Skip to main content
Log in

Optical parameters of the eyes of some benthic decapods as a function of habitat depth (Crustacea, Decapoda)

  • Published:
Zoomorphology Aims and scope Submit manuscript

Summary

Eye diameter relative to body length, and interommatidial angle, rhabdom length and rhabdom width as a function of eye size, were determined for specimens of 19 benthic macruran decapod species in 8 genera and 5 families, spanning a wide range of habitat depths. For these species, eye diameter relative to body length tends to increase with adult habitat. In addition, rate of eye growth relative to body growth increases with habitat depth, a trend opposite to that of pelagic crustaceans previously investigated. Interommatidial angle decreases with increasing eye diameter, and therefore with depth for an individual of a particular size. Rhabdom length and width tend to increase with eye diameter. Visual sensitivity may increase with depth among these species as a result of both larger eyes and the associated increase in rhabdom dimensions. Differences in energetic limitations and visual environments might produce the difference in trends of eye size relative to body size between benthic and pelagic crustaceans.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ball EE (1977) Fine structure of the compound eyes of the mid-water amphipod Phronima in relation to behavior and habitat. Tissue & Cell 9:521–536

    Google Scholar 

  • Barak M, Ulitzur S (1980) Bacteral bioluminescence as an early indication of marine fish spoilage. Eur J Appl Microbiol Biotechnol 10:155–165

    Google Scholar 

  • Beddard FE (1886) Report on the isopoda collected by the HMS Challenger during the years 1872–1876. Challenger Report, vol. 17

  • Beddard FE (1890) On the minute structure of the eye in some shallow-water and deep-sea species of the isopod genus Acturus. Proc Zool Soc London 26:365–375

    Google Scholar 

  • Bursey CR (1975) The microanatomy of the compound eye of Munida irrasa (Decapoda: Galatheida). Cell Tissue Res 160:505–514

    Google Scholar 

  • Childress JJ (1971) Respiratory rate and depth of occurrence of midwater animals. Limnol Oceanogr 16:104–106

    Google Scholar 

  • Childress JJ (1975) The respiratory rates of midwater crustaceans as a function of depth of occurrence and relation to the oxygen minimum layer off Southern California. Comp Biochem Physiol 50A:787–799

    Google Scholar 

  • Chun C (1896) Atlantis Biologische Studien über pelagische Organismen. Zoologica Stuttgart 7:1–260

    Google Scholar 

  • Cooper RA, Uzmann JR (1980) Ecology of juvenile and adult Homarus. In: Cobb JS, Phillips BF (eds) The biology and management of lobsters, vol. II. Academic Press, New York, pp 143–178

    Google Scholar 

  • Denton EJ, Gilpin-Brown JB, Wright PG (1972) The angular distribution of the light produced by some mesopelagic fish in relation to their camouflage. Proc R Soc London B182:145–158

    Google Scholar 

  • Dobkin S (1965) The early larval stages of Glyphocrangon spinicauda A. Milne Edwards. Bull Mar Sci 15:872–884

    Google Scholar 

  • Hanstrom B (1983) Neue Untersuchungen über Sinnesorgane und Nervensystem der Crustaceen. II. Zool Jahrb Abt Anat Ontog Tiere 56:387–520

    Google Scholar 

  • Hiller-Adams P, Case JF (1984) Optical parameters of euphausiid eyes as a function of habitat depth. J Comp Physiol 154:307–318

    Google Scholar 

  • Karl DM, LaRock PA, Morse JW, Sturges W (1976) Adenosine triphosphate in the North Atlantic Ocean and its relationship to the oxygen minimum. Deep-Sea Res 23:81–88

    Google Scholar 

  • Kampa EM (1965) The euphausiid eye — a re-evaluation. Vision Res 5:475–481

    Google Scholar 

  • Kirschfeld K (1974) The absolute sensitivity of lens and compound eyes. Zt Naturforsch 29C:592–596

    Google Scholar 

  • Land MF (1979) Optics and vision in invertebrates. In: Autrum H (ed) Handbook of sensory physiology, vol VII/6B. Springer, Berlin-Heidelberg-New York, pp 471–592

    Google Scholar 

  • Land MF (1981) Optics of the eyes of Phronima and other deep-sea amphipods. J Comp Physiol 145:209–226

    Google Scholar 

  • Land MF, Burton FA, Meyer-Rochow VB (1979) The optical geometry of euphausiid eyes. J Comp Physiol 130:49–62

    Google Scholar 

  • Latz MI, Case JF (1982) Light organ and eyestalk compensation to body tilt in the luminescent midwater shrimp, Sergestes similis. J Exp Biol 98:83–104

    Google Scholar 

  • Locket NA (1977) Adaptations to the deep-sea environment. In: Crescitelli F (ed) Handbook of sensory physiology, vol VII/5. Springer, Berlin — Heidelberg — New York, pp 67–192

    Google Scholar 

  • Loew ER (1976) Light, and photoreceptor degeneration in the Norway lobster, Nephrops norvegicus (L). Proc R Soc London B193:31–44

    Google Scholar 

  • Meyer-Rochow VB, Walsh S (1977) The eyes of mesopelagic crustaceans: I. Gennadus sp. (Penaeidae). Cell Tissue Res 184:87–101

    Google Scholar 

  • Mickel TJ, Childress JJ (1982) Effects of temperature, pressure, and oxygen concentration on the oxygen consumption rate of the hydrothermal vent crab Bythograea thermydron (Brachyura). Physiol Zool 55:199–207

    Google Scholar 

  • Murray J, Hjort J (1912) The depths of the ocean. MacMillan and Co., London, pp 821

    Google Scholar 

  • Schmitt WL (1921) The marine decapod crustacea of California. University of California Publications in Zoology, vol 23

  • Smith SI (1886) The abyssal decapod crustacea of the ‘Albatross’ dredgings in the North Atlantic. Ann Mag Nat Hist, Ser 5, 17:187–198

    Google Scholar 

  • Warner JA, Latz MI, Case JF (1979) Cryptic bioluminescence in a midwater shrimp. Science 203:1109–1110

    Google Scholar 

  • Welsh JH, Chace FA (1937) Eyes of deep-sea crustaceans. I. Acanthephyridae. Biol Bull 72:57–74

    Google Scholar 

  • Welsh JH, Chace FA (1938) Eyes of deep-sea crustaceans. II. Sergestidae. Biol Bull 74:364–375

    Google Scholar 

  • Wenner EL (1978) Comparative biology of four species of glyphocrangonid and crangonid shrimp from the continental slope of the middle Atlantic Bight. Can J Zool 56:1052–1065

    Google Scholar 

  • Widder EA, Latz MI, Case JF (1983) Marine bioluminescence spectra measured with an optical multichannel detection system. Biol Bull 165:791–810

    Google Scholar 

  • Zharkova IS (1970) Reduction of the organs of vision in deep-sea mysids. Zool Zh 49:685–693

    Google Scholar 

  • Zharkova IS (1973) Histological structure of the eye in three representatives of Munidopsis (Crustacea, Decapoda). Zool Zh 52:1643–1647

    Google Scholar 

  • Zharkova IS (1975) Reduction of organs of sight in deep-water Isopoda, Amphipoda and Decapoda. Zool Zh 54:200–208

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hiller-Adams, P., Case, J.F. Optical parameters of the eyes of some benthic decapods as a function of habitat depth (Crustacea, Decapoda). Zoomorphology 105, 108–113 (1985). https://doi.org/10.1007/BF00312145

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00312145

Keywords

Navigation