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Holland and Straub
Supports S-S. Food aversion when paired with noise
Holland
Supports S-S. Aversion to food when paired with tone, as tone was previously paired with illness
Cunningham and Rescorla
Supports S-S. Sensory preconditioning. Aversion to sugar, as acid was paired with illness and sugar and acid were previously paired together
Fudim
Sensory preconditioning. Ate more banana when craved salt as previously paired together
Rescorla and Freberg
S-S associations acquired during sensory preconditioning are subject to extinction
Colwill and Rescorla
Outcome devaluation to discriminate between R-O and S-R. Supports R-O
Verway
Supports S-R. Based on features (line orientation and colour). S-R was found for line orientation but not colour. Due to long term development
Mackintosh
Overshadowing in conditioned suppression. More fear to light if only light was paired with shock than if both light and noise were paired with shock
Kamin
Blocking in conditioned suppression. More fear to noise if both light and noise were paired with shock than if light had first been paired with shock
Rescorla (contingency)
High contingency = high fear
Rescorla and Wagner
Role of surprise. Based on summation
Westbrook and Lovibond
Disagrees with S-S models (due to expectancy differing from memory).
CR may not be the same UR (Preparatory vs protective, drug administration, context shift for fear)
CR varies as a function of the CS-US interval (Hierarchy of defensive distance)
Mixed evidence on failures of US revaluation (disagrees with S-R)
Expectancy = performed better than those with only food memory (challenges SoP A2 state)
The perruchet effect in humans (expectancy and gamblerās fallacy
Problems with HeiDI and other stimulus substitution models as a combination of factors determines which CRs are triggered by US
Ommission effect = suggests reflexive model
Overall = integrated expectancy model is most likely (supports S-S with the specific role of expectancy; allows for differences in CR and UR by suggesting a specific expectancy state)
Zimmerhart and Rescorla
Extinction of conditioned inhibition. Inhibitory properties donāt diminish when presented alone
Rescorla; Pearce and Redhead
Superconditioning. Increased response intensity when stimulus is really surprising
Kremer; Rescorla and Wagner
Overexpectation. Lambda<SumV = associative strength decreases
Reiss and Wagner
Preexposure retards acquisition of both excitatory and inhibitory conditioning
Pearce and Hall (attention)
Controlled and automatic attention. Greater attention if previous trial has large expectancy discrepency. Habituation and latent inhibition reflect decline in attention. Consistent consequences lead to latent inhibition. Partial condition = increased attention. BUT does not account for context specific latent inhibition
Lovibond, Preston and Mackintosh
Contextual specificity of latent inhibition. If rats with preexposure changed context, they no longer showed latent inhibition
Wagnerās SoP model
Inactive = waiting to be activated
A1 = elicts UR, initial reaction
A2 = less effective processing, secondary activation, like habituation and latent inhibition
Inactive ā A1 = Presentation of novel stimulus
Inactive ā A2 = multiple stimuli (e.g. tone and shock, tone goes to A1, memory of shock stored in A2)
A1 ā A2 = rapid decay. Short term habituation
A2 ā inactive = decay
If preexposure of a stimulus = will be in the A2 thus less likely to cause UR or be learnt about (habituation and latent inhibition)
Honey, Good and Manser; Honey and Good
Context specificity of habituation. Increased attention in different context but decreases quickly to same level as same condition
Pavlov (stimulus substitution)
CR to the CS often resembles UR of the US
Problem = CR does not always resemble UR and can be influenced by the natures of the CS
Problem = Different measures provide the basis of drawing potentially opposite conclusions about associative strength
HeiDI model
Solves Pavlovās stimulus substitution problems
Reciprocal associations allow conditioning to be affected by properties of both CS and US
Mitchell and Hall
Applications of discrimination learning to perceptual learning in humans
Strong evidence of Rescorla; Mackintosh; and Hebbian theories of discrimination
Presence of feedback links to human perceptual learning
Preexposure of a stimulus in rats leads to better performance of discrimination (particularly difficult to discriminate)
Likely partly due to latent inhibition (but cannot fully explain it)
Pavlov (stimulus generalisation)
If you create a CS then the CR will happen to a stimulus that's close enough to the CS (but to a lower extent)
Hilgard and Marquis
Discrimination is needed when it leads to different outcomes
Rescorla-Wagner rule
Elemental theory of discrimination
Discrimination occurs when the unique element leads to positive and the other unique element leads to negative (common element remains neutral)
Problems: does not explain negative patterning (except with configural cue); lack of catastrophic interference; does not account for similarity (based on summation)
Wilson and Pearce
Lack of catastrophic interference. If A+ and AB- (will respond less to AB-). Then B+. Does not remove discrimination of AB-
Redhead and Pearce
Similarity in discrimination learning. If A+, BC+, ABC-; then BC+ is harder to discriminate than A+ due to increased similarity to ABC-
Pearce (configural theory)
Compares stimulus to memory of stimuli
Strength of CR will depend on similarity
Smith et al
Suggests categorisation is due to a combination of exemplar and prototype theory with categorisation rules
Largely disagrees with exemplar because when prototype was directly compared to exemplar, prototype was almost always more accurate
However the XOR task forces exemplar and showed 75% accuracy
COVIS model uses neuroscience to suggest category rules (Similar to humans and that requires some verbal system so primates perform better than pigeons)
Neuroscience suggests that exemplar and prototype use distinct brain regions and starts with exemplar then moves to prototype as training continues
Transfer on rule-based task but not information-integration tasks suggesting categorisation rules
Lots of evidence of concrete categorisation
Hernstein et al
Cerella
Watanabe et al
Scarfa et al
Rote learning as an explanation for categorisation
Not a good explanation as categorisation occurs with novel stimuli
Feature learning as an explanation for categorisation
Most likely explanation.
