Carter;
Mapping
the Mind |
112 |
"Where"
path: V1 -- V2 -- V3 -- V5 -- V6 |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
112 |
"What"
path: V1 -- V2
-- V4 |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
115 |
Vast
majority
of the cortex
is given over to sensory processing --
only the frontal lobes are dedicated to non-sensual tasks. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
115 |
Thalamus acts as a relay station, shunting
incoming data onto appropriate cortical areas for processing. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
117 |
Recognizing
someone is a process,
most of which is done unconsciously. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
123 |
Cortical
"who?" recognition pathway
ends in the frontal area with the conscious acknowledgment that
a person is familiar. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
138 |
Language areas of the brain are mainly in
the left hemisphere. Wernicke's area
makes spoken language comprehensible. Broca's
area generates speech and may contain a "grammar module." Annular gyrus is concerned with meaning. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
147 |
Words and music
are processed in different parts of the brain. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
148 |
Brain responds
differently
to a word according to whether (1) hearing
it spoken, (2) seeing it written down, (3) speaking
it, (4) considering which other words it relates to. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
149 |
Switch in brain
activity from the language areas
to the parietal lobes where spatial tasks are processed. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
150 |
Reading activates
part of the visual cortex. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
150 |
Listening to speech makes the auditory
cortex light up. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
150 |
Thinking about
words makes Broca's area --
the articulation center -- light up. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
150 |
Thinking about words and speaking
generates widespread activity. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
155 |
Stuttering may be due to competition for dominance between left and
right hemispheres. Neither side
can decide which is in control, so that both
try to produce words. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
158 |
Human brain holds
billions of impressions, called memories. At night, memory fragments are replayed and
reassembled. Each
run-through etches them deeper into the neural
structure until there comes a time when memories and a person
who holds them are effectively one and the same. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
166 |
Hippocampus is activated when people are asked
to recall personal or 'episodic' memories. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
166 |
Finding your way
around a familiar
place involves the hippocampus, but
only on the right side. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
176 |
Alzheimer's
disease first area to go
tends to be the hippocampus. People with Alzheimer's dementia often get
lost. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
176 |
In semantic dimentia the temporal lobe
is affected first, so people tend to forget general things like the names
of objects. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
176 |
Memories are groups of neurons that fire
together in the same pattern each time
they are activated. The links
between individual neurons, which bind them into a single memory, are
formed through a process called long-term potentiation (LTP). |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
176 |
Sematic
dementia,
which involves loss of factual memory rather than loss of personal
memory, destroys the cortical area of the temporal
lobe first, where semantic memories are thought to be stored. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
178 |
In Alzheimer's disease, plaques of an insoluble protein fragment, beta amyloid,
accumulate in the cleft between neurons,
blocking communication. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
180 |
Frontal
lobes are where ideas
are created, plans constructed, thoughts join with their associations
to form new memories, fleeting perceptions held in mind until they are
dispatched to long-term memory. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
184 |
Blindsight first came to light on the battlefields
of the First World War when blinded soldiers
were seen to.duck bullets even though
they had no idea they were doing so. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
184 |
Blindsight is easiest to detect in people with
a form of blindness caused by damage to the primary visual cortex (V1). |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
189 |
Skilled tennis
and cricket players
have hit a speeding ball before its
existence can possibly be registered by the cortex, may be due to blindsight. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
192 |
Thinking requires a degree of attention, a focusing
of activity in which irrelevant stimuli are
ignored. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
192 |
Two types of
attention: (1) automatic engagement of the senses that occurs when
your eye is caught by a flash of movement, (2) deliberate turning of
the mind to a subject. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
192 |
Attention is created by a flood of neurotransmitters that turns important areas ON and unimportant ones OFF. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
195 |
Many
brain regions
are involved in directing and controlling attention. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
195 |
One brain region
controlling attention that is
especially concerned with holding internally generated stimuli in focus is
the anterior cingulate cortex, a region
on the inside front edge of the longitudinal fissure, the deep
chasm that runs from the front of the brain to the back. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
195 |
Anterior
cingulate cortex
is sensitive to information from the body and it is fiercely active
when a person feels pain, and also becomes active when we are conscious
of emotion. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
195 |
Thinking -- holding ideas in mind and
manipulating them -- takes place in the dorsolateral prefrontal cortex. This is the location of the closely related
