|
by Wikipedia

Closeup of a
blue-green human eye.

Closeup of a
hawk's eye
An eye is an organ
of vision that detects light. Different kinds of light-sensitive organs
are found in a variety of organisms. The simplest eyes do nothing but
detect whether the surroundings are light or dark, while more complex
eyes can distinguish shapes and colors. Many animals, including some
mammals, birds, reptiles and fish, have two eyes which may be placed on
the same plane to be interpreted as a single three-dimensional "image"
(binocular vision), as in humans; or on different planes producing two
separate "images" (monocular vision), such as in rabbits and chameleons.

The compound eyes
of a dragonfly.
In most vertebrates and some mollusks, the eye works by
allowing light to enter it and project onto a light-sensitive panel of
cells known as the retina at the rear of the eye, where the light is
detected and converted into electrical signals, which are then
transmitted to the brain via the optic nerve. Such eyes are typically
roughly spherical, filled with a transparent gel-like substance called
the vitreous humour, with a focusing lens and often an iris which
regulates the intensity of the light that enters the eye. The eyes of
cephalopods, fish, amphibians, and snakes usually have fixed lens
shapes, and focusing vision is achieved by telescoping the lens —
similar to how a camera focuses.
Compound eyes are
found among the arthropods and are composed of many simple facets which
give a pixelated image (not multiple images, as is often believed). Each
sensor has its own lens and photosensitive cell(s). Some eyes have up to
28,000 such sensors, which are arranged hexagonally, and which can give
a full 360 degree field of vision. Compound eyes are very sensitive to
motion. Some arthropods, including many Strepsiptera, have compound eye
composed of a few facets each, with a retina capable of creating an
image, which does provide multiple-image vision. With each eye viewing a
different angle, a fused image from all the eyes is produced in the
brain, providing a very wide-angle, high-resolution image.
Trilobites, which
are now extinct, had unique compound eyes. They used clear calcite
crystals to form the lenses of their eyes. In this, they differ from
most other arthropods, which have soft eyes. The number of lenses in
such an eye varied, however: some trilobites had only one, and some had
thousands of lenses in one eye.
Some of the
simplest eyes, called ocelli, can be found in animals like snails, who
cannot actually "see" in the normal sense. They do have photosensitive
cells, but no lens and no other means of projecting an image onto these
cells. They can distinguish between light and dark, but no more. This
enables snails to keep out of direct sunlight. Jumping spiders have
simple eyes that are so large, supported by an array of other, smaller
eyes, that they can get enough visual input to hunt and pounce on their
prey. Some insect larvae, like caterpillars, have a different type of
single eye (stemmata) which gives a rough image.
Evolution of eyes
Main article:
Evolution of the eye

Diagram of major
stages in the eye's evolution.
The common origin (monophyly) of all
animal eyes is now widely accepted as fact based on shared anatomical
and genetic features of all eyes; that is, all modern eyes, varied as
they are, have their origins in a proto-eye believed to have evolved
some 540 million years ago.[1][2][3] The majority of the advancements in
early eyes are believed to have taken only a few million years to
develop, as the first predator to gain true imaging would have touched
off an "arms race".[4] Prey animals and competing predators alike would
be forced to rapidly match or exceed any such capabilities to survive.
Hence multiple eye types and subtypes developed in parallel.
Eyes in various
animals show adaptation to their requirements. For example, birds of
prey have much greater visual acuity than humans, and some can see
ultraviolet light. The different forms of eyes in, for example,
vertebrates and mollusks are often cited as examples of parallel
evolution, despite their distant common ancestry.
The earliest eyes,
called "eyespots", were simple patches of photoreceptor cells,
physically similar to the receptor patches for taste and smell. These
eyespots could only sense ambient brightness: they could distinguish
light and dark, but not the direction of the lightsource.[5] This
gradually changed as the eyespot depressed into a shallow "cup" shape,
granting the ability to slightly discriminate directional brightness by
using the angle at which the light hit certain cells to identify the
source. The pit deepened over time, the opening diminished in size, and
the number of photoreceptor cells increased, forming an effective
pinhole camera that was capable of slightly distinguishing dim
shapes.[6]

