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Transcript
excitation
inhibition
loss
Quiz 3 2. Decision making in the honey bee model A)  Some'mes is exactly equivalent to the op'mal On optimal decision-making J. A. R. Marshall et al. 3
Figure 2. In the Usher–McClelland model of decision-making
diffusion model of decision making n the primate visual cortex, neural populations represent
;
accumulated evidence for each of the alternatives. TheseB) Always is exactly equivalent to the opEmal diffusion .
excitation
populations
y1 and y2 integrate noisy inputs I1 and
I2, but leak model of decision making g
inhibition
accumulated
evidence
at
rate
k.
Each
population
also
inhibits
loss
e
he
other
in
proportion
to
its
own
activation
level,
at
rate w.C) Never is exactly equivalent to the opEmal diffusion n
When
wZk and both are large, the Usher–McClelland model
e
model of decision making, but can be asymptoEcally Peduces to the diffusion model of decision-making (figure 3).
opEmal Figure 2. In the Usher–McClelland model of decision-making
e
in the16primate visual cortex, neural populations represent
s
accumulated evidence for each of the alternatives. These
g
14
populations
y and y integrate noisy inputs I and I , but leak
3. Decision making in the ant models e
accumulated evidence at rate k. Each population also inhibits
12
the other in proportion to its own activation level, at rate w.
t
A)  SomeEmes is exactly equivalent to the opEmal When wZk and both are large, the Usher–McClelland model
s
10
reduces to the diffusion model of decision-making (figure 3).
s
diffusion model of decision making 8
16
B) Always is exactly equivalent to the opEmal diffusion 6
14
model of decision making 4
12
C) Never is exactly equivalent to the op'mal diffusion 2 10
y
model of decision making, but can be asympto'cally 8
e
0
2
4
6
8 10 12 14 16
d
6
op'mal e
4
t
Figure
3.
The
expected
dynamics of the Usher–McClelland
0. G
ive y
our n
ame 2
f
model,
plotted as the activation of population y1 against the t
etypublishing.org on 14 April 2009
1
2
1
2
activation
of population
When
decay
0 what 2 this 4 y2.l6ower 8 fi
10gure 12 equals
16inhibition
s14hows in 2 sentences - 1. Explain wZk),
the
system
converges
to
a
line
(bold
arrow)
and
a (y1 and y2 are the same as in the figure above): diffuses
along
it,
until
a
movable
decision
threshold
is
reached
e
Figure 3. The expected dynamics of the Usher–McClelland
lines).
Along the
attracting line,
the Usher–McClelland
The n
egaEve elaEonship between the athe
cEvaEon of y1 and the acEvaEon of y2 indicates inhibiEon tdashed
model,
plotted asrthe
activation of population
y1 against
model
is
equivalent
to
the
optimal
diffusion
model
of
decisionr
activation of
population y2.yWhen
decay
equals inhibition
between psystem
opulaEon 1 and populaEon y2. The solid line is the result of decay equal to inhibiEon (k making
(figure
s
(wZk),
the1).
converges to a line (bold arrow) and
c
= w
, in along
which case the m
odel threshold
is equivalent diffuses
it, until
a movable
decision
is reached to the opEmal diffusion model of decision making.) Usher-­‐McClelland Model Leaky inhibitory integraEon Change in acEvaEon of a populaEon of neurons = input signal + noise – decay – inhibiEon from alternaEve populaEon Eqn 4.2 transforms Eqn 4.1 to decouple the Eqns and show the UM model approximates diffusion model & opEmal decision making when w = k & both are large How your brain makes decisions MoEon discriminaEon h[p://www.youtube.com/watch?v=hpvbZxDtXSY (1:40) Siegel et al FronEers in Human NeuroScience 5 (2011) h[p://www.economicswiki.com/economics-­‐tutorials/
pareto-­‐efficient-­‐pareto-­‐opEmal-­‐tutorial/ Bee decision-­‐making model Downloaded from rsif.royalsocietypublishing.org on 14 April 2009
On optimal decision-making
gradually increase their firing rate (Schall 2001;
Shadlen & Newsome 2001; Roitman & Shadlen 2002).
Detailed studies of their activity provide strong
evidence that the LIP neurons integrate input from the
corresponding MT neurons over time (Huk & Shadlen
2005; Hanks et al. 2006). Hence, as time progresses in the
task, the sensory evidence accumulated in the LIP
neurons becomes more and more accurate.
It has been observed that when the activity of the
LIP neurons exceeds a certain threshold, the decision is
made and an eye movement in the corresponding
direction is initiated (Schall 2001; Shadlen & Newsome
2001; Roitman & Shadlen 2002). This arrangement
of neural populations with decision thresholds lends
itself to representation through a simple model, as
described in §4.
J. A. R. Marshall et al.
3
excitation
inhibition
loss
Figure 2. In the Usher–McClelland model of decision-making
in the primate visual cortex, neural populations represent
accumulated evidence for each of the alternatives. These
populations y1 and y2 integrate noisy inputs I1 and I2, but leak
accumulated evidence at rate k. Each population also inhibits
the other in proportion to its own activation level, at rate w.
When wZk and both are large, the Usher–McClelland model
reduces to the diffusion model of decision-making (figure 3).
16
14
4. THE USHER–MCCLELLAND MODEL
12
The Usher–McClelland model represents decisionmaking using neural populations that act as mutually
inhibitory, leaky integrators of incoming evidence
(figure 2). In the moving-dots decision task described
above, these integrator populations would represent the
LIP neural populations corresponding to the different
possible eye movement decisions. Each population of
integrator neurons receives a noisy input signal that it
integrates, subject to some constant loss. Each population also inhibits the activation of the other to a
degree proportional to its own activation. So, as one
10
8
6
4
2
0
2
4
6
8
10
12
14
16
Figure 3. The expected dynamics of the Usher–McClelland
Ants: no direct switching Undecided Scouts choose y2 y2 commiCed scouts recruit new scouts y2 scouts decay from y2 Bee decision-­‐making model Undecided Scouts choose y2 y2 commiCed scouts recruit new scouts y2 scouts decay from y2 Y2 scouts directly switch to y1 InformaEon gathering, evaluaEon, deliberaEon, consensus, choice, implementaEon • 
• 
• 
• 
• 
Bees commit all at once; waggle dances are broadcast in a crowded hive (only a few see it at at Eme) Ants go one at a Eme with no opportunity (usually) to assess mulEple nests; commit based on a quorum at one nest site How ants assess nest size: Ant lays a trail; leaves, returns, counts number of Emes it crosses its trail Ants show preferences, consistent rankings, transiEvity, weighing of all a[ributes Ants use a 'weighted addiEve Strategy' prefer bright, thick and narrow over dark thin and wide (with constant area) even though dark is most important Pra[ showed quorum sensing -­‐-­‐-­‐switch from tandem running to carrying (full commitment) once a (changeable) threshold # of ants have chosen to stay in a nest