activity, working memory. Planning takes place in this area. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
203 |
Roger Penrose of
Oxford University believes that nonbiological machines can never cross
the chasm between computation and understanding. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
203 |
Roger Penrose has the strong feeling that the
conscious mind cannot work like a computer. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
204 |
Consciousness -- not a thing but a process -- Francis
Crick, Salk Institute for Biological Studies, San Diego. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
205 |
Episodic
memory, enabled by the hippocampal system, is not essential for
consciousness. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
205 |
Attention is caused either by sensory
input or by the planning parts of the brain. |
||||||||||||||||||||||||
Carter;
Mapping
the Mind |
207 |
Some illusions are programmed
so firmly in our brains that the mere knowledge that they are false does not stop us from seeing them. |
||||||||||||||||||||||||
Damasio; Self Comes to Mind |
118 |
The insular cortex is an important substrate of
feelings -- from those that are associated with emotions to those
that correspond to any shade of pleasure or pain, induced by a wide
ranges stimuli -- hearing music one likes or hates; viewing pictures
one loves, including erotic material, or pictures that can
cause disgust; drinking wine; having sex; being high on drugs;
being low on drugs and experiencing withdrawal; etc. |
|||||
Damasio; Self Comes to Mind |
141 |
Convergence
divergence zones (CDZs)
record the coincidence of activity in neurons hailing from different
brain sites, neurons that had been made active by, for example,
the mapping of a certain object. |
|||||
Damasio; Self Comes to Mind |
144 |
A convergence-divergence zone (CDZ) is an ensemble
of neurons within which many feedforward-feedback loops make contact. |
|||||
Damasio; Self Comes to Mind |
144 |
A CDZ receives feedforward connections from
sensory areas located earlier in the signal-processing chains, which begin at
the entry point of the sensory signals in the cerebral cortex. |
|||||
Damasio; Self Comes to Mind |
144 |
A CDZ sends reciprocal
feedback projections to the originating areas. |
|||||
Damasio; Self Comes to Mind |
144 |
A CDZ also sends
feedforward projections to regions located in the next connectional level of the chain and receives return projections from them. |
|||||
Damasio; Self Comes to Mind |
145 |
CDZs are microscopic and are
located within convergence-divergence regions (CDRegions),
which are macroscopic. |
|||||
Damasio; Self Comes to Mind |
145 |
Damasio envisions
the number of CDZs to be on the order
of many thousands. |
|||||
Damasio; Self Comes to Mind |
145 |
CDRegions play an important role in producing
and organizing critical components of the conscious mind, including
those that make up the autobiographical self. |
|||||
Damasio; Self Comes to Mind |
149 |
Images constructed during perception
are reconstructed during the process of imagery. They are approximations
rather than replicas, attempts at getting back at past reality and
thus not quite as vivid or accurate. |
|||||
Eichenbaum;
Neuroscience
of Memory |
41 |
All of us use habituation
every day to help us learn not to respond to irrelevant stimuli. |
|||
Eichenbaum;
Neuroscience
of Memory |
41 |
Habituation is a very simple form of learning,
but it has the lasting property that indicates it is indeed a form of long-term memory. |
|||
Eichenbaum;
Neuroscience
of Memory |
43 |
Sensitization is the opposite of a habituation --
it involves an increase in reflex magnitude as a result of prior
stimulation. |
|||
Eichenbaum;
Neuroscience
of Memory |
43 |
As the result of sensitization, when we encounter a fearful
stimulus, such as a loud noise, we've become for sometime more likely to startle, or startle more
vigorously. |
|||
Eichenbaum;
Neuroscience
of Memory |
46 |
Classical
conditioning
involves the acquisition of an association between the first, or conditioned
stimulus, and the second, unconditioned stimulus. |
|||
Fuster; Cortex and Mind |
45 |
Hippocampus, which is phylogenetically old cortex, plays a crucial
role in the acquisition and consolidation of memory and thus in the construction
of neocortical representations. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Memory
representations over 4 weeks old presumably have already been consolidated in the neocortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Hippocampus exerts its memory making role over
the neocortex probably through the connections that reciprocally link the two structures
through the parahippocampal gyrus. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Neocortical connectivity of the hippocampus is
limited to areas of association. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
No hippocampal
fibers terminate or
originate in primary sensory or motor
cortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Hippocampal connectivity reaches into large sectors of the posterior cortex of association, behind the central
sulcus, and also extends to association areas of the frontal lobe,
i.e. the prefrontal cortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Only the associative areas of the neocortex need the input from the hippocampus for the formation of new representations. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Primary sensory and motor cortices do
not need hippocampal inputs for the formation of elementary sensory and
motor representations. [Stereotyped
motor programs] [FAPs] |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
Cortex of association
needs hippocampal inputs in order to
accommodate the new memories, and also to retrieve them before
they are consolidated into long-term memory. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
46 |
A significant
implication of the hippocampal-prefrontal connections is that the hippocampus, in addition to its role in memory
formation, contributes to the formation of the neocortical
representation of the most complex actions
of the individual. [Stereotyped motor
programs] [FAPs] |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
47 |
Bidirectional
connectivity between
the hippocampus and the neocortex through the parahippocampal cortex.
