The human eye: structure and function
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| Main Author: | |
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| Format: | Book |
| Language: | English |
| Published: |
Sunderland, Mass.
Sinauer
1999
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| Subjects: | |
| Online Access: | Inhaltsverzeichnis |
| Physical Description: | XXVIII, 766, 16, 13 S. Ill. |
| ISBN: | 0878936459 |
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Record in the Search Index
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| adam_text | Contents
Preface xxiii
Acknowledgments xxviii
Prologue A Brief History of Eyes I
The Antiquity of Eyes and Vision I
Thinking about the eye gave Charles Darwin a cold shudder 1
The history of the eye is embedded in the history of animals and
molecules 2
Several of the eye s critical molecules are ancient 3
Eyes were invented by multicellular animals almost 600 million years
ago 5
Eyes arose not once, but numerous times, in different animal groups 6
Eyes are most common in groups of motile animals living in lighted
environments 8
The Diversity and Distribution of Eyes 9
The first step in vision is an eye that can sense the direction of incident
light 9
At least ten types of eyes can be distinguished by differences in their
optical systems 11
Vertebrates always have simple eyes, but invertebrates can have
compound eyes, simple eyes, or both 13
Paths and Obstacles to Perfection 16
Simple eyes improve as they become larger 16
Elaborate simple eyes may have evolved rapidly 18
Compound eyes have inherent optical limitations in their
performance 19
An Ocular Bestiary: Fourteen Eyes and Their Animals 21
I. Compound eye—focal apposition, terrestrial variety: Honeybee
(Apis mellifica) 21
II. Compound eye—focal apposition, aquatic variety: Horseshoe crab
(Limulus polyphemus) 23
III. Compound eye—afocal apposition: Monarch butterfly (Danaus
plexippus) 26
ix
X Contents
IV. Compound eye—apposition with neural
superposition: Housefly (Musca domestica) 29
V. Compound eye—refracting superposition: Firefly
(Photuris spp.) 31
VI. Compound eye—reflecting superposition:
Crayfish 33
VII. Compound eye—parabolic superposition: Crabs 36
VIII. Simple eye—pinhole: Nautilus 37
IX. Simple eye—refracting, aquatic variety: Octopus 38
X. Simple eye—refracting, aquatic variety: Goldfish 40
XL Simple eye—refracting, terrestrial variety: Pigeon
(Columba livia) 43
XII. Simple eye—refracting, terrestrial variety: Jumping
spiders (Metaphidippus spp.) 45
XIII. Simple eye—reflecting: Scallops 48
XIV. Simple eye—refracting, terrestrial variety: Humans
(Homo sapiens) 50
PART ONE
Ocular Systems
Chapter I Formation of the Human Eye 57
Some Developmental Strategies and Operations 57
Embryogenesis begins with cell proliferation, cell
movement, and changes in cell shape 57
Specialized tissues are formed by collections of cells that
have become specialized themselves 58
Proliferation, movement, and differentiation in a cell
group may require communication with other cells 58
Embryonic Events before the Eyes Appear 59
The blastocyst forms during the first week of
embryogenesis 59
The inner cell mass becomes the gastrula, which is
divided into different germinal tissues 60
Neurulation begins the development of the nervous
system 62
Formation of the Primitive Eye 64
Ocular development begins in the primitive forebrain 64
The optic vesicle induces formation of the lens 64
Elaboration of the Primitive Eye 65
The optic cup and the lens form from different germinal
tissues by changes in cell shape 65
The optic cup is initially asymmetric, with a deep groove
on its inferior surface 67
Closure of the choroidal fissure completes the optic
cup 67
The lens vesicle forms in synchrony with the optic cup 67
The primitive lens is the first ocular structure to exhibit
cell differentiation 68
All future growth of the lens comes from the early lens
cells, some of which are immortal stem cells 69
The precursors of the future retina, optic nerve, lens, and
cornea are present by the sixth week of gestation 69
In general, the eye develops from inside to outside 70
Failures of Early Development 71
If anything can go wrong, it will 71
One or both eyes may fail to develop completely 71
Congenital absence of the lens may be an early
developmental failure 71
Incomplete closure of the choroidal fissure can produce
segmental defects in the adult eye 74
VIGNETTE 1.1 The Eye of Mann 72
Chapter 2 Ocular Geometry and
Topography 77
Elements of Ocular Structure 77
The human eye is a simple eye 77
The outermost of the three coats of the eye consists of
cornea, limbus, and sclera 78
The middle coat—the uveal tract—includes the iris,
ciliary body, and choroid 78
The eye s innermost coat—the retina—communicates
with the brain via the optic nerve 79
Most of the volume of the eye is fluid or gel 81
Image Quality and Visual Performance 82
Images of point sources are always small discs of light
whose size is a measure of optical quality 82
The amount of smear or spread in the image of a point
source is related to the range of spatial frequencies
transmitted by the optical system 83
The contrast sensitivity function specifies how well
different spatial frequencies are seen by the visual
system 86
We can see flies when their images subtend about one
minute of visual angle 87
The Anatomy of Image Formation 90
The quality of a focused image is affected by pupil size,
curvatures of optical surfaces, and homogeneity of the
optical media 90
Defocusing produces large changes in the modulation
transfer function 92
The major anatomical factors that determine the
refractive power of the eye are the curvatures of the
cornea and lens and the depth of the anterior
chamber 93
Schematic eyes are approximations of the eye s optically
relevant anatomy 95
Eye Shape and Size 97
Vertebrate eyes vary considerably in shape 97
Both the cornea and the sclera are aspheric 97
On average, the adult human eye measures twenty four
millimeters in all dimensions 100
Axial lengths and other anatomical features vary among
individuals, but most eyes are emmetropic 101
Most refractive error is related to relatively large or small
axial lengths 102
The Eye s Axes and Planes of Reference 103
The eyes rotate around nearly fixed points 103
Like the head, the eyes have three sets of orthogonal
reference planes 104
The pupillary axis is a measure of the eye s optical
axis 106
The line of sight differs from the pupillary axis by the
angle kappa 107
The angles kappa in the two eyes should have the same
magnitude 107
Eye position is specified by the direction of the line of
sight in a coordinate system whose origin lies at the
eye s center of rotation 108
VIGNETTE 2.1 The Medieval Eye 80
BOX 2.1 Evaluating Visual Resolution 88
VIGNETTE 2.2 Fundamentum Opticum 98
Chapter 3 The Orbit 111
The Bony Orbit 111
The orbits are roughly pyramidal 111
The large bones of the face form the orbital margin and
much of the orbit s roof, floor, and lateral wall 112
The sphenoid bone fills the apex of the orbital pyramid
and contributes to the lateral and medial walls 114
The lacrimal and ethmoid bones complete the medial
wall between the maxillary bone in front and the
sphenoid in back 118
Three major and several minor foramina permit blood
vessels and nerves to enter or exit the orbital cavity 118
Blowout fractures of the orbit are a consequence of the
relative weakness of the orbital plates 119
Abnormal positioning of the eye relative to the orbital
margin may indicate local or systemic pathology 120
Infection and tumors can enter the orbital cavity through
