J. Devlin 1,2, C. Moore 1,3, C. Mummery 1, J. Phillips 1, M. Gorno-Tempini 1, U. Noppenney 1, K....
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Transcript of J. Devlin 1,2, C. Moore 1,3, C. Mummery 1, J. Phillips 1, M. Gorno-Tempini 1, U. Noppenney 1, K....
J. Devlin1,2, C. Moore1,3, C. Mummery1, J. Phillips1, M. Gorno-Tempini1, U. Noppenney1, K.
Friston1, R. Frackowiak1, and C. Price1
1Wellcome Department of Cognitive Neurology2Functional Magnetic Resonance Imaging of the Brain
3Institute of Psychiatry
Is there an anatomical basis category specificity?
Cognitive theories of category specificity
Semantic theories
Evolutionary account: Individual categories recruit distinct neural regions. (Caramazza & Shelton, 1998)
Perceptional/functional account: Perceptual and functional attributes localised in different regions. (Warrington & Shallice, 1984)
Cognitive structure account: Undifferentiated semantic system at a neural level (Tyler et al., in press)
Cognitive theories and neuroimaging
Anatomical hypotheses can be best evaluated by functional neuroimaging, however, the findings to date are very variable Living things > man-made items -- only three areas identified in more
than one study: 1) bilateral anterior temporal poles(refs), 2) right inferior parietal lobe (refs), and 3) left lingual gyrus (refs)
Man-made items > living things -- three areas seen in more than one study: 1) left posterior middle temporal cortex (refs), 2) left pre-motor cortex (refs), and 3) left lingual gyrus (refs)
All other areas have been seen in only a single study
We hypothesized that this variability was due to small, context-specific effects and investigated this using a multi-factorial analysis
Design
Data from 7 PET studies of category specificity
Study Categories Stimuli Task
1. Mummery et al (1996) A, T Spoken words Category fluency
2. Mummery et al (1998) A, T Written words Semantic & syllable
decisions
3. Moore & Price (1999a) A, F, T, V Pictures Naming
4. Moore & Price (1999b) A, F, T, V Written words Matching
and pictures
5. Moore & Price (1999b) A, F, T, V Pictures Naming
6. Gorno-Tempini (2000) Fa, A, T Pictures Naming
7. Phillips et al (submitted) F, T Written words Semantic & screen
and pictures size decisions
Abbreviations: A=animals, F=fruit, Fa=famous faces, T=tools, V=vehicles.
Analysis
Single multi-factorial analysis with three factors:
1) Category (man-made vs. living things)
2) Task (semantic vs. non-semantic)3) Stimulus type (words vs. pictures)
to evaluate the effects of category in different contexts
Data collected from 60 (53M, 7F) native English speakers on a single PET scanner.
Results
No main effects of Category and no significant interactions with Stimulus type
Highly significant Category x Task interactions
Tools > Living things for semantic tasks only
Peak in left posterior middle temporal gyrus at (-62 -58 0), SPM{Z}=5.30, p=0.005 (corrected)
z = 0
L L R
Contrasts1. Location decisions2. Color decisions3. Syllable decisions4. Action decisions5. Real Size decisions6. Screen size decisions7. Category fluency8. Naming color pictures9. Naming b/w pictures10. Naming pictures11. Reading words12. Word-Picture matching
Effect size (%rCBF)
L. post. middle temporal gyrus(-62 -58 0)
Manmade - Living Contrasts
2.5
2.0
1.5
1.0
0.5
0.0
-0.5
-1.0
-1.5 1 2 3 4 5 6 7 8 9 10 11 12
Semantic tasksNonsemantic tasks
Consistent tool advantage
Word-picture matching Picture naming
L. post. middle temporal gyrus(-62 -58 0)
KeyA AnimalsF FruitV VehiclesT ToolsB BaselineCN C. N. objectsSN S. N. objects
A F V T B A F V T CN SN
Relativeeffect sizes
Tool-specific? No.
Tools > living things and vehicles BUTSimple nonobjects also activated this region
T F T F Faces A T Body Parts
Relativeeffect sizes
Semantic decisions Picture naming
Action Perceptual
{ {
KeyA AnimalsF FruitT Tools
Combine this slide into last one?
In addition, this region is activated by:1) Action decisions (for both tools and fruit) and2) Naming pictures of body parts
Living things > manmade items(Tasks requiring identification only)
z = -8 y = 8 z = -24
R. anterio-medial TP extending along medial surface. SPM{Z}=5.2, p=0.01 (corrected)
L. insula extending into anterio-medial TP. SPM{Z}=4.1, p=0.086 (corrected)
R RL RLL
Consistent living things advantage
Effect size
(%rCBF)
Nam
ing
pict
ures
Ack
now
ledg
ing
Rea
ding
Ack
now
ledg
ing
Act
ion
deci
sion
sR
eal S
ize
deci
sion
sS
cree
n si
ze d
ecis
ions
Loc
atio
n de
cisi
ons
Col
or d
ecis
ions
Syl
labl
e de
cisi
ons
Nam
ing
colo
r pi
ctur
esN
amin
g b/
w p
ictu
res
W-P
mat
chin
gN
amin
g pi
ctur
esC
ateg
ory
flue
ncy
R. Ant. Temp. Pole(24 8 -24)
L. Ant. Temp. Pole(-30 6 -18)
6
5
4
3
2
1
0
-1
-2
-3
-4
6
5
4
3
2
1
0
-1
-2
-3
-4
Living - Manmade Contrasts
Requires identificationOther tasks
Left TP(-30 6 -18)
Right TP(24 8 -24)
Relativeeffect sizes
A F V T B A F V T Faces A T BP
W-P matching Picture naming Picture naming
Category-specific? No. Separate into 2 slides??
Animals, fruit, and faces all activate these regions
*
Left TP(-30 6 -18)
Right TP(24 8 -24)
Relativeeffect sizes
A F V T B A F V T Faces A T BP
W-P matching Picture naming Picture naming
Category-specific? No. Separate into 2 slides??
Animals, fruit, and faces all activate these regions
*
Summary
Robust evidence of anatomical specialisation for semantic categories: Tools activated left posterior middle temporal region Living things activated anterio-medial temporal poles
Small, context-specific effects: Tool activation only in semantic tasks Living thing activation for tasks requiring
identification
Q: How do these findings relate to cognitive theories of category specificity?
Conclusions
Results illustrate clear specialisation within the semantic system by demonstrating an anatomical double dissociation between living things and manmade items
Inconsistent with accounts based on an undifferentiated semantic system
Conclusions
Results were not specific to individual categories “Tool area” responded to action decisions for fruit,
naming body parts, and pictures of non-objects Temporal poles were activated by animals, fruit, and
famous faces
Inconsistent with evolutionary account of neural regions specialised for individual categories
Conclusions
Results were most consistent with distinct regions for different types of information
Posterior middle temporal region responds to actions associated with graspable objects
Anterior temporal poles may respond to greater semantic integrating information RLL
Replace thiswith an axialslice through antTPs (z=-20)
References