Compound eye of
Antarctic krill.
The thin overgrowth of transparent cells over the eye's
aperture, originally formed to prevent damage to the eyespot, allowed
the segregated contents of the eye chamber to specialize into a
transparent humour that optimized colour filtering, blocked harmful
radiation, improved the eye's refractive index, and allowed
functionality outside of water. The transparent protective cells
eventually split into two layers, with circulatory fluid in between that
allowed wider viewing angles and greater imaging resolution, and the
thickness of the transparent layer gradually increased, in most species
with the transparent crystallin protein.[7]
The gap between
tissue layers naturally formed a bioconvex shape, an ideal structure for
a normal refractive index. Independently, a transparent layer and a
nontransparent layer split forward from the lens: the cornea and iris.
Separation of the forward layer again forms a humour, the aqueous humour.
This increases refractive power and again eases circulatory problems.
Formation of a nontransparent ring allows more blood vessels, more
circulation, and larger eye sizes.[7]
Anatomy of the
mammalian eye

Schematic diagram
of the human eye.
The mammalian eye can be divided into two main
segments: the anterior segment and the posterior segment.[8]
Anterior segment
The anterior
segment is the front third of the eye that includes the structures in
front of the vitreous humour: the cornea, iris, ciliary body, and
lens.[9] [10] Within the anterior segment are two fluid-filled spaces:
the anterior chamber and the posterior chamber. The anterior chamber
between the posterior surface of the cornea (i.e. the corneal
endothelium) and the iris. The posterior chamber between the iris and
the front face of the vitreous.[9]
Posterior segment
The posterior
segment is the back two-thirds of the eye that includes the anterior
hyaloid membrane and all structures behind it: the vitreous humor,
retina, choroid, and optic nerve.[11] In some animals, the retina
contains a reflective layer (the tapetum lucidum) which increases the
amount of light each photosensitive cell perceives, allowing the animal
to see better under low light conditions.
The structure of
the mammalian eye owes itself completely to the task of focusing light
onto the retina. All of the individual components through which light
travels within the eye before reaching the retina are transparent,
minimising dimming of the light. The cornea and lens help to converge
light rays to focus onto the retina. This light causes chemical changes
in the photosensitive cells of the retina, the products of which trigger
nerve impulses which travel to the brain.
Light enters the
eye from an external medium such as air or water, passes through the
cornea, and into the first of two humours, the aqueous humour. Most of
the light refraction occurs at the cornea which has a fixed curvature.
The first humour is a clear mass which connects the cornea with the lens
of the eye, helps maintain the convex shape of the cornea (necessary to
the convergence of light at the lens) and provides the corneal
endothelium with nutrients. The iris, between the lens and the first
humour, is a coloured ring of muscle fibres. Light must first pass
though the centre of the iris, the pupil. The size of the pupil is
actively adjusted by the circular and radial muscles to maintain a
relatively constant level of light entering the eye. Too much light
being let in could damage the retina; too little light makes sight
difficult. The lens, behind the iris, is a convex, springy disk which
focuses light, through the second humour, onto the retina.

Diagram of a human
eye. Note that not all eyes have the same anatomy as a human eye.
The
lens is attached to the ciliary body via suspensory ligaments known as
the Zonules of Zinn. To clearly see an object far away, the circularly
arranged ciliary muscle will pull on the lens, flattening it. When the
ciliary muscle contracts, the lens will spring back into a thicker, more
convex, form. Humans gradually lose this flexibility with age, resulting
in the inability to focus on nearby objects, which is known as
presbyopia. There are other refraction errors arising from the shape of
the cornea and lens, and from the length of the eyeball. These include
myopia, hyperopia, and astigmatism.
On the other side
of the lens is the second humour, the vitreous humour, which is bounded
on all sides: by the lens, ciliary body, suspensory ligaments and by the
retina. It lets light through without refraction, helps maintain the
shape of the eye and suspends the delicate lens.
Light from a
single point of a distant object and light from a single point of a near
object being brought to a focus.Three layers, or tunics, form the wall
of the eyeball. The outermost is the sclera which gives the eye most of
its white colour. It consists of dense connective tissue filled with the
protein collagen to both protect the inner components of the eye and
maintain its shape. On the inner side of the sclera is the choroid,
which contains blood vessels that supply the retinal cells with
necessary oxygen and remove the waste products of respiration. The
choroid gives the inner eye a dark colour, which prevents disruptive
reflections within the eye. The inner most layer of the eye is the
retina, containing the photosensitive rod and cone cells, and neurons.
To maximise vision
and light absorption, the retina is a relatively smooth (but curved)
layer. It does have two points at which it is different; the fovea and
optic disc. The fovea is a dip in the retina directly opposite the lens,
which is densely packed with cone cells. It is largely responsible for
color vision in humans, and enables high acuity, such as is necessary in
reading. The optic disc, sometimes referred to as the anatomical blind
spot, is a point on the retina where the optic nerve pierces the retina
to connect to the nerve cells on its inside. No photosensitive cells
whatsoever exist at this point, it is thus "blind".
Other articles
regarding eye anatomy
Annulus of Zinn,
Conjunctiva, Fovea, Macula, Nictitating membrane, Schlemm's canal,
Trabecular meshwork.
Cytology

