Visual Pathways:
The Road to Vision
Anthony DeSimone LDO
Visual Pathway
   “Focus on the Eye”
    • Concerned about
       Cornea
       Lens

       Retina

   There is more to vision than meets
    the eye
Retinal Fields vs. Visual Fields
   What’s the difference
    • Retinal Field – describes the area that includes
      neural fibers of the retina that are receiving
      light from some object
    • Visual Field – describes the area in space
      where the object lies
   They are the reversal of one another
    • The nasal retinal field receives light from the
      temporal visual field
    • The temporal retinal field receives light from
      the nasal visual field
Temporal          Temporal
Visual field      Visual Field


Nasal Visual      Nasal Visual
Field             Field




  Temporal         Temporal
  Retinal field   Retinal Field

  Nasal Retinal     Nasal Retinal
  Field             Field
Optic Chiasm
   Partial decussation (cross-over) of
    Optic Nerve fibers occurs at the level
    of the Optic Chiasm
    • Only nasal retinal fibers (from the nasal
      retinal field) cross over
    • Temporal nasal fibers (from the
      temporal retinal field) do not.
Lateral Aspect
Inferior Aspect




1. Optic Nerve (stump)
2. Optic Chiasm
3. Optic Tract
Optic Tract
   Optic tract
   It is important for the sense of sight.
   By convention, the optic tract is defined as
    that extent of the visual system pathway
    from the optic chiasm to the lateral
    geniculate nucleus of the thalamus.
   Each optic tract contains axons from
    ganglion cells in the retinas of both the left
    and right eyes, but information from only
    one half (i.e either left or right) of each
    eye's visual field
Nerve Cells
Chiasm


LGN


               Optic Tracts
Lateral Geniculate Body
   After the optic tract, the next stop is
    the Lateral Geniculate Body (or
    Lateral Geniculate Nucleus)
LGN
• Optic nerve fibers from the optic
tracts terminate at two bodies in the
thalamus (a structure in the middle
of the brain) known as the Lateral
Geniculate Nuclei (or LGN for
short).
• One LGN lies in the left
hemisphere and the other lies in the
right hemisphere.
• Each has six layers
The optic tract wraps around the
cerebral peduncles of the
midbrain to get to the lateral
geniculate nucleus (LGN), which
is a part of the thalamic sensory
relay system.