the large sinuses that surround the orbit 120
Connections between the Eye and the Orbit 121
Connective tissue lines the interior surface of the
orbit 121
Connective tissue surrounds the eye and extraocular
muscles 121
Check ligaments connect Tenon s capsule to the
periorbita 124
Contents xi
All structures in the orbital cavity are lined and
interconnected with connective tissue 125
Abnormal development of the connective tissue may
affect movement of the eyes 125
Fat fills the spaces in the orbital cavity that are not
occupied by other structures 126
The septum orbitale prevents herniation of orbital fat into
the eyelids 127
Development of the Orbital Bones 127
Many bones form first as cartilage templates 127
Most orbital bones do not have cartilaginous
templates 127
The orbital plates begin to form during the sixth week of
gestation 130
The capacity of bone for growth, repair, and remodeling
lasts many years 130
The eyes and orbits rotate from lateral to frontal positions
during development 130
Most developmental anomalies of the orbital bones are
associated with anomalies of the facial bones 131
VIGNETTE 3.1 Sovereign of the Visible World 116
BOX 3.1 Visualizing the Orbit and Its Contents In
Vivo 122
VIGNETTE 3.2 The Anatomy of Vesalius 128
Chapter 4 The Extraocular Muscles 133
Patterns of Eye Movement 133
Our eyes are always moving, and some motion is
necessary for vision 133
Large, rapid eye movements are used for looking around,
for placing retinal images of interest on the fovea 135
Slow eye movements are used to track or follow movement
and to compensate for changes in head and body
position 136
Eye movement velocities may vary by a factor of 105 137
Since the eyes have overlapping fields of view, their
movements must be coordinated 137
Slow movements of the eyes in opposite directions help
keep corresponding images on the foveas in both
retinas simultaneously 138
Strabismus is a misalignment of the two visual axes
under binocular viewing conditions 139
Control of Eye Position 13 9
The extraocular muscles are arranged as three
reciprocally innervated agonist antagonist pairs 139
The eyes are stationary when the opposing forces exerted
by the extraocular muscles are in balance 141
Imbalanced forces produce eye rotations 142
Muscle force is related to muscle length 143
Most of the force that maintains eye position is passive
force 144
xii Contents
Equilibrium muscle lengths and forces for different gaze
positions are functions of the innervational
command 145
Different patterns of innervation are required for fast and
slow eye movements 146
Extraocular motor neurons are located in three
interconnected nuclei in the brainstem 146
Motor commands are the result of interactions between
visual and nonvisual inputs to the motor control
centers 147
A copy of the innervational command is used to verify
the system s operation 148
Extraocular motor neurons receive inputs from premotor
areas in the brainstem to generate appropriate signals
for saccadic eye movements 148
The pathways for smooth pursuit movements and for
vergences go through the cerebellum, but vergences
have a separate control center near the oculomotor
nucleus 149
Extraocular Muscle Structure and Contractile
Properties 153
Muscle fibers are the units from which muscles are
constructed 153
Striated muscle fibers have a parallel arrangement of
contractile proteins that interleave to cause
contraction 154
Striated muscle fibers differ in structural, histochemical,
and contractile properties 155
The extraocular muscles contain muscle fiber types not
found in skeletal muscles 156
Thick and thin extraocular muscle fibers differ in their
contractile properties 156
Different muscle fiber types are not randomly distributed
within the muscles 157
Different muscle fiber types may receive different
innervational commands 158
Extraocular muscles have very small motor units 159
Acetylcholine at the neuromuscular junctions depolarizes
the cell membrane by opening sodium channels 161
The spread of depolarization along the sarcolemma may
differ among muscle fiber types, producing different
contractile properties 161
Extraocular muscles exhibit high sensitivity to agents
that mimic or block the action of acetylcholine 162
Extraocular muscles often exhibit early symptoms of
myasthenia gravis 163
Neurotoxins that interfere with acetylcholine action can
be used to alleviate strabismus and blepharospasm 163
Sensory Endings in Extraocular Muscles and Tendons 165
Skeletal muscles have two major types of sensory
organs 165
Human extraocular muscles have anatomically
degenerate sensory organs and exhibit no stretch
reflexes 166
Passive extraocular muscle stretch may produce
bradycardia 167
Sensory endings in extraocular muscles probably do not
convey information about eye position 167
Sensory signals from the extraocular muscles may be
involved in motor learning, motor plasticity, and
development 168
Actions of the Extraocular Muscles 168
All of the extraocular muscles except the inferior oblique
have their anatomical origins at the apex of the
orbit 168
The anatomical origin of the inferior oblique and the
functional origin of the superior oblique are anterior
and medial in the orbit 169
The four rectus muscles are arranged as horizontal and
vertical pairs, all inserting onto the anterior portion of
the globe 170
The horizontal recti rotate the eye in the horizontal plane
around a vertical axis 170
The vertical recti are responsible for upward and
downward rotations of the eye 171
The recti define a muscle cone within the orbital cavity
that contains most of the ocular blood vessels and
nerves 172
The oblique muscles constitute a third functional pair,
inserting onto the posterior portion of the eye 172
Extraocular muscle actions cannot be measured
directly 174
The classic description of action of the extraocular
muscles is based on the geometry of their origins and
insertions 174
Boeder diagrams attempt to describe the actions of the
extraocular muscles completely 176
The presence of Tenon s capsule and muscle pulleys
invalidates the geometric model of extraocular muscle
actions 178
There is no simple way to describe the action of these
muscles on the eye! 180
A realistic model of the extraocular muscle system is
important for the diagnosis and treatment of muscle
paresis 182
Development of the Extraocular Muscles 183
Each muscle develops from several foci in the mesoderm
surrounding the optic cup 183
The extraocular muscles appear after the optic cup, but
before the orbital bones 185
Different muscle fiber types form late in gestation and
continue to develop postnatally 185
Most developmental anomalies are associated with the
connective tissue of the muscles or with their
innervation 186
The oculomotor system is not fully operational at
birth 186
BOX 4.1 Detecting Ocular Misalignment 140
BOX 4.2 Changing the Effects of Extraocular Muscle
Contraction 152
VIGNETTE 4.1 Locating the Extraocular Muscles 164
VIGNETTE 4.2 In the Service of the Eye 184
Chapter 5 The Nerves of the Eye and
Orbit 191
Elements of Neural Organization 19 /
The brain deals with information about the external
world and the body 191
Neurons are the anatomical elements of neural
systems 191
Neural circuits consist of neurons linked mostly by
unidirectional chemical synapses 193
The direction of neural information flow distinguishes
between sensory and motor nerves 194
Motor outputs are divided anatomically and functionally
into somatic and autonomic systems 194
The autonomic system is subdivided into the
sympathetic and parasympathetic systems 194
