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PROFESSOR: In the
last class we were

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talking about the
parasitic birds that

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lay their eggs in the
nest of another bird,

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and I asked you a question.

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Now how-- why wouldn't
these other birds

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evolve means of opposing that?

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Why don't they just
learn to recognize

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the eggs of the other bird?

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You can see here
that in many cases

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you can see that much
larger egg there,

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and yet they, generally,
will raise it.

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Raise the chick.

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In fact, it's often at the
expense of their own chicks,

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because the cuckoo is
an aggressive chick.

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Often you know pushes the
other, the smaller chicks

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out of the nest.

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And sometimes the foster
mother, and in this case,

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is raising only the cuckoo.

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But at least her
reproduction is considerably

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diminished by this problem.

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And one of the
reasons they do it

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has been investigated in a
study of the spotted cuckoo

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and magpies in Spain.

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At a time when the cuckoos moved
into an area the magpies were

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living-- or the magpies moved
in, I can't remember which.

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I think the cuckoos
came in later.

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OK.

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And so they started laying
their eggs in other birds' nest.

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But then they found out
that the birds often

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do destroy the cuckoo's egg.

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But when they do,
there's sort of a mag--

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a cuckoo mafia that comes
around and destroys their nest,

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so then they don't
reproduce at all.

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And it's better to reproduce
even a few than none.

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So that was the
mafia hypothesis,

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and it was verified in Spain.

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But there have been reports--

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and I don't know of any really
quantitative description

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of this, but were cases
when the song bird

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would build a decoy
nest above his real nest

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and lay eggs in both.

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And the cuckoo generally
will lay the agony--

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the conspicuous nest, the
nest at the top, and the next

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below is more hidden.

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But I don't know just
how often that happens.

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But they have to do
it in a way that this

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is group of cuckoos
couldn't force them,

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or couldn't destroy
their nest, because they

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destroyed their egg.

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So we saw this last time.

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Well so the cuckoo is
exploiting the innate releasing

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mechanism of the song birds that
they use to raise their young.

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It's because they can't resist
that big gap of the cuckoo

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chick.

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It elicits feeding
behavior, so they get fed.

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But this kind of thing
happens in humans, too.

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We discussed earlier how the
food industry and restaurants

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add extra fat, including
saturated fat, to foods--

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especially the fast
food industry--

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because people prefer the taste.

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They wanted to be fat.

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Think of all the people that
are eating the high fat potato--

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what do they call them?

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STUDENT: French fry?

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PROFESSOR: --the French fries.

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I never eat them, so I don't
even remember their name.

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All right.

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When you're diabetic
you know you really

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pay if you eat stuff like that.

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The high fat, because
fat digests very slowly

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and it raises blood sugar
for many hours afterwards.

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It has more than
double the number

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of calories of protein
and carbohydrate.

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But what-- I mentioned
here the doll industry.

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These are pictures from--

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[INAUDIBLE] one of his papers--

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and some of these
properties of infants

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were pointed out by
Lorenz and how you find it

00:05:30.700 --> 00:05:32.950 align:middle line:90%
in many different species--

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that babies have a
relatively larger head,

00:05:35.550 --> 00:05:37.460 align:middle line:90%
relatively larger eyes.

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They have short limbs--

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short usually chubby limbs,
and that appearance of the baby

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elicits care giving.

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You know even a
big, aggressive male

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will respond to babies
showing these properties,

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especially if the baby's
submitting the cute little

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sounds they make.

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We call them cute, because of
these stimuli that they have,

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and even men are affected by it.

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And the doll industry uses
that also in creating dolls.

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The cupie dolls normally
made with the, again,

00:06:21.360 --> 00:06:25.010 align:middle line:84%
relatively larger
head and large eyes.

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But if you overdo
that, what happens?

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There's a line between what's
cute and what's grotesque.

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OK?

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So obviously they simply
use human reactions

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to shape the way they
design those things.

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OK.

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Now we talk about
key stimuli, and we

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say that they can release
fixed action patterns.

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But we don't call
all key stimuli that

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engage the innate
releasing mechanisms,

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we don't call them releasers
generally, because that term is

00:07:10.640 --> 00:07:13.690 align:middle line:90%
used somewhat differently.

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A releaser is a
stimulus property

00:07:18.850 --> 00:07:22.890 align:middle line:84%
that has evolved for the
purpose of communicating,

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for the purpose of eliciting
behavior from members

00:07:27.050 --> 00:07:28.890 align:middle line:90%
of the same species.

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00:07:33.900 --> 00:07:35.640 align:middle line:90%
So this is the way it's defined.

00:07:35.640 --> 00:07:40.300 align:middle line:84%
"A structure or a movement,
most often a combination,

00:07:40.300 --> 00:07:43.970 align:middle line:84%
that's evolved in the
service of sending a signal."

00:07:43.970 --> 00:07:47.460 align:middle line:90%
So it is they emit key stimuli.

00:07:47.460 --> 00:07:52.540 align:middle line:84%
So in nature whenever you see
release showy color patterns

00:07:52.540 --> 00:07:56.853 align:middle line:84%
or structures, in
any vertebrate.

00:07:56.853 --> 00:07:58.520 align:middle line:84%
And they don't have
to be invertebrates,

00:07:58.520 --> 00:08:01.910 align:middle line:84%
they can be
invertebrates as well.

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And also any louder
or regular sound

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utterance, any regular
complicated and rhythmically

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perform movement, like evolves
in the rituals of courting.

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It functions as releaser.

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And I'm showing you the
cover of Smithsonian's--

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of a Smithsonian
publication there that shows

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the hamadryas baboon face.

00:08:28.570 --> 00:08:30.200 align:middle line:90%
But let's start with humans.

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Describe two releasers in human,
one involving a motor pattern.

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Well that's easy, smiling.

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Smiling is a movement, but it's
evolved because of the way it--

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the stimuli it that cause
a reaction in others.

00:08:49.590 --> 00:08:51.750 align:middle line:90%
OK?

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Almost all of us respond
positively to smiles.

00:08:55.970 --> 00:08:57.150 align:middle line:90%
OK?

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And we smile whether
we're aware of it or not

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in order to, you know, get
those positive responses.

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What other-- Can you
think of anything else?

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Think of babies
and their parents.

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They've evolved
not just the larger

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head and the short limbs--

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I mean there could be various
reasons for that-- but they've

00:09:21.380 --> 00:09:23.120 align:middle line:90%
evolved these chubby cheeks.

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They actually have fat
pads in their cheeks

00:09:25.260 --> 00:09:28.690 align:middle line:90%
that disappear later on.

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They've evolved specifically
to elicit a certain reaction.

00:09:36.380 --> 00:09:39.560 align:middle line:84%
And there's no doubt
that human breasts have

00:09:39.560 --> 00:09:42.750 align:middle line:84%
a similar function, that
is breasts don't have

00:09:42.750 --> 00:09:45.340 align:middle line:90%
to be as large as they are.

00:09:45.340 --> 00:09:50.264 align:middle line:84%
They evolved in order
to elicit response.

00:09:50.264 --> 00:09:51.260 align:middle line:90%
OK?

00:09:51.260 --> 00:09:55.470 align:middle line:90%
So these are what releaser are.

00:09:55.470 --> 00:09:58.100 align:middle line:84%
And there's of course many
others you can think of,

00:09:58.100 --> 00:10:01.090 align:middle line:84%
various emotional
expressions and things

00:10:01.090 --> 00:10:06.220 align:middle line:84%
that also have evolved as
these signals, social signals

00:10:06.220 --> 00:10:09.720 align:middle line:90%
of various sorts.

00:10:09.720 --> 00:10:11.740 align:middle line:84%
Now when we talk
about mimicry, we're

00:10:11.740 --> 00:10:13.620 align:middle line:84%
usually talking about
something that's

00:10:13.620 --> 00:10:16.030 align:middle line:84%
evolved to affect the
behavior of another species.

00:10:16.030 --> 00:10:19.030 align:middle line:84%
Like the monarch
butterfly has mimics,

00:10:19.030 --> 00:10:24.200 align:middle line:84%
because the monarch
tastes terrible.

00:10:24.200 --> 00:10:27.770 align:middle line:84%
Other, you know, birds won't
generally attack monarchs,

00:10:27.770 --> 00:10:29.990 align:middle line:90%
because they taste bad.

00:10:29.990 --> 00:10:33.030 align:middle line:90%
So they quickly learn, you know?

00:10:33.030 --> 00:10:36.530 align:middle line:84%
It only takes one experience
of a really horrible taste

00:10:36.530 --> 00:10:39.720 align:middle line:90%
and animals won't do it again.

00:10:39.720 --> 00:10:43.510 align:middle line:84%
But so other
butterflies and moths

00:10:43.510 --> 00:10:48.510 align:middle line:84%
have evolved to mimic
the bitter tasting ones,

00:10:48.510 --> 00:10:52.440 align:middle line:84%
and the same thing
happens in some insects.

00:10:52.440 --> 00:10:57.960 align:middle line:84%
But in some cases a species
evolves some way to mimic--

00:10:57.960 --> 00:11:02.210 align:middle line:90%


00:11:02.210 --> 00:11:05.750 align:middle line:84%
a mimic that affects
its own species.

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And these are the two examples,
I like the mouth breeder fish.

00:11:09.250 --> 00:11:10.710 align:middle line:90%
Let's look at that here.

00:11:10.710 --> 00:11:11.950 align:middle line:90%
The mouth breeder fish.

00:11:11.950 --> 00:11:13.130 align:middle line:90%
Here's the male.

00:11:13.130 --> 00:11:20.430 align:middle line:84%
And if you look here at the anal
fin you see the little spots.

00:11:20.430 --> 00:11:22.680 align:middle line:90%
What are those orange spots?

00:11:22.680 --> 00:11:26.790 align:middle line:84%
Well they look just like
the eggs of the female mouth

00:11:26.790 --> 00:11:28.040 align:middle line:90%
breeder.

00:11:28.040 --> 00:11:29.650 align:middle line:84%
Well what does the
mouth breeder do?

00:11:29.650 --> 00:11:33.610 align:middle line:84%
She lays her eggs and she
takes them up in her mouth.

00:11:33.610 --> 00:11:36.510 align:middle line:90%
She breeds them in her mouth.

00:11:36.510 --> 00:11:39.930 align:middle line:90%
So she tries to get these, too.

00:11:39.930 --> 00:11:42.590 align:middle line:90%
Perfect for the male.

