Fovea centralis

The fovea centralis is a small, central pit composed of closely packed cones in the eye. It is located in the center of the macula lutea of the retina.[1][2]

Fovea centralis
Schematic diagram of the human eye, with the fovea at the bottom. It shows a horizontal section through the right eye.
Details
Identifiers
Latinfovea centralis
MeSHD005584
TAA15.2.04.022
FMA58658
Anatomical terminology

The fovea is responsible for sharp central vision (also called foveal vision), which is necessary in humans for activities for which visual detail is of primary importance, such as reading and driving. The fovea is surrounded by the parafovea belt and the perifovea outer region.[2]

The parafovea is the intermediate belt, where the ganglion cell layer is composed of more than five layers of cells, as well as the highest density of cones; the perifovea is the outermost region where the ganglion cell layer contains two to four layers of cells, and is where visual acuity is below the optimum. The perifovea contains an even more diminished density of cones, having 12 per 100 micrometres versus 50 per 100 micrometres in the most central fovea. That, in turn, is surrounded by a larger peripheral area, which delivers highly compressed information of low resolution following the pattern of compression in foveated imaging.

Approximately half the nerve fibers in the optic nerve carry information from the fovea, while the remaining half carry information from the rest of the retina. The parafovea extends to a radius of 1.25 mm from the central fovea, and the perifovea is found at a 2.75 mm radius from the fovea centralis.[3]

The term fovea comes from the from Latin foves, meaning 'pit'.

Structure

The fovea is a depression in the inner retinal surface, about 1.5 mm wide, the photoreceptor layer of which is entirely cones and which is specialized for maximum visual acuity. Within the fovea is a region of 0.5mm diameter called the foveal avascular zone (an area without any blood vessels). This allows the light to be sensed without any dispersion or loss. This anatomy is responsible for the depression in the center of the fovea. The foveal pit is surrounded by the foveal rim that contains the neurons displaced from the pit. This is the thickest part of the retina.[4]

The fovea is located in a small avascular zone and receives most of its oxygen from the vessels in the choroid, which is across the retinal pigment epithelium and Bruch's membrane. The high spatial density of cones along with the absence of blood vessels at the fovea accounts for the high visual acuity capability at the fovea.[5]

The center of the fovea is the foveola – about 0.35 mm in diameter – or central pit where only cone photoreceptors are present and there are virtually no rods.[1] The central fovea consists of very compact cones, thinner and more rod-like in appearance than cones elsewhere. These cones are very densely packed (in a hexagonal pattern). Starting at the outskirts of the fovea, however, rods gradually appear, and the absolute density of cone receptors progressively decreases.

The anatomy of the foveola was recently reinvestigated, and it was discovered that outer segments from the central foveolar cones of monkeys are not straight and twice as long as those from the parafovea.[6]

Size

The size of the fovea is relatively small with regard to the rest of the retina. However, it is the only area in the retina where 20/20 vision is attainable, and is the area where fine detail and colour can be distinguished.[7][8]

Properties
Time-Domain OCT of the macular area of a retina at 800 nm, axial resolution 3 µm
Spectral-Domain OCT macula cross-section scan.
macula histology (OCT)
The diagram shows the relative acuity of the left human eye (horizontal section) in degrees from the fovea.
Photograph of the retina of the human eye, with overlay diagrams showing the positions and sizes of the macula, fovea, and optic disc
  • Anatomical macula / macula lutea / area centralis (clinical: posterior pole):
    • Diameter = 5.5mm (~3.5 disc-diameters) (about 18 deg of VF)
    • Demarcated by the superior and inferior temporal arterial arcades.
    • Has an elliptical shape horizontally.
    • Histologically the only region of the retina where GCL has >1 layer of ganglion cells
    • Yellowish appearance = luteal pigments (xanthophyll and beta-carotenoid (Beta-Carotene) in the outer nuclear layers inward.
  • Anatomical perifovea:
    • Region between parafovea (2.5mm) and edge of macula
    • GCL has 2–4 layers of cells.
    • 12 cones / 100 um
  • Anatomical parafovea:
    • Diameter = 2.5mm.
    • GCL has >5 layers of cells, and highest density of cones
  • Anatomical fovea / fovea centralis (clinical: macula)
    • Area of depression in the centre of the macula lutea.
    • Diameter = 1.5mm (~1 disc-diameter) (about 5 deg of VF)
  • Foveal avascular zone (FAZ)
    • Diameter = 0.5mm (about 1.5 deg of VF)
    • Approximately equal to the foveola
  • Anatomical foveola (clinical: fovea)
    • Diameter = 0.35mm (about 1 deg of VF)
    • the central floor of depression of fovea centralis
    • 50 cones / 100 um
    • Highest visual acuity
  • Anatomical umbo
    • Represents the precise center of the macula[9]
    • Diameter = 0.15mm
    • Corresponds to the clinical light reflex

