The adult cornea is 0.52 mm thick in the center and 0.65 mm thick in the periphery, and is about 12.6 mm in diameter horizontally and 11.7 mm vertically. It is composed of several layers, from anterior to posterior: the outer epithelium, the basement membrane, anterior limiting lamina (or the Bowman’s layer), corneal stroma, posterior limiting lamina (or the Descemet’s membrane), and the epithelium. The corneal stroma constitutes 90% of the corneal thickness and is composed of 50 layers, each with similarly oriented collagen fibers, with the fibers always parallel to the cornea surface. The cornea is transparent because it is uniform in structure, avascular (i.e., it has no blood vessels) except in the extreme periphery, and relatively dehydrated. (More on this below.) It is covered by a 7–m thick layer of tears, which, among other things, smoothes over optical irregularities on the anterior surface of the cornea and supplies the cornea with oxygen . The average radius of curvature of the anterior surface of the cornea is about 7.8 mm in the central region, with a variation among people of about mm, and is flatter in the periphery.
The aqueous humor fills the anterior chamber (with a volume of 0.3 cm) bounded by the cornea, iris, and the anterior surface of the crystalline lens, and the posterior chamber (0.2 cm) on the periphery of the lens. It has many fewer proteins (0.1 g/L) than blood plasma (60–70 g/L). The pupil in the iris is usually slightly nasal and inferior to the center of the iris, and can vary roughly from 1.5 to 10 mm in diameter . The diameter of the pupil is controlled by an opposing pair of smooth muscles: the sphincter pupillae (which is a ring of muscles that encircle the pupil) contracts it and the dilator pupillae (which has the form of a thin disc) widens it.
The crystalline lens is suspended from the ciliary body by zonular fibers and rests on the posterior surface of the iris. It is composed of about 66% water and 33% protein. This crystalline lens is about 4 mm thick and 9 mm in diameter. It continues to grow during life, with new layers growing on older layers, forming a layered structure like an onion (Fig. 11.1). At 30 years of age, the lens has a mass of 170 mg, which increases by about 1.2 mg per year; similarly the lens width is about 4 mm and increases by about 0.02 mm per year. The crystalline lens is avascular and almost completely transparent. Still, it is slightly birefractive (i.e., it has slightly different refractive indices for different polarizations of light), becomes more yellow with age, and can become opaque (and this forms a cataract). Aphakia describes the condition when the crystalline lens is absent. The vitreous humor is about 99% water, with the remaining 1% composed of collagen (0.5 g/L proteins) and hyaluronic acid; the latter gives it its gelatinous, viscous physical characteristics. This humor accounts for about 5 cm of the 7–8 cm volume of the eye.
As we will see below, the formation of an image on the retina is determined by the indices of refraction of each eye component that the light passes through and by the shapes of the surfaces of these elements. The cornea and crystalline lens are the actual focusing elements in the eye. The cornea performs about two-thirds of the focusing and the crystalline lens the remaining one-third. The shape and consequently the focal length of the crystalline lens are adjustable and do the fine-tuning of imaging for accommodation. The measured refractive index of the tears and the vitreous humor is about 1.336 and that of the aqueous humor is a bit higher, 1.3374. The refractive indices of the cornea, about 1.3771, and the crystalline lens are higher. At the center of the crystalline lens (which is called the nuclear region), the index is about 1.40–1.41 and it decreases to 1.385–1.388 in the direction towards the “poles” and to 1.375 in the direction toward the “equator”; it is 1.360 in the capsule, which is the elastic membrane that encloses the crystalline lens. There is still some uncertainty in these values; optical models of the eye use values close to these cited numbers.
Fig. 11.2
Schematic of the retina in the eye, with the arrangement of rods and cones and other neurons, along with electrical excitation by the shown light stimulus (From [50])
Only about 50% of visible light (400–700 nm) incident on the eye actually reaches the retina as direct light. Then light must pass through the (transparent) ganglion and other retinal neurons before reaching and forming an image on the backward-facing photoreceptors on the retina (Fig. 11.2). The fovea or fovea centralis is the central region of the retina, and the region of sharpest vision because it has the highest density of cone cells on the retina (Fig. 11.3). The visual axis of the eye is the line from the point you are focusing on, through the center of pupil, to the fovea. The optical axis of the eye is a line that passes through the centers of the cornea, pupil and crystalline lens to the retina. They are not parallel. The optic nerve leaves the eyeball at a blind spot (optic disk), a region with no rods or cones (Fig. 11.3); it is 13– away from the fovea in the “nasal” direction.