00:11:42.590 --> 00:11:45.060 align:middle line:84%
He comes after-- she
comes after the male,

00:11:45.060 --> 00:11:48.050 align:middle line:84%
her mouth is there trying
to get at those eggs,

00:11:48.050 --> 00:11:49.940 align:middle line:90%
and what does he do?

00:11:49.940 --> 00:11:54.150 align:middle line:84%
He injects semen
right into her mouth.

00:11:54.150 --> 00:11:57.190 align:middle line:90%
So he fertilizes her eggs.

00:11:57.190 --> 00:12:00.415 align:middle line:84%
So that's why the mouth breeder
fish has evolved that way.

00:12:00.415 --> 00:12:01.690 align:middle line:90%
The mouth breeder male.

00:12:01.690 --> 00:12:04.690 align:middle line:90%
Now let's take baboons.

00:12:04.690 --> 00:12:09.425 align:middle line:84%
Here's a female olive baboon,
and notice this pink patch

00:12:09.425 --> 00:12:10.620 align:middle line:90%
on her rump.

00:12:10.620 --> 00:12:13.130 align:middle line:90%
It's used as a signal.

00:12:13.130 --> 00:12:15.590 align:middle line:90%
It's evolved to affect the male.

00:12:15.590 --> 00:12:18.980 align:middle line:84%
But then look, males
evolve a patch, too.

00:12:18.980 --> 00:12:20.260 align:middle line:90%
And some of them--

00:12:20.260 --> 00:12:21.820 align:middle line:84%
I couldn't find a
really pink one,

00:12:21.820 --> 00:12:24.930 align:middle line:84%
but this one's pink
only at the edge.

00:12:24.930 --> 00:12:28.125 align:middle line:84%
But the hamadryas baboon,
it's even more obvious.

00:12:28.125 --> 00:12:30.500 align:middle line:84%
You know here's a
male hamadryas baboon,

00:12:30.500 --> 00:12:33.370 align:middle line:84%
and look at the pink
rump on that animal.

00:12:33.370 --> 00:12:37.020 align:middle line:84%
And here are two females
actually presenting to a male,

00:12:37.020 --> 00:12:38.800 align:middle line:90%
and you can see.

00:12:38.800 --> 00:12:40.853 align:middle line:84%
You know that's
what's being imitated.

00:12:40.853 --> 00:12:42.020 align:middle line:90%
Well why would they do that?

00:12:42.020 --> 00:12:45.560 align:middle line:90%
Why would a male do that?

00:12:45.560 --> 00:12:50.120 align:middle line:84%
Because if a female
appears and presents to him

00:12:50.120 --> 00:12:54.280 align:middle line:84%
it totally inhibits his
aggressive response.

00:12:54.280 --> 00:12:56.080 align:middle line:84%
These are pretty
aggressive animals.

00:12:56.080 --> 00:12:56.580 align:middle line:90%
OK?

00:12:56.580 --> 00:13:00.120 align:middle line:84%
And they need ways to
turn off the aggression,

00:13:00.120 --> 00:13:02.760 align:middle line:84%
so the males have taken
advantage of that.

00:13:02.760 --> 00:13:05.580 align:middle line:84%
They evolve a signal
where they can turn off

00:13:05.580 --> 00:13:08.610 align:middle line:84%
the aggression of a
more dominant male,

00:13:08.610 --> 00:13:11.630 align:middle line:90%
and it protects them.

00:13:11.630 --> 00:13:14.090 align:middle line:84%
And many rodents--
many of these things

00:13:14.090 --> 00:13:15.860 align:middle line:90%
are a little more subtle.

00:13:15.860 --> 00:13:21.465 align:middle line:84%
You know a hamster a
normal Syrian hamster--

00:13:21.465 --> 00:13:27.380 align:middle line:84%
has evolved these white
patches on his chest.

00:13:27.380 --> 00:13:27.880 align:middle line:90%
OK?

00:13:27.880 --> 00:13:32.000 align:middle line:84%
If those are exposed it reduces
the aggression of a male.

00:13:32.000 --> 00:13:32.500 align:middle line:90%
OK.

00:13:32.500 --> 00:13:34.500 align:middle line:84%
If he wants to
attack, he actually

00:13:34.500 --> 00:13:36.940 align:middle line:90%
covers them with his feet.

00:13:36.940 --> 00:13:37.440 align:middle line:90%
OK?

00:13:37.440 --> 00:13:39.950 align:middle line:84%
Because of the signal
property that they have,

00:13:39.950 --> 00:13:42.090 align:middle line:84%
and similarly their
white underbelly.

00:13:42.090 --> 00:13:45.640 align:middle line:84%
If they expose that, because
they're defeated in a fight,

00:13:45.640 --> 00:13:50.000 align:middle line:84%
it generally works pretty
well to inhibit the attack

00:13:50.000 --> 00:13:51.820 align:middle line:90%
so they won't get killed.

00:13:51.820 --> 00:13:55.530 align:middle line:84%
The only time I've had hamster
males kill or females--

00:13:55.530 --> 00:13:57.460 align:middle line:84%
they both are
pretty aggressive--

00:13:57.460 --> 00:14:02.080 align:middle line:84%
kill another animal is when
it's an artificial situation

00:14:02.080 --> 00:14:04.190 align:middle line:84%
in a cage where the
animal gets caught

00:14:04.190 --> 00:14:08.750 align:middle line:84%
and he can't expose
the right stimuli.

00:14:08.750 --> 00:14:14.330 align:middle line:84%
Like he's caught in the wire
mesh or where he's not--

00:14:14.330 --> 00:14:17.650 align:middle line:84%
they're in such close
quarters, he can't, you know,

00:14:17.650 --> 00:14:20.310 align:middle line:90%
actually expose those signals.

00:14:20.310 --> 00:14:21.823 align:middle line:90%
All right.

00:14:21.823 --> 00:14:23.490 align:middle line:84%
Just a couple of other
things, and we'll

00:14:23.490 --> 00:14:25.800 align:middle line:90%
get onto the next class here.

00:14:25.800 --> 00:14:28.020 align:middle line:84%
I want you to know
what the dummy rule is.

00:14:28.020 --> 00:14:33.440 align:middle line:84%
The rule is that if you
can make a simple model--

00:14:33.440 --> 00:14:37.420 align:middle line:84%
like those models of
the stickleback female--

00:14:37.420 --> 00:14:39.200 align:middle line:84%
that elicits a fixed
action pattern--

00:14:39.200 --> 00:14:41.550 align:middle line:84%
like following
response of the male--

00:14:41.550 --> 00:14:45.230 align:middle line:84%
then we're dealing with an
innate releasing mechanism.

00:14:45.230 --> 00:14:48.650 align:middle line:84%
Something that has--
on the sensory side--

00:14:48.650 --> 00:14:51.850 align:middle line:84%
that's evolved to
respond to those stimuli.

00:14:51.850 --> 00:14:57.100 align:middle line:84%
But if you can't find a
dummy stimulus that works,

00:14:57.100 --> 00:15:00.770 align:middle line:84%
it doesn't mean there's no
innate releasing mechanism.

00:15:00.770 --> 00:15:05.070 align:middle line:84%
And the reason is
this, learning.

00:15:05.070 --> 00:15:10.550 align:middle line:84%
The usual role of
learning in animals,

00:15:10.550 --> 00:15:12.660 align:middle line:84%
it does affect
instinctive behavior.

00:15:12.660 --> 00:15:13.440 align:middle line:90%
And the way it--

00:15:13.440 --> 00:15:16.550 align:middle line:84%
It usually doesn't affect
the motor side very much.

00:15:16.550 --> 00:15:19.530 align:middle line:84%
Different motor patterns can
be linked in specific ways

00:15:19.530 --> 00:15:22.580 align:middle line:84%
as we've talked about
with the attack behavior,

00:15:22.580 --> 00:15:24.990 align:middle line:90%
predatory attack in cats.

00:15:24.990 --> 00:15:28.450 align:middle line:84%
They do have to put the
various individual fix

00:15:28.450 --> 00:15:30.430 align:middle line:90%
motor patterns together.

00:15:30.430 --> 00:15:30.930 align:middle line:90%
OK?

00:15:30.930 --> 00:15:33.230 align:middle line:90%
They learn that.

00:15:33.230 --> 00:15:35.640 align:middle line:84%
But the selectivity
of the stimuli

00:15:35.640 --> 00:15:38.450 align:middle line:84%
that elicit the
fixed action pattern

00:15:38.450 --> 00:15:40.680 align:middle line:90%
can be increased with learning.

00:15:40.680 --> 00:15:41.180 align:middle line:90%
OK?

00:15:41.180 --> 00:15:46.670 align:middle line:84%
So in imprinting you
see that happening.

00:15:46.670 --> 00:15:50.390 align:middle line:84%
It can change with the
experience of the animal.

00:15:50.390 --> 00:15:52.530 align:middle line:84%
But even an animal that
doesn't have to imprint,

00:15:52.530 --> 00:15:55.010 align:middle line:84%
he responds innately
to something.

00:15:55.010 --> 00:15:59.550 align:middle line:84%
Like a novel box moved
overhead above turkeys

00:15:59.550 --> 00:16:05.290 align:middle line:84%
can elicit the anti-predatory
response of crouching

00:16:05.290 --> 00:16:08.726 align:middle line:84%
and freezing, but that
can become more specific

00:16:08.726 --> 00:16:09.393 align:middle line:90%
with experience.

00:16:09.393 --> 00:16:16.770 align:middle line:90%


00:16:16.770 --> 00:16:17.300 align:middle line:90%
OK.

00:16:17.300 --> 00:16:20.460 align:middle line:84%
Now this will take us the
rest of this hour and Monday.

00:16:20.460 --> 00:16:24.050 align:middle line:90%


00:16:24.050 --> 00:16:27.860 align:middle line:84%
I want to go through the
theoretical models of fixed

00:16:27.860 --> 00:16:30.360 align:middle line:84%
action patterns, and
the innate releasing

00:16:30.360 --> 00:16:34.150 align:middle line:84%
mechanisms of Lorenz
and Tinbergen,

00:16:34.150 --> 00:16:37.580 align:middle line:90%
which have been the major ones.

00:16:37.580 --> 00:16:43.980 align:middle line:84%
And you can easily see how their
models can be put into computer

00:16:43.980 --> 00:16:48.020 align:middle line:90%
models using information flow.

