Cerebrum rear {occipital lobe}| is for vision, perceptual judgment, memory, and association.
input
Occipital lobe receives from lateral geniculate nucleus, mostly onto layer 4 [Allman, 1998] [Allman and Kaas, 1971] [Zeki, 1974] [Zeki, 1993].
Layer 4 keeps input from two eyes separate. Alternating ocular-dominance-column bands, 0.5 millimeters wide, are for input from same ipsilateral side or opposite contralateral side.
Cortical layers above and below layer 4 have neurons that receive from both eyes. Binocular neurons differ slightly in eye connection alignment, allowing distance judgments.
Occipital lobe also receives from lower brain centers.
damage
Occipital lobe damage causes blindness. Cortical area V1, V2, and V3 damage affects perception and pattern recognition, leaving only ability to perceive intensity. Left-occipital lesion and corpus-callosum posterior-splenium lesion cause alexia without agraphia.
anatomy
Simple cells have well-defined excitatory and inhibitory regions in receptive fields [DeValois and DeValois, 1988] [Hubel and Wiesel, 1959] [Hubel and Wiesel, 1962] [Hubel, 1988] [Livingstone, 1998] [Spillman and Werner, 1990] [Wandell, 1995] [Wilson et al., 1990].
Complex cells do not have well-defined excitatory and inhibitory regions [Allman et al., 1985] [Gallant et al., 1997] [Lamme and Spekreijse, 2000] [Shapley and Ringach, 2000].
Complex-neuron receptive fields are larger than simple-neuron fields and have up to 100 degrees of visual angle.
processing
Some visual-cortex neurons distinguish between familiar and unfamiliar objects. Some neurons recognize faces. Some neurons respond only to face, hairbrush, or hand. Some neurons respond to face only if eyes point in direction. Some neurons store object locations. Some neurons predict eye-movement direction.
Visual-cortex layers 2 and 3 neuron groups {blob} and layers 4B, 5, and 6, separated by 0.4 to 1.0 millimeters, detect color and brightness, but not orientation, at space point [Conway et al., 2002] [Lennie, 2000] [Livingstone and Hubel, 1984] [Livingstone and Hubel, 1988] [Michael, 1978] [Michael, 1981]. Blob center-surround cells are for white-black and black-white, red-green and green-red opponent, and red-green and blue-yellow double opponent.
Visual-cortex layer-4 neurons {calcarine cortex} receive input from lateral geniculate nucleus and other brain sites. Cortical layers 3, 2, 1, and 6 repeat neural array in visual-cortex layer 4.
input
One quarter of neurons use input from right eye. One quarter use input from left eye. One quarter use input from both eyes with right eye dominant. One quarter use input from both eyes with left eye dominant.
Half have receptive fields with excitatory center. Half have inhibitory center.
Half are for shape and color detection. Half are for texture and motion detection.
100 billion neurons converge on 100 million output neurons in visual-cortex layer 5 and lower-4.
point processing
For space plane-surface points, brain has 30 neurons to detect features, such as line-segment orientation. The 30 neurons are in a circle and cover ranges, such as orientations.
receptive fields
Brain has neurons with different-size receptive fields, to detect different-size features, from point size, 0.1 millimeters, to whole-visual-field size, 1000 millimeters.
density
Neurons are denser at brain points corresponding to retina center and are less dense for retina edge.
maps
Visual cortex has maps for shape, depth, color, motion, and texture that interconnect. For features, visual cortex has repeated maps to represent different times in sequence.
number
Space plane-surface points have 4*2*2*30*5 = 2400 visual-cortex neurons. If point number is 1,000,000, then black-and-white representation requires 2,400,000,000 neurons. Color requires 7,200,000,000 neurons. If times differ by 200 milliseconds over three-second intervals, neuron number for visual information totals 100,000,000,000.
Occipital and temporal lobe region {circumstriate cortex} codes patterns and motion relations.
Visual-cortex superficial layers have color-sensitive neuron clusters {color blob}, at macrocolumnar intervals.
Region near ventral temporal lobe {dorsolateral visual area} {area DL} detects visual stimuli length, width, and stimulus position. It detects light-on-dark, dark-on-light, and contrast. It has large excitatory receptive fields, larger than optimum stimulus. It sends to inferotemporal cortex.
