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Arthropod eye

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"Fly eye" redirects here. For Calvin Harris's record label, see Fly Eye Records.

Apposition eyes are the most common form of eye, and are presumably the ancestral form of compound eye. They are found in all arthropod groups, although they may have evolved more than once within this phylum.[1] Some annelids and bivalves also have apposition eyes. They are also possessed by Limulus, the horseshoe crab, and there are suggestions that other chelicerates developed their simple eyes by reduction from a compound starting point.[1] Some caterpillars appear to have evolved compound eyes from simple eyes in the opposite fashion.[citation needed]

Insects and all mandibulates have compound eyes, with the exception of some myriapods that have stemmata
Although arachnids (like this spider) do not have compound eyes, xiphosurans and many other extinct chelicerates do

The arthropods ancestrally possessed compound eyes, but the type and origin of this eye varies between groups, and some taxa have secondarily developed simple eyes. The organ's development through the lineage can be estimated by comparing groups that branched early, such as the velvet worm and horseshoe crab to the advanced eye condition found in insects and other derived arthropods.

Eyes and functions

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Most arthropods have at least one of two types of eye: lateral compound eyes, and smaller median ocelli, which are simple eyes.[2] When both are present, the two eye types are used in concert because each has its own advantage.[3] Some insect larvae, e.g., caterpillars, have a different type of simple eye known as stemmata. These eyes usually provide only a rough image, but (as in sawfly larvae) they can possess resolving powers of 4 degrees of arc, be polarization sensitive and capable of increasing their absolute sensitivity at night by a factor of 1,000 or more.[4] Flying insects can remain level with either type of eye surgically removed, but the two types combine to give better performance.[3] Ocelli can detect lower light levels,[a][5] and have a faster response time, while compound eyes are better at detecting edges and are capable of forming images.[3]

Further information: Simple eye in invertebrates

Anatomical distribution of compound eyes

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    Many insects, such as the female Tabanus lineola, shown here, have dichoptic compound eyes
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    The male Tabanus lineola has holoptic compound eyes, with the dorsal ommatidia larger than the ventral ommatidia
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    In some male mayflies the eyes are split into separate organs for distinct visual functions
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    Stalked dichoptic eyes of a River Crab are typical of mature larger Crustacea. The reflection of the photographer in different regions of the surface of each eye indicate the basis for stereoscopic vision
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    Many copepods and other small Crustacea have their eyes combined into a single cycloptic compound eye in the middle of the head, visible here as the dark spot between the bases of the antennae

Most species of Arthropoda with compound eyes bear just two eyes that are located separately and symmetrically, one on each side of the head. This arrangement is called dichoptic. Examples include most insects, and most of the larger species of Crustacea, such as crabs. Many other organisms, such as vertebrates and Cephalopoda are similarly and analogously dichoptic, which is the common state in animals that are members of the Bilateria and have functionally elaborate eyes. However, there are variations on that scheme. In some groups of animals whose ancestors originally were dichoptic, the eyes of modern species may be crowded together in the median plane; examples include many of the Archaeognatha. In extreme cases such eyes may fuse, effectively into a single eye, as in some of the Copepoda, notably in the genus Cyclops. One term for such an arrangement of eyes is cycloptic.

On the other hand, some modes of life demand enhanced visual acuity, which in compound eyes demands a larger number of ommatidia, which in turn demands larger compound eyes. The result is that the eyes occupy most of the available surface of the head, reducing the area of the frons and the vertex and crowding the ocelli, if any. Though technically such eyes still may be regarded dichoptic, the result in the extreme case is that borders of such eyes meet, effectively forming a cap over most of the head. Such an anatomy is called holoptic. Spectacular examples may be seen in the Anisoptera and various flies, such as some Acroceridae and Tabanidae.

In contrast, the need for particular functions may not require extremely large eyes, but do require great resolution and good stereoscopic vision for precise attacks. Good examples may be seen in the Mantodea and Mantispidae, in which seeing prey from particular ommatidia in both compound eyes at the same time, indicates that it is in the right position to snatch in a close-range ambush. Their eyes accordingly are placed in a good position for all-round vision, plus particular concentration on the anterior median plane. The individual ommatidia are directed in all directions and accordingly, one may see a dark spot (the pseudopupil), showing which ommatidia are covering that field of view; from any position on the median plane, and nowhere else, the two dark spots are symmetrical and identical.