There are two geniculate nuclei,
located on either side of the rear
end of the thalamus. They each
consist of six cellular layers,
forming a threefold
representation of the opposite
binocular visual hemifield in
exact anatomic registration.
This apparently
complicated arrangement
is engineered so that the
right LGN receives
information about the left
visual field, and the left
LGN receives information
about the right visual
field.
LGN
   This layered structure is
    exquisitely precise in two
    ways.
    • First, cells in different layers
      that align (like the numbers in
      the picture) have receptive
      fields in the same area of
      retina.
    • Second, optic nerve fibers
      from the two eyes are
      segregated in different layers.
      If you look carefully at the
      projections to the LGN, you
      will see that ipsilateral fibers
      arrive in layers 2, 3, and 5,
      while contralateral fibers
      arrive in layers 1, 4, and 6
      (no-one knows why).
LGN Cell Types
   All cells in the LGN have concentric
    receptive fields, just like the ganglion cells
    whose fibers terminate in the LGN.
   Layers 1 and 2 are made up of cells with
    large bodies ("magnocellular") that have
    monochromatic responses (ie. mediate
    responses to light and dark)
   Layers 3 to 6 are made up of cells with
    small bodies ("parvocellular") that mediate
    color vision.
Optic Radiations
   Leaving the LGN are optic radiations
   Optic radiations are a collection of axons
    from relay neurons in the lateral
    geniculate nucleus of the thalamus.
   They carry visual information to the visual
    cortex (also called striate cortex) along
    the calcarine fissure.
   There is one such tract on each side of the
    brain.
Meyer’s Loop
   The optic radiations follow a very wide three
    dimensional arc. Here is how the radiations are
    conventionally drawn, and how they look from the
    side
   The longer loop actually dives into the temporal
    lobe before it heads back to the occipital lobe.
   This group of fibers is called Meyer's loop. Recall
    that, since the lens inverts all images, the lower
    half of the retina sees the upper half of the world.
    This orientation is preserved through the pathway,
    so that the lower optic radiations, or Meyer's loop,
    are carrying information from the upper visual
    world.
Meyer’s Loop
Striate Cortex (V1)
Retinotopic Mapping
   In lower visual areas (e.g., V1 through V5) the
    neurons are organized in an orderly fashion called
    topographic or retinotopic mapping
    • they form a 2D representation of the visual image
      formed on the retina in such a way that neighboring
      regions of the image are represented by neighboring
      regions of the visual area
   But this retinotopic representation in the cortical
    areas is distorted.
   The foveal area is represented by a relatively
    larger area in V1 than the peripheral areas.
Visual Cortex
   Much of the primate cortex is
    devoted to visual processing.
    • In the macaque monkey at least 50% of
      the neocortex appears to be directly
      involved in vision, with over twenty
      distinct areas.
    • Some of the areas concerned are quite
      well understood, others are still a
      complete mystery.
Visual Cortex
   Nearly all visual information reaches the
    cortex via V1, the largest and most
    important visual cortical area.
   Because of its stripey appearance this area
    is also known as striate cortex, amongst
    other things.
   Other areas of visual cortex are known as
    extrastriate visual cortex
    • the more important areas are V2, V3, V4 and
      MT (also known as .....V5!).
Areas of Visual Cortex
V1
   In primates nearly all visual
    information enters the cortex via
    area V1. This area is located in the
    occipital lobe at the back of the
    brain. It is also known as:

    -   primary visual cortex
    -   area 17
    -   striate cortex.
V1
 This region represents about 5% of
  the neocortex in man.
 It is the most complex region of the

  cortex with at least 6 identifiable
  layers
    • layer 1 is close to the cortical surface,
      layer 6 adjoins the white matter below
V1
Simple Cells
   Simple cell receptive fields contain sub-regions
    that exert an excitatory influence on the cell's
    response (light grey in the picture), and sub-
    regions that exert an inhibitory influence (dark
    grey in the picture). The blue lines in the picture
    are time traces that plot the onset and offset of
    stimulation. The black vertical lines below them
    indicate individual nerve impulses. The most
    effective stimulus for this particular receptive
    field (left) is one that puts a lot of light in the
    excitatory region, and only a little in the
    inhibitory region.
Response of Simple Cells
Simple Cells
   It must have the right orientation, the
    right position, and the right size. Stimuli
    that are non-optimal in terms of position
    (middle left), or orientation (middle right),
    or size (right) are less effective. Simple
    cell receptive fields could be 'built' in the
    cortex by collecting responses from LGN
    cells whose receptive fields fall along a line
    across the retina, but the exact wiring is
    still the subject of debate.
Complex Cells
   Complex cells are the most numerous in
    V1 (perhaps making up three-quarters of
    the population). Like Simple cells, they
    respond only to appropriately oriented
    stimuli, but unlike Simple cells, they are
    not fussy about the position of the
    stimulus, as along as it falls somewhere
    inside the receptive field (left and middle-
    left examples above). Many complex cells
    are also direction-selective, in the sense
    that they respond only when the stimulus
    moves in one direction and not when it
    moves in the opposite direction
Response of Complex Cells
Orientation Cells
   Hubel and Wiesel were the first to discover that cells in V1
    are arranged in a beautifully precise and orderly fashion.
   Hubel and Wiesel found that as one advances deeper into
    the cortex through successive layers perpendicular to the
    surface, all cells that have orientation tuning prefer the
    same orientation.
   On the other hand, moving across the surface of the
    cortex, orientation tuning mostly changes in an orderly
    fashion (as shown by the small lines in the picture).
   Hubel and Wiesel used the term "orientation columns" to
    describe this arrangement, but they are really slabs rather
    than columns.
Visual pathway
Visual pathway