Occipital regions {ectosylvian visual area} can send to superior colliculi.
Around striate cortex are areas V2, V3, and V4 {extrastriate cortex, brain} [Bullier et al., 1994] [Hadjikhani et al., 1998].
Visual-cortex neurons respond to orientation, size, contrast, motion direction, motion speed, color, length, and depth {feature detector} in visual space. Neurons are switches that route messages, and states contain messages. Nerve signals from other neurons, muscles, and glands affect feature detectors. Feature detection is generalized associative learning, which can cause actions.
Visual association area 18, area 19, and posterior area 37 {inferior occipital lobe} bilateral damage prevents unique object recognition and feature retrieval. Area 18 and 19 bilateral damage prevents color perception.
Visual-cortex left striate region {intermediate medial hyperstriatum ventrale} (IMHV) is for filial imprinting.
Occipital regions {left posterior occipital lobe} can combine individual letters into one chunk {visual word form} and discriminate between words and non-words 200 milliseconds after input.
Words and pseudo-words, but not consonant strings, excite occipital region {left ventral occipital lobe}.
Occipital-lobe and parietal-lobe regions {occipito-parietal lobe} can be for thinking about two seen things simultaneously.
Occipital-lobe region {parastriate cortex} damage can cause blindness or word blindness.
Occipital-lobe area V4 and V4A region {posterior lunate sulcus} analyzes color and color constancy.
Occipital-lobe regions {posterior occipital lobe} can be for concrete low-complexity knowledge.
Occipital regions {posterior prestriate area} can attend to color, motion, or form.
Occipital regions {V1 brain area} {area V1} {primary visual cortex} {Brodmann area 17} {striate cortex} {striate occipital cortex} {area OC} can be for primary vision perception [Brewer et al., 2002] [Dantzker and Callaway, 2000] [Preuss, 2000] [Preuss et al., 1999] [Sawatari and Callaway, 2000] [Vanduffel et al., 2002].
input
Area V1 receives from lateral geniculate nucleus.
output
Area V1 sends feedback {shifter circuit, vision} to lateral-geniculate-nucleus left-and-right-eye layers, which excite or inhibit cortical-area activity [Ahmed et al., 1994] [Budd, 1998] [Douglas et al., 1995] [Felleman and Van Essen, 1991] [Fries, 1990] [LeVay and Gilbert, 1976] [Saint-Cyr et al., 1990] [Sherk, 1986] [White, 1989].
Area V1 sends orientation information to area V2 and then to area V5.
Area V1 sends object recognition and color information to area V2, then to area V4, and then to inferotemporal cortex.
Area V1 sends object location and movement information to area V2, then to area V5, and then to inferior parietal cortex.
Area V1, area V2, area V3, and mediotemporal cortex layer-5 pyramidal cells send to superior colliculus superficial layers and to pons nuclei.
Layer-6 pyramidal-cell axon collaterals synapse on aspinous inhibitory interneurons [Callaway and Wiser, 1996].
anatomy
Striate occipital cortex has visual-field map accurate to one millimeter. Map has ocular dominance columns for both eyes. Map has orientation columns, in which preferred orientation shifts through complete cycle in 0.5 to 1 millimeter. Thousands of orientation and ocular dominance columns cross each other at right angles. Neurons that prefer particular spatial frequency, color, or size also cluster [Engel et al., 1997] [Gur and Snodderly, 1997].
Around striate cortex are areas V2, V3, and V4 {extrastriate cortex, vision} [Bullier et al., 1994] [Hadjikhani et al., 1998].
processing: edge
Most area-V1 neurons respond best to one light or dark edge-or-thin-bar orientation. Edge or bar can be stationary, moving, or flashing.
processing: line
Concentric circles on retina are parallel lines in V1.
processing: letters
Area V1 is active while visualizing letters, even with eyes closed. V1 anterior part, for parafoveal input, is more active for large size letters. V1 posterior part, for foveal input, is more active for small size letters.
processing: binocular
Striate cortex combines signals from both eyes, as do most cells in visual cortex.
processing: attention
Attention affects area V1 [Brefczynski and DeYoe, 1999] [Fries et al., 2001] [Gandhi et al., 1999] [Ito and Gilbert, 1999] [Ito et al., 1995] [Kastner and Ungerleider, 2000] [Motter, 1993] [Niebur and Koch, 1994] [Niebur et al., 1993] [Niebur et al., 2002] [O'Connor et al., 2002] [Roelfsema et al., 1998] [Somers et al., 1999] [Watanabe et al., 1998].
factors: saccade
Spontaneous area-V1-neuron activity decreases when eye moves {saccadic suppression, V1} [Bridgeman et al., 1975] [Burr et al., 1994] [Castet and Masson, 2000] [Haarmeier et al., 1997] [Ilg and Thier, 1996] [McConkie and Currie, 1996].
