance. The statistic procedures used for these purposes can be divided into two categories: descriptive statistics, which are used to summarize sets of data and inferential statistics, which help the researchers decide how confident they can be in judging that the results they observed are not due to chance.

The mean is the arithmetic average. The median is the centre score. Variability refers to the degree to which the numbers in the set differ from one another and their mean. A common measure of variability is the standard deviation. The further the most individual scores are from the mean, the greater the standard deviation is.

A correlation can be positive or negative. A positive correlation (>0) means that when variable A increases, variable B increases as well. A negative correlation (<0) means that when variable A increases, variable B decreases. If the correlation is near 0, it means that the two variables are unrelated.

Inferential statistic methods are procedures for calculating the probability that the observed effects could derive from chance alone. In a correlational study, p is the probability that a correlation coefficient as large as or larger than observed would occur by chance. If ‘p’ is <0.05 then it means that the results are statistically significant; the chance that the results occurred by chance is acceptably low.

When calculation ‘p’ the following things are needed in the calculations:

  • The size of the observed effect
    The larger the size of the effect, the higher the chance that the results are statistically significant.
  • The number of participants in the study
    The more participants, the less likely it is that the results occurred by chance.
  • The variability of data within each group
    The less variability of data within each group, the less likely it is that the results occurred by chance

Bias refers to non-random effects caused by some factor or factors extraneous to the researchers' hypothesis. Bias can lead researchers to false conclusions, while randomness (and thus error) only increases the chance of finding statistically insignificant results. With a bias, a factor, irrelevant to the hypothesis has influenced the results. Three types of bias are the sampling bias, the measurement bias and the expectancy bias.

If the members of a particular group are systematically different from those of another group or are different than the population the researcher is interested in there is a biased sample. When conducting research, participants should be assigned to a group randomly, because the initial differences will then merely be a source of error, otherwise, there will be a bias. It is not possible to draw conclusions about a population when there is a bias in the research. A sample is biased when it is not representative of the population that researchers are trying to describe.

A measure is reliable if the measurement is:

  • Replicable
    It yields about the same result every time it is used with a participant under a set of conditions, also known as replicability. Low reliability decreases the chance of finding statistical significance in research.
  • Interobserver reliability
    Two observers should come to the same result when measuring something and they should be able to observe the same behaviour. The behaviour should be carefully defined ahead of time. This is done by generating an operational definition.

A measurement procedure is valid if it measures or predicts what you want it to measure or predict. A lack of validity can be a source of bias. There are several types of validity:

  • Face validity
    Common sense should tell us that something is valid (it should be a reasonable way to measure what you want to measure)
  • Criterion validity
    Does the measurement correlate with a related variable?

In a previous experiment with autistic children who did not have language ability, but appeared to have exactly that because a facilitator would help them type things on a keyboard. This showed the observer-expectancy bias. The observers (in this case the facilitators) expected something and unintentionally helped the autistic children write exactly that.

The observer-expectancy bias reveals itself in two ways. If an observer expects something he acts (unintentionally) different towards the participants or if the observer expects something he is quicker to see what he expects. This can be prevented by keeping the observer blind from what is expected. Participants also have expectations. This is called subject-expectancy bias. This can also be prevented by conducting double-blind research in which both the observer and the participant don’t know what is expected of them. When administering drugs to participants some should receive a placebo, to make sure that the drug doesn’t only work because of the placebo effect.

In research with humans, ethical considerations revolve around three interrelated issues:

  1. A person’s right to privacy
  2. The possibility of discomfort or harm
    If there is a possibility of harm there must be made sure that there is no way to test what the researchers want to test with less or no chance of harm and should be outweighed by the human benefits. Besides that, participants have to be free to quit at any time.
  3. The use of deception
    Not all psychologists agree on this matter, but some psychologists believe that the use of deception is unethical and undermines the possibility of obtaining truly informed consent. Special considerations, in this case, must be given when the participants are children, have limited intellectual capabilities or have limited capabilities of their own (e.g: prisoners)

When animals are used in research the discomfort and the suffering of the animal has to be outweighed by the potential benefits of the research. Animals must be well cared for and not subjected to unnecessary deprivation or pain.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 3

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 3

Adaptation refers to modification as a result of changed life circumstances.

Genes never produce behaviour directly, so genes are technically not for a behavioural trait, but associated with that behavioural trait. All the effects that genes have on behaviour occur through their role in building and modifying the physical structures of the body.

Genes affect the body’s development through, and only through, their influence on the production of protein molecules. A class of proteins called structural proteins forms the structure of every cell in the body. Another, much larger class called enzymes controls the rate of every chemical reaction in every cell. Genes are components of extremely long molecules of a substance called DNA (deoxyribonucleic acid). A replica of your whole unique set of DNA molecules exists in the nucleus of your body’s cell, where it serves to code for and regulate the production of protein molecules. Each protein molecule consists of a long chain of smaller molecules called amino acids. There are two types of genes. Coding genes: genes that code for unique protein molecules and regulatory genes which help suppress or activate coding genes and thereby influences the body’s development.

The environment is everything except for the genes and this influences the genes. Behaviour is influenced by the genes through the interaction with the environment. The environment is everything except for the genes. The internal environment influences the genes by certain gene activations for example. The external environment influences the genes by eating, for example, a different kind of foods. The genes then go on to activate or suppress development in certain physiological areas and this affects the behaviour.

Experience can activate a certain gene which then goes on to affect behaviour. The experience activates genes, which produce proteins, which alter the function of some of the neural circuits in the brain and thereby changes how an individual behaves.

Genotype refers to the set of genes an individual possesses and phenotype refers to the observable properties of the body and behavioural traits. If two individuals with the same genotype are exposed to different environmental conditions, they will have different phenotypes.

The genetic material (strands of DNA) exists in each cell in structures called chromosomes. When cells divide, other than sperm or egg cells, they do so by a process called mitosis. In this process, the chromosome copies itself before the cell divides so there’s an identical copy of the cell. When cells divide to produce sperm or egg cells, they do so by a process called meiosis, which results in cells that are not genetically alike. During meiosis, each chromosome replicates itself once, but then the cell divides twice.

When a sperm and an egg cell unite, the result is a zygote, which contains the full complement of 23 paired chromosomes. The zygote then grows, through mitosis. By producing diverse offspring, parents are reducing the chance that all of their offspring will die as a result of an unforeseen change in the environment. The only people who are genetically identical to each other are identical twins. Fraternal twins originate from two zygotes, where identical twins originate from one.

Two genes that occupy the same locus (location) can be identical to each other. If they are, they are homozygous and if they’re not they’re heterozygous. Different genes that occupy the same locus and can potentially pair with each other are called alleles. A dominant gene is one that will produce its observable effects in either the homozygous or the heterozygous condition. A recessive gene is one that will produce its effects in homozygous conditions only. Not all genes are recessive or dominant. It is possible for them to blend.

It is possible that diseases that only occur in a heterozygous state will persist in a gene pool because the benefit comes from carrying the disease, not having it. That is why the gene with only one recessive gene for the disease will be passed on the most, instead of the genes without the recessive gene for the disease or genes in a homozygous state with the disease (people who have the disease).

Scott and Fuller show that fearfulness in a certain breed of dogs is controlled by a single gene locus, by crossing the dogs and keeping track of the fearfulness. This way they could determine whether it was a recessive or a dominant gene that played it’s part here. Fear in dogs is not completely controlled by a single gene locus, but this one particular type of fear, the one they tested under controlled conditions, is a fear which is controlled by a single gene locus. It is not safe to say that other types of fear or fear in other conditions in dogs will also be controlled by the same single gene locus. Genes and the environment interact.

Characteristics that derive from variation at a single gene locus are typically categorical in nature (e.g: seeds are either round-shaped or wrinkled), but most anatomical and behavioural differences among individuals of any species are measurable in degree, not in type. They are continuous, rather than categorical. Examples of this are aggressiveness in mice and maze learning in rats. They can fall anywhere on the scale and they are not either aggressive or non-aggressive. The scores are divided over a normal distribution. Characteristics that vary continuously are generally affected by many genes and are therefore called polygenic characteristics. These characteristics are the results of both genes and the environment.