00:16:48.020 --> 00:16:52.240 align:middle line:84%
And that has been done
fairly successfully.

00:16:52.240 --> 00:16:55.120 align:middle line:84%
The second thing is the
hierarchy and chains

00:16:55.120 --> 00:16:57.680 align:middle line:90%
of behavior.

00:16:57.680 --> 00:17:02.510 align:middle line:84%
The hierarchical organization
of instinctive behavior.

00:17:02.510 --> 00:17:09.520 align:middle line:84%
And then spatial
orientation by reflexes,

00:17:09.520 --> 00:17:11.050 align:middle line:90%
and an internal model.

00:17:11.050 --> 00:17:12.220 align:middle line:90%
We'll talk about that.

00:17:12.220 --> 00:17:15.099 align:middle line:84%
And then finally
what happens when

00:17:15.099 --> 00:17:19.430 align:middle line:84%
there are multiple motivations
arise simultaneously?

00:17:19.430 --> 00:17:20.940 align:middle line:90%
And that happens very commonly.

00:17:20.940 --> 00:17:26.829 align:middle line:84%
And sometimes two motivations
can be almost equally strong.

00:17:26.829 --> 00:17:28.190 align:middle line:90%
How does an animal handle that?

00:17:28.190 --> 00:17:30.490 align:middle line:90%


00:17:30.490 --> 00:17:30.990 align:middle line:90%
OK.

00:17:30.990 --> 00:17:36.370 align:middle line:90%
So Lorenz' model we call--

00:17:36.370 --> 00:17:38.950 align:middle line:84%
it's sometimes been called
a psycho-hydraulic model.

00:17:38.950 --> 00:17:42.500 align:middle line:84%
It's really a sort of
hydraulic mechanical model

00:17:42.500 --> 00:17:47.680 align:middle line:84%
of the motivational state,
the action specific potential

00:17:47.680 --> 00:17:49.210 align:middle line:90%
in his terms.

00:17:49.210 --> 00:17:50.360 align:middle line:90%
And he had two models.

00:17:50.360 --> 00:17:52.290 align:middle line:90%
He changed it after awhile.

00:17:52.290 --> 00:17:55.840 align:middle line:84%
On the left, there
you see his old model.

00:17:55.840 --> 00:18:01.490 align:middle line:84%
The action specific potential
was represented as reservoir.

00:18:01.490 --> 00:18:06.780 align:middle line:84%
The endogenous stimulus--
that is an internal stimulus--

00:18:06.780 --> 00:18:10.260 align:middle line:84%
is always there, and so
it's gradually building up

00:18:10.260 --> 00:18:14.620 align:middle line:90%
that level until its released.

00:18:14.620 --> 00:18:19.740 align:middle line:84%
And he has the
release there by the--

00:18:19.740 --> 00:18:23.160 align:middle line:84%
he throws this mechanical
thing where the spring there

00:18:23.160 --> 00:18:26.300 align:middle line:84%
represents some kind of
inertia of the system.

00:18:26.300 --> 00:18:32.680 align:middle line:84%
But the releasing stimuli
there caused the discharge

00:18:32.680 --> 00:18:34.800 align:middle line:90%
of that fluid.

00:18:34.800 --> 00:18:38.090 align:middle line:84%
But then his
observations on animals

00:18:38.090 --> 00:18:42.460 align:middle line:84%
made him realize that
it's not accurate enough,

00:18:42.460 --> 00:18:45.130 align:middle line:90%
so he revised it.

00:18:45.130 --> 00:18:52.480 align:middle line:84%
And he realized that there's
not only this endogenous input

00:18:52.480 --> 00:18:55.850 align:middle line:90%
that's gradually building up--

00:18:55.850 --> 00:18:58.870 align:middle line:84%
like our tendency to
blink our eyes gradually

00:18:58.870 --> 00:19:00.130 align:middle line:90%
builds up until we blink.

00:19:00.130 --> 00:19:02.738 align:middle line:84%
And we do it spontaneously, and
we don't even think about it.

00:19:02.738 --> 00:19:04.280 align:middle line:84%
Unless right now
I'm conscious of it,

00:19:04.280 --> 00:19:06.030 align:middle line:84%
and I realized that
I've now blinked twice

00:19:06.030 --> 00:19:08.110 align:middle line:90%
since I started talking.

00:19:08.110 --> 00:19:08.610 align:middle line:90%
OK.

00:19:08.610 --> 00:19:11.120 align:middle line:84%
But he's got other
stimuli there, too.

00:19:11.120 --> 00:19:16.190 align:middle line:84%
And these are, he calls,
readiness increasing stimuli.

00:19:16.190 --> 00:19:20.510 align:middle line:84%
They are stimuli that don't
act quite like the releasing--

00:19:20.510 --> 00:19:23.100 align:middle line:84%
they're not adequate to
actually release the movement,

00:19:23.100 --> 00:19:26.370 align:middle line:84%
but they do increase
the motivation.

00:19:26.370 --> 00:19:28.430 align:middle line:90%
OK?

00:19:28.430 --> 00:19:32.200 align:middle line:84%
And you can think how many
of those could be learned.

00:19:32.200 --> 00:19:33.940 align:middle line:84%
But then the
releasing stimulus--

00:19:33.940 --> 00:19:36.760 align:middle line:90%


00:19:36.760 --> 00:19:44.250 align:middle line:84%
the key stimuli that caused the
discharge of the fixed motor

00:19:44.250 --> 00:19:45.070 align:middle line:90%
pattern--

00:19:45.070 --> 00:19:49.580 align:middle line:84%
is like just pouring more
fluid rapidly into the cup.

00:19:49.580 --> 00:19:53.350 align:middle line:84%
So he sees the releasing
stimuli as just something that

00:19:53.350 --> 00:19:57.625 align:middle line:84%
raises the motivation to a high
level, and it does so rapidly.

00:19:57.625 --> 00:20:01.070 align:middle line:90%


00:20:01.070 --> 00:20:05.020 align:middle line:84%
And I've defined the
various things there below.

00:20:05.020 --> 00:20:08.160 align:middle line:84%
Now the major
difference, of course,

00:20:08.160 --> 00:20:14.660 align:middle line:84%
is the way the releasing stimuli
are acting, as I pointed out.

00:20:14.660 --> 00:20:15.450 align:middle line:90%
And the--

00:20:15.450 --> 00:20:18.490 align:middle line:90%


00:20:18.490 --> 00:20:21.980 align:middle line:84%
Where these things
are in the CNS--

00:20:21.980 --> 00:20:24.890 align:middle line:84%
this is very far from
any kind CNS model.

00:20:24.890 --> 00:20:26.540 align:middle line:90%
It's an analogous model.

00:20:26.540 --> 00:20:27.040 align:middle line:90%
OK?

00:20:27.040 --> 00:20:30.270 align:middle line:90%


00:20:30.270 --> 00:20:37.300 align:middle line:84%
It's a hydraulic mechanical
model that unfortunately looks

00:20:37.300 --> 00:20:39.910 align:middle line:84%
more like a flush toilet than
other things you can think of,

00:20:39.910 --> 00:20:46.270 align:middle line:84%
and so sometimes Lorenz
was made fun of for this.

00:20:46.270 --> 00:20:49.840 align:middle line:84%
But in fact the model was
useful in that it pointed out

00:20:49.840 --> 00:20:50.900 align:middle line:90%
properties.

00:20:50.900 --> 00:20:53.400 align:middle line:84%
He's basically
summarizing properties

00:20:53.400 --> 00:20:55.980 align:middle line:84%
that he observed for many
different fixed action

00:20:55.980 --> 00:20:57.570 align:middle line:90%
patterns.

00:20:57.570 --> 00:20:59.460 align:middle line:84%
And the one on the
right does a better job

00:20:59.460 --> 00:21:00.502 align:middle line:90%
than the one on the left.

00:21:00.502 --> 00:21:03.310 align:middle line:90%


00:21:03.310 --> 00:21:06.280 align:middle line:84%
Now if we talk about where
these things are in the brain,

00:21:06.280 --> 00:21:07.650 align:middle line:90%
it's interesting.

00:21:07.650 --> 00:21:12.460 align:middle line:90%
Because if we go here--

00:21:12.460 --> 00:21:14.960 align:middle line:84%
Now let's say you're
stimulating the spinal cord

00:21:14.960 --> 00:21:16.192 align:middle line:90%
or the hindbrain.

00:21:16.192 --> 00:21:20.240 align:middle line:84%
You can get various components
of fixed motor patterns.

00:21:20.240 --> 00:21:21.860 align:middle line:90%
OK?

00:21:21.860 --> 00:21:26.430 align:middle line:84%
But generally only when the
stimulus is on, you get them.

00:21:26.430 --> 00:21:31.980 align:middle line:84%
So it's not acting at all like
the action specific potential

00:21:31.980 --> 00:21:37.160 align:middle line:84%
in the reservoir here where
you get the whole sequence.

00:21:37.160 --> 00:21:37.660 align:middle line:90%
OK?

00:21:37.660 --> 00:21:40.690 align:middle line:90%


00:21:40.690 --> 00:21:44.160 align:middle line:84%
And when you suddenly
take the stimulus away,

00:21:44.160 --> 00:21:48.000 align:middle line:84%
the action doesn't just suddenly
stop, just like in the model.

00:21:48.000 --> 00:21:54.800 align:middle line:90%


00:21:54.800 --> 00:21:57.240 align:middle line:90%
So I just summarized that here.

00:21:57.240 --> 00:21:59.330 align:middle line:84%
For low levels, the
behavioral changes

00:21:59.330 --> 00:22:04.160 align:middle line:84%
occur only during the periods
of stimulation, then they stop.

00:22:04.160 --> 00:22:06.070 align:middle line:84%
And in fact if you
have an animal that's

00:22:06.070 --> 00:22:09.150 align:middle line:84%
had a transection of the
higher of the brain--

00:22:09.150 --> 00:22:11.240 align:middle line:90%
they've been totally separated.

00:22:11.240 --> 00:22:12.480 align:middle line:90%
They're no longer influence--

00:22:12.480 --> 00:22:14.850 align:middle line:84%
the hypothalamic region,
the whole forebrain

00:22:14.850 --> 00:22:18.380 align:middle line:84%
is cut off from
those lower regions--

00:22:18.380 --> 00:22:21.480 align:middle line:84%
you can still stimulate fixed
action patterns, but only

00:22:21.480 --> 00:22:22.450 align:middle line:90%
the motor component.