This image clearly
shows the pupil, iris, and blood vessels of the human eye.
The retina
contains two forms of photosensitive cells — rods and cones. Though
structurally and metabolically similar, their function is quite
different, though they are equally important to vision. Rod cells are
highly sensitive to light allowing them to respond in dim light and dark
conditions. These are the cells which allow humans and other animals to
see by moonlight, or with very little available light (as in a dark
room). However, they do not distinguish between colours, and have low
visual acuity (a measure of detail). This is why the darker conditions
become, the less colour objects seem to have. Cone cells, conversely,
need high light intensities to respond and have high visual acuity.
Different cone cells respond to different colours (wavelengths) of
light, which allows an organism to see colour.
The differences
are useful; apart from enabling sight in both dim and light conditions,
humans have given them further application. The fovea, directly behind
the lens, consists of mostly densely-packed cone cells. This gives
humans a highly detailed central vision, allowing reading, bird
watching, or any other task which primarily requires looking at things.
Its requirement for high intensity light does cause problems for
astronomers, as they cannot see dim stars, or other objects, using
central vision because the light from these is not enough to stimulate
cone cells. Because cone cells are all that exist directly in the fovea,
astronomers have to look at stars through the "corner of their eyes"
(averted vision) where rods also exist, and where the light is
sufficient to stimulate cells, allowing the individual to observe
distant stars.
Rods and cones are
both photosensitive, but respond differently to different frequencies of
light. They both contain different pigmented photoreceptor proteins. Rod
cells contain the protein rhodopsin and cone cells contain different
proteins for each colour-range. The process through which these proteins
go is quite similar — upon being subjected to electromagnetic radiation
of a particular wavelength and intensity (ie. a colour visible light),
the protein breaks down into two constituent products. Rhodopsin, of
rods, breaks down into opsin and retinal; iodopsin of cones breaks down
into photopsin and retinal. The opsin in both opens ion channels on the
cell membrane which leads to the generation of an action potential (an
impulse which will eventually get to the visual cortex in the brain).
This is the reason
why cones and rods enable organisms to see in dark and light conditions
— each of the photoreceptor proteins requires a different light
intensity to break down into the constituent products. Further, synaptic
convergence means that several rod cells are connected to a single
bipolar cell, which then connects to a single ganglion cell and
information is relayed to the visual cortex. Whereas, a single cone cell
is connected to a single bipolar cell. Thus, action potentials from rods
share neurons, where those from cones are given their own. This results
in the high visual acuity, or the high ability to distinguish between
detail, of cone cells and not rods. If a ray of light were to reach just
one rod cell this may not be enough to stimulate an action potential.
Because several "converge" onto a bipolar cell, enough transmitter
molecules reach the synapse of the bipolar cell to attain the threshold
level to generate an action potential.
Furthermore,
colour is distinguishable when breaking down the iodopsin of cone cells
because there are three forms of this protein. One form is broken down
by the particular EM wavelength that is red light, another green light,
and lastly blue light. In simple terms, this allows human beings to see
red, green and blue light. If all three forms of cones are stimulated
equally, then white is seen. If none are stimulated, black is seen. Most