Sometimes the needs for visual acuity in different functions conflict, and different parts of the eyes may be adapted to separate functions; for example, the Gyrinidae spend most of their adult lives on the surface of water, and have their two compound eyes split into four halves, two for underwater vision and two for vision in air. Again, particularly in some Diptera, ommatidia in different regions of the holoptic male eye may differ visibly in size; the upper ommatidia tend to be larger. In the case of some Ephemeroptera the effect is so exaggerated that the upper part of the eye is elevated like a risen cupcake, while its lower part that serves for routine vision looks like a separate organ.

Compound eyes are often not completely symmetrical in terms of ommatidia count. For example, asymmetries have been indicated in honeybees[6] and various flies.[7] This asymmetry has been correlated with behavioural lateralization in ants (turning bias).[8]

Genetic controls

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In the fruit fly Drosophila melanogaster (the best-studied arthropod species with respect to developmental biology), among the most important genes for patterning the eyes of insects are the Pax6 homologs eyeless (ey) and twin of eyeless (toy). Together, these genes drive the proliferation of cells early in eye development. Loss of either of these genes results in failure of eye formation. The activity of ey and toy includes the activation of the retinal determination genes sine oculis (so) and eyes absent (eya), which form a protein complex that regulates the transcription of downstream target genes.[9] Thereafter, the two visual systems of D. melanogaster are patterned differently. Anterior head patterning is controlled by orthodenticle (otd), a homeobox gene which demarcates the segments from the top-middle of the head to the more lateral aspects. The ocelli are in an otd-rich area and disruption of otd results in loss of the ocelli, but does not affect the compound eyes.[10] Inversely, the transcription factor dachshund (dac) is required for the patterning of compound eyes, but mutants lacking dac do not exhibit loss of the ocelli.[11] Different opsins are used in the ocelli of compound eyes.[12]

The visual systems of Chelicerata (the sister group to the remaining Arthropoda) are less well understood. It has been shown that homologs of many eye patterning genes are variably expressed in the eyes of different spider species, but the functional significance of these changes in expression is not well understood, due to lack of functional data.[13][14] In addition, it has been shown in horseshoe crabs and spiders that Pax6 homologs are not expressed in the same way as their counterparts in insects, suggesting that Pax6 may not be required as a top-level eye patterning switch in chelicerates.[15][16] Most of the functional data on eye patterning in Chelicerata is drawn from the daddy-longlegs Phalangium opilio, which has been used to show that eyes absent plays a conserved role in patterning both the visual systems of this species (an example of conservation of gene function, with respect to insects) and that dachshund affects the patterning of lateral eyes, but not median eyes (another example of conservation).[17]

Evolution

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Hexapods are currently thought to fall within the Crustacean crown group; while molecular work paved the way for this association, their eye morphology and development is also markedly similar.[18] The eyes are strikingly different from the myriapods, which were traditionally considered to be a sister group to the Hexapoda.

Both ocelli and compound eyes were probably present in the last common arthropod ancestor,[19] and may be apomorphic with ocelli in other phyla,[20] such as the annelids.[21] Median ocelli are present in chelicerates and mandibulates; lateral ocelli are also present in chelicerates.[20]

Origin

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No fossil organisms have been identified as similar to the last common ancestor of arthropods; hence the eyes possessed by the first arthropod remains a matter of conjecture. The largest clue into their appearance comes from the onychophorans: a stem group lineage that diverged soon before the first true arthropods. The eyes of these creatures are attached to the brain using nerves which enter into the centre of the brain, and there is only one area of the brain devoted to vision. This is similar to the wiring of the median ocelli (small simple eyes) possessed by many arthropods; the eyes also follow a similar pathway through the early development of organisms. This suggests that onychophoran eyes are derived from simple ocelli, and the absence of other eye structures implies that the ancestral arthropod lacked compound eyes, and only used median ocelli to sense light and dark.[2]

 
Fossilised eye of Anomalocaris daleyae from the Emu Bay Shale

A conflicting view notes, however, that compound eyes appeared in many early arthropods, including the trilobites and eurypterids. That suggests that the compound eye may have developed after the onychophoran and arthropod lineages split, but before the radiation of arthropods.[20] This view is supported if a stem-arthropod position is supported for compound-eye bearing Cambrian organisms such as the Radiodontids. Yet another alternative is that compound eyes independently evolved, multiple times within the arthropods.[21]

There were probably only a single pair of ocelli in the arthropod concestor, since Cambrian lobopod fossils display a single pair. And while many arthropods today have three, four, or even six, the lack of a common pathway suggests that a pair is the most probable ancestral state. The crustaceans and insects mainly have three ocelli, suggesting that such a formation was present in their concestor.[2]

It is deemed probable that the compound eye arose as a result of the 'duplication' of individual ocelli.[20] In turn, the dispersal of compound eyes seems to have created large networks of seemingly independent eyes in some arthropods, such as the larvae of certain insects.[20] In some other insects and myriapods, lateral ocelli appear to have arisen by the reduction of lateral compound eyes.[20]

Trilobite eyes

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Holochroal eye of Paralejurus sp.
 