00:22:22.450 --> 00:22:24.450 align:middle line:84%
And they just stop
immediately, just

00:22:24.450 --> 00:22:27.160 align:middle line:84%
like the effects of electrical
stimulation of those lower

00:22:27.160 --> 00:22:29.920 align:middle line:90%
levels.

00:22:29.920 --> 00:22:32.910 align:middle line:84%
But when you stimulate in
the caudal forebrain there,

00:22:32.910 --> 00:22:35.010 align:middle line:84%
the hypothalamic
area, then you do

00:22:35.010 --> 00:22:40.380 align:middle line:84%
elicit moods that
are very, very hard

00:22:40.380 --> 00:22:45.960 align:middle line:84%
to distinguish from the mood
that would occur normally.

00:22:45.960 --> 00:22:49.190 align:middle line:90%


00:22:49.190 --> 00:22:53.720 align:middle line:84%
And that's been done for both
the quiet, biting attack--

00:22:53.720 --> 00:23:00.160 align:middle line:84%
the predatory attack-- of a
cat, and for the more aggressive

00:23:00.160 --> 00:23:01.510 align:middle line:90%
defensive attack.

00:23:01.510 --> 00:23:03.100 align:middle line:84%
And you are all
familiar with that.

00:23:03.100 --> 00:23:08.000 align:middle line:84%
The cat that arches its back,
you know and extends its claws

00:23:08.000 --> 00:23:10.490 align:middle line:90%
and makes a lot of noise.

00:23:10.490 --> 00:23:11.200 align:middle line:90%
OK?

00:23:11.200 --> 00:23:13.890 align:middle line:84%
We call the other one
a quiet biting attack,

00:23:13.890 --> 00:23:16.680 align:middle line:90%
because he does not make noise.

00:23:16.680 --> 00:23:20.090 align:middle line:84%
It's designed
specifically to kill prey.

00:23:20.090 --> 00:23:24.980 align:middle line:90%


00:23:24.980 --> 00:23:28.610 align:middle line:84%
So I'm just pointing
out I want you

00:23:28.610 --> 00:23:32.490 align:middle line:84%
to give examples of the effects
of the inertia of excitation

00:23:32.490 --> 00:23:33.335 align:middle line:90%
in animal behavior.

00:23:33.335 --> 00:23:36.960 align:middle line:90%


00:23:36.960 --> 00:23:39.120 align:middle line:84%
Think of an example
from human behavior,

00:23:39.120 --> 00:23:41.760 align:middle line:90%
but it occurs with animals, too.

00:23:41.760 --> 00:23:43.600 align:middle line:84%
You suddenly remove
the stimulus--

00:23:43.600 --> 00:23:45.530 align:middle line:90%
you elicit the whole--

00:23:45.530 --> 00:23:48.300 align:middle line:84%
you increase the
level of motivation

00:23:48.300 --> 00:23:52.200 align:middle line:84%
that-- remember Lorenz'
model on the right there.

00:23:52.200 --> 00:23:57.140 align:middle line:84%
You cause the motivation
to go way, way up.

00:23:57.140 --> 00:24:00.580 align:middle line:84%
If you just suddenly
remove that stimulus,

00:24:00.580 --> 00:24:03.950 align:middle line:84%
the behavior doesn't
just go away.

00:24:03.950 --> 00:24:05.820 align:middle line:90%
OK?

00:24:05.820 --> 00:24:09.590 align:middle line:84%
I like the example from
a Disney movie of a bear.

00:24:09.590 --> 00:24:13.880 align:middle line:84%
They show the bear
that's high on a hill,

00:24:13.880 --> 00:24:16.700 align:middle line:84%
and he's trying to get
something in a log-- a big log.

00:24:16.700 --> 00:24:19.585 align:middle line:84%
And he crawls in to the
log as far as he can get,

00:24:19.585 --> 00:24:21.250 align:middle line:90%
and he gets stuck there.

00:24:21.250 --> 00:24:24.920 align:middle line:84%
And then the log starts
rolling downhill.

00:24:24.920 --> 00:24:29.690 align:middle line:84%
Bonding downhill until finally
it crashes against a tree

00:24:29.690 --> 00:24:31.340 align:middle line:90%
and breaks open the log.

00:24:31.340 --> 00:24:35.770 align:middle line:84%
And the bear comes
out angry as can be.

00:24:35.770 --> 00:24:37.480 align:middle line:90%
And he starts swatting.

00:24:37.480 --> 00:24:39.690 align:middle line:90%
He pulls little trees.

00:24:39.690 --> 00:24:42.580 align:middle line:84%
You know just like
an angry human,

00:24:42.580 --> 00:24:45.270 align:middle line:84%
that you don't get
over it suddenly,

00:24:45.270 --> 00:24:46.970 align:middle line:90%
even if the stimuli are gone.

00:24:46.970 --> 00:24:50.162 align:middle line:90%


00:24:50.162 --> 00:24:52.700 align:middle line:84%
If something on the TV
makes you very angry,

00:24:52.700 --> 00:24:54.905 align:middle line:84%
some people have been
known to break their TV.

00:24:54.905 --> 00:24:58.360 align:middle line:90%


00:24:58.360 --> 00:25:02.650 align:middle line:84%
This is the inertia of
excitation of a fixed action

00:25:02.650 --> 00:25:09.410 align:middle line:84%
pattern by this change in
the motivational level here

00:25:09.410 --> 00:25:11.160 align:middle line:90%
on the right.

00:25:11.160 --> 00:25:14.100 align:middle line:84%
You can remove that
stimulus there,

00:25:14.100 --> 00:25:19.100 align:middle line:84%
but the reservoir is so full
that the action continues

00:25:19.100 --> 00:25:19.935 align:middle line:90%
for some time.

00:25:19.935 --> 00:25:23.150 align:middle line:90%


00:25:23.150 --> 00:25:23.670 align:middle line:90%
All right.

00:25:23.670 --> 00:25:28.310 align:middle line:90%


00:25:28.310 --> 00:25:30.680 align:middle line:84%
So you see that with
fear, with aggression,

00:25:30.680 --> 00:25:32.720 align:middle line:84%
with sexual
excitement, certainly.

00:25:32.720 --> 00:25:35.290 align:middle line:84%
These are the areas
certainly in human behavior,

00:25:35.290 --> 00:25:40.840 align:middle line:84%
but also in many animals
that you see that the most.

00:25:40.840 --> 00:25:44.880 align:middle line:84%
How can we explain the fact
that the urination activities

00:25:44.880 --> 00:25:48.390 align:middle line:84%
of a male dog often don't
depend on the amount of urine

00:25:48.390 --> 00:25:49.485 align:middle line:90%
in the bladder?

00:25:49.485 --> 00:25:50.860 align:middle line:84%
You say, well,
why do we urinate?

00:25:50.860 --> 00:25:54.980 align:middle line:84%
Well we have an urge to urinate,
because the bladder's full.

00:25:54.980 --> 00:26:00.890 align:middle line:84%
But in the case of a dog,
urination has other functions.

00:26:00.890 --> 00:26:05.240 align:middle line:84%
So there's two very different
motivations that make,

00:26:05.240 --> 00:26:08.200 align:middle line:90%
at least, the male dog urinate.

00:26:08.200 --> 00:26:11.320 align:middle line:90%
In the case of female cats--

00:26:11.320 --> 00:26:12.570 align:middle line:90%
in the case of cats--

00:26:12.570 --> 00:26:13.890 align:middle line:90%
I don't know about--

00:26:13.890 --> 00:26:16.880 align:middle line:90%
I don't think dogs--

00:26:16.880 --> 00:26:19.230 align:middle line:90%
But what are they doing?

00:26:19.230 --> 00:26:20.560 align:middle line:90%
Why do they hold back?

00:26:20.560 --> 00:26:24.810 align:middle line:84%
They don't discharge
all their urine.

00:26:24.810 --> 00:26:28.080 align:middle line:84%
They need it for scent
marking behavior,

00:26:28.080 --> 00:26:31.450 align:middle line:90%
so that's a separate motivation.

00:26:31.450 --> 00:26:33.160 align:middle line:90%
OK?

00:26:33.160 --> 00:26:38.440 align:middle line:84%
And cats do it, too,
both male and female,

00:26:38.440 --> 00:26:40.320 align:middle line:90%
because of the odor.

00:26:40.320 --> 00:26:42.900 align:middle line:84%
These are very
olfactory animals,

00:26:42.900 --> 00:26:48.290 align:middle line:84%
and their whole world is
very different from ours.

00:26:48.290 --> 00:26:53.500 align:middle line:84%
It is visual and auditory, like
ours, but much more olfactory.

00:26:53.500 --> 00:26:57.350 align:middle line:84%
They come into an
area, they know

00:26:57.350 --> 00:27:00.340 align:middle line:84%
which other cats,
which individual cats

00:27:00.340 --> 00:27:02.500 align:middle line:84%
have been in that
region, and whether they

00:27:02.500 --> 00:27:04.060 align:middle line:90%
were male or female.

00:27:04.060 --> 00:27:04.560 align:middle line:90%
OK?

00:27:04.560 --> 00:27:05.670 align:middle line:90%
And they leave their mark.

00:27:05.670 --> 00:27:08.790 align:middle line:90%


00:27:08.790 --> 00:27:10.350 align:middle line:90%
Humans sometimes do that, too.

00:27:10.350 --> 00:27:13.415 align:middle line:84%
They write on walls
and things like that.

00:27:13.415 --> 00:27:13.915 align:middle line:90%
OK.

00:27:13.915 --> 00:27:21.230 align:middle line:90%


00:27:21.230 --> 00:27:24.080 align:middle line:84%
Let's talk about
chains of behavior,

00:27:24.080 --> 00:27:28.770 align:middle line:84%
and then the hierarchy of
the systems of fixed action

00:27:28.770 --> 00:27:30.300 align:middle line:90%
patterns.

00:27:30.300 --> 00:27:34.090 align:middle line:84%
So as an example here I'm
asking for a description

00:27:34.090 --> 00:27:36.400 align:middle line:84%
of the chain of
behavior patterns shown

00:27:36.400 --> 00:27:39.420 align:middle line:84%
by newborn kittens
in nursing behavior.

00:27:39.420 --> 00:27:40.420 align:middle line:90%
It's very interesting.

