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28th International Congress of Psychology August 8 ... - U-netSURF

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the two domains in the late ERP effects and some earlier differences, as well as interesting<br />

differences between musicians and non-musicians.<br />

1045.2 Spatially and temporally distributed representations <strong>of</strong> faces, J. Haxby, Green Hall<br />

Princeton University, Princeton, NJ, USA<br />

The neural representation <strong>of</strong> faces is distributed in space and time. Locally distributed<br />

representations <strong>of</strong> faces and other objects are found in ventral and lateral temporal cortex.<br />

Whereas the ventral temporal representation carries information about face identity, the lateral<br />

temporal representation carries information about how faces change with movement. The activity<br />

evoked by faces also extends across other cortical areas, reflecting activation <strong>of</strong> additional<br />

information, such as the direction <strong>of</strong> attention indicated by gaze direction. Neural responses to<br />

faces are also distributed in time, reflecting a differentiation between early feed-forward<br />

processing and later processing that is influenced by inter-regional interactions.<br />

1045.3 Brain electrical correlates <strong>of</strong> spatial, verbal and object representations, F. Roesler 1 , M.<br />

Heil 2 , P. Khader 1 , 1 Philipps-University Marburg, Marburg, Germany; 2 Institute <strong>of</strong> <strong>Psychology</strong>,<br />

Duesseldorf, Germany<br />

Slow waves <strong>of</strong> the EEG show that storage and retrieval <strong>of</strong> long-term memory (LTM) contents<br />

produce a material-specific topography which is by and large the same as when similar contents<br />

have to be manipulated in working memory (WM). Moreover, in both cases, the maximum<br />

amplitude <strong>of</strong> each slow wave pattern increases with increasing task demands. In sum, these studies<br />

not only prove a distinct topography for different representations but also that each topography is<br />

specifically modulated by the task demands. The congruent topography strongly supports the idea<br />

that WM and LTM contents are activated within the same cortical areas.<br />

1045.4 Associative learning signals in the medial temporal lobe, W.A. Suzuki, New York<br />

University, New York, NY, USA<br />

To examine the patterns <strong>of</strong> neural activity during associative memory formation, we trained two<br />

monkeys to perform a location-scene association task. The activity <strong>of</strong> individual hippocampal<br />

neurons was recorded as monkeys learned which one <strong>of</strong> four identical targets superimposed on a<br />

complex visual scene was associated with reward (Wirth et al., 2003). Hippocampal neurons<br />

signaled new learning with dramatic changes in their stimulus-selective response properties. This<br />

changing neural activity was significantly correlated with the animal’s behavioral learning curve.<br />

We call these cells “changing” cells. These findings provide new insights into how associative<br />

learning is represented within the medial temporal lobe.<br />

1045.5 Adaptive capacities <strong>of</strong> memory functions, B. Roeder 1 , F. Roesler 2 , H.J. Neville 3 ,<br />

1 University <strong>of</strong> Hamburg, Hamburg, Germany; 2 Philipps-University Marburg, Marburg, Germany;<br />

3<br />

University <strong>of</strong> Oregon at Eugene, Eugene, OR, USA<br />

Blind and sighted adults were compared in short- and long-term memory tasks to test if and if yes<br />

which memory functions are capable to adapt to specific requirements. We found higher<br />

short-term and long-term memory in the congenitally blind than in the sighted. Behavioral and<br />

ERP results showed that blind people encode auditory verbal material more efficiently than<br />

matched sighted controls and that this in turn allows them to recognize theses items with a higher<br />

91

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