Visual pathway

  • 1.
    Visual Pathways: The Roadto Vision Anthony DeSimone LDO
  • 2.
    Visual Pathway  “Focus on the Eye” • Concerned about  Cornea  Lens  Retina  There is more to vision than meets the eye
  • 4.
    Retinal Fields vs.Visual Fields  What’s the difference • Retinal Field – describes the area that includes neural fibers of the retina that are receiving light from some object • Visual Field – describes the area in space where the object lies  They are the reversal of one another • The nasal retinal field receives light from the temporal visual field • The temporal retinal field receives light from the nasal visual field
  • 5.
    Temporal Temporal Visual field Visual Field Nasal Visual Nasal Visual Field Field Temporal Temporal Retinal field Retinal Field Nasal Retinal Nasal Retinal Field Field
  • 6.
    Optic Chiasm  Partial decussation (cross-over) of Optic Nerve fibers occurs at the level of the Optic Chiasm • Only nasal retinal fibers (from the nasal retinal field) cross over • Temporal nasal fibers (from the temporal retinal field) do not.
  • 8.
  • 9.
    Inferior Aspect 1. OpticNerve (stump) 2. Optic Chiasm 3. Optic Tract
  • 10.
    Optic Tract  Optic tract  It is important for the sense of sight.  By convention, the optic tract is defined as that extent of the visual system pathway from the optic chiasm to the lateral geniculate nucleus of the thalamus.  Each optic tract contains axons from ganglion cells in the retinas of both the left and right eyes, but information from only one half (i.e either left or right) of each eye's visual field
  • 11.
  • 12.
    Chiasm LGN Optic Tracts
  • 13.
    Lateral Geniculate Body  After the optic tract, the next stop is the Lateral Geniculate Body (or Lateral Geniculate Nucleus)
  • 14.
    LGN • Optic nervefibers from the optic tracts terminate at two bodies in the thalamus (a structure in the middle of the brain) known as the Lateral Geniculate Nuclei (or LGN for short). • One LGN lies in the left hemisphere and the other lies in the right hemisphere. • Each has six layers
  • 15.
    The optic tractwraps around the cerebral peduncles of the midbrain to get to the lateral geniculate nucleus (LGN), which is a part of the thalamic sensory relay system. There are two geniculate nuclei, located on either side of the rear end of the thalamus. They each consist of six cellular layers, forming a threefold representation of the opposite binocular visual hemifield in exact anatomic registration.
  • 16.
    This apparently complicated arrangement isengineered so that the right LGN receives information about the left visual field, and the left LGN receives information about the right visual field.
  • 17.
    LGN  This layered structure is exquisitely precise in two ways. • First, cells in different layers that align (like the numbers in the picture) have receptive fields in the same area of retina. • Second, optic nerve fibers from the two eyes are segregated in different layers. If you look carefully at the projections to the LGN, you will see that ipsilateral fibers arrive in layers 2, 3, and 5, while contralateral fibers arrive in layers 1, 4, and 6 (no-one knows why).
  • 18.
    LGN Cell Types  All cells in the LGN have concentric receptive fields, just like the ganglion cells whose fibers terminate in the LGN.  Layers 1 and 2 are made up of cells with large bodies ("magnocellular") that have monochromatic responses (ie. mediate responses to light and dark)  Layers 3 to 6 are made up of cells with small bodies ("parvocellular") that mediate color vision.
  • 19.
    Optic Radiations  Leaving the LGN are optic radiations  Optic radiations are a collection of axons from relay neurons in the lateral geniculate nucleus of the thalamus.  They carry visual information to the visual cortex (also called striate cortex) along the calcarine fissure.  There is one such tract on each side of the brain.
  • 21.