00:27:40.420 --> 00:27:45.510 align:middle line:84%
It's a consistent chain of
behavior that they show.

00:27:45.510 --> 00:27:48.980 align:middle line:84%
And normally one behavior
leads to the next,

00:27:48.980 --> 00:27:51.840 align:middle line:84%
because it leads to the
stimulus that elicits the next.

00:27:51.840 --> 00:27:53.990 align:middle line:90%
And I've listed them here.

00:27:53.990 --> 00:27:57.080 align:middle line:84%
If he's awake, and
he's not suckling,

00:27:57.080 --> 00:28:01.190 align:middle line:84%
he shows this constant to and
fro sideways sweeping movement

00:28:01.190 --> 00:28:07.770 align:middle line:84%
of the head and foreparts of the
body while he creeps forward.

00:28:07.770 --> 00:28:12.070 align:middle line:84%
I know, of course, he's
normally near the mother.

00:28:12.070 --> 00:28:14.830 align:middle line:84%
And if he touches a
solid vertical surface,

00:28:14.830 --> 00:28:17.810 align:middle line:84%
even if it's not the
mother, he snuggles up to it

00:28:17.810 --> 00:28:23.090 align:middle line:84%
and maintains contact while he
continues that sweeping motion.

00:28:23.090 --> 00:28:26.020 align:middle line:84%
It's designed, of course--
even though it's a fixed motor

00:28:26.020 --> 00:28:28.030 align:middle line:90%
pattern--

00:28:28.030 --> 00:28:32.500 align:middle line:84%
it's designed to find
the teat of the mother.

00:28:32.500 --> 00:28:36.110 align:middle line:84%
So if he contacts fur, he
stops his forward motion.

00:28:36.110 --> 00:28:37.410 align:middle line:90%
OK?

00:28:37.410 --> 00:28:39.790 align:middle line:84%
But he continues the
sweeping motions, his nose

00:28:39.790 --> 00:28:40.835 align:middle line:90%
pressed against the fur.

00:28:40.835 --> 00:28:44.740 align:middle line:84%
If he touches a bare spot, then
he ceases the sweeping motion,

00:28:44.740 --> 00:28:47.290 align:middle line:84%
and initiates a
different behavior.

00:28:47.290 --> 00:28:49.050 align:middle line:90%
He's kind of snapping.

00:28:49.050 --> 00:28:51.365 align:middle line:84%
He's trying to get
the teat in his mouth.

00:28:51.365 --> 00:28:54.830 align:middle line:84%
So he finds it, he stops
his other movements,

00:28:54.830 --> 00:28:57.970 align:middle line:84%
and that initiates
the suckling behavior.

00:28:57.970 --> 00:28:59.790 align:middle line:90%
Sucking behavior.

00:28:59.790 --> 00:29:02.860 align:middle line:84%
And also milk treading
while he's sucking.

00:29:02.860 --> 00:29:04.915 align:middle line:84%
You see this movement
of the front paws.

00:29:04.915 --> 00:29:09.600 align:middle line:90%


00:29:09.600 --> 00:29:13.420 align:middle line:84%
So each motor pattern serves
as appetitive behaviour

00:29:13.420 --> 00:29:15.270 align:middle line:84%
for the next fixed
action pattern.

00:29:15.270 --> 00:29:17.850 align:middle line:90%


00:29:17.850 --> 00:29:22.990 align:middle line:84%
Or I would say the next
component of the sequence,

00:29:22.990 --> 00:29:24.495 align:middle line:90%
because these are always linked.

00:29:24.495 --> 00:29:27.310 align:middle line:90%


00:29:27.310 --> 00:29:33.290 align:middle line:84%
But Lorenz sees them as a
very different fixed action

00:29:33.290 --> 00:29:39.005 align:middle line:84%
patterns, because, in
fact, you don't have

00:29:39.005 --> 00:29:40.130 align:middle line:90%
to have the whole sequence.

00:29:40.130 --> 00:29:43.430 align:middle line:84%
If you put the animal
right next to the mother,

00:29:43.430 --> 00:29:45.330 align:middle line:84%
the he won't show the
earlier components.

00:29:45.330 --> 00:29:49.510 align:middle line:84%
He does not have to go
through the earlier ones,

00:29:49.510 --> 00:29:53.070 align:middle line:84%
because they're all somewhat
independent fixed action

00:29:53.070 --> 00:29:53.570 align:middle line:90%
patterns.

00:29:53.570 --> 00:29:56.225 align:middle line:84%
But they're normally linked
because of the situation.

00:29:56.225 --> 00:30:00.130 align:middle line:90%


00:30:00.130 --> 00:30:03.280 align:middle line:84%
And Tinbergen had described
these kinds of things

00:30:03.280 --> 00:30:08.830 align:middle line:84%
as examples of the hierarchical
organization of instinct.

00:30:08.830 --> 00:30:12.030 align:middle line:84%
And he has some very
well known diagrams

00:30:12.030 --> 00:30:13.630 align:middle line:84%
that you should
be familiar with.

00:30:13.630 --> 00:30:16.620 align:middle line:90%


00:30:16.620 --> 00:30:18.840 align:middle line:84%
He shows a view of
innate releasing

00:30:18.840 --> 00:30:22.970 align:middle line:84%
mechanisms that are quite a
bit different from Lorenz.

00:30:22.970 --> 00:30:26.030 align:middle line:84%
They did work together some,
but they had a different way

00:30:26.030 --> 00:30:28.350 align:middle line:90%
of picturing it.

00:30:28.350 --> 00:30:31.330 align:middle line:84%
And you can see that he doesn't
explain some of the aspects

00:30:31.330 --> 00:30:32.750 align:middle line:90%
that Lorenz was dealing with.

00:30:32.750 --> 00:30:35.940 align:middle line:84%
All that stuff about the
inertia behavior and so forth,

00:30:35.940 --> 00:30:37.950 align:middle line:90%
he didn't try to deal with.

00:30:37.950 --> 00:30:40.070 align:middle line:84%
But he did deal
with the hierarchy.

00:30:40.070 --> 00:30:43.205 align:middle line:84%
In this case we just
take one component of it.

00:30:43.205 --> 00:30:43.705 align:middle line:90%
OK?

00:30:43.705 --> 00:30:48.860 align:middle line:90%


00:30:48.860 --> 00:30:55.550 align:middle line:90%
And this is just for example.

00:30:55.550 --> 00:30:59.560 align:middle line:84%
We're dealing with an aspect
of reproductive behavior.

00:30:59.560 --> 00:31:01.485 align:middle line:90%
Hormones provide a major input.

00:31:01.485 --> 00:31:04.890 align:middle line:90%


00:31:04.890 --> 00:31:09.340 align:middle line:84%
The higher level could be coming
from the visual system that

00:31:09.340 --> 00:31:10.740 align:middle line:90%
signals the time of year.

00:31:10.740 --> 00:31:14.070 align:middle line:90%


00:31:14.070 --> 00:31:17.440 align:middle line:84%
Other input that
increase that motivation.

00:31:17.440 --> 00:31:22.740 align:middle line:84%
And then, unlike
Lorenz, he has a block

00:31:22.740 --> 00:31:26.520 align:middle line:84%
preventing the continuous
discharge of the motor

00:31:26.520 --> 00:31:28.100 align:middle line:90%
patterns.

00:31:28.100 --> 00:31:29.600 align:middle line:84%
And the innate
releasing mechanism--

00:31:29.600 --> 00:31:32.710 align:middle line:90%


00:31:32.710 --> 00:31:35.580 align:middle line:84%
and then the stimulus that
activates the innate releasing

00:31:35.580 --> 00:31:36.580 align:middle line:90%
mechanism--

00:31:36.580 --> 00:31:39.550 align:middle line:84%
its function is simply
to remove that block.

00:31:39.550 --> 00:31:42.610 align:middle line:84%
And then the block,
once it's removed,

00:31:42.610 --> 00:31:46.040 align:middle line:90%
can elicit a whole series.

00:31:46.040 --> 00:31:47.585 align:middle line:90%
And which one would be first?

00:31:47.585 --> 00:31:49.210 align:middle line:84%
Well the one with
the lowest threshold,

00:31:49.210 --> 00:31:52.250 align:middle line:84%
and normally that's
appetitive behavior.

00:31:52.250 --> 00:31:52.750 align:middle line:90%
OK.

00:31:52.750 --> 00:31:56.900 align:middle line:84%
And these different components
of the fixed action pattern

00:31:56.900 --> 00:31:59.190 align:middle line:84%
are normally
inhibiting each other.

00:31:59.190 --> 00:32:02.260 align:middle line:84%
And this shows a
more complete model

00:32:02.260 --> 00:32:05.650 align:middle line:84%
where he shows a
male stickleback

00:32:05.650 --> 00:32:07.350 align:middle line:90%
reproductive behavior.

00:32:07.350 --> 00:32:10.410 align:middle line:84%
Basically the whole hierarchy
starting with hormones

00:32:10.410 --> 00:32:13.310 align:middle line:90%
with the spring migration.

00:32:13.310 --> 00:32:17.130 align:middle line:84%
The nature of the
water has an influence,

00:32:17.130 --> 00:32:20.370 align:middle line:84%
the plants in the vicinity,
and various internal factors.

00:32:20.370 --> 00:32:22.060 align:middle line:90%
And then there's the block.

00:32:22.060 --> 00:32:24.950 align:middle line:84%
The innate releasing mechanisms
that can remove the block

00:32:24.950 --> 00:32:27.810 align:middle line:84%
and start these
various behaviors.

00:32:27.810 --> 00:32:30.500 align:middle line:84%
And note he has the
mutual inhibition shown

00:32:30.500 --> 00:32:33.090 align:middle line:90%
by the double arrows here.

00:32:33.090 --> 00:32:36.170 align:middle line:84%
He has fighting,
nesting, courtship,

00:32:36.170 --> 00:32:40.320 align:middle line:84%
and parental behavior, each
with somewhat different stimuli.

00:32:40.320 --> 00:32:43.020 align:middle line:84%
And so depending on
the stimuli there,

00:32:43.020 --> 00:32:45.820 align:middle line:90%
these will be discharged.

00:32:45.820 --> 00:32:49.060 align:middle line:84%
And then he shows the
lower levels, too.

00:32:49.060 --> 00:32:51.050 align:middle line:90%
The level of the actual action.