(diagram) |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
47 |
Brodmann's area
28 is a major node
of connections linking the hippocampus
with associative areas of the neocortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
49 |
In both
hippocampus and cortex, glutamate, through in NMDA receptors, may activate second
messengers in postsynaptic cells, and thus induced protein changes that sustain LTP as well
as other lasting phenomena of network formation. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
49 |
NMDA
receptors
are most common in layers 2 and 3, which are the preferred
terminations of corticocortical axons, and thus the potential site for
corticocortical network links. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
49 |
Neural network
representations
in the neocortex are a continuation of a process that began with cortical
evolution in ancestral mammalian species. The phylogenetically
oldest representations are those of the simplest physical
features of the world and of motor adaptations to it. They are present
at birth in the structure of the primary
sensory and motor cortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
49 |
The innate structure of primary sensory and
motor cortex can be considered a form of memory
that has been stored in evolution and
can be retrieved as needed by the organism for adaptation to its
surroundings. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
50 |
Neocortical
networks
for cognitive representation fan out
into more areas and higher areas, gaining width of distribution,
where they intersect other networks of different
origin. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
50 |
Cognitive
networks
are largely self-organized by auto-association. They are formed by inputs
arriving simultaneously, in temporal
correlation, to cell groups of existing networks of association
cortex, where those inputs established new
associations. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
60 |
The most obvious
characteristic of perceptual categories is their hierarchical organization. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
60 |
Perceptual
categories
are organized in cognitive hierarchies
of progressive integration and generality, with sensory percepts in lower
levels and abstract or symbolic percepts in higher ones. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
84 |
Every percept
is a historical event, a categorization
of current sensory impressions that is
entirely determined by previously established memory. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
84 |
Perception can be viewed as the interpretation of new
experiences based on assumptions from prior
experience. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
88 |
Gestalt
psychology developed
a number of principles of organization. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
88 |
Because of their
power to explain a great variety of configurations in human cognition, the laws of Gestalt psychology have been
generalized to several cognitive functions, including learning and thinking. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
91 |
Perceptual
processing will
be one of categorizing incoming information
in accord with prior experience, by matching the new to the old
and by modifying the old with the new. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
92 |
Degeneracy implies an approximate or highly
probable fit between the structure of the network, in connective
terms, and the structure of the external Gestalt in relational terms. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
92 |
Because of the
factors of approximation and probability, and because several cognits shared
common features, an incoming gestalt or part thereof can activate several
networks before the best match and categorization occur. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
93 |
Some of these categorization processes will be guided --
top-down -- by attention and may
occur consciously. The vast
majority will occur unconsciously in rapid succession. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
113 |
Bulk of individual memory is formed and stored in
neuronal networks of cortex of association. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
118 |
Short-term
memory is characterized
by limited storage capacity, estimated to be a maximum of about seven items, and
relatively rapid decay. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
118 |
Long-term
memory has unlimited
capacity and a little or no decay. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
118 |
Presented with a list
of words, and required to repeat the words regardless of the order
(free recall), can usually recall well the first
words in the list (primacy effect)
and the last words (recency effect), but not so well the words in the middle. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
118 |
Hippocampus is necessary for the transfer of a short-term memory to its long-term permanent store. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
119 |
The curve of forgetting is not inflected but
monotonically gradual. When plotted on
double-log graphs, the data become straight lines. They conform to a power
function. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
119 |
Remembering is reinforced by rehearsal and impeded by distraction. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
120 |
Information begins
to enter permanent storage as soon
as it comes in. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Evidence for the consolidation of memory in one store implicates
the entire cerebral cortex and synaptic
change in cortical networks as the essence of consolidation. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Concept of