Edited photos and removed features (pigeons categorised based on subtle colour feature)
Works for novel stimuli
Exemplar theory for categorisation
Similar to rote learning
Issue: scrambling is not catastrophically disruptive (suggesting feature or prototype theory)
Support: Scrambling can be disruptive even if features are preserved but breaks configuration (could be a potential support for prototype theory)
Abstract categorisation
Matching to sample = āsamenessā but could be rote learning
Evidence that only some species can do this (mainly primates)
Issues with matching to sample = could be based on familiarity
Inside/outside = relationship not familiarity, took a while until pigeons were able to learn so maybe not abstract
Bar height = took so long to learn it suggests rote
Anecdotal support
Second-order = forced relationship but not familiarity. Initially only those with language ability could do it but then non-language chimps were able to complete it, if it was adjusted
Harrison et al
Cultural evolutionary theory = adaptive value of information to naive individuals
Some evidence of normative conformity (similar to humans)
Homophily has been found
Imitation and mimicry improve social relations
Webster
Non-grouping animals also show social learning
Although method of doing so is more indirect (e.g. scent markers)
If direct observation they take longer to learn
Galef
Socially acquired food preferences
Stimulus enhancement (does not create preference but increases interaction with cue)
Mate selection (quails)
Social facilitation and stimulus enhancement not imitation (bottle caps)
Preferences can occur prenatally
Hayes and Hayes
Do as I do test (imitation)
Animals imitation as it caused them to be fed (methodological issue?)
Akins et al (imitation)
Move screen either left or right (only saw it moved one way)
Akins et al (two action control)
Showed imitation
Either jump or pecked treadle
Mineka and Cook; Cook and Mineka
Fear of predators
Found learning was necessary and the monkeys did not have an innate fear of snakes
Had experienced monkey react fearfully to snake and naive monket watched the experienced monkeyās reaction
However when replicated with neutral stimulus suggesting itās specialised
Suggesting āpreparednessā or āselectiveā learning
Selective Conditioned taste aversion
Does not matter what causes the illness, rejection of food still happens (e.g. even when the real source of illness is known people still dislike paired flavours)
Ease of association = itās easier to associate food with illness than light/etc
Palatability = looked at pairing sucrose with either LiCl or shock. Both led to rejection of the sucrose but the orofacial reactions differed (disgust for LiCl and positive for shock). Suggesting dissociation between taste reactivity and consumption reinforced idea that CTA is about rejecting foods paired with illness.
Similar findings have been found in humans
However, limited research and contrary evidence exists (such as context cues and learning about context blocks learning about tastes, suggesting there is something unique but not selective learning)
Foote et al
Rats showed metacognition (refused to do tasks that they deemed too difficult)
But failed to create a model to exclusively explain metacognitive behaviour
Krupenye
Suggests studying ToM has human applications as we are unsure if ToM is due to inhibitory control
Evidence of chimps showint ToM by hiding food
Blue jays food preference
When accounted for cognitive demands chimps were able to complete false belief tasks
Gallup et al (issue with mirror test)
Found issues with many self-recognition tasks (mainly mirror tests) i.e. misinterpreting results, ambiguous results
Acknowledges there is some strong evidence of chimps possessing self recognition
Hopkins
Cortical thickness = improves performance on mirror tests
Gallup (mirror test)
Apes, elephants and dolphins were able to complete mirror test (although elephants and dolphins required preexposure to mirror)
Some evidence of fish being able to pass the test
Studies for Associative structures in simple conditioning
Holland and Straub
Holland
Cunningham and Rescorla
Fudim
Rescorla and Freberg
Colwill and Rescorla
Verway
Studies for conditions of learning
Mackintosh
Kamin
Rescorla (contingency)
Rescorla and Wagner
Westbrook and Lovibond
Studies for introduction to theories of learning
Westbrook and Lovibond
Zimmerhart and Rescorla
Rescorla; Pearce and Redead
Kremer; Rescorla and Wagner
Studies for attention
Westbrook and Lovibond
Reiss and Wagner
Pearce and Hall (attention)
Lovibond, Preston and Mackintosh
Wagner (SoP)
Honey, Good and Manser; Honey and Good
Studies for the expression of learning in behaviour
Westbrook and Lovibond
Pavlov (stimulus substitution)
HeiDI
Studies for discrimination learning
Mitchell and Hall
Pavlov (stimulus generalisation)
Hilgard and Marquis
Rescorla-Wagner rule (elemental theory)
Wilson and Pearce
Redhead and Pearce (similarity)
Pearce (configural)
Studies for categorisation
Smith et al
Lots for concrete
Mixed for abstract
Studies for Social and selective learning
Harrison et al
Webster
Galef
Hayes and Hayes
Akins et al (imitation - screen door)
Akins et al (imitation - two action control)
Mineka and Cook; Cook and Mineka
Selective conditioned taste aversion
Studies for animal minds
Foote et al
Krupenye
Gallup et al (issues)
Gallup (mirror)
Hopkins
Ostojic et al
Ostojic et al
Scrub jays gave mate food that they showed a preference for