00:32:51.050 --> 00:32:54.095 align:middle line:84%
So here for fighting behavior he
has the displaying, the biting,

00:32:54.095 --> 00:32:55.750 align:middle line:90%
and the chasing.

00:32:55.750 --> 00:32:56.250 align:middle line:90%
OK?

00:32:56.250 --> 00:32:59.920 align:middle line:84%
And if you get the
display purring,

00:32:59.920 --> 00:33:03.180 align:middle line:84%
then you get whole
fins, raise of one

00:33:03.180 --> 00:33:08.850 align:middle line:84%
fin, muscle fibers of one
ray, and motor neurons.

00:33:08.850 --> 00:33:11.430 align:middle line:90%
For when the muscle fiber--

00:33:11.430 --> 00:33:13.470 align:middle line:84%
So he shows the
whole hierarchy here.

00:33:13.470 --> 00:33:16.200 align:middle line:84%
And this is often
reproduced, because--

00:33:16.200 --> 00:33:18.820 align:middle line:84%
Neuroscientists like it
because it sort of fits

00:33:18.820 --> 00:33:23.440 align:middle line:84%
the hierarchical organization
of the nervous system.

00:33:23.440 --> 00:33:26.230 align:middle line:84%
And this shows a
functional picture of that.

00:33:26.230 --> 00:33:29.160 align:middle line:90%


00:33:29.160 --> 00:33:29.660 align:middle line:90%
OK.

00:33:29.660 --> 00:33:30.160 align:middle line:90%
And I'm--

00:33:30.160 --> 00:33:32.780 align:middle line:90%


00:33:32.780 --> 00:33:34.920 align:middle line:84%
This is the level
of ethology up here,

00:33:34.920 --> 00:33:36.755 align:middle line:84%
and you are at the level
of neurophysiology.

00:33:36.755 --> 00:33:39.710 align:middle line:84%
They study different
aspects of it.

00:33:39.710 --> 00:33:43.000 align:middle line:84%
But in fact the physiologist
working on hypothalamus

00:33:43.000 --> 00:33:46.360 align:middle line:84%
have also studied
many of these things.

00:33:46.360 --> 00:33:50.590 align:middle line:90%


00:33:50.590 --> 00:33:53.760 align:middle line:84%
So the major difference then
between the Lorenz model

00:33:53.760 --> 00:33:58.560 align:middle line:84%
and the Tinbergen model
I've listed for you here.

00:33:58.560 --> 00:34:01.200 align:middle line:84%
Obviously Tinbergen's
view was the broader one.

00:34:01.200 --> 00:34:04.340 align:middle line:90%


00:34:04.340 --> 00:34:08.020 align:middle line:84%
It looks more like an
information flow scheme.

00:34:08.020 --> 00:34:12.790 align:middle line:84%
But Lorenz by focusing on
the dynamics of the drive

00:34:12.790 --> 00:34:15.340 align:middle line:84%
state, the action specific
potential, and the innate

00:34:15.340 --> 00:34:23.000 align:middle line:84%
releasing mechanism it's
showing very different aspects

00:34:23.000 --> 00:34:27.310 align:middle line:84%
of the properties
of innate behavior.

00:34:27.310 --> 00:34:29.665 align:middle line:84%
And here I just point out
the strengths and weaknesses.

00:34:29.665 --> 00:34:34.080 align:middle line:90%


00:34:34.080 --> 00:34:38.330 align:middle line:84%
And I also note that Tinbergen's
model has been more popular

00:34:38.330 --> 00:34:40.260 align:middle line:90%
among the neural people.

00:34:40.260 --> 00:34:43.130 align:middle line:90%


00:34:43.130 --> 00:34:46.719 align:middle line:84%
But it was the Lorenz
view that was actually

00:34:46.719 --> 00:34:50.235 align:middle line:84%
used in the modeling of real
behavior patterns in animals.

00:34:50.235 --> 00:34:53.600 align:middle line:90%


00:34:53.600 --> 00:34:57.340 align:middle line:84%
In the work of Bruce
Blumberg here at MIT when

00:34:57.340 --> 00:34:59.660 align:middle line:84%
he was doing that
in the media lab.

00:34:59.660 --> 00:35:00.160 align:middle line:90%
OK.

00:35:00.160 --> 00:35:04.580 align:middle line:90%


00:35:04.580 --> 00:35:10.120 align:middle line:84%
So let's go to the
discussion of Lorenz--

00:35:10.120 --> 00:35:11.590 align:middle line:90%
of the work of [INAUDIBLE].

00:35:11.590 --> 00:35:14.640 align:middle line:84%
And this is his work on
the female digger wasp,

00:35:14.640 --> 00:35:17.620 align:middle line:84%
because it points out another
aspect of innate behavior

00:35:17.620 --> 00:35:19.740 align:middle line:90%
that I think is quite important.

00:35:19.740 --> 00:35:23.740 align:middle line:84%
And this-- We're going to
come back to the digger wasp

00:35:23.740 --> 00:35:27.440 align:middle line:84%
next week when we
read a little bit

00:35:27.440 --> 00:35:33.070 align:middle line:84%
from Tinbergen and his
studies of orienting

00:35:33.070 --> 00:35:35.140 align:middle line:90%
behavior in that wasp.

00:35:35.140 --> 00:35:38.760 align:middle line:90%
How does he find things?

00:35:38.760 --> 00:35:39.260 align:middle line:90%
OK.

00:35:39.260 --> 00:35:48.160 align:middle line:84%
So he's doing experiments on
the influence of inspections

00:35:48.160 --> 00:35:51.000 align:middle line:90%
of the nest by the wasp.

00:35:51.000 --> 00:35:54.470 align:middle line:84%
It's a behavior that
has a lot of plasticity.

00:35:54.470 --> 00:35:55.900 align:middle line:90%
OK?

00:35:55.900 --> 00:36:01.366 align:middle line:84%
And this is what the
digger wasp is like.

00:36:01.366 --> 00:36:03.690 align:middle line:84%
And note there's a
hole in the sand.

00:36:03.690 --> 00:36:07.700 align:middle line:84%
And she's made that hole,
and it's basically a nest.

00:36:07.700 --> 00:36:12.890 align:middle line:84%
She makes nests in the sand,
little holes in the sand.

00:36:12.890 --> 00:36:17.030 align:middle line:84%
And she digs a separate
hole for every egg she lays.

00:36:17.030 --> 00:36:20.640 align:middle line:90%


00:36:20.640 --> 00:36:24.540 align:middle line:90%
And she has to--

00:36:24.540 --> 00:36:26.420 align:middle line:90%
The egg will hatch.

00:36:26.420 --> 00:36:28.030 align:middle line:90%
A larvae comes out.

00:36:28.030 --> 00:36:29.770 align:middle line:84%
And when the larvae
comes out, they

00:36:29.770 --> 00:36:32.040 align:middle line:90%
have to have food right away.

00:36:32.040 --> 00:36:36.890 align:middle line:90%
So she catches insects.

00:36:36.890 --> 00:36:40.550 align:middle line:84%
This wasp is catching
little insects and worms.

00:36:40.550 --> 00:36:44.570 align:middle line:84%
And brings them-- killing
them and bringing them,

00:36:44.570 --> 00:36:47.390 align:middle line:90%
putting them in these nests.

00:36:47.390 --> 00:36:49.080 align:middle line:84%
But she doesn't
have just one nest.

00:36:49.080 --> 00:36:51.390 align:middle line:90%
She has a bunch of them.

00:36:51.390 --> 00:36:56.260 align:middle line:84%
And so when she comes
to a nest she inspects--

00:36:56.260 --> 00:37:00.460 align:middle line:84%
Her first task is
just to inspect it.

00:37:00.460 --> 00:37:06.840 align:middle line:84%
And if it's already got some
food there, then she goes on.

00:37:06.840 --> 00:37:13.710 align:middle line:84%
And if it's empty,
then she will fly off,

00:37:13.710 --> 00:37:15.040 align:middle line:90%
and she will bring food back.

00:37:15.040 --> 00:37:18.620 align:middle line:84%
And she has to remember which
nest it was, and she does.

00:37:18.620 --> 00:37:21.390 align:middle line:90%
She does it pretty accurately.

00:37:21.390 --> 00:37:23.120 align:middle line:90%
OK?

00:37:23.120 --> 00:37:25.350 align:middle line:84%
And she can have a lot
of different nests.

00:37:25.350 --> 00:37:27.445 align:middle line:84%
So when you look at
the whole situation

00:37:27.445 --> 00:37:30.700 align:middle line:84%
it seems like quite complex
behavior that obviously

00:37:30.700 --> 00:37:32.150 align:middle line:90%
involves some learning.

00:37:32.150 --> 00:37:36.750 align:middle line:84%
And yet the whole structure
is innate behavior,

00:37:36.750 --> 00:37:38.760 align:middle line:84%
but with these
specific things she

00:37:38.760 --> 00:37:41.935 align:middle line:84%
has to remember in order to
carry out the whole sequence.

00:37:41.935 --> 00:37:46.470 align:middle line:90%


00:37:46.470 --> 00:37:49.950 align:middle line:84%
So what she detects in a nest
determines her next behavior.

00:37:49.950 --> 00:37:52.710 align:middle line:84%
Looks like my words
didn't all copy there.

00:37:52.710 --> 00:37:55.220 align:middle line:90%


00:37:55.220 --> 00:37:59.140 align:middle line:84%
So the behavior sequences
are complicated by the fact

00:37:59.140 --> 00:38:00.890 align:middle line:84%
that she digs and
uses multiple nests.

00:38:00.890 --> 00:38:06.360 align:middle line:90%


00:38:06.360 --> 00:38:11.460 align:middle line:84%
And that led in general
motivational states underlying

00:38:11.460 --> 00:38:14.110 align:middle line:84%
the feeding behavior
of chicks and geese

00:38:14.110 --> 00:38:19.190 align:middle line:84%
also show this relative
hierarchy of moods.

00:38:19.190 --> 00:38:22.360 align:middle line:84%
And a good example
is the feeding

00:38:22.360 --> 00:38:25.550 align:middle line:84%
of ducks, which we talked
about that a little bit.

00:38:25.550 --> 00:38:28.415 align:middle line:84%
But we didn't describe this
behavior, the upending behavior

00:38:28.415 --> 00:38:29.540 align:middle line:90%
of ducks and geese.

00:38:29.540 --> 00:38:31.650 align:middle line:90%
What's upending?