time-limited memory as an active and operant
state of cortical memory -- not a short-term memory per se but is memory
for the short-term. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Working
memory, a function of
fundamental importance for the temporal organization
of cognition, speech, and behavior. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Memory can take many forms, and any memory
has a mixture of contents. Heterogeneity is a universal trait of all memories. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Heterogeneity of memory
is a direct result of its associative
nature. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
121 |
Autobiographical
memory, which is
commonly characterized as episodic or declarative, illustrates
the heterogeneity of memory. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
124 |
All dated
experience is an extension of previous experience, an expansion
of old memory and of old knowledge. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
124 |
Any perceptual
memory is an associative conglomerate
of sensory and semantic features at many
levels of the cognitive hierarchy of perceptual knowledge. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
124 |
The network
representing a memory must tie together features of the same modality in unimodal association cortex
and of different modalities in cross
modal association cortex. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
133 |
It is well known
that memories can be more easily retrieved by recognition than by recall. |
|||||||||||||||||||||||||||||||
Fuster; Cortex and Mind |
139 |
Priming can be appropriately understood as
a result of the reactivation of the memory
network -- at a subliminal level of conscious awareness -- through an associative link within itself or with other
networks. |
|||||||||||||||||||||||||||||||
Gluck & Myers; Gateway to Memory |
86 |
The brain
generally represents information using distributed representations, in
which each
stimulus is encoded by many different neurons and each neuron may respond to conjunctions of features that may be present in many different stimuli. |
|||||||||||||||||||||
Gluck & Myers; Gateway to Memory |
87 |
Distributed
representation is efficient
because a large number of stimuli can be processed by smaller number of neurons, each of which encodes some
features of the stimuli. |
|||||||||||||||||||||
Gluck & Myers; Gateway to Memory |
87 |
Distributed
representations have the advantage
that if some of the units are lost or degraded, the remaining
units may be able to provide enough information to represent the stimuli adequately. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
9 |
A signature is the only universally accepted outward sign of an individual. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
59 |
Blindsight patients possess some kind of visual ability,
but this ability has become totally disassociated from conscious
awareness of events in the visual field.
Weiskrantz (1974) |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
68 |
Memory appears to be in inextricably
linked to consciousness. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
85 |
Consciousness is a property of many transient groupings of neurons. Our brains are a restless grouping
and re-grouping of temporarily relevant neurons with greater and lesser connectivity. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
88 |
A property of consciousness is its spatial
multiplicity combined with temporal unity. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
91 |
Consciousness can be focused on an internalized representation, such as a hope
or a memory. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
98 |
Idea behind the gestalt school of thought is that perception
is global, not local; objects or
features are perceived in relation to one another, giving a final
holistic view that cannot be
inferred from the individual components alone. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
104 |
Consciousness is an emergent
property of nonspecialized and divergent groups of
neurons that is continuously variable
with respect to, and always entailing, a stimulus epicenter. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
112 |
Gestalt is defined as a highly variable
aggregation of neurons that is temporarily
recruited around a triggering epicenter. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
112 |
Not
all neuronal assemblies are gestalts, but all
gestalts are neuronal assemblies. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
114 |
Columns are the basic modules of the
functionally complex cortex. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
114 |
In more highly evolved animals, the critical factor that
changes is not the number of layers and not necessarily the number of cells,
but the potential complexity of connections
among the cells. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
114 |
Neuronal
gestalts
are transient groupings of neurons
where the connections among them are only temporarily functional. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
120 |
Wolf Singer has shown that disparate neurons large distances apart in the
area of the cortex associated with vision can oscillate in their excitability in a synchronous fashion,
if they are processing respective parts of a pattern
with a common feature. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
120 |
Gestalts are ceaselessly at work,
shuffling and reorganizing their internal communications. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
120 |
Oscillations and neuronal groups can vary from one moment to the next, corresponding