of the time however, the three forms are stimulated to different extents
— resulting in different colours being seen. If, for example, the red
and green cones are stimulated to the same extent, and no blue cones are
stimulated, yellow is seen. For this reason red, green and blue are
called primary colours and the colours obtained by mixing two of them,
secondary colours. The secondary colours can be further complimented
with primary colours to see tertiary colours.
Acuity
Main article:
Visual acuity
Visual acuity can
be measured with several different metrics.
Cycles per degree
(CPD) measures how much an eye can differentiate one object from another
in terms of degree angles. It is essentially no different from angular
resolution. To measure CPD, first draw a series of black and white lines
of equal width on a grid (similar to a bar code). Next, place the
observer at a distance such that the sides of the grid appear one degree
apart. If the grid is 1 meter away, then the grid should be about 8.7
millimeters wide. Finally, increase the number of lines and decrease the
width of each line until the grid appears as a solid grey block. In one
degree, a human would not be able to distinguish more than about 12
lines without the lines blurring together. So a human can resolve
distances of about 0.93 millimeters at a distance of one meter. A horse
can resolve about 17 CPD (0.66 mm at 1 m) and a rat can resolve about 1
CPD (8.7 mm at 1 m).
A diopter is the
unit of measure of focus.
Dynamic range
At any given
instant, the retina can resolve a contrast ratio of around 100:1 (about
6 1/2 stops). As soon as your eye moves (saccades) it re-adjusts its
exposure both chemically and by adjusting the iris. Initial dark
adaptation takes place in approximately four seconds of profound,
uninterrupted darkness; full adaptation through adjustments in retinal
chemistry (the Purkinje effect) are mostly complete in thirty minutes.
Hence, over time, a contrast ratio of about 1,000,000:1 (about 20 stops)
can be resolved. The process is nonlinear and multifaceted, so an
interruption by light nearly starts the adaptation process over again.
Full adaptation is dependent on good blood flow; thus dark adaptation
may be hampered by poor circulation, and vasoconstrictors like alcohol
or tobacco.
Adnexa and related
parts
The orbit
In many species,
the eyes are inset in the portion of the skull known as the orbits or
eyesockets. This placement of the eyes helps to protect them from
injury.
Eyebrows
In humans, the
eyebrows redirect flowing substances (such as rainwater or sweat) away
from the eye. Water in the eye can alter the refractive properties of
the eye and blur vision. It can also wash away the tear fluid — along
with it the protective lipid layer — and can alter corneal physiology,
due to osmotic differences between tear fluid and freshwater. This is
made apparent when swimming in freshwater pools, as the osmotic gradient
draws 'pool water' into the corneal tissue, causing edema, and
subsequently leaving the swimmer with "cloudy" or "misty" vision for a
short period thereafter. It can be reversed by irrigating the eye with
hypertonic saline.
Eyelids
In many animals,
including humans, eyelids wipe the eye and prevent dehydration. They
spread tear fluid on the eyes, which contains substances which help
fight bacterial infection as part of the immune system. Some aquatic
animals have a second eyelid in each eye which refracts the light and
helps them see clearly both above and below water. Most creatures will
automatically react to a threat to its eyes (such as an object moving
straight at the eye, or a bright light) by covering the eyes, and/or by
turning the eyes away from the threat. Blinking the eyes is, of course,
also a reflex.
Eyelashes
In many animals,
including humans, eyelashes prevent fine particles from entering the
eye. Fine particles can be bacteria, but also simple dust which can
cause irritation of the eye, and lead to tears and subsequent blurred
vision.
Eye movement