The Optic Nerve and the Flow of Visual Information 195
In the optic nerve, the location of axons from retinal
ganglion cells corresponds to their location on the
retina 195
Axons from the two optic nerves are redistributed in the
optic chiasm 198
The decussation of axons in the chiasm is imperfect 199
Spatial ordering of axons changes in the optic tracts 200
In the lateral geniculate nuclei, which are primary targets
of axons in the optic tracts, inputs from the two eyes are
separated into different layers 200
Axons terminating in the lateral geniculate nuclei are
spatially ordered 201
Some axons leave the optic tracts for other
destinations 203
Axons terminating in the superior colliculi form
discontinuous retinotopic maps 204
Axons forming the afferent part of the pupillary light
reflex pathway terminate in the pretectal nuclear
complex 204
Retinal inputs to the accessory optic system may help
coordinate eye and head movement 205
Retinal axons may provide inputs to a biological
clock 205
Lesions of the optic nerves and tracts produce defects in
the visual fields 207
Lesions in the secondary visual pathways can be
observed only as motor deficits 212
The Trigeminal Nerve: Signals for Touch and Pain 212
Two of the three trigeminal divisions carry signals from
the eye and surrounding tissues 212
Contents xiii
All somatosensory information from the eye is conveyed
by the nasociliary nerve to the ophthalmic division of
the trigeminal 213
Sensory nerve fibers from the cornea, conjunctiva,
limbus, and anterior sclera join to form the long ciliary
nerves 213
Stimulation of corneal or conjunctival nerve endings
elicits sensations of touch or pain, a blink reflex, and
reflex lacrimation 215
Other sensory fibers from the eye are conveyed by the
short ciliary nerves and the sensory root of the ciliary
ganglion 215
Most other branches of the ophthalmic nerve carry
somatosensory fibers from the skin of the eyelids and
face 215
A few branches of the maxillary nerve pass through the
orbit from the facial skin and the maxillary sinus 217
Lesions in the branching hierarchy of the ophthalmic
nerve produce anesthesia that helps identify the lesion
site 218
Viral infection of the trigeminal system can produce
severe corneal damage 219
The Extraocular Motor Nerves 219
The three cranial nerves that innervate the extraocular
muscles contain axons from clusters of cells in the
brainstem 219
Cells in different parts of the oculomotor nerve nucleus
innervate the levator, the superior and inferior recti, the
medial rectus, and the inferior oblique 219
Axons destined for different muscles run together in the
oculomotor nerve until it exits the cavernous sinus just
behind the orbit 221
The oculomotor nerve contains parasympathetic fibers
bound for the ciliary ganglion 224
Cells in the trochlear nerve nucleus innervate the
contralateral superior oblique 224
Abducens nerve cells innervate the ipsilateral lateral
rectus 225
All of the oculomotor nerves pass through the cavernous
sinus on their way to the orbit 225
The extraocular motor nerves probably contain sensory
axons from muscle spindles and tendon organs 226
Innervation of the Muscles of the Eyelids 226
Three sets of muscles are associated with the eyelids 226
The orbicularis is innervated by the facial nerve 227
The superior and inferior tarsal muscles are innervated
by the sympathetic system 227
Ptosis may result from either oculomotor or sympathetic
lesions 228
Autonomic Innervation of Smooth Muscle within
the Eye 228
The superior cervical ganglion is the source of most
sympathetic innervation to the eye 228
xiv Contents
Sympathetic fibers enter the eye in the short ciliary
nerves 230
Sympathetic innervation of the dilator muscle acts at
alpha adrenergic receptors to dilate the pupils 230
The arterioles in the uveal tract receive sympathetic
innervation that produces vasoconstriction 231
Homer s syndrome is the result of a central lesion in the
sympathetic pathway 231
Parasympathetic fibers entering the eye originate in the
ciliary or the pterygopalatine ganglion 231
Axons from cells in the ciliary ganglion innervate the
sphincter and the ciliary muscle 232
Axons from the pterygopalatine ganglion cells innervate
vascular smooth muscle in the choroid 233
Accommodation and pupillary light reflexes share
efferent pathways from the Edinger Westphal nuclei to
the eyes; pupillary reflexes are mediated by retinal
signals reaching the Edinger Westphal nuclei through
the pretectal complex 233
Deficient pupillary reflexes may be associated with
midbrain lesions 234
Innervation of the Lacrimal Gland 235
Axons from cells in the pterygopalatine ganglion reach
the lacrimal gland via the zygomatic and lacrimal
nerves 235
The efferent pathway for lacrimal innervation begins in
the facial nerve nucleus 235
Basal tear production may require tonic innervation of
the lacrimal gland 236
Some Issues in Neural Development 236
Specialized growth cones guide the extension of axons
and dendrites 236
Pathfinding by growth cones depends on recognition of
local direction signs 237
Target recognition and acquisition may require specific
markers produced by the target cells 238
Many early neurons are eliminated as mature patterns of
connectivity are established 238
Adult connectivity patterns are not always complete at
birth, and postnatal development is subject to
modification 239
Ocular albinism is associated with a pathfinding error in
the development of optic nerve axons 239
Anomalous innervation of the extraocular muscles
may be the result of pathfinding or target recognition
errors 240
Some forms of amblyopia may be related to problems
with postnatal establishment and maintenance of
synaptic connections 240
Innervation of the extraocular muscles begins early in
gestation, sensory innervation much later 241
Postnatal Neuron Growth and Regeneration 241
Most postnatal neuron growth is interstitial growth 241
Neurons do not undergo mitosis postnatally 242
Spinal neurons in peripheral nerves can regenerate after
being damaged 242
Central nervous system neurons do not regenerate
following major damage 242
Corneal nerve endings will regenerate following local
damage 243
Neuronal degeneration can affect other, undamaged neu¬
rons 243
VIGNETTE 5.1 The Integrative Action of the Nervous
System 196
BOX 5.1 Tracing Neural Pathways: Degeneration and
Myelin Staining 206
VIGNETTE 5.2 Seeing One World with Two Eyes:
The Problem of Decussation 210
BOX 5.2 Tracing Neuronal Connections: Axonal
Transport Methods 222
Chapter 6 Blood Supply and Drainage 247
Distributing Blood to Tissues 247
Arteries control blood flow through capillary beds, and
veins regulate blood volume 247
Blood flow through capillary beds can be controlled
locally or systemically 248
Capillary beds in a tissue may be independent or
interconnected 251
The interchange between blood and cells depends partly
on the structure of the vascular endothelium 252
Capillary endothelium is renewable, and capillary beds
can change 253
Neovascularization is a response to altered functional
demands 253
Structurally weakened capillaries may be prone to
excessive neovascularization 254
The Ophthalmic Artery and Ophthalmic Veins 255
The ophthalmic artery distributes blood to the eye and its
surroundings 255
Blood supplied to tissues by the ophthalmic artery is
drained to the cavernous sinus by the ophthalmic
veins 257
Supply and Drainage of the Eye 260
Muscular arteries supply both the extraocular muscles
and the anterior segment of the eye 260
The anterior ciliary arteries contribute to the episcleral