to changes in the interactions within the network. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
120 |
The process
wherein gestalts are undergoing
shifting changes as further associations
are triggered and new associations made,
might constitute the behavior or phenomena of
thinking. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
128 |
Three published biological
descriptions of consciousness,
including those by Francis Crick and the physiologist Rudolfo
Llinás focus on a particular loop between the cortex
and the thalamus. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
131 |
Llinás focuses on another part of the thalamus,
the nucleus reticularis, which seems to be involved with more generalized
states of arousal during sleep and waking. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
134 |
Persistent
vegetative state
-- patients in this condition regain
sleep wake cycles
and are able to
regulate body temperature and successfully fight infection. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
161 |
Consciousness is an emergent
property of nonspecialized and divergent groups of
neurons (gestalts)
that is continuously variable with respect to, and
always entailing, a stimulus
epicenter. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
165 |
Small,
minimal gestalts,
produced artificially by Penfield but more normally during dreaming state,
could be regarded as scraps of consciousness
torn from seemingly cohesive fabric of our awareness. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
170 |
Daydreaming is an extreme example of consciousness
dominated by highly complex cognitive epicenters, when sensory input is
minimal. |
|||||||||||||||||||||
Greenfield;
Centers
of Mind |
171 |
A powerful epicenter could be cognitive,
such as an all-pervading worry, or it
could be external and strong, due to an intrinsic brightness or
loudness of an outside object or to a heightened arousal. |
|||||||||||||||||||||
Hobson; Consciousness |
45 |
Dreaming
may be our most creative conscious
state, one in which the chaotic,
spontaneous recombination of cognitive elements produces novel
configurations of information -- new ideas. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
59 |
Sleep-dream-wake
cycle is triggered and tuned by neuronal
circuits in the pons. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
59 |
Key brain
structure
involved in attention is the thalamus,
a large collection of cells
located atop the brainstem in the center of the upper
brain. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
60 |
Hypothalamus contains the
biological clock that times
the body's cycles of rest and activity and gates
the sleep-wake cycle in the pons. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
61 |
Brain
structures of emotion lie below the thalamus and cortex and above the spinal cord and
brainstem. Taken together, the amygdala,
hippocampus, and hypothalamus have been called the limbic lobe of the brain |
||||||||||||||||||||||||||||
Hobson; Consciousness |
62 |
Intimate
relationship
between the hippocampus, which is
essential to memory, and the structures
mediating emotion. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
62 |
Mental faculty of
orientation cannot properly be
considered apart from memory.
Knowing who one is, what day
it is, and where one is. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
67 |
Overall brain activation level changes
as little as 10
percent (or at most 20
percent), between waking and sleep. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
68 |
Spontaneously high
level of activation during sleeping and dreaming; such processing is not only automatic but
potentially self-organizing and autocreative. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
69 |
Reticular
formation, like a pair
of sausages, occupies the
central core on each side of the
brainstem as it ascends from the medulla upward through the pons and midbrain to the hypothalamus. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
69 |
A particularly
cogent example of the function of the reticular
formation is the coordination
of eye position, which involves visual processing
centers of the upper brain and spinal circuits mediating head
and body position. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
70 |
Pons and midbrain
are the very center of the reticular system because they so clearly coordinate
activation of the higher brain structures. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
70 |
When the activation level of
the brainstem falls, even a
little, the thalamocortical
circuits begin to oscillate. This kind of synchrony contributes
to the global loss of consciousness that occurs in NREM
sleep. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
71 |
Oscillations of the
thalamocortical circuits that occur at sleep
onset are robust and so highly synchronous
that they cause the
characteristic EEG pattern of slow wave sleep. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
68 |
A significant
amount of information processing occurs even when we are completely
unaware of it as we sleep. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
68 |
Spontaneously high
level of activation during sleeping and dreaming; such processing is not only automatic but
potentially self-organizing and autocreative. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
74 |
Memories are ultimately encoded as proteins in the
synapses. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
84 |
Primary
consciousness
comprises sensation, perception, emotion, learning, geographic orientation,
instinct, primary intention; all of these can be operationally defined in lower
animals. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
87 |
Neuronal
networks