Schizochroal eye of Phacops sp.

The eyes of trilobites came in three forms, called holochroal, schizochroal, and abathochroal eyes. The eye morphology of trilobites is useful for inferring their mode of life, and can function as indicators of the palaeo-environment conditions.[22]

The holochroal eye was the most common and most primitive. It consisted of many small lenses – between 100 and 15,000 – covered by a single corneal membrane. This was the most ancient kind of eye. This eye morphology was found in the Cambrian trilobites (the earliest) and survived until the Permian extinction.[22]

The more complex schizochroal eye was found only in one sub-order of trilobite, the Phacopina (Ordovician-Silurian). There is no exact counterpart to the schizochroal eye in modern animals, but a somewhat similar eye structure is found in adult male insects in the order Strepsiptera. Schizochroal eyes developed as an improvement on holochroal; they were more powerful, with overlapping visual fields, and were particularly useful for nocturnal vision and possibly for colour and depth perception. Schizochroal eyes have up to 700 large lenses (large compared to holochroal lenses). Each lens has a cornea, and each has an individual sclera that separates it from the surrounding lenses. The multiple lenses for the eye were each constructed from a single calcite crystal. Early schizochroal eye designs appear haphazard and irregular – possibly constrained by the geometrical complications of packing identical sized lenses on a curved surface. Later schizochroal eyes had size graduated lens.[22]

The abathochroal eye is the third eye morphology of trilobites, but it has found only within the Eodiscina. This form of eye consisted of up to 70 much smaller lenses. The cornea separated each lens, and the sclera on each lens terminated on top of each cornea.[22]

Horseshoe crab

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Horseshoe crabs have two primary compound eyes and seven secondary simple eyes. Two of the secondary eyes are on the underside.[23]

The horseshoe crab has traditionally been used in investigations into the eye, because it has relatively large ommatidia with large nerve fibres (making them easy to experiment on). It also falls nears the base of the chelicerates; its eyes are believed to represent the ancestral condition because they have changed so little over evolutionary time. Most other living chelicerates have lost their lateral compound eyes, evolving simple eyes in their place that vary in number.[24] Up to five pairs of lateral eyes occur in scorpions, whereas three pairs of lateral eyes are typical for Tetrapulmonata (e.g., spiders; Amblypygi).[25]

Horseshoe crabs have two large compound eyes on the sides of its head. An additional simple eye is positioned at the rear of each of these structures.[24] In addition to these obvious structures, it also has two smaller ocelli situated in the middle-front of its carapace, which may superficially be mistaken for nostrils.[24] A further simple eye is located beneath these, on the underside of the carapace; this eye is initially paired during embryonic stages and fuses later in development.[24][15] A further pair of simple eyes are positioned just in front of the mouth.[24] The simple eyes are probably important during the embryonic or larval stages of the organism, with the compound eyes and median ocelli becoming the dominant sight organs during adulthood.[24] These ocelli are less complex, and probably less derived, than those of the Mandibulata.[20] Unlike the compound eyes of trilobites, those of horseshoe crabs are triangular in shape; they also have a generative region at their base, but this elongates with time. Hence the one ommatidium at the apex of the triangle was the original "eye" of the larval organism, with subsequent rows added as the organism grew.[18]

Insects and crustaceans

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Eye of Triatoma infestans

It is generally thought that insects are a clade within the Crustacea, and that the Crustacea are monophyletic. This is consistent with the observation that their eyes develop in a very similar fashion. While most crustacean and some insect larvae possess only simple median eyes, such as the Bolwig organs of Drosophila and the naupliar eye of most crustaceans, several groups have larvae with simple or compound lateral eyes. The compound eyes of adults develop in a region of the head separate from the region in which the larval median eye develops.[18] New ommatidia are added in semicircular rows at the rear of the eye; during the first phase of growth, this leads to individual ommatidia being square, but later in development they become hexagonal. The hexagonal pattern will become visible only when the carapace of the stage with square eyes is molted.[18]

Although stalked eyes on peduncles occur in some species of crustaceans and some insects, only some of the Crustacea, such as crabs, bear their eyes on articulated peduncles that permit the eyes to be folded out of the way of trouble.