and intramuscular arterial circles 261
The conjunctiva and corneal arcades are supplied by
branches from the episcleral arterial circle and drained
by the episcleral and anterior ciliary veins 262
The system of episcleral veins drains the conjunctiva,
corneal arcades, and limbus 263
The posterior ciliary arteries divide into long and short
posterior ciliary arteries that supply different
regions 264
The intramuscular and major arterial circles are formed
in the ciliary body by branches from the anterior and
long posterior ciliary arteries 265
Blood supply to the anterior segment is redundant, but
there is some segmentation in supply to the iris 268
The short posterior ciliary arteries terminate in the
choriocapillaris, which supplies the retinal
photoreceptors 269
The short posterior ciliary arteries contribute to the
supply of the optic nerve through the circle of Zinn 272
The short posterior ciliary arteries sometimes contribute
to the supply of the inner retina 274
The central retinal artery enters the eye through the optic
nerve and ramifies to supply the inner retina 275
The central retinal vein exits the eye through the optic
nerve 277
The vortex veins drain most of the uveal tract 277
The vortex veins have segmented drainage fields, but
they are heavily anastomotic 278
Supply and Drainage of the Eyelids and Surrounding
Tissues 279
The lacrimal gland is supplied by the lacrimal artery and
drained by lacrimal veins 279
The eyelids are supplied by branches of the lacrimal,
ophthalmic, facial, and infraorbital arteries 279
The terminal branches of the ophthalmic artery leave the
orbit to supply the skin and muscles of the face 282
The infraorbital artery runs under the orbital floor 283
The orbital veins are connected to the veins of the face,
the pterygoid plexus, and the nose 283
Development of the Ocular Blood Vessels 284
Primitive embryonic blood vessels appear very early in
the eye s development 284
Several parts of the early ocular vasculature are transient
and do not appear in the mature eye 284
The anterior ciliary system forms later than the posterior
ciliary system 287
Remnants of normally transient, embryological
vasculature may persist in the mature eye 287
VIGNETTE 6.1 Circulation of the Blood 256
BOX 6.1 Tracing Hidden Blood Vessels: Vascular
Casting 270
VIGNETTE 6.2 Blood Vessels inside the Eye 280
Contents xv
Chapter 7 The Eyelids and the Lacrimal
System 291
Structure and Function of the Eyelids 291
Structural rigidity of the lids is provided by the tarsal
plates 291
The tarsal plates are made of dense connective tissue in
which glands are embedded 292
The palpebral fissure is opened by muscles inserting onto
or near the edges of the tarsal plates 294
The palpebral fissure is closed by contraction of the
orbicularis 296
Blinking may be initiated as a reflex response or as a
regular, spontaneous action 298
Lid movements during spontaneous blinks move tears
across the cornea 299
Overaction of the orbicularis may appear as
blepharospasm or as entropion 299
Paresis of the orbicularis produces ectropion and
epiphora 300
Other glands in the lids are associated with the
eyelashes 301
The skin on the lids is continuous with the conjunctiva
lining the posterior surface of the lids and covering the
anterior surface of the sclera 302
The orbital septum is a connective tissue sheet extending
from the orbital rim to the tarsal plates 303
The shape and size of the palpebral fissure vary 304
The overall structure of the lids consists of well defined
planes or layers of tissue 306
Tear Supply and Drainage 307
Most of the tear fluid is supplied by the main lacrimal
gland 307
Secretion by the lacrimal gland is regulated by autonomic
inputs operating through a second messenger
system 308
The composition of the lacrimal gland secretion varies
with the secretion rate 309
Dry eye may result from a decreased amount of tears,
abnormal tear composition, or both 310
Tears are drained off at the medial canthus and deposited
in the nasal cavity 311
Pressure gradients created by contraction of the
orbicularis during blinks move tears through the
canaliculi into the lacrimal sac 312
Formation of the Eyelids and the Lacrimal System 315
The eyelids first appear as folds in the surface ectoderm,
which gives rise to the lid glands 315
The lacrimal gland and the lacrimal drainage system
derive from surface ectoderm 316
Most developmental anomalies in the eyelids and
lacrimal system are problems in lid position or blockage
of the drainage channels 318
Anomalous innervation can produce eyelid movements
linked to contraction of muscles in the jaw 318
PART TWO
Components of the Eye
Chapter 8 The Cornea and the Sclera 325
Components and Organization of the Cornea and
Sclera 325
The cornea, sclera, and limbus are made primarily of
collagen fibrils 325
Collagen is embedded in a polysaccharide gel that forms
the extracellular matrix 326
The fibroblasts in the corneal and scleral stroma
constitute a small fraction of the stroma s volume 327
Collagen fibrils in the cornea are highly organized; those
in the sclera are not 328
The structure of the corneal stroma is altered in
Bowman s layer 331
Corneal transparency is a function of its regular
structure 332
Collagen organization in the stroma and corneal
transparency depend on intact epithelium and
endothelium 334
The corneal epithelium is a multilayered, renewable
barrier to water movement into the cornea 335
The corneal endothelium is a single layer of metabolically
active cells 339
The endothelial cell tiling changes with time because
cells that die cannot be replaced 340
Descemet s membrane separates the endothelium from
the stroma 345
Nerve endings in the cornea give rise to sensations of
touch or pain, a blink reflex, and reflex lacrimation 347
The epithelium contains a dense array of free terminals
of nerve fibers from the long ciliary nerves 347
Corneal sensitivity can be measured quantitatively 349
The dense innervation of the cornea makes it subject to
viral infection 349
The Cornea as a Refractive Surface 349
The optical surface of the cornea is the precorneal film
covering the surface of the epithelium 349
The cornea s outline is not circular, its thickness is not
uniform, and its radius of curvature is not constant 351
The shape of the cornea is determined by comparison to
a sphere 353
The cornea does not have a single, specifiable shape 354
Contact lenses can affect corneal shape and structure
directly or indirectly 356
The shape and optical properties of the cornea can be
permanently altered 358
Surgically reshaped corneas may change with time 359
Corneal shape can be changed by removing tissue 360
Stromal reshaping leaves the epithelium intact 361
Corneal grafts are used to repair optically damaged
corneas 361
Corneal Healing and Repair 365
The epithelium heals quickly and completely 365
Corneal healing may require limbal transplants 368
Repair of damage to the stroma produces translucent scar
tissue 368
The endothelium repairs itself by cell expansion and
migration 369
Corneal graft incisions are repaired by the normal
healing processes 369
Radial keratotomy incisions are repaired by epithelial
hyperplasia and collagen formation 370
Photorefractive keratectomy ablations are healed mostly
by the epithelium 371
Growth and Development of the Cornea 371
The epithelium and endothelium are the first parts of the
cornea to appear 371
The stroma is derived from neural crest cells associated
with the mesoderm 372
The regular arrangement of the stromal collagen appears
soon after collagen production begins 372
Corneal growth continues for a few years