Function
Illustration of the distribution of cone cells in the fovea of an individual with normal color vision (left), and a color blind (protanopic) retina. Note that the center of the fovea holds very few blue-sensitive cones.

In the primate fovea (including humans) the ratios of ganglion cells to photoreceptors is about 2.5; almost every ganglion cell receives data from a single cone, and each cone feeds onto between 1 and 3 ganglion cells.[10] Therefore, the acuity of foveal vision is limited only by the density of the cone mosaic, and the fovea is the area of the eye with the highest sensitivity to fine details.[11] Cones in the central fovea express pigments that are sensitive to green and red light. These cones are the 'midget' pathways that also underpin high acuity functions of the fovea.

The fovea is employed for accurate vision in the direction where it is pointed. It comprises less than 1% of retinal size but takes up over 50% of the visual cortex in the brain.[12] The fovea sees only the central two degrees of the visual field, (approximately twice the width of your thumbnail at arm's length).[13] If an object is large and thus covers a large angle, the eyes must constantly shift their gaze to subsequently bring different portions of the image into the fovea (as in reading).

Distribution of rods and cones along a line passing through the fovea and the blind spot of a human eye[14]

Since the fovea does not have rods, it is not sensitive to dim lighting. Hence, in order to observe dim stars, astronomers use averted vision, looking out of the side of their eyes where the density of rods is greater, and hence dim objects are more easily visible.

The fovea has a high concentration of the yellow carotenoid pigments lutein and zeaxanthin. They are concentrated in the Henle fiber layer (photoreceptor axons that go radially outward from the fovea) and to a lesser extent in the cones.[15][16] They are believed to play a protective role against the effects of high intensities of blue light which can damage the sensitive cones. The pigments also enhance the acuity of the fovea by reducing the sensitivity of the fovea to short wavelengths and counteracting the effect of chromatic aberration.[17] This is also accompanied by a lower density of blue cones at the center of the fovea.[18] The maximum density of blue cones occurs in a ring about the fovea. Consequently, the maximum acuity for blue light is lower than that of other colours and occurs approximately 1° off center.[18]

Angular size of foveal cones

On average, each square millimeter (mm) of the fovea contains approximately 147,000 cone cells,[19] or 383 cones per millimeter. The average focal length of the eye, i.e. the distance between the lens and fovea, is 17.1 mm.[20] From these values, one can calculate the average angle of view of a single sensor (cone cell), which is approximately 31.46 arc seconds.

The following is a table of pixel densities required at various distances so that there is one pixel per 31.5 arc seconds:

Example objectDistance from eye assumedPPI (PPCM) to match
avg. foveal cone density
(20/10.5 vision)
Phone or tablet10 inches (25.4 cm)655.6 (258.1)
Laptop screen2 feet (61 cm)273.2 (107.6)
42" (1.07 m) 16:9 HDTV, 30° view5.69 feet (1.73 m)96.0 (37.8)

Peak cone density varies highly between individuals, such that peak values below 100,000 cones/mm2 and above 324,000 cones/mm2 are not uncommon.[21] Assuming average focal lengths, this suggests that individuals with both high cone densities and perfect optics may resolve pixels with an angular size of 21.2 arc seconds, requiring PPI values at least 1.5 times those shown above in order for images not to appear pixelated.

It is worth noting that individuals with 20/20 (6/6 m) vision, defined as the ability to discern a 5x5 pixel letter that has an angular size of 5 arc minutes, cannot see pixels smaller than 60 arc seconds. In order to resolve a pixel the size of 31.5 and 21.2 arc seconds, an individual would need 20/10.5 (6/3.1 m) and 20/7.1 (6/2.1 m) vision, respectively. To find the PPI values discernible at 20/20, simply divide the values in the above table by the visual acuity ratio (e.g. 96 PPI / (20/10.5 vision) = 50.4 PPI for 20/20 vision).