To the degree that individuals within a species differ in any measurable characteristic because of differences in their genes, that characteristic can be modified over time over successive generations through selective breeding.

The field of epigenetics examines gene-regulating activity that doesn’t involve changes to the DNA-code and that can persist through one or more generations. Epigenetic mechanisms are responsible for making sure that the right genes are activated at the right places at the right time. Epigenetics seems to be the primary mechanism by which experience modifies gene-action and thus behaviour.

The difference between artificial selection and natural selection is that natural selection is not driven by the needs of humans, but rather by the obstacles to reproduction that are imposed by the natural environment. Animals that have characteristics to help them overcome the obstacles are more likely to have offspring than the ones that don’t. There are four core concepts of Darwin´s theory of natural selection:

  1. There is an overproduction of offspring in each generation
  2. There is variation in features or traits within members of a generation
  3. Individual differences are inherited from one generation to the next
  4. Individuals with traits and features that fit well with the local environment are more likely to survive and have more offspring than the ones who don’t.

The genetic variability on which natural selection acts has two main sources:

  • The reshuffling of genes that occur in sexual reproduction
  • Mutations (errors that occasionally and unpredictably occur during DNA replication)

August Weismann established the doctrine of the separation of the germ (sex cells) and somatic (body cells) lines. What happens to the body cells during the life of an animal does not affect that animal’s gametes (egg and sperm).

Environmental changes spur evolution by promoting natural selection. Evolution can happen so quickly that people can see it happen. If the natural selection conditions are harsh, evolution speeds up, but complex changes take longer than simple changes such as the change of thickness of the beak of a bird.

There are three common mistakes regarding evolution:

  1. Evolution has no foresight and does not move to a pre-determined plan
    There is no such thing as anticipating environmental changes. Only the immediate changes in the environment will make a difference in the natural selection and thus in the evolution.
  2. Organisms can’t be ranked on an evolutionary scale
    This would mean that organisms move towards a planned end, which is not true. This means that humans are not further evolved than chimpanzees.
  3. Natural selection is not a moral force
    There is no reason to call natural selection ‘good’ or ‘evil’. There is no moral ground for it. This is known as the naturalistic fallacy. Something is not good, because it is the way it is. It’s the same the other way around: something is not evil, because it is the way it is.

The mechanics underlying behaviour are products of natural selection. Functionalism refers to the attempt to explain behaviour in terms of what it accomplishes for the behaving individual. The functionalist’s approach explaining behaviour is the same as explaining anatomy. The functionalist believes that everything is to be seen in function: what does it accomplish for the individual; not only physical aspects but also behavioural aspects.

There are two kinds of explanations of behaviour in evolutionary terms:

  1. Distal explanations (function)
    These are explanations at evolutionary level. They are statements of how the behaviour helped the individual’s ancestors genes make it to the next generation.
  2. Proximate explanations (mechanism)
    These are explanations that are about the mechanism. They are statements of the immediate conditions; both inside and outside the animal, that bring on the behaviour.

Both these explanations are needed for the explanation of behaviour. It is needed to explain how come this behaviour is positive for the reproduction and what conditions bring out the behaviour, what’s the mechanism behind the behaviour.

There are four reasons why a trait or behaviour may not be functional.

  1. Vestigial characteristics
    Some traits or behaviours could have been functional in the past but are not functional anymore.
  2. Side effects
    Some traits or behaviours are the side-effects of natural selection for other traits.
  3. Chance
    Some traits or behaviours result simply from chance. These variations are inconsequential for survival or reproduction, so they are not filtered out.
  4. Traits or behaviours can’t always deal effectively with every situation
    Some traits of behaviours came into existence because they promoted survival and reproduction, but this does not mean that they always help survival and reproduction.

Species-typical behaviour are products of evolution, but that does not mean that they are necessarily rigid in form or uninfluenced by learning. Some species-specific behaviour is affected by learning: such as language and walking in young infants. It is species-specific behaviour to walk and talk, but it requires multiple hours of practice, so it is subject to learning and experience. Biological-preparedness is the manner in which an animal is physically prepared to perform a certain behaviour. Humans are well equipped to walk on two legs and they do it naturally, so they are biologically-prepared for it and it is species-specific behaviour. Dogs can walk on two legs, so they are (less) biologically-prepared for it, but it is not natural for them, so it is not species-specific behaviour for them.

Although species-specific behaviour is typical for species, it does require an impulse from the direct environment. Some sort of experience with the environment is always needed.

There are two conceptually different classes of similarity that exist across species.

  1. Homology
    This is a similarity between two species that exist because of a common ancestor.
  2. Analogy
    This is a similarity between two species that exist because of convergent evolution: two species have something in common (e.g: lifestyle, habitat) and independently develop a common characteristic.

Homologies are used for physiological research. A lot can be learned about physiological mechanisms regarding humans if we research another specie with a similar trait which happens to be a homology. Besides that, we can use homologies to research how certain animals evolved from simpler forms to the animals they are now.

Looking at analogies allows us to find out what may have caused the similarity between two species and what is the distant explanation of a certain behaviour, which could be for example the habitat or lifestyle.

There are four mating classes:

  1. Polygyny (high female, low male investment)
    One male mates with more than one female
  2. Polyandry (high male, low female investment)
    One female mates with more than one male
  3. Monogamy (equal investment)
    One male mates with one female
  4. Promiscuity (group investment, decreases violence -> paternal confusion)
    A group consisting of more than one male and one female mate with each other

In general, for species in which parental investment is inequal, the more parentally invested sex will be more vigorously competed for than the other and more discriminating than the other when choosing mates. This is Triver’s theory of parental investment.

Aggression is behaviour intended to harm another member of the same species. Most of the violence perpetrated by male primates has to do directly or indirectly with sex. Female primates do not only risk her life but also the offspring she’s nurturing because a female primate generally has a higher parental investment.

Helping can be defined as any behaviour that increases the survival chance or reproductive capacity of another individual. There are two categories of helping.

  1. Cooperation
    This is helping another individual while also helping oneself.
  2. Altruism
    This is helping another individual, while it decreases its survival chance or reproductive capacity.

The kin selection theory of altruism holds that behaviour that seems to be altruistic came about through natural selection because it preferentially helps close relatives, who are genetically most similar to the helper. The reciprocity theory of altruism holds that behaviours that seem altruistic are forms of long-term cooperation. If someone feeds another non-kin, that individual will be more likely to feed the one that’s fed him before if necessary.

There are two important fallacies:

  1. Naturalistic fallacy
    This is the idea that because things happen in nature, they’re good and they’re supposed to be like that. “It is good to be selfish because it happens in nature as well” is an example of the naturalistic fallacy. Evolution is not a moral force and neither is natural selection.
  2. Deterministic fallacy
    This is the assumption that genetic influences on our behaviour take the form of genetic control of our behaviour. This implies that the genes influence behaviour directly and not through the environment. This fallacy implies that genes control behaviour in ways that cannot be altered by environmental experiences or conscious decisions.
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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 4

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 4

The brain contains a lot of nerve cells or neurons. The points of communication between neurons are called synapses. The brain and the spinal cord make up the central nervous system. Extensions from the central nervous system, called nerves, make up the peripheral nervous system. The difference between a neuron and a nerve is that a nerve is a bundle of neurons within the peripheral nervous system.

There are three types of neurons:

  1. Sensory neurons
    These neurons carry information from sensory organs into the central nervous system.
  2. Motor neurons
    These neurons carry messages out from the central nervous system to operate muscles and glands.
  3. Interneurons
    These neurons exist entirely within the central nervous system and carry messages from one set of neurons to another. They collect, organize and integrate messages from various sources.

Neurons consist of the following things:

  • Cell body
    This is the widest part of the neuron. It contains the cell nucleus.
  • Dendrites
    These are thin, tube-like extensions that branch extensively and function to receive input for the neuron. In interneurons and motor neurons, the dendrites extend directly from the cell body. In sensory neurons, dendrites extend from one end of the axon rather than directly from the cell body.
  • Axon
    This is another thin, tube-like extension from the cell body. Its function is to carry messages to other neurons or, in the case of motor neurons, to muscle cells. Each branch of an axon with a small swelling is called an axon terminal. Axon terminals are designed to release chemical transmitter molecules onto other neurons (or onto muscle cells or glandular cells in the case of motor neurons). The axons of some neurons are surrounded by a casing called a myelin sheath. This is a fatty substance produced by supportive brain cells called glial cells.