postnatally 374
Anomalous corneal development can produce misshapen
or opaque corneas 375
BOX 8.1 Biomicroscopy of the Cornea 342
VIGNETTE 8.1 The Invisible Made Visible 350
BOX 8.2 Some Reservations about Corneal Refractive
Surgery 362
VIGNETTE 8.2 The Art of William Bowman 366
Chapter 9 The Limbus and the Anterior
Chamber 379
The Anterior Chamber and Aqueous Flow 379
The anterior chamber is the fluid filled space between the
cornea and the iris 379
The angle of the anterior chamber varies in
magnitude 380
Aqueous is formed by the ciliary processes and enters the
anterior chamber through the pupil 381
Aqueous drains from the eye at the angle of the anterior
chamber 383
Intraocular pressure depends on the rate of aqueous
production and the resistance to aqueous outflow 385
The Anatomy of Aqueous Drainage 390
The scleral spur is an anchoring structure for parts of the
limbus and the ciliary body 390
The trabecular meshwork is made of interlaced cords of
tissue extending from the apex of the angle to the
margin of the cornea 392
Schwalbe s ring separates the trabecular meshwork from
the cornea 393
The trabecular cords have a collagen core wrapped with
endothelial cells 393
The major source of outflow resistance is the juxta
canalicular tissue separating the canal of Schlemm from
the trabecular spaces 395
The canal of Schlemm encircles the anterior chamber
angle 395
Aqueous enters the canal of Schlemm by way of large
vacuoles in the endothelial lining of the canal 397
Aqueous drains out of the canal into venous plexuses in
the limbal stroma 399
Pilocarpine reduces intraocular pressure, probably by an
effect of ciliary muscle contraction on the structure of
the trabecular meshwork 400
An effective way to reduce intraocular pressure seems to
be to increase the uveoscleral outflow 402
Surgery for glaucoma aims to increase aqueous
outflow 402
The outer surface of the limbus is covered with episcleral
tissue and a heavily vascularized conjunctiva 403
Development of the Limbus 405
The anterior chamber is defined by the iris growing
between the developing cornea and lens 405
The angle of the anterior chamber opens during
development as the root of the iris shifts
posteriorly 406
The trabecular meshwork develops between the fourth
and eighth months 408
Most developmental anomalies in the limbus are
associated with structural anomalies that affect other
parts of the anterior chamber 408
BOX 9.1 Through the Looking Glass: Gonioscopy 382
BOX 9.2 Estimating the Pressure Within:
Tonometry 388
Chapter 10 The Iris and the Pupil 411
Functions of the Iris and Pupil 411
The iris is an aperture stop for the optical system of the
eye 411
The entrance pupil is a magnified image of the real
pupil 412
Variation of pupil size changes the amount of light
entering the eye, the depth of focus, and the quality of
the retinal image 413
Pupil size varies with illumination level, thereby helping
the retina cope with large changes in illumination 414
Pupil size varies with accommodation and
accommodative convergence 416
The pupillary near response is smaller in children than in
adults 417
The pupil is in constant motion, and it reacts quickly to
changes in retinal illumination 418
Decreased iris pigmentation in ocular albinism affects the
optical function of the iris 419
Contents xvii
Structure of the Iris 420
The pupils in the two eyes are normally the same size
and are decentered toward the nose 420
The iris is constructed in layers and regional differences
in the iris are related to the different muscles within
them 421
The anterior border layer is an irregular layer of
melanocytes and fibroblasts interrupted by large
holes 422
The iris stroma has the same cellular components as the
anterior border layer, but loosely arranged 423
Small blood vessels run radially through the stroma,
anastomosing to form the minor arterial circle and
supply the iris muscles 425
The sphincter and dilator occupy different parts of the
iris and have antagonistic actions 426
The sphincter is activated by the parasympathetic
system, the dilator by the sympathetic system 427
The anterior pigmented epithelium is a myoepithelium,
forming both the epithelial layer and the dilator
muscle 428
The posterior epithelial cells contact the anterior surface
of the lens 430
Surgery for closed angle glaucoma often involves the iris
rather than the limbus 432
Some Clinically Significant Anomalies of the Iris and
Pupil 432
Changes in iris color after maturity are potentially
pathological 432
Differences between the two eyes in pupil size or
pupillary responses to light are commonly associated
with neurological problems 433
Anisocoria and unresponsive pupils are often associated
with defects in the efferent part of the innervational
pathways 435
Clinically useful drugs affecting pupil size fall into four
functional groups 437
Development of the Iris 440
The iris stroma forms first by migration of
undifferentiated neural crest cells 440
The epithelial layers and the iris muscles develop from
the rim of the optic cup and are therefore of
neuroectodermal origin 440
The pupil is the last feature of the iris to appear 442
Most postnatal development of the iris is an addition of
melanin pigment 443
Segmental defects and holes in the iris result from
unsynchronized or failed growth of the optic cup rim 443
An ectopic pupil is improperly centered in an otherwise
normal iris 445
A persistent pupillary membrane may be the result of
either insufficient tissue atrophy or tissue
hyperplasia 445
xviii Contents
Chapter 11 The Ciliary Body and the
Choroid 447
Anatomical Divisions of the Ciliary Body 447
The ciliary processes characterize the pars plicata 447
The ciliary muscle extends through both pars plicata and
pars plana 449
The Ciliary Processes and Aqueous Formation 449
The ciliary processes are mostly filled with blood
vessels 449
The capillaries in the ciliary processes are highly
permeable 451
Two layers of epithelium lie between the capillaries and
the posterior chamber 452
Aqueous formation involves metabolically driven
transport systems 452
The ciliary epithelium is anatomically specialized as a
blood aqueous barrier 454
Ions are transported around the band of tight junctions to
produce an osmotic gradient in the basal folds of the
unpigmented epithelium 455
Aqueous production varies during the day and declines
with age 456
The major classes of drugs used to reduce aqueous
production interact either with adrenergic membrane
receptors or with the intracellular formation of
bicarbonate ions 458
The pars plana is covered by epithelial layers that are
continuous with the epithelial layers of the pars
plicata 459
The Ciliary Muscle and Accommodation 461
The ciliary muscle has three parts with a complex
geometry 461
Contraction of the ciliary muscle produces movement
inward toward the lens so that the muscle behaves like
a sphincter 463
The zonule provides a mechanical linkage between
ciliary muscle and lens 465
Accommodation is a result of ciliary muscle
contraction 468
The primary stimulus to accommodation is retinal image
blur 469
Accommodative amplitude decreases progressively with
age 472
Presbyopia is not a consequence of reduced innervation
to the ciliary muscle 473
Aging of the ciliary muscle is unlikely to be a significant
factor in presbyopia 474
The Choroid 477
The choroidal stroma consists of loose connective tissue
and dense melanin pigment 477
Blood vessels that supply and drain the capillary bed
supplying retinal photoreceptors make up the main
part of the choroid 478
The choriocapillaris is heavily anastomotic but has local