MRI scan of human
eye.
Main article: Eye movements
Animals with
compound eyes have a wide field of vision, allowing them to look in many
directions. To see more, they have to move their entire head or even
body.
The visual system
in the brain is too slow to process that information if the images are
slipping across the retina at more than a few degrees per second (Westheimer
and McKee, 1954). Thus, for humans to be able to see while moving, the
brain must compensate for the motion of the head by turning the eyes.
Another complication for vision in frontal-eyed animals is the
development of a small area of the retina with a very high visual
acuity. This area is called the fovea, and covers about 2 degrees of
visual angle in people. To get a clear view of the world, the brain must
turn the eyes so that the image of the object of regard falls on the
fovea. Eye movements are thus very important for visual perception, and
any failure to make them correctly can lead to serious visual
disabilities.
Having two eyes is
an added complication, because the brain must point both of them
accurately enough that the object of regard falls on corresponding
points of the two retinas; otherwise, double vision would occur. The
movements of different body parts are controlled by striated muscles
acting around joints. The movements of the eye are no exception, but
they have special advantages not shared by skeletal muscles and joints,
and so are considerably different.
How we see an
object
The steps of how
we see an object:
The light rays
enter the eye through the cornea (transparent front portion of eye to
focus the light rays)
Then, light rays move through the pupil, which is surrounded by Iris to
keep out extra light
Then, light rays move through the crystalline lens (Clear lens to
further focus the light rays )
Then, light rays move through the vitreous humor (clear jelly like
substance)
Then, light rays fall on the retina, which processes and converts
incident light to neuron signals using special pigments in rod and cone
cells.
These neuron signals are transmitted through the optic nerve,
Then, the neuron signals move through the visual pathway: Optic nerve →
Optic Chiasm → Optic Tract → Optic Radiations → Cortex
Then, the neuron signals reach the occipital (visual) cortex and its
radiations for the brain's processing.
The visual cortex interprets the signals as images and along with other
parts of the brain, interpret the images to extract form, meaning,
memory and context of the images.
Color vision
Main articles:
Color and Color vision
What is seen as
color is essentially different combinations of certain ranges of
wavelengths in the electromagnetic spectrum. In humans at least, there
are three different kinds of cones for three ranges of wavelengths,
roughly red, green and blue light. Each color of cone picks up the
intensity of light in its range of wavelengths, and the combination is
translated by the brain to a perceived color. Of course, some people
lack the ability to see some or all of the colour spectrum: they are
referred to as being 'color blind'.
Extraocular
muscles
Main article:
Extraocular muscles
Each eye has six
muscles that control its movements: the lateral rectus, the medial
rectus, the inferior rectus, the superior rectus, the inferior oblique,
and the superior oblique. When the muscles exert different tensions, a
torque is exerted on the globe that causes it to turn. This is an almost
pure rotation, with only about one millimeter of translation (Carpenter,
1988). Thus, the eye can be considered as undergoing rotations about a
single point in the center of the eye.
Rapid eye movement
Main article:
Rapid eye movement
Rapid eye movement
typically refers to the stage during sleep during which the most vivid
dreams occur. During this stage, the eyes move rapidly. It is not in
itself a unique form of eye movement.
Saccades
Main article:
Saccade
Saccades are
quick, simultaneous movements of both eyes in the same direction
controlled by the frontal lobe of the brain.
Microsaccades
Main article:
Microsaccade
Even when looking
intently at a single spot, the eyes drift around. This ensures that
individual photosensitive cells are continually stimulated in different
degrees. Without changing input, these cells would otherwise stop
generating output. Microsaccades move the eye no more than a total of
0.2° in adult humans.
Vestibulo-ocular
reflex
Main article:
Vestibulo-ocular reflex
Many animals, such
as humans, can look at something while turning their heads. The eyes are
automatically rotated to remain fixed on the object, directed by input
from the organs of balance near the ears.
Smooth pursuit
movement
Main article:
Pursuit movement
The eyes can also
follow a moving object around. This is less accurate than the vestibulo-ocular
reflex as it requires the brain to process incoming visual information
and supply feedback. Following an object moving at constant speed is
relatively easy, though the eyes will often make saccadic jerks to keep
up. The smooth pursuit movement can move the eye at up to 100°/s in
adult humans.
While still, the
eye can measure relative speed with high accuracy, however under
movement relative speed is highly distorted. Take for example, when
watching a plane while standing -- the plane has normal visual speed.
However, if an observer watches the plane while moving in the opposite
direction from the plane's movement, the plane will appear as if were
standing still or moving very slowly.
When an observer
views an object in motion moving away or towards himself, there is no
eye movement occurring as in the examples above, however the ability to
discern speed and speed difference is still present; although not as
severe. The intensity of light (e.g. night vs. day) plays a major role
in determining speed and speed difference. For example, no human can
with reasonable accuracy, visually determine the speed of an approaching
train in the evening as they could during the day. Similarly, while
moving, the ability is further diminished unless there is another point
of reference for determining speed; however the inaccuracy of speed or
speed difference will always be present.
Optokinetic reflex
The optokinetic
reflex is a combination of a saccade and smooth pursuit movement. When,
for example, looking out of the window in a moving train, the eyes can
focus on a 'moving' tree for a short moment (through smooth pursuit),
until the tree moves out of the field of vision. At this point, the
optokinetic reflex kicks in, and moves the eye back to the point where
it first saw the tree (through a saccade).
Vergence movement
Main article:
Vergence