Neurons exert their influence on other neurons and muscle cells by firing off all-or-none impulses called action potentials. In motor neurons and interneurons, action potentials are triggered at the junction between the cell body and the axon. In sensory neurons, they are triggered at the dendritic end of the axon. Each action potential produced by a given neuron is the same strength as any other action potential produced neuron and the action potential retains its full strength down the axon.

A cell membrane encloses each neuron. It is porous skin that permits certain chemicals to flow into and out of the cell while blocking others. Among the various chemicals dissolved in the intracellular and extracellular fluids are some that have electrical charges. These include soluble protein molecules (A-), which have negative charges and exist only in the intracellular fluid, and sodium ions (Na+) and chloride ions (Cl-) which are more concentrated in extracellular than intercellular fluid.

The charge (-70mv relative to the outside) across the membrane is called the resting potential. The action potential is a wave of change in the electrical charge across the membrane and it moves rapidly from one end of the axon to the other. When the action potential is ‘activated’ thousands of tiny channels that permits sodium ions to pass through open up. As a result, enough sodium moves inward to cause the electrical charge across the membrane to reverse itself and become momentarily positive relative to the outside. This sudden shift constitutes the depolarization phase of the action potential. As soon as depolarization occurs, the channels that permitted sodium to pass through close, but channels that permit potassium to pass through remain open. The electrical charge is pushed back to the resting potential and even for a short while below that. This is called the repolarization phase of the action potential. To maintain the original balance of ions across the membrane, each portion of the membrane contains a chemical mechanism, referred to as the sodium-potassium pump.

The speed at which an action potential moves down an axon is affected by two things:

  1. The axon’s diameter
    The larger the diameter, the less resistance there is, thus the faster the action potential moves down an axon.
  2. Presence of a myelin sheath
    If there is a myelin sheath present, the action potential moves faster down the axon.

Neurons generate action potentials are rates that are influenced by all the information that is sent to them from other neurons. The junction between each axon terminal and the cell body or dendrite of the receiving neuron is referred to as a synapse. When an action potential reaches an axon terminal, it causes the terminal to release packets of a chemical substance, called a neurotransmitter. Having too little or too many neurotransmitters can cause psychological disorders. A very narrow gap, the synaptic cleft separates the axon terminal from the membrane of the cell that it influences. The membrane of the axon terminal that abuts the cleft is the presynaptic membrane and that of the cell on the other side of the cleft in the postsynaptic membrane. Within the axon terminal are hundreds of tiny globe-like vesicles.

At an excitatory synapse, the transmitter opens sodium channels in the postsynaptic membrane. The movement of the positively charged sodium ions into the cell causes a slight depolarization of the receiving neuron which tends to increase the rate of action potentials triggered in that neuron. At an inhibitory synapse, the transmitter opens either chloride channels or potassium channels. This can cause hyperpolarization.

New-born infants have more neurons in their brains than adults do. The process of creating new neurons is referred to as neurogenesis. After a while neurons enter the last stage of their development: differentiation. During this time, neurons grow in size and increase their numbers of dendrites and axons terminals as well as the number of synapses they form. Neurons and synapses die during the development of the brain. This is called selective cell death, or apoptosis. The brain first overproduces neurons and synapses, but then just as a sculptor chisels them away.

Mirror neurons reflect an individual being able to recognize when another is doing something that the self can do. Human’s mirror neurons seem to code for movement forming an action and not only for the action itself. Mirror neurons are important for imitation.

Neurons in the central nervous system are organized into nuclei and tracts. A nucleus is a cluster of cell bodies in the central nervous system and a tract is a bundle of axons that course together from one nucleus to another.

There are three categories of identifying the functions of specific brain areas:

  1. Observing behavioural deficits that occur when a part of the brain is destroyed or temporarily inactivated
  2. Observing behavioural effects of artificially stimulating specific parts of the brain
  3. Recording changes in neural activity that occur in specific parts of the brain when an individual is engaged in a particular mental or behavioural task

Lesions in one area of the brain can also lead to changes in 0ther brain areas. Lesions are areas of damage. There are several ways of recording brain activity in humans:

Name

Function

Transcranial magnetic stimulation (TMS)

Disrupting brain activity with magnetic waves for a short while

Electroencephalogram (EEG)

Recording brain activity (just on the surface near the skull)

Positron emission tomography (PET)

Injecting a radioactive substance in the blood and measuring the radioactivity that is emitted from each part of the brain

Functional magnetic resonance imaging (fMRI)

Creating a magnetic field around the person’s head so haemoglobin molecules that are carrying oxygen give off radio waves

 

There are also several ways of studying the effects of certain areas in the brain using non-human animals:

  • Deliberately placing brain lesions (using surgery to destroy certain neurons)
  • Stimulating specific areas of the brain (using surgery to stimulate certain neurons)
  • Electrical recording of single neurons

The nervous system contains two distinct, but interacting hierarchies:

  • Sensory-perceptual hierarchy
    This is involved in the data processing. It perceives sensory data about a person’s internal and external environment and it analyses those data to make decisions. The flow is from the bottom (sensory receptors) to top (perceptual centres in the brain).
  • Motor-control hierarchy
    This is involved in movement. The flow is from top to bottom (brain to muscles).

The peripheral nervous system consists of the entire set of nerves, which connect the central nervous system to the body’s sensory organs, muscles and glands. Nerves are divided into two classes:

  • Cranial nerves
    Nerves that project directly from the brain (12 pairs)
  • Spinal nerves
    Nerves that project from the spinal cord (31 pairs)

Sensory neurons are activated at their dendritic ends by the effects of sensory stimuli (e.g: light on the eye, chemical son the tongue). They send their action potentials into the central nervous system. Somatosensation is all the sensory input that comes from the body, with the exception of specialized sensory organs of the head. The nervous system can control behaviour through motor neurons.

Motor neurons act on two broad classes of structures:

  1. Skeletal muscles
    These are the muscles that are attached to bones and produce externally observable movement of the body when contracted.
  2. Visceral muscles and glands
    Visceral muscles are muscles that are not connected to bones. They form walls of structures such as the heart. Glands are structures that produce secretions, such as sweat.

The peripheral nervous system consists of a skeletal portion and an autonomic portion. The skeletal muscles make up the skeletal portion and the visceral muscles and glands make up the autonomic portion. Most visceral muscles and glands receive two sets of neurons, which produce opposite effects and come from two anatomically distinct divisions of the autonomic system: sympathetic and parasympathetic. The sympathetic division responds especially to stressful stimulation helps prepare the body for fight or flight. The parasympathetic division serves regenerative, growth-promoting and energy-conserving functions.

The spinal cord has three categories of functions:

  1. The spinal cord contains pathways to and from the brain
    The ascending tracts carry somatosensory information and the descending tracts carry motor control commands.
  2. The spinal cord organizes simple reflex
    Simple reflexes, such as the flexion reflex do not require the brain but are operated by the spinal cord
  3. The spinal cord contains pattern generators for locomotion
    The spinal cord contains networks of neurons that stimulate one another in a cyclic manner and thereby produce a burst of action potentials that wax and wane in a regular, repeating rhythm. These networks are called pattern generators.

The lower, more primitive parts of the brain are referred to as subcortical structures. The spinal cord and the brainstem are alike. They both contain ascending (sensory) and descending (motor) tracts. The brainstem also organizes some reflexes and certain species-typical behaviour patterns, but the brainstem organizes more complex and sustained reflex, such as the postural reflexes. This is a reflex that helps an animal maintain balance and vital reflexes such as breathing rate and heart rate in response to input signalling the body’s metabolic needs.

The thalamus is a relay station that connects different parts of the brain with one another. It also plays a role in the arousal of the brain as a whole. The cerebral cortex is the outer layer of the major portion of the brain. The entire folded cerebral cortex is divided into left and right hemispheres. Each hemisphere is further divided into four lobes or segments. The lobes are, from back to front, the occipital lobe, the temporal lobe, the parietal lobe and the frontal lobe.