functional units 479
The choriocapillaris varies in capillary density and in the
ratio of arterioles to venules 480
Capillaries in the choriocapillaris are specialized for
ease of fluid movement across the capillary
endothelium 481
Bruch s membrane lies between capillaries and
pigmented epithelium in both the choroid and the pars
plana of the ciliary body 481
Development of the Ciliary Body and Choroid 482
The ciliary epithelium arises from the optic cup, the
ciliary muscle from neural crest cells 482
Formation of the ciliary epithelium may be induced by
the lens 483
Formation of the ciliary muscle may be induced by the
ciliary epithelium 484
The ciliary muscle begins to form during the fourth
month and continues to develop until term 485
The muscles associated with the eye originate from
different germinal tissues 486
The ciliary processes form in synchrony with the vascular
system in the ciliary body 486
The zonule is produced by the ciliary epithelium 486
The choroidal vasculature has two developmental
gradients: center to periphery and inside to outside 488
VIGNETTE 11.1 The Source 470
Chapter 12 The Lens and the Vitreous 491
Structure of the Lens 492
Some unusual proteins, the crystallins, are the dominant
structural elements in the lens 492
Dense, uniform packing of the crystallins within lens
cells is responsible for lens transparency 494
Crystallins are highly stable molecules, making them
some of the oldest proteins in the body, but they can be
changed by light absorption and altered chemical
environments 494
a Crystallins may play a special role in maintaining
native crystallin structure over time 496
The lens is formed of long, thin lens fibers arranged in
concentric shells to form a flattened spheroid 497
Lens fibers in each shell meet anteriorly and posteriorly
along irregular lines 498
Lens shells are bound together with miniature locks and
keys, a kind of biological Velcro 499
The anterior epithelium is the source of new cells for the
lens 501
Elongating epithelial cells at the equator become long
lens fibers that form new shells in the lens 503
The size of the lens and the number of lens fibers
increase throughout life 503
Each new lens shell has one more fiber than the previous
shell and about five new shells are added each year
after the age of five 504
An aged lens has about 2500 shells and 3.6 million lens
fibers 505
The lens capsule encloses the lens shells and
epithelium 507
The locations at which the zonule inserts onto the lens
change with age 510
The Lens as an Optical Element 513
The refractive index of the ocular lens varies from one
part of the lens to another 513
Lens transparency is related not only to protein
regularity but also to water content, which is
maintained by ion pumping in the epithelium 514
The lens contains several different optical zones 515
The lens surfaces are parabolic and therefore flatten
gradually from the poles to the equator 516
Both anterior and posterior lens surfaces become more
curved with accommodation, but the anterior surface
change is larger 519
The lens thickens with age and its curvatures increase, but
unaccommodated lens power does not increase with
age 520
The increased lens surface curvatures in accommodation
are primarily a consequence of tissue elasticity 522
The presbyopic lens is aging, fat, and unresponsive 523
Presbyopia is largely, if not solely, associated with age
related changes in the lens 525
Cataracts, most of which are age related, take different
forms and can affect any part of the lens 526
The Vitreous 530
The vitreous is the largest component of the eye 530
The primary structural components of the vitreous are
collagen and hyaluronic acid 530
The external layer of the vitreous—the vitreous cortex—
attaches the vitreous to surrounding structures 532
Inhomogeneity of the vitreous structure produces
internal subdivisions in the vitreous 533
The vitreous changes with age 533
Shrinkage of the vitreous gel may break attachments to
the retina 536
Altered activity of cells normally present in the vitreous
or the introduction of cells from outside the vitreous
may produce abnormal collagen production and scar
formation 537
Vitrectomy removes abnormal portions of the
vitreous 538
Development of the Lens and Vitreous 539
The lens forms from a single cell line 539
Most failures of lens development are manifest as
congenital cataracts 540
The primary vitreous forms around the embryonic
hyaloid artery 541
The secondary vitreous, initially acellular, forms outside
the vasa hyaloidea propria 541
Contents xix
Most developmental anomalies in the vitreous represent
incomplete regression of the hyaloid artery system 541
VIGNETTE 12.1 Putting the Lens in Its Proper
Place 512
BOX 12.1 Cataract Surgery 528
Chapter 13 Retina I: Photoreceptors and
Functional Organization 545
The Retina s Role in Vision 545
The retina detects light and tells the brain about aspects
of light that are related to objects in the world 545
Objects are defined visually by light and by variations in
light reflected from their surfaces 546
The retina makes sketches of the retinal image from
which the brain can paint pictures 547
Functional Organization of the Retina 549
Photoreceptors catch photons and produce chemical
signals to report photon capture 549
Photoreceptor signals are conveyed to the brain by
bipolar and ganglion cells 551
Lateral pathways connect neighboring parts of the
retina 552
Recurrent pathways may assist in adjusting the
sensitivity of the retina 554
The retina has anatomical and functional layers 555
Catching Photons: Photoreceptors and Their
Environment 560
Each photoreceptor contains one of four photopigments,
each of which differs in its spectral absorption 560
Color vision requires more than one photopigment 562
The photopigments are stacked in layers within the outer
segments of the photoreceptor 564
Light absorption produces a structural change in the
photopigments 565
Structural change in the photopigment activates an
intracellular second messenger system using cGMP as
the messenger 566
A decrease in cGMP concentration closes cation channels,
decreases the photocurrent, and hyperpolarizes the
photoreceptor 568
Absorption of one photon can produce a detectable rod
signal 570
Photocurrent in the outer segment decreases in
proportion to the number of absorbed photons 572
Photopigments activated by photon absorption are
inactivated, broken down, and then regenerated 573
Photoreceptor sensitivity is modulated by intracellular
Ca2+ 575
Changes in photoreceptor sensitivity account for less
than half of the retina s sensitivity increase in the dark
and sensitivity decrease in the light 578
xx Contents
The tips of photoreceptor outer segments are surrounded
by pigment epithelial cell processes 579
The pigment epithelium and the interphotoreceptor
matrix are necessary for photopigment regeneration 580
Both rods and cones undergo a continual cycle of
breakdown and renewal 583
The inner segments of photoreceptors assemble the
proteins to construct the outer segment membranes 585
The inner segments form tight junctions with Miiller s
cells; these junctions are the external limiting
membrane 586
Photoreceptors signal light absorption by decreasing the
rate of glutamate release from their terminals 590
Glutamate release from a photoreceptor is subject to
modification by activity in other photoreceptors 592
VIGNETTE 13.1 Everything in the Vertebrate Eye
Means Something 558
Chapter 14 Retina II: Editing Photoreceptor
Signals 595
The Editing Process 595
Interactions among Photoreceptors, Horizontal Cells, and
