Questão | Responda |
Psychophysics | The relationship between physical stimuli and their subjective or psychological correlates |
Transduction | Converting physical stimuli to nerve impulses |
Chemical senses | Gustation Olfaction |
Body Senses | Somatosensation Equilibrioception |
Somatosensation | Taction/Haptics Proprioception |
How much of the cortex is involved in visual processing? | 50% of the cortex |
Failure in recognition due to failure in perception | Apperceptive agnosia |
Failure in recognition despite successful perception | Associative agnosia |
Hierarchical Processing | Neural impulses travel "up" the system to the cortex |
Top down processing | Prior knowledge influences what is perceived |
Bottom-up or Top-down processing? | Forward, backward and lateral connections in the visual pathway demonstrate information can flow in all directions |
Selectivity | Cells respond most to stimuli with certain properties |
Tuning | A cell is "tuned" to the dimension of a stimulus that generates the strongest response |
Organisation | Within sensory brain regions there's often an orderly progression of stimulus preferences |
Cortical magnification | Larger amounts of cortex are devoted to processing more important stimulus values |
Doctrine of specific nerve energies | => Each sense projects onto a specific cortical area => The nature of sensation depends on which sensory fibres are stimulated (Müller, 1838) |
Noise | Neural firing is stochastic (random) -Noise interferes with measurement of responses to stimuli |
Spontaneous Activity | Cells fire a little even with no stimulus |
Detectability | How easy a stimulus is to detect. More intense stimuli are easier to detect |
Detection Threshold | The minimum intensity required for detection |
Absolute Threshold | The minimum intensity required for detection |
Sensitivity | Opposite of threshold (1/threshold) |
Method of Adjustment (MoA) Detection | Adjust a stimulus until subject can just see it =>Not reliable, people cheat |
Method of Constant Stimuli (MoCS) Yes-No Paradigm | -Vary stimulus intensity -Subjects respond if they can detect it -Plot the psychometric function (curved due to noise) =>Threshold is the point where detectability is 50% |
Method of Constant Stimuli (MoCS) 2AFC Paradigm | Subjects respond if stimuli was detected in one of two fields =Threshold at 75, as there is 50% chance of correct guesses |
Measuring Magnitude: Estimation Technique | "Modulus" stimuli presented, acts as a reference for sensory magnitude -Following stimuli rated by subject compared to modulus which is rated "10" |
Compressive non-linear functions | If intensity is increased 2x, sensory magnitude increases <2x (Except for electric shock) |
Discrimination | Perceiving the difference between two stimuli |
Discrimination threshold | The minimum difference between two stimuli for discrimination =>Just noticable difference |
Precision | Degree to which repeated measurements show the same result =>Relates to discrimination threshold |
Accuracy | Degree to which measurements match the true value of a stimulus =Relates to Bias |
Bias | Something external to stimulus which changes the way it is perceived =>Sometimes called the "point of subjective equality" (PSE) |
Method of adjustment (MOA) Matching | Measuring discrimination -Adjust a probe stimulus until it matches the test stimulus -Slightly different settings each time (noise) |
Method of adjustment (MOA) Matching => Accuracy | Represented by the mean of several settings -Good result if mean probe settings are close to true test setting -Poor results are said to be biased |
Method of Adjustment (MoA) Matching -Precision | Represented by the 'spread' of probe settings (eg. standard deviation) -Low spread = good discrimination ability |
Adaptation (4 consequences) | Prolonged stimulation decreases rate of firing => Increases detection threshold for similar stimuli =>Reduces perceived intensity =>Rate at which magnitude rises with stimulus intensity is increased =>Perceived properties of similar stimuli can appear biased |
Anatomical Research Methods | Examining dead brains |
Anatomical research methods: staining dead brains (3 features) | => Reveals axons/connections => Reveals cell body density & size => Reveals activity (cytochrome oxidase) |
Recording techniques: Single cell recording | Electrode attached to single brain cell -Invasive -Anaesthetised or awake (microstimulation) -High spatial and temporal resolution -limited information (only one cell) |
Recording techniques: Optical imaging | Filming a working brain with a colour sensitive camera -Blood flow increases to active areas => Active areas become more red -Invasive -Only a small area visible -Slow response to stimulus |
Visually evoked potential | Presenting a visual stimulus and measuring the brain's response |
Magnetoencephalography (MEG) | Superconducting quantum interference device (SQUID) -Non Invasive -Measures magnetic fields in the brain -High temporal resolution -Moderate spatial resolution |
Electroencephalography (EEG) | Electrodes on the scalp detect changes to electric fields in the brain -Non invasive -High interference from skull -Low spatial resolution -High temporal resolution |
Positron Emission Tomography (PET) | Injecting radioactive dye and tracking it through the brain -More radioactive blood goes to active areas so is detectable -Non invasive -Moderate spatial resolution -Low temporal resolution |
Functional Magnetic Resonance imaging (fMRI) | Use powerful magnet to detect differences between oxygenated & deoxygenated blood in brain -Moderate spatial resolution -Low temporal resolution -Non-Invasive |
Anatomical Research Methods: Lesions | Destroying (ablating) parts of the brain with neurotoxins (for specific pathways) or surgery (for specific areas) and studying what happens -Invasive |
Anatomical Research Methods: Human Brain Lesions (Neuropsychology) | Studying living humans with damaged brains. -Damage is usually diffuse -Damage to fibres can affect areas far from lesion -Brains recover from damage (plasticity) -Correct tests are neccessary |
Transcranial Magnetic Stimulation (TMS) (3 properties) | Temporary magnetic field "knocks out" cells over a broad area of the brain -Temporary -Temporally precise -Spatially imprecise |
Axon | Also known as Nerve Fibre -Long slender projection of a nerve cell (or neuron) -Conducts nerve impulses away from the cell body -In some sensory neurons, electrical impulses travel UP the axon to the cell body |
Action Potential | A nerve impulse -Electrical membrane potential rapidly rises and falls back to resting potential -ion channels on the axon open, allowing sodium ions to gush inside, causing a rise in the electrochemical gradient -The polarity of the plasma membrane then reverses, closing the ion channels -Sodium ions actively transported out -Potassium channels open and potassium ions are released (Repolarisation) |
Grey Matter | Neuronal cell bodies, with relatively few myelinated axons |
White matter | Mostly glial cells and myelinated axons that transmit signals from one region of the cerebrum to another and further on |
Neurotransmitters | Endogenous chemicals that transmit signals across a synapse from one neuron (nerve cell) to another "target" neuron |
Psychometric Function | Describes the relationship between a parameter of a physical stimulus and the subjective responses of the subject (eg. visual acuity) |
Suprathreshold | Stimulus of sufficient intensity to generate a response |
Thalamus | Symmetrical structure between the cerebral cortex and midbrain -Relays sensory and motor signals to the cortex -Regulates consciousness/sleep/alertness |
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