are associatively connected and sequentially activated by one another. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
88 |
Associative
learning --
building block of memory, of priming, and of word search must
be a mechanism shared by neuronal networks at all levels of phylogeny
(evolution of species) and ontogeny (individual development). |
||||||||||||||||||||||||||||
Hobson; Consciousness |
91 |
If an
invertebrate ganglionic neuron is to keep a record of its
experience, the neurotransmitter serotonin
must be released during its training-induced
activation. No serotonin, no learning. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
91 |
Conscious state
of waking, serotonin is released,
we perceive and can remember. In the conscious state of sleep (REM), serotonin is not released,
we can perceive but not remember. No serotonin, no
memory. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
96 |
Vision is a symbolic process; no real
pictures in the head, only neuronal patterns. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
99 |
Developmental
psychologists
postulate that consciousness emerges
gradually during the second year of human life and culminates at about
age 2 with
the gaining of awareness of the self as an
entity. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
99 |
Infant at age 7-8 mo learns to control
movement voluntarily. Called "will" by
developmental psychologists. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
99 |
Self arises when sensations associated with movement come to be
taken as causes of the movement. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
100 |
Recognition memory is evident at 8 months of age. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
100 |
Retrieval memory and inference
allow a 14 month old to detect logical
connection between past and present. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
101 |
Neural origin of primary
consciousness, thalamocortical system
of the forebrain. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
115 |
Working memory
neurons of the premotor cortex, receive dopamine and serotonin; Every
cortical neuron involved in the representation of working memory is
influenced by a variety of chemical modulators. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
135 |
Normal waking
conscious state;
aware of where we are, the date and approximate time, who is present in
our surroundings, goal or direction of our behavior. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
135 |
Orientational
instability during
dream consciousness is at the root of dream
bizarreness. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
135 |
Waking
consciousness;
we know, but we also know that we know. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
136 |
In dreams we are cognitively
adrift; no mooring to time, place, or person, no self-awareness,
no critical thought. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
137 |
Among the neuromodulators crucial to memory: (1) norepinephrine
(2) serotonin; both are conspicuously diminished
during dream consciousness. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
141 |
Thalamocortical
system - In its activated state, information
is rapidly and efficiently processed. Information can be either online data
from the real world or data about the real world that are stored in
the brain. |
||||||||||||||||||||||||||||
Hobson; Consciousness |
141 |
Consciousness at any instant is simply the integrated
product of the information represented in the activated
thalamocortical networks at that instant. That includes sense of self; awareness of body; and awareness of the world, be it real or
fictive. [Edelman's dynamic core] |
||||||||||||||||||||||||||||
Hobson; Consciousness |
141 |
Can define consciousness at any instant as the information
that is then represented in the working memory circuitry of the dorsolateral
prefrontal cortex (DLPFC).
[Edelman's dynamic core]
[Fuster's perception-action
cycle] |
||||||||||||||||||||||||||||
Houk;
Info Process in Basal Ganglia and Cortex |
4 |
The
input stage of the basal ganglia is the striatum, and the principal
neurons of the striatum are called spiny neurons because of the great
density of synaptic spines on their long dendrites. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
4 |
Each spiny neuron receives input
from about 10,000 different afferent fibers, a remarkable degree of convergence that is second only
to that for the Purkinje cells in the cerebellar cortex. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
5 |
Dopamine
fibers
provide a reinforcement input to the striatal spiny neurons that trains them
to recognize
patterns in their cerebral cortical input. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
5 |
Spiny
neurons have
abrupt
thresholds between "up" and "down" states, owing to the highly nonlinear ionic properties of their membranes. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
5 |
These
three features -- convergence of diverse inputs, specialized training signals, and dual-state behavior --
suggests that spiny neurons may be particularly well suited for pattern recognition tasks. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
5 |
The more
diffuse dopamine input is assumed to function as a training signal that reinforces
the synaptic
weights of cortical and frontal neuron inputs to guide the pattern recognition process. |
||||||
Houk;
Info Process in Basal Ganglia and Cortex |
6 |
Burst
discharges of spiny neurons relate to a variety of contextual situations that
the animal confronts in performing behavioral tasks. |
||||||
LeDoux; Synaptic Self |
31 |
The self is the totality of what an
organism is physically, biologically, psychologically, socially, and culturally.