Bipolar Cells 597
Horizontal cells integrate photoreceptor signals 597
Horizontal cells receive inputs from photoreceptors and
send signals of opposite sign back to the photoreceptor
terminals, using GABA as the neurotransmitter 601
Horizontal cell connections emphasize differences in
illumination between different photoreceptors 602
Different glutamate receptors on cone bipolar cells cause
increases and decreases in light intensity to be reported
by ON and OFF bipolar cells, respectively 605
Signals from both red and green cones go to midget
bipolar cells, which are specific for cone type, and to
diffuse bipolar cells, which are not cone specific 606
Blue cones have their own bipolar cells 608
Rods have sign inverting synapses to rod bipolar cells,
which do not contact ganglion cells but send signals to
the cone pathways through an amacrine cell 608
Interactions among Bipolar Cells, Amacrine Cells, and
Ganglion Cells 610
Bipolar cell terminals in the inner plexiform layer release
glutamate at synapses to amacrine or ganglion cells and
receive inputs from amacrine cells 610
Bipolar cells terminate at different levels within the inner
plexiform layer, thereby creating functional
sublayers 611
Amacrine cells vary in the extent over which they
promote lateral interactions among vertical pathways
and in the levels of the inner plexiform layer in which
they operate 616
Amacrine cells exert their effects mainly at glycine and
GABA synapses, while several other neurotransmitters
or neuromodulators play subsidiary roles 618
The effects of neurotransmission depend on postsynaptic
receptors 620
Amacrine cell connections centering on the All amacrine
cells illustrate difficulties in understanding amacrine
cell operations 621
Ganglion Cell Signals to the Brain: Dots for the Retinal
Sketches 624
Most ganglion cells are midget or parasol cells 624
The small region of the world seen by a ganglion cell is
its receptive field 628
The concentric organization of excitation and inhibition
makes ganglion cells sensitive to contrast rather than to
average light intensity 630
Ganglion cell receptive fields can be thought of as filters
that modify the retinal image 631
Sensitivity functions of ganglion cell receptive fields
differ in size and in the strength of their inhibitory
components 636
Ganglion cell signals differ in their reports on stimulus
duration and on the rate of intensity change 637
Midget ganglion cells have wavelength information
embedded in their signals, but only small bistratified
cells are known to convey specific wavelength
information 639
Axons from midget and parasol ganglion cells go to
different layers in the lateral geniculate nucleus 642
Ganglion cell responses are the elements of retinal
sketches 643
VIGNETTE 14.1 The Retina Comes to Light 612
VIGNETTE 14.2 The Shoemaker s Apprentice 626
BOX 14.1 Studying Individual Neurons 632
Chapter 15 Retina III: Regional Variation
and Spatial Organization 649
Making Retinal Sketches out of Dots: Limits and
Strategies 649
The detail in a sketch is limited by dot size and spacing,
and cones set the dot size in the central retina 649
The entire retinal image cannot be sketched in great
detail 652
Most retinas are organized around points or lines 653
Retinal sketches should be continuous, with no
unnecessary blank spots 654
Tilings do not need to be regular, and tiles do not have to
be the same size 657
Tilings formed by axonal or dendritic arbors at different
levels of the retina need not match precisely 659
Spatial Organization of the Retina 660
The fovea is a depression in the retina where the inner
retinal layers are absent 660
The spatial distribution of a pigment in and around the
fovea is responsible for entoptic images associated with
the fovea 661
Photoreceptor densities vary with respect to the center of
the fovea, where cones have their maximum density
and rods are absent 663
The human retina varies from center to periphery in
terms of the spatial detail in the retinal sketch 664
Maximum cone densities vary among different retinas by
a factor of three 666
The human retina has about 4.5 million cones and 91
million rods 666
Blue cones have a different distribution than red and green
cones have: the center of the fovea is dichromatic 667
There are more red cones than green cones, and more
green cones than blue cones 668
The distribution of different types of cones is neither
regular nor random 668
Cone pedicles probably tile the retina in and near the
fovea, but rod spherules probably never form a single
layered tiling 672
The pedicles of cones in and near the fovea are displaced
radially outward from the cone inner segments, but
spatial order is preserved 674
The density of horizontal cells is highest near the fovea
and declines in parallel with cone density 675
Neither HI nor H2 horizontal cells form tilings 676
All types of cone and rod bipolar cells are distributed like
their photoreceptor types 676
The different types of bipolar cells provide different
amounts of coverage with their dendrites 678
All bipolar cell terminals form tilings at different levels in
the inner plexiform layer 679
All amacrine cells tile the retina, varying in density as
ganglion cells do 681
Medium and large field amacrine cells are low density
populations whose processes generate high coverage
factors 682
Ganglion cell density declines steadily from the
parafovea to the periphery of the retina 685
Midget and parasol ganglion cell dendrites tile at
different levels in the inner plexiform layer 687
Spatial resolution is limited by cone spacing in the fovea
and parafovea and by midget ganglion cells elsewhere
in the retina 690
A Final Look at Three Small Pieces of Retina: Dots for the
Retinal Sketches 691
A sampling unit is the smallest retinal region containing
at least one representative from each type of ganglion
cell 691
Sampling units are smallest at the foveal center and are
dominated by cone signals 692
Rods and blue cones become significant in the parafoveal
sampling units 694
Rods and rod pathways dominate in peripheral sampling
units 695
Contents xxi
The problem of understanding how the retina works can
be reduced to the problem of understanding its
sampling units 698
The central representation of a sampling unit depends on
the number of ganglion cells it contains 698
BOX 15.1 Locating Species of Molecules: Immunohisto
chemistry 670
Chapter 16 The Retina In Vivo and
the Optic Nerve 701
Electrical Signals and Assessment of Retinal Function 702
A difference in electrical potential exists between the
vitreal and choroidal surfaces of the retina and between
the front and back of the eye 702
The electroretinogram measures a complex change in
voltage in response to retinal illumination 702
The a wave and off effect are generated by the photo
receptors, the c wave by the pigment epithelium 703
The b wave is either a direct reflection of ON bipolar cell
activity or is indirectly related to their activity by a
secondary potential arising from Muller s cells 704
The ERG is useful as a gross indicator of photoreceptor
function 706
Multifocal ERGs provide assessments of retinal function
within small areas of the retina 707
The Retinal Vessels and Assessment of Retinal Health 708
The retina in vivo is invisible 708
Since the choroidal circulation is usually not directly
visible, irregularities and nonuniformities on the
fundus are commonly indicators of pathology 711
The central retinal artery is an end arterial system 712
The capillaries supplied by the central retinal artery
ramify in the inner two thirds of the retina 713