Entoptic effects in the fovea

The presence of the pigment in the radially arranged axons of the Henle fiber layer causes it to be dichroic and birefringent[22] to blue light. This effect is visible through the Haidinger's brush when the fovea is pointed to a polarized light source.

The combined effects of the macular pigment and the distribution of short wavelength cones results in the fovea having a lower sensitivity to blue light (blue light scotoma). Though this is not visible under normal circumstances due to "filling in" of information by the brain, under certain patterns of blue light illumination, a dark spot is visible at the point of focus.[23] Also, if mixture of red and blue light is viewed (by viewing white light through a dichroic filter), the point of foveal focus will have a central red spot surrounded by a few red fringes.[23][24] This is called the Maxwell's spot after James Clerk Maxwell[25] who discovered it.

Bifoveal fixation

In binocular vision, the two eyes converge to enable bifoveal fixation, which is necessary for achieving high stereoacuity.

In contrast, in a condition known as anomalous retinal correspondence, the brain associates the fovea of one eye with an extrafoveal area of the other eye.

Other animals

The fovea is also a pit in the surface of the retinas of many types of fish, reptiles, and birds. Among mammals, it is found only in simian primates. The retinal fovea takes slightly different forms in different types of animals. For example, in primates, cone photoreceptors line the base of the foveal pit, the cells that elsewhere in the retina form more superficial layers having been displaced away from the foveal region during late fetal and early postnatal life. Other foveae may show only a reduced thickness in the inner cell layers, rather than an almost complete absence.

Most birds have a single fovea but hawks, swallows, and hummingbirds have a double fovea, the second is called the temporal fovea, which enables them to track slow movements.[26]. The density of cones in a typical bird's fovea has 400,000 cones per millimeter squared but some birds can reach a density of 1,000,000 cones per millimeter squared (e.g. Common Buzzard).[27]

Additional images
  • Illustration showing main structures of the eye including the fovea
  • Structures of the eye labeled
  • This image shows another labeled view of the structures of the eye
  • Schematic diagram of the macula lutea of the retina, showing perifovea, parafovea, fovea, and clinical macula
  • A fundus photograph showing the macula as a spot to the left. The optic disc is the area on the right where blood vessels converge. The grey, more diffuse spot in the centre is a shadow artifact.
gollark: Skynet has a web API - an interface for connecting to skynet - and a client library which uses it.
gollark: APIs provide access to some thingy or other. Libraries are just some code which may *use* APIs.
gollark: WRONG!
gollark: There definitely is one.
gollark: Easily, even.

See also
This article uses anatomical terminology.