Part of the brain

Function

Brainstem

Major functions (e.g: breathing, heartbeat, standing and walking)

Hypothalamus

Regulation of internal environment (e.g: sensations of hunger, thirst and sexual desire)

Prefrontal cortex

Making plans and interrupting current behaviour

Association cortex

Making associations (located in the parietal and temporal lobes)

Hippocampus

Saving new memories and spatial orientation

Premotor cortex

Making a plan of movement before (and during) the actual movement (sends it via the primary motor cortex, basal ganglia and cerebellum)

Visual cortex

Analysing visual information

Thalamus

Central hub for sensory information (except smell)

Amygdala

Plays a role in emotions (especially fear)

Cerebellum

Uses information of the senses to control precise, previously learned movements (without feedback, fast movements)

Somatosensory

Receives signals of tactile sense (via the thalamus)

Basal ganglia

Control precise previously learned movements using information of the senses (with feedback, slow movement)

Primary motor cortex

Delicate movements (active during the movement)

Broca’s area

A language centre used for syntax

Wernicke’s area

A language centre used for the meaning of sentences

Corpus callosum

Connecting the brain’s hemispheres

 

Hormones are chemical messengers that are secreted into the blood. They are carried by the blood to all parts of the body where they act on specific target tissues. Some effects of hormones are long term or irreversible. Hormones can influence the body on an anatomical level and this can influence behaviour. There are also short term effects of hormones, such as the effects of adrenaline.

The pituitary produces hormones that stimulates the production of other hormones in other glands.

The brain consists of two hemispheres. The areas in the left are specialized for language and comparable areas in the right are specialized for nonverbal, visuospatial analysis of information. Any loss of language resulting from brain damage is called aphasia.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 5

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 5

Slower changing components of the mind are referred to as behavioural states (e.g: variations in motivation, emotion).

Motivation refers to the entire constellation of factors, inside and outside of the organism, that causes an individual to behave in a particular way at a particular time. Motivational state or drive refers to an internal condition that orients an individual toward a specific category of goals that can change over time in a reversible way (the drive can increase and decrease).

Motivated behaviour is directed towards incentives or reinforcers. The motivational state for searching for food is hunger, but the incentive is the food itself. Drives and incentives complement each other and influence each other’s strength.

Homeostasis is the constancy of internal conditions that the body must actively maintain. The loss of homeostasis is the psychological foundation of drives because this loss acts on the nervous system to induce behaviour designed to correct the imbalance.

There are two general classes of drives: regulatory drives and nonregulatory drives. There are five categories of mammalian drives:

  1. Regulatory drives
    These are drives that promote survival by helping to maintain the body’s homeostasis.
  2. Safety drives
    These are drives that motivate an animal to stay safe (e.g: fear, anger).
  3. Reproductive drives
    These are drives that motivate an individual to reproduce and keep the offspring safe.
  4. Social drives
    These are drives that promote cooperation and friendship.
  5. Educative drives
    These are drives that motivate an individual to play and to explore.

Things such as art, music and literature can be seen as an extension of the educative drive, but it can also be seen as something that taps into our already existing drives.

The central-state theory of drives states that different drives correspond to neural activity in different sets of neurons in the brain. A set of neurons in which activity constitutes a drive is called a central drive system. For a set of neurons to be a central drive system, it must receive and integrate the various signals that can raise or lower the drive state. Besides that, it must act on all the neural processes that would be involved in carrying out the motivated behaviour; it must direct perceptual mechanisms toward stimuli related to the goal and motor mechanisms toward producing the appropriate movements. The hypothalamus is believed to be the hub of many central drive systems because it fits the exact description and has a strong connection with the pituitary gland.

The term ‘reward’ has three interrelated meanings.

  1. Wanting
    A reward is something that we want. Wanting is measured by the amount of effort an individual will exert to get the reward. Dopamine is crucial in the wanting part, as individuals show an increase of dopamine right before they get the reward, but not after they’ve received the reward.
  2. Liking
    A reward is something that we like. Liking refers to the subjective feeling of pleasure. Endorphin is crucial for an individual to like the reward.
  3. Reinforcer
    A reward is something that affects learning.

Animals will work the hardest to stimulate a tract in the brain called the medial forebrain bundle. The neurons of this tract that are most crucial for this rewarding effect have their cell bodies in nuclei in the midbrain and synaptic terminals in a large nucleus in the basal ganglia called the nucleus accumbens. Damage to the medial forebrain bundle or the nucleus accumbens destroys all motivated behaviour.

Dopamine release promotes long-term potentiation of neural connections with the nucleus accumbens and LTP is believed to be part of the cellular basis for learning throughout the brain, thus dopamine plays an important role in learning. When a reward is unexpected, the dopamine release immediately after the reward helps to reinforce an association between the reward and any stimulus or response that happened to precede it.

Drugs often release dopamine in the brain in a manner that normally only happens if a reward is unexpected. This causes some sort of ‘super-learning’, where the individual starts to learn all the environmental cues to the drug, which causes dopamine release and thus a strong urge to get the drug when they are in the same environment again. The liking of a drug reduces over time, but the wanting only grows stronger.

Regulatory drives make use of feedback control (e.g: a thermostat. It will increase the temperature if the temperature is below a certain level and it will do nothing if the temperature is above a certain level). The arcuate nucleus, which lies in the centre of the lowest portion of the hypothalamus, very close to the pituitary gland, is the master control centre for appetite and weight regulation. There are several ways the body tells a person that he’s either hungry or satiated:

  1. Hungry
    Appetite-stimulating neurons
    release the neurotransmitter NPY, which is the most potent appetite stimulator yet discovered.
  2. Satiated
    There is a higher body temperature. There is an increased blood level of glucose and the stomach temporarily grows. The release of certain hormones, such as PYY.  Appetite-suppressing neurons stimulate these effects. The hormone leptin produced by fat cells reduces appetite (individuals without the hormone leptin become incredibly obese). Leptin reduces appetite up to a certain level.

Within a culture, differences in body weight result mostly from the difference in genes, but across cultures, environment plays a larger role. The evidence for this statement comes from the following things: the weight of adopted children correlate much more strongly with the weight of their adoptive parents and genetically similar Indians in two different environments differed greatly in weight. The prenatal diet is very important for the future bodyweight of the offspring. Sensory-specific satiety is when an individual has had enough of one taste or type of food and will feel satiated, but the hunger mechanisms can easily be activated again because of the availability of other food. Classical conditioned cues can also cause the hunger mechanisms to be activated.

Testosterone is crucial for maintaining the sex drive in males. The amount of testosterone that men secrete into their blood is affected by psychological conditions. Estrogen and progesterone produce the menstrual cycle in humans and the oestrous cycle in other mammals. This cycle controls ovulation. The female sexual drive and behaviour are tightly controlled by the oestrous cycle.

In rats, the ventromedial area of the hypothalamus plays a role in sexual behaviour analogous to the preoptic area in the male. Most female animals seek a partner to copulate when they are fertile, while many primates also seek out sexual partners when they are not fertile. Their sexual drive during non-fertile times doesn’t depend on androgens, a category of hormones including testosterone. Arousability refers to the capacity to become sexually aroused in response to appropriate stimuli. Proceptivity refers to the person’s motivation to seek out and initiate sexual activity.

Sex hormones influence sexual drive and behaviour through two different kinds of effects on the brain: activating and differentiating. Activating effects are the kinds of effects that occur during and after puberty. Differentiating effects are effects that occur before and immediately after birth and cause the brain to develop in a male or female direction. They are responsible for the biological differences between males and females in sexual drive and orientation. The hormone testosterone causes the male to develop like a male during the foetal stage. It develops the male sex drive and develops the brain in a male-like manner.

A theory states that falling in love involves three primary emotional systems that evolved to support mating, reproduction and parenting:

  1. Lust
    This is becoming sexually excited by members of the opposite sex (driven by androgen hormones, such as testosterone)
  2. Attraction
    This consists of strong emotions toward the other
  3. Attachment
    This is the feeling of closeness and anxiety when separated (associated with the hormones vasopressin and oxytocin)

Sexual orientation consists of at least three components:

  1. Sexual / romantic attraction
    To which sex do people feel most attracted?
  2. Sexual behaviour
    With which sex do people have voluntary sexual acts?
  3. Sexual identity
    How do people describe themselves sexually?