    Meyer’s Loop  The optic radiations follow a very wide three dimensional arc. Here is how the radiations are conventionally drawn, and how they look from the side  The longer loop actually dives into the temporal lobe before it heads back to the occipital lobe.  This group of fibers is called Meyer's loop. Recall that, since the lens inverts all images, the lower half of the retina sees the upper half of the world. This orientation is preserved through the pathway, so that the lower optic radiations, or Meyer's loop, are carrying information from the upper visual world.
  • 22.
  • 23.
  • 24.
    Retinotopic Mapping  In lower visual areas (e.g., V1 through V5) the neurons are organized in an orderly fashion called topographic or retinotopic mapping • they form a 2D representation of the visual image formed on the retina in such a way that neighboring regions of the image are represented by neighboring regions of the visual area  But this retinotopic representation in the cortical areas is distorted.  The foveal area is represented by a relatively larger area in V1 than the peripheral areas.
  • 25.
    Visual Cortex  Much of the primate cortex is devoted to visual processing. • In the macaque monkey at least 50% of the neocortex appears to be directly involved in vision, with over twenty distinct areas. • Some of the areas concerned are quite well understood, others are still a complete mystery.
  • 26.
    Visual Cortex  Nearly all visual information reaches the cortex via V1, the largest and most important visual cortical area.  Because of its stripey appearance this area is also known as striate cortex, amongst other things.  Other areas of visual cortex are known as extrastriate visual cortex • the more important areas are V2, V3, V4 and MT (also known as .....V5!).
  • 27.
  • 28.
    V1  In primates nearly all visual information enters the cortex via area V1. This area is located in the occipital lobe at the back of the brain. It is also known as: - primary visual cortex - area 17 - striate cortex.
  • 30.
    V1  This regionrepresents about 5% of the neocortex in man.  It is the most complex region of the cortex with at least 6 identifiable layers • layer 1 is close to the cortical surface, layer 6 adjoins the white matter below
  • 32.
  • 33.
    Simple Cells  Simple cell receptive fields contain sub-regions that exert an excitatory influence on the cell's response (light grey in the picture), and sub- regions that exert an inhibitory influence (dark grey in the picture). The blue lines in the picture are time traces that plot the onset and offset of stimulation. The black vertical lines below them indicate individual nerve impulses. The most effective stimulus for this particular receptive field (left) is one that puts a lot of light in the excitatory region, and only a little in the inhibitory region.
  • 34.
  • 35.
    Simple Cells  It must have the right orientation, the right position, and the right size. Stimuli that are non-optimal in terms of position (middle left), or orientation (middle right), or size (right) are less effective. Simple cell receptive fields could be 'built' in the cortex by collecting responses from LGN cells whose receptive fields fall along a line across the retina, but the exact wiring is still the subject of debate.
  • 36.
    Complex Cells  Complex cells are the most numerous in V1 (perhaps making up three-quarters of the population). Like Simple cells, they respond only to appropriately oriented stimuli, but unlike Simple cells, they are not fussy about the position of the stimulus, as along as it falls somewhere inside the receptive field (left and middle- left examples above). Many complex cells are also direction-selective, in the sense that they respond only when the stimulus moves in one direction and not when it moves in the opposite direction
  • 37.
  • 38.
    Orientation Cells  Hubel and Wiesel were the first to discover that cells in V1 are arranged in a beautifully precise and orderly fashion.  Hubel and Wiesel found that as one advances deeper into the cortex through successive layers perpendicular to the surface, all cells that have orientation tuning prefer the same orientation.  On the other hand, moving across the surface of the cortex, orientation tuning mostly changes in an orderly fashion (as shown by the small lines in the picture).  Hubel and Wiesel used the term "orientation columns" to describe this arrangement, but they are really slabs rather than columns.