Fig. 11.4
Fixate on the using your left eye, with your right eye closed. Keep the book about 10 cm from your left eye, and then move it back and forth until you do not see the central dot. This dot is then on the blind spot. The dots above and below it are still visible, but fuzzy because of the lower visual acuity outside the fovea. (Also see Fig. 11.24) (Based on [63])
We are usually not aware of the blind spot when we use both eyes because the part of the image that forms on the blind spot in one eye is located in a functional region in the other eye and the brain fuses the images of the two eyes. It is easy to prove the existence of the blind spot. Close your right eye and use your left eye to look at the in Fig. 11.4. When you move the book about 10 cm from your left eye, you will find one position where the central dot disappears because of the blind spot in your left eye.
There are about 120 million rod cells per retina (Fig. 11.5). They have high sensitivity , low spatial acuity, and are relatively more numerous in the periphery of the retina. The sensitivity of rods peaks near 500 nm (Fig. 11.6). Vision using only rods results in various shades of gray. Night vision and peripheral vision are mostly due to rods. Rods are about m in diameter. Far from the fovea the rods become more widely spaced and many (in some cases several hundred) rods are connected to the same nerve fiber. Both factors decrease visual acuity in the outer portions of the retina.
Fig. 11.5
Scanning electron micrograph of rod and cone outer segments, with the cone seen (with its tapered end) in the center and the end and beginning of two rods (which are longer than the cones) seen beneath and to the left of it (Reprinted from [29]. Used with permission of Elsevier)
There are about 6.5 million cone cells per retina. They have low sensitivity—about 1,000 lower than rods—high spatial acuity, and are concentrated in the fovea. There are three types of cone cells, with spectral sensitivities peaking near 445 nm (blue or S cones—S for short wavelength peak sensitivity), 535 nm (green or M cones—M for middle wavelengths), and 570 nm (red or L cones—L for long wavelengths) (Fig. 11.6). The overall spectral sensitivity due to the rods and cones of humans closely matches the spectrum of solar light reaching land. Sharp vision and color vision are due to cones, and consequently damage to the fovea leads to visual images that are fuzzy. Cones are about 1.0–1.5 m in diameter and are about 2.0–2.5 m apart in the fovea. There are only about 1 million nerve fibers in the eye, so there are some cones (as well as rods) connected to the same nerve cells. We will not delve into the cellular structure of the rods and cones, but will focus on two physical aspects of these sensors: the absorption of light and acuity of vision.
The absorption of light by the rods and cones is a fundamental quantum-mechanical process in which one photon (or quantum) of light is absorbed by the pigment rhodopsin. Quantum mechanics is the physics of small-scale objects, and has features that are distinct from the physics of larger-scale objects, which is the classical physics we have been using throughout this book. One feature of quantum physics is the quantization of energy levels in molecules, which means that a molecule can have only distinct energies. Consequently, a molecule can absorb light only at those specific energies (or frequencies) corresponding to the differences of its energy levels. Moreover, in quantum mechanics, light acts like light packets, called photons. The energy of a photon is
where h is Planck’s constant ( J–s, as in (6.37)), (or f) is the frequency of the light, c is the speed of light ( m/s), and is the wavelength of light. The last two parts of this equation reflect the relationship between frequency, wavelength, and propagation speed for these electromagnetic waves,
as in (10.3). Absorption occurs when the photons have energy in ranges that can be absorbed by the photosensitive molecules in these cells.
(11.1)
(11.2)
Rhodopsin consists of a chromophore (i.e., the part of the molecule responsible for its color) covalently attached to the protein opsin. The chromophore is retinal, which is a derivative of vitamin A, and the absorption of a single photon of light isomerizes it (i.e., changes its molecular conformation) from 11-cis retinal to all-trans retinal. This isomerization triggers a change in the conformation of rhodopsin that starts a sequence of sensory transduction processes (Fig. 11.7). Proteins themselves have absorption bands in the ultraviolet, and cannot absorb in the visible. The absorption of free 11-cis retinal is in the near ultraviolet, 360–380 nm; however, the binding of the retinal to the protein red shifts the absorption by about 200 nm to the visible . Differences in the opsin proteins in the rods and the three cones cause the different wavelength responses for these four types of photoreceptor cells. (By the way, Ragnar Granit, Haldan Keffer Hartline, and George Wald were awarded the Nobel Prize in Physiology or Medicine in 1967 for their discoveries concerning the primary physiological and chemical visual processes in the eye.)
Fig. 11.7
The chromophore 11-cis retinal is photoisomerized by light to all-trans retinal (11-trans retinal)
Fig. 11.8
Imaging by a thin, positive lens
The pressure in the eyeball maintains its shape. It is normally about 15 mmHg (ranging from 10 to 20 mmHg), and is determined by the rates of formation of the aqueous humor (about 1% of the total volume is produced per minute) and drainage of the aqueous humor through the canal of Schlemm. If the exit of the aqueous humor is impaired, the eyeball pressure increases, leading to glaucoma and possible blindness (as is addressed below). Intraocular pressure (IOP) is measured by the amount of force needed to flatten to a given area (or the area flattened by a given force) by using a tonometer. (This is explored in Problem 11.53.)
