Localisation of brain function
Different areas of the brain are responsible for different behaviours, cognitive processes or activities
Brain lobes
Frontal lobe, parietal lobe, occipital lobe, temporal lobe
Frontal lobe
Front section of the brain, contains: Broca's area (left hemisphere), motor cortex.
Parietal lobe
Top middle section of the brain, contains: somatosensory cortex. Separated from frontal lobe by central sulcus
Occipital lobe
Back of the brain, contains: visual centres
Temporal lobe
Bottom middle of the brain (by your temples), contains: primary auditory cortex, Wernickes area (left hemisphere)
Somatosensory cortex
Processes input from sensory receptors in the body that are sensitive to touch. Produces sensations of touch, pressure, pain and temp which it localises to specific body regions
Visual centres
Receives and processes visual information, visual cortex contains several different areas, with each processing different types of visual info, e.g. colour, shape, movement
Auditory centres
Analyses speech-based info, i.e. hearing. Damage to auditory cortex may cause hearing loss; more extensive damage = more extensive loss
Motor cortex
Responsible for generation of voluntary motor movement. Different parts of it contain different parts of body, they're arranged logically next to each other.
Broca's area
Responsible for speech production
Broca's aphasia
Speech production is affected, not understanding. Often speak in short, not very fluid, but meaningful sentences which take great effort
Wernicke's area
Responsible for understanding language
Wernicke's aphasia
Speak fluidly but its often nonsense, words that don't make sense
Aphasia
Inability to use or understand language because of brain damage
Strengths of localisation of brain function
Supporting evidence - Phineas Gage (frontal lobe = personality = support); studies of people with Broca's and Wernicke's aphasia, had damage to that area = support as language areas are localised
Weaknesses of localisation of brain function
Undermining evidence - Lashley removed areas of cortex in rats that were learning to complete a maze, no part more important than another - learning is too complex to be localised = processes can be more holistic
Lateralisation of brain function
When some functions are dominated by one hemisphere
Functions of left hemisphere
Control of right side of body, right visual field, speech, understanding written + spoken language, logical thinking, analytical tasks
Functions of right hemisphere
Control of left side of body, left visual field, spatial awareness, creativity, recognising faces, musical ability, emotional content of language, drawing
Cerebral cortex
The outer layer of both hemispheres
Corpus callosum
The thick bundle of nerves that connects the two hemispheres
Sperry and Gazzinga's aim and method
11 individuals who had their corpus callosum severed to treat severe epilepsy. Showed stimuli to one hemisphere using a tachistoscope and compared how they did to a control who didn't have epilepsy.
Sperry and Gazzinga: describing what you see
Pic of object shown to left or right visual field, right = easily named, left = couldn't describe it - often said nothings there
Sperry and Gazzinga: recognition by touch
Object shown to left visual field, asked to choose matching object from a bag using only left hand - could select matching object but not describe it
Sperry and Gazzinga: composite words
2 words simultaneously show, 1 to left and 1 to right visual field, asked to say what it was or draw it if couldn't see it. Could write/draw left 1, say right 1
Sperry and Gazzinga: matching faces
Shown different faces to each visual field, asked to match it to one from a series of others, one shown to right hemisphere selected, one to left ignored. Also shown composite faces (made of 2) - half shown to left hemisphere dominated description, half shown to right selected more
Strength of split-brain research
Highly specialised, standardised procedure - using tachistoscope to flash image for 1/10th sec - ensured only one hemisphere saw the task/object = high internal validity and can be used to establish cause and effect
Weaknesses of split-brain research
Small sample, all of which had epilepsy, could have unique brain changes that effect the results = lacks validity + data = artificially produced = lacks mundane realism; lateralisation isn't fixed - healthy older adults had less lateralisation = older peoples brains recruit both hemispheres to maximise processing power
Plasticity
The brains tendency to change and adapt (functionally and structurally) as a result of experiences, new learning or training. Functional plasticity decreases with age
Functional recovery
The brains ability to redistribute or transfer functions usually performed by damaged areas, to not damaged area(s)
Spontaneous recovery
Functional recovery occurs quickly after trauma, but slows down after several weeks/months
Neural reorganisation
The transfer of functions to undamaged areas
Neural regeneration/axon sprouting
When new neurons may grow and/or new connections may form to compensate for the damaged areas where neurons are lost
Functional recovery plasticity
Allows the brain to cope better with the 'indirect' effects of brain damage, e.g. swelling, haemorrhaging
McGuire et al
Looked at the brains of London cab drivers who had taken 'The knowledge': found significantly more volume of grey matter in posterior hippocampus compared to a control
Draganski et al
Brain scanned students 3 months before and after an exam, found changes in the posterior hippocampus and parietal cortex, presumably because of the exams
Kuhn et al
Compared a control group with a group that trained for 2 months, playing super mario for at least 30mins per day: found they had significant increase in grey matter in the cortex and hippocampus compared to a control
Strengths of plasticity and functional recovery
Supporting evidence: McGuire et al, Kuhn, Draganski = suggest brain changes + adpats functionally = supports theory; real world application, can be used in neurorehabilitation =
Weaknesses of plasticity and functional recovery
Schneider et al found patients with college equivalent education were 7x more likely to be disability free 1 year after a moderate - severe brain injury than those who didn't finish high school = education may influence how the brain functionally adapts = moderating factor.