Genes play a role in sexual orientation, but not the sole role. The prenatal development can also play a role in the sexual orientation, as this can cause differences in the amount of testosterone available to the foetus’s brain. The most consistent, nongenetic influence on sexual orientation is the fraternal birth-order effect on male homosexuality. The more older brothers a man has, the greater is the likelihood of his sexual orientation being homosexual.

Alpha waves are relatively slow, large and regular waves. These waves occur when someone is awake but has his eyes closed. If a person concentrates on something, the EEG pattern changes to low amplitude, fast, irregular waves called beta waves. A slow, irregular, high-amplitude kind of wave is called a delta wave. When a person falls asleep they generally go through four stages:

  1. Stage 1 (brief transition)
  2. Stage 2 (sleep spindles)
  3. Stage 3 (delta waves start to occur)
  4. Stage 4 (delta waves)

After stage four, a sleeping person returns to stage 3 and 2 and then a new type of sleep occurs: REM sleep (rapid-eye-movement sleep). During REM sleep dreams occur and there are small twitches of muscles during this type of sleep. Also, the eyes move rapidly under the eyelids. REM sleep also marks the onset of a new sleep cycle. Stage 2, 3 and 4 are referred to as non-REM sleep. A person generally goes through five sleep cycles. At first, the non-REM-sleep will become deeper and after the second sleep cycle, the sleep will rapidly become lighter.

If a person is awakened during REM sleep, the person will often report a true dream. If a person is awakened during non-REM sleep, the person will often only report sleep thought, which lacks the vivid sensory and motor hallucinations of true dreams (more alike to daytime thinking). A person is not completely irresponsive during sleep and although the eyes are closed, the other sensory channels remain open (e.g: a parent can sleep through a thunderstorm but awakens when they hear their child cry). The sleeping person’s brain sorts out sounds by meaning to some degree. All mental activity during sleep is quickly forgotten. 

There are several theories about the functions of sleep:

  1. Preservation and protection theory
    This theory states that the function of sleep is to protect the individual and preserve energy at times when there is relatively little value to being awake and considerable danger. Evidence for this comes from the different time of awakening of animals with different feeding patterns and the amount of sleep they get.
  2. Body-Restoration theory
    This theory states that the body wears out during the day and needs sleep to restore it. There is little to no evidence that the amount of energy an individual uses in a day affects the number of hours that the individual sleeps.
  3. Brain-Maintenance theory of REM sleep
    This theory states that REM sleep provides regular exercise to groups of neurons in the brain. Synapses can degenerate if they go too long without being active, so neural activity during REM sleep may help preserve important circuits. Evidence for this theory is found in foetuses, which spend almost 24 hours a day in REM sleep.

It is unclear whether dreams serve any purpose, but it could just be the side effect of psychological changes that occur during REM sleep. Neurons in visual and motor areas of the brain become active during REM sleep and dreams could just be the result of those neurons activating.

Nonsomniacs are people who barely need any sleep. Insomniacs are people who need a normal amount of sleep but have great difficulty sleeping at night

The sleep drive is promoted by neural mechanisms located in the hypothalamus. A repetitive biological change that continues at close to a 24-hour cycle in the absence of external cues is called circadian rhythm. The clock that controls the circadian rhythm of sleep in all mammals is located in a specific nucleus of the hypothalamus called the suprachiasmatic nucleus. This nucleus contains rhythm generating neurons, controls a daily rhythm of the body temperature and secretes melatonin through the pineal gland. Light synchronizes the internal clock with the light-dark cycle.

An emotion is a subjective feeling that is mentally directed toward some object. That object can be another person, an object, an idea or concept. Self-conscious emotions are emotions
that depend on the individual’s self-awareness.

The feeling associated with emotion, independent of the object, is referred to as affect (tense). If an emotional feeling is not attached to an object but rather experienced as free-floating and it lasts for a sufficiently long period, it is referred to as a mood (e.g: depressed). It is possible to regulate emotions. Emotions can be recognized through facial expression, voice and body language. Emotions are also not independent of cognitions (e.g: heart rate that increases when someone is happy).

The discrete emotion theory states that basic emotions are innate and associated with distinctive bodily and facial reactions. Emotions could have an evolutionary purpose. They also promote our survival and reproduction through their capacity to communicate our intentions and needs to others. The social setting affects our emotions and our emotions affect our behaviour. Emotional states are accompanied by peripheral changes in the body.

James’s theory of emotion states that the bodily reaction precedes the emotion (e.g: we see a bear, we interpret the danger, there is a bodily reaction and then we feel fear). The common-sense theory states that the emotion precedes the bodily reaction (e.g: we see a bear, we interpret danger, we feel fear and there is a bodily reaction). In an emergency situation, there is no time for conscious reflection. The body reacts immediately.

Schachter’s Cognition-Plus-Feedback Theory states that the feeling of an emotion depends not just on sensory feedback pertaining to the body’s response, but also on the person’s perception and thoughts about the environmental event that presumably evoked that response. The perception and thought about the environment influence the type of emotion felt (e.g: we see a bear, we interpret danger and this causes a bodily reaction. We interpret danger and this causes us to feel fear and the strength of the bodily reaction determines the intensity of the fear. In other words, the interpretation determines bodily reaction, which determines the intensity and the interpretation also determines the type of emotion we feel).

Mimicking emotion causes people to feel that emotion earlier than people who do not mimic a certain emotion. The amygdala is the brain’s early warning system. It receives sensory input by way of two routes: a very rapid subcortical route and a slower cortical route. Through the subcortical route, it analyses information before it has been processed by sensory areas of the cerebral cortex. Through the cortical route, it analyses in more detail.

The removal of the amygdala causes psychic blindness. Individuals with physic blindness seem indifferent to the psychological significance of objects. Sensory areas of the cortex are essential for conscious perception of stimuli, but not for unconscious emotional responses to them. The amygdala is essential for unconscious emotional responses and the prefrontal cortex is essential for the full conscious experience of emotions and the ability to act in deliberate, planned ways based on those emotions. There is greater neural activity in the right prefrontal cortex when experiencing withdrawal emotions and there is greater neural activity in the left prefrontal cortex when experiencing approach emotions.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 7

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 7

Photoreceptors are specialized light-detecting cells. One possible evolutionary road of the eyes is the following: photoreceptors became concentrated in groups, they began to form light detecting organs and this light-detecting organ developed until it became the eye as we know it today.

The front of the eyeball is covered by the cornea, a transparent tissue. Here the light is focussed. Behind the cornea is the iris. Inside the iris is the pupil. Behind the iris is the lens, which adds to the focusing process began by the cornea. The lens is adjustable and the cornea is not. Light forms an image of the object on the retina. The image is on the retina is upside down, but the retina’s function is to trigger patterns of activity in neurons running to the brain.

The process by which a stimulus from the environment generates electrical changes in neurons is called transduction. Transduction is the function of photoreceptor cells. There are two types of photoreceptor cells on the retina:

  1. Cones
    These permit sharply focused colour vision in bright light. They are most concentrated in the fovea, the area of the retina that is in the most direct line of sight.
  2. Rods
    These permit vision in dim light. They exist everywhere in the retina except the fovea.

At the place on the retina where the axons of neurons converge to form the optic nerve, there is a blind spot. We normally don’t notice this. There are two separate, but interacting visual systems within the human eye:

  1. Cone vision (photopic vision)
    This is focused on high detail and colour perception. There are three types of cones, each with a different photochemical that makes it most sensitive to the light within a particular band of wavelengths.
  2. Rod vision (scotopic vision)
    This is focused on seeing very dim light but lacks the capacity to distinguish colours.

The three-primaries law states that three different wavelengths of light can be used to match any colour that the eye can see if they are mixed in the appropriate proportions. The primaries can be any colour, as long as one is from the longwave end of the spectrum, one from the shortwave and one from the middle. The law of complementarity states that pairs of wavelengths can be found that, when added together, produce the visual sensation of white.