References
  1. "Simple Anatomy of the Retina". Webvision. University of Utah. Archived from the original on 2011-03-15. Retrieved 2011-09-28.
  2. Iwasaki, M; Inomata, H (1986). "Relation between superficial capillaries and foveal structures in the human retina". Investigative Ophthalmology & Visual Science. 27 (12): 1698–705. PMID 3793399.
  3. "eye, human."Encyclopædia Britannica. 2008. Encyclopædia Britannica 2006 Ultimate Reference Suite DVD
  4. Emmett T. Cunningham; Paul Riordan-Eva (2011). Vaughan & Asbury's general ophthalmology (18th ed.). McGraw-Hill Medical. p. 13. ISBN 978-0-07-163420-5.
  5. Provis, Jan M; Dubis, Adam M; Maddess, Ted; Carroll, Joseph (2013). "Adaptation of the central retina for high acuity vision: Cones, the fovea and the avascular zone". Progress in Retinal and Eye Research. 35: 63–81. doi:10.1016/j.preteyeres.2013.01.005. PMC 3658155. PMID 23500068.
  6. Tschulakow, Alexander V; Oltrup, Theo; Bende, Thomas; Schmelzle, Sebastian; Schraermeyer, Ulrich (2018). "The anatomy of the foveola reinvestigated". PeerJ. 6: e4482. doi:10.7717/peerj.4482. PMC 5853608. PMID 29576957. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
  7. Gregory S. Hageman. "Age-Related Macular Degeneration (AMD)". Retrieved December 11, 2013.
  8. "Macular Degeneration Frequently Asked Questions". Archived from the original on December 15, 2018. Retrieved December 11, 2013.
  9. Yanoff M, Duker JS. 2014. Ophthalmology. In: Schubert HD, editor. Part 6 Retina and Vitreous, Section 1 Anatomy. 4th ed. China: Elsevier Saunders. p. 420.
  10. Ahmad, Kareem M; Klug, Karl; Herr, Steve; Sterling, Peter; Schein, Stan (2003). "Cell density ratios in a foveal patch in macaque retina" (PDF). Visual Neuroscience. 20 (2): 189–209. CiteSeerX 10.1.1.61.2917. doi:10.1017/s0952523803202091. PMID 12916740.
  11. Smithsonian/The National Academies, Light:Student Guide and Source Book. Carolina Biological Supply Company, 2002. ISBN 0-89278-892-5.
  12. Krantz, John H. (2012). "Chapter 3: The Stimulus and Anatomy of the Visual System" (PDF). Experiencing Sensation and Perception. Pearson Education. ISBN 978-0-13-097793-9. OCLC 711948862. Retrieved 6 April 2012.
  13. Fairchild, Mark. (1998), Color Appearance Models. Reading, Mass.: Addison, Wesley, & Longman, p. 7. ISBN 0-201-63464-3
  14. Foundations of Vision Archived 2013-12-03 at the Wayback Machine, Brian A. Wandell
  15. Krinsky, Norman I; Landrum, John T; Bone, Richard A (2003). "Biologic Mechanisms of the Protective Role of Lutein and Zeaxanthin in the Eye". Annual Review of Nutrition. 23: 171–201. doi:10.1146/annurev.nutr.23.011702.073307. PMID 12626691.
  16. Landrum, John T; Bone, Richard A (2001). "Lutein, Zeaxanthin, and the Macular Pigment". Archives of Biochemistry and Biophysics. 385 (1): 28–40. doi:10.1006/abbi.2000.2171. PMID 11361022.
  17. Beatty, S; Boulton, M; Henson, D; Koh, H-H; Murray, I J (1999). "Macular pigment and age related macular degeneration". British Journal of Ophthalmology. 83 (7): 867–877. doi:10.1136/bjo.83.7.867. PMC 1723114. PMID 10381676.
  18. Curcio, Christine A; Allen, Kimberly A; Sloan, Kenneth R; Lerea, Connie L; Hurley, James B; Klock, Ingrid B; Milam, Ann H (1991). "Distribution and morphology of human cone photoreceptors stained with anti-blue opsin". The Journal of Comparative Neurology. 312 (4): 610–624. doi:10.1002/cne.903120411. PMID 1722224.
  19. Shroff, Anand (2011). An Eye on Numbers: A Ready Reckoner in Ophthalmology. p. 97. ISBN 978-81-921123-1-2.
  20. Serpenguzel, Ali; Serpengüzel, Ali; Poon, Andrew W. (2011). Optical Processes in Microparticles and Nanostructures: A Festschrift Dedicated to Richard Kounai Chang on His Retirement from Yale University. ISBN 978-981-4295-77-2.
  21. Curcio, Christine A; Sloan, Kenneth R; Kalina, Robert E; Hendrickson, Anita E (1990). "Human photoreceptor topography". The Journal of Comparative Neurology. 292 (4): 497–523. doi:10.1002/cne.902920402. PMID 2324310.
  22. Vannasdale, D. A; Elsner, A. E; Weber, A; Miura, M; Haggerty, B. P (2009). "Determination of foveal location using scanning laser polarimetry". Journal of Vision. 9 (3): 21.1–17. doi:10.1167/9.3.21. PMC 2970516. PMID 19757960.
  23. Magnussen, Svein; Spillmann, Lothar; Stürzel, Frank; Werner, John S (2001). "Filling-in of the foveal blue scotoma". Vision Research. 41 (23): 2961–2967. doi:10.1016/S0042-6989(01)00178-X. PMC 2715890. PMID 11704235.
  24. Isobe, Kosaku; Motokawa, Koiti (1955). "Functional Structure of the Retinal Fovea and Maxwell's Spot". Nature. 175 (4450): 306–307. doi:10.1038/175306a0. PMID 13235884.
  25. Flom, M. C; Weymouth, F. W (1961). "Centricity of Maxwell's Spot in Strabismus and Amblyopia". Archives of Ophthalmology. 66 (2): 260–268. doi:10.1001/archopht.1961.00960010262018.
  26. "Birds Comparative Physiology of Vision". Retrieved December 29, 2019.
  27. "Avian Eye Tunics". Retrieved December 29, 2019.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.