Spatial resolution
The smallest feature (or measurement), greater spatial resolution to allow discrimination between different brain regions with greater accuracy
Temporal resolution
The accuracy of the scanner in relation to time (how quickly it can detect changes in brain activity)
fMRI
Measures the blood flow in the brain when a task is performed - most active neurons requires most energy = more oxygen needed = more blood flow. Creates dynamic 3D map of brain
Strengths of fMRIs
Non-invasive unlike PET scans = more patients able to have one = more data = more understanding of localisation of function; Good spatial resolution (1-2mm) = can determine areas of function with greater accuracy
Weaknesses of fMRIs
Poor temporal resolution (1-4 secs) = unable to predict with high accuracy the onset of brain activity; Don't provide direct measure of neural activity - changes in blood flow indicate activity, but can't associate it with a specific function
EEG
Measures electrical activity on surface of brain - electrodes placed on scalp, detecting small electrical charges from neural activity directly underneath them. Looks at general brain activity
ERP
Uses statistical averaging technique to show only the responses that relate to a specific stimulus presented to the patient. Repeated many times, with responses averaged together to eliminate extraneous activity
Strengths of EEGs
Used in clinical diagnosis, e.g. epilepsy = useful for diagnosing people = real world application; high temporal resolution (detect changes at 1 millisecond) = accurately measure particular task with associated brain activity; cheap = large sample sizes = higher external validity
Weaknesses of EEGs
Only detect superficial brain activity = can't look at deeper parts, e.g. hippocampus = can't ethically implant electrodes in brain to measure with humans, but can with animals; poor spatial resolution - can't pinpoint where electrical signal originated from = unable to distinguish between activities from different but adjacent parts
Strengths of ERPs
Measure processing of stimuli in absence of behavioural response, e.g. reaction to seeing an unfamiliar object = can monitor processing of stimulus without requiring person to respond
Weaknesses of ERPs
Lack validity as can't completely eliminate background noise, materials etc = could be influenced by extraneous variables, so cautious generalising
Post-mortems
Analysing the brains of someone after they've died, most likely if they have a rare disorder/have experienced unusual deficits in mental processes or behaviour. Areas of damage examined to try and correlate to structural abnormalities.
Strengths of post-mortems
More detailed exam of anatomical and neurochemical aspects of brain, e.g. areas like hippocampus and hypothalamus; Contributed massively towards understanding of key processes in the brain, e.g. making link between language and the Brocas and Wernickes areas
Weaknesses of post-mortems
Can't establish cause and effect as: only shows physiology, not actual brain activity; many confounding influences, e.g. disease, time between death and examination, medications, age. Retrospective = can't follow up on interesting findings = difficult to explain all behaviours
Biological rhythms
Cyclic changes in body activity
Circadian rhythms
Type of biological rhythm where a pattern of behaviour occurs, or reoccurs, approx. every 24 hours. Its set and reset by environment (light and temp), e.g. sleep wake cycle
Siffre (1962)
Spent time underground (no natural light, sounds) for 2 and 6 months (he did it twice). Found that his biological rhythm settled to 25 hours, with him falling asleep on a regular basis
Aschoff and Wever (1976)
Group of participants spent 4 weeks in a WWII bunker (no natural light). Most had a 24-25 hour circadian rhythm, but one had a 29 hour one
Strengths of circadian rhythms
Practical application to shift work - many practical + economic implications as can maintain worker productivity + prevent workplace accidents; Practical application to pharmacokinetics - can give drugs at optimal times using circadian rhythms = useful for timing drug dosing; supporting evidence (Siffre) = increased validity
Weaknesses of circadian rhythms
Issues with case studies (Siffre and Aschoff & Wever) = lacks external validity as small sample, doesn't look at gender or age influence; poor control in studies, e.g. only assuming natural not artificial light having an influence = lacks validity
Endogenous pacemakers
Internal body clocks, control the SCN and pineal gland for the circadian sleep-wake cycle
Exogenous zeitgebers
External cues that affect our biological rhythms, e.g. light on sleep-wake cycle
Ep supporting evidence
DeCoursey: destroyed SCN in 30 chipmunks = sleep-wake cycle disappeared; Ralph: bred mutant hampsters with 20 hour sleep wake cycle, transplated SCN tissue to normal ones and their sleep wake cycle became 20 hours
Ez supporting evidence