There are two theories of colour vision:

  1. Trichromatic theory
    Colour vision emerges from the combined activity of three different types of receptors, each most sensitive to a different range of wavelength.
  2. Opponent-Process theory
    Colour perception is mediated by neurons that can be either excited or inhibited, depending on the wavelength of the light and complementary wavelengths have opposite effects.

Most of what new-born sees is out of focus. Convergence (both eyes looking at the same object) and coordination (both eyes following a moving stimulus in a coordinated fashion) are poor at birth but develops rapidly. Synapses are formed and maintained when an organism has species-typical experience as experience-expectancy processes. As a result, functions will develop for all members of a species, given a species-typical environment.

The primary visual cortex is responsible for vision. Here, millions of neurons are involved in analysing the sensory input. In the primary visual cortex there are neurons called bar detectors, neurons called edge detectors and neurons called feature detectors.

The feature-integration theory, also called the two-stage theory states that any perceived stimulus consists of several distinct primitive sensory features (e.g: colour and the slant of its lines). The essence of this theory is that the detection and integration occur sequentially in two fundamentally different steps or stages of information processing.

  1. Detection of features
    This occurs instantaneously and involves parallel processing. Parallel processing means that this step operates simultaneously on all parts of the stimulus array (our visual system picks up all the primitive features of the objects whose light rays strike our retinas at once).
  2. Integration of features
    This requires more time and leads eventually to our perception of objects. This step involves serial processing, which occurs sequentially, at one spatial location at a time, rather than simultaneously (e.g: we can integrate the features of X and then an instant later the features of Y, but we can’t integrate the two sets of features simultaneously).

The Gestalt psychology stated that the whole is greater than the sum of its parts because the whole is defined by the way the parts are organized, not just by the parts themselves. They assume that we automatically perceive whole, organized patterns and objects (e.g: people perceive and recognize the chair as a whole before noticing its arms, legs and other components). The Gestalt principles of grouping are the following:

  1. Proximity
    We tend to see stimulus elements that are near each other as parts of the same object and those that are separated as parts of different objects.
  2. Similarity
    We tend to see stimulus elements that physically resemble each other as parts of the same objects and those that do not resemble each other as parts of different objects.
  3. Closure
    We tend to see forms as completely enclosed by a border and ignore gaps in the border.
  4. Good continuation
  5. Common movement
    When stimulus elements move in the same direction and at the same rate, we tend to see them as part of a single object.
  6. Good form
    Things that are simple, uncluttered, symmetrical, regular and predictable are more likely to be seen as a single object than as two objects.

Besides those six principles of grouping, we tend to automatically divide any visual scene in figure (the object that attracts attention) and ground (the background). This is mostly determined by circumscription. We tend to see the circumscribing form as ground and the circumscribed form as figure.

Once your visual system has hit upon a particular solution to the problem of ‘what is there’,
it may create or distort features in ways that are consistent with that inference. This is called unconscious inference, your visual system uses the sensory input from a scene to draw inferences about what is present.

Control that comes from higher up in the brain is called top-down control and they refer to control that comes more directly from the sensory input as bottom-up control. Perception always involves interplay between bottom-up and top-down control. Bottom-up processes bring in the sensory information that is actually present in the stimulus and top-down processes bring to bear the results of calculations based on that sensory information plus other information, such as that derived from previous experience and from larger context in which the stimulus appears.

The recognition-by-Components theory states that in order recognize an object, our visual system first organizes the stimulus information into a set of basic, three-dimensional components, which are called geons, and then it uses the arrangement of those components to recognize the object (e.g: an aeroplane, no matter how it is positioned relative to our eyes, always consists of the same set of geons). The theory posits that recognition of an object occurs through the following sequence:

Pick-up of sensory features -> detection of geons -> recognition of objects

People with visual agnosia can still see, but can no longer make sense of what they see. There are several types of visual agnosia:

  1. Visual form agnosia
    People with this condition can see that something is present and can identify some of its elements, such as its colour and brightness, but cannot perceive its shape.
  2. Visual object agnosia
    People with this condition have no problems seeing shapes, but they are unable to identify the object.

The visual areas beyond the primary area exist in two relatively distinct cortical pathways or streams, which serve different functions:

  1. “What” pathway
    This stream runs into the lower portion of the temporal lobe and is specialized for identifying objects.
  2. “Where-and-how” pathway
    This stream runs upward in the parietal lobe. This stream is specialized for maintaining a map of three-dimensional space and localizing objects within that space. This pathway is also crucial for the use of visual information to guide a person’s movement.

There are several cues for seeing depth. There are binocular cues and monocular cues.

Binocular cues:
There is binocular disparity, which refers to the slightly different views that the two eyes have of the same object or scene. This disparity can serve as a cue for seeing depth. The less the disparity, the greater the distance. The ability to see depth from binocular disparity is called stereopsis.

Monocular cues:
One of the monocular cues is motion parallax, which refers to the changed view one has of a scene or object when one’s head moves sideways. The smaller the change when moving your head, the greater the distance. Motion parallax depends on the geometry of true three-dimensionality. It cannot be used to depict depth in two-dimensional pictures.

There is a way to see depth in two-dimensional pictures. These cues are called pictorial cues for depth and there are several of them:

  1. Occlusion
  2. Relative size for familiar objects
  3. Linear perspective
  4. Texture gradient
  5. Position relative to the horizon
  6. Differential lightning of surface

The ability to see an object as unchanged in size, despite change in the image size as it moves farther away or closer, is called size constancy. Previous knowledge of the object’s usual size may contribute to size constancy.

Multisensory integration refers to the integration of information from different senses by the nervous system. When sight and sound are put in conflict with each other, vision usually wins. This is referred to as the visual dominance effect. The McGurk effect occurs when the sound is not correct according to the vision.

Multisensory integration is most apt to be perceived then the individual sensory stimuli come from the same location, arise at approximately the same time and evoke relatively weak responses when presented in isolation.

Synaesthesia is a condition in which sensory stimulation in one modality induces a sensation in a different modality.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 8

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 8

Animals need to learn to survive. Learning is any process through which experience at one time can alter an individual’s behaviour at another tie. Experience is any effects of the environment that are mediated by the individual’s sensory system. Future behaviour is any behaviour that is not part of the individual’s immediate response to the sensory stimulation during the learning experience.

Classical conditioning is a learning process that creates new reflexes. A reflex is a simple, relatively automatic, stimulus/response sequence mediated by the nervous system. Habituation is a decline in the magnitude of a reflexive response when the stimulus is repeated several times in succession. Not all reflexes undergo habituation.

With classical conditioning, several things should be taken into account:

  1. Unconditioned stimulus
    This is the original stimulus which should trigger the reflex
  2. Unconditioned response
    This is the reflex
  3. Conditioned stimulus
    This is the new stimulus
  4. Conditioned response
    This is the reflex

A conditioned response can be extinguished when the same conditioned stimulus is represented each time, without showing the unconditioned stimulus (e.g: ringing a bell without presenting food repeatedly). This is called extinction. The mere passage of time following extinction can partially renew the conditioned response. This is called spontaneous recovery. A single pairing of the conditioned stimulus with the unconditioned stimulus can fully renew the conditioned response. The response is somehow inhibited. It can be disinhibited by the passage of time or the recurrence of the unconditioned stimulus.

Individuals don’t only react to the conditioned stimulus, but also stimuli that resemble the unconditioned stimulus. This is called generalization. The less a stimuli resembles the original conditioned stimulus, the weaker the conditioned response is. Generalization between two stimuli can be abolished if the response to one is reinforced while the response to the other is extinguished. This is called discrimination training. (e.g: dogs were given food when a bell of 1000 hertz is heard, but not given food when a bell of 700 hertz is heard). For humans, interpretation is important for classical conditioning. When they are shown several words and a conditioned response is learned, they also show a similar response to words that have the same meaning as the original words but not to words that look similar to the original words.

The school of thought known as behaviourism argued that science should avoid terms that refer to mental entities because such entities cannot be directly observed. They believed that psychology should focus on the relationship between observable events (stimuli) in the environment and observable behavioural reactions to those events (responses). Behaviourism argued that all of behaviour is in essence reflex-like in nature.