Saccade target object excites some V1 cells and more V2 cells.
evolution
All mammals have areas V1 and V2, which combine visual, auditory, and tactile sense data. Perhaps, more trunk-and-neck flexibility and limb development allowed those areas.
Occipital regions {V2 brain area} {area V2} can be for stereoscopic vision [Engel et al., 1997] [Heydt et al., 2000] [Levitt et al., 1994] [Livingstone and Hubel, 1981] [Livingstone and Hubel, 1987] [Merigan et al., 1993] [Peterhans, 1997] [Roe and Ts'o, 1997] [Thomas et al., 2002] [Tootell et al., 1998] [Wong-Riley, 1994].
Almost all area V2 neurons receive input from both eyes. Color, location, and shape have alternating area-V2 bands. Nearness and farness cells detect distance. Area V2 neurons have bigger receptive fields than neurons in area V1. V2 neurons can respond to illusory edges, hidden and seen shapes, or figure-ground differences.
output
Almost as many neurons send to area V1 from area V2 as send from V1 to V2.
Occipital regions {V3 brain area} {area V3} can be for depth of vision [Burkhalter and Van Essen, 1986] [Lyon and Kass, 2002] [Newsome and Pare, 1988] [Newsome et al., 1986] [Newsome et al., 1989] [Tootell et al., 1997] [Zeki, 2003]. Nearness and farness cells detect distance. Some cortical-area-V3A neurons respond to gaze angle.
Ventral-system occipital regions {V4 brain area} {area V4} are for color perception and have topographic maps. Lunate sulcus posterior part and superior temporal sulcus anterior part are for color and color constancy. Area V4 responds to all wavelengths and line orientations but does not respond to movement. Some neurons are sensitive to spots or rectangles. Nearness and farness cells detect distance. Area-V4 visual neurons also respond to somatosensory stimuli [Burkhalter and Van Essen, 1986] [Newsome and Pare, 1988] [Newsome et al., 1986] [Newsome et al., 1989] [Tootell et al., 1997] [Wachtler et al., 2003] [Zeki, 1973] [Zeki, 1983] [Zeki, 1993]. Perhaps, cells are in color columns.
attention
Attention affects area V4 [DeWeerd et al., 1999] [Ghose and Maunsell, 2002] [McAdams and Maunsell, 1999] [Treue and Martinez-Trujillo, 1999].
color
Some cells are opponent, and some double-opponent. Some cells are for specific colors, orientations, and shapes. Some cells are for any color differences [DeValois and DeValois, 1975].
Ventromedial occipital-lobe regions {V6 occipital brain area} {area V6, occipital lobe} can be for color.
Ventral and medial occipital lobe region {ventromedial occipital lobe} damage causes color vision loss. Practice can reduce damaged region.
Ventral and posterior occipital regions {ventroposterior occipital lobe} {area VP} can be for color.
In occipital lobe, maps {visual buffer}, with retina input, can segregate figure from ground during perception and store images.
Vision cortex {visual cortex}| measures surface area and spatial frequency. It has same number of stellate neurons as pyramidal cells. Cerebral cortex has more than 30 visual or mixed areas, and half have maps with input from retina. Primates have more than 21 visual areas: V1, V2, MT, and M. V1 has calcarine fissure.
input
It receives excitatory axons one-third from same-side lateral geniculate nucleus and reticular nuclei. It receives inhibitory axons two-thirds from same-side locus coeruleus. It does not receive many axons from association areas or from other brain half.
output
It sends to superior colliculus, lateral geniculate nucleus, and area-17 and area-19 superficial pyramidal neurons, up to three millimeters away.
4-Zoology-Organ-Nerve-Brain-Cerebrum
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Date Modified: 2022.0225