Myriapods

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Eye of Lithobius forficatus

Most myriapods bear stemmata – single lensed eyes which are thought to have evolved by the reduction of a compound eye.[20] However, members of the chilopod genus Scutigera have a compound eye, which is composed of facets [26] and not, as earlier interpretations had it, of clustered stemmata.[21] that were thought to grow in rows, inserted between existing rows of ocelli.[18]

See also

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Footnotes

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  1. ^ Ocelli are about 5000 times more sensitive than apposition compound eyes. They can, for instance, respond to the position of the full moon.

References

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  1. ^ a b Land, Michael F.; Fernald, Russell D. (1992), "The Evolution of Eyes", Annual Review of Neuroscience, 15 (1): 1–29, doi:10.1146/annurev.ne.15.030192.000245, PMID 1575438.
  2. ^ a b c Mayer, G. (2006). "Structure and development of onychophoran eyes: What is the ancestral visual organ in arthropods?". Arthropod Structure & Development. 35 (4): 231–245. Bibcode:2006ArtSD..35..231M. doi:10.1016/j.asd.2006.06.003. PMID 18089073.
  3. ^ a b c Taylor, Charles P. (1981). "Contribution of compound eyes and ocelli to steering of locusts in flight. I. Behavioural analysis". J. Exp. Biol. 93: 1–18. doi:10.1242/jeb.93.1.1.[full citation needed]
  4. ^ Meyer-Rochow, V.B. (1974). "Structure and function of the larval eye of the sawfly larva Perga". Journal of Insect Physiology. 20 (8): 1565–1591. doi:10.1016/0022-1910(74)90087-0. PMID 4854430.
  5. ^ Wilson, M. (1978). "The functional organisation of locust ocelli". Journal of Comparative Physiology. 124 (4): 297–316. doi:10.1007/bf00661380. S2CID 572458.
  6. ^ Seidl, R.; Kaiser, W. (1981). "Visual field size, binocular domain and the ommatidial array of the compound eyes in worker honey bees". J. Comp. Physiol. 143: 17–26. doi:10.1007/bf00606065. S2CID 41150125.
  7. ^ Beersma, D.G.; et al. (1977). "Retinal lattice, visual field and binocularities in flies". J. Comp. Physiol. 119 (3): 207–220. doi:10.1007/bf00656634. S2CID 6384399.
  8. ^ Hunt, E.R.; et al. (2018). "Asymmetric ommatidia count and behavioural lateralization in the ant Temnothorax albipennis". Scientific Reports. 8 (5825): 5825. Bibcode:2018NatSR...8.5825H. doi:10.1038/s41598-018-23652-4. PMC 5895843. PMID 29643429.
  9. ^ Carthew, Richard W (August 2007). "Pattern formation in the Drosophila eye". Current Opinion in Genetics & Development. 17 (4): 309–313. doi:10.1016/j.gde.2007.05.001. PMC 2693403. PMID 17618111.
  10. ^ Royet, J; Finkelstein, R (1995), "Pattern formation in Drosophila head development: the role of the orthodenticle homeobox gene" (PDF), Development, 121 (11): 3561–3572, doi:10.1242/dev.121.11.3561, PMID 8582270
  11. ^ Mardon, G.; Solomon, N.M., N. M.; Rubin, G. M., G. M. (Dec 1994). "dachshund encodes a nuclear protein required for normal eye and leg development in Drosophila". Development. 120 (12): 3473–3486. doi:10.1242/dev.120.12.3473. ISSN 0950-1991. PMID 7821215.
  12. ^ S. Wehrhahn, William A. Zuker; Harris, WA; Kirschfeld, K; Wehrhahn, C; Zuker, CS (1988), "Targeted misexpression of a Drosophila opsin gene leads to altered visual function", Nature, 333 (6175): 737–41, Bibcode:1988Natur.333..737F, doi:10.1038/333737a0, PMID 2455230, S2CID 4248264
  13. ^ Schomburg, Christoph; Turetzek, Natascha; Schacht, Magdalena Ines; Schneider, Julia; Kirfel, Phillipp; Prpic, Nikola-Michael; Posnien, Nico (December 2015). "Molecular characterization and embryonic origin of the eyes in the common house spider Parasteatoda tepidariorum". EvoDevo. 6 (1): 15. doi:10.1186/s13227-015-0011-9. ISSN 2041-9139. PMC 4450840. PMID 26034574.