There are several theories of what is actually learned in classical conditioning:

  1. Stimulus-response theory
    The new reflex is learned because a connection between the unconditioned response and the conditioned stimulus is learned. (e.g: rats that have a connection between a light and a loud sound should still freeze when the light comes on, even though they are habituated to the sound)
  2. Stimulus-stimulus theory
    The new reflex is learned because a new stimulus represents the old stimulus.
    (e.g: rats that are conditioned to learn that a light signals a loud sound, which causes them to freeze. If they are habituated to the sound, they will not freeze at the sight of the light) This theory is cognitive because it holds that the observed stimulus-response relation is mediated by an inner, mental representation of the original unconditioned stimulus.
  3. Expectancy theory
    Individuals learn to expect the unconditioned stimulus when presented with the conditioned stimulus. This causes the conditioned response.

There are three conditions needed for classical conditioning:

  1. The conditioned stimulus must precede the unconditioned stimulus
  2. The conditioned stimulus must signal heightened probability of occurrence of the unconditioned stimulus
  3. Conditioning is ineffective when the animal already has a good predictor

The failure of conditioning is called the blocking effect. The already conditioned stimulus blocks conditioning to a new stimulus that has been paired with it.

Evaluative conditioning refers to changes in the strength of liking or disliking of a stimulus as a result of being paired with another positive or negative stimulus. (e.g: attractive women being placed in car commercials. Attractive women resemble arousal and the new product of the car company causes the same effect after a while, causing people to be more likely to purchase it

Drug tolerance refers to the decline in physiological and behavioural effects that occur with some drugs when they are taken repeatedly.

Operant responses are responses that operate on the world to produce some effect (e.g: asking for potatoes at dinner, a rat pushing a button to receive some food). They are also called instrumental responses, because they function like instruments or tools, to bring about some change in the environment. The process by which individuals learn to make operant responses is called operant conditioning or instrumental conditioning. Operant conditioning is the learning process by which the effect or consequence of a response influences the future rate of production of that response.

Animals often learn through a trial-and-error process, through which an individual gradually becomes more likely to make responses that produce beneficial effects. Thorndike formulated the law of effect: responses that produce a satisfying effect in a particular situation become more likely to occur again in that situation and responses that produce a discomforting effect become less likely to occur again in that situation.

Operant response is any behavioural act that has some effect on the environment. Reinforcer is a replacement for words such as satisfaction and reward and refers to a stimulus change that follows a response and increase in the subsequent frequency of that response. Conditioned reinforcers are reinforcers that have reinforcing value only because of previous learning, for example, money.

With operant conditioning, the individual generates behaviour that has some effect on the environment, whereas in classical conditioning a stimulus elicits a response from the organism. Operant conditioning can come without awareness of the conditioning and this shows us how people can learn motor skills. We are not aware of the conditioning, but certain behaviour gets reinforced, thus we show that behaviour (e.g: proper motor skills) more often.

If the never individual makes the desired response himself, he can never be reinforced. The solution to this problem is called shaping, in which successively closer approximations to the desired response are reinforced until the desired response finally occurs and can be reinforced. Operantly conditioned responses can be extinguished if the response is no longer reinforced. Just as with classical conditioning, there is no unlearning of the response and there can be a spontaneous recovery of responding and a single reinforced response following extinction can lead the individual to respond again at a rapid rate.

There is a difference between partial reinforcement, in which the response only sometimes produces a reinforcer, and continuous reinforcement, where the response is always reinforced. There are four basic types of partial reinforcement schedules:

  1. Fixed-ratio schedule
    A reinforcer occurs after every nth response.
  2. Variable-ratio schedule
    The number of responses required before reinforcement varies unpredictably around some average.
  3. Fixed-interval schedule
    A fixed period of time must elapse between one reinforced response and the next.
  4. Variable-interval schedule
    The amount of time required before the reinforcement varies unpredictably around some average.

The different schedules produce different response rates because individuals are striving to maximize the number of reinforced responses and minimize the number of unreinforced responses.

Positive reinforcement occurs when the arrival of some stimulus following a response makes the response more likely to occur. The stimulus is also known as a positive reinforcer. Negative reinforcement occurs when the removal of some stimulus following a response makes the response more likely to occur. The stimulus is also known as a negative reinforcer. An individual will work toward a positive reinforcer (money, food) and work to move away from a negative reinforcer (electric shocks, loud noises). Punishment is the opposite of reinforcement. It is the process through which the consequence of a response decreases the likelihood that the response will recur. Positive punishment occurs when the arrival of a stimulus (electric shocks) decreases the likelihood of that response. Negative punishment occurs when the removal of a stimulus (taking away food, money) decreases the likelihood that the response will occur again. Reinforcement always increases the likelihood of the response and punishment always decreases the likelihood of the response.

The overjustification effect is a decline in response because the reward presumably provides an unneeded extra justification for engaging in that behaviour. This causes individuals to show the behaviour for an external reward, not for its own sake. They start perceiving the task as work and when they no longer receive a reward for the task, why would they continue to do the task?

The primary purpose of play is to provide a means for young animals to practice their species-typical behaviour. There are five pieces of evidence for this theory:

  1. Young animals play more than adults do of their species
  2. Species of animals that have the most to learn play the most
  3. Young animals play most at those skills that they need to learn
  4. Play involves many repetitions
  5. Play is challenging

Learning can be divided at least roughly into two broad categories: learning to do (skill learning) and learning about (information learning). Exploration is used to learn about the environment and it differs from play learning because it is not used to learn any skills. Latent learning refers to learning that is not immediately demonstrated in the animal’s behaviour.

Observational learning is learning by watching others. Children learn important social behaviours (social learning) through a process of vicarious reinforcement, the ability to learn from the consequences of other’s actions.

Imitation is copying the observed individual. Stimulus enhancement refers to an increase in the salience or attractiveness of the object that the observed individual is acting upon. Goal enhancement refers to an increased drive to obtain rewards similar to what the observed individual is receiving (e.g: a kitten seeing its mother pressing a lever for food pellets may become attracted to the lever (stimulus enhancement) and motivated to eat food pellets (goal enhancement).

With stimulus and goal enhancement, the individual is not imitating the observed individual, but rather learning quickly, because of the increased attraction to a stimulus and motivated to obtain the same rewards.

Chimpanzees learn by emulation, which involves observing another individual achieve some goal, then reaching that same goal by their own means. With emulation individuals are more focussed on the goal than the means used to achieve it. Humans have mirror neurons; when we observe an individual, the same neurons that become active in the observed individual become active in ourselves. Gaze following is the reflexive action in which humans follow another person’s eyes to look at the same object the other person is looking at.

Food aversion is different from classical conditioning because with food aversion there is a much longer delay between the unconditioned stimulus and the conditioned stimulus. than with classical conditioning. Food aversion fails to occur if the gap between tasting the food and the induction of illness is less than a few minutes. In classical conditioning, almost every stimulus can serve as the conditioned stimulus, but with food aversion learning the stimulus must be a distinctive smell or taste. Some animals are prepared to make associations between food and nausea, so-called prepared behaviours. Unprepared behaviours are behaviours that are acquired through the normal processes of operant conditioning and usually take repeated trials to acquire. Contraprepared behaviours are behaviours that are impossible or difficult to learn despite extensive training. This shows that there are some biological constraints on learning.

There are a couple of evolutionary rules that omnivores use to determine what is safe to eat:

  1. Eat what your elders eat
  2. Remember the smell and taste of a food

Imprinting happens with animals such as chickens, that imprint on a moving object as soon as possible after they hatch.

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Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 9

Psychology by P. Gray and D. F., Bjorkland (eight edition) – Summary chapter 9

In a model on how the memory works there are three types of memory stores:

  1. Sensory memory
    There is some information stored here for a couple of seconds even when you are not paying attention to it (e.g: you can remember things you hear for approximately 4 seconds after you heard it, even if you are not paying attention to it). There is a separate sensory-memory store for each memory system.
  2. Short-term (working) memory
    Information in the working memory is lost within seconds when it is no longer actively attended to. Information can enter the working memory from long-term memory and sensory memory.
  3. Long-term memory
    We are not conscious of information in the long-term memory unless the information has been activated and moved into short-term memory. The long-term memory is passive.