Fig. 11.9
Special cases of imaging with positive lenses , and imaging with negative lenses
11.2 Focusing and Imaging with Lenses
11.2.1 Image Formation
Figure 11.8 shows how an object or source is imaged by a convex (converging or positive) lens . By convention in optics the object is placed a positive distance to the left of the lens and optical rays propagate from the left to the right. The object has a size (or height) . For a convex lens the focal length f is positive, hence the name positive lens. The central axis (the z-axis) is known as the optic axis. All rays passing through the lens form an image a positive distance to the right of the lens, where is given by the lens equation
A real image forms at when if you place a screen, such as a piece of paper, there. The image is inverted and its size is magnified by (the transverse magnification ). This can be seen from the triangles in Fig. 11.8 that give , so the magnification is
(Actually, it is magnified when .) When , parallel rays are incident on the lens and an image forms at (Fig. 11.9a). When the object is at the focus and so , the image is at (Fig. 11.9b). When the object is closer to the lens than the focal point and so , then and the image is to the left of the lens (Fig. 11.9c). This is a virtual image. Placing a screen there will give no image. However, if the light rays to the right of the lens are traced backward to the left of the lens, they will seem to emanate from this virtual image.
(11.3)
(11.4)
This same lens equation (11.3) can be used to determine the location of the image for a concave (diverging or negative) lens, which has a negative focal length f . Concave lenses produce virtual images (Fig. 11.9d).
Within the eye the cornea and crystalline lens are positive lenses, because they need to form a real image on the retina. Corrective lenses (eyeglass lenses and contact lenses) can have positive or negative focal lengths, depending on the necessary correction. We will explore this later in this chapter. Focal lengths are expressed as distances, in cm or m. We will see that in discussing the eye and corrective lenses it is very common to discuss 1 / f and use units of diopters (D), with 1 D = 1/m.
In a very simple model of the eye imaging system, the eye is treated as a thin lens with a 17 mm focal length in air ( Standard eye model ). For an image at , (11.3) shows that . We will see that two points are resolvable by at best m on the fovea. So for a source that is 10 m away, two points are resolvable when separated by at least m / 17 mm) (2 m) mm; this corresponds to an angle of 1.2 mm/10 m = 0.12 mrad = 25 s of arc. The 300 m foveal diameter corresponds to a lateral separation of m / 17 mmm) cm at 10 m or cm / 10 m mrad of arc.
In clinical, ophthalmic optics, the lens equation (11.3) is phrased and used differently. It is expressed in terms of vergences, which indicate the angles rays make with the optic axis and signify ray convergence with positive vergence and divergence with negative vergence. U is the object convergence, sometimes also known as the object proximity. If all optical elements are in a medium with refractive index n, then . The image vergence (or image proximity) is . The refractive power of the lens , as we will see. U, V, and P are expressed in diopters (1 D = 1/m). The lens equation (11.3) expressed in vergences is then:
This is interpreted as meaning that the propagation of light from an object through the lens to the image increases the ray vergence by an amount equal to the power of the lens (or more generally, the power of the optical interface or optical system).
(11.5)
We have assumed geometric optics, which ignores the wave-like features of light due to optical diffraction; this is a good approximation for very short wavelengths and for much of the imaging in the eye. Our analysis also assumes only paraxial rays , i.e., all rays are near the optic axis and make small angles to it. (Rays that are farther away from the optic axis—nearer where the maximum amount of light is transmitted—are called zonal rays, and those at the margin of the lens are marginal rays. We will evaluate the importance of diffraction and of these zonal and marginal rays later in this chapter.)
11.2.2 Scientific Basis for Imaging
We will trace rays by following how they propagate in straight lines in uniform media and how they refract at interfaces by using Snell’s Law. Snell’s Law of refraction shows that light from medium 1 with index of refraction impinging at an angle (relative to the normal) on a flat interface with medium 2 with refractive index , is refracted to an angle given by (Fig. 11.10).
and for small angles (, )
Some important indices of refraction are 1.0 for air, 1.33 for water, 1.5–1.6 for different types of glass, and 1.44–1.50 for plastics. Refractive indices actually vary some with wavelength and temperature, but we will ignore those variations at present.