Retinal detachment separates photoreceptors from their
blood supply 714
The foveal center lacks capillaries 715
Retinal capillaries are specialized to create a blood retina
barrier 715
Retinal blood flow is autoregulated 717
The arterial and venous branches on the retinal surface
can be distinguished ophthalmoscopically 717
Drainage of the inner retina is segmental 718
The Optic Nerve 719
All ganglion cell axons and all branches of the central
retinal artery and vein converge at the optic nerve
head 719
The nerve head and the optic nerve consist primarily of
axon bundles separated by sheaths of glial cells and
connective tissue 719
The blood supply and drainage differ between the pre
and postlaminar portions of the nerve head 721
xxii Contents
Ganglion cell axons form a stereotyped pattern as they
cross the retina to the optic nerve head 722
Axons from many widely separated ganglion cells are
collected in bundles in the nerve fiber layer 723
Axon bundles have an orderly arrangement in the nerve
head 724
Scotomas observed in advanced stages of glaucoma
correspond to those produced by lesions along the
superior and inferior temporal margin of the nerve
head 727
The lamina cribrosa is weaker than the rest of the
sclera 727
Field defects in glaucoma may be due to blockage of
axonal transport secondary to deformation of the
lamina cribrosa 728
Ganglion cell loss in experimental glaucoma does not
appear to be selective by cell type or axon diameter 730
Development of the Retina and Optic Nerve 732
The retina develops from the two layers of the optic
cup 732
Retinal development proceeds from the site of the future
fovea to the periphery 733
Retinal neurons have identifiable birthdays 733
Ganglion cells, horizontal cells, and cones are the first
cells in the retina to be born 733
As distance from the fovea increases, the firstborn cells
appear at progressively later dates 735
Synapse formation has a center to periphery gradient
superimposed on a gradient from inner retina to outer
retina 736
The location of the future fovea is specified very early;
the pit is created by cell migration 737
Foveal cones are incomplete at birth 737
Photoreceptor densities are shaped by cell migration and
retinal expansion 739
Ganglion cell density is shaped by migration, retinal
expansion, and cell death 740
The spatial organization of the retina may depend on
specific cell cell interactions and modifications of cell
morphology during development 741
Retinal blood vessels develop relatively late 743
Developing vessels are inhibited by too much
oxygen 744
The optic nerve forms as tissue in the optic stalk is
replaced with developing ganglion cell axons and glial
cells 745
Fusion of the optic stalks produces the optic chiasm,
where pioneering axons must choose the ipsilateral or
contralateral path 746
The last stages of development in the optic nerve are
axon loss and myelination 746
The inner retina seems relatively immune to congenital
anomalies 748
The most common developmental anomalies are failures
to complete embryonic structures or eliminate transient
structures 748
BOX 16.1 Fluorescein Angiography and the Adequacy
of Circulation 710
Epilogue Time and Change 753
Postnatal Growth and Development 753
The newborn eye increases in overall size for the next 15
years 753
Refractive error is quite variable among newborn infants,
but the variation decreases with growth 754
Visual functions mature at different rates during the first
6 years of life 756
Changes in the lens and vitreous that begin in infancy
continue throughout life 758
Maturation and Senescence 759
The average refractive error is stable from ages 20 to 50,
but the eye becomes more hyperopic and then more
myopic later in life 759
Although the gross structure of the eye is stable after the
age of 20, tissues and membranes are constantly
changing 760
Retinal illuminance and visual sensitivity decrease with
age 761
Visual acuity declines after age 50, largely because of
optical factors 763
Historical References and Additional
Reading HR I
Glossary G l
Index I 1
|
| any_adam_object | 1 |
| author | Oyster, Clyde W. |
| author_facet | Oyster, Clyde W. |
| author_role | aut |
| author_sort | Oyster, Clyde W. |
| author_variant | c w o cw cwo |
| building | Verbundindex |
| bvnumber | BV015428941 |
| callnumber-first | Q - Science |
| callnumber-label | QP475 |
| callnumber-raw | QP475 |
| callnumber-search | QP475 |
| callnumber-sort | QP 3475 |
| callnumber-subject | QP - Physiology |
| classification_rvk | WW 1784 |
| ctrlnum | (OCoLC)41070828 (DE-599)BVBBV015428941 |
| dewey-full | 612.8/4 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 612 - Human physiology |
| dewey-raw | 612.8/4 |
| dewey-search | 612.8/4 |
| dewey-sort | 3612.8 14 |
| dewey-tens | 610 - Medicine and health |
| discipline | Biologie Medizin |
| format | Book |
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| id | DE-604.BV015428941 |
| illustrated | Illustrated |
| indexdate | 2024-07-09T19:09:18Z |
| institution | BVB |
| isbn | 0878936459 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-010108078 |
| oclc_num | 41070828 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR |
| owner_facet | DE-355 DE-BY-UBR |
| physical | XXVIII, 766, 16, 13 S. Ill. |
| publishDate | 1999 |
| publishDateSearch | 1999 |
| publishDateSort | 1999 |
| publisher | Sinauer |
| record_format | marc |
| spelling | Oyster, Clyde W. Verfasser aut The human eye structure and function Clyde W. Oyster Sunderland, Mass. Sinauer 1999 XXVIII, 766, 16, 13 S. Ill. txt rdacontent n rdamedia nc rdacarrier Oeil - Anatomie ram Oeil - Physiologie ram Ogen gtt Oogheelkunde gtt Œil - Anatomie Œil - Physiologie Eye Anatomy Eye Physiology Ocular Physiological Phenomena Physiologie (DE-588)4045981-0 gnd rswk-swf Anatomie (DE-588)4001895-7 gnd rswk-swf Auge (DE-588)4122841-8 gnd rswk-swf Auge (DE-588)4122841-8 s Anatomie (DE-588)4001895-7 s DE-604 Physiologie (DE-588)4045981-0 s HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010108078&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Oyster, Clyde W. The human eye structure and function Oeil - Anatomie ram Oeil - Physiologie ram Ogen gtt Oogheelkunde gtt Œil - Anatomie Œil - Physiologie Eye Anatomy Eye Physiology Ocular Physiological Phenomena Physiologie (DE-588)4045981-0 gnd Anatomie (DE-588)4001895-7 gnd Auge (DE-588)4122841-8 gnd |
| subject_GND | (DE-588)4045981-0 (DE-588)4001895-7 (DE-588)4122841-8 |
| title | The human eye structure and function |
| title_auth | The human eye structure and function |
| title_exact_search | The human eye structure and function |
| title_full | The human eye structure and function Clyde W. Oyster |
| title_fullStr | The human eye structure and function Clyde W. Oyster |
| title_full_unstemmed | The human eye structure and function Clyde W. Oyster |
| title_short | The human eye |
| title_sort | the human eye structure and function |
| title_sub | structure and function |
| topic | Oeil - Anatomie ram Oeil - Physiologie ram Ogen gtt Oogheelkunde gtt Œil - Anatomie Œil - Physiologie Eye Anatomy Eye Physiology Ocular Physiological Phenomena Physiologie (DE-588)4045981-0 gnd Anatomie (DE-588)4001895-7 gnd Auge (DE-588)4122841-8 gnd |
| topic_facet | Oeil - Anatomie Oeil - Physiologie Ogen Oogheelkunde Œil - Anatomie Œil - Physiologie Eye Anatomy Eye Physiology Ocular Physiological Phenomena Physiologie Anatomie Auge |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010108078&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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