The model specifies a set of control processes, which govern the processing of information within stores and the movement of information from one store to another. The control processes are:

  1. Attention
    This is the process that controls the flow of information from the sensory memory into the working memory. Attention restricts the flow of information because the capacity of the short-term memory is small.
  2. Encoding
    This is the process that controls movement from the working memory to long-term memory.
  3. Retrieval
    This is the process that controls the flow of information from the long-term memory to short-term memory.

Individual mental operations can be placed on a continuum with respect to how much of one’s limited capacity each requires for its execution.

  1. Effortful processes (conscious)
    These processes are available to the consciousness, interfere with the execution of other effortful processes, improve with practice and are influenced by individual differences in intelligence, motivation and education.
  2. Automatic processes (unconscious)
    These processes occur without intention, are not available to the consciousness, don’t interfere with other processes, don’t improve with practice and are not influenced by individual differences in intelligence, motivation and education.

All the sensory information is briefly analysed at an unconscious level and this is called preattentive processing. The preattentive processing helps determine whether something is significant and should be paid attention to. People are able to select what they pay attention to. This is shown in a couple of ways:

  • Selective listening
    This includes the cocktail party phenomenon. We only hear the conversation we want to hear and are not disturbed by other conversations. We cannot fully select what we want to hear though, as we do hear our name the moment someone says it. In the preattentive processing part, this is determined as significant.
  • Selective viewing
    When we look at something we tend to ignore other visuals than the thing we are paying attention to. It is possible to miss a significant event or change because we are paying attention to something else. This is called inattentional blindness.

Auditory sensory memory is called echoic memory and visual sensory memory is called iconic memory. Sensory input can alter behaviour and conscious thought, without itself becoming conscious. This is called priming. Priming is the activation, by sensory input, of information that is already stored in the long-term memory. It is sometimes impossible to not process a stimuli (e.g: it is sometimes not possible to not read a word).

There are three general conclusions that can be drawn from brain studies concerning preattentive processing and attention:

  1. Stimuli that are not attended to nevertheless activate sensory and perceptual areas of the brain
  2. Attention magnifies the activity that task-relevant stimuli produce in sensory and perceptual areas of the brain, and it diminishes the activity that task-irrelevant stimuli produce.
  3. Neural mechanisms in anterior (forward) portions of the cortex are responsible for control of attention.

There are people with spatial neglect, meaning that they are unable to process information in the visual field opposite to the brain hemisphere in which they have a lesion.

The working memory consists of three separate, but interacting components:

  1. Phonological loop
    This is responsible for holding verbal information
  2. Visuospatial sketchpad
    This is responsible for holding visual and spatial information
  3. Central executive
    This is responsible for coordinating the mind’s activities and for bringing new information into working memory from the sensory and long-term stores.

The number of pronounceable items that a person can keep in mind and report back accurately after a brief delay is called the short-term memory span or the phonological loop of working memory. The phonological loop is the part of working memory that holds on to verbal information by subvocally repeating it.  The memory of the working memory is generally two items shorter than the phonological loop.

The working memory is part of executive functions, relatively basic and general-purpose information-processing mechanisms that, together, are important in planning and regulating behaviour and performing complex cognitive tasks. The executive functions consist of three related components:

  1. Working memory
    Updating, monitoring and rapidly adding/deleting the contents of the working memory.
  2. Switching
    Shifting flexibly between different tasks or mindsets.
  3. Inhibition
    Preventing a cognitive or behavioural response or keeping unwanted information out of mind.

There are four general conclusions about executive functions:

  1. Executive functions show both unity and diversity
    The executive functions are separate functions but correlate strongly with each other.
  2. There is a substantial genetic component to executive functions
    The heritability of executive functions is quite high.
  3. Executive functions are related to and predictive of important clinical and societal outcomes
    People who perform better on tasks of executive functions have fewer behavioural problems.
  4. There is substantial developmental stability of executive-function abilities
    Although the functions improve, children who perform well on tasks with executive functions tend to perform well on these tasks as adults.

Memory refers to all the information in a person´s mind and to the mind´s capacity to store and retrieve that information. There are two types of memory:

  1. Explicit memory
    This is the memory that can be brought into a person’s consciousness. It is also called declarative memory. This is memory we are aware of.
  2. Implicit memory
    This refers to memory that we are not aware of. Implicit memories are much more closely tied to the context of the specific stimuli, tasks or problems to which they pertain.

There are two types of explicit memory:

  1. Episodic memory
    This is memory from one’s own past experiences. Episodic memories have a personal quality.
  2. Semantic memory
    This is general knowledge. There is no personal quality attached to these memories. These memories are more stable and less often forgotten.

The spreading activation model of explicit memory shows that words that are related to words seen earlier are thought of more often than words that are not related (e.g: after hearing the colour red and then asked for a flower they say rose more often than when they are not presented with the colour red first).

There are two types of implicit memory:

  1. Classical conditioning effects
    These are memories that lead people to unconsciously react to certain conditioned stimuli.
  2. Procedural memory
    These include motor skills, habit and unconsciously learned rules (e.g: riding a bicycle).

Any loss of long-term memory, usually resulting from some sort of physical disruption, is called amnesia. The inability to create new memories is called temporal-lobe amnesia, which is strongly correlated with damage to the hippocampus. With temporal-lobe amnesia, skill learning is not affected. People can recall nothing or barely anything from their infant years and this is called infantile amnesia.

There are two types of rehearsal:

  1. Maintenance rehearsal
    This is the process by which a person holds information in working memory for a period of time
  2. Encoding rehearsal
    This is the process by which a person encodes information into the long-term memory

There are several ways in which encoding is promoted:

  1. Elaboration
    This is also called elaborative rehearsal and promotes encoding.
  2. Organization
    This can be done through the procedure known as chunking, grouping several single items together to make them a single item. (e.g: remembering the letters b b c u v a n b c is more difficult if trying to remember it letter by letter, but easier if trying to remember it as bbc, uva and nbc).

Anterograde amnesia is the loss of capacity to form long term memories of events occurring after the injury. Retrograde amnesia Is loss of memories of events that occurred before the injury. Long-term memories are encoded in the brain in two forms: a labile, easily disrupted form and a stable, not easily disrupted form. Consolidation occurs the labile memory form is converted into the stable form. 

Sleep is important for the consolidation of memories, especially the slow-wave in the deep sleep stage.

Memories are linked to each other through associations. A stimulus or thought that becomes a particular memory is a retrieval cue for that memory. There are two principles of association:

  1. Association by contiguity
    Some concepts are associated because they have occurred contiguously (e.g: plate is associated to napkin because they occur contiguously).
  2. Association by similarity
    Some concepts are associated because they are similar to each other (e.g: apple is associated with pear because they are similar. They are both fruits).

Schema refers to one’s generalized mental representation, or concept, of any given class of objects, scenes or events (e.g: western people might share a schema for a living room). Schemas that involve the organization of events in time, rather than objects in space, are called scripts (e.g: a typical night out).

Leading questions can cause false memories to be created. Memories are often adapted to the schemas and scripts in the mind of a person. The word choice is also important in memories and the word choice can determine memories.

There are two possible causes of false memory construction:

  1. Source confusion
    We hear many different stories of an event and may be confused about the hierarchy of the sources over time. This causes us to believe that a story about an event is closer to the truth than the first-hand experience you have yourself. Leading questions and implied meanings are important here (e.g: the roadworker said ‘crash’, so the speed must’ve been great, although you saw the cars just bump each other).
  2. Social pressure
    This can lead to the construction of false memories as well.

Prospective memory is memory about things we still have to do in the future. There are two types of prospective memory:

  1. Time-based prospective memory
    This involves remembering to perform a particular action when cued by a target time (e.g: answering e-mails in the evening).
  2. Event-based prospective memory
    This involves remembering to perform a particular action when cued by a target event (e.g: sending someone a text message next time you see them).

There are three phases in prospective memory: an intention, the intention must be maintained and there must be a switch from the ongoing task to execute the intention.

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Introduction to Psychology - Year 1 Psychology UvA

Introduction to Psychology

This page bundles the study guides and additional learning materials for the 'Introduction to Psychology' course at the University of Amsterdam as wirtten by JesperN, the material might be a little outdated for you. Therefore, please check the difference in edition to ensure there are no unforced errors in your own work.

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