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The dissemination of divination in roman republican times

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1963). Michotte had subjects watch a screen on which dots were mov<strong>in</strong>g. When they were<br />

mov<strong>in</strong>g freely, apparently self-propelled, and reacted to other dots, subjects were <strong>in</strong>cl<strong>in</strong>ed to<br />

<strong>in</strong>fer mental states to the dots such as chas<strong>in</strong>g, help<strong>in</strong>g etc. This obviously suggests some sort<br />

<strong>of</strong> hyperactive agency detection. A good portion <strong>of</strong> neurological research has been dedicated<br />

to this function (Blakemore et al. 2003; Blakemore & Decety 2001; Decety & Grezes 1999;<br />

Frith & Frith 2001; Grezes et al. 2001). It is usually referred to as detection <strong>of</strong> biological<br />

movement, and the neural structure responsible for this is the superior temporal sulcus, or<br />

STS. While most studies have focused on its activation by visual stimuli, a recent fMRI study<br />

has showed that part <strong>of</strong> the STS is also activated by auditory stimuli (Bidet-Caulet, Vois<strong>in</strong>,<br />

Bertrand, & Fonlupt 2005a). <strong>The</strong>re are lateral specializations <strong>in</strong> the STS (Blakemore et al.<br />

2003b), and also some substructures sub-serv<strong>in</strong>g specific sub-functions (Bidet-Caulet,<br />

Vois<strong>in</strong>, Bertrand, & Fonlupt 2005b; Goodale & Milner 1992; Grezes et al. 2001). Indeed this<br />

neural structure would account for B1, where someth<strong>in</strong>g is mov<strong>in</strong>g, but not B2-4, where<br />

noth<strong>in</strong>g is mov<strong>in</strong>g. Thus it cannot be the S expla<strong>in</strong><strong>in</strong>g the existence <strong>of</strong> the HADD. <strong>The</strong>re is<br />

also another problem, namely, that it is not unique to humans.<br />

Another possibility is that the so called mirror neuron circuit is responsible for the<br />

hyperactive agency detection. Mirror neurons are a type <strong>of</strong> neuron found <strong>in</strong> the ventral pre-<br />

motor cortex <strong>in</strong> macaque monkeys (Gallese et al. 1996). <strong>The</strong>y have the special property that<br />

they are activated both by the perception <strong>of</strong> a movement and the execution <strong>of</strong> a movement.<br />

This has been seen as the basis <strong>of</strong> mentaliz<strong>in</strong>g or empathy (Gallese 2001). 59 Comparable<br />

f<strong>in</strong>d<strong>in</strong>gs have been reported <strong>in</strong> homologous areas <strong>in</strong> humans. <strong>The</strong>se areas were found to be<br />

active dur<strong>in</strong>g perception <strong>of</strong> a movement, execution <strong>of</strong> the movement, but also <strong>in</strong> the<br />

imag<strong>in</strong>ation <strong>of</strong> the movement (Jeannerod 1999). Thus mirror neurons could enable us to<br />

simulate a non-present agent. This would account for B3- 4, where some sort <strong>of</strong> simulation <strong>of</strong><br />

an agent takes place, but it wouldn’t expla<strong>in</strong> B1. Mirror neurons are not either very<br />

hyperactive, and they seem to function at a very low and bor<strong>in</strong>g level <strong>of</strong> mere movements.<br />

Another problem is, as mentioned, they are found also <strong>in</strong> monkeys, even macaques.<br />

Consequently the mirror neuron circuit cannot be the S <strong>of</strong> the HADD<br />

We could then stipulate that the superior temporal sulcus (STS) and ventral pre-motor<br />

cortex (PMv) together formed a distributed neurological <strong>in</strong>stantiation <strong>of</strong> the HADD. <strong>The</strong>re<br />

are two objections to this. First, the mirror neuron circuit is not hyperactive at all; at least not<br />

59 For recent criticism <strong>of</strong> this see (Jacob & Jeannerod 2005)<br />

85

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