The two eyes
converge to point to the same object
When a creature with binocular
vision looks at an object, the eyes must rotate around a vertical axis
so that the projection of the image is in the centre of the retina in
both eyes. To look at an object closer by, the eyes rotate 'towards each
other' (convergence), while for an object farther away they rotate 'away
from each other' (divergence). Exaggerated convergence is called cross
eyed viewing (focussing on the nose for example) . When looking into the
distance, or when 'staring into nothingness', the eyes neither converge
nor diverge.
Vergence movements
are closely connected to accommodation of the eye. Under normal
conditions, changing the focus of the eyes to look at an object at a
different distance will automatically cause vergence and accommodation.
Accommodation
Main article:
Accommodation (eye)
To see clearly,
the lens will be pulled flatter or allowed to regain its thicker form.
Diseases,
disorders, and age-related changes
Main articles:
List of eye diseases and disorders and List of systemic diseases with
ocular manifestations

The stye is a
common irritating inflammation of the eyelid.
There are many diseases,
disorders, and age-related changes that may affect the eyes and
surrounding structures.
As the eye ages
certain changes occur that can be attributed solely to the aging
process. Most of these anatomic and physiologic processes follow a
gradual decline. With aging, the quality of vision worsens due to
reasons independent of aging eye diseases. While there are many changes
of significance in the nondiseased eye, the most functionally important
changes seem to be a reduction in pupil size and the loss of
accommodation or focusing capability (presbyopia). The area of the pupil
governs the amount of light that can reach the retina. The extent to
which the pupil dilates also decreases with age. Because of the smaller
pupil size, older eyes receive much less light at the retina. In
comparison to younger people, it is as though older persons wear
medium-density sunglasses in bright light and extremely dark glasses in
dim light. Therefore, for any detailed visually guided tasks on which
performance varies with illumination, older persons require extra
lighting. [12]
With aging a
prominent white ring develops in the periphery of the cornea- called
arcus senilis. Aging causes laxity and downward shift of eyelid tissues
and atrophy of the orbital fat. These changes contribute to the etiology
of several eyelid disorders such as ectropion, entropion,
dermatochalasis, and ptosis. The vitreous gel undergoes liquefaction
(posterior vitreous detachment or PVD) and its opacities — visible as
floaters — gradually increase in number.
Various eye care
professionals, including ophthalmologists, optometrists, and opticians,
are involved in the treatment and management of ocular and vision
disorders. A Snellen chart is one type of eye chart used to measure
visual acuity. At the conclusion of an eye examination, an eye doctor
may provide the patient with an eyeglass prescription for corrective
lenses.
References
-
Halder,
G., Callaerts, P. and Gehring, W.J. (1995). "New
perspectives on eye evolution." Curr. Opin.
Genet. Dev. 5 (pp. 602–609).
-
Halder,
G., Callaerts, P. and Gehring, W.J. (1995).
"Induction of ectopic eyes by targeted
expression of the eyeless gene in
Drosophila". Science 267 (pp.
1788–1792).
-
Tomarev,
S.I., Callaerts, P., Kos, L., Zinovieva, R.,
Halder, G., Gehring, W., and Piatigorsky, J.
(1997). "Squid Pax-6 and eye
development." Proc. Natl. Acad. Sci. USA, 94
(pp. 2421–2426).
-
Conway-Morris, S. (1998). The Crucible of
Creation. Oxford: Oxford University Press.
-
Land, M.F.
and Fernald, Russell D. (1992). "The evolution
of eyes." Annu Rev Neurosci 15 (pp.
1–29).
-
Eye-Evolution?
-
Fernald,
Russell D. (2001).
The Evolution of Eyes: Where Do Lenses Come
From? Karger Gazette 64: "The Eye in
Focus".
-
http://www.e-sunbear.com/anatomy_02.html
-
Cassin, B.
and Solomon, S. Dictionary of Eye Terminology.
Gainsville, Florida: Triad Publishing Company,
1990.
-
"Departments. Anterior segment." Cantabrian
Institute of Ophthalmology.
-
Posterior segment anatomy
-
AgingEye Times
Return to Table of Contents
|