  14. ^ Samadi, Leyli; Schmid, Axel; Eriksson, Bo Joakim (December 2015). "Differential expression of retinal determination genes in the principal and secondary eyes of Cupiennius salei Keyserling (1877)". EvoDevo. 6 (1): 16. doi:10.1186/s13227-015-0010-x. ISSN 2041-9139. PMC 4450993. PMID 26034575.
  15. ^ a b Blackburn, David C.; Conley, Kevin W.; Plachetzki, David C.; Kempler, Karen; Battelle, Barbara-Anne; Brown, Nadean L. (August 2008). "Isolation and expression of Pax6 and atonal homologues in the American horseshoe crab, Limulus polyphemus". Developmental Dynamics. 237 (8): 2209–2219. doi:10.1002/dvdy.21634. ISSN 1058-8388. PMC 2577597. PMID 18651657.
  16. ^ Friedrich, Markus (December 2022). "Coming into clear sight at last: Ancestral and derived events during chelicerate visual system development". BioEssays. 44 (12): e2200163. doi:10.1002/bies.202200163. ISSN 0265-9247. PMID 36317531. S2CID 253246397.
  17. ^ Gainett, Guilherme; Klementz, Benjamin C.; Blaszczyk, Pola; Setton, Emily V.W.; Murayama, Gabriel P.; Willemart, Rodrigo; Gavish-Regev, Efrat; Sharma, Prashant P. (February 2024). "Vestigial organs alter fossil placements in an ancient group of terrestrial chelicerates". Current Biology. 34 (6): 1258–1270.e5. doi:10.1016/j.cub.2024.02.011. PMID 38401545. S2CID 267821504.
  18. ^ a b c d e Harzsch, S.; Hafner, G. (2006), "Evolution of eye development in arthropods: Phylogenetic aspects", Arthropod Structure & Development, 35 (4): 319–340, Bibcode:2006ArtSD..35..319H, doi:10.1016/j.asd.2006.08.009, hdl:11858/00-001M-0000-0012-A87C-4, PMID 18089079
  19. ^ Friedrich, M (2006), "Ancient mechanisms of visual sense organ development based on comparison of the gene networks controlling larval eye, ocellus, and compound eye specification in Drosophila" (PDF), Arthropod Structure & Development, 35 (4): 357–378, Bibcode:2006ArtSD..35..357F, doi:10.1016/j.asd.2006.08.010, PMID 18089081
  20. ^ a b c d e f g h Bitsch, C.; Bitsch, J. (2005), "Evolution of eye structure and arthropod phylogeny", Crustacean Issues, 16: 185–214, doi:10.1201/9781420037548, ISBN 978-0-8493-3498-6
  21. ^ a b c Paulus, H.F. (2000), "Phylogeny of the Myriapoda-Crustacea-Insecta: a new attempt using photoreceptor structure*", Journal of Zoological Systematics & Evolutionary Research, 38 (3): 189–208, doi:10.1046/j.1439-0469.2000.383152.x
  22. ^ a b c d Clarkson, Euan (2009). Invertebrate Palaeontology and Evolution (4th ed.). John Wiley & Sons. ISBN 9781444313321 – via Google Books.
  23. ^ Barlow, R.B. (2009). "Vision in horseshoe crabs". In Tanacredi, J.T.; Botton, M.L.; Smith, D. (eds.). Biology and Conservation of Horseshoe Crabs. Springer. pp. 223–235. ISBN 9780387899589 – via Google Books.
  24. ^ a b c d e f Battelle, B.A. (December 2006), "The eyes of Limulus polyphemus (Xiphosura, Chelicerata) and their afferent and efferent projections.", Arthropod Structure & Development, 35 (4): 261–74, Bibcode:2006ArtSD..35..261B, doi:10.1016/j.asd.2006.07.002, PMID 18089075.
  25. ^ Miether, Sebastian T.; Dunlop, Jason A. (July 2016). "Lateral eye evolution in the arachnids". Arachnology. 17 (2): 103–119. doi:10.13156/arac.2006.17.2.103. ISSN 2050-9928. S2CID 89428386.
  26. ^ Müller, C.H.G.; Rosenberg, J.; Richter, S.; Meyer-Rochow, V.B. (2003). "The compound eye of Scutigera coleoptrata (Linnaeus, 1758) (Chilopoda; Notostigmophora): An ultrastructural re-investigation that adds support to the Mandibulata concept". Zoomorphology. 122 (4): 191–209. doi:10.1007/s00435-003-0085-0. S2CID 6466405.
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