Campbell and Murphy: 15 participants were woken by light being shone on back of knees = change in sleep-wake cycle without eyes seeing light; Burgess: exposure to bright light before east-west flight reduced period of jet lag
Strengths of Ep and Ez
Supporting evidence; real life applications to reducing jet lag
Weaknesses of Ep and Ez
Issue of generalising animal studies to humans, especially due to ethics; lack of reliability found for Ez results; total isolation of Ep and Ez unlikely = lacks validity
Infradian rhythms
Infrequent - biological rhythm with duration of over 24 hours, e.g. the menstrual cycle
Menstrual cycle
approx. 28 days, ovulation occurs in middle when oestrogen is highest, next progesterone increases to prep for pregnancy, if pregnancy doesn’t occur egg is absorbed and leaves with womb lining
Stern and McClintock
29 women with irregular periods, collected pheromones from 9 from armpit using cotton wool, other 20 had it rubbed on their upper lip; pads were collected on different days of the cycle: 68% experienced changes to their menstrual cycle which bought it closer to their ‘donors’
Ultradian rhytms
Biological rhythm that lasts less than 24 hours, e.g. stages of sleep
Sleep cycle
Has 5 stages it goes through (1-4, REM) that altogether spans 90-120 mins
Stage 1
Light sleep, easily awoken, mucscles less active, eye movement slows, can suddenly twitch; have alpha (restful) and theta (between sleep and wake) brainwaves
Stage 2
Between light and deep sleep, breathing + heartrate slows; slower brainwaves, mainly theta
Stage 3
Deep sleep begins, muscle activity decreases; slow delta waves, but also some fast ones
Stage 4
Deep sleep (very hard to be awoken); almost all delta waves
REM
Dreaming occurs, eyelids can be seen flickering; brainwaves reach similar levels to when awake
Strengths of ultradian/infradian rhythms
Supporting evidence (Derment and Kleitman stages of sleep + Ericsson BRAC + Stern and McClintock); evolutionary value to Stern and McClintock’s findings
Weaknesses of ultradian/infradian rhythms
Differences in sleep is often environmental not biological
Central nervous system
The brain and spinal cord - processes + interprets information and reacts to it
Peripheral nervous system
Transmits info to and from CNS, contains autonomic and somatic nervous system
Autonomic nervous system
Controls involuntary functions, includes: sympathetic and parasympathetic nervous system
Sympathetic nervous system
Mobilises the body for action, energy output and is primarily involved in responses that help us deal with emergencies (flight or fight)
Parasympathetic nervous system
Conserves energy, maintains quiet state - restores normal physiological functioning when danger has passed
Neuron
Cells of the nervous system that process and transmit messages through chemical and electrical messages/signals
Sensory neuron
Carry messages from sensory receptors via the PNS to the CNS
Relay neuron
Connect with other neurons, e.g. allow sensory and motor neurons to communicate with each other. When impulses reach brain, they're translated into sensations so the organism can work out how to respond
Motor neuron
Connect CNS to effectors, e.g. muscles, glands. Located in CNS and their axons spread outside it to directly or indirectly control muscles
Synaptic transmission
Action potential reaches presynaptic terminal, triggers synaptic vesicles, release neurotransmitters into synaptic gap, diffuses across, binds to post-synaptic receptor on post-synaptic dendrite, converts chemical to electrical impulses, repeats. Effects terminated by reuptake (neurotransmitters absorbed by pre-synaptic neuron, stored in vesicles for later use)
Excitatory neurons
Causes excitation of the post-synaptic membrane = more likely to fire an action potential (on switches), e.g. Noradrenaline
Inhibitory neurons
Causes inhibitory post-synaptic potentials (IPSPs) = less likely to fire an action potential (off switches), e.g. Serotonin
Summation
Exhibitory and inhibitory influences are summed together
Endocrine system
A network of glands throughout the body that manufacture and secrete hormones: 'a chemical system of communication'
Glands
A group of cells in an animals body that syntheses substances for release into the bloodstream
Hormones
Chemical messengers that travel throughout the bloodstream to target sites and cells
Key functions of pituitary gland
Produce hormones that control release of hormones from other glands; regulated many bodily functions
Hormones released by pituitary gland
Oxytocin, ACTH, LH + FSH
Effect of oxytocin on behaviour
Stimulates contraction of the womb in childbirth and is important for mother-infant bonding
Effect of ACTH on behaviour
Stimulates adrenal glands to release cortisol in response to stress
Effect of LH and FSH on behaviour
Stimulates the ovaries to produce oestrogen and progesterone. In males, stimulates testes to produces testosterone
Key functions of adrenal glands
Supports bodily functions, e.g. cardiovascular and anti-inflammatory functions; causes physiological changes associated with arousal + prepares body for fight or flight