|
||||||||||||||
LeDoux; Synaptic Self |
49 |
Every human
brain has billions of neurons that
together make trillions of synaptic
connections among one another. During wakefulness and during sleep,
during thoughtfulness and during boredom -- at any one moment, billions of synapses are active. |
||||||||||||||
LeDoux; Synaptic Self |
49 |
Projection
neurons have relatively long
axons that extend out of the area in which their cell bodies are located. |
||||||||||||||
LeDoux; Synaptic Self |
49 |
Interneurons link their short axons to nearby
neurons, often projection neurons, and are involved in information
processing. |
||||||||||||||
LeDoux; Synaptic Self |
49 |
Brain
circuits can
be thought of as hierarchically arranged
circuits linked together by synaptic connections. |
||||||||||||||
LeDoux; Synaptic Self |
50 |
Projection
neurons tend to be idle in the absence of inputs. Inhibitory interneurons are often active all the time. |
||||||||||||||
LeDoux; Synaptic Self |
53 |
Glutamate is a ubiquitous excitatory transmitter in the brain |
||||||||||||||
LeDoux; Synaptic Self |
53 |
GABA (an amino acid) is a neurotransmitter
of inhibitory neurons. |
||||||||||||||
LeDoux; Synaptic Self |
55 |
A neuron
receives many excitatory and inhibitory inputs form many other
cells; the likelihood of firing at any
one moment depends on the net balance
between excitation and inhibition
across all of the inputs at that particular
time. |
||||||||||||||
LeDoux; Synaptic Self |
57 |
Glutamate and GABA are fast-acting; they cause an electrical change in
the postsynaptic cell within milliseconds of being released from the presynaptic terminal,
and their effect is over in a matter
of milliseconds. |
||||||||||||||
LeDoux; Synaptic Self |
57 |
Peptides represent a large class of slow-acting
modulatory substances found throughout the brain. Made up of many
amino acids, and are larger molecules than simple amino acids
like glutamate and GABA. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Monoamines are a class of modulators
that include substances such as serotonin,
dopamine, epinephrine, and norepinephrine. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Cells that produce monoamines are found in only a few
areas, mostly in the brain stem. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Monoamines achieve their effects by facilitating
or inhibiting the actions of glutamate or GABA. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Many drugs used in the treatment of psychiatric disorders work by altering
monoamines. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Prozac prevents the removal of serotonin
from the synaptic space. |
||||||||||||||
LeDoux; Synaptic Self |
58 |
Amines are targets of recreational drugs -- cocaine and amphetamine
affect norepinephrine and dopamine levels, while LSD acts on serotonin receptors. |
||||||||||||||
LeDoux; Synaptic Self |
64 |
Prozac may reduce exaggerated fear and
anxiety in psychiatric disorders by enhancing the ability of serotonin
to facilitate GABA inhibition. |
||||||||||||||
LeDoux; Synaptic Self |
104 |
Reciprocal
connections between
hippocampus and neocortex, long-term storage of memories. |
||||||||||||||
LeDoux; Synaptic Self |
104 |
Rhinal areas, convergence zones, integrate information
across sensory modalities, mental representations go beyond perceptions
to become conceptions. |
||||||||||||||
LeDoux; Synaptic Self |
105 |
Hippocampus receives inputs from several convergence zones
in the rhinal region; it can be thought of as a superconvergence
zone. |
||||||||||||||
LeDoux; Synaptic Self |
105 |
Rhinal cortical
areas and hippocampus
are convergence zones, regions that
receive and integrate inputs from diverse regions. - (diagram) |
||||||||||||||
Douglas; Neocortex |
466 |
Thalamus
projects to all
cortical areas
and provides input to most layers of the cortex. The densest
projections are to the middle layers,
where they form about 5-10% of the synapses
in those layers. |
|||||||||
Douglas; Neocortex |
459 |
In all mammals the neocortex
consists of a sheet of cells, about 2 mm
thick. Conventionally, it is divided into 6 layers, but in many
regions more than 6 laminae are in evidence. Each cubic millimeter
contains approximately 50,000 neurons. |
|||||||||
Douglas; Neocortex |
477 |
Cortico-cortical
connections arise mainly from the superficial cortical layers, and the subcortical projections arise from the deep layers. |
|||||||||
Douglas; Neocortex |
477 |
Within the deep layers, there is an output to regions
that have a motor-related function,
e.g., the superior colliculus, basal ganglia,
brainstem nuclei, and spinal cord. |
|||||||||
Douglas; Neocortex |
477 |
Cortico-thalamic projection generally arises from the layer 6 pyramidal cells. |
|||||||||
Douglas; Neocortex |
484 |
Long
term potentiation --
brief tetanic stimulation of a set of input fibers potentiates synapses in hippocampal excitatory synapses for many
hours. |
|||||||||
Douglas; Neocortex |
469 |
Major
input from any
cortical area is from other cortical areas. |
|||||||||
Douglas; Neocortex |