(11.6)
(11.7)
Fig. 11.10
Snell’s law
Imaging can occur when the interfaces are curved. Let us consider the refraction of paraxial rays at the interface in Fig. 11.11 from medium 1 to medium 2, which has a spherical radius of curvature . (This region can be formed by slicing off a section from a sphere with radius , composed of material 2.) As shown here, this radius is defined to be positive (see the Fig. 11.11 inset) . Equation (11.6) still applies, but the angle of incidence for a light ray parallel to the optic axis varies with the distance y the ray is displaced from this axis . We see that . For (so ), (11.7) gives
This refracted ray makes an angle with the horizontal (Fig. 11.11). Geometry shows that it hits the optic axis a distance after the interface. This distance is independent of y, and so all parallel rays impinging on the curved surface hit the optic axis at this same distance, which is called the focal length f (or for this interface)
The last expression has been written in terms of the refractive power (or sometimes called the convergence) of the interface
The focal length is defined in terms of the refractive power of the interface and the refractive index of the medium the ray enters . The ratio of the indices of refraction of the two media is important and not their individual values. (For , we see that .) The units of the refractive power are diopters (1 D = 1/m).
(11.8)
(11.9)
(11.10)
Fig. 11.11
Refraction at a curved interface. The inset shows the convention for the radius of curvature. In this figure, n_{1}$$” src=”http://basicmedicalkey.com/wp-content/uploads/2017/06/A114622_2_En_11_Chapter_IEq86.gif”>, and so
We see that this derivation giving the focal length in (11.9) is similar to that for (11.3), except that the object and image are in regions with different refractive indices here. If and were interchanged, the sign of the focal length would change and its magnitude would change to . The analog of (11.3) at this refractive interface is
For , a real image occurs at , a real image occurs at
(11.11)
(11.12)
(11.13)
(11.14)
What happens when there are two refracting interfaces in succession (Fig. 11.12)? If they are separated by a distance D that is “very small,” the same reasoning gives an overall focal length f for this lens
where is given by (11.10) and
This is called the thin lens approximation. Equation (11.15) can be expressed as , where
so the refractive powers add in this approximation.
(11.15)
(11.16)
(11.17)
Fig. 11.12
Refraction at two spherical interfaces. As drawn here , the radii of curvature
For a thin lens of refractive index in air or vacuum (with refractive index , so ), (11.15) reduces to
which is known as the Lensmaker’s equation. Thisfocal length can also be expressed as
with and .
(11.18)
(11.19)
Lenses can have a range of shapes even for the same focal length (Fig. 11.13). For positive focal lengths, they can be either biconvex (as shown ), planoconvex (one side flat), or positive meniscus as shown ( and ). The isolated cornea is a negative meniscus lens and the crystalline lens is an asymmetric biconvex lens. We will see below that in the eye the cornea serves as a positive lens.
Fig. 11.13
Types of positive and negative lenses
The length of the eyeball is approximately 24 mm, so the distances from the cornea/crystalline lens to the retina and the focal length of optical rays focused by the cornea/crystalline lens propagating in the vitreous humor and imaging on the retina, are also about 24 mm. The refractive index of the vitreous humor is approximately 1.33. Equation (11.15) shows that a system with the same refractive power has a focal length that is proportional to this refractive index, so in air the focal length would be smaller by a factor of 1.33, or 24 mm/1.33 = 17 mm. That is why a model eyeball can be treated as if the cornea/crystalline lens system had an effective focal length of 17 mm, with the effective lens separated by 17 mm of air from the retina; we will call this the Standard eye model. (This differs from the eye models in Table 11.1.)
Moving Lenses
Two lenses have the same effectivity (i.e., effectiveness) if both can image the same object to the same image, placed at the appropriate distance between the object and image as given by (11.3). For example, an image forms 4 cm after a lens with focal length 2 cm that is placed 4 cm after an object. If you wanted move the lens to the left by 2 cm, you would have to change its focal lens to 1.5 cm for it to have the image at the same place and so have the same effectivity. (Why?)
Let us consider the special case of parallel rays hitting a converging lens with power P in a medium with refractive index n. They form an image a distance n / P after the lens. If we move the same lens a distance D to the left and want the rays to focus in the same place, we now need them to focus a distance after the lens and so the lens will need to have a power such that . Therefore we see that
This is known as the effectivity formula . (This equation is sometimes displayed with a negative sign in the denominator because the lens is being moved a distance D to the right.)
(11.20)
Why is this imaging effectivity important to us? The corrective powers for prescriptions for eyeglasses and contact lenses are different because eyeglasses are placed about 1.2 cm anterior to the cornea, while contact lenses sit right on the cornea, and so are different in two ways. We just addressed the consequences of this different lateral position and will address below those due to refractive power changes that occur because the contact lens is physically on the cornea. In any case, you want both prescriptions to have the same effectivity for objects at infinity, so (11.20) is used with .