00:38:31.650 --> 00:38:35.830 align:middle line:84%
Have you ever watched ducks
or geese feeding in a pond?

00:38:35.830 --> 00:38:39.130 align:middle line:84%
Much of the time you
only see their tail.

00:38:39.130 --> 00:38:41.080 align:middle line:90%
They're upended.

00:38:41.080 --> 00:38:43.880 align:middle line:84%
They're looking for
something down below.

00:38:43.880 --> 00:38:44.800 align:middle line:90%
OK?

00:38:44.800 --> 00:38:47.970 align:middle line:90%
And that's how they feed.

00:38:47.970 --> 00:38:54.600 align:middle line:84%
If you feed the geese, or
the ducks, on the ground then

00:38:54.600 --> 00:38:55.850 align:middle line:90%
they wouldn't have to do that.

00:38:55.850 --> 00:38:56.656 align:middle line:90%
Right?

00:38:56.656 --> 00:39:00.850 align:middle line:84%
Ah, but they're highly
motivated to do upending.

00:39:00.850 --> 00:39:03.700 align:middle line:90%
See it's a separate motivation.

00:39:03.700 --> 00:39:08.940 align:middle line:84%
So if you deprive them of food,
they will go out and upend.

00:39:08.940 --> 00:39:10.302 align:middle line:90%
OK?

00:39:10.302 --> 00:39:15.130 align:middle line:84%
They're not-- They're feeding
because they want to upend.

00:39:15.130 --> 00:39:17.410 align:middle line:84%
They're not upending
in order to feed.

00:39:17.410 --> 00:39:19.650 align:middle line:84%
And that's similar to
what we talked about

00:39:19.650 --> 00:39:24.110 align:middle line:84%
before when we talked about the
starling poking into things.

00:39:24.110 --> 00:39:26.420 align:middle line:84%
He's so highly
motivated to poke,

00:39:26.420 --> 00:39:28.460 align:middle line:84%
that even if he's well
fed, he will do it.

00:39:28.460 --> 00:39:32.320 align:middle line:84%
And similarly the cactus finch
would still find a cactus spine

00:39:32.320 --> 00:39:33.805 align:middle line:90%
and poke into things.

00:39:33.805 --> 00:39:36.180 align:middle line:84%
Because he's highly-- even if
he's well fed, because he's

00:39:36.180 --> 00:39:37.530 align:middle line:90%
highly motivated to do that.

00:39:37.530 --> 00:39:40.700 align:middle line:90%


00:39:40.700 --> 00:39:45.330 align:middle line:84%
So well fed birds
deprived of upending--

00:39:45.330 --> 00:39:48.420 align:middle line:90%
we'll do that.

00:39:48.420 --> 00:39:52.500 align:middle line:84%
Here's the picture of
what it looks like.

00:39:52.500 --> 00:39:53.390 align:middle line:90%
Two ducks upending.

00:39:53.390 --> 00:39:59.540 align:middle line:90%


00:39:59.540 --> 00:40:02.730 align:middle line:84%
And I just point out here that
the action specific potential

00:40:02.730 --> 00:40:06.127 align:middle line:84%
for that behavior is
separate than for hunger.

00:40:06.127 --> 00:40:08.750 align:middle line:90%


00:40:08.750 --> 00:40:11.675 align:middle line:84%
So to deprive them of it,
they will show the behavior.

00:40:11.675 --> 00:40:15.370 align:middle line:90%


00:40:15.370 --> 00:40:17.590 align:middle line:84%
Lorenz has this interesting
little discussion

00:40:17.590 --> 00:40:20.330 align:middle line:90%
of why the head--

00:40:20.330 --> 00:40:23.780 align:middle line:84%
which he says contains the
locus of superior command--

00:40:23.780 --> 00:40:28.320 align:middle line:90%
had to be invented in evolution.

00:40:28.320 --> 00:40:29.440 align:middle line:90%
So how is the function--

00:40:29.440 --> 00:40:33.070 align:middle line:90%


00:40:33.070 --> 00:40:35.360 align:middle line:84%
I'm asking, has the function
of the head ganglion

00:40:35.360 --> 00:40:37.395 align:middle line:84%
changed in higher
vertebrates with respect

00:40:37.395 --> 00:40:40.140 align:middle line:90%
to fixed action patterns?

00:40:40.140 --> 00:40:41.810 align:middle line:84%
And that's an
interesting question.

00:40:41.810 --> 00:40:45.390 align:middle line:84%
Lorenz says the head had
to evolve to limit behavior

00:40:45.390 --> 00:40:46.785 align:middle line:90%
to one motor pattern at a time.

00:40:46.785 --> 00:40:52.710 align:middle line:90%


00:40:52.710 --> 00:40:56.020 align:middle line:84%
It was to embody the innate
releasing mechanisms also,

00:40:56.020 --> 00:40:58.650 align:middle line:84%
because most innate
releasing mechanisms involve

00:40:58.650 --> 00:41:00.750 align:middle line:90%
stimuli coming into the head.

00:41:00.750 --> 00:41:04.680 align:middle line:84%
And the stimuli come in
through the cranial nerves.

00:41:04.680 --> 00:41:08.040 align:middle line:84%
Most of them do not come in
through the spinal nerves.

00:41:08.040 --> 00:41:10.450 align:middle line:90%
OK?

00:41:10.450 --> 00:41:14.560 align:middle line:84%
There are some components,
for example in that nursing

00:41:14.560 --> 00:41:18.750 align:middle line:84%
behavior of the kitten
looking for the opportunity

00:41:18.750 --> 00:41:21.855 align:middle line:84%
to nurse that do come in
through the spinal cord.

00:41:21.855 --> 00:41:23.855 align:middle line:84%
But most of them are
coming in through the head.

00:41:23.855 --> 00:41:27.950 align:middle line:90%


00:41:27.950 --> 00:41:29.760 align:middle line:84%
And I'm asking here
how the function has

00:41:29.760 --> 00:41:32.000 align:middle line:90%
changed in higher vertebrates?

00:41:32.000 --> 00:41:35.950 align:middle line:84%
I would say that the main
thing that's been changing

00:41:35.950 --> 00:41:38.410 align:middle line:84%
is increased linkage
between innate

00:41:38.410 --> 00:41:39.890 align:middle line:90%
and learned aspects of behavior.

00:41:39.890 --> 00:41:43.410 align:middle line:84%
And that reaches
a peak in humans,

00:41:43.410 --> 00:41:47.360 align:middle line:84%
but it's very prominent
in other animals.

00:41:47.360 --> 00:41:51.800 align:middle line:84%
And the other is initiation
of behavior patterns

00:41:51.800 --> 00:41:54.210 align:middle line:90%
by learned motivations.

00:41:54.210 --> 00:41:56.674 align:middle line:90%
Motivations can be learned.

00:41:56.674 --> 00:41:57.500 align:middle line:90%
OK?

00:41:57.500 --> 00:42:01.220 align:middle line:84%
And acquired
motivations are common.

00:42:01.220 --> 00:42:04.660 align:middle line:84%
We all know about, of
course, some of the bad ones,

00:42:04.660 --> 00:42:06.920 align:middle line:90%
the addictive behaviors.

00:42:06.920 --> 00:42:08.710 align:middle line:84%
But there are many
different motivations.

00:42:08.710 --> 00:42:12.290 align:middle line:84%
We become highly motivated
to do certain tasks.

00:42:12.290 --> 00:42:12.790 align:middle line:90%
OK?

00:42:12.790 --> 00:42:14.590 align:middle line:90%
Well that was not--

00:42:14.590 --> 00:42:19.030 align:middle line:84%
we didn't carry that
with us from the uterus.

00:42:19.030 --> 00:42:19.530 align:middle line:90%
OK?

00:42:19.530 --> 00:42:23.820 align:middle line:90%


00:42:23.820 --> 00:42:30.300 align:middle line:84%
But also our cognitive level,
we contain a model of the world.

00:42:30.300 --> 00:42:32.180 align:middle line:90%
And in that we make--

00:42:32.180 --> 00:42:34.750 align:middle line:84%
embodies choices we
make and so forth.

00:42:34.750 --> 00:42:41.240 align:middle line:90%


00:42:41.240 --> 00:42:43.660 align:middle line:84%
I just point out here
that the cognitive level

00:42:43.660 --> 00:42:47.430 align:middle line:84%
is at the top of a
neural hierarchy.

00:42:47.430 --> 00:42:50.400 align:middle line:84%
But it doesn't mean just
because it's at the top

00:42:50.400 --> 00:42:52.290 align:middle line:90%
that it's always dominant.

00:42:52.290 --> 00:42:54.460 align:middle line:90%
And we all know that for sure.

00:42:54.460 --> 00:42:58.510 align:middle line:84%
People can be totally
dominated by the drive

00:42:58.510 --> 00:43:06.590 align:middle line:84%
to enact revenge, drive to
feed, drive to acquire things.

00:43:06.590 --> 00:43:08.940 align:middle line:84%
These are innate
behavior patterns.

00:43:08.940 --> 00:43:17.110 align:middle line:84%
And that cognitive level
that's often not at the top.

00:43:17.110 --> 00:43:21.500 align:middle line:84%
Maybe in true
intellectuals it is.

00:43:21.500 --> 00:43:25.935 align:middle line:84%
I define a true intellectual as
somebody who, by what he knows

00:43:25.935 --> 00:43:28.530 align:middle line:90%
and what he learns--

00:43:28.530 --> 00:43:30.580 align:middle line:84%
the cognitions
that he acquires--

00:43:30.580 --> 00:43:34.230 align:middle line:84%
actually affect his
behavior in a major way.

00:43:34.230 --> 00:43:37.400 align:middle line:90%
It's not true of most people.

00:43:37.400 --> 00:43:42.360 align:middle line:84%
In fact when one student
working with Bruce and with me

00:43:42.360 --> 00:43:46.490 align:middle line:84%
here at MIT was
simulating human behavior,

00:43:46.490 --> 00:43:50.850 align:middle line:84%
everything in it, except
for some very simple spatial

00:43:50.850 --> 00:43:53.180 align:middle line:90%
things, was not learned.

00:43:53.180 --> 00:43:56.190 align:middle line:84%
It was all built
into the software.

00:43:56.190 --> 00:44:01.480 align:middle line:84%
And yet you show the
results of simulations

00:44:01.480 --> 00:44:04.080 align:middle line:84%
where you see people moving
around, making choices,

00:44:04.080 --> 00:44:07.175 align:middle line:84%
and this and that, it looks like
pretty normal human behavior.