469 |
Only 1:100 or
even 1:1000 in white matter is involved in subcortical
projection. |
|||||||||
Douglas; Neocortex |
469 |
Most of the
fibers in white matter are involved in intrahemispheric connections and interhemispheric connections. |
|||||||||
Douglas; Neocortex |
475 |
Axons of cortical neurons do not
extend more than a few
millimeters laterally in an area. |
|||||||||
Douglas; Neocortex |
475 |
Neurons with similar functional properties
are organized in 'columns' that extend from the cortical surface to the
white matter. |
|||||||||
Douglas; Neocortex |
477 |
Output neurons from the cortex are generally
pyramidal cells. |
|||||||||
Douglas; Neocortex |
477 |
Cortico-cortical
connections arise mainly from the superficial cortical layers, and the subcortical projections arise from the deep layers. |
|||||||||
Douglas; Neocortex |
477 |
Within the deep layers, there is an output to regions
that have a motor-related function,
e.g., the superior colliculus, basal ganglia,
brainstem nuclei, and spinal cord. |
|||||||||
Sherman and Koch; Thalamus |
295 |
Major
input to thalamus originates
among layer 6 pyramidal cells of the cortex. There seems to be at least an order of magnitude more corticothalamic axons
than thalamocortical ones. |
|||||||||
Sherman and Koch; Thalamus |
295 |
Each
cortical axon innervates
many thalamic neurons. |
|||||||||
Sherman and Koch; Thalamus |
295 |
Strong reciprocity exists in thalamocortical connections. |
|||||||||
Zeman; Consciousness |
60 |
Widespread damage to the thalamus can underlie the condition of 'wakefulness
without awareness', which is
known as the 'permanent vegetative state'. |
||||||||||||||||||
Zeman; Consciousness |
66 |
Cortical parts of the limbic
system have a relatively primitive microscopic
structure, hinting at their ancient evolutionary origins; this kind of cortex dominates the brain of 'lower'
vertebrates. |
||||||||||||||||||
Zeman; Consciousness |
66 |
Link between memory
and emotion; remember
what excites us, whether with pleasure
or pain;
what bores us is safely forgotten. |
||||||||||||||||||
Zeman; Consciousness |
66 |
Large overlap
between limbic system and the cortical
areas concerned with smell; scent can sometimes evoke long-buried memories. |
||||||||||||||||||
Zeman; Consciousness |
68 |
A sensory neuron in the spinal cord may signal to as many as 1000 target neurons
by way of axonal arborization. |
||||||||||||||||||
Zeman; Consciousness |
70 |
Approximately 10
'small molecule' neurotransmitters. Most
are amino acids, or are derived from amino acids: acetylcholine, dopamine, adrenaline,
serotonin, histamine; glutamate, glycine, GABA. |
||||||||||||||||||
Zeman; Consciousness |
70 |
Small protein
neurotransmitters: endorphins
act to modulate the perception of
pain; opium and its derivatives
mimic the action of the endorphins. |
||||||||||||||||||
Zeman; Consciousness |
70 |
Substances that mimic,
oppose, boost or otherwise modify the action of neurotransmitters
are
among the most widely used drugs in medicine; epilepsy, schizophrenia, depression, Parkinson's disease. |
||||||||||||||||||
Zeman; Consciousness |
70 |
A
single neuron releases the same
chemicals at all its
synapses. |
||||||||||||||||||
Zeman; Consciousness |
70 |
Receptor
variety creates a third
source of complexity at the synapse. |
||||||||||||||||||
Zeman; Consciousness |
71 |
Great
variety of receptor
types at the synapses. |
||||||||||||||||||
Zeman; Consciousness |
71 |
Second
messengers, cascade of chemical reactions
in a cell. |
||||||||||||||||||
Zeman; Consciousness |
72 |
At
birth, brain possesses more or less the final complement of neurons, but synapse adjustments continue
briskly. |
||||||||||||||||||
Zeman; Consciousness |
73 |
Long
Term Potentiation (LTP), occurs in the hippocampus, formation of new conscious memories. |
||||||||||||||||||
Zeman; Consciousness |
73 |
Nervous system, network
of nerve cells that communicate at synapses; transforms patterns of sensory input into patterns of motor output;
adapt behavior to experience, present and past. |
||||||||||||||||||
Zeman; Consciousness |
73 |
Much of the complexity of the human brain depends on the endless
elaboration of simple elements. |
||||||||||||||||||
Zeman; Consciousness |
130 |
Tendency for
anaesthetics
to provide analgesia - relief from pain - at doses that are not high
enough to suppress
awareness altogether. |
||||||||||||||||||
Zeman; Consciousness |
131 |
It is possible to
be conscious during anaesthesia but free of pain. |
||||||||||||||||||
Zeman; Consciousness |
175 |
In gestalt psychology, the brain tends to group items that are close, similar
to one another, that create
a closed space, or achieve a smooth continuity of line. [Gestalt laws] |
||||||||||||||||||
Zeman; Consciousness |
289 |
Crick
and Koch
anticipate that at any given moment the NCC will be comprised of a sparse but widespread
network of neurons, whose activity will stand out above
background neuron firing for at least 100-200
milliseconds. [Edelman's
dynamic core] |
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