00:44:07.175 --> 00:44:09.800 align:middle line:90%


00:44:09.800 --> 00:44:12.330 align:middle line:84%
So a lot of times when we're
observing human behavior,

00:44:12.330 --> 00:44:14.340 align:middle line:84%
we're just looking at
fixed action patterns.

00:44:14.340 --> 00:44:18.110 align:middle line:90%


00:44:18.110 --> 00:44:18.610 align:middle line:90%
All right.

00:44:18.610 --> 00:44:22.160 align:middle line:90%


00:44:22.160 --> 00:44:26.445 align:middle line:84%
Next topic here concerns what
we call taxis and reflexes.

00:44:26.445 --> 00:44:29.330 align:middle line:84%
This involves
spatial orientation.

00:44:29.330 --> 00:44:32.825 align:middle line:84%
And that leads to a discussion
of thinking in higher animals.

00:44:32.825 --> 00:44:35.400 align:middle line:90%


00:44:35.400 --> 00:44:38.700 align:middle line:84%
First of all-- and we won't
have time for too much more than

00:44:38.700 --> 00:44:40.540 align:middle line:90%
this--

00:44:40.540 --> 00:44:43.280 align:middle line:84%
explain how the
mantle of reflexes--

00:44:43.280 --> 00:44:49.460 align:middle line:84%
the term I've used from
Fromholtz and Lorenz uses it,

00:44:49.460 --> 00:44:50.010 align:middle line:90%
I believe.

00:44:50.010 --> 00:44:52.540 align:middle line:90%


00:44:52.540 --> 00:44:56.718 align:middle line:84%
It tends to conceal the rigidity
of fixed motor patterns.

00:44:56.718 --> 00:44:57.990 align:middle line:90%
You know?

00:44:57.990 --> 00:45:00.760 align:middle line:84%
When we walk, for
example, we know

00:45:00.760 --> 00:45:02.300 align:middle line:90%
that's a fixed motor pattern.

00:45:02.300 --> 00:45:05.250 align:middle line:84%
It appears at a certain age
when the neural mechanisms

00:45:05.250 --> 00:45:07.350 align:middle line:90%
of the spinal cord mature.

00:45:07.350 --> 00:45:10.240 align:middle line:84%
And the various gaits
are walking and running.

00:45:10.240 --> 00:45:13.250 align:middle line:84%
The various gaits of a
horse, which are multiple.

00:45:13.250 --> 00:45:15.050 align:middle line:90%
They're all inherited.

00:45:15.050 --> 00:45:18.280 align:middle line:84%
And yet at least,
especially for humans,

00:45:18.280 --> 00:45:22.840 align:middle line:84%
when we're walking around
it seems to vary a lot.

00:45:22.840 --> 00:45:25.315 align:middle line:84%
It depends on what
we're walking on.

00:45:25.315 --> 00:45:26.970 align:middle line:90%
It depends on the terrain.

00:45:26.970 --> 00:45:30.320 align:middle line:84%
Even horses change the way
they walk, even though--

00:45:30.320 --> 00:45:32.720 align:middle line:84%
much less than, say, the
more sure footed animals

00:45:32.720 --> 00:45:35.470 align:middle line:90%
like goats and donkeys.

00:45:35.470 --> 00:45:40.210 align:middle line:84%
But it's being adjusted
by the reflexes.

00:45:40.210 --> 00:45:41.420 align:middle line:90%
You know?

00:45:41.420 --> 00:45:45.810 align:middle line:84%
If I'm walking along here, I'm
responding visually here, too.

00:45:45.810 --> 00:45:47.350 align:middle line:84%
And I don't even
look here, but I

00:45:47.350 --> 00:45:48.860 align:middle line:90%
can see the edge of this table.

00:45:48.860 --> 00:45:51.710 align:middle line:84%
And I will walk around it
without even thinking about it.

00:45:51.710 --> 00:45:58.550 align:middle line:84%
This is just an example of
simple spatial orientation

00:45:58.550 --> 00:46:03.000 align:middle line:84%
reflexes that alter the way
the locomotion is expressed.

00:46:03.000 --> 00:46:06.040 align:middle line:84%
And there's much
simpler examples.

00:46:06.040 --> 00:46:08.840 align:middle line:84%
Like the egg rolling behavior
of the graylag goose.

00:46:08.840 --> 00:46:12.300 align:middle line:84%
Every time you see a graylag
goose rolling an egg back

00:46:12.300 --> 00:46:14.830 align:middle line:84%
into the nest, it looks
a little different

00:46:14.830 --> 00:46:16.400 align:middle line:90%
than other times you see it.

00:46:16.400 --> 00:46:19.620 align:middle line:84%
Because the egg is
rolling this way and that.

00:46:19.620 --> 00:46:22.060 align:middle line:84%
It's meeting little
stones and he

00:46:22.060 --> 00:46:27.045 align:middle line:84%
has to keep adjusting how he's
getting his beak over the egg

00:46:27.045 --> 00:46:29.300 align:middle line:84%
and pulling it back
towards the nest.

00:46:29.300 --> 00:46:31.235 align:middle line:84%
So it looks like it's
complex, and yet it's

00:46:31.235 --> 00:46:32.550 align:middle line:90%
a fixed motor pattern.

00:46:32.550 --> 00:46:34.950 align:middle line:84%
That's basically the
same motor pattern,

00:46:34.950 --> 00:46:39.435 align:middle line:84%
but it's working at a higher
level than all these reflexes

00:46:39.435 --> 00:46:41.440 align:middle line:84%
that are constantly
adjusting it.

00:46:41.440 --> 00:46:43.590 align:middle line:90%
And the reflexes never stop.

00:46:43.590 --> 00:46:46.730 align:middle line:84%
Remember they don't
depend on the motivation.

00:46:46.730 --> 00:46:47.560 align:middle line:90%
They always act.

00:46:47.560 --> 00:46:50.310 align:middle line:90%


00:46:50.310 --> 00:46:52.160 align:middle line:84%
So it looks variable
and complex,

00:46:52.160 --> 00:46:58.730 align:middle line:84%
because it's superimposed
on the behavior

00:46:58.730 --> 00:47:00.100 align:middle line:90%
of these various reflexes.

00:47:00.100 --> 00:47:01.030 align:middle line:90%
They're vestibular.

00:47:01.030 --> 00:47:02.360 align:middle line:90%
They're tactile.

00:47:02.360 --> 00:47:06.000 align:middle line:90%
They're visual, and so forth.

00:47:06.000 --> 00:47:09.320 align:middle line:90%


00:47:09.320 --> 00:47:11.220 align:middle line:90%
Last topic.

00:47:11.220 --> 00:47:15.640 align:middle line:90%
A goldfish behind a barrier.

00:47:15.640 --> 00:47:19.140 align:middle line:90%
Let's say these are thick weeds.

00:47:19.140 --> 00:47:22.370 align:middle line:84%
He can't swim through,
but he can see through it

00:47:22.370 --> 00:47:24.755 align:middle line:84%
well enough to see that
there's food on the other side.

00:47:24.755 --> 00:47:28.940 align:middle line:90%


00:47:28.940 --> 00:47:30.520 align:middle line:90%
How does he solve that problem?

00:47:30.520 --> 00:47:33.670 align:middle line:84%
And actually goldfish
do pretty well.

00:47:33.670 --> 00:47:37.220 align:middle line:90%
Better than dogs actually.

00:47:37.220 --> 00:47:38.690 align:middle line:90%
Here's what he does.

00:47:38.690 --> 00:47:41.740 align:middle line:90%
He swims right for it.

00:47:41.740 --> 00:47:46.970 align:middle line:84%
And as soon as he touches
it, he's got another reflex.

00:47:46.970 --> 00:47:47.470 align:middle line:90%
OK?

00:47:47.470 --> 00:47:50.080 align:middle line:84%
We call it a
negative thigmotaxis.

00:47:50.080 --> 00:47:54.030 align:middle line:84%
A negative response to touching
with his snot, and that

00:47:54.030 --> 00:47:56.020 align:middle line:90%
causes him to pull back.

00:47:56.020 --> 00:47:58.690 align:middle line:84%
Now of course the algorithm
can vary among fish,

00:47:58.690 --> 00:48:00.420 align:middle line:90%
and it's very different in dogs.

00:48:00.420 --> 00:48:02.890 align:middle line:84%
But normally he will keep
trying to get at the food,

00:48:02.890 --> 00:48:05.510 align:middle line:84%
but he will keep
moving like this

00:48:05.510 --> 00:48:09.180 align:middle line:90%
until he can get at the food.

00:48:09.180 --> 00:48:11.940 align:middle line:90%
So just two reflexes are enough.

00:48:11.940 --> 00:48:15.850 align:middle line:84%
Positive telotaxis is
what we call his moving

00:48:15.850 --> 00:48:17.320 align:middle line:90%
towards the food.

00:48:17.320 --> 00:48:20.000 align:middle line:84%
It's just a technical name
for it, positive telotaxis.

00:48:20.000 --> 00:48:23.860 align:middle line:84%
Telo means the end,
taxis movement.

00:48:23.860 --> 00:48:24.560 align:middle line:90%
OK?

00:48:24.560 --> 00:48:28.652 align:middle line:84%
Directed towards the prey,
or towards the other food

00:48:28.652 --> 00:48:29.860 align:middle line:90%
that he was trying to get to.

00:48:29.860 --> 00:48:33.140 align:middle line:84%
And then the
negative thigmotaxis

00:48:33.140 --> 00:48:37.740 align:middle line:84%
causes him to avoid the
obstacles, branches, plants,

00:48:37.740 --> 00:48:39.110 align:middle line:90%
so forth.

00:48:39.110 --> 00:48:40.735 align:middle line:84%
So it looks like
intelligent behavior.

00:48:40.735 --> 00:48:43.590 align:middle line:90%


00:48:43.590 --> 00:48:46.510 align:middle line:84%
He seems to figure out
how to reach the food,

00:48:46.510 --> 00:48:50.480 align:middle line:84%
but in fact it's just
two reflexes running on.

00:48:50.480 --> 00:48:51.530 align:middle line:90%
OK?

00:48:51.530 --> 00:48:53.845 align:middle line:84%
So now think about
how a dog does it.

00:48:53.845 --> 00:48:57.390 align:middle line:84%
And we'll come back
here next time.